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The impact of chronic pain on adolescents and their families: A qualitative investigation of parental perspectives. 慢性疼痛对青少年及其家庭的影响:父母视角的定性调查。
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-12-08 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2562440
Lindsay Sullivan, Ellie Ferguson, Harrison Vriese, Kathleen Lemanek, Lindsey Vater, Sharon Wrona, Lauren Renner, Megan Armstrong, Hannah Williams, Henry Xiang

Background: Understanding the experiences of parents of adolescents with chronic pain is crucial in creating a better experience for all involved throughout the adolescent's chronic pain journey. However, limited qualitative research has explored the experiences of parents of adolescents with chronic pain.

Aims: This qualitative study explored the lived experiences of parents of adolescents with chronic pain, with a focus on the impact of chronic pain on their child and family life. Methods: We conducted 12 semi-structured interviews with parents of adolescents with chronic pain receiving care through a pain management program. Data were transcribed and analyzed using inductive thematic analysis.

Results: Seven key themes were generated and divided into two groups: (1) adolescent and (2) family (including both parents and siblings). Groups were determined based on whether the theme referred to the effect of chronic pain on the adolescent or the caregiver or family. The adolescent group included four themes: (1) physical, (2) psychological, (3) social interaction, and (4) school functioning. The family group included three themes: (1) disruption to daily life, (2) emotional, and (3) relationship dynamics.

Conclusions: This study provides a deeper understanding of the negative effect chronic pain can have on adolescents and family life. Our findings call for interventions to mitigate the physical, psychological, and social impact of chronic pain on adolescents. Family level interventions are also needed to support families of adolescents with chronic pain. More research is needed to explore adolescents' own views of their experiences with chronic pain.

背景:了解患有慢性疼痛的青少年父母的经历对于在青少年的慢性疼痛之旅中为所有参与者创造更好的体验至关重要。然而,有限的定性研究已经探讨了青少年慢性疼痛的父母的经验。目的:本定性研究探讨慢性疼痛青少年父母的生活经历,重点关注慢性疼痛对他们的孩子和家庭生活的影响。方法:我们对接受疼痛管理项目治疗的青少年慢性疼痛患者的父母进行了12次半结构化访谈。对数据进行转录和归纳主题性分析。结果:产生了七个关键主题,并分为两组:(1)青少年和(2)家庭(包括父母和兄弟姐妹)。分组是根据主题是否涉及慢性疼痛对青少年或照顾者或家庭的影响来确定的。青少年组包括四个主题:(1)身体,(2)心理,(3)社会互动,(4)学校功能。家庭组包括三个主题:(1)日常生活的中断,(2)情感,(3)关系动态。结论:本研究对慢性疼痛对青少年和家庭生活的负面影响提供了更深入的了解。我们的研究结果呼吁采取干预措施来减轻慢性疼痛对青少年的身体、心理和社会影响。家庭层面的干预也需要支持患有慢性疼痛的青少年的家庭。需要更多的研究来探索青少年自己对慢性疼痛经历的看法。
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引用次数: 0
What can the Global South learn from Canada's innovations in pain science? 全球南方国家可以从加拿大在疼痛科学方面的创新中学到什么?
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-09-25 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2541108
Jose Eric M Lacsa

Canada's advancements in pain research, characterized by innovative education, clinical care, and trainee-led scholarship, offer valuable insights for the Global South. This article examines key initiatives highlighted in a recent Canadian Journal of Pain special issue, including multidisciplinary approaches, patient-centered care, and the development of accessible pain assessment tools. By contextualizing these innovations within the Philippine healthcare landscape, the article explores challenges such as limited access, cultural perceptions of pain, and under-resourced pain management systems. Emphasizing the importance of narrative-driven and culturally sensitive methodologies, it advocates for integrating indigenous knowledge and community participation into pain research and care. Furthermore, the article underscores the critical role of nurturing early-career researchers and fostering cross-sector collaboration to build sustainable pain research ecosystems. Ultimately, this reflection invites Global South countries to adapt and co-create pain science innovations, contributing to a more inclusive and globally connected understanding of pain management. The article serves as a call to reimagine pain research that bridges local realities with global expertise, fostering equitable health outcomes across diverse populations.

加拿大在疼痛研究方面的进步,以创新教育、临床护理和实习生主导的奖学金为特征,为全球南方提供了宝贵的见解。本文探讨了最近加拿大疼痛杂志特刊中突出的关键举措,包括多学科方法,以患者为中心的护理,以及可访问的疼痛评估工具的发展。通过将菲律宾医疗保健领域的这些创新置于背景下,本文探讨了诸如有限的访问、对疼痛的文化认知和资源不足的疼痛管理系统等挑战。它强调叙述驱动和文化敏感方法的重要性,倡导将土著知识和社区参与纳入疼痛研究和护理。此外,文章强调了培养早期职业研究人员和促进跨部门合作以建立可持续的疼痛研究生态系统的关键作用。最终,这一反思邀请全球南方国家适应并共同创造疼痛科学创新,促进对疼痛管理的更具包容性和全球联系的理解。这篇文章呼吁重新构想疼痛研究,将当地现实与全球专业知识联系起来,在不同人群中促进公平的健康结果。
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引用次数: 0
Winner of the Ronald Melzack-Canadian Journal of Pain Paper of the Year Award for 2024/Récipiendaire du Prix Ronald Melzack Pour L'Année 2024 Des Articles Parus Dans La Revue Canadienne de La Douleur. 获得Ronald Melzack-加拿大杂志2024年年度疼痛纸奖/获得Ronald Melzack Pour L' Annee 2024年Des Articles Parus Dans La Revue Canadienne de La Douleur奖。
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-09-04 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2544489
Joel Katz, Heather Lumsden-Ruegg, Anna Waisman
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引用次数: 0
The effects of traumatic pain memories on current pain experience in men with hemophilia. 创伤性疼痛记忆对血友病患者当前疼痛体验的影响。
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-09-04 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2530966
Anna Wells, Debra Gray, Margaret Husted, David Stephensen

Hemophilia is a bleeding disorder characterized by recurrent bleeding into muscles and joints. Many people with hemophilia experience multiple traumatic painful bleeding episodes, meaning that pain is often a significant problem for people with hemophilia, with a potentially high prevalence of posttraumatic stress and posttraumatic stress disorder symptoms. Current pain treatments are often ineffective and do not consider pain memories, which are experienced by almost half of people with posttraumatic stress disorder and which has not been explored in people with hemophilia. To fill this gap, 14 semistructured interviews with men with hemophilia were completed between November 2022 and January 2023 to explore their lived experiences of pain relating to their hemophilia. Data were analyzed using reflexive thematic analysis. Three overarching themes were constructed from the data: "trauma histories," "pain management," and "impact on the present." Findings show that pain experienced by people with hemophilia is complex and does include a memory element for many individuals. Pain memories are clear and vivid and include visual, somatic, and emotional elements in intricate detail. Pain can also be experienced in the present when experiencing a pain flashback, and pain in the present can be a trigger to recalling and re-experiencing pain memories from the past. Self-taught active dissociation from pain, imagery, and distraction were described as useful pain management strategies. Findings from this study have implications for clinicians and service providers because current pharmacological and physical pain management techniques may be ineffective when pain memory is involved. Future interventions should consider how pain management is advanced for people with hemophilia and how hemophilia services become trauma informed.

血友病是一种以反复出血进入肌肉和关节为特征的出血性疾病。许多血友病患者会经历多次创伤性疼痛出血,这意味着疼痛通常是血友病患者的一个重要问题,可能会导致创伤后应激障碍和创伤后应激障碍症状的高发。目前的疼痛治疗通常是无效的,而且没有考虑到疼痛记忆,几乎一半的创伤后应激障碍患者都经历过疼痛记忆,而在血友病患者中还没有进行过探索。为了填补这一空白,研究人员在2022年11月至2023年1月期间完成了对血友病男性患者的14次半结构化访谈,以探索他们与血友病相关的疼痛生活经历。数据分析采用反身性主题分析。从数据中构建了三个主要主题:“创伤历史”、“疼痛管理”和“对现在的影响”。研究结果表明,血友病患者所经历的疼痛是复杂的,对许多人来说确实包括记忆因素。疼痛记忆清晰而生动,包括视觉、身体和情感的复杂细节。当经历疼痛闪回时,也可以在现在体验到疼痛,并且现在的疼痛可以触发回忆和重新体验过去的疼痛记忆。自学主动分离疼痛、想象和分心被描述为有用的疼痛管理策略。这项研究的发现对临床医生和服务提供者具有启示意义,因为当涉及疼痛记忆时,当前的药物和物理疼痛管理技术可能无效。未来的干预措施应考虑如何对血友病患者进行先进的疼痛管理,以及血友病服务如何成为创伤知情的。
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引用次数: 0
Editorial to accompany the special issue: Social and health inequities in chronic pain across the life span. 特刊附社论:慢性疼痛在整个生命周期中的社会和健康不平等。
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-08-21 eCollection Date: 2024-01-01 DOI: 10.1080/24740527.2025.2533301
Fiona Webster, Leigha Comer, Abhimanyu Sud, Kara Turcotte, Joel Katz
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引用次数: 0
Opioid analgesics for chronic noncancer pain in patients prescribed opioid agonist therapy or with opioid use disorder: A systematic review. 阿片类镇痛药用于处方阿片类激动剂治疗或阿片类药物使用障碍患者的慢性非癌性疼痛:一项系统综述。
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-07-31 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2499553
Vahid Ashoorion, Tushar Sood, Shezel Muneer, Jason W Busse, Danielle Rice, Jaris Swidrovich, Umair Majid, James Abesteh, Randi Q Mao, Abhimanyu Sud

Background: Opioid use disorder (OUD) is a growing public health concern in North America, often coexisting with chronic noncancer pain (CNCP). Managing both conditions presents unique challenges, highlighting the need for evidence to guide decision making.

Aim: The study aimed to conduct a systematic review that summarizes evidence on the efficacy, effectiveness, and safety of opioid analgesics alone or in combination with opioid agonist therapy (OAT) to manage CNCP in people with OUD or with a history of OUD.

Methods: We searched MEDLINE, Embase, PsycINFO, CINAHL and AMED from inception to July 2023 for randomized studies and up to January 2025 for non-randomized studies that explored the efficacy, effectiveness, and safety of opioids for people living with chronic pain and current or prior OUD. We assessed the risk of bias in included studies, evaluated the quality of evidence using the GRADE approach, and provided a narrative summary of treatment effects.

Results: Our search identified 15,988 unique citations, of which six observational studies were deemed eligible to inform safety outcomes for review, while no observational studies or RCTs met the eligibility criteria for efficacy or effectiveness outcomes. The likelihood of suicidality was twice as high in CNCP patients with OUD receiving long-term opioid analgesics compared to those without OUD (absolute risk increase: 127; 95% CI: 36 to 249 more participants with suicidality in 1,000 participants; moderate certainty evidence). Compared to opioid analgesics alone, the risk of fatal opioid-related overdose may decrease in patients with CNCP and OUD who receive both opioid analgesics and OAT (absolute risk reduction: 60; 95%CI: 18 to 94 fewer deaths in 1,000 participants; low certainty evidence).

Conclusions: There is a paucity of evidence to inform practice and policy regarding opioid analgesic prescribing amongst people with OUD. Existing evidence suggests that such prescribing is associated with a higher risk of suicidality, while the use of OAT together with opioid analgesics in this population may be protective against fatal overdose. Further observational and trial research is needed to clarify the benefits and harms of opioid analgesics for CNCP patients with OUD.

背景:阿片类药物使用障碍(OUD)在北美是一个日益严重的公共卫生问题,通常与慢性非癌性疼痛(CNCP)共存。管理这两种情况带来了独特的挑战,突出表明需要证据来指导决策。目的:本研究旨在进行系统综述,总结阿片类镇痛药单独或联合阿片类激动剂治疗(OAT)对OUD患者或OUD病史患者CNCP的疗效、有效性和安全性的证据。方法:我们检索MEDLINE、Embase、PsycINFO、CINAHL和AMED,检索从成立到2023年7月的随机研究,检索到2025年1月的非随机研究,这些研究探讨了阿片类药物对慢性疼痛患者和当前或既往OUD患者的疗效、有效性和安全性。我们评估了纳入研究的偏倚风险,使用GRADE方法评估了证据质量,并提供了治疗效果的叙述性总结。结果:我们的搜索确定了15,988个独特的引用,其中6个观察性研究被认为有资格为安全性结果提供审查,而没有观察性研究或随机对照试验符合疗效或有效性结果的资格标准。接受长期阿片类镇痛药的CNCP OUD患者的自杀可能性是未接受OUD患者的两倍(绝对风险增加:127;95%置信区间:在1000名参与者中,有自杀倾向的参与者多出36至249人;中等确定性证据)。与单独使用阿片类镇痛药相比,同时使用阿片类镇痛药和OAT的CNCP和OUD患者发生致命性阿片类药物过量的风险可能会降低(绝对风险降低:60;95%可信区间:1000名参与者中死亡人数减少18至94人;低确定性证据)。结论:在OUD患者中,关于阿片类镇痛药处方的实践和政策缺乏证据。现有证据表明,这种处方与较高的自杀风险有关,而在这一人群中,OAT与阿片类镇痛药一起使用可能对致命的过量服用有保护作用。需要进一步的观察和试验研究来阐明阿片类镇痛药对CNCP合并OUD患者的利弊。
{"title":"Opioid analgesics for chronic noncancer pain in patients prescribed opioid agonist therapy or with opioid use disorder: A systematic review.","authors":"Vahid Ashoorion, Tushar Sood, Shezel Muneer, Jason W Busse, Danielle Rice, Jaris Swidrovich, Umair Majid, James Abesteh, Randi Q Mao, Abhimanyu Sud","doi":"10.1080/24740527.2025.2499553","DOIUrl":"10.1080/24740527.2025.2499553","url":null,"abstract":"<p><strong>Background: </strong>Opioid use disorder (OUD) is a growing public health concern in North America, often coexisting with chronic noncancer pain (CNCP). Managing both conditions presents unique challenges, highlighting the need for evidence to guide decision making.</p><p><strong>Aim: </strong>The study aimed to conduct a systematic review that summarizes evidence on the efficacy, effectiveness, and safety of opioid analgesics alone or in combination with opioid agonist therapy (OAT) to manage CNCP in people with OUD or with a history of OUD.</p><p><strong>Methods: </strong>We searched MEDLINE, Embase, PsycINFO, CINAHL and AMED from inception to July 2023 for randomized studies and up to January 2025 for non-randomized studies that explored the efficacy, effectiveness, and safety of opioids for people living with chronic pain and current or prior OUD. We assessed the risk of bias in included studies, evaluated the quality of evidence using the GRADE approach, and provided a narrative summary of treatment effects.</p><p><strong>Results: </strong>Our search identified 15,988 unique citations, of which six observational studies were deemed eligible to inform safety outcomes for review, while no observational studies or RCTs met the eligibility criteria for efficacy or effectiveness outcomes. The likelihood of suicidality was twice as high in CNCP patients with OUD receiving long-term opioid analgesics compared to those without OUD (absolute risk increase: 127; 95% CI: 36 to 249 more participants with suicidality in 1,000 participants; moderate certainty evidence). Compared to opioid analgesics alone, the risk of fatal opioid-related overdose may decrease in patients with CNCP and OUD who receive both opioid analgesics and OAT (absolute risk reduction: 60; 95%CI: 18 to 94 fewer deaths in 1,000 participants; low certainty evidence).</p><p><strong>Conclusions: </strong>There is a paucity of evidence to inform practice and policy regarding opioid analgesic prescribing amongst people with OUD. Existing evidence suggests that such prescribing is associated with a higher risk of suicidality, while the use of OAT together with opioid analgesics in this population may be protective against fatal overdose. Further observational and trial research is needed to clarify the benefits and harms of opioid analgesics for CNCP patients with OUD.</p>","PeriodicalId":53214,"journal":{"name":"Canadian Journal of Pain-Revue Canadienne de la Douleur","volume":"9 1","pages":"2499553"},"PeriodicalIF":2.1,"publicationDate":"2025-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12320809/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144785914","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The efficacy of a clustered group-based acceptance and commitment therapy for patients with chronic pain - a randomized controlled semi-crossover trial. 基于集群组的接受和承诺治疗对慢性疼痛患者的疗效——一项随机对照半交叉试验。
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-07-31 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2515106
Lena Danielsson, Svein Bergvik, Are Hugo Pripp, Gunnvald Kvarstein

Purpose: The efficacy of Acceptance and Commitment Therapy (ACT) for chronic pain when provided as weekly sessions, is well documented. In scarcely populated areas, the traveling distance may be a barrier to weekly attendance. This study aimed to test the efficacy of a group-based ACT intervention, clustered into three bouts of three consecutive days, separated by 4 weeks.

Patients and methods: A total of 122 patients, recruited from a university hospital pain clinic, were randomized to either a clustered ACT or Treatment As Usual (TAU) provided by the primary health care services. The study had a semi-crossover design. Group effects of ACT versus TAU were assessed 3 months after the start of ACT by using linear mixed models for repeated measures. Outcome measures included pain intensity, health-related quality of life, pain acceptance, catastrophizing, and psychological distress.

Results: A total of 81 patients completed the ACT intervention. No statistically significant effects were observed on the primary outcome variables, pain intensity and health-related quality of life.

Significant group differences in favor of ACT were detected in pain acceptance (modified Cohen`s d = 0.32), including pain willingness (modified Cohen`s d = 0.30) and activity engagement (modified Cohen`s d = 0.23). The treatment effect remained at the 6- and 12-month follow-ups with a trend toward improvement.

Conclusion: A group-based ACT for chronic pain clustered into 3-day bouts may strengthen pain acceptance processes, including pain willingness and activity engagement. Reasons why the intervention did not affect pain intensity and health-related quality of life are discussed.

目的:接受与承诺疗法(ACT)对慢性疼痛的治疗效果是有文献记载的。在人口稀少的地区,旅行距离可能成为每周出席会议的障碍。本研究旨在测试以组为基础的ACT干预的有效性,分为三组,连续三天,间隔4周。患者和方法:从一所大学医院疼痛门诊招募的122名患者被随机分配到由初级卫生保健服务提供的聚集性ACT或常规治疗(TAU)组。该研究采用半交叉设计。ACT与TAU的组效应在ACT开始3个月后通过线性混合模型进行重复测量。结果测量包括疼痛强度、健康相关生活质量、疼痛接受度、灾难化和心理困扰。结果:共有81例患者完成了ACT干预。在主要结局变量、疼痛强度和健康相关生活质量方面未观察到统计学上显著的影响。在疼痛接受(修正Cohen’s d = 0.32)、疼痛意愿(修正Cohen’s d = 0.30)和活动投入(修正Cohen’s d = 0.23)方面,ACT组间存在显著差异。在6个月和12个月的随访中,治疗效果仍有改善的趋势。结论:以小组为基础的ACT治疗慢性疼痛,集中在3天的疗程中,可以增强疼痛接受过程,包括疼痛意愿和活动参与。讨论了干预不影响疼痛强度和健康相关生活质量的原因。
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引用次数: 0
Correction. 修正。
IF 2.1 Q3 CLINICAL NEUROLOGY Pub Date : 2025-07-25 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2533718

[This corrects the article DOI: 10.1080/24740527.2024.2425596.].

[这更正了文章DOI: 10.1080/24740527.2024.2425596.]。
{"title":"Correction.","authors":"","doi":"10.1080/24740527.2025.2533718","DOIUrl":"10.1080/24740527.2025.2533718","url":null,"abstract":"<p><p>[This corrects the article DOI: 10.1080/24740527.2024.2425596.].</p>","PeriodicalId":53214,"journal":{"name":"Canadian Journal of Pain-Revue Canadienne de la Douleur","volume":"9 1","pages":"2533718"},"PeriodicalIF":2.1,"publicationDate":"2025-07-25","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12309528/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144755109","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Percutaneous auricular neuromodulation to treat pain after ambulatory breast surgery: A randomized, double-masked, sham-controlled pilot study. 经皮耳神经调节治疗门诊乳房手术后疼痛:一项随机、双盲、假对照的初步研究。
IF 2 Q3 CLINICAL NEUROLOGY Pub Date : 2025-07-10 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2521117
Brian M Ilfeld, Wendy B Abramson, Engy T Said, Jacklynn F Sztain, John J Finneran, Jonna L Griggs, Baharin Abdullah, Evan J Jensen, Adam Schaar, Anne M Wallace

Introduction: Percutaneous auricular neuromodulation involves implanting electrodes around the ear and administering an electric current. A device is currently available that is cleared to treat symptoms from opioid withdrawal, and multiple reports suggest a possible postoperative analgesic effect. This randomized, controlled pilot study aimed to (1) assess the feasibility of a postoperative auricular neuromodulation protocol and (2) provide an estimate of its treatment effects on postoperative pain and opioid consumption.

Methods: Adults undergoing unilateral or bilateral ambulatory breast surgery with anticipated moderate-severe pain and a single-injection paravertebral nerve block(s) received an auricular neuromodulation device (NSS-2 Bridge, Masimo) following surgery. Participants were randomized to 5 days of electrical stimulation or sham in a double-masked fashion.

Results: In the first 5 days, the median pain for those receiving active stimulation (n = 15) was 0 (interquartile range [IQR] = 0, 0.5] versus 1.5 (IQR = 0, 3.8) for the sham group (n = 15, P = 0.084). Concurrently, the median oxycodone use for active stimulation was 0 mg (IQR = 0, 2.5) compared to 0 mg (IQR = 0, 3) for the sham group (P = 0.905). Various secondary outcomes reached statistical significance, including maximum and average daily pain scores.

Conclusions: This pilot study demonstrates that percutaneous auricular neuromodulation is a feasible approach for managing pain in ambulatory surgical procedures and shows potential as an effective analgesic following discharge. Considering its ease of application, absence of systemic side effects, and lack of significant complications, conducting a definitive clinical trial seems justified because the current study was underpowered, which possibly resulted in the lack of statistical significance for the primary outcome.Registry: Clinicaltrials.gov NCT05521516.

导读:经皮耳神经调节包括在耳周围植入电极并施加电流。目前有一种装置可用于治疗阿片类药物戒断症状,多份报告表明可能具有术后镇痛作用。这项随机、对照的先导研究旨在(1)评估术后耳廓神经调节方案的可行性,(2)评估其对术后疼痛和阿片类药物消耗的治疗效果。方法:接受单侧或双侧门诊乳房手术的成年人,预期中-重度疼痛和单次注射椎旁神经阻滞,术后接受耳穴神经调节装置(NSS-2 Bridge, Masimo)。参与者被随机分为5天的电刺激或假手术。结果:前5天,主动刺激组(n = 15)的中位疼痛为0(四分位间距[IQR] = 0,0.5),假手术组(n = 15, P = 0.084)的中位疼痛为1.5 (IQR = 0,3.8)。同时,主动刺激中位羟考酮用量为0 mg (IQR = 0,2.5),而假手术组为0 mg (IQR = 0,3) (P = 0.905)。各种次要结局均有统计学意义,包括最大和平均每日疼痛评分。结论:这项初步研究表明,经皮耳神经调节是一种可行的方法来管理门诊手术过程中的疼痛,并显示出潜在的有效镇痛出院后。考虑到其易于应用,无系统性副作用,无显著并发症,进行明确的临床试验似乎是合理的,因为目前的研究力度不足,这可能导致主要结果缺乏统计学意义。注册:Clinicaltrials.gov NCT05521516。
{"title":"Percutaneous auricular neuromodulation to treat pain after ambulatory breast surgery: A randomized, double-masked, sham-controlled pilot study.","authors":"Brian M Ilfeld, Wendy B Abramson, Engy T Said, Jacklynn F Sztain, John J Finneran, Jonna L Griggs, Baharin Abdullah, Evan J Jensen, Adam Schaar, Anne M Wallace","doi":"10.1080/24740527.2025.2521117","DOIUrl":"10.1080/24740527.2025.2521117","url":null,"abstract":"<p><strong>Introduction: </strong>Percutaneous auricular neuromodulation involves implanting electrodes around the ear and administering an electric current. A device is currently available that is cleared to treat symptoms from opioid withdrawal, and multiple reports suggest a possible postoperative analgesic effect. This randomized, controlled pilot study aimed to (1) assess the feasibility of a postoperative auricular neuromodulation protocol and (2) provide an estimate of its treatment effects on postoperative pain and opioid consumption.</p><p><strong>Methods: </strong>Adults undergoing unilateral or bilateral ambulatory breast surgery with anticipated moderate-severe pain and a single-injection paravertebral nerve block(s) received an auricular neuromodulation device (NSS-2 Bridge, Masimo) following surgery. Participants were randomized to 5 days of electrical stimulation or sham in a double-masked fashion.</p><p><strong>Results: </strong>In the first 5 days, the median pain for those receiving active stimulation (<i>n</i> = 15) was 0 (interquartile range [IQR] = 0, 0.5] versus 1.5 (IQR = 0, 3.8) for the sham group (<i>n</i> = 15, <i>P</i> = 0.084). Concurrently, the median oxycodone use for active stimulation was 0 mg (IQR = 0, 2.5) compared to 0 mg (IQR = 0, 3) for the sham group (<i>P</i> = 0.905). Various secondary outcomes reached statistical significance, including maximum and average daily pain scores.</p><p><strong>Conclusions: </strong>This pilot study demonstrates that percutaneous auricular neuromodulation is a feasible approach for managing pain in ambulatory surgical procedures and shows potential as an effective analgesic following discharge. Considering its ease of application, absence of systemic side effects, and lack of significant complications, conducting a definitive clinical trial seems justified because the current study was underpowered, which possibly resulted in the lack of statistical significance for the primary outcome.<b>Registry</b>: Clinicaltrials.gov NCT05521516.</p>","PeriodicalId":53214,"journal":{"name":"Canadian Journal of Pain-Revue Canadienne de la Douleur","volume":"9 1","pages":"2521117"},"PeriodicalIF":2.0,"publicationDate":"2025-07-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12247084/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144627714","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Editorial commitment to trust and integrity in science: Implications for pain and anesthesiology research. 对科学信任和诚信的编辑承诺:对疼痛和麻醉学研究的影响。
IF 2 Q3 CLINICAL NEUROLOGY Pub Date : 2025-07-10 eCollection Date: 2025-01-01 DOI: 10.1080/24740527.2025.2506941
Tonya M Palermo, Didier Bouhassira, Karen D Davis, Hugh C Hemmings, Robert W Hurley, Joel Katz, Jaideep J Pandit, Theodore J Price, Michael E Schatman, Stephan K W Schwarz, Dennis C Turk, Marc Van de Velde, Matthew D Wiles, Tony L Yaksh, David Yarnitsky
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引用次数: 0
期刊
Canadian Journal of Pain-Revue Canadienne de la Douleur
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