Abraham William T, Compton Steven, Haas Garrie, Foreman Blair, Canby Robert C, Fishel Robert, McRae Scott, Toledo Gloria B, Sarkar Shantanu, Hettrick Douglas A
Division of Cardiovascular Medicine, Ohio State University, 473 West 12th Avenue, Columbus, OH 43210-1252, USA.
Congest Heart Fail. 2011 Mar-Apr;17(2):51-5. doi: 10.1111/j.1751-7133.2011.00220.x. Epub 2011 Mar 21.
The relative sensitivity and unexplained detection rate of changes in intrathoracic impedance has not been compared with standard heart failure (HF) monitoring using daily weight changes. The Fluid Accumulation Status Trial (FAST) prospectively followed 156 HF patients with implanted cardioverter-defibrillator or cardiac resynchronization therapy defibrillator devices modified to record daily changes in intrathoracic impedance in a blinded fashion for 537±312 days. Daily impedance changes were used to calculate a fluid index that could be compared with a prespecified threshold. True positives were defined as adjudicated episodes of worsening HF occurring within 30 days of a fluid index above threshold or an acute weight gain. Unexplained detections were defined as threshold crossings or acute weight gains not associated with worsening HF. Impedance measurements were performed on >99% of follow-up days, compared with only 76% of days for weight measurements. Sixty-five HF events occurred during follow-up (0.32/patient-year). Forty HF events were detected by impedance but not weight, whereas 5 were detected by weight but not impedance. Sensitivity was greater (76% vs 23%; P<.0001) and unexplained detection rate was lower (1.9 vs 4.3/patient-year; P<.0001) for intrathoracic impedance monitoring at the threshold of 60Ω days compared with acute weight increases of 3 lbs in 1 day or 5 lbs in 3 days and also over a wide range of fluid index and weight thresholds. The sensitivity and unexplained detection rate of intrathoracic impedance monitoring was superior to that seen for acute weight changes. Intrathoracic impedance monitoring represents a useful adjunctive clinical tool for managing HF in patients with implanted devices.
尚未将胸内阻抗变化的相对敏感性和无法解释的检测率与使用每日体重变化的标准心力衰竭(HF)监测进行比较。液体蓄积状态试验(FAST)前瞻性地跟踪了156例植入心脏复律除颤器或心脏再同步治疗除颤器装置的HF患者,这些装置经过改良,以盲法记录537±312天内的每日胸内阻抗变化。每日阻抗变化用于计算一个可与预先设定阈值进行比较的液体指数。真阳性定义为在液体指数高于阈值或急性体重增加后30天内判定的HF恶化发作。无法解释的检测定义为与HF恶化无关的阈值跨越或急性体重增加。在超过99%的随访日进行了阻抗测量,而体重测量仅在76%的日子进行。随访期间发生了65例HF事件(0.32/患者-年)。40例HF事件通过阻抗检测到但未通过体重检测到,而5例通过体重检测到但未通过阻抗检测到。与1天内急性体重增加3磅或3天内急性体重增加5磅以及在广泛的液体指数和体重阈值范围内相比,在60Ω日的阈值下,胸内阻抗监测的敏感性更高(76%对23%;P<0.0001),无法解释的检测率更低(1.9对4.3/患者-年;P<0.0001)。胸内阻抗监测的敏感性和无法解释的检测率优于急性体重变化。胸内阻抗监测是管理植入装置患者HF的一种有用的辅助临床工具。