在门诊乳房重建手术后减少阿片类药物处方
Nkechi J Fearon1,2, Joey Kurtzman3, Nicole Benfante3
1Josie Robertson Surgical Center, Memorial Sloan Kettering Cancer Center, New York, New York, USA.
Journal of surgical oncology
|September 1, 2023
概括
乳房重建后的阿片类药物处方标准化显著减少了处方药的数量,但没有影响疼痛控制或早期身体健康. 这个倡议解决了人们对阿片类药物滥用和滥用的担忧.
科学领域:
- 整形外科 整形外科 整形外科
- 疼痛管理 疼痛管理
- 药理学 药理学是指药理学的学科.
背景情况:
- 乳房重建后术后阿片类药物处方缺乏基于证据的指导方针导致实践变化.
- 这种变化增加了阿片类药物滥用和滥用的可能性.
研究的目的:
- 评估标准化阿片类药物处方减少计划对乳腺重建患者的可行性和影响.
- 评估阿片类药物使用,疼痛控制和患者报告结果的变化.
主要方法:
- 在实施标准化阿片类药物处方减少倡议之前 (n=97) 和之后 (n=101) 进行了一项调查,用于门诊乳房重建.
- 术后阿片类药物使用,疼痛控制 (恢复追踪器) 和身体健康 (BREAST-Q) 在两组之间进行了比较.
主要成果:
- 处方阿片类药物的中位数从30下降到8.
- 实际的阿片类药物消费在两组中都保持稳定,仅为3片.
- 在中度至非常严重的疼痛或早期的BREAST-Q身体健康得分中没有发现显著差异.
结论:
- 标准化和减少用于乳腺重建的阿片类药物处方是可行的,并且有效地减少了多余的药丸.
- 该计划没有对早期身体健康产生不利影响.
- 建议进行更大规模的研究以进一步获取数据.
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