处方阿片类药物与抑郁途径队列研究。

Journal of psychiatry and brain science Pub Date : 2020-01-01 Epub Date: 2020-04-28 DOI:10.20900/jpbs.20200009
Jeffrey F Scherrer, Brian Ahmedani, Kirsti Autio, Lynn Debar, Patrick J Lustman, Lisa R Miller-Matero, Joanne Salas, Scott Secrest, Mark D Sullivan, Lauren Wilson, Sarah Skiold-Hanlin
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引用次数: 8

摘要

背景:使用医疗记录数据的研究结果表明,长期(>90天)使用阿片类镇痛药(非统)与新的抑郁发作(NDE)、抑郁恶化和抑郁复发风险相关。这些证据是基于回顾性队列研究和医疗记录数据。现有研究的局限性,克服了新的前瞻性队列研究阿片类抑郁症的关系。方法:从两个卫生保健系统招募的1500名成年患者的前瞻性队列。符合条件的受试者开始一个新的非统组织时期,并有30至90天的非统组织基线。将在基线、6个月和12个月的随访中获得精神疾病的诊断评估、疼痛的结构化测量、疼痛功能、阿片类药物使用、社会支持、睡眠和冲动。基线参与者将被邀请参加12个月的疼痛相关功能、抑郁症状和阿片类药物使用的简短评估。创新:通过抑郁症和阿片类药物使用障碍的适应症和详细表型对混淆进行强有力的控制。预期结果:慢性非统组织将与以快感缺乏和躯体症状为特征的抑郁表型的新发病有关。这种关系可以用功能受损和社会支持不足来部分解释,但不能完全解释。结论:尽管美国每年的阿片类药物处方数量有所减少,但每年仍有超过1.9亿患者患有非统组织。如果慢性非统组织导致临床有意义的情感障碍,独立于疼痛,那么我们需要考虑抑郁症是慢性非统组织的一个重要不利影响,并相应地调整慢性疼痛的护理。
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The Prescription Opioids and Depression Pathways Cohort Study.

Background: Results from studies using medical record data indicate chronic (>90 days) opioid analgesic use (OAU) is associated with new depressive episodes (NDE), worsening depression and risk for depression recurrence. This body of evidence is based on retrospective cohort studies and medical record data. Limitations of existing research are overcome in a new prospective cohort study of the opioid-depression relationship.

Methods: Prospective cohort of 1500 adult patients recruited from two health care systems. Eligible subjects started a new period of OAU and have 30 to 90 days of OAU at baseline. Diagnostic assessments for psychiatric disorders, structured measures of pain, pain functioning, opioid use, social support, sleep and impulsivity will be obtained at baseline, 6-month and 12-month follow-up. Baseline participants will be invited to 12 monthly brief assessments of pain-related functioning, depression symptoms and opioid use.

Innovation: Robust control for confounding by indication and detailed phenotyping of depression and opioid use disorder.

Anticipated results: Chronic OAU will be associated with new onset of a depression phenotype characterized by anhedonia and somatic symptoms. This relationship will be partly, but not completely explained by impaired functioning and low social support.

Conclusions: Although the annual number of opioid prescriptions in the United States has decreased, over 190 million patients have OAU each year. If chronic OAU leads to a clinically meaningful affective disorder, independent of pain, then we need to consider depression an important adverse effect of chronic OAU and adjust care for chronic pain accordingly.

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