Effect of Low-Dose Vs Standard-Dose Valganciclovir in the Prevention of Cytomegalovirus Disease in Kidney Transplantation Recipients: A Systemic Review and Meta-Analysis

被引:18
作者
Hwang, S. D. [1 ]
Lee, J. H. [2 ]
Lee, S. W. [1 ]
Kim, J. K. [2 ]
Kim, M. -J. [1 ]
Song, J. H. [1 ]
机构
[1] Inha Univ, Coll Med, Dept Internal Med, Div Nephrol & Hypertens, Incheon, South Korea
[2] Bong Seng Mem Hosp, Dept Internal Med, Divison Nephrol, Busan, South Korea
关键词
SOLID-ORGAN TRANSPLANTATION; ORAL GANCICLOVIR; PROPHYLAXIS; EFFICACY; RISK; INFECTION; SAFETY; VALACYCLOVIR; MANAGEMENT; BIAS;
D O I
10.1016/j.transproceed.2018.01.023
中图分类号
R392 [医学免疫学]; Q939.91 [免疫学];
学科分类号
100102 ;
摘要
Background. Valganciclovir is widely used to prevent post-transplant cytomegalovirus (CMV) infection in kidney transplant patients. However, the currently used dose remains controversial because the continuous use of this drug decreases kidney function and can induce leukopenia. Objective. The purpose of this study was to measure the appropriate dose of valganciclovir required to prevent CMV infection. Methods. A systematic review and meta-analysis were performed by using a random effects model. The Cochrane Central Register, MEDLINE, EMBASE, and PubMed databases were searched up to April 15, 2017. We conducted analysis on low-dose (450 mg) and standard-dose (900 mg) valganciclovir groups. Results. After completion of the research, the analysis revealed that the glomerular filtration rate, graft loss, tacrolimus level, antibody-mediated rejection, and fungal and Candida infection rates did not differ between the 2 groups. However, the incidence of CMV tended to decrease in the low-dose group (0.584 [95% confidence interval [CI], 0.352-0.967]; P = .036). The biopsy-proven rejection rate decreased by 0.427 times in the low-dose group compared with the standard-dose group (95% CI, 0.274-0.667; P = .002). Furthermore, the incidence of leukopenia decreased by 0.371 times in the low-dose group compared with the standard-dose group (95% CI, 0.264-0.523; P = .001). Conclusions. The 450-mg dose of valganciclovir effectively prevented post-transplantation CMV infection and decreased drug-induced side effects such as leukopenia. In the future, the lower dose of valganciclovir should be considered to prevent CMV infection and enhance cost-effectiveness.
引用
收藏
页码:2473 / 2478
页数:6
相关论文
共 33 条
[1]  
[Anonymous], THYM RABB ANT GLOB P
[2]  
Atkins D, 2004, BMJ-BRIT MED J, V328, P1490
[3]   Efficacy of allergen-specific immunotherapy for atopic dermatitis: A systematic review and meta-analysis of randomized controlled trials [J].
Bae, Jung Min ;
Choi, Yoon Young ;
Park, Chang Ook ;
Chung, Kee Yang ;
Lee, Kwang Hoon .
JOURNAL OF ALLERGY AND CLINICAL IMMUNOLOGY, 2013, 132 (01) :110-117
[4]   Endoscopic submucosal dissection of gastric subepithelial tumors: a systematic review and meta-analysis [J].
Bang, Chang Seok ;
Baik, Gwang Ho ;
Shin, In Soo ;
Suk, Ki Tae ;
Yoon, Jai Hoon ;
Kim, Dong Joon .
KOREAN JOURNAL OF INTERNAL MEDICINE, 2016, 31 (05) :860-+
[5]   OPERATING CHARACTERISTICS OF A BANK CORRELATION TEST FOR PUBLICATION BIAS [J].
BEGG, CB ;
MAZUMDAR, M .
BIOMETRICS, 1994, 50 (04) :1088-1101
[6]   Pharmacokinetics of valganciclovir and ganciclovir following multiple oral dosages of valganciclovir in HIV- and CMV-seropositive volunteers [J].
Brown, F ;
Banken, L ;
Saywell, K ;
Arum, I .
CLINICAL PHARMACOKINETICS, 1999, 37 (02) :167-176
[7]   METAANALYSIS IN CLINICAL-TRIALS [J].
DERSIMONIAN, R ;
LAIRD, N .
CONTROLLED CLINICAL TRIALS, 1986, 7 (03) :177-188
[8]   Trim and fill: A simple funnel-plot-based method of testing and adjusting for publication bias in meta-analysis [J].
Duval, S ;
Tweedie, R .
BIOMETRICS, 2000, 56 (02) :455-463
[9]   Bias in meta-analysis detected by a simple, graphical test [J].
Egger, M ;
Smith, GD ;
Schneider, M ;
Minder, C .
BMJ-BRITISH MEDICAL JOURNAL, 1997, 315 (7109) :629-634
[10]   2009 Updated Method Guidelines for Systematic Reviews in the Cochrane Back Review Group [J].
Furlan, Andrea D. ;
Pennick, Victoria ;
Bombardier, Claire ;
van Tulder, Maurits .
SPINE, 2009, 34 (18) :1929-1941