• Cincinnati Children's Hospital Medical Center. Evidence based clinical practice guideline for fever of uncertain source in infants 60 days of age or less. Cincinnati (OH): Cincinnati Children's Hospital Medical Center; 2003 Jun. 12 p. [49 references]

This is the current release of the guideline.

This guideline updates a previous version: Cincinnati Children's Hospital Medical Center. Evidence based clinical protocol guideline for fever of uncertain source in infants 60 days of age or less. Cincinnati (OH): Cincinnati Children's Hospital Medical Center; 1998. 32 p.

The guideline was reviewed for currency in September 2006 using updated literature searches and was determined to be current.

Each recommendation is followed by evidence grades (A-X) identifying the type of supporting evidence. Definitions of the evidence grades are presented at the end of the Major Recommendations field.

Clinical Assessment

1. It is recommended that rectal temperatures are preferred to axillary or other temperature measures (Center for Reviews and Dissemination Reviewers, 1996 [M]; Hooker, 1993 [C]; Reisinger, Kao, & Grant, 1979 [C]).

   Note 1: A parental report of fever detected only by touch is likely to be accurate (sensitivity 82--89%, specificity 76--86%) (Graneto & Soglin, 1996 [C]; Hooker et al., 1996 [C]; Singhi & Sood, 1990 [C]).

   Note 2: The magnitude of fever may not be useful for predicting illness source or severity (Bonadio et al., 1991 [C]; Kluger, 1992 [S]).

2. It is recommended and essential that a thorough history and physical examination be performed. In the history and the physical examination it is important to elicit high risk clinical elements. See Table 1 below for points of consideration.

Table 1: Definitions (Baraff et al.,1993 [E]) unless otherwise specified

Fever

Rectal temperature >38ºC (100.4ºF) (Bonadio, Smith, & Sabnis, 1994 [D])

Fever of Uncertain Source (FUS)

An acute febrile illness in which the etiology of the fever is not apparent after a thorough history and physical exam

Serious Bacterial Infection (SBI)

• Meningitis
• Bone and joint infections
• Soft tissue infections (cellulitis)
• Pneumonia
• Urinary tract infections (UTI)
• Sepsis/bacteremia
• Enteritis

Toxic Appearance -- "Yale Observation Scale" (for study population <24 months of age); see also (Baker, Bell, & Avner, 1993 [A]; McCarthy et al., 1982 [C])

• Lethargy
• Poor or absent eye contact
• Failure of child to recognize parents or failure to interact with persons or objects in the environment
• Poor perfusion of the extremities
• Acrocyanosis
• Mottling
• Slow capillary refill time of >2 seconds in "warm" environment (Gorelick, Shaw, & Baker, 1993 [C]; Schriger & Baraff, 1988 [C])
• Hyperventilation or marked hypoventilation or cyanosis

Low Risk for SBI -- "Rochester Criteria"; see also (Baker, Bell, & Avner, 1993 [A]; Jaskiewicz et al., 1994 [C]; McCarthy et al., 1982 [C])

• Prior history of being healthy
  • born at term (>37 weeks gestation)
  • has not been previously hospitalized
  • has no chronic or underlying illness
  • was not hospitalized longer than mother
  • was not treated for unexplained hyperbilirubinemia
  • has not received and was not receiving antimicrobial agents
  • no intrapartum history of mother for fever, Group B streptococcus, or antibiotic treatment
• No focal bacterial infection on physical exam
• No evidence of purulent otitis media, skin or soft tissue infection, or bone or joint skeletal infection
• Negative laboratory screen

Laboratory Studies

1. It is recommended that the following five laboratory tests be performed in all infants with FUS (Klassen & Rowe, 1992 [M]; Jaskiewicz et al., 1994 [C]; Dagan et al., 1988 [C]; Dagan et al., 1985 [C]; Kadish et al., 2000 [D]; Baraff et al., 1993 [E]).
   1. Complete blood count (CBC) with differential

      Note 1: An abnormal CBC is defined as: white blood cells (WBC) >15,000/microliter or <5,000/microliter; WBC band forms >1,500/microliter (Dagan et al., 1988 [C]; Dagan et al., 1985 [C]; Bonadio, Smith, & Carmody, 1992 [D]).

      Note 2: WBC lab values have no predictive value in determining the risk of meningitis (Bonsu & Harper, 2003 [Q]).

      Note 3: A band-to-neutrophil ratio <0.2 improves the negative predictive value for SBI to 98% or greater when added to the screening criteria (Baker, Bell, & Avner, 1993 [A]).

   2. Blood culture
   3. Urinalysis (Herr et al., 2001 [D])

      Note 1: Abnormal microscopy defined as spun urine >10 WBC/high-power field (hpf).

      Note 2: Gram stain of sample for organisms is more sensitive (94%) and specific (92%) than simple urinalysis or "dip sticks" as quick indicator of infection (Lockhart et al., 1995 [C]).

   4. Urine culture

      It is recommended that urine samples be collected by catheter, as they are less likely to be contaminated than "clean catch" urine samples (Weinberg & Gan, 1991 [D]).

   5. Lumbar puncture (LP)
      • It is recommended that all infants receive a lumbar puncture.
      • Exception: In infants 31 to 60 days AND with the presence of all of the following, delaying or omitting a lumbar puncture may be considered (Jaskiewicz et al.,1994 [C]; Dagan et al., 1988 [C]; Local Expert Consensus [E]):
        • Low risk as identified with strict screening criteria utilizing both clinical assessment and diagnostic testing (see Table 1 above and in the original guideline document)
        • Available reliable follow-up in 12 to 24 hours
        • Healthcare provider(s) confident that parent will use appropriate observational and follow-up skills
        • Primary care physician (PCP) and family agree with plan of care
        • Antibiotic therapy will not be initiated
      • It is recognized that an acceptable cerebrospinal fluid (CSF) specimen might not be obtained secondary to failed procedure, traumatic lumbar puncture, or parental refusal. If the decision to start antibiotics has already been made, then it is recommended that treatment be initiated (Local Expert Consensus [E]).
2. It is recommended that the following also be considered:
   • Stool culture (if child has diarrhea)
   • Viral cultures in selected patients and as appropriate to season
   • Chest x-ray (if respiratory signs)
3. A. For infants 0 to 30 days with FUS, it is recommended that a laboratory evaluation for neonatal herpes simplex virus (HSV) infections be considered:
   • If risk factor(s) are present (see Appendix in the guideline document), or
   • If the patient is not improving on antibiotic therapy (Local Expert Consensus [E])

   The following laboratory tests are recommended if an evaluation for neonatal HSV infection is performed.

   • Blood viral culture
   • CSF viral culture
   • CSF polymerase chain reaction (PCR)
   • Conjunctiva viral culture
   • Skin lesion viral culture
   • Nasopharyngeal (NP) viral culture
   • Rectal viral culture
   • Also consider
     • Chest x-ray
     • Liver function studies

   B. For infants 31 to 60 days with FUS, it is recommended that laboratory evaluation for neonatal HSV infections be reserved primarily for those with clinical findings suggestive of an HSV infection or a prior history of HSV.

   Note: In the infant beyond one month of age there is a considerably reduced risk for neonatal HSV infection; 95 to 98% present prior to 22 days of age (Koskiniemi et al., 1989 [D]; Sullivan-Bolyai et al.,1986 [D]).

   See Appendix in the original guideline document) for information which may help when deciding on the appropriateness of evaluating for and treating neonatal HSV infections.

4. It is recommended that the following laboratory tests be considered selectively in non-low-risk infants:
   • PCR. A positive PCR does not rule out SBI. Consider applicable specificity, sensitivity and turnaround time for specific PCR at the time of testing (Local Expert Consensus [E]).
     • Enterovirus (summer and fall). At present, test results are available within 24 hours.

       Note 1: CSF and blood sources for PCR are the most sensitive for diagnosis of enterovirus infection (Byington et al., 1999 [C]; Rotbart et al.,1999 [C]).

       Note 2: PCR is more sensitive than viral culture in detecting enterovirus (Rotbart et al., 1999 [C]).

     • Human herpes virus 6 (HHV-6) (Byington et al., 2002 [C])
   • Rapid plasma reagin (RPR)

Admission Criteria

1. It is recommended that all infants 0 to 30 days of age with FUS be hospitalized (Kadish et al., 2000 [D]).

   Note: 3.2 to 3.5% of febrile infants 0 to 30 days identified as low-risk [by the Philadelphia or Boston protocols] will have SBI (Kadish et al., 2000 [D]).

2. It is recommended that any infant 31 to 60 days of age with FUS identified as high-risk clinically or by laboratory data be hospitalized (Baraff et al., 1993 [E]).
3. It is recommended that low-risk infants 31 to 60 days may be managed as outpatients or inpatients (Baker, Bell, & Avner, 1993 [A]; Baker, Bell, & Avner, 1999 [C]; Baskin, O’Rourke, & Fleisher, 1992 [C]; Dagan et al., 1988 [C]; Wasserman & White, 1990 [D]). This decision must take into consideration:
   • The needs of the family
   • The judgment of the primary care physician
   • Excellent outpatient follow-up
   • Excellent communication with care provider as an outpatient assured.

     Note: Low-risk infants may be identified using strict screening criteria utilizing both clinical assessment and diagnostic testing. Use of these criteria has 98.9 to 100% negative predictive value for SBI (Baker, Bell, & Avner, 1993 [A]; Jaskiewicz et al.; 1994 [C], Herr et al.; 2001 [D]).

Medications

Antibiotics

1. It is recommended that all infants 0 to 30 days with FUS be treated with intravenous ampicillin plus a 3rd generation cephalosporin or gentamicin.

   Note: About 138 such infants need to be treated with ampicillin to prevent one case of Listeria monocytogenes or enterococcal infection (number needed to treat [NNT] = 138) (Brown, Burns, & Cummings, 2002 [M]).

2. Recommendations for treatment of infants 31 to 60 with FUS vary depending on laboratory and clinical findings.
   • It is recommended that the first line treatment for this group is intravenous 3rd generation cephalosporin alone (Byington et al., 2003 [D]; Sadow, Derr, & Teach, 1999 [D]).
   • It is recommended that intravenous ampicillin be considered as an addition to the antibiotic regimen for febrile infants 31 to 60 days in severely ill infants or with findings suggestive of UTI to assure coverage for rare organisms such as L. monocytogenes, gram-positive cocci, or enterococcus (Brown, Burns, & Cummings, 2002 [M]; Byington et al., 2003 [D]; Sadow, Derr, & Teach, 1999 [D]).

     Note: About 527 infants 31 to 60 days with FUS need to be treated with ampicillin to prevent one case of L. monocytogenes or enterococcal infection (number needed to treat = 527) (Brown, Burns, & Cummings, 2002 [M]).

   • Inpatient and outpatient low-risk infants may be managed without antibiotics pending culture results and/or a change in clinical status (Baker, Bell, & Avner, 1993 [A]; Baker, Bell & Avner, 1999 [C]; Jaskiewicz et al., 1994 [C]; Dagan et al.,1988 [C]).
   • It is recommended that those infants managed as outpatients and treated with antibiotics receive parenteral ceftriaxone (Baskin et al., 1992 [C]).

See Table 2 in the original guideline document for summary of recommended doses for antibiotics.

3. It is recommended that the duration of initial antibiotic therapies cover a treatment period of 24 to 48 hours with discontinuance or continuation of therapy based on result of cultures or other tests and review of history and clinical response.

   Cultures must be checked after a true minimum incubation period of 36 hours, which begins when the inoculated culture is placed in the incubator.

   Note 1: The probability of identifying SBI in febrile infants (28--90 days) after 24 hours is about 1.1% among all patients and 0.3% among low risk patients (Kaplan et al., 2000 [D]).

   Note 2: In blood cultures of infants 0 to 6 months, mean time to positivity for true pathogens is about 17.5 hours and for contaminants is about 27.9 hours (McGowan, Foster, & Coffin, 2000 [C]). Median times to positivity for urine and CSF cultures are 16 and 18 hours, respectively, in febrile infants 28 to 90 days (Kaplan et al., 2000 [D]).

Antiviral

1. It is recommended that acyclovir not be added routinely to standard antimicrobial therapy for infants with FUS. Benefit is moderated by the rarity of neonatal HSV infection, especially with an FUS presentation, and drug therapy is not without risk (Local Expert Consensus [E]).
2. Acyclovir is recommended when the decision is made to initiate therapy for the treatment of possible neonatal HSV infection. Appropriate diagnostic specimens must be collected before therapy is initiated (Kimberlin et al.,2001 [C]).

See Table 2 in the original guideline document for recommended doses.

Nutrition

1. Diet for age as tolerated
2. Supplemental hydration as required. This is especially recommended for <1-week-old breastfeeding infant with decreased urine output if on drugs (e.g., acyclovir) that are dependent on good renal function for excretion.

Infection Control

Follow infection control precautions (droplet, contact, or standard) as appropriate to presumptive diagnosis.

Consults and Referrals

Consider consult with Infectious Diseases if:

1. Diagnosis or clinical course of infection is unusual
2. There are questions regarding continuation or discontinuation of acyclovir in situations where neither the cultures nor the PCR are positive for HSV; or
3. HSV culture or HSV PCR results are positive

Education

Family education and review is recommended on the following topics.

1. Fever:
   • Observing signs, including taking an accurate temperature measurement
   • Causes
   • Therapies
2. Indications to call their physician
3. Anticipated course of the illness

(O'Neill-Murphy, Liebman, & Barnsteiner, 2001 [O])

Discharge Criteria

(Note: Begin discharge planning on admission.)

1. Well-appearing
2. Eating well
3. Antimicrobial therapies complete or can be continued in the home environment
4. Culture results negative when checked after a true minimum incubation period of 36 hours (which begins when the inoculated culture is placed in the incubator)
5. Hospitalized infant observed without antibacterial treatment is well-appearing at 24 hours
6. Family:
   • Has participated in the discharge planning and decision processes
   • Understands and agrees to any prescribed therapies or follow-up needs
   • Is confident in ability to care for infant at home
7. Home environment considered appropriate for continuing care prescriptions
8. Follow-up physician:
   • Is identified
   • Has participated in generating the discharge plan
   • Agrees with the discharge plan

Definitions:

Evidence Based Grading Scale:

A: Randomized controlled trial: large sample
B: Randomized controlled trial: small sample
C: Prospective trial or large case series
D: Retrospective analysis
E: Expert opinion or consensus
F: Basic laboratory research
S: Review article
M: Meta-analysis
Q: Decision analysis
L: Legal requirement
O: Other evidence
X: No evidence

Clinical algorithms are provided in the original guideline document for:

• Managing Fever of Uncertain Source in Infants Age 0-60 Days
• Serious Bacterial Infection (SBI) Risk Assessment

The type of evidence is identified and classified for each recommendation (see "Major Recommendations").

Evidence Based Grading Scale:

A: Randomized controlled trial: large sample
B: Randomized controlled trial: small sample
C: Prospective trial or large case series
D: Retrospective analysis
E: Expert opinion or consensus
F: Basic laboratory research
S: Review article
M: Meta-analysis
Q: Decision analysis
L: Legal requirement
O: Other evidence
X: No evidence

• Cincinnati Children's Hospital Medical Center. Evidence based clinical practice guideline for fever of uncertain source in infants 60 days of age or less. Cincinnati (OH): Cincinnati Children's Hospital Medical Center; 2003 Jun. 12 p. [49 references]

Not applicable: The guideline was not adapted from another source.

1998 May 15 (revised 2003 Jun; reviewed 2006 Sep)

Cincinnati Children's Hospital Medical Center - Hospital/Medical Center

Cincinnati Children's Hospital Medical Center

Fever 0 to 60 Days Team Members 2003

Community Physicians: *Bob Siegel, MD, Chair (General Pediatrics); *Joseph Gibbons, MD (General Pediatrics); *Evelyn Joseph, MD (General Pediatrics)

Cincinnati Children's Hospital Medical Center Physicians: *Mary Patterson, MD (Emergency Medicine); Michael Gerber, MD (Infectious Disease)

Residents: Hamilton Schwartz, MD

Patient Services: Michelle Widecan, RN, MSN, CPNP; Melissa Catania, RN; *Cyndy Jackman, RN

Laboratory: Joel Mortensen, PhD

Pharmacist: Dawn Butler, PharmD

Parent Advisors: Takisha Thompson

Division of Health Policy Clinical Effectiveness Support: *Uma Kotagal, MBBS, MSc (VP, Division Director); Eloise Clark, MPH (Facilitator); Wendy Engstrom Gerhardt, RN, MSN (Lead Administrator, Evidence Based Practice); Mindy Muenich, RN (Education Coordinator); Terri Byczkowski, PhD (Lead Administrator, Data); Kate Rich (Senior Analyst); Angela Booth-Jones, PhD, MS (Senior Outcomes Coordinator); Carol Frese, RN (Clinical Data Reviewer)

Ad Hoc Advisors: *Michael Farrell, MD (Chief of Staff); *Tom DeWitt, MD (Director, General and Community Pediatrics); *Richard Ruddy, MD (Director, Emergency Medicine); *Beverly Connelly, MD (Director, Infection Control Program); Keith Powell, MD (Children’s Hospital Medical Center of Akron); Irwin Light, MD (IRB); Scott Reeves, MD (Emergency Medicine); *Mel Rutherford (VP, Legal Services); *Dorine Sequist, RN (VP, Patient Services); Mike McKibben (Performance Improvement); Barbarie Hill (Pratt Library); Kim Collins (Medical Education); Ajit Sarnaik (Resident); Kieran Phelan, MD (Clinical Effectiveness)

*Members of 1997-1998 Development Team or Ad Hoc Advisor

The guideline was developed without external funding. All Team Members and Clinical Effectiveness support staff listed have declared whether they have any conflict of interest.

This is the current release of the guideline.

This guideline updates a previous version: Cincinnati Children's Hospital Medical Center. Evidence based clinical protocol guideline for fever of uncertain source in infants 60 days of age or less. Cincinnati (OH): Cincinnati Children's Hospital Medical Center; 1998. 32 p.

The guideline was reviewed for currency in September 2006 using updated literature searches and was determined to be current.

This summary was completed by ECRI on September 1, 1998. The information was verified by the guideline developer on December 1, 1998. This summary was updated by ECRI on March 11, 2004. This summary was updated by ECRI Institute on October 3, 2007 following the U.S. Food and Drug Administration (FDA) advisory on Rocephin (ceftriaxone sodium).