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Motivations behind complementary and alternative medicine use in patients with Crohn's disease and ulcerative colitis. 克罗恩病和溃疡性结肠炎患者使用补充和替代药物的动机。
Pub Date : 2024-07-31 eCollection Date: 2024-10-01 DOI: 10.1093/jcag/gwae020
Natasha Klemm, Roberto Trasolini, Brian Bressler, Gregory Rosenfeld, Gina Almasan, Yvette Leung

Background: Complementary and alternative medicine (CAM) use is common in inflammatory bowel disease (IBD) patients and impacts compliance with conventional treatment. Gastroenterologists should understand the motivational factors of CAM use-factors that push patients away from standard therapy or pull towards CAM. Our study describes the motivations behind CAM use for IBD and evaluates differences between Crohn's disease (CD) and ulcerative colitis (UC) patients.

Methods: Retrospective cohort survey of patients over 18 years old with IBD, evaluated by gastroenterologists at a tertiary care referral centre from January 1 to December 31, 2019. Only patients who reported CAM use were included. Chi-square and independent t-tests were performed and P-value <0.05 was significant.

Results: Of the 230 completed surveys, 193 reported CAM use (CD: 57.5% vs UC: 42.5%). Demographics, disease duration, and hospitalizations were similar, but CD patients had lower SIBDQ scores (CD: 48.1 vs UC: 53.5, P < 0.001). Both groups were largely influenced by their social network to use CAM (CD: 33% vs UC: 31.3%) and did not feel well informed about CAM (87.4%). CD and UC patients had similar push and pull factors. Push factors included lack of improvement (39%) and side effects (20%) with conventional treatment. Pull factors included the desire for a holistic approach (21%) and to improve mood (35%). UC patients wanted a natural approach to treat their IBD, which nearly reached significance (P = 0.049). Most patients hoped fatigue 62.7%, and diarrhoea 61.7% would improve with CAM, but more CD patients wanted to improve their appetite (P = 0.043).

Conclusion: Despite differences in QoL, push and pull motivations for CAM use did not differ between CD and UC patients. Most users do not feel well informed of CAM and ongoing dialogue is important for patient-centred care.

背景:在炎症性肠病(IBD)患者中,使用补充和替代医学(CAM)很常见,而且会影响患者对常规治疗的依从性。肠胃病学家应该了解使用 CAM 的动机因素,即促使患者放弃标准疗法或转向 CAM 的因素。我们的研究描述了使用 CAM 治疗 IBD 的动机,并评估了克罗恩病(CD)和溃疡性结肠炎(UC)患者之间的差异:对18岁以上的IBD患者进行回顾性队列调查,由一家三级医疗转诊中心的消化科医生在2019年1月1日至12月31日期间进行评估。仅纳入报告使用 CAM 的患者。进行了卡方检验和独立 t 检验,并得出了 P 值:在完成的 230 份调查问卷中,有 193 份报告了 CAM 的使用情况(CD:57.5% vs UC:42.5%)。人口统计学、病程和住院情况相似,但 CD 患者的 SIBDQ 分数较低(CD:48.1 vs UC:53.5,P <0.001)。两组患者在很大程度上都受其社交网络的影响而使用 CAM(CD:33% vs UC:31.3%),并且都不太了解 CAM(87.4%)。CD 和 UC 患者的推拉因素相似。推动因素包括传统治疗效果不佳(39%)和副作用(20%)。拉动因素包括希望采用整体方法(21%)和改善情绪(35%)。UC 患者希望采用自然方法治疗他们的 IBD,这一点几乎达到了显著性水平(P = 0.049)。大多数患者希望通过 CAM 改善疲劳(62.7%)和腹泻(61.7%),但更多的 CD 患者希望改善食欲(P = 0.043):尽管 QoL 存在差异,但 CD 和 UC 患者使用 CAM 的推拉动机并无不同。大多数使用者并不了解 CAM,而持续的对话对于以患者为中心的护理非常重要。
{"title":"Motivations behind complementary and alternative medicine use in patients with Crohn's disease and ulcerative colitis.","authors":"Natasha Klemm, Roberto Trasolini, Brian Bressler, Gregory Rosenfeld, Gina Almasan, Yvette Leung","doi":"10.1093/jcag/gwae020","DOIUrl":"https://doi.org/10.1093/jcag/gwae020","url":null,"abstract":"<p><strong>Background: </strong>Complementary and alternative medicine (CAM) use is common in inflammatory bowel disease (IBD) patients and impacts compliance with conventional treatment. Gastroenterologists should understand the motivational factors of CAM use-factors that <i>push</i> patients away from standard therapy or <i>pull</i> towards CAM. Our study describes the motivations behind CAM use for IBD and evaluates differences between Crohn's disease (CD) and ulcerative colitis (UC) patients.</p><p><strong>Methods: </strong>Retrospective cohort survey of patients over 18 years old with IBD, evaluated by gastroenterologists at a tertiary care referral centre from January 1 to December 31, 2019. Only patients who reported CAM use were included. Chi-square and independent <i>t</i>-tests were performed and <i>P</i>-value <0.05 was significant.</p><p><strong>Results: </strong>Of the 230 completed surveys, 193 reported CAM use (CD: 57.5% vs UC: 42.5%). Demographics, disease duration, and hospitalizations were similar, but CD patients had lower SIBDQ scores (CD: 48.1 vs UC: 53.5, <i>P</i> < 0.001). Both groups were largely influenced by their social network to use CAM (CD: 33% vs UC: 31.3%) and did not feel well informed about CAM (87.4%). CD and UC patients had similar push and pull factors. Push factors included lack of improvement (39%) and side effects (20%) with conventional treatment. Pull factors included the desire for a holistic approach (21%) and to improve mood (35%). UC patients wanted a natural approach to treat their IBD, which nearly reached significance (<i>P</i> = 0.049). Most patients hoped fatigue 62.7%, and diarrhoea 61.7% would improve with CAM, but more CD patients wanted to improve their appetite (<i>P</i> = 0.043).</p><p><strong>Conclusion: </strong>Despite differences in QoL, push and pull motivations for CAM use did not differ between CD and UC patients. Most users do not feel well informed of CAM and ongoing dialogue is important for patient-centred care.</p>","PeriodicalId":17263,"journal":{"name":"Journal of the Canadian Association of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-07-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11477972/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142468653","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
Correction to: Quality of life, clinical outcomes and cost utilization of endoscopic therapy in patients with Barrett's esophagus and early esophageal cancer-an 8-year Canadian experience. 更正为巴雷特食管和早期食管癌患者的生活质量、临床疗效和内窥镜疗法的成本使用--8 年加拿大经验。
Pub Date : 2024-07-30 eCollection Date: 2024-10-01 DOI: 10.1093/jcag/gwae026

[This corrects the article DOI: 10.1093/jcag/gwae018.].

[This corrects the article DOI: 10.1093/jcag/gwae018.].
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引用次数: 0
An incidental choledochoduodenal fistula discovered during gastroscopy 胃镜检查中意外发现的胆总管十二指肠瘘
Pub Date : 2024-07-25 DOI: 10.1093/jcag/gwae023
Andrea M Kulyk, Justin Flood, Jennifer Jin
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引用次数: 0
The usefulness of head computed tomography in patients with known cirrhosis presenting to emergency department with suspected hepatic encephalopathy. 头部计算机断层扫描对急诊科疑似肝性脑病的已知肝硬化患者的作用。
Pub Date : 2024-07-10 eCollection Date: 2024-10-01 DOI: 10.1093/jcag/gwae022
David Yi Yang, Joel Bowron, Mohammed Ahmed, Juan G Abraldes, Sander Veldhuyzen van Zanten

Background: Computed tomography of the head (CT head) is frequently used for patients with cirrhosis presenting with suspected hepatic encephalopathy (HE).

Aims: The primary aims of this study were to assess the frequency of CT head usage in this patient population and to determine whether these scans yielded significant findings. Our secondary aims were to identify factors associated with the decision to order CTs and whether patients who received CTs had different outcomes.

Methods: A single-centre, retrospective chart review was performed. Patients presenting to the University of Alberta Hospital with cirrhosis and common liver disease aetiologies over a 27-month period were identified via discharge diagnosis codes. Charts of patients with suspected HE were manually identified. The use of a CT head was documented, as were patient demographics, cirrhosis aetiology, MELD, and outcomes. Comparisons were made between patients with and without CT head.

Results: A total of 119 encounters from 100 patients met our inclusion criteria. In 57% of encounters, a CT scan was performed on presentation. None of these CT scans had significant findings. Patient factors associated with the decision to order CT included older age, more preserved liver function, and longer length of time between patient's current and previous presentations. Patients who did not receive CT head had higher in-hospital mortality, which was likely reflective of more severe underlying liver dysfunction in this group.

Conclusions: The frequency of CT head usage in the studied patient population was high while the yield was low. This calls into question the usefulness of CT head in this population.

背景:头部计算机断层扫描(CT头部计算机断层扫描(CT)常用于疑似肝性脑病(HE)的肝硬化患者。我们的次要目的是确定与下达 CT 命令的决定相关的因素,以及接受 CT 检查的患者是否会有不同的结果:我们进行了一项单中心回顾性病历审查。通过出院诊断代码确定了在 27 个月内到阿尔伯塔大学医院就诊的肝硬化和常见肝病患者。对疑似 HE 患者的病历进行人工识别。记录了头部 CT 的使用情况、患者人口统计学特征、肝硬化病因、MELD 和结果。对使用和未使用 CT 头颅的患者进行了比较:共有 100 名患者的 119 次就诊符合我们的纳入标准。57%的患者在就诊时进行了 CT 扫描。这些 CT 扫描均无重大发现。与决定进行 CT 检查相关的患者因素包括年龄较大、肝功能较好以及患者本次就诊与前次就诊间隔时间较长。未接受头部CT检查的患者院内死亡率较高,这可能反映出这组患者潜在的肝功能异常更为严重:结论:在所研究的患者群体中,头部 CT 的使用频率很高,而收益率却很低。结论:在所研究的患者群体中,头部 CT 的使用频率很高,而收益率却很低,这让人怀疑头部 CT 在这一人群中的实用性。
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引用次数: 0
Quality of life, clinical outcomes and cost utilization of endoscopic therapy in patients with Barrett's esophagus and early esophageal cancer-an 8-year Canadian experience. 巴雷特食管和早期食管癌患者的生活质量、临床疗效和内窥镜疗法的成本使用--8 年加拿大经验。
Pub Date : 2024-06-26 eCollection Date: 2024-10-01 DOI: 10.1093/jcag/gwae018
Joel David, Matthew Woo, Stephen Congly, Christopher N Andrews, Thurarshen Jeyalingam, Paul J Belletrutti, Milli Gupta

Background and aims: Endoscopic treatment is a definitive and cost-effective management strategy for early neoplasia in Barrett's oesophagus (BE). However, little is known of its impact on quality of life (QoL). This study reports outcomes of endoscopic eradication treatment (EET), focusing on QoL and costs in a Canadian tertiary referral centre.

Methods: A retrospective cohort study using a prospectively maintained clinical database captured validated QoL metrics during and at the end of EET, risk factors for BE, treatment response, complications, costs, and follow-up response of all treated Barrett patients in Calgary and Southern Alberta, Canada.

Results: A total of 147 BE patients were treated from 2013 to 2021. All patients showed significant improvement in almost all QoL parameters except depression. There was significant improvement in 7 of the 8 QoL metrics in those who achieved complete eradication of intestinal metaplasia (CEIM). EET was successful in achieving complete eradication of dysplasia (CED) and CEIM in 93.4% and 74.3% of patients, respectively, with a median of 3 radio frequency ablation treatments. Longer circumferential segments of BE (Cx) predicted a lower likelihood of achieving CEIM. The average total cost to achieve CED and CEIM were $10 414.58 and $9347.93CAD, respectively (compared to oesophagectomy estimated at $58 332.30 CAD).

Conclusion: This Canadian cohort reports significant post-treatment improvement in QoL parameters in patients treated to CEIM or CED over an 8-year period. EET for BE eradication is cost-effective compared to oesophagectomy. There was a low rate of complications and recurrence post-CEIM.

背景和目的:内镜治疗是治疗巴雷特食管(BE)早期肿瘤的一种确切且经济有效的方法。然而,人们对其对生活质量(QoL)的影响知之甚少。本研究报告了加拿大一家三级转诊中心的内镜根除治疗(EET)结果,重点关注QoL和成本:一项回顾性队列研究使用了一个前瞻性维护的临床数据库,该数据库收集了加拿大卡尔加里和南阿尔伯塔省所有接受治疗的巴雷特患者在 EET 治疗期间和结束时的有效 QoL 指标、BE 的风险因素、治疗反应、并发症、费用和随访反应:2013年至2021年期间,共有147名BE患者接受了治疗。除抑郁外,所有患者的几乎所有生活质量参数都有明显改善。在 8 项 QoL 指标中,有 7 项指标在完全根除肠化生(CEIM)后有明显改善。射频消融治疗成功实现完全根除发育不良(CED)和CEIM的患者比例分别为93.4%和74.3%,中位数为3次射频消融治疗。较长的BE(Cx)圆周段预示着实现CEIM的可能性较低。实现CED和CEIM的平均总费用分别为10 414.58加元和9347.93加元(相比之下,食管切除术的费用估计为58 332.30加元):该加拿大队列报告显示,在 8 年的时间里,接受 CEIM 或 CED 治疗的患者在治疗后的生活质量参数方面有了明显改善。与食道切除术相比,EET根除BE具有成本效益。CEIM术后并发症和复发率较低。
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引用次数: 0
Outcomes of patients admitted with acute, severe ulcerative colitis on biologic therapy: a retrospective analysis from a tertiary referral hospital. 急性重度溃疡性结肠炎患者接受生物疗法的疗效:一家三级转诊医院的回顾性分析。
Pub Date : 2024-05-31 eCollection Date: 2024-08-01 DOI: 10.1093/jcag/gwae017
Nasruddin Sabrie, Manisha Jogendran, Rohit Jogendran, Laura E Targownik

Background: In steroid-refractory acute, severe, ulcerative colitis (ASUC), salvage medical therapy with infliximab is recommended to reduce the risk of colectomy. However, the evidence supporting this practice is based on cohorts naïve to biologics. Consequently, the management of patients on biologic or small molecule therapy (BST) with ASUC is not well defined.

Methods: We conducted a retrospective chart review of patients admitted with ASUC to Mount Sinai Hospital (MSH) in Toronto, Ontario from January 2018 until January 2022. Included subjects were considered to be on BST if they had received a dose of these agents within 56 days prior to admission. Our outcomes of interest included the mean difference in hospital length of stay (HLOS), rates of surgical consultation, rates of inpatient colectomies, and 90-day readmission rates between the 2 groups.

Results: Of the 185 admissions for ASUC, 76 were on BST prior to admission and 109 were not. Baseline characteristics were similar between the 2 groups. There were no significant differences in hospital length of stay (7.46 days vs 7.45 days P = .52) or in-hospital colectomy rates between the 2 groups. Patients on BST had higher rates of surgical consultation (36.8% vs 8.3% P < .01) and 90-day readmission rates (26.3% vs 13.8% P = .03).

Conclusions: We did not identify significant differences in the majority of our outcomes between the 2 groups. However, patients on BST were more likely to receive a surgical consultation during their admission and had higher rates of readmission at 90 days. Further studies evaluating the underlying factors that contribute to readmission in patients on BST in hospitals are needed.

背景:对于类固醇难治性急性重度溃疡性结肠炎(ASUC),建议使用英夫利西单抗进行挽救性治疗,以降低结肠切除术的风险。然而,支持这种做法的证据是基于对生物制剂不了解的人群。因此,对接受生物制剂或小分子疗法(BST)的 ASUC 患者的管理尚无明确定义:我们对安大略省多伦多西奈山医院(MSH)从 2018 年 1 月至 2022 年 1 月收治的 ASUC 患者进行了回顾性病历审查。纳入的受试者如果在入院前 56 天内接受过一剂 BST,则被视为正在接受 BST 治疗。我们关注的结果包括两组患者住院时间(HLOS)、手术咨询率、住院结肠切除率和90天再入院率的平均差异:在 185 名入院的 ASUC 患者中,76 人在入院前服用过 BST,109 人未服用。两组患者的基线特征相似。两组患者的住院时间(7.46 天 vs 7.45 天,P = .52)和院内结肠切除率无明显差异。接受 BST 治疗的患者的手术会诊率(36.8% vs 8.3% P < .01)和 90 天再入院率(26.3% vs 13.8% P = .03)均较高:我们没有发现两组患者在大多数结果上存在明显差异。然而,接受 BST 治疗的患者更有可能在入院时接受外科会诊,90 天后的再入院率也更高。我们需要进一步研究评估导致接受 BST 患者再次入院的潜在因素。
{"title":"Outcomes of patients admitted with acute, severe ulcerative colitis on biologic therapy: a retrospective analysis from a tertiary referral hospital.","authors":"Nasruddin Sabrie, Manisha Jogendran, Rohit Jogendran, Laura E Targownik","doi":"10.1093/jcag/gwae017","DOIUrl":"10.1093/jcag/gwae017","url":null,"abstract":"<p><strong>Background: </strong>In steroid-refractory acute, severe, ulcerative colitis (ASUC), salvage medical therapy with infliximab is recommended to reduce the risk of colectomy. However, the evidence supporting this practice is based on cohorts naïve to biologics. Consequently, the management of patients on biologic or small molecule therapy (BST) with ASUC is not well defined.</p><p><strong>Methods: </strong>We conducted a retrospective chart review of patients admitted with ASUC to Mount Sinai Hospital (MSH) in Toronto, Ontario from January 2018 until January 2022. Included subjects were considered to be on BST if they had received a dose of these agents within 56 days prior to admission. Our outcomes of interest included the mean difference in hospital length of stay (HLOS), rates of surgical consultation, rates of inpatient colectomies, and 90-day readmission rates between the 2 groups.</p><p><strong>Results: </strong>Of the 185 admissions for ASUC, 76 were on BST prior to admission and 109 were not. Baseline characteristics were similar between the 2 groups. There were no significant differences in hospital length of stay (7.46 days vs 7.45 days <i>P</i> = .52) or in-hospital colectomy rates between the 2 groups. Patients on BST had higher rates of surgical consultation (36.8% vs 8.3% <i>P</i> < .01) and 90-day readmission rates (26.3% vs 13.8% <i>P</i> = .03).</p><p><strong>Conclusions: </strong>We did not identify significant differences in the majority of our outcomes between the 2 groups. However, patients on BST were more likely to receive a surgical consultation during their admission and had higher rates of readmission at 90 days. Further studies evaluating the underlying factors that contribute to readmission in patients on BST in hospitals are needed.</p>","PeriodicalId":17263,"journal":{"name":"Journal of the Canadian Association of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-05-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11317625/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"141975968","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
Practical guidance for managing patients with moderate-to-severe ulcerative colitis using small molecule therapies. 使用小分子疗法治疗中重度溃疡性结肠炎患者的实用指南。
Pub Date : 2024-05-15 eCollection Date: 2024-08-01 DOI: 10.1093/jcag/gwae013
Vipul Jairath, Waqqas Afif, Brian Bressler, Janet E Pope, Daniel Selchen, Laura E Targownik, Remo Panaccione

Ulcerative colitis (UC) is a severe and debilitating illness that affects the quality of life and physical health of many Canadians. Given the dynamic and progressive nature of the disease, advanced therapies are required to support its long-term management. The emergence of small molecule therapies offers novel treatment options that target mechanisms central to the immunopathology of UC. Sphingosine-1-phosphate (S1P) receptor modulators and Janus-activated kinase inhibitors are 2 classes of therapies that target unique pathways to attenuate inflammation and modulate the immune response characteristic of UC. This review aims to provide practical guidance on how these therapeutic options can best be used to optimize treatment management and highlight the emerging role of small molecule therapies as a treatment strategy for UC.

溃疡性结肠炎(UC)是一种严重的衰弱性疾病,影响着许多加拿大人的生活质量和身体健康。鉴于该病的动态和进展性,需要先进的疗法来支持其长期治疗。小分子疗法的出现提供了针对UC免疫病理核心机制的新型治疗方案。两性鞘氨醇-1-磷酸(S1P)受体调节剂和 Janus 激活激酶抑制剂是两类靶向独特途径的疗法,可减轻炎症反应并调节 UC 特有的免疫反应。本综述旨在就如何更好地利用这些治疗方案优化治疗管理提供实用指导,并强调小分子疗法作为 UC 治疗策略的新兴作用。
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引用次数: 0
Indication for endoscopic retrograde cholangiopancreatography and development of hemorrhage: a systematic review and meta-analysis. 内镜逆行胰胆管造影术的适应症与出血的发生:系统回顾和荟萃分析。
Pub Date : 2024-04-26 eCollection Date: 2024-10-01 DOI: 10.1093/jcag/gwae014
Michael K Parvizian, Mitchell V Edwards, Prem Bhoey, Melanie C Zhang, Lawrence C Hookey, David M Rodrigues

Background: Hemorrhage is a common complication associated with endoscopic retrograde cholangiopancreatography (ERCP), usually following sphincterotomy. Studies investigating risk factors for hemorrhage including ERCP indication have been conflicting. Therefore, we conducted a systematic review and meta-analysis to characterize the association between the ERCP indication and hemorrhage.

Methods: Database searches of MEDLINE, EMBASE, and CENTRAL were conducted to identify articles up to December 12, 2022. Randomized trials or observational studies of adult patients undergoing ERCP were included. Quality assessment using the Cochrane Risk of Bias 2.0 and Newcastle-Ottawa Scales for randomized trials and observational studies respectively was conducted. A random effects meta-analysis generating pooled odds ratios with 95% confidence intervals was conducted.

Results: A total of 1323 articles were identified of which 26 were included with up to 25 121 subjects in each meta-analysis. Rates of sphincterotomy (median 96.1%; IQR 60.5-100), biliary stent placement (median 17.2%; IQR 10.6-34.4), antiplatelet use (median 6.0%; IQR 0-10.1), and anticoagulant use (median 1.9%; IQR 0%-3.2%) varied among included studies. No specific indication was associated with hemorrhage in the meta-analyses including cholangitis (OR 1.50; 95% CI 0.97-2.32), choledocholithiasis/biliary stone (OR 1.28; 95% CI 0.95-1.73), malignancy (OR 0.97; 95% CI 0.66-1.42), sphincter of Oddi dysfunction (OR 1.32; 95% CI 0.72-2.40), and acute pancreatitis (OR 0.81; 95% CI 0.44-1.49).

Conclusions: Overall, no indication was significantly associated with increased hemorrhage following ERCP. However, given limitations in the included studies (ie, significant heterogeneity between studies), additional research to better characterize these associations is needed.

Protocol registration number: PROSPERO (CRD42021283978).

背景:出血是内镜逆行胰胆管造影术(ERCP)的常见并发症,通常发生在括约肌切开术之后。有关出血风险因素(包括ERCP适应症)的研究结果相互矛盾。因此,我们进行了一项系统回顾和荟萃分析,以确定ERCP适应症与出血之间的关系:方法:对 MEDLINE、EMBASE 和 CENTRAL 进行数据库检索,以确定截至 2022 年 12 月 12 日的文章。研究纳入了对接受ERCP治疗的成人患者进行的随机试验或观察性研究。对随机试验和观察性研究分别采用 Cochrane Risk of Bias 2.0 和 Newcastle-Ottawa Scales 进行了质量评估。进行随机效应荟萃分析,得出汇总的几率比及 95% 的置信区间:结果:共发现了 1323 篇文章,其中 26 篇被纳入荟萃分析,每篇荟萃分析的受试者多达 25 121 人。括约肌切开术(中位数 96.1%;IQR 60.5-100)、胆道支架置入术(中位数 17.2%;IQR 10.6-34.4)、抗血小板使用(中位数 6.0%;IQR 0-10.1)和抗凝剂使用(中位数 1.9%;IQR 0%-3.2%)的比率在纳入的研究中各不相同。在包括胆管炎(OR 1.50;95% CI 0.97-2.32)、胆总管结石/胆道结石(OR 1.28;95% CI 0.95-1.73)、恶性肿瘤(OR 0.97;95% CI 0.66-1.42)、Oddi括约肌功能障碍(OR 1.32;95% CI 0.72-2.40)和急性胰腺炎(OR 0.81;95% CI 0.44-1.49):总体而言,ERCP术后出血量增加与适应症无明显关联。然而,鉴于纳入研究的局限性(即研究之间存在明显的异质性),需要进行更多的研究以更好地描述这些关联:prospero(CRD42021283978)。
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引用次数: 0
The relationship among vedolizumab drug concentrations, biomarkers of inflammation, and clinical outcomes in a Canadian real-world study 加拿大一项真实世界研究中的维多珠单抗药物浓度、炎症生物标志物和临床结果之间的关系
Pub Date : 2024-03-24 DOI: 10.1093/jcag/gwae010
C. H. Seow, J. K. Marshall, Stewart Erin, Christopher Pettengell, Ryan Ward, W. Afif
Therapeutic drug monitoring is used to optimize anti-tumour necrosis factor biologic effectiveness in inflammatory bowel disease, but its role with other biological classes is unclear. This study explores relationships between post-induction vedolizumab trough concentrations and biochemical outcomes in a real-world study of individuals with inflammatory bowel disease. This retrospective analysis of data from a national patient support program between 2018 and 2020, included 436 individuals with Crohn’s disease or ulcerative colitis receiving vedolizumab. Optimal vedolizumab concentration thresholds (at weeks 6 and 14) were determined based on their ability to predict biochemical normalization (week 30 faecal calprotectin [<250 µg/g], C-reactive protein [<5 mg/l]). Thresholds best associated with each outcome were evaluated in multivariate analyses. Among patients with Crohn’s disease, week 6 serum vedolizumab concentrations (>41.65 µg/ml) predicted normalization defined by C-reactive protein: Spearman correlation coefficient [ρ] = −0.26, P = 0.002 and multivariate analysis (MVA)—OR: 3.22, 95% CI: 1.32–7.87, P = 0.01, and at week 14 (>22.25 µg/ml): ρ = −0.38, P < 0.0001, and MVA—OR: 3.21, 95% CI: 1.26–8.17 but not faecal calprotectin. Similarly, among patients with ulcerative colitis, week 6 vedolizumab concentrations (>39.65 g/ml) predicted normalization defined by C-reactive protein: ρ = −0.26, P = 0.005 and MVA—OR: 4.03, 95% CI: 1.30–12.52, P = 0.016, and at week 14 (>17.35 µg/ml): ρ = −0.39, P = 0.0001 and MVA—OR: 6.95, 95% CI: 1.81–26.77, P = 0.005, but not faecal calprotectin. Induction and post-induction serum vedolizumab were not consistently associated with biochemical normalization. As such, proactive therapeutic drug monitoring for vedolizumab should not be routinely incorporated in a treat to target strategy for inflammatory bowel disease. NCT04567628.
治疗药物监测用于优化抗肿瘤坏死因子生物制剂在炎症性肠病中的疗效,但其在其他生物制剂中的作用尚不明确。本研究在一项针对炎症性肠病患者的真实世界研究中,探讨了诱导后韦多珠单抗谷浓度与生化结果之间的关系。 该研究对2018年至2020年间一项全国性患者支持计划的数据进行了回顾性分析,纳入了436名接受维多珠单抗治疗的克罗恩病或溃疡性结肠炎患者。最佳维多珠单抗浓度阈值(第6周和第14周)是根据其预测生化指标正常化的能力确定的(第30周粪便钙蛋白[41.65 µg/ml]预测了C反应蛋白定义的正常化:斯皮尔曼相关系数[ρ] = -0.26,P = 0.002,多变量分析(MVA)-OR:3.22,95% CI:1.32-7.87,P = 0.01;第 14 周(>22.25 µg/ml):ρ = -0.38,P <0.0001,MVA-OR:3.21,95% CI:1.26-8.17,但不能预测粪便钙蛋白。同样,在溃疡性结肠炎患者中,第 6 周维多利珠单抗浓度(>39.65 g/ml)可预测由 C 反应蛋白定义的正常化:ρ = -0.26,P = 0.005,MVA-OR:4.03,95% CI:1.30-12.52,P = 0.016;第 14 周(>17.35 µg/ml):ρ = -0.39,P = 0.0001,MVA-OR:6.95,95% CI:1.81-26.77,P = 0.005,但不能预测粪便钙蛋白。 诱导和诱导后血清维多珠单抗与生化指标正常化的关系并不一致。因此,在炎症性肠病的靶向治疗策略中,不应常规纳入对维多珠单抗的主动治疗药物监测。 NCT04567628。
{"title":"The relationship among vedolizumab drug concentrations, biomarkers of inflammation, and clinical outcomes in a Canadian real-world study","authors":"C. H. Seow, J. K. Marshall, Stewart Erin, Christopher Pettengell, Ryan Ward, W. Afif","doi":"10.1093/jcag/gwae010","DOIUrl":"https://doi.org/10.1093/jcag/gwae010","url":null,"abstract":"\u0000 \u0000 \u0000 Therapeutic drug monitoring is used to optimize anti-tumour necrosis factor biologic effectiveness in inflammatory bowel disease, but its role with other biological classes is unclear. This study explores relationships between post-induction vedolizumab trough concentrations and biochemical outcomes in a real-world study of individuals with inflammatory bowel disease.\u0000 \u0000 \u0000 \u0000 This retrospective analysis of data from a national patient support program between 2018 and 2020, included 436 individuals with Crohn’s disease or ulcerative colitis receiving vedolizumab. Optimal vedolizumab concentration thresholds (at weeks 6 and 14) were determined based on their ability to predict biochemical normalization (week 30 faecal calprotectin [<250 µg/g], C-reactive protein [<5 mg/l]). Thresholds best associated with each outcome were evaluated in multivariate analyses.\u0000 \u0000 \u0000 \u0000 Among patients with Crohn’s disease, week 6 serum vedolizumab concentrations (>41.65 µg/ml) predicted normalization defined by C-reactive protein: Spearman correlation coefficient [ρ] = −0.26, P = 0.002 and multivariate analysis (MVA)—OR: 3.22, 95% CI: 1.32–7.87, P = 0.01, and at week 14 (>22.25 µg/ml): ρ = −0.38, P < 0.0001, and MVA—OR: 3.21, 95% CI: 1.26–8.17 but not faecal calprotectin. Similarly, among patients with ulcerative colitis, week 6 vedolizumab concentrations (>39.65 g/ml) predicted normalization defined by C-reactive protein: ρ = −0.26, P = 0.005 and MVA—OR: 4.03, 95% CI: 1.30–12.52, P = 0.016, and at week 14 (>17.35 µg/ml): ρ = −0.39, P = 0.0001 and MVA—OR: 6.95, 95% CI: 1.81–26.77, P = 0.005, but not faecal calprotectin.\u0000 \u0000 \u0000 \u0000 Induction and post-induction serum vedolizumab were not consistently associated with biochemical normalization. As such, proactive therapeutic drug monitoring for vedolizumab should not be routinely incorporated in a treat to target strategy for inflammatory bowel disease.\u0000 \u0000 \u0000 \u0000 NCT04567628.\u0000","PeriodicalId":17263,"journal":{"name":"Journal of the Canadian Association of Gastroenterology","volume":null,"pages":null},"PeriodicalIF":0.0,"publicationDate":"2024-03-24","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"140385366","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
Outcomes of a mandatory non-medical switch of infliximab to a biosimilar for inflammatory bowel disease in British Columbia, Canada 加拿大不列颠哥伦比亚省在炎症性肠病治疗中强制将英夫利西单抗转为生物仿制药的结果
Pub Date : 2024-03-23 DOI: 10.1093/jcag/gwae011
T. T. Hoang, J. Reid, C. Galorport, Brian Bressler, Y. Leung, G. Rosenfeld
Despite infliximab biosimilars becoming widely used in inflammatory bowel disease (IBD) patients, real-world non-medical switching is sparse. A biosimilar non-medical switch was launched in British Columbia in 2019, the first Canadian province to do so, from Remicade to an approved biosimilar (CT-P13 or SB2). This study aims to obtain real-world evidence evaluating the clinical outcomes of non-medical switching from Remicade to the infliximab biosimilars. This is a retrospective observational study of stable IBD patients from the IBD Centre of BC who underwent the non-medical infliximab switch. The primary outcome is treatment continuation at 12 ± 2 months post-switch. Secondary outcomes include frequency of loss of response, adverse events, and immunogenicity within the first 12 months post-switch. A control group of patients maintained on the originator served as a comparison. Patients in the biosimilar switch group (n = 264) and originator group (n = 99), show similar demographics and disease characteristics. There was no difference in infliximab continuation between the biosimilar group (94.9%) and the originator group (90.1%) (P = 0.18). Reasons for discontinuation of infliximab included loss of response (4.04% vs 4.91%), immunogenicity (1.01% vs 0.75%), or adverse effect (1.01% vs 2.3%) in the infliximab originator vs biosimilar switch group, respectively. Similarly, no differences in safety or efficacy were observed between patients switched to CT-P13 or SB2. Non-medical biosimilar switch of infliximab demonstrates similar clinical outcomes compared to originator molecule continuation for therapy of IBD. These data support the safety and efficacy of non-medical infliximab switching in IBD patients.
尽管英夫利西单抗生物仿制药在炎症性肠病(IBD)患者中得到了广泛应用,但现实世界中的非医疗转换却很少。不列颠哥伦比亚省于2019年启动了生物类似物非医疗转换,从Remicade转换为已获批准的生物类似物(CT-P13或SB2),这是加拿大第一个这样做的省份。 本研究旨在获得真实世界的证据,评估从 Remicade 非医疗转换到英夫利西单抗生物仿制药的临床效果。 这是一项回顾性观察研究,研究对象是不列颠哥伦比亚省 IBD 中心接受非药物英夫利西单抗转换治疗的稳定型 IBD 患者。主要结果是转换后 12±2 个月的持续治疗情况。次要结果包括转换后前 12 个月内的应答丧失频率、不良事件和免疫原性。由继续使用原研药的患者组成的对照组作为对比。 生物仿制药转换组(264 人)和原研药组(99 人)的患者显示出相似的人口统计学特征和疾病特征。生物仿制药组(94.9%)和原研药组(90.1%)在继续使用英夫利西单抗方面没有差异(P = 0.18)。英夫利西单抗原研药组和生物类似药转换组的停药原因分别包括反应消失(4.04% vs 4.91%)、免疫原性(1.01% vs 0.75%)或不良反应(1.01% vs 2.3%)。同样,转用 CT-P13 或 SB2 的患者在安全性或疗效方面也未发现差异。 与继续使用原研分子治疗 IBD 相比,英夫利西单抗的非医用生物仿制药转换具有相似的临床疗效。这些数据支持对IBD患者进行非医用英夫利西单抗转换治疗的安全性和有效性。
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Journal of the Canadian Association of Gastroenterology
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