影响参与儿科麻醉临床研究意愿的因素(FILIPPA):基于小故事的结构化访谈研究。

IF 1.7 4区 医学 Q2 ANESTHESIOLOGY Pediatric Anesthesia Pub Date : 2024-08-01 Epub Date: 2024-05-17 DOI:10.1111/pan.14922
Clemens Miller, Jan Scholand, Johannes Wieditz, Carlo Pancaro, Hendrik Rosewich, Marcus Nemeth
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引用次数: 0

摘要

背景:知情同意是开展临床试验(尤其是涉及儿童的临床试验)的相关背景。虽然已知有几个因素会影响儿童麻醉研究的同意意愿,但研究设计对同意行为的影响尚不清楚。目的:量化研究复杂性对儿童麻醉研究同意意愿的影响:我们进行了一项基于小故事的访谈研究,向 106 名子女计划接受麻醉的家长或法定监护人介绍了三项假设研究。这些研究的复杂程度各不相同,包括一项前瞻性观察研究、一项随机对照试验和一项二期药理学研究。主要结果是同意的意愿,采用李克特五点量表,从 "绝对同意 "到 "绝对拒绝"。次要结果是儿童相关因素(如性别、年龄、之前的麻醉经历、研究接触)和邻近相关因素的影响:观察研究中 "绝对同意 "的应答概率为 90.9% [95% CI 85.3-96.5],随机对照试验中为 48.6% [95% CI 38.3-58.9],II 期药理学研究中为 32.7% [95% CI 23.9-41.6]。绝对下降 "的应答概率分别为 1.6% [95% CI 0.3-2.8]、14.4% [95% CI 8.3-20.5]和 24.7% [95% CI 16.6-32.7]。研究发现,以前接触过研究(OR = 0.486 [95% CI 0.256-0.923],p = .027)、年龄较大(OR = 0.963 [95% CI 0.927-0.999],p = .045)和父母或法定监护人的性别对同意的意愿有显著影响,因为母亲同意的意愿较低(OR = 0.234 [95% CI 0.107-0.512],p 结论:母亲同意的意愿随着研究水平的提高而降低:同意的意愿随着研究复杂程度的增加而降低。在进行更复杂的研究时,需要加大力度增加儿科患者的入组人数。
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Factors Influencing Willingness to Participate in Clinical Studies in Pediatric Anesthesia (FILIPPA): A vignette-based, structured interview study.

Background: Informed consent is a relevant backdrop for conducting clinical trials, particularly those involving children. While several factors are known to influence the willingness to consent to pediatric anesthesia studies, the influence of study design on consenting behavior is unknown.

Aims: To quantify the impact of study complexity on willingness to consent to pediatric anesthesia studies.

Methods: We conducted a vignette-based interview study by presenting three hypothetical studies to 106 parents or legal guardians whose children were scheduled to undergo anesthesia. These studies differed in level of complexity and included an example of a prospective observational study, a randomized controlled trial, and a phase-II-pharmacological study. Primary outcome was the willingness to consent, using a 5-point Likert scale ranging from "absolutely consent" to "absolutely decline". Secondary outcomes were the effects of child-related (such as sex, age, previous anesthesia, research exposure) and proxy-related factors.

Results: Response probabilities for "absolute consent" were 90.9% [95% CI 85.3-96.5] for the observational study, 48.6% [95% CI 38.3-58.9] for the randomized controlled trial, and 32.7% [95% CI 23.9-41.6] for the phase-II-pharmacological study. Response probabilities for "absolutely decline" were 1.6% [95% CI 0.3-2.8], 14.4% [95% CI 8.3-20.5], and 24.7% [95% CI 16.6-32.7], respectively. Significant effects were found for previous research exposure (OR = 0.486 [95% CI 0.256-0.923], p = .027), older age (OR = 0.963 [95% CI 0.927-0.999], p = .045) and the gender of the parent or legal guardian, as mothers were less willing to consent (OR = 0.234 [95% CI 0.107-0.512], p < .001).

Conclusions: Willingness to consent decreased with increasing level of study complexity. When conducting more complex studies, greater efforts need to be made to increase the enrollment of pediatric patients.

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来源期刊
Pediatric Anesthesia
Pediatric Anesthesia 医学-麻醉学
CiteScore
3.20
自引率
11.80%
发文量
222
审稿时长
3-8 weeks
期刊介绍: Devoted to the dissemination of research of interest and importance to practising anesthetists everywhere, the scientific and clinical content of Pediatric Anesthesia covers a wide selection of medical disciplines in all areas relevant to paediatric anaesthesia, pain management and peri-operative medicine. The International Editorial Board is supported by the Editorial Advisory Board and a team of Senior Advisors, to ensure that the journal is publishing the best work from the front line of research in the field. The journal publishes high-quality, relevant scientific and clinical research papers, reviews, commentaries, pro-con debates, historical vignettes, correspondence, case presentations and book reviews.
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