eMedicine Specialties > Pediatrics: General Medicine > Infectious Disease

Varicella: Treatment & Medication

Author: Parang N Mehta, MD, Consulting Staff, Department of Pediatrics, Mehta Hospital, Surat, India
Coauthor(s): Archana Chatterjee, MD, PhD, Professor of Pediatrics, Medical Microbiology and Immunology, and Pharmacy, Division of Pediatric Infectious Diseases, Chief of Division of Pediatric Infectious Diseases, Creighton University School of Medicine; Hospital Epidemiologist and Medical Director of Infection Control, Children's Hospital
Contributor Information and Disclosures

Updated: Jul 31, 2009

Treatment

Medical Care

  • Manage pruritus in patients with varicella with cool compresses and regular bathing.
  • Discourage scratching to avoid scarring. Trimming the child's fingernails and having the child wear mittens while sleeping may reduce scratching.

Consultations

  • Consult with an infectious disease specialist in the following situations:
    • Progressive or severe varicella
    • Life-threatening complications (eg, encephalitis, pneumonia)
    • Serious secondary bacterial infections, especially group A streptococcal superinfections, which may evolve rapidly into necrotizing fasciitis and toxic shock syndrome
  • Children who develop severe and life-threatening varicella complications may require hospitalization in an ICU.

Diet

  • Advise parents to provide a full and unrestricted diet to the child.
  • Some children with varicella have reduced appetite and should be encouraged to take sufficient fluids to maintain hydration. Adequate hydration is especially important if the child is receiving acyclovir because the drug can crystallize in the renal tubules if administered to dehydrated individuals.

Activity

  • No activity restrictions are needed for young children with uncomplicated varicella.

Medication

Antivirals

Chickenpox is not always benign. In certain well-defined groups, varicella can be severe and even fatal. Antiviral drugs are recommended for adolescents, adults, and children on steroid or salicylate therapy and for children who are otherwise immunocompromised. Acyclovir is the only adequately studied drug of this class.


Acyclovir (Zovirax)

Antiviral that acts by inhibiting herpes virus DNA polymerase and terminating viral replication. It reduces the number of lesions and duration of fever if started within 24 h of appearance of rash. In young children with uncomplicated varicella, benefit is only marginal and use is not routinely recommended. It does not affect incidence of pruritus, complications, or secondary transmission. It is always used for complications of varicella (eg, encephalitis, pneumonia) and for immunocompromised individuals with varicella. Available as cap (200-800 mg), PO liquid (400 mg/5 mL), and parenteral injection (500 mg/mL).

Adult

800 mg PO 5 times/d for 7 d
1500 mg/m2/d IV divided q8h for 7-10 d for encephalitis, pneumonia, or infection in immunocompromised patients

Pediatric

80 mg/kg/d PO divided in 4-5 doses for 5 d; not to exceed 3200 mg/d
Encephalitis or pneumonia: Administer as in adults

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; may cause malaise, GI upset, and rash; PO bioavailability is poor, making IV administration essential for patients with severe varicella and for immunocompromised patients

Antipyretics

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

Fever is usually low grade but may be elevated. Acetaminophen is probably the safest drug to use for this purpose. Salicylate usage for varicella is associated with Reye syndrome; therefore, never prescribe these agents. Nonsteroidal anti-inflammatory drugs (NSAIDs) have been suspected of suppressing immune function and promoting infection progress in patients infected with invasive group A streptococci.


Acetaminophen (Tylenol, Feverall, Tempra, Aspirin-Free Anacin)

DOC because has no association with Reye syndrome; available as gtt containing 80 mg/0.8 mL, susp containing 160 mg/5 mL, chewable tab or cap containing 80 mg, and tab containing 160 mg, 325 mg, and 500 mg.

Adult

500-650 mg/dose PO q4-6h prn for fever; not to exceed 4 g/d

Pediatric

10-15 mg/kg PO q4-6h prn for fever; not to exceed 60 mg/kg/d

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

Pregnancy

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

Precautions

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


Ibuprofen (Motrin, Ibuprin)

A propionic acid–derivative NSAID; acts by inhibiting prostaglandin synthesis; also has anti-inflammatory and analgesic properties; available as an PO suspension (100 mg/5 mL) and tab containing 300 mg, 400 mg, 600 mg, or 800 mg.

Adult

200-400 mg PO q4-6h prn for fever

Pediatric

6 months to 12 years: 4-10 mg/kg/dose PO tid/qid; not to exceed 40 mg/kg/d
>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; closely monitor PT (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

C - 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

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; causes nausea, stomach upset, and rashes in 3-9% of patients; causes maculopapular rash and pruritus in 1-3% of recipients; may confuse clinical picture of varicella

Antihistamines

These agents may control pruritus by blocking effects of endogenous release of histamine. Pruritus can be severe in varicella, preventing sleep and possibly leading to scarring or secondary infection. Nonsedating antihistaminics lack sufficient antipruritic action. The value of local preparations (eg, calamine, antihistamines) is unproved. Topical antihistamines can cause significant sedation from absorption through injured skin.


Diphenhydramine (Benadryl)

Antihistamine has a sedating effect and is effective for pruritus; available as a liquid containing 12.5 mg/5 mL, cap containing 25 and 50 mg, and injections containing 10 and 50 mg/mL.

Adult

25-50 mg PO tid/qid

Pediatric

5 mg/kg/d PO divided tid/qid; not to exceed 300 mg/d

Potentiates effect of CNS depressants; because of alcohol content, do not administer syrup form to patient taking medications that can cause disulfiramlike reactions

Documented hypersensitivity; MAOIs

Pregnancy

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

Precautions

May exacerbate angle-closure glaucoma, hyperthyroidism, peptic ulcer, and urinary tract obstruction

More on Varicella

Overview: Varicella
Differential Diagnoses & Workup: Varicella
Treatment & Medication: Varicella
Follow-up: Varicella
Multimedia: Varicella
References

References

  1. Kouwabunpat D, Hoffman J, Adler R. Varicella complicated by group A streptococcal sepsis and osteonecrosis. Pediatrics. Oct 1999;104(4 Pt 1):967-9. [Medline][Full Text].

  2. [Guideline] Update: recommendations from the Advisory Committee on Immunization Practices (ACIP) regarding administration of combination MMRV vaccine. MMWR Morb Mortal Wkly Rep. Mar 14 2008;57(10):258-60. [Medline].

  3. Matsukura H, Murakami M, Sakaki H, Mitani T, Shimura S. Varicella glomerulonephritis preceding the cutaneous lesions. Clin Nephrol. Aug 2009;72(2):161-2. [Medline].

  4. Arbeter AM, Granowetter L, Starr SE, et al. Immunization of children with acute lymphoblastic leukemia with live attenuated varicella vaccine without complete suspension of chemotherapy. Pediatrics. Mar 1990;85(3):338-44. [Medline].

  5. Buchholz U, Moolenaar R, Peterson C, Mascola L. Varicella outbreaks after vaccine licensure: should they make you chicken?. Pediatrics. Sep 1999;104(3 Pt 1):561-3. [Medline][Full Text].

  6. CDC. National, state, and urban area vaccination coverage among children aged 19-35 months--United States, 2004. MMWR Morb Mortal Wkly Rep. Jul 29 2005;54(29):717-21. [Medline][Full Text].

  7. Chaves SS, Gargiullo P, Zhang JX, et al. Loss of vaccine-induced immunity to varicella over time. N Engl J Med. Mar 15 2007;356(11):1121-9. [Medline].

  8. Derrick CW Jr, Lord L. In utero varicella-zoster infections. South Med J. Nov 1998;91(11):1064-6. [Medline].

  9. Dowell SF, Bresee JS. Severe varicella associated with steroid use. Pediatrics. Aug 1993;92(2):223-8. [Medline].

  10. Galil K, Lee B, Strine T, et al. Outbreak of varicella at a day-care center despite vaccination. N Engl J Med. Dec 12 2002;347(24):1909-15. [Medline][Full Text].

  11. Jaamaa S, Salonen M, Seppala I, et al. Varicella zoster and Borrelia burgdorferi are the main agents associated with facial paresis, especially in children. J Clin Virol. Jul 2003;27(2):146-51. [Medline].

  12. Pastuszak AL, Levy M, Schick B, et al. Outcome after maternal varicella infection in the first 20 weeks of pregnancy. N Engl J Med. Mar 31 1994;330(13):901-5. [Medline][Full Text].

  13. Verstraeten T, Jumaan AO, Mullooly JP, et al. A retrospective cohort study of the association of varicella vaccine failure with asthma, steroid use, age at vaccination, and measles-mumps-rubella vaccination. Pediatrics. Aug 2003;112(2):e98-103. [Medline][Full Text].

  14. Zhou F, Harpaz R, Jumaan AO, et al. Impact of varicella vaccination on health care utilization. JAMA. Aug 17 2005;294(7):797-802. [Medline][Full Text].

Further Reading

Keywords

varicella, chickenpox, chicken pox, waterpox, water pox, varicellovirus, varicella-zoster virus, varicella pneumonia, varicella encephalitis, group A streptococcal disease, Reye syndrome, congenital varicella syndrome, growth retardation, microcephaly, cortical atrophy, limb hypoplasia, microphthalmia, cataracts, chorioretinitis, infantile zoster, neonatal varicella, maternal varicella, diagnosis, treatment 

Contributor Information and Disclosures

Author

Parang N Mehta, MD, Consulting Staff, Department of Pediatrics, Mehta Hospital, Surat, India
Disclosure: Nothing to disclose.

Coauthor(s)

Archana Chatterjee, MD, PhD, Professor of Pediatrics, Medical Microbiology and Immunology, and Pharmacy, Division of Pediatric Infectious Diseases, Chief of Division of Pediatric Infectious Diseases, Creighton University School of Medicine; Hospital Epidemiologist and Medical Director of Infection Control, Children's Hospital
Archana Chatterjee, MD, PhD is a member of the following medical societies: American Academy of Pediatrics, American Society for Microbiology, International Society for Infectious Diseases, Pediatric Infectious Diseases Society, and Society for Pediatric Research
Disclosure: GlaxosmithKline Honoraria Speaking and teaching; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; Sanofi-Pasteur Honoraria Speaking and teaching; Wyeth Honoraria Speaking and teaching; GlaxoSmithKline Grant/research funds Other; MedImmune  Other; Merck Grant/research funds Other; Novartis Grant/research funds Other; Sanofi-Pasteur Grant/research funds Other

Medical Editor

Leonard R Krilov, MD, Chief of Pediatric Infectious Diseases, Vice Chair, Department of Pediatrics, Professor of Pediatrics, Winthrop University Hospital
Leonard R Krilov, MD is a member of the following medical societies: American Academy of Pediatrics, American Pediatric Society, Infectious Diseases Society of America, Pediatric Infectious Diseases Society, and Society for Pediatric Research
Disclosure: Medimmune Grant/research funds Cliinical trials; Medimmune Honoraria Speaking and teaching; Medimmune Consulting fee Consulting

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

Leslie L Barton, MD, Professor, Program Director, Department of Pediatrics, University of Arizona School of Medicine
Leslie L Barton, MD is a member of the following medical societies: American Academy of Pediatrics, Association of Pediatric Program Directors, Infectious Diseases Society of America, and Pediatric Infectious Diseases Society
Disclosure: Nothing to disclose.

CME Editor

Robert W Tolan Jr, MD, Chief, Division 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, MD 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
Disclosure: GlaxoSmithKline Honoraria Speaking and teaching; MedImmune Honoraria Speaking and teaching; Merck Honoraria Speaking and teaching; sanofi pasteur Honoraria Speaking and teaching; Baxter Healthcare Honoraria Speaking and teaching

Chief Editor

Russell W Steele, MD, Head, Division of Pediatric Infectious Diseases, Ochsner Children's Health Center; Clinical Professor, Department of Pediatrics, Tulane University School of Medicine
Russell W Steele, MD is a member of the following medical societies: American Academy of Pediatrics, American Association of Immunologists, American Pediatric Society, American Society for Microbiology, Infectious Diseases Society of America, Louisiana State Medical Society, Pediatric Infectious Diseases Society, Society for Pediatric Research, and Southern Medical Association
Disclosure: None None None

 
 
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