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DOI: 10.1055/s-0038-1665300
Rapid Quantitation of Plasma Heparin and Antithrombin III Levels for Cardiopulmonary Bypass Monitoring, Using Fluorometric Substrate Assays
Publication History
Received 14 February 1983
Accepted 26 August 1983
Publication Date:
18 July 2018 (online)
Summary
Plamsa heparin and AT III levels were determined using recently developed fluorometric substrate techniques on serial samples taken from 9 unselected patients undergoing open-heart surgery on cardiopulmonary bypass. The fluorometric assay for AT III and established clotting and immunological methods showed a highly significant correlation (p <0.001). Heparin recovery was reduced in all cases, and plasma levels (fluorometric assay) demonstrated poor correlation to Whole Blood Activated Clotting Time (Hemochron) estimations. AT III levels were dramatically reduced during bypass, and in 3 cases reached levels below 0.08 iu/ml. Heparin reversal schedules based upon empirical dosage led to excessive protamine administration by a mean factor of 3.3, as assessed by in vitro neutralization of standardized heparin concentrations.
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References
- 1 Bull BS, Huse WM, Brauer FS, Korpman RA. Heparin during extracorporeal circulation: II. The use of a dose-response curve to individualise heparin and protamine dosage. J Thorac Cardiovasc Surg 1975; 69: 685-689
- 2 Culliford AT, Sanford NG, Starr N, Thomas ST, Baumann FG, Wessler S, Spencer FC. Lack of correlation between activated clotting time and plasma heparin during cardiopulmonary bypass. Ann Surg 1981; 193: 105-111
- 3 Effeney DJ, Goldstone J, Chin D, Krupski WC, Ellis RJ. Intraoperative anticoagulation in carciovascular surgery. Surgery 1981; 90: 1068-1074
- 4 Bull BS, Korpman RA, Huse WM, Briggs BD. Heparin therapy during extracorporeal circulation: I. Problems inherent in existing heparin protocols. J Thorac Cardiovasc Surg 1975; 69: 674-684
- 5 Harker LA, Malpass TW, Branson HE, Hessel EA, Slichter SJ. Mechanism of abnormal bleeding in patients undergoing cardiopulmonary bypass: Acquired transient platelet dysfunction associated with selective α-granule release. Blood 1980; 56: 824-834
- 6 Austen DE G, Rhymes IL. A laboratory manual of blood coagulation. Oxford Blackwell; 1975. p 38
- 7 Hardisty RM, Ingram GI C. Bleeding disorders - Investigation and Management. Oxford Blackwell; 1965. pp 274-277
- 8 Biggs R. Human blood coagulation, haemostasis and thrombosis. Oxford Blackwell; 1972. p 320
- 9 Mitchell GA, Gargiulo RJ, Huseby RM, Lawson DE, Pochron SP, Sehuanes JA. Assay for plasma heparin using a synthetic peptide substrate for thrombin - Introduction of the fluophor aminoisopthalic acid: dimethyl ester. Thromb Res 1978; 13: 47-52
- 10 Mitchell GA, Hudson DM, Huseby RM, Pochron SP, Gargiulo RJ. Fluorescent substrate assay for antithrombin. Thromb Res 1978; 12: 219-225
- 11 The determination of antithrombin III in plasma. Sigma Technical Bulletin. Sigma Chemical Co.; USA: 1981. p 855
- 12 Laurell C-B. Quantitative estimation of proteins by electrophoresis in agarose gel containing antibodies. Anal Biochem 1966; 15: 45-52
- 13 Nadler SB, Hidalgo JU, Block T. Prediction of blood volume in normal human adults. Surgery 1962; 51: 224-232
- 14 Marciniak E. Thrombin-induced proteolysis of human antithrombin III: an outstanding contribution of heparin. Br J Haematol 1981; 48: 325-336
- 15 Kolkka R, Hilberman M. Neurological dysfunction following cardiac operations with low-flow, low pressure cardiopulmonary bypass. J Thorac Cardiovasc Surg 1980; 79: 432-437
- 16 Taylor KM, Devlin BJ, Mittra SM, Gillan JG, Brannan JJ, McKenna JM. Assessment of cerebral damage during open-heart surgery. A new experimental model Scand J Thorac Cardiovasc Surg 1980; 14: 197-203
- 17 Cees AM, Nijmeyer B, Roelofs JM, Sixma JJ. Kinetics of intravenously administered heparin in normal humans. Blood 1982; 60: 1251-1258