++
The management of the child with acute fever is discussed in
Chapter 227. Management of the child with chronic fever of unknown
origin is discussed in Chapter 228, and of fever in the immunocompromised
child in Chapter 229. An algorithm for the management of infants
and children with acute fever is shown in Figure
227-1.
+++
Infant Less
Than 3 Months of Age
++
Traditionally, the majority of clinicians in the United States
investigated aggressively any infant who presented with fever before
2 to 3 months of age,2 including a broad laboratory
investigation for bacterial disease, hospitalization, and empirical
parenteral administration of antibiotics. In the 1990s, this approach
became tempered by a series of large clinical studies3,4 that
established new screening tools to identify febrile infants at low
risk of having a serious bacterial infection (Table 105-1).
Of the three screening tools developed,3,5,6 the
model created at the Children’s Hospital of Philadelphia5 was
the most conservative and had the highest negative predictive value.
++
++
The application of screening tools has diminished the number
of febrile infants who are admitted to the hospital or who leave
the emergency room with antibiotics. However, the approach to managing
fever in the young infant is far from uniform, and many pediatric
practitioners continue to rely on long-established personal practices.7
++
A few principles are well accepted. In the presence of fever,
the clinician should conduct a thorough history and physical examination,
including an assessment of well or ill appearance. The latter must
prompt aggressive investigation for possible bacterial infection
and empirical administration of antibiotics as an inpatient regardless
of initial results of diagnostic tests.
++
Well appearance, while reassuring, does not necessarily indicate
absence of bacterial disease. Even when validated objective criteria
for clinical appearance are applied,8 many senior, experienced
clinicians will describe infants who have culture-proven serious
bacterial infections as appearing well.
++
The minimum diagnostic testing for evaluating fever in young
infants consists of a complete blood count with differential, blood
culture, urinalysis with microscopy, urine culture, and usually
spinal fluid analysis and culture. To minimize contamination, the
urine sample should be obtained via urine catheterization or bladder
puncture, and not by bag collection.9
++
A lumbar puncture is indicated in febrile infants less than 1
month of age and in any ill-appearing older infants. Performing
a lumbar puncture in well-appearing febrile infants who are 1 to
2 months of age has become a source of debate over the past few
years. Some studies suggest that lumbar puncture can be delayed
or omitted provided that the infant meets all low-risk clinical
and laboratory criteria and that the parents are reliable observers
and have appropriate follow-up skills.7 However,
recent data has shown that 40% of infants with bacterial meningitis
had total white blood cell counts in the usually acceptable range
(5000–15,000), so this was not a reliable predictor of
absence of bacterial meningitis.1 In another study
of the performance of clinical criteria for infants at very low
risk of bacterial meningitis, all failures of the tool to predict
absence of bacterial meningitis involved infants younger than 2
months of age.10
++
The necessity of obtaining a chest radiograph in every infant
with fever is also a debatable issue. Several clinical studies have
shown that the chest film has a low yield in those infants who do not
have specific signs of respiratory disease.11
++
The use of acute phase reactants such as C-reactive protein (CRP)
and procalcitonin (PCT) as predictors of bacterial infection has
come into vogue in recent years.4,12 Both CRP and
PCT are produced by the liver in response to cytokines like tumor
necrosis factor alpha and interleukin-6. Their values increase 3
to 4 and 4 to 6 hours, respectively and peak within hours after the
onset of fever. While valuable as a screening tool, none of these
acute phase reactants is reliable as a sole predictor of bacterial
infection.
++
It is a widely held concept that children develop acute illnesses
as single and distinct events, one at a time. Reports of some groups of
infants, such as those with clinical bronchiolitis (defined as presence
of fever and wheezing), cite very low rates of concurrent bacterial infection.13 However,
rapid testing and identification of viral agents is not useful to
rule out the possibility of bacterial infection since evidence suggests
that young infants can test positive for two infecting agents at
the same time. During the past two decades, studies of large cohorts
of febrile infants and preschool-age children have consistently
demonstrated that 6% to 7% will test positive
for the simultaneous presence of viral and bacterial pathogens.14,15This
is true of infants with documented respiratory syncytial virus infections16 and
with other common viral infections.17 In infants
who have documented viral disease, the most common location for
simultaneous bacterial infection is the urinary tract. However,
bacteremia occurs in approximately 1% of infants who test
positive for the presence of common viruses.
+++
Infants and
Young Children (3 to 36 Months of Age)
++
The rates of bacterial infection in older infants and toddlers
lie in between the higher rates for newborns and the lower rates
for school-age children. As is the case for those younger and older,
the urinary tract is the most common site of bacterial infection
associated with fever in this age group, with a reported incidence
of approximately 5%. Responsiveness of fever to antipyretics
does not correlate with likelihood of presence of bacterial disease.
While several prospective design studies have disproved any such
correlation, many parents continue to value this myth.
++
Occult bacteremia, which is defined as a positive blood culture
in a well-appearing febrile child who has no discernable focus of
infection on clinical evaluation, has become less of a concern for
children younger than 36 months. This is in great part attributable
to the introduction of modern vaccination practices for strains of Haemophilusinfluenza type
b (in 1986) and Streptococcus pneumococcus (in
2000).
++
Clinical examination alone will also fail to identify all instances
of bacterial disease in older infants. McCarthy and colleagues at
Yale University have developed a workable objective clinical tool
to help identify the likelihood of serious bacterial disease in
the face of fever.11 Sensitivity (74%)
and specificity (75%) of the tool are very good but are
not perfect. Many children with potentially serious illnesses can
appear well on clinical examination and vice versa. For the toxic-appearing
older infant or toddler, there is uniformity of opinion and approach:
All should have thorough investigation for possible bacterial sources
of infection and should receive parenteral antimicrobial therapy
(ie, a third-generation cephalosporin and possibly vancomycin) as
inpatients. The choice of antibiotic(s) should be tailored to combat
the pathogens most commonly identified through institutional and
community surveillance. It is the well-appearing child with insidious
infection who benefits most from additional laboratory testing.
++
Numerous investigators have studied the utility of commonly
available laboratory tests in identifying children at increased
risk for occult bacteremia. One study of febrile children between
3 and 36 months of age demonstrated that increased risk of occult
bacteremia correlated with total white blood cell counts above 15,000
per microliter.18 In this study, the risk of occult
bacteremia reached 10.8% for those children who had a peripheral
blood white blood cell of 25,000 per microliter or
higher. However, the sensitivity of the white cell count alone was
low, at 21%.
++
Numerous investigators have studied the utility of commonly available
laboratory tests in identifying children at increased risk for occult
bacteremia. One study of febrile children between 3 and 36 months
of age demonstrated that increased risk of occult bacteremia correlated with
total white blood cell counts above 15,000 per microliter.18
++
In this study, the risk of occult bacteremia was 10.8% for
those children who had two peripheral blood white blood cell counts
of 25,000 per microliter or higher. However, the sensitivity of
that single parameter was only 21%.
++
Urinary tract infections (UTIs) occur in up to 7% of
boys younger than 6 months and in up to 8% of girls younger
than 1 year of age.19 Overall, girls are about
twice as likely to have UTIs as boys, and white children are almost
10 times more likely to have UTIs than nonwhites. Unfortunately,
dipstick urinalysis is not a reliable means of detecting presence
of bacteriuria; sensitivities approximate 80% in large
cohorts of young children. In infants younger than 6 months of age,
there is evidence to suggest that Gram stain has excellent (> 90%)
correlation with presence of bacteriuria. Thus, many experts recommend
that a specimen of urine for culture be obtained in otherwise asymptomatic febrile
boys younger than 6 months of age and in otherwise asymptomatic
girls younger than 1 year of age. The means of obtaining the urine sample
is important, as bag technique in younger children is much more
prone to contamination than clean catch, catheterization, or needle aspiration
of the bladder.
++
The value of spinal fluid analysis and culture in children has
decreased as the occurrence rates of different types of meningitis have
decreased with the advent of new vaccinations. However, while the
overall rates of occurrence of different types of bacterial meningitis
have been substantially reduced, the incidence remains highest in
children younger than 2 years and in adults older than 60 years
of age. Clinical appearances can at times be misleading. Whenever
meningitis is suspected, a sample of cerebrospinal fluid should
be obtained for analysis and culture, and a prudent decision should
be made about early administration of antibiotics.
++
The majority of older infants and toddlers who acquire bacterial
meningitis will have either suggestive historical or physical findings (ie,
ill-appearance, seizure activity) or abnormal laboratory test results
(ie, positive CSF Gram stain, elevated CSF protein, elevated peripheral
blood, or CSF ANC).
++
A recent multicenter retrospective review of data from febrile
children younger than 20 years of age identified a five-component
clinical tool that assigns very low risk of bacterial meningitis
to children who meet all five very-low-risk criteria (negative CSF
Gram stain, CSF ANC < 1000, CSF protein < 80, peripheral CBC
ANC < 10,000, no evidence of acute associated seizure activity).
This clinical tool has not yet been prospectively tested for reliability.
++
Published fever-management protocols have called for empirical
administration of antibiotics to certain cohorts of infants and
children who have higher temperatures (ie, 39 °C or higher) or to
those in the higher temperature range who also have an elevated
peripheral white blood cell count (ie, 15,000 or higher).20-22 However,
the relatively low prevalence of occult bacteremia and the even
lower prevalence of serious sequelae, such as bacterial meningitis,
has led to a physician practices trend toward less diagnostic and
therapeutic intervention and closer outpatient observation. Thus,
a thorough history, physical examination, and assessment of general
appearance along with parental observation and reliable follow-up
remain the mainstay of management for well-appearing febrile children
without an identifiable source of infection. The management of occult
bacteremia (positive blood culture without an obvious source of
infection) is discussed in Chapter 227.