Pub Date : 2025-09-26eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0007
Maria Belen Garay, Rasmus Hagn-Meincke, Lili Fekete, Zoltan Hajnády, Peter Hegyi, Misbah Unnisa, Rupjyoti Talukdar, Imran Khan Niazi, Imran Amjad, Soumiya J Mahapatra, Pramod Garg, Enrique De-Madaria, Søren S Olesen, Asbjørn M Drewes, Rasmus B Nedergaard
Objectives: The cold pressor test, in which subjects immerse part of an extremity in cold water for a specified amount of time, evokes both pain and unpleasantness. As it is low cost and readily available, it is widely used in pain research. However, data on the impact of race, area of exposure, and the effects of instructions are lacking.
Methods: Cold pressure test data were recorded in a mixed Asian and European healthy population. Trial 1 was a randomised crossover trial varying the extent of hand submersion (two fingers, four fingers, and whole hand) (n = 54). Trial 2 was a randomised cross-sectional design, investigating instructed and non-instructed pain expectations, n = 40.
Results: European subjects tolerated the cold pressor test longer than Asian subjects (116 ± 14 versus 93 ± 36 s, p < 0.001), and fewer subjects withdrew their hand in less than two minutes (9% vs 43%, p = 0.007). Stimulation area influenced pain tolerance, with more subjects able to maintain two-finger immersion in cold water for 2 min compared to whole-hand immersion (p < 0.001). The instruction or no instruction did not affect the numeric rating scale when comparing instruction levels (p = 0.88). Additionally, pain tolerance was not affected either (p = 1).
Conclusion: The cold pressor test is a robust tool across genders, race, and instruction levels. Significant differences were found in pain perception and tolerance across different locations and stimulation intensities. However, instructions in expected pain did not affect the outcomes, reflecting the robustness of the test.
{"title":"Robustness of the cold pressor test: Study across geographic locations on pain perception and tolerance.","authors":"Maria Belen Garay, Rasmus Hagn-Meincke, Lili Fekete, Zoltan Hajnády, Peter Hegyi, Misbah Unnisa, Rupjyoti Talukdar, Imran Khan Niazi, Imran Amjad, Soumiya J Mahapatra, Pramod Garg, Enrique De-Madaria, Søren S Olesen, Asbjørn M Drewes, Rasmus B Nedergaard","doi":"10.1515/sjpain-2025-0007","DOIUrl":"10.1515/sjpain-2025-0007","url":null,"abstract":"<p><strong>Objectives: </strong>The cold pressor test, in which subjects immerse part of an extremity in cold water for a specified amount of time, evokes both pain and unpleasantness. As it is low cost and readily available, it is widely used in pain research. However, data on the impact of race, area of exposure, and the effects of instructions are lacking.</p><p><strong>Methods: </strong>Cold pressure test data were recorded in a mixed Asian and European healthy population. Trial 1 was a randomised crossover trial varying the extent of hand submersion (two fingers, four fingers, and whole hand) (<i>n</i> = 54). Trial 2 was a randomised cross-sectional design, investigating instructed and non-instructed pain expectations, <i>n</i> = 40.</p><p><strong>Results: </strong>European subjects tolerated the cold pressor test longer than Asian subjects (116 ± 14 versus 93 ± 36 s, <i>p</i> < 0.001), and fewer subjects withdrew their hand in less than two minutes (9% vs 43%, <i>p</i> = 0.007). Stimulation area influenced pain tolerance, with more subjects able to maintain two-finger immersion in cold water for 2 min compared to whole-hand immersion (<i>p</i> < 0.001). The instruction or no instruction did not affect the numeric rating scale when comparing instruction levels (<i>p</i> = 0.88). Additionally, pain tolerance was not affected either (<i>p</i> = 1).</p><p><strong>Conclusion: </strong>The cold pressor test is a robust tool across genders, race, and instruction levels. Significant differences were found in pain perception and tolerance across different locations and stimulation intensities. However, instructions in expected pain did not affect the outcomes, reflecting the robustness of the test.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-09-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145151444","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}
Pub Date : 2025-09-22eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0047
Paulin Andréll, Axel Wolf
{"title":"Transcutaneous electrical nerve stimulation - an important tool in person-centered multimodal analgesia.","authors":"Paulin Andréll, Axel Wolf","doi":"10.1515/sjpain-2025-0047","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0047","url":null,"abstract":"","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-09-22","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145114671","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}
Introduction: Trigeminal neuralgia (TN) caused by a dolichoectatic vertebral artery is a rare and atypical form of TN, where an enlarged and tortuous vertebral artery compresses the trigeminal nerve at its root entry zone. The term dolichoectatic is of Greek origin and means elongated, torturous or dilated. The vascular anomaly may lead to the characteristic severe, stabbing facial pain. This type of TN is often identified through advanced imaging techniques such as magnetic resonance imaging or angiography, which reveal the vascular anomaly impinging on the nerve. Treatment options for the type of TN secondary to dolichoectatic vertebrobasilar artery include primarily microvascular decompression or Gamma knife treatment to alleviate nerve compression and reduce symptoms.
Case reports: The authors present two illustrative cases of elderly patients: an 82-year-old with the right-sided and a 68-year-old patient with the left-sided facial pain, respectively. Both patients presented with lancinating and irritating facial pain. Magnetic resonance imaging in both patients confirmed compression of the trigeminal nerve secondary to a vertebrobasilar dolichoectatic artery. The authors performed microvascular decompression in both patients, which resulted in instant pain relief.
Conclusion: Early diagnosis and surgical intervention are crucial for effective pain management and improved patient outcomes.
{"title":"Trigeminal neuralgia caused by dolichoectatic vertebral artery: Reports of two cases.","authors":"Nenad Koruga, Alen Rončević, Tajana Turk, Tatjana Rotim, Domagoj Kretić, Vedran Farkaš, Tomislav Ištvanić, Anamarija Soldo Koruga","doi":"10.1515/sjpain-2025-0034","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0034","url":null,"abstract":"<p><strong>Introduction: </strong>Trigeminal neuralgia (TN) caused by a dolichoectatic vertebral artery is a rare and atypical form of TN, where an enlarged and tortuous vertebral artery compresses the trigeminal nerve at its root entry zone. The term <i>dolichoectatic</i> is of Greek origin and means elongated, torturous or dilated. The vascular anomaly may lead to the characteristic severe, stabbing facial pain. This type of TN is often identified through advanced imaging techniques such as magnetic resonance imaging or angiography, which reveal the vascular anomaly impinging on the nerve. Treatment options for the type of TN secondary to dolichoectatic vertebrobasilar artery include primarily microvascular decompression or Gamma knife treatment to alleviate nerve compression and reduce symptoms.</p><p><strong>Case reports: </strong>The authors present two illustrative cases of elderly patients: an 82-year-old with the right-sided and a 68-year-old patient with the left-sided facial pain, respectively. Both patients presented with lancinating and irritating facial pain. Magnetic resonance imaging in both patients confirmed compression of the trigeminal nerve secondary to a vertebrobasilar dolichoectatic artery. The authors performed microvascular decompression in both patients, which resulted in instant pain relief.</p><p><strong>Conclusion: </strong>Early diagnosis and surgical intervention are crucial for effective pain management and improved patient outcomes.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-09-16","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145087701","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}
Pub Date : 2025-09-15eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0024
Katarina Eklund, Britt-Marie Stålnacke, Paul Enthoven, Magnus Zingmark, Gunilla Stenberg
Objectives: Most patients with chronic pain are identified and managed in primary care (PC). Chronic pain management is challenging, which is manifested by increased healthcare utilization (HCU) in this patient group. The interdisciplinary pain rehabilitation program (IPRP) is the gold standard treatment for patients with chronic pain but is scarcely used in PC. The aim of this study was to evaluate the HCU of patients with chronic pain in PC 1 year before and 1 year after an IPRP by examining the distribution of costs and resources.
Methods: This retrospective cohort study combined data from a national pain registry and HCU data from regional administrative registries, including 146 patients who participated in an IPRP in PC. The outcome measure was the number of outpatient healthcare contacts. Costs and the distribution of resources were compared across the two measurement intervals using paired t-tests. HCU costs were described from a healthcare provider perspective.
Results: HCU decreased by 16% in the year following IPRP compared to the year before. Costs for outpatient visits dropped by 12% or €434 per participant. Visits to physiotherapists and general practitioners decreased the most, by 31% (p = 0.048) and 23% (p < 0.001) respectively. Visits to nurses, occupational therapists, and psychologists/social workers in turn increased marginally (6%, 5% vs 10%).
Conclusions: IPRP in PC may lead to reduced HCU, freed resources, and streamlined chronic pain management. The study offers valuable insights into expected changes in HCU for chronic pain patients after an IPRP and how these changes may impact daily activities at the PC center.
目的:大多数慢性疼痛患者在初级保健(PC)中被识别和管理。慢性疼痛管理具有挑战性,这表现在该患者组中医疗保健利用率(HCU)的增加。跨学科疼痛康复计划(IPRP)是治疗慢性疼痛患者的金标准,但很少用于PC。本研究的目的是通过检查成本和资源的分配,评估慢性疼痛PC患者在IPRP术前和术后1年的HCU。方法:这项回顾性队列研究结合了来自国家疼痛登记处的数据和来自地区行政登记处的HCU数据,包括146名在PC参加IPRP的患者。结果测量是门诊医疗接触的次数。使用配对t检验比较两个测量区间的成本和资源分布。从医疗保健提供者的角度描述了HCU成本。结果:与前一年相比,IPRP后一年HCU下降了16%。门诊费用下降了12%,即每位参与者434欧元。对物理治疗师和全科医生的访问减少最多,分别减少了31% (p = 0.048)和23% (p < 0.001)。护士、职业治疗师和心理学家/社会工作者的就诊人数依次略有增加(6%,5% vs 10%)。结论:PC患者的IPRP可减少HCU,释放资源,简化慢性疼痛管理。该研究为IPRP后慢性疼痛患者HCU的预期变化以及这些变化如何影响PC中心的日常活动提供了有价值的见解。
{"title":"Healthcare utilization and resource distribution before and after interdisciplinary pain rehabilitation in primary care.","authors":"Katarina Eklund, Britt-Marie Stålnacke, Paul Enthoven, Magnus Zingmark, Gunilla Stenberg","doi":"10.1515/sjpain-2025-0024","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0024","url":null,"abstract":"<p><strong>Objectives: </strong>Most patients with chronic pain are identified and managed in primary care (PC). Chronic pain management is challenging, which is manifested by increased healthcare utilization (HCU) in this patient group. The interdisciplinary pain rehabilitation program (IPRP) is the gold standard treatment for patients with chronic pain but is scarcely used in PC. The aim of this study was to evaluate the HCU of patients with chronic pain in PC 1 year before and 1 year after an IPRP by examining the distribution of costs and resources.</p><p><strong>Methods: </strong>This retrospective cohort study combined data from a national pain registry and HCU data from regional administrative registries, including 146 patients who participated in an IPRP in PC. The outcome measure was the number of outpatient healthcare contacts. Costs and the distribution of resources were compared across the two measurement intervals using paired <i>t</i>-tests. HCU costs were described from a healthcare provider perspective.</p><p><strong>Results: </strong>HCU decreased by 16% in the year following IPRP compared to the year before. Costs for outpatient visits dropped by 12% or €434 per participant. Visits to physiotherapists and general practitioners decreased the most, by 31% (<i>p</i> = 0.048) and 23% (<i>p</i> < 0.001) respectively. Visits to nurses, occupational therapists, and psychologists/social workers in turn increased marginally (6%, 5% vs 10%).</p><p><strong>Conclusions: </strong>IPRP in PC may lead to reduced HCU, freed resources, and streamlined chronic pain management. The study offers valuable insights into expected changes in HCU for chronic pain patients after an IPRP and how these changes may impact daily activities at the PC center.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-09-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145087676","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}
Pub Date : 2025-09-02eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0028
Kine Gjesdal, Svetlana Skurtveit, Ane Djuv, Aksel Paulsen, Cille Sevild, Torgeir Gilje Lid
Objectives: Chronic pain represents a major public health challenge, substantially affecting daily functioning and overall well-being. While self-management strategies can be effective, they are often introduced only after pharmacological or surgical treatments have proven insufficient, highlighting the need for more personalized, accessible, and early interventions in primary care. However, the feasibility and practical implementation of such approaches remain insufficiently explored. Considering these challenges, the aims of this study were to co-create and to evaluate the feasibility of a personalized, multidisciplinary, and coordinated intervention for chronic pain management within municipal healthcare services.
Methods: The intervention included a generic pain management course (part one) and a personalized second part offering various group-based courses. Participants (n = 70) were recruited through an orthopedic outpatient clinic and general practitioners. Individual consultations with course leaders were conducted before, during, and after the intervention. Questionnaires assessing health-related quality of life, alcohol consumption, medication use, and sleep were administered at baseline, midway, and post-intervention, along with a self-reported evaluation of the intervention after completion.
Results: Among the total participants (n = 70), 81% completed Part 1 of the intervention, while 61% completed the entire intervention. At baseline, participants had a mean EQ-5D-5L score of 0.65 and an EQ-VAS score of 48.8. Regarding alcohol use, 47% were drinking once a month or less, and no participants were drinking alcohol four or more times a week. Insomnia was reported by 84%. Paracetamol was the most used daily medication (41%), followed by non-steroidal anti-inflammatory drugs and weak opioids (26% each). In Part 2 of the intervention, stress management courses were the most frequently selected (26%), followed closely by physical activity and body-mind activity at 23%. Most participants reported benefit, with 63% (Part 1) and 56% (Part 2) indicating good or very good benefit, and 98% would recommend it to others.
Conclusion: This feasibility study demonstrates the potential for addressing the complex needs of individuals with chronic pain through a personalized and multidisciplinary intervention in primary care. The high completion rates indicate feasibility and acceptability. The findings support further evaluation of resource use, implementation, and effectiveness in future controlled trials.
{"title":"A feasibility study of a co-developed, multidisciplinary, tailored intervention for chronic pain management in municipal healthcare services.","authors":"Kine Gjesdal, Svetlana Skurtveit, Ane Djuv, Aksel Paulsen, Cille Sevild, Torgeir Gilje Lid","doi":"10.1515/sjpain-2025-0028","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0028","url":null,"abstract":"<p><strong>Objectives: </strong>Chronic pain represents a major public health challenge, substantially affecting daily functioning and overall well-being. While self-management strategies can be effective, they are often introduced only after pharmacological or surgical treatments have proven insufficient, highlighting the need for more personalized, accessible, and early interventions in primary care. However, the feasibility and practical implementation of such approaches remain insufficiently explored. Considering these challenges, the aims of this study were to co-create and to evaluate the feasibility of a personalized, multidisciplinary, and coordinated intervention for chronic pain management within municipal healthcare services.</p><p><strong>Methods: </strong>The intervention included a generic pain management course (part one) and a personalized second part offering various group-based courses. Participants (<i>n</i> = 70) were recruited through an orthopedic outpatient clinic and general practitioners. Individual consultations with course leaders were conducted before, during, and after the intervention. Questionnaires assessing health-related quality of life, alcohol consumption, medication use, and sleep were administered at baseline, midway, and post-intervention, along with a self-reported evaluation of the intervention after completion.</p><p><strong>Results: </strong>Among the total participants (<i>n</i> = 70), 81% completed Part 1 of the intervention, while 61% completed the entire intervention. At baseline, participants had a mean EQ-5D-5L score of 0.65 and an EQ-VAS score of 48.8. Regarding alcohol use, 47% were drinking once a month or less, and no participants were drinking alcohol four or more times a week. Insomnia was reported by 84%. Paracetamol was the most used daily medication (41%), followed by non-steroidal anti-inflammatory drugs and weak opioids (26% each). In Part 2 of the intervention, stress management courses were the most frequently selected (26%), followed closely by physical activity and body-mind activity at 23%. Most participants reported benefit, with 63% (Part 1) and 56% (Part 2) indicating good or very good benefit, and 98% would recommend it to others.</p><p><strong>Conclusion: </strong>This feasibility study demonstrates the potential for addressing the complex needs of individuals with chronic pain through a personalized and multidisciplinary intervention in primary care. The high completion rates indicate feasibility and acceptability. The findings support further evaluation of resource use, implementation, and effectiveness in future controlled trials.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144974044","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}
Pub Date : 2025-09-02eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0018
Elisabeth Ørskov Rotevatn, Mette Engan, Emilie Stensaker, Karl Ove Hufthammer, Lars Jørgen Rygh
Objectives: Pain assessment is challenging given its subjective nature, and existing assessment tools have limitations, especially for patients having problems with verbal communication. A prior study evaluated the Grasp, a handheld device for assessing pain intensity through squeezing, showing a moderate association with the numeric rating scale (NRS). This study examined an improved version of the Grasp with instant visual feedback through color-coded categories and compared it to NRS.
Methods: Healthy adults underwent two consecutive cold pressor tests (CPTs), reporting pain intensity via NRS or Grasp with colour-coded feedback. Two additional CPTs assessed the association of repeated measurements with both instruments. The Grasp was calibrated to individual strength before CPTs.
Results: Forty-six subjects completed all tests. Pain intensity association between Grasp and NRS was moderate with a mean Kendall's τ-b coefficient (τ-b) of 0.45, 95% confidence interval (CI) 0.35-0.56. Repeated Grasp measurements showed a moderate association (τ-b = 0.37, 95% CI 0.27-0.48), while repeated NRS measurements had a stronger association (τ-b = 0.71, 95% CI 0.64-0.78). After adjusting Grasp to individual squeeze strength (resulting in a 0.0-1.0 scale), a simple equation relating NRS value and mean Grasp value was identified: Grasp = 0.091 × NRS. Grouping reports into mild, moderate, and severe pain resulted in agreement proportions across two CPTs of 69% for Grasp and 79% for NRS.
Conclusions: The moderately high agreement proportions for pain intensity categories suggest that the Grasp method with colour-coded feedback may be useful for categorical pain intensity assessment, especially in settings where conventional tools (i.e., NRS) are inconvenient or not feasible.
目的:疼痛评估具有主观性,现有评估工具存在局限性,特别是对于有语言交流问题的患者。一项先前的研究评估了Grasp,一种通过挤压来评估疼痛强度的手持设备,显示出与数字评定量表(NRS)的适度关联。本研究通过颜色编码的分类检查了具有即时视觉反馈的抓握的改进版本,并将其与NRS进行了比较。方法:健康成人接受两次连续的冷压试验(CPTs),通过NRS或grip报告疼痛强度,并进行颜色编码反馈。另外两项CPTs评估了两种仪器重复测量的相关性。在CPTs之前,Grasp被校准为个人力量。结果:46名受试者完成了所有测试。握力与NRS之间的疼痛强度相关性为中等,平均肯德尔τ-b系数(τ-b)为0.45,95%可信区间(CI)为0.35-0.56。重复的Grasp测量结果显示中度相关性(τ-b = 0.37, 95% CI 0.27-0.48),而重复的NRS测量结果具有较强的相关性(τ-b = 0.71, 95% CI 0.64-0.78)。将Grasp调整为个体挤压强度(产生0.0-1.0的量表)后,确定了NRS值与平均Grasp值之间的简单方程:Grasp = 0.091 × NRS。将报告分为轻度、中度和重度疼痛,两个cpt的一致性比例在Grasp组为69%,在NRS组为79%。结论:对疼痛强度类别的中等高的一致性比例表明,具有颜色编码反馈的Grasp方法可能对分类疼痛强度评估有用,特别是在传统工具(即NRS)不方便或不可行的情况下。
{"title":"Measuring pain intensity in categories through a novel electronic device during experimental cold-induced pain.","authors":"Elisabeth Ørskov Rotevatn, Mette Engan, Emilie Stensaker, Karl Ove Hufthammer, Lars Jørgen Rygh","doi":"10.1515/sjpain-2025-0018","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0018","url":null,"abstract":"<p><strong>Objectives: </strong>Pain assessment is challenging given its subjective nature, and existing assessment tools have limitations, especially for patients having problems with verbal communication. A prior study evaluated the Grasp, a handheld device for assessing pain intensity through squeezing, showing a moderate association with the numeric rating scale (NRS). This study examined an improved version of the Grasp with instant visual feedback through color-coded categories and compared it to NRS.</p><p><strong>Methods: </strong>Healthy adults underwent two consecutive cold pressor tests (CPTs), reporting pain intensity via NRS or Grasp with colour-coded feedback. Two additional CPTs assessed the association of repeated measurements with both instruments. The Grasp was calibrated to individual strength before CPTs.</p><p><strong>Results: </strong>Forty-six subjects completed all tests. Pain intensity association between Grasp and NRS was moderate with a mean Kendall's <i>τ</i>-<i>b</i> coefficient (<i>τ</i>-<i>b</i>) of 0.45, 95% confidence interval (CI) 0.35-0.56. Repeated Grasp measurements showed a moderate association (<i>τ</i>-<i>b</i> = 0.37, 95% CI 0.27-0.48), while repeated NRS measurements had a stronger association (<i>τ</i>-<i>b</i> = 0.71, 95% CI 0.64-0.78). After adjusting Grasp to individual squeeze strength (resulting in a 0.0-1.0 scale), a simple equation relating NRS value and mean Grasp value was identified: Grasp = 0.091 × NRS. Grouping reports into mild, moderate, and severe pain resulted in agreement proportions across two CPTs of 69% for Grasp and 79% for NRS.</p><p><strong>Conclusions: </strong>The moderately high agreement proportions for pain intensity categories suggest that the Grasp method with colour-coded feedback may be useful for categorical pain intensity assessment, especially in settings where conventional tools (i.e., NRS) are inconvenient or not feasible.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-09-02","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144973991","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}
Pub Date : 2025-08-28eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2024-0073
Sigfridur Inga Karlsdottir, Eva Halapi, Gudmundur Kristjan Oskarsson, Hafdis Skuladottir, Thorbjorg Jonsdottir
Objectives: The purpose of the study was to assess the prevalence of both non-chronic and chronic pain among women of childbearing age and describe the impact that pain has on their health-related quality of life (HRQoL).
Methods: This is a cross-sectional cohort study, and the data were collected as part of the ICEPAIN nationwide study. Participants were recruited from a randomised sample, stratified by age and residence to secure a proportional sample, by email invitation. Women between 18 and 45 years of age participated, and data were collected through a web-based platform with questionnaires that measured sociodemographic characteristics, lifestyle factors, sleep quality, pain severity, characteristics of pain, pain interference (Brief Pain Inventory), and HRQoL (SF-12-v2). Spearman correlation was used when assessing relationships between demographic and lifestyle factors, and HRQoL and pain. Chi-square, Mann-Whitney U, ANOVA, and multivariate general linear model were used to assess group differences.
Results: In total, 969 women of childbearing age (18-45 years) participated in the study, and the response rate was 34.8%. The average age was 36.1 ± 6.3 years, and the majority (82.5%) were married, cohabiting, or in a steady relationship. Altogether, 45.9% of the sample reported having pain during the past week (n = 445); the vast majority, 80.4% (n = 366), had chronic pain. The majority of the participants, 57.3%, had moderate or severe pain. Chronic pain was significantly correlated with higher age, higher BMI, experiencing pain during the period, and poorer sleep quality. In contrast, no significant correlation was found between chronic pain and parity, residence, education, physical exercise, smoking, or alcohol drinking. Both non-chronic and chronic pain interfered with mood, sleep, general activities, and other aspects of daily life, and the effect of pain was significantly greater among women with chronic pain. Among these, pain severity was strongly correlated with the level of pain interference (0.79). A negative correlation between pain interference and HRQoL (physical component score, -0.64, and mental component score, -0.34) was observed among women with chronic pain.
Conclusions: Both non-chronic and chronic pain are common among women of childbearing age in Iceland. It interferes with daily life and affects their HRQoL.
{"title":"Pain and health-related quality of life among women of childbearing age in Iceland: ICEPAIN, a nationwide survey.","authors":"Sigfridur Inga Karlsdottir, Eva Halapi, Gudmundur Kristjan Oskarsson, Hafdis Skuladottir, Thorbjorg Jonsdottir","doi":"10.1515/sjpain-2024-0073","DOIUrl":"https://doi.org/10.1515/sjpain-2024-0073","url":null,"abstract":"<p><strong>Objectives: </strong>The purpose of the study was to assess the prevalence of both non-chronic and chronic pain among women of childbearing age and describe the impact that pain has on their health-related quality of life (HRQoL).</p><p><strong>Methods: </strong>This is a cross-sectional cohort study, and the data were collected as part of the ICEPAIN nationwide study. Participants were recruited from a randomised sample, stratified by age and residence to secure a proportional sample, by email invitation. Women between 18 and 45 years of age participated, and data were collected through a web-based platform with questionnaires that measured sociodemographic characteristics, lifestyle factors, sleep quality, pain severity, characteristics of pain, pain interference (Brief Pain Inventory), and HRQoL (SF-12-v2). Spearman correlation was used when assessing relationships between demographic and lifestyle factors, and HRQoL and pain. Chi-square, Mann-Whitney <i>U</i>, ANOVA, and multivariate general linear model were used to assess group differences.</p><p><strong>Results: </strong>In total, 969 women of childbearing age (18-45 years) participated in the study, and the response rate was 34.8%. The average age was 36.1 ± 6.3 years, and the majority (82.5%) were married, cohabiting, or in a steady relationship. Altogether, 45.9% of the sample reported having pain during the past week (<i>n</i> = 445); the vast majority, 80.4% (<i>n</i> = 366), had chronic pain. The majority of the participants, 57.3%, had moderate or severe pain. Chronic pain was significantly correlated with higher age, higher BMI, experiencing pain during the period, and poorer sleep quality. In contrast, no significant correlation was found between chronic pain and parity, residence, education, physical exercise, smoking, or alcohol drinking. Both non-chronic and chronic pain interfered with mood, sleep, general activities, and other aspects of daily life, and the effect of pain was significantly greater among women with chronic pain. Among these, pain severity was strongly correlated with the level of pain interference (0.79). A negative correlation between pain interference and HRQoL (physical component score, -0.64, and mental component score, -0.34) was observed among women with chronic pain.</p><p><strong>Conclusions: </strong>Both non-chronic and chronic pain are common among women of childbearing age in Iceland. It interferes with daily life and affects their HRQoL.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-08-28","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144974009","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}
Pub Date : 2025-08-26eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0001
Jasmin Klick, Cui Yang, Armin Azimi, Christel Weiß, Christoph Reissfelder, Martin Schmelz, Erfan Ghanad
Objectives: Pressure algometry is a validated method for objectively quantifying pain sensitivity in musculoskeletal disorders, particularly useful for diagnosis and monitoring of treatment responses. However, its application to abdominal pain sensitivity remains insufficiently standardized, especially regarding the influence of physiological factors such as respiration. This study investigated the impact of respiratory phase (inhalation vs exhalation) on abdominal pressure pain thresholds (PT) to support the development of standardized assessment protocols.
Methods: Thirty-one healthy medical students were recruited for the study. Each participant underwent three assessments of the abdominal PT with varying respiration phases. Furthermore, intraclass correlation coefficients (ICCs) were estimated to quantify the reliability of PT measurements.
Results: The respiration phase has a significant impact on the PT, which was found to be significantly lower during exhalation than during inhalation (431 ± 177 vs 492 ± 186 kPa, p = 0.0003). The pressure application rate (PAR) for the expiratory measurements was significantly lower compared to the inspiratory PAR (112 ± 56 vs 130 ± 63 kPa/s, p = 0.0007). Both ICCs had similar magnitudes (close to 0.9). No significant difference in PT was found between sexes.
Conclusions: Our study underscores the impact of respiration on pain perception, revealing increased abdominal PT during inhalation. A standardized approach is needed for abdominal PT assessment to guarantee its success in diagnostic and therapeutic evaluations.
目的:压力测量法是一种有效的方法,用于客观量化肌肉骨骼疾病的疼痛敏感性,特别适用于诊断和监测治疗反应。然而,它在腹痛敏感性方面的应用仍然不够规范,特别是关于呼吸等生理因素的影响。本研究探讨了呼吸期(吸气与呼气)对腹压痛阈值(PT)的影响,以支持标准化评估方案的制定。方法:招募31名健康的医学生进行研究。每位参与者在不同的呼吸阶段进行了三次腹部PT评估。此外,估计类内相关系数(ICCs)来量化PT测量的可靠性。结果:呼吸相对PT有显著影响,呼气时PT明显低于吸气时(431±177 vs 492±186 kPa, p = 0.0003)。呼气测量的压力施加率(PAR)明显低于吸气PAR(112±56 vs 130±63 kPa/s, p = 0.0007)。两次icc的震级相似(接近0.9)。PT在性别间无显著差异。结论:我们的研究强调了呼吸对疼痛感知的影响,揭示了吸入过程中腹部PT的增加。需要一个标准化的方法来评估腹部PT,以保证其诊断和治疗评价的成功。
{"title":"Impact of respiration on abdominal pain thresholds in healthy subjects - A pilot study.","authors":"Jasmin Klick, Cui Yang, Armin Azimi, Christel Weiß, Christoph Reissfelder, Martin Schmelz, Erfan Ghanad","doi":"10.1515/sjpain-2025-0001","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0001","url":null,"abstract":"<p><strong>Objectives: </strong>Pressure algometry is a validated method for objectively quantifying pain sensitivity in musculoskeletal disorders, particularly useful for diagnosis and monitoring of treatment responses. However, its application to abdominal pain sensitivity remains insufficiently standardized, especially regarding the influence of physiological factors such as respiration. This study investigated the impact of respiratory phase (inhalation vs exhalation) on abdominal pressure pain thresholds (PT) to support the development of standardized assessment protocols.</p><p><strong>Methods: </strong>Thirty-one healthy medical students were recruited for the study. Each participant underwent three assessments of the abdominal PT with varying respiration phases. Furthermore, intraclass correlation coefficients (ICCs) were estimated to quantify the reliability of PT measurements.</p><p><strong>Results: </strong>The respiration phase has a significant impact on the PT, which was found to be significantly lower during exhalation than during inhalation (431 ± 177 vs 492 ± 186 kPa, <i>p</i> = 0.0003). The pressure application rate (PAR) for the expiratory measurements was significantly lower compared to the inspiratory PAR (112 ± 56 vs 130 ± 63 kPa/s, <i>p</i> = 0.0007). Both ICCs had similar magnitudes (close to 0.9). No significant difference in PT was found between sexes.</p><p><strong>Conclusions: </strong>Our study underscores the impact of respiration on pain perception, revealing increased abdominal PT during inhalation. A standardized approach is needed for abdominal PT assessment to guarantee its success in diagnostic and therapeutic evaluations.</p>","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-08-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144973965","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}
Pub Date : 2025-08-06eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0044
Robin Bekrater-Bodmann
{"title":"When pain meets hope: Case report of a suspended assisted suicide trajectory in phantom limb pain and its broader biopsychosocial implications.","authors":"Robin Bekrater-Bodmann","doi":"10.1515/sjpain-2025-0044","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0044","url":null,"abstract":"","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144795843","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}
Pub Date : 2025-08-06eCollection Date: 2025-01-01DOI: 10.1515/sjpain-2025-0041
Ulf E Kongsgaard, Mads U Werner
{"title":"Stellate ganglion block for mental disorders - too good to be true?","authors":"Ulf E Kongsgaard, Mads U Werner","doi":"10.1515/sjpain-2025-0041","DOIUrl":"https://doi.org/10.1515/sjpain-2025-0041","url":null,"abstract":"","PeriodicalId":47407,"journal":{"name":"Scandinavian Journal of Pain","volume":"25 1","pages":""},"PeriodicalIF":1.9,"publicationDate":"2025-08-06","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144790398","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}