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논문 기본 정보

자료유형
학술저널
저자정보
변정현 (경상대학교병원) 장인석 (경상대학교) 김종우 (경상대학교) 고은하 (경상대학교)
저널정보
대한혈액학회 Blood Research Blood Research Vol.51 No.3
발행연도
2016.1
수록면
171 - 174 (4page)

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BackgroundUnfractionated heparin (UFH) has unstable pharmacokinetics and requires close monitoring. The activated partial thromboplastin time (aPTT) test has been used to mon-itor UFH therapy for decades in Korea, but its results can be affected by numerous variables. We established an aPTT heparin therapeutic range (HTR) corresponding to ther-apeutic anti-Xa levels for continuous intravenous UFH administration, and used appro-priate monitoring to determine if an adequate dose of UFH was applied.MethodsA total of 134 ex vivo samples were obtained from 71 patients with a variety of thromboembolisms. All patients received intravenous UFH therapy and were enrolled from June to September 2015 at Gyeongsang National University Hospital. All laboratory protocols were in accordance with the Clinical and Laboratory Standards Institute guide-lines and the College of American Pathologist requirements for aPTT HTR. ResultsAn aPTT range of 87.1 sec to 128.7 sec corresponded to anti-Xa levels of 0.3 IU/mL to 0.7 IU/mL for HTR under our laboratory conditions. Based on their anti-Xa levels, blood specimen distribution were as follows: less than 0.3 IU/mL, 65.7%; 0.3‒0.7 IU/mL (ther-apeutic range), 33.6%; and more than 0.7 IU/mL, 0.7%. No evidence of recurring throm-boembolism was observed. ConclusionUsing the conventional aPTT target range may lead to inappropriate dosing of UFH. Transitioning from the aPTT test to the anti-Xa assay is required to avoid the laborious validation of the aPTT HTR test, even though the anti-Xa assay is more expensive.

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