Study Design and Outcome Measures in Studies on Aneurysmal Subarachnoid Hemorrhage

I. van der Schaaf, Y. Ruigrok, G. Rinkel, A. Algra, J. van Gijn
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引用次数: 38

Abstract

Background and Purpose— Methods of performing and reporting randomized clinical trials (RCTs) are available, but weaknesses still occur. For observational studies, methodology is less well described, and weaknesses are even more likely. In recent guidelines for patients with subarachnoid hemorrhage (SAH), 25% of treatment recommendations are based on clinical trials. To interpret the results of research on the therapeutic effect of treatment modalities, definition of outcome measures is essential. We assessed quality of study design and outcome measures and presence and precision of definitions concerning major complications of SAH in studies evaluating treatment strategies in patients with aneurysmal SAH. Methods— We retrieved and reviewed all articles on treatment strategies in patients with SAH that fulfilled a prespecified set of criteria and were published during 1990–1999 in 10 general, neurosurgical, or neurological journals. We categorized articles into RCTs, observational studies with a control group, and observational studies without a control group. We assessed study design by means of a prespecified set of methodological criteria. For outcome measures we assessed whether a prespecified outcome measurement was defined and whether any handicap scale was used. For complications after SAH we assessed whether the definition included a description of the clinical features and a technical investigation with criteria for abnormal results. Results— We identified 18 RCTs, 24 observational studies with a control group, and 41 uncontrolled observational studies. Two RCTs, no observational studies with a control group, and 15 observational studies without a control group met all criteria for study design. A primary outcome measure was specified in 67 of the 83 studies and was defined in 59. Any measure of handicap or information on degree of dependence was given in 65 of 83 studies. A complete definition of delayed cerebral ischemia was given in 13 of 66 studies, of rebleeding in 2 of 26 studies, and of hydrocephalus in 2 of 14 studies. Conclusions— Most studies on treatment strategies in SAH suffer from methodological weaknesses. This implies that current management of patients with SAH is based on weak evidence.
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动脉瘤性蛛网膜下腔出血的研究设计和结果评价
背景和目的-随机临床试验(rct)的执行和报告方法是可用的,但仍然存在弱点。对于观察性研究,方法描述得不太好,更有可能出现弱点。在最近的蛛网膜下腔出血(SAH)患者指南中,25%的治疗建议是基于临床试验。为了解释治疗方式治疗效果的研究结果,结果测量的定义是必不可少的。在评估动脉瘤性SAH患者治疗策略的研究中,我们评估了研究设计和结果测量的质量,以及SAH主要并发症定义的存在和准确性。方法:我们检索并回顾了1990-1999年间发表在10个普通、神经外科或神经学期刊上的所有关于SAH患者治疗策略的文章,这些文章符合预先设定的标准。我们将文章分为随机对照试验、有对照组的观察性研究和没有对照组的观察性研究。我们通过预先指定的一套方法学标准来评估研究设计。对于结果测量,我们评估了是否定义了预先指定的结果测量以及是否使用了任何残疾量表。对于SAH后的并发症,我们评估了定义是否包括临床特征的描述和异常结果标准的技术调查。结果:我们确定了18项随机对照试验、24项对照组观察性研究和41项非对照观察性研究。两项随机对照试验、无对照组观察性研究和15项无对照组观察性研究符合研究设计的所有标准。在83项研究中,67项研究明确了主要结局指标,59项研究确定了主要结局指标。83项研究中有65项给出了残疾或依赖程度的衡量标准。66项研究中有13项给出了延迟性脑缺血的完整定义,26项研究中有2项给出了再出血的定义,14项研究中有2项给出了脑积水的定义。结论:大多数关于SAH治疗策略的研究都存在方法学上的缺陷。这意味着目前对SAH患者的管理是基于薄弱的证据。
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