Preservation of myocardial functions by pentoxyphylline cardioplegia during and after cardiopulmonary bypass

Citation
At. Ulus et al., Preservation of myocardial functions by pentoxyphylline cardioplegia during and after cardiopulmonary bypass, PANMIN MED, 42(4), 2000, pp. 253-256
Citations number
15
Categorie Soggetti
General & Internal Medicine
Journal title
PANMINERVA MEDICA
ISSN journal
00310808 → ACNP
Volume
42
Issue
4
Year of publication
2000
Pages
253 - 256
Database
ISI
SICI code
0031-0808(200012)42:4<253:POMFBP>2.0.ZU;2-5
Abstract
Background. The aim of the presented study was to evaluate the preservation effect of the pentoxyphylline-blood cardioplegia on myocardial functions d uring and after the cardiopulmonary bypass in an experimental dog model. Methods. Central hemodynamics and metabolic variables such as creatine phos phokinase, myocardial oxygen extraction and myocardial lactate extraction w ere obtained during and following 4 hours after the cardiopulmonary bypass after the baseline scores were recorded. Twelve mongrel dogs were divided i nto two equal groups. The first group of animals served as controls. The se cond group of animals was treated with pentoxyphylline cardioplegia that wa s added to each blood cardioplegia as 15 mg/100 ml, Results. After bypass, the hemodynamic parameters were better in the pentox yphylline group. Cardiac index fell in all animals, but it was significantl y less in the control group. Pulmonary capillary wedge pressure was lower i n the pentoxyphylline group as an index of better preservation of ventricul ar filling pressure. CPK-MB was significantly higher in the control group b oth at 2 and 4 hours after the bypass. It was 79+/-13 iu/L in the control g roup and 41+/-9 iu/L in the pentoxyphylline group 4 hours after cardiopulmo nary bypass. MLE was also higher both on bypass and following bypass in the control group. Conclusions, In conclusion, pentoxyphylline usage may reduce the risks of i schemic-reperfusion injury during and following cardiopulmonary bypass and aortic cross-damping. It can be an administered drug during cardioplegia.