eMedicine Specialties > Emergency Medicine > Pediatric

Pediatrics, Fever: Treatment & Medication

Author: John W Graneto, DO, FACEP, FAAP, Clinical Assistant Professor of Emergency Medicine, Chicago College of Osteopathic Medicine of Midwestern University; Consulting Staff, Department of Emergency Medicine, Swedish Covenant Hospital
Contributor Information and Disclosures

Updated: Aug 6, 2009

Treatment

Prehospital Care

Prehospital care provided by emergency medical technicians (EMTs) and paramedics may vary from region to region on the basis of regional differences in education, training, and transport times.

  • Children with fever alone may require no specific intervention in the EMS setting, except for those other conditions that exist in the presence of fever.
  • Assessment of and attention to airway, breathing, and circulation is recommended first for all ill children.
  • Those children who have had prolonged, or very high, fever may become dehydrated, and assessment of the hydration status is indicated.
  • Some children may be prone to febrile seizures and seizure precautions should be followed in those with a history of febrile seizures.

Emergency Department Care

Vital signs recorded in triage should routinely include a temperature in young children. This should be recorded on all neonates and infants presenting with fever or other potentially infectious complaints (eg, not eating well, not breathing well, color changes, behavior changes). A rectal temperature is the most accurate for infants.

The nursing triage includes an accurate assessment of the patient's weight to ascertain the correct dose of an antipyretic or other medications.

  • An antipyretic should be given as early as possible during the ED visit. Reduction of fever is used to help comfort the child as well as provide for the optimal examination conditions. Triage protocols are developed to facilitate this.
    • The ED staff should be educated that a positive response to antipyretics (evidenced by a drop in the measured temperature) is not predictive of the absence of a potentially serious bacterial disease.27,28
    • Criteria for discharge from the ED do not necessarily include reduction of the child's fever to a certain level before discharge. No evidence indicates that fever reduction is necessary for the child to be discharged from the ED.29
  • Neonates with fever who undergo the previously described routine workup to rule out sepsis should then receive 2 antibiotics as treatment for their potential septicemia: an aminopenicillin (eg, ampicillin) and a cephalosporin (eg, cefotaxime). Neonates may also receive antiviral treatment with acyclovir if they are at risk for neonatal herpes infection.
  • Older children with a low-grade fever, no risk factors, no localized signs of infection, a good appearance, and no irritability may require only symptomatic treatment and close follow-up care. These patients do not routinely need laboratory evaluation, radiography, or empiric antibiotics.

Consultations

Contact with the patient's primary care provider or designee helps ensure a continuum of care and enables effective follow-up care.

Medication

The goals of pharmacotherapy are to reduce morbidity and prevent complications.

Antipyretics

These agents provide patient comfort during the ED visit and are used liberally in febrile children. A child whose temperature has been reduced is more comfortable and more likely to have an optimal examination.

Acetaminophen and ibuprofen have both been used for fever control.9

  • These drugs are sometimes alternated to achieve an overlapping period of fever control. However, no data support the safety of this practice of alternating medications.29,28
  • Some studies have shown that acetaminophen works faster by initially lowering elevations in temperature.27
  • Some studies have shown that ibuprofen takes longer to initially result in fever reduction but that its effect may last longer than that of acetaminophen.8
  • Hay et al studied whether administering a combination of acetaminophen and ibuprofen for fever in children was superior to administration of acetaminophen alone or ibuprofen alone.30 Dosage was calculated as acetaminophen 15 mg/kg/dose and ibuprofen 10 mg/kg/dose. Children aged 6 months to 6 years whose fever could be managed at home (37.5-41ºC) were included. Use of acetaminophen and ibuprofen improved time without fever during the first 4 hours and was superior to acetaminophen alone, but not ibuprofen alone. The combination also decreased fever 23 minutes faster than acetaminophen alone, but no faster than ibuprofen alone. Time without fever during the first 24 hours was improved with the combination compared with either acetaminophen or ibuprofen.


Acetaminophen (Tylenol, Feverall, Panadol)

Reduces fever by directly acting on hypothalamic heat-regulating centers, increasing dissipation of body-heat via vasodilation and sweating.

Adult

Pediatric

10-15 mg/kg/dose PO q4-6h prn; not to exceed 2.6 g/d

Rifampin can reduce analgesic effects; coadministration with barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity

Documented hypersensitivity; liver failure; known G-6-PD deficiency

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Hepatotoxicity possible following various dose levels in persons with chronic alcoholism; severe or recurrent pain or high or continued fever may indicate serious illness; contained in many OTC products and combined use may result in cumulative doses exceeding recommended maximum


Ibuprofen (Advil, Motrin)

One of few NSAIDs indicated for reduction of fever. Inhibits prostaglandin formation.

Adult

Pediatric

5-10 mg/kg/dose PO q6-8h prn; not to exceed 40 mg/kg/d or 2.4 g/d

Coadministration with aspirin increases risk of inducing serious NSAID-related adverse effects; probenecid may increase concentrations and, possibly, toxicity of NSAIDs; may decrease effect of hydralazine, captopril, and beta-blockers; may decrease diuretic effects of furosemide and thiazides; monitor PT closely (instruct patients to watch for signs of bleeding); may increase risk of methotrexate toxicity; phenytoin levels may be increased when administered concurrently

Documented hypersensitivity; peptic ulcer disease, recent GI bleeding or perforation, renal insufficiency, or high risk of bleeding

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Category D in third trimester of pregnancy; caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in anticoagulation abnormalities or during anticoagulant therapy

Antimicrobial agents

Antibiotics are used to treat occult bacterial infection. Empiric antimicrobial therapy must be comprehensive and should cover all likely pathogens in the clinical setting. Whenever feasible, select antibiotics based upon blood culture sensitivity. Consider initiating acyclovir for suspected HSV or VSV infections.


Cefotaxime (Claforan)

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 1 or more penicillin-binding proteins.

Adult

Pediatric

Infants and children: 150-200 mg/kg/d IV/IM divided q4-6h

Probenecid may increase levels; coadministration with furosemide and aminoglycosides may increase nephrotoxicity

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in severe renal impairment; has been associated with severe colitis


Ampicillin (Omnipen, Marcillin, Principen)

Bactericidal activity against susceptible organisms.

Adult

Pediatric

50-100 mg/kg/d PO divided q4-6h or 100-400 mg/kg/d IV/IM divided q4-6h

Probenecid and disulfiram elevate levels; allopurinol decreases effects and has additive effects on ampicillin rash; may decrease effects of oral contraceptives

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal failure; evaluate rash and differentiate from hypersensitivity reaction


Ceftriaxone (Rocephin)

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 1 or more penicillin-binding proteins.

Adult

Pediatric

Neonates >7 days: 25-50 mg/kg/d IV/IM; not to exceed 125 mg/d
Infants and children: 50-75 mg/kg/d IV/IM divided q12h; not to exceed 2 g/d

Probenecid may increase levels; coadministration with ethacrynic acid, furosemide, and aminoglycosides may increase nephrotoxicity

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Adjust dose in renal impairment; caution in breastfeeding women and patients with penicillin allergy


Oxacillin (Bactocill, Prostaphlin)

Bactericidal antibiotic that inhibits cell wall synthesis. Used in the treatment of infections caused by penicillinase-producing staphylococci. May be used to initiate therapy when a staphylococcal infection is suspected.

Adult

Pediatric

50-100 mg/kg/d PO divided q6h or 150-200 mg/kg/d IV/IM divided q6h; not to exceed 12 g/d

Oxacillin decreases effects of contraceptives and tetracycline; administered concomitantly with disulfiram and probenecid, may increase oxacillin levels; effect of anticoagulants increase when large IV doses of oxacillin given

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in renal impairment


Acyclovir (Zovirax)

Prodrug activated by phosphorylation by virus-specific thymidine kinase (TK) that inhibits viral replication. Herpes virus TK, but not host cells TK, uses acyclovir as a purine nucleoside, converting it into acyclovir monophosphate, a nucleotide analogue. Guanylate kinase converts the monophosphate form into diphosphate and triphosphate analogues that inhibit viral DNA replication.
Has affinity for viral TK and once phosphorylated causes DNA chain termination when acted on by DNA polymerase. Inhibits activity of both HSV-1 and HSV-2. Patients experience less pain and faster resolution of cutaneous lesions when used within 48 h from rash onset. May prevent recurrent outbreaks. Early initiation of therapy is imperative.
IV therapy is treatment of choice for neonatal HSV infection regardless of clinical presentation.
Also used in VZV meningitis. Activated by herpes-specific TK; prevents viral replication by inhibiting viral DNA polymerase. Excreted primarily by kidneys; modify dose in patients with renal impairment.

Adult

Pediatric

1500 mg/m2/d divided q8h or 10 mg/kg/dose IV q8h for 14-28 d; typically infused over 1 h (smaller doses may be appropriate in very premature infants)

Concomitant use of probenecid or zidovudine prolongs half-life and increases CNS toxicity of acyclovir

Pregnancy

B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals

Precautions

Caution in renal failure or when using nephrotoxic drugs

More on Pediatrics, Fever

Overview: Pediatrics, Fever
Differential Diagnoses & Workup: Pediatrics, Fever
Treatment & Medication: Pediatrics, Fever
Follow-up: Pediatrics, Fever
References

References

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Further Reading

Keywords

fever in children, fever in kids, high temperature, febrile, pyrexia, feverish, febrile child, febrile infant, infant with fever, child with fever, infection, meningitis, bacteremia or sepsis, enteritis, pneumonia, pericarditis, osteomyelitis, septic arthritis, cellulitis, otitis media, pharyngitis, sinusitis, urinary tract infections, enteritis, appendicitis, viral illnesses, upper respiratory infections, bronchiolitis, enteroviral exanthems, gastroenteritis, flulike illnesses

Contributor Information and Disclosures

Author

John W Graneto, DO, FACEP, FAAP, Clinical Assistant Professor of Emergency Medicine, Chicago College of Osteopathic Medicine of Midwestern University; Consulting Staff, Department of Emergency Medicine, Swedish Covenant Hospital
John W Graneto, DO, FACEP, FAAP is a member of the following medical societies: American Academy of Pediatrics, American College of Emergency Physicians, American College of Osteopathic Emergency Physicians, American College of Osteopathic Pediatricians, and American Osteopathic Association
Disclosure: Nothing to disclose.

Medical Editor

William G Gossman, MD, Associate Clinical Professor of Emergency Medicine, Creighton University School of Medicine; Consulting Staff, Department of Emergency Medicine, Creighton University Medical Center
William G Gossman, MD is a member of the following medical societies: American Academy of Emergency Medicine
Disclosure: Nothing to disclose.

Pharmacy Editor

Mary L Windle, PharmD, Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy, Pharmacy Editor, eMedicine
Disclosure: Pfizer Inc Stock Investment from financial planner; Avanir Pharma Stock Investment from financial planner ; WebMD Salary and stock Employment and investment from financial planner

Managing Editor

Wayne Wolfram, MD, MPH, 
Wayne Wolfram, MD, MPH is a member of the following medical societies: American Academy of Emergency Medicine, American Academy of Pediatrics, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

CME Editor

John D Halamka, MD, MS, Associate Professor of Medicine, Harvard Medical School, Beth Israel Deaconess Medical Center; Chief Information Officer, CareGroup Healthcare System and Harvard Medical School; Attending Physician, Division of Emergency Medicine, Beth Israel Deaconess Medical Center
John D Halamka, MD, MS is a member of the following medical societies: American College of Emergency Physicians, American Medical Informatics Association, Phi Beta Kappa, and Society for Academic Emergency Medicine
Disclosure: Nothing to disclose.

Chief Editor

Richard G Bachur, MD, Associate Professor of Pediatrics, Harvard Medical School; Associate Chief and Fellowship Director, Attending Physician, Division of Emergency Medicine, Children's Hospital of Boston
Richard G Bachur, MD is a member of the following medical societies: American Academy of Pediatrics, Society for Academic Emergency Medicine, and Society for Pediatric Research
Disclosure: Nothing to disclose.

 
 
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