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Safety in primary care (SAP-C): a randomised, controlled feasibility study in two different healthcare systems

机译:初级保健的安全性(SAP-C):在两个不同的保健系统中进行的随机对照可行性研究

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Patient safety research is conducted predominantly in hospital settings, with a dearth of insight from primary care, despite suggestions that 2.2% of primary care consultations result in a patient safety incident. This study aimed to assess the feasibility of an intervention intended to improve patient safety in general practice. A randomised controlled feasibility study was conducted with general practices in the Republic of Ireland (N?=?9) and Northern Ireland (N?=?2), randomly assigned to the intervention (N?=?5) or control (N?=?6) group. The nine-month intervention consisted of: 1) repeated safety climate (SC) measurement (using GP-SafeQuest questionnaire) and feedback (comparative anonymised practice-level SC data), and 2) patient record reviews using a specialised trigger tool to identify instances of undetected patient harm. For control practices, SC was measured at baseline and study end only. The intervention’s perceived usefulness and feasibility were explored via an end-of-study questionnaire and semi-structured interviews. Thirteen practices were invited; 11 participated; 10 completed the study. At baseline, 84.8% of intervention practice staff (39/46) and 77.8% (42/54) of control practice staff completed the SC questionnaire; at the study terminus, 78.3% (36/46) of intervention practice staff and 68.5% (37/54) of control practice staff did so. Changes in SC scores, indicating improvement, were observed among the intervention practices but not in the control group. The trigger tool was applied to 188 patient records; patient safety incidents of varying severity were detected in 19.1% (36/188). Overall, 59% of intervention practice team members completed the end-of-study questionnaire, with the majority in both healthcare systems responding positively about the intervention. Interviews (N?=?9) identified the intervention’s usefulness in informing practice management and patient safety issues, time as a barrier to its use, and the value of group discussion of feedback. This feasibility study suggests that a definitive randomised controlled trial of the intervention is warranted. Our findings suggest that the intervention is feasible, useful, and sustainable. Practices were willing to be recruited into the study, response and retention rates were acceptable, and there is possible evidence of a positive effect of the intervention.
机译:尽管有2.2%的初级保健咨询会导致患者安全事件,但主要在医院环境中进行患者安全研究,而缺乏初级保健的见识。本研究旨在评估旨在提高一般实践中患者安全性的干预措施的可行性。在爱尔兰共和国(N = 9)和北爱尔兰(N == 2),按照常规进行了一项随机对照可行性研究,随机分配给干预措施(N = 5)或对照组(N = 5)。 =?6)组。为期9个月的干预措施包括:1)反复进行安全气候(SC)测量(使用GP-SafeQuest问卷)和反馈(比较匿名的实践水平SC数据),以及2)使用专门的触发工具来确定患者病历,以识别实例未发现的患者伤害。对于对照实践,仅在基线和研究结束时测量SC。通过研究结束后的问卷调查和半结构化访谈,探讨了干预措施的有用性和可行性。邀请了十三种做法; 11人参加; 10完成研究。基线时,干预实践人员的84.8%(39/46)和对照实践人员的77.8%(42/54)完成了SC调查表;在研究终点,干预实践人员的占78.3%(36/46),对照实践人员的占68.5%(37/54)。在干预措施中观察到SC得分的变化,表明有改善,但在对照组中未观察到。触发工具已应用于188位患者记录;发生不同严重程度的患者安全事件的发生率为19.1%(36/188)。总体而言,干预实践团队成员中有59%完成了研究结束调查问卷,两个医疗保健系统中的大多数都对该干预做出了积极回应。访谈(N?=?9)指出了干预措施在告知执业管理和患者安全问题方面的有用性,时间阻碍了干预措施的使用以及小组讨论反馈的价值。这项可行性研究表明,必须对干预措施进行明确的随机对照试验。我们的发现表明,干预是可行,有用和可持续的。愿意参加研究的实践者,其反应率和保留率是可以接受的,并且有可能证明该干预措施具有积极作用。

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