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探索急救药物、数据插补与研究结果之间的相互作用:急性疼痛数据集的概念性综述与定性分析

Exploring the Interplay between Rescue Drugs, Data Imputation, and Study Outcomes: Conceptual Review and Qualitative Analysis of an Acute Pain Data Set.

作者信息

Singla Neil K, Meske Diana S, Desjardins Paul J

机构信息

Lotus Clinical Research, Huntington Hospital, Department of Anesthesiology, Pasadena, CA, USA.

Collegium Pharmaceutical, Inc., Canton, MA, USA.

出版信息

Pain Ther. 2017 Dec;6(2):165-175. doi: 10.1007/s40122-017-0074-5. Epub 2017 Jul 4.

Abstract

In placebo-controlled acute surgical pain studies, provisions must be made for study subjects to receive adequate analgesic therapy. As such, most protocols allow study subjects to receive a pre-specified regimen of open-label analgesic drugs (rescue drugs) as needed. The selection of an appropriate rescue regimen is a critical experimental design choice. We hypothesized that a rescue regimen that is too liberal could lead to all study arms receiving similar levels of pain relief (thereby confounding experimental results), while a regimen that is too stringent could lead to a high subject dropout rate (giving rise to a preponderance of missing data). Despite the importance of rescue regimen as a study design feature, there exist no published review articles or meta-analysis focusing on the impact of rescue therapy on experimental outcomes. Therefore, when selecting a rescue regimen, researchers must rely on clinical factors (what analgesics do patients usually receive in similar surgical scenarios) and/or anecdotal evidence. In the following article, we attempt to bridge this gap by reviewing and discussing the experimental impacts of rescue therapy on a common acute surgical pain population: first metatarsal bunionectomy. The function of this analysis is to (1) create a framework for discussion and future exploration of rescue as a methodological study design feature, (2) discuss the interplay between data imputation techniques and rescue drugs, and (3) inform the readership regarding the impact of data imputation techniques on the validity of study conclusions. Our findings indicate that liberal rescue may degrade assay sensitivity, while stringent rescue may lead to unacceptably high dropout rates.

摘要

在安慰剂对照的急性外科疼痛研究中,必须为研究对象提供充分的镇痛治疗。因此,大多数方案允许研究对象根据需要接受预先指定的开放标签镇痛药(救援药物)治疗方案。选择合适的救援方案是关键的实验设计选择。我们假设,过于宽松的救援方案可能导致所有研究组获得相似程度的疼痛缓解(从而混淆实验结果),而过于严格的方案可能导致高受试者脱落率(导致大量缺失数据)。尽管救援方案作为研究设计特征很重要,但尚无已发表的综述文章或荟萃分析关注救援治疗对实验结果的影响。因此,在选择救援方案时,研究人员必须依靠临床因素(在类似手术场景中患者通常接受何种镇痛药)和/或轶事证据。在以下文章中,我们试图通过回顾和讨论救援治疗对常见急性外科疼痛人群(第一跖骨拇囊炎切除术)的实验影响来弥合这一差距。本分析的作用是:(1)创建一个框架,用于讨论和未来探索救援作为一种方法学研究设计特征;(2)讨论数据插补技术与救援药物之间的相互作用;(3)让读者了解数据插补技术对研究结论有效性的影响。我们的研究结果表明,宽松的救援可能会降低检测灵敏度,而严格的救援可能会导致高得不可接受的脱落率。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/3809/5693805/aefea67a4ad0/40122_2017_74_Fig1_HTML.jpg

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