Systematic review and meta-analysis of secondary prophylaxis for prevention of HIV-related toxoplasmic encephalitis relapse using trimethoprim-sulfamethoxazole

被引:18
作者
Connolly, Mark P. [1 ,2 ]
Haitsma, Gertruud [1 ,2 ]
Hernandez, Adrian V. [3 ,4 ,5 ]
Vidal, Jose E. [6 ,7 ]
机构
[1] Univ Groningen, Dept Pharm, Unit PharmacoEpidemiol & PharmacoEcon, Groningen, Netherlands
[2] Global Market Access Solut LLC, Hlth Econ, Mooresville, NC 28117 USA
[3] Hartford Hosp, UCONN Evidence Based Practice Ctr, Hartford, CT 06115 USA
[4] Univ Peruana Ciencias Aplicadas UPC, Sch Med, Lima, Peru
[5] Cleveland Clin, Hlth Outcomes & Clin Epidemiol Sect, Dept Quantitat Hlth Sci, Cleveland, OH 44106 USA
[6] Emilio Ribas Inst Infectol, Dept Neurol, Sao Paulo, Brazil
[7] Univ Sao Paulo, Hosp Clin, Dept Infect Dis, Sch Med,LIM 49, Sao Paulo, Brazil
关键词
Trimethoprim-sulfamethoxazole; secondary prevention; toxoplasmic encephalitis; cerebral toxoplasmosis; secondary prophylaxis; meta-analysis; HIV; relapse rates; CEREBRAL TOXOPLASMOSIS; COTRIMOXAZOLE; THERAPY;
D O I
10.1080/20477724.2017.1377974
中图分类号
R1 [预防医学、卫生学];
学科分类号
1004 ; 120402 ;
摘要
A recent systematic literature and meta-analysis reported relative efficacy of trimethoprim-sulfamethoxazole (TMP-SMX) for the treatment of toxoplasmic encephalitis (TE) in HIV-infected adults. Here, we estimated relapse rates during secondary prophylaxis with TMP-SMX, and further explored differences in relapse rates prior to introduction of highly active antiretroviral therapy (HAART) and the widespread adoption of HAART. A systematic search of PubMed, Embase, and Cochrane Central Register of Controlled Trials yielded 707 studies whereby 663 were excluded after abstract screening, and 38 were excluded after full review leaving 6 studies for extraction. We performed double data extraction with a third-party adjudicator. Study designs varied with only one randomized study, four prospective cohorts and one retrospective cohort. Relapse rates were transformed using the Freeman-Tukey method and pooled using both fixed-effect and random-effects meta-analysis models. The TMP-SMX relapse rate was 16.4% (95% CI = 6.2% to 30.3%) based on random-effects models. When the disaggregated pre-HAART studies (n = 4) were included, the relapse rate was 14.9% (random effects; 95% CI = 3.7% to 31.9%). Analysis of two post-HAART studies indicated a relapse rate of 19.2% (random effects; 95% CI = 2.8% to 45.6%). Comparing the relapse rates between pre- and post-HAART studies were contrary to what might be expected based on known benefits of HAART therapy in this population. Nevertheless, cautious interpretation is necessary considering the heterogeneity of the included studies and a limited number of subjects receiving TMP-SMX reported in the post-HAART era.
引用
收藏
页码:327 / 331
页数:5
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