Scherrer Jeffrey F, Salas Joanne, Sullivan Mark D, Schneider F David, Bucholz Kathleen K, Burroughs Thomas, Copeland Laurel, Ahmedani Brian, Lustman Patrick J
Department of Family and Community Medicine, Saint Louis University School of Medicine, St. Louis, MO 63104, United States; Harry S. Truman Veterans Administration Medical Center, Columbia, MO, United States.
Department of Family and Community Medicine, Saint Louis University School of Medicine, St. Louis, MO 63104, United States; Harry S. Truman Veterans Administration Medical Center, Columbia, MO, United States.
Prev Med. 2016 Oct;91:110-116. doi: 10.1016/j.ypmed.2016.08.003. Epub 2016 Aug 3.
Long-term prescription opioid use is associated both with new-onset and recurrence of depression. Whether chronic opioid use interferes with depression management has not been reported, therefore we determined whether patients' longer duration of opioid use and higher opioid dose are associated with new-onset treatment resistant depression (TRD) after controlling for confounding from pain and other variables. Data was obtained from Veteran Health Administration (VHA) de-identified patient medical records. We used a retrospective cohort design from 2000-2012. Eligible subjects (n=6169) were 18-80years of age, free of cancer and HIV, diagnosed with depression and opioid-free for the 24-month interval prior to the observation period. Duration of a new prescription for opioid analgesic was categorized as 1-30days, 31-90days and >90days. Morphine-equivalent dose (MED) during follow-up categorized as ≤50mg versus >50mg per day. Pain and other sources of confounding were controlled by propensity scores and inverse probability of treatment weighting. Cox proportional hazard models were computed to estimate the association between duration and dose of opioid and onset of TRD. After controlling for confounding by weighting data, opioid use for 31-90days and for >90days, compared to 1-30days, was significantly associated with new onset TRD (HR=1.25; 95% CI: 1.09-1.45 and HR=1.52; 95% CI: 1.32-1.74, respectively). MED was not associated with new onset TRD. The risk of developing TRD increased as time spent on opioid analgesics increased. Long-term opioid treatment of chronic pain may interfere with treatment of depression.
长期使用处方阿片类药物与抑郁症的新发和复发均有关联。慢性阿片类药物的使用是否会干扰抑郁症的治疗尚未见报道,因此,我们在控制了疼痛和其他变量的混杂因素后,确定患者使用阿片类药物的时间越长以及剂量越高是否与新发难治性抑郁症(TRD)有关。数据来自退伍军人健康管理局(VHA)已去识别化的患者病历。我们采用了2000年至2012年的回顾性队列设计。符合条件的受试者(n = 6169)年龄在18至80岁之间,无癌症和艾滋病毒感染,在观察期前的24个月内被诊断为抑郁症且未使用阿片类药物。阿片类镇痛药新处方的持续时间分为1至30天、31至90天和> 90天。随访期间的吗啡等效剂量(MED)分为每天≤50mg和> 50mg。疼痛和其他混杂因素通过倾向评分和治疗权重的逆概率进行控制。计算Cox比例风险模型以估计阿片类药物的持续时间和剂量与TRD发作之间的关联。在通过加权数据控制混杂因素后,与1至30天相比,使用阿片类药物31至90天和> 90天与新发TRD显著相关(HR = 1.25;95%CI:1.09 - 1.45和HR = 1.52;95%CI:1.32 - 1.74)。MED与新发TRD无关。随着使用阿片类镇痛药时间的增加,发生TRD的风险也增加。慢性疼痛的长期阿片类药物治疗可能会干扰抑郁症的治疗。