Charach Gideon, Rubalsky Olga, Charach Lior, Rabinovich Alexander, Argov Ori, Rogowski Ori, George Jacob
Department of Internal Medicine "C", Tel Aviv Sourasky Medical Center, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel.
Department of Internal Medicine "C", Tel Aviv Sourasky Medical Center, affiliated to the Sackler Faculty of Medicine, Tel Aviv University, Tel Aviv, Israel; Cardiology Department Kaplan Medical Center, affiliated to Hebrew University Medical Center, Jerusalem, Israel.
PLoS One. 2015 Apr 28;10(4):e0122576. doi: 10.1371/journal.pone.0122576. eCollection 2014.
Measurement of internal thoracic impedance (ITI) is sensitive and accurate in detecting acute pulmonary edema even at its preclinical stage. We evaluated the suitability of the highly sensitive and noninvasive RS-207 monitor for detecting pleural effusion and for demonstrating increased ITI during its resolution. This prospective controlled study was performed in a single department of internal medicine of a university-affiliated hospital between 2012-2013. One-hundred patients aged 25–96 years were included, of whom 50 had bilateral or right pleural effusion of any etiology (study group) and 50 had no pleural effusion (controls). ITI, the main component of which is lung impedance, was continuously measured by the RS-207 monitor. The predictive value of ITI monitoring was determined by 8 measurements taken every 8 hours. Pleural effusion was diagnosed according to well-accepted clinical and roentgenological criteria. During treatment, the ITI of the study group increased from 32.9±4.2 ohm to 42.8±3.8 ohm (p<0.0001) compared to non-significant changes in the control group (59.6±6.6 ohm, p = 0.24). Prominent changes were observed in the respiratory rate of the study group: there was a decrease from 31.2±4.0 to 19.5±2.4 ohm (35.2%) compared to no change for the controls, and a mean increase from 83.6± 5.3%-92.5±1.6% (13.2%) in O2 saturation compared to 94.2±1.7% for the controls. Determination of ITI for the detection and monitoring of treatment of patients with pleural effusion enables earlier diagnosis and more effective therapy, and can prevent hospitalization and serious complications, such as respiratory distress, and the need for mechanical ventilation.
The study is registered at ClinicalTrials.gov NCT01601444.
测量胸廓内阻抗(ITI)对于检测急性肺水肿甚至在其临床前期阶段都具有敏感性和准确性。我们评估了高度敏感且无创的RS - 207监测仪在检测胸腔积液以及在其消退过程中显示ITI增加方面的适用性。这项前瞻性对照研究于2012 - 2013年在一家大学附属医院的单一内科进行。纳入了100名年龄在25 - 96岁的患者,其中50名患有任何病因引起的双侧或右侧胸腔积液(研究组),50名没有胸腔积液(对照组)。ITI的主要成分是肺阻抗,通过RS - 207监测仪持续测量。ITI监测的预测价值通过每8小时进行8次测量来确定。胸腔积液根据公认的临床和放射学标准进行诊断。在治疗期间,研究组的ITI从32.9±4.2欧姆增加到42.8±3.8欧姆(p<0.0001),而对照组无显著变化(59.6±6.6欧姆,p = 0.24)。研究组的呼吸频率有显著变化:从31.2±4.0降至19.5±2.4(下降35.2%),而对照组无变化,氧饱和度平均从83.6±5.3%增加到92.5±1.6%(增加13.2%),而对照组为94.2±1.7%。测定ITI用于检测和监测胸腔积液患者的治疗能够实现更早的诊断和更有效的治疗,并可预防住院以及严重并发症,如呼吸窘迫和机械通气的需求。
该研究已在ClinicalTrials.gov注册,注册号为NCT01601444。