|
|
||||||||
The Journal of Thoracic and Cardiovascular Surgery, Vol 87, 678-686, Copyright © 1984 by The American Association for Thoracic Surgery and The Western Thoracic Surgical Association
HJ Stefaniszyn, RJ Novick and TA Salerno
Hemodynamic changes have been documented during protamine infusion into
heparinized but not unheparinized pigs and suggest that a protamine-
heparin interaction might be responsible. This hypothesis was tested in
four groups of pigs by varying the dosage and order of administration of
these two drugs: Group I (n = 9) received heparin (3 mg/kg) followed by
protamine (3 mg/kg); Group II (n = 9) received protamine (3 mg/kg) followed
by heparin (3 mg/kg); Group III (n = 9) received protamine (25 mg/kg)
followed by heparin (3 mg/kg); and Group IV (n = 16) received
protamine-heparin complex (protamine 3 mg/kg and heparin 3 mg/kg mixed
immediately prior to injection). Systemic and pulmonary arterial pressures,
systemic and pulmonary vascular resistances, left ventricular end-diastolic
pressure, central venous pressure, cardiac output, and heart rate were
measured before and at 1.0, 2.5, 5.0, and 15 minutes after protamine,
heparin, or protamine-heparin complex infusions. Immediately following
protamine infusion, Group I pigs exhibited transiently but significantly
increased pulmonary artery pressure, pulmonary vascular resistance,
systemic vascular resistance, and central venous pressure and decreased
cardiac output with (Group Ib, n = 5) or without (Group Ia, n = 4) systemic
hypotension. The fact that no hemodynamic changes occurred in Group II
confirms that infusion of clinical doses of protamine produces no
hemodynamic changes in unheparinized pigs. Protamine alone in high doses
(Group III) produced hemodynamic changes similar to clinical-dose protamine
reversal of heparin (Group I). This effect suggests that the presence of
heparin in the circulation lowers the threshold for protamine-mediated
hemodynamic responses. Infusion of heparin (3 mg/kg) into pigs 15 minutes
after treatment with high (25 mg/kg) (Group III) but not clinical (3 mg/kg)
(Group II) doses of protamine produced hemodynamic effects similar to
clinical-dose protamine reversal of heparin (Group I), suggesting that a
protamine-heparin interaction may be responsible. These results also
suggest a rapid inactivation in vivo of clinical doses (3 mg/kg) (Group II)
of infused protamine. Protamine-heparin complex formed in vitro (Group IV)
also produced hemodynamic changes similar to clinical-dose protamine
reversal of heparin (Group I), suggesting that formation of this complex in
vivo may be the protamine-heparin interaction responsible.
Protamine-heparin complex may well be a useful tool in further elucidating
the full effects of protamine reversal of heparin.
ARTICLES
Toward a better understanding of the hemodynamic effects of protamine and heparin interaction
This article has been cited by other articles:
![]() |
P. Kesteven Haemostatic changes during cardiopulmonary bypass Perfusion, January 1, 1990; 5(1_suppl): 9 - 19. [PDF] |
||||
![]() |
C. Aren Review article : Heparin and protamine during cardiac surgery Perfusion, July 1, 1989; 4(3): 171 - 181. [PDF] |
||||
| HOME | HELP | FEEDBACK | SUBSCRIPTIONS | ARCHIVE | SEARCH | TABLE OF CONTENTS |
| ANN THORAC SURG | ASIAN CARDIOVASC THORAC ANN | EUR J CARDIOTHORAC SURG |
| J THORAC CARDIOVASC SURG | ICVTS | ALL CTSNet JOURNALS |