Parvovirus B19 infection after transplantation: a review of 98 cases

TitleParvovirus B19 infection after transplantation: a review of 98 cases
Publication TypeJournal Article
Year of Publication2006
AuthorsEid AJ, Brown RA, Patel R, Razonable RR
JournalClinical infectious diseases : an official publication of the Infectious Diseases Society of America
Pagination40 - 8
Date PublishedJul 1
Type of ArticleCase Reports Research Support, Non-U.S. Gov't Review
ISSN1537-6591 (Electronic) 1058-4838 (Linking)
Accession Number16758416
Keywords*Parvovirus B19, Human, Adult, Anemia / etiology, DNA, Viral, Female, Hematopoietic Stem Cell Transplantation / *adverse effects, Humans, Male, Middle Aged, Organ Transplantation / *adverse effects, Parvoviridae Infections / epidemiology / *etiology, Polymerase Chain Reaction, Retrospective Studies

BACKGROUND: Infections with parvovirus B19 (PVB19) can cause significant morbidity in transplant recipients. METHODS: To characterize the epidemiology and clinical spectrum of posttransplant PVB19 infection, we reviewed all cases at our institution during a 16-year period, summarized the data from 91 cases published in the medical literature, and performed longitudinal molecular surveillance for PVB19 DNAemia among 47 solid organ and hematopoietic stem cell transplant recipients. RESULTS: The median time to onset of PVB19 disease was 7 weeks after transplantation. Anemia, leukopenia, and thrombocytopenia were present in 98.8%, 37.5%, and 21.0% of patients, respectively. Hepatitis, myocarditis, and pneumonitis were also reported in association with PVB19 disease. Allograft tissue loss or dysfunction was observed at the time of PVB19 disease in 10% of cases. At the onset of disease, PVB19 IgM serological test results were negative in 29% of cases. Almost all patients (96%) with anti-PVB19 IgM had a positive PVB19 polymerase chain reaction assay result. Intravenous immunoglobulin was the most commonly used treatment modality. Three of 98 patients died of myocarditis and cardiogenic shock associated with PVB19 disease. Molecular surveillance throughout the first year after transplantation did not reveal PVB19 DNAemia in 47 anemic solid organ and hematopoietic stem cell transplant patients. CONCLUSIONS: PVB19 is a rare but clinically significant infection that manifests as refractory anemia during the posttransplantation period. The use of polymerase chain reaction for diagnosis is particularly helpful in immunosuppressed transplant patients who may fail to mount antibodies against PVB19 during active infection.

Alternate JournalClin Infect Dis
Notify Library Reference ID474

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