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基于 SOLOIST-WHF 试验纳入标准,真实世界心力衰竭人群中索格列净的资格:来自瑞典心力衰竭注册登记处的数据。

Eligibility for sotagliflozin in a real-world heart failure population based on the SOLOIST-WHF trial enrolment criteria: data from the Swedish heart failure registry.

机构信息

Division of Cardiology, Department of Medicine, Karolinska Institutet, Stockholm 17177, Sweden.

Department of Cardiology, University Heart and Vascular Centre Hamburg, University Medical Centre Hamburg-Eppendorf, Hamburg 20246, Germany; German Centre of Cardiovascular Research (DZHK), Partner Site Hamburg/Kiel/Lübeck, Germany.

出版信息

Eur Heart J Cardiovasc Pharmacother. 2023 Jun 2;9(4):343-352. doi: 10.1093/ehjcvp/pvad012.

Abstract

AIMS

The SOLOIST-WHF trial demonstrated efficacy of sotagliflozin in patients with type 2 diabetes mellitus (T2DM) and recent worsening heart failure (HF) regardless of ejection fraction (EF). Selection criteria in trials may limit their generalizability. Therefore, we aimed to investigate eligibility for sotagliflozin based on the SOLOIST-WHF criteria in a real-world HF population.

METHODS AND RESULTS

SOLOIST-WHF criteria were applied to patients stabilized after HF hospitalization in the Swedish HF Registry according to (i) literal scenario (all inclusion/exclusion criteria) or (ii) pragmatic scenario (only criteria likely to influence treatment decisions). Of 5453 inpatients with T2DM and recent worsening HF, 51.4% had reduced EF (HFrEF), 19.1% mildly reduced (HFmrEF), and 29.5% preserved EF (HFpEF). Eligibility (literal) was: 27.2% (32.4% in HFrEF, 24.7% in HFmrEF, 19.7% in HFpEF) and eligibility (pragmatic) was 62.8% (69.1%, 60.3%, 53.4%, respectively). In the literal scenario, criteria limiting eligibility were HF duration <3 months, eGFR <30 ml/min/1.73 m2, age >85 years, acute coronary syndrome <3 months, and insufficiently high N-terminal pro-B-type natriuretic peptide levels. Eligible vs. non-eligible patients had more severe HF, higher cardiovascular (CV) comorbidity burden, higher use of HF treatments, and higher event rates (all-cause death 30.8 vs. 27.2 per 100 patient-years, CV death 19.1 vs. 16.6, and HF hospitalization 36.7 vs. 24.0).

CONCLUSION

In this large, real-world HF cohort with T2DM, ∼1/3 of patients were eligible for sotagliflozin in the literal and ∼2/3 of patients in the pragmatic scenario. Eligible patients had more severe HF and higher event rates, in particular CV and HF events.

摘要

目的

SOLOIST-WHF 试验表明,无论射血分数(EF)如何,索格列净均可有效治疗 2 型糖尿病(T2DM)合并近期恶化的心力衰竭(HF)患者。临床试验的入选标准可能限制了其普遍性。因此,我们旨在根据 SOLOIST-WHF 标准,在真实世界的 HF 人群中调查索格列净的入选资格。

方法和结果

根据(i)字面情况(所有纳入/排除标准)或(ii)实用情况(仅纳入可能影响治疗决策的标准),将 SOLOIST-WHF 标准应用于瑞典 HF 登记处中 HF 住院后稳定的 T2DM 患者。在 5453 例伴有近期恶化 HF 的住院患者中,51.4%存在射血分数降低(HFrEF),19.1%存在轻度降低(HFmrEF),29.5%存在射血分数保留(HFpEF)。入选标准(字面)为:27.2%(HFrEF 为 32.4%,HFmrEF 为 24.7%,HFpEF 为 19.7%),入选标准(实用)为 62.8%(分别为 69.1%、60.3%、53.4%)。在字面情况下,限制入选标准的因素为 HF 持续时间<3 个月、eGFR<30 ml/min/1.73 m2、年龄>85 岁、急性冠状动脉综合征<3 个月以及 NT-proBNP 水平不够高。与不符合入选标准的患者相比,符合入选标准的患者 HF 更严重,心血管(CV)合并症负担更重,HF 治疗使用率更高,且事件发生率更高(全因死亡 30.8/100 患者年 vs. 27.2/100 患者年,CV 死亡 19.1/100 患者年 vs. 16.6/100 患者年,HF 住院 36.7/100 患者年 vs. 24.0/100 患者年)。

结论

在这项伴有 T2DM 的大型真实世界 HF 队列中,字面情况下约 1/3的患者符合索格列净的入选标准,实用情况下约 2/3的患者符合入选标准。符合入选标准的患者 HF 更严重,且事件发生率更高,尤其是 CV 和 HF 事件。

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