首页 > 最新文献

Pain management最新文献

英文 中文
Transforaminal epidural steroid injection for radiculopathy and the evolution to surgical treatment: a pragmatic prospective observational multicenter study. 经椎间孔硬膜外注射类固醇治疗根神经病和手术治疗的演变:一项务实的前瞻性多中心观察研究。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-03-05 DOI: 10.2217/pmt-2023-0121
Vincent Raymaekers, Gert Roosen, Eric Put, Steven Vanvolsem, Salah-Eddine Achahbar, Sacha Meeuws, Maarten Wissels, Sven Bamps, Dirk De Ridder, Tomas Menovsky, Mark Plazier

Aim: The aim of this study is to analyze the real-world outcomes of transforaminal epidural steroid injections (TFESIs) in all patients with radiculopathy and their long-term outcomes. Methods: Patients with radiculopathy and failure of conservative treatment were included in a prospective, multicenter, observational cohort study. Results: In total, 117 patients were treated with one or two TFESIs. The mean duration of follow-up was 116 (±14) weeks. In total 19,6% (95% CI: 12.9-28.0%) patients were treated with surgery after insufficient symptom improvement. The evolution to surgery was not associated with etiology, symptom duration or previous spine surgery. Conclusion: Real-world data confirms that TFESIs is an effective treatment with satisfactory results in about 80% of patients for a period of 2 years.

目的:本研究旨在分析所有根神经根病患者接受经椎间孔硬膜外类固醇注射(TFESI)的实际效果及其长期疗效。方法:一项前瞻性、多中心、观察性队列研究纳入了保守治疗失败的根神经病患者。研究结果共有 117 名患者接受了一种或两种 TFESI 治疗。平均随访时间为 116 (±14) 周。共有19.6%(95% CI:12.9-28.0%)的患者在症状未得到充分改善后接受了手术治疗。手术的演变与病因、症状持续时间或之前的脊柱手术无关。结论真实世界的数据证实,TFESIs 是一种有效的治疗方法,约 80% 的患者在 2 年内获得了满意的疗效。
{"title":"Transforaminal epidural steroid injection for radiculopathy and the evolution to surgical treatment: a pragmatic prospective observational multicenter study.","authors":"Vincent Raymaekers, Gert Roosen, Eric Put, Steven Vanvolsem, Salah-Eddine Achahbar, Sacha Meeuws, Maarten Wissels, Sven Bamps, Dirk De Ridder, Tomas Menovsky, Mark Plazier","doi":"10.2217/pmt-2023-0121","DOIUrl":"10.2217/pmt-2023-0121","url":null,"abstract":"<p><p><b>Aim:</b> The aim of this study is to analyze the real-world outcomes of transforaminal epidural steroid injections (TFESIs) in all patients with radiculopathy and their long-term outcomes. <b>Methods:</b> Patients with radiculopathy and failure of conservative treatment were included in a prospective, multicenter, observational cohort study. <b>Results:</b> In total, 117 patients were treated with one or two TFESIs. The mean duration of follow-up was 116 (±14) weeks. In total 19,6% (95% CI: 12.9-28.0%) patients were treated with surgery after insufficient symptom improvement. The evolution to surgery was not associated with etiology, symptom duration or previous spine surgery. <b>Conclusion:</b> Real-world data confirms that TFESIs is an effective treatment with satisfactory results in about 80% of patients for a period of 2 years.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11229444/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140028673","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: 0
Artificial intelligence and pain management: cautiously optimistic. 人工智能与疼痛管理:谨慎乐观。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-09-11 DOI: 10.1080/17581869.2024.2392483
Bhargav Srinivasan, Archana Venkataraman, Srinivasa N Raja
{"title":"Artificial intelligence and pain management: cautiously optimistic.","authors":"Bhargav Srinivasan, Archana Venkataraman, Srinivasa N Raja","doi":"10.1080/17581869.2024.2392483","DOIUrl":"10.1080/17581869.2024.2392483","url":null,"abstract":"","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11485867/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142293118","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: 0
Multidevice spinal cord stimulation trials: shared decision making in the era of multiple neuromodulation paradigms. 多设备脊髓刺激试验:多种神经调节范例时代的共同决策。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-09-26 DOI: 10.1080/17581869.2024.2401767
Soun Sheen, John Markman, Michael Sohn, Anuj Bhatia, Ram Haddas, Paul Geha, Jennifer Gewandter

Aim: There is a lack of evidence-based standards for matching spinal cord stimulation (SCS) paradigm to individual patients. We aim to determine the feasibility and safety of a new alternative trial strategy, a sequential multidevice trial.Materials & methods: A retrospective analysis was performed on 116 patients who underwent SCS trials, single device or sequential multidevice (tonic and high-frequency), for chronic low back pain to assess feasibility and compare trial-to-implantation rate and explantation rate.Results: Multidevice SCS trials are feasible and safe. There was no statistically significant difference in the trial-to-implantation and explantation rates between the two groups.Conclusion: Multidevice SCS trial, prioritizing patient preference, may serve as an alternative trial strategy to improve long-term success of SCS.

目的:脊髓刺激(SCS)范例与个体患者的匹配缺乏循证标准。我们旨在确定一种新的替代试验策略--多装置顺序试验--的可行性和安全性:我们对116名因慢性腰背痛接受SCS试验的患者进行了回顾性分析,这些患者接受了单装置或顺序多装置(强直和高频)试验,以评估可行性并比较试验到植入率和切除率:多装置 SCS 试验可行且安全。结果:多器械 SCS 试验是可行和安全的,两组的植入试验率和切除率在统计学上没有明显差异:结论:多装置 SCS 试验优先考虑患者的偏好,可作为提高 SCS 长期成功率的另一种试验策略。
{"title":"Multidevice spinal cord stimulation trials: shared decision making in the era of multiple neuromodulation paradigms.","authors":"Soun Sheen, John Markman, Michael Sohn, Anuj Bhatia, Ram Haddas, Paul Geha, Jennifer Gewandter","doi":"10.1080/17581869.2024.2401767","DOIUrl":"10.1080/17581869.2024.2401767","url":null,"abstract":"<p><p><b>Aim:</b> There is a lack of evidence-based standards for matching spinal cord stimulation (SCS) paradigm to individual patients. We aim to determine the feasibility and safety of a new alternative trial strategy, a sequential multidevice trial.<b>Materials & methods:</b> A retrospective analysis was performed on 116 patients who underwent SCS trials, single device or sequential multidevice (tonic and high-frequency), for chronic low back pain to assess feasibility and compare trial-to-implantation rate and explantation rate.<b>Results:</b> Multidevice SCS trials are feasible and safe. There was no statistically significant difference in the trial-to-implantation and explantation rates between the two groups.<b>Conclusion:</b> Multidevice SCS trial, prioritizing patient preference, may serve as an alternative trial strategy to improve long-term success of SCS.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11487958/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142351884","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: 0
Dual effects of dulaglutide on glycemic control and knee osteoarthritis pain in elderly patients with Type 2 diabetes. 度拉鲁肽对老年 2 型糖尿病患者血糖控制和膝关节骨关节炎疼痛的双重影响。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-09-20 DOI: 10.1080/17581869.2024.2402214
Shambo Samrat Samajdar, Gaurab Bhaduri, Pradip Kumar Ghoshal, Shatavisa Mukherjee, Jyotirmoy Pal, Nandini Chatterjee, Shashank R Joshi

Aim: This study aims to evaluate the dual benefits of dulaglutide in improving glycemic control and reducing knee OA pain.Patients & methods: Elderly T2DM patients diagnosed with bilateral knee OA on conventional OA treatment for at least 3 months were studied for their glycemic metrics, OA pain scores and NSAID consumption at baseline, 3 months and 6 months.Results: Significant improvements in glycemic control were observed, HbA1c decreased from 8.7% to 6.5% over 6 months. Pain scores, NSAID, body weight and BMI showed substantial reductions over time. Positive correlation (r = 0.73, p < 0.001) was found between glycemic control and pain reduction.Conclusion: Dulaglutide improves glycemic control, knee joint OA pain and weight management in elderly patients with T2DM.

目的:本研究旨在评估度拉鲁肽在改善血糖控制和减轻膝关节OA疼痛方面的双重功效:研究对象: 被诊断为双侧膝关节 OA 的老年 T2DM 患者,接受常规 OA 治疗至少 3 个月,分别在基线、3 个月和 6 个月对其血糖指标、OA 疼痛评分和非甾体抗炎药消耗量进行研究:结果:血糖控制明显改善,6 个月内 HbA1c 从 8.7% 降至 6.5%。随着时间的推移,疼痛评分、非甾体抗炎药、体重和体重指数均大幅下降。正相关性(r = 0.73,p 结论:杜拉鲁肽可改善疼痛评分、非甾体抗炎药、体重和体重指数:度拉鲁肽可改善 T2DM 老年患者的血糖控制、膝关节 OA 疼痛和体重管理。
{"title":"Dual effects of dulaglutide on glycemic control and knee osteoarthritis pain in elderly patients with Type 2 diabetes.","authors":"Shambo Samrat Samajdar, Gaurab Bhaduri, Pradip Kumar Ghoshal, Shatavisa Mukherjee, Jyotirmoy Pal, Nandini Chatterjee, Shashank R Joshi","doi":"10.1080/17581869.2024.2402214","DOIUrl":"10.1080/17581869.2024.2402214","url":null,"abstract":"<p><p><b>Aim:</b> This study aims to evaluate the dual benefits of dulaglutide in improving glycemic control and reducing knee OA pain.<b>Patients & methods:</b> Elderly T2DM patients diagnosed with bilateral knee OA on conventional OA treatment for at least 3 months were studied for their glycemic metrics, OA pain scores and NSAID consumption at baseline, 3 months and 6 months.<b>Results:</b> Significant improvements in glycemic control were observed, HbA1c decreased from 8.7% to 6.5% over 6 months. Pain scores, NSAID, body weight and BMI showed substantial reductions over time. Positive correlation (r = 0.73, <i>p</i> < 0.001) was found between glycemic control and pain reduction.<b>Conclusion:</b> Dulaglutide improves glycemic control, knee joint OA pain and weight management in elderly patients with T2DM.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11485723/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142293120","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: 0
The use of naltrexone in the treatment of chronic pain: a systematic review. 纳曲酮在慢性疼痛治疗中的应用:系统综述。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-09-20 DOI: 10.1080/17581869.2024.2401769
Victor Rassi-Mariani, Eduardo Silva Reis Barreto, César Romero Antunes, Vinicius Borges Alencar, Liliane Elze Falcão Lins-Kusterer, Liana Maria Torres de Araujo Azi, Durval Campos Kraychete

This study aims to assess the efficacy of low-dose naltrexone (LDN) in treating chronic pain. We conducted a systematic review using the PICO strategy: (P) Patients with chronic pain, (I) Use of oral naltrexone, (C) Placebo or active drug and (O) Pain relief and quality of life. We included articles from PubMed, Scopus, Cochrane CENTRAL and EMBASE databases. Seven randomized clinical trials involving 406 patients were analyzed. The doses ranging from 2 to 4.5 mg once daily across all studies. Various chronic pain conditions were evaluated. The results suggest that low-dose naltrexone is not effective in managing chronic pain and improving the quality of life in patients with diverse chronic pain conditions. However, further research with larger sample sizes and standardized methodologies is necessary.

本研究旨在评估低剂量纳曲酮(LDN)治疗慢性疼痛的疗效。我们采用 PICO 策略进行了系统综述:(P)慢性疼痛患者;(I)口服纳曲酮的使用;(C)安慰剂或活性药物;(O)疼痛缓解和生活质量。我们从 PubMed、Scopus、Cochrane CENTRAL 和 EMBASE 数据库中收录了相关文章。对涉及 406 名患者的七项随机临床试验进行了分析。所有研究的剂量从 2 毫克到 4.5 毫克不等,每天一次。对各种慢性疼痛病症进行了评估。研究结果表明,小剂量纳曲酮不能有效控制慢性疼痛并改善各种慢性疼痛患者的生活质量。不过,有必要使用更大样本量和标准化方法开展进一步研究。
{"title":"The use of naltrexone in the treatment of chronic pain: a systematic review.","authors":"Victor Rassi-Mariani, Eduardo Silva Reis Barreto, César Romero Antunes, Vinicius Borges Alencar, Liliane Elze Falcão Lins-Kusterer, Liana Maria Torres de Araujo Azi, Durval Campos Kraychete","doi":"10.1080/17581869.2024.2401769","DOIUrl":"10.1080/17581869.2024.2401769","url":null,"abstract":"<p><p>This study aims to assess the efficacy of low-dose naltrexone (LDN) in treating chronic pain. We conducted a systematic review using the PICO strategy: (P) Patients with chronic pain, (I) Use of oral naltrexone, (C) Placebo or active drug and (O) Pain relief and quality of life. We included articles from PubMed, Scopus, Cochrane CENTRAL and EMBASE databases. Seven randomized clinical trials involving 406 patients were analyzed. The doses ranging from 2 to 4.5 mg once daily across all studies. Various chronic pain conditions were evaluated. The results suggest that low-dose naltrexone is not effective in managing chronic pain and improving the quality of life in patients with diverse chronic pain conditions. However, further research with larger sample sizes and standardized methodologies is necessary.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11487945/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142293122","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: 0
Hip and waist circumference correlations with demographic factors and pain intensity in patients with chronic pain. 慢性疼痛患者的臀围和腰围与人口统计学因素和疼痛强度的相关性。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-10-03 DOI: 10.1080/17581869.2024.2403961
Frank A Trujillo, Hannah A Thomas, Deepak Berwal, Nikhil Rajulapati, Marisa DiMarzio, Julie G Pilitsis

Aim: This study aimed to investigate how demographic factors such as race, age, sex and ethnicity can impact hip circumference (HC) and waist circumference (WC) in patients with chronic pain.Materials & methods: We queried the NIH-sponsored All of Us database for patients with documented HC, WC and waist/hip ratio (WHR) data. This cross-sectional study categorized participants into four groups: total cohort, no chronic pain, mild/moderate chronic pain (numeric rating scale < 7) and severe chronic pain (numeric rating scale > 7). Further subgroup analyses were performed based on race, age, sex and ethnicity. We examined the correlation between chronic pain and WC, HC and WHR. ANCOVA analysis was used to determine to investigate demographics.Results: This study included 204,013 participants, with 25.22% having a chronic pain diagnoses. In most subgroups, females had significantly greater HC, while males had greater WC and WHR. WC (p < 0.001 in females, p < 0.01 in males), HC (p < 0.001 in females) and WHR (p < 0.001 in females, p < 0.05 in males) were significantly greater in the severe pain group compared with the mild/moderate pain group.Conclusion: These findings suggest that when assessing HC and WC, demographic variables need to be considered to develop more personalized and comprehensive treatment plans for chronic pain patients.

目的:本研究旨在调查种族、年龄、性别和民族等人口统计学因素如何影响慢性疼痛患者的臀围(HC)和腰围(WC):我们查询了美国国立卫生研究院赞助的 "我们所有人 "数据库,以获得有记录的患者臀围、腰围和腰臀比(WHR)数据。这项横断面研究将参与者分为四组:总人群、无慢性疼痛、轻度/中度慢性疼痛(数字评分量表 < 7)和重度慢性疼痛(数字评分量表 > 7)。此外,还根据种族、年龄、性别和民族进行了分组分析。我们研究了慢性疼痛与体重指数(WC)、血压指数(HC)和体重指数(WHR)之间的相关性。方差分析用于确定调查人口统计学:这项研究包括 204 013 名参与者,其中 25.22% 的人被诊断为慢性疼痛。在大多数亚组中,女性的 HC 明显高于男性,而男性的 WC 和 WHR 则高于女性。WC (p p p p p 结论:这些研究结果表明,在评估HC和WC时,需要考虑人口统计学变量,以便为慢性疼痛患者制定更加个性化和全面的治疗方案。
{"title":"Hip and waist circumference correlations with demographic factors and pain intensity in patients with chronic pain.","authors":"Frank A Trujillo, Hannah A Thomas, Deepak Berwal, Nikhil Rajulapati, Marisa DiMarzio, Julie G Pilitsis","doi":"10.1080/17581869.2024.2403961","DOIUrl":"10.1080/17581869.2024.2403961","url":null,"abstract":"<p><p><b>Aim:</b> This study aimed to investigate how demographic factors such as race, age, sex and ethnicity can impact hip circumference (HC) and waist circumference (WC) in patients with chronic pain.<b>Materials & methods:</b> We queried the NIH-sponsored All of Us database for patients with documented HC, WC and waist/hip ratio (WHR) data. This cross-sectional study categorized participants into four groups: total cohort, no chronic pain, mild/moderate chronic pain (numeric rating scale < 7) and severe chronic pain (numeric rating scale > 7). Further subgroup analyses were performed based on race, age, sex and ethnicity. We examined the correlation between chronic pain and WC, HC and WHR. ANCOVA analysis was used to determine to investigate demographics.<b>Results:</b> This study included 204,013 participants, with 25.22% having a chronic pain diagnoses. In most subgroups, females had significantly greater HC, while males had greater WC and WHR. WC (<i>p</i> < 0.001 in females, <i>p</i> < 0.01 in males), HC (<i>p</i> < 0.001 in females) and WHR (<i>p</i> < 0.001 in females, <i>p</i> < 0.05 in males) were significantly greater in the severe pain group compared with the mild/moderate pain group.<b>Conclusion:</b> These findings suggest that when assessing HC and WC, demographic variables need to be considered to develop more personalized and comprehensive treatment plans for chronic pain patients.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11487955/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142372520","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: 0
Perioperative N-acetylcysteine: evidence and indications. 围手术期 N-乙酰半胱氨酸:证据和适应症。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-08-21 DOI: 10.1080/17581869.2024.2388504
Phillip Ryan Wilson, Kathryn H Bridges, Michael Scofield, Sylvia H Wilson

Nonopioid analgesics serve to improve analgesia and limit side effects and risks of perioperative opioids. N-acetylcysteine (NAC), the primary treatment of acetaminophen toxicity, may have perioperative indications, including analgesia. NAC impacts glutathione synthesis, oxidant scavenging, glutamate receptor modulation and neuroinflammation. Potential perioperative benefits include arrhythmia prevention after cardiac surgery, decreased contrast-induced nephropathy, improved post-transplant liver function and superior pulmonary outcomes with general anesthesia. NAC may improve perioperative analgesia, with some studies displaying a reduction in postoperative opioid use. NAC is generally well tolerated with an established safety profile. NAC administration may predispose to gastrointestinal effects, while parenteral administration may carry a risk of anaphylactoid reactions, including bronchospasm. Larger randomized trials may clarify the impact of NAC on perioperative analgesic outcomes.

非阿片类镇痛药可改善镇痛效果,限制围手术期阿片类药物的副作用和风险。N-乙酰半胱氨酸(NAC)是治疗对乙酰氨基酚毒性的主要药物,也可用于围手术期,包括镇痛。NAC 可影响谷胱甘肽的合成、氧化剂清除、谷氨酸受体调节和神经炎症。围手术期的潜在益处包括预防心脏手术后的心律失常、减少造影剂诱发的肾病、改善移植后的肝功能以及在全身麻醉时获得更好的肺部效果。NAC 可改善围术期镇痛,一些研究显示可减少术后阿片类药物的使用。NAC 一般具有良好的耐受性和公认的安全性。NAC 给药可能会引起胃肠道反应,而肠道外给药可能会有过敏反应的风险,包括支气管痉挛。更大规模的随机试验可能会明确 NAC 对围术期镇痛效果的影响。
{"title":"Perioperative N-acetylcysteine: evidence and indications.","authors":"Phillip Ryan Wilson, Kathryn H Bridges, Michael Scofield, Sylvia H Wilson","doi":"10.1080/17581869.2024.2388504","DOIUrl":"10.1080/17581869.2024.2388504","url":null,"abstract":"<p><p>Nonopioid analgesics serve to improve analgesia and limit side effects and risks of perioperative opioids. N-acetylcysteine (NAC), the primary treatment of acetaminophen toxicity, may have perioperative indications, including analgesia. NAC impacts glutathione synthesis, oxidant scavenging, glutamate receptor modulation and neuroinflammation. Potential perioperative benefits include arrhythmia prevention after cardiac surgery, decreased contrast-induced nephropathy, improved post-transplant liver function and superior pulmonary outcomes with general anesthesia. NAC may improve perioperative analgesia, with some studies displaying a reduction in postoperative opioid use. NAC is generally well tolerated with an established safety profile. NAC administration may predispose to gastrointestinal effects, while parenteral administration may carry a risk of anaphylactoid reactions, including bronchospasm. Larger randomized trials may clarify the impact of NAC on perioperative analgesic outcomes.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11486111/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142018281","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: 0
A population-based survey of Americans with frequent migraine and acute medication use: A plain language summary. 对经常偏头痛和急性用药的美国人进行的人群调查:通俗易懂的摘要。
IF 1.4 Q4 CLINICAL NEUROLOGY Pub Date : 2024-01-01 Epub Date: 2024-09-18 DOI: 10.1080/17581869.2024.2392466
Amaal J Starling, Roger Cady, Dawn C Buse, Meghan Buzby, Kevin Lenaburg

What is this summary about?: The Harris Poll Migraine Report Card was a survey about people's experiences and challenges with headaches and migraine. The survey was conducted from December 9, 2021, to January 10, 2022, in the United States. The people who took the survey had frequent headaches/migraine attacks (on 8 or more days per month) and used acute headache/migraine medication to relieve head pain and other symptoms (on 10 or more days per month). This summary focuses on the responses of adults with frequent headaches and frequent acute medication use at the time of the survey or within the few months (not specified) before the survey (and not those who previously had frequent headaches and frequent acute medication use at some point in their life prior to the survey). The group of people who took the survey will be called 'respondents'. The term 'headaches' can mean any type of headache including as part of a migraine attack, a tension type headache, or another unknown headache type. All respondents screened positive for having migraine, so many of the headaches they reported on may have been a migraine headache or part of a migraine attack.

What were the results?: Over 50% of respondents said their headaches affected their overall quality of life. Many respondents wished their healthcare provider who was managing their headaches understood more about how headaches affect their mental well-being, how much pain their headaches cause, and why they get headaches. 80% of respondents had concerns about their overall health. Over 60% of respondents said they have experienced anxiety and/or depression. In this survey, although all respondents were eligible to receive a preventive headache/migraine medication because of their headache frequency, only 15% were taking one.

What do the results of the survey mean?: The findings from this survey showed many ways that headaches/migraine care can improve, including talking about mental and emotional well-being, making sure the treatment plan works and does not have side effects that cannot be tolerated, and trying to prevent headaches/migraine from occurring.

本摘要是关于什么的? Harris Poll偏头痛报告卡是一项关于人们在头痛和偏头痛方面的经历和挑战的调查。调查于 2021 年 12 月 9 日至 2022 年 1 月 10 日在美国进行。参加调查的人经常头痛/偏头痛发作(每月发作 8 天或以上),并使用急性头痛/偏头痛药物缓解头部疼痛和其他症状(每月发作 10 天或以上)。本摘要主要针对在接受调查时或调查前几个月内(未具体说明)经常头痛和经常使用急性药物的成年人(而不是那些在接受调查前的某个时期经常头痛和经常使用急性药物的成年人)。参与调查的人群将被称为 "受访者"。头痛 "一词可以指任何类型的头痛,包括偏头痛发作、紧张型头痛或其他未知类型的头痛。所有受访者的偏头痛筛查结果均为阳性,因此他们报告的许多头痛可能是偏头痛或偏头痛发作的一部分:50%以上的受访者表示,头痛影响了他们的整体生活质量。许多受访者希望管理他们头痛的医疗服务提供者能更多地了解头痛如何影响他们的精神健康、头痛造成的疼痛程度以及他们为什么会头痛。80% 的受访者对自己的整体健康感到担忧。超过 60% 的受访者表示他们曾经历过焦虑和/或抑郁。在这次调查中,尽管所有受访者都有资格因头痛频率而接受预防性头痛/偏头痛药物治疗,但只有15%的人在服用这种药物。 调查结果有何意义? 调查结果显示,头痛/偏头痛护理有许多可以改进的方法,包括谈论心理和情绪健康、确保治疗方案有效且不会产生无法忍受的副作用,以及努力预防头痛/偏头痛的发生。
{"title":"A population-based survey of Americans with frequent migraine and acute medication use: A plain language summary.","authors":"Amaal J Starling, Roger Cady, Dawn C Buse, Meghan Buzby, Kevin Lenaburg","doi":"10.1080/17581869.2024.2392466","DOIUrl":"10.1080/17581869.2024.2392466","url":null,"abstract":"<p><strong>What is this summary about?: </strong>The Harris Poll Migraine Report Card was a survey about people's experiences and challenges with headaches and migraine. The survey was conducted from December 9, 2021, to January 10, 2022, in the United States. The people who took the survey had frequent headaches/migraine attacks (on 8 or more days per month) and used acute headache/migraine medication to relieve head pain and other symptoms (on 10 or more days per month). This summary focuses on the responses of adults with frequent headaches and frequent acute medication use at the time of the survey or within the few months (not specified) before the survey (and not those who previously had frequent headaches and frequent acute medication use at some point in their life prior to the survey). The group of people who took the survey will be called 'respondents'. The term 'headaches' can mean any type of headache including as part of a migraine attack, a tension type headache, or another unknown headache type. All respondents screened positive for having migraine, so many of the headaches they reported on may have been a migraine headache or part of a migraine attack.</p><p><strong>What were the results?: </strong>Over 50% of respondents said their headaches affected their overall quality of life. Many respondents wished their healthcare provider who was managing their headaches understood more about how headaches affect their mental well-being, how much pain their headaches cause, and why they get headaches. 80% of respondents had concerns about their overall health. Over 60% of respondents said they have experienced anxiety and/or depression. In this survey, although all respondents were eligible to receive a preventive headache/migraine medication because of their headache frequency, only 15% were taking one.</p><p><strong>What do the results of the survey mean?: </strong>The findings from this survey showed many ways that headaches/migraine care can improve, including talking about mental and emotional well-being, making sure the treatment plan works and does not have side effects that cannot be tolerated, and trying to prevent headaches/migraine from occurring.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.4,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11495521/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142293117","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: 0
IonicRF™: a novel step in technology for radiofrequency ablation treatments. IonicRF™:射频消融治疗技术的新进展。
IF 1.7 Q2 Medicine Pub Date : 2024-01-01 Epub Date: 2022-01-10 DOI: 10.2217/pmt-2021-0068
Harjot S Bhandal, Chau Vu, Jason E Pope

Radiofrequency ablation (RFA) has been utilized since the 1970s to treat various painful conditions. The technology has evolved from its initial use to treat lumbar facet mediated pain with monopolar lesioning to now treat a plethora of chronic pain conditions. This article reviews Abbott Corporation's (IL, USA) IonicRF™ generator. The IonicRF generator utilizes an intelligent power algorithm that improves efficiency and reduces procedure time. The generator also carries a wide range of RFA therapies such as monopolar, bipolar, pulsed or pulsed dose radiofrequency. Additionally, the IonicRF RFA generator is compatible with the Simplicity™ RF probe (Abbott) which allows for efficient and effective denervation of the sacroiliac joint.

射频消融术(RFA)自 20 世纪 70 年代以来一直被用于治疗各种疼痛病症。该技术从最初用于治疗腰椎面神经介导的单极病变疼痛,发展到现在可以治疗多种慢性疼痛病症。本文回顾了雅培公司(美国伊利诺伊州)的 IonicRF™ 发生器。IonicRF 发生器采用智能功率算法,可提高效率并缩短手术时间。该发生器还可进行单极、双极、脉冲或脉冲剂量射频等多种射频消融治疗。此外,IonicRF 射频发生器与 Simplicity™ 射频探头(雅培)兼容,可对骶髂关节进行高效、有效的去神经支配。
{"title":"IonicRF™: a novel step in technology for radiofrequency ablation treatments.","authors":"Harjot S Bhandal, Chau Vu, Jason E Pope","doi":"10.2217/pmt-2021-0068","DOIUrl":"10.2217/pmt-2021-0068","url":null,"abstract":"<p><p>Radiofrequency ablation (RFA) has been utilized since the 1970s to treat various painful conditions. The technology has evolved from its initial use to treat lumbar facet mediated pain with monopolar lesioning to now treat a plethora of chronic pain conditions. This article reviews Abbott Corporation's (IL, USA) IonicRF™ generator. The IonicRF generator utilizes an intelligent power algorithm that improves efficiency and reduces procedure time. The generator also carries a wide range of RFA therapies such as monopolar, bipolar, pulsed or pulsed dose radiofrequency. Additionally, the IonicRF RFA generator is compatible with the Simplicity™ RF probe (Abbott) which allows for efficient and effective denervation of the sacroiliac joint.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"39676018","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
Treatment characteristics of chronic low back pain patients treated with buprenorphine buccal film or transdermal patch. 使用丁丙诺啡口腔胶片或透皮贴剂治疗慢性腰背痛患者的治疗特点。
IF 1.7 Q2 Medicine Pub Date : 2024-01-01 Epub Date: 2024-01-18 DOI: 10.2217/pmt-2023-0124
Filip Stanicic, Dimitrije Grbic, Djurdja Vukicevic, Vladimir Zah

Aims: Retrospective insurance claims analysis exploring treatment characteristics in chronic low back pain patients prescribed buprenorphine buccal film (Belbuca®) or transdermal patches. Patients and methods: The first buprenorphine prescription (buccal film or transdermal patch) was an index event. Patients were observed over 6 month pre- and post-index periods. Propensity score matching minimized the selection bias. Results: Buccal film patients had a higher buprenorphine daily dose (501.7 vs 270.9 µg; p < 0.001). The patch-to-film switching rate was higher than vice versa (11.5 vs 3.8%; p < 0.001). The buccal film showed a greater reduction in opioid prescriptions (-1.1 vs -0.7; p = 0.012), daily morphine milligram equivalents (-12.6 vs -7.3; p < 0.001) and opioid treatment duration (-13.4 vs -7.6 days; p = 0.022). Conclusion: Buccal film was associated with higher buprenorphine doses and a greater reduction of opioid burden.

目的:回顾性保险理赔分析,探讨慢性腰背痛患者接受丁丙诺啡口腔胶片(Belbuca®)或透皮贴剂治疗的特点。患者和方法:首次开具丁丙诺啡处方(丁丙诺啡口腔胶片或透皮贴剂)为指标事件。对患者进行为期 6 个月的指标前和指标后观察。倾向评分匹配将选择偏差降至最低。结果颊黏膜患者的丁丙诺啡日剂量更高(501.7 微克对 270.9 微克;P丁丙诺啡口腔胶片与更高的丁丙诺啡剂量和更大程度地减轻阿片类药物负担有关。
{"title":"Treatment characteristics of chronic low back pain patients treated with buprenorphine buccal film or transdermal patch.","authors":"Filip Stanicic, Dimitrije Grbic, Djurdja Vukicevic, Vladimir Zah","doi":"10.2217/pmt-2023-0124","DOIUrl":"10.2217/pmt-2023-0124","url":null,"abstract":"<p><p><b>Aims:</b> Retrospective insurance claims analysis exploring treatment characteristics in chronic low back pain patients prescribed buprenorphine buccal film (Belbuca<sup>®</sup>) or transdermal patches. <b>Patients and methods:</b> The first buprenorphine prescription (buccal film or transdermal patch) was an index event. Patients were observed over 6 month pre- and post-index periods. Propensity score matching minimized the selection bias. <b>Results:</b> Buccal film patients had a higher buprenorphine daily dose (501.7 vs 270.9 µg; p < 0.001). The patch-to-film switching rate was higher than vice versa (11.5 vs 3.8%; p < 0.001). The buccal film showed a greater reduction in opioid prescriptions (-1.1 vs -0.7; p = 0.012), daily morphine milligram equivalents (-12.6 vs -7.3; p < 0.001) and opioid treatment duration (-13.4 vs -7.6 days; p = 0.022). <b>Conclusion:</b> Buccal film was associated with higher buprenorphine doses and a greater reduction of opioid burden.</p>","PeriodicalId":20000,"journal":{"name":"Pain management","volume":null,"pages":null},"PeriodicalIF":1.7,"publicationDate":"2024-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"139485647","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
期刊
Pain management
全部 Acc. Chem. Res. ACS Applied Bio Materials ACS Appl. Electron. Mater. ACS Appl. Energy Mater. ACS Appl. Mater. Interfaces ACS Appl. Nano Mater. ACS Appl. Polym. Mater. ACS BIOMATER-SCI ENG ACS Catal. ACS Cent. Sci. ACS Chem. Biol. ACS Chemical Health & Safety ACS Chem. Neurosci. ACS Comb. Sci. ACS Earth Space Chem. ACS Energy Lett. ACS Infect. Dis. ACS Macro Lett. ACS Mater. Lett. ACS Med. Chem. Lett. ACS Nano ACS Omega ACS Photonics ACS Sens. ACS Sustainable Chem. Eng. ACS Synth. Biol. Anal. Chem. BIOCHEMISTRY-US Bioconjugate Chem. BIOMACROMOLECULES Chem. Res. Toxicol. Chem. Rev. Chem. Mater. CRYST GROWTH DES ENERG FUEL Environ. Sci. Technol. Environ. Sci. Technol. Lett. Eur. J. Inorg. Chem. IND ENG CHEM RES Inorg. Chem. J. Agric. Food. Chem. J. Chem. Eng. Data J. Chem. Educ. J. Chem. Inf. Model. J. Chem. Theory Comput. J. Med. Chem. J. Nat. Prod. J PROTEOME RES J. Am. Chem. Soc. LANGMUIR MACROMOLECULES Mol. Pharmaceutics Nano Lett. Org. Lett. ORG PROCESS RES DEV ORGANOMETALLICS J. Org. Chem. J. Phys. Chem. J. Phys. Chem. A J. Phys. Chem. B J. Phys. Chem. C J. Phys. Chem. Lett. Analyst Anal. Methods Biomater. Sci. Catal. Sci. Technol. Chem. Commun. Chem. Soc. Rev. CHEM EDUC RES PRACT CRYSTENGCOMM Dalton Trans. Energy Environ. Sci. ENVIRON SCI-NANO ENVIRON SCI-PROC IMP ENVIRON SCI-WAT RES Faraday Discuss. Food Funct. Green Chem. Inorg. Chem. Front. Integr. Biol. J. Anal. At. Spectrom. J. Mater. Chem. A J. Mater. Chem. B J. Mater. Chem. C Lab Chip Mater. Chem. Front. Mater. Horiz. MEDCHEMCOMM Metallomics Mol. Biosyst. Mol. Syst. Des. Eng. Nanoscale Nanoscale Horiz. Nat. Prod. Rep. New J. Chem. Org. Biomol. Chem. Org. Chem. Front. PHOTOCH PHOTOBIO SCI PCCP Polym. Chem.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
0
微信
客服QQ
Book学术公众号 扫码关注我们
反馈
×
意见反馈
请填写您的意见或建议
请填写您的手机或邮箱
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
现在去查看 取消
×
提示
确定
Book学术官方微信
Book学术文献互助
Book学术文献互助群
群 号:481959085
Book学术
文献互助 智能选刊 最新文献 互助须知 联系我们:info@booksci.cn
Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。
Copyright © 2023 Book学术 All rights reserved.
ghs 京公网安备 11010802042870号 京ICP备2023020795号-1