HEV infection in stem cell transplant recipients-retrospective study of EBMT Infectious Diseases Working Party
Publication date
2022-02
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Abstract
HEV infection is an emerging cause of acute and chronic hepatitis in stem cell transplant (SCT) recipients. We performed a retrospective observational study among EBMT centers with the aim of describing characteristics, management and outcome of HEV after SCT. There were 34 cases of HEV infection from 12 centers in 6 countries, diagnosed in median 4.5 months after SCT; 20 of acute and 14 of chronic infection. Non-hepatic findings possibly associated with HEV infection were present in 9 (26%). Patients with chronic infection had more characteristics associated with severely immunocompromised status. Ribavirin was provided to 16 patients (47%; 40% with acute and 57% with chronic infection), in median for 75 days. Three (19%) patients discontinued it due to side effects. HEV-RNA clearance occurred in 29 patients (85%; 85% in acute and 86% in chronic infection). HEV was considered a cause of death in 3 (9%), with 2 cases with late diagnosis. Reduction of immunosuppression in those receiving it, and ribavirin treatment in those with chronic infection were associated with shorter time to HEV-RNA clearance. Policy on HEV testing varied between the centers. In conclusion, acute and chronic HEV hepatitis should be promptly diagnosed and managed in SCT recipients.
Keywords
Communicable Diseases, Hepatitis E virus/genetics, Humans, Immunocompromised Host, RNA, Retrospective Studies, Ribavirin/therapeutic use, Stem Cell Transplantation/adverse effects, Transplant Recipients, Taverne, Transplantation, Hematology, Observational Study, Journal Article
Citation
Mikulska, M, Penack, O, Wendel, L, Knelange, N, Cornelissen, J J, Blijlevens, N, Passweg, J, Kroger, N, Bruns, A, Koenecke, C, Bierings, M, Piñana, J L, Labussiere-Wallet, H, Ghesquieres, H, Diaz, M A, Sampol, A, Averbuch, D, de la Camara, R & Styczynski, J 2022, 'HEV infection in stem cell transplant recipients-retrospective study of EBMT Infectious Diseases Working Party', Bone Marrow Transplantation, vol. 57, no. 2, pp. 167-175. https://doi.org/10.1038/s41409-021-01497-2