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NOVEL METHOD OF PROGNOSIS ASSOCIATED WITH CASES OF POSTPARTUM HEMORRHAGE

机译:产后出血预后的新方法

摘要

The present invention relates to an in vitro method of prognosis for the arrest of bleeding in a patient suffering from postpartum haemorrhage in the absence of an invasive procedure, comprising the following steps: (a) determining, using a biological sample from said patient, the plasma fibrinogen concentration, the blood troponin concentration and also the prothrombin time; (b) studying at least two clinical markers for said patient, selected from the group comprising heart rate and the presence of placentation abnormalities; (c) calculating a score Z according to the following equation: Z=a+b+v+d+e; where a is associated with the existence of placentation abnormalities in said patient, with a being 0 when no placentation abnormality is observed in said patient and a being 1 when one or more placentation abnormalities are observed in said patient; where b is associated with the heart rate of said patient, with b being 0 when the heart rate of said patient is less than or equal to 115 bpm (beats per minute) and b being 1 when the heart rate is greater than 115 bpm; where c is associated with the plasma fibrinogen concentration of said patient, with c being 0 when said concentration is greater than or equal to 2 g/L and c being 1 when said concentration is less than 2 g/L; where d is associated with the blood troponin concentration of said patient, with d being 0 when said concentration is less than the detection cut-off and d being 1 when said concentration is grater than or equal to the detection cut-off; where e is associated with the prothrombin time (PT) of said patient, with e being 0 when said prothrombin time is greater than or equal to 50% and e being 1 when said prothrombin time is less than 50%; where a score Z of greater than or equal to a value of 2 is an indication of the need to perform an invasive procedure in order to stop the bleeding in said patient suffering from postpartum haemorrhage.
机译:本发明涉及在没有侵入性程序的情况下在产后出血患者中止血的体外预后方法,其包括以下步骤:(a)使用来自所述患者的生物样品确定血浆纤维蛋白原浓度,血液肌钙蛋白浓度以及凝血酶原时间; (b)为所述患者研究至少两种临床标记,选自心率和胎盘异常的组; (c)根据以下等式计算分数Z:Z = a + b + v + d + e;其中a与所述患者中存在胎盘异常有关,当在所述患者中未观察到胎盘异常时为0,而在所述患者中观察到一个或多个胎盘异常时为1;其中b与所述患者的心率相关,当所述患者的心率小于或等于115bpm(每分钟心跳数)时b为0,而当心率大于115bpm时b为1。其中c与所述患者的血浆纤维蛋白原浓度有关,当所述浓度大于或等于2g / L时c为0,而当所述浓度小于2g / L时c为1;其中d与所述患者的血液肌钙蛋白浓度相关,当所述浓度小于检测极限时d为0,而当所述浓度大于或等于检测极限时d为1;其中e与所述患者的凝血酶原时间(PT)相关,当所述凝血酶原时间大于或等于50%时,e为0,而当所述凝血酶原时间小于50%时,e为1。其中评分Z大于或等于2的值表示需要执行侵入性程序以停止患有产后出血的所述患者的出血。

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