Díaz-Cremades J M, Lorenzo R, Sánchez M, Moreno M J, Alsar M J, Bosch J M, Fajardo L, González D, Guerrero D
Department of Hematology, Hospital Insular, Las Palmas de Gran Canaria, Spain.
Intensive Care Med. 1994 Nov;20(8):577-80. doi: 10.1007/BF01705725.
To evaluate the effect of the AT III concentrates upon the clinical evolution and hemostatic parameters.
Prospective, open, randomized trial.
Septic and multiple trauma patients admitted to our Intensive Care Unit.
Levels of AT III below 70% were used as criteria to choose 36 patients, 20 of whom received treatment with AT III and 16 did not.
AT III concentrates were administered at an initial dose of 60 U/kg followed by 10 U/kg every six hours.
The administration of AT III neither contributes to alterations in haemostasis, nor the clinical evolution (evaluated according to Apache II score).
The results suggest that the administration of AT III concentrates to critical patients with acquired low levels, but without manifest DIC, may not be justified; although further studies on a larger population are required to establish definite conclusions.
评估抗凝血酶III(AT III)浓缩物对临床病程及止血参数的影响。
前瞻性、开放性、随机试验。
入住我院重症监护病房的脓毒症和多发性创伤患者。
以AT III水平低于70%为标准选取36例患者,其中20例接受AT III治疗,16例未接受治疗。
AT III浓缩物初始剂量为60 U/kg,随后每6小时给予10 U/kg。
AT III的应用既未导致止血功能改变,也未影响临床病程(根据急性生理学及慢性健康状况评分系统II [Apache II]评分评估)。
结果表明,对于获得性低水平但无明显弥散性血管内凝血(DIC)的重症患者,应用AT III浓缩物可能并无依据;尽管需要对更多人群进行进一步研究以得出确切结论。