Center on Mindfulness and Integrative Health Intervention Development, University of Utah, United States; College of Social Work, University of Utah, United States.
Center on Mindfulness and Integrative Health Intervention Development, University of Utah, United States; College of Social Work, University of Utah, United States; Salt Lake City Veterans Administration Medical Center, United States.
Drug Alcohol Depend. 2020 Dec 1;217:108351. doi: 10.1016/j.drugalcdep.2020.108351. Epub 2020 Oct 12.
Chronic pain patients on long-term opioid therapy (LTOT) may be at elevated risk for developing conditioned opioid cue-reactivity as their prescribed dosing schedules simultaneously function as fixed reinforcement schedules. Since opioids are typically consumed orally during LTOT, it stands to reason that opioid cue exposure might elicit conditioned salivary responses. However, no study has examined salivary cue-reactivity among opioid users during in-vivo exposure to their own prescription opioid medication.
Two samples (N = 68, N = 39) of chronic pain patients on LTOT were recruited from primary care and specialty care clinics. Study 1 aimed to determine whether chronic pain patients receiving LTOT exhibited salivary cue-reactivity to their prescribed opioid. Study 2 was a pilot study that aimed to assess the effects of behavioral treatment on chronic pain patients' salivary cue-reactivity.
In Study 1, exposure to the patient's own prescribed opioid resulted in significantly greater increases in salivation and cue-elicited craving than exposure to a neutral cue. In Study 2 participants who were randomized to an 8-week Mindfulness-Oriented Recovery Enhancement intervention evidenced significantly greater decreases in opioid cue-reactivity than participants in an active control condition as evidenced by both reduced salivation and craving ratings.
Study findings demonstrate salivation may serve as a useful, objective index of opioid cue-reactivity. With further refinement of this task, conditioned salivary response could be used to identify especially vulnerable patients, who then could be targeted with a personalized medicine approach for selective and intensive prevention/treatment interventions to preempt escalation of opioid use to opioid misuse and OUD.
长期接受阿片类药物治疗(LTOT)的慢性疼痛患者可能面临更高的风险,因为他们的处方剂量方案同时作为固定强化方案,从而发展出条件性阿片类药物线索反应。由于 LTOT 期间通常口服阿片类药物,因此可以合理地假设阿片类药物线索暴露可能会引起条件性唾液反应。然而,尚无研究在慢性疼痛患者接受自身处方阿片类药物的体内暴露期间检查过唾液线索反应。
从初级保健和专科诊所招募了两个接受 LTOT 的慢性疼痛患者样本(N=68,N=39)。研究 1 旨在确定接受 LTOT 的慢性疼痛患者是否表现出对其处方阿片类药物的唾液线索反应。研究 2 是一项试点研究,旨在评估行为治疗对慢性疼痛患者唾液线索反应的影响。
在研究 1 中,与暴露于中性线索相比,暴露于患者自身处方阿片类药物会导致唾液分泌和线索诱发的渴求显著增加。在研究 2 中,与积极对照组的参与者相比,被随机分配到 8 周正念导向康复增强干预的参与者在阿片类药物线索反应方面表现出明显更大的降低,这表现在唾液分泌和渴求评分均降低。
研究结果表明,唾液分泌可能是阿片类药物线索反应的有用客观指标。通过进一步改进此任务,可以使用条件性唾液反应来识别特别脆弱的患者,然后可以针对这些患者采用个性化医学方法进行有针对性和强化的预防/治疗干预,以预防阿片类药物使用升级为阿片类药物滥用和 OUD。