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See our publications catalogue at:http://europa.eu.int/comm/environment/pubs/home.htm
European Commission
RADIATION PROTECTION 118
Referral guidelinesfor imaging
ISBN 92-828-9454-1
OFFICE FOR OFFICIAL PUBLICATIONSOF THE EUROPEAN COMMUNITIES
L-2985 Luxembourg
Price (excluding VAT) in Luxembourg: EUR 16
9 789282 894545
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Abstract
The newly revised medical exposuredirective (97/43/Euratom) lays down thegeneral principles of radiation protectionof individuals in relation to medicalexposure. Member States had totranspose it into national legislationuntil 13 May 2000. Article 6(2) of thedirective requires Member States toensure that recommendat ionsconcerning referral criteria for medicalexposure are available to the prescribersof medical exposure.
This booklet sets out referral guidelinesthat can be used by health professionalsqualified to refer patients for imaging,in order to ensure that all examinationsare well justified and optimised.
This booklet has evolved from thatpreviously published by the UK RoyalCollege of Radiologists in 1998 and isentitled: Making the best use of adepartment of clinical radiology:guidelines for doctors. These referralguidelines have been adapted by expertsrepresenting European radiology andnuclear medicine, in conjunction withthe UK Royal College of Radiologists,and may now be adopted as modelsfor the Member States.
These referral guidelines are not bindingon Member States, and form part of anumber of technical guides drawn upto facilitate implementation of themedical exposure directive. Localvariations may be required accordingto healthcare practice and provision.
Continued use of recommendations ofthis kind should improve clinical practiceand lead to a reduction in the numberof referrals for investigation andconsequently to a reduction inassociated medical radiation exposure.
Radiation Protection 118
Referral guidelines for imaging
Adapted by experts representingEuropean radiology and nuclear
medicine
In conjunction with the UK Royal College of Radiologists
Co-ordinated bythe European Commission
European CommissionDirectorate-General for the Environment
2000
A great deal of additional information on theEuropean Union is available on the Internet.
It can be accessed through the Europa server(http://europa.eu.int).
Cataloguing data can be found at the end of thispublication.
Luxembourg: Office for Official Publications ofthe European Communities, 2001
ISBN 92-828-9454-1
© European Communities, 2001
Reproduction is authorised provided the source isacknowledged.
Printed in Italy
PRINTED ON WHITE CHLORINE-FREE PAPER
Any views expressed in this document do notnecessarily reflect the views of the EuropeanCommission. Neither the European Commissionnor any person acting on behalf of theCommission is responsible for the use whichmight be made of the following information.
Preface
These referral guidelines for imaging have evolvedfrom the booklet ‘Making the best use of adepartment of clinical radiology: guidelines fordoctors’, which was published by the UK RoyalCollege of Radiologists in 1998 (1). They have beenadapted by various expert groups from severalcountries and comments have also been gathered fromradiological societies and nuclear medicine societiesof Member States through the European Associationfor Radiology and Nuclear Medicine. The EuropeanCommission co-ordinated this process. The referralguidelines may now be adopted as models for theMember States, even though it is recognised thatfurther local adaptation may be needed according tovarying health care practice and provision. The nextedition of the guidelines will be prepared by theRoyal College of Radiologists (Chairman of theworking party: Professor Gillian Needham,Aberdeen), in conjunction with the EuropeanCommission and the various expert bodies within theEuropean Community. They will be even moreevidence-based and take into account European aswell as UK practice.
The EU Council Directive 1997/43/Euratom (2)declared that Member States shall promote theestablishment and use of diagnostic reference levels forradiological examinations and guidance thereof. Thesereferral guidelines can be used for the above purposes.
This publication would not have been possiblewithout the work of a sub-committee which met threetimes in 1999:
Professor Dr W Becker, Nuclear Medicine, Göttingen, DE
Professor Angelika Bischof Delaloye, President,European Association of Nuclear Medicine,Lausanne, CH
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Dr Vittorio Ciani, European Commission, Directorate-General for Environment, Brussels, B
Professor Adrian K Dixon, Royal College ofRadiologists, Cambridge, UK
Mr Steve Ebdon-Jackson, Department of Health,London, UK
Dr Keith Harding, Nuclear Medicine, Birmingham,UK
Dr Elisabeth Marshall-Depommier, Paris, F
Professor Iain McCall, President, UEMS RadiologySection, Oswestry, UK
Professor Gillian Needham, Royal College ofRadiologists, Aberdeen, UK
Professor Hans Ringertz, European Association ofRadiology, Stockholm, S
Dr Bruno Silberman, Hon. General Secretary, UEMS,Paris, F
Dr Diederik Teunen, European Commission,Directorate-General for Environment, Brussels, B
Dr Ciska Zuur, Ministry of Housing, Spatial Planningand the Environment, The Hague, NL
We owe them all a lot of thanks.
P Armstrong Prof Hans Ringertz,President President (1999), Royal College European Associationof Radiologists of Radiology,London, UK Stockholm, SE
Prof. Angelika Bischof Delaloye,President (1999),European Associationof Nuclear MedicineLausanne, CH
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ContentsForeword to the fourth edition (1998) of theRoyal College of Radiologists (RCR)guidelines (1)..................................................... 7
Introduction ....................................................... 11
Why are guidelines and referral criterianeeded?........................................................ 11
What advice is available? ........................... 12
What images are taken?.............................. 14
For whom are the guidelines designed? ..... 14
Using the guidelines.................................... 14
Pregnancy and protection of the foetus ............ 16
Optimising radiation dose ................................. 18
Typical effective doses from diagnosticmedical exposures in the 1990s.................. 19
Communications with a department of clinicalradiology............................................................ 22
Technique-based imaging.................................. 23
Computed tomography (CT)....................... 23
Interventional radiology (includingangiography and minimal access therapy) ... 24
Magnetic resonance imaging (MRI)........... 25
Nuclear medicine (NM) .................................... 27
Nuclear medicine therapy ........................... 28
Ultrasound (US) ................................................ 29
Glossary............................................................. 31
5
Clinical problems, investigations,recommendations and comments ...................... 32
A. Head (including ENT problems)........... 32
B. Neck....................................................... 37
C. The spine ............................................... 40
D. Musculoskeletal system......................... 45
E. Cardiovascular system........................... 53
F. Thoracic system..................................... 57
G. Gastrointestinal system ......................... 60
H. Urological, adrenal and genito-urinarysystems .................................................. 73
I. Obstetrics and gynaecology .................. 77
J. Breast disease ........................................ 80
K. Trauma................................................... 84
L. Cancer.................................................... 99
M. Paediatrics.............................................. 110
Selected bibliography........................................ 121
Appendix ........................................................... 124
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7
Foreword to the fourthedition (1998) of the RoyalCollege of Radiologists(RCR) guidelines (1)
This booklet has been prepared to help referringclinicians make the best use of a department ofclinical radiology. Continued use of recommendationsof this kind leads to a reduction in the number ofreferrals for investigation and also to a reduction inmedical radiation exposure (3–7). Nevertheless theprimary objective of this booklet is to improveclinical practice. Such recommendations work best ifthey are used in conjunction with clinico-radiologicaldialogue and as part of the audit process. They areintended to be used by both hospital doctors (allgrades) and primary care physicians. The editor(Adrian Dixon, Cambridge) has been assisted by theother members of the working party: Dr JohnBradshaw (Bristol), Dr Michael Brindle (President ofthe Royal College of Radiologists, King’s Lynn), thelate Dr Claire Dicks-Mireaux (London), Dr RayGodwin (Bury St Edmunds), Dr Adrian Manhire(Chairman of the RCR audit sub-committee,Nottingham), Dr Gillian Needham (Aberdeen), DrDonald Shaw (London), Mr Chris Squire (RCRclinical audit advisor), Dr Iain Watt (Bristol) andProfessor J Weir (Dean of the Faculty of Radiology,Aberdeen). Mr Barry Wall from the NationalRadiological Protection Board (NRPB) has againkindly provided data regarding radiation doses for avariety of investigations.
Since the third edition there has been yet furtheradvance within magnetic resonance imaging (MRI),and this is reflected in the recommendations. Thisedition also includes recommendations for some ofthe new niche roles for ultrasound (US), computed
8
tomography (CT) and nuclear medicine (NM),including positron emission tomography (PET). Thesystem based approach introduced in 1995 has beenretained; most feedback has suggested that this formatwas more useful than the previous arrangement.
Once again we have indicated whether the statementsincluded within the booklet are based on rigorousscientific evidence. In line with UK National HealthService Executive policy on the development ofclinical guidelines (8), we have adopted the followingclassification:
(A) randomised controlled trials (RCTs), meta-analyses, systematic reviews; or
(B) robust experimental or observational studies; or
(C) other evidence where the advice relies on expertopinion and has the endorsement of respectedauthorities.
Interestingly, such grading systems have now becomequite commonplace in many aspects of health care,now that ‘evidence-based medicine’ has becomeaccepted practice (9–10). Review of the evidence hasbeen very time consuming. The working party is verygrateful to Dr Rachael Harrison who did much of theinitial data trawl as part of the REALM projectfunded by the Royal College of Radiologists (RCR).Subsequent literature searches have been performedby individual members of the working party and byvarious members of specialist imaging groups whohave provided very useful data.
Around 85 000 copies of the third edition (1995) ofthe booklet have been distributed and the contentshave, at various times, been commended by theNational Health Service Executive (NHSE) (8,11), theUK chief medical officers and the Audit Commission(12). It is of note that they have been adopted byseveral purchasers, many of whom now link the use
of the RCR’s recommendations to contracts withdepartments of clinical radiology. They have beenadopted in the private sector and adopted andtranslated by the radiological societies of othercountries. The recommendations are also extensivelyused as a standard for audit studies (13). A number offorward-looking hospitals have obtained electronicversions of these recommendations which can beincorporated into hospital information systems. Thisfourth edition has already been endorsed by theAcademy of Medical Royal Colleges and beenapproved by the Guidelines Appraisal Unit at StGeorge’s Hospital, London, in the United Kingdom.
With such serious implications now attached to theserecommendations, the working party has been fullyaware of the importance of getting it ‘as right asreasonably achievable’. We believe that this fourthedition, which has been produced following wideconsultation (see Appendix), represents a currentreasonable view of how departments of clinicalradiology should be used for some of the morecommon clinical problems. There will, undoubtedly,be some unpopular decisions; we have occasionallyreceived diametrically opposite advice. However, thisis probably inevitable in one of the most rapidlydeveloping specialties within medicine.
We hope that this fourth edition will prove useful andtrust that we will continue to receive advice andreferenced comments so that the development ofthese recommendations can continue. The nextedition of the RCR guidelines is planned for 2002.
Adrian K Dixon on behalf of the RCR guidelinesworking party
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Introduction
Why are guidelines and referral criterianeeded?A useful investigation is one in which the result —positive or negative — will alter management or addconfidence to the clinician’s diagnosis. A significantnumber of radiological investigations do not fulfilthese aims and may add unnecessarily to patientirradiation (14). The chief causes of the wasteful useof radiology are:
(1) Repeating investigations which have alreadybeen done: e.g. at another hospital, in anoutpatient department, or in the accident andemergency department.HAS IT BEEN DONE ALREADY? Everyattempt should be made to get previous films.Transfer of digital data through electronic linksmay assist in this respect in future years.
(2) Investigation when results are unlikely toaffect patient management: because theanticipated ‘positive’ finding is usuallyirrelevant, e.g. degenerative spinal disease (as‘normal’ as grey hairs from early middle age) orbecause a positive finding is so unlikely.DO I NEED IT?
(3) Investigating too often: i.e. before the diseasecould have progressed or resolved or before theresults could influence treatment. DO I NEED ITNOW?
(4) Doing the wrong investigation. Imagingtechniques are developing rapidly. It is oftenhelpful to discuss an investigation with aspecialist in clinical radiology or nuclearmedicine before it is requested. IS THIS THEBEST INVESTIGATION?
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(5) Failing to provide appropriate clinicalinformation and questions that the imaginginvestigation should answer. Deficiencies heremay lead to the wrong technique being used (e.g.the omission of an essential view). HAVE IEXPLAINED THE PROBLEM?
(6) Over-investigating. Some clinicians tend to relyon investigations more than others. Somepatients take comfort in being investigated.ARE TOO MANY INVESTIGATIONS BEINGPERFORMED?
What advice is available?In some clinical situations firm guidelines have beenestablished. Guidelines are:
systematically developed statements to assistpractitioner and patient decisions aboutappropriate health care for specific clinicalcircumstances... (Field & Lohr 1992, 15).
Just as the term implies, a guideline is not a rigidconstraint on clinical practice, but a concept of goodpractice against which the needs of the individualpatient can be considered. So while there have to begood reasons for ignoring them they are not absoluterules. No set of recommendations will commanduniversal support and you should discuss anyproblems with your radiologists.
The preparation of guidelines has become something ofa science, with numerous papers emerging within theevolving guidelines discipline. In particular, expertshave provided detailed methodology as to howguidelines should be developed, produced andappraised (8, 15–21). Using such methodology, thedevelopment of a single scientifically robust guidelinerepresents a major piece of academic endeavour. Forthe 280 clinical problems in this booklet, suchexpenditure of time and resources is somewhatimpractical. Nevertheless much of the philosophy of themethodology for the preparation of guidelines has been
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followed during the preparation of theserecommendations. In particular there has been extensiveliterature review with key references analysed. TheRoyal College of Radiologists holds an archive ofreferences upon which statements within the text arebased. Every opportunity has been given to workers inother disciplines and those representing patients to putforward their views. Many groups have beenencouraged to comment on points of fact, local policies,etc. In particular appropriate specialty imaging groupshave provided active support. There has been extensivedialogue with other professional groups, includingpatients’ representatives and all the royal colleges,culminating in endorsement by the Academy ofMedical Royal Colleges (see Appendix). Indeed one ofthe strongest features of these recommendations is thatthey have been reviewed and modified during thedevelopment of four editions since 1989.
Another concurrent development has been theproduction of ‘appropriateness criteria’ by theAmerican College of Radiologists (22). Rather thanpronouncing on what is perceived to be the optimalinvestigation, the ACR lists all possible investigationsand awards an appropriateness score (out of 10).These have been developed using a modified Delphitechnique with consensus reached amongst experts.The RCR has kept a watching brief on this interestingdevelopment and has incorporated some of the ACRconclusions.
Throughout the booklet the strength of the evidence(8) for the various statements is indicated by:
(A) randomised controlled trials (RCTs), meta-analyses, systematic reviews; or
(B) robust experimental or observational studies; or
(C) other evidence where the advice relies on expertopinion and has the endorsement of respectedauthorities.
14
In some clinical situations (e.g. the role of US innormal pregnancy) there are conflicting data within alarge body of excellent scientific reports. Thus nofirm recommendations are given and the evidence isclassified as C. It should also be noted that there arevery few randomised trials comparing differentradiological diagnostic procedures – they are difficultto perform and ethical approval may be denied.
What images are taken?All imaging departments should have protocols foreach common clinical situation. Therefore no definiterecommendations are given about this aspect. Sufficeit to say that all examinations should be optimised toobtain maximum information with the minimum ofradiation. It is important to be aware of this as thepatient may not get what the referring clinicianexpects.
For whom are the guidelines designed?These guidelines are intended to be used by all healthprofessionals entitled to refer patients for imaging. Inthe hospital setting they are likely to be of most useto newly qualified doctors and many hospitals give acopy to each newly appointed junior doctor tostimulate good practice.
The range of investigations available to differenthealth professionals must be determined inconsultation with local specialists in radiology andnuclear medicine, bearing in mind the availableresources. The recommendations are also of value tothose interested in audit of a department’s referralpattern and workload (13).
Using the guidelinesThis booklet tends to highlight areas of difficulty orcontroversy. The pages are mostly composed of fourcolumns: the first sets the clinical situation forrequesting an examination; the next lists somepossible imaging techniques (and the band of
15
radiation exposure involved); the third gives therecommendation (and the grade of availableevidence) on whether or not the investigation isappropriate; and the fourth provides explanatorycomments.
The recommendations used are:
(1) Indicated. This shows the investigation(s) mostlikely to contribute to clinical diagnosis andmanagement. This may differ from theinvestigation requested by the clinician: e.g. USrather than venography for deep vein thrombosis.
(2) Specialised investigation. These are complex orexpensive investigations which will usually beperformed only for doctors who have therelevant clinical expertise to evaluate the clinicalfindings and act on the imaging results. Theyusually justify individual discussion with aspecialist in radiology or nuclear medicine.
(3) Not indicated initially. This includes situationswhere experience shows that the clinical problemusually resolves with time; we therefore suggestdeferring the study for three to six weeks andonly performing it then if symptoms continue.Shoulder pain is a typical example.
(4) Not indicated routinely. This emphasises thatwhile no recommendation is absolute, the requestwill only be carried out if a clinician givescogent arguments for it. An example of such ajustification would be plain radiography in apatient with backache in whom there wereclinical findings to suggest something more thana degenerative disease (e.g.? Osteoporoticvertebral fracture).
(5) Not indicated. Examinations in this group arethose where the supposed rationale for theinvestigation is untenable (e.g. intravenousurogram (IVU) for hypertension).
Pregnancy and protectionof the foetus
• Irradiation of a foetus should be avoidedwhenever possible (23–25). This includessituations where pregnancy is not suspected bythe woman herself. The prime responsibility foridentifying such patients lies with the referringclinician.
• Women of reproductive age presenting for anexamination in which the primary beamirradiates directly, or by scatter, the pelvic area(essentially any ionising irradiation between thediaphragm and the knees), or for a procedureinvolving radioactive isotopes, should be askedwhether they are or may be pregnant. If thepatient cannot exclude the possibility ofpregnancy, she should be asked if her period isoverdue.
• If there is no possibility of pregnancy theexamination can proceed, but if the patient isdefinitely, or probably, pregnant (i.e. menstrualperiod overdue) the justification for the proposedexamination should be reviewed by theradiologist and the referring clinician, with adecision taken on whether to defer theinvestigation until after delivery or until the nextmenstrual period has occurred. However, aprocedure of clinical benefit to the mother mayalso be of indirect benefit to her unborn childand a delay in an essential procedure until laterin pregnancy may increase the risk to the foetusas well as to the mother.
• If pregnancy cannot be excluded, but themenstrual period is NOT overdue and theprocedure gives a relatively low dose to theuterus the examination may proceed. However, if
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the examination gives relatively high doses (inmost departments, the common examinations inthis category will probably be abdominal andpelvic CT, IVUs, fluoroscopy and NM studies),there will be discussion in line with locallyagreed recommendations.
• In all cases, if the radiologist and referringclinician agree that irradiation of the pregnant orpossibly pregnant uterus is clinically justified,this decision should be recorded. The radiologistmust then ensure that exposure is limited to theminimum required to acquire the necessaryinformation.
• If it becomes obvious that a foetus has beeninadvertently exposed, despite the abovemeasures, the small risk to the foetus of theexposure is unlikely to justify, even at the higherdoses, the greater risks of invasive fetaldiagnostic procedures (e.g. amniocentesis) orthose of a termination of the pregnancy. Whensuch inadvertent exposure has occurred, anindividual risk assessment should be made by aradiation physicist and the results discussed withthe patient.
• The RCR has recently co-authored (with theNRPB and the College of Radiographers) aguidance booklet on the protection of the foetusduring the diagnostic investigation of its mother(25).
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Optimising radiation dose
The use of radiological investigations is an acceptedpart of medical practice, justified in terms of clearclinical benefits to the patient which should faroutweigh the small radiation risks. However, evensmall radiation doses are not entirely without risk. Asmall fraction of the genetic mutations and malignantdiseases occurring in the population can be attributedto natural background radiation. Diagnostic medicalexposures, being the major source of man-maderadiation exposure of the population, add about onesixth to the population dose from backgroundradiation.
The 1997 EU directive (2) requires all concerned toreduce unnecessary exposure of patients to radiation.Responsible organisations and individuals usingionising radiation must comply with these regulations.One important way of reducing the radiation dose isto avoid undertaking investigations unnecessarily(especially repeat examinations).
The effective dose for a radiological investigation isthe weighted sum of the doses to a number of bodytissues, where the weighting factor for each tissuedepends upon its relative sensitivity to radiationinduced cancer or severe hereditary effects. It thusprovides a single dose estimate related to the totalradiation risk, no matter how the radiation dose isdistributed around the body.
Typical effective doses for some common diagnosticradiology range over a factor of about 1 000 from theequivalent of a day or two of natural backgroundradiation (0.02 mSv for a chest radiograph) to 4.5years (eg, for computed tomography of the abdomen).However, there is substantial variation in thebackground radiation between and within countries.The doses for conventional x-ray examinations arebased on results compiled by the NRPB from patient
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Typical effective doses from diagnosticmedical exposures in the 1990s
Diagnostic procedure Typical Equivalent Approximateeffective No. of equivalent
dose chest period of(mSv) x-rays natural
backgroundradiation (1)
X-ray examinations:
Limbs and joints(except hip) <0.01 <0.5 <1.5 days
Chest (single PA film) 0.02 1 3 days
Skull 0.07 3.5 11 days
Thoracic spine 0.7 35 4 months
Lumbar spine 1.3 65 7 months
Hip 0.3 15 7 weeks
Pelvis 0.7 35 4 months
Abdomen 1.0 50 6 months
IVU 2.5 125 14 months
Barium swallow 1.5 75 8 months
Barium meal 3 150 16 months
Barium follow through 3 150 16 months
Barium enema 7 350 3.2 years
CT head 2.3 115 1 year
CT chest 8 400 3.6 years
CT abdomen or pelvis 10 500 4.5 years
Radionuclide studies:
Lung ventilation (Xe-133) 0.3 15 7 weeks
Lung perfusion (Tc-99m) 1 50 6 months
Kidney (Tc-99m) 1 50 6 months
Thyroid (Tc-99m) 1 50 6 months
Bone (Tc-99m) 4 200 1.8 years
Dynamic cardiac (Tc-99m) 6 300 2.7 years
PET head (F-18 FDG) 5 250 2.3 years
(1) UK average background radiation = 2.2 mSv per year: regionalaverages range from 1.5 to 7.5 mSv per year.
With advice from Wall, B. National Radiological Protection Board.
dose measurements made in 380 hospitals throughoutthe UK from 1990 to 1995. They are mostly lowerthan those given in earlier editions of this bookletwhich were based on data from the early 1980s,indicating a gratifying trend towards improved patientprotection. The doses for CT examinations andradionuclide studies are based on national surveysconducted by the NRPB and BNMS and are unlikelyto have changed significantly since then.
Low-dose examinations of the limbs and chest are themost common radiological investigations butrelatively infrequent high-dose examinations such asbody CT and barium studies make the majorcontribution to the collective population dose. Thedoses from some CT examinations are particularlyhigh, show no sign of decreasing and the use of CT isstill rising. CT now probably contributes almost halfof the collective dose from all x-ray examinations. Itis thus particularly important that requests for CT arethoroughly justified and that techniques are adoptedwhich minimise dose while retaining essentialdiagnostic information. Indeed some authoritiesestimate the additional lifetime risk of fatal cancer foran abdominal CT examination in an adult is around 1in 2 000 (compared with the risk for a chest x-ray at1 in a million) (26). However, this is a small excessrisk compared with the very high overall risk ofcancer (nearly 1 in 3) and is usually more than offsetby the benefit gained from the CT examination.
In these referral guidelines the doses have beengrouped into broad bands to help the referrerunderstand the order of magnitude of radiation doseof the various investigations.
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TABLE Classification of the typicaleffective doses of ionisingradiation from common imagingprocedures
Class Typical effective ExamplesDose (mSv)
0 0 US, MRI
I <1 CXR, limb XR, pelvisXR
II* 1–5 IVU, lumbar spine XR,NM (e.g. skeletalscintigram), CT head &neck
III 5–10 CT chest and abdomen,NM (e.g. cardiac)
IV >10 Some NM studies (e.g.PET)
* The average annual background dose in most parts of Europe fallsin Band II.
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Communications with adepartment of clinicalradiology
Referral for an imaging examination is generallyregarded as a request for an opinion from a specialistin radiology or nuclear medicine. The outcome of thisrequest for opinion should be presented in the form ofa report to assist in the management of a clinicalproblem.
Request forms should be completed accurately andlegibly in order to avoid any misinterpretation. Youshould state clearly the reasons for the request andgive sufficient clinical details to enable the imagingspecialist to understand the particular diagnostic orclinical problems that you are attempting to resolveby radiological investigation.
In some cases the best investigation for resolving theproblem may be an alternative imaging examination.
If you are in doubt as to whether an investigation isrequired or which investigation is best, you shouldconsult with an appropriate specialist in radiology ornuclear medicine. Indeed imaging departments arealways pleased to discuss investigations withreferring doctors. Regular clinico-radiologicalmeetings provide a useful format for such discussionand are considered good practice (27).
While it should be noted that these recommendationshave been widely endorsed, it is recognised that afew departments will adapt them according to localcircumstances and policies.
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Technique-based imaging
Computed tomography (CT)CT is now quite widely available throughout Europe.Furthermore there have been recent importantadvances due to the development of spiral andmultislice CT which allows breath-hold volume dataacquisition. Such advances have opened up newdiagnostic opportunities, such as the use of spiral CTin the diagnosis of pulmonary embolism. Neverthelessdifferent hospitals will have their own policies aboutaccepting CT requests. It is worth remembering thatCT is a relatively expensive study and imparts a highx-irradiation dose. Thus it is always worth consideringalternatives, especially in view of the increasing roleof MRI. Indeed the UK National RadiologicalProtection Board have published several generalrecommendations with regard to CT in Protection ofthe patient in x-ray computed tomography (26), someextracts from which are reproduced here:
In view of the potential high doses CT should onlybe carried out after proper clinical justification byan experienced radiologist. Examinations onchildren require a higher level of justification, sincesuch patients are at greater risk from radiation.
When clinically appropriate, the alternative use ofsafer non-ionising techniques (US and MRI) or oflow dose x-ray techniques should be considered.
CT should not be carried out on the abdomen orpelvis of pregnant patients without sound clinicalreasons and particular attention to low-dosetechniques.
Care should always be taken to minimise exposureto the eyes, particularly for patients likely toundergo multiple examinations.
As for all radiological requests, any CT referralwhich falls outside established guidelines should bediscussed with a radiologist. Because of the need to
minimise the extent of the examination (and therebythe cost and radiation dose), it is helpful if theclinical notes and previous imaging investigations areavailable for review at the time of CT.
A few further points:
• CT remains the optimal investigation for manyclinical problems within the chest and abdomen,despite the radiation risks.
• CT is still widely used for intracranial problems,especially CVA and trauma.
• CT remains a simple method of staging manymalignant diseases (e.g. lymphoma) and inmonitoring the response to therapy.
• CT provides valuable pre-operative informationabout complex masses and is widely used forpost-operative complications.
• CT allows accurate guidance for drainageprocedures, biopsies and anaesthetic nerveblocks.
• CT has an important role in trauma.
• CT images may be degraded by prostheses,fixation devices, etc.
• CT provides better anatomical detail in obesepatients than US. In thinner patients andchildren, US should be used wherever possible.
• CT of the abdomen imparts a radiation doseequivalent to about 500 CXRs.
Interventional radiology (includingangiography and minimal accesstherapy)
This area of radiology is currently undergoing rapidexpansion. While all departments of clinical radiologyhave been undertaking angiography and associated
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25
procedures (e.g. angioplasty) for many years, severalnew techniques have emerged recently. Most abscessesin the abdomen are now treated by percutaneousdrainage procedures using radiological guidance.Likewise the majority of liver biopsies are nowperformed by radiologists (using US guidance). Lymphnode biopsies are routine in most US and CT units.
New technology is rapidly widening the range ofinterventional radiology yet further. Theseinnovations include:
• percutaneous diskectomy for lumbar diskherniation (often using CT control);
• percutaneous insertion of grafts for abdominalaortic aneurysms;
• various techniques to treat inoperable hepaticlesions (e.g. laser ablation under imagingcontrol);
• interventional MRI with ‘real-time’ imaging toallow monitoring of therapeutic manoeuvres.
These examples of recent innovations require closecollaboration with clinical colleagues. The precisearrangements vary considerably according to localexpertise and availability of equipment. There iscontinuing discussion at national level about the bestarrangement for these interventional procedures.Inevitably requests for all such procedures involvedetailed discussion between various specialists.
Magnetic resonance imaging (MRI)
There has been a substantial recent increase in thenumber of MRI systems across Europe. Accordinglythere are numerous recommendations for the use ofMRI. Indeed, with the recent technical advances andincreasing experience, the role of MRI continues toexpand and the limiting factor for further expansionis now often financial.
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Because MRI does not use ionising radiation, MRIshould be preferred where both CT and MRI wouldprovide similar information and when both areavailable. However MRI is in danger of beingsubjected to inappropriate demands which may leadto long waiting times. Thus, all requests for MRIshould be agreed with a radiologist.
A few further points:
• MRI usually provides more information than CTabout intracranial, head and neck, spinal andmusculoskeletal disorders because of highcontrast sensitivity and multiplanar imagingcapability. This helps to establish the diagnosisand institute appropriate management withgreater confidence. It is increasingly being usedin oncology.
• Major recent advances include: breast andcardiac MR imaging; angiographic andinterventional techniques; MRCP and other fluid-sensitive MR techniques; functional MR imagingof the brain. However, many of these techniquesawait full evaluation.
• MRI is not approved during the first trimester ofpregnancy. However it may well prove to besafer than some of the alternative options.Discuss all imaging in pregnancy with theradiology department.
• There are some definite contraindications to theuse of MRI: metallic foreign bodies (FBs) in theorbits, aneurysm clips, pacemakers, cochlearimplants, etc. Furthermore MRI will givereduced image quality close to prostheses, etc.The full list of contraindications is provided inseveral textbooks and monographs. Anyuncertainty about contraindications should bediscussed with the imaging department well inadvance.
Nuclear medicine (NM)
In EU countries NM is an independent specialty, theuse of unsealed sources of radionuclides for diagnosisand therapy being restricted to NM specialists. Insome countries other specialists, usually radiologists,can also provide NM services. Whatever the localarrangements, an experienced specialist will beavailable to discuss the appropriate NM techniques ina given clinical situation. They will also be able toadvise on which particular NM investigation shouldbe used. Accordingly referring clinicians shouldindicate the precise clinical problem requiringinvestigation, because this will determine whichradionuclide (or alternative) investigation is used.
Despite some misconceptions, the radiation dosesimparted by most NM techniques comparefavourably with those of many other imaginginvestigations which are regarded as ‘safe’. As shownin the chart displayed in the section on minimisingradiation dose, the effective dose associated withmost routine NM studies is considerably less thanthat for abdominal CT.
There is particular value in the functional data whichcan be provided by NM techniques. At a basic level,NM can determine whether a distended renal pelvisshown by US is merely due to a capacious collectingsystem, or caused by an obstructing lesion. The sameinvestigation can provide data on the percentage ofoverall renal function provided by each kidney. Morecomplex studies can indicate the ejection fraction ofthe left ventricle or the distribution of blood flow tothe cerebral cortex.
PET has recently made large strides and there is agradual increase in its availability. Because of theshort-lived nature of the key radionuclides (theglucose analogue F-18 fluorodeoxyglucose, FDG, iswidely used), PET can only be offered close to a
27
28
cyclotron and radionuclide pharmacy. However, thedevelopment of double-headed gamma cameras withmodified PET capabilities is a significant advancewhich should increase availability; it is currently thefocus of much research. Because PET can identifysmall foci of viable tumours, it offers exceptionalopportunities in the staging of various cancers (e.g.bronchus) and in cancer follow-up (e.g. lymphoma),where other imaging techniques may be unable todistinguish between residual fibrotic masses andactive disease. PET can also provide unique dataabout brain metabolism and myocardial viability andthere are several research units studying theseaspects. Over the next few years there will be anincreasing uptake of PET into clinical practice and itspotential use is flagged for certain clinical problemsin the ensuing recommendations.
Nuclear medicine therapyAlthough not considered further in these referralguidelines, it is worth considering the important roleof NM in the treatment of both benign and malignantdisease. The thyroid gland is still the most importanttarget but the field is rapidly expanding. Otherindications include neuroendocrine tumours, painfulskeletal metastases, some arthropathies,polycythaemia, malignant effusions. NM treatmentoptions are being investigated in theleukaemias/lymphomas and some liver tumours.
29
Ultrasound (US)Since the previous edition of these guidelines, mostdepartments of clinical radiology have experienced alarge increase in referrals for US examinations.During this period US equipment and expertise haveadvanced and the scope of referrals (Colour Doppler,Power Doppler, transvaginal (TV) gynaecologicalwork, etc.) has widened. These trends are to bewelcomed because US does not employ ionisingradiation. However there is scant evidence that theincrease in US has been accompanied by muchreduction in referrals for other radiologicalinvestigations and a consequent reduction in totalradiation dose to the public.
In fact, the rising US workload has developed whilethe demand for other radiological investigations hasalso continued to increase. The one notable exceptionis the IVU which is required much less often since theadvent of US. However, because US is non-invasive,the total number of patients investigated withuroradiological problems has increased. Departmentsof clinical radiology have developed different localpolicies for dealing with the increasing US workload.
The actual acquisition of US images has to beundertaken by an experienced operator; even such anoperator may not be able to gain perfect images inevery patient. For example US can be difficult andunsatisfactory in obese patients. Furthermore thedistribution of bowel gas may mask certain features.Nevertheless the cheap, quick, reliable and non-invasive nature of US make it an excellent initialinvestigation for a wide range of clinical referrals.Accordingly US has been recommended as theappropriate investigation wherever possible.
Because US avoids ionising radiation and is relativelyinexpensive, it is often recommended where moreexpensive studies (e.g. CT) cannot be justified or
resources are limited. Conversely, it is difficult torefuse a request for US on grounds of invasiveness orexpense. There is thus a danger of US departmentsbeing overloaded with requests which may be on themargins of appropriateness. Accordingly, referringclinicians still have a duty to consider carefullywhether each request for US is justified and whetherthe result (e.g. the presence of gallstones) will affectmanagement (see Introduction, why are guidelinesneeded?).
30
31
GLOSSARY
ABBREVIATION DEFINITION
XR Plain radiography one or morefilms
CXR Chest radiograph
AXR Abdominal radiograph
US Ultrasound
Skeletal survey A series of XRs to show thepresence and extent of involvedskeleton
Mammogram Breast radiography
Ba swallow/ meal/FT Barium swallow/ meal/followthrough
Small bowel enema Detailed Barium study vianasoduodenal intubation
Ba enema Barium enema
IVU Intravenous urogram
CT Computed tomography
CTA CT angiography
HRCT High resolution CT
NM Nuclear medicine
SPECT Single photon emissiontomography
MRI Magnetic resonance imaging
MRA MR angiography
MRCP Magnetic resonance cholangiopancreatography
DSA Digital subtraction angiography
ERCP Endoscopic retrograde cholangiopancreatography
PET Positron emission tomography
A.
Hea
d (
incl
ud
ing
ENT
pro
ble
ms)
Con
geni
tal
diso
rder
s M
RI
(0)
Indi
cate
d (C
)D
efin
itive
exa
m f
or a
ll m
alfo
rmat
ions
and
avo
ids
x-ir
radi
atio
n. 3
D C
Tm
ay b
e ne
eded
for
bon
e
(for
chi
ldre
n se
ean
omal
ies.
Sed
atio
n us
ually
req
uire
d fo
r yo
ung
Se
ctio
n M
)A
1ch
ildre
n. C
onsi
der
US
in n
eona
tes.
Cer
ebro
vasc
ular
acc
iden
t C
T(I
I)In
dica
ted
(C)
CT
adeq
uate
ly a
sses
ses
mos
t ca
ses
and
(CV
A);
str
oke
show
s ha
emor
rhag
e.
MR
I (0
) an
dSp
ecia
lised
M
RI
and
NM
mor
e se
nsiti
ve t
han
CT
in e
arly
N
M (
II)
inve
stig
atio
n (B
)in
farc
tion
and
for
post
erio
r fo
ssa
lesi
ons.
US
caro
tids
(0)
Not
ind
icat
ed
Exc
eptio
ns f
or:
(a)
thos
e w
ith f
ull
reco
very
in
who
m
rout
inel
y (C
)ca
rotid
sur
gery
is
cont
empl
ated
. (b)
an
evol
ving
CV
AA
2w
here
dis
sect
ion
or e
mbo
lus
susp
ecte
d.
Tra
nsie
nt i
scha
emic
U
S ca
roti
ds (
0)In
dica
ted
(B)
If d
oubt
abo
ut d
iagn
osis
or
surg
ery
cont
empl
ated
. at
tack
(T
IA)
Muc
h de
pend
s on
loc
al p
olic
y an
d av
aila
ble
expe
rtis
e.
US
(with
Col
our
Dop
pler
) pr
ovid
es f
unct
iona
l da
ta
abou
t bi
furc
atio
n di
seas
e. A
ngio
grap
hy, M
RA
and
CTA
are
mor
e ex
pens
ive
alte
rnat
ives
to
show
the
(s
ee a
lso
B5)
A3
vess
els.
MR
I an
d N
M c
an b
e us
ed t
o sh
ow f
unct
ion.
32
A. HeadC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Dem
yelin
atin
g an
d ot
her
MR
I (0
)In
dica
ted
(A)
MR
I m
uch
mor
e se
nsiti
ve t
han
CT
for
dem
yelin
atin
gw
hite
mat
ter
dise
ase
dise
ase.
But
MR
I m
ay s
till
be n
egat
ive
in u
p to
25
%of
tho
se w
ith e
stab
lishe
d m
ultip
le s
cler
osis
. MR
I al
sosu
peri
or t
o C
Tin
del
inea
ting
exte
nt a
nd l
ocat
ion
of
A4
othe
r w
hite
-mat
ter
dise
ase.
Spac
e-oc
cupy
ing
CT
(II)
or
Indi
cate
d (B
)M
RI
mor
e se
nsiti
ve f
or e
arly
tum
ours
, in
reso
lvin
g le
sion
(SO
L)
MR
I (0
)ex
act
posi
tion
(use
ful
for
surg
ery)
and
for
pos
teri
or
foss
a le
sion
s. M
RI
may
mis
s ca
lcif
icat
ion.
CT
mor
ew
idel
y av
aila
ble;
and
oft
en s
uffi
cien
t in
sup
rate
ntor
ial
lesi
ons
and
subd
ural
hae
mat
omas
. MR
I su
peri
or i
n th
epo
ster
ior
foss
a an
d fo
r va
scul
ar l
esio
ns. N
M m
ay b
eus
eful
in
cert
ain
circ
umst
ance
s —
tum
our
viab
ility
A
5po
st-t
hera
py, e
spec
ially
pos
t-ra
diot
hera
py.
Hea
dach
e: a
cute
, sev
ere
CT
(II)
Indi
cate
d (B
)C
Tpr
ovid
es a
dequ
ate
data
in
mos
t ca
ses
of
suba
rach
noid
and
oth
er i
ntra
cran
ial
haem
orrh
age
and
asso
ciat
ed h
ydro
ceph
alus
. NB
:Ane
gativ
e C
Tdo
es n
ot
excl
ude
SAH
and
whe
re s
uspe
cted
lum
bar
punc
ture
sh
ould
fol
low
, ass
umin
g no
con
trai
ndic
atio
ns(e
.g. o
bstr
uctiv
e hy
droc
epha
lus)
. Lum
bar
punc
ture
m
ay a
lso
be n
eede
d to
exc
lude
men
ingi
tis.
MR
I (0
) or
Sp
ecia
lised
M
RI
bette
r th
an C
Tfo
r in
flam
mat
ory
caus
es. N
M m
ayN
M (
II)
inve
stig
atio
n (C
)be
the
mos
t se
nsiti
ve i
nves
tigat
ion
for
ence
phal
itis
and
can
prov
ide
evid
ence
of
circ
ulat
ion
dera
ngem
ent
in
A6
mig
rain
e.
33
A. Head
Hea
dach
e: c
hron
ic
XR
sku
ll, s
inus
, N
ot i
ndic
ated
R
adio
grap
hy o
f lit
tle u
se i
n th
e ab
senc
e of
foc
al
C s
pine
(I)
rout
inel
y (B
)si
gns/
sym
ptom
s. S
ee A
13 b
elow
.
(for
chi
ldre
nC
T(I
I) o
rN
ot i
ndic
ated
So
me
exce
ptio
ns f
or s
peci
alis
ts o
r if
evi
denc
e of
rai
sed
see
Sect
ion
M)
A7
MR
I (0
)ro
utin
ely
(B)
intr
acra
nial
pre
ssur
e, p
oste
rior
fos
sa o
r ot
her
sign
s.
Pitu
itary
and
M
RI
(0)
Spec
ialis
edD
emon
stra
tion
of m
icro
aden
omas
may
not
be
help
ful
juxt
a-se
llar
prob
lem
sin
vest
igat
ion
(B)
for
man
agem
ent.
CT
if M
RI
not
avai
labl
e. U
rgen
t re
ferr
al w
hen
visi
on d
eter
iora
ting.
Som
e ce
ntre
s us
e sp
ecif
ic N
M a
gent
s.
SXR
(I)
Not
ind
icat
ed
Patie
nts
who
req
uire
inv
estig
atio
n ne
ed M
RI
or C
T.A
8ro
utin
ely
(C)
Post
erio
r fo
ssa
sign
sM
RI
(0)
Indi
cate
d (A
)M
RI
muc
h be
tter
than
CT.
CT
imag
es o
ften
deg
rade
d A
9by
bea
m h
arde
ning
art
efac
ts.
Hyd
roce
phal
us
CT
(II)
Indi
cate
d (B
)C
Tad
equa
te f
or m
ost
case
s; M
RI
som
etim
es
nece
ssar
y an
d m
ay b
e m
ore
appr
opri
ate
in c
hild
ren.
U
S fi
rst
choi
ce f
or i
nfan
ts. N
M u
sed
in s
ome
cent
res,
(for
chi
ldre
n se
ees
peci
ally
for
shu
nt f
unct
ion.
Sect
ion
M)
A10
XR
Indi
cate
d (C
)X
R c
an d
emon
stra
te w
hole
val
ve s
yste
m.
34
A. HeadC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Mid
dle
or i
nner
-ear
C
T(I
I)Sp
ecia
lised
E
valu
atio
n of
the
se s
ympt
oms
requ
ires
EN
T,sy
mpt
oms
(inc
ludi
ng
inve
stig
atio
n (B
)ne
urol
ogic
al o
r ne
uros
urgi
cal
expe
rtis
e.ve
rtig
o)A
11
Sens
orin
eura
l de
afne
ss
MR
I (0
)Sp
ecia
lised
M
RI
muc
h be
tter
than
CT,
esp
ecia
lly f
or a
cous
tic
(for
chi
ldre
n se
ein
vest
igat
ion
(B)
neur
omas
. For
dea
fnes
s in
chi
ldre
n se
e M
4.Se
ctio
n M
)A
12
Sinu
s di
seas
e Si
nus
XR
(I)
Not
ind
icat
edT
hick
ened
muc
osa
is a
non
-spe
cifi
c fi
ndin
g an
d m
ay
rout
inel
y (B
)oc
cur
in a
sym
ptom
atic
pat
ient
s.
CT
(II)
Spec
ialis
ed
CT
is m
ore
rew
ardi
ng a
nd p
rovi
des
uniq
ue
inve
stig
atio
n (B
)in
form
atio
n ab
out
ostia
l an
atom
y. L
ow d
ose
tech
niqu
ede
sira
ble.
Ind
icat
ed w
hen
max
imal
med
ical
tre
atm
ent
(for
chi
ldre
n se
eha
s fa
iled,
whe
n co
mpl
icat
ions
ari
se o
r if
mal
igna
ncy
Sect
ion
M)
A13
susp
ecte
d.
Dem
entia
and
mem
ory
SXR
(I)
Not
ind
icat
ed
Con
side
r in
vest
igat
ion
if c
linic
al c
ours
e un
usua
l or
in
diso
rder
s, f
irst
ons
et
rout
inel
y (B
)yo
unge
r pa
tient
. ps
ycho
sis
CT
(II)
or
Spec
ialis
ed
CT
and
SPE
CT
a go
od c
ombi
natio
n fo
r A
lzhe
imer
’s
MR
I (0
) or
in
vest
igat
ion
(B)
dise
ase.
MR
I be
tter
for
stru
ctur
al c
hang
es a
nd
NM
(II
I)as
sess
men
t of
‘no
rmal
pre
ssur
e hy
droc
epha
lus’
. PE
Tan
d SP
EC
Tre
adily
pro
vide
fun
ctio
nal
data
. C
ereb
ral
bloo
d fl
ow s
tudi
es m
ay d
iffe
rent
iate
A
14A
lzhe
imer
’s f
rom
oth
er f
orm
s of
dem
entia
.
35
A. Head
Orb
ital
lesi
ons
CT
(II)
or
Spec
ialis
ed
CT
prov
ides
bet
ter
anat
omic
al d
etai
l, pa
rtic
ular
ly o
f M
RI
(0)
inve
stig
atio
n (B
)bo
ny s
truc
ture
s (e
.g. n
asol
acri
mal
duc
t). M
RI
avoi
ds
radi
atio
n do
se t
o le
ns (
but
cont
rain
dica
ted
whe
n fe
rrom
agne
tic F
B s
uspe
cted
). C
onsi
der
US
for
A15
intr
a-oc
ular
les
ions
.
Orb
itsX
R o
rbit
s (I
)In
dica
ted
(B)
Esp
ecia
lly f
or t
hose
who
hav
e w
orke
d w
ith m
etal
lic
Met
allic
FB
(be
fore
MR
I)m
ater
ials
, pow
er t
ools
, etc
. Som
e ce
ntre
s us
e C
T.
A16
(see
Tra
uma
Sect
ion
K f
or a
cute
inj
ury.
Vis
ual
dist
urba
nces
SXR
(I)
Not
ind
icat
ed
Plai
n X
Rs
rare
ly c
ontr
ibut
ory.
Spe
cial
ists
may
req
uire
A17
rout
inel
y (C
)C
Tor
MR
I.
Epi
leps
y (a
dult)
SX
R (
I)N
ot i
ndic
ated
E
valu
atio
n re
quir
es s
peci
alis
t ex
pert
ise.
Lat
e on
set
rout
inel
y (B
)se
izur
es s
houl
d no
rmal
ly b
e in
vest
igat
ed b
ut i
mag
ing
may
be
unne
cess
ary
if c
lear
ly a
lcoh
ol-r
elat
ed.
CT
(II)
, MR
ISp
ecia
lised
Pa
rtia
l/foc
al s
eizu
res
may
req
uire
det
aile
d ev
alua
tion
(0)
or N
M (
III)
inve
stig
atio
n (B
)if
sur
gery
is
bein
g co
nsid
ered
. Ict
al S
PEC
Tm
axim
ises
lik
elih
ood
of l
ocal
isin
g fo
cus.
Int
eric
tal
func
tiona
l (f
or c
hild
ren
see
imag
ing
also
im
port
ant.
Muc
h de
pend
s on
loc
al p
olic
ySe
ctio
n M
)A
18w
hich
will
det
erm
ine
com
bina
tions
of
proc
edur
es.
36
A. HeadC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
B.
Nec
k (f
or
the
spin
e se
e Se
ctio
ns
C [
Th
e sp
ine]
an
d K
[Tr
aum
a])
Soft
tis
sues
Thy
roid
nod
ules
US
(0)
and
Indi
cate
d (B
)D
emon
stra
tes
mor
phol
ogy;
allo
ws
guid
ed a
spir
atio
nan
d en
larg
emen
tN
M (
I)fo
r cy
tolo
gy o
r bi
opsy
for
his
tolo
gy. S
ome
clin
icia
ns
will
pro
ceed
to
aspi
ratio
n w
ith n
o im
agin
g.
B1
Con
tem
pora
ry C
XR
nee
ded
to s
how
tra
chea
.
Thy
roto
xico
sis
NM
(I)
, US
(0)
Indi
cate
d (B
)C
an d
iffe
rent
iate
bet
wee
n G
rave
s’di
seas
e, t
oxic
no
dula
r go
itre
and
suba
cute
thy
roid
itis.
Pro
vide
s fu
nctio
nal
info
rmat
ion
abou
t no
dule
s. A
lso
usef
ul i
n B
2th
yroi
ditis
.
Ect
opic
thy
roid
tis
sue
NM
(I)
Indi
cate
d (C
)N
M e
xcel
lent
for
sm
all
ecto
pic
rest
s of
thy
roid
tis
sue.
(e.g
. lin
gual
thy
roid
)In
gen
eral
ised
thy
roid
enl
arge
men
t or
mul
tinod
ular
goitr
e U
S re
adily
sho
ws
retr
oste
rnal
ext
ensi
on;
real
time
stud
ies
show
eff
ect
of n
eck
exte
nsio
n, e
tc.
CT
/MR
I ne
eded
to
dem
onst
rate
ful
l re
tros
tern
al e
xten
tB
3an
d tr
ache
al c
ompr
omis
e.
Hyp
erpa
rath
yroi
dism
Imag
ing
Spec
ialis
edSe
ek a
dvic
e. D
iagn
osis
mad
e on
clin
ical
/bio
chem
ical
inve
stig
atio
n (C
)gr
ound
s. I
mag
ing
can
assi
st i
n pr
e-op
erat
ive
loca
lisat
ion
but
may
not
be
need
ed b
y ex
peri
ence
dsu
rgeo
ns. M
uch
depe
nds
on l
ocal
pol
icy
and
avai
labl
ete
chno
logy
and
exp
ertis
e. U
S, N
M, C
Tan
d M
RI
all
B4
accu
rate
in
the
un-o
pera
ted
neck
.
37
B. Neck
Asy
mpt
omat
ic c
arot
idU
S ca
roti
ds (
0)N
ot i
ndic
ated
Sign
ific
ant
inte
rnal
car
otid
art
ery
lesi
ons
are
rare
lybr
uit
B5
rout
inel
y (B
)fo
und.
Swal
low
ed o
r in
hale
dSe
e T
raum
a K
30.
fore
ign
body
(FB
)B
6
Mas
s of
unk
now
n or
igin
US
(0)
Indi
cate
d (C
)U
S fi
rst-
line
inve
stig
atio
n w
hich
can
als
o di
rect
biop
sy. M
RI
or C
Tus
ually
onl
y if
rec
omm
ende
d af
ter
B7
radi
olog
ical
or
spec
ialis
t cl
inic
al o
pini
on.
Saliv
ary
obst
ruct
ion
US
(0)
orIn
dica
ted
(C)
For
inte
rmitt
ent,
food
rel
ated
sw
ellin
g. M
Rsi
alog
ram
(II
)si
alog
raph
y m
ay b
e pr
efer
red
in s
ome
cent
res.
XR
Not
ind
icat
edE
xcep
t in
cal
culu
s in
flo
or o
f m
outh
, whe
re X
R m
ayB
8ro
utin
ely
(C)
be a
ll th
at i
s re
quir
ed.
Saliv
ary
mas
sU
S (0
)In
dica
ted
(B)
US
extr
emel
y se
nsiti
ve a
nd, d
epen
dent
on
loca
lex
pert
ise,
sho
uld
be f
irst
-lin
e in
vest
igat
ion.
MR
Iex
celle
nt f
or e
xten
sive
or
recu
rren
t di
seas
e. C
Tno
w o
fB
9lim
ited
use.
No
indi
catio
n fo
r C
Tsi
alog
raph
y.
Dry
mou
th —
con
nect
ive
US
(0)
orSp
ecia
lised
Not
com
mon
ly r
equi
red.
Sia
logr
am m
ay b
e di
agno
stic
tissu
e di
seas
esi
alog
ram
(II
)in
vest
igat
ion
(C)
but
NM
pro
vide
s be
tter
func
tiona
l as
sess
men
t. M
RB
10or
NM
(II
)si
alog
raph
y al
so u
sed
here
.
38
B. NeckC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Tem
poro
-man
dibu
lar
join
tX
R (
I)Sp
ecia
lised
Rad
iogr
aphs
will
dem
onst
rate
bon
y ab
norm
aliti
es, b
utdy
sfun
ctio
nin
vest
igat
ion
(B)
are
norm
al i
n gr
eat
maj
ority
, as
prob
lem
s ar
e us
ually
rela
ted
to a
rtic
ular
dis
k dy
sfun
ctio
n.
MR
I (0
) or
Spec
ialis
edFo
llow
ing
failu
re o
f co
nser
vativ
e tr
eatm
ent
whe
nar
thro
grap
hy (
II)
inve
stig
atio
n (B
)in
tern
al d
eran
gem
ent
susp
ecte
d. A
rthr
ogra
phy
offe
rs a
B11
true
dyn
amic
dem
onst
ratio
n.
39
B. Neck
C.
Th
e sp
ine
Gen
eral
(fo
r tr
aum
a se
e Se
ctio
n K
)C
onge
nita
l di
sord
ers
XR
(I)
Spec
ialis
ede.
g. F
ull-
leng
th s
tand
ing
radi
ogra
ph f
or s
colio
sis.
See
inve
stig
atio
n (C
)Se
ctio
n M
for
bac
k pa
in (
M10
).
MR
I (0
)Sp
ecia
lised
MR
I de
fine
s al
l sp
inal
mal
form
atio
ns a
nd e
xclu
des
inve
stig
atio
n (B
)as
soci
ated
the
cal
abno
rmal
ity. C
Tm
ay b
e re
quir
ed t
o(f
or c
hild
ren
delin
eate
bon
y de
tail,
but
rem
embe
r la
rge
radi
atio
nse
e Se
ctio
n M
)C
1bu
rden
.
Mye
lopa
thy:
tum
ours
,M
RI
(0)
Indi
cate
d (B
)M
RI
clea
r fi
rst
choi
ce f
or a
ll sp
inal
cor
d le
sion
s an
din
flam
mat
ion,
inf
ectio
n,to
eva
luat
e co
rd c
ompr
essi
on. C
Tm
ay b
e ne
eded
if
infa
rctio
n, e
tc.
bette
r bo
ny d
etai
l is
req
uire
d. M
yelo
grap
hy o
nly
ifM
RI
is u
nava
ilabl
e or
im
poss
ible
. NM
stil
l w
idel
yus
ed t
o sc
reen
for
met
asta
ses
and
for
iden
tifyi
ng f
ocal
C2
skel
etal
les
ions
(su
ch a
s os
teoi
d os
teom
a).
40
C. The spineC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Cer
vica
l sp
ine
Poss
ible
atla
nto-
axia
lX
R (
I)In
dica
ted
(C)
Asi
ngle
lat
eral
cer
vica
l sp
ine
XR
with
the
pat
ient
in
subl
uxat
ion
supe
rvis
ed c
omfo
rtab
le f
lexi
on s
houl
d re
veal
any
sign
ific
ant
subl
uxat
ion
in p
atie
nts
with
rhe
umat
oid
arth
ritis
, Dow
n’s
Synd
rom
e, e
tc. M
RI
(fle
xion
/ext
ensi
on)
show
s ef
fect
on
cord
whe
n X
RC
3po
sitiv
e or
neu
rolo
gica
l si
gns
pres
ent.
Nec
k pa
in, B
rach
algi
a,X
R (
I)N
ot i
ndic
ated
Deg
ener
ativ
e ch
ange
s be
gin
in e
arly
mid
dle-
age
and
dege
nera
tive
chan
gero
utin
ely
(B)
are
ofte
n un
rela
ted
to s
ympt
oms
whi
ch a
re u
sual
ly d
ueto
dis
k/lig
amen
tous
cha
nges
und
etec
tabl
e on
pla
in X
R.
MR
I in
crea
sing
ly b
eing
use
d, e
spec
ially
whe
nbr
acha
lgia
is
pres
ent.
MR
I (0
)Sp
ecia
lised
Con
side
r M
RI
and
spec
ialis
t re
ferr
al w
hen
pain
inve
stig
atio
n (B
)af
fect
ing
lifes
tyle
or
whe
n th
ere
are
neur
olog
ical
sign
s. M
yelo
grap
hy (
with
CT
) m
ay o
ccas
iona
lly b
ere
quir
ed t
o pr
ovid
e fu
rthe
r de
linea
tion
or w
hen
MR
I is
C4
unav
aila
ble
or i
mpo
ssib
le.
41
C. The spine
Th
ora
cic
spin
ePa
in w
ithou
t tr
aum
a:X
R (
I)N
ot i
ndic
ated
Deg
ener
ativ
e ch
ange
s ar
e in
vari
able
fro
m m
iddl
e-ag
ede
gene
rativ
e di
seas
ero
utin
ely
(B)
onw
ards
. Exa
min
atio
n ra
rely
use
ful
in t
he a
bsen
ce o
fne
urol
ogic
al s
igns
or
poin
ters
to
met
asta
ses
orin
fect
ion.
Con
side
r m
ore
urge
nt r
efer
ral
in e
lder
lypa
tient
s w
ith s
udde
n pa
in t
o sh
ow o
steo
poro
ticco
llaps
e or
oth
er f
orm
s of
bon
e de
stru
ctio
n. C
onsi
der
NM
for
pos
sibl
e m
etas
tatic
les
ions
.
MR
I (0
)Sp
ecia
lised
MR
I m
ay b
e in
dica
ted
if l
ocal
pai
n pe
rsis
ts, d
iffi
cult
C5
inve
stig
atio
n (B
)to
man
age
or i
f th
ere
are
long
tra
ct s
igns
.
Lum
bar
sp
ine
Chr
onic
bac
k pa
in w
ithX
R (
II)
Not
ind
icat
edD
egen
erat
ive
chan
ges
are
com
mon
and
non
-spe
cifi
c.no
poi
nter
s to
inf
ectio
nro
utin
ely
(C)
Mai
n va
lue
in y
oung
er p
atie
nts
(e.g
. les
s th
an 2
0,or
neo
plas
msp
ondy
lolis
thes
is, a
nkyl
osin
g sp
ondy
litis
, etc
.) o
r in
olde
r pa
tient
s e.
g. >
55.
MR
I (0
) or
CT
Spec
ialis
edIn
cas
es w
here
man
agem
ent
is d
iffi
cult.
Neg
ativ
eC
6(I
I) o
r N
M (
II)
inve
stig
atio
n (C
)fi
ndin
gs m
ay b
e he
lpfu
l.
42
C. The spineC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Bac
k pa
in w
ith p
ossi
ble
Imag
ing
Indi
cate
d (B
)To
geth
er w
ith u
rgen
t sp
ecia
list
refe
rral
; M
RI
is u
sual
lyse
riou
s fe
atur
es s
uch
as:
the
best
inv
estig
atio
n. I
mag
ing
shou
ld n
ot d
elay
•on
set
< 2
0, >
55
yrs
spec
ialis
t re
ferr
al. N
M i
s al
so w
idel
y us
ed f
or p
ossi
ble
•sp
hinc
ter
or g
ait
bone
des
truc
tion,
and
in
case
s of
chr
onic
pai
n or
•sp
hinc
ter
or g
ait
whe
re i
nfec
tion
is s
uspe
cted
.di
stur
banc
e•
sadd
le a
naes
thes
ia•
seve
re o
r pr
ogre
ssiv
em
otor
los
s(‘
NO
RM
AL’
PLA
IN X
R M
AY
BE
FA
LSE
LY•
wid
espr
ead
neur
olog
ical
RE
ASS
UR
ING
).de
fici
t•
prev
ious
car
cino
ma
•sy
stem
atic
ally
unw
ell
•H
IV•
wei
ght
loss
•in
trav
enou
s dr
ug a
buse
•st
eroi
ds•
stru
ctur
al d
efor
mity
•no
n-m
echa
nica
l pa
in
C7
(for
chi
ldre
n se
e Se
ctio
n M
)
43
C. The spine
Acu
te b
ack
pain
: di
skX
R (
II)
Not
ind
icat
edA
cute
bac
k pa
in i
s us
ually
due
to
cond
ition
s w
hich
hern
iatio
n; s
ciat
ica
with
rout
inel
y (C
)ca
nnot
be
diag
nose
d on
pla
in X
R (
oste
opor
otic
no a
dver
se f
eatu
res
colla
pse
an e
xcep
tion)
. ‘N
orm
al’
plai
n X
Rs
may
be
(see
abo
ve).
fals
ely
reas
suri
ng. D
emon
stra
tion
of d
isk
hern
iatio
nre
quir
es M
RI
or C
Tan
d sh
ould
be
cons
ider
edim
med
iate
ly a
fter
fai
led
cons
erva
tive
man
agem
ent.
MR
I (0
) or
CT
Not
ind
icat
edM
RI
gene
rally
pre
ferr
ed (
wid
er f
ield
of
view
, con
us,
(II)
initi
ally
(B
)po
st-o
pera
tive
chan
ges
etc.
) an
d av
oids
x-i
rrad
iatio
n.E
ither
MR
I or
CT
is n
eede
d be
fore
int
erve
ntio
n (e
.g.
epid
ural
inj
ectio
n). M
RI
bette
r th
an C
Tfo
r po
st-
C8
oper
ativ
e pr
oble
ms.
44
C. The spineC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
D.
Mu
scu
losk
elet
al s
yste
mO
steo
mye
litis
XR
(I)
+N
M (
II)
Indi
cate
d (B
)T
he 2
–3 p
hase
ske
leta
l sc
intig
ram
is
mor
e se
nsiti
veor
MR
I (0
)th
an X
R. H
owev
er, f
indi
ngs
are
not
spec
ific
and
furt
her
spec
ialis
ed N
M w
ith a
ltern
ativ
e ag
ents
may
be
need
ed. F
at-s
uppr
esse
d M
RI
is b
ecom
ing
rega
rded
as
the
optim
al i
nves
tigat
ion.
CT
(II)
or
Spec
ialis
edC
Tus
ed t
o id
entif
y se
ques
tra.
Bot
h C
Tan
d U
S ca
nU
S (0
)in
vest
igat
ions
(C
)de
mon
stra
te a
ppro
pria
te s
ite f
or g
uide
d pe
rcut
aneo
usbi
opsy
. US
may
be
help
ful,
espe
cial
ly i
n ch
ildre
n, i
fm
etal
war
e ca
uses
art
efac
ts o
n M
RI/
CT
or i
f N
M n
onD
1sp
ecif
ic d
ue t
o re
cent
sur
gery
.
Prim
ary
bone
tum
our
XR
(I)
Indi
cate
d (B
)X
R m
ay c
hara
cter
ise
the
lesi
on.
MR
I (0
) or
Spec
ialis
edM
RI
usef
ul f
or f
urth
er c
hara
cter
isat
ion
and
nece
ssar
yC
T(I
I)in
vest
igat
ions
(B
)fo
r su
rgic
al s
tagi
ng;
shou
ld b
e pe
rfor
med
bef
ore
any
biop
sy. C
Tca
n sh
ow b
ony
deta
il be
tter
at s
ome
site
s(e
.g. s
pine
) an
d fo
r so
me
smal
l le
sion
s an
d is
nee
ded
if M
RI
unav
aila
ble.
MR
I m
ore
usef
ul f
or a
sses
smen
tof
ext
ent.
CT
ches
t if
CX
R n
egat
ive
to a
sses
spu
lmon
ary
met
asta
ses
for
man
y pr
imar
y m
alig
nant
lesi
ons.
(se
e L
41).
The
se s
tate
men
ts a
pply
to
adul
tsD
2an
d ch
ildre
n.
45
D. Musculoskeletal system
Kno
wn
prim
ary
tum
our.
NM
(II
)In
dica
ted
(B)
NM
rea
dily
ass
esse
s th
e w
hole
ske
leto
n an
d is
muc
hSk
elet
al m
etas
tase
sm
ore
sens
itive
tha
n pl
ain
XR
, tho
ugh
less
spe
cifi
c.L
ocal
ised
XR
s m
ay b
e ne
eded
to
excl
ude
othe
r ca
uses
of i
ncre
ased
act
ivity
, e.g
. deg
ener
ativ
e di
seas
e. I
npr
osta
tic c
ance
r bi
oche
mic
al m
arke
rs (
PSA
) ca
n be
used
to
follo
w u
p pr
ogre
ss o
f sk
elet
al i
nvol
vem
ent.
NM
can
als
o he
lp c
hara
cter
ise
the
lesi
on. (
e.g.
ost
eoid
oste
oma)
and
is
usef
ul i
n fo
llow
-up.
Skel
etal
sur
vey
Not
ind
icat
ed(I
I)ro
utin
ely
(C)
MR
I (0
)Sp
ecia
lised
MR
I m
ore
sens
itive
and
spe
cifi
c th
an N
M, e
spec
ially
inve
stig
atio
n (C
)fo
r m
arro
w-b
ased
les
ions
. How
ever
, fie
ld o
f vi
ew i
sD
3lim
ited.
46
D. Musculoskeletal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Soft
tis
sue
mas
s tu
mou
r,M
RI
(0)
Indi
cate
d (B
)M
RI
bette
r th
an C
Tfo
r ex
clus
ion,
det
ectio
n an
dpo
ssib
le r
ecur
renc
est
agin
g of
sof
t tis
sue
tum
ours
(su
peri
or c
ontr
ast
reso
lutio
n, m
ultip
lana
r ca
pabi
lity,
del
inea
tion
ofne
urov
ascu
lar
bund
le a
nd m
uscl
e/co
mpa
rtm
ent
invo
lvem
ent)
. CT
has
grea
ter
sens
itivi
ty f
orca
lcif
icat
ion.
Inc
reas
ing
inte
rest
in
US
for
som
ean
atom
ical
site
s. M
R a
ccep
ted
as i
nves
tigat
ion
ofch
oice
for
pos
sibl
e re
curr
ence
alth
ough
US
has
itspr
opon
ents
and
can
be
used
for
bio
psy.
Con
side
r N
MD
4(e
.g. P
ET
).
Bon
e pa
inX
R (
I)In
dica
ted
(B)
Loc
al v
iew
of
sym
ptom
atic
are
as o
nly.
NM
(II
) or
Indi
cate
d (B
)W
hen
sym
ptom
s pe
rsis
t an
d pl
ain
XR
s ne
gativ
e.D
5M
RI
(0)
Mye
lom
aSk
elet
al s
urve
yIn
dica
ted
(C)
For
stag
ing
and
iden
tifyi
ng l
esio
ns w
hich
may
ben
efit
(II)
from
rad
ioth
erap
y. S
urve
y ca
n be
ver
y lim
ited
for
follo
w-u
p.
NM
(II
)N
ot i
ndic
ated
Skel
etal
sci
ntig
raph
y is
oft
en n
egat
ive
and
rout
inel
y (B
)un
dere
stim
ates
dis
ease
ext
ent;
cons
ider
bon
e m
arro
wst
udie
s.
MR
I (0
)Sp
ecia
lised
MR
I ve
ry s
ensi
tive,
eve
n lim
ited
to s
pine
, pel
vis
and
inve
stig
atio
n (B
)pr
oxim
al f
emor
a. P
artic
ular
ly u
sefu
l in
non
-sec
reto
rym
yelo
ma
or i
n th
e pr
esen
ce o
f di
ffus
e os
teop
enia
. Can
D6
be u
sed
for
tum
our-
mas
s as
sess
men
t an
d fo
llow
-up.
47
D. Musculoskeletal system
Met
abol
ic b
one
dise
ase
Skel
etal
sur
vey
Not
ind
icat
edB
ioch
emic
al t
ests
usu
ally
suf
fice
. If
need
ed, t
his
(II)
rout
inel
y (C
)sh
ould
be
limite
d (e
.g. h
ands
, CX
R, p
elvi
s an
d la
tera
llu
mba
r sp
ine)
. Bon
e de
nsito
met
ry m
ay b
e ne
eded
.(s
ee D
9).
NM
(II
)In
dica
ted
(C)
Skel
etal
sci
ntig
ram
goo
d fo
r co
mpl
icat
ions
Ost
eom
alac
iaX
R (
0)In
dica
ted
(B)
Loc
alis
ed X
R t
o es
tabl
ish
caus
e of
loc
al p
ain
orD
7eq
uivo
cal
lesi
on o
n N
M.
NM
(II
)Sp
ecia
lised
NM
can
sho
w i
ncre
ased
‘ac
tivity
’an
d so
me
loca
lco
mpl
icat
ions
. Bon
e de
nsito
met
ry m
ay b
e ne
eded
.D
8(s
ee D
9).
Pain
— o
steo
poro
ticX
R (
II)
late
ral
Indi
cate
d (B
)L
ater
al v
iew
s w
ill d
emon
stra
te c
ompr
essi
on f
ract
ures
.co
llaps
eth
orac
ic a
ndN
M o
r M
RI
mor
e us
eful
in
dist
ingu
ishi
ng b
etw
een
lum
bar
spin
ere
cent
and
old
fra
ctur
es a
nd c
an h
elp
excl
ude
path
olog
ical
fra
ctur
es. B
one
dens
itom
etry
(du
al e
nerg
yX
R a
psor
ptio
met
ry (
DE
XA
) or
qua
ntita
tive
CT
)pr
ovid
es o
bjec
tive
mea
sure
men
ts o
f bo
ne m
iner
alco
nten
t; ca
n al
so b
e us
ed f
or m
etab
olic
bon
e di
seas
eD
9(s
ee D
7, D
8).
48
D. Musculoskeletal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Art
hrop
athy
, pre
sent
atio
nX
R (
I) a
ffec
ted
Indi
cate
d (C
)M
ay b
e he
lpfu
l to
det
erm
ine
caus
e al
thou
gh e
rosi
ons
join
tar
e a
rela
tivel
y la
te f
eatu
re.
XR
(I)
Indi
cate
d (C
)In
pat
ient
s w
ith s
uspe
cted
rhe
umat
oid
arth
ritis
, XR
hand
s/fe
etfe
et m
ay s
how
ero
sion
s ev
en w
hen
sym
ptom
atic
hand
(s)
appe
ar n
orm
al.
XR
(II
) m
ulti
ple
Not
ind
icat
edjo
int(
s)ro
utin
ely
(C)
US
(0)
orSp
ecia
lised
All
can
show
acu
te s
ynov
itis.
NM
can
sho
wN
M (
II)
orin
vest
igat
ions
(C
)di
stri
butio
n. M
RI
can
show
art
icul
ar c
artil
age.
D10
MR
I (0
)
Art
hrop
athy
, fol
low
-up
XR
(I)
Not
ind
icat
edX
Rs
need
ed b
y sp
ecia
lists
to
assi
st m
anag
emen
tD
11ro
utin
ely
(C)
deci
sion
s.
Pain
ful
shou
lder
joi
ntX
R (
I)N
ot i
ndic
ated
Deg
ener
ativ
e ch
ange
s in
the
acr
omio
-cla
vicu
lar
join
tsin
itial
ly (
C)
and
rota
tor
cuff
are
com
mon
. Ear
lier
XR
if
soft
tis
sue
D12
calc
ific
atio
n is
exp
ecte
d.
Pain
ful
pros
thes
isX
R (
I)+
NM
(II
)In
dica
ted
(B)
Ano
rmal
NM
stu
dy e
xclu
des
mos
t la
te c
ompl
icat
ions
.Fu
rthe
r sp
ecia
lised
NM
stu
dies
can
hel
p di
stin
guis
hlo
osen
ing
from
inf
ectio
n.
US
(0)
orSp
ecia
lised
Usu
ally
cou
pled
with
asp
irat
ion/
biop
sy/a
rthr
ogra
phy.
fluo
rosc
opy
(II)
inve
stig
atio
n (C
)Su
ch i
nter
vent
ion
whi
ch p
rovi
des
a de
fini
tive
resu
lt is
D13
incr
easi
ngly
bei
ng u
sed.
49
D. Musculoskeletal system
Shou
lder
im
ping
emen
tM
RI
(0)
Spec
ialis
edA
lthou
gh i
mpi
ngem
ent
is a
clin
ical
dia
gnos
is, i
mag
ing
inve
stig
atio
n (B
)is
ind
icat
ed w
hen
surg
ery
is b
eing
con
side
red
and
prec
ise
delin
eatio
n of
ana
tom
y is
req
uire
d. B
utde
gene
rativ
e ch
ange
s al
so c
omm
on i
n th
eas
ympt
omat
ic p
opul
atio
n.
US
(0)
Spec
ialis
edSu
bacr
omia
l an
d ac
rom
iocl
avic
ular
joi
nt i
mpi
ngem
ent
D14
inve
stig
atio
n (B
)ar
e dy
nam
ic p
roce
sses
whi
ch c
an b
e as
sess
ed b
y U
S.
Shou
lder
ins
tabi
lity
CT
Spec
ialis
edG
leno
id l
abru
m a
nd s
ynov
ial
cavi
ty a
re w
ell
arth
rogr
aphy
(II
)in
vest
igat
ion
(B)
delin
eate
d by
bot
h te
chni
ques
. Som
e gr
adie
nt e
cho
MR
tec
hniq
ues
can
show
lab
rum
wel
l w
ithou
tar
thro
grap
hy.
MR
Spec
ialis
edD
15ar
thro
grap
hy (
0)in
vest
igat
ion
(C)
Rot
ator
cuf
f te
arA
rthr
ogra
phy
Spec
ialis
edM
uch
depe
nds
on l
ocal
exp
ertis
e an
d su
rgic
al p
lans
.(I
I) o
r U
S (0
)in
vest
igat
ion
(B)
All
thre
e te
chni
ques
dem
onst
rate
rot
ator
cuf
f te
ars.
D16
or M
RI
(0)
50
D. Musculoskeletal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
SI j
oint
les
ion
XR
SI
join
ts (
II)
Indi
cate
d (B
)M
ay h
elp
in i
nves
tigat
ion
of s
ero-
nega
tive
arth
ropa
thy.
SI j
oint
s us
ually
ade
quat
ely
dem
onst
rate
d on
AP
lum
bar
spin
e.
MR
I (0
) or
Spec
ialis
edM
RI
or N
M o
r C
Tw
hen
plai
n X
Rs
equi
voca
l; M
RI
NM
(II
) or
inve
stig
atio
n (C
)ca
rrie
s no
rad
iatio
n do
se.
D17
CT
(II)
Hip
pai
n: f
ull
mov
emen
tX
R p
elvi
s (I
)N
ot i
ndic
ated
XR
onl
y if
sym
ptom
s an
d si
gns
pers
ist
or c
ompl
exro
utin
ely
(C)
hist
ory
(e.g
. cha
nce
of a
vasc
ular
nec
rosi
s, s
ee D
20)
(for
chi
ldre
n se
eSe
ctio
n M
)D
18N
B:T
his
reco
mm
enda
tion
does
not
app
ly t
o ch
ildre
n.
Hip
pai
n: l
imite
dX
R p
elvi
s (I
)N
ot i
ndic
ated
Sym
ptom
s of
ten
tran
sien
t. X
R i
f hi
p re
plac
emen
tm
ovem
ent
initi
ally
(C
)m
ight
be
cons
ider
ed o
r sy
mpt
oms
pers
ist.
PET
may
be h
elpf
ul, i
f X
R, M
RI
stan
dard
NM
all
norm
al.
(for
chi
ldre
n se
eSe
ctio
n M
)D
19N
B:T
his
reco
mm
enda
tion
does
not
app
ly t
o ch
ildre
n.
Hip
pai
n: a
vasc
ular
XR
Pel
vis
(I)
Indi
cate
d (B
)A
bnor
mal
in
esta
blis
hed
dise
ase.
necr
osis
MR
I (0
)Sp
ecia
lised
MR
I us
eful
whe
n X
R n
orm
al, e
spec
ially
in
high
ris
kin
vest
igat
ion
(B)
patie
nts.
NM
and
CT
can
also
pro
vide
inf
orm
atio
nD
20he
re.
51
D. Musculoskeletal system
Kne
e pa
in:
with
out
XR
(I)
Not
ind
icat
edSy
mpt
oms
freq
uent
ly a
rise
fro
m s
oft
tissu
es a
nd t
hese
lock
ing
or r
estr
ictio
n in
rout
inel
y (C
)w
ill n
ot b
e de
mon
stra
ted
on X
R. O
Ach
ange
sm
ovem
ent
com
mon
. XR
s ne
eded
whe
n co
nsid
erin
g su
rger
y.D
21
Kne
e pa
in:
with
loc
king
,X
R (
I)In
dica
ted
(C)
To i
dent
ify
radi
o-op
aque
loo
se b
odie
s.re
stri
cted
mov
emen
t or
effu
sion
(lo
ose
body
) D22
Kne
e pa
in:
arth
rosc
opy
MR
I (0
)Sp
ecia
lised
MR
I ca
n as
sist
the
man
agem
ent
deci
sion
as
to w
heth
erbe
ing
cons
ider
edin
vest
igat
ion
(B)
or n
ot t
o pr
ocee
d w
ith a
rthr
osco
py. E
ven
in t
hose
patie
nts
with
def
inite
clin
ical
abn
orm
aliti
es,
war
rant
ing
inte
rven
tion,
sur
geon
s fi
nd p
re-o
pera
tive
D23
MR
I he
lpfu
l in
ide
ntif
ying
uns
uspe
cted
les
ions
.
Hal
lux
valg
usX
R (
I)Sp
ecia
lised
For
asse
ssm
ent
befo
re s
urge
ry.
D24
inve
stig
atio
n (C
)
Plan
tar
fasc
iitis
—X
R (
I)N
ot i
ndic
ated
Plan
tar
spur
s ar
e co
mm
on i
ncid
enta
l fi
ndin
gs. T
heca
lcan
eal
spur
rout
inel
y (B
)ca
use
of t
he p
ain
is s
eldo
m d
etec
tabl
e on
XR
. US,
NM
and
MR
I ar
e m
ore
sens
itive
in
show
ing
infl
amm
ator
y ch
ange
but
the
maj
ority
of
patie
nts
can
D25
be m
anag
ed w
ithou
t im
agin
g.
52
D. Musculoskeletal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
E. C
ard
iova
scu
lar
syst
emC
entr
al c
hest
pai
nC
XR
(I)
Indi
cate
d (B
)C
XR
mus
t no
t de
lay
adm
issi
on t
o a
spec
ialis
ed u
nit.
myo
card
ial
infa
rctio
nC
XR
can
ass
ess
hear
t si
ze, p
ulm
onar
y oe
dem
a, e
tc.
and
can
excl
ude
othe
r ca
uses
. Dep
artm
ent
film
pref
erab
le. S
ubse
quen
t im
agin
g in
volv
es s
peci
alis
edin
vest
igat
ions
(N
M, c
oron
ary
angi
ogra
phy,
etc
.) a
ndde
pend
on
loca
l po
licy.
NM
off
ers
myo
card
ial
perf
usio
n an
d ve
ntri
culo
grap
hy d
ata.
Inc
reas
ing
E1
inte
rest
in
MR
I.
Che
st p
ain:
aor
ticC
XR
(I)
Indi
cate
d (B
)M
ainl
y to
exc
lude
oth
er c
ause
s; r
arel
y di
agno
stic
.di
ssec
tion:
acu
te
CT
(III
) or
Indi
cate
d (B
)Se
ek a
dvic
e fr
om l
ocal
rad
iolo
gist
s. M
uch
vari
atio
n.U
S (0
) or
Mod
ern
CT
syst
ems
prov
ide
very
acc
urat
e re
sults
.M
RI
(0)
Oft
en c
oupl
ed w
ith t
rans
-tho
raci
c U
S or
, bet
ter,
tran
s-oe
soph
agea
l U
S. M
RI
prob
ably
the
mos
tac
cura
te a
nd i
ncre
asin
gly
used
, des
pite
log
istic
prob
lem
s an
d co
nstr
aint
s w
ith s
ome
life-
supp
ort
syst
ems.
Ang
iogr
aphy
rar
ely
nece
ssar
y un
less
abo
veE
2ex
amin
atio
ns a
re e
quiv
ocal
.
Aor
tic d
isse
ctio
n: c
hron
icM
RI
(0)
Spec
ialis
edM
RI
best
inv
estig
atio
n to
ass
ess
chan
ge i
nin
vest
igat
ion
(B)
long
itudi
nal
exte
nt. T
rans
-oes
opha
geal
US
and
CT
E3
reco
mm
ende
d.
53
E. Cardiovascular system
Pulm
onar
y em
bolu
sN
M (
II)
orIn
dica
ted
(B)
Inte
rpre
ted
alon
g w
ith c
onte
mpo
rary
CX
R. E
quiv
ocal
CT
(III
)fi
ndin
gs (
e.g.
int
erm
edia
te p
roba
bilit
y) m
ay n
eces
sita
tefu
rthe
r cl
arif
icat
ion.
Som
e ce
ntre
s us
e U
S to
sho
wth
rom
bus
in l
eg v
eins
for
fur
ther
pro
of. A
norm
alpe
rfus
ion
NM
stu
dy e
xclu
des
pulm
onar
y em
bolis
m i
nm
ost
case
s. S
pira
l C
Tus
ed i
ncre
asin
gly
as t
he i
nitia
lte
st, e
spec
ially
in
patie
nts
with
co-
exis
ting
card
iore
spir
ator
y di
seas
e, a
nd a
head
of
pulm
onar
yE
4an
giog
raph
y.
Peri
card
itis
— p
eric
ardi
alC
XR
(I)
Indi
cate
d (B
)M
ay b
e no
rmal
; ef
fusi
on v
olum
e/ef
fect
not
effu
sion
dete
rmin
ed.
US
(0)
Indi
cate
d (B
)E
xtre
mel
y ac
cura
te:
may
be
need
ed u
rgen
tly f
orta
mpo
nade
; ca
n sh
ow b
est
acce
ss f
or d
rain
age.
CT
E5
som
etim
es n
eede
d fo
r ca
lcif
icat
ion,
loc
ulat
ion,
etc
.
Susp
ecte
d va
lvul
arC
XR
(I)
and
Indi
cate
d (B
)U
sed
for
initi
al a
sses
smen
t an
d w
hen
ther
e is
a c
hang
eca
rdia
c di
seas
eca
rdia
c U
S (0
)in
the
clin
ical
pic
ture
.E
6
Clin
ical
det
erio
ratio
nC
ardi
ac U
S (0
)In
dica
ted
(B)
US
may
sho
w r
emed
iabl
e co
mpl
icat
ions
(V
SD,
follo
win
g m
yoca
rdia
lpa
pilla
ry r
uptu
re, a
neur
ysm
, etc
.).
infa
rctio
n E
7
54
E. Cardiovascular systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Follo
w-u
p of
pat
ient
sC
XR
(I)
Not
ind
icat
edO
nly
if s
igns
or
sym
ptom
s ha
ve c
hang
ed, w
hen
with
hea
rt d
isea
se o
rro
utin
ely
(B)
com
pari
son
with
the
CX
R o
btai
ned
at p
rese
ntat
ion
hype
rten
sion
E8
may
be
help
ful.
Abd
omin
al a
ortic
US
(0)
aort
aIn
dica
ted
(A)
Use
ful
in d
iagn
osis
, det
erm
inat
ion
of m
axim
alan
eury
smdi
amet
er a
nd f
ollo
w-u
p. C
Tpr
efer
able
for
sus
pect
edle
ak b
ut s
houl
d no
t de
lay
urge
nt s
urge
ry.
CT
(III
) or
Indi
cate
d (A
)C
Tan
d M
RI
for
rela
tions
hip
to r
enal
ves
sels
and
M
RI
(0)
iliac
s. I
ncre
asin
g de
man
d fo
r de
taile
d an
atom
ical
info
rmat
ion
beca
use
of i
ncre
asin
g co
nsid
erat
ion
E9
for
perc
utan
eous
ste
ntin
g.
Dee
p-ve
in t
hrom
bosi
sU
S (0
) lo
wer
Indi
cate
d (A
)M
ore
sens
itive
with
col
our-
flow
Dop
pler
. Mos
tli
mb
vein
scl
inic
ally
sig
nifi
cant
thr
ombi
are
det
ecte
d. I
ncre
asin
gex
peri
ence
with
US
for
calf
vei
n th
rom
bi. M
ay s
how
othe
r le
sion
s.
Veno
grap
hy (
II)
Not
ind
icat
edE
xten
sive
var
iatio
n ac
cord
ing
to U
S ex
pert
ise
and
E10
rout
inel
y (C
)lo
cal
ther
apeu
tic s
trat
egy.
Isch
aem
ic l
egA
ngio
grap
hySp
ecia
lised
Loc
al p
olic
y ne
eds
to b
e de
term
ined
in
agre
emen
t(I
II)
inve
stig
atio
n (A
)w
ith v
ascu
lar
surg
eons
, esp
ecia
lly w
ith r
egar
d to
ther
apeu
tic i
nter
vent
ions
. US
used
in
som
e ce
ntre
s as
firs
t in
vest
igat
ion.
Spi
ral
CT
and
MR
I ar
e be
ing
E11
deve
lope
d.
55
E. Cardiovascular system
Myo
card
ial
eval
uatio
nN
M (
III)
Indi
cate
d (A
)N
M i
s th
e m
ost
esta
blis
hed
inve
stig
atio
n fo
r as
sess
ing
E12
myo
card
ial
perf
usio
n. C
ardi
ac M
RI
only
ava
ilabl
e in
afe
w c
entr
es.
56
E. Cardiovascular systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
F. T
ho
raci
c sy
stem
Non
-spe
cifi
c ch
est
pain
CX
R (
I)N
ot i
ndic
ated
Con
ditio
ns s
uch
as T
ietz
e’s
dise
ase
show
no
F1
initi
ally
(C
)ab
norm
ality
on
CX
R. M
ain
purp
ose
is r
eass
uran
ce.
Che
st t
raum
aC
XR
(I)
Not
ind
icat
edSh
owin
g a
rib
frac
ture
aft
er m
inor
tra
uma
does
not
rout
inel
y (C
)al
ter
man
agem
ent
F2
(see
Tra
uma
Sect
ion
K).
Pre-
empl
oym
ent
orC
XR
(I)
Not
ind
icat
edN
ot j
ustif
ied
exce
pt i
n a
few
hig
h-ri
sk c
ateg
orie
s (e
.g.
scre
enin
g m
edic
als
at r
isk
imm
igra
nts
with
no
rece
nt C
XR
). S
ome
have
to
be d
one
for
occu
patio
nal
(e.g
. div
ers)
or
emig
ratio
nF
3pu
rpos
es (
UK
cat
egor
y 2)
.
Pre-
oper
ativ
eC
XR
(I)
Not
ind
icat
edE
xcep
tions
bef
ore
card
io-p
ulm
onar
y su
rger
y, l
ikel
yro
utin
ely
(B)
adm
issi
on t
o IT
U, s
uspe
cted
mal
igna
ncy
or p
ossi
ble
TB
. Ana
esth
etis
ts m
ay a
lso
requ
est
CX
Rs
for
dysp
noei
c pa
tient
s, t
hose
with
kno
wn
card
iac
dise
ase
and
the
very
eld
erly
. Man
y pa
tient
s w
ith c
ardi
ore
spir
ator
y di
seas
e ha
ve r
ecen
t C
XR
ava
ilabl
e; a
F4
repe
at C
XR
is
then
not
usu
ally
nee
ded.
Upp
er r
espi
rato
ry-t
ract
C
XR
(I)
Not
ind
icat
edin
fect
ion
F5
rout
inel
y (C
)
Chr
onic
obs
truc
tive
CX
R (
I)N
ot i
ndic
ated
Onl
y if
sig
ns o
r sy
mpt
oms
have
cha
nged
.ai
rway
s di
seas
e or
rout
inel
y (B
)as
thm
a; f
ollo
w-u
pF
6
57
F. Thoracic system
Pneu
mon
ia a
dults
:C
XR
(I)
Indi
cate
d (A
)To
con
firm
cle
arin
g, e
tc. P
oint
less
to
re-e
xam
ine
atfo
llow
-up
less
tha
n 10
-day
int
erva
ls a
s cl
eari
ng c
an b
e sl
ow(f
or c
hild
ren
see
(esp
ecia
lly i
n th
e el
derl
y).
Sect
ion
M)
F7
Pleu
ral
effu
sion
CX
R (
I)In
dica
ted
(B)
Smal
l ef
fusi
on c
an b
e m
isse
d, e
spec
ially
on
a fr
onta
lC
XR
.
US
(0)
Indi
cate
d (B
)To
pro
ve f
luid
con
sist
ency
; to
gui
de a
spir
atio
n. C
Toc
casi
onal
ly n
eede
d fo
r be
tter
loca
lisat
ion,
ass
essm
ent
F8
of s
olid
com
pone
nts,
etc
.
Hae
mop
tysi
sC
XR
(I)
Indi
cate
d (B
)PA
plus
lat
eral
vie
w.
CT
(III
)Sp
ecia
lised
Man
y ce
ntre
s us
e C
Tan
d th
en p
roce
ed t
oin
vest
igat
ion
(B)
bron
chos
copy
; in
crea
sing
use
of
CT
firs
t (s
ee C
ance
rL
7). C
onsi
der
bron
chia
l ar
teri
ogra
phy
in m
assi
veF
9ha
emop
tysi
s.
ITU
/HD
U p
atie
ntC
XR
(I)
Indi
cate
d (B
)A
CX
R i
s m
ost
help
ful
whe
n th
ere
has
been
a c
hang
ein
sym
ptom
s or
ins
ertio
n or
rem
oval
of
a de
vice
. The
valu
e of
the
rou
tine
daily
CX
R i
s be
ing
incr
easi
ngly
F10
ques
tione
d.
58
F. Thoracic systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Occ
ult
lung
dis
ease
CT
(II)
Indi
cate
d (B
)H
igh
reso
lutio
n C
Tca
n sh
ow a
bnor
mal
ities
not
evid
ent
on C
XR
, esp
ecia
lly i
nter
stiti
al d
isea
se.
NM
(II
)Sp
ecia
lised
NM
can
ass
ess
dise
ase
activ
ity (
e.g.
mea
sure
inve
stig
atio
n (B
)pe
rmea
bilit
y in
alv
eolit
is)
and
mon
itor
effe
cts
ofF
11th
erap
y.
59
F. Thoracic system
G.
Gas
tro
inte
stin
al s
yste
mG
astr
oin
test
inal
tra
ctD
iffi
culty
in
swal
low
ing
Ba
swal
low
(II
)In
dica
ted
(B)
Ba
stud
ies
are
still
rec
omm
ende
d be
fore
pos
sibl
een
dosc
opy;
the
y w
ill a
ccur
atel
y lo
calis
e le
sion
s an
dsh
ow t
he d
egre
e of
obs
truc
tion
caus
ed b
y a
stri
ctur
ean
d its
len
gth.
Web
s an
d po
uche
s ar
e w
ell
NM
(I)
Spec
ialis
edde
mon
stra
ted.
Sub
tle s
tric
ture
s m
ay b
e de
mon
stra
ted
inve
stig
atio
n (B
)by
a m
arsh
mal
low
(or
oth
er b
olus
) st
udy.
Det
aile
dfl
uoro
scop
y or
NM
nee
ded
for
mot
ility
dis
orde
rs.
Vid
eo s
wal
low
s fo
r su
spec
ted
phar
ynge
al d
ysfu
nctio
nG
1in
con
junc
tion
with
spe
ech
ther
apis
ts.
Che
st p
ain
— h
iatu
sB
a sw
allo
wN
ot i
ndic
ated
Alth
ough
Ba
swal
low
use
ful
to d
emon
stra
te h
erni
a,he
rnia
or
refl
ux/m
eal
(III
)ro
utin
ely
(C)
refl
ux a
nd t
heir
com
plic
atio
ns, n
ot a
ll su
ch p
atie
nts
need
inv
estig
atio
n. R
eflu
x is
com
mon
and
not
nece
ssar
ily th
e ca
use
of p
ain.
NM
may
be
over
sens
itive
;pH
mon
itori
ng i
s ge
nera
lly r
egar
ded
as t
he ‘
gold
stan
dard
’fo
r ac
id r
eflu
x bu
t gi
ves
no a
nato
mic
alin
form
atio
n. M
etap
lasi
a an
d oe
soph
agiti
s ar
e be
stde
tect
ed b
y en
dosc
opy
whi
ch a
lso
allo
ws
biop
sy.
G2
Incr
easi
ng u
se o
f B
a st
udie
s be
fore
ant
i-re
flux
sur
gery
.
60
G. Gastrointestinal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Oes
opha
geal
per
fora
tion
CX
R (
I)In
dica
ted
(B)
CX
R m
ay b
e su
ffic
ient
, unl
ess
loca
lisat
ion
for
surg
ical
repa
ir i
s pl
anne
d.
Swal
low
(II
)Sp
ecia
lised
Swal
low
sho
uld
be p
erfo
rmed
with
wat
er-s
olub
leG
3in
vest
igat
ion
(B)
non-
ion
ic c
ontr
ast
agen
ts. S
ome
cent
res
use
CT.
Acu
te G
I bl
eedi
ng:
AX
R (
II)
Not
ind
icat
edO
f no
val
ue.
haem
atem
esis
rout
inel
y (B
)
Ba
stud
ies
(II)
Not
ind
icat
edE
ndos
copy
pro
vide
s di
agno
sis
of u
pper
GI
lesi
ons,
rout
inel
y (A
)al
low
s in
ject
ion
of v
aric
es, e
tc. B
a st
udie
s pr
eclu
dean
giog
raph
y.
NM
(II
)Sp
ecia
lised
Aft
er e
ndos
copy
. NM
can
det
ect
blee
ding
rat
es a
s lo
w(r
ed c
ell
stud
y)in
vest
igat
ion
(B)
as 0
.1 m
l/min
; m
ore
sens
itive
tha
n an
giog
raph
y. R
edce
ll st
udy
is m
ost
usef
ul i
n in
term
itten
t bl
eedi
ng.
Ang
iogr
aphy
Spec
ialis
edW
hen
cons
ider
ing
surg
ery
or i
nter
vent
ion
(e.g
.G
4(I
II)
inve
stig
atio
n (B
)em
bolis
atio
n) f
or u
ncon
trol
labl
e bl
eedi
ng.
61
G. Gastrointestinal system
Dys
peps
ia i
n th
e yo
unge
r Im
agin
gN
ot i
ndic
ated
Mos
t pa
tient
s un
der
45 y
rs c
an b
e tr
eate
d w
ithou
tpa
tient
(e.
g. u
nder
45
yrs)
(Ba
mea
l (I
I)/
rout
inel
y (C
)co
mpl
ex i
nves
tigat
ions
and
will
und
ergo
a t
rial
of
End
osco
py (
0))
ther
apy
(ant
i-ul
cer
or r
eflu
x). E
ither
Ba
mea
l or
endo
scop
y fo
r th
ose
who
fai
l to
res
pond
. Oth
er a
larm
feat
ures
poi
ntin
g to
ear
ly i
nves
tigat
ion
incl
ude
unin
tent
iona
l w
eigh
t lo
ss, a
naem
ia, a
nore
xia,
GI
blee
ding
, pai
n re
quir
ing
hosp
italis
atio
n, n
on-s
tero
idan
ti-in
flam
mat
ory
drug
s, v
omiti
ng, n
o im
prov
emen
tfo
llow
ing
trea
tmen
t in
tho
se p
ositi
ve f
or H
elic
obac
ter
G5
pylo
ri.
Dys
peps
ia i
n th
e ol
der
Imag
ing
(Ba
Indi
cate
d (C
)E
ndos
copy
is
ofte
n th
e fi
rst
line
inve
stig
atio
n.pa
tient
(e.
g. o
ver
45 y
rs)
mea
l (I
I)/
How
ever
, Ba
mea
l re
mai
ns a
rea
sona
ble
alte
rnat
ive.
endo
scop
y (0
))T
he a
ltern
ativ
e in
vest
igat
ion
shou
ld b
e co
nsid
ered
whe
neve
r sy
mpt
oms
cont
inue
aft
er n
egat
ive
resu
lt.T
he m
ain
conc
ern
is t
he d
etec
tion
of e
arly
can
cer,
G6
espe
cial
ly s
ubm
ucos
al t
umou
rs.
Ulc
er f
ollo
w-u
pB
a st
udie
s (I
I)N
ot i
ndic
ated
Scar
ring
pre
clud
es a
ccur
ate
asse
ssm
ent.
End
osco
pyro
utin
ely
(B)
pref
erre
d to
con
firm
com
plet
e he
alin
g an
d to
obt
ain
biop
sies
(e.
g. H
elic
obac
ter
pylo
ri, e
tc.)
whe
re n
eces
sary
.So
me
cent
res
use
NM
stu
dies
(C
arbo
n-14
bre
ath
test
)G
7to
ass
ess
effe
ct o
f tr
eatm
ent
of H
elic
obac
ter
pylo
ri.
62
G. Gastrointestinal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Prev
ious
upp
er G
I su
rger
yW
ater
sol
uble
Indi
cate
d (B
)To
ass
ess
anas
tom
osis
and
tra
nsit
thro
ugh
to s
mal
l(r
ecen
t)co
ntra
st m
ediu
mbo
wel
.G
8st
udy
(II)
Prev
ious
upp
er G
IB
a st
udie
s (I
I)N
ot i
ndic
ated
Gas
tric
rem
nant
bes
t as
sess
ed b
y en
dosc
opy
(gas
triti
s,su
rger
y (o
ld)
rout
inel
y (B
)ul
cera
tion,
rec
urre
nt t
umou
r, et
c.).
Cro
ss-s
ectio
nal
imag
ing
(US,
CT,
etc
.) m
ay b
e ne
eded
to
asse
ssex
tram
ural
dis
ease
. End
osco
pic
US
can
dem
onst
rate
subm
ucos
al r
ecur
renc
e.
NM
(II
)Sp
ecia
lised
NM
can
pro
vide
fun
ctio
nal
data
abo
ut e
mpt
ying
.G
9in
vest
igat
ion
(B)
Inte
stin
al b
lood
los
s,B
a sm
all
bow
elN
ot i
ndic
ated
Onl
y af
ter
uppe
r an
d lo
wer
tra
ct i
mag
ing
(Ba
stud
ies
chro
nic
or r
ecur
rent
stud
y (I
I)in
itial
ly(C
)or
end
osco
py).
NM
(II
) (r
edSp
ecia
lised
Whe
n al
l ot
her
inve
stig
atio
ns a
re n
egat
ive.
cell
or
Mec
kel’s
inve
stig
atio
n (B
)st
udy)
and
/or
G10
angi
ogra
phy
(III
)
Acu
te a
bdom
inal
pai
n —
CX
R (
I) (
erec
t)In
dica
ted
(B)
Dec
ubitu
s A
XR
to
show
fre
e ai
r if
CX
R s
upin
e.pe
rfor
atio
n— o
bstr
uctio
nan
d A
XR
(II
)Su
pine
AX
R u
sual
ly s
uffi
cien
t to
est
ablis
h di
agno
sis
and
poin
t to
an
anat
omic
al l
evel
of
obst
ruct
ion.
CT
(II)
Spec
ialis
edC
onsi
der
erec
t AX
R i
f su
pine
AX
R n
orm
al a
ndIn
vest
igat
ion
(B)
stro
ng c
linic
al s
uspi
cion
of
obst
ruct
ion.
The
re i
sin
crea
sing
use
of
CT
here
– e
.g. t
o es
tabl
ish
site
and
G11
caus
e of
obs
truc
tion.
63
G. Gastrointestinal system
Smal
l bo
wel
Con
tras
t st
udie
sSp
ecia
lised
Stud
ies
with
non
-ion
ic a
gent
s ca
n de
term
ine
both
the
obst
ruct
ion
(II)
or
CT
(III
)in
vest
igat
ion
(B)
site
and
com
plet
enes
s of
obs
truc
tion.
Som
e ce
ntre
s us
eC
Tin
thi
s si
tuat
ion
whi
ch c
an d
eter
min
e le
vel
and
G12
likel
y ca
use.
Smal
l bo
wel
obs
truc
tion:
Smal
l bo
wel
Indi
cate
d (B
)Sm
all
bow
el e
nem
a is
the
exa
min
atio
n of
cho
ice.
chro
nic
or r
ecur
rent
Ba
stud
y (I
I)G
13
Smal
l bo
wel
dis
ease
Ba
smal
l bo
wel
Indi
cate
d (C
)B
a fo
llow
thr
ough
ten
ds t
o gi
ve a
low
er r
adia
tion
dose
susp
ecte
d (e
.g. C
rohn
’sst
udy
(II)
than
sm
all
bow
el e
nem
a. S
ome
cent
res
use
US
and/
ordi
seas
e)C
Tto
ass
ess
bow
el w
all.
NM
(w
hite
cel
lSp
ecia
lised
Lab
elle
d w
hite
cel
l sc
intig
raph
y re
veal
s ac
tivity
and
stud
y) (
III)
inve
stig
atio
n (B
)ex
tent
of
dise
ase.
Com
plem
enta
ry t
o B
a st
udie
s. C
TG
14an
d M
RI
rese
rved
for
com
plic
atio
ns.
64
G. Gastrointestinal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Lar
ge b
owel
tum
our
or
Ba
enem
a (I
II)
Indi
cate
d (B
)N
B:
Dou
ble
cont
rast
Ba
is o
nly
usef
ul i
f th
e bo
wel
is
infl
amm
ator
y bo
wel
prop
erly
pre
pare
d. F
urth
erm
ore
all
patie
nts
shou
lddi
seas
e: p
ain,
ble
edin
g,un
derg
o re
ctal
exa
min
atio
n to
ass
ess
suita
bilit
y fo
r B
ach
ange
in
bow
el h
abit,
enem
a an
d to
exc
lude
a l
ow r
ecta
l tu
mou
r. G
ood
etc.
prac
tice
requ
ires
a s
igm
oido
scop
y be
fore
Ba
enem
a.D
efer
Ba
enem
a fo
r se
ven
days
aft
er f
ull
thic
knes
sbi
opsy
via
a r
igid
sig
moi
dosc
ope.
Bio
psie
s ta
ken
duri
ng f
lexi
ble
sigm
oido
scop
y ar
e us
ually
sup
erfi
cial
and
the
risk
of
subs
eque
nt p
erfo
ratio
n is
low
(id
eally
a48
hou
r de
lay)
. Som
e ce
ntre
s us
e co
lono
scop
yin
itial
ly, r
eser
ving
Ba
enem
a fo
r di
ffic
ult
orin
com
plet
e ex
amin
atio
ns. S
ome
cent
res
use
CT
for
the
frai
l el
derl
y pa
tient
. Alth
ough
the
irr
itabl
e bo
wel
synd
rom
e is
the
mos
t co
mm
on c
ause
of
a ch
ange
in
bow
el h
abit,
Ba
enem
a or
col
onos
copy
is
need
ed t
oG
15ex
clud
e ot
her
caus
es.
Lar
ge b
owel
obs
truc
tion:
Ene
ma
(III
)Sp
ecia
lised
Sing
le c
ontr
ast
(ide
ally
wat
er-s
olub
le c
ontr
ast
acut
ein
vest
igat
ion
(B)
med
ium
) st
udy
can
show
nar
row
ed a
rea
and
excl
ude
‘pse
udo-
obst
ruct
ion’
. Som
e ce
ntre
s us
e C
Tw
hich
can
G16
poin
t to
the
lik
ely
caus
e.
65
G. Gastrointestinal system
Infl
amm
ator
y bo
wel
AX
R (
II)
Indi
cate
d (B
)O
ften
suf
fici
ent
for
eval
uatio
n.di
seas
e of
col
on
NM
(w
hite
cel
lIn
dica
ted
(B)
Lab
elle
d w
hite
cel
l st
udy
best
exa
m —
will
rev
eal
stud
y) (
III)
activ
ity a
nd e
xten
t of
dis
ease
.
Ba
enem
a (I
II)
Not
ind
icat
edB
a en
ema
is d
ange
rous
whe
n to
xic
meg
acol
on p
rese
nt;
rout
inel
y (B
)un
prep
ared
ene
ma
in s
elec
ted
case
s af
ter
disc
ussi
onG
17w
ith r
adio
logi
sts.
Infl
amm
ator
y bo
wel
Ba
enem
a (I
II)
Not
ind
icat
edC
olon
osco
py f
ollo
w-u
p pr
efer
red
to i
dent
ify
dise
ase
of c
olon
:ro
utin
ely
(B)
deve
lopi
ng c
arci
nom
a in
tho
se a
t hi
gh r
isk,
alth
ough
long
-ter
m f
ollo
w-u
pB
a en
ema
is s
till
ofte
n us
ed, p
artic
ular
ly a
fter
com
plex
inte
stin
al s
urge
ry. L
ikew
ise
Ba
enem
a pr
efer
red
for
G18
eval
uatin
g fi
stul
ae e
tc.
Gen
eral
ab
do
min
al p
rob
lem
sA
cute
abd
omen
pai
n;A
XR
(II
) pl
usIn
dica
ted
(B)
Loc
al p
olic
y w
ill d
eter
min
e st
rate
gy. S
upin
e A
XR
(fo
r(w
arra
ntin
g ho
spita
ler
ect
CX
R (
I)ga
s pa
ttern
, etc
.) i
s us
ually
suf
fici
ent.
Ere
ct A
XR
not
adm
issi
on a
nd s
urgi
cal
indi
cate
d ro
utin
ely.
Inc
reas
ing
use
of C
Tas
a ‘
catc
h-co
nsid
erat
ion)
all’
inve
stig
atio
n he
re. U
S w
idel
y us
ed a
s a
G19
prel
imin
ary
surv
ey.
66
G. Gastrointestinal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Palp
able
mas
sA
XR
(II
)N
ot i
ndic
ated
rout
inel
y (C
)
US
(0)
Indi
cate
d (B
)U
S us
ually
sol
ves
the
prob
lem
and
is
very
rel
iabl
e in
thin
pat
ient
s, r
ight
upp
er q
uadr
ant
and
pelv
is.
G20
CT
(III
)In
dica
ted
(A)
CT
is a
n al
tern
ativ
e an
d us
eful
to
excl
ude
a le
sion
;pa
rtic
ular
ly g
ood
in f
at p
atie
nts.
Mal
abso
rbtio
nB
a st
udy
ofN
ot i
ndic
ated
Imag
ing
is n
ot r
equi
red
for
the
diag
nosi
s of
coe
liac
smal
l bo
wel
(II
)ro
utin
ely
(B)
dise
ase
but
may
be
indi
cate
d fo
r je
juna
l di
vert
icul
osis
or w
hen
biop
sy i
s no
rmal
/equ
ivoc
al. C
Tm
ay b
e be
tter
if l
ymph
oma
susp
ecte
d.
NM
(I)
Spec
ialis
edN
umer
ous
NM
inv
estig
atio
ns a
vaila
ble
whi
ch s
houl
din
vest
igat
ion
(B)
esta
blis
h pr
esen
ce o
f m
alab
sorp
tion.
Som
e of
the
se a
reG
21no
n-ra
diol
ogic
al (
e.g.
bre
ath
test
).
App
endi
citis
Imag
ing
Spec
ialis
edW
ide
rang
e of
pol
icy
vary
ing
acco
rdin
gly
to l
ocal
inve
stig
atio
n (C
)av
aila
bilit
y of
equ
ipm
ent
and
expe
rtis
e an
d th
e bo
dyha
bitu
s of
the
pat
ient
.App
endi
citis
is
usua
lly a
clin
ical
dia
gnos
is. I
mag
ing
(e.g
. US
with
gra
ded
com
pres
sion
) ca
n he
lp i
n eq
uivo
cal
case
s or
in
diff
eren
tiatio
n fr
om g
ynae
colo
gica
l le
sion
s. S
o to
o ca
nN
M (
whi
te c
ell
stud
y) a
nd f
ocus
ed a
ppen
dix
CT
(FA
CT
). U
S re
com
men
ded
in c
hild
ren
and
youn
gG
22w
omen
.
67
G. Gastrointestinal system
Con
stip
atio
nA
XR
(II
)N
ot i
ndic
ated
Man
y no
rmal
adu
lts s
how
ext
ensi
ve f
aeca
l m
ater
ial;
rout
inel
y (C
)al
thou
gh t
his
may
be
rela
ted
to p
rolo
nged
tra
nsit
time
it is
im
poss
ible
to
asse
ss s
igni
fica
nce
on A
XR
alo
ne.
(for
chi
ldre
nB
ut A
XR
can
hel
p ce
rtai
n sp
ecia
lists
(e.
g.se
e Se
ctio
n M
)G
23ge
riat
rici
ans)
in
refr
acto
ry c
ases
.
Abd
omin
al s
epsi
s;
US
(0)
or C
TIn
dica
ted
(C)
Seek
rad
iolo
gica
l ad
vice
; m
uch
depe
nds
on l
ocal
pyre
xia
of u
nkno
wn
orig
in(I
II)
or N
M (
III)
avai
labi
lity
and
expe
rtis
e. U
S of
ten
used
fir
st (
spee
d,(P
UO
)co
st)
and
may
be
defi
nitiv
e, p
artic
ular
ly w
hen
ther
ear
e lo
calis
ing
sign
s; e
spec
ially
goo
d fo
rsu
bphr
enic
/sub
hepa
tic s
pace
s an
d pe
lvis
. CT
prob
ably
best
tes
t ov
eral
l: in
fect
ion
and
tum
our
usua
llyid
entif
ied
and
excl
uded
. Als
o al
low
s bi
opsy
of
node
sor
tum
our
and
drai
nage
of
colle
ctio
ns (
espe
cial
lyre
cent
pos
t-op
erat
ive)
. NM
par
ticul
arly
goo
d w
hen
ther
e ar
e no
loc
alis
ing
feat
ures
: la
belle
d W
BC
goo
dfo
r ch
roni
c po
st-o
pera
tive
seps
is;
galli
um w
illac
cum
ulat
e at
site
s of
tum
our
(e.g
. lym
phom
a) a
ndG
24in
fect
ion.
68
G. Gastrointestinal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Live
r, g
allb
lad
der
an
d p
ancr
eas
Hep
atic
met
asta
ses
US
(0)
Indi
cate
d (B
)T
he m
ajor
ity o
f m
etas
tase
s w
ill b
e de
mon
stra
ted
byU
S w
hich
als
o al
low
s bi
opsy
. US
shou
ld b
e th
e in
itial
inve
stig
atio
n bu
t m
etas
tase
s m
ay s
how
the
sam
ere
flec
tivity
as
the
hepa
tic p
aren
chym
a an
d th
us b
eC
T(I
I) o
rSp
ecia
lised
mis
sed.
CT
/MR
I us
ed f
or f
urth
er e
xclu
sion
, whe
re U
SM
RI
(0)
inve
stig
atio
n (B
)eq
uivo
cal
or s
urpr
isin
gly
norm
al a
nd w
here
ful
lst
agin
g is
nee
ded
or h
epat
ic r
esec
tion
is p
lann
ed (
see
also
Can
cer
L13
). R
ecen
t in
tere
st i
n du
al-p
hase
spi
ral
CT.
MR
I be
ing
incr
easi
ngly
use
d he
re. S
ome
rece
ntG
25in
tere
st i
n N
M (
som
atos
tatin
ana
logu
es a
nd P
ET
).
Hep
atic
hae
man
giom
aM
RI
(0)
orIn
dica
ted
(B)
MR
I, C
Tan
d N
M r
elia
bly
show
fur
ther
cha
ract
eris
tic(e
.g. o
n U
S)C
T(I
II)
feat
ures
of
haem
angi
oma
and
man
y ot
her
solit
ary
hepa
tic l
esio
ns.
NM
(re
d ce
llSp
ecia
lised
G26
stud
y) (
III)
inve
stig
atio
n (B
)
Jaun
dice
US
(0)
Indi
cate
d (B
)Se
nsiti
ve f
or b
ile d
uct
dila
tatio
n. B
ut d
ilata
tion
may
be s
ubtle
in
earl
y ob
stru
ctio
n an
d sc
lero
sing
chol
angi
tis. S
how
s ga
llsto
nes
and
mos
t fo
rms
ofhe
patic
dis
ease
. US
also
sho
ws
the
leve
l an
d ca
use
ofan
y ob
stru
ctio
n to
com
mon
bile
duc
t. D
iscu
sssu
bseq
uent
inv
estig
atio
ns (
CT,
ER
CP,
MR
CP,
etc
.)G
27w
ith r
adio
logi
st.
69
G. Gastrointestinal system
Bili
ary
dise
ase,
AX
R (
II)
Not
ind
icat
edPl
ain
XR
s on
ly s
how
abo
ut 1
0%
of
galls
tone
s.(e
.g. g
alls
tone
s)ro
utin
ely
(C)
US
(0)
Indi
cate
d (B
)U
S al
low
s ev
alua
tion
of o
ther
org
ans
too.
Cho
lecy
stog
raph
y is
now
rar
ely
need
ed (
e.g.
poo
rvi
ews
at U
S). C
T/e
ndos
copy
may
be
need
ed f
orfu
rthe
r de
linea
tion.
Inc
reas
ing
inte
rest
in
MR
CP.
NM
(II
)Sp
ecia
lised
Bili
ary
scin
tigra
phy
show
s cy
stic
duc
t ob
stru
ctio
n in
G28
inve
stig
atio
n (B
)ac
ute
chol
ecys
titis
. Als
o us
eful
in
chro
nic
chol
ecys
titis
.
Panc
reat
itis:
acu
teA
XR
(II
)N
ot i
ndic
ated
Unl
ess
diag
nosi
s in
dou
bt;
then
AX
R n
eede
d to
rout
inel
y (C
)ex
clud
e ot
her
caus
es o
f ac
ute
abdo
men
pai
n (s
eeG
19).
Som
e pa
tient
s pr
esen
ting
with
acu
te p
ancr
eatit
isha
ve u
nder
lyin
g ch
roni
c pa
ncre
atiti
s w
hich
may
cau
seca
lcif
icat
ion
evid
ent
on A
XR
.
US
(0)
Indi
cate
d (B
)To
sho
w g
alls
tone
s an
d to
dia
gnos
e an
d fo
llow
pseu
docy
st d
evel
opm
ent,
espe
cial
ly g
ood
in t
hin
patie
nts.
70
G. Gastrointestinal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
CT
(III
) or
Not
ind
icat
edR
eser
ved
for
clin
ical
ly s
ever
e ca
ses
(to
asse
ss e
xten
tM
RI
(0)
rout
inel
y (B
)of
nec
rosi
s), i
n pa
tient
s w
ho d
o no
t im
prov
e on
trea
tmen
t or
if
ther
e is
unc
erta
inty
as
to t
he d
iagn
osis
.C
Tca
n he
lp p
redi
ct m
orbi
dity
and
mor
talit
y. S
ome
cent
res
use
MR
I, e
spec
ially
if
repe
ated
fol
low
-up
G29
likel
y.
Panc
reat
itis:
chr
onic
AX
R (
II)
Indi
cate
d (B
)To
sho
w c
alci
fica
tion.
US
(0)
orIn
dica
ted
(B)
US
may
be
defi
nitiv
e in
thi
n pa
tient
s; C
Tw
ill s
how
CT
(IV
)ca
lcif
icat
ion
to g
ood
effe
ct.
ER
CP
(II)
or
Spec
ialis
edE
RC
Psh
ows
duct
mor
phol
ogy,
but
con
side
rabl
e ri
skG
30M
RC
P(0
)in
vest
igat
ion
(C)
of a
cute
pan
crea
titis
. Hen
ce c
urre
nt i
nter
est
in M
RC
P.
Post
-ope
rativ
e bi
liary
lea
kN
M (
II)
Indi
cate
d (C
)U
S w
ill u
sual
ly h
ave
show
n th
e an
atom
y of
the
colle
ctio
ns, e
tc. N
M s
tudy
(H
IDA
) w
ill s
how
act
ivity
at s
ite o
f le
ak. M
RC
Pal
so u
sed
here
. ER
CP
will
sho
wth
e an
atom
y of
the
lea
k an
d m
ay a
llow
int
erve
ntio
nG
31(e
.g. s
tent
).
Panc
reat
ic t
umou
rU
S (0
)In
dica
ted
(B)
Esp
ecia
lly i
n th
in p
atie
nts
and
for
lesi
ons
in t
he h
ead
CT
(III
)an
d bo
dy. I
ncre
asin
g us
e of
end
osco
pic
and
or M
RI
(0)
lapa
rosc
opic
US.
CT
(or
MR
I) g
ood
in t
he f
atte
rpa
tient
and
whe
re U
S eq
uivo
cal
or w
here
pre
cise
stag
ing
need
ed. E
RC
P/M
RC
Pm
ay a
lso
be i
ndic
ated
.N
M (
eg P
ET
) m
ay h
elp
dist
ingu
ish
carc
inom
a fr
omG
32pa
ncre
atiti
s.
71
G. Gastrointestinal system
Insu
linom
aIm
agin
gSp
ecia
lised
Whe
n bi
oche
mic
al t
ests
are
con
vinc
ing.
MR
Iem
ergi
ng a
s th
e be
st e
xam
inat
ion
alth
ough
art
eria
lph
ase
spir
al C
Tpr
omis
ing.
Mos
t ce
ntre
s se
ek t
wo
posi
tive
inve
stig
atio
ns b
efor
e su
rger
y (o
ut o
fC
T/N
M/M
RI
/ang
iogr
aphy
). E
ndos
copi
c an
d in
tra-
G33
oper
ativ
e U
S al
so u
sefu
l.
72
G. Gastrointestinal systemC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
H.
Uro
logi
cal,
ad
ren
al a
nd
gen
ito
-uri
nar
y sy
stem
s
Hae
mat
uria
mac
ro-
US
(0)
+A
XR
In
dica
ted
(B)
The
re i
s a
wid
e va
riat
ion
in l
ocal
pol
icy.
Im
agin
gor
mic
rosc
opic
(II)
or
IVU
(II
)st
rate
gies
sho
uld
be a
gree
d w
ith t
he l
ocal
neph
rolo
gist
s an
d ur
olog
ists
. In
man
y ce
ntre
sU
S+
AX
R a
re t
he i
nitia
l st
udie
s, b
ut i
f ne
gativ
e, I
VU
is s
till
indi
cate
d in
pat
ient
s w
ith c
ontin
uing
mac
rosc
opic
hae
mat
uria
or
in t
he o
ver
40s
with
mic
rosc
opic
hae
mat
uria
. Con
vers
ely,
pat
ient
s in
who
mIV
U a
nd c
ysto
scop
y ar
e no
rmal
who
con
tinue
to
blee
dsh
ould
und
ergo
US,
as
IVU
can
fai
l to
sho
w a
ren
altu
mou
r an
d U
S w
ill o
ccas
iona
lly d
emon
stra
te a
H1
blad
der
lesi
on n
ot s
een
at c
ysto
scop
y. I
ncre
asin
g us
eof
CT.
Hyp
erte
nsio
n (w
ithou
tIV
U (
II)
Not
ind
icat
edIV
U i
s in
sens
itive
for
ren
al a
rter
y st
enos
is. S
ee H
3.ev
iden
ce o
f re
nal
dise
ase)
rout
inel
y (A
)H
2
Hyp
erte
nsio
n: i
n th
eU
S (0
) ki
dney
sIn
dica
ted
(B)
To a
sses
s re
lativ
e re
nal
size
and
par
ench
ymal
pat
tern
.yo
ung
adul
t or
in
patie
nts
Dop
pler
US
is n
ot s
ensi
tive
enou
gh f
or u
se a
s a
unre
spon
sive
to
med
icat
ion
scre
enin
g to
ol.
NM
(II
)In
dica
ted
(B)
Cap
topr
il re
nogr
aphy
is
an e
stab
lishe
d m
etho
d of
reno
gram
dete
rmin
ing
func
tiona
lly s
igni
fica
ntre
nal
arte
ryst
enos
is.
73
H. Urological systems
Ang
iogr
aphy
Spec
ialis
edTo
sho
w s
teno
sis
if s
urge
ry o
r an
giop
last
y is
(D
SA(I
II),
inve
stig
atio
n (C
)co
nsid
ered
as
a po
ssib
le t
reat
men
t.C
TA(I
II)
orH
3M
RA
(0))
Ren
al f
ailu
reU
S (0
)+
Indi
cate
d (B
)Fo
r re
nal
size
, str
uctu
re, o
bstr
uctio
n, e
tc. N
B:
aA
XR
(II
)no
rmal
US
does
not
exc
lude
obs
truc
tion.
NM
(II
)In
dica
ted
(B)
Whe
n ap
prop
riat
e, r
enog
raph
y ca
n as
sess
ren
alH
4pe
rfus
ion,
fun
ctio
n an
d ob
stru
ctio
n.
Ren
al c
olic
, loi
n pa
inIV
U (
II)
or U
S In
dica
ted
(B)
Imag
ing
shou
ld b
e pe
rfor
med
as
an e
mer
genc
y(0
) an
d A
XR
(II
)ex
amin
atio
n w
hils
t th
e pa
in i
s pr
esen
t, as
rad
iolo
gica
lor
CT
(III
)si
gns
disa
ppea
r ra
pidl
y af
ter
pass
age
of a
sto
ne.
Del
ayed
film
s (u
p to
24
hrs)
may
be
need
ed t
o sh
owth
e si
te o
f ob
stru
ctio
n. A
plai
n A
XR
on
its o
wn
is o
flit
tle v
alue
. Bot
h C
Tan
d U
S ar
e in
crea
sing
ly
bein
g us
ed, e
spec
ially
in
thos
e w
ith c
ontr
aind
icat
ions
H5
to c
ontr
ast
med
ium
.
Ren
al c
alcu
li (i
n th
eU
S (0
)+
Indi
cate
d (C
)A
XR
alo
ne m
ay b
e ap
prop
riat
e fo
llow
-up
for
prev
ious
lyab
senc
e of
acu
te c
olic
)A
XR
(II
)de
mon
stra
ted
calc
uli
afte
r an
unc
ompl
icat
ed a
cute
atta
ck. A
n IV
U m
ay b
e re
quir
ed b
efor
e tr
eatm
ent
tosh
ow a
nato
my.
NM
may
be
need
ed t
o de
term
ine
H6
rela
tive
func
tion.
74
H. Urological systemsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Ren
al m
ass
US
(0)
Indi
cate
d (B
)U
S is
goo
d at
dis
tingu
ishi
ng b
etw
een
cyst
ic a
nd s
olid
mas
ses.
AX
R (
II)
+N
ot i
ndic
ated
CT
or M
RI
pref
erab
le f
or f
urth
er e
valu
atio
n. N
M m
ayH
7IV
U (
II)
rout
inel
y (C
)be
nee
ded
to d
eter
min
e re
lativ
e fu
nctio
n.
Pros
tatis
mU
S 0)
Indi
cate
d (B
)U
S ca
n al
so a
sses
s up
per
trac
t an
d bl
adde
r vo
lum
esIV
U (
II)
Not
ind
icat
edbe
fore
and
aft
er v
oidi
ng, p
refe
rabl
y w
ith f
low
rat
es. I
tH
8ro
utin
ely
(B)
can
also
sho
w b
ladd
er c
alcu
li.
Pros
tatic
mal
igna
ncy
US
(0)
Spec
ialis
edT
rans
rect
al U
S w
ith g
uide
d bi
opsi
es a
fter
clin
ical
H9
inve
stig
atio
n (B
)ex
amin
atio
n. S
ome
inte
rest
in
MR
I an
d PE
The
re.
Uri
nary
ret
entio
nU
S (0
)In
dica
ted
(C)
US
to e
valu
ate
the
uppe
r tr
acts
(af
ter
cath
eter
isat
ion
IVU
(II
)N
ot i
ndic
ated
and
relie
f of
bla
dder
dis
tens
ion)
, par
ticul
arly
if
urea
H10
rout
inel
y (C
)le
vels
rem
ain
rais
ed.
Scro
tal
mas
s or
pai
nU
S (0
)In
dica
ted
(B)
Allo
ws
diff
eren
tiatio
n of
tes
ticul
ar f
rom
ext
ra-
H11
test
icul
ar l
esio
ns.
Test
icul
ar t
orsi
onU
S (0
)Sp
ecia
lised
Tors
ion
is u
sual
ly a
clin
ical
dia
gnos
is. I
mag
ing
inve
stig
atio
n (C
)in
vest
igat
ions
mus
t no
t de
lay
the
prio
rity
tha
t m
ust
begi
ven
to s
urgi
cal
expl
orat
ion.
Dop
pler
US
can
be u
sed,
whe
n cl
inic
al f
indi
ngs
are
equi
voca
l in
the
pos
tpu
bert
al t
estis
.
NM
(II
)Sp
ecia
lised
NM
tec
hniq
ues
can
assi
st w
ith t
his
diag
nosi
s bu
tH
12in
vest
igat
ion
(C)
prom
pt r
esul
ts e
ssen
tial.
75
H. Urological systems
Uri
nary
tra
ct i
nfec
tion
US
(0)
+N
ot i
ndic
ated
The
maj
ority
do
not
need
inv
estig
atio
n un
less
the
rein
adu
ltsA
XR
(II
) or
rout
inel
y (C
)ar
e re
curr
ent
infe
ctio
ns, r
enal
col
ic o
r fa
ilure
to
IVU
(II
)re
spon
d to
ant
ibio
tics.
Slig
htly
low
er t
hres
hold
to
(for
chi
ldre
n se
ein
vest
igat
e m
ale
patie
nts.
Sect
ion
M)
H13
NB
:T
his
does
not
app
ly t
o ch
ildre
n.
Adr
enal
med
ulla
ryC
T(I
II)
orSp
ecia
lised
Whi
lst
US
may
ide
ntif
y le
sion
s of
thi
s ty
pe, C
Tan
dtu
mou
rsM
RI
(0)
inve
stig
atio
n (B
)M
RI
prov
ide
the
best
ana
tom
ical
del
inea
tion.
Im
agin
gis
rar
ely
indi
cate
d in
the
abs
ence
of
bioc
hem
ical
evid
ence
of
such
tum
ours
.
NM
(II
)Sp
ecia
lised
MIB
G l
ocat
es f
unct
ioni
ng t
umou
rs a
nd i
s pa
rtic
ular
lyH
14in
vest
igat
ion
(B)
usef
ul f
or e
ctop
ic s
ites
and
met
asta
ses.
Adr
enal
cor
tical
les
ions
,C
T(I
II),
NM
Spec
ialis
edL
ocal
adv
ice
on t
he m
ost
appr
opri
ate
exam
inat
ion
Cus
hing
’s a
nd C
onn’
s(I
V)
or M
RI
(0)
inve
stig
atio
n (B
)sh
ould
be
soug
ht. B
oth
CT
and
MR
I ca
n di
ffer
entia
tedi
seas
e an
d sy
ndro
me
betw
een
the
diff
eren
t le
sion
s. N
M c
an d
istin
guis
hbe
twee
n fu
nctio
ning
and
non
-fun
ctio
ning
ade
nom
as.
H15
So t
oo c
an v
ario
us M
RI
tech
niqu
es.
76
H. Urological systemsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
I. O
bst
etri
cs a
nd
gyn
aeco
logy
NB
:T
rans
vagi
nal
(TV
) U
S eq
uipm
ent
shou
ld b
e av
aila
ble
in a
ll de
part
men
ts p
erfo
rmin
g pe
lvic
US
Scre
enin
g in
pre
gnan
cyU
S (0
)In
dica
ted
(C)
Scre
enin
g U
S ha
s no
t be
en s
how
n to
alte
r pe
rina
tal
mor
talit
y, e
xcep
t w
here
sel
ectiv
e te
rmin
atio
n of
preg
nanc
y is
app
lied
in t
he p
rese
nce
of g
ross
foe
tal
abno
rmal
ity. I
t do
es p
rovi
de u
sefu
l in
form
atio
n ab
out
datin
g an
d m
ultip
le p
regn
anci
es. U
S is
als
o of
pro
ven
valu
e in
ass
essi
ng p
lace
nta
prae
via
and
intr
a-ut
erin
egr
owth
. In
the
spec
ialis
t ca
re o
f hi
gh-r
isk
preg
nanc
ies,
Dop
pler
US
of t
he u
mbi
lical
art
ery
assi
sts
man
agem
ent.
The
re i
s w
ide
vari
atio
n in
the
use
of
I1ob
stet
ric
US
in d
iffe
rent
cou
ntri
es.
Susp
ecte
d pr
egna
ncy
US
(0)
Not
ind
icat
edPr
egna
ncy
test
ing
mos
t ap
prop
riat
e. U
S va
luab
leI2
rout
inel
y (C
)w
here
mol
ar p
regn
ancy
sus
pect
ed.
Susp
ecte
d ec
topi
cU
S (0
)In
dica
ted
(B)
Aft
er p
ositi
ve p
regn
ancy
tes
t. T
VU
S pr
efer
red.
preg
nanc
yI3
Col
our
flow
Dop
pler
inc
reas
es s
ensi
tivity
.
Poss
ible
non
-via
ble
US
(0)
Indi
cate
d (C
)R
epea
t U
S af
ter
a w
eek
may
be
need
ed (
espe
cial
lypr
egna
ncy
whe
n ge
stat
iona
l sa
c <
20
mm
or
crow
n ru
mp
leng
th<
6 m
m).
Pre
gnan
cy t
est
requ
ired
. Whe
re d
oubt
exi
sts
abou
t th
e vi
abili
ty o
f a
preg
nanc
y, d
elay
in
evac
uatio
nI4
of t
he u
teru
s is
ess
entia
l.
77
I. Obstetrics and gynaecology
Susp
ecte
d pe
lvic
mas
sU
S (0
)In
dica
ted
(C)
Com
bina
tion
of t
rans
-abd
omin
al a
nd T
VU
S of
ten
requ
ired
. US
shou
ld c
onfi
rm a
les
ion’
s pr
esen
ce a
ndde
term
ine
likel
y or
gan
of o
rigi
n. S
ee C
ance
r Se
ctio
nL
. MR
I is
the
bes
t se
cond
lin
e in
vest
igat
ion,
alth
ough
I5C
Tst
ill w
idel
y us
ed.
Pelv
ic p
ain,
inc
ludi
ngU
S (0
)In
dica
ted
(C)
Esp
ecia
lly w
hen
clin
ical
exa
min
atio
n di
ffic
ult
orsu
spec
ted
pelv
icim
poss
ible
.in
flam
mat
ory
dise
ase
and
susp
ecte
d en
dom
etri
osis
MR
I (0
)Sp
ecia
lised
Can
be
usef
ul t
o lo
calis
e th
e la
rger
foc
i of
I6in
vest
igat
ion
(B)
endo
met
rios
is.
Los
t IU
CD
US
(0)
Indi
cate
d (C
)
AX
R (
II)
Not
ind
icat
edU
nles
s IU
CD
is
not
seen
in
uter
us o
n U
S.I7
rout
inel
y (C
)
Rec
urre
nt m
isca
rria
ges
US
(0)
Indi
cate
d (C
)W
ill s
how
the
maj
or c
onge
nita
l an
d ac
quir
edpr
oble
ms.
MR
I (0
)Sp
ecia
lised
Supp
lem
ents
US
for
uter
ine
anat
omy.
Som
e ce
ntre
sI8
inve
stig
atio
n (C
)us
e hy
ster
osal
ping
ogra
phy.
78
I. Obstetrics and gynaecologyC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Infe
rtili
tyU
S (0
)In
dica
ted
(C)
For
folli
cle-
trac
king
dur
ing
trea
tmen
t. Fo
r as
sess
men
tof
tub
al p
aten
cy. S
ome
cent
res
use
MR
I an
d/or
I9hy
ster
osal
ping
ogra
phy.
Susp
ecte
d ce
phal
opel
vic
XR
(II
)N
ot i
ndic
ated
The
nee
d fo
r pe
lvim
etry
is
incr
easi
ngly
bei
ngdi
spro
port
ion
Pel
vim
etry
rout
inel
y (B
)qu
estio
ned.
Loc
al p
olic
y sh
ould
be
dete
rmin
ed i
nag
reem
ent
with
obs
tetr
icia
ns. F
urth
erm
ore
MR
I or
CT
MR
I (0
) or
Spec
ialis
edsh
ould
be
used
whe
reve
r po
ssib
le. M
RI
is b
est
as i
tC
T(I
I)in
vest
igat
ion
(C)
avoi
ds x
-irr
adia
tion.
CT
gene
rally
off
ers
a lo
wer
dos
eI1
0th
an s
tand
ard
XR
pel
vim
etry
.
79
I. Obstetrics and gynaecology
J. B
reas
t d
isea
seA
sym
pto
mat
ic p
atie
nts
Bre
ast
scre
enin
gM
amm
ogra
phy
Var
ious
Var
ious
str
ateg
ies
have
bee
n ad
opte
d in
dif
fere
ntJ1
–4(I
)in
dica
tions
coun
trie
s. T
his
topi
c is
not
con
side
red
furt
her.
Fam
ily h
isto
ry o
f br
east
Mam
mog
raph
ySp
ecia
lised
A
t pr
esen
t th
ere
is n
o ev
iden
ce o
f be
nefi
t bu
t th
ere
isca
ncer
(I)
exam
inat
ion
(C)
som
e ev
iden
ce o
f ha
rm. S
cree
ning
sho
uld
only
be
cont
empl
ated
aft
er g
enet
ic r
isk
asse
ssm
ents
and
appr
opri
ate
coun
selli
ng a
s to
the
ris
ks a
nd u
npro
ven
bene
fits
. Con
sens
us a
t th
e m
omen
t is
tha
t sc
reen
ing
shou
ld o
nly
be c
onte
mpl
ated
whe
n th
e lif
etim
e ri
sk o
fbr
east
can
cer
is g
reat
er t
han
2.5
times
ave
rage
. Uni
tssh
ould
col
lect
and
aud
it th
eir
wor
k. T
his
topi
c is
bei
ngri
goro
usly
dis
cuss
ed a
t th
e pr
esen
t tim
e. F
urth
erev
alua
tion
is u
sual
ly o
btai
ned
by U
S, N
M a
nd M
RI
J5ac
cord
ing
to l
ocal
exp
ertis
e an
d av
aila
bilit
y.
Wom
en <
50
yrs
havi
ngM
amm
ogra
phy
Not
ind
icat
edA
met
a-an
alys
is h
as s
how
n w
omen
< 5
0 yr
s w
ho h
ave
or b
eing
con
side
red
for
(I)
rout
inel
y (A
)re
ceiv
ed H
RT
for
> 1
1 yr
s ar
e no
t at
inc
reas
ed r
isk
ofH
RT
brea
st c
ance
r co
mpa
red
to a
pee
r gr
oup.
Wom
en o
nH
RT
50 y
rs a
nd o
ver
can
be a
ppro
pria
tely
mon
itore
dJ6
by b
reas
t sc
reen
ing
prog
ram
mes
.
80
J. Breast diseaseC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Asy
mpt
omat
ic w
omen
Mam
mog
raph
yB
est
cons
ider
ed a
s pa
rt o
f w
hate
ver
natio
nal
brea
stw
ith a
ugm
enta
tion
(I)
scre
enin
g po
licy
appl
ies
(see
J1–
4).
mam
mop
last
yJ7
Sym
pto
mat
ic p
atie
nts
Clin
ical
sus
pici
on o
fM
amm
ogra
phy
Indi
cate
d (B
)R
efer
ral
to a
bre
ast
clin
ic s
houl
d pr
eced
e an
ybr
east
can
cer
(dia
gnos
is)
(I),
radi
olog
ical
inv
estig
atio
n.
US
(0)
Spec
ialis
edM
amm
ogra
phy
±U
S sh
ould
be
used
in
the
cont
ext
ofin
vest
igat
ion
(B)
trip
le a
sses
smen
t —
i.e
. clin
ical
exa
min
atio
n, i
mag
ing
and
cyto
logy
/bio
psy.
Ultr
asou
nd c
an r
eadi
ly d
irec
tbi
opsy
.
NM
(II
I) o
rSp
ecia
lised
NM
or
MR
I so
met
imes
a u
sefu
l ad
junc
t to
tri
ple
J8M
RI
(0)
inve
stig
atio
n (B
)as
sess
men
t of
an
equi
voca
l le
sion
.
Gen
eral
ised
lum
pine
ss,
Mam
mog
raph
yN
ot i
ndic
ated
In t
he a
bsen
ce o
f ot
her
sign
s su
gges
tive
ofge
nera
lised
bre
ast
pain
,(I
) or
US
(0)
rout
inel
y (C
)m
alig
nanc
y, i
mag
ing
is u
nlik
ely
to i
nflu
ence
or t
ende
rnes
s, o
rm
anag
emen
t. Fo
cal,
rath
er t
han
gene
ralis
ed p
ain
may
long
stan
ding
nip
ple
war
rant
inv
estig
atio
n.re
trac
tion
J9
Cyc
lical
mas
talg
iaM
amm
ogra
phy
Not
ind
icat
edIn
the
abs
ence
of
othe
r cl
inic
al s
igns
sug
gest
ive
of(I
)ro
utin
ely
(B)
mal
igna
ncy
and
loca
lised
pai
n, i
nves
tigat
ion
isJ1
0un
likel
y to
inf
luen
ce m
anag
emen
t.
81
J. Breast disease
Aug
men
tatio
nU
S (0
)In
dica
ted
(B)
The
ass
essm
ent
of i
nteg
rity
of
brea
st i
mpl
ants
or
mam
mop
last
yco
inci
dent
mas
ses
requ
ires
spe
cial
ist
skill
s an
dfa
cilit
ies.
MR
I (0
) or
Spec
ialis
edM
RI
is n
ow a
n es
tabl
ishe
d in
vest
igat
ion
for
impl
ant
NM
(II
I)in
vest
igat
ion
(B)
leak
age.
It
can
also
sho
w t
umou
rs.
Scin
timam
mog
raph
y an
d PE
Tal
so h
ave
a ro
le w
hen
J11
othe
r in
vest
igat
ions
are
unh
elpf
ul.
Page
t’s d
isea
se o
f th
eM
amm
ogra
phy
Indi
cate
d (C
)T
he p
reva
lenc
e of
coe
xist
ent
brea
st c
ance
r va
ries
in
nipp
le(I
)pu
blis
hed
stud
ies,
but
its
ass
ocia
tion
is c
lear
and
J12
just
ifie
s sp
ecia
list
refe
rral
.
Bre
ast
infl
amm
atio
nU
S (0
)In
dica
ted
(B)
US
can
dist
ingu
ish
betw
een
an a
bsce
ss r
equi
ring
drai
nage
and
dif
fuse
inf
lam
mat
ion,
and
can
gui
deas
pira
tion
whe
n ap
prop
riat
e. M
amm
ogra
phy
may
be
J13
of v
alue
whe
re m
alig
nanc
y is
pos
sibl
e.
82
J. Breast diseaseC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Bre
ast
canc
erB
reas
t/ax
illa
Spec
ialis
edT
he r
ole
of s
entin
el n
ode
scin
tigra
phy
and
loca
lisat
ion
Stag
ing:
axi
llabr
east
NM
inve
stig
atio
n (C
)is
cur
rent
ly b
eing
eva
luat
ed.
axil
la (
III)
Stag
ing:
gen
eral
NM
ske
leta
lIn
dica
ted
(B)
For
patie
nts
with
a p
rim
ary
tum
our
>2c
m a
nd t
hose
(II)
with
bon
e pa
in.
US
live
r (0
)N
ot r
outin
ely
J14
indi
cate
d (C
)
Bre
ast
canc
erM
amm
ogra
phy
Indi
cate
d (A
)Pr
inci
ples
of
trip
le a
sses
smen
t ap
ply.
For
loc
oreg
iona
lFo
llow
-up
(sur
veill
ance
)(I
)re
curr
ence
, NM
sci
ntim
amm
ogra
phy
and
MR
I ha
ve a
J15
role
.
83
J. Breast disease
K.
Trau
ma
Hea
d:
gen
eral
Hea
d in
jury
:Pr
otoc
ols
for
man
agem
ent
of h
ead
inju
ries
are
con
stan
tly u
nder
rev
iew
and
will
var
y ac
cord
ing
to l
ocal
avai
labi
lity
of C
T, d
ista
nces
inv
olve
d in
tra
nspo
rtat
ion
to n
euro
surg
ical
cen
tres
, etc
. The
rec
omm
enda
tions
give
n he
re m
ay n
eed
to b
e ad
apte
d fo
llow
ing
cons
ulta
tion
with
the
neu
rosu
rgic
al c
entr
e fo
r yo
ur a
rea
in t
helig
ht o
f lo
cal
circ
umst
ance
s an
d po
licie
s.
The
key
man
agem
ent
and
clin
ical
que
stio
ns i
n he
ad i
njur
y ar
e:
Clin
ical
:Is
the
re e
vide
nce
of b
rain
inj
ury?
Is t
here
evi
denc
e of
int
racr
ania
l ha
emor
rhag
e or
rai
sed
intr
acra
nial
pre
ssur
e?Is
the
re c
lini
cal
evid
ence
of
a sk
ull
frac
ture
and
, if
so, i
s it
dep
ress
ed?
Are
oth
er s
yste
ms/
area
s in
volv
ed?
Man
agem
ent:
Doe
s th
e pa
tien
t ne
ed a
dmis
sion
to
hosp
ital
for
obs
erva
tion
?Is
CT
requ
ired
?Is
a n
euro
surg
ical
opi
nion
req
uire
d?
The
se q
uest
ions
und
erlin
e ke
y po
licie
s co
ncer
ning
man
agem
ent
of p
atie
nts.
Dec
isio
ns a
bout
im
agin
g re
quir
emen
tsca
nnot
be
sepa
rate
d fr
om n
on-i
mag
ing
issu
es s
uch
as a
dmis
sion
.
84
K. Trauma
The
usu
al i
ndic
atio
ns f
or a
dmis
sion
inc
lude
: co
nfus
ion
or d
epre
ssed
con
scio
usne
ss;
frac
ture
on
SXR
; ne
urol
ogic
al s
ympt
oms
or s
igns
; se
izur
es;
CSF
or
bloo
d fr
om n
ose
or e
ar;
coag
ulat
ion
diso
rder
s; l
ack
of a
dult
supe
rvis
ion
at h
ome;
pat
ient
dif
ficu
lt to
asse
ss (
non-
acci
dent
al i
njur
y (N
AI)
, dru
gs, a
lcoh
ol, e
tc.)
. If
a de
cisi
on i
s m
ade
to a
dmit
for
obse
rvat
ion,
im
agin
g be
com
es l
ess
urge
nt, a
nd t
he p
atie
nt w
ill b
e be
tter
exam
ined
whe
n so
ber
and
mor
e co
oper
ativ
e. C
Tis
inc
reas
ingl
y be
ing
used
as
the
firs
tin
vest
igat
ion
in t
hose
whe
re t
here
is
a m
ediu
m r
isk
of i
ntra
cran
ial
inju
ry, i
n w
hich
cas
e SX
R i
s us
ually
unn
eces
sary
.D
iffi
culti
es w
ith i
mag
e in
terp
reta
tion
or t
he m
anag
emen
t of
the
pat
ient
may
be
reso
lved
by
refe
rral
s vi
a im
age
tran
sfer
syst
ems
to d
esig
nate
d ne
uros
cien
ce c
entr
es.
Intr
acra
nial
abn
orm
alit
ies
sugg
esti
ng n
eed
for
urge
nt n
euro
surg
ical
man
agem
ent
incl
ude:
Hig
h or
mix
ed a
ttenu
atio
n in
trac
rani
al l
esio
nSh
ift
of m
id-l
ine
stru
ctur
es (
e.g.
thi
rd v
entr
icle
)O
blite
ratio
n of
thi
rd v
entr
icle
Rel
ativ
e di
lata
tion
of a
lat
eral
ven
tric
le(s
)O
blite
ratio
n of
bas
al c
iste
rns
Intr
acra
nial
air
Sub-
arac
hnoi
d or
int
rave
ntri
cula
r ha
emor
rhag
e.
Chi
ldre
nH
ead
inju
ries
are
rel
ativ
ely
com
mon
in
child
ren;
in
the
maj
ority
of
case
s, t
here
is
no s
erio
us i
njur
y: i
mag
ing
and
hosp
italis
atio
n ar
e un
nece
ssar
y. I
f th
ere
is a
his
tory
of
loss
of
cons
ciou
snes
s, n
euro
logi
cal
sign
s or
sym
ptom
s (e
xclu
ding
asi
ngle
vom
it) o
r an
ina
dequ
ate
or i
ncon
sist
ent
hist
ory,
im
agin
g is
req
uire
d. C
Tis
the
sim
ples
t w
ay o
f ex
clud
ing
sign
ific
ant
brai
n in
jury
. If
non-
acci
dent
al i
njur
y is
sus
pect
ed, a
sku
ll SX
R a
s pa
rt o
f a
skel
etal
sur
vey
is r
equi
red.
In
addi
tion,
MR
I of
the
brai
n m
ay b
e re
quir
ed l
ater
to
furt
her
docu
men
t tim
ing
of t
he i
njur
y.
85
K. Trauma
Hea
d:
low
ris
k o
f in
trac
ran
ial
inju
ry•
Fully
ori
enta
ted
SXR
(I)
Not
ind
icat
edT
hese
pat
ient
s ar
e us
ually
sen
t ho
me
with
hea
d in
jury
•N
oam
nesi
aro
utin
ely
(C)
inst
ruct
ions
to
the
care
of
a re
spon
sibl
e ad
ult.
The
y•
No
neur
olog
ical
def
ects
CT
(II)
Not
ind
icat
edm
ay b
e ad
mitt
ed t
o ho
spita
l if
no
such
adu
lt is
•N
ose
riou
s sc
alp
rout
inel
y (C
)av
aila
ble.
lace
ratio
n•
No
haem
atom
aK
1
Hea
d:
med
ium
-ris
k o
f in
trac
ran
ial
inju
ry•
Los
s of
con
scio
usne
ssC
T(I
I) o
rIn
dica
ted
(B)
CT
is i
ncre
asin
gly
bein
g us
ed a
s th
e fi
rst
and
ON
LYor
am
nesi
aSX
R (
I)in
vest
igat
ion
in t
his
grou
p of
pat
ient
s, t
o co
nfid
ently
•V
iole
nt m
echa
nism
sex
clud
e cr
ania
l in
jury
. If
no f
ract
ure
is s
een,
pat
ient
sof
inj
ury
will
usu
ally
be
sent
hom
e w
ith h
ead
inju
ry i
nstr
uctio
ns•
Scal
p br
uise
, sw
ellin
gto
the
car
e of
a r
espo
nsib
le a
dult.
If
no r
espo
nsib
leor
lac
erat
ion
dow
n to
adul
t is
ava
ilabl
e or
if
a fr
actu
re i
s pr
esen
t, th
e pa
tient
bone
or
> 5
cm
will
usu
ally
be
adm
itted
. See
Sec
tion
M (
M13
) fo
r•
Neu
rolo
gica
l sy
mpt
oms
non-
acci
dent
al i
njur
y in
chi
ldre
n. M
RI
of t
he b
rain
or s
igns
(in
clud
ing
is t
he p
refe
rred
inv
estig
atio
n fo
r in
trac
rani
al i
njur
ies
head
ache
, vom
iting
tw
ice
in N
AI,
but
SX
R m
ay s
till
be n
eede
d to
exc
lude
or m
ore,
ret
urn
visi
t)fr
actu
res
mis
sed
on C
T.
86
K. TraumaC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
•In
adeq
uate
his
tory
or
exam
inat
ion
(epi
leps
y/a
lcoh
ol/c
hild
/etc
.)
•C
hild
bel
ow 5
yrs
:su
spec
ted
NA
I, t
ense
font
anel
le, f
all
mor
e th
an60
cm
or
on t
o ha
rdsu
rfac
eK
2
Hea
d:
hig
h r
isk
of
intr
acra
nia
l in
jury
•Su
spec
ted
FB o
rC
T(I
I)In
dica
ted
(B)
The
se p
atie
nts
will
usu
ally
hav
e be
en a
dmitt
ed f
orpe
netr
atin
g in
jury
to
skul
lob
serv
atio
n. I
f th
ere
is a
ny d
elay
in
getti
ng C
Ton
an
•D
isor
ient
ated
or
urge
nt b
asis
, see
k ne
uros
urgi
cal
opin
ion.
depr
esse
d co
nsci
ousn
ess
NB
:C
Tsh
ould
be
avai
labl
e w
ithi
n fo
urho
urs
of•
Foca
l ne
urol
ogic
alad
mis
sion
in
all
pati
ents
wit
h a
skul
l fr
actu
re.
sym
ptom
s or
sig
nsSX
R is
not
req
uire
d be
fore
CT.
In
rhin
orrh
oea/
otor
rhoe
a•
Seiz
ure
NM
can
ide
ntif
y si
te o
f le
akag
e in
chr
onic
pha
se.
•Sk
ull
frac
ture
or
sutu
ral
dias
tasi
s sh
own
on S
XR
•C
SF f
rom
nos
e or
CSF
/bl
ood
from
ear
•U
nsta
ble
syst
emic
sta
tepr
eclu
ding
tra
nsfe
r to
neur
olog
ical
uni
t•
Dia
gnos
is u
ncer
tain
K3
87
K. Trauma
Hea
d:
very
hig
h r
isk
of
intr
acra
nia
l in
jury
•D
eter
iora
ting
CT
(II)
Indi
cate
d (B
)U
RG
EN
TN
EU
RO
SUR
GIC
AL
AN
D A
NA
EST
HE
TIC
cons
ciou
snes
s or
RE
FER
RA
LIN
DIC
AT
ED
, whi
ch s
houl
d no
t be
neur
olog
ical
sig
nsde
laye
d by
im
agin
g.(e
.g. p
upil
chan
ges)
•C
onfu
sion
or
com
aN
B:
CT
shou
ld b
e pe
rfor
med
as
an e
mer
genc
y (s
eepe
rsis
tent
des
pite
K3
abov
e).
resu
scita
tion
•Te
nse
font
anel
le o
rsu
tura
l di
asta
sis
•O
pen
or p
enet
ratin
g in
jury
•D
epre
ssed
or
com
poun
dfr
actu
re•
Frac
ture
of
skul
l ba
se K4
Nas
al t
raum
aSX
R (
I)N
ot i
ndic
ated
Unl
ess
requ
este
d by
a s
peci
alis
t. Po
or c
orre
latio
nX
R f
acia
l bo
nes
rout
inel
y (B
)be
twee
n ra
diol
ogic
al f
indi
ngs
and
pres
ence
of
(I),
XR
nas
alex
tern
al d
efor
mity
. Man
agem
ent
of t
he b
ruis
ed n
ose
bone
s (I
)w
ill d
epen
d on
loc
alpo
licy:
usu
ally
fol
low
-up
at a
nE
NT
or m
axill
o-fa
cial
clin
ic w
ill d
eter
min
e th
e ne
edK
5fo
r X
R.
88
K. TraumaC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Orb
ital
trau
ma:
XR
fac
ial
bone
sIn
dica
ted
(B)
Esp
ecia
lly i
n th
ose
whe
re ‘
blow
-out
’in
jury
pos
sibl
ebl
unt
inju
ry(I
)M
RI
or l
ow d
ose
CT
may
eve
ntua
lly b
e re
quir
ed b
ysp
ecia
lists
, esp
ecia
lly w
hen
XR
s or
clin
ical
sig
nsK
6eq
uivo
cal.
Orb
ital
trau
ma:
XR
orb
its
(I)
Indi
cate
d (C
)W
hen:
(1)
Rad
io-o
paqu
e in
tra-
ocul
ar F
B i
s a
pene
trat
ing
inju
rypo
ssib
ility
(se
e A
16).
(2)
Inv
estig
atio
n re
ques
ted
byop
htha
lmol
ogis
t. (3
) Su
spic
ion
of d
amag
e to
orb
ital
wal
ls.
US
(0)
orSp
ecia
lised
US
or l
ow-d
ose
CT
may
be
requ
ired
; M
RI
K7
CT
(II)
inve
stig
atio
n (B
)co
ntra
indi
cate
d w
ith m
etal
lic F
B (
see
A16
).
Mid
dle
thir
d fa
cial
inj
ury
XR
fac
ial
bone
sIn
dica
ted
(B)
But
pat
ient
coo
pera
tion
esse
ntia
l. A
dvis
able
to
dela
y(I
)X
R i
n un
coop
erat
ive
patie
nts.
In
child
ren,
XR
oft
enun
help
ful.
Low
-dos
e C
TSp
ecia
lised
Dis
cuss
with
max
illof
acia
l su
rgeo
n w
ho m
ay r
equi
reK
8(I
I)in
vest
igat
ion
(B)
low
-dos
e C
Tat
an
earl
y st
age.
Man
dibu
lar
trau
ma
XR
Man
dibl
e (I
)In
dica
ted
(C)
For
non-
trau
mat
ic T
MJ
prob
lem
s se
e B
11.
or o
rtho
pant
omo-
K9
gram
(O
PG
) (I
)
89
K. Trauma
Cer
vica
l sp
ine
Con
scio
us p
atie
nt w
ithX
R C
spi
ne (
I)N
ot i
ndic
ated
In t
hose
who
mee
t al
l of
the
fol
low
ing
crite
ria:
head
and
/or
face
inj
ury
rout
inel
y (B
)(1
) Fu
lly c
onsc
ious
.on
ly(2
) N
ot i
ntox
icat
ed.
(3)
No
abno
rmal
neu
rolo
gica
l fi
ndin
gs.
K10
(4)
No
neck
pai
n or
ten
dern
ess.
Unc
onsc
ious
hea
d in
jury
XR
C s
pine
(I)
Indi
cate
d (B
)M
ust
be o
f go
od q
ualit
y to
allo
w a
ccur
ate
eval
uatio
n.(s
ee K
3/4)
But
rad
iogr
aphy
may
be
very
dif
ficu
lt in
the
sev
erel
ytr
aum
atis
ed p
atie
nt a
nd m
ust
avoi
d m
anip
ulat
ion
(see
K11
also
K12
).
Nec
k in
jury
: w
ith p
ain
XR
C s
pine
(I)
Indi
cate
d (B
)C
ervi
cal
spin
e X
Rs
can
be v
ery
diff
icul
t to
eva
luat
e.R
adio
grap
hy a
lso
diff
icul
t an
d:1.
Mus
t sh
ow C
7/T
1.2.
Sho
uld
show
odo
ntoi
d pe
g (n
ot a
lway
s po
ssib
le a
ttim
e of
ini
tial
stud
y).
3. M
ay n
eed
spec
ial
view
s, C
Tor
MR
I es
peci
ally
whe
n X
R e
quiv
ocal
or
com
plex
les
ions
.
CT
(II)
or
MR
ISp
ecia
lised
Dis
cuss
with
dep
artm
ent
of c
linic
al r
adio
logy
.K
12(0
)in
vest
igat
ion
(B)
90
K. TraumaC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Nec
k in
jury
: w
ithX
R (
I)In
dica
ted
(B)
For
orth
opae
dic
asse
ssm
ent.
neur
olog
ical
def
icit
MR
I (0
)In
dica
ted
(B)
Som
e co
nstr
aint
s w
ith l
ife
supp
ort
syst
ems.
MR
I be
stan
d sa
fest
met
hod
of d
emon
stra
ting
intr
insi
c co
rdda
mag
e, c
ord
com
pres
sion
, lig
amen
tous
inj
urie
s an
dve
rteb
ral
frac
ture
s at
mul
tiple
lev
els.
CT
mye
logr
aphy
K13
may
be
cons
ider
ed i
f M
RI
not
avai
labl
e.
Nec
k in
jury
: w
ith p
ain
XR
C s
pine
;Sp
ecia
lised
Vie
ws
take
n in
fle
xion
and
ext
ensi
on (
cons
ider
but
XR
ini
tially
nor
mal
;fl
exio
n an
din
vest
igat
ion
(B)
fluo
rosc
opy)
as
achi
eved
by
the
patie
nt w
ith n
osu
spec
ted
ligam
ento
usex
tens
ion
(I)
assi
stan
ce a
nd u
nder
med
ical
sup
ervi
sion
. MR
I m
ayin
jury
K14
be h
elpf
ul h
ere.
Th
ora
cic
and
lu
mb
ar s
pin
eT
raum
a: n
o pa
in, n
oX
R (
II)
Not
ind
icat
edPh
ysic
al e
xam
inat
ion
is r
elia
ble
in t
his
regi
on. W
hen
neur
olog
ical
def
icit
rout
inel
y (B
)th
e pa
tient
is
awak
e, a
lert
and
asy
mpt
omat
ic, t
heK
15pr
obab
ility
of
inju
ry i
s lo
w.
Tra
uma:
with
pai
n, n
oX
R p
ainf
ulIn
dica
ted
(B)
Alo
w t
hres
hold
to
XR
whe
n th
ere
is p
ain/
tend
erne
ss,
neur
olog
ical
def
icit
orar
ea (
II)
a si
gnif
ican
t fa
ll, a
hig
h im
pact
RTA
, oth
er s
pina
lpa
tient
not
abl
e to
be
frac
ture
pre
sent
or
it is
not
pos
sibl
e to
clin
ical
lyev
alua
ted
eval
uate
the
pat
ient
. Inc
reas
ing
use
of C
Tan
d M
RI
K16
here
.
91
K. Trauma
Tra
uma:
with
neu
rolo
gica
lX
R (
II)
Indi
cate
d (B
)de
fici
t —
pai
nM
RI
(0)
Indi
cate
d (B
)W
here
tec
hnic
ally
pos
sibl
e. C
Tof
ten
used
as
patie
ntun
derg
oing
CT
for
othe
r re
ason
s. B
ut M
RI
best
met
hod
of d
emon
stra
ting
intr
insi
c co
rd d
amag
e, c
ord
K17
com
pres
sion
and
ver
tebr
al f
ract
ures
at
mul
tiple
lev
els.
Pel
vis
and
sac
rum
Fall
with
ina
bilit
y to
XR
pel
vis
(I)
Indi
cate
d (C
)Ph
ysic
al e
xam
inat
ion
may
be
unre
liabl
e. C
heck
for
bear
wei
ght
plus
lat
eral
XR
fem
oral
nec
k fr
actu
res,
whi
ch m
ay n
ot s
how
on
initi
alhi
p (I
)X
R, e
ven
with
goo
d la
tera
l vi
ews.
In
sele
cted
cas
esN
M o
r M
RI
or C
Tca
n be
use
ful
whe
n X
R n
orm
al o
rK
18eq
uivo
cal.
Ure
thra
l bl
eedi
ng a
ndR
etro
grad
eIn
dica
ted
(C)
To s
how
ure
thra
l in
tegr
ity, l
eak,
rup
ture
. Con
side
rpe
lvic
inj
ury
uret
hrog
ram
(II
)cy
stog
ram
if
uret
hra
norm
al a
nd s
uspi
cion
of
blad
der
K19
leak
.
Tra
uma
to c
occy
x or
XR
coc
cyx
(I)
Not
ind
icat
edN
orm
al a
ppea
ranc
es o
ften
mis
lead
ing
and
find
ings
do
cocc
ydyn
iaK
20ro
utin
ely
(C)
not
alte
r m
anag
emen
t.
92
K. TraumaC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Up
per
lim
bSh
ould
er i
njur
yX
R s
houl
der
(I)
Indi
cate
d (B
)So
me
disl
ocat
ions
pre
sent
sub
tle f
indi
ngs.
As
am
inim
um, o
rtho
gona
l vi
ews
are
requ
ired
. US,
MR
Ian
d C
Tar
thro
grap
hy a
ll ha
ve a
rol
e in
sof
t tis
sue
K21
inju
ry.
Elb
ow i
njur
yX
R e
lbow
(I)
Indi
cate
d (B
)To
sho
w a
n ef
fusi
on. R
outin
e fo
llow
-up
XR
s no
tin
dica
ted
in ‘
effu
sion
, no
obvi
ous
frac
ture
’(s
ee a
lso
K22
Sect
ion
M).
Inc
reas
ing
use
of C
Tan
d M
RI
here
.
Wri
st i
njur
yX
R w
rist
(I)
Indi
cate
d (B
)Sc
apho
id f
ract
ures
can
be
invi
sibl
e at
pre
sent
atio
n.N
M (
II)
orSp
ecia
lised
Mos
t ce
ntre
s re
peat
XR
at
10–1
4 da
ys i
f th
ere
are
MR
I (0
)in
vest
igat
ion
(B)
stro
ng c
linic
al s
igns
and
ini
tial
XR
neg
ativ
e. S
ome
depa
rtm
ents
use
CT,
NM
or
MR
I to
exc
lude
fra
ctur
eea
rlie
r th
an t
his.
Inc
reas
ing
use
of M
RI
as t
he o
nly
K23
exam
inat
ion.
Low
er l
imb
Kne
e in
jury
XR
kne
e (I
)N
ot i
ndic
ated
Esp
ecia
lly w
here
phy
sica
l si
gns
of i
njur
y ar
e m
inim
al.
(fal
l/blu
nt t
raum
a)ro
utin
ely
(B)
Inab
ility
to
bear
wei
ght
or p
rono
unce
d bo
nyte
nder
ness
, par
ticul
arly
at
pate
lla a
nd h
ead
of f
ibul
a,m
erit
radi
ogra
phy.
CT
/MR
I m
ay b
e ne
eded
whe
reK
24fu
rthe
r in
form
atio
n is
req
uire
d (s
ee D
23).
93
K. Trauma
Ank
le i
njur
yX
R a
nkle
(I)
Not
ind
icat
edFe
atur
es w
hich
jus
tify
XR
inc
lude
: th
e el
derl
y pa
tient
,ro
utin
ely
(B)
mal
leol
ar t
ende
rnes
s, m
arke
d so
ft t
issu
e sw
ellin
g an
dK
25in
abili
ty t
o be
ar w
eigh
t.
Foot
inj
ury
XR
foo
t (I
)N
ot i
ndic
ated
Unl
ess
ther
e is
tru
e bo
ny t
ende
rnes
s. E
ven
then
the
rout
inel
y (B
)de
mon
stra
tion
of a
fra
ctur
e ra
rely
inf
luen
ces
man
agem
ent.
Onl
y ra
rely
are
XR
s of
foo
t an
d an
kle
indi
cate
d to
geth
er;
both
will
not
be
done
with
out
good
reas
on. C
linic
al a
bnor
mal
ities
are
usu
ally
con
fine
d to
K26
foot
or
ankl
e.
Stre
ss f
ract
ure
XR
(I)
Indi
cate
d (B
)A
lthou
gh o
ften
unr
ewar
ding
.
NM
(II
) or
Indi
cate
d (B
)Pr
ovid
es a
mea
ns o
f ea
rly
dete
ctio
n as
wel
l as
vis
ual
MR
I (0
)ac
coun
t of
the
bio
mec
hani
cal
prop
ertie
s of
the
bon
e.K
27So
me
cent
res
use
US
here
.
Th
e Fo
reig
n B
od
y (F
B)
Soft
tis
sue
inju
ry:
XR
(I)
Indi
cate
d (B
)A
ll gl
ass
is r
adio
-opa
que;
som
e pa
int
is r
adio
-opa
que.
FB (
met
al, g
lass
, pai
nted
Rad
iogr
aphy
and
int
erpr
etat
ion
may
be
diff
icul
t;w
ood)
rem
ove
bloo
d-st
aine
d dr
essi
ngs
firs
t. C
onsi
der
US,
K28
espe
cial
ly i
n ar
eas
whe
re r
adio
grap
hy d
iffi
cult.
94
K. TraumaC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Soft
tis
sue
inju
ry:
XR
(I)
Not
ind
icat
edFB
(pl
astic
, woo
d)ro
utin
ely
(B)
Plas
tic is
not
rad
io-o
paqu
e: w
ood
is r
arel
y ra
dio-
opaq
ue.
K29
US
(0)
Indi
cate
d (B
)So
ft-t
issu
e U
S m
ay s
how
non
-opa
que
FB.
Swal
low
ed F
B s
uspe
cted
XR
sof
tIn
dica
ted
(C)
Aft
er d
irec
t ex
amin
atio
n of
oro
phar
ynx
(whe
re m
ost
in p
hary
ngea
l or
upp
erti
ssue
s of
FBs
lodg
e), a
nd i
f FB
lik
ely
to b
e op
aque
.oe
soph
agea
l re
gion
neck
(I)
Dif
fere
ntia
tion
from
cal
cifi
ed c
artil
age
can
be d
iffi
cult.
Mos
t fi
sh b
ones
inv
isib
le o
n X
R. M
aint
ain
a lo
wA
XR
(II
)N
ot i
ndic
ated
thre
shol
d fo
r la
ryng
osco
py o
r en
dosc
opy,
esp
ecia
lly i
f(f
or c
hild
ren
see
rout
inel
y (B
)pa
in p
ersi
sts
afte
r 24
hou
rs (
see
K33
). N
B:
for
Sect
ion
M)
K30
poss
ible
inh
aled
FB
in
child
ren
see
Sect
ion
M (
M23
).
Swal
low
ed F
B:
smoo
than
d sm
all
(e.g
. coi
n)C
XR
(I)
Indi
cate
d (B
)T
he m
inor
ity o
f sw
allo
wed
FB
s w
ill b
e ra
dio-
opaq
ue.
In c
hild
ren
a si
ngle
, slig
htly
ove
r-ex
pose
d, f
ront
alC
XR
to
incl
ude
neck
sho
uld
suff
ice.
In
adul
ts, a
late
ral
CX
R m
ay b
e ne
eded
in
addi
tion
if f
ront
al C
XR
nega
tive.
Maj
ority
of
FBs
that
im
pact
, do
so a
t cr
ico
phar
ynge
us. I
f th
e FB
has
not
pas
sed
(say
with
in 6
days
), A
XR
may
be
usef
ul f
or l
ocal
isat
ion.
AX
R (
II)
Not
ind
icat
edK
31ro
utin
ely
(B)
95
K. Trauma
Shar
p or
pot
entia
llyA
XR
(II
)In
dica
ted
(B)
Mos
t sw
allo
wed
for
eign
bod
ies
that
pas
s th
epo
ison
ous
swal
low
ed F
B:
oeso
phag
us e
vent
ually
pas
s th
roug
h th
e re
mai
nder
of
(e.g
. bat
tery
)th
e ga
stro
inte
stin
al t
ract
with
out
com
plic
atio
n. B
utlo
catio
n of
bat
teri
es i
s im
port
ant
as l
eaka
ge c
an b
eda
nger
ous.
CX
R (
I)N
ot i
ndic
ated
Unl
ess
AX
R n
egat
ive.
K32
rout
inel
y (B
)
Swal
low
ed F
B:
larg
eC
XR
(I)
Indi
cate
d (B
)D
entu
res
vary
in
radi
o-op
acity
; m
ost
plas
tic d
entu
res
obje
ct (
e.g.
den
ture
s)ar
e ra
diol
ucen
t. A
XR
may
be
need
ed i
f C
XR
neg
ativ
e,as
may
bar
ium
sw
allo
w o
r en
dosc
opy.
Lat
CX
R m
ayK
33be
hel
pful
.
Ch
est
Che
st t
raum
a: m
inor
CX
R (
I)N
ot i
ndic
ated
The
dem
onst
ratio
n of
a r
ib f
ract
ure
does
not
alte
rK
34ro
utin
ely
(B)
man
agem
ent.
Che
st t
raum
a: m
oder
ate
CX
R (
I)In
dica
ted
(B)
Fron
tal
CX
R f
or p
neum
otho
rax,
flu
id o
r lu
ngco
ntus
ion.
Ano
rmal
CX
R d
oes
not
excl
ude
aort
icin
jury
and
art
erio
grap
hy/C
T/M
RI
shou
ld b
eK
35co
nsid
ered
.
96
K. TraumaC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Stab
inj
ury
CX
R (
I)In
dica
ted
(C)
PAan
d/or
oth
er v
iew
s to
sho
w p
neum
otho
rax,
lun
gda
mag
e or
flu
id. U
S us
eful
for
ple
ural
and
per
icar
dial
K36
flui
d.
Ster
nal
frac
ture
XR
lat
eral
In
dica
ted
(C)
In a
dditi
on t
o C
XR
. Thi
nk o
f th
orac
ic s
pina
l an
dK
37st
ernu
m (
I)ao
rtic
inj
urie
s to
o.
Abd
omen
(in
clud
ing
Supi
ne A
XR
(II
)In
dica
ted
(B)
US
valu
able
for
det
ectin
g ha
emat
oma
and
poss
ible
kidn
ey).
Blu
nt o
r st
ab+
erec
t C
XR
(I)
inju
ry t
o so
me
orga
ns, e
.g. s
plee
n, l
iver
. CT
may
be
inju
ryK
38ne
eded
(se
e K
40–K
42).
Ren
al t
raum
aIm
agin
gIn
dica
ted
(B)
Dis
cuss
with
rad
iolo
gist
. In
agre
emen
t w
ith l
ocal
polic
y an
d av
aila
bilit
y. U
S of
ten
suff
icie
nt f
or m
inor
loca
l in
jury
. Man
y ce
ntre
s us
e a
limite
d IV
U, m
erel
yto
ens
ure
norm
ality
of
cont
rala
tera
l ki
dney
. Som
epa
tient
s w
ith m
ajor
inj
ury
(see
bel
ow)
unde
rgo
CT,
mak
ing
IVU
unn
eces
sary
. Con
side
r re
nal
arte
ryda
mag
e, e
spec
ially
in
dece
lera
tion
inju
ries
;ar
teri
ogra
phy
may
be
need
ed. N
M m
ay b
e he
lpfu
l to
K39
asse
ss r
esid
ual
func
tion.
97
K. Trauma
Maj
or
trau
ma
Maj
or t
raum
a —
gen
eral
C-s
pine
XR
(I)
,In
dica
ted
(B)
Stab
ilise
pat
ient
’s c
ondi
tion
as a
pri
ority
. Per
form
onl
ysc
reen
in
the
unco
nsci
ous
CX
R (
I),
the
min
imum
XR
s ne
cess
ary
at i
nitia
l as
sess
men
t.or
con
fuse
d pa
tient
pelv
is X
R (
I),
C-s
pine
XR
can
wai
t so
lon
g as
spi
ne a
nd c
ord
CT
head
(II
)su
itabl
y pr
otec
ted,
but
CT
C-s
pine
may
be
com
bine
dw
ith C
The
ad. P
elvi
c fr
actu
res
ofte
n as
soci
ated
with
K40
maj
or b
lood
los
s. S
ee H
ead
Inju
ry K
1–K
4.
Maj
or t
raum
a —
CX
R (
I),
Indi
cate
d (B
)Pn
eum
otho
rax
mus
t be
exc
lude
d. P
elvi
c fr
actu
res
abdo
men
/pel
vis
Pel
vis
XR
(I)
whi
ch i
ncre
ase
pelv
ic v
olum
e of
ten
asso
ciat
ed w
ithm
ajor
blo
od l
oss.
CT
abdo
(II
I)In
dica
ted
(B)
Sens
itive
and
spe
cifi
c, b
ut t
ime-
cons
umin
g an
d m
ayde
lay
surg
ery.
CT
shou
ld p
rece
de p
erito
neal
lav
age.
Incr
easi
ng i
nter
est
in t
he u
se o
f U
S in
em
erge
ncy
K41
room
to
show
fre
e fl
uid
plus
sol
id o
rgan
-inj
ury.
Maj
or t
raum
a –
ches
tC
XR
(I)
Indi
cate
d (B
)A
llow
s im
med
iate
man
agem
ent
(e.g
. pne
umot
hora
x).
CT
Che
st (
III)
Indi
cate
d (B
)E
spec
ially
use
ful
to e
xclu
de m
edia
stin
al h
aem
orrh
age.
K42
Low
thr
esho
ld f
or p
roce
edin
g to
art
erio
grap
hy.
98
K. TraumaC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
L. C
ance
r
Par
oti
dD
iagn
osis
US
(0)
Indi
cate
d (B
)To
est
ablis
h pr
esen
ce o
f a
mas
s, p
artic
ular
ly i
nsu
perf
icia
l le
sion
s.
MR
I (0
) or
Indi
cate
d (B
)U
sefu
l in
the
dee
p po
rtio
n of
the
gla
nd a
nd b
efor
eL
1C
T(I
I)co
mpl
ex s
urge
ry.
Stag
ing
MR
I (0
) or
Indi
cate
d (B
)E
spec
ially
whe
n co
mpl
ex s
urge
ry c
onte
mpl
ated
; to
see
L2
CT
(II)
rela
tions
and
inv
olve
men
t of
dee
p lo
be.
Lary
nx
Dia
gnos
isIm
agin
gN
ot i
ndic
ated
Thi
s is
a c
linic
al d
iagn
osis
.L
3ro
utin
ely
(B)
Stag
ing
CT
(II)
or
Indi
cate
d (B
)M
RI
has
the
adva
ntag
e of
dir
ect
coro
nal
imag
ing.
L4
MR
I (0
)M
RI
will
eve
ntua
lly s
uper
sede
.
99
L. Cancer
Man
y of
the
clin
ical
pro
blem
s re
late
d to
the
diag
nosi
s of
can
cer
have
alr
eady
par
tly b
een
cove
red
with
in th
e in
divi
dual
sys
tem
sec
tions
. Bri
efno
tes
are
prov
ided
her
e ab
out
the
use
of i
mag
ing
in t
he d
iagn
osis
, st
agin
g an
d fo
llow
-up
of s
ome
of t
he c
omm
on p
rim
ary
mal
igna
ncie
s.Pa
edia
tric
mal
igna
ncie
s ar
e no
t in
clud
ed a
s th
eir
man
agem
ent
is a
lway
s at
spe
cial
ist
leve
l. Fo
r br
east
can
cer
see
Sect
ion
J. A
CX
R i
sne
cess
ary
at p
rese
ntat
ion
for
mos
t m
alig
nant
les
ions
to
iden
tify
pos
sibl
e pu
lmon
ary
Met
asta
ses.
Con
cern
abo
ut r
adia
tion
in
diag
nost
ic i
mag
ing
is g
ener
ally
les
s re
leva
nt i
n th
is s
ecti
on.
CX
R i
s al
so p
art
of m
any
follo
w-u
p pr
otoc
ols
(e.g
. te
stic
ular
lesi
ons)
.F
ollo
w-u
p in
vest
igat
ions
to
mon
itor
prog
ress
(e.
g. p
ost-
chem
othe
rapy
) ar
e of
ten
requ
ired
; so
me
are
driv
en b
y tr
ial
prot
ocol
s ra
ther
than
clin
ical
nee
d an
d th
us s
houl
d be
app
ropr
iate
ly f
unde
d.
Th
yro
idD
iagn
osis
US
(0)
and
Indi
cate
d (A
)Se
e N
eck
Sect
ion
B1.
US
guid
ed c
ore
biop
sy i
sN
M (
I)in
crea
sing
ly b
eing
use
d, e
spec
ially
for
‘co
ld’
nodu
les
L5
on N
M.
Stag
ing
CT
(II)
or
Indi
cate
d (B
)To
ass
ess
loca
l ex
tent
(e.
g. r
etro
ster
nal
exte
nsio
n an
dM
RI
(0)
node
s).
NM
(IV
)In
dica
ted
(B)
Aft
er t
hyro
idec
tom
y. N
M i
s al
so u
sed
in f
ollo
w-u
pL
6w
hen
recu
rren
ce i
s su
spec
ted.
Lun
gD
iagn
osis
CX
R P
Aan
dIn
dica
ted
(B)
But
can
be
norm
al, p
artic
ular
ly w
ith c
entr
al t
umou
rs.
Lat
(I)
CT
(III
)In
dica
ted
(B)
Man
y ce
ntre
s pr
ocee
d di
rect
ly t
o br
onch
osco
py w
hich
allo
ws
biop
sy. C
Tis
sup
erio
r in
ide
ntif
ying
les
ions
L7
resp
onsi
ble
for
haem
opty
sis.
Stag
ing
CT
ches
t, up
per
Indi
cate
d (B
)D
espi
te l
imita
tions
in
spec
ific
ity o
f no
dal
abdo
men
(II
I)in
volv
emen
t, et
c. S
ome
cent
res
perf
orm
NM
for
poss
ible
ske
leta
l m
etas
tase
s.
100
L. CancerC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
MR
I (0
)Sp
ecia
lised
Ass
ists
in
estim
atin
g lo
cal
inva
sion
of
ches
t w
all,
inve
stig
atio
n (B
)pa
rtic
ular
ly f
or a
pica
l an
d pe
riph
eral
les
ions
and
med
iast
inal
inv
asio
n. H
elps
dis
tingu
ish
adre
nal
aden
oma
from
met
asta
sis.
NM
(IV
)Sp
ecia
lised
FDG
-PE
Tas
a s
ingl
e ex
pens
ive
inve
stig
atio
n ca
nin
vest
igat
ion
(B)
iden
tify
smal
l m
etas
tatic
foc
i; m
ay s
ave
a lo
t of
oth
erL
8in
vest
igat
ions
and
ina
ppro
pria
te s
urge
ry.
Oes
op
hag
us
Dia
gnos
isB
ariu
m s
wal
low
Indi
cate
d (B
)B
efor
e en
dosc
opy
in d
ysph
agia
.L
9(I
I)
Stag
ing
CT
(III
)In
dica
ted
(B)
Des
pite
lim
itatio
ns i
n se
nsiti
vity
and
spe
cifi
city
of
noda
l in
volv
emen
t. Si
mpl
er t
han
MR
I fo
r lu
ng, l
iver
and
intr
a-ab
dom
inal
nod
es.
Tran
soes
o-In
dica
ted
(A)
Incr
easi
ng u
se o
f tr
anso
esop
hage
al U
S fo
r lo
cal
L10
phag
eal
US
(0)
stag
ing
whe
re a
vaila
ble.
Live
r: p
rim
ary
lesi
on
Dia
gnos
isU
S (0
)In
dica
ted
(B)
The
maj
ority
of
lesi
ons
will
be
iden
tifie
d.
MR
I (0
) or
In
dica
ted
(B)
If b
ioch
emic
al m
arke
rs e
leva
ted
and
US
nega
tive
orC
T(I
II)
liver
ver
y ci
rrho
tic. E
nhan
ced
MR
I an
d ar
teri
al p
hase
L11
CT
mos
t ac
cura
te i
n de
linea
ting
tum
our
exte
nt.
101
L. Cancer
Stag
ing
MR
I (0
) or
Indi
cate
d (B
)M
RI
prob
ably
the
opt
imal
inv
estig
atio
n in
ass
essi
ngC
T(I
II)
invo
lved
seg
men
ts a
nd l
obes
. Int
ra-o
pera
tive
US
L12
usef
ul w
here
ava
ilabl
e.
Live
r: s
eco
nd
ary
lesi
on
Dia
gnos
isU
S (0
)In
dica
ted
(B)
US
will
sho
w t
he m
ajor
ity o
f m
etas
tase
s an
d gu
ides
biop
sy.
CT
(III
) or
Indi
cate
d (B
)W
hen
US
nega
tive
and
clin
ical
sus
pici
on h
igh.
MR
IM
RI
(0)
bette
r fo
r ch
arac
teri
sing
les
ions
. CT
arte
rial
port
ogra
phy
is s
ensi
tive
but
not
spec
ific
, but
man
yno
w u
se t
ripl
e ph
ase
spir
al C
Tte
chni
ques
fol
low
ing
intr
aven
ous
enha
ncem
ent.
CT
and
MR
I of
ten
part
of
othe
r st
agin
g an
d fo
llow
-up
prot
ocol
s. I
ncre
asin
gL
13in
tere
st i
n PE
Tfo
r ve
ry s
mal
l m
etas
tatic
foc
i.
102
L. CancerC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Pan
crea
sD
iagn
osis
Imag
ing
Indi
cate
d (B
)M
uch
depe
nds
on l
ocal
exp
ertis
e an
d bo
dy h
abitu
s.U
S us
ually
suc
cess
ful
in t
hin
patie
nts;
CT
bette
r in
the
mor
e ob
ese.
MR
I fo
r cl
arif
icat
ion
of p
robl
ems.
Bio
psy
usin
g U
S or
CT.
ER
CP
or M
RC
Pm
ay a
lso
be n
eede
d.E
ndos
copi
c U
S, w
here
ava
ilabl
e, m
ost
sens
itive
.L
14In
crea
sing
int
eres
t in
PE
T.
Stag
ing
CT
(III
) or
Indi
cate
d (B
)E
spec
ially
if
radi
cal
surg
ery
cont
empl
ated
. Wid
e lo
cal
MR
I (0
)va
riat
ion:
som
e ce
ntre
s us
e an
giog
raph
y, o
ther
s sp
iral
L15
abdo
men
CT;
lap
aros
copi
c U
S al
so u
sed.
Co
lon
an
d r
ectu
mD
iagn
osis
Ba
enem
a (I
II)
Indi
cate
d (B
)M
uch
depe
nds
on l
ocal
pol
icy,
exp
ertis
e an
dor
col
onos
copy
avai
labi
lity.
See
Sec
tion
G. I
ncre
asin
g in
tere
st i
n C
Tan
d M
RI
of t
he c
olon
, esp
ecia
lly w
ith v
irtu
alL
16en
dosc
opic
tec
hniq
ues.
Stag
ing
US
(0)
Indi
cate
d (B
)Fo
r liv
er m
etas
tase
s. E
ndol
umin
al U
S us
eful
for
loc
alre
ctal
spr
ead.
CT
(II)
or
Indi
cate
d (B
)L
ocal
pre
-ope
rativ
e st
agin
g to
ass
ess
rect
al l
esio
nsM
RI
(0)
befo
re p
re-o
pera
tive
radi
othe
rapy
. Man
y ce
ntre
s no
wab
dom
en, p
elvi
str
eat
liver
sec
onda
ries
ver
y ag
gres
sive
ly, w
hich
may
nece
ssita
te M
RI
and/
or d
etai
led
CT.
MR
I an
d C
Tof
ten
com
plem
enta
ry;
both
can
ass
ess
othe
r ab
dom
inal
L17
spre
ad. I
ncre
asin
g in
tere
st i
n PE
The
re.
103
L. Cancer
Rec
urre
nce
US
(0)
live
rIn
dica
ted
(B)
For
liver
met
asta
ses.
Som
e de
bate
abo
ut t
he v
alue
of
rout
ine
US
follo
w-u
p in
asy
mpt
omat
ic p
atie
nts.
CT
(III
) or
Indi
cate
d (B
)Fo
r liv
er m
etas
tase
s an
d lo
cal
recu
rren
ce.
MR
I (0
)ab
dom
en, p
elvi
s
NM
(IV
)Sp
ecia
lised
PET
and
mon
oclo
nal
antib
odie
s ca
n id
entif
y liv
erL
18in
vest
igat
ion
(B)
met
asta
ses
and
loca
l re
curr
ence
.
Kid
ney
Dia
gnos
isL
19U
S (0
)In
dica
ted
(B)
See
Ren
al M
ass
H7.
Stag
ing
CT
(III
) or
MR
IIn
dica
ted
(B)
For
loca
l ex
tent
, ven
ous,
nod
al a
nd u
rete
ric
(0)
abdo
men
invo
lvem
ent,
oppo
site
kid
ney
etc.
CT
(III
) C
hest
Not
ind
icat
edT
he p
rese
nce
of l
ung
met
asta
ses
does
not
usu
ally
rout
inel
y (B
)in
flue
nce
man
agem
ent.
NM
(I)
Spec
ialis
edC
onve
ntio
nal
NM
can
ass
ess
cont
rala
tera
l fu
nctio
n.L
20in
vest
igat
ion
(C)
Incr
easi
ng i
nter
est
in P
ET.
104
L. CancerC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Rec
urre
nce
CT
(III
)In
dica
ted
(B)
For
sym
ptom
s su
gges
ting
rela
pse
arou
nd n
ephr
ecto
my
L21
abdo
men
bed.
Rou
tine
follo
w-u
p no
t re
com
men
ded.
Bla
dd
erD
iagn
osis
Imag
ing
Not
ind
icat
edC
ysto
scop
y is
the
opt
imal
(al
thou
gh n
ot i
nfal
lible
, e.g
.L
22ro
utin
ely
(B)
dive
rtic
ulum
) in
vest
igat
ion.
Stag
ing
IVU
(II
)In
dica
ted
(B)
To a
sses
s ki
dney
s an
d ur
eter
s fo
r fu
rthe
r ur
othe
lial
tum
ours
.
CT
(III
) or
MR
IIn
dica
ted
(B)
Whe
n ra
dica
l th
erap
y co
ntem
plat
ed. M
RI
is p
roba
bly
(0)
abdo
men
mor
e se
nsiti
ve. C
Tw
idel
y us
ed f
or r
adio
ther
apy
L23
and
pelv
ispl
anni
ng.
Pro
stat
eD
iagn
osis
Tran
srec
tal
Indi
cate
d (B
)So
me
vari
atio
n ac
cord
ing
to l
ocal
ava
ilabi
lity
and
US
(0)
expe
rtis
e. T
rans
rect
al U
S is
wid
ely
used
tog
ethe
r w
ithL
24gu
ided
bio
psie
s. S
ome
inte
rest
in
MR
I an
d PE
The
re.
Stag
ing
MR
I (0
)/C
T(I
II)
Spec
ialis
edSo
me
vari
atio
n in
ran
ge o
f in
vest
igat
ive
and
pelv
is,
inve
stig
atio
n (B
)th
erap
eutic
pol
icie
s. S
tagi
ng c
ontin
ued
into
the
abdo
men
whe
n pe
lvic
dis
ease
fou
nd.
NM
(II
)In
dica
ted
(A)
To a
sses
s sk
elet
al m
etas
tase
s, w
hen
PSA
isL
25si
gnif
ican
tly e
leva
ted.
105
L. Cancer
Test
icle
Dia
gnos
isL
26U
S (0
)In
dica
ted
(B)
Esp
ecia
lly w
hen
clin
ical
fin
ding
s eq
uivo
cal
or n
orm
al.
Stag
ing
CT
(III
) ch
est,
Indi
cate
d (B
)M
anag
emen
t no
w d
epen
ds h
eavi
ly o
n ac
cura
teL
27ab
dom
en, p
elvi
sra
diol
ogic
al s
tagi
ng. I
ncre
asin
g in
tere
st i
n PE
T.
Follo
w-u
pC
T(I
II)
Indi
cate
d (B
)So
me
cent
res
still
rou
tinel
y ex
amin
e th
e ch
est
as w
ell,
abdo
men
espe
cial
ly f
or p
atie
nts
with
out
bioc
hem
ical
evi
denc
eof
dis
ease
. Som
e de
bate
as
to w
heth
er w
hole
pel
vis
isne
eded
at
follo
w-u
p un
less
the
re a
re i
dent
ifie
d ri
skfa
ctor
s.
NM
(IV
)Sp
ecia
lised
PET
can
asse
ss v
iabi
lity
of r
esid
ual
mas
ses.
L28
inve
stig
atio
n (C
)
Ova
ryD
iagn
osis
US
(0)
Indi
cate
d (B
)T
he m
ajor
ity o
f le
sion
s ar
e di
agno
sed
by U
S(i
nclu
ding
TV
with
Dop
pler
), l
apar
osco
py o
rla
paro
tom
y. S
ome
are
iden
tifie
d by
CT
/MR
Iin
vest
igat
ions
for
abd
omin
al s
ympt
oms.
MR
I us
eful
L29
for
eluc
idat
ing
prob
lem
s.
106
L. CancerC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Stag
ing
CT
(III
)/M
RI
(0)
Spec
ialis
edM
any
spec
ialis
ts r
equi
re C
Tor
MR
I in
add
ition
to
abdo
men
, pel
vis
inve
stig
atio
n (B
)st
agin
g by
lap
arot
omy.
CT
is s
till
mor
e w
idel
yL
30av
aila
ble.
Follo
w-u
pC
T(I
II)
Spec
ialis
edU
sual
ly t
o as
sess
res
pons
e to
adj
uvan
t th
erap
y. A
lso
L31
abdo
men
, pel
vis
inve
stig
atio
n (B
)us
ed, a
long
with
mar
kers
, to
dete
ct r
elap
se.
Ute
rus:
cer
vix
Dia
gnos
isIm
agin
gN
ot i
ndic
ated
Usu
ally
a c
linic
al d
iagn
osis
. MR
I m
ay a
ssis
t in
L32
rout
inel
y (B
)co
mpl
ex c
ases
.
Stag
ing
MR
I (0
) or
CT
Indi
cate
d (B
)M
RI
prov
ides
bet
ter
dem
onst
ratio
n of
tum
our
and
(III
) ab
dom
enlo
cal
exte
nt. A
lso
bette
r fo
r pe
lvic
nod
es. P
ara-
aort
ican
d pe
lvis
node
s an
d ur
eter
s m
ust
also
be
exam
ined
. Som
eL
33ce
ntre
s no
w u
se t
rans
rect
al U
S fo
r lo
cal
inva
sion
.
Rel
apse
MR
I (0
) or
CT
Spec
ialis
edM
RI
prov
ides
bet
ter
info
rmat
ion
in t
he p
elvi
s. B
iops
y(I
II)
abdo
men
inve
stig
atio
n (B
)(e
.g. o
f no
dal
mas
s) e
asie
r w
ith C
T.L
34an
d pe
lvis
Ute
rus:
bo
dy
Dia
gnos
isU
S (0
) or
Indi
cate
d (B
)M
RI
can
give
val
uabl
e in
form
atio
n ab
out
beni
gn a
ndL
35M
RI
(0)
mal
igna
nt l
esio
ns.
Stag
ing
MR
I (0
) or
Spec
ialis
edB
oth
CT
and
MR
I ca
n sh
ow e
xtra
-ute
rine
dis
ease
. But
L36
CT
(III
)in
vest
igat
ion
(B)
MR
I ca
n al
so d
emon
stra
te i
ntra
-ute
rine
ana
tom
y.
107
L. Cancer
Lym
ph
om
aD
iagn
osis
CT
(III
)In
dica
ted
(B)
CT
good
at
eval
uatin
g no
dal
site
s th
roug
hout
the
bod
y.A
lso
allo
ws
biop
sy a
lthou
gh e
xcis
ion
of w
hole
nod
epr
efer
able
whe
re p
ossi
ble.
NM
(II
I)Sp
ecia
lised
NM
(ga
llium
) ca
n sh
ow f
oci
of o
ccul
t di
seas
e (e
.g.
L37
inve
stig
atio
n (B
)m
edia
stin
um).
PE
Tus
ed i
n so
me
cent
res.
Stag
ing
CT
(III
) ch
est,
Indi
cate
d (B
)D
epen
ding
on
site
of
dise
ase,
hea
d an
d ne
ck m
ay a
lso
L38
abdo
men
, pel
vis
need
to
be e
xam
ined
. Inc
reas
ing
inte
rest
in
PET
here
.
Follo
w-u
pC
T(I
II)
orIn
dica
ted
(B)
Incr
easi
ng r
ole
for
MR
I in
lon
g te
rm f
ollo
w-u
p an
dM
RI
(0)
resi
dual
mas
ses.
NM
(II
I)Sp
ecia
lised
Con
side
r N
M f
or g
alliu
m p
ositi
ve d
isea
se. S
ome
L39
inve
stig
atio
n (B
)ce
ntre
s us
e PE
T.
108
L. CancerC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Mu
scu
losk
elet
al t
um
ou
rsD
iagn
osis
XR
(I)
+In
dica
ted
(B)
Imag
ing
and
hist
olog
y co
mpl
emen
tary
. Bes
t be
fore
MR
I (0
)bi
opsy
: Se
e M
uscu
losk
elet
al S
ectio
n D
. NM
nee
ded
toL
40en
sure
tha
t le
sion
is
solit
ary.
Stag
ing
MR
I (0
) lo
cal
Spec
ialis
edSe
e M
uscu
losk
elet
al S
ectio
n D
. CT
for
lung
dise
ase
+C
Tin
vest
igat
ion
(C)
met
asta
ses.
L41
ches
t (I
II)
Met
asta
ses
fro
m u
nkn
ow
n p
rim
ary
tum
ou
rD
iagn
osis
of
prim
ary
Imag
ing
Not
ind
icat
edR
arel
y be
nefi
cial
. Som
e ex
cept
ions
for
spe
cial
ists
,le
sion
L42
rout
inel
y (C
)yo
unge
r pa
tient
s or
fav
oura
ble
hist
olog
y.
Bre
ast
— s
ee S
ecti
on
J
109
L. Cancer
M.
Pae
dia
tric
sM
inim
ise
x-ir
rad
iati
on
in
ch
ild
ren
, es
pec
iall
y th
ose
wit
h l
on
g te
rm p
rob
lem
s
(for
hea
d in
jury
in
child
ren
see
Tra
uma
Sect
ion
K)
CN
SC
onge
nita
l di
sord
ers
MR
I (0
)In
dica
ted
(C)
Def
initi
ve e
xam
for
all
mal
form
atio
ns a
nd a
void
sx-
irra
diat
ion.
Sed
atio
n us
ually
req
uire
d fo
r yo
ung
child
ren.
Con
side
r U
S in
neo
nate
s. 3
D C
Tm
ay b
eM
1ne
eded
for
bon
e an
omal
ies.
Abn
orm
al h
ead
US
(0)
Indi
cate
d (B
)U
S in
dica
ted
whe
re a
nter
ior
font
anel
le i
s op
en.
appe
aran
ce —
SXR
(I)
Spec
ialis
edW
here
sut
ures
are
clo
sed/
clos
ing.
MR
I in
dica
ted
for
hydr
ocep
halu
s —
inve
stig
atio
n (C
)ol
der
child
ren.
(C
Tm
ay b
e ap
prop
riat
e if
MR
I no
tod
d su
ture
sM
2av
aila
ble.
)
Epi
leps
ySX
R (
I)N
ot i
ndic
ated
Poor
yie
ld.
rout
inel
y (B
)
MR
I (0
) or
Spec
ialis
edM
RI
usua
lly m
ore
appr
opri
ate
than
CT.
Ict
al a
nd i
nter
-M
3N
M (
II)
inve
stig
atio
n (B
)ic
tal
SPE
CT
also
use
d to
ide
ntif
y fo
cus
befo
re s
urge
ry.
110
M. PaediatricsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Dea
fnes
s in
chi
ldre
nC
T(I
I)Sp
ecia
lised
Bot
h C
Tan
d M
RI
may
be
nece
ssar
y in
chi
ldre
n w
ithM
4M
RI
(0)
inve
stig
atio
n (C
)co
ngen
ital
and
post
-inf
ectiv
e de
afne
ss.
Hyd
roce
phal
us —
shun
tX
R (
I)In
dica
ted
(B)
XR
sho
uld
incl
ude
who
le v
alve
sys
tem
.m
alfu
nctio
n (s
ee A
10)
US
(0)
orIn
dica
ted
(B)
US
if p
ract
ical
, MR
I in
old
er c
hild
ren
(or
CT
if M
RI
M5
MR
I (0
)un
avai
labl
e). N
M u
sed
to e
valu
ate
shun
t fu
nctio
n.
Dev
elop
men
tal
dela
y —
Cra
nial
MR
I (0
)Sp
ecia
lised
See
also
M15
for
ske
leta
l in
vest
igat
ion
of g
row
thce
rebr
al p
alsy
M6
inve
stig
atio
n (B
)fa
ilure
.
Hea
dach
esSX
R (
I)N
ot i
ndic
ated
If p
ersi
sten
t or
ass
ocia
ted
with
clin
ical
sig
ns r
efer
for
rout
inel
y (B
)sp
ecia
lised
inv
estig
atio
ns.
MR
I (0
) or
Spec
ialis
edIn
chi
ldre
n M
RI
is p
refe
rabl
e if
ava
ilabl
e be
caus
e of
CT
(II)
inve
stig
atio
n (B
)ab
senc
e of
x-i
rrad
iatio
n. S
ee a
lso
A6
for
poss
ible
M7
men
ingi
tis a
nd e
ncep
halit
is
Sinu
sitis
see
als
o A
13Si
nus
XR
(I)
Not
ind
icat
edN
ot i
ndic
ated
bef
ore
5 ye
ars
as t
he s
inus
es a
re p
oorl
yro
utin
ely
(B)
deve
lope
d; m
ucos
al t
hick
enin
g ca
n be
a n
orm
alfi
ndin
g in
chi
ldre
n. A
sing
le u
nder
-tilt
ed O
M v
iew
may
be
mor
e ap
prop
riat
e th
an t
he s
tand
ard
OM
vie
wM
8de
pend
ing
on t
he c
hild
’s a
ge.
111
M. Paediatrics
Nec
k an
d s
pin
e —
Fo
r tr
aum
a se
e Se
ctio
n K
Tort
icol
lis w
ithou
t tr
aum
aX
R (
I)N
ot i
ndic
ated
Def
orm
ity i
s us
ually
due
to
spas
m w
ith n
o si
gnif
ican
tbo
ne c
hang
es. I
f pe
rsis
tent
, fur
ther
im
agin
g (e
.g. C
T)
M9
may
be
indi
cate
d fo
llow
ing
cons
ulta
tion.
Bac
k or
nec
k pa
inX
R (
I)In
dica
ted
(B)
Bac
k pa
in i
s un
com
mon
in
child
ren
with
out
a ca
use.
Follo
w-u
p is
nee
ded
if i
nfec
tion
is s
uspe
cted
.
NM
(II
)Sp
ecia
lised
Whe
n pa
in c
ontin
ues
and
XR
s ar
e no
rmal
. Use
ful
inin
vest
igat
ion
(B)
pain
ful
scol
iosi
s.
MR
I (0
)Sp
ecia
lised
See
also
The
Spi
ne S
ectio
n C
. MR
I de
fine
s sp
inal
inve
stig
atio
n (B
)m
alfo
rmat
ions
and
exc
lude
s as
soci
ated
the
cal
abno
rmal
ity. M
RI
can
also
dem
onst
rate
juv
enile
dis
cM
10le
sion
s.
Spin
a bi
fida
occ
ulta
XR
(I)
Not
ind
icat
edA
com
mon
var
iatio
n an
d no
t in
its
elf
sign
ific
ant
(eve
nro
utin
ely
(B)
in e
nure
sis)
. How
ever
, neu
rolo
gica
l si
gns
wou
ldM
11re
quir
e in
vest
igat
ion.
Hai
ry p
atch
, sac
ral
dim
ple
XR
(I)
Not
ind
icat
edM
ay b
e he
lpfu
l in
old
er c
hild
ren.
rout
inel
y (B
)
112
M. PaediatricsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
US
(0)
Indi
cate
d (B
)U
S m
ay b
e us
eful
in
the
neon
atal
per
iod
to s
cree
n fo
run
derl
ying
tet
here
d co
rd, e
tc.
MR
I (0
)Sp
ecia
lised
MR
I pa
rtic
ular
ly i
f ne
urol
ogic
al s
igns
are
pre
sent
.M
12in
vest
igat
ion
(B)
Mu
scu
losk
elet
alN
on a
ccid
enta
l in
jury
—X
R (
I) o
fIn
dica
ted
(B)
Loc
al p
olic
ies
will
app
ly;
clos
e cl
inic
al/r
adio
logi
cal
child
abu
se (
for
head
affe
cted
par
tslia
ison
ess
entia
l. Sk
elet
al s
urve
y fo
r th
ose
unde
r tw
oin
jury
see
Sec
tion
K)
year
s af
ter
clin
ical
con
sulta
tion.
May
occ
asio
nally
be
requ
ired
in
the
olde
r ch
ild. C
T/M
RI
of b
rain
may
be
need
ed, e
ven
in t
he a
bsen
ce o
f cr
ania
l ap
pare
nt i
njur
y.
M13
NM
(II
)In
dica
ted
(B)
Sens
itive
for
occ
ult
spin
e/ri
b fr
actu
re.
Lim
b in
jury
: op
posi
te s
ide
XR
(I)
Not
ind
icat
edSe
ek r
adio
logi
cal
advi
ce.
for
com
pari
son
M14
rout
inel
y (B
)
Shor
t st
atur
e,X
R (
I) f
or b
one
Indi
cate
d at
2–18
yrs
: le
ft (
or n
on-d
omin
ant)
han
d/w
rist
onl
y.gr
owth
fai
lure
age
appr
opri
ate
Prem
atur
e in
fant
s an
d ne
onat
es:
knee
(sp
ecia
lised
inte
rval
s (B
)in
vest
igat
ion)
. May
nee
d to
be
supp
lem
ente
d w
ith a
skel
etal
sur
vey
and
MR
I fo
r hy
poth
alam
us a
ndM
15pi
tuita
ry f
ossa
(sp
ecia
lised
inv
estig
atio
ns).
113
M. Paediatrics
Irri
tabl
e hi
pU
S (0
)In
dica
ted
(B)
US
will
del
inea
te e
ffus
ions
whi
ch c
an b
e as
pira
ted
for
diag
nost
ic a
nd t
hera
peut
ic p
urpo
ses.
XR
s ca
n be
dela
yed,
but
sho
uld
be c
onsi
dere
d w
hen
the
sym
ptom
sar
e pe
rsis
tent
. Con
side
r N
M o
r M
RI
whe
n Pe
rthe
s’M
16di
seas
e is
sus
pect
ed a
nd p
lain
XR
s ar
e no
rmal
.
Lim
pX
R p
elvi
s (I
)In
dica
ted
(C)
Gon
ad p
rote
ctio
n is
use
d ro
utin
ely
unle
ss s
hiel
ds w
illob
scur
e ar
ea o
f cl
inic
al s
uspi
cion
. If
slip
ped
epip
hyse
sis
lik
ely,
lat
eral
XR
s of
bot
h hi
ps a
re n
eede
d.
US
(0)
orSp
ecia
lised
Acc
ordi
ng t
o lo
cal
polic
y, e
xper
tise
and
avai
labi
lity.
NM
(II
) or
inve
stig
atio
n (B
)M
17M
RI
(0)
Foca
l bo
ne p
ain
XR
(I)
and
Indi
cate
d (B
)X
R m
ay b
e no
rmal
ini
tially
. US
can
be h
elpf
ulU
S (0
)pa
rtic
ular
ly i
n os
teom
yelit
is.
NM
(II
) or
Spec
ialis
edIn
crea
sing
use
of
MR
I he
re.
M18
MR
I (0
)in
vest
igat
ion
(B)
Clic
king
hip
—U
S (0
)In
dica
ted
(B)
XR
may
be
used
to
supp
lem
ent
US
exam
inat
ion
ordi
sloc
atio
nw
here
exp
ertis
e is
not
ava
ilabl
e. X
R i
ndic
ated
in
the
M19
olde
r in
fant
.
114
M. PaediatricsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Osg
ood–
Schl
atte
r’s
XR
kne
e (I
)N
ot i
ndic
ated
Alth
ough
bon
y ra
diol
ogic
al c
hang
es a
re v
isib
le i
ndi
seas
ero
utin
ely
(C)
Osg
ood–
Schl
atte
r’s
dise
ase
thes
e ov
erla
p w
ith n
orm
alap
pear
ance
s. A
ssoc
iate
d so
ft t
issu
e sw
ellin
g sh
ould
be
M20
asse
ssed
clin
ical
ly r
athe
r th
an r
adio
grap
hica
lly.
Car
dio
tho
raci
cA
cute
che
st i
nfec
tion
CX
R (
I)N
ot i
ndic
ated
Initi
al a
nd f
ollo
w-u
p fi
lms
are
indi
cate
d in
the
rout
inel
y (B
)pr
esen
ce o
f pe
rsis
ting
clin
ical
sig
ns o
r sy
mpt
oms
or i
nth
e se
vere
ly i
ll ch
ild. C
onsi
der
the
need
for
CX
R i
nfe
ver
of u
nkno
wn
orig
in. C
hild
ren
may
hav
eM
21pn
eum
onia
with
out
clin
ical
sig
ns.
Rec
urre
nt p
rodu
ctiv
eC
XR
(I)
Not
ind
icat
edC
hild
ren
with
rec
urre
nt c
hest
inf
ectio
n te
nd t
o ha
veco
ugh
rout
inel
y (C
)no
rmal
CX
Rs
(apa
rt f
rom
bro
nchi
al w
all
thic
keni
ng).
Rou
tine
follo
w-u
p C
XR
not
ind
icat
ed u
nles
s co
llaps
epr
esen
t on
ini
tial
CX
R. S
uspe
cted
cys
tic f
ibro
sis
M22
requ
ires
spe
cial
ist
refe
rral
.
Inha
led
FB (
susp
ecte
d)C
XR
(I)
Indi
cate
d (B
)H
isto
ry o
f in
hala
tion
ofte
n no
t cl
ear.
Bro
ncho
scop
y is
(see
Sec
tion
K)
indi
cate
d, e
ven
in t
he p
rese
nce
of a
nor
mal
CX
R.
NM
/CT
may
be
help
ful
to s
how
sub
tle a
ir t
rapp
ing.
Wid
e va
riat
ion
in l
ocal
pol
icy
abou
t ex
pira
tory
film
s,M
23fl
uoro
scop
y, C
Tan
d N
M (
vent
ilatio
n sc
intig
raph
y).
115
M. Paediatrics
Whe
eze
CX
R (
I)N
ot i
ndic
ated
Chi
ldre
n w
ith a
sthm
a us
ually
hav
e no
rmal
CX
R a
part
rout
inel
y (B
)fr
om b
ronc
hial
wal
l th
icke
ning
. Sud
den
unex
plai
ned
whe
eze
CX
R i
ndic
ated
, may
be
due
to i
nhal
ed F
BM
24(a
bove
).
Acu
te s
trid
orX
R n
eck
(I)
Not
ind
icat
edE
pigl
ottit
is i
s a
clin
ical
dia
gnos
is, b
ut c
onsi
der
FBM
25ro
utin
ely
(B)
(abo
ve).
Hea
rt m
urm
urC
XR
(I)
Not
ind
icat
edSp
ecia
list
refe
rral
may
be
need
ed;
card
iac
US
ofte
nM
26ro
utin
ely
(C)
may
be
indi
cate
d.
Gas
tro
inte
stin
al —
see
als
o Se
ctio
n G
for
mor
e ge
nera
l ab
dom
inal
pro
blem
s
Intu
ssus
cept
ion
AX
R (
II)
Indi
cate
d (C
)L
ocal
pol
icie
s re
quir
e cl
ose
paed
iatr
ic, r
adio
logi
cal
and
surg
ical
lia
ison
. Whe
re e
xper
tise
is a
vaila
ble,
bot
hU
S an
d co
ntra
st e
nem
a (a
ir o
r ba
rium
) ca
n co
nfir
mdi
agno
sis
and
guid
e re
duct
ion.
Fur
ther
im
agin
gSp
ecia
lised
M27
inve
stig
atio
n (B
)
116
M. PaediatricsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Swal
low
ed F
Bs
AX
R (
II)
Not
ind
icat
edE
xcep
t fo
r sh
arp
or p
oten
tially
poi
sono
us F
Bs,
e.g
.(s
ee S
ectio
n K
)ro
utin
ely
(C)
batte
ries
. See
Sec
tion
K. I
f th
ere
is d
oubt
whe
ther
the
FB h
as p
asse
d, a
n A
XR
aft
er 6
day
s m
ay b
e in
dica
ted.
CX
R (
I)In
dica
ted
(C)
If t
here
is
doub
t w
heth
er t
he F
B h
as p
asse
d, a
n A
XR
M28
(inc
ludi
ng n
eck)
afte
r 6
days
may
be
indi
cate
d.
Min
or t
raum
a to
abd
omen
AX
R (
II)
Not
ind
icat
edU
S m
ay b
e us
ed a
s in
itial
inv
estig
atio
n bu
t C
Tis
rout
inel
y (C
)m
ore
spec
ific
, par
ticul
arly
in
visc
eral
tra
uma.
XR
sm
ay s
how
bon
e in
jury
in
seve
re t
raum
a. T
hepr
inci
ples
for
the
inv
estig
atio
n of
maj
or t
raum
a in
child
ren
sim
ilar
to t
hose
in
adul
ts (
see
Maj
or T
raum
a,M
29K
40–K
42).
Proj
ectil
e vo
miti
ngU
S (0
)In
dica
ted
(A)
US
can
conf
irm
the
pre
senc
e of
hyp
ertr
ophi
c py
lori
cst
enos
is, e
spec
ially
whe
re c
linic
al f
indi
ngs
are
M30
equi
voca
l.
Rec
urre
nt v
omiti
ngU
pper
GI
Not
ind
icat
edT
his
sym
ptom
cov
ers
a w
ide
rang
e fr
om o
bstr
uctio
n in
cont
rast
stu
dyro
utin
ely
(C)
the
neon
atal
per
iod
to r
eflu
x, p
osse
ters
and
chi
ldre
nw
ith m
igra
ine.
US
may
be
help
ful
to c
onfi
rmm
alro
tatio
n. H
owev
er, u
pper
GI
cont
rast
stu
dies
may
be i
ndic
ated
to
excl
ude
mal
rota
tion
even
with
nor
mal
abdo
min
al X
R. C
ontr
ast
stud
ies
in n
eona
tes
shou
ld b
eun
dert
aken
as
a sp
ecia
lised
inv
estig
atio
n. C
onsi
der
NM
for
gas
tric
em
ptyi
ng a
nd g
astr
o-oe
soph
agea
lM
31re
flux
.
117
M. Paediatrics
Pers
iste
nt n
eona
tal
US
(0)
Indi
cate
d (B
)E
arly
(<
10
wee
ks)
and
prom
pt i
nves
tigat
ion
isja
undi
cees
sent
ial.
The
abs
ence
of
dila
tatio
n in
the
int
rahe
patic
NM
(II
)In
dica
ted
(B)
bile
duc
t do
es n
ot e
xclu
de a
n ob
stru
ctiv
eM
32ch
olan
giop
athy
.
Rec
tal
blee
ding
NM
(II
)Sp
ecia
lised
If M
ecke
l’s d
iver
ticul
um i
s a
poss
ibili
ty d
o N
M f
irst
.in
vest
igat
ion
(B)
Smal
l bo
wel
con
tras
t st
udie
s m
ay a
lso
be n
eces
sary
.N
M a
lso
usef
ul i
n in
vest
igat
ion
of i
nfla
mm
ator
ybo
wel
dis
ease
. End
osco
py i
s pr
efer
able
to
Ba
enem
afo
r as
sess
men
t of
pol
yps
and
infl
amm
ator
y bo
wel
M33
dise
ase.
US
can
be u
sed
to d
iagn
ose
dupl
icat
ion
cyst
s.
Con
stip
atio
nA
XR
(II
)N
ot i
ndic
ated
Man
y no
rmal
chi
ldre
n sh
ow e
xten
sive
fae
cal
mat
eria
l;ro
utin
ely
(C)
impo
ssib
le t
o as
sess
sig
nifi
canc
e of
rad
iolo
gica
l si
gns.
But
AX
R c
an h
elp
spec
ialis
ts i
n re
frac
tory
cas
es.
Con
tras
t en
ema
Not
ind
icat
edIf
Hir
schs
prun
g’s
dise
ase
is s
uspe
cted
, spe
cial
ist
M34
rout
inel
y (B
)re
ferr
al p
lus
biop
sy i
s pr
efer
red
to r
adio
logi
cal
stud
ies.
Palp
able
abd
omin
al/
US
(0)
and
Indi
cate
d (B
)If
mal
igna
ncy
is s
uspe
cted
, fur
ther
im
agin
g sh
ould
be
pelv
ic m
ass
M35
AX
R (
II)
perf
orm
ed i
n a
spec
ialis
ed c
entr
e.
118
M. PaediatricsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Uro
rad
iolo
gyE
nure
sis
Imag
ing
Not
ind
icat
edU
S an
d ur
odyn
amic
stu
dies
may
be
need
ed i
n ca
ses
ofM
36ro
utin
ely
(B)
pers
iste
nt e
nure
sis.
Con
tinuo
us w
ettin
gU
S (0
)In
dica
ted
(B)
Bot
h ex
amin
atio
ns m
ay b
e ne
eded
to
eval
uate
dup
lex
syst
em w
ith e
ctop
ic u
rete
r.
M37
IVU
(II
)In
dica
ted
Impa
lpab
le t
estis
US
(0)
Indi
cate
d (B
)To
loc
ate
ingu
inal
tes
tis. M
RI
may
be
help
ful
to l
ocat
ean
int
ra-a
bdom
inal
tes
tis, b
ut i
ncre
asin
gly
lapa
rosc
opy
M38
is t
he i
nves
tigat
ion
of c
hoic
e.
Ant
enat
al d
iagn
osis
of
US
(0)
Indi
cate
d (B
)L
ocal
pro
toco
ls s
houl
d be
est
ablis
hed.
Mild
dila
tatio
nur
inar
y tr
act
dila
tatio
nca
n no
rmal
ly b
e m
onito
red
by U
S. L
ow t
hres
hold
for
M39
spec
ialis
t re
ferr
al.
119
M. Paediatrics
Prov
en u
rina
ry t
ract
Imag
ing
US
(0)
Spec
ialis
edT
here
is
wid
e va
riat
ion
in l
ocal
pol
icy.
Muc
h de
pend
sin
fect
ion
//NM
(II
)/in
vest
igat
ions
(C
)on
loc
al t
echn
olog
y an
d ex
pert
ise.
Mos
t pa
tient
scy
stog
raph
y (I
II)
shou
ld r
emai
n on
pro
phyl
actic
ant
ibio
tics
pend
ing
the
resu
lts o
f in
vest
igat
ions
. The
age
of
the
patie
nt a
lso
infl
uenc
es d
ecis
ions
. The
re i
s m
uch
curr
ent
emph
asis
on m
inim
isin
g ra
diat
ion
dose
; he
nce
AX
R i
s no
tin
dica
ted
rout
inel
y (c
alcu
li ra
re).
Exp
ert
US
is t
he k
eyin
vest
igat
ion
in a
ll im
agin
g st
rate
gies
at
this
age
.T
here
afte
r N
M p
rovi
des
data
abo
ut r
enal
str
uctu
re(D
MSA
) an
d ha
s vi
rtua
lly r
epla
ced
the
IVU
her
e. N
Mw
ill e
stab
lish
func
tion,
exc
lude
obs
truc
tion
and
can
also
be
used
for
cys
togr
aphy
(di
rect
or
indi
rect
) to
show
ref
lux.
For
mal
dir
ect
XR
cys
togr
aphy
is
still
need
ed i
n th
e yo
ung
(e.g
. < 2
yrs
) m
ale
patie
nt w
here
delin
eatio
n of
the
ana
tom
y (e
.g. u
reth
ral
valv
es)
isM
40cr
itica
l.
120
M. PaediatricsC
LIN
ICA
L PR
OBL
EMIN
VES
TIG
ATIO
N{D
OSE
}RE
CO
MM
END
ATIO
N{G
RAD
E}C
OM
MEN
T
Selected bibliography
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2 European Union. Council directive 97/43/Euratomof 30 June 1997 on health protection ofindividuals against the dangers of ionisingradiation in relation to medical exposure(OJ L 180, 9.7.1997, p. 22).
3 Roberts, C. J, ‘Towards the more effective use ofdiagnostic radiology. A review of the work of theRCR working party of the more effective use ofdiagnostic radiology 1976–86’. Clin Radiol 1988,39:3–6.
4 National Radiological Protection board and TheRoyal College of Radiologists. Patient dosereduction in diagnostic radiology(ISBN 0 85951 327 0). HMSO London, 1990.
5 RCR working party. ‘A multi-centre audit ofhospital referral for radiological investigation inEngland and Wales’. BMJ 1991, 303:809–12.
6 RCR working party. ‘Influence of the RoyalCollege of Radiologists’ guidelines on hospitalpractice: a multi-centre study’. BMJ 1992,304:740–43.
7 Roberts, C. J., ‘The RCR multi-centre guidelinestudy. Implications for clinical practice’. ClinRadiol 1992, 45:365–8.
8 NHS Executive. Clinical guidelines: usingclinical guidelines to improve patient care withinthe NHS (96CC0001). NHS Executive, Leeds,1996.
121
9 Sackett, D. L., Richardson, W. S., Rosenberg, W.,Haynes, R. B., Evidence-based medicine(ISBN 0 443 05686 2). Churchill Livingstone,Edinburgh, 1997.
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Appendix
List of bodies involved in the consultation exercisefor the 1998 UK RCR guidelines
Royal Colleges, etcAcademy of Medical Royal CollegesFaculty of Accident and Emergency MedicineFaculty of Dental Surgery, RCSFaculty of Clinical Oncology, RCRFaculty of Occupational MedicineFaculty of Public Health MedicineRoyal College of AnaesthetistsRoyal College of General PractitionersRoyal College of Paediatrics and Child HealthRoyal College of Physicians of LondonRoyal College of Physicians and Surgeons of GlasgowRoyal College of Physicians of EdinburghRoyal College of Physicians of IrelandRoyal College of PsychiatristsRoyal College of Obstetricians and GynaecologistsRoyal College of OphthalmologistsRoyal College of PathologistsRoyal College of Surgeons of EdinburghRoyal College of Surgeons of EnglandRoyal College of Surgeons of Ireland
Other organisationsBritish Institute of RadiologyBritish United Provident AssociationMedical Defence UnionMedical Protection SocietyNational Radiological Protection BoardThe Patients’ Association
Speciality groupsAssociation of Chest RadiologistsBritish Society of Nuclear MedicineBritish Society of GastroenterologyBritish Society of Interventional RadiologyBritish Society of NeuroradiologistsBritish Medical Ultrasound SocietyBritish Society of Skeletal RadiologistsDental Radiology Group
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Paediatric RadiologistsMagnetic Resonance Radiologists Association UKRCR Cardiac GroupRCR Breast GroupRCR Clinical Directors’ GroupRCR Interventional Radiology Sub-CommitteeRCR Nuclear Medicine Sub-CommitteeRCR Paediatric GroupRCR/RCOG Standing Committee on Obstetric USRCR/RCP Standing Committee on Nuclear MedicineUK Children’s Cancer Study GroupUK Neurointervention Group
The adaptation of the 1998 UK RCR guidelines into EU2000 referral criteria was performed in consultation with:
European Association of Nuclear MedicineEuropean Association of RadiologyUnion of European Medical Specialists
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European Commission
Referral guidelines for imagingRadiation Protection 118
Luxembourg: Office for Official Publications of theEuropean Communities
2001 —125 pp. — 10 x 19 cm
ISBN 92-828-9454-1
Price (excluding VAT) in Luxembourg: EUR 16