eMedicine Specialties > Dermatology > Viral Infections
Erythema Infectiosum (Fifth Disease): Treatment & Medication
Updated: Dec 8, 2009
- Overview
- Differential Diagnoses & Workup
- Treatment & Medication
- Follow-up
- Multimedia
Treatment
Medical Care
Because erythema infectiosum (fifth disease) most often is a benign self-limited disease, reassuring the parents often is the only intervention necessary.12 For patients with arthralgias or pruritus, symptomatic relief can be obtained using oral analgesics and antihistamines or topical antipruritic lotions.
Consultations
- Dermatologist: Refer patients for diagnosis and dermatologic care.
- Internal medicine specialist: Refer patients for associated conditions.
- Obstetrician/gynecologist: Due to potential complications from intrauterine parvovirus B-19 (PV-B19) infection, refer pregnant women who have IgM antibodies to PV-B19 or who have been exposed to the virus. Maternal alpha-fetoprotein levels and serial ultrasounds followed through the pregnancy may help predict complications.
Activity
Activities may be pursued as tolerated, with sun protection or avoidance.
Medication
Symptomatic relief of erythema infectiosum (fifth disease) may be provided using nonsteroidal anti-inflammatory drugs (NSAIDs), antihistamines, and topical antipruritics, along with plenty of fluids and rest. For an acute aplastic crisis, supplemental oxygen and blood transfusions may be necessary. Intravenous immunoglobulin (IVIG) is helpful for chronic anemia in patients who are immunocompromised.
Nonsteroidal anti-inflammatory drugs
Provide relief for fever, malaise, headache, and arthralgia. Although the effects of NSAIDs in the treatment of pain tend to be patient specific, ibuprofen usually is the drug of choice (DOC) for initial therapy. Other options include fenoprofen, flurbiprofen, mefenamic acid, ketoprofen, indomethacin, and piroxicam.
Ibuprofen (Ibuprin, Advil, Motrin)
Has analgesic, anti-inflammatory, and antipyretic properties. Inhibits inflammatory reactions and pain, possibly by decreasing prostaglandin synthesis.
Adult
200-400 mg PO tid/qid
Pediatric
5-10 mg/kg PO tid/qid (100 mg/5 mL susp)
Coadministration 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
Documented hypersensitivity; peptic ulcer disease; recent GI tract bleeding or perforation; renal insufficiency; patients at high risk for bleeding
Pregnancy
B - Fetal risk not confirmed in studies in humans but has been shown in some studies in animals
D - Fetal risk shown in humans; use only if benefits outweigh risk to fetus
Precautions
FDA category D (unsafe in pregnancy) in third trimester of pregnancy; caution in congestive heart failure, hypertension, and decreased renal and hepatic function; caution in coagulation abnormalities or during anticoagulant therapy
Antihistamines
Provide symptomatic relief of pruritus.
Hydroxyzine (Atarax, Vistaril)
Antihistamine with antipruritic, anxiolytic, and mild sedative effects. Antagonizes H1 receptors in periphery. May suppress histamine activity in subcortical region of CNS.
Adult
25-50 mg PO tid/qid prn for pruritus
Pediatric
2-3 mg/kg/d PO divided tid/qid prn for pruritus (10 mg/5 mL syr)
CNS depression may increase with alcohol or other CNS depressants
Documented hypersensitivity
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
Associated with clinical exacerbations of porphyria (may not be safe for patients with porphyria); ECG abnormalities (alterations in T waves) may occur; may cause drowsiness; caution patients regarding operating automobiles and other dangerous machinery because of possible sedation; anticholinergic effects (eg, dry mouth) may occur
Topical antipruritics
Help relieve the discomfort of itching skin.
0.5% camphor/0.5% menthol lotion
Cooling, soothing, moisturizing lotion used to help alleviate pruritus.
Adult
Apply topically to affected areas bid/tid prn for pruritus
Pediatric
<2 years: Not recommended
>2 years: Administer as in adults
None reported
Documented hypersensitivity
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
For topical use only; avoid contact with eyes; discontinue if irritation occurs
More on Erythema Infectiosum (Fifth Disease) |
| Overview: Erythema Infectiosum (Fifth Disease) |
| Differential Diagnoses & Workup: Erythema Infectiosum (Fifth Disease) |
Treatment & Medication: Erythema Infectiosum (Fifth Disease) |
| Follow-up: Erythema Infectiosum (Fifth Disease) |
| Multimedia: Erythema Infectiosum (Fifth Disease) |
| References |
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References
Veraldi S, Rizzitelli G. Erythematous exanthem associated with primary infection by human parvovirus B19. Int J Dermatol. Feb 1995;34(2):119. [Medline].
van Rijckevorsel GG, Sonder GJ, Schim van der Loeff MF, van den Hoek JA. Population-based study on the seroprevalence of parvovirus B19 in Amsterdam. J Med Virol. Jul 2009;81(7):1305-9. [Medline].
Nicolay N, Cotter S. Clinical and epidemiological aspects of parvovirus B19 infections in Ireland, January 1996-June 2008. Euro Surveill. Jun 25 2009;14(25):[Medline].
Frydenberg A, Starr M. Slapped cheek disease. How it affects children and pregnant women. Aust Fam Physician. 2003;32:589-92. [Medline].
McCarter-Spaulding D. Parvovirus B19 in pregnancy. J Obstet Gynecol Neonatal Nurs. Jan-Feb 2002;31(1):107-12. [Medline].
Keeler ML. Human parvovirus B-19: not just a pediatric problem. J Emerg Med. Jan-Feb 1992;10(1):39-44. [Medline].
Magro CM, Dawood MR, Crowson AN. The cutaneous manifestations of human parvovirus B19 infection. Hum Pathol. Apr 2000;31(4):488-97. [Medline].
Takeda S, Takaeda C, Takazakura E, Haratake J. Renal involvement induced by human parvovirus B19 infection. Nephron. Nov 2001;89(3):280-5. [Medline].
Broliden K, Tolfvenstam T, Norbeck O. Clinical aspects of parvovirus B19 infection. J Intern Med. 2006;260:285-304. [Medline].
Yamada Y, Itoh M, Yoshida M. Sensitive and rapid diagnosis of human parvovirus B19 infection by loop-mediated isothermal amplification. Br J Dermatol. 2006;155:50-5. [Medline].
Corcoran A, Doyle S. Advances in the biology, diagnosis and host-pathogen interactions of parvovirus B19. J Med Microbiol. Jun 2004;53(Pt 6):459-75. [Medline].
Revilla Grande AI, Carro Garcia T, Sanchez de Dios M, Galan Calvo MJ, Nebreda Mayoral T. [Outbreak of infectious erythema at a urban health center]. Aten Primaria. Jul-Aug 2000;26(3):172-5. [Medline].
Fattet S, Cassinotti P, Popovic MB. Persistent human parvovirus B19 infection in children under maintenance chemotherapy for acute lymphocytic leukemia. J Pediatr Hematol Oncol. 2004;26:497-503. [Medline].
Aractingi S, Bakhos D, Flageul B, Vérola O, Brunet M, Dubertret L, et al. Immunohistochemical and virological study of skin in the papular- purpuric gloves and socks syndrome. Br J Dermatol. Oct 1996;135(4):599-602. [Medline].
Harms M, Feldmann R, Saurat JH. Papular-purpuric "gloves and socks" syndrome. J Am Acad Dermatol. Nov 1990;23(5 Pt 1):850-4. [Medline].
McNeely M, Friedman J, Pope E. Generalized petechial eruption induced by parvovirus B19 infection. J Am Acad Dermatol. May 2005;52(5 Suppl 1):S109-13. [Medline].
Colmegna I, Alberts-Grill N. Parvovirus B19: its role in chronic arthritis. Rheum Dis Clin North Am. Feb 2009;35(1):95-110. [Medline].
Magro CM, Wusirika R, Frambach GE, Nuovo GJ, Ferri C, Ross P. Autoimmune-like pulmonary disease in association with parvovirus B19: a clinical, morphologic, and molecular study of 12 cases. Appl Immunohistochem Mol Morphol. 2006;14:208-16. [Medline].
Douvoyiannis M, Litman N, Goldman DL. Neurologic manifestations associated with parvovirus B19 infection. Clin Infect Dis. Jun 15 2009;48(12):1713-23. [Medline].
Barah F, Vallely PJ, Cleator GM, Kerr JR. Neurologic manifestations of human parvovirus B19 infection. Rev Med Virol. 2003;13:185-99. [Medline].
Hsu D, Sandborg C, Hahn JS. Frontal lobe seizures and uveitis associated with acute human parvovirus B19 infection. J Child Neurol. 2004;19:304-6. [Medline].
Peter G. School policies for children with erythema infectiosum. Pediatr Infect Dis J. 1989;8 (1):64.
Jarvi JF. Pediatric exanthems: recognize the rash. JAAPA. Apr 2001;14(4):29-32, 35-6. [Medline].
Meyer O. Parvovirus B19 and autoimmune diseases. Joint Bone Spine. 2003;70:6-11. [Medline].
Prcic S, Jakovijevic A, Duran V, Gajinov Z. Erythema infectiosum in children. A Clinical study. Med Pregl. 2006;59:5-10. [Medline].
Qari M, Qadri SM. Parvovirus B19 infection. Associated diseases, common and uncommon. Postgrad Med. Jul 1996;100(1):239-43, 246, 252. [Medline].
Stiefel L. Erythema infectiosum (fifth disease). Pediatr Rev. Dec 1995;16(12):474-5. [Medline].
Wyndham M. Parvovirus. Practitioner. Oct 1996;240(1567):606. [Medline].
Young NS. Parvovirus infection and its treatment. Clin Exp Immunol. May 1996;104 Suppl 1:26-30. [Medline].
Further Reading
Keywords
erythema infectiosum, fifth disease, slapped-cheek disease, academy rash, Sticker's disease, Sticker disease, childhood exanthem, Parvovirus B19, PV-B19, PV-B19 infection, Parvoviridae family, acute arthropathy, acute polyarthropathy, coryza, pharyngitis, arthralgias, malar rash
Treatment & Medication: Erythema Infectiosum (Fifth Disease)