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首页> 外文期刊>Circulation. Heart failure >Assessment of long-term effects of irbesartan on heart failure with preserved ejection fraction as measured by the minnesota living with heart failure questionnaire in the irbesartan in heart failure with preserved systolic function (I-PRESERVE) trial.
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Assessment of long-term effects of irbesartan on heart failure with preserved ejection fraction as measured by the minnesota living with heart failure questionnaire in the irbesartan in heart failure with preserved systolic function (I-PRESERVE) trial.

机译:评估厄贝沙坦对射血分数保留的心力衰竭的长期影响,该评估通过明尼苏达州心衰患者调查问卷在厄贝沙坦具有维持收缩功能的心衰中进行测量(I-PRESERVE)。

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摘要

The Minnesota Living with Heart Failure Questionnaire (MLHFQ) was used in a large, multinational, randomized, placebo-controlled trial to measure adverse effects of heart failure with preserved ejection fraction (HF-PEF) on patients' lives and the effects of irbesartan.Patients with symptomatic HF-PEF were randomly assigned to irbesartan (up to 300 mg daily) or placebo. The MLHFQ was administered at baseline (n=3605), month 6 (n=3137), month 14 (n=2904), and the end of study (median, 56 months, n=2205). Baseline MLHFQ scores of 43±21 indicated that HF-PEF had a substantial adverse effects. Estimated retest reliability was 0.80. Baseline MLHFQ scores were associated with other measures of the severity of heart failure including symptoms, signs of congestion, cardiac structure, and time to hospitalizations or deaths attributed to heart failure. Slight improvement in shortness of breath or fatigue was associated with significant improvement in MLHFQ scores (-5.9 and -5.0, P<0.0001). Compared with placebo, further improvement in MLHFQ scores was not observed with irbesartan after 6 months (mean adjusted difference, 0.4; 95% confidence interval, -0.8 to 1.7), 14 months (0.5; 95% confidence interval, -0.9 to 1.8), or the end of study (2.0; 95% confidence interval, -4.1 to 0.01).The MLHFQ scores are a reliable, valid, and sensitive measure of the adverse impact of HF-PEF on patients' lives. Irbesartan did not substantially improve MLHFQ scores during a long period of follow-up. Clinical Trial Registration- URL: http://www.clinicaltrials.gov. Unique identifier: NCT00095238.
机译:明尼苏达州心衰患者生存调查表(MLHFQ)被用于一项大型,跨国,随机,安慰剂对照试验中,以保留射血分数(HF-PEF)的心衰对患者生活和厄贝沙坦的不良影响。有症状的HF-PEF患者随机分配厄贝沙坦(每日最多300 mg)或安慰剂。 MLHFQ在基线(n = 3605),第6个月(n = 3137),第14个月(n = 2904)和研究结束(中位数56个月,n = 2205)时给药。基线MLHFQ得分为43±21,表明HF-PEF具有明显的不良反应。估计的重测可靠性为0.80。基线MLHFQ评分与心力衰竭严重程度的其他指标相关,包括症状,充血迹象,心脏结构以及因心力衰竭而住院或死亡的时间。呼吸急促或疲劳的轻微改善与MLHFQ评分的显着改善相关(-5.9和-5.0,P <0.0001)。与安慰剂相比,厄贝沙坦在6个月(均值调整差异,0.4; 95%置信区间,-0.8至1.7),14个月(0.5; 95%置信区间,-0.9至1.8)后未观察到MLHFQ评分的进一步改善。 ,即研究结束(2.0; 95%置信区间,-4.1至0.01)。MLHFQ评分是对HF-PEF对患者生活的不良影响的可靠,有效且敏感的指标。在长期的随访中,厄贝沙坦并未显着改善MLHFQ评分。临床试验注册-URL:http://www.clinicaltrials.gov。唯一标识符:NCT00095238。

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