The Newcastle upon Tyne Hospitals NHS Foundation Trust, Freeman Hospital, Newcastle upon Tyne, UK.
Institute of Health & Society, Newcastle University, Newcastle upon Tyne, UK.
Health Technol Assess. 2020 Mar;24(12):1-176. doi: 10.3310/hta24120.
Heavy alcohol consumption is associated with an increased risk of postoperative complications and extended hospital stay. Alcohol consumption therefore represents a modifiable risk factor for surgical outcomes. Brief behavioural interventions have been shown to be effective in reducing alcohol consumption among increased risk and risky drinkers in other health-care settings and may offer a method of addressing preoperative alcohol consumption.
To investigate the feasibility of introducing a screening process to assess adult preoperative drinking levels and to deliver a brief behavioural intervention adapted for the target population group. To conduct a two-arm (brief behavioural intervention plus standard preoperative care vs. standard preoperative care alone), multicentre, pilot randomised controlled trial to assess the feasibility of proceeding to a definitive trial. To conduct focus groups and a national web-based survey to establish current treatment as usual for alcohol screening and intervention in preoperative assessment.
A single-centre, qualitative, feasibility study was followed by a multicentre, two-arm (brief behavioural intervention vs. treatment as usual), individually randomised controlled pilot trial with an embedded qualitative process evaluation. Focus groups and a quantitative survey were employed to characterise treatment as usual in preoperative assessment.
The feasibility study took place at a secondary care hospital in the north-east of England. The pilot trial was conducted at three large secondary care centres in the north-east of England.
Nine health-care professionals and 15 patients (mean age 70.5 years, 86.7% male) participated in the feasibility study. Eleven health-care professionals and 68 patients (mean age 66.2 years, 80.9% male) participated in the pilot randomised trial. An additional 19 health-care professionals were recruited to one of three focus groups, while 62 completed an electronic survey to characterise treatment as usual.
The brief behavioural intervention comprised two sessions. The first session, delivered face to face in the preoperative assessment clinic, involved 5 minutes of structured brief advice followed by 15-20 minutes of behaviour change counselling, including goal-setting, problem-solving and identifying sources of social support. The second session, an optional booster, took place approximately 1 week before surgery and offered the opportunity to assess progress and boost self-efficacy.
Feasibility was assessed using rates of eligibility, recruitment and retention. The progression criteria for a definitive trial were recruitment of ≥ 40% of eligible patients and retention of ≥ 70% at 6-month follow-up. Acceptability was assessed using themes identified in qualitative data.
The initial recruitment of eligible patients was low but improved with the optimisation of recruitment processes. The recruitment of eligible participants to the pilot trial (34%) fell short of the progression criteria but was mitigated by very high retention (96%) at the 6-month follow-up. Multimethod analyses identified the methods as acceptable to the patients and professionals involved and offers recommendations of ways to further improve recruitment.
The evidence supports the feasibility of a definitive trial to assess the effectiveness of brief behavioural intervention in reducing preoperative alcohol consumption and for secondary outcomes of surgical complications if recommendations for further improvements are adopted.
Current Controlled Trials ISRCTN36257982.
This project was funded by the National Institute for Health Research Health Technology Assessment programme and will be published in full in ; Vol. 24, No. 12. See the National Institute for Health Research Journals Library website for further project information.
大量饮酒与术后并发症风险增加和住院时间延长有关。因此,酒精摄入是手术结果的一个可改变的危险因素。在其他医疗保健环境中,简短的行为干预已被证明可以有效减少高危和风险饮酒者的酒精摄入量,并可能提供一种解决术前酒精摄入问题的方法。
调查引入一种评估成人术前饮酒水平的筛选流程并提供针对目标人群的简短行为干预措施的可行性。开展一项两臂(简短行为干预加标准术前护理与标准术前护理)、多中心、随机对照试点试验,以评估进行确定性试验的可行性。开展焦点小组和全国性网络调查,以确定术前评估中酒精筛查和干预的现行常规治疗方法。
一项单中心、定性、可行性研究之后,进行了一项多中心、两臂(简短行为干预与常规治疗)、个体随机对照试点试验,并嵌入了定性过程评估。采用焦点小组和定量调查来描述术前评估中的常规治疗方法。
可行性研究在英格兰东北部的一家二级保健医院进行。试点试验在英格兰东北部的三家大型二级保健中心进行。
九名医疗保健专业人员和 15 名患者(平均年龄 70.5 岁,86.7%为男性)参加了可行性研究。11 名医疗保健专业人员和 68 名患者(平均年龄 66.2 岁,80.9%为男性)参加了随机试点试验。另外 19 名医疗保健专业人员参加了三个焦点小组中的一个,而 62 名医疗保健专业人员完成了电子调查,以描述常规治疗方法。
简短行为干预包括两个阶段。第一阶段在术前评估诊所面对面进行,包括 5 分钟的结构化简短建议,然后进行 15-20 分钟的行为改变咨询,包括设定目标、解决问题和确定社会支持来源。第二阶段是可选的助推器,大约在手术前一周进行,提供评估进展和提高自我效能的机会。
通过资格、招募和保留的比率评估可行性。确定性试验的进展标准是招募≥40%的合格患者和在 6 个月随访时保留≥70%的患者。可接受性通过定性数据中确定的主题进行评估。
最初合格患者的招募率较低,但通过优化招募流程得到了改善。试点试验中合格参与者的招募率(34%)低于进展标准,但在 6 个月随访时保留率非常高(96%)得到了缓解。多方法分析表明,这些方法可被涉及的患者和专业人员接受,并提出了进一步改进的建议。
如果采用进一步改进的建议,该证据支持进行确定性试验以评估简短行为干预在减少术前饮酒和手术并发症等次要结局方面的有效性。
当前对照试验 ISRCTN36257982。
该项目由英国国家卫生研究院健康技术评估计划资助,将在英国国家卫生研究院期刊图书馆网站上全文发表;第 24 卷,第 12 期。请访问英国国家卫生研究院期刊图书馆网站以获取更多项目信息。