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Outcomes of Pain Management Training for the Fourth- and Fifth-Year Medical Students. 四年级和五年级医学生疼痛管理培训的结果。
IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-08-25 eCollection Date: 2023-01-01 DOI: 10.1155/2023/6080769
Ayano Saeki, Yumiko Takao, Keiichiro Suzuki, Munetaka Hirose

Pain management is a major medical issue. However, current medical education in Japan is inadequate with regard to training students to properly assess patients with acute and chronic pain and plan their treatment. Therefore, starting in 2019, Hyogo Medical University established a multidisciplinary educational system to better train medical students to provide pain care. The course, called clinical pain study, is offered to fourth- and fifth-year medical students. Fourth-year students learn the scientific aspects of pain through clinical practice. In this study, we assessed students' understanding of pain management based on the results of pretests and posttests performed before and after their practicum. These tests were administered from November 2019 to April 2022 to 263 fourth- and fifth-year medical students who took the clinical pain study class. The test results were compared in terms of the percentage of correct answers and the total score for each question using McNemar's chi-square test and paired t-tests, respectively. The results showed a significant improvement in the mean of the total score, confirming the improvement in medical students' knowledge (6.43 vs. 7.35 points; p < 0.001). Based on the results, overall, pain education at the university has had positive outcomes and will therefore be continued in the future.

疼痛管理是一个主要的医学问题。然而,日本目前的医学教育不足以培训学生正确评估急性和慢性疼痛患者并计划他们的治疗。因此,从2019年开始,兵库医科大学建立了多学科教育体系,以更好地培训医学生提供疼痛护理。该课程名为临床疼痛研究,面向四年级和五年级的医学生。四年级学生通过临床实践学习疼痛的科学方面。在这项研究中,我们根据实习前后的前测和后测结果,评估了学生对疼痛管理的理解。这些测试于2019年11月至2022年4月对263名参加临床疼痛研究班的四年级和五年级医学生进行。分别使用McNemar卡方检验和配对t检验,根据每个问题的正确答案百分比和总分对测试结果进行比较。结果显示,总分的平均值有了显著提高,证实了医学生知识的提高(6.43分对7.35分;p<0.001)。根据结果,总体而言,该大学的疼痛教育取得了积极成果,因此将在未来继续下去。
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引用次数: 0
Effectiveness of Dry Needling in Improving Pain and Function in Comparison with Other Techniques in Patients with Chronic Neck Pain: A Systematic Review and Meta-Analysis. 与其他技术相比,干针在改善慢性颈部疼痛患者疼痛和功能方面的有效性:系统综述和荟萃分析。
IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-08-23 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1523834
Mar Hernández-Secorún, Hugo Abenia-Benedí, Sergio Borrella-Andrés, Isabel Marqués-García, María Orosia Lucha-López, Pablo Herrero, Isabel Iguacel, José Miguel Tricás-Moreno, César Hidalgo-García

The purpose of this systematic review and meta-analysis was to assess the short-, mid-, and long-term effectiveness of dry needling in improving pain and functional capacity of patients with chronic neck pain. Search strategy was performed on PubMed, Web of Science, Scopus, PEDro, and Cochrane Library Plus biomedical databases. The risk of bias was assessed using the RoB2 tool. Randomised controlled clinical trials in which at least 1 of the groups received dry needling were included. 662 studies were found; 14 clinical trials were selected for qualitative analysis and 13 for quantitative analysis. The quality of most of the studies included was "high." All the studies reported improvements in cervical pain and/or disability, regardless of the protocol followed and the muscles targeted. No serious adverse effects were reported. Dry needling showed to be more effective when compared with other therapies in both women and men, without differences by sex. When the analysis was carried out by age, patients over 40 years old benefitted more than those below 40 years old. Our meta-analysis supports the use of dry needling to improve pain and functional capacity in patients with chronic neck pain at short- and mid-term intervals.

本系统综述和荟萃分析的目的是评估干针在改善慢性颈部疼痛患者疼痛和功能能力方面的短期、中期和长期有效性。搜索策略在PubMed、Web of Science、Scopus、PEDro和Cochrane Library Plus生物医学数据库上执行。使用RoB2工具评估偏倚风险。随机对照临床试验包括其中至少1组接受干针治疗。发现662项研究;选择14项临床试验进行定性分析,13项进行定量分析。大多数研究的质量都是“高”的。所有研究都报告了宫颈疼痛和/或残疾的改善,无论遵循的方案和针对的肌肉如何。未报告严重不良反应。与其他疗法相比,干针在女性和男性中都更有效,没有性别差异。当按年龄进行分析时,40岁以上的患者 老年人比40岁以下的人受益更多 岁我们的荟萃分析支持在中短期使用干针来改善慢性颈部疼痛患者的疼痛和功能能力。
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引用次数: 0
Influence of Temperament on the Acceptance of Two Conscious Sedation Techniques in Toddlers Undergoing Dental Treatment: A Randomised Cross Over Trial. 气质对接受牙科治疗的幼儿接受两种有意识镇静技术的影响:一项随机交叉试验。
IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-08-22 eCollection Date: 2023-01-01 DOI: 10.1155/2023/6655628
Palak Janiani, Deepa Gurunathan, Sivakumar Nuvvula

Background: Pediatric dentists often find it challenging to handle pediatric patients due to their fear, unease, and anxiety toward dental procedures. To address this, sedation agents such as intranasal midazolam and nitrous oxide are commonly used as pharmacological behavior management methods. A child's temperament affects their behavior in unfamiliar settings.

Aim: To study the effect of child temperament on the acceptance of the nasal mask and intranasal drug administration in children undergoing dental treatment.

Methods: Thirty-two anxious children aged three to five were randomly assigned to two groups. During the first visit, one group received intranasal midazolam sedation, while the other group received nitrous oxide administered through a mask. On the subsequent visit, the groups crossed over. The parent assessed the child's temperament, and the acceptance of the sedation methods was recorded. The Ohio State University Behavioral Rating Scale (OSUBRS) was employed to assess behavior during the administration of local anesthesia. Statistical analysis was carried out using the chi-square test and Mann-Whitney U test (p value <0.05).

Results: Children exhibited greater acceptance of the nasal mask compared to using the intranasal route for delivering midazolam during the induction process. A significant statistical influence of temperament was observed on the acceptance of the nasal mask and the intranasal atomisation device (p value <0.05). The mean OSUBRS scores did not show any statistically significant differences between the sedation groups (p = 0.14).

Conclusion: Most children demonstrated a more favorable acceptance of the nasal mask during the induction process; however, intranasal midazolam can serve as an effective alternative for anxious patients who struggle to keep the nitrous oxide mask on during the dental procedure. The adoption of these methods is influenced directly by the child's temperament.

背景:由于儿科患者对牙科手术的恐惧、不安和焦虑,儿科牙医经常发现处理他们很有挑战性。为了解决这一问题,镇静剂,如鼻内咪唑安定和一氧化二氮,通常被用作药理学行为管理方法。孩子的气质会影响他们在陌生环境中的行为。目的:研究儿童气质对接受牙科治疗的儿童接受鼻罩和鼻内给药的影响。方法:将32名3~5岁的焦虑儿童随机分为两组。在第一次就诊期间,一组接受了咪达唑仑鼻内镇静,而另一组则通过面罩给予一氧化二氮。在随后的访问中,这些小组进行了交叉访问。父母评估了孩子的气质,并记录了对镇静方法的接受程度。俄亥俄州立大学行为评定量表(OSUBRS)用于评估局部麻醉期间的行为。使用卡方检验和Mann-Whitney U检验进行统计分析(p值结果:与诱导过程中使用鼻内途径递送咪达唑仑相比,儿童对鼻面罩的接受度更高。观察到气质对鼻面罩和鼻内雾化装置的接受度有显著的统计影响(p值p = 0.14)。结论:大多数儿童在诱导过程中对鼻面罩表现出更有利的接受度;然而,对于那些在牙科手术中难以戴上一氧化二氮口罩的焦虑患者,咪达唑仑可以作为一种有效的替代品。这些方法的采用直接受到孩子气质的影响。
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引用次数: 0
Application of Ketamine in Pain Management and the Underlying Mechanism. 氯胺酮在疼痛管理中的应用及其潜在机制。
IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-08-16 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1928969
Xiaofan Ma, Jia Yan, Hong Jiang

Since ketamine was approved by the FDA as an intravenous anesthetic, it has been in clinical use for more than 50 years. Apart from its anesthetic effects, ketamine is one of the few intravenous anesthetics with potent analgesic properties. As part of the effort to develop pain management, renewed interest has focused on the use of ketamine for the treatment of acute and chronic pain. Ketamine is commonly used to treat various kinds of chronic pain syndromes and is also applied to control perioperative pain and reduce the consumption of postoperative analgesics. However, its precise mechanisms of action remain mysterious for a large part. Despite extensive research in the field, the mechanism of ketamine is still unclear. Its analgesic effect appears to be largely mediated by blockade of NMDARs, but opioid, GABA, and monoaminergic system seem to partly participate in the pain transmission procedure. Its metabolites also have an analgesic effect, which may prolong pain relief. More recently, the antidepressant effect of ketamine has been considered to reduce pain-related aversion to relieve chronic pain. Overall, the analgesic mechanism of ketamine seems to be a complex combination of multiple factors. Due to its potent analgesic properties, ketamine is an analgesic with great clinical application prospects. Exploring the precise mechanism of action of ketamine will help guide clinical medication and confirm indications for ketamine analgesia. This review aims to list the application of ketamine in pain management and discuss its analgesic mechanism.

自从氯胺酮被美国食品药品监督管理局批准为静脉麻醉药以来,它已经在临床上使用了50多年 年。除了麻醉作用外,氯胺酮是为数不多的具有强效镇痛特性的静脉麻醉药之一。作为开发疼痛管理的努力的一部分,人们重新关注氯胺酮用于治疗急性和慢性疼痛。氯胺酮通常用于治疗各种慢性疼痛综合征,也用于控制围手术期疼痛和减少术后镇痛药的消耗。然而,它的确切作用机制在很大程度上仍然是神秘的。尽管在该领域进行了广泛的研究,但氯胺酮的作用机制仍不清楚。其镇痛作用似乎主要由NMDARs的阻断介导,但阿片类药物、GABA和单胺类系统似乎部分参与了疼痛传递过程。其代谢产物还具有镇痛作用,可以延长疼痛缓解时间。最近,氯胺酮的抗抑郁作用被认为可以减少与疼痛相关的厌恶,从而缓解慢性疼痛。总体而言,氯胺酮的镇痛机制似乎是多种因素的复杂组合。氯胺酮具有较强的镇痛作用,是一种具有良好临床应用前景的镇痛药。探讨氯胺酮的确切作用机制将有助于指导临床用药和确定氯胺酮镇痛的适应证。本综述旨在列举氯胺酮在疼痛管理中的应用,并讨论其镇痛机制。
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引用次数: 0
The Efficacy of Manual Therapy and Pressure Biofeedback-Guided Deep Cervical Flexor Muscle Strength Training on Pain and Functional Limitations in Individuals with Cervicogenic Headaches: A Randomized Comparative Study. 手动治疗和压力生物反馈引导的颈深屈肌力量训练对颈源性头痛患者疼痛和功能限制的疗效:一项随机比较研究。
IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-08-14 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1799005
Shahnaz Hasan, Nasrin Bharti, Ahmad H Alghadir, Amir Iqbal, Naiyer Shahzad, Abeer R Ibrahim

Objective: This study aimed to compare the efficacy of manual therapy and pressure biofeedback-guided DCFM strength training on pain intensity and functional limitations in individuals with CGH. Trial Design. A double-blinded, two-arm parallel group randomized comparative design.

Methods: After applying the eligibility criteria, sixty out of eighty-nine CGH patients were recruited from King Saud University Medical Center in Riyadh and randomly allocated to intervention groups using simple random sampling. Group 1 underwent pressure biofeedback-guided DCFM strength training and conventional treatment, while Group 2 received manual therapy and conventional treatment for three consecutive weeks. The main outcome measures were scores on the visual analog scale (VAS) and the headache disability index (HDI). One assessor and two physical therapists were blinded to group allocation.

Results: Sixty out of eighty participants aged 29-40 years were randomized into intervention groups (n = 30/group; age (mean ± standard deviation): group 1 = 35.0 ± 2.82; group 2 = 34.87 ± 2.60), and their data were analyzed. A significant improvement (95% CI, p < 0.05) was observed within each group when comparing the VAS and HDI scores between baseline and postintervention. In contrast, between-group comparisons for the outcome score of VAS and HDI revealed nonsignificant differences in the first, second, and third weeks after intervention, except for the VAS score, which showed a significant difference in weeks 2 and 3 after intervention. Cohen's d-value indicated that the intervention effect size for reducing pain was larger in group 1 than in group 2 at weeks 2 and 3.

Conclusion: Compared with manual therapy, pressure biofeedback-guided DCFM strength training showed a greater reduction in pain intensity (assessed using the VAS) at weeks two and three. However, both treatments were equally effective in lowering headache-related functional limitations in patients with CGH. This trial is registered with ClinicalTrial.gov PRS (Identifier ID: NCT05692232).

目的:本研究旨在比较手法治疗和压力生物反馈引导的DCFM力量训练对CGH患者疼痛强度和功能限制的疗效。试验设计。双盲、双臂平行组随机对照设计。方法:在应用资格标准后,从利雅得沙特国王大学医学中心招募了89名CGH患者中的60名,并使用简单随机抽样将其随机分配到干预组。第1组接受了压力生物反馈指导的DCFM力量训练和常规治疗,而第2组接受了连续三周的手动治疗和常规治疗。主要的结果指标是视觉模拟评分(VAS)和头痛残疾指数(HDI)。一名评估员和两名物理治疗师对小组分配视而不见。结果:80名参与者中有60名年龄在29-40岁之间 年被随机分为干预组(n = 30/组;年龄(平均值 ± 标准偏差):组1 = 35 ± 2.82;第2组 = 34.87 ± 2.60),并对其数据进行了分析。当比较基线和干预后的VAS和HDI评分时,观察到各组有显著改善(95%CI,p<0.05)。相反,VAS和HDI结果评分的组间比较显示,在干预后的第一、第二和第三周,除了VAS评分外,没有显著差异,VAS评分在干预后第2和第3周显示出显著差异。Cohen的d值表明,在第2周和第3周,第1组减轻疼痛的干预效果大于第2组。然而,两种治疗方法在降低CGH患者头痛相关功能限制方面同样有效。该试验已在ClinicalTrial.gov PRS注册(标识符ID:NCT05692232)。
{"title":"The Efficacy of Manual Therapy and Pressure Biofeedback-Guided Deep Cervical Flexor Muscle Strength Training on Pain and Functional Limitations in Individuals with Cervicogenic Headaches: A Randomized Comparative Study.","authors":"Shahnaz Hasan,&nbsp;Nasrin Bharti,&nbsp;Ahmad H Alghadir,&nbsp;Amir Iqbal,&nbsp;Naiyer Shahzad,&nbsp;Abeer R Ibrahim","doi":"10.1155/2023/1799005","DOIUrl":"10.1155/2023/1799005","url":null,"abstract":"<p><strong>Objective: </strong>This study aimed to compare the efficacy of manual therapy and pressure biofeedback-guided DCFM strength training on pain intensity and functional limitations in individuals with CGH. <i>Trial Design</i>. A double-blinded, two-arm parallel group randomized comparative design.</p><p><strong>Methods: </strong>After applying the eligibility criteria, sixty out of eighty-nine CGH patients were recruited from King Saud University Medical Center in Riyadh and randomly allocated to intervention groups using simple random sampling. Group 1 underwent pressure biofeedback-guided DCFM strength training and conventional treatment, while Group 2 received manual therapy and conventional treatment for three consecutive weeks. The main outcome measures were scores on the visual analog scale (VAS) and the headache disability index (HDI). One assessor and two physical therapists were blinded to group allocation.</p><p><strong>Results: </strong>Sixty out of eighty participants aged 29-40 years were randomized into intervention groups (<i>n</i> = 30/group; age (mean ± standard deviation): group 1 = 35.0 ± 2.82; group 2 = 34.87 ± 2.60), and their data were analyzed. A significant improvement (95% CI, <i>p</i> < 0.05) was observed within each group when comparing the VAS and HDI scores between baseline and postintervention. In contrast, between-group comparisons for the outcome score of VAS and HDI revealed nonsignificant differences in the first, second, and third weeks after intervention, except for the VAS score, which showed a significant difference in weeks 2 and 3 after intervention. Cohen's <i>d</i>-value indicated that the intervention effect size for reducing pain was larger in group 1 than in group 2 at weeks 2 and 3.</p><p><strong>Conclusion: </strong>Compared with manual therapy, pressure biofeedback-guided DCFM strength training showed a greater reduction in pain intensity (assessed using the VAS) at weeks two and three. However, both treatments were equally effective in lowering headache-related functional limitations in patients with CGH. This trial is registered with ClinicalTrial.gov PRS (Identifier ID: NCT05692232).</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2023 ","pages":"1799005"},"PeriodicalIF":2.9,"publicationDate":"2023-08-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10442171/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10433384","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}
引用次数: 0
Artificial Intelligence for Automatic Pain Assessment: Research Methods and Perspectives. 用于自动疼痛评估的人工智能:研究方法与展望
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-06-28 eCollection Date: 2023-01-01 DOI: 10.1155/2023/6018736
Marco Cascella, Daniela Schiavo, Arturo Cuomo, Alessandro Ottaiano, Francesco Perri, Renato Patrone, Sara Migliarelli, Elena Giovanna Bignami, Alessandro Vittori, Francesco Cutugno

Although proper pain evaluation is mandatory for establishing the appropriate therapy, self-reported pain level assessment has several limitations. Data-driven artificial intelligence (AI) methods can be employed for research on automatic pain assessment (APA). The goal is the development of objective, standardized, and generalizable instruments useful for pain assessment in different clinical contexts. The purpose of this article is to discuss the state of the art of research and perspectives on APA applications in both research and clinical scenarios. Principles of AI functioning will be addressed. For narrative purposes, AI-based methods are grouped into behavioral-based approaches and neurophysiology-based pain detection methods. Since pain is generally accompanied by spontaneous facial behaviors, several approaches for APA are based on image classification and feature extraction. Language features through natural language strategies, body postures, and respiratory-derived elements are other investigated behavioral-based approaches. Neurophysiology-based pain detection is obtained through electroencephalography, electromyography, electrodermal activity, and other biosignals. Recent approaches involve multimode strategies by combining behaviors with neurophysiological findings. Concerning methods, early studies were conducted by machine learning algorithms such as support vector machine, decision tree, and random forest classifiers. More recently, artificial neural networks such as convolutional and recurrent neural network algorithms are implemented, even in combination. Collaboration programs involving clinicians and computer scientists must be aimed at structuring and processing robust datasets that can be used in various settings, from acute to different chronic pain conditions. Finally, it is crucial to apply the concepts of explainability and ethics when examining AI applications for pain research and management.

虽然正确的疼痛评估是确定适当疗法的必要条件,但自我报告的疼痛程度评估存在一些局限性。数据驱动的人工智能(AI)方法可用于自动疼痛评估(APA)研究。我们的目标是开发客观、标准化和可推广的工具,用于不同临床环境下的疼痛评估。本文旨在讨论 APA 在研究和临床场景中应用的研究现状和前景。本文将讨论人工智能功能的原理。为了便于叙述,本文将人工智能方法分为基于行为学的方法和基于神经生理学的疼痛检测方法。由于疼痛通常伴随着自发的面部行为,因此有几种 APA 方法是基于图像分类和特征提取的。通过自然语言策略、身体姿势和呼吸衍生元素获得的语言特征是其他基于行为的研究方法。基于神经生理学的疼痛检测是通过脑电图、肌电图、皮肤电活动和其他生物信号获得的。最近的方法通过将行为与神经生理学发现相结合,采用了多模式策略。在方法方面,早期的研究采用机器学习算法,如支持向量机、决策树和随机森林分类器。最近,卷积神经网络和递归神经网络等人工神经网络算法也开始应用,甚至是结合使用。临床医生和计算机科学家的合作计划必须以构建和处理强大的数据集为目标,这些数据集可用于从急性疼痛到不同慢性疼痛的各种情况。最后,在研究人工智能在疼痛研究和管理中的应用时,应用可解释性和伦理概念至关重要。
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引用次数: 0
Scraping Therapy Improved Muscle Regeneration through Regulating GLUT4/Glycolytic and AMPK/mTOR/4EBP1 Pathways in Rats with Lumbar Multifidus Injury. 刮痧疗法通过调节GLUT4/糖酵解和AMPK/mTOR/4EBP1通路促进腰椎多裂肌损伤大鼠肌肉再生。
IF 2.9 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-06-22 eCollection Date: 2023-01-01 DOI: 10.1155/2023/8870256
Bin Zou, Juan Du, Qiwen Xuan, Yajing Wang, Zixiao Wang, Wen Zhang, Lianghua Wang, Wei Gu

Background: High morbidity of nonspecific low back pain (NLBP) and large consumption of medical resources caused by it have become a heavy social burden. There are many factors inducing NLBP, among which the damage and atrophy of multifidus (MF) are most closely related to NLBP. Scraping therapy can have significant treatment effects on NLBP with fewer adverse reactions and less medical fund input than other modalities or medications. However, the mechanism of scraping therapy treating NLBP remains unclarified. Here, we wanted to investigate the effects of scraping therapy on promoting MF regeneration and the underlying mechanisms.

Methods: A total of 54 male rats (SD, 6-7 weeks old) were randomly divided into nine groups, namely, K, M6h, M1d, M2d, M3d, G6h, G1d, G2d, and G3d, with six rats in each group. They were injected with bupivacaine (BPVC) to intentionally induce MF injury. We then performed scraping therapy on the rats that had been randomly chosen and compared treatment effects at different time points. In vitro data including skin temperature and tactile allodynia threshold were collected and histological sections were analyzed. mRNA sequencing was applied to distinguish the genes or signaling pathways that had been altered due to scraping therapy, and the results were further verified through reverse transcription polymerase chain reaction and Western blot analysis.

Results: Transitory petechiae and ecchymosis both on and beneath the rats' skin raised by scraping therapy gradually faded in about 3 d. Cross-sectional area (CSA) of MF was significantly smaller 30 h, 2 d, and 4 d after modeling (P=0.007, P=0.001, and P=0.015, respectively, vs. the blank group) and was significantly larger in the scraping group 1 d after treatment (P=0.002 vs. the model 1d group). Skin temperature significantly increased immediately after scraping (P < 0.001) and hindlimb pain threshold increased on the 2nd day after scraping (P=0.046 and P=0.028, respectively). 391 differentially expressed genes and 8 signaling pathways were characterized 6 h after scraping; only 3 differentially expressed genes and 3 signaling pathways were screened out 2 d after treatment. The amounts of mRNAs or proteins for GLUT4, HK2, PFKM, PKM, LDHA (which belong to the GLUT4/glycolytic pathway), p-mTOR, p-4EBP1 (which belong to the AMPK/mTOR/4EBP1 pathway), and BDH1 were enhanced, and p-AMPKα was decreased after scraping therapy.

Conclusions: Scraping therapy has therapeutic effects on rats with multifidus injury by promoting muscle regeneration via regulating GLUT4/glycolytic and AMPK/mTOR/4EBP1 signaling pathways.

背景:非特异性腰痛(NLBP)发病率高,医疗资源消耗大,已成为一种沉重的社会负担。诱发NLBP的因素很多,其中多裂肌的损伤和萎缩与NLBP关系最为密切。与其他方式或药物相比,刮痧疗法可以对NLBP产生显著的治疗效果,不良反应更少,医疗资金投入更少。然而,刮痧疗法治疗NLBP的机制尚不明确。在这里,我们想研究刮痧疗法对促进MF再生的影响及其潜在机制。方法:共54只雄性大鼠(SD,6-7 周龄)随机分为K、M6h、M1d、M2d、M3d、G6h、G1d、G2d和G3d 9组,每组6只。他们被注射了布比卡因(BPVC)以故意诱导MF损伤。然后,我们对随机选择的大鼠进行刮痧治疗,并比较不同时间点的治疗效果。收集体外数据,包括皮肤温度和触觉异常性疼痛阈值,并分析组织学切片。应用信使核糖核酸测序来区分因刮削治疗而改变的基因或信号通路,并通过逆转录聚合酶链式反应和蛋白质印迹分析进一步验证了结果。结果:刮痧法引起的大鼠皮肤上下的短暂性瘀点和瘀斑在3年左右逐渐消退 d.MF的横截面积(CSA)明显较小30 h、 2 d、 和4 建模后第d天(与空白组相比,分别为P=0.007、P=0.001和P=0.015),刮除组1中明显更大 d(与模型1d组相比P=0.002)。刮削后皮肤温度立即显著升高(P<0.001),后肢疼痛阈值在刮削后第2天升高(分别为P=0.046和P=0.028)。391个差异表达基因和8个信号通路被鉴定6 h刮除后;仅筛选出3个差异表达基因和3个信号通路 d。刮除治疗后,GLUT4、HK2、PFKM、PKM、LDHA(属于GLUT4/糖酵解途径)、p-mTOR、p-4EBP1(属于AMPK/mTOR/4EBP1途径)和BDH1的mRNA或蛋白质数量增加,p-AMPKα减少。结论:刮痧疗法通过调节GLUT4/糖酵解和AMPK/mTOR/4EBP1信号通路促进肌肉再生,对多裂肌损伤大鼠具有治疗作用。
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引用次数: 0
Analgesic Effect of Passive Range-of-Motion Exercise on the Healthy Side for Pain after Total Knee Arthroplasty: A Prospective Randomized Trial. 全膝关节置换术后健侧被动活动范围锻炼对疼痛的镇痛效果:前瞻性随机试验。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-06-14 eCollection Date: 2023-01-01 DOI: 10.1155/2023/1613116
Shuichi Eto, Motoki Sonohata, Yasuo Takei, Masaya Ueno, Norio Fukumori, Masaaki Mawatari

Background: Exercise can reduce the pain threshold momentarily and induce analgesia, which is called exercise-induced hypoalgesia (EIH). Exercise therapy for inducing EIH may be an effective treatment option for pain. We aimed at investigating whether continuous passive motion (CPM) on both healthy and affected sides could induce EIH and reduce pain in the operated knee in patients after unilateral total knee arthroplasty (TKA). Patients and Methods. In this prospective randomized controlled trial, participants were randomly assigned to two groups: a bilateral group that received bilateral exercise on the operated and healthy sides and a unilateral group that received exercise therapy only on the affected side. We enrolled 40 patients aged ≥60 years who were scheduled to undergo unilateral TKA. Visual analogue scale (VAS) scores and range of motion (ROM) on the operated side were measured immediately before and after CPM on postoperative days 2, 4, 7, and 14. The primary outcome was the difference in the VAS scores before and after CPM on postoperative day 14. The secondary outcome was the difference in the ROM before and after CPM on postoperative day 14.

Results: Comparison of VAS scores before and after CPM showed no significant intergroup differences on all measurement dates. However, there was a significant difference in values on day 14 (P < 0.05). Both groups showed an increase in ROM after CPM, with significant increments observed on days 2 and 4 in the bilateral group and on day 14 in the unilateral group. There was no significant difference in values on postoperative day 14.

Conclusion: Post-TKA pain was reduced by performing the same exercise on the healthy knee during CPM therapy. This could be due to EIH, and the results indicated that EIH can also influence postoperative pain immediately after surgery.

背景:运动可瞬间降低疼痛阈值并诱导镇痛,这被称为运动诱导低镇痛(EIH)。诱导 EIH 的运动疗法可能是一种有效的疼痛治疗方法。我们的目的是研究单侧全膝关节置换术(TKA)后患者在健侧和患侧进行持续被动运动(CPM)是否能诱导 EIH 并减轻手术膝关节的疼痛。患者和方法。在这项前瞻性随机对照试验中,参与者被随机分配到两组:一组为双侧组,在手术侧和健康侧接受双侧运动;另一组为单侧组,仅在受累侧接受运动疗法。我们招募了 40 名年龄≥60 岁、计划接受单侧 TKA 手术的患者。在术后第 2、4、7 和 14 天,分别在 CPM 之前和之后测量手术侧的视觉模拟量表 (VAS) 评分和活动范围 (ROM)。主要结果是术后第 14 天 CPM 前后 VAS 评分的差异。次要结果是术后第 14 天 CPM 前后 ROM 的差异:结果:CPM前后的VAS评分比较显示,在所有测量日期,组间差异均不显著。然而,第 14 天的数值有明显差异(P < 0.05)。两组患者在 CPM 后的 ROM 均有增加,双侧组在第 2 天和第 4 天,单侧组在第 14 天均有显著增加。术后第14天的数值无明显差异:结论:在 CPM 治疗期间,对健康膝关节进行相同的锻炼可减轻 TKA 术后疼痛。结论:在 CPM 治疗期间对健康膝关节进行相同的锻炼可减轻 TKA 术后疼痛,这可能是 EIH 的作用,结果表明 EIH 也可影响术后疼痛。
{"title":"Analgesic Effect of Passive Range-of-Motion Exercise on the Healthy Side for Pain after Total Knee Arthroplasty: A Prospective Randomized Trial.","authors":"Shuichi Eto, Motoki Sonohata, Yasuo Takei, Masaya Ueno, Norio Fukumori, Masaaki Mawatari","doi":"10.1155/2023/1613116","DOIUrl":"10.1155/2023/1613116","url":null,"abstract":"<p><strong>Background: </strong>Exercise can reduce the pain threshold momentarily and induce analgesia, which is called exercise-induced hypoalgesia (EIH). Exercise therapy for inducing EIH may be an effective treatment option for pain. We aimed at investigating whether continuous passive motion (CPM) on both healthy and affected sides could induce EIH and reduce pain in the operated knee in patients after unilateral total knee arthroplasty (TKA). <i>Patients and Methods</i>. In this prospective randomized controlled trial, participants were randomly assigned to two groups: a bilateral group that received bilateral exercise on the operated and healthy sides and a unilateral group that received exercise therapy only on the affected side. We enrolled 40 patients aged ≥60 years who were scheduled to undergo unilateral TKA. Visual analogue scale (VAS) scores and range of motion (ROM) on the operated side were measured immediately before and after CPM on postoperative days 2, 4, 7, and 14. The primary outcome was the difference in the VAS scores before and after CPM on postoperative day 14. The secondary outcome was the difference in the ROM before and after CPM on postoperative day 14.</p><p><strong>Results: </strong>Comparison of VAS scores before and after CPM showed no significant intergroup differences on all measurement dates. However, there was a significant difference in values on day 14 (<i>P</i> < 0.05). Both groups showed an increase in ROM after CPM, with significant increments observed on days 2 and 4 in the bilateral group and on day 14 in the unilateral group. There was no significant difference in values on postoperative day 14.</p><p><strong>Conclusion: </strong>Post-TKA pain was reduced by performing the same exercise on the healthy knee during CPM therapy. This could be due to EIH, and the results indicated that EIH can also influence postoperative pain immediately after surgery.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2023 ","pages":"1613116"},"PeriodicalIF":2.5,"publicationDate":"2023-06-14","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10284656/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"10089686","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}
引用次数: 0
Analgesic Efficacy of Ketoprofen Transdermal Patch versus Ibuprofen Oral Tablet on Postendodontic Pain in Patients with Irreversible Pulpitis: A Randomized Clinical Trial. 酮洛芬透皮贴剂与布洛芬口服片剂对不可逆牙髓炎患者根管治疗后疼痛的镇痛效果:随机临床试验。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-06-07 eCollection Date: 2023-01-01 DOI: 10.1155/2023/8549655
Saeede Zadsirjan, Amirhossein Toghrolian, Nazanin Zargar

Materials and methods: In this randomized clinical trial, 64 patients who had mandibular first and second molars with irreversible pulpitis were randomly divided into two groups (n = 32) by stratified permuted block randomization. The experimental group used 60 mg KTP every 6 hours, and the control group received 400 mg ibuprofen tablets every 6 hours for 1 day. The severity of pain experienced by patients was quantified before and at 2, 4, 8, 12, 24, and 48 hours after endodontic treatment, using the numerical rating scale (NRS). Data were analyzed by using the t-test, Mann-Whitney test, and generalized estimating equation (GEE) (alpha = 0.05).

Results: The pain score was not significantly different between the two groups at the baseline or any other postoperative time point (P > 0.05). The reduction in the pain score was significant in both groups from 2 to 10 hours and 10 to 48 hours, postoperatively (P < 0.001). The interaction effect of time and group was not significant on the postoperative pain score in the abovementioned time intervals, and the pattern of pain reduction was the same over time in both groups (P > 0.05).

Conclusion: Both KTP and ibuprofen effectively decreased postendodontic pain. Considering the comparable pattern of pain reduction, KTP can be used as an alternative to ibuprofen tablets for effective pain control after endodontic treatment of mandibular first and second molars with irreversible pulpitis.

材料和方法:在这项随机临床试验中,64 名患有下颌第一和第二磨牙不可逆牙髓炎的患者通过分层包块随机法被随机分为两组(n = 32)。实验组每 6 小时服用 60 毫克 KTP,对照组每 6 小时服用 400 毫克布洛芬片,共服用 1 天。在牙髓治疗前和治疗后 2、4、8、12、24 和 48 小时,使用数字评分量表(NRS)对患者疼痛的严重程度进行量化。数据分析采用 t 检验、曼-惠特尼检验和广义估计方程(GEE)(α = 0.05):结果:两组患者的疼痛评分在基线和术后其他时间点均无明显差异(P>0.05)。在术后 2 至 10 小时和 10 至 48 小时内,两组的疼痛评分均有显著降低(P < 0.001)。在上述时间间隔内,时间和组别的交互作用对术后疼痛评分的影响不显著,两组的疼痛减轻模式随时间变化相同(P > 0.05):结论:KTP和布洛芬都能有效减轻牙髓术后疼痛。结论:KTP 和布洛芬都能有效减轻牙髓治疗后的疼痛,考虑到两者减轻疼痛的模式具有可比性,KTP 可作为布洛芬片的替代药物,用于不可逆性牙髓炎下颌第一和第二磨牙牙髓治疗后的有效止痛。
{"title":"Analgesic Efficacy of Ketoprofen Transdermal Patch versus Ibuprofen Oral Tablet on Postendodontic Pain in Patients with Irreversible Pulpitis: A Randomized Clinical Trial.","authors":"Saeede Zadsirjan, Amirhossein Toghrolian, Nazanin Zargar","doi":"10.1155/2023/8549655","DOIUrl":"10.1155/2023/8549655","url":null,"abstract":"<p><strong>Materials and methods: </strong>In this randomized clinical trial, 64 patients who had mandibular first and second molars with irreversible pulpitis were randomly divided into two groups (<i>n</i> = 32) by stratified permuted block randomization. The experimental group used 60 mg KTP every 6 hours, and the control group received 400 mg ibuprofen tablets every 6 hours for 1 day. The severity of pain experienced by patients was quantified before and at 2, 4, 8, 12, 24, and 48 hours after endodontic treatment, using the numerical rating scale (NRS). Data were analyzed by using the <i>t</i>-test, Mann-Whitney test, and generalized estimating equation (GEE) (alpha = 0.05).</p><p><strong>Results: </strong>The pain score was not significantly different between the two groups at the baseline or any other postoperative time point (<i>P</i> > 0.05). The reduction in the pain score was significant in both groups from 2 to 10 hours and 10 to 48 hours, postoperatively (<i>P</i> < 0.001). The interaction effect of time and group was not significant on the postoperative pain score in the abovementioned time intervals, and the pattern of pain reduction was the same over time in both groups (<i>P</i> > 0.05).</p><p><strong>Conclusion: </strong>Both KTP and ibuprofen effectively decreased postendodontic pain. Considering the comparable pattern of pain reduction, KTP can be used as an alternative to ibuprofen tablets for effective pain control after endodontic treatment of mandibular first and second molars with irreversible pulpitis.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2023 ","pages":"8549655"},"PeriodicalIF":2.5,"publicationDate":"2023-06-07","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10266914/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9653946","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}
引用次数: 0
Neuropathic Pain Was Associated with Central Sensitivity Syndrome in Patients with Preoperative Lumbar Spinal Stenosis Using the painDETECT and Central Sensitization Inventory Questionnaires: A Cross-Sectional Study. 使用painDETECT和中枢敏感性量表问卷调查术前腰椎管狭窄症患者的神经性疼痛与中枢敏感综合征有关:一项横断面研究。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2023-05-10 eCollection Date: 2023-01-01 DOI: 10.1155/2023/9963627
Rintaro Iwasaki, Takahiro Miki, Mizuki Miyazaki, Chifumi Kanetaka, Tetsuryu Mitsuyama, Kaiji Ota

Background: Lumbar spinal stenosis (LSS) patients have been reported to have neuropathic pain and central sensitivity syndrome (CSS). These associations have been reported in other diseases but are unknown in preoperative LSS patients. We aimed to investigate the association between neuropathic pain and CSS in preoperative LSS patients using the painDETECT and the Central Sensitization Inventory (CSI) questionnaires.

Methods: This cross-sectional study was conducted from November 2021 to March 2022. The data were collected regarding demographics and pain, including neuropathic pain, numbness, LSS severity, physical function, quality of life, and CSS. Patients were divided into two groups, patients with acute and chronic pain, and further classified into three categories based on the clinical phenotype of patients in each group. Independent variables included age, gender, type of LSS (bilateral or unilateral symptoms), Numerical Rating Scale of leg pain, CSI, and the Zurich Claudication Questionnaire (ZCQ) for symptom severity and physical function. The dependent variable was painDETECT. Multiple regression analysis using the forced entry method examined the association between painDETECT and CSI.

Results: Of the 119 patients with preoperative LSS, 106 were included. The mean age of the participants was 69.9 years, and 45.3% were female. Neuropathic pain was present in 19.8%, and CSS was present in 10.4%. The CSI (β = 0.468, p < 0.001) and ZCQ for symptom severity (β = 0.304, p < 0.01) were significantly associated with the painDETECT, explaining 47.8% of the variance in the painDETECT score.

Conclusions: There is an association between neuropathic pain and CSS in patients with preoperative LSS using the painDETECT and CSI questionnaires.

背景:据报道,腰椎管狭窄症(LSS)患者会出现神经性疼痛和中枢敏感综合征(CSS)。这些关联在其他疾病中也有报道,但在术前腰椎管狭窄症患者中尚属未知。我们的目的是使用疼痛检测法(painDETECT)和中枢敏感性量表(CSI)问卷调查术前 LSS 患者的神经病理性疼痛和 CSS 之间的关联:这项横断面研究于 2021 年 11 月至 2022 年 3 月进行。研究收集了有关人口统计学和疼痛的数据,包括神经病理性疼痛、麻木、LSS 严重程度、身体功能、生活质量和 CSS。患者被分为急性疼痛和慢性疼痛两组,并根据每组患者的临床表型进一步分为三类。自变量包括年龄、性别、LSS 类型(双侧或单侧症状)、腿痛数字评分量表、CSI 和苏黎世跛行问卷 (ZCQ),用于评估症状严重程度和身体功能。因变量为 painDETECT。使用强制进入法进行的多元回归分析检验了 painDETECT 和 CSI 之间的关联:结果:在 119 名术前 LSS 患者中,有 106 人被纳入研究。参与者的平均年龄为 69.9 岁,45.3% 为女性。19.8%的患者存在神经性疼痛,10.4%的患者存在 CSS。CSI (β = 0.468, p < 0.001)和症状严重程度 ZCQ (β = 0.304, p < 0.01)与疼痛DETECT显著相关,解释了47.8%的疼痛DETECT得分差异:结论:使用painDETECT和CSI问卷调查术前LSS患者的神经性疼痛与CSS之间存在关联。
{"title":"Neuropathic Pain Was Associated with Central Sensitivity Syndrome in Patients with Preoperative Lumbar Spinal Stenosis Using the painDETECT and Central Sensitization Inventory Questionnaires: A Cross-Sectional Study.","authors":"Rintaro Iwasaki, Takahiro Miki, Mizuki Miyazaki, Chifumi Kanetaka, Tetsuryu Mitsuyama, Kaiji Ota","doi":"10.1155/2023/9963627","DOIUrl":"10.1155/2023/9963627","url":null,"abstract":"<p><strong>Background: </strong>Lumbar spinal stenosis (LSS) patients have been reported to have neuropathic pain and central sensitivity syndrome (CSS). These associations have been reported in other diseases but are unknown in preoperative LSS patients. We aimed to investigate the association between neuropathic pain and CSS in preoperative LSS patients using the painDETECT and the Central Sensitization Inventory (CSI) questionnaires.</p><p><strong>Methods: </strong>This cross-sectional study was conducted from November 2021 to March 2022. The data were collected regarding demographics and pain, including neuropathic pain, numbness, LSS severity, physical function, quality of life, and CSS. Patients were divided into two groups, patients with acute and chronic pain, and further classified into three categories based on the clinical phenotype of patients in each group. Independent variables included age, gender, type of LSS (bilateral or unilateral symptoms), Numerical Rating Scale of leg pain, CSI, and the Zurich Claudication Questionnaire (ZCQ) for symptom severity and physical function. The dependent variable was painDETECT. Multiple regression analysis using the forced entry method examined the association between painDETECT and CSI.</p><p><strong>Results: </strong>Of the 119 patients with preoperative LSS, 106 were included. The mean age of the participants was 69.9 years, and 45.3% were female. Neuropathic pain was present in 19.8%, and CSS was present in 10.4%. The CSI (<i>β</i> = 0.468, <i>p</i> < 0.001) and ZCQ for symptom severity (<i>β</i> = 0.304, <i>p</i> < 0.01) were significantly associated with the painDETECT, explaining 47.8% of the variance in the painDETECT score.</p><p><strong>Conclusions: </strong>There is an association between neuropathic pain and CSS in patients with preoperative LSS using the painDETECT and CSI questionnaires.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2023 ","pages":"9963627"},"PeriodicalIF":2.5,"publicationDate":"2023-05-10","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10191751/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9562354","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}
引用次数: 0
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Pain Research & Management
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