1. Impact of prosthesis-patient mismatch on early haemodynamic status after aortic valve replacement
- Author
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Hélène Petit-Eisenmann, Stéphanie Perrier, Tam Hoang Minh, Jonathan Bentz, Mircea Cristinar, Michel Kindo, Gharib Ajob, Olivier Collange, and Jean-Philippe Mazzucotelli
- Subjects
Pulmonary and Respiratory Medicine ,Male ,medicine.medical_specialty ,Mean arterial pressure ,Time Factors ,Hemodynamics ,030204 cardiovascular system & hematology ,03 medical and health sciences ,Coronary artery bypass surgery ,0302 clinical medicine ,Aortic valve replacement ,Internal medicine ,Prosthesis Fitting ,Troponin I ,Natriuretic Peptide, Brain ,medicine ,Humans ,Prospective Studies ,Coronary Artery Bypass ,Aged ,Heart Valve Prosthesis Implantation ,business.industry ,Central venous pressure ,Aortic Valve Stenosis ,Middle Aged ,medicine.disease ,Brain natriuretic peptide ,Treatment Outcome ,030228 respiratory system ,Aortic valve stenosis ,Heart Valve Prosthesis ,Cardiology ,Surgery ,Female ,Cardiology and Cardiovascular Medicine ,business - Abstract
Objectives Prosthesis-patient mismatch (PPM) has been reported to impact early haemodynamic status and early mortality after prosthetic aortic valve replacement (AVR) in patients with aortic stenosis (AS). The aim of this study was to assess the impact of PMM on early haemodynamic status after AVR using vasoactive-inotropic dependency index (VDI), postoperative pressures and end-organ perfusion. Methods A total of 183 patients with AS were included in this prospective cohort study, and underwent elective AVR with or without combined coronary artery bypass graft surgery. PPM was defined as a projected indexed effective orifice area of ≤0.85 cm2/m2, and was present in 27.9% of the patients. The primary end-point was the VDI [VDI = vasoactive-inotropic score/mean arterial pressure] measured upon admission to the intensive care unit (POD0) and on the morning of the first postoperative day (POD1). The secondary end-points were the following: mean left atrial pressure, mean central venous pressure, fluid balance, brain natriuretic peptide, troponin I, glomerular filtration rate and lactate levels on POD0 and POD1. Results No significant differences in VDI were observed between the no PPM and PPM groups on POD0 (0.08 ± 0.48 vs 0.05 ± 0.13, respectively, P = 0.622) or on POD1 (0.09 ± 0.40 vs 0.06 ± 0.13, respectively; P = 0.583). The mean arterial pressure, mean left atrial pressure, central venous pressure, troponin I, glomerular filtration rate and lactate levels did not differ between the two groups on POD0 and POD1, as well as fluid balance and brain natriuretic peptide on POD1. Conclusions PPM is not associated with early haemodynamic status impairment and end-organ perfusion after AVR. Clinical trial number ClinicalTrials.gov number, NCT00699673.
- Published
- 2016