Nenke Marni A, Haylock Clare L, Rankin Wayne, Inder Warrick J, Gagliardi Lucia, Eldridge Crystal, Rolan Paul, Torpy David J
Endocrine and Metabolic Unit, Royal Adelaide Hospital, Adelaide, Australia; School of Medicine, University of Adelaide, Adelaide, Australia.
Northern Adelaide Geriatrics Service, Modbury Hospital, Modbury, Australia; School of Medical Sciences, University of Adelaide, Adelaide, Australia.
Psychoneuroendocrinology. 2015 Jun;56:157-67. doi: 10.1016/j.psyneuen.2015.03.015. Epub 2015 Mar 14.
Long-term opioid therapy has been associated with low cortisol levels due to central suppression of the hypothalamic-pituitary-adrenal axis. The implications of hypocortisolism on wellbeing have not been established. Our aim was to determine whether intervention with physiologic glucocorticoid replacement therapy improves wellbeing and analgesic responses in patients with chronic non-cancer pain on long-term opioid therapy with mild cortisol deficiency. We performed a pilot randomized, double-blind, placebo-controlled crossover study of oral hydrocortisone replacement therapy in 17 patients recruited from a Pain Clinic at a single tertiary center in Adelaide, Australia. Patients were receiving long-term opioid therapy (≥ 20 mg morphine equivalents per day for ≥ 4 weeks) for chronic non-cancer pain with mild hypocortisolism, as defined by a plasma cortisol response ≤ 350 nmol/L at 60 min following a cold pressor test. The crossover intervention included 28-day treatment with either 10mg/m(2)/day of oral hydrocortisone in three divided doses or placebo. Improvement in wellbeing was assessed using Version 2 of the Short Form-36 (SF-36v2), Brief Pain Inventory-Short Form, and Addison's disease quality of life questionnaires; improvement in analgesic response was assessed using cold pressor threshold and tolerance times. Following treatment with hydrocortisone, the bodily pain (P=0.042) and vitality (P=0.013) subscales of the SF-36v2 were significantly better than scores following treatment with placebo. There was also an improvement in pain interference on general activity (P=0.035), mood (P=0.03) and work (P=0.04) following hydrocortisone compared with placebo. This is the first randomized, double-blind placebo-controlled trial of glucocorticoid replacement in opioid users with chronic non-cancer pain and mild hypocortisolism. Our data suggest that physiologic hydrocortisone replacement produces improvements in vitality and pain experiences in this cohort compared with placebo.
Therapeutic Goods Administration Clinical Trials Notification Scheme (Drugs), Trial Number 2012/0476.
长期使用阿片类药物治疗与下丘脑-垂体-肾上腺轴的中枢抑制导致皮质醇水平降低有关。低皮质醇血症对健康的影响尚未明确。我们的目的是确定生理性糖皮质激素替代疗法干预是否能改善长期接受阿片类药物治疗且伴有轻度皮质醇缺乏的慢性非癌性疼痛患者的健康状况和镇痛反应。我们在澳大利亚阿德莱德一个单一三级中心的疼痛诊所招募了17名患者,进行了一项口服氢化可的松替代疗法的试点随机、双盲、安慰剂对照交叉研究。患者因慢性非癌性疼痛接受长期阿片类药物治疗(每天≥20毫克吗啡当量,持续≥4周),且伴有轻度低皮质醇血症,定义为冷加压试验后60分钟血浆皮质醇反应≤350纳摩尔/升。交叉干预包括为期28天的治疗,治疗药物为每日10毫克/平方米的口服氢化可的松,分三次服用,或安慰剂。使用简明健康状况调查量表第2版(SF-36v2)、简明疼痛问卷简表和艾迪生病生活质量问卷评估健康状况的改善情况;使用冷加压阈值和耐受时间评估镇痛反应的改善情况。接受氢化可的松治疗后,SF-36v2的身体疼痛(P = 0.042)和活力(P = 0.013)分量表明显优于接受安慰剂治疗后的得分。与安慰剂相比,氢化可的松治疗后在一般活动(P = 0.035)、情绪(P = 0.03)和工作(P = 0.04)方面的疼痛干扰也有所改善。这是第一项针对患有慢性非癌性疼痛且伴有轻度低皮质醇血症的阿片类药物使用者进行糖皮质激素替代治疗的随机、双盲、安慰剂对照试验。我们的数据表明,与安慰剂相比,生理性氢化可的松替代疗法可改善该队列患者的活力和疼痛体验。
治疗用品管理局临床试验通知计划(药品),试验编号2012/0476。