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RespiratoryRespiratoryDiseasesDiseases
caused bycaused byVirusesViruses
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MEASLES
RUBEOLAORMORBILLI
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DEFINITION
Measles is an acute highly contagiousviral disease caused by measles virus.It is characterized by fever, URTcatarrhal inflammation, kopliks spotsand maculopapules .
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ETIOLOGY1 . Measles virus.
2 .Site
of
the
measles
virus
exists
measles can be detected from blood and nasal, pharyngeal secretions.
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EPI DEMIOLOGY1.Source of infection
The patients are the only source of infection.2 .Routes of transmission
air-borne
3. Susceptibility of population3.1 All age person is susceptible; 90% of contact people acquire the disease.3.2 The permanent immunity acquire after
disease.4. Epidemic features
season:winter and spiringage:6 months to 5 years old
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CLINIC ALMANIFESTATIONS
Typical type1 . Incubation period is approximately 10-1 2 days.
2 . predromal phase 3~4 days.
2 .1 F ever;2 .2 C atarrhal inflammation of URT;
2 .3 K opliks spots;2 .4 Transient prodromal rashes.
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3. E ruption stage3 .1 . Time: the 3~5 days after fever;but the 4 th day is most common;
3 .2 . Shape:maculopapular3 .3 . Seuqence:behind the ear along the hairline face neck chest back abdomen
limbs hand and feet(palm,sole)3 .4 . The temperature rise continously and
companied w ith the toxic symptoms exaggerate
4 . C onvalescent stage
bro w n staining.fine branny desquamation.course: 10-14 days
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LABORATORY FINDINGSBlood routineSerum A b measurementcomplement combining antibody;hemagglutinin inhibiting antibody;
neutralizing antibody;specific antibody IgM.UA
Nose and throat sw abbing
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treatment1 .General therapy: rest and diet2. Symptomatic therapy: fever and
cough,3.Support threapy:r-globulin
traditional chinese herbsmay be used ;
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Amild viral illness caused by rubellavirus. It causes mild feverish illness
associated with rashes and aches in joints. It has a teratogenic effect onthe fetus
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Infectious Agent
Rubella virus (family-togaviridae;genus-
rubivirus)
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Incubationperiod
From exposure toappearance of rashUsually 14 to 21 days
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P eriod of communicability Th e virus is communicable
approximately 1 week before and fourdays before t h e onset of ras h es butis at worst w h en t h e ras h is at peak
High ly communicable infants wit h congenital rubella may s h ed virus formonth s after birt h
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C linicalManifestations
a. Prodromal stage L ow grade fever H eadac h e M alaise M ild coryza C
onjunctivitis P ost- auricular, sub occipital andposterior cervicallymph adenopat h y( 3 rd -5 t h dayonset1/21/2011 22
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B.Eruptive stage Forsc hh eimers spot
ras h es T esticular pain in youngadultsPolyart h ralgia andpolyart h ritis
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Very little treatment is
necessary:T reatment issymptomatic
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C omplicationsEnceph alitis
Neuritis Art h ritis
Art h ralgiasRubella syndrome manifested by: M icrocep h ally M ental retardation C ataract D eaf-mutism H eart disease
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Clinical mani f estati o n
(Co ngenital Rub ella)Classic congenital rubella syndrome I ntrauterine growt h retardation ( LBW ) Th rombocytopenic purpura blueberry
muffin skin
L et h argy and h ypot h ermia
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I ntrauterine infection M ay result to spontaneous abortion Birt h anomalies
Cleft palate, h are lip, talipes and eruptionof teet h
Cardiac defectsEye defectsEar defects
neurologic1/21/2011 27
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P reventi o n
Administration of live attenuatedvaccine ( MM R)
Pregnant women s h ould avoidexposure to patients infected wit h Rubella
Administration of I mmune SerumGlobulin one week after exposure toRubella.
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Nu rsing
managemento I solationo Bed rest until fever subsides
o D arken room to avoid p h otop h obiao M ild liquid diet but nouris h ingo I rrigate eyes wit h warm normal saline to relieve
irritation .
o Care of t h e ears do not apply h eat or cold unless soordered .o Good ventilationo Prevent spread of infection
o Prevent occurrence of complications1/21/2011 29
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Ch ickenpox (varicella)
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An acute h igh ly contagious disease ofviral etiology t h at is c h aracterized byvesicular eruptions on t h e skin andmucous membrane wit h mildconstitutional symptoms
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E tiologicagent
H erpesvirusvaricellae
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Incubationperiod
10-21 days or maybe prolonged after
passive immunization against chickenpox
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Mod e of
transmissi o nD irect contactI
ndirect contact AirborneD roplet infection
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P eri od of
c o mm u nica b ility Th e patient is capable oftransmitting t h e disease about a daybefore t h e eruption of t h e firstlesion up to about 5 days after t h eappearance of t h e last crop
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C linical
ManifestationsM ild fever and malaise- pre- eruptivestageEruptive stage Rash starts on t h e trunk M ilky and pus like papules ( 4 days) P ruritic vesicular lesions C elestial map M
ucule-papule-vesicles-pustule-crust1/21/2011 36
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Diagn o stic test
Complement fixation test
Electron microscopic examination ofvesicular fluid
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Treatment
mod alities Oral acyclovir O
ral antih
istamineCalamine lotion Antipyretics
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Nu rsing management
Respiratory isolationPrevent secondary infectionLinens must be disinfected
Cut fingernails s h ort and was h h ands A ch ild must wear mittensProvide alternative activities
Oral and nasal care1/21/2011 40
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S mallpox
(variola)1/21/2011 41
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An infectious and h igh lycommunicable disease c h aracterizedby marked symptoms during t h eprodromal period and appearance ofskin eruption, w h ich progressest h rough t h e stages of macule, papule,vesicle, pustule and crust, to end andputting scar formation
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Eti o l o gic agent
Variola virus- remains viable formonth s in a dry climate
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Inc ub ati o n peri od
8 to 17 days; 10 -12 days
(average); 1- 3 weeks
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Mod e of
Transmissi o nD irect contactD ropletinfection andsecretions
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Clinical mani f estati o ns
Fever, h eadac h e, weakness and
backac h e, abdominal pain, nausea andvomiting, severe muscular and jointpains
ras h
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STAGES..1. MUCUL AR STA GE2 . PA PUL AR STA GE3 . VESICUL AR STA GE4 . PAST UL AR STA GE
5 . CRU ST I N G STA GE
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CLINIC AL TYPES1. Variola minor or alatrim (kaffir pox,amaos)
A mild type of variola wit h low mortalityand was believed by some to be due to adifferent or mild type of virus .
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2 . V arill o id o r
Eruption proceed rapidly t h rough t h edifferent stages and said to be to apartial immunity or previousvaccination
Few and more superficial skin lesions
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3. Variolasine eruption
I n wh ich t h e eruptions occur after
a recent small pox vaccination andt h e lesions disappear after t h epopular stage or no eruptiveappears at all .
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4 . Flat type
Pre- eruptive illness- severe wit h
fever Focal lesion mature slowlyVesicles- flat, projecting little
surrounding skin and soft andvelvety to touc h
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5 . Hemorrhagic
type Hemorr h ages occur in t h e vesicles orin t h e surrounding areas .M ost serious clinical type of variolaPre- eruptive illness- severe2 nd
-3rd
day- bleeding from mouth
,conjunctiva, skinD eat h (5- 7 days) wit h maculopapular
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D iagnostic
ProceduresElectro M icroscopyM icroscopic Exam ofSmearsPrecipitation in GelC
omplementF
ixationT estLaboratory D ata
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ComplicationsSecondary skin infection wit h septicemia
F urunculosis- inflammation of furuncles A
bscess formation C ellulitis Gangrene
Laryngitis, pleurisy and emp h ysema Keritis and laryngeal ulcerations wit h edemaEnceph alitis and bronc h opneumonia maydevelop later .
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T reatmentSymptomatic
and supportive
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HES PES ZOSTE R
Sh ingles/ AcutePosterior Ganglionitis
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D efinition
An acute viral infection of t h esensory nerve caused by variety ofch icken pox virus
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E tiologic AgentVaricella Agent (V-Z virus) Th is agent h as been found two diseases,
varicella and h erpes zoster . Th e virus still occurs in partially immune
individuals due to previous varicella
infection .
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Period ofC
ommunicability Herpes zoster is communicable a daybefore t h e appearance of t h e firstras h until five to six days after t h elast crust
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M ode of transmission
D irect contactD roplet infection
AirborneI ndirect contact
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Clinical manifestationEryt h ematous base of skin lesionPain
Fever, malaise, anorexia and h eadac h eRegional lymph nodesParalysis of t h e facial nerve(ramsayh unt syndrome)Gasserian ganglionitis
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D iagnostic exam
T issue cultureSmear of vesicle fluidM icroscopySkin ras h may be diagnostic
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Complications
Enceph alitisParalytic ileus, bladder paralysis
Opt h almic h erpes may lead toblindness
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M odalities of
treatmentSymptomatic Antiviral drugs Analgesic to control pain Anti-inflammatory
antiviral
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N ursing management
Keep patient comfortable, maintainmeticulous h ygieneStrict isolation
Apply cool, wet dressing wit h N SS topruritic lesionsEfforts s h ould be made to preventsecondary infection
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Prevent entrance of microorganismsinto t h e lesions especially if t h eybreak
Assess degree of pain and to avoidneuralgic pain do not delay t h eadministration of pain relievers asprescribed
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INFLU E N ZA
La Grippe, F lu
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An acute viral infectious diseaseaffecting t h e respiratory system
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RNA containing myxoviruses,influenza virus types A , B and C
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I N CU BAT I ON PER
I O D
24 to 3 8 h ours (in some books 3 days)
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Period of
communicability Th e disease is communicable until t h e5 t h day of illness and up to 7 days inch ildren
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M ode of transmission
Airborne spreadD irect contactD roplet I nfluenza virus persists for h ours in
dried mucus
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Clinical
manifestationsCh illy sensation, h yperpyrexia,malaise . Sore t h roat,coryza,rinorr h ea, myalgia and h eadac h eBack pain, severe sweatingVomiting
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Complications
Hemorr h agic pneumoniaEnceph alitisM yocarditisS ID S
myoglobinuria
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D iagnostic
proceduresBlood examinations Oroph aryngeal swab cultureViral serology C omplement fixation test H emo-agglutination test
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A contagious disease of animalscaused by viruses t h at normallyinfect only birds and less commonlypigs.
Avian influenza viruses are h igh lyspecies specific but h ave on rareoccasions, caused t h e species barrierto infect h uman
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Causative agent
Avian influenza A (H 5N 1) virus
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M ode of transmission
D irect contact wit h infected poultryor surfaces and objects contaminatedby t h eir feces .
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I ncubation period
2 to 8 days and possibly as long as 17 days .
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P i d f
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Period of
communicability15 to 17 days after illness onset .I n t h e absence of corticosteroidadministration, immunocompetent A (H 5N 1) infected persons probablycease to excrete t h e infectious virusin 3 weeks after illness onset .
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F orms:
Low pat h ogenic form- may comeunnoticed .
High ly pat h ogenic form- h igh mortality rate often wit h in 48 h ours
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D iagnostic test
Collection of multiple respiratoryspecimensBlood and stool samples
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Complications
BacteremiaBacterial pneumoniaSh ockRenal failure
Respiratory failure
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N i
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N ursing
interventionsM onitor clinical status includingoxygenationEducation on personal h ygiene andinfection control measures
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Sw ine I nfluenza
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A very contagious acute viralrespiratory disease of pigs
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Causative agent
Swine influenza virus H 1N 1
H 1N 2 H 3N 1 H 3N 2
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M ode of transmission
D irect contactRespiratory secretions and bodilyfluids
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I ncubation period
U nknown; 1 to 7 days
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Period of
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Period ofC
ommunicability One day before until 7 days aftert h e case onset of illness
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C d fi i i f i f i i h
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Case definition for infection wit h swine-origin influenza A (H 1N 1)
Confirmed caseProbable caseSuspected case
***reverse transcriptase polymerasech ain reaction (R T -PCR)
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S I GN S AN D
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S I GN S AN D
SYMP TO M
S Fever Headac h eU pper respiratory tract symptomsM yalgia
FatigueVomiting
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treatment
Oseltamivir (tamiflu) and zanamivir(relenza)- initiated as soon as
possible after t h e onset of symptomsfor 5 days
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Complications
Exacerbation of underlying c h ronicmedical conditionU pper respiratory tract diseaseLower respiratory tract diseaseCardiac complication
Neurologic complication
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A void close contact( 6 feet away) P roper disposal of articles used by
infected person D isinfection W ash linens in h ot water
C ontact h ealt h provider if a sick personh as t h e ff symptoms:Ch est pain
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D O B
Purplush / bluish lip discolorationV
omitingSeizuresConfused / less responsivedeh ydrated
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M U M PS
I nfectious Parotitis/Epidemic Parotitis
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D efinition
An active viral disease manifested byt h e swelling of one or bot h parotid
glands, wit h occasional involvement ofot h er glandular structures,particularly t h e testes in male
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Etiologic A gent
Paramyxovirus group t h at is usuallyfound in saliva of an infected person
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I ncubation Period
14 to 2 5 days (t h e average is 18 days)
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Period of
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Period ofC
ommunicability Th e disease is communicable 6 daysbefore and 9 days after t h e onset of
parotid gland swelling Th e 48 - h our period immediatelypreceding onset of swelling isconsidered t h e time of h igh estcommunicability
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Clinical
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Clinical
manifestations Headac h e J oint pains*Pain on c
hewing and swallowing(earliestsymptom)
Earac h e*Back pain*loss of appetiteLow grade fever
swelling of th
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Complications Orc h itis in male Ooph oritis in femaleM astitis
Nuch al rigidityD eafness
J uvenile DMLow or absent sperm countCongenital malformations in pregnantwomen
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D iagnostic test
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D iagnostic test
Blood exam- h igh leukocyte countComplement fixationViral culture
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T reatment
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T reatment
modalitiesSupportive care Hot or cold compressanalgesics
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N ursing management
1. M edical aseptic protective careA . I solation
B. W ash h ands regularlyC. D isinfectionD . O ral and personal h ygiene
2 . General managementa. Bed restb. D iversional activities
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3 . D ieta. no restriction to foodb. soft and semisolid food
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VI RAL E N CE PH ALI T I S
Brain F ever
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O
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D EF I N I T I ON
An inflammation of t h e centralnervous system resulting in abnormal
function of t h e different parts oft h e brain and t h e spinal cord .
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I b P d
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I ncubation Period
5- 15 days wit h a range from 4 to 21 days
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Classification and
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lassification andPat h ology
PRIM ARY EN CEPHA LI T I S Eastern Equine Encep h alitis W estern Equine Encep h alitis J apanese B St . Louise Encep h alitis
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PO ST I NF ECT I O U S / SECON D ARY EN CEPHA LI T I S U sually a complication or a sequelae to
some viral diseases like measles, c h ickenpox and mumps
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General
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GeneralM anifestations
Fever, h eadac h e, dizziness, vomitingad apat h y
Sore t h roat, conjunctivitis, at h ralgia,myalgia and abdominal pain
Nuch al rigidity, ataxia, tremors,mental confusion, speec h difficulties,stupor and h yper-excitability,convulsions, coma, deat h
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D isturbances in swallowing,movements of t h e muscles of t h e
eyes and faceM uscle twitc h ing
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D i i
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D iagnostic exams
CSF analysis Neutralization test
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T
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T reatment T reatment must be symptomatic andsupportiveC
onvulsions must be controlled Nose and t h roat secretions s h ouldbe sanitarily disposed
T SB Oral fluid s h ould be encouraged Oral care
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Cli i l
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Clinical management
Provide comfort Keep patient in a quiet, well ventilated
room Stretc h linens Encourage or do oral h ygiene D o bed bat h if not contraindicated
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Prevention from complication T urn patient to sides at least every 3 to
4 h ours Encourage increase oral fluid intake Encourage h igh caloric intake M onitor intake and output
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Th ank y ou