Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Protamine titration to optimize heparin antagonization after cardiopulmonary bypass

View through CrossRef
Objectives To optimize protamine titration for heparin antagonization after weaning from cardiopulmonary bypass (CPB). Design A prospective, observational trial. Setting Single-center, non-university teaching hospital. Participants Forty patients presenting for elective on-pump coronary artery bypass grafting with or without single valve surgery. Interventions At the end of CPB, the residual amount of heparin in the patient was estimated using a Bull-curve. The total protamine dose was calculated as 1 unit of protamine for 1 unit of heparin. Protamine was administered as 5 aliquots containing 20% of the total protamine dose each, with 2-min intervals. Measurements and main results Activated Clotting Time (ACT) values were measured 2 min after administration of each aliquot. ROTEM(®)-analysis was performed after the full dose of protamine had been administered. After 60% of the total protamine dose had been administered, ACT values were normalized in 86.5% of patients. After the complete dose of protamine had been administered, 61.1% of patients displayed signs of protamine overdose on ROTEM(®)-analysis. Conclusions In patients who present for on-pump coronary artery bypass grafting with or without single valve surgery, a 0.6-to-1 ratio of protamine-to-heparin to antagonize heparin may be sufficient and beneficial for patients.
Title: Protamine titration to optimize heparin antagonization after cardiopulmonary bypass
Description:
Objectives To optimize protamine titration for heparin antagonization after weaning from cardiopulmonary bypass (CPB).
Design A prospective, observational trial.
Setting Single-center, non-university teaching hospital.
Participants Forty patients presenting for elective on-pump coronary artery bypass grafting with or without single valve surgery.
Interventions At the end of CPB, the residual amount of heparin in the patient was estimated using a Bull-curve.
The total protamine dose was calculated as 1 unit of protamine for 1 unit of heparin.
Protamine was administered as 5 aliquots containing 20% of the total protamine dose each, with 2-min intervals.
Measurements and main results Activated Clotting Time (ACT) values were measured 2 min after administration of each aliquot.
ROTEM(®)-analysis was performed after the full dose of protamine had been administered.
After 60% of the total protamine dose had been administered, ACT values were normalized in 86.
5% of patients.
After the complete dose of protamine had been administered, 61.
1% of patients displayed signs of protamine overdose on ROTEM(®)-analysis.
Conclusions In patients who present for on-pump coronary artery bypass grafting with or without single valve surgery, a 0.
6-to-1 ratio of protamine-to-heparin to antagonize heparin may be sufficient and beneficial for patients.

Related Results

Impact of Common Anticoagulants on Complete Blood Count Parameters Among Humans
Impact of Common Anticoagulants on Complete Blood Count Parameters Among Humans
Abstract Introduction Among the most frequently used anticoagulants in hematological testing are tetra-acetic acid (EDTA), sodium citrate, and sodium heparin. However, there is a n...
Heparin-protamine management: a comparison study of three different heparin-protamine management protocols
Heparin-protamine management: a comparison study of three different heparin-protamine management protocols
In a prospective randomized open study, 180 patients underwent open-heart surgery using cardiopulmonary bypass (CPB) and were divided into three different heparin-protamine managem...
Novel ELISA-Based Assay for Detection of Complement Activation By PF4/Heparin Complexes
Novel ELISA-Based Assay for Detection of Complement Activation By PF4/Heparin Complexes
Abstract The immune response to platelet factor 4 (PF4)/heparin complexes is a frequent iatrogenic complication of heparin therapy associated with development of hep...
Protamine inhibits platelet derived growth factor receptor activity but not epidermal growth factor activity
Protamine inhibits platelet derived growth factor receptor activity but not epidermal growth factor activity
AbstractProtamine sulfate blocked 125I‐PDGF binding to its specific physiological receptor on Swiss mouse 3T3 cells. Reduced 125I‐PDGF binding in the presence of protamine sulfate ...
HEPARIN BINDING TO HUMAN MONOCYTES: MODULATION BY HISTIDINE-RICH GLYCOPROTEIN
HEPARIN BINDING TO HUMAN MONOCYTES: MODULATION BY HISTIDINE-RICH GLYCOPROTEIN
Heparin and its related glycosaminoglycans interact with a variety of cell types and, irrespective of their anticoagulant activities, have a complex and biologically important infl...
KINETICS OF LOW MOLECULAR WEIGHT HEPARIN IN MAN DETERMINED BY PROTAMINE CHLORIDE
KINETICS OF LOW MOLECULAR WEIGHT HEPARIN IN MAN DETERMINED BY PROTAMINE CHLORIDE
Low molecular weight (LMW) heparin is characterized by a higher affinity to antithrombin HI, less inhibition of thrombin and increased inhibition of factor Xa. The half life of the...

Back to Top