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Document Details :

Title: Effect of haematocrit on pump and kidney dysfunction after myocardial revascularization
Author(s): F.P. Taniguchi , A.S. Martins
Journal: Acta Cardiologica
Volume: 64    Issue: 1   Date: 2009   
Pages: 41-45
DOI: 10.2143/AC.64.1.2034360

Abstract :
Objective — Kidney dysfunction is a common complication after cardiac surgery. It occurs in 7 to 31% of the patients. The lowest haematocrit after cardiopulmonary bypass surgery (LHCT) has been identified as a risk factor for kidney dysfunction after cardiac surgery. The aim of this study is to determine whether different levels of haematocrit during cardiopulmonary bypass surgery are related to kidney dysfunction.
Methods and results — A prospective study was conducted on consecutive adult patients undergoing myocardial revascularization. Preoperative renal function was assessed by baseline serum creatinine level (CrPre). Peak postoperative creatinine (CrPost) was defined as the highest daily in-hospital postoperative value. Peak fractional change in creatinine (%ΔCr) was defined as the difference between the CrPre and CrePost represented as a percentage of the preoperative value. The LHTC was defined as the lowest recorded haematocrit prior to weaning from the initial pump run. A category variable was created for haematocrit based on the distribution of values. The category variable had the following cut-off points: less than 23%, 23.1 to 28% and greater than 28.1%. Lowest haematocrit (26.62 ± 4.15%), CPB (74.71 ± 24.90 min), CrPre (1.23 ± 0.37 mg/dl) and highest CrPost (1.52 ± 0.47 mg/dl) data varied in near-normal fashion. Statistical significance has been observed in the < 23% lowest haematocrit group (Cr1POD and Cr5POD; P = 0.006) and the 23.1-28% lowest haematocrit level group (CrPre and Cr2POD; P = 0.047). CrPre and Cr5POD did not differ between groups (P > 0.05). The multiple linear regression model confirmed that the determinants for higher %ΔCr were age, body surface area and preoperative serum creatinine level.
Conclusion — The LHTC was not identified as a risk factor for kidney dysfunction after myocardial revascularization.