The aim of the study is to determine whether cardiac output measurements obtained using APCO are comparable with those obtained using intermitted thermodilution cardiac output in critical ill patients.
ID
Bron
Aandoening
Septic Shock or dynamic hemodynamic profiles
Ondersteuning
Onderzoeksproduct en/of interventie
Uitkomstmaten
Primaire uitkomstmaten
1. Bias, percision, limits of agreement;<br>
2. Percentage of error, Bland altman plot.<br>
Grouped measurements of cardiac output derived from PAC and waveform analysis are performed in triplets, and averaged. Before and after therapeutic interventions in ICU, before and after fluid challenge, before and after changing inotropes, like vasodialition drugs.
Achtergrond van het onderzoek
During the progress of organ failure in critical ill patients often it is unclear whether the patient is adequately fluid resuscitated. To facilitate optimal fluid resuscitation cardiac output is measured by either using an invasive pulmonary artery catheter or a less invasive device. A new minimal invasive technique has become available. Cardiac output measured by arterial pressure waveform (APCO) analysis without manual calibration, the FloTrac/VigileoTM system Edwards Lifesciences. Since its launch there have been three software updates. The cardiac output derived from the arterial waveform analysis of the two latest versions showed good agreements when compared to pulmonary artery catheter under stable haemodynamic conditions [1,2]. In septic shock the bias has been improved with introduction of the 1.10 version of the software (unpublished data). Only recently the newest software version has been released (3.02).
The aim of the study is to determine whether cardiac output measurements obtained using APCO are comparable with those obtained using intermitted thermodilution cardiac output in critical ill patients.
Doel van het onderzoek
The aim of the study is to determine whether cardiac output measurements obtained using APCO are comparable with those obtained using intermitted thermodilution cardiac output in critical ill patients.
Onderzoeksopzet
Power analysis after 8 patients.
Onderzoeksproduct en/of interventie
N/A
Algemeen / deelnemers
Department of Anesthesiology
Marcel A Leeuw, de
Koningin Julianaplein 58
Zaanstad 1502 DV
The Netherlands
+ 31 75-6425529
ma.deleeuw@planet.nl
Wetenschappers
Department of Anesthesiology
Marcel A Leeuw, de
Koningin Julianaplein 58
Zaanstad 1502 DV
The Netherlands
+ 31 75-6425529
ma.deleeuw@planet.nl
Belangrijkste voorwaarden om deel te mogen nemen (Inclusiecriteria)
1. Sinus Rhythm;
2. Septic Shock;
3. Inotropic support including Noradrenalin;
4. PA Catheter;
5. Informed consent.
Belangrijkste redenen om niet deel te kunnen nemen (Exclusiecriteria)
1. Non sinus rhythm;
2. No informed consent.
Opzet
Deelname
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