Martí-Carvajal Arturo J, Solà Ivan, Agreda-Pérez Luis H
Iberoamerican Cochrane Network, Valencia, Venezuela.
Cochrane Database Syst Rev. 2014 Jul 10(7):CD004344. doi: 10.1002/14651858.CD004344.pub5.
Avascular necrosis of bone is a frequent and severe complication of sickle cell disease and its treatment is not standardised.
To determine the impact of any surgical procedure compared with other surgical interventions or non-surgical procedures, on avascular necrosis of bone in people with sickle cell disease in terms of efficacy and safety.
We searched the Cochrane Cystic Fibrosis and Genetic Disorders Group Haemoglobinopathies Trials Register, comprising references identified from comprehensive electronic database searches and handsearches of relevant journals and abstract books of conference proceedings. Additional trials were sought from the reference lists of papers identified by the search strategy.Date of the most recent search of the Group's Haemoglobinopathies Trials Register: 17 March 2014.
Randomised clinical trials comparing specific therapies for avascular necrosis of bone in people with sickle cell disease.
Each author independently extracted data and assessed trial quality. Since only one trial was identified, meta-analysis was not possible.
One trial (46 participants) was eligible for inclusion. After randomisation eight participants were withdrawn, mainly because they declined to participate in the trial. Data were analysed for 38 participants at the end of the trial. After a mean follow up of three years, hip core decompression and physical therapy did not show clinical improvement when compared with physical therapy alone using the score from the original trial (an improvement of 18.1 points for those treated with intervention therapy versus an improvement of 15.7 points with control therapy). There was no significant statistical difference between groups regarding major complications (hip pain, relative risk (RR) 0.95 (95% confidence interval (CI) 0.56 to 1.60; vaso-occlusive crises, RR 1.14 (95% CI 0.72 to 1.80; very low quality of evidence); and acute chest syndrome, RR 1.06 (95% CI 0.44 to 2.56; very low quality of evidence)). This trial did not report results on mortality or quality of life.
AUTHORS' CONCLUSIONS: We found no evidence that adding hip core decompression to physical therapy achieves clinical improvement in people with sickle cell disease with avascular necrosis of bone compared to physical therapy alone. However, we highlight that our conclusion is based on one trial with high attrition rates. Further randomised controlled trials are necessary to evaluate the role of hip-core depression for this clinical condition. Endpoints should focus on participants' subjective experience (e.g. quality of life and pain) as well as more objective 'time-to-event' measures (e.g. mortality, survival, hip longevity). The availability of participants to allow adequate trial power will be a key consideration for endpoint choice.
骨缺血性坏死是镰状细胞病常见且严重的并发症,其治疗尚无标准化方案。
确定与其他手术干预或非手术治疗相比,任何手术操作对镰状细胞病患者骨缺血性坏死在疗效和安全性方面的影响。
我们检索了Cochrane囊性纤维化和遗传性疾病组血红蛋白病试验注册库,其中包括通过全面电子数据库检索、相关期刊手工检索以及会议论文摘要书籍检索得到的参考文献。通过检索策略确定的论文参考文献列表中还查找了其他试验。该组血红蛋白病试验注册库的最新检索日期为2014年3月17日。
比较镰状细胞病患者骨缺血性坏死特定治疗方法的随机临床试验。
每位作者独立提取数据并评估试验质量。由于仅识别出一项试验,因此无法进行荟萃分析。
一项试验(46名参与者)符合纳入标准。随机分组后,8名参与者退出,主要原因是他们拒绝参加试验。试验结束时对38名参与者的数据进行了分析。平均随访三年后,与单纯物理治疗相比,髋关节核心减压联合物理治疗在使用原始试验评分时未显示出临床改善(干预治疗组改善18.1分,对照治疗组改善15.7分)。两组在主要并发症方面无显著统计学差异(髋关节疼痛,相对危险度(RR)0.95(95%置信区间(CI)0.56至1.60);血管闭塞性危机,RR 1.14(95%CI 0.72至1.80;证据质量极低);急性胸部综合征,RR 1.06(95%CI 0.44至2.56;证据质量极低))。该试验未报告死亡率或生活质量结果。
我们没有发现证据表明,与单纯物理治疗相比,在镰状细胞病合并骨缺血性坏死患者中,物理治疗联合髋关节核心减压能实现临床改善。然而,我们强调我们的结论基于一项失访率高的试验。需要进一步的随机对照试验来评估髋关节核心减压在这种临床情况下的作用。终点应关注参与者的主观体验(如生活质量和疼痛)以及更客观的“事件发生时间”指标(如死亡率、生存率、髋关节使用寿命)。选择终点时,能否获得足够数量的参与者以保证试验效能将是一个关键考虑因素。