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Transcript
Dr. Osama Kentab, MD, FAAP, FACEP
Assistant Professor of Paediatrics and emergency Medicine
King Saud Bin Abdulaziz university for Health sciences
Riyadh
Epidemiology
 Very common sign and symptom of illness in
childhood
 May be indicative of an infection that is local or
systemic; benign or invasive & life threatening
 Normal body physiological reaction to pyrogen
( infective, inflammatory)
Implications of body temperature
 Is it beneficial?
 Rate of bacteraemia is 2-3% in all febrile infants <
2months (Baker 1999; Kadesh et al 1998)
 Infants < 2 months differ are less immunocompetent
unique group of bacteria (GBS, Gram. Neg bacteria &
listeria)
 Young infants show relative inability to demonstrate
clinical evidence of illness
Assessment: Relevant history
 Duration of fever
 Pattern of fever: intermittent or continuous
 Hx of contact: family members, friends, school
mates
 Hx travel abroad: country visited
 Malaria endemic regions, enteric fever (Africa, Asia)
Travel immunization, malaria prophylaxis
 Travel to mountainous region, camping in forest
(Rickettsial infection, Lyme disease)
 Hx of Immunization
Relevant symptoms
 Systemic symptoms: Resp, ENT, Renal, GI
 Rash: Pattern/type (macular, papular, ulcerative,
erythematous, blanching)
 Distribution (mucosal involvement-conjuctivitis,
mucositis, buttocks and extremities(HSP) Oral ulcers
(aphthous, herpes gingivostomatitis)
Relevant clinical signs
 Unwell – Toxic
 Haemodynamic instability
 Rash
 Lower Respiratory signs
 Joint involvement: Arthritis/ Athralgia: Reactive
viral arthritis, Septic arthritis, HSP, Rheumatic
fever, Chronic arthritis of childhood
 Organomegaly: Hepatomegaly, Splenomegaly, +/Anaemia: Systemic illness, Septicaemia,
Lymphoproliferative disorders
Causes of febrile illnesses in
childhood
 Common causes
 URTI (viral or bact.)
 LRTI
 Gastroenteritis
 UTI
 Oral (dental abscess,
hyperangina, herpetic
gingivitis, mumps)
 MSS (septic arthritis,
osteomyelitis,
cellulitis
 Serious causes
 URTI (epiglottitis,
croup,
retropharyngeal
abscess)
 LRTI
 GI (appendicitis)
 CNS (Meningitis,
encephalitis)
 Systemic
(meningococcaemia,
toxic shock syndrome
Management of fever in young
children
Protocols for Identification of Low Risk Infants
Rochester
1985-1988
Boston
1992
Philadelphia
1993-1999
Pittsburgh
1999-2000
28-89
29-56
0-60
-
No known immundef.
Rochester
38.0
38.0
38.0
Yes
Yes
no
<20,000
<15,000
<5>15
<1.5x10/L
<0.2 BNR
no
Yes
Yes <8 wbc
Yes  5
10WBC/hpf
-
10WBC/hpf
EUA  9
5 wbc/hpf
-
-
<5
-
-
Yes
Neg if sx
Age(days)
0-60
Past health
>37 wk,home with or before mom,no susequent hosp,no
prenatal, post,or current ATB,no treatment for unexplained
hyperbole,no chronic diseases
Temp C
Infant Obs.score
WBC
Bands/BNR
LP
urine
Stool(if diarrhea)
CXR
38.0
no
5-15,000
No
ATB(Ceftrx)
No
Yes
No
34.7%??
SBI in low risk
Pts (%)
1.1
5.4
0
0
NPV(%)
98.9
94.6
100
100
Sens (%)
92.4
Not stated
100
100 8
Age < 29 days
 CBCD,glucose,BUN,Creat,lytes, +/- cap.gasses
 Blood culture
 Urine cath (microscopy and culture)
 LP (if infant unstable defer)
 CXR (suspected respiratory disease)
 NPW (suspected viral respiratory disease)
 Stool for WBC, culture and heme test (suspected
eneteric infection)
Management of fever in young children
9
Age < 29 days
Cont’d
 Supportive care
 Antibiotics:
Ampicillin AND
Gentamycin OR Ceftriaxone/Cefotaxime
Consider Acyclovir
 Admit
Management of fever in young children
10
29 to 60 days
 CBCD, BNR
 Blood culture
 LP (if infant unstable defer)
 Urine cath (microscopy and culture)
 CXR (suspected respiratory disease)
 Stool for WBC, heme test and culture (suspected
enteric infection)
Management of fever in young children
11
29-60 days
Low risk
Past history
 Born >37 wks
 Home with or before the mother
 No subsequent admission
 No prenatal,postnatal,or current antibiotics
 No treatment for unexplained hyperbilirubinemia
 No known immune deficiency
Management of fever in young children
12
29-60 days
Low risk
P/E
 Appears generally well (non-toxic)
 No evidence of skin,soft tissue,bone,
joint,or ear infection
Management of fever in young children
13
29-60 days
Low risk
Laboratory
 WBC >5k <15k
 ANC <10K or band/neutrophil ratio < 0.2
 Urine <10 WBC/hpf, spun and negative Gram stain
 CSF: Non-bloody ,< 8 WBC , normal glucose,
protein, negative Gram stain and latex agg.test
 Normal CXR (if it was done)
 Stool (if diarrhea) <5 wbc/hpf
Management of fever in young children
14
29-60 days
Low Risk
Option I
 No antibiotics
 Admit for observation OR
 Re-evaluate in 24 & 48
hours
Discharge only if:
Reliable caregiver
Has nearby telephone
Adequate transportation
Management of fever in young children
Option II
 Ceftriaxone 50 mg/kg
IV or IM
 Re-evaluate in 24 hours
and 48 hours
 Optional second dose
of ceftriaxone at second
visit
15
61-90 days
Low Risk
Option I
 No LP
 No antibiotics
 Admit for observation OR
 Re-evaluate in 24 hours
Discharge only if:
Reliable caregiver
Has nearby telephone
Adequate transportation
Management of fever in young children
Option II
 LP & if normal:
 Ceftriaxone 50 mg/kg (IV
or IM) OR
 NO antibiotics
 Admit for observation.
OR
 Re-evaluate in 24 hours
16
29-90 days
High risk
 Toxic
 Positive labs
 Concerning history
/social factors
 Admit
 Supportive care
 Meningitis
Ceftriaxone and
Vancomycin
 Non-meningitis
Ampicillin and
Ceftriaxone OR
Gentamycin
Management of fever in young children
17
3-36 months
 Toxic looking
Fever, meningeal signs, lethargic, limb, mottled
 Admit, septic work-up, parenteral antibiotics
 Focal bacterial infection
OM, pharyngitis, sinusitis, etc (excluding SBI).
 Oral/parenteral antibiotics, outpatient care
 Well looking
Risk for occult bacteremia and serious bacterial infection
 Previous decision analysis( Pre-H. flu immunization)
 Current decision analysis
Management of fever in young children
18
3-36 months
High risk/toxic
 Admit
 Supportive care
 Septic work-up
 IV antibiotics

Meningitis---->Vanco + Ceftriaxone

Non-meningitis ----> Ceftriaxone
Management of fever in young children
19
3-36 months
 Non-toxic
 If <3 yrs,temp >39 :
 Obtain CBC,Blood culture,Urinalysis & culture
 Stool culture,CXR as indicated
 If WBC>15k --->Empiric antibiotics
(Ceftriaxone,Clavulin,Biaxin, omnicef or Suprax )
 If urine is positive treat as UTI
 If WBC normal ,urine is negative no therapy
needed
Management of fever in young children
20
3-36 months
Cont’d
 IF Temp < 39, Non-toxic, No focus of infection
NO INVESTIGATIONS ARE REQUIRED
 Follow up all in 24 hours
Management of fever in young children
21
Management of fever in children with
underlying illness
Management of fever in young children
22
Oncology patients
At risk of overwhelming sepsis
 CBC, CXR, blood culture, urine culture, and LP when
clinically indicated
 Neutropenic patients at risk for Pseudomonas and
other gram negative
 Broad spectrum antibiotics
Management of fever in young children
23
Acquired Immunodeficiency Syndrome
 Repeated risk of infection with common bacterial
pathogens, risk of Pneumocytsis carinii, mycobacterial
infections, cryptococcosis, CMV, Ebstein-Barr virus.
 Low CD4; septic work up and broad spectrum
antibiotic
Management of fever in young children
24
Sickle Cell Anemia
 Functional asplenia susceptible to overwhelming
infection esp. encapsulated organisms such as
pneumococci and H. flu
 Parvovirus can cause aplastic crisis
 Osteomyelitis should be suspected in fever and
bone pain
 CBC, retics,blood culture, stool culture, and urine
culture recommended
 Ceftriaxone
 Hospitalization recommended
Management of fever in young children
25
Congenital Heart Diseases
 Children with valvular heart disease are at risk for
endocarditis
 Fever without obvious source with a new or
changing murmur; hospitalization, serial blood
cultures, echo, antibiotics against: S.viridans,
S
aureus, S. fecalis, S. pneumo, enterococci,
H.
flu, and other gram neg rods
 Suggested antibiotics include Vancomycin and
Gentamycin until cultures are known
Management of fever in young children
26
Ventriculoperitoneal shunts
 Must be evaluated for shunt infection esp if patient
displays headache, stiff neck, vomiting, or irritability
 Shunt reservoir should be aspirated and examined for
pleocytosis and bacteria
 Most common pathogen is S. epidermidis
 CT head also warranted
Management of fever in young children
27
Febrile Seizures
 455 children with simple febrile seizure
-1.3% with bacteremia
-5.9% UTI
- 12.5% with abnormal chest x-ray
-Normal CSF in all who had an LP (135)
Trainor J, et al: Clin Pediatr Emerg Med 1999
Management of fever in young children
28
Febrile Seizures
486 children with bacterial meningitis
-complex seizures present in 79%
-93% of those with seizures were obtunded
-of the few with “normal” LOC, 78% had nuchal
rigidity
Green SM, et al: Pediatrics 1993
Management of fever in young children
29
Febrile Seizures
 Synopsis of the American Academy of Pediatric
practices parameters on the evaluation and
treatment of children with febrile seizures
 LP strongly considered in the first seizure in infants less
than 12 month because signs and symptoms of
meningitis may be absent in this age group
 12-18 months LP should be considered because sign of
meningitis may be subtle in this age group
 18+ months LP only if signs and symptoms of meningitis
(Peditrics 1999)
Management of fever in young children
30
Febrile Seizures
 Routine lab (CBC, lytes, Ca, phos, Mg, or glucose)
should not be performed in simple febrile seizure
 Neuro-imaging should not be performed routinely
on simple febrile seizure
 EEG is not performed in a neurologically healthy
child with simple febrile seizure
 Anticonvulsant therapy is not recommended in
simple febrile seizure
Management of fever in young children
31
DDx Fever with rash
 Viral exanthems
 Streptococcal infection
 Staphylococcal scalded skin syndrome / Toxic
shock syndrome
 Kawasaki disease
 Meningococcal disease
 Henoch Schonlein purpura (HSP)
Measles
 paramyxo virus
 Spread by respiratory droplets
 Incubation period: 7 – 12 days
 CF: prodromal period (fever, conjuctivitis, coryza, dry
cough, koplik spots +/- lymphadenopathy) florid
maculopapular rash appearing over head and neck
spreading to cover the whole body X 3-4 days
 Infectious from the prodromal period until 4 days
after rash appeared
 Dx: Measles Antibodies in saliva or serum
 Complications: OM, pneumonia, encephalitis,
subacute sclerosing pan encephalitis
Chicken pox (Varicella)
 varicella zoster DNA virus
 Incubation period 14 – 21 days
 Fever & malaise X 5-6 days followed by crops of skin
lesions that go through stages of macules, papules,
vesicles, and crusting
 Infectious 2 days before rash until vesicles dry/crust
 Complications: Secondary bact. Infection of lesions,
haemorrhagic varicella, pneumonia, encephalitis,
ataxia at 7-10 days after rash
 Severe illness in immunocompromised adults, preg.
Women & neonates
Rubella (german measles)
 RNA rubella virus
 Incubation period: 14 – 21 days
 Fever, rash, posterior cervical lymph node
 Complications: Deafness,encephalitus, Congenital
rubella syndrome
 Rx: Symptomatic
Roseola infantum (Human herpes
virus type 6)
Roseola infantum
 Caused by Human herpes DNA virus type 6 & 7
 Many children already infected by 2 years
 Incubation period: 5- 15 days
 CF: short febrile illness x 3- 5 days and an
erythematous rash
 Complication: Meningoencephalitis & Sz
Fifth Disease
Erythema infectiosum (Fifth ds/
Slapped cheek ds)
 Human parvo virus B19
 Incubation period: 7 – 17 days
 Head ache & malaise
 rash on face ( slapped cheek app.) spreading to
the trunk and limbs with maculopapular lesion
evolving to a lace- like reticular pattern
 Complications: Aplastic crisis with underlying
chronic haemolytic anaemia, Aseptic
meningitis, Hydrops fetalis
Hand, Foot & Mouth disease
 Caused by coxsackie A16, A19 and Enterovirus 71
RNA viruses
 Incubation period: 4 – 7 days
 CF: fever, malaise , head ache, pharyngitis,
vesicular lesions on the hands and feet including
palms & soles
 May be complicated by chronic recurrent skin
lesions
 Rx: Symptomatic
Infectious mononucleosis
(Glandular fever)
 Ebstein Barr (DNA) virus
 CF: fever, lymphadenopathy, tonsillitis, headache,
malaise, myalgia, splenomegaly, petechiae on soft
palate, rash (macular, maculopapular, urticarial or
erythema multiforme)
 DX: EBV specific IgM; Paul Bunnell test
 Complication: Splenic rupture, ataxia, facial nerve
palsy, aplastic anaemia, interstitial pneumonia
 Rx: Symptomatic
UTI in childhood
 UTI is common
 VUR is assoc with renal scarring particularly in the
1st year pf life
 chronic renal failure
 Neonates – irritability, refusal of feeds, vomiting,
FTT, prolonged NNJ, toxic/extremely unwell
 Pre-school: vomiting, poor wt. Gain, fever, malaise,
freq, dysuria, enuresis, haematuria, loin pain
UTI (2)
 Inv: Urine m/c/s x 2 (or 1 SPA urine sample) –
mid stream, clean catch, bag, SPA urine sample
 Pyuria, organism on microscopy
 Significant bacteruria > 10 5 org/ml or and growth
from SPA
 Treatment: Antibiotics PO or iv
 Commence low dose prophylactic antibiotic
 Refer to the Paediatrician for further investigations
Meningococcal disease




Gram neg. diplococci
Nasopharyngeal carriage in 25%
Invasive disease in 1% carriers
15% meningitis; 60% Septicaemia + endotoxaemia;
fulminant septicaemic shock with circulatory failure &
wide spread purpura
 Rx: Antibiotics; management of shock, anticipate
ventilatory failure
 Transfer to PICU and contact public health dept
 Prognosis: Poor if <1 year, better if evolution of ds slower;
overall mortality approx. 30%
Kawasaki disease
 Systemic vasculitis of early childhood
 80% cases < 4 years & M:F ratio = 1.5:1
 No single diagnostic test; 5/6 clinical criteria
 fever >5 days
 Changes in the mucous membrane of URT
 Changes in the peripheral extremities (oedema,




desquamation
Polymorphous rash (urticarial, maculopapular,
multiforme)
Cervical lymph adenopathy
Exclusion of staphylococcal & streptococcal infection &
others (Measles, drug reaction, JCA)
Coronary aneurysm +fever + 3 / 4 criteria
Kawasaki disease (2)
 Other features: irritability, arthritis, aseptic
meningitis, hepatitis, hydropic gall bladder
 20-30% Myocarditis, pericarditis, arthymia, cardiac
failure, coronary aneurysm
 Rx: High dose IV Ig 2g/Kg over 12-18 hrs
 High dose Aspirin 30mg/Kg/day until fever resolves
then 3-5mg/Kg/day
 Cardiac echo for coronary aneurysm
Investigation
 According to the differential diagnosis
 Indicated if child is unwell and or no cause
identified
 full infection screen
 Urinalysis & Urine m/c/s
 where no focus of infection
 All children <2 years where S&S of UTI is non
specific and diagnosis has implication for future
management
 With urinary symptoms
 Before starting antibiotics
Complete Infection Screen
 FBC & blood film; WBC differential, band
neutrophil ratio
 CRP
 Throat swab: virology, m/c/s
 Urine m/c/s
 Blood c/s
 Blood for PCR and rapid antigen screen:
meningococcal, pneumococcal,
 Stool m/c/s & virology
 CXR
 LP for CSF analysis: protein, glucose, m/c/s
Treatment
 Temp control: antipyretics (paracetamol,
Ibuprofen) exposure & avoid dehydration
 Sick / deteriorating child: supportive mx with best
guess antimicrobial therapy
 Specific cause
 Indication for referral to paediatric team
 Unwell/ toxic
 Unknown source or cause of fever particularly in early
childhood
 Associated systemic symptoms & signs
 Fever > 14 days (PUO)