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应用处方药物监测项目以发现接受肝移植评估患者中未报告的受控物质使用情况。

Application of Prescription Drug Monitoring Program to detect underreported controlled substance use in patients evaluated for liver transplant.

机构信息

Department of Surgery, Hospital of the University of Pennsylvania, Philadelphia, Pennsylvania.

Department of Surgery, Rutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey.

出版信息

Am J Transplant. 2019 Dec;19(12):3398-3404. doi: 10.1111/ajt.15548. Epub 2019 Aug 22.

Abstract

Presurgical controlled substance use predicts postoperative complications, increased readmissions, and mortality. We aimed to examine if a Prescription Drug Monitoring Program (PDMP) would detect underreported controlled substance use in patients undergoing liver transplant evaluation. We performed a retrospective cohort study at a tertiary referral center of patients undergoing liver transplant evaluation in 2017. PDMP reviews were performed on all 360 patients and urine drug screen (UDS) results were reviewed when available to evaluate dispensed controlled substances. These results were compared to the patient's self-reported medication list at evaluation to identify any underreporting. The primary outcome was the number of self-reported controlled substance discrepancies on the medication list identified by PDMP and UDS at the time of evaluation. Among the 360 patients, 87 (24%) had a discrepancy where PDMP revealed a controlled substance prescription that the patient did not report on their medication list. Seventy-seven (67/87) of these discrepancies involved opiates. Of the 360 patients, 219 (61%) had a negative UDS, but 70 (32%) of these patients had at least one controlled substance listed on PDMP. PDMP is a promising screening tool when used in conjunction with the UDS for detecting underreported controlled substance use in liver transplant candidates.

摘要

术前受控物质的使用情况可预测术后并发症、再入院率增加和死亡率。我们旨在研究处方药物监测计划(PDMP)是否可以检测到接受肝移植评估的患者中报告不足的受控物质使用情况。我们在一家三级转诊中心对 2017 年接受肝移植评估的患者进行了回顾性队列研究。对所有 360 名患者进行了 PDMP 审查,当有尿液药物筛查(UDS)结果时,也对其进行了审查,以评估开出的受控物质。将这些结果与患者在评估时自我报告的药物清单进行比较,以确定是否存在漏报。主要结果是 PDMP 和 UDS 在评估时在药物清单上识别出的自我报告受控物质差异数量。在 360 名患者中,有 87 名(24%)存在差异,即 PDMP 显示出患者未在其药物清单上报告的受控物质处方。这些差异中有 77 个(67/87)涉及阿片类药物。在 360 名患者中,有 219 名(61%)的 UDS 为阴性,但 PDMP 上列出了至少一种受控物质的有 70 名(32%)患者。PDMP 是一种很有前途的筛查工具,与 UDS 联合使用时可用于检测肝移植候选者中报告不足的受控物质使用情况。

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