Chronic musculoskeletal pain

慢性肌肉骨骼痛
  • 文章类型: Journal Article
    COVID-19大流行增加了细菌厌恶,对病原体传播的高可能性的厌恶情感反应。虽然心理因素与慢性疼痛有关,细菌厌恶与慢性疼痛之间的关系仍未被研究。这项研究旨在使用在COVID-19大流行期间收集的纵向数据来检查细菌厌恶与慢性疼痛的新发和预后之间的关系。我们在基线和三个月后对全职员工进行了基于网络的调查。收集了有关人口统计特征的数据,心理因素,和慢性疼痛。使用改良的感知疾病易感性量表评估细菌厌恶。我们分析了两次完成调查的1265名小组成员的回答。慢性腰背痛(CLBP)和慢性颈肩痛(CNSP)的患病率与性别有关,睡眠时间短,心理困扰,孤独,和细菌厌恶。分层分析表明,在基线时,细菌厌恶是有和没有CLBP的个体三个月时CLBP的危险因素。对于CNSP在基线时的三个月,即使在对混杂因素进行调整之后。总之,这项初步研究表明,高细菌厌恶是中青年工人CLBP和CNSP的危险因素。
    The COVID-19 pandemic has increased germ aversion, an aversive affective response to a high likelihood of pathogen transmission. While psychological factors are associated with chronic pain, the relationship between germ aversion and chronic pain remains unexplored. This study aimed to examine the relationship between germ aversion and new-onset and prognosis of chronic pain using longitudinal data collected during the COVID-19 pandemic. We conducted web-based surveys of full-time workers at baseline and after three months. Data were collected on demographic characteristics, psychological factors, and chronic pain. Germ aversion was assessed using a modified Perceived Vulnerability to Disease scale. We analyzed responses from 1265 panelists who completed the survey twice. The prevalence of chronic low back pain (CLBP) and chronic neck and shoulder pain (CNSP) was associated with sex, short sleep duration, psychological distress, loneliness, and germ aversion. Stratified analyses showed that germ aversion was a risk factor for CLBP at three months in both individuals with and without CLBP at baseline, and for CNSP at three months in those with CNSP at baseline, even after adjustment for confounders. In conclusion, this preliminary study suggests that high germ aversion is a risk factor for CLBP and CNSP in young and middle-aged workers.
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  • 文章类型: Systematic Review
    背景:移动技术越来越多地用于医疗保健和公共卫生实践中,用于患者沟通,监测,和教育。移动健康(mHealth)工具也已用于促进坚持慢性肌肉骨骼疼痛(CMP)管理,这对实现改善疼痛结果至关重要,生活质量,和具有成本效益的医疗保健。
    目的:本系统综述的目的是评估有关依从性的文献的25年趋势,可用性,可行性,以及患者和医疗保健提供者在CMP管理中的mHealth干预措施的可接受性。
    方法:我们搜索了PubMed,科克伦中部,MEDLINE,EMBASE,和WebofScience数据库,用于评估1999年1月至2023年12月mHealth在CMP管理中的作用的研究。感兴趣的结果包括mHealth干预对患者依从性的影响;干预后疼痛特异性临床结果;和可用性,可行性,以及目标最终用户在慢性疼痛管理中mHealth工具和平台的可接受性。
    结果:共89篇(26,429名参与者)纳入系统评价。在纳入的研究中,移动应用程序是最常用的mHealth工具(78/89,88%)。其次是移动应用程序加显示器(5/89,6%),移动应用程序加可穿戴传感器(4/89,4%),和基于网络的移动应用程序加显示器(1/89,1%)。可用性,可行性,在26%(23/89)的研究中评估了mHealth干预措施的可接受性或患者偏好,并观察到总体较高.总的来说,30%(27/89)的研究使用随机对照试验(RCT),队列,或试点设计,以评估m健康干预对患者依从性的影响,在93%(25/27)的这些研究中观察到显著改善(所有P<0.05)。在测量mHealth对CMP特异性临床结果的影响的29个RCT中,有27个(93%)报告了组间差异的显着(在P<0.05时判断)。
    结论:mHealth工具有很大的潜力来更好地促进对CMP管理的坚持,目前支持其有效性的证据普遍很高。进一步的研究应集中在mHealth干预措施的成本效益上,以更好地将这些工具纳入医疗保健实践。
    背景:国际前瞻性系统审查注册(PROSPERO)CRD42024524634;https://www.crd.约克。AC.uk/prospro/display_record.php?RecordID=524634。
    BACKGROUND: Mobile technologies are increasingly being used in health care and public health practice for patient communication, monitoring, and education. Mobile health (mHealth) tools have also been used to facilitate adherence to chronic musculoskeletal pain (CMP) management, which is critical to achieving improved pain outcomes, quality of life, and cost-effective health care.
    OBJECTIVE: The aim of this systematic review was to evaluate the 25-year trend of the literature on the adherence, usability, feasibility, and acceptability of mHealth interventions in CMP management among patients and health care providers.
    METHODS: We searched the PubMed, Cochrane CENTRAL, MEDLINE, EMBASE, and Web of Science databases for studies assessing the role of mHealth in CMP management from January 1999 to December 2023. Outcomes of interest included the effect of mHealth interventions on patient adherence; pain-specific clinical outcomes after the intervention; and the usability, feasibility, and acceptability of mHealth tools and platforms in chronic pain management among target end users.
    RESULTS: A total of 89 articles (26,429 participants) were included in the systematic review. Mobile apps were the most commonly used mHealth tools (78/89, 88%) among the included studies, followed by mobile app plus monitor (5/89, 6%), mobile app plus wearable sensor (4/89, 4%), and web-based mobile app plus monitor (1/89, 1%). Usability, feasibility, and acceptability or patient preferences for mHealth interventions were assessed in 26% (23/89) of the studies and observed to be generally high. Overall, 30% (27/89) of the studies used a randomized controlled trial (RCT), cohort, or pilot design to assess the impact of the mHealth intervention on patients\' adherence, with significant improvements (all P<.05) observed in 93% (25/27) of these studies. Significant (judged at P<.05) between-group differences were reported in 27 of the 29 (93%) RCTs that measured the effect of mHealth on CMP-specific clinical outcomes.
    CONCLUSIONS: There is great potential for mHealth tools to better facilitate adherence to CMP management, and the current evidence supporting their effectiveness is generally high. Further research should focus on the cost-effectiveness of mHealth interventions for better incorporating these tools into health care practices.
    BACKGROUND: International Prospective Register of Systematic Reviews (PROSPERO) CRD42024524634; https://www.crd.york.ac.uk/prospero/display_record.php?RecordID=524634.
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  • 文章类型: Journal Article
    背景:患有慢性肌肉骨骼疼痛(CMSP)的人通常体力活动较少。各种因素可以影响活动水平。这项研究的目的是监测身体活动,以每天的步数来评估,随着时间的推移,在患有CMSP的人群中,并确定可能与此活动功能相关的因素。
    方法:这项前瞻性研究涉及骨科创伤导致CMSP的康复患者。在入境时,参与者完成了评估疼痛的自我报告问卷,焦虑,抑郁症,灾难性的,运动恐惧症,和行为活动模式(回避,起搏和过度)。他们还进行了功能测试,评估步行耐力和身体素质。要确定每日步数,参与者在康复期间和康复后3个月佩戴加速度计1周.在三个时间点之间比较了每天的步数:康复周末(对康复前活动的估计;T1),康复工作日(T2),和康复后(T3)。线性回归模型用于分析T2和T3时的每日步数与自我报告和基于性能的参数之间的关联。
    结果:分析了来自145名参与者的数据。T2期间的平均步数明显高于T1和T3(7323[3047]与4782[2689],p<0.001,科恩的d=0.769,和4757[2680],p<0.001,科恩的d=0.693),而T1和T3结果相似(p=0.92,Cohen'sd=0.008)。时间点之间每天步数的相关性较低(r≤0.4)。多变量回归模型揭示了T2时的每日步数与干扰行走的疼痛之间的关联,焦虑和过度行为。T3时的每日步数与过度行为和身体健康有关。
    结论:尽管有慢性疼痛,如果给予激励措施,骨科创伤后康复的人们会增加体力活动。当这些激励措施消失时,大多数人恢复到以前的活动水平。多模式随访方法可以包括治疗和环境激励措施,以帮助维持该人群的身体活动。
    BACKGROUND: People with chronic musculoskeletal pain (CMSP) often have low physical activity. Various factors can influence the activity level. The aim of this study was to monitor physical activity, assessed by the number of steps per day, over time in people with CMSP and identify factors that could be associated with this activity feature.
    METHODS: This prospective study involved people undergoing rehabilitation following an orthopedic trauma that had led to CMSP. At entry, participants completed self-reported questionnaires assessing pain, anxiety, depression, catastrophyzing, kinesiophobia, and behavioural activity patterns (avoidance, pacing and overdoing). They also underwent functional tests, assessing walking endurance and physical fitness. To determine daily step counts, participants wore an accelerometer for 1 week during rehabilitation and 3 months post-rehabilitation. The number of steps per day was compared among three time points: weekend of rehabilitation (an estimate of pre-rehabilitation activity; T1), weekdays of rehabilitation (T2), and post-rehabilitation (T3). Linear regression models were used to analyze the association between daily steps at T2 and at T3 and self-reported and performance-based parameters.
    RESULTS: Data from 145 participants were analyzed. The mean number of steps was significantly higher during T2 than T1 and T3 (7323 [3047] vs. 4782 [2689], p < 0.001, Cohen\'s d = 0.769, and 4757 [2680], p < 0.001, Cohen\'s d = 0.693), whereas T1 and T3 results were similar (p = 0.92, Cohen\'s d = 0.008). Correlations of number of steps per day among time points were low (r ≤ 0.4). Multivariable regression models revealed an association between daily steps at T2 and pain interfering with walking, anxiety and overdoing behaviour. Daily steps at T3 were associated with overdoing behaviour and physical fitness.
    CONCLUSIONS: Despite chronic pain, people in rehabilitation after an orthopedic trauma increased their physical activity if they were given incentives to do so. When these incentives disappeared, most people returned to their previous activity levels. A multimodal follow-up approach could include both therapeutic and environmental incentives to help maintain physical activity in this population.
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  • 文章类型: Journal Article
    背景:开发了疼痛敏感性问卷(PSQ)来评估一般的疼痛敏感性。
    目的:本研究旨在验证希腊语版本的PSQ。
    方法:问卷被翻译成希腊语(PSQ-GR),并在一小部分慢性疼痛患者(n=35)中进行试验。共有146名慢性疼痛患者和健康志愿者完成了PSQ-GR,疼痛突变量表(PCS),医院焦虑抑郁量表(HADS)和中央敏感量表(CSI)。为了评估重测可靠性,36名志愿者在7±2天内两次完成PSQ-GR。
    结果:PSQ-total的内部一致性非常好(Cronbach的alpha0.90-0.96),PSQ-小调,和PSQ-中等。PSQ-total的组内相关系数估计为0.90-0.96,PSQ-次要和PSQ-中等,PSQ-总计的SEM为0.59-0.90,PSQ-次要和PSQ-中等大约。PSQ-total的最小可检测变化为0.48,PSQ次要为0.47,PSQ中等为0.44。PSQ-GR与HADS呈显著正相关(r=0.38,p<0.01),PCS(r=0.41,p<0.01)和CSI(r=0.30,p<0.01)。在健康志愿者和慢性疼痛患者之间,PSQ-GR评分具有统计学上的显着差异。
    结论:PSQ-GR是一种可靠且有效的工具,可以评估健康个体和慢性肌肉骨骼疼痛患者的疼痛敏感性。
    BACKGROUND: The Pain Sensitivity Questionnaire (PSQ) was developed to assess general pain sensitivity.
    OBJECTIVE: This study aimed to validate the Greek version of PSQ.
    METHODS: The questionnaire was translated into Greek (PSQ-GR) and piloted in a small sample of patients with chronic pain (n = 35). A total of 146 chronic pain patients and healthy volunteers completed the PSQ-GR, the Pain Catastrophizing Scale (PCS), Hospital Anxiety and Depression Scale (HADS) and Central Sensitization Inventory (CSI). To evaluate the test-retest reliability, 36 volunteers completed the PSQ-GR twice over 7 ± 2 days.
    RESULTS: Internal consistency was excellent (Cronbach\'s alpha 0.90-0.96) for PSQ-total, PSQ-minor, and PSQ-moderate. The Intraclass Correlation Coefficient was estimated at 0.90-0.96 for PSQ-total, PSQ-minor and PSQ-moderate and the SEM was 0.59-0.90 for PSQ-total, PSQ-minor and PSQ-moderate approximately. The smallest detectable change was 0.48 for PSQ-total, 0.47 for PSQ-minor and 0.44 for PSQ-moderate. Positive and significant correlations were observed between PSQ-GR and HADS (r = 0.38, p < 0.01), PCS (r = 0.41, p < 0.01) and CSI (r = 0.30, p < 0.01). Statistically significant differences in PSQ-GR scores were identified between the healthy volunteers and the chronic pain patients.
    CONCLUSIONS: The PSQ-GR is a reliable and valid tool that can assess pain sensitivity in healthy individuals and chronic musculoskeletal pain patients.
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  • 文章类型: Journal Article
    遭受政治暴力(PV)的人有患精神疾病的风险,慢性非传染性疾病,慢性疼痛,预期寿命下降。然而,这些指标主要在退伍军人和难民中进行了研究。这项研究的目的是估计1973年至1990年独裁统治期间智利PV受害者中慢性肌肉骨骼疼痛(CMP)和中枢致敏相关症状(CSRS)的患病率。进行了一项横断面观察性多中心研究。来自智利卫生部计划的六个中心的三百二十五人参加了会议。CMP的存在是由≥3个月的疼痛史确定的。CSRS是使用中央敏化清单确定的。约69.23%的样本具有CMP(76.85%的女性和56.56%的男性)。大约60%的CMP患者表现出高水平的CSRS严重程度(66.67%的女性和44.93%的男性)。女性的CMP比例明显更高(p<.001),CSRS严重程度与女性之间存在关联(p=.004)。1973年至1990年独裁统治期间,智利PV的受害者表现出CMP的高流行率和高水平的CSRS严重性。这两种情况对女性的影响大于男性。未来的研究需要进一步深入研究这些变量的行为及其对该人群生活质量的影响。
    People who suffer political violence (PV) are at risk of developing mental illness, chronic noncommunicable diseases, chronic pain, and decreased life expectancy. However, these indicators have been studied primarily in war veterans and refugees. The objective of this study was to estimate the prevalence of chronic musculoskeletal pain (CMP) and central sensitization-related symptoms (CSRS) in Chilean victims of PV during the 1973 to 1990 dictatorship. A cross-sectional observational multicenter study was conducted. Three hundred twenty-five people from six centers of a Ministry of Health of Chile program participated. The presence of CMP was determined by a history of pain ≥3 months, and CSRS was determined using the central sensitization inventory. About 69.23% of the sample had CMP (76.85% of females and 56.56% of males). About 60% of people with CMP showed a high level of CSRS severity (66.67% females and 44.93% males). Females presented significantly higher proportions of CMP (p < .001), and there was an association between CSRS severity and being female (p = .004). Chilean victims of PV during the 1973 to 1990 dictatorship presented a high prevalence of CMP and high-level CSRS severity. Both conditions affected females more than males. Future studies are needed to further delve into these variables\' behavior and their influence on the quality of life in this population.
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  • 文章类型: Journal Article
    运动是慢性非特异性下腰痛(CNSLBP)的一线治疗方法。运动结合特定的呼吸技术有可能改善多因素结果。没有以前的研究,然而,在统一的临床研究环境中,比较了有或没有特定呼吸方案的相同运动之间的结果。
    1)调查将同步呼吸与运动控制练习相结合的可行性,并评估合格标准,随机化程序,和辍学率。2)研究干预措施对多因素结局指标的初步疗效。
    将30名CNSLBP患者随机分为两组。两组都进行了四次接触诊所访问,在那里他们接受了个性化的家庭运动控制练习,并进行了两个月的练习。实验组包括运动控制运动干预结合同步呼吸技术。试用注册号:NCT05268822。
    通过在预先规定的时间框架内达到30个科目的招募目标,入学率为24.8%(30/121),证明了可行性。参与者成功地遵守了同步呼吸技术。两组之间的家庭锻炼依从性几乎相同,没有任何不良事件。疼痛强度的初步疗效发现,残疾,实验组的自我效能超过了最小的临床重要差异。在对照组的任何结果测量中未观察到此类发现。总的来说,多因素差异是一致的,因为11项结局指标中有9项显示实验组有更大的改善.
    与运动控制锻炼方案同步呼吸是可行的,与单独的相同锻炼相比,可能更有利于改善多因素结果。结果表明进展为全面试验。
    UNASSIGNED: Exercise is a first-line treatment for chronic non-specific low back pain (CNSLBP). Exercise combined with specific breathing techniques have the potential to improve multifactorial outcomes. No previous studies, however, have compared outcomes between identical exercises with or without a specific breathing protocol in a uniform clinical study setting.
    UNASSIGNED: 1) To investigate the feasibility of combining synchronized breathing with movement control exercises and evaluate eligibility criteria, randomization procedures, and dropout rates. 2) To study the preliminary efficacy of the interventions on multifactorial outcome measures.
    UNASSIGNED: Thirty subjects with CNSLBP were randomized into two groups. Both groups had four contact clinic visits where they received personalized home movement control exercises to practice over two months. The experimental group included a movement control exercise intervention combined with synchronized breathing techniques. Trial registration number: NCT05268822.
    UNASSIGNED: Feasibility was demonstrated by meeting the recruitment goal of 30 subjects within the pre-specified timeframe with enrolment rate of 24.8% (30/121). Synchronized breathing techniques were successfully adhered by participants. Home exercise adherence was nearly identical between the groups without any adverse events. Preliminary efficacy findings on pain intensity, disability, and self-efficacy in the experimental group exceeded the minimal clinically important difference. No such findings were observed in any outcome measures within the control group. Overall, multifactorial differences were consistent because nine out of eleven outcome measures showed greater improvements for the experimental group.
    UNASSIGNED: The synchronized breathing with movement control exercises protocol was feasible and may be more beneficial for improving multifactorial outcomes compared to identical exercises alone. Results suggested progression to a full-scale trial.
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  • 文章类型: Journal Article
    背景:中枢敏化(CS)在慢性肌肉骨骼(MSK)疼痛中具有重要作用,这是全球残疾的主要原因之一。
    目的:探讨慢性MSK疼痛中CS相关症状与残疾的关系。
    方法:多中心横断面调查。
    方法:人口统计学和临床变量,包括位置,持续时间,记录疼痛的严重程度。在残疾检查中,伊斯坦布尔下腰痛残疾指数下腰痛,颈部疼痛和残疾量表,手臂的快速残疾,肩膀,手用于肩部/上肢疼痛,使用膝关节损伤和骨关节炎对膝关节疼痛的预后评分。通过中枢致敏量表(CSI)调查CS相关症状。根据CSI得分,使用T检验和ANOVA比较患者数据.使用Pearson相关和多元回归分析研究CSI与所选变量之间的关联。
    结果:500名参与者的平均CSI得分为40.46(SD:15.87)。发现CSI≥40的患者疼痛和残疾水平较高,生活质量较差(p<0.05)。在方差分析中,两组间的CS严重程度有显著差异,症状持续时间,和所有临床评分(p<0.01)。在多元回归分析中,发现CSI和VAS评分与所有疼痛组的残疾有关,而疼痛持续时间仅对膝关节残疾的变化有效。
    结论:CS相关症状,与疼痛和残疾增加有关,慢性MSK疼痛患者应密切监测。
    Central sensitization (CS) has an important role in chronic musculoskeletal (MSK) pain, which is one of the leading causes of disability worldwide.
    To investigate the relationship between CS-related symptoms and disability in chronic MSK pain.
    Multi-center cross-sectional survey.
    Demographic and clinical variables including location, duration, and severity of pain were recorded. In the examination of disability, Istanbul Low Back Pain Disability Index for low back pain, Neck Pain and Disability Scale for neck pain, Quick Disability of the Arm, Shoulder, and Hand for shoulder/upper extremity pain, and Knee Injury and Osteoarthritis Outcome Score for knee pain were used. CS-related symptoms were investigated via the central sensitization inventory (CSI). Based on CSI scores, patient data were compared using the T test and an ANOVA. The association between CSI and selected variables was investigated using Pearson correlation and multivariate regression analysis.
    The mean CSI score of five hundred participants was 40.46 (SD: 15.87). Patients with CSI≥40 were found to have higher levels of pain and disability and a poorer quality of life (p < 0.05). In ANOVA, significant differences between groups were observed in CS severity levels for VAS, symptom duration, and all clinical scores (p < 0.01). In the multivariate regression analysis, CSI and VAS scores were found to be related to disability in all pain groups, while pain duration was effective only in the change of knee disability.
    CS-related symptoms, which are related to increased pain and disability, should be closely monitored in patients with chronic MSK pain.
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  • 文章类型: Journal Article
    目的:评估耳穴贴压(AA)在治疗慢性肌肉骨骼疼痛患者疼痛和残疾方面的有效性。材料和方法:从开始到2023年5月7日,对六个电子数据库进行了系统搜索,以确定相关的随机对照试验(RCT)。两名独立审稿人筛选了摘要和全文,提取的数据,并使用RoB2评估偏倚风险。主要结果是疼痛强度和残疾。次要结果是疼痛压力阈值,痛苦灾难化水平,和避免恐惧的信念。使用随机效应模型进行荟萃分析。使用建议分级评估来评估证据的确定性,发展,和评价。去除低质量纸张后进行敏感性分析。结果:在633条确定的记录中,纳入了6项涉及496名参与者的研究.所有纳入的研究比较了AA与假对照治疗各种慢性肌肉骨骼疼痛的有效性。进行了四个荟萃分析,以比较AA与假对照的有效性。低质量证据支持AA对干预后主观疼痛减轻有很大影响(标准化平均差[SMD]=-0.95;95%置信区间[CI]:-1.36至-0.54;p=0.00;I2=52.61%);中等质量证据证实AA对提高干预后压力疼痛阈值有很大影响(SMD=-0.55;95%CI:-0.88至-0.23;p=0;有低质量的证据表明AA对减少干预后残疾有很大影响(SMD=-0.68;95%CI:-1.24至-0.12;p=0.02;I2=51.33%)。我们的敏感性分析重申了关于干预后立即减轻疼痛的相同结论。14名参与者报告了最小的不良事件,包括酸痛,压痛,刺激,和发红,它在1-7天内消失了。讨论:我们的系统评价显示,AA显著改善疼痛,压力疼痛阈值,与假治疗相比,治疗后立即患有各种慢性肌肉骨骼疼痛状况的个体的残疾。鉴于缺乏研究和不一致的协议,未来的随机对照试验有必要评估AA在慢性肌肉骨骼疼痛患者中的有效性,并在更长时间的随访中使用详细的方案,这允许研究人员和临床医生优化AA干预。结论:AA对慢性肌肉骨骼疼痛具有立即的治疗后益处,而其在1个月或6个月随访时的效果仍不确定。
    Objectives: To assess the effectiveness of auricular acupressure (AA) in managing pain and disability in individuals with chronic musculoskeletal pain. Materials and Methods: A systematic search on six electronic databases was performed from their inception to May 7, 2023, to identified relevant randomized controlled trials (RCTs). Two independent reviewers screened the abstracts and full texts, extracted data, and assessed risk of bias using RoB 2. The primary outcomes were pain intensity and disability. The secondary outcomes were pain pressure thresholds, pain catastrophizing level, and fear avoidance beliefs. A random-effects model was used for meta-analyses. The certainty of evidence was evaluated using the Grading of Recommendations Assessment, Development, and Evaluation. Sensitivity analyses were conducted after removing low-quality papers. Results: Of 633 identified records, six studies involving 496 participants were included. All included studies compared the effectiveness of AA with sham controls in treating various chronic musculoskeletal pain. Four meta-analyses were conducted to compare the effectiveness of AA with sham controls. Low-quality evidence supported that AA had a large effect size on postintervention subjective pain reduction (standardized mean difference [SMD] = -0.95; 95% confidence interval [CI]: -1.36 to -0.54; p = 0.00; I2 = 52.61%); moderate-quality evidence substantiated that AA had a large effect size on enhancing postintervention pressure pain threshold (SMD = -0.55; 95% CI: -0.88 to -0.23; p = 0.00; I2 = 0%). There was low-quality evidence that AA had a large effect on reducing postintervention disability (SMD = -0.68; 95% CI: -1.24 to -0.12; p = 0.02; I2 = 51.33%). Our sensitivity analysis reaffirmed the same conclusion regarding pain reduction immediately after the intervention. Fourteen participants reported minimal adverse events, including soreness, tenderness, irritation, and redness, which disappeared within 1-7 days. Discussion: Our systematic review revealed that AA significantly improved pain, pressure pain thresholds, and disability in individuals with various chronic musculoskeletal pain conditions immediately post-treatment compared with sham treatment. Given the paucity of studies and inconsistent protocols, future RCTs are warranted to evaluate the effectiveness of AA in people with chronic musculoskeletal pain at a longer follow-up with detailed protocols, which allows researchers and clinicians to optimize AA intervention. Conclusion: AA has immediate post-treatment benefits for chronic musculoskeletal pain, whereas its effects at the 1- or 6-month follow-up remain uncertain.
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  • 文章类型: Journal Article
    慢性肌肉骨骼(MSK)疼痛在老年人中普遍存在,并具有丧失独立性和生活质量低下的巨大风险。虽然肥胖被认为是慢性MSK疼痛的危险因素,高体重指数和低体重指数(BMI)在老年人中与较高的疼痛报告相关.区分脂肪量和瘦体重的身体成分测量可能有助于澄清该高危人群中BMI和MSK疼痛之间看似矛盾的关联。
    24名老年人(平均年龄:78.08±5.1岁)完成了双能X射线吸收法(DEXA),和疼痛措施(慢性疼痛分级量表,解剖疼痛部位的数量,压力痛阈值,机械时间求和)。皮尔逊相关性和多元线性回归检查了体重指数(BMI)、身体成分指数,和痛苦。
    发现疼痛部位数量与BMI(b=0.37)和总脂肪量(b=0.42)之间存在显著正相关,考虑年龄和性别。全身瘦体重与压力疼痛敏感性相关(b=0.65),提示较大的瘦体重与较低的机械性疼痛敏感性相关。
    这项探索性试点研究的结果表明,瘦体重可能为老年人疼痛处理的适应不良变化提供额外的弹性,并强调了区分身体成分指数和总体体重指数的重要性,以更好地了解老年人肥胖和MSK疼痛之间的复杂关系。
    UNASSIGNED: Chronic musculoskeletal (MSK) pain is prevalent in older adults and confers significant risk for loss of independence and low quality of life. While obesity is considered a risk factor for developing chronic MSK pain, both high and low body mass index (BMI) have been associated with greater pain reporting in older adults. Measures of body composition that distinguish between fat mass and lean mass may help to clarify the seemingly contradictory associations between BMI and MSK pain in this at-risk group.
    UNASSIGNED: Twenty-four older adults (mean age: 78.08 ± 5.1 years) completed dual-energy x-ray absorptiometry (DEXA), and pain measures (Graded Chronic Pain Scale, number of anatomical pain sites, pressure pain threshold, mechanical temporal summation). Pearson correlations and multiple liner regression examined associations between body mass index (BMI), body composition indices, and pain.
    UNASSIGNED: Significant positive associations were found between number of pain sites and BMI (b = 0.37) and total fat mass (b = 0.42), accounting for age and sex. Total body lean mass was associated with pressure pain sensitivity (b = 0.65), suggesting greater lean mass is associated with less mechanical pain sensitivity.
    UNASSIGNED: The results from this exploratory pilot study indicate lean mass may provide additional resilience to maladaptive changes in pain processing in older adults, and highlights the importance of distinguishing body composition indices from overall body mass index to better understand the complex relationship between obesity and MSK pain in older adults.
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  • 文章类型: Journal Article
    背景:大麻具有镇痛和抗炎特性的信念继续吸引患有慢性肌肉骨骼(MSK)疼痛的患者使用。然而,大麻在慢性MSK疼痛治疗中的作用尚待确定.这项研究检查了1)比率,使用模式,和自我报告的慢性MSK疼痛患者使用大麻的功效,以及2)目前未使用大麻的慢性MSK疼痛患者对大麻使用的兴趣和潜在障碍。
    方法:前瞻性收集了向大学健康网络骨科诊所就诊的慢性MSK疼痛患者的自我报告大麻使用和感知疗效,多伦多,加拿大。主要因变量是当前或过去使用大麻来治疗慢性MSK疼痛;使用双变量和多变量逻辑回归来识别与该结果独立相关的患者特征。次要结果进行了描述性总结,包括大麻使用者的自我感知效能,和兴趣以及大麻非使用者使用大麻的障碍。
    结果:样本包括629名患有慢性MSK疼痛的患者(平均年龄:56±15.7岁;56%为女性)。总的来说,144(23%)报告过去或现在使用大麻来管理其MSK疼痛,63.7%的人认为大麻非常有效或有点有效,26.6%的人认为大麻稍微有效。在这项研究人群中,大麻使用的最强预测因素是娱乐性大麻使用史(OR12.7,p<0.001)。在非大麻使用者中(N=489),65%表示有兴趣使用大麻来管理他们的慢性MSK疼痛,但是使用的常见障碍包括缺乏关于获取的知识,使用和证据,和耻辱。
    结论:五分之一的患者出现慢性MSK疼痛的整形外科医生正在使用或已经使用大麻来控制疼痛。大多数人报告说它是有效的。在非用户中,三分之二的人表示有兴趣使用大麻来管理他们的MSK疼痛,但是存在共同的使用障碍。未来的双盲安慰剂对照试验需要了解这种报告的疗效是否准确,什么角色,如果有的话,大麻可能在慢性MSK疼痛的管理中起作用。
    BACKGROUND: The belief that cannabis has analgesic and anti-inflammatory properties continues to attract patients with chronic musculoskeletal (MSK) pain towards its use. However, the role that cannabis will play in the management of chronic MSK pain remains to be determined. This study examined 1) the rate, patterns of use, and self-reported efficacy of cannabis use among patients with chronic MSK pain and 2) the interest and potential barriers to cannabis use among patients with chronic MSK pain not currently using cannabis.
    METHODS: Self-reported cannabis use and perceived efficacy were prospectively collected from chronic MSK pain patients presenting to the Orthopaedic Clinic at the University Health Network, Toronto, Canada. The primary dependent variable was current or past use of cannabis to manage chronic MSK pain; bivariate and multivariable logistic regression were used to identify patient characteristics independently associated with this outcome. Secondary outcomes were summarized descriptively, including self-perceived efficacy among cannabis users, and interest as well as barriers to cannabis use among cannabis non-users.
    RESULTS: The sample included 629 patients presenting with chronic MSK pain (mean age: 56±15.7 years; 56% female). Overall, 144 (23%) reported past or present cannabis use to manage their MSK pain, with 63.7% perceiving cannabis as very or somewhat effective and 26.6% considering it as slightly effective. The strongest predictor of cannabis use in this study population was a history of recreational cannabis use (OR 12.7, p<0.001). Among cannabis non-users (N=489), 65% expressed interest in using cannabis to manage their chronic MSK pain, but common barriers to use included lack of knowledge regarding access, use and evidence, and stigma.
    CONCLUSIONS: One in five patients presenting to an orthopaedic surgeon with chronic MSK pain are using or have used cannabis with the specific intent to manage their pain, and most report it to be effective. Among non-users, two-thirds reported an interest in using cannabis to manage their MSK pain, but common barriers to use existed. Future double-blind placebo-controlled trials are required to understand if this reported efficacy is accurate, and what role, if any, cannabis may play in the management of chronic MSK pain.
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