Narayana Arvind, Katz Nathaniel, Shillington Alicia C, Stephenson Judith J, Harshaw Qing, Frye Carla B, Portenoy Russell K
Teva Pharmaceuticals, Frazer, PA, USA Tufts University School of Medicine, Boston, MA, USA Analgesic Solutions, Natick, MA, USA EPI-Q, Inc, Oak Brook, IL, USA HealthCore, Inc, Wilmington, DE, USA Thayer County Health Services, Hebron, NE, USA MJHS Institute for Innovation in Palliative Care, New York, NY, USA.
Pain. 2015 Feb;156(2):252-259. doi: 10.1097/01.j.pain.0000460305.41078.7d.
The National Breakthrough Pain Study is a large observational study that assessed breakthrough pain (BTP) in a population of commercially insured community-dwelling patients with opioid-treated chronic pain. Eligible patients were identified from an administrative claims database, and consenting patients were asked to complete a structured telephone interview and several validated questionnaires. Questionnaires assessed pain interference with function (Brief Pain Inventory-Short Form), health status (Short Form 12 [SF-12] Health Survey), disability (Sheehan Disability Scale), work performance (World Health Organization Health and Work Performance Questionnaire), and mood (Generalized Anxiety Disorder-7 Screener [GAD-7] and Patient Health Questionnaire-2 [PHQ-2]). Of 2198 patients interviewed, 1278 patients had persistent pain controlled with opioid therapy; 1023 (80%) of these patients reported BTP. Patients had a median of 2.0 episodes of BTP per day (range, 1-50) and a median duration of BTP of 45 minutes (range, 1-720). Compared with patients without BTP, patients with BTP had more pain-related interference in function (Brief Pain Inventory, mean ± SD: 34.2 ± 15.6 vs 25.0 ± 15.7 [P < 0.001]), worse physical health (SF-12 physical component score: 29.9 ± 9.6 vs 35.1 ± 10.4 [P < 0.001]) and mental health (SF-12 mental component score: 47.4 ± 11.3 vs 49.3 ± 10.4 [P < 0.001]), more disability (Sheehan Disability Scale global impairment score: 15.1 ± 9.1 vs 10.6 ± 8.5; World Health Organization Health and Work Performance Questionnaire absolute absenteeism: 12.4 ± 59.9 vs 7.7 ± 44.9 hours [both P < 0.001]), and worse mood (GAD-7 score: 7.4 ± 5.9 vs 5.9 ± 5.4; PHQ-2 anhedonia score: 1.2 ± 1.1 vs 0.9 ± 1.0 [both P < 0.001]). In this population of community-dwelling patients with opioid-treated chronic pain, BTP was highly prevalent and associated with negative outcomes. This burden of illness suggests the need for specific treatment plans.
国家突破性疼痛研究是一项大型观察性研究,评估了在接受阿片类药物治疗慢性疼痛的商业保险社区居住患者群体中的突破性疼痛(BTP)。符合条件的患者从行政索赔数据库中识别出来,同意参与的患者被要求完成一次结构化电话访谈以及几份经过验证的问卷。问卷评估了疼痛对功能的干扰(简明疼痛量表简表)、健康状况(12项简短健康调查[SF-12])、残疾情况(希恩残疾量表)、工作表现(世界卫生组织健康与工作表现问卷)以及情绪(广泛性焦虑障碍7项筛查量表[GAD-7]和患者健康问卷2[PHQ-2])。在接受访谈的2198名患者中,1278名患者的持续性疼痛通过阿片类药物治疗得到控制;其中1023名(80%)患者报告有突破性疼痛。患者每天突破性疼痛发作的中位数为2.0次(范围为1 - 50次),突破性疼痛的持续时间中位数为45分钟(范围为1 - 720分钟)。与无突破性疼痛的患者相比,有突破性疼痛的患者在功能方面有更多与疼痛相关的干扰(简明疼痛量表,均值±标准差:34.2±15.6 vs 25.0±15.7[P < 0.001]),身体健康状况更差(SF-12身体成分得分:29.9±9.6 vs 35.1±10.4[P < 0.001])以及心理健康状况更差(SF-12心理成分得分:47.4±11.3 vs 49.3±10.4[P < 0.001]),残疾情况更多(希恩残疾量表总体损伤得分:15.1±9.1 vs 10.6±8.5;世界卫生组织健康与工作表现问卷绝对缺勤时间:12.4±59.9 vs 7.7±44.9小时[两者P < 0.001]),并且情绪更差(GAD-7得分:7.4±5.9 vs 5.9±5.4;PHQ-2快感缺失得分:1.2±1.1 vs 0.9±