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Fear Avoidance Beliefs and Risk of Long-Term Sickness Absence: Prospective Cohort Study among Workers with Musculoskeletal Pain. 恐惧回避信念和长期缺勤的风险:肌肉骨骼疼痛工人的前瞻性队列研究。
Q2 Medicine Pub Date : 2018-09-02 eCollection Date: 2018-01-01 DOI: 10.1155/2018/8347120
Kenneth Jay, Sannie Vester Thorsen, Emil Sundstrup, Ramon Aiguadé, Jose Casaña, Joaquin Calatayud, Lars Louis Andersen

Background and objective: Musculoskeletal pain is common in the population. Negative beliefs about musculoskeletal pain and physical activity may lead to avoidance behavior resulting in absence from work. The present study investigates the influence of fear avoidance beliefs on long-term sickness absence.

Methods: Workers of the general working population with musculoskeletal pain (low back, neck/shoulder, and/or arm/hand pain; n = 8319) from the Danish Work Environment Cohort Study were included. Long-term sickness absence data were obtained from the Danish Register for Evaluation and Marginalization (DREAM). Time-to-event analyses (cox regression) controlled for various confounders estimated the association between fear avoidance beliefs (very low, low, moderate [reference category], high, and very high) at baseline and long-term sickness absence (LTSA; ≥6 consecutive weeks) during a 2-year follow-up.

Results: During the 2-year follow-up, 10.2% of the workers experienced long-term sickness absence. In the fully adjusted model, very high-level fear avoidance increased the risk of LTSA with hazard ratio (HR) of 1.48 (95% CI 1.15-1.90). Similar results were seen analyses stratified for occupational physical activity, i.e., sedentary workers (HR 1.72 (95% CI 1.04-2.83)) and physically active workers (HR 1.48 (95% CI 1.10-2.01)).

Conclusion: A very high level of fear avoidance is a risk factor for long-term sickness absence among workers with musculoskeletal pain regardless of the level of occupational physical activity. Future interventions should target fear avoidance beliefs through information and campaigns about the benefits of staying active when having musculoskeletal pain.

背景与目的:肌肉骨骼疼痛在人群中很常见。对肌肉骨骼疼痛和体力活动的消极看法可能导致回避行为,从而导致缺勤。本研究探讨了恐惧回避信念对长期疾病缺勤的影响。方法:有肌肉骨骼疼痛(腰背、颈/肩和/或手臂/手疼痛)的普通工人;来自丹麦工作环境队列研究的n = 8319)。长期疾病缺勤数据来自丹麦评估和边缘化登记册(DREAM)。控制各种混杂因素的事件时间分析(cox回归)估计了基线时恐惧回避信念(非常低、低、中等[参考类别]、高和非常高)与长期疾病缺勤(LTSA;≥连续6周),随访2年。结果:在2年的随访中,10.2%的员工经历了长期病假。在完全调整的模型中,非常高的恐惧回避增加了LTSA的风险,风险比(HR)为1.48 (95% CI 1.15-1.90)。对职业体力活动的分层分析也看到了类似的结果,即久坐工人(HR 1.72 (95% CI 1.04-2.83))和体力活动工人(HR 1.48 (95% CI 1.10-2.01))。结论:无论职业体力活动水平如何,高水平的恐惧回避是肌肉骨骼疼痛工人长期缺勤的一个危险因素。未来的干预措施应该针对恐惧避免信念,通过信息和运动,当有肌肉骨骼疼痛时保持运动的好处。
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引用次数: 12
Preemptive Analgesia in Total Knee Arthroplasty: Comparing the Effects of Single Dose Combining Celecoxib with Pregabalin and Repetition Dose Combining Celecoxib with Pregabalin: Double-Blind Controlled Clinical Trial. 全膝关节置换术中的先期镇痛:比较单剂量联合塞来昔布和普瑞巴林以及重复剂量联合塞来昔布和普瑞巴林的效果:双盲对照临床试验。
Q2 Medicine Pub Date : 2018-08-07 eCollection Date: 2018-01-01 DOI: 10.1155/2018/3807217
Andri M T Lubis, Rangga B V Rawung, Aida R Tantri

Acute pain is the most common early complication after total knee arthroplasty causing delayed mobilization and increased demands of morphine, leading to higher operative cost. Several studies have assessed the effectiveness, side-effects, and ease of use of various analgesics. Preemptive analgesia with combined celecoxib and pregabalin has been reported to yield positive outcomes. In this randomized, double-blind controlled clinical trial, 30 subjects underwent surgery for total knee arthroplasty using 15-20mg bupivacaine 5% epidural anesthesia. All subjects were divided into three groups. Group 1 was given celecoxib 400mg and pregabalin 150mg 1 hour before the operation, Group 2 was given celecoxib 200mg and pregabalin 75mg twice daily starting from 3 days before the operation, and Group 3 was given a placebo. The outcome was measured with Visual Analog Scale, knee range of motion, and postoperative mobilization. There was a significant difference in postoperative morphine usage between the groups that were administered with preemptive analgesia and the placebo group, but no significant difference was found between Group 1 and Group 2 that were given preemptive analgesia at different doses. ROM and postoperative mobilization were not significantly different among the three groups. Two patients in the first group, one patient in the second group, and one patient in the third group developed nausea. Preemptive analgesia is proven to reduce postoperative usage of morphine independent of the dosage. We recommend the use of combined celecoxib and pregabalin as preemptive analgesia after the total knee arthroplasty procedure. This trial is registered with NCT03523832 (ClinicalTrials.gov).

急性疼痛是全膝关节置换术后最常见的早期并发症,会导致活动延迟和吗啡用量增加,从而增加手术费用。多项研究对各种镇痛药的有效性、副作用和易用性进行了评估。据报道,联合使用塞来昔布和普瑞巴林进行先期镇痛可取得良好效果。在这项随机、双盲对照临床试验中,30 名受试者接受了全膝关节置换手术,使用了 15-20 毫克 5%布比卡因硬膜外麻醉。所有受试者被分为三组。第一组在手术前 1 小时服用塞来昔布 400 毫克和普瑞巴林 150 毫克;第二组在手术前 3 天开始服用塞来昔布 200 毫克和普瑞巴林 75 毫克,每天两次;第三组服用安慰剂。结果通过视觉模拟量表、膝关节活动范围和术后活动能力进行测量。术后吗啡用量方面,给予抢先镇痛的组别与安慰剂组别存在显著差异,但给予不同剂量抢先镇痛的第一组和第二组之间没有发现显著差异。三组患者的 ROM 和术后活动能力无明显差异。第一组有两名患者、第二组有一名患者、第三组有一名患者出现恶心症状。事实证明,先期镇痛可以减少术后吗啡用量,而与剂量无关。我们建议在全膝关节置换术后使用塞来昔布和普瑞巴林联合疗法作为术前镇痛。该试验已在 NCT03523832(ClinicalTrials.gov)上注册。
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引用次数: 0
The Role of Nurses' Uncertainty in Decision-Making Process of Pain Management in People with Dementia. 护士不确定性在痴呆患者疼痛管理决策过程中的作用。
Q2 Medicine Pub Date : 2018-08-01 eCollection Date: 2018-01-01 DOI: 10.1155/2018/7281657
Mohammad Rababa

Pain in people with dementia (PWD) is underassessed and undertreated. Treatment of pain in people with dementia goes awry because of poor assessment, poor treatment, and factors related to nursing decision-making skills. Several theoretical models addressed the role of nurses' critical thinking and decision-making skills in pain treatment, like the cognitive continuum theory (CCT) and the adaptive pain management (APT). Only the Response to Certainty of Pain (RCP) model was the first model to posit relationships between nurses' uncertainty, pain assessment, and patient outcomes. Gilmore-Bykovskyi and Bowers developed the RCP, which incorporates the concept of uncertainty and how it relates to the problem of unrelieved pain in PWD. The RCP model has the potential to provide good understanding of the problem of unrelieved pain in people with dementia. It also could help to develop a research study that brings comfort to an often neglected and vulnerable population.

痴呆症患者(PWD)的疼痛被低估和治疗不足。由于评估不佳、治疗不佳以及与护理决策技能相关的因素,痴呆症患者的疼痛治疗出现了问题。一些理论模型解决了护士的批判性思维和决策技能在疼痛治疗中的作用,如认知连续统理论(CCT)和适应性疼痛管理(APT)。只有疼痛确定性反应(RCP)模型是第一个假设护士不确定性、疼痛评估和患者预后之间关系的模型。Gilmore-Bykovskyi和Bowers开发了RCP,其中包含了不确定性的概念以及它与PWD中未缓解的疼痛问题的关系。RCP模型有可能为痴呆症患者无法缓解的疼痛问题提供更好的理解。它还可以帮助开展一项研究,为经常被忽视和脆弱的人群带来安慰。
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引用次数: 14
The Consumption of Cannabis by Fibromyalgia Patients in Israel. 以色列纤维肌痛患者的大麻消费量。
Q2 Medicine Pub Date : 2018-07-22 eCollection Date: 2018-01-01 DOI: 10.1155/2018/7829427
George Habib, Irit Avisar

Objective: To report on the habits of cannabis consumption among fibromyalgia patients in Israel.

Patients and methods: An Internet-based questionnaire was posted to three large fibromyalgia Facebook groups in our country. The questionnaire was anonymous and included demographic, clinical, and cannabis-related questions, including acquisition of a license for medical cannabis (MC) method and amount of cannabis consumption; need to buy cannabis beyond the medical allowance; effect of cannabis on pain, sleep, depression, and anxiety; adverse effects of cannabis; feelings of dependence on cannabis or other meds; the involvement of family members; tendency to drive after using cannabis; and employment and social disability status.

Results: Of 2,705 people, 383 (14%) responded to the questionnaire, with a mean age of 42.2±14.2 years. Of the responders, 84% reported consuming cannabis, and 44% were licensed for MC. The mean amount per month of cannabis consumed was 31.4±16.3g, and 80% of cannabis consumers (CC) smoked pure cannabis or cannabis mixed with tobacco. Pain relief was reported by 94% of CC, while 93% reported improved sleep quality, 87% reported improvement in depression, and 62% reported improvement in anxiety. Of MC-licensed CC, 55% bought cannabis beyond the medical allowance on the black market. Adverse effects were reported by 12% of CC. Only 8% reported dependence on cannabis. Most CC (64%) worked either full- or part-time jobs, and 74% reported driving "as usual" under cannabis use.

Conclusions: Cannabis consumption among fibromyalgia patients in our country is very common and is mostly not licensed. Nearly all CC reported favorable effects on pain and sleep, and few reported adverse effects or feeling of dependence on cannabis.

目的:报道以色列纤维肌痛患者的大麻消费习惯。患者和方法:将一份基于互联网的问卷发布到我国三个大型纤维肌痛Facebook群组。问卷是匿名的,包括人口统计、临床和大麻相关问题,包括获得医用大麻许可证的方法和大麻消费量;需要购买超过医疗津贴的大麻;大麻对疼痛、睡眠、抑郁和焦虑的影响;大麻的不良影响;对大麻或其他药物的依赖感;家庭成员的参与;吸食大麻后驾车的倾向;就业和社会残疾状况。结果:2705人中,383人(14%)回复问卷,平均年龄42.2±14.2岁。在应答者中,84%的人报告吸食大麻,44%的人有大麻执照。每月平均吸食大麻量为31.4±16.3克,80%的大麻消费者(CC)吸食纯大麻或大麻与烟草混合。94%的CC患者报告疼痛缓解,93%的CC患者报告睡眠质量改善,87%的CC患者报告抑郁改善,62%的CC患者报告焦虑改善。在mc许可的CC中,55%的人在黑市上购买了超出医疗补贴的大麻。12%的CC报告了不良反应,只有8%报告了对大麻的依赖。大多数CC(64%)有全职或兼职工作,74%的人报告说吸食大麻后开车“像往常一样”。结论:我国纤维肌痛患者吸食大麻现象普遍,且大多未获许可。几乎所有的CC都报告了对疼痛和睡眠的有利影响,很少有人报告了对大麻的不良影响或依赖感。
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引用次数: 21
The Effectiveness of Orofacial Pain Therapy in Indonesia: A Cross-Sectional Study. 印度尼西亚口腔面部疼痛治疗的有效性:一项横断面研究。
Q2 Medicine Pub Date : 2018-07-18 DOI: 10.1155/2018/6078457
T Maulina, G Yubiliana, R Rikmasari

Objectives: As the most complained oral problems in Indonesia, the therapy of orofacial pain has to be constantly evaluated. The objective of the current study was to evaluate the effectiveness of orofacial pain therapy in Indonesia.

Methods: This study recruited 5412 (3816 female; 1596 male) participants from 27 districts in West Java province. Half of the participants (2714) were recruited from those who were treated at community health centers whilst the rest were those who were treated at private dental clinics. A Likert-scale questionnaire that consists of nine questions that were divided to three subsections was used. The first subsection of the questionnaire evaluated the participants' post-therapy basic oral functions (three questions), and the second part evaluated the participants' post-therapy pain intensity and frequency (three questions), whilst the last part evaluated the participants' post-therapy activities (three questions). All data were then cross-tabulated and correlated by using Spearman correlation.

Result: The current study revealed that out of 5412 participants, 4023 (74.33%) participants claimed that the therapy has enabled them to perform their work activity as usual, whilst 2576 (59.2%) claimed that the therapy has decreased the intensity of the pain moderately. A significant (p < 0.01) correlation (r = 0.1) between the type of dental facility visited and the total score of the therapy effectiveness was revealed.

Conclusion: The therapy of orofacial pain in Indonesian sample was proven to be effective. Further study evaluating the reasons underlying the current results is of importance.

目的:作为印尼最受投诉的口腔问题,必须不断评估口腔面部疼痛的治疗方法。本研究的目的是评估印度尼西亚口腔面部疼痛治疗的有效性。方法:本研究招募了来自西爪哇省27个区的5412名参与者(3816名女性;1596名男性)。一半的参与者(2714人)是从在社区卫生中心接受治疗的人中招募的,其余的是在私人牙科诊所接受治疗的。Likert量表由九个问题组成,分为三个小节。问卷的第一小节评估了参与者治疗后的基本口腔功能(三个问题),第二部分评估了参与者的治疗后疼痛强度和频率(三个问),而最后一部分评估了与会者的治疗后活动(三个答问)。然后将所有数据交叉制成表格,并使用Spearman相关性进行关联。结果:目前的研究显示,在5412名参与者中,4023名(74.33%)参与者声称该疗法使他们能够像往常一样进行工作活动,而2576名(59.2%)声称该疗法适度降低了疼痛强度。就诊的牙科机构类型与治疗有效性总分之间存在显著(p<0.01)相关性(r=0.1)。结论:印尼样本口腔面部疼痛的治疗已被证明是有效的。进一步研究评估当前结果背后的原因具有重要意义。
{"title":"The Effectiveness of Orofacial Pain Therapy in Indonesia: A Cross-Sectional Study.","authors":"T Maulina,&nbsp;G Yubiliana,&nbsp;R Rikmasari","doi":"10.1155/2018/6078457","DOIUrl":"10.1155/2018/6078457","url":null,"abstract":"<p><strong>Objectives: </strong>As the most complained oral problems in Indonesia, the therapy of orofacial pain has to be constantly evaluated. The objective of the current study was to evaluate the effectiveness of orofacial pain therapy in Indonesia.</p><p><strong>Methods: </strong>This study recruited 5412 (3816 female; 1596 male) participants from 27 districts in West Java province. Half of the participants (2714) were recruited from those who were treated at community health centers whilst the rest were those who were treated at private dental clinics. A Likert-scale questionnaire that consists of nine questions that were divided to three subsections was used. The first subsection of the questionnaire evaluated the participants' post-therapy basic oral functions (three questions), and the second part evaluated the participants' post-therapy pain intensity and frequency (three questions), whilst the last part evaluated the participants' post-therapy activities (three questions). All data were then cross-tabulated and correlated by using Spearman correlation.</p><p><strong>Result: </strong>The current study revealed that out of 5412 participants, 4023 (74.33%) participants claimed that the therapy has enabled them to perform their work activity as usual, whilst 2576 (59.2%) claimed that the therapy has decreased the intensity of the pain moderately. A significant (p < 0.01) correlation (r = 0.1) between the type of dental facility visited and the total score of the therapy effectiveness was revealed.</p><p><strong>Conclusion: </strong>The therapy of orofacial pain in Indonesian sample was proven to be effective. Further study evaluating the reasons underlying the current results is of importance.</p>","PeriodicalId":19786,"journal":{"name":"Pain Research and Treatment","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2018-07-18","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2018/6078457","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36401373","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 5
Liposome Bupivacaine Compared to Plain Local Anesthetics to Reduce Postsurgical Pain: An Updated Meta-Analysis of Randomized Controlled Trials. 脂质体布比卡因与普通局麻药相比减少术后疼痛:一项随机对照试验的最新荟萃分析。
Q2 Medicine Pub Date : 2018-07-15 eCollection Date: 2018-01-01 DOI: 10.1155/2018/5710169
Mark C Kendall, Lucas Jorge Castro Alves, Gildasio De Oliveira

Objective: Peripheral nerve blocks for postoperative analgesia have improved block success, but analgesia efficacy has been limited by the short duration of traditional local anesthetics. The results of randomized trials comparing liposome bupivacaine with conventional local anesthetic formulations (e.g., plain bupivacaine and ropivacaine) have generated conflicting results. This study was conducted to systematically review the effectiveness of analgesic efficacy of liposome bupivacaine infiltration at the surgical site versus plain local anesthetic bupivacaine or ropivacaine in patients undergoing surgery.

Methods: PRISMA statement guidelines were followed. A search of electronic databases National Library of Medicine's PubMed database, Cochrane Database of Systematic Reviews, Embase, and Google Scholar from January 2012 to September 2017 was performed. Among the 1,612 records identified, 9 randomized controlled trials involving 779 patients were eligible for data extraction and meta-analysis.

Results: Liposome bupivacaine did not reduce postsurgical pain at rest compared to plain local anesthetics at 24 and 48 hours after surgery. Moreover, liposome bupivacaine did not reduce postoperative opioid consumption at 24, 48, or 72 hours when compared to plain local anesthetics. Liposome bupivacaine did reduce postoperative nausea when compared to plain local anesthetics (P =<0.3). There was no significant difference in hospital length of stay between study groups, the use of plain bupivacaine or ropivacaine, or among orthopedic or nonorthopedic procedures. No manifestations of local anesthetic toxicity were reported.

Conclusions: Our results suggest that liposome bupivacaine does not have an analgesic advantage when compared to plain local anesthetics at the surgical site for patients undergoing surgical procedures.

目的:周围神经阻滞用于术后镇痛提高了阻滞成功率,但传统局麻药持续时间短,限制了镇痛效果。比较脂质体布比卡因与常规局部麻醉制剂(如普通布比卡因和罗哌卡因)的随机试验结果产生了相互矛盾的结果。本研究旨在系统回顾布比卡因脂质体在手术部位浸润与普通局麻布比卡因或罗哌卡因在手术患者中的镇痛效果。方法:遵循PRISMA声明指南。检索2012年1月至2017年9月美国国家医学图书馆PubMed数据库、Cochrane系统评价数据库、Embase和Google Scholar等电子数据库。在确定的1,612项记录中,9项随机对照试验涉及779名患者,符合数据提取和荟萃分析的条件。结果:与普通局麻药相比,脂质体布比卡因在术后24和48小时内并没有减轻术后休息时的疼痛。此外,与普通局麻药相比,脂质体布比卡因并没有减少术后24、48或72小时的阿片类药物消耗。与普通局麻药相比,布比卡因脂质体确实减少了术后恶心(P =结论:我们的研究结果表明,与普通局麻药相比,布比卡因脂质体在手术部位对接受外科手术的患者没有镇痛优势。
{"title":"Liposome Bupivacaine Compared to Plain Local Anesthetics to Reduce Postsurgical Pain: An Updated Meta-Analysis of Randomized Controlled Trials.","authors":"Mark C Kendall,&nbsp;Lucas Jorge Castro Alves,&nbsp;Gildasio De Oliveira","doi":"10.1155/2018/5710169","DOIUrl":"https://doi.org/10.1155/2018/5710169","url":null,"abstract":"<p><strong>Objective: </strong>Peripheral nerve blocks for postoperative analgesia have improved block success, but analgesia efficacy has been limited by the short duration of traditional local anesthetics. The results of randomized trials comparing liposome bupivacaine with conventional local anesthetic formulations (e.g., plain bupivacaine and ropivacaine) have generated conflicting results. This study was conducted to systematically review the effectiveness of analgesic efficacy of liposome bupivacaine infiltration at the surgical site versus plain local anesthetic bupivacaine or ropivacaine in patients undergoing surgery.</p><p><strong>Methods: </strong>PRISMA statement guidelines were followed. A search of electronic databases National Library of Medicine's PubMed database, Cochrane Database of Systematic Reviews, Embase, and Google Scholar from January 2012 to September 2017 was performed. Among the 1,612 records identified, 9 randomized controlled trials involving 779 patients were eligible for data extraction and meta-analysis.</p><p><strong>Results: </strong>Liposome bupivacaine did not reduce postsurgical pain at rest compared to plain local anesthetics at 24 and 48 hours after surgery. Moreover, liposome bupivacaine did not reduce postoperative opioid consumption at 24, 48, or 72 hours when compared to plain local anesthetics. Liposome bupivacaine did reduce postoperative nausea when compared to plain local anesthetics (<i>P</i> =<0.3). There was no significant difference in hospital length of stay between study groups, the use of plain bupivacaine or ropivacaine, or among orthopedic or nonorthopedic procedures. No manifestations of local anesthetic toxicity were reported.</p><p><strong>Conclusions: </strong>Our results suggest that liposome bupivacaine does not have an analgesic advantage when compared to plain local anesthetics at the surgical site for patients undergoing surgical procedures.</p>","PeriodicalId":19786,"journal":{"name":"Pain Research and Treatment","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2018-07-15","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1155/2018/5710169","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"36401372","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 32
Incidence and Health Related Quality of Life of Opioid-Induced Constipation in Chronic Noncancer Pain Patients: A Prospective Multicentre Cohort Study. 慢性非癌性疼痛患者阿片类药物引起便秘的发生率和健康相关生活质量:一项前瞻性多中心队列研究
Q2 Medicine Pub Date : 2018-07-10 eCollection Date: 2018-01-01 DOI: 10.1155/2018/5704627
Dalila R Veiga, Liliane Mendonça, Rute Sampaio, José C Lopes, Luís F Azevedo

Background: High rates of opioid use for chronic noncancer pain (CNCP) have been reported worldwide, despite its association with adverse events, inappropriate use, and limited analgesic effect. Opioid-induced constipation (OIC) is the most prevalent and disabling adverse effect associated with opioid therapy. Our aim was to assess the incidence, health related quality of life (HRQOL), and disability in OIC patients.

Methods: A prospective cohort study was performed, with 6 months of follow-up, of adult CNCP patients consecutively admitted in 4 multidisciplinary pain clinics (MPC). Demographic and clinical data have been collected. Brief Pain Inventory (BPI) and Short version of Treatment Outcomes in Pain Survey (S-TOPS) were used to measure functional outcomes and HRQOL. OIC was assessed using Bowel Function Index (BFI).

Results: 694 patients were recruited. OIC prevalence at baseline was 25.8%. At 6 months, OIC incidence was 24.8%. Female gender (OR = 1.65, p = 0.039), opioid therapy (OR 1.65, p = 0.026), and interference pain score on BPI (OR 1.10, p = 0.009) were identified as OIC independent predictors. OIC patients presented higher disability and pain interference and severity scores. OIC patients reported less satisfaction with outcome (p = 0.038).

Discussion: Constipation is a common adverse event among opioid users with major functional and quality of life impairment. These findings emphasise the need of OIC adequate assessment and management.

背景:阿片类药物用于慢性非癌性疼痛(CNCP)的发生率很高,尽管其与不良事件、不当使用和有限的镇痛效果有关。阿片类药物引起的便秘(OIC)是与阿片类药物治疗相关的最普遍和致残性的不良反应。我们的目的是评估OIC患者的发病率、健康相关生活质量(HRQOL)和残疾。方法:对4家多学科疼痛诊所(MPC)连续收治的CNCP成人患者进行前瞻性队列研究,随访6个月。已经收集了人口统计和临床数据。使用简短疼痛量表(BPI)和简短疼痛调查治疗结果量表(S-TOPS)来衡量功能结局和HRQOL。OIC采用肠功能指数(BFI)评估。结果:共纳入694例患者。OIC基线患病率为25.8%。6个月时OIC发生率为24.8%。女性性别(OR = 1.65, p = 0.039)、阿片类药物治疗(OR 1.65, p = 0.026)和BPI干扰性疼痛评分(OR 1.10, p = 0.009)被确定为OIC的独立预测因素。OIC患者表现出较高的残疾、疼痛干扰和严重程度评分。OIC患者对预后的满意度较低(p = 0.038)。讨论:便秘是阿片类药物使用者中常见的不良事件,主要是功能和生活质量受损。这些调查结果强调伊斯兰会议组织需要进行充分的评估和管理。
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引用次数: 13
Burn Pain Management at Burn Unit of Yekatit 12 Hospitals, Addis Ababa. 亚的斯亚贝巴Yekatit 12医院烧伤科的烧伤疼痛管理。
Q2 Medicine Pub Date : 2018-07-04 eCollection Date: 2018-01-01 DOI: 10.1155/2018/1092650
Negashu Dadi Mengistu, Mohammed Suleiman Obsa, Leulayehu Akalu Gemeda

Background: Burn pain is a unique and complex challenge for all health professionals and the patients. The only way to insure quality burn pain relief is the patient's self-report. Thus, assessment of severity of pain and its associated factors are important in treatment plan.

Objective: To assess severity of burn pain and associated factors in Yekatit 12 Hospitals burn unit from January 1, 2017, to March 30, 2017.

Methods: Hospital based cross sectional study design was conducted. Data was collected by using structural questionnaires from all eligible patients, those admitted to burn unit of Yekatit 12 Hospital during the study period. Severity of burn pain was assessed by using numerical, facial, and behavioral pain scale measurement tools. Pain assessment scale was deployed for patients by data collectors before medication and dressing change. Multivariate logistic regression analysis was conducted to identify significant predictors based on p value less than 0.05 with 95% confidence interval.

Results: A total of 62 burn patients were included in the study. 87.1% of the patients feel severe pain and 12.9% of the patients feel moderate pain. Pediatrics age groups were about 11 times more likely to feel severe pain than adults, and patients with TBSA ≥ 25% were about 8 times more likely to feel severe burn pain than those with TBSA < 25% [AOR = 7.773; CI 1.184, 51.043] (P = 0.033).

Conclusion and recommendation: Majorities of burn patients had severe pain and burn pain was not appropriately treated. Therefore, appropriate pain management was strongly recommended.

背景:烧伤疼痛是所有卫生专业人员和患者面临的独特而复杂的挑战。确保烧伤疼痛缓解质量的唯一方法是病人的自我报告。因此,评估疼痛的严重程度及其相关因素在治疗计划中是重要的。目的:评估2017年1月1日至2017年3月30日在Yekatit 12医院烧伤科的烧伤疼痛严重程度及相关因素。方法:采用基于医院的横断面研究设计。数据收集采用结构化问卷调查的所有符合条件的患者,这些患者在研究期间住在Yekatit 12医院的烧伤科。采用数字、面部和行为疼痛量表测量工具评估烧伤疼痛的严重程度。在给药和换药前,由数据收集人员对患者进行疼痛评估量表。采用多因素logistic回归分析,以p值< 0.05,置信区间为95%为判别显著性预测因子。结果:共纳入62例烧伤患者。87.1%的患者感到重度疼痛,12.9%的患者感到中度疼痛。儿科年龄组感到严重疼痛的可能性约为成人的11倍,TBSA≥25%的患者感到严重烧伤疼痛的可能性约为TBSA < 25%的患者的8倍[AOR = 7.773;[Ci 1.184, 51.043] (p = 0.033)。结论与建议:大多数烧伤患者有严重的疼痛,烧伤疼痛没有得到适当的治疗。因此,强烈建议适当的疼痛管理。
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引用次数: 8
Sphenopalatine Ganglion Block for the Treatment of Acute Migraine Headache. 蝶腭神经节阻滞治疗急性偏头痛。
Q2 Medicine Pub Date : 2018-05-07 eCollection Date: 2018-01-01 DOI: 10.1155/2018/2516953
Mohamed Binfalah, Eman Alghawi, Eslam Shosha, Ali Alhilly, Moiz Bakhiet

Transnasal sphenopalatine ganglion block is emerging as is an attractive and effective treatment modality for acute migraine headaches, cluster headache, trigeminal neuralgia, and several other conditions. We assessed the efficacy and safety of this treatment using the Sphenocath® device. 55 patients with acute migraine headaches underwent this procedure, receiving 2 ml of 2% lidocaine in each nostril. Pain numeric rating scale (baseline, 15 minutes, 2 hours, and 24 hours) and patient global impression of change (2 hours and 24 hours after treatment) were recorded. The majority of patients became headache-free at 15 minutes, 2 hours, and 24 hours after procedure (70.9%, 78.2%, and 70.4%, resp.). The rate of headache relief (50% or more reduction in headache intensity) was 27.3% at 15 minutes, 20% at 2 hours, and 22.2% at 24 hours. The mean pain numeric rating scale decreased significantly at 15 minutes, 2 hours, and 24 hours, respectively. Most patients rated the results as very good or good. The procedure was well-tolerated with few adverse events. This treatment is emerging as an effective and safe option for management of acute migraine attacks.

经鼻蝶腭神经节阻滞是急性偏头痛、丛集性头痛、三叉神经痛和其他一些疾病的一种有吸引力和有效的治疗方式。我们使用Sphenocath®装置评估了这种治疗的有效性和安全性。55名急性偏头痛患者接受了这种治疗,每个鼻孔注射2ml 2%利多卡因。记录疼痛数值评定量表(基线、15分钟、2小时和24小时)和患者总体印象变化(治疗后2小时和24小时)。大多数患者在手术后15分钟、2小时和24小时(分别为70.9%、78.2%和70.4%)头痛消失。头痛缓解率(头痛强度降低50%或更多)在15分钟时为27.3%,在2小时时为20%,在24小时时为22.2%。平均疼痛数值评分分别在15分钟、2小时和24小时显著下降。大多数患者认为结果非常好或很好。该手术耐受性良好,几乎没有不良事件。这种治疗方法正在成为治疗急性偏头痛发作的一种有效和安全的选择。
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引用次数: 52
Prevalence and Characterization of Breakthrough Pain Associated with Chronic Low Back Pain in the South of Spain: A Cross-Sectional, Multicenter, Observational Study. 西班牙南部与慢性腰痛相关的突破性疼痛的患病率和特征:一项横断面、多中心、观察性研究。
Q2 Medicine Pub Date : 2018-04-23 eCollection Date: 2018-01-01 DOI: 10.1155/2018/4325271
Luis Miguel Torres, Antonio Javier Jiménez, Ana Cabezón, Manuel Jesús Rodríguez

Chronic low back pain (CLBP) is highly prevalent in industrialized countries, where it is one of the main causes of disability. Patients with CLBP in treatment with opioids often experience episodes of breakthrough pain (BTP), but data on prevalence and treatment preferences are scarce. The objectives of this study were, first, the evaluation of the prevalence of BTP in patients with CLBP in the South of Spain (N = 1,868) and, second, the characterization of BTP in these patients (N = 295). Data was collected on presence of BTP, type and location of pain, treatment, compliance, and patient satisfaction. We found a prevalence of BTP in patients with CLBP of 37.5% (95% CI: 35.3%-39.7%), similar in men and women. 75% of the patients were older than 50 years. The preferred drug of patients who control BTP with opioids is fentanyl (78.3%) and its most common form of administration is nasal (53.2%). Therapeutic compliance was high and 46.3% of patients considered the control of their BTP very satisfactory. Our study showed that BTP is common in patients with CLBP and that current treatments seem adequate.

慢性腰痛(CLBP)在工业化国家非常普遍,是致残的主要原因之一。使用阿片类药物治疗的CLBP患者经常经历突破性疼痛(BTP)发作,但关于患病率和治疗偏好的数据很少。本研究的目的首先是评估西班牙南部CLBP患者中BTP的患病率(N = 1868),其次是这些患者中BTP的特征(N = 295)。收集BTP的存在,疼痛的类型和位置,治疗,依从性和患者满意度的数据。我们发现BTP在CLBP患者中的患病率为37.5% (95% CI: 35.3%-39.7%),男性和女性相似。75%的患者年龄在50岁以上。用阿片类药物控制BTP的患者首选芬太尼(78.3%),最常见的给药方式是鼻腔给药(53.2%)。治疗依从性高,46.3%的患者认为BTP控制非常满意。我们的研究表明BTP在CLBP患者中很常见,目前的治疗似乎是足够的。
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Pain Research and Treatment
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