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1.
J Cardiovasc Med (Hagerstown) ; 10(2): 135-42, 2009 Feb.
Article in English | MEDLINE | ID: mdl-19377380

ABSTRACT

OBJECTIVE: This prospective randomized study compares full and reduced heparinization on novel hyaluronan-based heparin-bonded circuits vs. uncoated controls under challenging clinical setting including biomaterial evaluation. METHODS: 100 patients undergoing reoperation for coronary artery bypass grafting were allocated into two equal groups (n = 50): Group one was treated with hyaluronan-based heparin bonded preconnected circuits (Vision HFOGBS, Gish, California, USA) and Group two with identical uncoated controls (Vision HFO, Gish, USA). In the study group, half of the patients (n = 25) received low-systemic heparin (125 IU/kg, ACT >250 s) or full dose like control group. Blood samples were collected after induction of anesthesia (T1) and heparin administration before cardiopulmonary bypass (CPB) (T2), 15 min after initiation of CPB (T3), before cessation of CPB (T4), 15 min after reversal with protamine (T5), and the first postoperative day at 08: 00 h (T6). RESULTS: Platelet counts were preserved significantly better at T5, T6 in hyaluronan groups (P < 0.05 vs. control). Serum IL-2 levels were significantly lower at T4, T5 in both hyaluronan groups and C3a levels at T4 and T5 only in low-dose group (P < 0.05). Troponin-T levels in coronary sinus blood demonstrated well preserved myocardium in hyaluronan groups. No significant differences in thrombin-antithrombin levels were observed between full and low-dose heparin groups at any time point. Amount of desorbed protein was 1.41 +/- 0.01 in full and 1.43 +/- 0.01 in low dose vs. 1.78 +/- 0.01 mg/dl in control (P < 0.05). CONCLUSION: Hyaluronan-based heparin-bonded circuits provided better clinical outcome and less inflammatory response compared with uncoated surfaces. Reduced systemic heparinization combined with hyaluronan-based heparin-bonded circuits is feasible and clinically well tolerated.


Subject(s)
Anticoagulants/administration & dosage , Cardiopulmonary Bypass/instrumentation , Coated Materials, Biocompatible , Coronary Artery Bypass , Heparin/administration & dosage , Hyaluronic Acid , Antithrombin III , Cardiopulmonary Bypass/adverse effects , Complement C3a/metabolism , Equipment Design , Feasibility Studies , Female , Heparin Antagonists/administration & dosage , Humans , Inflammation/blood , Inflammation/etiology , Inflammation/prevention & control , Interleukin-2/blood , Male , Materials Testing , Middle Aged , Peptide Hydrolases/blood , Platelet Count , Prospective Studies , Protamines/administration & dosage , Reoperation , Time Factors , Treatment Outcome , Troponin T/blood
2.
J Biomater Sci Polym Ed ; 14(6): 589-600, 2003.
Article in English | MEDLINE | ID: mdl-12901440

ABSTRACT

In this study, attachment and growth of Baby Hamster Kidney (BHK) cells on ethylene diamine (EDA)-plasma-treated poly(L-lactide/epsilon-caprolactone) biodegradable copolymer films were investigated. The co-polymer (Mw: 58000; Mn: 35000 and PI 1.60) was synthesised by ring-opening polymerization of the respective dimers with using stannous octoate as the catalyst. The final ratio of L-lactide to epsilon-caprolactone obtained by 1H-NMR was 87:13. The co-polymer films were treated with the EDA-plasma in a glow-discharge apparatus. The BHK-30 cell line was cultured on plain and EDA-plasma-treated films and their pre-wetted forms (with ethanol and/or cell culture medium before use). Cell attachment and growth were followed. Alkaline phosphatase (ALP) activity and glucose uptake in cell culture medium were also investigated. There was no attachment in the first 12 h. Glow-discharge treatment increased significantly the attachment and growth. Pre-wetting with ethanol and cell culture medium was also increase significantly both the attachment and growth.


Subject(s)
Biocompatible Materials/chemistry , Epithelial Cells/metabolism , Ethylenediamines/chemistry , Lactones/chemistry , Polyesters/chemistry , Polymers/chemistry , Alkaline Phosphatase/analysis , Animals , Biocompatible Materials/chemical synthesis , Cell Adhesion , Cell Division , Cell Line , Cricetinae , Culture Media , Ethanol/chemistry , Glucose/pharmacokinetics , Isoelectric Point , Kidney/cytology , Magnetic Resonance Spectroscopy , Membranes, Artificial , Molecular Weight , Polymers/chemical synthesis , Time Factors
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