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新生儿维生素K:如何给药、何时给药以及给谁给药。

Vitamin K in neonates: how to administer, when and to whom.

作者信息

Autret-Leca E, Jonville-Béra A P

机构信息

Department of Clinical Pharmacology, H pital Bretonneau, University François Rabelais, Tours, France.

出版信息

Paediatr Drugs. 2001;3(1):1-8. doi: 10.2165/00128072-200103010-00001.

Abstract

Vitamin K-dependent factors are lower in neonates than in adults, and these anomalies are more prevalent in preterm neonates and in breast-fed infants. Vitamin K deficiency can account for vitamin K deficiency bleeding (VKDB) which occurs in 3 forms--early, classic and late. Vitamin K should be administered to all neonates at birth or immediately afterwards. However, the protocols for administration (route of administration, dosage, number of doses) remain a subject of discussion. Oral administration of a single dose of vitamin K protects against classical and early VKDB, but is less effective than intramuscular (IM) prophylaxis for the prevention of late VKDB. Although an increased risk of solid tumour, associated vitamin K administration, can be definitively excluded, a low potential risk of lymphoblastic leukaemia in childhood can not be ruled out. For formula-fed neonates without risk of haemorrhage, a 2 mg oral dose of vitamin K at birth, followed by a second 2 mg oral dose between day 2 and 7, is probably sufficient to prevent VKDB. For infants who are exclusively or nearly exclusively breast-fed, weekly oral administration of 2mg (or 25 microg/day) vitamin K after the initial 2 oral doses is justified at completion of breast-feeding. For neonates at high risk of haemorrhage (premature, neonatal disease, birth asphyxia, difficult delivery, any illness which will delay feeding, known hepatic disease, maternal drugs inhibiting vitamin K activity), the first dose must be administered by the IM or slow intravenous route. Doses should be repeated, particularly in premature infants, by a route of administration decided for each dose according to the clinical state of the infant. For infants of mothers treated with drugs inhibiting vitamin K activity, antenatal maternal prophylaxis (10 to 20 mg/day orally for 15 to 30 days before delivery) prevents early VKDB. After neonatal prophylaxis, as for infants at high risk of haemorrhage, doses need to be repeated at a rate and route of administration decided for each dose, according to the clotting factor profile specific for each infant.

摘要

新生儿体内维生素K依赖因子的水平低于成年人,这些异常情况在早产儿和母乳喂养的婴儿中更为普遍。维生素K缺乏可导致维生素K缺乏性出血(VKDB),其有三种形式——早期、典型和晚期。所有新生儿都应在出生时或出生后立即给予维生素K。然而,给药方案(给药途径、剂量、给药次数)仍是一个讨论的话题。口服单剂量维生素K可预防典型和早期VKDB,但在预防晚期VKDB方面不如肌肉注射(IM)预防有效。虽然可以明确排除与维生素K给药相关的实体瘤风险增加,但儿童期淋巴细胞白血病的低潜在风险不能排除。对于无出血风险的配方奶喂养新生儿,出生时口服2mg维生素K,然后在第2天至第7天之间再口服2mg,可能足以预防VKDB。对于纯母乳喂养或几乎纯母乳喂养的婴儿,在最初两次口服剂量后,在母乳喂养结束时每周口服2mg(或每天25μg)维生素K是合理的。对于出血风险高的新生儿(早产儿、新生儿疾病、出生时窒息、难产、任何会延迟喂养的疾病、已知的肝脏疾病、抑制维生素K活性的母体药物),首剂必须通过肌肉注射或缓慢静脉注射途径给药。应重复给药,特别是早产儿,根据婴儿的临床状态为每一剂确定给药途径。对于接受抑制维生素K活性药物治疗的母亲所生的婴儿,产前母体预防(分娩前15至30天每天口服10至20mg)可预防早期VKDB。新生儿预防后,与出血风险高的婴儿一样,需要根据每个婴儿特定的凝血因子情况,按为每一剂确定的速率和途径重复给药。

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