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Prehospital administration of blood products: experiences from a Finnish physician-staffed helicopter emergency medical service

机译:血液产品的预孢子管理:来自芬兰医师 - 人员的直升机紧急医疗服务的经验

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Massive infusions of crystalloids into bleeding hypotensive patients can worsen the outcome. Military experience suggests avoiding crystalloids using early damage control resuscitation with blood components in out of hospital setting. Civilian emergency medical services have since followed this idea. We describe our red blood cell protocol in helicopter emergency medical services (HEMS) and initial experience with prehospital blood products from the first 3 years after implementation. We performed an observational study of patients attended by the HEMS unit between 2015 and 2018 to whom packed red blood cells, freeze-dried plasma, or both were transfused. The Student’s two-sided T-test was used to compare vitals in prehospital phase with those at the hospital’s emergency department. A p-value ?0.05 was considered significant. Altogether, 62 patients received prehospital transfusions. Of those, 48 (77%) were trauma patients and most (n?=?39, 81%) suffered blunt trauma. The transfusion began at a median of 33 (IQR 21–47) minutes before hospital arrival. Median systolic blood pressure showed an increase from 90?mmHg (IQR 75–111?mmHg) to 107?mmHg (IQR 80–124?mmHg; P??0.026) during the prehospital phase. Four units of red blood cells were handled incorrectly when unused red blood cells were returned and required disposal during a three-year period. There were no reported adverse effects from prehospital transfusions. We treated two patients per month with prehospital blood products. A prehospital physician-staffed HEMS unit carrying blood products is a feasible and safe method to start transfusion roughly 30?min before arrival to the hospital. The study was retrospectively registered by the Tampere University Hospital’s Medical Director (R19603) 5.11.2019.
机译:将晶体输送到出血低血压患者的巨大输注可以恶化结果。军事经验表明,使用早期损伤控制复苏与医院环境中的血液成分避免了晶状体。平民紧急医疗服务遵循这个想法。我们在直升机紧急医疗服务(HEMS)中描述了我们的红细胞协议,并在实施后的前3年从初始血液产品初始经验。我们对2015年和2018年在2015年至2018年之间进行的患者进行了观察性研究,填充了红细胞,冷冻干燥的血浆或两者均转移。学生的双面T检验用于与医院的急诊部门的预孢子阶段进行比较。 p值<?0.05被认为是显着的。共有62名患者接受了急性输血。其中48例(77%)是创伤患者,大多数(n?=?39,81%)遭受钝的创伤。在医院到来之前,输血开始于33分钟的中位数(IQR 21-47)分钟。中位数收缩压显示在预孢子期期间90?mmHg(IQR 75-111?mmhg)至107毫升(IQR 80-124?mmhg;p≤026)。在返回未使用的红细胞并在为期三年期间返回并要求所需的处理时,4个单位的红细胞进行了不正确。没有报告的报告从前孢子输血产生的不利影响。我们每月治疗两名患者,血液产品每月治疗。携带血液产品的携带血液制品的一款血液制品是一种可行和安全的方法,在抵达医院前大约30次开始输血。该研究由Tampere University医院的医疗总监(R19603)第5.11.2019号回顾性。

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