Clinician Perspectives on Increased Gabapentinoid Prescribing in Nursing Homes

IF 4.5 2区 医学 Q1 GERIATRICS & GERONTOLOGY
Jonathan D. Winter, J. William Kerns, Danya M. Qato, Katherine M. Winter, Nicole Brandt, Linda Wastila, Christopher Winter, Yu-Hua Fu, Eposi Elonge, Alex H. Krist, Sarah R. Reves, Rebecca S. Etz
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These surveys revealed that gabapentinoids are increasingly applied off-label not only for all neuropathic pain but also for every form of pain. Most clinicians also perceive gabapentinoids as helpful in moderating behavioral and psychological symptoms, and neuropsychiatric treatment goals influence prescribing. Furthermore, clinicians directly linked gabapentinoid gains with opioid and psychotropic reduction policies as gabapentinoids are viewed as reasonable but unmonitored alternatives to these medications [<span>3</span>]. In addition to these structured responses, results also included 111 clinician free-text responses, offering granular insights into gabapentinoid prescribing practices unobtainable by descriptive statistics alone. 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引用次数: 0

Abstract

Gabapentinoid use in nursing homes (NHs) is rapidly increasing, though the reasons for this evolving trend remain opaque [1, 2]. To bridge this knowledge gap, we conducted two iterative surveys of NH prescribing clinicians. The first survey focused on why gabapentinoids are prescribed in NHs; the second assessed the magnitude of prescribing for each identified indication. Both explored provider perspectives on factors influencing gabapentinoid increases and barriers to deprescribing [3]. These surveys revealed that gabapentinoids are increasingly applied off-label not only for all neuropathic pain but also for every form of pain. Most clinicians also perceive gabapentinoids as helpful in moderating behavioral and psychological symptoms, and neuropsychiatric treatment goals influence prescribing. Furthermore, clinicians directly linked gabapentinoid gains with opioid and psychotropic reduction policies as gabapentinoids are viewed as reasonable but unmonitored alternatives to these medications [3]. In addition to these structured responses, results also included 111 clinician free-text responses, offering granular insights into gabapentinoid prescribing practices unobtainable by descriptive statistics alone. This qualitative analysis of that free-text response data deepens our understanding of NH prescribers' increasing reliance on gabapentinoids.

In October 2023 and May 2024, we used SurveyMonkey to anonymously survey NH clinicians about their gabapentinoid prescribing practices, exploring the indications for use and the factors driving prevalence gains. The first survey inventoried why gabapentinoids are prescribed in NHs, the second iteratively quantified the relative scope of such prescribing [3]. A multidisciplinary team developed the surveys, grounding them in existing literature and emerging data [4-6]. We employed convenience sampling through crowdsourcing, engaging with NH clinician networks to reach a diverse range of clinicians. Participants had four opportunities to provide open-ended insights to enrich responses. Both surveys included the open-ended question “Is there anything else you feel is important for us to know about your use of gabapentin or the challenges of managing behavioral symptoms related to dementia?” Two additional questions also allowed free responses, “I would use gabapentin less if…,” and “I use pregabalin (Lyrica) less often than gabapentin because….” From these observations, themes were identified through an iterative process of immersive crystallization using codes that emerged during data collection and early immersion/crystallization, with differences reconciled by team consensus [7]. Both survey instruments and additional methodological detail are available as online supplements.

One-hundred-eighty-seven NH clinicians participated in the surveys of which 78 provided 111 free responses. All major geographic regions in the United States were represented by free respondents. About 30% were from rural regions, two-thirds were from middle-income areas, and a quarter was from high-income areas. Clinicians who volunteered free responses were more likely to be physicians and had greater NH experience than those who gave no free responses; otherwise no important differences were detected. The characteristics of the free responders are summarized in Table 1 and reasonably approximate the NH clinician population [8]. Five themes emerged regarding increased gabapentinoid use in NHs where respondents generally agreed. Table 2 outlines exemplar quotes.

Theme 1: Polarized beliefs about safety and efficacy. Clinicians displayed divergent opinions about gabapentinoids. Some viewed them as low-risk and beneficial for various off-label uses; others described significant potential for harm and minimal benefits. Notably, there were no meaningful differences in characteristics between these clinician subgroups.

Theme 2: Influence of opioid and psychotropic reduction policies. Gabapentinoids are appealing as less scrutinized alternatives to opioids and psychotropics since they are not included in federal reporting mandates or quality-measure grading.

Theme 3: Challenges of deprescribing. Gabapentinoids are easily initiated for diverse reasons yet difficult to stop. Once prescribed, clinical inertia tends to prevail, regardless of initial intent.

Theme 4: Payor influences. Many clinicians prefer pregabalin to gabapentin but economic factors, including cost and coverage, limit application. Lack of payor support for non-pharmacologic treatment options also contributes to all psychotropic and pain prescribing, a situation exacerbated by NH staffing deficiencies.

Theme 5: Initiation of gabapentinoids outside NHs. Most gabapentinoids prescribed in NHs are started by non-NH clinicians, linking NH increases to broader prescribing trends. Emerging application for postoperative analgesia was highlighted.

Though limited in scope, this study offers insights into increased NH gabapentinoid use, a subject lacking concrete data. Most NH prescriptions are started in other care settings, underscoring that NH prescribing increases are not siloed but rather engrained in global prescribing trends. To curb NH gabapentinoid increases, deprescribing existing prescriptions must be emphasized as much as limiting new NH prescriptions. Moreover, strategies reducing gabapentinoid use in other settings could positively impact downstream NH prescribing.

Deprescribing is complicated by the “sticky” nature of gabapentinoids, often initiated without clearly defined therapeutic goals or discontinuation criteria [9]. Expanding federal mandates for gradual dose reductions to include gabapentinoids might aid in navigating these difficult decisions. Including gabapentinoids under current regulations for long-stay psychotropics would also discourage their use as substitutes for other medications targeted by reduction measures, promoting accountability [10].

The preference for gabapentin over pregabalin highlights the influence of payors on prescribing practices. Many clinicians preferred pregabalin, yet financial and coverage constraints limited its application. Similar factors limit non-drug therapies, which are time- and labor-intensive. These are essential for reducing medication overuse but lack payor support. Until effective non-pharmacologic solutions become as affordable and accessible as drugs, the over-reliance on potentially harmful medications—and inequity in such prescribing—will persist.

The stark divergence of NH clinician opinions on gabapentinoid safety and efficacy is striking and could affect efforts to moderate NH increases. This underscores the need for regularly updated, consensus-driven policy development considerate of different viewpoints and encourages ongoing research into effective, evidence-based alternatives for managing pain and behavioral symptoms in NH residents.

Drs. Jonathan D. Winter, J. William Kerns, Danya M. Qato, Nicole Brandt, Linda Wastila, Rebecca S. Etz, and Alex H. Krist, as well as Mrs. Katherine M. Winter all significantly contributed to design, acquisition, interpretation, and drafting of this submission while Mrs. Sarah R. Reves, Ms. Eposi Elonge, Ms. Yu-Hua Fu, and Mr. Christopher Winter significantly contributed to design, analysis, drafting, and revision.

The authors declare no conflicts of interest.

临床医生对养老院加巴喷丁类药物处方增加的看法。
加巴喷丁类药物在疗养院(NHs)的使用正在迅速增加,尽管这种发展趋势的原因尚不清楚[1,2]。为了弥合这一知识差距,我们对NH处方临床医生进行了两次反复调查。第一项调查的重点是为什么加巴喷丁类药物在NHs开处方;第二项评估了每个确定适应症的处方规模。双方都探讨了提供者对影响加巴喷丁类增加的因素和处方[3]障碍的观点。这些调查显示,加巴喷丁类药物越来越多地应用于标签外,不仅用于所有神经性疼痛,而且用于各种形式的疼痛。大多数临床医生也认为加巴喷丁类药物有助于缓解行为和心理症状,神经精神治疗目标影响处方。此外,临床医生直接将加巴喷丁类药物的增加与阿片类药物和精神药物减少政策联系起来,因为加巴喷丁类药物被视为这些药物的合理但未经监测的替代品[10]。除了这些结构化的回复,结果还包括111个临床医生的自由文本回复,提供了对加巴喷丁类药物处方实践的细致见解,这是单独通过描述性统计无法获得的。这种对自由文本响应数据的定性分析加深了我们对NH处方者越来越依赖加巴喷丁类药物的理解。在2023年10月和2024年5月,我们使用SurveyMonkey对NH临床医生进行了匿名调查,了解他们的加巴喷丁类药物处方实践,探索使用适应症和推动患病率上升的因素。第一次调查列出了为什么加巴喷丁类药物在NHs中被开处方,第二次调查迭代量化了这种处方的相对范围。一个多学科团队根据现有文献和新出现的数据开发了这些调查[4-6]。我们通过众包的方式进行方便抽样,与NH临床医生网络合作,接触到不同范围的临床医生。与会者有四次机会提供开放式见解,以丰富答复。这两项调查都包括一个开放式的问题:“关于您使用加巴喷丁或管理与痴呆症相关的行为症状的挑战,您认为还有其他重要的事情需要我们了解吗?”另外两个问题也允许自由回答,“如果……我会少用加巴喷丁”和“我比加巴喷丁少用普瑞巴林(Lyrica),因为....”。根据这些观察结果,通过使用在数据收集和早期浸泡/结晶过程中出现的代码的沉浸式结晶的迭代过程确定主题,并通过团队共识[7]协调差异。调查工具和额外的方法细节可作为在线补充。187名NH临床医生参与了调查,其中78名提供了111份免费回复。美国所有主要地理区域均由自由受访者代表。大约30%来自农村地区,三分之二来自中等收入地区,四分之一来自高收入地区。自愿提供免费回答的临床医生更有可能是医生,比那些没有提供免费回答的临床医生有更多的NH经验;除此之外,没有检测到重要的差异。表1总结了自由应答者的特征,并合理地近似于NH临床医生群体[8]。五个主题出现关于增加加巴喷丁类使用在国民保健制度,受访者普遍同意。表2列出了典型的引用。主题1:关于安全性和有效性的两极分化观念。临床医生对加巴喷丁类药物表现出不同的看法。一些人认为它们风险低,对各种标签外用途有益;其他人则描述了巨大的潜在危害和最小的好处。值得注意的是,这些临床亚组之间的特征没有显著差异。主题2:阿片类药物和精神药物减少政策的影响。加巴喷丁类药物作为阿片类药物和精神药物的替代品受到较少的审查,因为它们不包括在联邦报告要求或质量测量分级中。主题3:处方的挑战。加巴喷丁类药物很容易因各种原因开始使用,但很难停止。一旦开了处方,不管最初的意图如何,临床惯性往往占上风。主题4:付款人的影响。许多临床医生更喜欢普瑞巴林而不是加巴喷丁,但经济因素,包括成本和覆盖范围,限制了应用。对非药物治疗选择的支付方支持的缺乏也导致了所有精神药物和疼痛处方,这种情况因国家卫生组织人员不足而加剧。主题5:在NHs之外启动加巴喷丁类药物。大多数加巴喷丁类药物在NHs中是由非NH临床医生开出的,将NH的增加与更广泛的处方趋势联系起来。重点介绍了术后镇痛的新应用。 虽然范围有限,但这项研究提供了增加NH加巴喷丁类药物使用的见解,这是一个缺乏具体数据的主题。大多数NH处方是从其他医疗机构开始的,这强调了NH处方的增加不是孤立的,而是根深蒂固的全球处方趋势。为了抑制NH加巴喷丁类药物的增加,必须像限制新的NH处方一样强调减少现有处方。此外,在其他情况下减少加巴喷丁类药物使用的策略可能对下游NH处方产生积极影响。加巴喷丁类药物的“粘性”性质使处方解除变得复杂,通常在没有明确定义的治疗目标或停药标准的情况下开始。将加巴喷丁类药物纳入逐步减少剂量的联邦授权范围,可能有助于做出这些艰难的决定。将加巴喷丁类药物纳入长效精神药物的现行法规,也将阻止它们作为减少措施所针对的其他药物的替代品,从而促进问责制。加巴喷丁对普瑞巴林的偏好突出了付款人对处方实践的影响。许多临床医生更喜欢普瑞巴林,但财政和覆盖范围限制了它的应用。类似的因素限制了非药物治疗,这是时间和劳动密集型的。这些措施对于减少药物过度使用至关重要,但缺乏付款人的支持。除非有效的非药物解决方案变得像药物一样便宜和容易获得,否则对潜在有害药物的过度依赖以及此类处方的不平等将会持续下去。NH临床医生对加巴喷丁类药物安全性和有效性的看法存在明显分歧,这可能会影响缓和NH增加的努力。这强调了定期更新、共识驱动的政策制定需要考虑到不同的观点,并鼓励对有效的、基于证据的替代方案进行研究,以管理NH居民的疼痛和行为症状。Jonathan D. Winter、J. William Kerns、Danya M. Qato、Nicole Brandt、Linda Wastila、Rebecca S. Etz和Alex H. Krist以及Katherine M. Winter女士都对该文件的设计、获取、解释和起草做出了重要贡献,而Sarah R. Reves女士、Eposi Elonge女士、Yu-Hua Fu女士和Christopher Winter先生对设计、分析、起草和修改做出了重要贡献。作者声明无利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
10.00
自引率
6.30%
发文量
504
审稿时长
3-6 weeks
期刊介绍: Journal of the American Geriatrics Society (JAGS) is the go-to journal for clinical aging research. We provide a diverse, interprofessional community of healthcare professionals with the latest insights on geriatrics education, clinical practice, and public policy—all supporting the high-quality, person-centered care essential to our well-being as we age. Since the publication of our first edition in 1953, JAGS has remained one of the oldest and most impactful journals dedicated exclusively to gerontology and geriatrics.
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