Pub Date : 2025-08-30eCollection Date: 2025-01-01DOI: 10.1155/prm/8823617
Yi Liang, Huajian Peng, Xinxin Huang, Guanbiao Liang
Background: Pectus excavatum is a common congenital chest wall deformity that can lead to significant cardiopulmonary compression and psychological distress. The minimally invasive Nuss procedure is the standard treatment, but it often results in severe postoperative pain. Effective perioperative pain management is essential to enhance recovery and improve patient outcomes. Objectives: This study aimed to synthesize the most effective evidence on perioperative pain management in patients with pectus excavatum and to provide evidence-based management methods for clinical teams and patients undergoing this surgery. Methods: Guided by the "6S" pyramid model, we retrieved evidence on perioperative pain management from relevant websites, databases, and unpublished gray literature. The search timeframe ranged from 2014 to December 2024. Two researchers independently evaluated the literature quality using the Appraisal of Guidelines for Research and Evaluation II (AGREE II) for guidelines and the Joanna Briggs Institute (JBI) critical appraisal tool for other types of literature. Two researchers independently extracted and summarized the evidence according to the principle of high-quality evidence and newly published evidence. Results: A total of 39 articles were retrieved, of which 6 were guidelines, 6 were expert consensus, 7 were systematic reviews, 1 was a clinical decision, 11 were randomized controlled trials, and 8 were cohort studies. Overall, 35 pieces of evidence from seven dimensions-general principles, education and counseling, pain assessment, preemptive analgesia, intraoperative analgesia, postoperative pain management, and pain management after discharge-were summarized. Conclusions: This study summarized the best evidence on perioperative pain management in patients with pectus excavatum, providing a comprehensive and scientific approach to enhance recovery and patient satisfaction.
{"title":"Best Evidence Summary for Perioperative Pain Management in Patients With Pectus Excavatum.","authors":"Yi Liang, Huajian Peng, Xinxin Huang, Guanbiao Liang","doi":"10.1155/prm/8823617","DOIUrl":"10.1155/prm/8823617","url":null,"abstract":"<p><p><b>Background:</b> Pectus excavatum is a common congenital chest wall deformity that can lead to significant cardiopulmonary compression and psychological distress. The minimally invasive Nuss procedure is the standard treatment, but it often results in severe postoperative pain. Effective perioperative pain management is essential to enhance recovery and improve patient outcomes. <b>Objectives:</b> This study aimed to synthesize the most effective evidence on perioperative pain management in patients with pectus excavatum and to provide evidence-based management methods for clinical teams and patients undergoing this surgery. <b>Methods:</b> Guided by the \"6S\" pyramid model, we retrieved evidence on perioperative pain management from relevant websites, databases, and unpublished gray literature. The search timeframe ranged from 2014 to December 2024. Two researchers independently evaluated the literature quality using the Appraisal of Guidelines for Research and Evaluation II (AGREE II) for guidelines and the Joanna Briggs Institute (JBI) critical appraisal tool for other types of literature. Two researchers independently extracted and summarized the evidence according to the principle of high-quality evidence and newly published evidence. <b>Results:</b> A total of 39 articles were retrieved, of which 6 were guidelines, 6 were expert consensus, 7 were systematic reviews, 1 was a clinical decision, 11 were randomized controlled trials, and 8 were cohort studies. Overall, 35 pieces of evidence from seven dimensions-general principles, education and counseling, pain assessment, preemptive analgesia, intraoperative analgesia, postoperative pain management, and pain management after discharge-were summarized. <b>Conclusions:</b> This study summarized the best evidence on perioperative pain management in patients with pectus excavatum, providing a comprehensive and scientific approach to enhance recovery and patient satisfaction.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"8823617"},"PeriodicalIF":3.0,"publicationDate":"2025-08-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12413950/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145016096","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-29eCollection Date: 2025-01-01DOI: 10.1155/prm/5547227
Nathan Skidmore, Cormac G Ryan, Jagjit Mankelow, Denis Martin
Background: Persistent pain is a complex global issue, which has a significant impact on quality of life. Poor health literacy further impacts the quality of life in people with persistent pain. It is recommended that education be provided to improve health-related knowledge. VR is an engaging learning tool and could improve health literacy. Research exploring the feasibility of physiotherapists using VR to develop health literacy is minimal. Objectives: To determine the feasibility of a VR-based pain education system among physiotherapists and understand barriers and facilitators to its adoption in clinical practice. Methods: Semistructured interviews were conducted with physiotherapists in the United Kingdom after they used a VR-based pain education system, which combines sensory-altering experiences with pain science education. Thematic analysis was used to identify considerations related to its feasibility and its potential to influence health literacy in patients with persistent pain. Results: All participants (n = 12) believed that the VR system could develop several aspects of health literacy, such as information understanding and appraisal. Challenges to clinical integration include allowing for increased clinical time and system training and ensuring the use of VR represents both personalized and evidence-based care. Conclusion: The VR pain management system was considered a feasible adjunct to address health literacy by increasing the plausibility of information and addressing health-related understanding, appraisal, and application. Future research is required to validate the effectiveness of VR-based education systems to improve health literacy.
{"title":"Expectations for Adopting Virtual Reality to Promote Health Literacy in Patients With Persistent Pain: Qualitative Analysis of UK-Based Physiotherapists.","authors":"Nathan Skidmore, Cormac G Ryan, Jagjit Mankelow, Denis Martin","doi":"10.1155/prm/5547227","DOIUrl":"10.1155/prm/5547227","url":null,"abstract":"<p><p><b>Background:</b> Persistent pain is a complex global issue, which has a significant impact on quality of life. Poor health literacy further impacts the quality of life in people with persistent pain. It is recommended that education be provided to improve health-related knowledge. VR is an engaging learning tool and could improve health literacy. Research exploring the feasibility of physiotherapists using VR to develop health literacy is minimal. <b>Objectives:</b> To determine the feasibility of a VR-based pain education system among physiotherapists and understand barriers and facilitators to its adoption in clinical practice. <b>Methods:</b> Semistructured interviews were conducted with physiotherapists in the United Kingdom after they used a VR-based pain education system, which combines sensory-altering experiences with pain science education. Thematic analysis was used to identify considerations related to its feasibility and its potential to influence health literacy in patients with persistent pain. <b>Results:</b> All participants (<i>n</i> = 12) believed that the VR system could develop several aspects of health literacy, such as information understanding and appraisal. Challenges to clinical integration include allowing for increased clinical time and system training and ensuring the use of VR represents both personalized and evidence-based care. <b>Conclusion:</b> The VR pain management system was considered a feasible adjunct to address health literacy by increasing the plausibility of information and addressing health-related understanding, appraisal, and application. Future research is required to validate the effectiveness of VR-based education systems to improve health literacy.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"5547227"},"PeriodicalIF":3.0,"publicationDate":"2025-08-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12413278/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145016106","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-22eCollection Date: 2025-01-01DOI: 10.1155/prm/6610938
Parbati Thapa, Raj Kumar Thapa, Bhuvan K C, Sudesh Gyawali, Shaun Wen Huey Lee
Background: Chronic pain is one of the most common reasons for seeking medical care and is associated with depression and reduced quality of life. This study aims to explore the association of depression and quality of life with chronic pain, and medication management among patients with chronic pain. Methods: A cross-sectional study was conducted among patients visiting the outpatient departments of two tertiary care hospitals in Pokhara, Nepal. Validated questionnaires were used to collect information regarding socio-demographics, pain intensity (face pain scale), quality of life (EQ-5D-3L), depression (PROMIS depression questionnaire) and medications prescribed for pain management. Descriptive statistics, univariate analysis, correlation and multiple regression were used to analyse the data. Results: Three hundred eighty-five participants were enrolled in the study, and most were females 248 (64.4%). Low back pain (n = 96; 24.9%) was the most commonly reported pain condition. The participants' mean pain and quality of life scores were 4.5 ± 1.97 and 0.59 ± 0.37, respectively. NSAIDs were the most prescribed medication. About 25.2% of the participants had mild, 25.5% moderate and 3.4% severe depression. A significant difference in depression and quality of life score was observed between genders (p < 0.001), among participants with different education levels (p < 0.001), with comorbidity (p < 0.001) and pain duration (p < 0.001). A significant reverse association of quality of life with depression (β = -0.326, p < 0.001), pain score (β = -0.292, p < 0.001) and duration of pain (β = -0.208, p < 0.001) was observed. Conclusion: The quality of life among patients with chronic pain was correlated with the pain score, depression score and duration of pain.
背景:慢性疼痛是就医最常见的原因之一,并与抑郁和生活质量下降有关。本研究旨在探讨慢性疼痛患者的抑郁和生活质量与慢性疼痛的关系,以及慢性疼痛患者的药物治疗。方法:对尼泊尔博卡拉两家三级医院门诊的患者进行横断面研究。采用有效问卷收集社会人口统计学、疼痛强度(面部疼痛量表)、生活质量(EQ-5D-3L)、抑郁(PROMIS抑郁问卷)和疼痛管理处方药物等信息。采用描述性统计、单因素分析、相关及多元回归等方法对数据进行分析。结果:385名参与者被纳入研究,其中大多数为女性248(64.4%)。腰痛(n = 96, 24.9%)是最常见的疼痛状况。参与者的平均疼痛和生活质量评分分别为4.5±1.97和0.59±0.37。非甾体抗炎药是最常用的处方药。约25.2%的参与者患有轻度抑郁症,25.5%为中度抑郁症,3.4%为重度抑郁症。抑郁和生活质量评分在性别、受教育程度、合并症和疼痛持续时间上均存在显著差异(p < 0.001)。生活质量与抑郁(β = -0.326, p < 0.001)、疼痛评分(β = -0.292, p < 0.001)和疼痛持续时间(β = -0.208, p < 0.001)呈显著负相关。结论:慢性疼痛患者的生活质量与疼痛评分、抑郁评分和疼痛持续时间有关。
{"title":"Depression, Quality of Life and Medication Use Among Patients With Chronic Pain: A Cross-Sectional Study.","authors":"Parbati Thapa, Raj Kumar Thapa, Bhuvan K C, Sudesh Gyawali, Shaun Wen Huey Lee","doi":"10.1155/prm/6610938","DOIUrl":"10.1155/prm/6610938","url":null,"abstract":"<p><p><b>Background:</b> Chronic pain is one of the most common reasons for seeking medical care and is associated with depression and reduced quality of life. This study aims to explore the association of depression and quality of life with chronic pain, and medication management among patients with chronic pain. <b>Methods:</b> A cross-sectional study was conducted among patients visiting the outpatient departments of two tertiary care hospitals in Pokhara, Nepal. Validated questionnaires were used to collect information regarding socio-demographics, pain intensity (face pain scale), quality of life (EQ-5D-3L), depression (PROMIS depression questionnaire) and medications prescribed for pain management. Descriptive statistics, univariate analysis, correlation and multiple regression were used to analyse the data. <b>Results:</b> Three hundred eighty-five participants were enrolled in the study, and most were females 248 (64.4%). Low back pain (<i>n</i> = 96; 24.9%) was the most commonly reported pain condition. The participants' mean pain and quality of life scores were 4.5 ± 1.97 and 0.59 ± 0.37, respectively. NSAIDs were the most prescribed medication. About 25.2% of the participants had mild, 25.5% moderate and 3.4% severe depression. A significant difference in depression and quality of life score was observed between genders (<i>p</i> < 0.001), among participants with different education levels (<i>p</i> < 0.001), with comorbidity (<i>p</i> < 0.001) and pain duration (<i>p</i> < 0.001). A significant reverse association of quality of life with depression (<i>β</i> = -0.326, <i>p</i> < 0.001), pain score (<i>β</i> = -0.292, <i>p</i> < 0.001) and duration of pain (<i>β</i> = -0.208, <i>p</i> < 0.001) was observed. <b>Conclusion:</b> The quality of life among patients with chronic pain was correlated with the pain score, depression score and duration of pain.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"6610938"},"PeriodicalIF":3.0,"publicationDate":"2025-08-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12396909/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144964643","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Introduction: Labor pain is a well-known physiological phenomenon considered to be the most severe pain experienced by women of childbearing age. One nonpharmacological method used to alleviate labor pain is acupressure. This study aimed to examine the impact of acupressure on the BL23 points on pain intensity during the active phase of the first stage of labor. Method: This randomized, sham-controlled clinical trial took place at Tehran Baharlu Hospital in Iran from August 23 to October 21, 2023. Ninety first-time pregnant women in active labor were randomly assigned to one of three groups: acupressure on BL23 (n = 30), sham acupressure (between the seventh and eighth thoracic vertebra, 2 Cun from the midline) (n = 30), and a control group (n = 30). The sham and acupressure groups received 60 min of acupressure at three different time points during cervical dilatation at 4-5 cm, 6-7 cm, and 8-10 cm. The control group received standard labor care. Pain severity was assessed using a Numerical Rating Scale before, 10 min after, and 20 min after the intervention at each time point. Result: Pain intensity was significantly lower in the BL23 acupressure group compared to the control and sham groups at all three time points (p < 0.0001). Pain intensity decreased in the BL23 acupressure group after 10 min of intervention at all time points (p < 0.001) and continued to decrease throughout the intervention (p < 0.001). The reduction in pain in the BL23 acupressure group was evident before the start of the second and third interventions (p=0.33 andp=0.36, respectively). Twenty minutes of pressure on BL23 points at different dilatation stages were equally effective in reducing pain (p=0.13). No adverse effects on maternal and neonatal outcomes were observed in the BL23 acupressure group compared to the other groups (p > 0.05). Conclusion: This study demonstrates that applying acupressure to the BL23 points during the active phase of the first stage of labor significantly reduces labor pain. However, the pain relief provided by this intervention is temporary, with its effects diminishing over time rather than offering permanent relief. Trial Registration: Iranian Registry of Clinical Trials (IRCT): IRCT20230513058166N1.
{"title":"Effect of BL23 Acupressure on Pain Among Primiparous Women During the First Stage of Labor: A Randomized, Sham-Controlled Trial.","authors":"Fahimeh Pishva, Reza Heshmat, Sedigheh Sedigh Mobarakabadi","doi":"10.1155/prm/4486038","DOIUrl":"https://doi.org/10.1155/prm/4486038","url":null,"abstract":"<p><p><b>Introduction:</b> Labor pain is a well-known physiological phenomenon considered to be the most severe pain experienced by women of childbearing age. One nonpharmacological method used to alleviate labor pain is acupressure. This study aimed to examine the impact of acupressure on the BL23 points on pain intensity during the active phase of the first stage of labor. <b>Method:</b> This randomized, sham-controlled clinical trial took place at Tehran Baharlu Hospital in Iran from August 23 to October 21, 2023. Ninety first-time pregnant women in active labor were randomly assigned to one of three groups: acupressure on BL23 (<i>n</i> = 30), sham acupressure (between the seventh and eighth thoracic vertebra, 2 Cun from the midline) (<i>n</i> = 30), and a control group (<i>n</i> = 30). The sham and acupressure groups received 60 min of acupressure at three different time points during cervical dilatation at 4-5 cm, 6-7 cm, and 8-10 cm. The control group received standard labor care. Pain severity was assessed using a Numerical Rating Scale before, 10 min after, and 20 min after the intervention at each time point. <b>Result:</b> Pain intensity was significantly lower in the BL23 acupressure group compared to the control and sham groups at all three time points (<i>p</i> < 0.0001). Pain intensity decreased in the BL23 acupressure group after 10 min of intervention at all time points (<i>p</i> < 0.001) and continued to decrease throughout the intervention (<i>p</i> < 0.001). The reduction in pain in the BL23 acupressure group was evident before the start of the second and third interventions (<i>p</i>=0.33 <i>and</i> <i>p</i>=0.36, respectively). Twenty minutes of pressure on BL23 points at different dilatation stages were equally effective in reducing pain (<i>p</i>=0.13). No adverse effects on maternal and neonatal outcomes were observed in the BL23 acupressure group compared to the other groups (<i>p</i> > 0.05). <b>Conclusion:</b> This study demonstrates that applying acupressure to the BL23 points during the active phase of the first stage of labor significantly reduces labor pain. However, the pain relief provided by this intervention is temporary, with its effects diminishing over time rather than offering permanent relief. <b>Trial Registration:</b> Iranian Registry of Clinical Trials (IRCT): IRCT20230513058166N1.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"4486038"},"PeriodicalIF":3.0,"publicationDate":"2025-08-20","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12390697/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144964615","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-18eCollection Date: 2025-01-01DOI: 10.1155/prm/8881632
Mahmoud Kandeel, Mohamed Marzok, Sheryar Afzal, Ahmed Meligy, Maryam Mahmoud, Ibrahim Albokhadaim, Khalid M Al Khodair, Sameer Alhojaily
Myofascial pain syndrome (MPS) is a prevalent musculoskeletal disorder characterized by myofascial trigger points (MTrPs), which can significantly impact an individual's quality of life. This study aimed to evaluate the efficacy of Kinesio taping (KT) in reducing pain intensity and increasing pressure pain threshold (PPT) in individuals with MPS. A comprehensive search was performed across five electronic databases (PubMed, Web of Science, Cochrane Library, Embase, and SCOPUS) from inception to May 2024. Randomized controlled trials (RCTs) comparing KT to a control group, including no intervention, placebo, or sham taping, in individuals with MPS were included. Data on pain intensity and PPT were extracted and pooled using RevMan 5.4 software. A total of 15 RCTs were included in the systematic review and meta-analysis. The pooled analysis showed a significant reduction in pain intensity in the KT group compared to the control group immediately after intervention (mean difference [MD] = -1.07, 95% confidence interval (CI) [-1.93, -0.20], p = 0.02), within the first week (standardized mean difference [SMD] = -1.44, 95% CI [-2.39, -0.49], p = 0.003), and after 2-3 weeks (SMD = -0.97, 95% CI [-1.46, -0.49], p < 0.0001). However, the effect diminished after 4-6 weeks (MD = -0.90, 95% CI [-1.65, -0.14], p = 0.02). Regarding PPT, KT significantly increased PPT within the first week (MD = 4.32, 95% CI [2.47, 6.16], p < 0.00001) but not immediately after intervention or after 2-3 and 4-6 weeks. This meta-analysis provides evidence that KT is effective in reducing pain intensity and increasing PPT in individuals with MPS, particularly in the immediate and short-term periods. However, the effects on pain reduction and PPT diminish over time, suggesting a need for reapplication or combination with other interventions for sustained long-term benefits.
肌筋膜疼痛综合征(MPS)是一种以肌筋膜触发点(MTrPs)为特征的普遍肌肉骨骼疾病,它可以显著影响个体的生活质量。本研究旨在评估肌内效贴敷(KT)对MPS患者减轻疼痛强度和增加压力痛阈(PPT)的疗效。从成立到2024年5月,对五个电子数据库(PubMed, Web of Science, Cochrane Library, Embase和SCOPUS)进行了全面的搜索。随机对照试验(rct)将MPS患者的KT与对照组进行比较,包括不干预、安慰剂或假胶带。采用RevMan 5.4软件对疼痛强度和PPT数据进行提取和汇总。系统评价和荟萃分析共纳入15项随机对照试验。综合分析显示,与对照组相比,KT组在干预后立即(平均差值[MD] = -1.07, 95%可信区间(CI) [-1.93, -0.20], p = 0.02)、第一周内(标准化平均差值[SMD] = -1.44, 95% CI [-2.39, -0.49], p = 0.003)和2-3周后(SMD = -0.97, 95% CI [-1.46, -0.49], p < 0.0001)疼痛强度显著降低。然而,4-6周后效果减弱(MD = -0.90, 95% CI [-1.65, -0.14], p = 0.02)。在PPT方面,KT在第一周内显著提高PPT (MD = 4.32, 95% CI [2.47, 6.16], p < 0.00001),但在干预后立即或2-3周和4-6周后没有显著提高PPT。这项荟萃分析提供了证据,证明KT在减轻MPS患者的疼痛强度和增加PPT方面是有效的,特别是在即时和短期内。然而,随着时间的推移,疼痛减轻和PPT的效果逐渐减弱,这表明需要重新应用或与其他干预措施联合使用以获得持续的长期益处。
{"title":"A Systematic Review and Meta-Analysis of the Efficacy of Kinesio Taping for Pain Management and Pressure Pain Threshold in Myofascial Pain Syndrome.","authors":"Mahmoud Kandeel, Mohamed Marzok, Sheryar Afzal, Ahmed Meligy, Maryam Mahmoud, Ibrahim Albokhadaim, Khalid M Al Khodair, Sameer Alhojaily","doi":"10.1155/prm/8881632","DOIUrl":"10.1155/prm/8881632","url":null,"abstract":"<p><p>Myofascial pain syndrome (MPS) is a prevalent musculoskeletal disorder characterized by myofascial trigger points (MTrPs), which can significantly impact an individual's quality of life. This study aimed to evaluate the efficacy of Kinesio taping (KT) in reducing pain intensity and increasing pressure pain threshold (PPT) in individuals with MPS. A comprehensive search was performed across five electronic databases (PubMed, Web of Science, Cochrane Library, Embase, and SCOPUS) from inception to May 2024. Randomized controlled trials (RCTs) comparing KT to a control group, including no intervention, placebo, or sham taping, in individuals with MPS were included. Data on pain intensity and PPT were extracted and pooled using RevMan 5.4 software. A total of 15 RCTs were included in the systematic review and meta-analysis. The pooled analysis showed a significant reduction in pain intensity in the KT group compared to the control group immediately after intervention (mean difference [MD] = -1.07, 95% confidence interval (CI) [-1.93, -0.20], <i>p</i> = 0.02), within the first week (standardized mean difference [SMD] = -1.44, 95% CI [-2.39, -0.49], <i>p</i> = 0.003), and after 2-3 weeks (SMD = -0.97, 95% CI [-1.46, -0.49], <i>p</i> < 0.0001). However, the effect diminished after 4-6 weeks (MD = -0.90, 95% CI [-1.65, -0.14], <i>p</i> = 0.02). Regarding PPT, KT significantly increased PPT within the first week (MD = 4.32, 95% CI [2.47, 6.16], <i>p</i> < 0.00001) but not immediately after intervention or after 2-3 and 4-6 weeks. This meta-analysis provides evidence that KT is effective in reducing pain intensity and increasing PPT in individuals with MPS, particularly in the immediate and short-term periods. However, the effects on pain reduction and PPT diminish over time, suggesting a need for reapplication or combination with other interventions for sustained long-term benefits.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"8881632"},"PeriodicalIF":3.0,"publicationDate":"2025-08-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12377969/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144964549","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Objective: Despite the availability of studies, there is a lack of available literature on the treatment of psychological and gastrointestinal causes of noncardiac chest pain (NCCP). Physiotherapeutic techniques involving diaphragmatic breathing, Jacobson's relaxation and dynamic neuromuscular stabilization (DNS) could address these causes through the activation of parasympathetic system. Hence, this study aims to evaluate the combined effect of diaphragmatic breathing, Jacobson's relaxation and DNS along with pharmacological therapy on patients with gastrointestinal and psychological causes of NCCP. Design: Randomized controlled trial. Setting: Cardiology OPD of a tertiary care hospital. Subjects: Eighty-eight subjects with NCCP. Methods: The intervention group received diaphragmatic breathing, Jacobson's relaxation technique, DNS and pharmacological treatment for 4 weeks. The control group was given pharmacological treatment with patient education. The Beck Depression Inventory (BDI) score, Hamilton Depression Rating Scale (HDRS) score, gastroesophageal reflux disease (GERD) questionnaire score and Numerical Pain Rating Scale (NPRS) score were measured at baseline and after 4 weeks of intervention. Results: The baseline characteristics and outcome measures were assessed, and no significant differences were noted in their mean values (p > 0.05). After 4 weeks of intervention, a statistically significant difference was observed in BDI, HDRS, GERD questionnaire score and NPRS in both the groups (p < 0.001). However, the GERD questionnaire and NPRS showed statistically significant decrease in the intervention group (GERD questionnaire: 28.39 ± 9.74 and NPRS: 4.57 ± 0.91) compared with the control group (GERD questionnaire: 35.54 ± 12.23 and NPRS: 4.95 ± 0.96) with p < 0.05. Conclusion: The diaphragmatic breathing exercises, Jacobson's relaxation technique and DNS are beneficial for reducing GERD symptoms and pain in patients with NCCP. These techniques are safe and cost-effective treatment for addressing the psychological and gastrointestinal causes of NCCP. These can be incorporated along with the pharmacological treatment to enhance the outcomes. However, future researches with long-term follow-ups are required. Trial Registration: Clinical Trials Registry - India: CTRI/2025/02/081294.
{"title":"Effect of Diaphragmatic Breathing Exercise, Jacobson's Relaxation Technique and Dynamic Neuromuscular Stabilization on Gastrointestinal and Psychological Causes of Noncardiac Chest Pain: A Randomized Controlled Trial.","authors":"Anusha Rajesh Suryavanshi, Prem Venkatesan, Ranjan Shetty, Mrudula Pawar","doi":"10.1155/prm/8124858","DOIUrl":"10.1155/prm/8124858","url":null,"abstract":"<p><p><b>Objective:</b> Despite the availability of studies, there is a lack of available literature on the treatment of psychological and gastrointestinal causes of noncardiac chest pain (NCCP). Physiotherapeutic techniques involving diaphragmatic breathing, Jacobson's relaxation and dynamic neuromuscular stabilization (DNS) could address these causes through the activation of parasympathetic system. Hence, this study aims to evaluate the combined effect of diaphragmatic breathing, Jacobson's relaxation and DNS along with pharmacological therapy on patients with gastrointestinal and psychological causes of NCCP. <b>Design:</b> Randomized controlled trial. <b>Setting:</b> Cardiology OPD of a tertiary care hospital. <b>Subjects:</b> Eighty-eight subjects with NCCP. <b>Methods:</b> The intervention group received diaphragmatic breathing, Jacobson's relaxation technique, DNS and pharmacological treatment for 4 weeks. The control group was given pharmacological treatment with patient education. The Beck Depression Inventory (BDI) score, Hamilton Depression Rating Scale (HDRS) score, gastroesophageal reflux disease (GERD) questionnaire score and Numerical Pain Rating Scale (NPRS) score were measured at baseline and after 4 weeks of intervention. <b>Results:</b> The baseline characteristics and outcome measures were assessed, and no significant differences were noted in their mean values (<i>p</i> > 0.05). After 4 weeks of intervention, a statistically significant difference was observed in BDI, HDRS, GERD questionnaire score and NPRS in both the groups (<i>p</i> < 0.001). However, the GERD questionnaire and NPRS showed statistically significant decrease in the intervention group (GERD questionnaire: 28.39 ± 9.74 and NPRS: 4.57 ± 0.91) compared with the control group (GERD questionnaire: 35.54 ± 12.23 and NPRS: 4.95 ± 0.96) with <i>p</i> < 0.05. <b>Conclusion:</b> The diaphragmatic breathing exercises, Jacobson's relaxation technique and DNS are beneficial for reducing GERD symptoms and pain in patients with NCCP. These techniques are safe and cost-effective treatment for addressing the psychological and gastrointestinal causes of NCCP. These can be incorporated along with the pharmacological treatment to enhance the outcomes. However, future researches with long-term follow-ups are required. <b>Trial Registration:</b> Clinical Trials Registry - India: CTRI/2025/02/081294.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"8124858"},"PeriodicalIF":3.0,"publicationDate":"2025-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12373466/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144964565","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-07eCollection Date: 2025-01-01DOI: 10.1155/prm/4405696
Jasmine Heath Hearn, Areeba Rafiq, John Greenwood, Jordan Wilkey, Faith Johnson, Christopher McCarthy
Objective: Patient adherence to treatment recommendations is less than optimal within chronic pain management. Behaviour change techniques (BCTs) and frameworks can be used to maximise engagement with desired behaviours but are also underused. This study sought the perceptions of nurses to explore the perceived barriers and facilitators to utilising BCTs in clinical practice in chronic pain settings. Methods: Eight qualified nurses participated in semi-structured interviews. Reflexive thematic analysis was conducted to understand barriers and facilitators to the use of BCTs in practice. Results: Three themes were identified (1) behaviour change embedded in current practice, (2) complexities in chronic pain as barriers in implementing behaviour change and (3) from experience to expertise: training and supervision needs. Findings suggest that nurses engage in some BCTs (17 were discussed across all interviews), without explicit knowledge of specific BCTs and how to use them. The use of BCTs is restricted by patients' medical complexities, including mental health comorbidities, unhelpful biomedical beliefs about pain and opioid reliance. Furthermore, the opportunity to effectively utilise BCTs is impeded by a lack of training and clinical supervision. Conclusions: Improving nurses' capabilities by enhancing BCT training and clinical supervision is required. Furthermore, organisational change is recommended to create the opportunity for nurses to effectively utilise BCTs. Specifically, organisations should devote necessary resources, backed by effective implementation strategies, to enhance such engagement.
{"title":"Challenges in Nurses' Use of Behaviour Change Techniques in Chronic Pain Management.","authors":"Jasmine Heath Hearn, Areeba Rafiq, John Greenwood, Jordan Wilkey, Faith Johnson, Christopher McCarthy","doi":"10.1155/prm/4405696","DOIUrl":"10.1155/prm/4405696","url":null,"abstract":"<p><p><b>Objective:</b> Patient adherence to treatment recommendations is less than optimal within chronic pain management. Behaviour change techniques (BCTs) and frameworks can be used to maximise engagement with desired behaviours but are also underused. This study sought the perceptions of nurses to explore the perceived barriers and facilitators to utilising BCTs in clinical practice in chronic pain settings. <b>Methods:</b> Eight qualified nurses participated in semi-structured interviews. Reflexive thematic analysis was conducted to understand barriers and facilitators to the use of BCTs in practice. <b>Results:</b> Three themes were identified (1) behaviour change embedded in current practice, (2) complexities in chronic pain as barriers in implementing behaviour change and (3) from experience to expertise: training and supervision needs. Findings suggest that nurses engage in some BCTs (17 were discussed across all interviews), without explicit knowledge of specific BCTs and how to use them. The use of BCTs is restricted by patients' medical complexities, including mental health comorbidities, unhelpful biomedical beliefs about pain and opioid reliance. Furthermore, the opportunity to effectively utilise BCTs is impeded by a lack of training and clinical supervision. <b>Conclusions:</b> Improving nurses' capabilities by enhancing BCT training and clinical supervision is required. Furthermore, organisational change is recommended to create the opportunity for nurses to effectively utilise BCTs. Specifically, organisations should devote necessary resources, backed by effective implementation strategies, to enhance such engagement.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"4405696"},"PeriodicalIF":3.0,"publicationDate":"2025-08-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12352990/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144874550","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: Peripheral sensitization mediated by the Transient Receptor Potential Vanilloid 4-Calcium/calmodulin-dependent protein kinase II (TRPV4-CaMKII) signaling pathway plays a fundamental role in the generation and maintenance of neuropathic pain (NP). Tuina, a safe and effective therapy in traditional Chinese medicine, shows analgesic effects; however, the underlying mechanisms remain unclear. We aimed to investigate whether Tuina alleviates pain by modulating the TRPV4-CaMKII/CREB/NLRP3 signaling pathway. Methods: The Chronic Constriction Injury (CCI) model of the sciatic nerve was used to simulate clinical NP. Tuina was applied to the Yinmen (BL37), Yanglingquan (GB34), and Chengshan (BL57) acupoints once daily for 14 days. Mechanical Withdrawal Threshold (MWT) and Thermal Withdrawal Latency (TWL) were assessed to evaluate the analgesic effect of Tuina. Its protective effects on dorsal root ganglion (DRG) neurons were evaluated using Nissl staining. The whole-cell patch clamp technique recorded excitability changes in DRG neurons and assess the effects of Tuina on peripheral sensitization. Western blot (WB), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA) helped detect changes in the TRPV4-CaMKII/CREB/NLRP3 pathway and expression of inflammation-related cytokines in DRG neurons. Results: Tuina significantly alleviated mechanical allodynia and thermal hyperalgesia in CCI rats and exerted a protective effect on DRG neurons. Patch clamp recordings showed that Tuina inhibited hyperexcitability in DRG neurons. Mechanistically, Tuina downregulated the expression of the TRPV4-CaMKII/CREB/NLRP3 signaling pathway and reduced the secretion of TNF-α, IL-1β, and IL-18. Conclusion: The analgesic effect of Tuina in CCI rats is associated with reduced peripheral sensitization via modulation of the TRPV4-calcium signaling cascade.
背景:瞬时受体电位香草样蛋白4-钙/钙调素依赖性蛋白激酶II (TRPV4-CaMKII)信号通路介导的外周致敏在神经性疼痛(NP)的产生和维持中起着重要作用。推拿是一种安全有效的中医疗法,具有镇痛作用;然而,潜在的机制仍不清楚。我们的目的是研究推拿是否通过调节TRPV4-CaMKII/CREB/NLRP3信号通路来缓解疼痛。方法:采用坐骨神经慢性收缩损伤(CCI)模型模拟临床NP。推拿于阴门(BL37)、阳陵泉(GB34)、成山(BL57)穴,每日1次,连用14天。采用机械戒断阈值(MWT)和热戒断潜伏期(TWL)评价推拿镇痛效果。采用尼氏染色法观察其对背根神经节(DRG)神经元的保护作用。全细胞膜片钳技术记录了DRG神经元的兴奋性变化,并评估了推拿对外周致敏的影响。Western blot (WB)、免疫荧光(IF)和酶联免疫吸附试验(ELISA)有助于检测DRG神经元中TRPV4-CaMKII/CREB/NLRP3通路和炎症相关细胞因子表达的变化。结果:推拿可明显减轻CCI大鼠机械异常痛和热痛觉过敏,并对DRG神经元有保护作用。膜片钳记录显示,推拿可抑制DRG神经元的高兴奋性。机制上,推拿可下调TRPV4-CaMKII/CREB/NLRP3信号通路的表达,降低TNF-α、IL-1β、IL-18的分泌。结论:推拿对CCI大鼠的镇痛作用可能通过调节trpv4 -钙信号级联降低外周致敏性有关。
{"title":"Tuina Alleviates Neuropathic Pain in CCI Rats by Regulating the TRPV4-CaMKII Signaling Pathway in Dorsal Root Ganglion.","authors":"Rentuya Na, Yue Xu, Tianyuan Yu, Yingqi Zhang, Jiawang Yan, Hongzheng Zhang, Hanyu Zhang, Jiawei Sun, Jiayue Liu","doi":"10.1155/prm/3697374","DOIUrl":"10.1155/prm/3697374","url":null,"abstract":"<p><p><b>Background:</b> Peripheral sensitization mediated by the Transient Receptor Potential Vanilloid 4-Calcium/calmodulin-dependent protein kinase II (TRPV4-CaMKII) signaling pathway plays a fundamental role in the generation and maintenance of neuropathic pain (NP). Tuina, a safe and effective therapy in traditional Chinese medicine, shows analgesic effects; however, the underlying mechanisms remain unclear. We aimed to investigate whether Tuina alleviates pain by modulating the TRPV4-CaMKII/CREB/NLRP3 signaling pathway. <b>Methods:</b> The Chronic Constriction Injury (CCI) model of the sciatic nerve was used to simulate clinical NP. Tuina was applied to the Yinmen (BL37), Yanglingquan (GB34), and Chengshan (BL57) acupoints once daily for 14 days. Mechanical Withdrawal Threshold (MWT) and Thermal Withdrawal Latency (TWL) were assessed to evaluate the analgesic effect of Tuina. Its protective effects on dorsal root ganglion (DRG) neurons were evaluated using Nissl staining. The whole-cell patch clamp technique recorded excitability changes in DRG neurons and assess the effects of Tuina on peripheral sensitization. Western blot (WB), immunofluorescence (IF), and enzyme-linked immunosorbent assay (ELISA) helped detect changes in the TRPV4-CaMKII/CREB/NLRP3 pathway and expression of inflammation-related cytokines in DRG neurons. <b>Results:</b> Tuina significantly alleviated mechanical allodynia and thermal hyperalgesia in CCI rats and exerted a protective effect on DRG neurons. Patch clamp recordings showed that Tuina inhibited hyperexcitability in DRG neurons. Mechanistically, Tuina downregulated the expression of the TRPV4-CaMKII/CREB/NLRP3 signaling pathway and reduced the secretion of TNF-α, IL-1β, and IL-18. <b>Conclusion:</b> The analgesic effect of Tuina in CCI rats is associated with reduced peripheral sensitization via modulation of the TRPV4-calcium signaling cascade.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"3697374"},"PeriodicalIF":3.0,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12350020/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144848253","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Pub Date : 2025-08-04eCollection Date: 2025-01-01DOI: 10.1155/prm/7880611
Lisa Bernaerts, Ella Roelant, Maarten Moens, Huynh Giao Ly, Jean-Pierre Van Buyten, Bart Billet, Bart Bryon, Martine Puylaert, Turgay Tuna, Maureen Malone, Tom Theys, Anne Berquin, Johan Vangeneugden, Guy Hans
Background: Spinal cord stimulation (SCS) serves as a treatment option for neuropathic pain conditions. Despite its widespread use and technological advancements over the last decade, the long-term efficacy of SCS remains a topic of debate. Consequently, there is an increasing demand for real-world, long-term data regarding its effectiveness. Material and Methods: In 2018, the Belgian government launched a nationwide platform to monitor all SCS therapies. Five and a half years after its start, a full data extraction was conducted. In the present study, we update the findings of Bernaerts et al. (2024) from the 3-week trial period and the long-term follow-up of patients with persistent spinal pain syndrome and focus on the completion rates of the follow-ups and the battery lifetime of the implantable pulse generators (IPGs). Results: Findings indicate that "yellow flags" or psychological variables can be confirmed as significant predictors of recovery and satisfaction following the trial. Additionally, these yellow flags were able to predict long-term disability. Analysis revealed that patients who completed the follow-up module displayed more active and less passive coping strategies for their pain, along with lower levels of illness anxiety prior to the trial's start, better physical and psychological functioning, and greater recovery and satisfaction with the trial's outcomes. However, adherence to the chronic follow-up module declined over time. Moreover, we investigated the battery life of both rechargeable and nonrechargeable batteries across various indication types. The real-world dataset indicated no significant differences in battery lifetime between rechargeable and nonrechargeable IPGs for each indication type. Conclusions: The long-term outcomes of neuromodulation are intricate and influenced by various factors. Data extracted from the Neuro-Pain® registry increasingly enable us to identify confounding factors and predictors of treatment success with greater precision. Trial Registration: ClinicalTrials.gov identifier: NCT06835868.
背景:脊髓刺激(SCS)是神经性疼痛的一种治疗选择。尽管在过去十年中,SCS的广泛使用和技术进步,但其长期疗效仍然是一个有争议的话题。因此,对其有效性的真实世界长期数据的需求越来越大。材料和方法:2018年,比利时政府启动了一个全国性的平台,监测所有SCS疗法。在启动五年半后,进行了全面的数据提取。在本研究中,我们更新了Bernaerts et al.(2024)对持续性脊柱疼痛综合征患者进行的为期3周的试验和长期随访的研究结果,并重点关注随访完成率和植入式脉冲发生器(IPGs)的电池寿命。结果:研究结果表明,“黄旗”或心理变量可以被确认为试验后恢复和满意度的重要预测因子。此外,这些黄旗能够预测长期残疾。分析显示,完成后续模块的患者对疼痛表现出更积极和更少被动的应对策略,在试验开始前,他们的疾病焦虑水平较低,身体和心理功能更好,康复程度更高,对试验结果也更满意。然而,慢性随访模块的依从性随着时间的推移而下降。此外,我们研究了不同指示类型的可充电和非可充电电池的电池寿命。实际数据集表明,对于每种指示类型,可充电和不可充电ipg之间的电池寿命没有显着差异。结论:神经调节的远期疗效复杂,受多种因素影响。从neuropain®注册表中提取的数据越来越多地使我们能够更精确地识别治疗成功的混杂因素和预测因素。试验注册:ClinicalTrials.gov标识符:NCT06835868。
{"title":"Multidisciplinary Approach to Spinal Cord Stimulation for Persistent Spinal Pain Syndromes: A 65-Month Integrated Data Collection From the Belgian Neuro-Pain® Real-World Data Register.","authors":"Lisa Bernaerts, Ella Roelant, Maarten Moens, Huynh Giao Ly, Jean-Pierre Van Buyten, Bart Billet, Bart Bryon, Martine Puylaert, Turgay Tuna, Maureen Malone, Tom Theys, Anne Berquin, Johan Vangeneugden, Guy Hans","doi":"10.1155/prm/7880611","DOIUrl":"10.1155/prm/7880611","url":null,"abstract":"<p><p><b>Background:</b> Spinal cord stimulation (SCS) serves as a treatment option for neuropathic pain conditions. Despite its widespread use and technological advancements over the last decade, the long-term efficacy of SCS remains a topic of debate. Consequently, there is an increasing demand for real-world, long-term data regarding its effectiveness. <b>Material and Methods:</b> In 2018, the Belgian government launched a nationwide platform to monitor all SCS therapies. Five and a half years after its start, a full data extraction was conducted. In the present study, we update the findings of Bernaerts et al. (2024) from the 3-week trial period and the long-term follow-up of patients with persistent spinal pain syndrome and focus on the completion rates of the follow-ups and the battery lifetime of the implantable pulse generators (IPGs). <b>Results:</b> Findings indicate that \"yellow flags\" or psychological variables can be confirmed as significant predictors of recovery and satisfaction following the trial. Additionally, these yellow flags were able to predict long-term disability. Analysis revealed that patients who completed the follow-up module displayed more active and less passive coping strategies for their pain, along with lower levels of illness anxiety prior to the trial's start, better physical and psychological functioning, and greater recovery and satisfaction with the trial's outcomes. However, adherence to the chronic follow-up module declined over time. Moreover, we investigated the battery life of both rechargeable and nonrechargeable batteries across various indication types. The real-world dataset indicated no significant differences in battery lifetime between rechargeable and nonrechargeable IPGs for each indication type. <b>Conclusions:</b> The long-term outcomes of neuromodulation are intricate and influenced by various factors. Data extracted from the Neuro-Pain® registry increasingly enable us to identify confounding factors and predictors of treatment success with greater precision. <b>Trial Registration:</b> ClinicalTrials.gov identifier: NCT06835868.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"7880611"},"PeriodicalIF":3.0,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12339138/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144822210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
Background: The quadratus lumborum block (QLB) and erector spinae plane (ESP) block are relatively new regional analgesic techniques that provide analgesia to the abdominal wall and reduce postoperative opioid consumption. We compared the effectiveness of ultrasound-guided bilateral ESP block versus bilateral QLB in patients undergoing laparoscopic kidney surgery. Methods: Adult patients who underwent laparoscopic nephrectomy or nephron-sparing surgery (NSS) within the study period were included. Patients were randomly assigned to one of two groups: group I received an ultrasound-guided ESP block with 30 mL of 0.35% ropivacaine on each side and group II received an ultrasound-guided QLB 1 with 30 mL of 0.35% ropivacaine on each side. Results: A total of 84 patients were included, with 45 patients in the ESP block group and 39 in the QLB group. The mean dosage of oxycodone in the ESP block group was 22.66 mg and in the QLB group was 22.66 mg. There was no difference in oxycodone consumption within the first 24 h after surgery between the groups (p=0.77). Conclusion: The effect of ultrasound-guided bilateral QLB and ESP blocks in patients undergoing laparoscopic kidney surgery was found to be similar in terms of postoperative pain and opioid consumption. There were no significant differences between the blocks in opioid consumption or pain scores. Both techniques appear to be effective and safe components of multimodal analgesia strategy for laparoscopic nephrectomy. Trial Registration: ClinicalTrials.gov identifier: NCT05446727.
背景:腰方肌阻滞(QLB)和脊直肌平面阻滞(ESP)是一种相对较新的局部镇痛技术,可提供腹壁镇痛并减少术后阿片类药物的消耗。我们比较了超声引导下双侧ESP阻滞与双侧QLB在腹腔镜肾手术患者中的有效性。方法:纳入研究期间接受腹腔镜肾切除术或保留肾元手术(NSS)的成年患者。患者被随机分为两组:第一组接受超声引导的ESP阻滞,每侧30 mL 0.35%罗哌卡因;第二组接受超声引导的QLB 1阻滞,每侧30 mL 0.35%罗哌卡因。结果:共纳入84例患者,其中ESP阻滞组45例,QLB组39例。ESP阻滞组羟考酮平均剂量为22.66 mg, QLB组平均剂量为22.66 mg。两组术后24 h内羟考酮用量差异无统计学意义(p=0.77)。结论:超声引导下双侧QLB阻滞和ESP阻滞对腹腔镜肾手术患者术后疼痛和阿片类药物消耗的影响相似。两组在阿片类药物消耗和疼痛评分方面没有显著差异。这两种技术似乎是腹腔镜肾切除术多模式镇痛策略的有效和安全的组成部分。试验注册:ClinicalTrials.gov标识符:NCT05446727。
{"title":"Effects of Erector Spinae Plane Block and Quadratus Lumborum Block on Postoperative Opioid Consumption in Laparoscopic Kidney Surgery: A Randomized Controlled Clinical Trial.","authors":"Skladzien Tomasz, Maciejewski Pawel, Cicio Michal, Wojciech Szpunar, Szpor Jan, Lonc Tomasz, Kwinta Anna, Bugielska Renata, Szkudlarek Olga, Drygalski Tomasz, Terlecki Michal","doi":"10.1155/prm/8869716","DOIUrl":"10.1155/prm/8869716","url":null,"abstract":"<p><p><b>Background:</b> The quadratus lumborum block (QLB) and erector spinae plane (ESP) block are relatively new regional analgesic techniques that provide analgesia to the abdominal wall and reduce postoperative opioid consumption. We compared the effectiveness of ultrasound-guided bilateral ESP block versus bilateral QLB in patients undergoing laparoscopic kidney surgery. <b>Methods:</b> Adult patients who underwent laparoscopic nephrectomy or nephron-sparing surgery (NSS) within the study period were included. Patients were randomly assigned to one of two groups: group I received an ultrasound-guided ESP block with 30 mL of 0.35% ropivacaine on each side and group II received an ultrasound-guided QLB 1 with 30 mL of 0.35% ropivacaine on each side. <b>Results:</b> A total of 84 patients were included, with 45 patients in the ESP block group and 39 in the QLB group. The mean dosage of oxycodone in the ESP block group was 22.66 mg and in the QLB group was 22.66 mg. There was no difference in oxycodone consumption within the first 24 h after surgery between the groups (<i>p</i>=0.77). <b>Conclusion:</b> The effect of ultrasound-guided bilateral QLB and ESP blocks in patients undergoing laparoscopic kidney surgery was found to be similar in terms of postoperative pain and opioid consumption. There were no significant differences between the blocks in opioid consumption or pain scores. Both techniques appear to be effective and safe components of multimodal analgesia strategy for laparoscopic nephrectomy. <b>Trial Registration:</b> ClinicalTrials.gov identifier: NCT05446727.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"8869716"},"PeriodicalIF":3.0,"publicationDate":"2025-08-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12339145/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144822209","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}