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Autologous cord blood cell infusion in preterm neonates safely reduces respiratory support duration and potentially preterm complications

机译:早产新生儿的自体脐带血细胞输注安全地减少呼吸支持持续时间和潜在的早产并发症

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Preterm birth and its complications are the leading cause of neonatal death. The main underlying pathological mechanisms for preterm complications are disruption of the normal maturation processes within the target tissues, interrupted by premature birth. Cord blood, as a new and convenient source of stem cells, may provide new, promising options for preventing preterm complications. This prospective, nonrandomized placebo controlled study aimed at investigating the effect of autologous cord blood mononuclear cells (ACBMNC) for preventing preterm associated complications. Preterm infants less than 35?weeks gestational age were assigned to receive ACBMNC (5?×?10sup7/sup cells/kg) intravenous or normal saline within 8 hours after birth. Preterm complication rates were compared between two groups to demonstrate the effect of ACBMNC infusion in reducing preterm complications. Fifteen preterm infants received ACBMNC infusion, and 16 infants were assigned to the control group. There were no significant differences when comparing mortality and preterm complication rates before discharge. However, ACBMNC infusion demonstrated significant decreases in duration of mechanical ventilation (3.2?days vs 6.41?days, P = .028) and oxygen therapy (5.33?days vs 11.31?days, P = .047). ACBMNC infusion was effective in reducing respiratory support duration in very preterm infants. Due to the limited number of patients enrolled, powered randomized controlled trials are needed to better define its efficacy.
机译:早产及其并发症是新生儿死亡的主要原因。早产并发症的主要潜在病理机制是靶组织内的正常成熟过程中断,因早产而中断。脐带血,作为一种新的干细胞来源,可为预防早产并发症提供新的,有希望的选择。这种前景,非andoMized安慰剂受控研究旨在研究自体脐带血单核细胞(ACBMNC)的影响,防止早产相关并发症。早产儿少于35?周的胎儿在出生后8小时内分配静脉内或生理盐水的ACBMNC(5?×10 7℃)。在两组之间比较了早产并发症率,以证明ACBMNC输注在降低早产并发症中的作用。十五个早产儿接受了ACBMNC输注,16名婴儿被分配给对照组。在放电前比较死亡率和早产并发症率时没有显着差异。然而,ACBMNC输注在机械通气持续时间内表现出显着降低(3.2?天与6.41.天,P = .028)和氧疗法(5.33?天与11.31?天,P = .047)。 ACBMNC输注在非常早产儿减少呼吸支撑持续时间。由于注册数量有限的患者,需要动力随机对照试验以更好地定义其功效。

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