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Efficacy and Safety of Bupivacaine Liposomal in Intercostal Nerve Block for Postoperative Pain Management Following Uniportal Thoracoscopy: A Randomized Trial. 布比卡因脂质体用于肋间神经阻滞治疗单门胸腔镜术后疼痛的有效性和安全性:一项随机试验。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-07-09 eCollection Date: 2025-01-01 DOI: 10.1155/prm/8816879
Lingjun Dong, Xiang Wang, Linhai Fu, Zongming Jiang, Yulong Wang, Aixia Chen, Jianyi Ding, Guangmao Yu

Background: Postoperative pain in thoracic surgery often requires opioids, yet can be poorly managed with short-acting anesthetics. Liposomal bupivacaine (LB) offers prolonged analgesia, potentially improving pain control and reducing opioid use. This study evaluates LB's effectiveness and safety in thoracic postoperative pain management, aiming to provide an alternative to current practices. Methods: In this single-center, double-blind, prospective, randomized controlled trial, patients undergoing uniportal lobectomy, segmentectomy, or wedge resection from November 2023 to May 2024 were enrolled. Participants were randomly assigned in a 1:1 ratio to receive either 0.375% ropivacaine (control group, n = 57) or LB (LB group, n = 56) for intercostal nerve blocks (ICNBs). Postoperative visual analog scale (VAS) scores, opioid consumption, overall benefit of analgesia score (OBAS), chest tube duration, length of hospital stay, and adverse events (AEs) were recorded and analyzed. Results: Data from 57 patients in the control group and 56 patients in the LB group were included in the analysis, with no significant demographic differences between the groups. The LB group demonstrated lower VAS scores at rest and during activity (p > 0.05), reduced opioid consumption (p=0.021), and higher OBAS (p < 0.01) compared with the control group. No significant differences were observed in chest tube duration, length of hospital stay, or AEs between the groups. Conclusion: LB is safe and effective for ICNB, providing significant postoperative pain relief for patients undergoing uniportal thoracoscopic surgery. Trial Registration: Chinese Registry of Clinical Trials: chiCTR2300075463.

背景:胸外科术后疼痛通常需要阿片类药物,但短效麻醉药可能管理不善。布比卡因脂质体(LB)提供延长的镇痛,潜在地改善疼痛控制和减少阿片类药物的使用。本研究评估了LB在胸部术后疼痛管理中的有效性和安全性,旨在为目前的实践提供一种替代方案。方法:在这项单中心、双盲、前瞻性、随机对照试验中,纳入了从2023年11月至2024年5月接受单门叶切除术、节段切除术或楔形切除术的患者。参与者以1:1的比例随机分配,接受0.375%罗哌卡因(对照组,n = 57)或LB (LB组,n = 56)用于肋间神经阻滞(icnb)。记录并分析术后视觉模拟量表(VAS)评分、阿片类药物消耗、镇痛总获益评分(OBAS)、胸管持续时间、住院时间和不良事件(ae)。结果:对照组57例患者和LB组56例患者的数据被纳入分析,两组间无显著人口统计学差异。与对照组相比,LB组在休息和活动时VAS评分较低(p < 0.05),阿片类药物消耗减少(p=0.021), OBAS较高(p < 0.01)。两组间胸管时间、住院时间或ae均无显著差异。结论:LB治疗ICNB安全有效,可显著缓解单门胸腔镜手术患者术后疼痛。试验注册:中国临床试验注册中心:chiCTR2300075463。
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引用次数: 0
Treatment of Migraine With Phytocannabinoids, the Involvement of Endocannabinoids in Migraine, and Potential Mechanisms of Action. 植物大麻素治疗偏头痛,内源性大麻素在偏头痛中的作用,以及潜在的作用机制。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-07-01 eCollection Date: 2025-01-01 DOI: 10.1155/prm/7181066
Roger Gregory Biringer

The American Migraine Foundation estimates that over 39 million Americans and over 1 billion people worldwide suffer from some form of migraine. Treatment of migraine generally falls into two categories: treatment of attacks once they have begun, and prophylactic prevention, including lifestyle changes. The use of phytocannabinoids to reduce both the frequency and severity of migraine is widely documented in scientific, grey, and popular literature. This review provides descriptions of both preclinical and clinical studies involving the treatment of migraines with phytocannabinoids as well as the involvement of endocannabinoids and endocannabinoid-like compounds in migraine pathology, including the receptors and associated mechanisms. Currently unanswered questions and areas for further exploration are discussed.

美国偏头痛基金会估计,超过3900万美国人和全球超过10亿人患有某种形式的偏头痛。偏头痛的治疗通常分为两类:一是开始发作时的治疗,二是预防性预防,包括改变生活方式。使用植物大麻素可以减少偏头痛的频率和严重程度,这在科学文献、灰色文献和通俗文献中都有广泛的记载。本文综述了植物大麻素治疗偏头痛的临床前和临床研究,以及内源性大麻素和内源性大麻素样化合物在偏头痛病理中的作用,包括受体和相关机制。讨论了目前尚未解决的问题和有待进一步探索的领域。
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引用次数: 0
How Does Self-Declared Chronic Pain Compare to Other Definitions? A Prospective Multicenter Study. 自我宣称的慢性疼痛与其他定义相比如何?一项前瞻性多中心研究。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-06-19 eCollection Date: 2025-01-01 DOI: 10.1155/prm/5556400
Raoul Daoust, Jean Paquet, Jeffrey J Perry, Justin W Yan, David Williamson, Véronique Castonguay, Gilles Lavigne, Dominique Rouleau, Justine Lessard, Alexis Cournoyer

Background: Self-declared chronic pain has not been compared to existing definitions. Our objective was to evaluate the agreement between self-declared chronic pain and different chronic pain definitions, three months after an emergency department (ED) visit. Methods: In this planned substudy of a prospective multicenter cohort study, we included consecutive patients aged ≥ 18 years with an acute pain condition discharged from the ED with an opioid prescription. Three months after their ED visit, participants were asked about their pain intensity, pain frequency, pain disability, and self-declared chronic pain. Agreement between self-declared chronic pain and five other definitions were calculated with kappas. Results: A total of 1411 participants were included; mean age was 52 (±16) years, and 53% were female. Prevalence of self-declared chronic pain was 23.0% and varied from 16.9% to 45.3% for other definitions. Agreement of self-declared chronic pain was moderate (0.57-0.60) with most definitions but lower with the pain intensity ≥ 1 definition (0.47). The proportion of chronic pain participants using opioids ( ⁓20%) or other analgesics (⁓80%) was similar with all definitions except for the pain intensity ≥ 1 definition which was associated with a lower proportion of analgesic use (11%, 64%). Conclusion: In summary, self-declared chronic pain displayed moderate agreement with other chronic pain definitions and similar analgesic consumption but lower with the pain intensity ≥ 1 definition. Nonetheless, chronic pain prevalence varied greatly depending on how it was defined. Self-declared chronic pain might be a more patient-centered outcome and could be easily applied to standardize chronic pain definition. Trial Registration: ClinicalTrials.gov identifier: NCT03953534.

背景:自我宣称的慢性疼痛尚未与现有的定义进行比较。我们的目的是评估自我宣称的慢性疼痛和不同的慢性疼痛定义之间的一致性,三个月后急诊科(ED)访问。方法:在一项前瞻性多中心队列研究的计划亚研究中,我们纳入了年龄≥18岁、急性疼痛且服用阿片类药物从急诊科出院的连续患者。在急诊科就诊三个月后,参与者被问及他们的疼痛强度、疼痛频率、疼痛残疾和自述的慢性疼痛。自我宣称的慢性疼痛和其他五种定义之间的一致性用卡帕计算。结果:共纳入1411名受试者;平均年龄52(±16)岁,女性占53%。自述慢性疼痛的患病率为23.0%,其他定义的患病率从16.9%到45.3%不等。自述慢性疼痛与大多数定义的一致性为中等(0.57-0.60),但与疼痛强度≥1定义的一致性较低(0.47)。慢性疼痛参与者使用阿片类药物(⁓20%)或其他镇痛药(⁓80%)的比例与所有定义相似,但疼痛强度≥1的定义与较低的镇痛药使用比例相关(11%,64%)。结论:综上所述,自述慢性疼痛与其他慢性疼痛定义和类似的镇痛药物消耗有中等程度的一致性,但与疼痛强度≥1定义的一致性较低。然而,慢性疼痛的流行程度因其定义的不同而有很大差异。自我宣称的慢性疼痛可能是一个更以患者为中心的结果,可以很容易地应用于标准化慢性疼痛的定义。试验注册:ClinicalTrials.gov标识符:NCT03953534。
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引用次数: 0
Reduced Cortical Surface Area in the Frontal Operculum as a Causal Risk Predictor for Chronic Pain. 额盖皮层表面积减少作为慢性疼痛的因果风险预测因子。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-06-05 eCollection Date: 2025-01-01 DOI: 10.1155/prm/4687197
Xiuzhi Wang, Yipeng Le, Xichen Wang, Yingchao Song, Qian Su, Xiaoxiao Xiao, Yifan Li, Wen Qin, Chunshui Yu, Meng Liang

Chronic pain is a prevalent and debilitating condition that imposes substantial personal and societal burdens. Despite its significance, the neural mechanisms underlying individual susceptibility to chronic pain remain inadequately understood. In this study, we examined the prospective associations between 1325 brain structural imaging phenotypes and the future risk of developing chronic pain in a UK Biobank cohort of 5754-5756 participants. These phenotypes encompassed regional and tissue volume, cortical surface area and thickness. General linear models (GLMs) were employed to identify brain structural variations associated with the risk of developing chronic pain, and then Mendelian randomization (MR) was employed to explore potential causal relationships between brain structure and chronic pain development. GLMs identified three significant associations between imaging phenotypes and the future development of chronic pain. All three imaging phenotypes pertained to the cortical surface area of the frontal operculum, albeit derived from three different brain atlases. Specifically, reduced cortical surface area in the frontal operculum was significantly associated with an increased risk of developing chronic pain: BA atlas area 44 (T=-4.10, p=4.24 × 10-5), Desikan atlas pars opercularis (T=-4.21, p=2.55 × 10-5), and DKT atlas pars opercularis (T=-3.96, p=7.47 × 10-5). Subsequent MR analysis further demonstrated a causally protective effect of larger cortical area in the prefrontal operculum against the risk of developing chronic pain (OR = 0.91, p=1.91 × 10-2). These results indicate a critical role of the surface area of frontal operculum in individual chronic pain susceptibility and provide a potential risk predictor for chronic pain development.

慢性疼痛是一种普遍的、使人衰弱的疾病,给个人和社会带来了沉重的负担。尽管其意义重大,但个体对慢性疼痛易感性的神经机制仍未充分了解。在这项研究中,我们在英国生物银行的5754-5756名参与者队列中检查了1325种脑结构成像表型与未来发展为慢性疼痛风险之间的前瞻性关联。这些表型包括区域和组织体积、皮质表面积和厚度。采用一般线性模型(GLMs)来识别与慢性疼痛发生风险相关的脑结构变化,然后采用孟德尔随机化(MR)来探索脑结构与慢性疼痛发生之间的潜在因果关系。GLMs确定了成像表型与慢性疼痛未来发展之间的三个重要关联。所有三种成像表型都与额叶盖皮层表面积有关,尽管来自三种不同的脑图谱。具体来说,额盖皮质表面积的减少与发生慢性疼痛的风险增加显著相关:BA寰椎面积44 (T=-4.10, p=4.24 × 10-5)、Desikan寰椎小部(T=-4.21, p=2.55 × 10-5)和DKT寰椎小部(T=-3.96, p=7.47 × 10-5)。随后的MR分析进一步证明前额叶包皮层面积较大对慢性疼痛风险的因果保护作用(OR = 0.91, p=1.91 × 10-2)。这些结果表明额盖表面积在个体慢性疼痛易感性中起着关键作用,并为慢性疼痛的发展提供了潜在的风险预测因子。
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引用次数: 0
Investigation of the Relationship Between Type D Personality and Depression, Anxiety and Somatosensory Amplification in Patients With Fibromyalgia. D型人格与纤维肌痛患者抑郁、焦虑、躯体感觉放大的关系研究。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-05-15 eCollection Date: 2025-01-01 DOI: 10.1155/prm/5315083
Meltem Hazel Şimşek, Ulaş Korkmaz, Fatma Gül Helvacı Çelik, Nurçe Çilesizoğlu Yavuz, Çiçek Hocaoğlu

Objective: This study aimed to investigate differences in depression, anxiety and somatosensory amplification between fibromyalgia (FM) patients with and without type D personality (TDP) and healthy controls and to examine the mediating role of somatosensory amplification in the relationship between TDP and FM severity. Methods: A total of 159 participants were included in the cross-sectional case-control study and divided into three groups: FM patients with TDP (n = 56, mean age = 45.93 ± 11.01), FM patients without TDP (n = 48, mean age = 49.17 ± 11.18) and healthy controls (n = 55, mean age = 46.1 ± 9.64). Participants were assessed with the Fibromyalgia Impact Questionnaire (FIQ; administered only to FM patients), TDP Scale, Beck Depression Inventory, Beck Anxiety Inventory and Somatosensory Amplification Scale. Mediation analysis was performed to determine the mediating role of somatosensory amplification. Results: FM patients with TDP had significantly higher levels of depression, anxiety and somatosensory amplification compared to both FM patients without TDP and healthy controls (p < 0.001). Correlation analyses showed strong positive associations between TDP and anxiety (r = 0.729, p < 0.001) and depression (r = 0.794, p < 0.001). Somatosensory amplification was found to have a significant mediating role in the relationship between TDP and FM severity (b = 0.084, 95% CI = 0.018-0.172, p < 0.05). Conclusion: These results highlight TDP as an important psychological risk factor associated with increased depression, anxiety, and somatosensory amplification in FM patients. The apparent mediating role of somatosensory amplification suggests that addressing this mechanism and psychological stress with targeted psychosocial interventions may improve the efficacy of FM treatment.

目的:探讨伴有和不伴有D型人格(TDP)的纤维肌痛(FM)患者与健康对照者在抑郁、焦虑和躯体感觉放大方面的差异,并探讨躯体感觉放大在TDP与FM严重程度之间的中介作用。方法:将159例患者纳入横断面病例对照研究,分为伴有TDP的FM患者(n = 56,平均年龄为45.93±11.01)、无TDP的FM患者(n = 48,平均年龄为49.17±11.18)和健康对照组(n = 55,平均年龄为46.1±9.64)。通过纤维肌痛影响问卷(FIQ;(仅适用于FM患者)、TDP量表、Beck抑郁量表、Beck焦虑量表和躯体感觉放大量表。通过中介分析来确定体感放大的中介作用。结果:伴TDP的FM患者抑郁、焦虑和体感放大水平明显高于无TDP的FM患者和健康对照(p < 0.001)。相关分析显示,TDP与焦虑(r = 0.729, p < 0.001)和抑郁(r = 0.794, p < 0.001)呈正相关。体感放大在TDP和FM严重程度之间具有显著的中介作用(b = 0.084, 95% CI = 0.018-0.172, p < 0.05)。结论:这些结果强调TDP是一个重要的心理危险因素,与FM患者抑郁、焦虑和体感放大增加有关。躯体感觉放大的明显中介作用表明,通过有针对性的社会心理干预来解决这一机制和心理应激可能会提高FM治疗的疗效。
{"title":"Investigation of the Relationship Between Type D Personality and Depression, Anxiety and Somatosensory Amplification in Patients With Fibromyalgia.","authors":"Meltem Hazel Şimşek, Ulaş Korkmaz, Fatma Gül Helvacı Çelik, Nurçe Çilesizoğlu Yavuz, Çiçek Hocaoğlu","doi":"10.1155/prm/5315083","DOIUrl":"10.1155/prm/5315083","url":null,"abstract":"<p><p><b>Objective:</b> This study aimed to investigate differences in depression, anxiety and somatosensory amplification between fibromyalgia (FM) patients with and without type D personality (TDP) and healthy controls and to examine the mediating role of somatosensory amplification in the relationship between TDP and FM severity. <b>Methods:</b> A total of 159 participants were included in the cross-sectional case-control study and divided into three groups: FM patients with TDP (<i>n</i> = 56, mean age = 45.93 ± 11.01), FM patients without TDP (<i>n</i> = 48, mean age = 49.17 ± 11.18) and healthy controls (<i>n</i> = 55, mean age = 46.1 ± 9.64). Participants were assessed with the Fibromyalgia Impact Questionnaire (FIQ; administered only to FM patients), TDP Scale, Beck Depression Inventory, Beck Anxiety Inventory and Somatosensory Amplification Scale. Mediation analysis was performed to determine the mediating role of somatosensory amplification. <b>Results:</b> FM patients with TDP had significantly higher levels of depression, anxiety and somatosensory amplification compared to both FM patients without TDP and healthy controls (<i>p</i> < 0.001). Correlation analyses showed strong positive associations between TDP and anxiety (<i>r</i> = 0.729, <i>p</i> < 0.001) and depression (<i>r</i> = 0.794, <i>p</i> < 0.001). Somatosensory amplification was found to have a significant mediating role in the relationship between TDP and FM severity (<i>b</i> = 0.084, 95% CI = 0.018-0.172, <i>p</i> < 0.05). <b>Conclusion:</b> These results highlight TDP as an important psychological risk factor associated with increased depression, anxiety, and somatosensory amplification in FM patients. The apparent mediating role of somatosensory amplification suggests that addressing this mechanism and psychological stress with targeted psychosocial interventions may improve the efficacy of FM treatment.</p>","PeriodicalId":19913,"journal":{"name":"Pain Research & Management","volume":"2025 ","pages":"5315083"},"PeriodicalIF":2.5,"publicationDate":"2025-05-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12097857/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144128258","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
Radiation Synovectomy: An Enticing Treatment Option for Inflammatory Joint Pain. 放射滑膜切除术:炎性关节疼痛的诱人治疗选择。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-05-13 eCollection Date: 2025-01-01 DOI: 10.1155/prm/8887391
Ashutosh Dash, Tapas Das

Radiosynovectomy (RSV) represents an advanced therapeutic modality in nuclear medicine, designed to treat chronic inflammatory joint disorders that are unresponsive to conventional therapies. This targeted approach involves the intra-articular administration of radioactive microparticles containing a β--emitting radionuclide, selectively eradicating the inflamed synovial membrane while preserving surrounding tissues. As a minimally invasive, nonsurgical procedure routinely performed in outpatient settings, RSV offers a compelling alternative to more invasive interventions. Over time, RSV has evolved significantly, transitioning from the empirical use of radiocolloids to the development of specialized agents tailored for different joint types. Advancements in this field continue to explore a variety of β--emitting radionuclides with unique emission characteristics, integrated into novel microparticles to improve both specificity and therapeutic efficacy. The selection of an optimal radionuclide hinges on critical nuclear and chemical properties, ensuring effective binding to microparticles and delivering favorable clinical outcomes. This review examines the evolution of RSV in joint disorder management, detailing its mechanisms of action, key factors influencing radionuclide and microparticle selection, and the methodologies involved in their development and production. Additionally, it provides an overview of commonly used radionuclides and microparticles, evaluating their effectiveness within the ever-evolving landscape of RSV.

放射滑膜切除术(RSV)代表了核医学中一种先进的治疗方式,旨在治疗对传统治疗无反应的慢性炎性关节疾病。这种有针对性的方法包括关节内给药含有β-放射核素的放射性微粒,选择性地根除发炎的滑膜,同时保留周围组织。RSV作为一种微创、非手术的常规治疗方法,在门诊环境中进行,提供了一种令人信服的替代更具侵入性的干预措施。随着时间的推移,RSV发生了重大演变,从放射性胶体的经验使用过渡到针对不同关节类型量身定制的专门药物的开发。该领域的进展继续探索各种具有独特发射特性的β-放射核素,整合到新型微颗粒中,以提高特异性和治疗效果。最佳放射性核素的选择取决于关键的核和化学性质,确保与微粒的有效结合并提供良好的临床结果。本文综述了RSV在联合疾病管理中的演变,详细介绍了其作用机制,影响放射性核素和微粒选择的关键因素,以及它们的开发和生产所涉及的方法。此外,它还概述了常用的放射性核素和微粒,评估了它们在RSV不断发展的环境中的有效性。
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引用次数: 0
Effect of a Multimodal Pain Therapy Concept Including Intensive Physiotherapy on the Perception of Pain and the Quality of Life of Patients With Chronic Back Pain: A Prospective Observational Multicenter Study Named "RütmuS". 包括强化物理治疗在内的多模式疼痛治疗概念对慢性背痛患者疼痛感知和生活质量的影响:一项名为“r<s:1> tmus”的前瞻性观察性多中心研究。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-05-10 eCollection Date: 2025-01-01 DOI: 10.1155/prm/6693678
Katharina Zaglauer, Andrea Kunsorg, Vanessa Jakob, Lara Görg, Arndt Oehlschlägel, Rainer Riedel, Ursula Marschall, Dieter Welsink, Horst Schuhmacher, Maria Wittmann
<p><p><b>Question and Outcome Measures:</b> In this study, an intervention group (multimodal therapy for chronic back pain) and a control group (standard outpatient treatment) were compared with regard to the primary endpoint of pain (NRS) at rest and the secondary endpoints pain (NRS) during movement, general health status (Short Form 12 (SF-12)), health-related quality of life (EQ-5D-5L), pain disability index (PDI), Hospital Anxiety and Depression Scale-Germany (HADS-D), and Hannover Functional Ability Questionnaire for Measuring Back Pain-Related Disability (FFbH-R). <b>Design and Participants:</b> The total patient cohort of this prospective observational multicenter study consisted of 477 patients who were initially enrolled in the study from January 2019 to September 2020. <b>Intervention:</b> The intervention group received physiotherapy, pain therapy (pain-therapeutic, body-related, and patient-specific treatment), and control examinations from the responsible physician in a 6-month structured interdisciplinary program. The evaluation points used in the analysis are the baseline survey, 6 months and 12 months after the start of the study. <b>Results:</b> A total of 477 patients (243 in the intervention group and 234 in the control group) were included in the analysis; 42 patients in the intervention group deviated from the eligibility criteria due to insufficient adherence to study participation. Nonetheless, they were included in the analysis in line with the ITT principle. The primary endpoint, pain at rest (NRS), showed greater reductions in the intervention group compared to the control group, with mean differences of -0.492 (95% CI: [-0.866, -0.118], <i>p</i> = 0.010) at 6 months (EVA 3) and -0.463 (95% CI: [-0.837, -0.089], <i>p</i> = 0.015) at 12 months (EVA 5), respectively. Regarding the secondary endpoints, pain during movement exhibited a significantly greater reduction in the intervention group compared to the control group (<i>p</i> < 0.001). Quality of life, measured via the EQ-5D-5L index, improved significantly more in the intervention group than in the control group, as did functional capacity (FFbH-R) and physical health (SF-12 KSK) (<i>p</i> < 0.001). In contrast, mental health (SF-12 PSK) declined significantly during the intervention (<i>p</i> < 0.001). Disability (PDI) exhibited a significantly greater reduction in the intervention group compared to the control group (<i>p</i> < 0.001), whereas anxiety and depression levels (HADS-D) showed only slight changes in both groups, with anxiety being significant at <i>p</i> = 0.0164 and depression not significant at <i>p</i> = 0.1093. These results underscore the intervention's effectiveness across multiple health dimensions, particularly pain reduction and quality of life. <b>Conclusion:</b> Multimodal pain therapy over a 6-month period is an effective intervention to improve the perception of pain at rest and during movement while enhancing the subjective quality of life
问题和结果测量:在本研究中,对干预组(多模式治疗慢性背痛)和对照组(标准门诊治疗)在休息时疼痛的主要终点(NRS)和运动时疼痛的次要终点(NRS)、一般健康状况(SF-12)、健康相关生活质量(EQ-5D-5L)、疼痛残疾指数(PDI)、医院焦虑和抑郁量表-德国(HADS-D)、汉诺威背痛相关残疾功能能力问卷(FFbH-R)。设计和参与者:这项前瞻性观察性多中心研究的总患者队列包括477名患者,这些患者最初于2019年1月至2020年9月入组。干预:干预组接受物理治疗、疼痛治疗(疼痛治疗、身体相关治疗和患者特异性治疗),并由负责医生进行为期6个月的结构化跨学科项目的对照检查。分析中使用的评价点是基线调查、研究开始后6个月和12个月。结果:共纳入477例患者(干预组243例,对照组234例);干预组中有42例患者因参与研究的依从性不足而偏离了入选标准。尽管如此,它们还是按照国际电话咨询公司的原则列入了分析。主要终点,静止疼痛(NRS),干预组与对照组相比,在6个月(EVA 3)时的平均差异为-0.492 (95% CI: [-0.866, -0.118], p = 0.010),在12个月(EVA 5)时的平均差异为-0.463 (95% CI: [-0.837, -0.089], p = 0.015)。至于次要终点,与对照组相比,干预组在运动过程中的疼痛明显减少(p < 0.001)。通过EQ-5D-5L指数测量的生活质量,干预组的改善明显大于对照组,功能能力(FFbH-R)和身体健康(SF-12 KSK)的改善也明显大于对照组(p < 0.001)。相比之下,心理健康(SF-12 PSK)在干预期间显著下降(p < 0.001)。与对照组相比,干预组的残疾(PDI)显著降低(p < 0.001),而两组的焦虑和抑郁水平(HADS-D)仅略有变化,焦虑显著(p = 0.0164),抑郁无显著(p = 0.1093)。这些结果强调了干预措施在多个健康方面的有效性,特别是减轻疼痛和提高生活质量。结论:为期6个月的多模式疼痛治疗是一种有效的干预措施,可以改善休息和运动时的疼痛感觉,同时提高主观生活质量。这些益处持续超过治疗期,强调了干预的持久影响。试验注册:德国临床试验注册:DRKS00015800。
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引用次数: 0
Identifying Latent Profiles of Healthy Adults' Biopsychosocial Pain Concepts. 确定健康成人的生物心理社会疼痛概念的潜在特征。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-05-09 eCollection Date: 2025-01-01 DOI: 10.1155/prm/5706849
Catherina Lenhof, Laura Dukek, Linda Wickering, Lena Hitschler, Michael Schneider, Tanja Hechler

Objectives: To develop effective, individualized pain science education for people with chronic (primary) pain, underlying pain concepts, defined as the understanding of what pain is, what function it serves, and what processes are thought to underpin it, are essential. Pain concepts and misconcepts of chronic pain can influence its development and maintenance. This study explores whether profiles of healthy adults' biopsychosocial pain concepts can be identified using a newly developed tool, the biopsychosocial pain concept matrix (BiPS matrix), and if adults assigned to the profiles differ regarding sociodemographic and pain-related variables. Methods: N = 229 healthy adults (75% female, M = 22.66 years, SD = 3.61) participated in an online survey. The BiPS matrix assesses biopsychosocial pain concepts through 40 items on the biological, psychological, and social domains combined with the five content dimensions of the common-sense model of self-regulation. Results: A latent profile analysis (LPA) revealed a five-profile solution with distinct patterns of biopsychosocial pain concepts. Participants assigned to Profile 1 demonstrated strongly developed biopsychosocial pain concepts, Profile 2 showed weakly developed concepts, and Profiles 3 to 5 showed different levels of pain concepts. General and neurophysiological pain knowledge differed between profiles, with higher scores being associated with Profile 1 and lower scores with Profile 5. There were no differences in sociodemographic variables in adults assigned to the different profiles. Discussion: Results provide preliminary evidence for distinct profiles of biopsychosocial pain concepts among healthy adults. Further research should replicate these findings in clinical samples to better understand biopsychosocial pain concepts and their use for individualized pain science education.

目标:为慢性(原发性)疼痛患者发展有效的、个性化的疼痛科学教育,基本的疼痛概念,定义为理解疼痛是什么,它的功能是什么,以及什么过程被认为是支撑疼痛的基础,是必不可少的。疼痛的概念和误解慢性疼痛可以影响其发展和维持。本研究探讨了健康成人的生物心理社会疼痛概念是否可以使用一种新开发的工具来识别,即生物心理社会疼痛概念矩阵(BiPS矩阵),以及分配给这些特征的成年人是否在社会人口学和疼痛相关变量方面存在差异。方法:对229名健康成人进行在线调查,其中女性占75%,M = 22.66岁,SD = 3.61。BiPS矩阵通过生物、心理和社会领域的40个项目,结合自我调节常识模型的五个内容维度,评估生物心理社会疼痛概念。结果:潜在特征分析(LPA)揭示了具有不同生物心理社会疼痛概念模式的五特征解决方案。1组的参与者表现出强烈的生物心理社会疼痛概念,2组的参与者表现出较弱的疼痛概念,3 - 5组的参与者表现出不同程度的疼痛概念。一般的和神经生理性的疼痛知识在不同的概况之间存在差异,较高的分数与概况1相关,较低的分数与概况5相关。在分配到不同概况的成年人中,社会人口学变量没有差异。讨论:研究结果为健康成人中不同的生物心理社会疼痛概念提供了初步证据。进一步的研究应该在临床样本中复制这些发现,以更好地理解生物心理社会疼痛概念及其在个性化疼痛科学教育中的应用。
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引用次数: 0
Clinical Efficacy of Acupuncture Combined With Conventional Therapy for C5 Nerve Root Palsy After Posterior Cervical Decompression Surgery: A Randomized Controlled Study. 针刺联合常规治疗颈后减压术后C5神经根麻痹的临床疗效:一项随机对照研究。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-05-04 eCollection Date: 2025-01-01 DOI: 10.1155/prm/2625552
Hua Wei, Qingfeng Shen, Yuang Fu, Yubo Tan, Junwei Gao, Yingpeng Xia

Objectives: To observe the clinical efficacy of Tiaokou acupoint-penetrating Chengshan combined with conventional therapy for C5 nerve root palsy after posterior cervical decompression surgery. Methods: A total of 52 patients undergoing posterior cervical decompression surgery at Tianjin Union Medical Center from March 2020 to March 2023 were grouped using computer-generated random numbers. Group A (n = 26) received the treatment of acupuncture combined with conventional therapy. Group B (n = 26) received only conventional therapy. Results: The VAS scores of the two groups after treatment were significantly lower than scores before treatment (p < 0.01). The JOA scores, Lovett muscle strength grade, and shoulder ROM of the two groups after treatment were significantly higher than those before treatment (p < 0.01). After treatment, the VAS scores of Group A were significantly lower than those in Group B (p < 0.01) while the JOA scores, Lovett muscle strength grade, and shoulder ROM were significantly higher than those in Group B (p < 0.01). There were significant differences in VAS difference (p < 0.01) and JOA difference (p < 0.01) after 2 weeks of intervention treatment in Group A compared to Group B. There was a significant difference in the improvement of shoulder ROM in Group A after 2 weeks of intervention compared to Group B. Conclusions: The acupuncture method of Tiaokou acupoint-penetrating Chengshan combined with conventional nutritional support therapy was more effective in patients with C5 nerve root palsy after posterior cervical decompression surgery compared to conventional nutritional support therapy. Trial Registration: Clinical Trial Registry identifier: ChiCTR2300073583.

目的:观察调口透成山穴配合常规疗法治疗颈后减压术后C5神经根麻痹的临床疗效。方法:选取2020年3月至2023年3月在天津市协和医疗中心行颈椎后路减压手术的患者52例,采用计算机生成的随机数进行分组。A组(n = 26)采用针刺结合常规疗法治疗。B组(n = 26)仅接受常规治疗。结果:两组患者治疗后VAS评分均显著低于治疗前(p < 0.01)。治疗后两组患者JOA评分、Lovett肌力评分、肩关节活动度均显著高于治疗前(p < 0.01)。治疗后,A组VAS评分显著低于B组(p < 0.01), JOA评分、Lovett肌力分级、肩关节活动度显著高于B组(p < 0.01)。干预治疗2周后A组VAS差异(p < 0.01)、JOA差异(p < 0.01)与b组比较差异有统计学意义。干预治疗2周后A组肩关节活动度改善情况与b组比较差异有统计学意义。针刺调口透成山法联合常规营养支持治疗颈后减压术后C5神经根麻痹患者较常规营养支持治疗更有效。试验注册:临床试验注册标识:ChiCTR2300073583。
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引用次数: 0
Predicting Postcesarean Pain: A Prospective Cohort Study Using a 3-Question Questionnaire, Local Anesthesia Infiltration, and Observer Rating. 预测剖宫产后疼痛:一项使用3题问卷、局部麻醉浸润和观察者评分的前瞻性队列研究。
IF 2.5 3区 医学 Q2 CLINICAL NEUROLOGY Pub Date : 2025-04-21 eCollection Date: 2025-01-01 DOI: 10.1155/prm/6903333
Unyime S Ituk, Sapna Ravindranath

Purpose: Acute postoperative pain is a typical complaint following cesarean delivery (CD). The current standard for postcesarean pain management is the use of a multimodal analgesia regimen which is beneficial for many but may be inadequate for some patients. This study aimed to determine if combining patients' response to a pain rating questionnaire, their pain score during local anesthetic infiltration (LAI) preceding spinal anesthesia for CD, and an anesthesiologist's prediction of postcesarean pain severity can predict the intensity of postcesarean pain. Methods: This was a prospective study of ninety women undergoing scheduled CD under spinal anesthesia. Patients completed a pain rating questionnaire preoperatively and rated pain on LAI before spinal injection, and an anesthesiologist predicted the severity of postcesarean pain. Postoperative pain scores were assessed at rest and with movement at 6, 24, and 48 h after surgery. Results: The patient's expected postoperative pain (β = 0.39, p=0.0011), perceived analgesic requirements (β = 0.34, p=0.0002), pain on LAI (β = 0.22, p=0.004), and anesthesiologist's predicted postoperative pain severity (β = 0.22, p=0.01) were associated with mean postoperative pain after CD. The multivariate model analysis found that the pain rating questionnaire and the an anesthesiologist's prediction of postcesarean pain severity contributed to postoperative pain modeling (R 2 = 0.27). Conclusion: Combining a preoperative pain rating questionnaire with an anesthesiologist's prediction of postcesarean pain severity accounted for 27% of the variance in mean postoperative pain with movement and may be a useful tool in predicting postcesarean pain. Implications: This study highlights the potential of a combined preoperative pain rating questionnaire and anesthesiologist's predictions to improve postcesarean pain management. By accounting for 27% of the variance in mean postcesarean pain with movement, this approach could enhance pain management outcomes for CD patients.

目的:急性术后疼痛是剖宫产(CD)后的典型主诉。目前剖宫产后疼痛管理的标准是使用多模式镇痛方案,这对许多人有益,但对某些患者可能不够。本研究旨在确定结合患者对疼痛评分问卷的反应,他们在CD脊髓麻醉前局部麻醉浸润(LAI)期间的疼痛评分,以及麻醉师对剖宫产后疼痛严重程度的预测是否可以预测剖宫产后疼痛的强度。方法:这是一项前瞻性研究,90名妇女在脊髓麻醉下接受预定的CD。患者术前完成疼痛评定问卷,脊柱注射前用LAI评定疼痛,麻醉医师预测剖宫产后疼痛的严重程度。术后疼痛评分分别于术后6、24和48小时静息和活动时进行评估。结果:患者术后预期疼痛(β = 0.39, p=0.0011)、感知镇痛需求(β = 0.34, p=0.0002)、LAI疼痛(β = 0.22, p=0.004)和麻醉师预测的术后疼痛严重程度(β = 0.22, p=0.01)与CD术后平均疼痛相关。多因素模型分析发现,疼痛评分问卷和麻醉师预测的剖宫产后疼痛严重程度有助于术后疼痛建模(r2 = 0.27)。结论:将术前疼痛评分问卷与麻醉师对剖宫产后疼痛严重程度的预测相结合,可占术后平均运动疼痛方差的27%,可能是预测剖宫产后疼痛的有用工具。意义:本研究强调了术前疼痛评分问卷和麻醉师的预测对改善剖宫产后疼痛管理的潜力。剖宫产后平均疼痛随运动的差异占27%,这种方法可以提高CD患者的疼痛管理结果。
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引用次数: 0
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Pain Research & Management
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