Effects of opioid rotation to buprenorphine/naloxone on pain, pain thresholds, pain tolerance, and quality of life in patients with chronic pain and opioid use disorder

被引:12
作者
Veldman, Stijn [1 ]
van Beek, Maria [1 ,2 ]
van Rijswijk, Steffie [1 ]
Ellerbroek, Hannah [1 ]
Timmerman, Hans [3 ,4 ]
van der Wal, Selina [4 ]
Steegers, Monique [4 ,5 ]
Schellekens, Arnt [1 ,2 ,6 ]
机构
[1] Radboud Univ Nijmegen, Med Ctr, Dept Psychiat, Reinier Postlaan 10, NL-6525 GC Nijmegen, Netherlands
[2] Radboud Univ Nijmegen, Donders Inst Brain Cognit & Behav, Nijmegen, Netherlands
[3] Univ Med Ctr Groningen, Dept Anesthesiol, Pain Ctr, Groningen, Netherlands
[4] Radboud Univ Nijmegen, Dept Anesthesiol Pain & Palliat Med, Med Ctr, Nijmegen, Netherlands
[5] Univ Amsterdam, Med Ctr, Dept Anesthesiol, Amsterdam, Netherlands
[6] Nijmegen Inst Scientist Practitioners Addict NISP, Nijmegen, Netherlands
关键词
Buprenorphine; naloxone; Suboxone; Chronic pain; Opioid induced hyperalgesia; Pain threshold; Pain tolerance; Quality of life; Opioid use disorder; Pain; HEROIN-DEPENDENT PATIENTS; PLACEBO-CONTROLLED TRIAL; CHRONIC NONCANCER PAIN; LOW-BACK-PAIN; DOUBLE-BLIND; INDUCED HYPERALGESIA; SUBLINGUAL BUPRENORPHINE; MAINTENANCE TREATMENT; SUBSTANCE USE; TRANSDERMAL BUPRENORPHINE;
D O I
10.1097/j.pain.0000000000002462
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Long-term opioid use in patients with chronic noncancer pain (CNCP) can lead to opioid use disorder (OUD) and has been associated with hyperalgesia and reduced quality of life (QoL). Studies suggest antihyperalgesic properties of buprenorphine, and buprenorphine or naloxone (BuNa) has shown beneficial effects on QoL in patients with OUD without CNCP. This study investigated the added value of BuNa in patients with CNCP with OUD on self-reported pain, pain thresholds, pain tolerance, and QoL. In the current study, 43 outpatients with CNCP and OUD were included for inpatient conversion from full mu-receptor agonist opioids to BuNa. Self-reported pain, pain thresholds, pain tolerance, and QoL were determined at baseline and after 2 months of follow-up, using, respectively, a Visual Analogue Scale (VAS-pain and VAS-QoL), quantitative sensory testing, and EuroQol-5 dimensions. In total, 37 participants completed the protocol, and their data were analyzed. The mean VAS-pain score decreased from 51.3 to 37.2 (27.5%, F = 3.3; P = 0.044), whereas the pressure pain threshold and electric pain threshold or tolerance increased after substitution (F = 7.8; P = 0.005 and F = 44.5; P < 0.001, respectively), as well as QoL (EuroQol-5 dimensions questionnaire: F = 10.4; P = 0.003 and VAS-QoL: F = 4.4; P = 0.043). We found that conversion of full mu-receptor agonists to BuNa, in patients with CNCP with OUD, was accompanied with lower self-reported pain, higher pain thresholds, higher pain tolerance, and improved QoL. Despite several study limitations, these data suggest that BuNa might be of value in patients with CNCP with OUD. Future studies should investigate long-term effects of BuNa in randomized trials.
引用
收藏
页码:955 / 963
页数:9
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