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一种按照洛格里波方法灭菌的新型凝血酶原复合物制剂的肝炎安全性。一项前瞻性临床试验的结果。

Hepatitis safety of a new prothrombin complex preparation, sterilized according to the method of LoGrippo. Results of a prospective clinical trial.

作者信息

Hoppe I

出版信息

Blut. 1985 Jun;50(6):363-8. doi: 10.1007/BF00320930.

Abstract

In a controlled, prospective clinical trial with almost 300 patients undergoing cardiovascular surgery, the hepatitis risk was examined of a new prothrombin complex (PPSB) preparation produced from pooled plasma, which was cold sterilized according to the method of LoGrippo with beta-propiolactone and UV-light. Of 268 evaluable patients, 102 belonged to a group receiving PPSB and 166 belonged to a control group without PPSB. 25 batches of PPSB in dosages of up to 4,500 units per patient, in total, were used. The mean requirement for transfusion of blood or plasma was 10 units per patient in the group receiving PPSB and slightly more than 2 units per patient in the control group. In both of the groups, 3 hepatitis infections occurred (5 cases of non-A, non-B, 1 case of type B), corresponding to hepatitis incidences of 2.9 and 1.8%, respectively. The difference in hepatitis incidence between both groups was statistically not significant. This demonstrates, on the one hand, the hepatitis safety of the sterilized PPSB and, on the other, that multiple transfusion is no longer associated with a high risk of hepatitis when the guidelines of modern donor screening are followed.

摘要

在一项针对近300例接受心血管手术患者的前瞻性对照临床试验中,对一种由混合血浆制备的新型凝血酶原复合物(PPSB)制剂的肝炎风险进行了研究,该制剂采用洛格里波方法,用β-丙内酯和紫外线进行冷灭菌。在268例可评估患者中,102例属于接受PPSB的组,166例属于未接受PPSB的对照组。总共使用了25批PPSB,每位患者的剂量最高达4500单位。接受PPSB的组中,每位患者输血或血浆的平均需求量为10单位,而对照组中每位患者略多于2单位。两组均发生了3例肝炎感染(5例非甲非乙型,1例乙型),肝炎发病率分别为2.9%和1.8%。两组之间肝炎发病率的差异在统计学上无显著意义。这一方面证明了灭菌PPSB的肝炎安全性,另一方面表明,遵循现代献血者筛查指南时,多次输血不再与高肝炎风险相关。

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