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慢性非癌性疼痛阿片类药物的合理、安全与有效处方:美国介入性疼痛医师协会(ASIPP)指南

Responsible, Safe, and Effective Prescription of Opioids for Chronic Non-Cancer Pain: American Society of Interventional Pain Physicians (ASIPP) Guidelines.

作者信息

Manchikanti Laxmaiah, Kaye Adam M, Knezevic Nebojsa Nick, McAnally Heath, Slavin Konstantin, Trescot Andrea M, Blank Susan, Pampati Vidyasagar, Abdi Salahadin, Grider Jay S, Kaye Alan D, Manchikanti Kavita N, Cordner Harold, Gharibo Christopher G, Harned Michael E, Albers Sheri L, Atluri Sairam, Aydin Steve M, Bakshi Sanjay, Barkin Robert L, Benyamin Ramsin M, Boswell Mark V, Buenaventura Ricardo M, Calodney Aaron K, Cedeno David L, Datta Sukdeb, Deer Timothy R, Fellows Bert, Galan Vincent, Grami Vahid, Hansen Hans, Helm Ii Standiford, Justiz Rafael, Koyyalagunta Dhanalakshmi, Malla Yogesh, Navani Annu, Nouri Kent H, Pasupuleti Ramarao, Sehgal Nalini, Silverman Sanford M, Simopoulos Thomas T, Singh Vijay, Solanki Daneshvari R, Staats Peter S, Vallejo Ricardo, Wargo Bradley W, Watanabe Arthur, Hirsch Joshua A

机构信息

Vice Chair for Research and Education, Department of Anesthesiology and Pain Management, Advocate Illinois Masonic Medical Center, Clinical Associate Professor of Anesthesiology and Surgery at University of Illinois, Chicago, IL.

Northern Anesthesia & Pain Medicine, LLC.

出版信息

Pain Physician. 2017 Feb;20(2S):S3-S92.

Abstract

BACKGROUND

Opioid use, abuse, and adverse consequences, including death, have escalated at an alarming rate since the 1990s. In an attempt to control opioid abuse, numerous regulations and guidelines for responsible opioid prescribing have been developed by various organizations. However, the US opioid epidemic is continuing and drug dose deaths tripled during 1999 to 2015. Recent data show a continuing increase in deaths due to natural and semisynthetic opioids, a decline in methadone deaths, and an explosive increase in the rates of deaths involving other opioids, specifically heroin and illicit synthetic fentanyl. Contrary to scientific evidence of efficacy and negative recommendations, a significant proportion of physicians and patients (92%) believe that opioids reduce pain and a smaller proportion (57%) report better quality of life. In preparation of the current guidelines, we have focused on the means to reduce the abuse and diversion of opioids without jeopardizing access for those patients suffering from non-cancer pain who have an appropriate medical indication for opioid use.

OBJECTIVES

To provide guidance for the prescription of opioids for the management of chronic non-cancer pain, to develop a consistent philosophy among the many diverse groups with an interest in opioid use as to how appropriately prescribe opioids, to improve the treatment of chronic non-cancer pain and to reduce the likelihood of drug abuse and diversion. These guidelines are intended to provide a systematic and standardized approach to this complex and difficult arena of practice, while recognizing that every clinical situation is unique.

METHODS

The methodology utilized included the development of objectives and key questions. The methodology also utilized trustworthy standards, appropriate disclosures of conflicts of interest, as well as a panel of experts from various specialties and groups. The literature pertaining to opioid use, abuse, effectiveness, and adverse consequences was reviewed, with a best evidence synthesis of the available literature, and utilized grading for recommendation as described by the Agency for Healthcare Research and Quality (AHRQ).Summary of Recommendations:i. Initial Steps of Opioid Therapy 1. Comprehensive assessment and documentation. (Evidence: Level I; Strength of Recommendation: Strong) 2. Screening for opioid abuse to identify opioid abusers. (Evidence: Level II-III; Strength of Recommendation: Moderate) 3. Utilization of prescription drug monitoring programs (PDMPs). (Evidence: Level I-II; Strength of Recommendation: Moderate to strong) 4. Utilization of urine drug testing (UDT). (Evidence: Level II; Strength of Recommendation: Moderate) 5. Establish appropriate physical diagnosis and psychological diagnosis if available. (Evidence: Level I; Strength of Recommendation: Strong) 6. Consider appropriate imaging, physical diagnosis, and psychological status to collaborate with subjective complaints. (Evidence: Level III; Strength of Recommendation: Moderate) 7. Establish medical necessity based on average moderate to severe (≥ 4 on a scale of 0 - 10) pain and/or disability. (Evidence: Level II; Strength of Recommendation: Moderate) 8. Stratify patients based on risk. (Evidence: Level I-II; Strength of Recommendation: Moderate) 9. Establish treatment goals of opioid therapy with regard to pain relief and improvement in function. (Evidence: Level I-II; Strength of Recommendation: Moderate) 10. Obtain a robust opioid agreement, which is followed by all parties. (Evidence: Level III; Strength of Recommendation: Moderate)ii. Assessment of Effectiveness of Long-Term Opioid Therapy 11. Initiate opioid therapy with low dose, short-acting drugs, with appropriate monitoring. (Evidence: Level II; Strength of Recommendation: Moderate) 12. Consider up to 40 morphine milligram equivalent (MME) as low dose, 41 to 90 MME as a moderate dose, and greater than 91 MME as high dose. (Evidence: Level II; Strength of Recommendation: Moderate) 13. Avoid long-acting opioids for the initiation of opioid therapy. (Evidence: Level I; Strength of Recommendation: Strong) 14. Recommend methadone only for use after failure of other opioid therapy and only by clinicians with specific training in its risks and uses, within FDA recommended doses. (Evidence: Level I; Strength of Recommendation: Strong) 15. Understand and educate the patients of the effectiveness and adverse consequences. (Evidence: Level I; Strength of Recommendation: Strong) 16. Similar effectiveness for long-acting and short-acting opioids with increased adverse consequences of long-acting opioids. (Evidence: Level I-II; Strength of recommendation: Moderate to strong) 17. Periodically assess pain relief and/or functional status improvement of ≥ 30% without adverse consequences. (Evidence: Level II; Strength of recommendation: Moderate) 18. Recommend long-acting or high dose opioids only in specific circumstances with severe intractable pain. (Evidence: Level I; Strength of Recommendation: Strong)iii. Monitoring for Adherence and Side Effects 19. Monitor for adherence, abuse, and noncompliance by UDT and PDMPs. (Evidence: Level I-II; Strength of Recommendation: Moderate to strong) 20. Monitor patients on methadone with an electrocardiogram periodically. (Evidence: Level I; Strength of Recommendation: Strong). 21. Monitor for side effects including constipation and manage them appropriately, including discontinuation of opioids when indicated. (Evidence: Level I; Strength of Recommendation: Strong)iv. Final Phase 22. May continue with monitoring with continued medical necessity, with appropriate outcomes. (Evidence: Level I-II; Strength of Recommendation: Moderate) 23. Discontinue opioid therapy for lack of response, adverse consequences, and abuse with rehabilitation. (Evidence: Level III; Strength of Recommendation: Moderate) CONCLUSIONS: These guidelines were developed based on comprehensive review of the literature, consensus among the panelists, in consonance with patient preferences, shared decision-making, and practice patterns with limited evidence, based on randomized controlled trials (RCTs) to improve pain and function in chronic non-cancer pain on a long-term basis. Consequently, chronic opioid therapy should be provided only to patients with proven medical necessity and stability with improvement in pain and function, independently or in conjunction with other modalities of treatments in low doses with appropriate adherence monitoring and understanding of adverse events.Key words: Chronic pain, persistent pain, non-cancer pain, controlled substances, substance abuse, prescription drug abuse, dependency, opioids, prescription monitoring, drug testing, adherence monitoring, diversionDisclaimer: The guidelines are based on the best available evidence and do not constitute inflexible treatment recommendations. Due to the changing body of evidence, this document is not intended to be a "standard of care."

摘要

背景

自20世纪90年代以来,阿片类药物的使用、滥用及其不良后果(包括死亡)呈惊人的速度上升。为了控制阿片类药物滥用,各组织制定了许多关于负责任阿片类药物处方的法规和指南。然而,美国的阿片类药物流行仍在继续,1999年至2015年期间药物过量死亡人数增加了两倍。最近的数据显示,天然和半合成阿片类药物导致的死亡人数持续上升,美沙酮死亡人数下降,而涉及其他阿片类药物(特别是海洛因和非法合成芬太尼)的死亡率则呈爆发式增长。与疗效的科学证据和负面建议相反,很大一部分医生和患者(92%)认为阿片类药物能减轻疼痛,而较小比例(57%)的人报告生活质量有所改善。在制定本指南时,我们重点关注了减少阿片类药物滥用和转移的方法,同时不影响那些有适当医学指征使用阿片类药物治疗非癌性疼痛患者的用药机会。

目的

为慢性非癌性疼痛管理中阿片类药物的处方提供指导,在众多关注阿片类药物使用的不同群体中形成一致的合理处方理念,改善慢性非癌性疼痛的治疗,并降低药物滥用和转移的可能性。这些指南旨在为这个复杂且困难的实践领域提供系统和标准化的方法,同时认识到每个临床情况都是独特的。

方法

所采用的方法包括制定目标和关键问题。该方法还采用了可靠的标准、对利益冲突的适当披露,以及来自不同专业和群体的专家小组。对与阿片类药物使用、滥用、有效性和不良后果相关的文献进行了综述,并对现有文献进行了最佳证据综合,并采用了医疗保健研究与质量局(AHRQ)描述的推荐分级。

推荐摘要

i. 阿片类药物治疗的初始步骤

  1. 全面评估和记录。(证据:I级;推荐强度:强)

  2. 筛查阿片类药物滥用以识别阿片类药物滥用者。(证据:II - III级;推荐强度:中等)

  3. 利用处方药监测计划(PDMPs)。(证据:I - II级;推荐强度:中等至强)

  4. 利用尿液药物检测(UDT)。(证据:II级;推荐强度:中等)

  5. 如有可能,进行适当的体格诊断和心理诊断。(证据:I级;推荐强度:强)

  6. 考虑适当的影像学、体格诊断和心理状态,以与主观症状相佐证。(证据:III级;推荐强度:中等)

  7. 根据平均中度至重度(0 - 10分制中≥4分)疼痛和/或残疾确定医疗必要性。(证据:II级;推荐强度:中等)

  8. 根据风险对患者进行分层。(证据:I - II级;推荐强度:中等)

  9. 确定阿片类药物治疗在缓解疼痛和改善功能方面的治疗目标。(证据:I - II级;推荐强度:中等)

  10. 达成一份各方都应遵守的有力的阿片类药物协议。(证据:III级;推荐强度:中等)

ii. 长期阿片类药物治疗有效性评估

  1. 以低剂量、短效药物开始阿片类药物治疗,并进行适当监测。(证据:II级;推荐强度:中等)

  2. 将高达40毫克吗啡当量(MME)视为低剂量,41至90 MME视为中等剂量,大于91 MME视为高剂量。(证据:II级;推荐强度:中等)

  3. 避免在阿片类药物治疗开始时使用长效阿片类药物。(证据:I级;推荐强度:强)

  4. 仅在其他阿片类药物治疗失败后,且仅由对其风险和用途有特定培训的临床医生在FDA推荐剂量内使用美沙酮。(证据:I级;推荐强度:强)

15.让患者了解并知晓有效性和不良后果。(证据:I级;推荐强度:强)

  1. 长效和短效阿片类药物有效性相似,但长效阿片类药物不良后果增加。(证据:I - II级;推荐强度:中等至强)

  2. 定期评估疼痛缓解和/或功能状态改善≥30%且无不良后果。(证据:II级;推荐强度:中等)

  3. 仅在特定的严重顽固性疼痛情况下推荐使用长效或高剂量阿片类药物。(证据:I级;推荐强度:强)

iii. 依从性和副作用监测

  1. 通过UDT和PDMPs监测依从性、滥用和不依从情况。(证据:I - II级;推荐强度:中等至强)

  2. 定期对服用美沙酮的患者进行心电图监测。(证据:I级;推荐强度:强)

  3. 监测包括便秘在内的副作用并进行适当处理,包括在必要时停用阿片类药物。(证据:I级;推荐强度:强)

iv. 最后阶段

  1. 如有持续的医疗必要性且有适当结果,可继续进行监测。(证据:I - II级;推荐强度:中等)

  2. 因无反应、不良后果和滥用且需康复而停用阿片类药物治疗。(证据:III级;推荐强度:中等)

结论

这些指南是基于对文献的全面综述、专家小组的共识、符合患者偏好、共同决策以及有限证据下的实践模式制定的,基于随机对照试验(RCTs),旨在长期改善慢性非癌性疼痛的疼痛和功能。因此,慢性阿片类药物治疗应仅提供给有已证实的医疗必要性且病情稳定、疼痛和功能有所改善的患者,可单独或与其他治疗方式联合使用,采用低剂量并进行适当的依从性监测以及了解不良事件。

关键词

慢性疼痛、持续性疼痛、非癌性疼痛、管制物质、药物滥用、处方药滥用、依赖性、阿片类药物、处方监测、药物检测、依从性监测、转移

免责声明

本指南基于现有最佳证据,并不构成僵化的治疗建议。由于证据不断变化,本文件无意成为“护理标准”。

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