Evidence map›Paper›PMID 40896599›Full record

ArticleIndian journal of nephrology

Parvovirus B19 Infection as a Cause of Refractory Anemia in Kidney Transplant Recipients: A Case Series.

Umapati N Hegde, Ankur Mittal, Sishir Gang, Abhijit Konnur, Hardik Patel

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Article in Indian journal of nephrology. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
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1 · What the graph read from it

What it found

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The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

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3 · Its place in the literature

Who cites it

4 citing papers in PubMed.

  1. Observational
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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Umapati N HegdeDepartment of Nephrology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, India.ORCID https://orcid.org/0000-0002-4076-6153
Ankur MittalDepartment of Nephrology, Medanta Institute of Kidney and Urology, Medanta-The Medicity, Gurgaon, India.
Sishir GangDepartment of Nephrology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, India.
Abhijit KonnurDepartment of Nephrology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, India.ORCID https://orcid.org/0000-0001-7101-8169
Hardik PatelDepartment of Nephrology, Muljibhai Patel Urological Hospital, Nadiad, Gujarat, India.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Kidney transplant recipients (KTRs) are at higher risk for infections, including parvovirus B19 (PVB19). This virus typically presents within the first-year posttransplant, causing anemia and potentially leading to increased morbidity and graft dysfunction. Materials and Methods: Charts of patients undergoing kidney transplantation between May 2013 and March 2022 were reviewed. Twenty-one patients had PVB19. Their clinical presentation, laboratory parameters, and outcomes were studied. The diagnosis of PVB19 was established by PVB19 DNA Polymerase Chain Reaction (PCR) and bone marrow examination (BME). Results: Prevalence of PVB19 disease was 1.9% (21/1164) with a median onset time of 39 days posttransplantation. The most frequent clinical symptoms were fatigue reported by 76% of patients, followed by fever (47%), dyspnea (23%), and myalgia (33%). All patients (100%) developed anemia, while leukopenia and thrombocytopenia were observed in 14% and 9.5% of patients, respectively. Graft dysfunction was observed in 61.9% (13/21) patients. Diagnosis was confirmed by PCR in 20 out of 21 patients. One patient had a typical viral inclusion on BME. Immunosuppression, especially antiproliferative, was reduced in all patients. Eight patients received intravenous immunoglobulin, eight received packed cell blood transfusion, and seven received erythropoietin therapy. All patients recovered, with a median time of 30 days for hemoglobin levels to normalize. One patient had graft loss secondary to graft rejection. Conclusion: PVB19, while uncommon, can be a significant cause of refractory anemia, particularly within the first-year posttransplant. Diagnosing PVB19 infection with PCR is crucial, and the primary treatment involves reducing immunosuppressants, especially antiproliferative agents.

Indexed as

AnemiaKidney transplantParvovirus B19 infection

Identifiers

PMID40896599
PMCPMC12392229

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