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纸质出版:2013
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孙国林,李生德,齐萍,文仁国,肖颖彬.婴幼儿体外循环期间氨甲环酸血液浓度研究[J].陆军军医大学学报(原第三军医大学学报),2013,35(01):69-72.
Sun Guolin,Li Shengde,Qi Ping,Wen Renguo,Xiao Yingbin.Study of plasma concentration of tranexamic acid during cardiopulmonary bypass in infants with tetralogy of Fallot[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(01):69-72.
孙国林,李生德,齐萍,文仁国,肖颖彬.婴幼儿体外循环期间氨甲环酸血液浓度研究[J].陆军军医大学学报(原第三军医大学学报),2013,35(01):69-72. DOI:
Sun Guolin,Li Shengde,Qi Ping,Wen Renguo,Xiao Yingbin.Study of plasma concentration of tranexamic acid during cardiopulmonary bypass in infants with tetralogy of Fallot[J].J Amry Med Univ (J Third Mil Med Univ),2013,35(01):69-72. DOI:
目的 研究婴幼儿法洛四联症(tetralogy of fallot
TOF)根治术体外循环(cardiopulmonary bypaass
CPB)期间应用氨甲环酸(tranexamic acid,TA)的血液浓度。 方法 5例先天性TOF患儿,体质量(7.36±2.08)kg,在开胸前应用TA 100 mg/kg,单次静脉缓慢注射(10 min),CPB开始前再次注射100 mg/kg。应用磁共振波谱仪(
1
H-NMR)方法,检测不同时间段TA的血液浓度。 结果 CPB开始前(负荷剂量用药后约20 min)、CPB开始后1 h、手术结束时的血液TA浓度分别为(224.61±195.28)、(509.58±181.57)、(243.95±32.30)μg/mL。CPB开始前与CPB开始后1 h及手术结束时TA浓度比较均无统计学差异(P=0.052、0.83);CPB开始后1 h与手术结束时TA浓度有统计学差异(P=0.02)。 结论
1
H-NMR能够检测出TA的血液浓度。TA大于抑制有高度出血风险可能需要的血液浓度125 μg/mL时,提示可降低剂量。
Objective To study the plasma concentration of tranexamic acid (TA) during cardiopulmonary bypass in infants with tetralogy of Fallot (TOF). Methods Five TOF infants with body weight of (7.36±2.08) kg were given an slow intravenous injection of initial dose of TA (100 mg/kg
10 min) before thoracotomy
following by another 100 mg/kg TA before the initiation of cardiopulmonary bypass (CPB). The concentration of TA was measured in blood plasma using
1
H-NMR spectroscopy. Results Plasma TA concentration
s were (224.61±195.28) μg/mL before CPB (at 20 min after TA administration)
(509.58±181.57) μg/mL at 60 min after CPB initiation
and (243.95±32.30) μg/mL at the end of operation
respectively. The plasma TA concentration before CPB was not significantly different from that at 60 min after CPB initiation (P=0.052) and that at the end of operation (P=0.83)
but there was significant difference between plasma TA concentration at 60 min after CPB initiation and that at the end of operation (P=0.02). Conclusion A 100 mg/kg initial dose of TA followed by an infusion of 100 mg/kg before the initiation of CPB is sufficient enough to provide an effective plasma concentration
which is higher than 125 μg/mL for patients with high risk of bleeding
indicating the dose of TA can be decreased.
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