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Noninvasive Hemodynamic Monitoring in Emergency Patients with Suspected Heart Failure, Sepsis and Stroke: The Premium Registry

机译:疑似心力衰竭,败血症和中风的急诊患者的无创血流动力学监测:Premium Registry

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Introduction: Noninvasive hemodynamic (HD) assessments in the emergency department (ED) might assist in the diagnosis, therapeutic plan development and risk stratification of acutely ill patients. This multinational observational study was designed to initiate noninvasive HD measurements prior to any ED patient therapeutic interventions and broadly evaluate them for potential diagnostic, therapeutic and predictive value. Methods: We enrolled patients with suspected acute heart failure (AHF), sepsis or stroke. Continuous noninvasive HD monitoring was begun using the Nexfin finger cuff device (Edwards LifeSciences, BMEYE, Amsterdam, Netherlands). Beat-to-beat HD measurements were averaged for the initial 15 minutes, prior to therapeutic intervention. We performed suspected disease group comparisons and evaluated HD predictors of 30-day mortality. Results: Of 510 patients enrolled: 185 (36%) AHF, 194 (38%) sepsis and 131 (26%) stroke. HD variables were significantly different (p<0.05) amongst the groups. Cardiac output and index and stroke volume index (SVI) were highest in sepsis (6.5, 3.5, 36), followed by stroke (5.5, 2.7, 35.8), and lowest in AHF (5.4, 2.7, 33.6). The in-group HD standard deviations and ranges measurements were large, indicating heterogeneous underlying HD profiles. Presenting SVI predicted 30-day mortality for all groups. Conclusion: Presenting ED noninvasive HD data has not been previously reported in any large patient population. Our data suggest a potential role for early noninvasive HD assessments aiding in diagnosing of patients, individualizing therapy based on each person’s unique HD values and predicting 30-day mortality. Further studies and analyses are needed to determine how HD assessments should be best used in the ED. [West J Emerg Med. 2014;15(7):-0.].
机译:简介:急诊科(ED)的无创血流动力学(HD)评估可能有助于急性病患者的诊断,治疗计划制定和风险分层。这项多国观察性研究旨在在进行任何ED患者治疗干预之前启动非侵入性HD测量,并广泛评估其潜在的诊断,治疗和预测价值。方法:我们招募了疑似急性心力衰竭(AHF),败血症或中风的患者。开始使用Nexfin指套设备(Edwards LifeSciences,BMEYE,阿姆斯特丹,荷兰)进行连续的无创高清监测。在治疗干预之前的最初15分钟内,逐次高清测量的平均值是平均的。我们进行了可疑疾病组比较,并评估了30天死亡率的高清预测因素。结果:在510名患者中,有185名(36%)AHF,194名(38%)败血症和131名(26%)中风。各组间HD变量差异显着(p <0.05)。脓毒症的心输出量和指数以及中风量指数(SVI)最高(6.5、3.5、36),其次是中风(5.5、2.7、35.8),而AHF最低(5.4、2.7、33.6)。组内高清标准偏差和范围测量值较大,表明基础高清配置文件不均。提出SVI预测所有组的30天死亡率。结论:以前在任何大型患者中均未报告过ED无创高清数据。我们的数据表明,早期无创HD评估可能有助于诊断患者,根据每个人的独特HD值进行个性化治疗并预测30天死亡率。需要进一步的研究和分析,以确定在ED中应如何最好地使用HD评估。 [西急救医学杂志。 2014; 15(7):-0。]。

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