口服FXai治疗颅内出血的经济负担和死亡率:德国索赔数据分析。

Q2 Medicine
Hagen B Huttner, Felix Scherg, Katarina Kopke, Michael Schultze, Nils Kossack, Stefan T Gerner, Joji B Kuramatsu, Stefan Schwab
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引用次数: 0

摘要

背景:颅内出血(ICH)是口服Xa因子抑制剂(FXai)抗凝治疗最严重的并发症之一。为了满足优化治疗途径的迫切医疗需求,我们评估了口服FXai治疗期间脑出血的频率,以及德国卫生保健系统的相关负担。方法:我们的研究基于一个索赔数据库,该数据库包括德国超过400万拥有法定健康保险的人。该研究包括在2016年至2021年期间首次开始口服FXai治疗的人,以及在三年治疗期间经历过脑出血的人。为了平衡住院、费用和死亡率的比较,对有脑出血和没有脑出血的患者进行倾向评分匹配。结果:在研究期间,78,086例患者开始口服FXai治疗,其中530例患者在治疗期间出现脑出血。随访期间,脑出血发生率在口服FXai治疗开始后90天内最高,为0.64例/ 100患者年(PY;95% ci: 0.52-0.77%)。经历过脑出血事件的患者的三个月死亡率明显更高(39.4%;95% CI: 35.4-43.8%),而非脑出血患者(5.9%;95% ci: 4.2-8.3%)。这种差异在随访期间普遍存在,而两组患者的死亡率大致相同。脑出血患者在事件发生后的第一年平均住院时间为40.4天/年(95% CI: 35.7天- 45.2天);无脑出血的可比患者住院时间为10.8天/周(95% CI: 8.3天- 13.2天)。每位脑出血患者的年总成本为37,328欧元(95% CI: 32,243- 42,412欧元),非脑出血患者的年总成本为10,564欧元(95% CI: 9,298- 11,831欧元)。住院费用是主要原因,分别为86.1%和50.8%。结论:口服FXai治疗期间脑出血的发生率在其他已发表的真实数据范围内。脑出血患者的住院时间、相关费用和死亡率都很高,且明显高于非脑出血患者。卫生保健系统的高负担突出表明,需要采取预防措施,并为接受口服氟化辛治疗的脑出血患者提供更有效的治疗途径。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Economic burden of disease and mortality of intracranial haemorrhage under oral FXai: a German claims data analysis.

Background: Intracranial haemorrhage (ICH) is one of the most serious complications of anticoagulant therapy with oral factor Xa inhibitors (FXai). To meet an urgent medical need of optimising treatment pathways, we assessed the frequency of ICH during oral FXai treatment, as well as the associated burden on the German healthcare system.

Methods: Our study was based on a claims database comprising over 4 million people with statutory health insurance in Germany. The study included people initiating oral FXai treatment for the first time between 2016 and 2021, and who experienced ICH during a three-year treatment period. For a balanced comparison of hospitalisations, costs, and mortality, propensity score matching between patients with and without ICH was performed.

Results: During the study period, 78,086 patients had started oral FXai therapy, of which 530 experienced ICH during the therapy. The incidence rate of ICH was highest within the first 90 days after the start of oral FXai therapy during follow-up with 0.64 events per 100 patient-years (PY; 95% CI: 0.52-0.77%). Three-month mortality rates were significantly higher among patients who had experienced an ICH event (39.4%; 95% CI: 35.4-43.8%), as opposed to patients without ICH (5.9%; 95% CI: 4.2-8.3%). This difference prevailed during follow-up, while mortality increased at roughly equal rates in both patient groups. Patients with ICH were on average hospitalised for 40.4 days/PY (95% CI: 35.7 days - 45.2 days) in the first year after the event; comparable patients without ICH were hospitalised for 10.8 days/PY (95% CI: 8.3 days - 13.2 days). Annual total costs per patient were €37,328 (95% CI: €32,243-€42,412) for patients with ICH, and €10,564 (95% CI: €9,298-€11,831) for patients without ICH. Hospitalisation costs were the main driver with 86.1% versus 50.8%, respectively.

Conclusions: Incidence rates of ICH during oral FXai therapy were within the range of other published real-world data. Duration of hospitalisations, associated costs, and mortality were high and significantly higher for patients with ICH than for comparable patients without ICH. The high burden on the healthcare system highlights the need for preventive measures and more efficient treatment pathways for patients with ICH under oral FXai therapy.

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