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首页> 外文期刊>Canadian journal of anesthesia: Journal canadien d'anesthesie >Factors associated with refusal to enter a clinical trial: epidural anesthesia is a deterrent to participation: (Les facteurs associes au refus de participer a un essai clinique : l'anesthesie peridurale est un element dissuasif).
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Factors associated with refusal to enter a clinical trial: epidural anesthesia is a deterrent to participation: (Les facteurs associes au refus de participer a un essai clinique : l'anesthesie peridurale est un element dissuasif).

机译:与拒绝参加临床试验相关的因素:硬膜外麻醉会阻碍参与:

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摘要

PURPOSE: To compare patients who participate in a clinical trial for pain management involving epidural anesthesia to those who refuse and document their reasons for refusing. METHODS: Demographic and health history information was collected from 621 female patients who were screened for inclusion in a pain management trial involving epidural anesthesia. Patients who completed the clinical trial (n = 149) were compared to those who consented to provide screening information but did not enter the trial (n = 472). RESULTS: Sixty-seven percent of women who refused cited unwillingness to have an epidural as the reason for their decision. Non-Caucasians (P < 0.01), patients with no history of mood/anxiety disorders (P < 0.016) or systemic disease (P < 0.02), and patients with certain types of pain (P < 0.02) were more likely to refuse to participate in the clinical trial. A longer duration between recruitment and surgery was also found to be associated with higher participation rates (P < 0.01). A logistic regression equation significantly predicted which patients would participate or refuse (P < 0.0001), indicating that a specific set of health and demographic factors strongly influence the decision to participate in a trial. CONCLUSIONS: The decision to participate in a clinical trial is viewed as a risk/benefit analysis. Factors such as short recruitment to surgery intervals and pre-existing pain, which increase the salience of risks associated with the trial, may result in lower participation rates. Overall, epidural anesthesia is a strong deterrent to participation in a clinical trial.
机译:目的:比较参与硬膜外麻醉的疼痛治疗临床试验的患者与拒绝并记录拒绝原因的患者。方法:从621名女性患者中收集了人口统计学和健康史信息,这些患者经过筛查是否包含在涉及硬膜外麻醉的疼痛管理试验中。将完成临床试验的患者(n = 149)与同意提供筛查信息但未参加试验的患者(n = 472)进行比较。结果:拒绝接受治疗的女性中有67%表示不愿意接受硬膜外麻醉是她们做出决定的原因。非高加索人(P <0.01),无情绪/焦虑症病史(P <0.016)或系统性疾病(P <0.02)以及某些类型的疼痛(P <0.02)的患者更倾向于拒绝参加临床试验。还发现招募和手术之间更长的时间与更高的参与率相关(P <0.01)。逻辑回归方程显着预测了哪些患者会参加或拒绝(P <0.0001),表明一组特定的健康和人口统计学因素强烈影响了参加试验的决定。结论:参与临床试验的决定被视为风险/收益分析。诸如缩短手术间隔时间和预先存在的疼痛等因素增加了与试验相关的风险的显着性,可能导致参与率降低。总体而言,硬膜外麻醉对参加临床试验具有强大的威慑力。

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