Hearn Jasmine H, Cotter Imogen, Fine Philip, A Finlay Katherine
a Department of Psychology , The University of Buckingham , Buckingham , UK and.
b Department of Clinical Psychology , The National Spinal Injuries Centre, Stoke Mandeville Hospital , Aylesbury , UK.
Disabil Rehabil. 2015;37(23):2203-11. doi: 10.3109/09638288.2014.1002579. Epub 2015 Jan 20.
This article presents an in-depth, idiographic study examining the lived experience of chronic pain following spinal cord injury (SCI). Neuropathic pain (NP) occurs in a large majority of the SCI population and is particularly intractable to treatment. It can be both psychologically and physically debilitating. This study examines how the experience of NP is mediated by its meaning to the sufferer.
Semi-structured interviews were conducted with eight people with SCI and chronic NP, attending outpatient clinics at a specialist SCI Centre in the UK. Verbatim transcripts were subjected to interpretative phenomenological analysis to further understand the experience.
Analysis suggested that NP has powerful consequences upon the sufferer's physical, psychological and social well-being, in line with a biopsychosocial understanding of pain. Three super-ordinate themes were identified: a perceived gap between treatments received and participants' views of what they wanted and needed; a fight for life control and acceptance; and feeling understood by others with SCI, but isolated from the non-understanding able-bodied.
The results are discussed in terms of the possible application of acceptance-based therapy to NP and the potential for the alleviation of the debilitating consequences of NP.
Chronic NP after SCI is often described as worse than the injury itself, often impacting upon the sufferers physical and psychological health. The experiences of persons with SCI-specific NP highlight the impact of pain on their physical, psychological and social health. This indicates that healthcare professionals should incorporate a biopsychosocial approach for managing pain post-SCI. Routine clinical follow-up of SCI patients with chronic NP, as well as comprehensive pain management treatment programmes, could address the three themes evidenced in the current study, by moving routine intervention with NP away from pain relief, towards pain management. Continued education for patients, friends, family members and healthcare professionals may be beneficial in promoting understanding and awareness of NP and its consequences following SCI.
本文呈现了一项深入的、个案研究,考察脊髓损伤(SCI)后慢性疼痛的生活体验。大多数脊髓损伤患者会出现神经性疼痛(NP),且这种疼痛尤其难以治疗。它会在心理和生理上使人衰弱。本研究考察神经性疼痛的体验是如何通过其对患者的意义来调节的。
对八名患有脊髓损伤和慢性神经性疼痛的患者进行了半结构化访谈,这些患者在英国一家专科脊髓损伤中心的门诊就诊。逐字记录的访谈内容进行了解释现象学分析,以进一步理解这种体验。
分析表明,根据对疼痛的生物心理社会理解,神经性疼痛对患者的身体、心理和社会幸福感有重大影响。确定了三个上位主题:所接受的治疗与参与者对他们想要和需要的治疗的看法之间存在明显差距;为生活控制和接受而抗争;感觉被其他脊髓损伤患者理解,但与不理解的健全人隔绝。
从基于接受的疗法对神经性疼痛的可能应用以及减轻神经性疼痛使人衰弱的后果的可能性方面讨论了研究结果。
脊髓损伤后的慢性神经性疼痛通常被描述为比损伤本身更严重,常常影响患者的身心健康。脊髓损伤特异性神经性疼痛患者的经历凸显了疼痛对他们身体、心理和社会健康的影响。这表明医疗保健专业人员应采用生物心理社会方法来管理脊髓损伤后的疼痛。对患有慢性神经性疼痛的脊髓损伤患者进行常规临床随访以及全面的疼痛管理治疗方案,可以通过将对神经性疼痛的常规干预从疼痛缓解转向疼痛管理来解决本研究中证明的三个主题。对患者、朋友、家人和医疗保健专业人员的持续教育可能有助于促进对神经性疼痛及其脊髓损伤后果的理解和认识。