ESTABLISHING A THERAPEUTIC RANGE FOR HEPARIN-THERAPY

被引:263
作者
BRILLEDWARDS, P [1 ]
GINSBERG, JS [1 ]
JOHNSTON, M [1 ]
HIRSH, J [1 ]
机构
[1] HAMILTON CIVIC HOSP, RES CTR, HAMILTON, ON, CANADA
关键词
HEPARIN; PARTIAL THROMBOPLASTIN TIME; THROMBOEMBOLISM; DOSE-RESPONSE RELATIONSHIP; DRUG; ANTICOAGULANTS;
D O I
10.7326/0003-4819-119-2-199307150-00002
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Objective: To compare two methods of determining a therapeutic range of activated partial thromboplastin time (aPTT) results. Design: Cohort studies. Setting: Referral teaching hospital. Patients: Inpatients who received unfractionated heparin intravenously for venous thromboembolic disease. Measurements: A therapeutic range determined by aPTT ratios of 1.5 to 2.5 times the control value as compared with a therapeutic range determined by protamine titration heparin levels of 0.2 to 0.4 U/mL. Results: For all aPTT reagents studied, a ratio of 1.5 times the control value is much less than a minimum protamine titration heparin level of 0.2 U/mL. Various manufacturers' aPTT reagents and reagent lots from the same manufacturer show considerable variation in response to heparin and therefore have different therapeutic ranges. Conclusions: A different dose of heparin would be required to produce an aPTT ratio of 1.5 times the control value, depending on the reagent used. Establishing a therapeutic range for aPTT results using protamine titration heparin levels of 0.2 to 0.4 U/mL as a reference standard is practical and compensates for the variable response of aPTT reagents to heparin.
引用
收藏
页码:104 / 109
页数:6
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