Uthman Olalekan A, Abdulmalik Jubril O
Save the Youth Initiative, P. O. Box 5146, Ilorin, Kwara State, Nigeria, 240-001.
Cochrane Database Syst Rev. 2008 Jul 16;2008(3):CD006496. doi: 10.1002/14651858.CD006496.pub2.
AIDS dementia complex is a common complication of human immunodeficiency virus type 1 (HIV-1) that continues to exist despite the current use of potent antiretroviral therapy. It is a source of great morbidity and, when severe, is associated with limited survival.
To determine efficacy and safety of adjunctive therapies for AIDS dementia complex
We searched the Cochrane HIV/AIDS group trials Specialized Register (December 2006), the Cochrane Central Register of Controlled Trials (The Cochrane Library Issue 1, 2007), MEDLINE (January 1980 to February 2007), EMBASE (January 1980 to February 2007), AIDSearch (January 1980 to February 2007), PsycINFO (January 1980 to February 2007), PSYCHLIT (January 1980 to February 2007), LILACS (January 1980 to February 2007), conference proceedings, trial registers, theses databases, and reference lists of the articles. We also contacted manufacturers and researchers in the field.
Randomized controlled trials, either published or published, that compared one type of adjunctive therapy to no therapy or placebo in adults with AIDS dementia complex
Two authors independently assessed trials quality, extracted data and entered data into RevMan 4.2 software. Where possible intention-to-treat data were used and we contacted study authors for additional information. We collected neurocognitive performance, adverse effects, tolerability and all-cause mortality information from the trials.
Ten trials involving 711 people were included. All the studies were phase 2 trials. Six studies used adequate methods for allocation of sequence generation and unclear in the remaining four trials. Allocation concealment was adequate in five trials and unclear in the remaining trials. The trials were heterogeneous in terms of types, dosages, routes and frequencies of administration of the adjunctive therapies. There were no significant differences between the treated and placebo groups on neuropsychological test scores, number of those that complete the assign dosage of experimental medication, adverse effects, and all-cause mortality.
AUTHORS' CONCLUSIONS: This review confirms the absence of evidence that any of the adjunctive therapies improves cognitive performance or quality of life, or both for patients with ADC, though they were well tolerated and safe.
艾滋病痴呆综合征是1型人类免疫缺陷病毒(HIV-1)常见的并发症,尽管目前使用了强效抗逆转录病毒疗法,但该并发症仍持续存在。它是高发病率的一个来源,严重时与生存期受限相关。
确定艾滋病痴呆综合征辅助治疗的疗效和安全性。
我们检索了Cochrane HIV/AIDS小组试验专门注册库(2006年12月)、Cochrane对照试验中心注册库(《Cochrane图书馆》2007年第1期)、MEDLINE(1980年1月至2007年2月)、EMBASE(1980年1月至2007年2月)、AIDSearch(1980年1月至2007年2月)、PsycINFO(1980年1月至2007年2月)、PSYCHLIT(1980年1月至2007年2月)、LILACS(1980年1月至2007年2月)、会议论文集、试验注册库、学位论文数据库以及文章的参考文献列表。我们还联系了该领域的制造商和研究人员。
将一种辅助治疗与无治疗或安慰剂进行比较的已发表或未发表的随机对照试验,受试对象为患有艾滋病痴呆综合征的成人。
两位作者独立评估试验质量、提取数据并将数据录入RevMan 4.2软件。尽可能使用意向性治疗数据,我们还联系了研究作者以获取更多信息。我们从试验中收集神经认知表现、不良反应、耐受性和全因死亡率信息。
纳入了10项涉及711人的试验。所有研究均为2期试验。6项研究采用了适当的随机序列生成方法,其余4项试验方法不明。5项试验的分配隐藏充分,其余试验情况不明。辅助治疗的类型、剂量、给药途径和频率方面,试验具有异质性。治疗组和安慰剂组在神经心理学测试分数、完成试验药物指定剂量的人数、不良反应和全因死亡率方面无显著差异。
本综述证实,没有证据表明任何一种辅助治疗能改善艾滋病痴呆综合征患者的认知表现或生活质量,或两者兼具,不过这些治疗耐受性良好且安全。