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[基于血管外科患者实例的肝素长期静脉给药剂量]

[Heparin dosage in long-term intravenous administration based on the example of vascular surgery patients].

作者信息

Braun V, Homann B, Sperling M

出版信息

Anaesthesist. 1986 May;35(5):291-8.

PMID:3740376
Abstract

For prophylaxis of deep-vein thrombosis, 23 male and 7 female patients received intravenous 15 000 IE/24 h sodium-heparin continuously after different operations for blood-vessel surgery. The plasma heparin concentration was measured with chromogenic substrate at 0, 1, 2, 4, 8 and 12-18 hours after beginning of heparin application. Each patient's hematocrit, sex, height, weight and parameters of liver and renal function were measured at the same time. The aim of this investigation was to find a general model for intravenous heparin application which would allow the best individual therapeutic plasma heparin concentration to be obtained. At the latest eight hours after the beginning of heparin-infusion the steady state of plasma heparin concentration was reached in 100%, but only in 56.67% it equalled the therapeutical factor Xa inhibition-level of 0.10 IE/ml to 0.20 IE/ml (= 0.077 USP-E/ml to 0.154 USP-E/ml). It was found that the plasma heparin concentration correlates negatively with the plasma volume. The heparin halftime depends on the dosage. Plasma heparin concentrations from 0.04 IE/ml to 0.20 IE/ml (= 0.031 USP-E/ml to 0.154 USP-E/ml) correlate to heparin halftimes of 9 min to 38 min. With this results formulae for calculating the quantity of the bolus and the daily heparin application were obtained. As opposed to the liver function the kidney function does not have any significant effect on the plasma concentration of biological active heparin. Furthermore it was found that the actual weight is unreliable for determination of the dosage. Instead calculated weight (height minus 100) is to be used.

摘要

为预防深静脉血栓形成,23名男性和7名女性患者在接受不同血管手术后,连续24小时静脉输注15000国际单位的肝素钠。在应用肝素开始后的0、1、2、4、8以及12 - 18小时,用发色底物法测定血浆肝素浓度。同时测量每位患者的血细胞比容、性别、身高、体重以及肝肾功能参数。本研究的目的是找到一种静脉应用肝素的通用模型,以便获得最佳的个体治疗性血浆肝素浓度。在肝素输注开始后最迟8小时,100%的患者达到了血浆肝素浓度的稳态,但只有56.67%的患者其血浆肝素浓度等于0.10国际单位/毫升至0.20国际单位/毫升(= 0.077美国药典单位/毫升至0.154美国药典单位/毫升)的治疗性因子Xa抑制水平。发现血浆肝素浓度与血浆容量呈负相关。肝素半衰期取决于剂量。血浆肝素浓度在0.04国际单位/毫升至0.20国际单位/毫升(= 0.031美国药典单位/毫升至0.154美国药典单位/毫升)之间时,肝素半衰期为9分钟至38分钟。根据这些结果得出了计算推注量和每日肝素用量的公式。与肝功能不同,肾功能对生物活性肝素的血浆浓度没有任何显著影响。此外,发现实际体重对于确定剂量不可靠。相反,应使用计算体重(身高减去100)。

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