A Pneumocystis jirovecii pneumonia outbreak in a single kidney-transplant center: role of cytomegalovirus co-infection.

Details

Serval ID
serval:BIB_5B282AC3529B
Type
Article: article from journal or magazin.
Collection
Publications
Institution
Title
A Pneumocystis jirovecii pneumonia outbreak in a single kidney-transplant center: role of cytomegalovirus co-infection.
Journal
European Journal of Clinical Microbiology and Infectious Diseases
Author(s)
Pliquett R.U., Asbe-Vollkopf A., Hauser P.M., Presti L.L., Hunfeld K.P., Berger A., Scheuermann E.H., Jung O., Geiger H., Hauser I.A.
ISSN
1435-4373 (Electronic)
ISSN-L
0934-9723
Publication state
Published
Issued date
2012
Volume
31
Number
9
Pages
2429-2437
Language
english
Notes
Publication types: Journal ArticlePublication Status: ppublish. Authors' contributions H.G., E.H.S., R.U.P., and I.A.H. conceived the study. R.U.P. and A.A.-V. collected the data and performed the analysis. R.U.P., A.A.-V., and I.A.H. interpreted the data. O.J., K.P.H., and A.B. contributed to the collection of data. P.M.H. and L.L.P. contributed to the analysis and gave critical input to the interpretation of data. I.A.H., P.M.H., and R.U.P. drafted the manuscript.
Abstract
Pneumocystis jirovecii pneumonia (PCP) and cytomegalovirus (CMV) infection represent possible complications of medical immunosuppression. Between 2005 and 2010, non-human immunodeficiency virus (HIV) PCP patients admitted to a nephrology unit were analyzed for outcome, CMV comorbidity, and patient-to-patient contacts prior to PCP. In contrast to 2002-2004 (no cases) and 2008-2010 (10 cases), a PCP outbreak of 29 kidney-transplant recipients and one patient with anti-glomerular basement membrane disease occurred between 2005 and 2007. None of the patients were on PCP chemoprophylaxis. In four PCP patients, the genotyping data of bronchoalveolar lavage specimen showed an identical Pneumocystis strain. PCP cases had a higher incidence of CMV infection (12 of 30 PCP patients) and CMV disease (four patients) when compared to matched PCP-free controls (p < 0.05). Cotrimoxazole and, if applicable, ganciclovir were started 2.0 ± 4.0 days following admission, and immunosuppressive medication was reduced. In-hospital mortality was 10% and the three-year mortality was 20%. CMV co-infection did not affect mortality. CMV co-infection more frequently occurred during a cluster outbreak of non-HIV PCP in comparison to PCP-free controls. Here, CMV awareness and specific therapy of both CMV infection and PCP led to a comparatively favorable patient outcome. The role of patient isolation should be further investigated in incident non-HIV PCP.
Pubmed
Web of science
Create date
20/09/2012 18:07
Last modification date
20/08/2019 14:14
Usage data