Cytomegalovirus Treatment Strategy After a Liver Transplant: Preemptive Therapy or Prophylaxis for Cytomegalovirus Seropositive Donor and Recipient

被引:7
作者
Lindner, Kirsten [1 ]
Anthoni, Christoph [2 ]
Beckebaum, Susanne [3 ]
Senninger, Norbert [1 ]
Hoelzen, Jens Peter [4 ]
Wolters, Heiner [5 ]
机构
[1] Muenster Univ Hosp, Dept Gen & Visceral Surg, Waldeyerstr 1, D-48149 Munster, Germany
[2] St Josephs Hosp, Dept Gen & Visceral Surg, Beethovenstr 20, D-65189 Wiesbaden, Germany
[3] St Joseph Krankenhaus Kupferdreh, Dept Gastroenterol, Heidbergerweg 22-24, D-45257 Essen, Germany
[4] Katharinen Hosp, Dept Gen & Visceral Surg, Obere Husemannstr 2, D-59423 Unna, Germany
[5] St Josefs Hosp, Dept Gen & Visceral Surg, Wilhelm Schmidt Str 4, D-44263 Dortmund, Germany
关键词
Cytomegalovirus treatment; Preemptive therapy; CMV prophylaxis; Liver transplant; SOLID-ORGAN TRANSPLANTATION; INFECTION; DISEASE; METAANALYSIS; MANAGEMENT; IMPACT; RISK;
D O I
10.6002/ect.2015.0240
中图分类号
R3 [基础医学]; R4 [临床医学];
学科分类号
1001 ; 1002 ; 100602 ;
摘要
Objectives: Cytomegalovirus infections cause the most frequent infection after solid-organ transplant. While Cytomegalovirus prophylaxis is established in high-risk patients (donor+/ recipient-), data on Cytomegalovirus prophylaxis in other serostatus constellation are rare. The aim of this study was to evaluate the influence of Cytomegalovirus treatment strategy after a liver transplant (preemptive therapy vs general prophylaxis) in the largest group of patients: Cytomegalovirus seropositive donor and recipient. Materials and Methods: Forty-seven seropositive recipients of seropositive donor liver transplants (D+/R+, 2005-2012) were included in this retrospective study. Twenty-one patients received oral valganciclovir as Cytomegalovirus prophylaxis 100 days after transplant. Cytomegalovirus infection and Cyto megalovirus disease were monitored during the first 6 months. Results: A Cytomegalovirus infection could be detected in 4 out of 47 patients (8.5%), including Cytomegalovirus disease in 2 patients (Cytomegalovirus pneumonia and Cytomegalovirus-CNS disease). Three of these patients received no Cytomegalovirus prophylaxis (P =.408). Eight patients developed a graft failure; this occurred more frequently among patients without Cyto megalovirus prophylaxis (P =.044). Patients receiving Cytomegalovirus prophylaxis more often developed leukopenia. No difference was seen regarding the number of platelets, hemoglobin, and creatinine. Conclusions: Cytomegalovirus prophylaxis can minimize the risk of Cytomegalovirus reactivation and graft failure. However, disadvantages of the prophylaxis as leukopenia should be considered.
引用
收藏
页码:419 / 423
页数:5
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