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通过结合生物电阻抗分析仪的数字体重秤在随访期间检测已确诊心力衰竭患者的临床前体液潴留情况。

Detection of preclinical body fluid retention in established heart failure patients during follow-up by a digital weight scale incorporating a bioelectrical impedance analyzer.

作者信息

Kataoka Hajime

机构信息

Division of Internal Medicine, Nishida Hospital, Oita, Japan.

出版信息

Congest Heart Fail. 2012 Jan-Feb;18(1):37-42. doi: 10.1111/j.1751-7133.2011.00230.x. Epub 2011 Jul 4.

DOI:10.1111/j.1751-7133.2011.00230.x
PMID:22277176
Abstract

This study examined the characteristics of asymptomatic worsening heart failure (HF) events and validated the role of a novel HF monitoring method (measuring body weight [BW] and percent body fat [BF%]) to identify such worsening HF events. A clinician determined worsening HF status by evaluating symptoms, physical signs, and pleural effusion on ultrasonography. A criterion of significant fluid weight gain was defined as BW gain ≥1.5 kg with a concomitant decrease in BF%. A total of 74 HF patients were included. During a mean follow-up of 20.8 months, 1588 visits were evaluated. A total of 79 worsening HF events occurred in 50 patients, in which worsening was symptomatic in 46 events (58%) and asymptomatic in 33 events (42%). Novel method eliminated 42 of 73 (58%) false-positive indications of worsening HF events based only on the BW criterion (≥1.5 kg) without excluding true worsening HF events. The test characteristics of this method in the diagnosis of overall HF events were sensitivity 65.8% (95% confidence interval [CI], 54.3-76.1), specificity 97.9% (95%, CI 97.1-98.6), positive predictive value 62.7% (95% CI, 51.3-73.0), and negative predictive value 98.2% (95% CI, 97.4-98.8). Preclinical fluid retention occurs frequently in established HF patients, and novel monitoring method can specifically identify preclinical worsening HF.

摘要

本研究调查了无症状性心力衰竭(HF)事件的特征,并验证了一种新型HF监测方法(测量体重[BW]和体脂百分比[BF%])在识别此类HF病情恶化事件中的作用。临床医生通过评估症状、体征以及超声检查发现的胸腔积液来确定HF病情恶化情况。显著液体体重增加的标准定义为BW增加≥1.5 kg且BF%同时下降。共纳入74例HF患者。在平均20.8个月的随访期间,共评估了1588次就诊情况。50例患者共发生79次HF病情恶化事件,其中46次(58%)病情恶化有症状,33次(42%)无症状。仅基于BW标准(≥1.5 kg),新方法消除了73例(58%)HF病情恶化事件的假阳性指征,且未排除真正的HF病情恶化事件。该方法在诊断总体HF事件中的检测特征为灵敏度65.8%(95%置信区间[CI],54.3 - 76.1),特异度97.9%(95% CI,97.1 - 98.6),阳性预测值62.7%(95% CI,51.3 - 73.0),阴性预测值98.2%(95% CI,97.4 - 98.8)。临床前液体潴留常见于已确诊的HF患者,新型监测方法可特异性识别临床前HF病情恶化情况。

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