From the Departments of Plastic Surgery, Psychiatry and Behavioral Sciences, and Population Health, University of Kansas Medical Center.
Plast Reconstr Surg. 2020 Oct;146(4):734-741. doi: 10.1097/PRS.0000000000007150.
Current rates of opioid prescribing have deleterious consequences on both patient and societal levels. This study aims to evaluate responsible opioid prescribing and predictors of opioid consumption in immediate implant-based breast reconstruction.
Patients undergoing consultation for immediate, implant-based breast reconstruction were enrolled in a prospective, cohort survey study. A survey was administered at the preoperative and postoperative appointment to collect data on pain expectations and opioid use. A medical record review was performed.
Of 100 enrolled patients, 97 (97.0 percent) underwent surgery and 85 (85.0 percent) completed the postoperative survey. Preoperatively, 27 patients (27.0 percent) had a history of a chronic pain syndrome, 34 (34.0 percent) had a history of a mental health comorbidity, and nine (9.0 percent) had a history of active preoperative opioid use. A total of 85 tissue expander (87.6 percent) and 12 direct-to-implant (12.4 percent) reconstructions were completed. Patients were prescribed an average of 36.0 5-mg oxycodone tablets postoperatively. Patients reported consuming an average of 20.6 tablets, or 57.0 percent of the average prescription amount. The majority of patients (75.3 percent) reported taking an opioid less than once per day at the time of survey completion, and 24 patients (28.2 percent) reported that they did not use any opioids postoperatively. Preoperative opioid use (p = 0.004), inpatient opioid consumption (p < 0.0001), and patient-reported anxiety related to pain control (p < 0.05) were predictors of opioid consumption.
Patients undergoing mastectomy and implant-based breast reconstruction are prescribed nearly twice as many opioid tablets as consumed, and one in three patients report not using any opioids postoperatively. Clinical factors may help guide prescribing practices.
CLINICAL QUESTION/LEVEL OF EVIDENCE: Risk, III.
目前阿片类药物的处方率对患者和社会层面都产生了有害影响。本研究旨在评估即刻植入乳房重建中负责任的阿片类药物处方和阿片类药物消耗的预测因素。
接受即刻、植入式乳房重建咨询的患者被纳入前瞻性队列调查研究。术前和术后就诊时进行问卷调查,收集疼痛预期和阿片类药物使用的数据。进行了病历回顾。
在 100 名入组患者中,97 名(97.0%)接受了手术,85 名(85.0%)完成了术后调查。术前,27 名(27.0%)患者有慢性疼痛综合征病史,34 名(34.0%)有精神健康合并症病史,9 名(9.0%)有术前阿片类药物使用史。共完成 85 例组织扩张器(87.6%)和 12 例直接植入物(12.4%)重建。患者术后平均开 36.0 片 5mg 羟考酮片。患者报告平均服用 20.6 片,即平均处方量的 57.0%。大多数患者(75.3%)在调查完成时报告每天服用阿片类药物少于一次,24 名患者(28.2%)报告术后未使用任何阿片类药物。术前阿片类药物使用(p=0.004)、住院期间阿片类药物消耗(p<0.0001)和患者报告的与疼痛控制相关的焦虑(p<0.05)是阿片类药物消耗的预测因素。
接受乳房切除术和植入式乳房重建的患者开的阿片类药物片剂几乎是消耗的两倍,三分之一的患者报告术后不使用任何阿片类药物。临床因素可能有助于指导处方实践。
临床问题/证据水平:风险,III 级。