Continually Updated Clinical Reference
 
 
  All Sources     eMedicine     Medscape     Drug Reference     MEDLINE
 
eMedicine - Fever Without a Focus : Article by

Quick Find
Authors & Editors
Introduction
Clinical
Differentials
Workup
Treatment
Medication
Follow-up
Miscellaneous
References

Related Articles
Bacteremia

Bronchitis, Acute and Chronic

Croup

Dehydration

Diarrhea

Fever in the Toddler

Fever in the Young Infant

Leukocytosis

Measles

Meningitis, Aseptic

Meningitis, Bacterial

Neonatal Sepsis

Otitis Media

Parainfluenza Virus Infections

Pharyngitis

Pneumococcal Bacteremia

Pneumococcal Infections

Pneumonia

Pyelonephritis

Respiratory Syncytial Virus Infection

Urinary Tract Infection

Varicella




Patient Education
Children's Health Center

Fever in Children Overview

Fever in Children Causes

Fever in Children Symptoms

Fever in Children Treatment




Author: Robert W Tolan Jr, MD, Chief of Allergy, Immunology and Infectious Diseases, The Children's Hospital at Saint Peter's University Hospital; Clinical Associate Professor of Pediatrics, Drexel University College of Medicine

Robert W Tolan, Jr, is a member of the following medical societies: American Academy of Pediatrics, American Medical Association, American Society for Microbiology, American Society of Tropical Medicine and Hygiene, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, Phi Beta Kappa, and Physicians for Social Responsibility

Coauthor(s): Ann G Egland, MD, Consulting Staff, Department of Operational and Emergency Medicine, Walter Reed Army Medical Center; Terrance K Egland, MD, Director, Business Planning and Development, Bureau of Medicine and Surgery

Editors: Ashir Kumar, MBBS, MD, FAAP, Professor, Department of Pediatrics and Human Development, College of Human Medicine, Michigan State University; Consulting Staff, Department of Pediatrics, EW Sparrow Hospital; Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine.com, Inc; Mark R Schleiss, MD, American Legion Chair of Pediatrics, Professor of Pediatrics, Division Director, Division of Infectious Diseases and Immunology, Department of Pediatrics, University of Minnesota School of Medicine; Daniel Rauch, MD, FAAP, Director, Pediatric Hospitalist Program, Associate Professor, Department of Pediatrics, New York University School of Medicine; Russell W Steele, MD, Professor and Vice Chairman, Department of Pediatrics, Head, Division of Infectious Diseases, Louisiana State University Health Sciences Center

Author and Editor Disclosure

Synonyms and related keywords: fever without a focus, fever without a source, fever without localizing signs, pediatric fever, childhood fever, occult bacteremia, meningitis, urinary tract infection, UTI, pneumonia, Streptococcus pneumoniae, Streptococcus agalactiae, Neisseria meningitidis, Haemophilus influenzae type b, Listeria monocytogenes, Escherichia coli, hypoventilation, hyperventilation, cyanosis, otitis media, pharyngitis, sinusitis, bronchiolitis, croup, gingivostomatitis, viral gastroenteritis, varicella, hand-foot-and-mouth disease, pyelonephritis, renal scarring, renal failure, preeclampsia, end-stage renal disease

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 occult bacteremia or other serious bacterial infections. Address the following questions:

  • What laboratory studies are indicated for various age ranges?
  • Which patients need in-depth evaluation and treatment?
  • Which patients need treatment with antibiotics?
  • Which patients should be hospitalized?
  • Which patients can be sent home safely and what follow-up is appropriate for them?
  • Are the diagnosis and treatment modalities for each patient cost-effective?
  • What is the potential morbidity associated with testing and treatment?
  • What are the parental (and patient) preferences for testing and treatment?

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.

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. 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:

  • Streptococcus pneumoniae
  • Streptococcus agalactiae
  • Neisseria meningitidis
  • Haemophilus influenzae type b
  • Listeria monocytogenes
  • Escherichia coli

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

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.

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; the history obtained should include the following information:

  • Fever history: What was child's temperature prior to presentation and how was temperature measured? Consider fever documented at home by a reliable parent or caregiver the same as fever found upon presentation. Accept parental reports of maximum temperature.
  • Fever at presentation
    • If the physician believes the infant has been excessively bundled, and if a repeat temperature taken 15-30 minutes after unbundling is normal, the infant should be considered afebrile.
    • Always remember that normal or low temperature does not preclude serious, even life-threatening, infectious disease.
  • Current level of activity or lethargy
  • Activity level prior to fever onset (ie, active, lethargic)
  • Current eating and drinking pattern
  • Eating and drinking pattern prior to fever onset
  • Appearance: Fever sometimes makes a child appear rather ill.
  • Vomiting or diarrhea
  • Ill contacts
  • Medical history
  • Immunization history (especially recent immunizations)
  • Urinary output: Inquire as to the number of wet diapers.

Physical

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

  • Record vital signs.
    • Temperature: Rectal temperature is the standard. Temperature obtained via tympanic, axillary, or oral methods may not truly reflect the patient's temperature.
    • Pulse rate
    • Respiratory rate
    • Blood pressure
  • Measure pulse oximetry levels.
    • Pulse oximetry may be a more sensitive predictor of pulmonary infection than respiratory rate in patients of all ages, but especially in infants and young children.
    • Pulse oximetry is mandatory for any child with abnormal lung examination findings, respiratory symptoms, or abnormal respiratory rate, although keep in mind that the respiratory rate increases when children are febrile.
  • Record an accurate weight on every chart.
    • All pharmacologic and procedural treatments are based on the weight in kilograms.
    • In urgent situations, estimating methods (eg, Broselow tape, weight based on age) may be used.
  • During the examination, concentrate on identifying any of the following:
    • Toxic appearance, which suggests possible signs of lethargy, poor perfusion, hypoventilation or hyperventilation, or cyanosis (ie, shock)
    • A focus of infection that is the apparent cause of the fever
    • Minor foci (eg, otitis media [OM], pharyngitis, sinusitis, skin or soft tissue infection)
    • Identifiable viral infection (eg, bronchiolitis, croup, gingivostomatitis, viral gastroenteritis, varicella, hand-foot-and-mouth disease)
    • Petechial or purpuric rashes, often associated with bacteremia
    • Purpura, which is associated more often with meningococcemia than is the presence of petechiae alone
  • For all patients aged 3-36 months, management decisions are mostly based on the degree of toxicity and the height of temperature.
  • The Yale Observation Scale is a reliable method for determining degree of illness.3, 4
    • 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.
    • 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 UTI and that white females with that temperature had a 17% incidence of UTI.5 In this age group, the prevalence of bacteremia correlates with the height of fever.
    • Children with temperatures from 39-39.5°C (102.2-103°F) have an approximate 2-4% risk of having occult bacteremia. Those with temperatures higher than 39.5°C (103°F) have an approximate 5% chance of having occult bacteremia.
    • The impact of the conjugated pneumococcal vaccine on these findings and predictions has not been evaluated.
    • Summary of the Yale Observation Scale

      Observation Items1 (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)

Causes

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

  • S pneumoniae
    • S pneumoniae is the leading cause of nearly all common bacterial upper respiratory tract infections (eg, pneumonia, sinusitis, OM).
    • This organism is the most common cause of meningitis in the United States, although the use of the pneumococcal vaccine will likely change this.
    • It is the most common cause of occult bacteremia, the incidence of which is decreasing.
  • N meningitidis
  • H influenzae type b
  • L monocytogenes
  • E coli
    • E coli is the most common cause of UTIs.
    • Among febrile children with UTIs, 75% have pyelonephritis, with consequences that, if missed, include renal scarring in 27-64% of patients, a 23% risk of hypertension, a 10% risk of renal failure, and a 13% risk of preeclampsia as adults.
    • Approximately 13-15% of end-stage renal disease is believed to be related to undertreated childhood UTIs.



Bacteremia
Bronchitis, Acute and Chronic
Croup
Dehydration
Diarrhea
Fever in the Toddler
Fever in the Young Infant
Leukocytosis
Measles
Meningitis, Aseptic
Meningitis, Bacterial
Neonatal Sepsis
Otitis Media
Parainfluenza Virus Infections
Pharyngitis
Pneumococcal Bacteremia
Pneumococcal Infections
Pneumonia
Pyelonephritis
Respiratory Syncytial Virus Infection
Urinary Tract Infection
Varicella


Lab Studies

  • Recommended laboratory studies for children with fever without a focus are based on the child's appearance, age, and temperature.
  • 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 a CBC count with manual differential.
    • Obtain and hold blood cultures, pending receipt of CBC count results. Send blood culture for analysis if WBC count exceeds 15,000/μL or if the absolute neutrophil count exceeds 10,000/μL.
    • Perform urinalysis (UA) by bladder catheterization and urine culture based on the following criteria:
      • All males younger than 6 months and all uncircumcised males younger than 12 months
      • All females younger than 24 months and older female children if symptoms suggest a UTI
    • Consider cerebrospinal fluid (CSF) studies and culture. Obtain CSF if meningitis is suspected.
    • Consider obtaining stool for WBCs and guaiac if diarrhea is present.
  • Perform the following for children who appear toxic:
    • Perform a CBC count with manual differential.
    • Obtain blood cultures.
    • Consider obtaining a chest radiograph. Chest radiography should be performed for patients with a WBC count greater than 20,000/μL.
    • Perform UA by bladder catheterization and urine culture based on the following criteria:
      • All males younger than 6 months and all uncircumcised males younger than 12 months
      • All females younger than 24 months and older female children if symptoms suggest a UTI
    • Obtain CSF and perform studies and culture if meningitis is suspected. Administer antibiotics before performing the lumbar puncture (LP) if any delay is anticipated.
    • Consider obtaining stool for WBCs and guaiac if diarrhea is present.
    • Admit these patients for further treatment; pending culture results, administer parenteral antibiotics (see Treatment).
    • Rapid testing for viruses (eg, influenza, respiratory syncytial virus) may be useful to decrease the need for other studies and/or antibiotic therapy.

Imaging Studies

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

  • 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.
  • Chest radiographs should be obtained if the WBC count is more than 20,000/μL. One study found a high correlation with WBC greater than 20,000/μL and pneumonia, even with a lack of clinical findings suggestive of pneumonia.6

Procedures

  • Bladder catheterization
  • Suprapubic aspiration
  • LP



Medical Care

For children 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.

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

  • Patient was healthy prior to onset of fever.
  • Patient has no significant risk factors.
  • Patient appears nontoxic and otherwise healthy.
  • Patient's laboratory results are within reference ranges defined as low risk.
  • Patient's parents (or caregivers) appear reliable and have access to transportation if the child's symptoms should worsen.

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:
    • Consider no antibiotics; however, if absolute neutrophil count is greater than 10,000/μL, consider ceftriaxone (50 mg/kg/dose).
    • Schedule a follow-up appointment within 24-48 hours and instruct parents to return with the child sooner if the condition worsens.
    • Hospital admission is indicated for children whose condition worsens or whose evaluation findings suggest a serious infection.
  • For children who appear toxic, treatment recommendations are as follows:
    • Admit child for further treatment; pending culture results, administer parenteral antibiotics.
    • Initially administer ceftriaxone, cefotaxime, or ampicillin/sulbactam (50 mg/kg/dose).

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).



Treatment with antipyretics is somewhat controversial because fever is a defensive response to infection. 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.

Drug Category: Antibiotics

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

Drug NameCeftriaxone (Rocephin)
DescriptionThird-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.
Adult Dose1-2 g IV q12-24h; not to exceed 4 g/d
Pediatric Dose>1-2 months and children: 50-100 mg/kg/d IV/IM divided q12h; not to exceed 2 g/d
ContraindicationsDocumented hypersensitivity
InteractionsProbenecid may increase levels; coadministration with ethacrynic acid, furosemide, or aminoglycosides may increase nephrotoxicity
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsAdjust dose in renal impairment; caution in breastfeeding women and those allergic to penicillin; displaces bilirubin from serum protein-binding sites and should be used with caution in infants <2 mo and in those with hyperbilirubinemia or gallbladder problems

Drug NameCefotaxime (Claforan)
DescriptionFor 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.
Adult DoseModerate-to-severe infections: 1-2 g IV/IM q6-8h
Life-threatening infections: 1-2 g IV/IM q4h
Pediatric DoseInfants and children: 50-200 mg/kg/d IV/IM divided q4-6h
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity
InteractionsProbenecid may increase levels; coadministration with furosemide and aminoglycosides may increase nephrotoxicity
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsUse with caution in patients with documented hypersensitivity to beta-lactams; adjust dose in severe renal impairment; has been associated with severe colitis

Drug NameAmpicillin/sulbactam (Unasyn)
DescriptionDrug combination of beta-lactamase inhibitor with ampicillin. Covers skin, enteric flora, and anaerobes. Not ideal for nosocomial pathogens.
Adult Dose1.5 (1 g ampicillin + 0.5 g sulbactam) to 3 g (2 g ampicillin + 1 g sulbactam) IV/IM q6-8h; not to exceed 4 g/d sulbactam or 8 g/d ampicillin
Pediatric Dose3 months to 12 years: 100-200 mg ampicillin/kg/d (150-300 mg Unasyn) IV divided q6h
>12 years: Administer as in adults; not to exceed 4 g/d sulbactam or 8 g/d ampicillin
ContraindicationsDocumented hypersensitivity
InteractionsProbenecid and disulfiram elevate ampicillin levels; allopurinol decreases ampicillin effects and has additive effects on ampicillin rash; may decrease effects of PO contraceptives
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsAdjust dose in renal failure; evaluate rash and differentiate from hypersensitivity reaction

Drug Category: Antipyretic agents

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.

Drug NameIbuprofen (Advil, Motrin)
DescriptionAmong the few NSAIDs indicated for reduction of fever; produces anti-inflammatory, antipyretic, and analgesic effects by inhibiting prostaglandin synthesis.
Adult Dose200-800 mg PO q6-8h prn; not to exceed 3.2 g/d
Pediatric Dose4-10 mg/kg/dose PO tid/qid; not to exceed 40 mg/kg/d or 2.4 g/d
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity; peptic ulcer disease; recent GI bleeding or perforation; renal insufficiency; high risk of bleeding
InteractionsCoadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effects of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; may increase PT when taking anticoagulants (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently
PregnancyC - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
PrecautionsCaution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy

Drug NameAcetaminophen (Tempra, Tylenol)
DescriptionReduces fever by acting directly on hypothalamic heat-regulating centers, which increases dissipation of body heat via vasodilation and sweating.
Adult Dose325-650 mg PO q4-6h or 1000 mg PO tid/qid; not to exceed 4 g/d
Pediatric Dose<12 years: 10-15 mg/kg/dose PO q4-6h prn; not to exceed 2.6 g/d
>12 years: Administer as in adults
ContraindicationsDocumented hypersensitivity; known G-6-PD deficiency
InteractionsRifampin can reduce analgesic effects; coadministration with barbiturates, carbamazepine, hydantoins, or isoniazid may increase hepatotoxicity
PregnancyB - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
PrecautionsHepatotoxicity possible following various dose levels in individuals with chronic alcoholism; severe or recurrent pain or high or continued fever may indicate a serious illness; contained in many OTC products; combined use with these products may result in cumulative doses exceeding recommended maximum dose



Further Inpatient Care

  • Patients who appear toxic or who fail to improve with outpatient treatment require hospital admission for further evaluation and treatment.

Further Outpatient Care

  • All children and infants with a febrile illness without a focus of bacterial infection require close follow-up care and instructions to return if the patient's condition deteriorates.
  • Follow-up visits should be arranged within 24-48 hours after the initial visit.

In/Out Patient Meds

  • Tailor medication choice to the source of infection, if known. Administer empiric treatment based on the most likely organisms.
  • A second dose of long-acting parenteral antibiotic may be given at the follow-up visit pending culture results.

Complications

  • When an occult infection is not suspected and diagnosed in a timely manner, a small but very real possibility that the infection may progress to bacteremia, meningitis, or other life-threatening illness is present.

Prognosis

  • Prognosis for an appropriately treated patient is excellent.

Patient Education



Medical/Legal Pitfalls

  • The biggest pitfall is failing to consider the possibility of a life-threatening illness. Physicians who approach their patients as if this is a possibility and who provide appropriate evaluation and treatment have done their best to avoid a poor outcome.
  • Stress to parents the criticality of their child returning for follow-up care and stress that they must seek immediate medical attention if their child's condition worsens.
  • Failure to evaluate and/or treat an ill-appearing infant or child because of a CBC count within the reference range considered normal is a serious pitfall.

Special Concerns

  • Even low-risk infants who meet criteria for discharge require close follow-up care. Instruct parents or caregivers to return before the next scheduled appointment if the infant's condition should worsen.
  • Admit to the hospital all 2- to 36-month-old febrile patients who have sickle cell anemia.



  1. Baraff LJ. Management of fever without source in infants and children. Ann Emerg Med. Dec 2000;36(6):602-14. [Medline].
  2. Benito-Fernandez J, Raso SM, Pocheville-Gurutzeta I, SanchezEtxaniz J, Azcunaga-Santibanez B, Capape-Zache S. Pneumococcal bacteremia among infants with fever without known source before and after introduction of pneumococcal conjugate vaccine in the Basque Country of Spain. Pediatr Infect Dis J. Aug 2007;26(8):667-71. [Medline].
  3. McCarthy PL, Sharpe MR, Spiesel SZ. Observation scales to identify serious illness in febrile children. Pediatrics. Nov 1982;70(5):802-9. [Medline].
  4. Bonadio WA. The history and physical assessments of the febrile infant. Pediatr Clin North Am. Feb 1998;45(1):65-77. [Medline].
  5. Hoberman A, Wald ER, Reynolds EA. Pyuria and bacteriuria in urine specimens obtained by catheter from young children with fever. J Pediatr. Apr 1994;124(4):513-9. [Medline].
  6. Murphy CG, van de Pol AC, Harper MB, Bachur RG. Clinical predictors of occult pneumonia in the febrile child. Acad Emerg Med. Mar 2007;14(3):243-9. [Medline].
  7. ACEP. Clinical policy for children younger than three years presenting to the emergency department with fever. ACEP Clinical Policies Committee; ACEP Clinical Policies Subcommittee on Pediatric Fever. Ann Emerg Med. Oct 2003;42(4):530-45. [Medline].
  8. Akintemi OB, Roberts KB. Evaluation and management of the febrile child in the conjugated vaccine era. Adv Pediatr. 2006;53:255-78. [Medline].
  9. Andreola B, Bressan S, Callegaro S, Liverani A, Plebani M, Da Dalt L. Procalcitonin and C-reactive protein as diagnostic markers of severe bacterial infections in febrile infants and children in the emergency department. Pediatr Infect Dis J. Aug 2007;26(8):672-7. [Medline].
  10. Baker MD, Bell LM, Avner JR. Outpatient management without antibiotics of fever in selected infants. N Engl J Med. Nov 11 1993;329(20):1437-41. [Medline].
  11. Baraff LJ, Bass JW, Fleisher GR, et al. Practice guideline for the management of infants and children 0 to 36 months of age with fever without source. Agency for Health Care Policy and Research. Ann Emerg Med. Jul 1993;22(7):1198-210. [Medline].
  12. Bergman DA, Mayer ML, Pantell RH, Finch SA, Wasserman RC. Does clinical presentation explain practice variability in the treatment of febrile infants?. Pediatrics. Mar 2006;117(3):787-95. [Medline].
  13. Bonadio WA, Hagen E, Rucka J, et al. Efficacy of a protocol to distinguish risk of serious bacterial infection in the outpatient evaluation of febrile young infants. Clin Pediatr (Phila). Jul 1993;32(7):401-4. [Medline].
  14. Bonadio WA, Lehrmann M, Hennes H, et al. Relationship of temperature pattern and serious bacterial infections in infants 4 to 8 weeks old 24 to 48 hours after antibiotic treatment. Ann Emerg Med. Sep 1991;20(9):1006-8. [Medline].
  15. Chinnock R, Butto J, Fernando N. Hot tots: current approach to the young febrile infant. Compr Ther. 1995;21(3):109-14. [Medline].
  16. Grubb NS, Lyle S, Brodie JH, et al. Management of infants and children 0 to 36 months of age with fever without source. J Am Board Fam Pract. Mar-Apr 1995;8(2):114-9. [Medline].
  17. Herd D. In children under age three does procalcitonin help exclude serious bacterial infection in fever without focus?. Arch Dis Child. Apr 2007;92(4):362-4. [Medline].
  18. Ishimine P. Fever without source in children 0 to 36 months of age. Pediatr Clin North Am. Apr 2006;53(2):167-94. [Medline].
  19. Ishimine P. The evolving approach to the young child who has fever and no obvious source. Emerg Med Clin North Am. Nov 2007;25(4):1087-115, vii. [Medline].
  20. Jaskiewicz JA, McCarthy CA. Evaluation and management of the febrile infant 60 days of age or younger. Pediatr Ann. Aug 1993;22(8):477-80, 482-3. [Medline].
  21. Jaskiewicz JA, McCarthy CA, Richardson AC, et al. Febrile infants at low risk for serious bacterial infection--an appraisal of the Rochester criteria and implications for management. Febrile Infant Collaborative Study Group. Pediatrics. Sep 1994;94(3):390-6. [Medline].
  22. Kramer MS, Tange SM, Drummond KN. Urine testing in young febrile children: a risk-benefit analysis. J Pediatr. Jul 1994;125(1):6-13. [Medline].
  23. Lee GM, Harper MB. Risk of bacteremia for febrile young children in the post-Haemophilus influenzae type b era. Arch Pediatr Adolesc Med. Jul 1998;152(7):624-8. [Medline].
  24. Lieu TA, Baskin MN, Schwartz JS, Fleisher GR. Clinical and cost-effectiveness of outpatient strategies for management of febrile infants. Pediatrics. Jun 1992;89(6 Pt 2):1135-44. [Medline].
  25. Maheshwari N. How useful is C-reactive protein in detecting occult bacterial infection in young children with fever without apparent focus?. Arch Dis Child. Jun 2006;91(6):533-5. [Medline].
  26. Massin MM, Montesanti J, Lepage P. Management of fever without source in young children presenting to an emergency room. Acta Paediatr. Nov 2006;95(11):1446-50. [Medline].
  27. McCarthy PL, Lembo RM, Baron MA. Predictive value of abnormal physical examination findings in ill-appearing and well-appearing febrile children. Pediatrics. Aug 1985;76(2):167-71. [Medline].
  28. McCarthy PL, Lembo RM, Fink HD. Observation, history, and physical examination in diagnosis of serious illnesses in febrile children less than or equal to 24 months. J Pediatr. Jan 1987;110(1):26-30. [Medline].
  29. Myers C, Gervaix A. Streptococcus pneumoniae bacteraemia in children. Int J Antimicrob Agents. Nov 2007;30 Suppl 1:S24-8. [Medline].
  30. Nozicka CA. Evaluation of the febrile infant younger than 3 months of age with no source of infection. Am J Emerg Med. Mar 1995;13(2):215-8. [Medline].
  31. Oppenheim PI, Sotiropoulos G, Baraff LJ. Incorporating patient preferences into practice guidelines: management of children with fever without source. Ann Emerg Med. Nov 1994;24(5):836-41. [Medline].
  32. Pena BM, Harper MB, Fleisher GR. Occult bacteremia with group B streptococci in an outpatient setting. Pediatrics. Jul 1998;102(1 Pt 1):67-72. [Medline].
  33. Perrott DA, Piira T, Goodenough B, Champion GD. Efficacy and safety of acetaminophen vs ibuprofen for treating children's pain or fever: a meta-analysis. Arch Pediatr Adolesc Med. Jun 2004;158(6):521-6. [Medline].
  34. Richardson M, Lakhanpaul M. Assessment and initial management of feverish illness in children younger than 5 years: summary of NICE guidance. BMJ. Jun 2 2007;334(7604):1163-4. [Medline].
  35. Rothrock SG, Harper MB, Green SM, et al. Do oral antibiotics prevent meningitis and serious bacterial infections in children with Streptococcus pneumoniae occult bacteremia? A meta- analysis. Pediatrics. Mar 1997;99(3):438-44. [Medline].
  36. Seow VK, Lin AC, Lin IY, Chen CC, Chen KC, Wang TL. Comparing different patterns for managing febrile children in the ED between emergency and pediatric physicians: impact on patient outcome. Am J Emerg Med. Nov 2007;25(9):1004-8. [Medline].
  37. Shaikh N, Morone NE, Lopez J, et al. Does this child have a urinary tract infection?. JAMA. Dec 26 2007;298(24):2895-904. [Medline].
  38. Vega R. Rapid viral testing in the evaluation of the febrile infant and child. Curr Opin Pediatr. Jun 2005;17(3):363-7. [Medline].
  39. Wasserman GM, White CB. Evaluation of the necessity for hospitalization of the febrile infant less than three months of age. Pediatr Infect Dis J. Mar 1990;9(3):163-9. [Medline].

Fever Without a Focus excerpt

Article Last Updated: Feb 5, 2008