Department of Surgery, Temple University Hospital, Philadelphia, Pennsylvania.
Lewis Katz School of Medicine at Temple University, Philadelphia, Pennsylvania.
J Surg Res. 2024 Sep;301:686-695. doi: 10.1016/j.jss.2024.07.089. Epub 2024 Aug 20.
Buprenorphine is a Food and Drug Administration-approved therapy for opioid use disorder, with proven efficacy in treatment retention and reduction in opioid use and mortality. Low-dose buprenorphine initiation or microinduction is a novel means of initiation that may allow for an easier transition in patients. Trauma patients have high rates of opioid use disorder and patient directed discharges (PDD). We hypothesized that patients initiated on a buprenorphine microinduction program would have increased protocol completion and fewer PDD compared with patients initiated historically on a traditional induction.
Our retrospective cohort study compared buprenorphine microinduction and traditional induction in trauma patients at an urban level one trauma center between December 2020 and June 2022. Patients aged 18-89 y with traumatic injuries who received buprenorphine were included. Our primary outcome was in-hospital protocol completion, defined as reaching 16 mg of buprenorphine within 24 h or a documented stable dose. Statistical analysis was performed using chi-square for categorical variables and two sample t-tests for continuous variables.
Ninety-eight patients were included, with 46 initiating with microinduction and 52 initiating with traditional induction. There was no difference in protocol completion, (P = 0.29) and 83% of subjects who started an induction protocol completed it. Those who completed a protocol were more likely to be discharged home (P = 0.0002), had less PDD (P = 0.001), and had an increased likelihood of attending outpatient addiction clinic follow-up (P = 0.038).
Regardless of the protocol type, buprenorphine induction can be implemented in trauma patients with high protocol completion rates. In our population, those who complete a protocol had a higher likelihood of discharge home and postdischarge follow-up in addiction medicine clinic.
丁丙诺啡是一种获得美国食品和药物管理局批准的阿片类药物使用障碍治疗药物,已被证实能提高治疗保留率、减少阿片类药物使用和降低死亡率。低剂量丁丙诺啡起始或微诱导是一种新的起始方法,可能使患者更容易过渡。创伤患者阿片类药物使用障碍和患者导向出院(PDD)的发生率很高。我们假设,与历史上传统诱导相比,接受丁丙诺啡微诱导方案的患者完成方案的比例更高,PDD 更少。
我们的回顾性队列研究比较了 2020 年 12 月至 2022 年 6 月在一家城市一级创伤中心的创伤患者中丁丙诺啡微诱导和传统诱导。纳入年龄在 18-89 岁之间、有创伤性损伤且接受丁丙诺啡治疗的患者。我们的主要结局是住院期间完成方案,定义为在 24 小时内达到 16 毫克丁丙诺啡或记录到稳定剂量。使用卡方检验进行分类变量分析,使用两样本 t 检验进行连续变量分析。
共纳入 98 例患者,其中 46 例接受微诱导,52 例接受传统诱导。两组方案完成率无差异(P=0.29),83%接受诱导方案的患者完成了方案。完成方案的患者更有可能出院回家(P=0.0002),PDD 更少(P=0.001),更有可能参加门诊成瘾医学诊所的随访(P=0.038)。
无论方案类型如何,创伤患者都可以实施丁丙诺啡诱导,且方案完成率较高。在我们的人群中,完成方案的患者出院回家和接受成瘾医学诊所随访的可能性更高。