Inserm, CHRU Nancy, Université de Lorraine, CIC-1433, Epidémiologie Clinique, F-54000, Nancy, France; Université de Lorraine, EA 4360 Apemac, F-54000, Nancy, France.
Université de Lorraine, EA 4360 Apemac, F-54000, Nancy, France.
Eur J Intern Med. 2018 May;51:53-60. doi: 10.1016/j.ejim.2017.12.005. Epub 2018 Jan 2.
We aimed to assess the effectiveness of recommended drug prescriptions at hospital discharge on 1-year mortality in patients with heart failure (HF) and reduced ejection fraction (HFREF).
We used data from the EPICAL2 cohort study. HF patients ≥18years old with left ventricular ejection fraction (LVEF) <40% and alive at discharge were included and followed up for mortality. Socio-demographic, clinical and therapeutic data were collected at admission. Therapeutic data were collected at discharge and at 6month. Prescription of an angiotensin-converting enzyme (ACE) inhibitor (or an angiotensin II receptor blocker [ARB] in case of ACE inhibitor intolerance) and a β-blocker at discharge were considered "guideline-consistent discharge prescription" (GCDP). A frailty Cox model after propensity score (PS) matching was used to assess the association of GCDP with survival.
Among 624 patients included, the mean (SD) age was 73.6 (12.8) years; 65% were male. A total of 412 (65.6%) patients received GCDP, and 82.8% still had guideline consistent prescription at 6months. A total of 166 patients died during the follow-up, 78 in the GCDP group and 88 in the other group. Before PS matching, patients with GCDP were younger (|StDiff|=48.32%) and had higher body mass index (BMI) (|StDiff|=11.71%), lower LVEF (|StDiff|=23.13%) and lower Charlson index (|StDiff|=55.27%) than patients without GCDP. After PS matching, all characteristics were balanced between the two treatment groups, and GCDP was associated with reduced mortality (pooled HR=0.51, 95% CI [0.35-0.73]).
Prescription of ACE (or ARB) inhibitors and β-blockers for patients with HFREF may be low despite the evidence for morbidity and mortality improvement with these medications but remains associated with reduced 1-year mortality in unselected HFREF patients.
我们旨在评估心力衰竭(HF)和射血分数降低(HFREF)患者出院时推荐药物治疗对 1 年死亡率的影响。
我们使用了 EPICAL2 队列研究的数据。纳入了年龄≥18 岁、左心室射血分数(LVEF)<40%且出院时存活的 HF 患者,并进行了死亡率随访。在入院时收集了社会人口统计学、临床和治疗数据。在出院时和 6 个月时收集了治疗数据。出院时处方血管紧张素转换酶(ACE)抑制剂(或 ACE 抑制剂不耐受时的血管紧张素 II 受体阻滞剂[ARB])和β受体阻滞剂被认为是“指南一致的出院处方”(GCDP)。使用倾向评分(PS)匹配后的脆弱性 Cox 模型评估 GCDP 与生存的关系。
在 624 名纳入的患者中,平均(SD)年龄为 73.6(12.8)岁;65%为男性。共有 412 名(65.6%)患者接受了 GCDP,其中 82.8%在 6 个月时仍有指南一致的处方。随访期间共有 166 名患者死亡,GCDP 组 78 例,其他组 88 例。在 PS 匹配之前,GCDP 组患者的年龄更小(|StDiff|=48.32%),体重指数(BMI)更高(|StDiff|=11.71%),左心室射血分数(LVEF)更低(|StDiff|=23.13%),Charlson 指数更低(|StDiff|=55.27%)。PS 匹配后,两组患者的所有特征均达到平衡,GCDP 与死亡率降低相关(合并 HR=0.51,95%CI [0.35-0.73])。
尽管 ACE(或 ARB)抑制剂和β受体阻滞剂治疗可改善 HFREF 患者的发病率和死亡率,但 HFREF 患者出院时处方 ACE(或 ARB)抑制剂和β受体阻滞剂的情况可能仍然较低,但仍与未选择的 HFREF 患者 1 年死亡率降低相关。