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生物医学风险评估辅助戒烟的有效性:一项系统综述。

Effectiveness of biomedical risk assessment as an aid for smoking cessation: a systematic review.

作者信息

Bize Raphaël, Burnand Bernard, Mueller Yolanda, Cornuz Jacques

机构信息

Department of Ambulatory Care and Community Medicine, University of Lausanne, 44 Rue du Bugnon, CH-1011 Lausanne, Switzerland.

出版信息

Tob Control. 2007 Jun;16(3):151-6. doi: 10.1136/tc.2006.017731.

Abstract

OBJECTIVE

To determine the efficacy of biomedical risk assessment (eg, exhaled carbon monoxide (CO), or genetic susceptibility to lung cancer) as an aid for smoking cessation.

DATA SOURCES

Cochrane Tobacco Addiction Group Specialized Register, Cochrane Central Register of Controlled Trials, Medline (1966-2004) and EMBASE (1980-2004).

STUDY SELECTION

Randomised controlled smoking cessation interventions using biomedical tests with at least 6 months follow-up.

DATA EXTRACTION

Two reviewers independently screened all search results (titles and abstracts) for possible inclusion. Each reviewer then extracted data from the selected studies, and assessed their methodological quality based on the CONSORT (Consolidated Standards of Reporting Trials) statement criteria.

DATA SYNTHESIS

Of 4049 retrieved references, eight trials were retained for data extraction and analysis. Three trials isolated the effect of exhaled CO on smoking cessation rates resulting in the following ORs and 95% CIs: 0.73 (0.38 to 1.39), 0.93 (0.62 to 1.41) and 1.18 (0.84 to 1.64). Measurement of exhaled CO and spirometry were used together in three trials, resulting in the following ORs (95% CI): 0.60 (0.25 to 1.46), 2.45 (0.73 to 8.25) and 3.50 (0.88 to 13.92). Spirometry results alone were used in one other trial with an OR (95% CI) of 1.21 (0.60 to 2.42). Ultrasonography of carotid and femoral arteries performed on light smokers gave an OR (95% CI) of 3.15 (1.06 to 9.31).

CONCLUSIONS

Scarcity and limited quality of the current evidence does not support the hypothesis that biomedical risk assessment increases smoking cessation as compared with the standard treatment.

摘要

目的

确定生物医学风险评估(如呼出一氧化碳(CO)或肺癌遗传易感性)作为辅助戒烟手段的疗效。

数据来源

Cochrane烟草成瘾小组专业注册库、Cochrane对照试验中心注册库、Medline(1966 - 2004年)和EMBASE(1980 - 2004年)。

研究选择

采用生物医学检测且随访至少6个月的随机对照戒烟干预措施。

数据提取

两名评审员独立筛选所有检索结果(标题和摘要)以确定可能纳入的研究。然后,每位评审员从选定的研究中提取数据,并根据CONSORT(试验报告统一标准)声明标准评估其方法学质量。

数据综合

在检索到的4049篇参考文献中,保留了八项试验用于数据提取和分析。三项试验分离出呼出CO对戒烟率的影响,得出以下比值比(OR)和95%可信区间(CI):0.73(0.38至1.39)、0.93(0.62至1.41)和1.18(0.84至1.64)。三项试验同时使用了呼出CO测量和肺功能测定,得出以下OR(95%CI):0.60(0.25至1.46)、2.45(0.73至8.25)和3.50(0.88至13.92)。另一项试验仅使用了肺功能测定结果,OR(95%CI)为1.21(0.60至2.42)。对轻度吸烟者进行的颈动脉和股动脉超声检查得出的OR(95%CI)为3.15(1.06至9.31)。

结论

现有证据稀缺且质量有限,不支持生物医学风险评估与标准治疗相比能提高戒烟率这一假设。

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