Caddell J L
Section on Disorders of Carbohydrate Metabolism, National Institute of Child Health and Human Department, Bethesda, Maryland 20892.
J Am Coll Nutr. 1988 Feb;7(1):5-16. doi: 10.1080/07315724.1988.10720215.
Apnea, bradycardia, and neuromuscular hyperirritability have been associated with magnesium (Mg) deficiency in young human infants and weanling animals. This is a retrospective review of a clinical experience of Mg therapy among 200 premature neonates who showed physical and clinical chemical changes compatible with Mg deficiency. The 200 infants all had idiopathic apnea neonatorum, and 93% also had the respiratory distress syndrome (RDS). This review was conducted to learn whether Mg therapy was associated with a significant reduction in apnea. The author suggested that the dose of Mg be 0.4 mEq/kg body weight/day, as 50% MgSO4.7H2O intramuscularly (IM) for 5 days; or as 1.0 mEq/kg/day, as 10% MgCl2.6H2O by mouth for 2 or more weeks, with appropriate monitoring of plasma Mg values in all infants. Sixty-one infants received a minimum of 5 days of Mg by either route (mean, 11.4 +/- 0.9, Group A); five received 3-4 doses IM (mean, 3.6 +/- 0.2, Group B); and 134 received 0-2 doses IM (0.5 +/- 0.1, Group C). Group A infants Mg-treated before Day 20 showed earlier cessation of apnea and bradycardia than those treated after Day 20. In Group A patients, 7 dose-days [corrected] of Mg therapy was associated with continuation of apnea; 14 dose-days [corrected], with cessation of apnea. Compared with Group A, Group C continued to develop apnea (P less than .003) and bradycardia (P less than 0.03) over longer periods of time. Group A infants showed no record of death or of hospital readmission for recurrent apnea, while 32 of 134 Group C infants had one or both of those unfavorable outcomes (P less than 0.001), with four of the five deaths in Group C (NS) as the sudden infant death syndrome (SIDS). In conclusion, Mg was associated with a reduction of apnea in this population. Emphasis was placed on the need to closely observe infants receiving supplementary Mg, with monitoring of plasma Mg levels.
呼吸暂停、心动过缓和神经肌肉兴奋性增高与幼龄人类婴儿及断奶动物的镁(Mg)缺乏有关。本文回顾性分析了200例有与镁缺乏相符的体格及临床化学变化的早产儿镁治疗的临床经验。这200例婴儿均患有特发性新生儿呼吸暂停,93%还患有呼吸窘迫综合征(RDS)。本研究旨在了解镁治疗是否能显著减少呼吸暂停。作者建议镁的剂量为0.4 mEq/kg体重/天,以50% MgSO4·7H2O肌肉注射(IM),共5天;或以1.0 mEq/kg/天,以10% MgCl2·6H2O口服,持续2周或更长时间,并对所有婴儿的血浆镁值进行适当监测。61例婴儿通过任何一种途径接受了至少5天的镁治疗(平均,11.4±0.9,A组);5例接受了3 - 4次肌肉注射(平均,3.6±0.2,B组);134例接受了0 - 2次肌肉注射(0.5±0.1,C组)。在出生后20天之前接受镁治疗的A组婴儿呼吸暂停和心动过缓的停止时间比20天之后治疗的婴儿更早。在A组患者中,7个剂量日[校正后]的镁治疗与呼吸暂停持续有关;14个剂量日[校正后],呼吸暂停停止。与A组相比,C组在更长时间内持续出现呼吸暂停(P < 0.003)和心动过缓(P < 0.03)。A组婴儿无死亡记录,也没有因反复呼吸暂停再次入院的情况,而134例C组婴儿中有32例出现了上述不良结局中的一种或两种(P < 0.001),C组5例死亡中有4例(无显著性差异)为婴儿猝死综合征(SIDS)。总之,镁与该人群呼吸暂停的减少有关。强调了密切观察接受补充镁的婴儿并监测血浆镁水平的必要性。