Fever Without a Focus

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Background

Infants or young children who have a fever with no obvious source of infection present a diagnostic dilemma. Health care providers see these patients on a daily basis. As many as 20% of childhood fevers have no apparent cause.[1] A small but significant number of these patients may have a serious bacterial infection; the risk is greatest among febrile infants and children younger than 36 months, making proper diagnosis and management important. Physical examination and patient history do not always identify patients with occult bacteremia or serious bacterial infection. Serious infections that are not recognized promptly and treated appropriately can cause significant morbidity or mortality.

This article focuses primarily on infants and young children aged 2-36 months and reflects the significant changes in the care of the febrile infant and child over the past 10 years. The article Fever in the Young Infant addresses the diagnosis and treatment of febrile infants younger than 2 months.

Fever is defined as a rectal temperature that exceeds 38°C (100.4°F). Direct the initial evaluation of these patients toward identifying or ruling out serious bacterial infections (SBI), most commonly urinary tract infections. The following questions are important to consider:

A great deal of time and effort has been spent on research to help identify the febrile infant and young child with a serious bacterial infection. However, evaluation and treatment of febrile infants and young children vary, despite nationally published treatment guidelines.

Note also, this article primarily addresses children who are completely immunized, and in particular who have received full Hib and PCV7 vaccine series. Unimmunized children are at higher risk for bacteremia, pneumonia, and other SBI's.

Pathophysiology

Meningitis, pneumonia, urinary tract infection (UTI), and bacteremia are serious etiologies of fever in infants and young children.

Neonates' immature immune systems place them at greater risk of systemic infection. Hematogenous spread of infection is most common in this age group or in patients who are immunocompromised or unimmunized. For these same reasons, infants who have a focal bacterial infection have a greater risk of developing metastatic infection or bacteremia.

The following are among the most common bacterial etiologies of serious bacterial infection in this age group:

Historically, approximately 2.5-3% of highly febrile children younger than 3 years have occult bacteremia, which is typically caused by S pneumoniae.[2] The advent of conjugate pneumococcal vaccine has resulted in a decrease in pneumococcal occult bacteremia and other disease.[3] Viral infections are common in the young child as well[4] ; however, exclude serious bacterial infection prior to assuming a viral etiology for the fever.[5]

Epidemiology

Frequency

United States

Fever accounts for 10-20% of pediatric visits to health care providers.

Mortality/Morbidity

Patients with no easily identified source of infection have a small but significant risk of a serious bacterial infection. If not recognized and treated appropriately and promptly, this can cause morbidity or mortality.

Race

There is no racial difference in incidence of fever.

Sex

There is no difference in incidence of fever in males vs. females.

Age

This article focuses on the diagnosis and treatment of febrile children aged 2-36 months.

History

Obtaining an accurate history from the parent or caregiver is important when assessing fever without a focus; the history obtained should include the following information:

Physical

While performing a complete physical examination, pay particular attention to assessing hydration status and identifying the source of infection.[6, 7] Physical examination of every febrile child should include the following:

Record vital signs.

Measure pulse oximetry levels.

Record an accurate weight on every chart.

During the examination, concentrate on identifying any of the following:

For all patients aged 2-36 months, management decisions are based on the degree of toxicity and the identification of serious bacterial infection.

The Yale Observation Scale is a reliable method for determining degree of illness.[8, 9] It consists of 6 variables: quality of cry, reaction to parent stimulation, state variation, color, hydration, and response. A score of 10 or less has a 2.7% risk of serious bacterial infection. A score of 16 or greater has a 92% risk of serious bacterial infection. It is important to remember that this scale was validated in the occult bacteremia era, prior to widespread pneumococcal conjugate vaccination.

Regarding the height of temperature, Hoberman et al found that 6.5% of patients with a temperature of 39.0°C (102.2°F) or more had a urinary tract infection (UTI) and that white females with that temperature had a 17% incidence of UTI.[10]

Table. Summary of the Yale Observation Scale



View Table

See Table

Causes

Several common bacteria cause serious bacterial infections, including the following:

Laboratory Studies

Recommended laboratory studies for children with fever without a focus are based on the child's appearance, age, and temperature.[12]

Begin intravenous (IV) or intramuscular (IM) antibiotic administration for all infants who appear ill once urine and blood specimens are obtained.

Perform the following for children who do not appear toxic:

Perform the following for children who appear toxic:

See the list below:

Imaging Studies

Chest radiography is part of any thorough evaluation of a febrile child.[14]

Chest radiography is indicated when the patient has tachypnea, retractions, focal auscultatory findings, or oxygen saturation level in room air of less than 95%.

Although viral etiologies are considered the cause of most pediatric pneumonias, establishing a viral or bacterial etiology may be challenging.

Procedures

See the list below:

Medical Care

For children with fever without a focus who appear ill, conduct a complete evaluation to identify occult sources of infection. Follow the evaluation with empiric antibiotic treatment and admit the patient to a hospital for further monitoring and treatment pending culture results. Because children presenting with fever and leukopenia are also a concern, consider leukocytosis and leukopenia in making decisions about empiric antibiotic therapy. According to a recent study by Gomez et al, isolated leukopenia, especially in children without leukocyturia suggestive of a UTI, may not be a significant risk factor for SBI and viral etiologies may be considered more strongly.[17]

Patients aged 2-36 months may not require admission if they meet the following criteria:

Treatment recommendations for children with fever without a focus are based on the child's appearance, age, and temperature.

For children who do not appear toxic, treatment recommendations are as follows:

For children who appear toxic, treatment recommendations are as follows:

Consultations

The need to consult with specialists depends on the specialty of the physician who initially evaluated the patient and the ultimate source of fever. Typically, general pediatricians easily manage febrile infants on both an inpatient and outpatient follow-up basis.

Diet

Patient tolerance is the only restriction on diet. Physicians should monitor intake and output as an indication of the patient's status because these measurements may provide the first evidence of a disturbance that indicates illness.

Activity

Patient tolerance also determines activity level, which should be monitored for changes (eg, lethargy, irritability).

Medication Summary

Treatment with antipyretics is somewhat controversial because fever is a defensive response to infection (Sullivan, 2011). Base the decision to treat a fever without a focus on age, presentation, and laboratory results. If antibiotics are administered empirically, close follow-up is required. Parenteral antibiotics are the drugs of choice.

Ceftriaxone (Rocephin)

Clinical Context:  Third-generation cephalosporin with broad-spectrum, gram-negative activity; lower efficacy against gram-positive organisms; higher efficacy against resistant organisms; arrests bacterial growth by binding to one or more penicillin-binding proteins.

Cefotaxime (Claforan)

Clinical Context:  For septicemia and treatment of gynecologic infections caused by susceptible organisms. Arrests bacterial cell wall synthesis, which, in turn, inhibits bacterial growth. Third-generation cephalosporin with gram-negative spectrum. Lower efficacy against gram-positive organisms. Useful in pediatric infections as an alternative to ceftriaxone in infants in the first month or two of life, in whom bilirubin displacement from protein-binding sites by the latter antibiotic may be harmful.

Ampicillin/sulbactam (Unasyn)

Clinical Context:  Drug combination of beta-lactamase inhibitor with ampicillin. Covers skin, enteric flora, and anaerobes. Not ideal for nosocomial pathogens.

Class Summary

Empiric antimicrobial therapy must be comprehensive and should cover likely pathogens in the clinical setting.

Ibuprofen (Advil, Motrin)

Clinical Context:  Among the few NSAIDs indicated for reduction of fever; produces anti-inflammatory, antipyretic, and analgesic effects by inhibiting prostaglandin synthesis.

Acetaminophen (Tempra, Tylenol)

Clinical Context:  Reduces fever by acting directly on hypothalamic heat-regulating centers, which increases dissipation of body heat via vasodilation and sweating.

Class Summary

These agents inhibit central synthesis and release of prostaglandins that mediate the effect of endogenous pyrogens in the hypothalamus and, thus, promote the return of the set-point temperature to normal.

Further Outpatient Care

See the list below:

Further Inpatient Care

See the list below:

Inpatient & Outpatient Medications

See the list below:

Complications

See the list below:

Prognosis

See the list below:

Patient Education

See the list below:

Author

Saul R Hymes, MD, FAAP, Director, Pediatric Lyme and Tick-Borne Diseases Center, Department of Pediatrics, Division of Pediatric Infectious Diseases, Stony Brook Children’s Hospital; Assistant Professor of Clinical Pediatrics, Department of Pediatrics, Division of Pediatric Infectious Diseases, Stony Brook University School of Medicine

Disclosure: Nothing to disclose.

Specialty Editors

Mary L Windle, PharmD, Adjunct Associate Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Nothing to disclose.

Mark R Schleiss, MD, Minnesota American Legion and Auxiliary Heart Research Foundation Chair of Pediatrics, Professor of Pediatrics, Division Director, Division of Infectious Diseases and Immunology, Department of Pediatrics, University of Minnesota Medical School

Disclosure: Nothing to disclose.

Chief Editor

Russell W Steele, MD, Clinical Professor, Tulane University School of Medicine; Staff Physician, Ochsner Clinic Foundation

Disclosure: Nothing to disclose.

Additional Contributors

Ashir Kumar, MD, MBBS, FAAP, Professor Emeritus, Department of Pediatrics and Human Development, Michigan State University College of Human Medicine

Disclosure: Nothing to disclose.

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Observation Items 1 (Normal) 3 (Moderate Impairment) 5 (Severe Impairment)
Quality of cryStrong with normal tone or contentment without cryingWhimpering or sobbingWeak cry, moaning, or high-pitched cry
Reaction to parent stimulationBrief crying that stops or contentment without cryingIntermittent cryingContinual crying or limited response
ColorPinkAcrocyanotic or pale extremitiesPale or cyanotic or mottled or ashen
State variationIf awake, stays awake; if asleep, wakes up quickly upon stimulationEyes closed briefly while awake or awake with prolonged stimulationFalls asleep or will not arouse
HydrationSkin normal, eyes normal, and mucous membranes moistSkin and eyes normal and mouth slightly drySkin doughy or tented, dry mucous membranes, and/or sunken eyes
Response (eg, talk, smile) to social overturesSmiling or alert (< 2 mo)Briefly smiling or alert briefly (< 2 mo)Unsmiling anxious face or dull, expressionless, or not alert (< 2 mo)