...
首页> 外文期刊>Circulation. Heart failure >Markers of decongestion, dyspnea relief, and clinical outcomes among patients hospitalized with acute heart failure.
【24h】

Markers of decongestion, dyspnea relief, and clinical outcomes among patients hospitalized with acute heart failure.

机译:急性心力衰竭住院患者的充血,呼吸困难缓解和临床结局指标。

获取原文
获取原文并翻译 | 示例
   

获取外文期刊封面封底 >>

       

摘要

Congestion is a primary driver of symptoms in patients with acute heart failure, and relief of congestion is a critical goal of therapy. Monitoring of response to therapy through the assessment of daily weights and net fluid loss is the current standard of care, yet the relationship between commonly used markers of decongestion and both patient reported symptom relief and clinical outcomes are unknown.We performed a retrospective analysis of the randomized clinical trial, diuretic optimization strategy evaluation in acute heart failure (DOSE-AHF), enrolling patients hospitalized with a diagnosis of acute decompensated heart failure. We assessed the relationship among 3 markers of decongestion at 72 hours-weight loss, net fluid loss, and percent reduction in serum N terminal B-type natriuretic peptide (NT-proBNP) level-and relief of symptoms as defined by the dyspnea visual analog scale area under the curve. We also determined the relationship between each marker of decongestion and 60-day clinical outcomes defined as time to death, first rehospitalization or emergency department visit. Mean age was 66 years, mean ejection fraction was 35%, and 27% had ejection fraction ≥50%. Of the 3 measures of decongestion assessed, only percent reduction in NT-proBNP was significantly associated with symptom relief (r=0.13; P=0.04). There was no correlation between either weight loss or net fluid loss and symptom relief, (r=0.04; P=0.54 and r=0.07; P=0.27, respectively). Favorable changes in each of the 3 markers of decongestion were associated with improvement in time to death, rehospitalization, or emergency department visit at 60 days (weight: hazard ratio, 0.91; 95% confidence interval, 0.85-0.97 per 4 lbs; weight lost; fluid hazard ratio, 0.94; 95% confidence interval, 0.90-0.99 per 1000 mL fluid loss; NT-proBNP hazard ratio, 0.95; 95% confidence interval, 0.91-0.99 per 10% reduction). These associations were unchanged after multivariable adjustment with the exception that percent reduction in NT-proBNP was no longer a significant predictor (hazard ratio, 0.97; 95% confidence interval, 0.93-1.02). The rates of death, HF hospitalization, or emergency department visit at 60 days for patients with 0, 1, 2, and 3 markers of decongestion (above the median) were 67%, 64%, 46%, and 38%, respectively (log rank P value=0.05).Weight loss, fluid loss, and NT-proBNP reduction at 72 hours are poorly correlated with dyspnea relief. However, favorable improvements in each of the 3 markers were associated with improved clinical outcomes at 60 days. These data suggest the need for ongoing research to understand the relationships among symptom relief, congestion, and outcomes in patients with acute decompensated heart failure.URL: http://www.clinicaltrials.gov. UNIQUE IDENTIFIER: NCT00577135.
机译:充血是急性心力衰竭患者症状的主要驱动力,缓解充血是治疗的关键目标。通过评估每日体重和净液体流失来监测对治疗的反应是目前的护理标准,但尚不常用的充血指标与患者报告的症状缓解和临床结果之间的关系尚不清楚。随机临床试验,急性心力衰竭的利尿剂优化策略评估(DOSE-AHF),招募住院诊断为急性代偿性心力衰竭的患者。我们评估了72小时体重减轻,净液体流失和血清N末端B型利尿钠肽(NT-proBNP)水平降低百分率与缓解呼吸困难视觉类似物所定义的症状的3种减充指标之间的关系曲线下的比例区域。我们还确定了充血的每个指标与60天临床结果之间的关系,这些结果定义为死亡时间,首次住院或急诊就诊。平均年龄为66岁,平均射血分数为35%,而射血分数≥50%的为27%。在评估的3种充血措施中,仅NT-proBNP降低的百分比与症状缓解显着相关(r = 0.13; P = 0.04)。体重减轻或净液体流失与症状缓解之间没有相关性(分别为r = 0.04; P = 0.54和r = 0.07; P = 0.27)。充血的3个指标中的每一个的有利变化都与60天时的死亡时间,重新住院或急诊就诊时间相关(体重:危险比,0.91; 95%置信区间,每4磅0.85-0.97;体重减轻) ;液体危险比,0.94; 95%置信区间,每1000 mL液体损失0.90-0.99; NT-proBNP危险比,0.95; 95%置信区间,每降低10%0.91-0.99)。这些关联在多变量调整后没有改变,只是NT-proBNP的降低百分比不再是重要的预测指标(危险比,0.97; 95%置信区间,0.93-1.02)。充血标记为0、1、2和3(高于中位数)的患者在60天时的死亡率,心衰住院率或急诊就诊率分别为67%,64%,46%和38%(对数秩P值= 0.05).72小时体重减轻,体液减少和NT-proBNP减少与呼吸困难缓解相关性很弱。但是,这三种标记物的每一种的有利改善与60天时的临床结局都有改善。这些数据表明需要进行持续的研究以了解急性失代偿性心力衰竭患者症状缓解,充血​​和预后之间的关系。URL:http://www.clinicaltrials.gov。唯一标识符:NCT00577135。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号