eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease
Yellow Fever: Treatment & Medication
Updated: Sep 15, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Treatment
Medical Care
No specific treatment for yellow fever (YF) is noted. Monitor for signs of organ failure and other infections and be prepared to manage them.
- Supportive care is the mainstay of management.
- Monitor fluid status and hydrate to maintain organ perfusion.
- Monitor electrolyte status and promptly correct any abnormalities.
- Monitor and be prepared to manage organ failure secondary to direct organ injury from yellow fever virus leading to cardiogenic shock, hepatic coma, and renal failure requiring dialysis.
- Monitor coagulation profile and correct abnormalities. Blood products may be required. Anticipate disseminated intravascular coagulation (DIC).
- Anticipate secondary bacterial infections, particularly pneumonia.
- Exclude concurrent malaria.
- Indicators of poor prognosis include the following:
- Early onset of bilirubinemia
- Marked albuminuria
- Prothrombin time increased by more than 25%
- Severe hemorrhage
- Shock
- Intractable hiccough (hiccup)
Consultations
- Infectious diseases specialist
- Additional training in tropical medicine is preferred.
- Diagnose and manage yellow fever.
- Diagnose and manage concurrent malaria.
- Diagnose and manage concurrent tropical disease other than malaria or yellow fever.
- Critical care specialist
- Consultation is preferred early in the course of illness in order to anticipate problems.
- Manage organ failure.
- Manage hemorrhagic diathesis.
- Nephrologist, if dialysis is required
Diet
- Diet is based on the patient's general status, the presence of any organ failure, and the development of a hemorrhagic diathesis.
Activity
- Activity is based on the patient's general status, the presence of any organ failure, and the development of a hemorrhagic diathesis.
Medication
No specific medication is indicated in the treatment of yellow fever (YF). Medication selection is based on the control of symptoms, secondary infections, and organ failure.
Analgesic and antipyretic agents
Antipyretics should be used only with caution, if at all, because of their metabolic effects on the liver and kidney. Do not use acetaminophen in the presence of hepatic compromise. Do not use ibuprofen in the presence of hepatic or renal compromise.
Acetaminophen (Tylenol, Feverall, Tempra)
Safe, well-tolerated, familiar agent with analgesic and antipyretic properties. Primary mechanism of action for analgesia and antipyresis is inhibition of prostaglandin synthesis. Available as tab, cap, liquid, powder, and supp.
Adult
325-650 mg PO/PR q4-6h prn
Alternative: 1000 mg PO q6h; not to exceed 4 g/d
Pediatric
15 mg/kg PO/PR q4h; not to exceed 2.6 g/d
Rifampin can reduce analgesic effects; coadministration with barbiturates, carbamazepine, hydantoins, and isoniazid may increase hepatotoxicity; hypothermia may occur when used concomitantly with phenothiazines
Documented hypersensitivity; known G-6-PD; hepatic compromise (because of potential for increased injury)
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
Precautions
Hepatotoxicity possible with overdose or long-term use of high doses; severe or recurrent pain or high or continued fever may indicate serious illness; contained in many OTC products, and their combined use may result in cumulative doses exceeding recommended maximum dose
Ibuprofen (Advil, Motrin)
Drug of choice (DOC) for mild-to-moderate pain; also used to reduce fever. Inhibits inflammatory reactions and pain by decreasing prostaglandin synthesis.
Adult
200-400 mg PO q4-6h while symptoms persist; not to exceed 3.2 g/d
Pediatric
<6 months: Not established
6 months to 12 years: 4-10 mg/kg PO q6-8h
>12 years: Administer as in adults
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 prothrombin time (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; 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
Vaccines
Active immunization increases resistance to infection. Vaccines consist of microorganisms or cellular components, which act as antigens. Administration of the vaccine stimulates the production of antibodies with specific protective properties.
YF vaccine (YF-Vax)
Live, attenuated virus preparation prepared by culturing 17D strain virus in living chick embryo. Immunity may start 7-10 d after vaccination. WHO requires revaccination q10y to maintain travelers' vaccination certificates which are valid in the United States for 10 y beginning 10 d after initial vaccination or revaccination.
Adult
0.5 mL SC at least 10 d before travel; reimmunization recommended q10y
Pediatric
<9 months: Contraindicated
>9 months: Administer as in adults
Cholera and YF vaccinations reduce response to each other and should be administered at least 3 wk apart, if possible (may be administered on same day if not feasible); concurrent hepatitis B vaccination may reduce response expected from YF vaccination and should be administered 1 mo apart, if possible; immunosuppressants, including steroids, or radiation may predispose patients to disseminated infections or insufficient response to immunization; patients may remain susceptible despite immunization
Documented hypersensitivity; age <9 mo, except when in high-risk areas or with immunodeficiency syndrome
Pregnancy
C - Fetal risk revealed in studies in animals but not established or not studied in humans; may use if benefits outweigh risk to fetus
Precautions
Preservative-free diluents should be used to avoid inactivating vaccine; caution in immunosuppressed patients or patients taking immunosuppressants; delay vaccination with YF vaccine for 8 wk after blood or plasma transfusion; may produce drowsiness, blurred vision, or sensitivity to light (due to dilated pupils); caution while driving or performing other tasks requiring alertness, coordination, or physical dexterity
More on Yellow Fever |
| Overview: Yellow Fever |
| Differential Diagnoses & Workup: Yellow Fever |
Treatment & Medication: Yellow Fever |
| Follow-up: Yellow Fever |
| Multimedia: Yellow Fever |
| References |
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References
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Further Reading
Keywords
yellow fever, YF, Flaviviridae, tropical infections, viral infections, yellow fever virus, yellow jack, proteinuria, mosquito, disseminated intravascular coagulation, DIC, high temperatures, chills, anxiety, confusion, lethargy, prostration, jaundice, epistaxis, anorexia, epigastric pain, nausea, vomiting, hematemesis, melena, lumbosacral pain, pneumonia, sepsis, infection, treatment, diagnosis
Treatment & Medication: Yellow Fever