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在严重休克中,生理盐水扩容组使用O型未交叉配血的浓缩红细胞作为初始复苏液体。

Saline-expanded group O uncrossmatched packed red blood cells as an initial resuscitation fluid in severe shock.

作者信息

Schwab C W, Civil I, Shayne J P

出版信息

Ann Emerg Med. 1986 Nov;15(11):1282-7. doi: 10.1016/s0196-0644(86)80609-6.

Abstract

Despite an excellent military experience with the use of the "universal donor" as an immediately available blood component, considerable reluctance to use uncrossmatched Group O packed cells (TOB) remains. In addition, problems continue with rapid blood acquisition in the emergency department. To study the safety of TOB used as an immediate resuscitation component, a 30-month prospective study of all patients arriving at a single trauma unit was undertaken. By protocol TOB (O-, female; O+, male) was delivered to the shock room prior to patient arrival and was expanded to 500 mL by adding 250 mL prewarmed saline (39.4 C) to the existing RBC unit. Transfusion was ordered on clinical signs of Class III or Class IV hemorrhage. Ninety-nine patients entered the protocol, receiving a total of 1,136 units of blood (11.5 units/patient). Four hundred ten units (4.1 units/patient) of uncrossmatched blood were administered on patient arrival--322 units of TOB and 88 units of type-specific blood (TSB). Seven patients (7.4%) had prior transfusions, and 14 (58%) women had prior pregnancies. Complications included disseminated intravascular coagulation, 12%; adult respiratory distress syndrome, 8%; and hepatitis, 1%. Forty-nine patients (49%) required massive transfusion (greater than 10 units/24 hr). All patients were followed clinically and by the blood bank for any signs of transfusion reactions or incompatibility throughout their hospital courses; none developed. There were no deaths related to transfusion incompatibility. We conclude that TOB used as an immediate resuscitative blood component is safe.(ABSTRACT TRUNCATED AT 250 WORDS)

摘要

尽管在将“通用供血者”作为即时可用血液成分使用方面有出色的临床经验,但对于使用未经交叉配血的O型浓缩红细胞(TOB)仍存在相当大的抵触情绪。此外,急诊科快速采血的问题依然存在。为研究将TOB用作即时复苏成分的安全性,对所有送至单个创伤单元的患者进行了一项为期30个月的前瞻性研究。按照方案,在患者到达之前将TOB(O型阴性,女性;O型阳性,男性)送至休克室,并通过向现有的红细胞单位中加入250 mL预热盐水(39.4℃)将其扩容至500 mL。根据Ⅲ级或Ⅳ级出血的临床体征下令输血。99名患者进入该方案,共接受了1136单位血液(每位患者11.5单位)。在患者到达时输注了410单位(每位患者4.1单位)未经交叉配血的血液——322单位TOB和88单位同型特异性血液(TSB)。7名患者(7.4%)曾接受过输血,14名(58%)女性曾怀孕。并发症包括弥散性血管内凝血,12%;成人呼吸窘迫综合征,8%;以及肝炎,1%。49名患者(49%)需要大量输血(超过10单位/24小时)。在患者整个住院期间,对所有患者进行临床随访并由血库监测是否有任何输血反应或不相容迹象;均未出现。没有与输血不相容相关的死亡病例。我们得出结论,将TOB用作即时复苏血液成分是安全的。(摘要截选至250词)

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