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Characteristics and Outcomes of Patients Receiving Physical Therapy for Low Back Pain with a Nociplastic Pain Presentation: A Secondary Analysis. 以伤害性疼痛为表现的腰痛患者接受物理治疗的特点和结果:一项次要分析。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/5326261
Abigail T Wilson, Joseph L Riley, Mark D Bishop, Jason M Beneciuk, Yenisel Cruz-Almeida, Joel E Bialosky

Introduction: Individuals with low back pain (LBP) may be classified based on mechanistic descriptors, such as a nociplastic pain presentation (NPP). The purpose of this secondary analysis was to examine the frequency and characteristics of patients with a NPP referred to physical therapy with LBP. Additionally, we characterized patients with LBP meeting the criteria for NPP by demographic, clinical, psychological, and pain sensitivity variables. Finally, we examined short- and long-term clinical outcomes in patients with a NPP compared to those without a NPP.

Materials and methods: Patients referred to physical therapy for LBP completed the Patient Self-report Survey for the Assessment of Fibromyalgia. Participants were categorized as "LBP with NPP" or "LBP without NPP" based on the threshold established in this measure. A rank sum test examined for differences in pain-related psychological factors and pressure-pain threshold between groups. Next, a Friedman test examined if LBP intensity and disability trajectories differed by groups at one and six months after initiation of physical therapy.

Results: 22.2% of patients referred to physical therapy for LBP met the criteria for a NPP. Patients with a NPP reported significantly greater disability, pain catastrophizing, depression, anxiety, and somatization compared to individuals without a NPP (p < 0.05). Pressure-pain threshold did not differ between groups (p > 0.05). Individuals with LBP with a NPP demonstrated nonsignificant, small to medium reductions in pain and disability at one and six months. Individuals experiencing LBP without a NPP demonstrated significant reductions in pain and disability in the short- and long term.

Conclusion: Patients with LBP with a NPP displayed greater negative pain-related psychological factors but similar pain sensitivity compared to LBP without NPP.

摘要:下腰痛(LBP)患者可根据机制描述进行分类,如致伤性疼痛表现(NPP)。这一次要分析的目的是检查NPP患者采用腰痛物理治疗的频率和特征。此外,我们通过人口统计学、临床、心理和疼痛敏感性变量来描述符合NPP标准的LBP患者。最后,我们比较了NPP患者与非NPP患者的短期和长期临床结果。材料与方法:经物理治疗的腰痛患者完成《纤维肌痛患者自我报告调查》。根据该测量中建立的阈值,将参与者分为“有NPP的LBP”或“没有NPP的LBP”。秩和检验检验了组间疼痛相关心理因素和压痛阈值的差异。接下来,弗里德曼测试检查了在物理治疗开始后1个月和6个月各组的腰痛强度和残疾轨迹是否不同。结果:22.2%的腰痛患者接受物理治疗符合NPP标准。与没有NPP的患者相比,NPP患者报告的残疾、疼痛灾难化、抑郁、焦虑和躯体化显著增加(p < 0.05)。压痛阈值组间差异无统计学意义(p > 0.05)。在1个月和6个月时,具有NPP的LBP患者在疼痛和残疾方面表现出不显著的、小到中等程度的减轻。在没有NPP的情况下经历LBP的个体在短期和长期内都表现出疼痛和残疾的显著减少。结论:与未发生NPP的LBP患者相比,有NPP的LBP患者表现出更多的负性疼痛相关心理因素,但疼痛敏感性相似。
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引用次数: 1
Erector Spinae Plane (ESP) Block for Postoperative Pain Management after Open Oncologic Abdominal Surgery. 直立脊柱平面(ESP)阻滞用于腹部开放性肿瘤手术术后疼痛管理。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9010753
Michael Dubilet, Benjamin F Gruenbaum, Michael Semyonov, Shlomo Yaron Ishay, Anton Osyntsov, Michael Friger, Alexander Geftler, Alexander Zlotnik, Evgeni Brotfain

Patients undergoing abdominal oncologic surgical procedures require particular surgical and anesthesiologic considerations. Traditional pain management, such as opiate treatment, continuous epidural analgesia, and non-opioid drugs, may have serious side effects in this patient population. We evaluated erector spinae plane (ESP) blocks for postoperative pain management following elective oncologic abdominal surgeries. In this single-center, prospective, and randomized study, we recruited 100 patients who underwent elective oncological abdominal surgery between December 2020 and January 2022 at Soroka University Medical Center in Beer Sheva, Israel. We compared postoperative pain levels in patients who were treated with a preincisional ESP block in addition to traditional pain management with intravenous opioids, non-steroidal anti-inflammatory drugs (NSAIDs), and acetaminophen, compared to patients who were only given traditional pain management (control). Patients who were treated with a preincisional ESP block demonstrated significantly lower Visual Analog Scale scores at 60 minutes and 4, 8, and 12 hours following the surgery, compared to the control group (p < 0.001). Accordingly, patients in the ESP group required less morphine from 60 minutes to 12 hours after surgery, but they required increased non-opioid postoperative analgesia management at 4, 8, and 12 hours after surgery (p from 0.002 to <0.001) compared to the control group. In this study, we found ESP blocks to be a safe, technically simple, and effective treatment for postoperative pain management after elective oncologic abdominal procedures.

接受腹部肿瘤外科手术的患者需要特殊的手术和麻醉考虑。传统的疼痛管理,如阿片类药物治疗、持续硬膜外镇痛和非阿片类药物,可能对这类患者有严重的副作用。我们评估了直立脊柱平面(ESP)阻滞在选择性腹部肿瘤手术后疼痛管理中的作用。在这项单中心、前瞻性、随机研究中,我们招募了100名患者,他们于2020年12月至2022年1月在以色列比尔舍瓦的索罗卡大学医学中心接受了选择性腹部肿瘤手术。我们比较了除传统的静脉注射阿片类药物、非甾体抗炎药(NSAIDs)和对乙酰氨基酚镇痛外,还接受手术前ESP阻滞治疗的患者与仅接受传统疼痛治疗(对照组)的患者的术后疼痛水平。与对照组相比,接受手术前ESP阻断治疗的患者在手术后60分钟、4小时、8小时和12小时的视觉模拟量表评分显著降低(p < 0.001)。因此,ESP组患者在术后60分钟至12小时内需要较少的吗啡,但在术后4、8和12小时,他们需要增加非阿片类药物的术后镇痛管理(p从0.002到0.002)
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引用次数: 0
Comparison of the Postoperative Analgesic Effects between Ultrasound-Guided Transmuscular Quadratus Lumborum Block and Thoracic Paravertebral Block in Laparoscopic Partial Nephrectomy Patients: A Randomized, Controlled, and Noninferiority Study. 超声引导下经腰方肌阻滞与胸椎旁阻滞在腹腔镜部分肾切除术患者术后镇痛效果的比较:一项随机、对照、非效性研究。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/8652596
Jin Wang, Xulei Cui, Liying Ren, Xu Li, Yuelun Zhang, Yi Xie, Zhigang Ji, Yuguang Huang

Background: This prospective, randomized, double-blinded, noninferiority study aimed to compare the effects of analgesia and recovery between transmuscular quadratus lumborum block (TMQLB) and paravertebral block (PVB).

Methods: Sixty-eight, American Society of Anesthesiologists level I-III patients, who underwent laparoscopic partial nephrectomy in Peking Union Medical College Hospital were randomly allocated to either TMQLB or PVB group (independent variable) in a 1 : 1 ratio. The TMQLB and PVB groups received corresponding regional anesthesia preoperatively with 0.4 ml/kg of 0.5% ropivacaine and follow-up at postoperative 4, 12, 24, and 48 hours. The participants and outcome assessors were blinded to group allocation. We hypothesized that the primary outcome, postoperative 48-hour cumulative morphine consumption, in the TMQLB group was not more than 50% of that in the PVB group. Secondary outcomes including pain numerical rating scales (NRS) and postoperative recovery data were dependent variables.

Results: Thirty patients in each group completed the study. The postoperative 48-hour cumulative morphine consumption was 10.60 ± 5.28 mg in the TMQLB group and 6.40 ± 3.40 mg in the PVB group. The ratio (TMQLB versus PVB) of postoperative 48-hour morphine consumption was 1.29 (95% CI: 1.13-1.48), indicating a noninferior analgesic effect of TMQLB to PVB. The sensory block range was wider in the TMQLB group than in the PVB group (difference 2 dermatomes, 95% CI 1 to 4 dermatomes, P=0.004). The intraoperative analgesic dose was higher in the TMQLB group than in the PVB group (difference 32 µg, 95% CI: 3-62 µg, P=0.03). The postoperative pain NRS at rest and on movement, incidences of side effects, anesthesia-related satisfaction, and quality of recovery scores were similar between the two groups (all P  >  0.05).

Conclusions: The postoperative 48-hour analgesic effect of TMQLB was noninferior to that of PVB in laparoscopic partial nephrectomy. This trial is registered with NCT03975296.

背景:这项前瞻性、随机、双盲、非低效性研究旨在比较经肌腰方肌阻滞(TMQLB)和椎旁阻滞(PVB)在镇痛和恢复方面的效果。方法:68例在北京联合医院行腹腔镜肾部分切除术的美国麻醉师学会I-III级患者按1:1的比例随机分为TMQLB组和PVB组(自变量)。TMQLB组和PVB组术前给予0.5%罗哌卡因0.4 ml/kg相应区域麻醉,术后4、12、24、48小时随访。参与者和结果评估者对分组分配不知情。我们假设TMQLB组的主要结局,术后48小时吗啡累积用量,不超过PVB组的50%。次要结局包括疼痛数值评定量表(NRS)和术后恢复数据是因变量。结果:每组30例患者完成研究。TMQLB组术后48小时吗啡累计用量为10.60±5.28 mg, PVB组术后48小时吗啡累计用量为6.40±3.40 mg。术后48小时吗啡用量之比(TMQLB与PVB)为1.29 (95% CI: 1.13-1.48),表明TMQLB对PVB具有非劣效镇痛作用。TMQLB组感觉阻滞范围较PVB组宽(差异2个皮节,95% CI 1 ~ 4个皮节,P=0.004)。TMQLB组术中镇痛剂量高于PVB组(差异32µg, 95% CI: 3 ~ 62µg, P=0.03)。两组患者术后静息、运动疼痛NRS、不良反应发生率、麻醉相关满意度、恢复质量评分比较,差异均无统计学意义(P > 0.05)。结论:TMQLB在腹腔镜部分肾切除术后48h的镇痛效果不逊于PVB。本试验注册号为NCT03975296。
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引用次数: 0
Ultrasound-Guided Rhomboid Block versus Paravertebral Block in Postoperative Analgesia for Video-Assisted Thoracoscopic Surgery: A Prospective Randomized Controlled Clinical Trial. 超声引导下菱形阻滞与椎旁阻滞在视频胸腔镜手术术后镇痛中的对比:一项前瞻性随机对照临床试验。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/3924511
Yan Wang, Xiaoping Gu, Simin Huang, Minke Shi, Xiaofeng He, Zhengliang Ma

Introduction: The anesthetic efficacy of the ultrasound-guided rhomboid intercostal block (RIB) in alleviating postoperative pain has been well concerned. This study aims to compare the effectiveness between ultrasound-guided RIB and paravertebral block (PVB) in alleviating acute pain following video-assisted thoracic surgery.

Methods: It was a prospective, randomized, double-blinded clinical trial involving 132 patients with video-assisted thoracic surgery divided into three groups: the general anesthesia (GA) group, RIB group, and PVB group on T5 vertebra, using 0.4% ropivacaine at 3 mg/kg, registered in the Chinese Clinical Trial Registry (ChiCTR2100054057, "https://www.chictr.org.cn"). The visual analogue scale (VAS) scores at rest and cough during 48 h postoperatively and the postoperative consumption of pain rescue were the primary outcomes, and the QoR15 score 48 h postoperatively, the usage of opioids during and after operation, and nerve block-related complications were the secondary outcomes. Demographic characteristics, surgery characteristics, and primary outcomes between the groups were compared.

Results: A total of 120 eligible patients were recruited, including 40 in each group. Baseline and surgery characteristics between the groups were comparable (all p > 0.05). The PVB and RIB groups were better than the GA group in the primary and secondary outcomes (p < 0.05). The static VAS score, QoR15 score, and block-related complications within 48 hours after surgery were better in the RIB group than in the PVB group (p < 0.001).

Conclusion: Both PVB and RIB can provide adequate analgesia and accelerate the recovery of patients. Compared with PVB, RIB has a better analgesic effect, especially to avoid paravertebral pain caused by block, and the operation of RIB is more straightforward and the safety is higher.

超声引导下菱形肋间阻滞(rhomboid interbrial block, RIB)减轻术后疼痛的麻醉效果一直备受关注。本研究旨在比较超声引导下肋骨与椎旁阻滞(PVB)在缓解电视胸外科手术后急性疼痛方面的效果。方法:采用前瞻性、随机、双盲临床试验,纳入132例胸腔镜手术患者,分为T5椎体全麻(GA)组、RIB组和PVB组,使用罗哌卡因0.4%,剂量为3 mg/kg,已在中国临床试验注册中心注册(ChiCTR2100054057,“https://www.chictr.org.cn”)。术后48 h休息和咳嗽时视觉模拟评分(VAS)评分及术后疼痛抢救消耗为主要观察指标,术后48 h QoR15评分、术中及术后阿片类药物使用情况、神经阻滞相关并发症为次要观察指标。比较两组患者的人口学特征、手术特征和主要结局。结果:共纳入符合条件的患者120例,每组40例。两组间基线和手术特征具有可比性(均p > 0.05)。PVB组和RIB组的主要和次要结局均优于GA组(p < 0.05)。术后48 h内,RIB组的静态VAS评分、QoR15评分、阻滞相关并发症均优于PVB组(p < 0.001)。结论:PVB和RIB均能提供充分的镇痛,促进患者的康复。与PVB相比,RIB具有更好的镇痛效果,尤其可以避免因阻滞引起的椎旁疼痛,并且RIB的操作更直接,安全性更高。
{"title":"Ultrasound-Guided Rhomboid Block versus Paravertebral Block in Postoperative Analgesia for Video-Assisted Thoracoscopic Surgery: A Prospective Randomized Controlled Clinical Trial.","authors":"Yan Wang,&nbsp;Xiaoping Gu,&nbsp;Simin Huang,&nbsp;Minke Shi,&nbsp;Xiaofeng He,&nbsp;Zhengliang Ma","doi":"10.1155/2023/3924511","DOIUrl":"https://doi.org/10.1155/2023/3924511","url":null,"abstract":"<p><strong>Introduction: </strong>The anesthetic efficacy of the ultrasound-guided rhomboid intercostal block (RIB) in alleviating postoperative pain has been well concerned. This study aims to compare the effectiveness between ultrasound-guided RIB and paravertebral block (PVB) in alleviating acute pain following video-assisted thoracic surgery.</p><p><strong>Methods: </strong>It was a prospective, randomized, double-blinded clinical trial involving 132 patients with video-assisted thoracic surgery divided into three groups: the general anesthesia (GA) group, RIB group, and PVB group on T5 vertebra, using 0.4% ropivacaine at 3 mg/kg, registered in the Chinese Clinical Trial Registry (ChiCTR2100054057, \"https://www.chictr.org.cn\"). The visual analogue scale (VAS) scores at rest and cough during 48 h postoperatively and the postoperative consumption of pain rescue were the primary outcomes, and the QoR15 score 48 h postoperatively, the usage of opioids during and after operation, and nerve block-related complications were the secondary outcomes. Demographic characteristics, surgery characteristics, and primary outcomes between the groups were compared.</p><p><strong>Results: </strong>A total of 120 eligible patients were recruited, including 40 in each group. Baseline and surgery characteristics between the groups were comparable (all <i>p</i> > 0.05). The PVB and RIB groups were better than the GA group in the primary and secondary outcomes (<i>p</i> < 0.05). The static VAS score, QoR15 score, and block-related complications within 48 hours after surgery were better in the RIB group than in the PVB group (<i>p</i> < 0.001).</p><p><strong>Conclusion: </strong>Both PVB and RIB can provide adequate analgesia and accelerate the recovery of patients. Compared with PVB, RIB has a better analgesic effect, especially to avoid paravertebral pain caused by block, and the operation of RIB is more straightforward and the safety is higher.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9995189/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9697711","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
Mechanism and Pharmacodynamic Substance Basis of Raw and Wine-Processed Evodia rutaecarpa on Smooth Muscle Cells of Dysmenorrhea Mice. 枸杞子生、酒对痛经小鼠平滑肌细胞的作用机制及药效物质基础。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7711988
Yeqian Liu, Hong Li, Lei Chen, Hongxia Zhao, Jian Liu, Shan Gong, Danfeng Ma, Chunming Chen, Shuiqing Zeng, Hongping Long, Weiqiong Ren
Objectives Evodia rutaecarpa (ER) is a well-known herbal Chinese medicine traditionally used for analgesia in dysmenorrhea, headaches, abdominal pain, etc. Notably, the analgesic effect of wine-processed Evodia rutaecarpa (PER) was more potent than that of raw ER. This research aimed to investigate the mechanism and pharmacodynamic substance basis of raw ER and PER on smooth muscle cells of dysmenorrhea mice. Methods Metabolomics methods based on UPLC-Q-TOF-MS were utilized to analyse the differential components of ER before and after wine processing. Afterwards, the uterine smooth muscle cells were isolated from the uterine tissue of dysmenorrhea and normal mice. The isolated dysmenorrhea uterine smooth muscle cells were randomly divided into four groups: model group, 7-hydroxycoumarin group (1 mmol/L), chlorogenic acid (1 mmol/L), and limonin (50 μmol/L). The normal group consisted of the isolated normal mouse uterine smooth muscle cells, which were repeated 3 times in each group. The cell contraction and the expression of P2X3 and Ca2+ in vitro were determined using immunofluorescence staining and laser confocal; ELISA was used for detection of PGE2, ET-1, and NO content after 7-hydroxycoumarin, chlorogenic acid, and limonin administered for 24 h. Results The metabolomics results suggested that seven differential compounds were identified in the extracts of raw ER and PER, including chlorogenic acid, 7-hydroxycoumarin, hydroxy evodiamine, laudanosine, evollionines A, limonin, and 1-methyl-2-[(z)-4-nonenyl]-4 (1H)-quinolone. The in vitro results showed that 7-hydroxycoumarin, chlorogenic acid, and limonin were able to inhibit cell contraction and PGE2, ET-1, P2X3, and Ca2+ in dysmenorrhea mouse uterine smooth muscle cells and increase the content of NO. Conclusion Our finding suggested that the compounds of the PER were different from those of the raw ER, and 7-hydroxycoumarin, chlorogenic acid, and limonin could improve dysmenorrhea in mice whose uterine smooth muscle cell contraction was closed with endocrine factors and P2X3-Ca2+ pathway.
目的:吴茱萸(ER)是一种著名的中药,用于镇痛痛经、头痛、腹痛等。值得注意的是,酒炙的吴茱萸(PER)的镇痛作用比生的吴茱萸更强。本研究旨在探讨生ER和PER对痛经小鼠平滑肌细胞的作用机制和药效学物质基础。方法:采用基于UPLC-Q-TOF-MS的代谢组学方法,分析葡萄酒加工前后ER的差异成分。然后分别从痛经小鼠和正常小鼠的子宫组织中分离子宫平滑肌细胞。将离体痛经子宫平滑肌细胞随机分为4组:模型组、7-羟基香豆素组(1 mmol/L)、绿原酸组(1 mmol/L)、柠檬素组(50 μmol/L)。正常组取离体正常小鼠子宫平滑肌细胞,每组重复3次。采用免疫荧光染色和激光共聚焦法检测细胞收缩及P2X3、Ca2+的体外表达;采用ELISA法检测7-羟基香豆素、绿原酸和柠檬苦素作用24 h后血清中PGE2、ET-1和NO含量。结果:代谢组学分析结果表明,从粗ER和PER提取物中鉴定出绿原酸、7-羟基香豆素、羟基evolodiamine、laudanosine、evollionines A、limonin和1-甲基-2-[(z)-4-壬烯基]-4 (1H)-喹诺酮等7种差异化合物。体外实验结果显示,7-羟基香豆素、绿原酸和柠檬素均能抑制痛经小鼠子宫平滑肌细胞的细胞收缩,抑制PGE2、ET-1、P2X3和Ca2+,增加NO含量。结论:我们的研究结果表明,PER的化合物与生ER不同,7-羟基香豆素、绿原酸和柠檬苦素可以改善受内分泌因子和P2X3-Ca2+途径封闭的子宫平滑肌细胞收缩小鼠的痛经。
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引用次数: 1
Artificial Intelligence for Automatic Pain Assessment: Research Methods and Perspectives. 人工智能用于疼痛自动评估:研究方法与展望。
IF 2.9 3区 医学 Q2 Medicine Pub 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.

虽然适当的疼痛评估是建立适当的治疗的必要条件,自我报告的疼痛水平评估有几个局限性。数据驱动的人工智能(AI)方法可以用于疼痛自动评估(APA)的研究。目标是开发客观、标准化和可推广的工具,用于不同临床情况下的疼痛评估。本文的目的是讨论APA在研究和临床应用方面的研究现状和前景。将讨论人工智能的功能原理。出于叙述目的,基于人工智能的方法分为基于行为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,一些基于图像分类和特征提取的APA方法。通过自然语言策略,身体姿势和呼吸衍生元素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、皮电活动和其他生物信号获得的。最近的方法包括将行为与神经生理学发现相结合的多模式策略。在方法上,早期的研究是通过支持向量机、决策树、随机森林分类器等机器学习算法进行的。最近,人工神经网络,如卷积和循环神经网络算法被实现,甚至组合在一起。涉及临床医生和计算机科学家的合作项目必须致力于构建和处理可用于各种情况的可靠数据集,从急性疼痛到不同的慢性疼痛。最后,在检查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的概念至关重要。
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引用次数: 4
Effects of a Rehabilitation Program Combined with Pain Management That Targets Pain Perception and Activity Avoidance in Older Patients with Acute Vertebral Compression Fracture: a Randomised Controlled Trial. 针对老年急性椎体压缩性骨折患者疼痛感知和活动回避的康复计划与疼痛管理相结合的效果:一项随机对照试验
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/1383897
Hideki Kataoka, Tatsuya Hirase, Kyo Goto, Yutaro Nomoto, Yutaro Kondo, Koichi Nakagawa, Junichiro Yamashita, Kaoru Morita, Yuichiro Honda, Junya Sakamoto, Minoru Okita

This study aimed to investigate the effect of a rehabilitation program combined with pain management targeting pain perception and activity avoidance on multifaceted outcomes in older patients with acute vertebral compression fractures (VCFs). We randomised 65 older adults with acute VCFs to either an intervention group (n = 32), involving usual rehabilitation combined with pain management that targeted pain perception and activity avoidance, or a control group (n = 33), involving only usual rehabilitation. The usual rehabilitation was initiated immediately after admission. All patients were treated conservatively. Pain management aimed to improve the patients' daily behaviour by increasing their daily activities despite pain, rather than by focusing on eliminating the pain. Pain intensity and psychological statuses such as depression, pain catastrophising, and physical activity levels were assessed on admission. Two weeks postadmission and at discharge, physical performance measures were assessed along with the above-given measurements. A significant main effect of the group was observed for the intensity of lower back pain, favouring the intervention group (F = 5.135, p = 0.027). At discharge, it was significantly better in the intervention group than in the control group (p = 0.011). A time-by-group interaction emerged for magnification of the pain catastrophising scale (p = 0.012), physical activity levels (p < 0.001), and six-minute walking distance (p = 0.006), all favouring the intervention group. Rehabilitation programs combined with pain management targeting pain perception and activity avoidance could be an effective conservative treatment for older patients with acute VCFs.

本研究旨在探讨针对疼痛感知和活动回避的康复方案结合疼痛管理对老年急性椎体压缩性骨折(vcf)患者多方面预后的影响。我们将65名患有急性vcf的老年人随机分为干预组(n = 32)和对照组(n = 33),干预组包括常规康复和针对疼痛感知和活动避免的疼痛管理,对照组只包括常规康复。入院后立即进行常规康复治疗。所有患者均采用保守治疗。疼痛管理旨在通过增加患者的日常活动来改善他们的日常行为,而不是专注于消除疼痛。入院时评估疼痛强度和心理状态,如抑郁、疼痛灾难和身体活动水平。入院后两周和出院时,身体表现测量与上述测量一起进行评估。干预组对腰痛强度有显著的主效应,对干预组有利(F = 5.135, p = 0.027)。出院时,干预组明显优于对照组(p = 0.011)。在疼痛灾难化量表(p = 0.012)、体力活动水平(p < 0.001)和6分钟步行距离(p = 0.006)的放大上,出现了按时间分组的相互作用,这些都有利于干预组。康复方案结合疼痛管理,针对疼痛感知和活动避免可能是有效的保守治疗老年急性vcf患者。
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引用次数: 0
Soluble Epoxide Hydrolase Inhibitor TPPU Alleviates Nab-Paclitaxel-Induced Peripheral Neuropathic Pain via Suppressing NF-κB Signalling in the Spinal Cord of a Rat. 可溶性环氧化合物水解酶抑制剂TPPU通过抑制大鼠脊髓NF-κB信号通路减轻nab -紫杉醇诱导的周围神经性疼痛。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/9058774
Xing Wei, Lijun Jia, Yaqing Zhou, Weimiao Li, Changyou Shan, Shuqun Zhang, Yonglin Zhao

Objective: Paclitaxel-induced peripheral neuropathy (PIPN) is a debilitating and difficult-to-treat side effect of paclitaxel. Soluble epoxide hydrolase (sEH) can rapidly metabolize the endogenous anti-inflammatory mediators' epoxyeicosatrienoic acids (EETs) to dihydroxyeicosatrienoic acids. This study aimed to assess whether the sEH inhibitor N-(1-(1-oxopropy)-4-piperidinyl]-N'-(trifluoromethoxy) phenyl)-urea (TPPU) plays a critical role in PIPN of rats and provides a new target for treatment.

Methods: A Sprague-Dawley male rat model of PIPN induced by nab-paclitaxel was established. Rats were randomly divided into a control group, nab-paclitaxel group, and nab-paclitaxel + TPPU (sEH inhibitor) group, with 36 rats in each group. The effects of the sEH inhibitor TPPU on behavioural assays, apoptosis, glial activation, axonal injury, microstructure, and permeability of the blood-spinal cord barrier were detected, and the underlying mechanisms were explored by examining the expression of NF-κB signalling pathways, inflammatory cytokines, and oxidative stress.

Results: The results showed that the mechanical and thermal pain thresholds of rats were decreased after nab-paclitaxel treatment, accompanied by an increased expression of axonal injury-related proteins, enhanced cell apoptosis, aggravated destruction of vascular permeability, intense glial responses, and elevated inflammatory cytokines and oxidative stress in the L4-L6 spinal cord. TPPU restored the mechanical and thermal thresholds, decreased cell apoptosis, alleviated axonal injury and glial responses, and protected vascular permeability by increasing the expression of tight junction proteins. TPPU relieved PIPN by inhibiting the activation of the sEH and NF-κB signalling pathways by decreasing the levels of inflammatory cytokines and oxidative stress.

Conclusion: These findings support a role for sEH in PIPN and suggest that the inhibition of sEH represents a potential new therapeutic target for PIPN.

目的:紫杉醇诱导的周围神经病变(PIPN)是紫杉醇致衰弱且难以治疗的副作用。可溶性环氧化物水解酶(sEH)能将内源性抗炎介质环氧二十碳三烯酸(EETs)快速代谢为二羟基二十碳三烯酸。本研究旨在评估sEH抑制剂N-(1-(1-氧丙基)-4-哌替啶基)- N'-(三氟甲氧基)苯基)-尿素(TPPU)是否在大鼠PIPN中起关键作用,并为治疗提供新的靶点。方法:建立nab-紫杉醇诱导PIPN雄性大鼠Sprague-Dawley模型。将大鼠随机分为对照组、nab-紫杉醇组和nab-紫杉醇+ TPPU (sEH抑制剂)组,每组36只。研究人员检测了sEH抑制剂TPPU对大鼠行为、细胞凋亡、神经胶质活化、轴突损伤、微观结构和血脊髓屏障通透性的影响,并通过检测NF-κB信号通路、炎症细胞因子和氧化应激的表达来探讨其潜在机制。结果:nab-紫杉醇治疗后大鼠机械痛阈和热痛阈降低,轴突损伤相关蛋白表达增加,细胞凋亡增强,血管通透性破坏加剧,神经胶质反应强烈,L4-L6脊髓炎症因子和氧化应激升高。TPPU恢复了机械和热阈值,降低了细胞凋亡,减轻了轴突损伤和胶质反应,并通过增加紧密连接蛋白的表达来保护血管通透性。TPPU通过降低炎症细胞因子和氧化应激水平,抑制sEH和NF-κB信号通路的激活,从而缓解PIPN。结论:这些发现支持了sEH在PIPN中的作用,并提示抑制sEH可能是PIPN的一个新的治疗靶点。
{"title":"Soluble Epoxide Hydrolase Inhibitor TPPU Alleviates Nab-Paclitaxel-Induced Peripheral Neuropathic Pain via Suppressing NF-<i>κ</i>B Signalling in the Spinal Cord of a Rat.","authors":"Xing Wei,&nbsp;Lijun Jia,&nbsp;Yaqing Zhou,&nbsp;Weimiao Li,&nbsp;Changyou Shan,&nbsp;Shuqun Zhang,&nbsp;Yonglin Zhao","doi":"10.1155/2023/9058774","DOIUrl":"https://doi.org/10.1155/2023/9058774","url":null,"abstract":"<p><strong>Objective: </strong>Paclitaxel-induced peripheral neuropathy (PIPN) is a debilitating and difficult-to-treat side effect of paclitaxel. Soluble epoxide hydrolase (sEH) can rapidly metabolize the endogenous anti-inflammatory mediators' epoxyeicosatrienoic acids (EETs) to dihydroxyeicosatrienoic acids. This study aimed to assess whether the sEH inhibitor N-(1-(1-oxopropy)-4-piperidinyl]-N'-(trifluoromethoxy) phenyl)-urea (TPPU) plays a critical role in PIPN of rats and provides a new target for treatment.</p><p><strong>Methods: </strong>A Sprague-Dawley male rat model of PIPN induced by nab-paclitaxel was established. Rats were randomly divided into a control group, nab-paclitaxel group, and nab-paclitaxel + TPPU (sEH inhibitor) group, with 36 rats in each group. The effects of the sEH inhibitor TPPU on behavioural assays, apoptosis, glial activation, axonal injury, microstructure, and permeability of the blood-spinal cord barrier were detected, and the underlying mechanisms were explored by examining the expression of NF-<i>κ</i>B signalling pathways, inflammatory cytokines, and oxidative stress.</p><p><strong>Results: </strong>The results showed that the mechanical and thermal pain thresholds of rats were decreased after nab-paclitaxel treatment, accompanied by an increased expression of axonal injury-related proteins, enhanced cell apoptosis, aggravated destruction of vascular permeability, intense glial responses, and elevated inflammatory cytokines and oxidative stress in the L4-L6 spinal cord. TPPU restored the mechanical and thermal thresholds, decreased cell apoptosis, alleviated axonal injury and glial responses, and protected vascular permeability by increasing the expression of tight junction proteins. TPPU relieved PIPN by inhibiting the activation of the sEH and NF-<i>κ</i>B signalling pathways by decreasing the levels of inflammatory cytokines and oxidative stress.</p><p><strong>Conclusion: </strong>These findings support a role for sEH in PIPN and suggest that the inhibition of sEH represents a potential new therapeutic target for PIPN.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9931472/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9702377","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
Positive Preemptive Analgesia Effectiveness of Pregabalin Combined with Celecoxib in Total Knee Arthroplasty: A Prospective Controlled Randomized Study. 普瑞巴林联合塞来昔布在全膝关节置换术中的积极先发制人镇痛效果:一项前瞻性对照随机研究。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/7088004
Yi Zhou, Xiaoyan Liu, Chuan Ding, Bingyan Xiang, Ling Yan

Objective: The purpose of the present study (a randomized clinical trial) was to evaluate the preemptive analgesic effects of pregabalin combined with celecoxib in total knee arthroplasty (TKA).

Methods: From January 2019 to June 2021, we enrolled 149 patients who underwent TKA and divided them into four groups: the placebo group (n = 36), celecoxib group (n = 38), pregabalin group (n = 38), and combination group (n = 37). Each group was given the corresponding preemptive analgesia regimen at 12 and 2 hours before surgery. The pain score at rest and upon movement, cumulative dosage of sufentanil, knee range of motion (ROM), high-sensitivityC-reactive protein (hs-CRP) level, and adverse effects were evaluated after TKA to compare the effects of the preemptive analgesia regimens among the four groups.

Results: The pain scores upon movement were significantly lower in the combination group than in the other three groups at 6, 12, 24, and 48 hours after surgery (P < 0.05). The cumulative dose of sufentanil within 48 hours after surgery was lowest in the combined group among the four groups (P < 0.05). Hs-CRP, ROM, and postoperative nausea and vomiting (PONV) were within 72 hours after surgery significantly improved in the combination group compared with those of the three other groups (P < 0.05).

Conclusion: The preemptive analgesia regimen of pregabalin combined with celecoxib had positive effects on improving acute pain and reducing the cumulative dose of opioids after TKA. This trial is registered with ChiCTR2100041595.

目的:本研究(一项随机临床试验)旨在评价普瑞巴林联合塞来昔布在全膝关节置换术(TKA)中的先发制人镇痛效果。方法:2019年1月至2021年6月,我们招募了149例接受TKA的患者,并将其分为4组:安慰剂组(n = 36)、塞来昔布组(n = 38)、普瑞巴林组(n = 38)和联合组(n = 37)。各组分别于术前12、2小时给予相应的先发制人镇痛方案。评估静息和运动时疼痛评分、舒芬太尼累积剂量、膝关节活动度(ROM)、高敏c反应蛋白(hs-CRP)水平及TKA后不良反应,比较四组患者先发制人镇痛方案的效果。结果:联合组术后6、12、24、48 h运动疼痛评分明显低于其他三组(P < 0.05)。联合用药组术后48 h内舒芬太尼累积剂量最低(P < 0.05)。联合用药组术后72 h内Hs-CRP、ROM、术后恶心呕吐(PONV)较其他三组明显改善(P < 0.05)。结论:普瑞巴林联合塞来昔布先发制人镇痛方案对改善TKA后急性疼痛、减少阿片类药物累积剂量有积极作用。该试验注册号为ChiCTR2100041595。
{"title":"Positive Preemptive Analgesia Effectiveness of Pregabalin Combined with Celecoxib in Total Knee Arthroplasty: A Prospective Controlled Randomized Study.","authors":"Yi Zhou,&nbsp;Xiaoyan Liu,&nbsp;Chuan Ding,&nbsp;Bingyan Xiang,&nbsp;Ling Yan","doi":"10.1155/2023/7088004","DOIUrl":"https://doi.org/10.1155/2023/7088004","url":null,"abstract":"<p><strong>Objective: </strong>The purpose of the present study (a randomized clinical trial) was to evaluate the preemptive analgesic effects of pregabalin combined with celecoxib in total knee arthroplasty (TKA).</p><p><strong>Methods: </strong>From January 2019 to June 2021, we enrolled 149 patients who underwent TKA and divided them into four groups: the placebo group (<i>n</i> = 36), celecoxib group (<i>n</i> = 38), pregabalin group (<i>n</i> = 38), and combination group (<i>n</i> = 37). Each group was given the corresponding preemptive analgesia regimen at 12 and 2 hours before surgery. The pain score at rest and upon movement, cumulative dosage of sufentanil, knee range of motion (ROM), high-sensitivityC-reactive protein (hs-CRP) level, and adverse effects were evaluated after TKA to compare the effects of the preemptive analgesia regimens among the four groups.</p><p><strong>Results: </strong>The pain scores upon movement were significantly lower in the combination group than in the other three groups at 6, 12, 24, and 48 hours after surgery (<i>P</i> < 0.05). The cumulative dose of sufentanil within 48 hours after surgery was lowest in the combined group among the four groups (<i>P</i> < 0.05). Hs-CRP, ROM, and postoperative nausea and vomiting (PONV) were within 72 hours after surgery significantly improved in the combination group compared with those of the three other groups (<i>P</i> < 0.05).</p><p><strong>Conclusion: </strong>The preemptive analgesia regimen of pregabalin combined with celecoxib had positive effects on improving acute pain and reducing the cumulative dose of opioids after TKA. This trial is registered with ChiCTR2100041595.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":null,"pages":null},"PeriodicalIF":2.9,"publicationDate":"2023-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9851777/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"9133733","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: 1
The Effectiveness of Various Types of Electrical Stimulation of the Spinal Cord for Chronic Pain in Patients with Postherpetic Neuralgia: A Literature Review. 不同类型脊髓电刺激治疗带状疱疹后神经痛慢性疼痛的疗效:文献综述。
IF 2.9 3区 医学 Q2 Medicine Pub Date : 2023-01-01 DOI: 10.1155/2023/6015680
Emil Isagulyan, Vasily Tkachenko, Denis Semenov, Svetlana Asriyants, Evgeny Dorokhov, Elizaveta Makashova, Karina Aslakhanova, Alexei Tomskiy

Introduction: Postherpetic neuralgia (PHN) is a severe condition that remains a challenge to treat. Spinal cord stimulation (SCS) is used in cases of insufficient efficacy of conservative treatment. However, in contrast to many other neuropathic pain syndromes, there is a huge problem in reaching long-term stable pain relief in patients with PHN using conventional tonic SCS. The objective of this article was to present a review of the current management strategies of PHN, their efficacy, and safety.

Materials and methods: We searched for articles containing the keywords "spinal cord stimulation AND postherpetic neuralgia," "high-frequency stimulation AND postherpetic neuralgia," "burst stimulation AND postherpetic neuralgia" and "dorsal root ganglion stimulation AND postherpetic neuralgia" in Pubmed, Web of Science, and Scopus databases. The search was limited to human studies published in the English language. There were no publication period limitations. Bibliographies and references of selected publications on neurostimulation for PHN were further manually screened. The full text of each article was studied once the abstract was analyzed by the searching reviewer and found appropriate. The initial search yielded 115 articles. Initial screening based on abstract and title allowed us to exclude 29 articles (letters, editorials, and conference abstracts). The full-text analysis allowed us to exclude another 74 articles (fundamental research articles, research utilizing animal subjects, and systemic and nonsystemic reviews) and results of PHN treatment presented with other conditions, leaving 12 articles for the final bibliography.

Results: 12 articles reporting on the treatment of 134 patients with PHN were analyzed, with a disproportionally large amount of traditional SCS treatment than that to alternative SCS: DRGS (13 patients), burst SCS (1 patient), and high-frequency SCS (2 patients). Long-term pain relief was achieved in 91 patients (67.9%). The mean VAS score improvement was 61.4% with a mean follow-up time of 12.85 months. Although the number of patients in alternative SCS studies was very limited, almost all of them showed good responses to therapy with more than 50% VAS improvement and reduction of analgesic dosage. The article contains a review analysis of 12 articles concerning the current methods of treatment for postherpetic neuralgia including conservative treatment, spinal cord stimulation, and novel neuromodulation strategies. Available information on the pathophysiology of PHN and the effect or stimulation on its course, together with a number of technical nuances concerning various types of neurostimulation are also elucidated in this article. A number of alternative invasive treatments of PHN are also discussed.

Conclusions: Spinal cord stimulation is an established treatment option for patients with pharmacologically resistant PHN. High-

带状疱疹后神经痛(PHN)是一种严重的疾病,治疗仍然是一个挑战。脊髓刺激(SCS)用于保守治疗效果不足的病例。然而,与许多其他神经性疼痛综合征不同的是,在PHN患者中,使用常规的强直性SCS实现长期稳定的疼痛缓解存在巨大的问题。本文的目的是回顾目前PHN的管理策略,它们的有效性和安全性。材料与方法:我们在Pubmed、Web of Science和Scopus数据库中检索包含关键词“脊髓刺激与带状疱疹后神经痛”、“高频刺激与带状疱疹后神经痛”、“突发刺激与带状疱疹后神经痛”和“背根神经节刺激与带状疱疹后神经痛”的文章。这项研究仅限于用英语发表的人类研究。没有出版期限限制。进一步人工筛选有关PHN神经刺激的选定出版物的参考书目和参考文献。一旦检索审稿人对摘要进行分析并认为合适,就研究每篇文章的全文。最初的搜索产生了115篇文章。基于摘要和标题的初步筛选使我们排除了29篇文章(信件、社论和会议摘要)。通过全文分析,我们排除了另外74篇文章(基础研究文章、动物实验研究、系统和非系统综述)以及PHN治疗伴有其他情况的结果,留下12篇文章作为最终参考书目。结果:我们分析了关于134例PHN患者治疗的12篇文章,其中传统SCS治疗的数量比替代SCS多得多:DRGS(13例)、burst SCS(1例)和高频SCS(2例)。91例(67.9%)患者获得长期疼痛缓解。VAS评分平均改善61.4%,平均随访时间12.85个月。虽然替代SCS研究的患者数量非常有限,但几乎所有患者都对治疗表现出良好的反应,VAS改善超过50%,镇痛剂量减少。本文回顾分析了目前治疗带状疱疹后神经痛的12篇文献,包括保守治疗、脊髓刺激和新的神经调节策略。本文还阐述了关于PHN的病理生理学和刺激对其过程的影响的现有信息,以及关于各种类型神经刺激的一些技术上的细微差别。本文还讨论了一些侵袭性治疗PHN的方法。结论:脊髓刺激是药物耐药PHN患者的治疗选择。高频刺激、爆裂刺激和背根神经节刺激是治疗PHN的有希望的选择,因为没有感觉异常,而感觉异常会给PHN患者带来痛苦。但仍需要更多的研究来推荐这些新方法的广泛使用。
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引用次数: 2
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Pain Research & Management
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