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引用次数: 10

摘要

许多治疗性分离技术已经被引进并成功开发。此外,这些技术的几种也已应用于重症监护。然而,与连续血液滤过、连续血液滤过、单滤血浆滤过和血浆吸附等治疗相比,双滤血浆置换(DFPP)在该领域的应用很少。本文综述了DFPP在重症监护中的应用特点。在DFPP治疗期间,由于补充液中白蛋白输注不足导致白蛋白丢失,患者的血容量(BV)往往随着时间的推移而减少。在对9例患者的体内研究中,我们通过连续红细胞压积监测仪Crit-Line检测了BV的变化。因此,白蛋白损失在DFPP治疗中相当普遍。患者BV的降低是由白蛋白丢失引起的肿瘤性血压下降引起的,通常导致血压下降。这是DFPP在重症监护中的一个严重问题。如果病人正在遭受这些不良反应,我们应该避免白蛋白输注不足。为了确定补充白蛋白溶液的最佳浓度C(S)和体积V(S)值,我们引入了可变血容量模型,用于白蛋白在DFPP中的运输。
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Double filtration plasmapheresis in critical care.
Many kinds of technologies have been introduced and successfully developed for therapeutic apheresis. Furthermore, several kinds of these technologies have also been applied in critical care. Double filtration plasmapheresis (DFPP), however, is rarely applied in this field in comparison with other treatments such as continuous hemofiltration, continuous hemodiafiltration, single filtration plasmapheresis, and plasma adsorption therapies. In this paper, the characteristics of the DFPP treatments for critical care are summarized. During the DFPP treatments, the patient's blood volume (BV) often decreases with time due to albumin loss induced by inadequate albumin infusion in a supplementation fluid. We examined the change of BV by a continuous hematocrit monitor, Crit-Line, during an in vivo study for 9 patients. As a result, albumin loss fairly occurred in DFPP treatments. The decrease of patient BV was induced by an oncotic pressure drop due to albumin loss and often resulted in a blood pressure drop. This is a serious problem for DFPP in critical care. We should avoid inadequate albumin infusion if the patient is suffering from these adverse effects. In order to determine the optimal concentration C(S) and volume V(S) values of a supplemented albumin solution, we introduced a variable blood volume model for albumin transport in DFPP.
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Presidential Address: PRESIDENTIAL ADDRESS Fluctuations in the peripheral blood leukocyte and platelet counts in leukocytapheresis in healthy volunteers. Mobilization factors of peripheral blood stem cells in healthy donors. Cytokine removal by plasma exchange with continuous hemodiafiltration in critically ill patients. In vitro evaluation of newly developed adsorbent for selective removal of glycosylated low-density lipoprotein.
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