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Correction: Operative team critical incident debriefing in a community hospital: a mixed methods study. 更正:社区医院手术小组危急事件汇报:一项混合方法研究。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-12-22 DOI: 10.1007/s12630-025-03054-7
Maira Quintanilha, Breanne Aylward, Patrick Feng, Ariane Fielding
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引用次数: 0
Correction: Association between postpartum depression and chronic postsurgical pain after Cesarean delivery: a secondary analysis of a randomized trial. 更正:产后抑郁与剖宫产后慢性术后疼痛的关系:一项随机试验的二次分析。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-12-22 DOI: 10.1007/s12630-025-03043-w
Asish Subedi, Sharon Orbach-Zinger, Alexandra M J V Schyns-van den Berg
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引用次数: 0
Seeking guidance in preoperative cardiac assessment guidelines. 寻求术前心脏评估指南的指导。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-12-01 DOI: 10.1007/s12630-025-03039-6
Kevin Venus, Duminda N Wijeysundera
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引用次数: 0
Cardiac risk assessment after noncardiac surgery: a historical cohort study on guideline adherence at a Canadian quaternary care centre. 非心脏手术后心脏风险评估:加拿大四级护理中心指南依从性的历史队列研究。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-12-01 DOI: 10.1007/s12630-025-03040-z
Dean Noutsios, Amanda Marino, Matthew Anacleto-Dabarno, Gabriele Baldini, Amal Bessissow

Purpose: Cardiac complications after noncardiac surgery remain a leading source of postoperative morbidity and mortality. In 2016, the Canadian Cardiovascular Society (CCS) published guidelines that outlined an approach to perioperative cardiac risk assessment for noncardiac surgery, integrating biomarkers. We sought to evaluate the adherence to these guidelines at McGill University Health Centre, a quaternary care hospital in Montreal, QC, Canada.

Methods: We conducted a historical cohort study of all patients undergoing elective noncardiac surgery requiring overnight stay between January 2018 and December 2019. The primary outcome was adherence to preoperative B-type natriuretic peptide (BNP) measurement. Secondary outcomes included adherence to postoperative troponin and electrocardiogram (ECG) acquisition, and 30-day postoperative outcomes.

Results: Among our cohort of 3,623 patients, BNP measurement adherence was 52.4%. Troponin and ECG acquisition adherence was 34.6% and 30.5%, respectively. Patients with an elevated preoperative BNP had higher incidences of 30-day myocardial injury after noncardiac surgery (20.2% vs 4.3%; P < 0.001), myocardial infarction (5.2% vs 0.5%; P < 0.001), mortality (2.5% vs 0.6%; P < 0.001), and to a lesser extent, cardiac arrest and heart failure decompensation. Patients with elevated postoperative troponin levels had higher incidences of 30-day myocardial infarction (20.7% vs 0.0%; P < 0.001), mortality (7.8% vs 0.6%; P < 0.001), and to a lesser extent, cardiac arrest and heart failure decompensation. Elevated BNP and troponin levels were associated with higher physician follow-up rates.

Conclusions: About half of the patients undergoing noncardiac surgery in our cohort underwent BNP screening as recommended by CCS guidelines; troponin and ECG acquisition adherence was even lower. While postoperative cardiac ischemia is associated with increased 30-day morbidity and mortality, more studies exploring physician risk stratification practice and the impact of increased testing on long-term outcomes are needed.

目的:非心脏手术后心脏并发症仍然是术后发病率和死亡率的主要来源。2016年,加拿大心血管学会(CCS)发布了指南,概述了整合生物标志物的非心脏手术围手术期心脏风险评估方法。我们试图评估麦吉尔大学健康中心对这些指南的遵守情况,麦吉尔大学健康中心是加拿大蒙特利尔的一家四级护理医院。方法:我们对2018年1月至2019年12月期间需要过夜的所有接受选择性非心脏手术的患者进行了一项历史队列研究。主要终点是术前b型利钠肽(BNP)测量的依从性。次要结果包括术后肌钙蛋白和心电图(ECG)采集的依从性,以及术后30天的结果。结果:在我们的3623例患者队列中,BNP测量依从性为52.4%。肌钙蛋白和心电图获取依从性分别为34.6%和30.5%。术前BNP升高的患者在非心脏手术后30天心肌损伤发生率更高(20.2% vs 4.3%); P结论:在我们的队列中,约有一半接受非心脏手术的患者按照CCS指南的建议进行了BNP筛查,肌钙蛋白和ECG获取依从性更低。虽然术后心脏缺血与30天发病率和死亡率增加有关,但需要更多的研究来探索医生风险分层实践和增加检测对长期结果的影响。
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引用次数: 0
Editorial commitment to trust and integrity in science: implications for pain and anesthesiology research. 对科学信任和诚信的编辑承诺:对疼痛和麻醉学研究的影响。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-11-01 Epub Date: 2026-01-13 DOI: 10.1007/s12630-025-03052-9
Tonya M Palermo, Didier Bouhassira, Karen D Davis, Hugh C Hemmings, Robert W Hurley, Joel Katz, Jaideep J Pandit, Theodore J Price, Michael E Schatman, Stephan K W Schwarz, Dennis C Turk, Marc Van de Velde, Matthew D Wiles, Tony L Yaksh, David Yarnitsky
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引用次数: 0
Risk factors for a central-to-peripheral arterial blood pressure gradient in adults: a systematic review. 成人中央到外周动脉血压梯度的危险因素:系统综述。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-11-01 Epub Date: 2026-01-13 DOI: 10.1007/s12630-025-03058-3
Hakim Chala, Nicolas Daccache, Louis Morisson, André Denault, Pascal Laferrière-Langlois

Purpose: Accurate hemodynamic monitoring is essential for personalized care in surgical and intensive care unit (ICU) settings, and radial artery catheters are the gold standard. Nevertheless, central-to-peripheral arterial blood pressure gradients (CPAPGs) have been reported in up to 77% of patients, potentially leading to misinformed clinical decisions. Identifying patients at risk of CPAPGs is crucial to adapt monitoring strategies. We aimed to identify the risk factors contributing to CPAPGs and assess their level of consensus in a systematic review of the literature.

Methods: For this systematic review, we searched MEDLINE/PubMed®, Embase, and Cochrane databases (CENTRAL and Database of Systematic Reviews) from inception to 15 July 2024. Studies on adult patients with simultaneous radial and central arterial pressure monitoring were included. We extracted and analyzed risk factors and assessed the consistency of the literature for each.

Results: From 741 retrieved articles, we included 55 studies (N = 5,598) evaluating the presence of CPAPGs during cardiopulmonary bypass, hepatic transplant, ICU stay, and other settings. Overall, 90 unique potential risk factors were evaluated, with 36 showing a statistically significant association with CPAPGs. Complex procedures and smaller radial artery diameter were the most consistent predictors, with both showing significant association with CPAPGs in the 3 studies evaluating them. Vasopressor usage showed statistical significance in half the studies evaluating it, and demographic factors, potentially associated with smaller radial artery diameter, such as older age, shorter stature, and female sex, were also statistically significant risk factors in some studies.

Conclusions: The present systematic review identified numerous risk factors for CPAPGs. In patients with multiple contributing factors, clinicians should consider using more central arterial cannulation to minimize the risk of inaccurate pressure measurements.

Study registration: PROSPERO ( CRD42024561474 ); first submitted 10 July 2024.

目的:精确的血流动力学监测对于外科和重症监护病房(ICU)的个性化护理至关重要,桡动脉导管是金标准。然而,据报道,高达77%的患者存在中央到外周动脉血压梯度(capgs),这可能导致错误的临床决策。识别有capgs风险的患者对于调整监测策略至关重要。我们的目的是确定导致capgs的风险因素,并通过对文献的系统回顾评估其共识水平。方法:在本系统综述中,我们检索了MEDLINE/PubMed®、Embase和Cochrane数据库(CENTRAL and Database of systematic Reviews),检索时间从建立到2024年7月15日。同时监测桡动脉和中心动脉压力的成人患者的研究被纳入。我们提取并分析了危险因素,并评估了每个因素的文献一致性。结果:从741篇检索到的文章中,我们纳入了55项研究(N = 5598),评估了在体外循环、肝移植、ICU住院和其他情况下capgs的存在。总的来说,我们评估了90个独特的潜在危险因素,其中36个与capgs有统计学意义的关联。复杂的手术和较小的桡动脉直径是最一致的预测因素,在评估它们的3项研究中,两者都显示出与capgs的显著关联。血管加压素的使用在一半的评估研究中显示出统计学意义,而人口统计学因素,如年龄较大、身材较矮和女性,可能与较小的桡动脉直径相关,在一些研究中也是统计学上显著的危险因素。结论:本系统综述确定了许多capgs的危险因素。对于有多种因素的患者,临床医生应考虑使用更多的中心动脉插管,以尽量减少血压测量不准确的风险。研究注册:PROSPERO (CRD42024561474);首次提交于2024年7月10日。
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引用次数: 0
Use of sedation for adults admitted to the intensive care unit during noninvasive ventilation: an international survey. 在无创通气期间入住重症监护病房的成人使用镇静:一项国际调查。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-11-01 Epub Date: 2025-10-13 DOI: 10.1007/s12630-025-03038-7
Josiah Butt, Yahya Shehabi, Yaseen M Arabi, Morten Hylander Møller, Eddy Fan, Sangeeta Mehta, Dan Perri, Deborah Cook, John Basmaji, Vincent I Lau, Kallirroi Laiya Carayannopoulos, Waleed Alhazzani, Kimberley Lewis

Purpose: Noninvasive positive pressure ventilation (NIV) is a common intervention used to treat acute respiratory failure. Unfortunately, many patients find NIV intolerable, ultimately leading to NIV failure, and the need for escalation to intubation and invasive mechanical ventilation (IMV). Hypothetically, sedation may treat NIV intolerance, thereby preventing the need for IMV. We hypothesized that there may be variability in practice regarding the use of sedation to treat NIV intolerance. Our primary aim was to assess if sedatives are used during NIV, and if so, which agents.

Methods: We created an 18-question survey that addressed demographics, the use of sedatives during NIV, the use of dexmedetomidine specifically, and attitudes and beliefs towards sedative use during NIV. The Hamilton Integrated Research Ethics Board (Hamilton, ON, Canada) approved the survey for global distribution. We used REDCap™ to electronically disseminate the survey in four countries (Australia, Canada, New Zealand, and Saudi Arabia).

Results: We received 140 responses from active practicing adult intensivists for an approximate response rate of 8%. Most intensivists (88%) reported that they would not administer a sedative to prevent NIV intolerance when a patient is not agitated. Overall, 44% of intensivists rarely or never give a sedative to treat NIV intolerance, 18% prescribe a sedative half the time, and 38% usually or always prescribe a sedative to improve NIV intolerance.

Conclusions: This international survey showed variability and equipoise on beliefs and attitudes regarding the use of sedatives to treat NIV intolerance. This must be considered in the context of a low response rate and may not represent the whole spectrum of opinions. Nevertheless, our findings likely justify the need for comprehensive research to outline the potential benefit and harm of using sedation in critically ill patients receiving NIV who are intolerant.

目的:无创正压通气(NIV)是治疗急性呼吸衰竭的常用干预手段。不幸的是,许多患者无法忍受NIV,最终导致NIV失败,需要升级到插管和有创机械通气(IMV)。假设,镇静可以治疗NIV不耐受,从而防止需要IMV。我们假设在使用镇静治疗NIV不耐受的实践中可能存在差异。我们的主要目的是评估在NIV中是否使用镇静剂,如果使用,使用哪种药物。方法:我们创建了一项18个问题的调查,涉及人口统计学,NIV期间镇静剂的使用,右美托咪定的具体使用,以及对NIV期间镇静剂使用的态度和信念。汉密尔顿综合研究伦理委员会(Hamilton, ON, Canada)批准了全球分布的调查。我们使用REDCap™在四个国家(澳大利亚、加拿大、新西兰和沙特阿拉伯)以电子方式传播调查结果。结果:我们收到140份来自积极执业的成人重症医师的回复,回复率约为8%。大多数强化医师(88%)报告说,当患者不激动时,他们不会给患者镇静剂以防止NIV不耐受。总体而言,44%的重症医师很少或从不使用镇静剂来治疗NIV不耐受,18%的人在一半的时间里使用镇静剂,38%的人通常或总是使用镇静剂来改善NIV不耐受。结论:这项国际调查显示,关于使用镇静剂治疗NIV不耐受的信念和态度存在差异和平衡。这必须在低回复率的背景下考虑,可能不能代表所有的意见。然而,我们的研究结果可能证明需要进行全面的研究,以概述在接受NIV治疗的不耐受的危重患者中使用镇静的潜在益处和危害。
{"title":"Use of sedation for adults admitted to the intensive care unit during noninvasive ventilation: an international survey.","authors":"Josiah Butt, Yahya Shehabi, Yaseen M Arabi, Morten Hylander Møller, Eddy Fan, Sangeeta Mehta, Dan Perri, Deborah Cook, John Basmaji, Vincent I Lau, Kallirroi Laiya Carayannopoulos, Waleed Alhazzani, Kimberley Lewis","doi":"10.1007/s12630-025-03038-7","DOIUrl":"10.1007/s12630-025-03038-7","url":null,"abstract":"<p><strong>Purpose: </strong>Noninvasive positive pressure ventilation (NIV) is a common intervention used to treat acute respiratory failure. Unfortunately, many patients find NIV intolerable, ultimately leading to NIV failure, and the need for escalation to intubation and invasive mechanical ventilation (IMV). Hypothetically, sedation may treat NIV intolerance, thereby preventing the need for IMV. We hypothesized that there may be variability in practice regarding the use of sedation to treat NIV intolerance. Our primary aim was to assess if sedatives are used during NIV, and if so, which agents.</p><p><strong>Methods: </strong>We created an 18-question survey that addressed demographics, the use of sedatives during NIV, the use of dexmedetomidine specifically, and attitudes and beliefs towards sedative use during NIV. The Hamilton Integrated Research Ethics Board (Hamilton, ON, Canada) approved the survey for global distribution. We used REDCap™ to electronically disseminate the survey in four countries (Australia, Canada, New Zealand, and Saudi Arabia).</p><p><strong>Results: </strong>We received 140 responses from active practicing adult intensivists for an approximate response rate of 8%. Most intensivists (88%) reported that they would not administer a sedative to prevent NIV intolerance when a patient is not agitated. Overall, 44% of intensivists rarely or never give a sedative to treat NIV intolerance, 18% prescribe a sedative half the time, and 38% usually or always prescribe a sedative to improve NIV intolerance.</p><p><strong>Conclusions: </strong>This international survey showed variability and equipoise on beliefs and attitudes regarding the use of sedatives to treat NIV intolerance. This must be considered in the context of a low response rate and may not represent the whole spectrum of opinions. Nevertheless, our findings likely justify the need for comprehensive research to outline the potential benefit and harm of using sedation in critically ill patients receiving NIV who are intolerant.</p>","PeriodicalId":56145,"journal":{"name":"Canadian Journal of Anesthesia-Journal Canadien D Anesthesie","volume":" ","pages":"1681-1689"},"PeriodicalIF":3.3,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145287899","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Safer oxygenation through flexible optical scopes during airway management: an in vitro study. 在气道管理中通过柔性光学镜进行更安全的氧合:一项体外研究。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-11-01 Epub Date: 2026-01-19 DOI: 10.1007/s12630-025-03059-2
Alexandre Garioud, Michael Seltz Kristensen

Purpose: Oxygen insufflation through the working channel of flexible optical scopes improves oxygenation and visibility during tracheal intubation but potentially causes barotrauma when not pressure-restricted. Pressure limited to 30-40 cm H2O improves safety. We sought to conduct an in vitro study to develop a setup that delivers oxygen at desired pressures while maintaining sufficient flows to achieve the documented benefits.

Methods: In the present in vitro study, we constructed a setup with equipment readily available in anesthesia locations, allowing regulation of the pressure at which oxygen is delivered at the distal end of the flexible optical scope. Pressure was regulated via the adjustable pressure-limiting valve and measured by immersion in water. We identified which combinations of set flow from the anesthesia machine and set pressure resulted in distal pressures of 10, 15, 30, and 40 cm H2O, respectively. We measured the resulting flows.

Results: In flexible scopes with a channel diameter ≥ 2 mm, we obtained clinically relevant flows > 3 L·min-1 at pressure of 30-40 cm H2O.

Conclusions: Oxygen insufflation through a flexible optical scope at a targeted distal pressure is possible with ubiquitous anesthesia equipment. Scopes with a suction-/working-channel diameter ≥ 2 mm delivered clinically relevant flows > 3 L·min-1 at a pressure of 30-40 cm H2O. Thinner scopes delivered lower flows. These findings will guide future studies and the implementation of this setup in clinical practice.

目的:在气管插管过程中,通过柔性光学镜的工作通道进行氧气注入可改善氧合和能见度,但在不限制压力的情况下可能导致气压损伤。压力限制在30-40 cm H2O,提高了安全性。我们试图进行一项体外研究,以开发一种装置,在所需压力下输送氧气,同时保持足够的流量,以实现文献记载的好处。方法:在目前的体外研究中,我们构建了一个装置,在麻醉位置有现成的设备,允许调节在柔性光学镜远端输送氧气的压力。压力通过可调节的限压阀调节,并通过浸入水中测量。我们确定了麻醉机的固定流量和固定压力的组合分别导致远端压力为10、15、30和40 cm H2O。我们测量了结果流。结果:在通道直径≥2mm的柔性范围内,在30-40 cm H2O压力下,我们获得了临床相关的流量> 3 L·min-1。结论:在无所不在的麻醉设备下,通过柔性光学镜在目标远端压力下进行氧气注入是可能的。吸力/工作通道直径≥2mm的范围,在30-40 cm H2O的压力下,提供临床相关的流量> 3 L·min-1。更薄的范围提供更低的流量。这些发现将指导未来的研究和在临床实践中实施这种设置。
{"title":"Safer oxygenation through flexible optical scopes during airway management: an in vitro study.","authors":"Alexandre Garioud, Michael Seltz Kristensen","doi":"10.1007/s12630-025-03059-2","DOIUrl":"10.1007/s12630-025-03059-2","url":null,"abstract":"<p><strong>Purpose: </strong>Oxygen insufflation through the working channel of flexible optical scopes improves oxygenation and visibility during tracheal intubation but potentially causes barotrauma when not pressure-restricted. Pressure limited to 30-40 cm H<sub>2</sub>O improves safety. We sought to conduct an in vitro study to develop a setup that delivers oxygen at desired pressures while maintaining sufficient flows to achieve the documented benefits.</p><p><strong>Methods: </strong>In the present in vitro study, we constructed a setup with equipment readily available in anesthesia locations, allowing regulation of the pressure at which oxygen is delivered at the distal end of the flexible optical scope. Pressure was regulated via the adjustable pressure-limiting valve and measured by immersion in water. We identified which combinations of set flow from the anesthesia machine and set pressure resulted in distal pressures of 10, 15, 30, and 40 cm H<sub>2</sub>O, respectively. We measured the resulting flows.</p><p><strong>Results: </strong>In flexible scopes with a channel diameter ≥ 2 mm, we obtained clinically relevant flows > 3 L·min<sup>-1</sup> at pressure of 30-40 cm H<sub>2</sub>O.</p><p><strong>Conclusions: </strong>Oxygen insufflation through a flexible optical scope at a targeted distal pressure is possible with ubiquitous anesthesia equipment. Scopes with a suction-/working-channel diameter ≥ 2 mm delivered clinically relevant flows > 3 L·min<sup>-1</sup> at a pressure of 30-40 cm H<sub>2</sub>O. Thinner scopes delivered lower flows. These findings will guide future studies and the implementation of this setup in clinical practice.</p>","PeriodicalId":56145,"journal":{"name":"Canadian Journal of Anesthesia-Journal Canadien D Anesthesie","volume":" ","pages":"1650-1660"},"PeriodicalIF":3.3,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12855237/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"146004775","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Association between extreme weather events and postoperative adverse outcomes: a systematic review. 极端天气事件与术后不良后果之间的关系:一项系统综述。
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-11-01 Epub Date: 2026-01-06 DOI: 10.1007/s12630-025-03051-w
Mark Hwang, Hiten Naik, Lindsay Blake, Michelle Dusko Biferie, Janny X C Ke

Purpose: Extreme weather events have been increasing in frequency and intensity globally. Surgical patients may be particularly susceptible to the impact of extreme weather on health outcomes and health care delivery. Our primary objective was to synthesize the available evidence on the association between extreme weather events and postoperative adverse outcomes within thirty days after surgery.

Methods: We performed a systematic review of the literature, searching MEDLINE on PubMed®, Embase, CINAHL, Web of Science, and the Cochrane Database of Systematic Reviews for English-language, full-text articles published prior to 30 May 2024. We included studies that involved surgical patients, exposure to an extreme weather event thirty days pre- or postoperatively, and had one or more adverse outcome within thirty days postoperatively. Screening and extraction were performed by two independent reviewers. We also performed thematic analysis to summarize the impact of extreme weather events on postoperative health care delivery.

Results: Our search identified 8,422 articles, of which 4 studies encompassing 117,804 surgical patients qualified for inclusion (3 on heatwave or extreme heat, and 1 on wildfire smoke). Retrospective studies linked temperatures > 40 °C to increased perioperative complications in trauma patients (1 study), temperatures > 30 °C to increased length of hospital stay in patients older than 60 yr (1 study), and wildfire smoke to respiratory complications in pediatric patients with prematurity or respiratory conditions (1 study). Health delivery domains that were affected were patients (3 studies), care processes and infrastructure (2 studies), and capacity (2 studies). The studies were limited by heterogenous definitions of exposure, confounding, and bias.

Conclusions: Our review revealed major research gaps in the impact of extreme weather events on postoperative outcomes and health care delivery. Existing literature is scant and limited by substantial methodologic issues, and further research is urgently required.

Study registration: PROSPERO ( CRD42023435273 ); first submitted 26 June 2023.

目的:全球极端天气事件的频率和强度都在增加。手术患者可能特别容易受到极端天气对健康结果和卫生保健服务的影响。我们的主要目的是综合关于极端天气事件与术后30天内不良后果之间关系的现有证据。方法:我们对文献进行了系统综述,在PubMed®、Embase、CINAHL、Web of Science和Cochrane系统综述数据库的MEDLINE上搜索2024年5月30日之前发表的英文全文文章。我们纳入的研究涉及手术患者,术前或术后30天暴露于极端天气事件,并在术后30天内有一个或多个不良后果。筛选和提取由两名独立审稿人进行。我们还进行了专题分析,总结了极端天气事件对术后医疗服务的影响。结果:我们检索了8,422篇文章,其中4篇研究纳入了117,804例手术患者(3篇关于热浪或极端高温,1篇关于野火烟雾)。回顾性研究表明,温度> ~ 40℃与创伤患者围手术期并发症增加有关(1项研究),温度> ~ 30℃与60岁以上患者住院时间延长有关(1项研究),野火烟雾与早产或呼吸系统疾病儿科患者呼吸系统并发症有关(1项研究)。受影响的卫生服务领域包括患者(3项研究)、护理流程和基础设施(2项研究)以及能力(2项研究)。这些研究受到暴露、混淆和偏倚的不同定义的限制。结论:我们的综述揭示了极端天气事件对术后结局和医疗服务的影响方面的主要研究空白。现有的文献很少,而且受到大量方法论问题的限制,迫切需要进一步的研究。研究注册:PROSPERO (CRD42023435273);首次提交于2023年6月26日。
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引用次数: 0
The association of point-of-care coagulation testing with bleeding symptoms in patients with Ehlers-Danlos syndrome: an exploratory cross-sectional study. ehers - danlos综合征患者即时凝血试验与出血症状的相关性:一项探索性横断面研究
IF 3.3 3区 医学 Q1 ANESTHESIOLOGY Pub Date : 2025-11-01 Epub Date: 2025-12-19 DOI: 10.1007/s12630-025-03048-5
Austin L Lam, Nimish Mittal, Michelle Vinod, Keyvan Karkouti, Hance Clarke, Justyna Bartoszko

Purpose: Ehlers-Danlos syndromes (EDS) are a group of connective tissue disorders associated with an increased risk of bleeding. We examined the association between point-of-care (POC) testing parameters with bleeding history in a cohort cared for at the GoodHope EDS Clinic at Toronto General Hospital.

Methods: We conducted an exploratory cross-sectional study at the Toronto General Hospital GoodHope EDS Clinic, recruiting adult patients with a diagnosis of EDS from 27 April 2022 to 7 October 2024. Patients provided samples for rotational thromboelastometry (ROTEM) and functional platelet testing (PlateletWorks), and were administered the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool (ISTH-BAT) to calculate the Bleeding Severity Score (BSS). The association between the BSS and POC parameters was examined using descriptive statistics and Spearman correlation analysis.

Results: We recruited 17 patients (hypermobile subtype, n = 10; classical subtype, n = 7). Clinically significant bleeding (BSS ≥ 4 in males; ≥ 6 in females) was reported in the majority (classical group, 86%; hypermobile group, 90%). Nine (53%) patients had major surgery or trauma at a median age of 23 (range, 8-39) yr. There were no significant abnormalities detected using ROTEM. Lower functional platelet percentages were observed in the hypermobile subgroup, with no association with BSS.

Conclusions: Point-of-care functional platelet testing using aggregation in response to an exogenous collagen agonist may detect inherent platelet dysfunction in patients with hypermobile subtype. We did not detect any ROTEM parameter abnormalities that were associated with elevated BSS scores. This supports a multifactorial etiology of bleeding in this patient population.

目的:ehers - danlos综合征(EDS)是一组与出血风险增加相关的结缔组织疾病。我们研究了在多伦多综合医院GoodHope EDS诊所护理的队列中,护理点(POC)检测参数与出血史之间的关系。方法:我们在多伦多总医院GoodHope EDS诊所进行了一项探索性横断面研究,招募了2022年4月27日至2024年10月7日诊断为EDS的成年患者。患者提供样本进行旋转血栓弹性测量(ROTEM)和血小板功能测试(PlateletWorks),并使用国际血栓和止血学会出血评估工具(ISTH-BAT)计算出血严重程度评分(BSS)。采用描述性统计和Spearman相关分析检验BSS和POC参数之间的关系。结果:我们招募了17例患者(过度运动亚型,n = 10;经典亚型,n = 7)。大多数患者报告有临床意义的出血(男性BSS≥4,女性BSS≥6)(经典组,86%;过度运动组,90%)。9例(53%)患者在中位年龄23岁(范围8-39岁)时进行了重大手术或创伤。使用ROTEM未发现明显异常。在高运动亚组中观察到较低的功能性血小板百分比,与BSS无关。结论:对外源性胶原受体激动剂使用聚集法进行的即时功能性血小板检测可以检测出超移动亚型患者固有的血小板功能障碍。我们没有发现任何与BSS评分升高相关的ROTEM参数异常。这支持了该患者群体出血的多因素病因学。
{"title":"The association of point-of-care coagulation testing with bleeding symptoms in patients with Ehlers-Danlos syndrome: an exploratory cross-sectional study.","authors":"Austin L Lam, Nimish Mittal, Michelle Vinod, Keyvan Karkouti, Hance Clarke, Justyna Bartoszko","doi":"10.1007/s12630-025-03048-5","DOIUrl":"10.1007/s12630-025-03048-5","url":null,"abstract":"<p><strong>Purpose: </strong>Ehlers-Danlos syndromes (EDS) are a group of connective tissue disorders associated with an increased risk of bleeding. We examined the association between point-of-care (POC) testing parameters with bleeding history in a cohort cared for at the GoodHope EDS Clinic at Toronto General Hospital.</p><p><strong>Methods: </strong>We conducted an exploratory cross-sectional study at the Toronto General Hospital GoodHope EDS Clinic, recruiting adult patients with a diagnosis of EDS from 27 April 2022 to 7 October 2024. Patients provided samples for rotational thromboelastometry (ROTEM) and functional platelet testing (PlateletWorks), and were administered the International Society on Thrombosis and Haemostasis Bleeding Assessment Tool (ISTH-BAT) to calculate the Bleeding Severity Score (BSS). The association between the BSS and POC parameters was examined using descriptive statistics and Spearman correlation analysis.</p><p><strong>Results: </strong>We recruited 17 patients (hypermobile subtype, n = 10; classical subtype, n = 7). Clinically significant bleeding (BSS ≥ 4 in males; ≥ 6 in females) was reported in the majority (classical group, 86%; hypermobile group, 90%). Nine (53%) patients had major surgery or trauma at a median age of 23 (range, 8-39) yr. There were no significant abnormalities detected using ROTEM. Lower functional platelet percentages were observed in the hypermobile subgroup, with no association with BSS.</p><p><strong>Conclusions: </strong>Point-of-care functional platelet testing using aggregation in response to an exogenous collagen agonist may detect inherent platelet dysfunction in patients with hypermobile subtype. We did not detect any ROTEM parameter abnormalities that were associated with elevated BSS scores. This supports a multifactorial etiology of bleeding in this patient population.</p>","PeriodicalId":56145,"journal":{"name":"Canadian Journal of Anesthesia-Journal Canadien D Anesthesie","volume":" ","pages":"1661-1668"},"PeriodicalIF":3.3,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145795350","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":3,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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Canadian Journal of Anesthesia-Journal Canadien D Anesthesie
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