Centre for Research on Inner City Health, The Keenan Research Centre in the Li Ka Shing Knowledge Institute of St, Michael's Hospital, Toronto, Canada.
BMC Fam Pract. 2011 Jul 8;12:73. doi: 10.1186/1471-2296-12-73.
Little information is available on the problem of chronic pain among homeless individuals. This study aimed to describe the characteristics of and treatments for chronic pain, barriers to pain management, concurrent medical conditions, and substance use among a representative sample of homeless single adult shelter users who experience chronic pain in Toronto, Canada.
Participants were randomly selected at shelters for single homeless adults between September 2007 and February 2008 and screened for chronic pain, defined as having pain in the body for ≥ 3 months or receiving treatment for pain that started ≥ 3 months ago. Cross-sectional surveys obtained information on demographic characteristics, characteristics of and treatments for chronic pain, barriers to pain management, concurrent medical conditions, and substance use. Whenever possible, participants' physicians were also interviewed.
Among 152 homeless participants who experienced chronic pain, 11 (8%) were classified as Chronic Pain Grade I (low disability-low intensity), 47 (32%) as Grade II (low disability-high intensity), 34 (23%) as Grade III (high disability-moderately limiting), and 54 (37%) as Grade IV (high disability-severely limiting). The most common self-reported barriers to pain management were stress of shelter life, inability to afford prescription medications, and poor sleeping conditions. Participants reported using over-the-counter medications (48%), street drugs (46%), prescribed medications (43%), and alcohol (29%) to treat their pain. Of the 61 interviewed physicians, only 51% reported treating the patient's pain. The most common physician-reported difficulties with pain management were reluctance to prescribe narcotics due to the patient's history of substance abuse, psychiatric comorbidities, frequently missed appointments, and difficulty getting the patient to take medications correctly.
Clinicians who provide healthcare for homeless people should screen for chronic pain and discuss barriers to effective pain management with their patients.
有关无家可归者慢性疼痛问题的信息很少。本研究旨在描述在加拿大多伦多,一个有代表性的无家可归的成年单人间收容所使用者群体中,患有慢性疼痛的个体的疼痛特征和治疗方法、疼痛管理障碍、并存的医疗状况和物质使用情况。
2007 年 9 月至 2008 年 2 月期间,在无家可归的成年单人收容所中随机选择参与者,并对其进行慢性疼痛筛查,定义为身体疼痛持续≥3 个月或因≥3 个月前开始的疼痛而接受治疗。横断面调查获得了人口统计学特征、慢性疼痛的特征和治疗方法、疼痛管理障碍、并存的医疗状况和物质使用情况的信息。在可能的情况下,还对参与者的医生进行了访谈。
在 152 名患有慢性疼痛的无家可归者中,11 名(8%)被归类为慢性疼痛 I 级(低残疾-低强度),47 名(32%)为 II 级(低残疾-高强度),34 名(23%)为 III 级(高残疾-中度限制),54 名(37%)为 IV 级(高残疾-严重限制)。自我报告的疼痛管理障碍最常见的是收容所生活的压力、无法负担处方药和睡眠条件差。参与者报告使用非处方药物(48%)、街头毒品(46%)、处方药物(43%)和酒精(29%)来治疗疼痛。在接受访谈的 61 名医生中,只有 51%的医生报告治疗了患者的疼痛。医生报告的疼痛管理最常见的困难是由于患者滥用药物、精神共病、经常错过预约和难以正确服药,不愿开麻醉性镇痛药。
为无家可归者提供医疗保健的临床医生应该对慢性疼痛进行筛查,并与患者讨论有效的疼痛管理障碍。