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能否让患者在医院睡觉?一项针对外科肿瘤患者实用睡眠方案的随机对照试验。

Can we let our patients sleep in the hospital? A randomized controlled trial of a pragmatic sleep protocol in surgical oncology patients.

机构信息

Department of General Surgery, Spectrum Health/Michigan State University College of Human Medicine General, Grand Rapids, Michigan, USA.

Department of Graduate Medical Education, Michigan State College of Human Medicine, Grand Rapids, Michigan, USA.

出版信息

J Surg Oncol. 2024 Mar;129(4):827-834. doi: 10.1002/jso.27565. Epub 2023 Dec 19.

Abstract

BACKGROUND

Postoperative inpatients experience increased stress due to pain and poor restorative sleep than non-surgical inpatients.

OBJECTIVES AND METHODS

A total of 101 patients, undergoing major oncologic surgery, were randomized to a postoperative sleep protocol (n = 50) or standard postoperative care (n = 51), between August 2020 and November 2021. The primary endpoint of the study was postoperative sleep time after major oncologic surgery. Sleep time and steps were measured using a Fitbit Charge 4®.

RESULTS

There was no statistically significant difference found in postoperative sleep time between the sleep protocol and standard group (median sleep time of 427 min vs. 402 min; p = 0.852, respectively). Major complication rates were similar in both groups (7.4% vs. 8.9%). Multivariate analysis found sex and Charlson Comorbidity Index to be significant factors affecting postoperative sleep time and step count. Postoperative delirium was only observed in the standard group, although this did not reach statistical significance. There were no in hospital mortalities.

CONCLUSION

The use of a sleep protocol was found to be safe in our study population. There was no statistical difference in postoperative sleep time or major complications. Institution of a more humane sleep protocol for postoperative inpatients should be considered.

摘要

背景

与非手术住院患者相比,术后住院患者由于疼痛和睡眠质量差而承受更大的压力。

目的和方法

2020 年 8 月至 2021 年 11 月期间,共有 101 名接受大肿瘤手术的患者被随机分为术后睡眠方案组(n=50)或标准术后护理组(n=51)。本研究的主要终点是大肿瘤手术后的术后睡眠时间。使用 Fitbit Charge 4® 测量睡眠时间和步数。

结果

睡眠方案组和标准组之间的术后睡眠时间没有统计学差异(中位数睡眠时间分别为 427 分钟和 402 分钟;p=0.852)。两组的主要并发症发生率相似(7.4%与 8.9%)。多变量分析发现,性别和 Charlson 合并症指数是影响术后睡眠时间和步数的重要因素。仅在标准组观察到术后谵妄,但无统计学意义。无院内死亡。

结论

在本研究人群中,使用睡眠方案是安全的。术后睡眠时间或主要并发症无统计学差异。应考虑为术后住院患者制定更人性化的睡眠方案。

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