第一个因素!血友病患者的急诊管理:一项单中心研究

IF 2.3 4区 医学 Q2 HEMATOLOGY
Kelsey Uminski, Natalia Rydz, Dawn Goodyear
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引用次数: 0

摘要

背景:当血友病患者(PwH)出现在急诊科(ED)时,及时止血治疗是必不可少的,指南建议在怀疑出血时进行治疗(“因素优先”策略)。研究设计和方法:本研究调查了2014年至2022年南阿尔伯塔省PwH的ED管理,重点关注指导方针的遵守情况。结果:191例成人A型或B型血友病患者共就诊393次。大多数就诊(86%)需要紧急或紧急护理。从ED登记到开处方和给药的中位时间分别为2.9小时和4.2小时,少数病例在2小时内给予治疗。在近一半的就诊中,预约了实验室检查,预约时间的中位数为65分钟。个性化应急管理方案的使用率随着时间的推移而增加,到2022年达到91.4%。中位急诊科住院时间为3.4小时,约25%的就诊与血友病相关。结论:这些发现突出了持续的延误和不遵守最佳实践建议,强调需要有针对性的质量改进干预措施,以确保在紧急情况下对PwH进行及时的、符合指南的护理。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Factor first! Emergency department management of persons with hemophilia: a single-center study.

Background: Timely hemostatic therapy is essential when persons with hemophilia (PwH) present to the emergency department (ED), with guidelines recommending treatment at the time a bleed is suspected ('Factor First' strategy).

Research design and methods: This study examined ED management of PwH in Southern Alberta from 2014 to 2022, focusing on adherence to guidelines.

Results: A total of 393 ED visits from 191 adults with hemophilia A or B were identified. Most visits (86%) required emergent or urgent care. Median times from ED registration to ordering and administering hemostatic therapy were 2.9 and 4.2 hours, respectively, with treatment given within 2 hours in a minority of cases. Laboratory tests were ordered in nearly half of visits, with a median ordering time of 65 minutes. Use of individualized emergency management protocols increased over time, reaching 91.4% in 2022. Median ED stay was 3.4 hours, and approximately 25% of visits had a hemophilia-related admission diagnosis.

Conclusions: These findings highlight persistent delays and nonadherence to best practice recommendations, emphasizing the need for targeted quality improvement interventions to ensure timely, guideline-concordant care for PwH in emergency settings.

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来源期刊
CiteScore
4.70
自引率
3.60%
发文量
98
审稿时长
6-12 weeks
期刊介绍: Advanced molecular research techniques have transformed hematology in recent years. With improved understanding of hematologic diseases, we now have the opportunity to research and evaluate new biological therapies, new drugs and drug combinations, new treatment schedules and novel approaches including stem cell transplantation. We can also expect proteomics, molecular genetics and biomarker research to facilitate new diagnostic approaches and the identification of appropriate therapies. Further advances in our knowledge regarding the formation and function of blood cells and blood-forming tissues should ensue, and it will be a major challenge for hematologists to adopt these new paradigms and develop integrated strategies to define the best possible patient care. Expert Review of Hematology (1747-4086) puts these advances in context and explores how they will translate directly into clinical practice.
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