PRESBYTR UNIVERSIT MEDICAL
B P.K.K CLINICIAN/ANA EXP
TRIAN SITY OUTSPAN L COLLEGE
BY K.KUBAI NAESTHETIST/MPH XPERT
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PRESBYTR TRIAN UNIVERSIT SITY OUTSPAN MEDICAL L COLLEGE B BY - - PDF document
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B P.K.K CLINICIAN/ANA EXP
BY K.KUBAI NAESTHETIST/MPH XPERT
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n An acute systemic vir
by inhalation of infect by inhalation of infect virus viral infection transmitted ective droplets of measles ective droplets of measles
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n Highly infectious dise n Humans are the only
Humans are the only
n Average incubation p
days, varying from 7- to onset of fever. isease ly reservoir ly reservoir period 10-12
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§ Direct contact with nasa
infected persons.
§ Spreads slightly before
4 days after the appear
§ All people who have no
immunized are suscept immunized are suscept asal or throat secretions of re the onset of symptoms to arance of rash. not had the disease or not ptible. ptible.
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1500 134 1500 2000 2500 1200 1243 134 500 1000 2002 2003 2004 20005 Reported measles cases Confirm
1344 1677 1344 1877 2100 1344 1344 2006 2007 2008 2009 irmed measles cases Unvaccinated children
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n Its highest incidence
permanent immunity ce is in young children and measles one acquires measles one acquires ity (natural immunity)
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n Its more virulence (co
greater during eruptio long as the rash rema (communicability) is tion/rapturing stage or as mains
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n Kopliks spots- unique
membrane esp. on bu
n Conjunctivitis – inflam n Cough n Cough n Coryza/flu n Rash- maculo papura
****KC3R
ue spots on mucous buccal cavity lamed conjunctiva ura in character
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n Usually 10 – 12/7 n Time taken before the
the onset of s/s
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n Route nasal – pharyn
droplets from an infe crying, sneezing and
rynx by the infective fected person during nd oughing
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Person
Age Measles vaccination
Time
Date of rash onset
Place
Residence at onset Potential exposures
ion status et es (places, persons)
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n .
Maculopapular Rash
+
Fever
+
Clinician Susp
Cough OR Runny nose (Coryza) OR
+
OR Red eyes (Conjunctivitis)
+
uspects Measles
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v Divided into various stag q Prodromal Phase
v High fever v Cough, v runny nose (coryza) an v red eyes (conjunctivitis
ages and/or itis)
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.
Incubation Period (7-18 days before Rash)
Rash minus 18 days is earliest possible exposure date Rash minus 4 days is probable start of infectiousness
5
+1 + +3 +4 +5 +6 +7 +8
Prodrome (about 4 days) Rash (about 4-8 days)
5
+1 + 2 +3 +4 +5 +6 +7 +8
Onset of rash Rash plus 4 days is probable end of infectiousness Communicable Period
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n
Its characterized by:
q Catarrhal Rash
v Onset 2-4 days after onset v Incubation period: 14 days v Red, blotchy (maculopapula v Moves from face to trunk of v Lasts 5-6 days v Fades in order of appearan
q
Common S/S in this stage
1.
Coryza – occurs between day 2
2.
Conjunctivitis which may have
3.
Running nose
4.
Apathy/malaise
5.
Fever
et of prodrome s (range, 7-18 days) ular)
ance
y 2 -4 /7 after infection (range ) e secondary bacterial infection
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n Most of the time this s
because the s/s are li except for Kopliks spo except for Kopliks spo greyish, white dots us sand/table salt, reddis haemorrhagic on the is stage passes unnoticed e like for other disease spots – Nb. they are spots – Nb. they are usually like grains of dish and sometimes the palate/buccal cavity
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n Kopliks spots may als
grains on the margin
also appear on the embranes embranes e coated with reddish gins is common r (40 – 41 Oc ) and rash -
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n Begins as faint macu n Starts from lateral sid
along the hairline
n Post auricular / cheek n Post auricular / cheek n Individual lesions late
papular rash
n Then it later spreads
then upper limbs, che lower limbs cules side of the neck/head eks eks ater changes to macular – ds to the whole face, neck hest abdomen , back and
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n Rash which appears
fades off by 2-3/7
n Itching may occur as n The rash affects all b n The rash affects all b
externally and interna rs first on face and necks as it fades off l body systems i.e. l body systems i.e. rnally
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n General condition of t n Vital signs n S/E or Regional Exam
am
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n P/A – splenomegally
some patients
n
GIT – Symptoms - d common common
n R/S: Are common w
like Otitis media and
n Lab. CBC – Low WBC
lly may be an evidence in diarrhea and vomiting are with assoc. complications d pneumonia BCS with lymphocytosis
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n Purely by hx and exa n Throat swab for lab b
virus because of late xamination but it rarely yields the te diagnosis or lack of it
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DDX of measles are d with with
e diseases which present ith RASH ith RASH
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Rubella Dengue Measle
Roseola Infantu Toxoplasmosis Scarlet Fever
Other Viral Exanthems Kawasaki
tum Meningococcemia Mononucleosis
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n Common in pregnant
very severe and fatal
n Mild and transient in n n The rash has same a n The rash has same a
but no constitutional s in measles morbili i.e , diarrhoe, conjunctivi
nt women and usually tal in non pregnant women appearance and pattern appearance and pattern al signs and symptoms like i.e. fever tivitis and vommiting
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n Common in malnouris
n In normal children the
they have antibodies they have antibodies
a) Conjunctivitis – ulce b)
Otitis Media – Bact
urished children because ne system/HIV or ISS there may be non because es from their parents es from their parents lcerations/neuritis/blindness acterial infxn may occur
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c) Cervical adenitis in 1 d) Mouth ulcers – sepsi bacterial 15% of children psis of kopliks spots by
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n Viral/bacterial bronch
OF children with mea leads to high mortality
n Tracheo- bronchiolitis
Tracheo- bronchiolitis may lead to LTB
n Flaring of T.B. n Bronchitis - rare n Lung abscess - rare
ncho pneumonia in 50% easles associated RDS lity litis – due edema of R/S litis – due edema of R/S
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cases of children with
high mortality or perm
urs in 1 out of every 1000 ith measles al signs and rx its assoc. with rmanent disability
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is encephalitis rare
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n Thrombocytopenia –
– leads to parpura
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n Gastro enteritis asso
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n Rare n Myocarditis may occu
ccur leading to heart failure
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v Manage case (give vitam
treat symptoms or compl
v Report case to District D v Collect a blood serum sp
v Quantity-4-8mls of blo v Quantity-4-8mls of blo v Container v Reverse cold chain
v Fill out a case investigati
amin A, encourage fluids, and plications, if present) t Disease Surveillance Officer specimen blood blood ation form (IDSR)
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n By virtue of it being a
no definitive managem
n Mnx and treat and pr
a viral infection there is gement prevent complications i.e. ial infxn Rx with antibiotics ial infxn Rx with antibiotics
f G.E/Pneumonia
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n Conjunctivitis – T.E.O 1 n Otitis Media - Broad sp
BSA) chloramphenicol ciproflaxin etc Pneumonia - Broad sp
n Pneumonia - Broad sp n Tracheo bronchiolitis –
& cough suppressants/ linctus
n
NB never give expecto O 1% TID/BID spectrum antibioticxs (
spectrum antibioticxs ( BSA) spectrum antibioticxs ( BSA) – steam inhalation /inhalers ts/linctuses e.g. actifed ctorant
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n T.B. – After confirmin
scoring Ant T.B regimen ma Diet is key Diet is key
n G.E. – Rehydrate with
depending on degree
n SUB acute sclerosing
nursing care ing the DXX by T.B ay be started ith ORS or I.V.F ee of dehydration ing Panencephalitis -
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Heart Failure - Antifailu & vasodilators ilure regimen i.e. diuretic
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Vaccinations/immunizations
immunization
v Strengthening of v Conduct Supplem v Conduct Supplem
up) immunizatio
and mnx of meas
management.
n/education – on
lemental (catch-up,Follow- lemental (catch-up,Follow- ation. g of measles surveillance easles outbreaks g of measles case
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After 1st dose at 9 m wit 1.0 x 0.80 x 0.85 = After 2nd opportunity wit 0.32 x 0.90 x 0.95 = 0.32 x 0.90 x 0.95 = 1st + 2nd dose = 0.6 immunity)
Ł
Herd immunity th
with 80% coverage: 0.68 immune with 90% coverage: = 0.27 immune = 0.27 immune 0.68 + 0.27 = 0.95 (95% threshold achieved
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against measles (do n
against measles throu immunization service
not develop protection
id not get vaccinated id not get vaccinated rough routine ices (drop-outs)
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measles control
tions or areas at high-risk stigate outbreaks stigate outbreaks ation strategies to improve
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1) Complete case investigation fo confirmation for every su
incase of cluster 2) Notify DDSC/DMOH/DPHN
the area the area 3) Conduct active case finding in identify other suspected c 4) Investigate other suspected ca
status) 5) Analyze data and give feedba
n form and collect blood for laboratory suspected case after first 5-10 with key information ice should notify all health facilities in in health facilities and villages to d cases cases key information (age, vaccination back to community
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n Disease s of Children
653 – 657
n Diseases of children
17/11/ 17/11/
n MoH policy framewor n WHO recommendatio
ren by Vellard & Mac pgs n by Hugh Jolly pgs
tions
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