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The effect of social exclusion on pain perception and heart rate variability in healthy controls and somatoform pain patients. 社会排斥对健康对照和躯体型疼痛患者疼痛感知和心率变异性的影响。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-12-04 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0042
Fabrice Kleber, Andreas Reif, Moritz de Greck

Objectives: The overlapping neural networks of social and physical pain have been investigated intensively in recent years. It was postulated that triggering social pain might result in greater physical pain. Nonetheless, how this affects somatoform pain disorder has not yet been considered. Since an increased pain processing activity is reported in these patients, the investigation of social exclusion and its effect on this group seems interesting. Hence, the aim of this study was to compare the influence of social exclusion on healthy controls and patients with somatoform pain disorder.

Methods: Nineteen patients with somatoform pain disorder and 19 healthy controls were examined. Cyberball, a virtual ball-tossing paradigm, was used to experimentally induce social exclusion and inclusion. To measure effects on pain perception, pressure pain thresholds and heart rate variability (HRV) were recorded after each round of cyberball. Demographic data, pain medication, and potential psychosocial moderators were collected by questionnaires.

Results: After social exclusion, pressure pain thresholds were significantly reduced in healthy controls (p < 0.01) as well as somatoform pain patients (p < 0.05), while HRV increased only in patients with somatoform pain disorder (p < 0.05) indicating increased parasympathetic activity.

Conclusion: This study is the first to analyse the effects of social exclusion on pain perception in somatoform pain disorder. While the reduction in pressure pain thresholds is in line with the social pain literature, the effects on HRV could be interpreted as a form of pain regulation mechanism. However, further research is needed to investigate the role of parasympathetic activity in socially excluded somatoform pain patients.

目的:近年来,人们对社会和身体疼痛的重叠神经网络进行了深入的研究。据推测,引发社交痛苦可能会导致更大的身体痛苦。然而,这如何影响躯体形式的疼痛障碍尚未被考虑。由于在这些患者中有增加的疼痛处理活动的报道,社会排斥及其对这一群体的影响的调查似乎很有趣。因此,本研究的目的是比较社会排斥对健康对照和躯体形式疼痛障碍患者的影响。方法:对19例躯体型疼痛障碍患者和19例健康对照者进行分析。赛博球(Cyberball)是一种虚拟投球范式,用于诱导社会排斥和包容的实验。为了测量对疼痛感知的影响,在每轮赛博球后记录压力疼痛阈值和心率变异性(HRV)。通过问卷调查收集人口统计数据、止痛药和潜在的社会心理调节因子。结果:社会排斥后,健康对照组和躯体型疼痛患者的压力痛阈值均显著降低(p < 0.01),而HRV仅在躯体型疼痛障碍患者中升高(p < 0.05),表明副交感神经活动增加。结论:本研究首次分析了社会排斥对躯体型疼痛障碍患者疼痛感知的影响。虽然压力疼痛阈值的降低与社会疼痛文献一致,但对HRV的影响可以被解释为一种疼痛调节机制。然而,需要进一步的研究来调查副交感神经活动在社会排斥的躯体型疼痛患者中的作用。
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引用次数: 0
Pain catastrophizing levels differentiate between common diseases with pain: HIV, fibromyalgia, complex regional pain syndrome, and breast cancer survivors. 疼痛灾难化水平可区分常见的疼痛疾病:艾滋病、纤维肌痛、复杂性区域疼痛综合症和乳腺癌幸存者。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-11-05 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0049
Reetta Sipilä, Eija Kalso, Harriet Kemp, Teemu Zetterman, Fabiola Escolano Lozano, Andrew S C Rice, Frank Birklein, Violeta Dimova

Objectives: Pain catastrophizing is a core psychological factor determining pain experience. We addressed the question of whether patients with different pain syndromes group into different pain catastrophizing phenotypes.

Methods: A total of 727 patients with chronic pain associated with four primary syndromes: Breast cancer (BC) survivors (n = 400), fibromyalgia (FM, n = 52), complex regional pain syndrome (CRPS, n = 155), and HIV (n = 120) were first studied for differences in levels of pain catastrophizing (Pain Catastrophizing Scale, PCS) and pain intensity by analysis of variance. Subsequently, individual scores of the PCS subscales "rumination", "magnification," and "helplessness" from the pooled cohorts were submitted to multivariate k-means clustering to explore subgroups.

Results: Three clusters defined by the level of catastrophizing were identified. The "low catastrophizing" cluster (n = 377) included most of the BC patients (71.0%) and the "moderate catastrophizing" cluster (n = 256) most of the FM patients (61.5%). HIV (31.9%) and CRPS (44.7%) patients were over-represented in the "high catastrophizing" cluster (n = 94) with the highest catastrophizing tendencies in all dimensions. These patients reported more helplessness than the patients in the two other clusters.

Conclusions: The primary syndrome causing the pain has an impact on self-reported pain-related catastrophizing. Helplessness is a predominant feature in HIV and CRPS patients and therefore an important target in pain rehabilitation.

目的:疼痛灾难化是决定疼痛体验的核心心理因素:疼痛灾难化是决定疼痛体验的核心心理因素。我们研究了不同疼痛综合征的患者是否会形成不同的疼痛灾难化表型:共有 727 名患者患有与四种主要综合征相关的慢性疼痛:乳腺癌(BC)幸存者(n = 400)、纤维肌痛(FM,n = 52)、复杂区域疼痛综合征(CRPS,n = 155)和艾滋病病毒(HIV,n = 120)患者的疼痛灾难化程度(疼痛灾难化量表,PCS)和疼痛强度的差异首先通过方差分析进行了研究。随后,对汇总队列中的 PCS 子量表 "反刍"、"放大 "和 "无助 "的个人得分进行多元 K-均值聚类,以探索亚群:结果:根据灾难化程度确定了三个群组。低度灾难化 "群组(n = 377)包括大多数 BC 患者(71.0%),"中度灾难化 "群组(n = 256)包括大多数 FM 患者(61.5%)。艾滋病毒(31.9%)和 CRPS(44.7%)患者在 "高度灾难化 "群组(n = 94)中所占比例较高,在所有维度上都具有最高的灾难化倾向。这些患者比其他两个群组的患者报告了更多的无助感:结论:引起疼痛的主要综合征对自我报告的疼痛相关灾难化有影响。无助感是 HIV 和 CRPS 患者的主要特征,因此也是疼痛康复的一个重要目标。
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引用次数: 0
To speak or not to speak? A secondary data analysis to further explore the context-insensitive avoidance scale. 说还是不说?通过二手数据分析进一步探索对情境不敏感的回避量表。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0039
Pernilla Abrahamsson, Katja Boersma, Monica Buhrman

Objectives: Inflexibly relying on avoidance of expression may increase and perpetuate pain-related emotional distress in patients with chronic pain. The context-insensitive avoidance (CIA) scale was recently developed to measure the degree to which patients avoid expressing their pain and distress in social situations. This study explored the psychometric properties of the CIA scale in a new sample.

Methods: This study uses baseline data from a treatment trial for n = 115 patients with chronic pain and co-occurring emotional distress. Reliability and construct and criteria validity were studied using the same instruments as in the original psychometric study and further explored in two new measures. A series of multiple regression analyses were conducted to assess the relationship between the CIA scale and criteria variables compared to the other psychological constructs.

Results: The CIA scale showed good reliability. Significant correlations between high scores on the CIA scale and low scores on self-compassion and activity engagement could be replicated. Significant correlations between high scores on the CIA scale and high scores of pain intensity and pain interference could also be replicated. In the exploring part of this study, validity was extended to general problems with emotion regulation and to satisfaction with life in general and contact with friends but not to satisfaction with family, partner, or sexual life. Avoidance of expression was the only significant predictor of pain intensity.

Conclusion: This study could replicate acceptable psychometric properties of a scale measuring CIA of expression. As in the original study, avoidance of expression was associated with increased suffering. Clinically, this instrument may be used to identify patients who may otherwise remain in aggravating silence. Theoretically, it introduces the important concept of context sensitivity to the field of chronic pain. Limitations include uncertainty about causal relationships, and that several important social situations were not examined.

目的:在慢性疼痛患者中,一味地回避表达可能会增加和延续与疼痛相关的情绪困扰。最近开发了情境敏感回避量表(CIA),用于测量患者在社交场合回避表达疼痛和痛苦的程度。本研究在一个新样本中探讨了 CIA 量表的心理测量特性:本研究使用的基线数据来自一项治疗试验,试验对象为 n = 115 名患有慢性疼痛并同时伴有情绪困扰的患者。使用与原始心理测量研究相同的工具研究了信度、结构效度和标准效度,并在两个新的测量工具中进行了进一步探讨。我们进行了一系列多元回归分析,以评估 CIA 量表和标准变量与其他心理结构之间的关系:结果:CIA量表显示出良好的可靠性。CIA量表的高分与自我同情和活动参与度的低分之间的显著相关性可以被复制。CIA 量表的高分与疼痛强度和疼痛干扰的高分之间的显著相关性也可以被复制。在本研究的探索部分,有效性扩展到了情绪调节的一般问题以及对生活和与朋友接触的满意度,但不包括对家庭、伴侣或性生活的满意度。避免表达是唯一能显著预测疼痛强度的因素:结论:本研究复制了一个测量 CIA 表达的量表,其心理测量特性是可以接受的。与最初的研究一样,回避表达与疼痛加剧有关。在临床上,该工具可用于识别那些可能会保持沉默的患者。从理论上讲,它将情境敏感性这一重要概念引入了慢性疼痛领域。不足之处包括因果关系的不确定性,以及没有对几种重要的社会情境进行研究。
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引用次数: 0
Dimensionality, reliability, and validity of the Finnish version of the pain catastrophizing scale in chronic low back pain. 芬兰版慢性腰背痛患者疼痛灾难化量表的维度、可靠性和有效性。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-11-04 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0034
Jani Mikkonen, Ville Leinonen, Tuomas Lähdeoja, Riikka Holopainen, Kristian Ekström, Petteri Koho, Olavi Airaksinen, Juan V Luciano, Jaime Navarrete, Randy Neblett

Objectives: The 13-item pain catastrophizing scale (PCS) is the most commonly used measure of pain catastrophizing. A validated Finnish version of the PCS has previously been unavailable. The objectives were to translate the original English version of the PCS into Finnish (PCS-FI), then to evaluate (i) structural validity of the PCS-FI with a confirmatory factor analysis (CFA), (ii) internal reliability with Cronbach's alpha, Omega, and Omega hierarchical, (iii) convergent validity with measures of well-being, quality of life, sleep quality, symptoms of central sensitization, and anxiety, and (iv) known-groups validity between participants with chronic low back pain (CLBP) and pain-free controls.

Methods: The translation process was performed with established guidelines. The PCS-FI was psychometrically validated using 92 participants with CLBP and 53 pain-free controls.

Results: Structural validity with CFA supported a bifactor solution. However, low reliability was found for the three specific factors (ω h ranging from 0.14 to 0.18) compared to the general factor (ω h = 0.88) suggesting that only the total score should be used. Convergent validity analysis showed satisfactory correlations and medium effect sizes with the other patient-reported outcome measures. Participants with CLBP had significantly higher total PCS-FI scores than pain-free controls.

Conclusions: The PCS-FI appears to be a valid and reliable instrument for assessing pain-related catastrophizing in Finnish-speaking populations. Ethical approval for this study was obtained from the Research Ethics Committee of the Northern Savo Hospital District, identification number 2131/2022, on the 31st of January 2022.

目的:13 项疼痛灾难化量表(PCS)是最常用的疼痛灾难化测量方法。以前一直没有经过验证的芬兰语版 PCS。我们的目标是将最初的英语版疼痛灾难化量表翻译成芬兰语(PCS-FI),然后评估:(i) PCS-FI 的结构效度,采用确证因子分析 (CFA);(ii) 内部可靠性,采用 Cronbach's alpha、Omega 和 Omega 层次分析;(iii) 与幸福感、生活质量、睡眠质量、中枢敏感症状和焦虑等测量指标的收敛效度;(iv) 患有慢性腰背痛 (CLBP) 的参与者与无痛对照组之间的已知组效度:方法:翻译过程按照既定准则进行。方法:翻译过程按照既定准则进行,并使用 92 名慢性腰背痛患者和 53 名无痛对照者对 PCS-FI 进行了心理计量学验证:结果:CFA 的结构效度支持双因素解决方案。然而,与一般因子(ω h = 0.88)相比,三个特定因子的信度较低(ω h 在 0.14 至 0.18 之间),这表明只应使用总分。聚合效度分析表明,该量表与其他患者报告的结果量表之间存在令人满意的相关性和中等效应大小。CLBP患者的PCS-FI总分明显高于无痛对照组:PCS-FI似乎是一种有效、可靠的工具,可用于评估芬兰语人群中与疼痛相关的灾难化程度。本研究于2022年1月31日获得了北萨沃医院区研究伦理委员会的伦理批准,批准号为2131/2022。
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引用次数: 0
Intrathecal pain treatment for severe pain in patients with terminal cancer: A retrospective analysis of treatment-related complications and side effects. 鞘内镇痛治疗晚期癌症患者的剧烈疼痛:治疗相关并发症和副作用的回顾性分析。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-10-04 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0041
Linda Bengtsson, Sven-Egron Thörn, Lars-Erik Dyrehag, Olaf Gräbel, Paulin Andréll

Objectives: Two-thirds of patients with advanced cancer experience pain. Some of these patients have severe pain refractory to oral and parenteral medication, for whom intrathecal pain treatment could be an option. While intrathecal therapy is presently used with good results in clinical practice, the current evidence is limited. Hence, increased knowledge of intrathecal pain treatment is needed. This retrospective study aimed to assess complications and side effects related to intrathecal pain treatment in patients with terminal cancer.

Methods: A retrospective study on all patients who received intrathecal treatment with morphine and bupivacaine through externalized catheters for cancer-related pain at a single university hospital during a 5-year period.

Results: Treatment-related complications were reported in 24 out of 53 patients. The most common complications were catheter dislocation (13%), catheter occlusion (9%), falls due to bupivacaine-related numbness or weakness (9%), and reversible respiratory depression (8%). There were five serious complications, i.e., meningitis or neurological impairment, of which four were reversible. Side effects related to intrathecal drugs, or the implantation procedure were observed in 35 patients. The most common were bupivacaine-related numbness or weakness (57%) and reversible post-dural puncture headache (19%). Systemic opioid doses decreased during the first 3 weeks of intrathecal treatment, from a median daily dose of 681 to 319 oral morphine milligram equivalents. The median treatment duration time was 62 days.

Conclusions: Complications related to intrathecal treatment are common, but mostly minor and reversible. Side effects are predominantly related to unwanted pharmacological effects from intrathecal drugs. Intrathecal treatment enables the reduction of systemic opioid doses, which indicates a good treatment effect on pain. Hence, intrathecal therapy can be considered a safe pain-relieving treatment in patients with severe refractory cancer-related pain. Future research is warranted on patient acceptability and satisfaction of intrathecal pain treatment.

目标三分之二的晚期癌症患者会感到疼痛。其中一些患者的剧烈疼痛是口服和肠外药物治疗的难治性症状,鞘内止痛治疗对这些患者来说不失为一种选择。虽然鞘内治疗目前在临床实践中取得了良好的效果,但目前的证据还很有限。因此,需要增加对鞘内疼痛治疗的了解。这项回顾性研究旨在评估晚期癌症患者鞘内止痛治疗的相关并发症和副作用:方法:对一家大学医院在 5 年内通过外置导管接受吗啡和布比卡因鞘内治疗以治疗癌症相关疼痛的所有患者进行回顾性研究:53 名患者中有 24 名出现了与治疗相关的并发症。最常见的并发症是导管脱位(13%)、导管闭塞(9%)、布比卡因相关麻木或无力导致的跌倒(9%)以及可逆性呼吸抑制(8%)。有五种严重并发症,即脑膜炎或神经功能损伤,其中四种是可逆的。35名患者出现了与鞘内药物或植入手术有关的副作用。最常见的副作用是布比卡因相关的麻木或无力(57%)和可逆的硬膜穿刺后头痛(19%)。在鞘内治疗的前三周,全身阿片类药物剂量有所减少,从每日中位剂量 681 毫克口服吗啡当量降至 319 毫克口服吗啡当量。中位治疗持续时间为62天:与鞘内治疗相关的并发症很常见,但大多较轻且可逆。副作用主要与鞘内药物的不良药理作用有关。鞘内治疗可减少全身阿片类药物的剂量,这表明对疼痛有良好的治疗效果。因此,鞘内治疗可被视为严重难治性癌症相关疼痛患者的一种安全止痛治疗方法。有关患者对鞘内镇痛治疗的接受度和满意度的研究还需进一步开展。
{"title":"Intrathecal pain treatment for severe pain in patients with terminal cancer: A retrospective analysis of treatment-related complications and side effects.","authors":"Linda Bengtsson, Sven-Egron Thörn, Lars-Erik Dyrehag, Olaf Gräbel, Paulin Andréll","doi":"10.1515/sjpain-2024-0041","DOIUrl":"10.1515/sjpain-2024-0041","url":null,"abstract":"<p><strong>Objectives: </strong>Two-thirds of patients with advanced cancer experience pain. Some of these patients have severe pain refractory to oral and parenteral medication, for whom intrathecal pain treatment could be an option. While intrathecal therapy is presently used with good results in clinical practice, the current evidence is limited. Hence, increased knowledge of intrathecal pain treatment is needed. This retrospective study aimed to assess complications and side effects related to intrathecal pain treatment in patients with terminal cancer.</p><p><strong>Methods: </strong>A retrospective study on all patients who received intrathecal treatment with morphine and bupivacaine through externalized catheters for cancer-related pain at a single university hospital during a 5-year period.</p><p><strong>Results: </strong>Treatment-related complications were reported in 24 out of 53 patients. The most common complications were catheter dislocation (13%), catheter occlusion (9%), falls due to bupivacaine-related numbness or weakness (9%), and reversible respiratory depression (8%). There were five serious complications, i.e., meningitis or neurological impairment, of which four were reversible. Side effects related to intrathecal drugs, or the implantation procedure were observed in 35 patients. The most common were bupivacaine-related numbness or weakness (57%) and reversible post-dural puncture headache (19%). Systemic opioid doses decreased during the first 3 weeks of intrathecal treatment, from a median daily dose of 681 to 319 oral morphine milligram equivalents. The median treatment duration time was 62 days.</p><p><strong>Conclusions: </strong>Complications related to intrathecal treatment are common, but mostly minor and reversible. Side effects are predominantly related to unwanted pharmacological effects from intrathecal drugs. Intrathecal treatment enables the reduction of systemic opioid doses, which indicates a good treatment effect on pain. Hence, intrathecal therapy can be considered a safe pain-relieving treatment in patients with severe refractory cancer-related pain. Future research is warranted on patient acceptability and satisfaction of intrathecal pain treatment.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"24 1","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142373173","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Psychometric evaluation of the Danish version of the Pain Self-Efficacy Questionnaire in patients with subacute and chronic low back pain. 亚急性和慢性腰背痛患者疼痛自我效能问卷丹麦语版的心理计量学评估。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-10-04 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0032
Mette Errebo, Martin Oxfeldt, Heidi Tegner, Jan Christensen

Objective: The Pain Self-Efficacy Questionnaire (PSEQ) is a widely used patient-reported outcome measure designed to assess the level of pain self-efficacy in patients with low back pain (LBP). Although the PSEQ has been translated into Danish, its measurement properties remain unknown in patients with subacute and chronic LBP in Danish outpatient clinics. The aim of this study was to investigate the construct validity, internal consistency, test-retest reliability, and measurement error of the Danish version of the PSEQ in a group of Danish patients with subacute and chronic LBP in a hospital outpatient setting.

Methods: Patients with LBP referred to two Danish outpatient clinics were recruited for this study. Two days after the consultation, the participants were emailed a link to a survey that included the following outcome measures: the PSEQ, the Oswestry Disability Index, the Numeric Pain Rating Scale, and the Tampa Scale of Kinesiophobia. Five days after completion of the survey, a new survey that included the PSEQ was sent to the participants.

Results: In total, 109 participants were included for the analysis of construct validity and internal consistency, with 94 participants included for the analysis of test-retest reliability and measurement error. Construct validity was found to be high and internal consistency was acceptable, with Cronbach's alpha = 0.93 (95% confidence interval [CI] = 0.91-0.93). Test-retest reliability was found to be good, with an intraclass correlation coefficient (ICC2.1) of 0.89 (95% CI = 0.82-0.92). The standard error of measurement was calculated to be 4.52 and the smallest detectable change was 12.5 points.

Conclusions: The Danish version of the PSEQ showed acceptable measurement properties in terms of construct validity, internal consistency, and test-retest reliability in a group of patients with subacute and chronic LBP. However, further studies are needed to investigate other aspects of the measurement properties.

目的:疼痛自我效能问卷(PSEQ)是一种广泛使用的患者报告结果测量方法,旨在评估腰背痛(LBP)患者的疼痛自我效能水平。尽管 PSEQ 已被翻译成丹麦语,但其在丹麦门诊部亚急性和慢性腰背痛患者中的测量特性仍不为人所知。本研究旨在调查丹麦语版 PSEQ 的构建效度、内部一致性、重测信度以及测量误差,调查对象为在医院门诊就诊的亚急性和慢性腰痛患者:本研究招募了在丹麦两家门诊部就诊的枸杞痛患者。就诊两天后,参与者通过电子邮件收到一份调查问卷的链接,其中包括以下结果测量:PSEQ、Oswestry 残疾指数、数字疼痛评分量表和运动恐惧症坦帕量表。在完成调查五天后,又向参与者发送了一份包含 PSEQ 的新调查:共有 109 名参与者参与了结构效度和内部一致性分析,94 名参与者参与了重测信度和测量误差分析。结构效度很高,内部一致性也可以接受,Cronbach's alpha = 0.93(95% 置信区间 [CI] = 0.91-0.93)。测试-再测可靠性良好,类内相关系数(ICC2.1)为 0.89(95% 置信区间 = 0.82-0.92)。计算得出的测量标准误差为 4.52,可检测到的最小变化为 12.5 分:结论:丹麦版 PSEQ 在亚急性和慢性腰背痛患者群体中的构建效度、内部一致性和测试-再测可靠性方面显示出了可接受的测量特性。不过,还需要进一步研究测量特性的其他方面。
{"title":"Psychometric evaluation of the Danish version of the Pain Self-Efficacy Questionnaire in patients with subacute and chronic low back pain.","authors":"Mette Errebo, Martin Oxfeldt, Heidi Tegner, Jan Christensen","doi":"10.1515/sjpain-2024-0032","DOIUrl":"10.1515/sjpain-2024-0032","url":null,"abstract":"<p><strong>Objective: </strong>The Pain Self-Efficacy Questionnaire (PSEQ) is a widely used patient-reported outcome measure designed to assess the level of pain self-efficacy in patients with low back pain (LBP). Although the PSEQ has been translated into Danish, its measurement properties remain unknown in patients with subacute and chronic LBP in Danish outpatient clinics. The aim of this study was to investigate the construct validity, internal consistency, test-retest reliability, and measurement error of the Danish version of the PSEQ in a group of Danish patients with subacute and chronic LBP in a hospital outpatient setting.</p><p><strong>Methods: </strong>Patients with LBP referred to two Danish outpatient clinics were recruited for this study. Two days after the consultation, the participants were emailed a link to a survey that included the following outcome measures: the PSEQ, the Oswestry Disability Index, the Numeric Pain Rating Scale, and the Tampa Scale of Kinesiophobia. Five days after completion of the survey, a new survey that included the PSEQ was sent to the participants.</p><p><strong>Results: </strong>In total, 109 participants were included for the analysis of construct validity and internal consistency, with 94 participants included for the analysis of test-retest reliability and measurement error. Construct validity was found to be high and internal consistency was acceptable, with Cronbach's alpha = 0.93 (95% confidence interval [CI] = 0.91-0.93). Test-retest reliability was found to be good, with an intraclass correlation coefficient (ICC<sub>2.1</sub>) of 0.89 (95% CI = 0.82-0.92). The standard error of measurement was calculated to be 4.52 and the smallest detectable change was 12.5 points.</p><p><strong>Conclusions: </strong>The Danish version of the PSEQ showed acceptable measurement properties in terms of construct validity, internal consistency, and test-retest reliability in a group of patients with subacute and chronic LBP. However, further studies are needed to investigate other aspects of the measurement properties.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"24 1","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-10-04","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142373174","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
The relationship between changes in pain intensity and functional disability in persistent disabling low back pain during a course of cognitive functional therapy. 在认知功能治疗过程中,持续性致残腰背痛患者的疼痛强度变化与功能障碍之间的关系。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-10-03 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0040
Kasper Ussing, Anne Smith, Peter O'Sullivan

Objectives: Pain relief and reduced disability are both common treatment targets for persistent disabling low back pain (LBP). Cross-sectional studies show a moderate relationship between functional disability and pain intensity, but little is known about the relationship between changes in pain intensity and functional disability over multiple time points. The objective of this study was to investigate the associations between changes in functional disability and pain intensity and whether changes occurred simultaneously or differentially during a course of cognitive functional therapy for people with persistent disabling LBP.

Methods: Self-reported measures of pain intensity and patient-specific functional disability were collected prior to each treatment session from 40 participants during a 12-week intervention period. Linear mixed modeling was used to assess simultaneous and lagged associations between pain intensity and functional disability over time. Sensitivity analysis using nonparametric subject-specific methods (simulation modeling analysis) was also performed.

Results: Thirty-five participants had sufficient data for analysis. Using the linear mixed-model approach, there was evidence of a moderate and simultaneous association between pain intensity and functional disability over time (regression coefficient = 0.56, 95% confidence interval: 0.44-0.68, p < 0.001). Simulation modeling analysis supported weak to mostly strong associations and supported for simultaneous change in pain and disability for the majority of participants (22 of 35, 64%).

Conclusion: Changes in pain intensity and functional disability were moderately related across the intervention. Visual inspection of graphs indicated a very close relationship in some individuals and a decoupling of pain intensity and functional disability in others. The changes in pain intensity and functional disability seem to occur simultaneously in most individuals.

目的:缓解疼痛和减少残疾是治疗持续性致残性腰背痛(LBP)的共同目标。横断面研究显示,功能性残疾与疼痛强度之间存在一定的关系,但对于疼痛强度的变化与功能性残疾在多个时间点之间的关系却知之甚少。本研究的目的是调查功能性残疾的变化与疼痛强度之间的关系,以及在对持续性致残性腰背痛患者进行认知功能治疗的过程中,两者的变化是同时发生还是有差异:方法: 在为期 12 周的干预期间,每次治疗前收集 40 名参与者对疼痛强度和患者特定功能障碍的自我报告。采用线性混合模型评估疼痛强度和功能障碍随时间变化的同步和滞后关联。此外,还使用非参数受试者特定方法进行了敏感性分析(模拟建模分析):35 名参与者有足够的数据进行分析。使用线性混合模型方法,有证据表明疼痛强度和功能障碍之间存在中度的同时关联(回归系数 = 0.56,95% 置信区间:0.44-0.68,p < 0.001)。模拟建模分析表明,大多数参与者(35 人中有 22 人,占 64%)的疼痛和残疾程度同时发生变化,且相关性由弱到强:结论:在整个干预过程中,疼痛强度和功能性残疾的变化呈中度相关。对图表的目测表明,一些人的疼痛强度和功能障碍之间的关系非常密切,而另一些人的疼痛强度和功能障碍之间的关系则脱钩。在大多数人身上,疼痛强度和功能障碍的变化似乎是同时发生的。
{"title":"The relationship between changes in pain intensity and functional disability in persistent disabling low back pain during a course of cognitive functional therapy.","authors":"Kasper Ussing, Anne Smith, Peter O'Sullivan","doi":"10.1515/sjpain-2024-0040","DOIUrl":"10.1515/sjpain-2024-0040","url":null,"abstract":"<p><strong>Objectives: </strong>Pain relief and reduced disability are both common treatment targets for persistent disabling low back pain (LBP). Cross-sectional studies show a moderate relationship between functional disability and pain intensity, but little is known about the relationship between changes in pain intensity and functional disability over multiple time points. The objective of this study was to investigate the associations between changes in functional disability and pain intensity and whether changes occurred simultaneously or differentially during a course of cognitive functional therapy for people with persistent disabling LBP.</p><p><strong>Methods: </strong>Self-reported measures of pain intensity and patient-specific functional disability were collected prior to each treatment session from 40 participants during a 12-week intervention period. Linear mixed modeling was used to assess simultaneous and lagged associations between pain intensity and functional disability over time. Sensitivity analysis using nonparametric subject-specific methods (simulation modeling analysis) was also performed.</p><p><strong>Results: </strong>Thirty-five participants had sufficient data for analysis. Using the linear mixed-model approach, there was evidence of a moderate and simultaneous association between pain intensity and functional disability over time (regression coefficient = 0.56, 95% confidence interval: 0.44-0.68, <i>p</i> < 0.001). Simulation modeling analysis supported weak to mostly strong associations and supported for simultaneous change in pain and disability for the majority of participants (22 of 35, 64%).</p><p><strong>Conclusion: </strong>Changes in pain intensity and functional disability were moderately related across the intervention. Visual inspection of graphs indicated a very close relationship in some individuals and a decoupling of pain intensity and functional disability in others. The changes in pain intensity and functional disability seem to occur simultaneously in most individuals.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"24 1","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-10-03","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142373175","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Comparison of ultrasound-guided continuous erector spinae plane block versus continuous paravertebral block for postoperative analgesia in patients undergoing proximal femur surgeries. 股骨近端手术患者术后镇痛中超声引导下连续竖脊肌平面阻滞与连续椎旁阻滞的比较。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-09-23 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0028
Aditya Mehrotra, Madhu Dayal, Sushmita Bairagi

Background: Proximal femur fracture surgeries have become increasingly prevalent, presenting unique challenges for postoperative pain management due to patient demographics and comorbidities. Erector spinae plane block (ESPB) has emerged as a relatively safe alternative to paravertebral block (PVB). Our aim was to compare ultrasound-guided continuous ESPB with continuous PVB for postoperative analgesia in patients undergoing proximal femur surgeries under spinal anesthesia.

Methods: A prospective randomized interventional study was conducted on 60 patients between 18 and 60 years of age undergoing proximal femur surgeries under spinal anesthesia with American Society of Anesthesiologists physical status I and II between January 2019 and April 2020. Patients were randomly assigned to receive either ultrasound-guided continuous ESPB (Group E, n = 30) or ultrasound-guided continuous PVB (Group P, n = 30) using a computer-generated randomization table. The mean maximum visual analog scale (VAS) score, VAS score in the first 24 h, the time of rescue analgesia, and total requirement of rescue analgesia were assessed.

Results: The maximum VAS score within the first 24 h was numerically higher in Group P but statistically insignificant (p-value 0.279). VAS scores at 0, 1, 2, 6, and 18 h postoperatively were comparable in both groups. However, at the 24-h mark, the VAS score between Group E and Group P was statistically significant (p-value 0.018) but not clinically relevant. The mean paracetamol and tramadol requirements were comparable between the two groups.

Conclusion: Continuous ESPB is as effective as continuous PVB for postoperative analgesia in proximal femur surgeries. The enhanced safety profile of erector spinae block underscores its significance in postoperative pain management.

背景:股骨近端骨折手术越来越普遍,由于患者的人口统计学特征和合并症,给术后疼痛治疗带来了独特的挑战。脊柱后凸面阻滞(ESPB)已成为椎旁阻滞(PVB)的一种相对安全的替代方法。我们的目的是比较超声引导下连续ESPB和连续PVB对脊髓麻醉下股骨近端手术患者术后镇痛的效果:在2019年1月至2020年4月期间,对60名年龄在18岁至60岁之间、在脊髓麻醉下接受股骨近端手术、美国麻醉医师协会身体状况为I级和II级的患者进行了前瞻性随机干预研究。通过计算机生成的随机分配表,患者被随机分配到接受超声引导下连续ESPB(E组,n = 30)或超声引导下连续PVB(P组,n = 30)。对平均最大视觉模拟量表(VAS)评分、头24小时的VAS评分、镇痛抢救时间和镇痛抢救总需求进行了评估:结果:P 组在最初 24 小时内的最大 VAS 评分在数值上较高,但在统计学上并不显著(P 值为 0.279)。两组在术后 0、1、2、6 和 18 小时的 VAS 评分相当。然而,在术后 24 小时,E 组和 P 组之间的 VAS 评分有统计学意义(p 值 0.018),但与临床无关。两组的平均扑热息痛和曲马多需求量相当:在股骨近端手术的术后镇痛中,连续ESPB与连续PVB同样有效。竖脊肌阻滞安全性的提高凸显了其在术后疼痛治疗中的重要性。
{"title":"Comparison of ultrasound-guided continuous erector spinae plane block versus continuous paravertebral block for postoperative analgesia in patients undergoing proximal femur surgeries.","authors":"Aditya Mehrotra, Madhu Dayal, Sushmita Bairagi","doi":"10.1515/sjpain-2024-0028","DOIUrl":"10.1515/sjpain-2024-0028","url":null,"abstract":"<p><strong>Background: </strong>Proximal femur fracture surgeries have become increasingly prevalent, presenting unique challenges for postoperative pain management due to patient demographics and comorbidities. Erector spinae plane block (ESPB) has emerged as a relatively safe alternative to paravertebral block (PVB). Our aim was to compare ultrasound-guided continuous ESPB with continuous PVB for postoperative analgesia in patients undergoing proximal femur surgeries under spinal anesthesia.</p><p><strong>Methods: </strong>A prospective randomized interventional study was conducted on 60 patients between 18 and 60 years of age undergoing proximal femur surgeries under spinal anesthesia with American Society of Anesthesiologists physical status I and II between January 2019 and April 2020. Patients were randomly assigned to receive either ultrasound-guided continuous ESPB (Group E, <i>n</i> = 30) or ultrasound-guided continuous PVB (Group P, <i>n</i> = 30) using a computer-generated randomization table. The mean maximum visual analog scale (VAS) score, VAS score in the first 24 h, the time of rescue analgesia, and total requirement of rescue analgesia were assessed.</p><p><strong>Results: </strong>The maximum VAS score within the first 24 h was numerically higher in Group P but statistically insignificant (<i>p</i>-value 0.279). VAS scores at 0, 1, 2, 6, and 18 h postoperatively were comparable in both groups. However, at the 24-h mark, the VAS score between Group E and Group P was statistically significant (<i>p</i>-value 0.018) but not clinically relevant. The mean paracetamol and tramadol requirements were comparable between the two groups.</p><p><strong>Conclusion: </strong>Continuous ESPB is as effective as continuous PVB for postoperative analgesia in proximal femur surgeries. The enhanced safety profile of erector spinae block underscores its significance in postoperative pain management.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"24 1","pages":""},"PeriodicalIF":1.5,"publicationDate":"2024-09-23","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142298547","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
ADHD-pain: Characteristics of chronic pain and association with muscular dysregulation in adults with ADHD. ADHD-疼痛:多动症成人慢性疼痛的特征及其与肌肉调节失调的关系。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-09-09 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2024-0015
Anne Beate Helseth Udal, Liv Larsen Stray, Torstein Stray, Thomas Bjerregaard Bertelsen, Are Hugo Pripp, Jens Egeland

Objectives: A high incidence of attention-deficit hyperactivity disorder (ADHD) has been reported in chronic pain (ChP) patients. Furthermore, an association between ChP and muscular dysregulation has been reported in adults with ADHD. The present study investigated whether ADHD was more prevalent among psychiatric outpatients with ChP than those without ChP, and if there was an association between ChP, muscular dysregulation and characteristics of pain in patients with ADHD.

Methods: One-hundred and twenty-one individuals remitted to an outpatient psychiatry unit took part in this naturalistic epidemiological cross-sectional study. They were assessed with a pain self-report form (localization, intensity, and onset) and a test of muscle dysregulation (the Motor Function Neurological Assessment). Prevalence of ADHD among patients with ChP, as well as the qualitative characteristics of ChP within the ADHDgroup are reported. Both ChP and pain intensity correlated with muscular dysregulation through Spearman's rho analysis. Additionally, the relationship between various diagnostic categories (ADHD, affective disorders, anxiety, or personality disorders) and incidence of axial pain was evaluated in logistic regression.

Results: ADHD was significantly more prevalent in patients with ChP, than in patients without ChP. In the ADHD group, ChP and pain intensity was associated with muscular dysregulation, particularly with high muscle tone. ChP was more axial and widespread, than for the patients without ADHD, and started at an early age. ADHD diagnosis predicted axial pain, whereas affective-, anxiety-, or personality disorders did not.

Conclusions: The study suggests that ChP in ADHD is associated with muscular dysregulation and is qualitatively different from ChP in psychiatric patients without ADHD. These findings may lead to further understanding of potential mechanisms involved in ADHD and ChP, and in turn to new treatment strategies for both disorders.

目的:据报道,慢性疼痛(ChP)患者中注意力缺陷多动障碍(ADHD)的发病率很高。此外,在患有多动症的成人中,也有慢性疼痛与肌肉调节障碍之间存在关联的报道。本研究调查了患有慢性疼痛的精神病门诊患者中多动症的发病率是否高于无慢性疼痛的患者,以及多动症患者的慢性疼痛、肌肉调节障碍和疼痛特征之间是否存在关联:方法:121 名精神科门诊病人参加了这项自然流行病学横断面研究。他们接受了疼痛自我报告表(定位、强度和发病情况)和肌肉失调测试(运动功能神经评估)的评估。报告了慢性阻塞性脉搏障碍患者中多动症的发病率,以及多动症组中慢性阻塞性脉搏障碍的定性特征。通过 Spearman's rho 分析,ChP 和疼痛强度都与肌肉失调相关。此外,还通过逻辑回归评估了各种诊断类别(多动症、情感障碍、焦虑症或人格障碍)与轴性疼痛发生率之间的关系:结果:多动症在脊髓灰质炎患者中的发病率明显高于非脊髓灰质炎患者。在多动症组中,慢性阻塞性脉管炎和疼痛强度与肌肉调节失调有关,尤其是与高肌张力有关。与无多动症的患者相比,慢性阻塞性脉搏停滞症更具有轴向性和广泛性,而且起病年龄较小。多动症诊断可预测轴性疼痛,而情感、焦虑或人格障碍则不能:研究表明,ADHD 患者的轴性疼痛与肌肉调节失调有关,与非 ADHD 精神病患者的轴性疼痛有本质区别。这些发现可能有助于进一步了解多动症和ChP的潜在机制,进而为这两种疾病找到新的治疗策略。
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引用次数: 0
Neck and shoulder pain and inflammatory biomarkers in plasma among forklift truck operators - A case-control study. 叉车操作员的颈肩疼痛与血浆中的炎症生物标志物--一项病例对照研究。
IF 1.5 Q4 CLINICAL NEUROLOGY Pub Date : 2024-08-28 eCollection Date: 2024-01-01 DOI: 10.1515/sjpain-2023-0142
Bijar Ghafouri, Bo Rolander, Björn Gerdle, Charlotte Wåhlin

Objectives: The aim of this study was to investigate a panel of inflammatory biomarkers in plasma from forklift truck operators (FLTOs) and healthy controls, and their relation to neck pain characteristics.

Methods: From employees in a warehouse, 26 FLTOs were recruited and 24 healthy age- and sex-matched controls (CONs) were recruited via advertisement. The inclusion criterion for FLTOs was that they should operate reach decker and/or counterbalanced tilting mast forklift trucks. All participants were asked to answer a questionnaire covering demographic data, pain intensity numeric rating scale (NRS), anatomical spread, psychological distress, and health aspects. Pain sensitivity was measured using a pressure algometer. Blood samples were collected and analyzed for inflammatory proteins in plasma using a panel of 71 cytokines and chemokines. Multivariate data analysis including orthogonal partial least square-discriminant analysis (OPLS-DA) was performed to identify significant biomarkers.

Results: Thirty percent of FLTOs reported NRS > 3 in the neck. Shoulder pain was common in 26% of the FLTOs. Pain and discomfort that most often prevented completion of activities were in the neck (20%), lower back (32%), and hips (27%). The FLTOs reported significantly (p = 0.04) higher levels of anxiety than the CON group and they had significantly lower pressure pain thresholds in the trapezius muscle on both right (p < 0.001) and left sides (p = 0.003). A significant OPLS-DA model could discriminate FLTOs from CON based on nine inflammatory proteins where the expression levels of four proteins were upregulated and five proteins were downregulated in FLTOs compared to CONs. Twenty-nine proteins correlated multivariately with pain intensity.

Conclusions: The profile of self-reported health, pain intensity, sensitivity, and plasma biomarkers can discriminate FLTOs with pain from healthy subjects. A combination of both self-reported and objective biomarker measurements can be useful for better understanding the pathophysiological mechanisms underlying work-related neck and shoulder pain.

研究目的本研究旨在调查叉车操作员(FLTO)和健康对照者血浆中的一系列炎症生物标志物及其与颈部疼痛特征的关系:方法:从一家仓库的员工中招募了 26 名 FLTO,并通过广告招募了 24 名年龄和性别匹配的健康对照组(CON)。纳入 FLTO 的标准是他们必须操作前移式叉车和/或平衡倾斜桅杆式叉车。所有参与者均需回答一份调查问卷,内容包括人口统计学数据、疼痛强度数字评分量表(NRS)、解剖学分布、心理困扰和健康状况。疼痛敏感度是通过压力测力计测量的。采集血样并使用 71 种细胞因子和趋化因子分析血浆中的炎症蛋白。进行了包括正交偏最小二乘法判别分析(OPLS-DA)在内的多变量数据分析,以确定重要的生物标志物:30%的 FLTO 报告颈部 NRS > 3。26%的 FLTO 肩部疼痛。最常导致无法完成活动的疼痛和不适部位是颈部(20%)、腰部(32%)和臀部(27%)。FLTO 报告的焦虑程度明显高于 CON 组(p = 0.04),而且他们右侧(p < 0.001)和左侧(p = 0.003)斜方肌的压痛阈值明显较低。基于9种炎症蛋白的OPLS-DA模型可将FLTO与CON区分开来,与CON相比,FLTO中4种蛋白的表达水平上调,5种蛋白的表达水平下调。29种蛋白质与疼痛强度存在多变量相关性:结论:自我报告的健康状况、疼痛强度、敏感性和血浆生物标志物的概况可将患有疼痛的 FLTO 患者与健康受试者区分开来。将自我报告和客观生物标志物测量相结合,有助于更好地了解与工作相关的颈肩疼痛的病理生理机制。
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引用次数: 0
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Scandinavian Journal of Pain
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