PURPOSE: To assess the use and validity of a mean systemic filling pressure analogue (Pmsa) in the closed-loop control of fluid replacement in continuous hemodiafiltration. METHODS: Cardiovascular variables were computer acquired from bedside monitor. Pmsa was calculated and compared with a target value. Gravitational fluid replacement to the extracorporeal hemodiafiltration circuit was regulated with a computer-controlled clamp. RESULTS: Ten patients (mean acute physiology and chronic health evaluation II score, 29.7; range, 21-33) received continuous venovenous hemodiafiltration for acute renal failure. Fluid replacement therapy was closed loop controlled to a target Pmsa for a total of 601 hours. During this period, 417 L of ultradiafiltrate were lost, and 409 L of replacement and nutritional fluids were administered. Despite such large fluid shifts, measured hemodynamic variables were kept within a narrow range (hour to hour variability: right atrial pressure, 1 +/- 0.1 mm Hg; mean arterial pressure 5.9 +/- 0.5 mm Hg; cardiac index, 0.44 +/- 0.05 L/m2/min). No complications of the technique occurred. CONCLUSIONS: The stability of cardiovascular variables achieved during Pmsa-based fluid replacement of critically ill patients with major fluid losses supports the validity of the use of the Pmsa as a measure of intravascular volume status. Such an analogue may be useful in nondialytic environments. The use of Pmsa as the basis for automated fluid replacement was safe.
PURPOSE: To assess the use and validity of a mean systemic filling pressure analogue (Pmsa) in the closed-loop control of fluid replacement in continuous hemodiafiltration. METHODS: Cardiovascular variables were computer acquired from bedside monitor. Pmsa was calculated and compared with a target value. Gravitational fluid replacement to the extracorporeal hemodiafiltration circuit was regulated with a computer-controlled clamp. RESULTS: Ten patients (mean acute physiology and chronic health evaluation II score, 29.7; range, 21-33) received continuous venovenous hemodiafiltration for acute renal failure. Fluid replacement therapy was closed loop controlled to a target Pmsa for a total of 601 hours. During this period, 417 L of ultradiafiltrate were lost, and 409 L of replacement and nutritional fluids were administered. Despite such large fluid shifts, measured hemodynamic variables were kept within a narrow range (hour to hour variability: right atrial pressure, 1 +/- 0.1 mm Hg; mean arterial pressure 5.9 +/- 0.5 mm Hg; cardiac index, 0.44 +/- 0.05 L/m2/min). No complications of the technique occurred. CONCLUSIONS: The stability of cardiovascular variables achieved during Pmsa-based fluid replacement of critically illpatients with major fluid losses supports the validity of the use of the Pmsa as a measure of intravascular volume status. Such an analogue may be useful in nondialytic environments. The use of Pmsa as the basis for automated fluid replacement was safe.
Authors: Maurizio Cecconi; Hollmann D Aya; Martin Geisen; Claudia Ebm; Nick Fletcher; R Michael Grounds; Andrew Rhodes Journal: Intensive Care Med Date: 2013-05-08 Impact factor: 17.440
Authors: Kapil Gupta; Soren Sondergaard; Geoffrey Parkin; Mark Leaning; Anders Aneman Journal: Intensive Care Med Date: 2015-01-08 Impact factor: 17.440
Authors: Marije Wijnberge; Daniko P Sindhunata; Michael R Pinsky; Alexander P Vlaar; Else Ouweneel; Jos R Jansen; Denise P Veelo; Bart F Geerts Journal: Ann Intensive Care Date: 2018-06-20 Impact factor: 6.925
Authors: Jacinta J Maas; Michael R Pinsky; Bart F Geerts; Rob B de Wilde; Jos R Jansen Journal: Intensive Care Med Date: 2012-05-15 Impact factor: 17.440