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提高初级保健中戒烟率的策略。

Strategies to improve smoking cessation rates in primary care.

机构信息

Nuffield Department of Primary Care Health Sciences, University of Oxford, Oxford, UK.

Division of Prevention and Rehabilitation, University of Ottawa Heart Institute, Ottawa, Canada.

出版信息

Cochrane Database Syst Rev. 2021 Sep 6;9(9):CD011556. doi: 10.1002/14651858.CD011556.pub2.

Abstract

BACKGROUND

Primary care is an important setting in which to treat tobacco addiction. However, the rates at which providers address smoking cessation and the success of that support vary. Strategies can be implemented to improve and increase the delivery of smoking cessation support (e.g. through provider training), and to increase the amount and breadth of support given to people who smoke (e.g. through additional counseling or tailored printed materials).

OBJECTIVES

To assess the effectiveness of strategies intended to increase the success of smoking cessation interventions in primary care settings. To assess whether any effect that these interventions have on smoking cessation may be due to increased implementation by healthcare providers.

SEARCH METHODS

We searched the Cochrane Tobacco Addiction Group's Specialized Register, the Cochrane Central Register of Controlled Trials (CENTRAL), MEDLINE, Embase, and trial registries to 10 September 2020.

SELECTION CRITERIA

We included randomized controlled trials (RCTs) and cluster-RCTs (cRCTs) carried out in primary care, including non-pregnant adults. Studies investigated a strategy or strategies to improve the implementation or success of smoking cessation treatment in primary care. These strategies could include interventions designed to increase or enhance the quality of existing support, or smoking cessation interventions offered in addition to standard care (adjunctive interventions). Intervention strategies had to be tested in addition to and in comparison with standard care, or in addition to other active intervention strategies if the effect of an individual strategy could be isolated. Standard care typically incorporates physician-delivered brief behavioral support, and an offer of smoking cessation medication, but differs across studies. Studies had to measure smoking abstinence at six months' follow-up or longer.

DATA COLLECTION AND ANALYSIS

We followed standard Cochrane methods. Our primary outcome - smoking abstinence - was measured using the most rigorous intention-to-treat definition available. We also extracted outcome data for quit attempts, and the following markers of healthcare provider performance: asking about smoking status; advising on cessation; assessment of participant readiness to quit; assisting with cessation; arranging follow-up for smoking participants. Where more than one study investigated the same strategy or set of strategies, and measured the same outcome, we conducted meta-analyses using Mantel-Haenszel random-effects methods to generate pooled risk ratios (RRs) and 95% confidence intervals (CIs).

MAIN RESULTS

We included 81 RCTs and cRCTs, involving 112,159 participants. Fourteen were rated at low risk of bias, 44 at high risk, and the remainder at unclear risk. We identified moderate-certainty evidence, limited by inconsistency, that the provision of adjunctive counseling by a health professional other than the physician (RR 1.31, 95% CI 1.10 to 1.55; I = 44%; 22 studies, 18,150 participants), and provision of cost-free medications (RR 1.36, 95% CI 1.05 to 1.76; I = 63%; 10 studies,7560 participants) increased smoking quit rates in primary care. There was also moderate-certainty evidence, limited by risk of bias, that the addition of tailored print materials to standard smoking cessation treatment increased the number of people who had successfully stopped smoking at six months' follow-up or more (RR 1.29, 95% CI 1.04 to 1.59; I = 37%; 6 studies, 15,978 participants). There was no clear evidence that providing participants who smoked with biomedical risk feedback increased their likelihood of quitting (RR 1.07, 95% CI 0.81 to 1.41; I = 40%; 7 studies, 3491 participants), or that provider smoking cessation training (RR 1.10, 95% CI 0.85 to 1.41; I = 66%; 7 studies, 13,685 participants) or provider incentives (RR 1.14, 95% CI 0.97 to 1.34; I = 0%; 2 studies, 2454 participants) increased smoking abstinence rates. However, in assessing the former two strategies we judged the evidence to be of low certainty and in assessing the latter strategies it was of very low certainty. We downgraded the evidence due to imprecision, inconsistency and risk of bias across these comparisons. There was some indication that provider training increased the delivery of smoking cessation support, along with the provision of adjunctive counseling and cost-free medications. However, our secondary outcomes were not measured consistently, and in many cases analyses were subject to substantial statistical heterogeneity, imprecision, or both, making it difficult to draw conclusions. Thirty-four studies investigated multicomponent interventions to improve smoking cessation rates. There was substantial variation in the combinations of strategies tested, and the resulting individual study effect estimates, precluding meta-analyses in most cases. Meta-analyses provided some evidence that adjunctive counseling combined with either cost-free medications or provider training enhanced quit rates when compared with standard care alone. However, analyses were limited by small numbers of events, high statistical heterogeneity, and studies at high risk of bias. Analyses looking at the effects of combining provider training with flow sheets to aid physician decision-making, and with outreach facilitation, found no clear evidence that these combinations increased quit rates; however, analyses were limited by imprecision, and there was some indication that these approaches did improve some forms of provider implementation.

AUTHORS' CONCLUSIONS: There is moderate-certainty evidence that providing adjunctive counseling by an allied health professional, cost-free smoking cessation medications, and tailored printed materials as part of smoking cessation support in primary care can increase the number of people who achieve smoking cessation. There is no clear evidence that providing participants with biomedical risk feedback, or primary care providers with training or incentives to provide smoking cessation support enhance quit rates. However, we rated this evidence as of low or very low certainty, and so conclusions are likely to change as further evidence becomes available. Most of the studies in this review evaluated smoking cessation interventions that had already been extensively tested in the general population. Further studies should assess strategies designed to optimize the delivery of those interventions already known to be effective within the primary care setting. Such studies should be cluster-randomized to account for the implications of implementation in this particular setting. Due to substantial variation between studies in this review, identifying optimal characteristics of multicomponent interventions to improve the delivery of smoking cessation treatment was challenging. Future research could use component network meta-analysis to investigate this further.

摘要

背景

初级保健是治疗烟草成瘾的重要场所。然而,提供者解决吸烟问题的频率和支持的成功程度各不相同。可以实施策略来改善和增加戒烟支持的提供(例如通过提供者培训),并增加给予吸烟者的支持的数量和广度(例如通过额外的咨询或定制的印刷材料)。

目的

评估旨在增加初级保健环境中戒烟干预成功率的策略的有效性。评估这些干预措施对戒烟的任何影响是否归因于医疗保健提供者实施的增加。

检索方法

我们检索了 Cochrane 烟草成瘾组的专业注册库、Cochrane 中心对照试验注册库(CENTRAL)、MEDLINE、Embase 和试验注册库,检索时间截至 2020 年 9 月 10 日。

选择标准

我们纳入了在初级保健中进行的随机对照试验(RCT)和群组随机对照试验(cRCT),包括非孕妇成年人。研究调查了改善或提高初级保健中戒烟治疗实施或成功率的策略或策略。这些策略可以包括旨在增加或增强现有支持质量的干预措施,或除标准护理之外提供的戒烟干预措施(附加干预措施)。干预策略必须在标准护理之外进行测试和比较,或者在可以隔离单个策略的效果的情况下,与其他积极的干预策略一起进行测试。标准护理通常包括医生提供的简短行为支持,以及提供戒烟药物,但在研究中有所不同。研究必须在六个月或更长时间的随访中测量吸烟戒断情况。

数据收集和分析

我们遵循了标准的 Cochrane 方法。我们的主要结局——吸烟戒断——使用可用的最严格的意向治疗定义进行测量。我们还提取了戒烟尝试的结果数据,以及以下医疗保健提供者绩效的指标:询问吸烟状况;建议戒烟;评估参与者戒烟的准备情况;协助戒烟;为吸烟参与者安排随访。如果同一策略或一组策略有多个研究进行调查,并且测量了相同的结果,我们将使用 Mantel-Haenszel 随机效应方法进行荟萃分析,以生成汇总风险比(RR)和 95%置信区间(CI)。

主要结果

我们纳入了 81 项 RCT 和 cRCT,涉及 112159 名参与者。14 项研究被评为低偏倚风险,44 项研究为高偏倚风险,其余研究为不确定偏倚风险。我们发现,在一致性存在局限性的情况下,中等确定性证据表明,除医生以外的健康专业人员提供的附加咨询(RR 1.31,95%CI 1.10 至 1.55;I = 44%;22 项研究,18150 名参与者),以及提供免费药物(RR 1.36,95%CI 1.05 至 1.76;I = 63%;10 项研究,7560 名参与者)可以增加初级保健中的吸烟戒烟率。还有中等确定性证据表明,将定制印刷材料添加到标准戒烟治疗中可以增加在六个月或更长时间的随访中成功戒烟的人数(RR 1.29,95%CI 1.04 至 1.59;I = 37%;6 项研究,15978 名参与者)。没有明确的证据表明向吸烟者提供生物医学风险反馈会增加他们戒烟的可能性(RR 1.07,95%CI 0.81 至 1.41;I = 40%;7 项研究,3491 名参与者),或者提供提供者戒烟培训(RR 1.10,95%CI 0.85 至 1.41;I = 66%;7 项研究,13685 名参与者)或提供者激励(RR 1.14,95%CI 0.97 至 1.34;I = 0%;2 项研究,2454 名参与者)可以提高吸烟率。然而,在评估前两项策略时,我们认为证据的确定性较低,在评估后两项策略时,证据的确定性非常低。我们根据这些比较的不准确性、不一致性和偏倚风险降低了证据的等级。有一些迹象表明,提供者培训增加了戒烟支持的提供,以及提供附加咨询和免费药物。然而,我们的次要结局没有得到一致的测量,在许多情况下,分析受到严重的统计学异质性、不准确性或两者的影响,使得难以得出结论。34 项研究调查了改善戒烟率的多成分干预措施。所测试的策略组合和由此产生的个别研究效应估计值存在很大差异,在大多数情况下无法进行荟萃分析。荟萃分析提供了一些证据表明,附加咨询与免费药物或提供者培训相结合可以提高与单独标准护理相比的戒烟率。然而,分析受到事件数量少、高度统计学异质性和偏倚风险高的限制。分析着眼于将提供者培训与帮助医生决策的流程图和外展促进相结合的效果,发现这些方法并没有明显提高戒烟率;然而,分析受到不准确性的限制,并且有一些迹象表明这些方法确实改善了某些形式的提供者实施。

作者结论

有中等确定性证据表明,在初级保健中提供由联合健康专业人员提供的附加咨询、免费戒烟药物和定制印刷材料作为戒烟支持的一部分,可以增加戒烟成功的人数。没有明确证据表明向参与者提供生物医学风险反馈,或向初级保健提供者提供培训或激励以提供戒烟支持会提高戒烟率。然而,我们将此证据评为低或非常低确定性,因此随着更多证据的出现,结论可能会发生变化。本综述中的大多数研究都评估了已经在普通人群中广泛测试过的戒烟干预措施。未来的研究应该评估旨在优化已经在初级保健环境中证明有效的干预措施实施的策略。这类研究应该采用群组随机化以考虑实施在这一特定环境中的影响。由于本综述中的研究之间存在很大差异,因此确定改善戒烟治疗提供的多成分干预措施的最佳特征具有挑战性。未来的研究可以使用组件网络荟萃分析进一步研究这一点。

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