Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Division of Cardiology, Department of Medicine, Johns Hopkins University School of Medicine, Baltimore, Maryland.
Am J Cardiol. 2020 Mar 15;125(6):916-923. doi: 10.1016/j.amjcard.2019.12.027. Epub 2019 Dec 27.
The pulse amplitude ratio (PAR), the ratio of pulse pressure at the end of the Valsalva maneuver to before the onset, correlates with cardiac filling pressure. We have developed a handheld device that uses finger photoplethysmography to measure PAR and estimate left ventricular end diastolic pressure (LVEDP). Patients hospitalized with heart failure (HF) performed three 10-second trials of a standardized Valsalva maneuver (at 20 mm Hg measured via pressure transducer), while photoplethysmography waveforms were recorded, at admission and discharge. Combined primary outcome was 30-day HF hospitalization, intravenous diuresis, or death. Fifty-two subjects had discharge PAR testing; 12 met the primary outcome. Median PAR on admission was 0.55 (interquartile range: 0.40 to 0.70, n = 48) and on discharge was 0.50 (interquartile range: 0.36 to 0.69). Mean PAR-estimated LVEDP was significantly higher in subjects that had an event (20.2 vs 16.9 mm Hg, p = 0.043). Subjects with PAR-estimated LVEDP >19.5 mm Hg had an event rate hazard ratio of 4.57 (95% confidence interval 1.37, 15.19, p = 0.013) compared with patients with LVEDP 19.5 mm Hg or below, with significantly lower 30-day event-free survival (log-rank p = 0.006). In conclusion, noninvasively estimated LVEDP using the pulse amplitude response to a Valsalva maneuver in patients hospitalized for HF changes with diuresis and identifies patients at high risk for 30-day HF events. Detection of elevated filling pressures before hospital discharge may be useful in guiding HF management to reduce HF events.
脉压幅度比(PAR),即瓦尔萨尔瓦动作结束时的脉压与开始时的脉压之比,与心脏充盈压相关。我们开发了一种手持式设备,它使用手指光体积描记法来测量 PAR 并估计左心室舒张末期压(LVEDP)。因心力衰竭(HF)住院的患者进行了三次 10 秒的标准化瓦尔萨尔瓦动作试验(通过压力传感器测量 20mmHg),同时记录光体积描记波,在入院时和出院时。联合主要结局为 30 天 HF 住院、静脉利尿剂治疗或死亡。52 名患者出院时进行了 PAR 检测;12 名患者符合主要结局。入院时 PAR 的中位数为 0.55(四分位距:0.40 至 0.70,n=48),出院时为 0.50(四分位距:0.36 至 0.69)。发生事件的患者 PAR 估计的 LVEDP 显著更高(20.2 与 16.9mmHg,p=0.043)。PAR 估计的 LVEDP >19.5mmHg 的患者事件发生率风险比为 4.57(95%置信区间:1.37,15.19,p=0.013),与 LVEDP 19.5mmHg 或以下的患者相比,30 天无事件生存率显著降低(对数秩检验,p=0.006)。总之,HF 住院患者使用瓦尔萨尔瓦动作的脉搏幅度反应无创估计 LVEDP 随利尿剂而变化,并确定了 30 天 HF 事件风险较高的患者。在出院前检测到升高的充盈压可能有助于指导 HF 管理以减少 HF 事件。