Mazumder Premasish, Dutta Sourabh, Kaur Jaswinder, Narang Anil
Department of Pediatrics, Postgraduate Institute of Medical Education and Research, Chandigarh, India.
Indian Pediatr. 2008 Aug;45(8):661-7.
This study compared the beneficial and adverse neonatal effects of a single versus repeated courses of antenatal betamethasone.
Tertiary care hospital
Open labeled, randomized controlled trial.
Pregnant women (26-33 weeks) at risk of preterm delivery, who received one course of antenatal betamethasone and remained undelivered for 7 days. Those with uncertain gestation, major malformations and frank chorioamnionitis were excluded.
Subjects were randomized to receive weekly antenatal betamethasone until 34 weeks or no further betamethasone.
Primary: incidence of severe respiratory distress syndrome (RDS). Secondary: incidence of non-severe RDS and other neonatal morbidity; birth weight, length and occipito-frontal circumference (OFC); and, development and growth at 6 mo corrected age.
38 subjects were allocated to each group. Severe RDS was similar in multiple and single course groups (7% vs. 3% respectively, P=0.34), as was incidence of other morbidity. Composite outcome of RDS and or death within 28 days tended to be less in multiple course group (P=0.07). Birth anthropometry was similar in the 2 groups. At 6 mo corrected age (n=44), weight and length were significantly lower in multiple course group (p=0.003 and P=0.007, respectively), whereas OFC was not different (P=0.1). There were no differences vis a vis neurodevelopmental outcomes.
A single course of antenatal betamethasone was as efficacious as multiple courses, with respect to prevention of neonatal morbidity. Multiple antenatal betamethasone courses have long-term adverse effects on infant weight and length growth, but not on OFC and neurodevelopment.
本研究比较了单疗程与重复疗程产前倍他米松对新生儿的有益和不良影响。
三级护理医院
开放标签、随机对照试验。
有早产风险的孕妇(26 - 33周),接受过一个疗程的产前倍他米松治疗且7天内未分娩。排除妊娠不确定、严重畸形和明显绒毛膜羊膜炎的孕妇。
将受试者随机分为两组,一组每周接受产前倍他米松治疗直至34周,另一组不再接受倍他米松治疗。
主要指标:严重呼吸窘迫综合征(RDS)的发生率。次要指标:非严重RDS和其他新生儿发病率;出生体重、身长和枕额周长(OFC);以及矫正年龄6个月时的发育和生长情况。
每组分配38名受试者。多疗程组和单疗程组的严重RDS发生率相似(分别为7%和3%,P = 0.34),其他发病率也相似。多疗程组28天内RDS和/或死亡的综合结局倾向于更低(P = 0.07)。两组的出生人体测量指标相似。在矫正年龄6个月时(n = 44),多疗程组的体重和身长显著更低(分别为P = 0.003和P = 0.007),而枕额周长无差异(P = 0.1)。神经发育结局方面无差异。
就预防新生儿发病而言,单疗程产前倍他米松与多疗程同样有效。多疗程产前倍他米松对婴儿体重和身长增长有长期不良影响,但对枕额周长和神经发育无影响。