生命最后一年维生素K拮抗剂治疗的质量

IF 7.6 2区 医学 Q1 HEMATOLOGY
HemaSphere Pub Date : 2025-05-19 DOI:10.1002/hem3.70135
Chantal Visser, Eva K. Kempers, Jamilla Goedgebuur, Denise Abbel, Sarah J. Aldridge, Adrian Edwards, Michelle Edwards, Geert-Jan Geersing, Anne Gulbech Ording, Sjef J. C. M. van de Leur, Kate J. Lifford, Isabelle Mahé, Simon P. Mooijaart, Melchior C. Nierman, Johanneke E. A. Portielje, Mette Søgaard, Sebastian Szmit, Nynke M. Wiersma, Simon I. R. Noble, Frederikus A. Klok, Qingui Chen, Suzanne C. Cannegieter, Eric C. T. Geijteman, Marieke J. H. A. Kruip, SERENITY Consortium
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引用次数: 0

摘要

关于临终患者抗凝治疗质量的数据有限。本研究评估了生命最后一年的维生素K拮抗剂(VKA)抗凝控制,使用荷兰统计局的全国数据,与抗凝诊所数据和荷兰癌症登记处相关联。我们纳入了2013年1月1日至2019年12月31日期间因严重医疗状况住院并死亡的流行VKA用户。采用治疗范围内时间(TTR)、治疗范围以上时间(TAR)、治疗范围以下时间(TBR)和反映INR变异性的国际归一化比率(INR)方差增长率(VGR)来评估抗凝控制。通过两种方法检查抗凝控制:(1)超过4个时间间隔(死亡前0-12个月、0-9个月、0-6个月和0-3个月),(2)每隔3个月(死亡前9-12个月、6-9个月、3-6个月和0-3个月)来描述时间变化。在6874名生命最后一年的VKA使用者中(中位年龄82岁[四分位数间距:76-87]岁,46.9%为女性),最常见的严重疾病是心脏病(60.4%)、癌症(16.2%)和髋部骨折(15.2%)。随着死亡的临近,TTR和TBR下降,而TAR和平均VGR增加,特别是在生命的最后3个月。这种下降在癌症患者和阿塞诺古玛洛服用者中更为明显。综上所述,危重患者的VKA抗凝质量在生命的最后一年下降,表现为TTR降低,TAR和VGR升高,提示出血风险增加。这些发现强调了重新评估VKA使用的重要性,并考虑在接近生命终点的患者中停用VKA。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Quality of vitamin K antagonist treatment during the last year of life

Limited data exist on the quality of anticoagulation in patients approaching the end of life. This study evaluated vitamin K antagonist (VKA) anticoagulation control during the last year of life, using nationwide data from Statistics Netherlands, linked to anticoagulation clinics' data and the Netherlands Cancer Registry. We included prevalent VKA users who were hospitalized with a severe medical condition and died between January 1, 2013, and December 31, 2019. Anticoagulation control was assessed using time in therapeutic range (TTR), time above therapeutic range (TAR), and time below therapeutic range (TBR) and the international normalized ratio (INR) variance growth rate (VGR), which reflects INR variability. Anticoagulation control was examined by two approaches: (1) over four intervals (0–12 months, 0–9 months, 0–6 months, and 0–3 months preceding death), and (2) in 3-month intervals (9–12, 6–9, 3–6, and 0–3 months before death) to describe temporal changes. Among 6874 VKA users in their last year of life (median age 82 [Interquartile range: 76–87] years, 46.9% female), the most prevalent severe medical conditions were heart disease (60.4%), cancer (16.2%), and hip fracture (15.2%). As death approached, TTR and TBR decreased, while TAR and mean VGR increased, particularly in the last 3 months of life. This decline was more pronounced in cancer patients and acenocoumarol users. In conclusion, the quality of VKA anticoagulation declined in the last year of life in severely ill patients, marked by reduced TTR and increased TAR and VGR, suggesting an increased bleeding risk. These findings highlight the importance of reassessing VKA use and considering discontinuation in patients approaching the end of life.

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来源期刊
HemaSphere
HemaSphere Medicine-Hematology
CiteScore
6.10
自引率
4.50%
发文量
2776
审稿时长
7 weeks
期刊介绍: HemaSphere, as a publication, is dedicated to disseminating the outcomes of profoundly pertinent basic, translational, and clinical research endeavors within the field of hematology. The journal actively seeks robust studies that unveil novel discoveries with significant ramifications for hematology. In addition to original research, HemaSphere features review articles and guideline articles that furnish lucid synopses and discussions of emerging developments, along with recommendations for patient care. Positioned as the foremost resource in hematology, HemaSphere augments its offerings with specialized sections like HemaTopics and HemaPolicy. These segments engender insightful dialogues covering a spectrum of hematology-related topics, including digestible summaries of pivotal articles, updates on new therapies, deliberations on European policy matters, and other noteworthy news items within the field. Steering the course of HemaSphere are Editor in Chief Jan Cools and Deputy Editor in Chief Claire Harrison, alongside the guidance of an esteemed Editorial Board comprising international luminaries in both research and clinical realms, each representing diverse areas of hematologic expertise.
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