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研究设计和报告质量对慢性特发性或自身免疫性荨麻疹随机对照试验的影响:综述。

Study design and quality of reporting of randomized controlled trials of chronic idiopathic or autoimmune urticaria: review.

机构信息

CHRU de Tours, Service de Dermatologie, Tours, France.

出版信息

PLoS One. 2013 Aug 5;8(8):e70717. doi: 10.1371/journal.pone.0070717. Print 2013.

Abstract

BACKGROUND

The recommended first-line therapy of chronic urticaria is second-generation antihistamines, but the modalities of treatment remains unclear. Numerous recommendations with heterogeneous conclusions have been published. We wondered whether such heterogeneous conclusions were linked to the quality of published studies and their reporting.

OBJECTIVE

To review the study design and quality of reporting of randomized control trials investigating pharmacological treatment of autoimmune or idiopathic chronic urticaria.

METHODOLOGY/PRINCIPAL FINDINGS: MEDLINE and EMBASE were searched for pharmacological randomized controlled trials involving patients with chronic autoimmune or idiopathic urticaria, with the main outcome being treatment efficacy. Data were collected on general characteristics of the studies, internal validity, studied treatments, design of the trial, outcome measures and "spin" strategy in interpreting results. Spin was defined as use of specific reporting strategies to highlight that the experimental treatment is beneficial, despite statistically nonsignificant results. We evaluated 52 articles that met our criteria. Patients were reported as blinded in 42 articles (81%) and the outcome assessor was blinded in 37 (71%). A placebo was the only comparator in 13 (25%) studies. The study duration was <8 weeks in 39 articles (75%), with no follow-up after discontinuation of treatment in 37 (71%). In 4 articles (8%), blinding was clear because they described blinding of the outcome assessor, the treatment was not recognizable (identical or double-dummy) or had no major secondary effects, and computed randomization was centralized. The primary outcome was specified in 33 articles (63%) and was a score in 31. In total, 15 different scores were used. A spin strategy was used for 10 of 12 studies with a nonsignificant primary outcome.

CONCLUSION

For establishing guidelines in treatment of chronic urticaria, studies should focus on choosing clinically relevant and reproducible primary outcomes, long-term follow-up, limited use of placebo and avoiding spin strategies.

摘要

背景

慢性荨麻疹的推荐一线治疗方法是第二代抗组胺药,但治疗方法仍不清楚。已经发表了许多结论不同的建议。我们想知道这些不同的结论是否与发表研究的质量及其报告有关。

目的

综述评价自身免疫性或特发性慢性荨麻疹药物治疗的随机对照试验的研究设计和报告质量。

方法/主要发现:在 MEDLINE 和 EMBASE 上搜索涉及慢性自身免疫性或特发性荨麻疹患者的药物随机对照试验,主要结局为治疗效果。收集研究的一般特征、内部有效性、研究治疗、试验设计、结局测量和解释结果的“spin”策略的数据。spin 被定义为使用特定的报告策略来强调尽管统计学上无显著意义,但实验治疗是有益的。我们评估了符合我们标准的 52 篇文章。在 42 篇文章(81%)中报告了患者接受盲法治疗,在 37 篇文章(71%)中报告了结局评估者接受盲法治疗。在 13 篇研究(25%)中,只有安慰剂作为对照。在 39 篇文章(75%)中,研究持续时间<8 周,在 37 篇文章(71%)中治疗停止后没有随访。在 4 篇文章(8%)中,由于描述了结局评估者的盲法、治疗不可识别(相同或双盲)或没有主要的次要作用,以及集中计算了随机化,因此盲法是明确的。在 33 篇文章(63%)中指定了主要结局,在 31 篇文章中指定了评分。总共使用了 15 种不同的评分。在 12 项具有非显著主要结局的研究中有 10 项使用了 spin 策略。

结论

为了制定慢性荨麻疹的治疗指南,研究应侧重于选择临床相关且可重复的主要结局、长期随访、限制安慰剂的使用和避免 spin 策略。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/159e/3733774/eaa0697dfc70/pone.0070717.g001.jpg

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