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胸痛评估预防急诊入院的有效性和安全性:ESCAPE 整群随机试验

Effectiveness and safety of chest pain assessment to prevent emergency admissions: ESCAPE cluster randomised trial.

作者信息

Goodacre Steve, Cross Elizabeth, Lewis Cath, Nicholl Jon, Capewell Simon

机构信息

Medical Care Research Unit, University of Sheffield, Sheffield S1 4DA.

出版信息

BMJ. 2007 Sep 29;335(7621):659. doi: 10.1136/bmj.39325.624109.AE. Epub 2007 Sep 18.

Abstract

OBJECTIVE

To determine whether introducing chest pain unit care reduces emergency admissions without increasing reattendances and admissions over the next 30 days.

DESIGN

Cluster randomised before and after intervention trial.

SETTING

14 diverse acute hospitals in the United Kingdom.

PARTICIPANTS

Patients attending the emergency department with acute chest pain during the year before and the year after the intervention started.

INTERVENTION

Establishment of chest pain unit care compared with continuation of routine care.

MAIN OUTCOME MEASURES

Proportion of chest pain attendances resulting in admission; reattendances and admissions over the next 30 days; daily emergency medical admissions (all causes); and proportion of emergency department attendances with chest pain.

RESULTS

The introduction of chest pain unit care was associated with weak evidence of an increase in emergency department attendances with chest pain (16% v 3.5%; P=0.08); no change in the proportion of chest pain attendances resulting in admission (odds ratio 0.998, 95% confidence interval 0.940 to 1.059; P=0.945); small increases in the proportion reattending (odds ratio 1.10, 1.00 to 1.21; P=0.036) or being admitted (1.30, 0.97 to 1.74; P=0.083) over the next 30 days; and evidence of increased daily medical admissions (1.7 per day, 95% confidence interval 0.8 to 2.5; P<0.001). However, this last finding was highly sensitive to changes in the method used to handle missing data.

CONCLUSION

The introduction of chest pain unit care did not reduce the proportion of patients with chest pain admitted and may have been associated with increased emergency department attendances with chest pain.

TRIAL REGISTRATION

Current Controlled Trials ISRCTN55318418.

摘要

目的

确定引入胸痛单元护理是否能减少急诊入院人数,同时不增加未来30天内的再次就诊和入院人数。

设计

干预前后的整群随机试验。

地点

英国14家不同的急症医院。

参与者

干预开始前一年和后一年期间因急性胸痛到急诊科就诊的患者。

干预措施

建立胸痛单元护理,并与继续常规护理进行比较。

主要观察指标

因胸痛就诊导致入院的比例;未来30天内的再次就诊和入院人数;每日急诊医疗入院人数(所有原因);以及因胸痛到急诊科就诊的比例。

结果

引入胸痛单元护理后,因胸痛到急诊科就诊人数增加的证据较弱(16%对3.5%;P=0.08);胸痛就诊导致入院的比例没有变化(优势比0.998,95%置信区间0.940至1.059;P=0.945);未来30天内再次就诊(优势比1.10,1.00至1.21;P=0.036)或入院(1.30,0.97至1.74;P=0.083)的比例略有增加;有证据表明每日医疗入院人数增加(每天1.7人,95%置信区间0.8至2.5;P<0.001)。然而,最后这一发现对处理缺失数据所用方法的变化高度敏感。

结论

引入胸痛单元护理并未降低胸痛患者的入院比例,且可能与因胸痛到急诊科就诊人数增加有关。

试验注册号

Current Controlled Trials ISRCTN55318418 。

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