Department of Surgery, Royal Glamorgan Hospital, Ynysmaerdy, Llantrisant, Rhondda Cynon Taf, CF37 1JL, UK.
Int J Surg. 2010;8(3):212-5. doi: 10.1016/j.ijsu.2009.12.009. Epub 2010 Jan 11.
The aim of this study was to assess the role of adding gabapentin (Neurontin) to the prescription of patients with opiate resistant pain as a result of critical limb ischaemia (CLI).
An observational pilot study was performed on 20 consecutive patients with CLI who were taking all experiencing rest pain despite high dose opiate analgesia. None of the patients were candidates for reconstructive surgery or angioplasty due to the anatomical distribution of their vascular disease or presence of co-morbidities. Gabapentin was commenced at 300 mg daily and titrated to 300 mg tds over 3 days. Doses were then increased up to 600 mg tds as indicated. Pain was assessed by visual analogue scoring at baseline, 4, 7, 14 and 28 days. Improvements in night pain and need for opiates were also noted. The primary end point was pain score at 28 days or until surgical intervention/death if these points occurred sooner.
Nineteen of 20 reported significant night pain, 15 had gangrene or ulceration. Seventeen of 20 patients completed the full observation period of 28 days. Two patients required an operation and 1 patient died of a myocardial infarct. The pain scores fell from a median of 9 (inter-quartile range [IQR]) (7-9) at baseline to 5 (3-6) at 28 days. Improvement in pain scores was observed in 15/17 patients. Of the 17 completing the study, 16 had experienced rest pain at the time of referral of which 15 had significant benefit with gabapentin.
The study has demonstrated that gabapentin is a useful adjuvant in the management of CLI and leads to significant reductions in pain scores and improves night pain for most patients.
本研究旨在评估在因严重肢体缺血(CLI)而对阿片类药物耐药的疼痛患者处方中添加加巴喷丁(Neurontin)的作用。
对 20 例连续 CLI 患者进行了观察性试点研究,这些患者均在接受高剂量阿片类药物镇痛治疗的情况下仍有静息痛。由于血管疾病的解剖分布或合并症的存在,没有患者适合进行重建手术或血管成形术。加巴喷丁从每天 300mg 开始,并在 3 天内滴定至每天 3 次,每次 300mg。然后根据需要将剂量增加至每天 3 次,每次 600mg。在基线、4、7、14 和 28 天时通过视觉模拟评分评估疼痛。还记录夜间疼痛和对阿片类药物的需求改善情况。主要终点是 28 天的疼痛评分或更早出现手术干预/死亡的时间。
20 例中有 19 例报告夜间疼痛明显,15 例有坏疽或溃疡。20 例中有 17 例完成了 28 天的完整观察期。2 例患者需要手术,1 例患者死于心肌梗死。疼痛评分从基线时的中位数 9(四分位距 [IQR])(7-9)降至第 28 天的 5(3-6)。17 例患者中有 15 例观察到疼痛评分改善。在完成研究的 17 例患者中,16 例在转诊时就有静息痛,其中 15 例使用加巴喷丁有明显获益。
该研究表明,加巴喷丁是 CLI 管理的有用辅助药物,可显著降低疼痛评分并改善大多数患者的夜间疼痛。