RESPI CAUSED BY VIRUS

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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

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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

    lesions 53

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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

    e parotid gland* 110

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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