Muhihi Alfa, Sudfeld Christopher R, Smith Emily R, Noor Ramadhani A, Mshamu Salum, Briegleb Christina, Bakari Mohamed, Masanja Honorati, Fawzi Wafaie, Chan Grace Jean-Yee
Ifakara Health Institute, Kiko Avenue, Mikocheni, Dar es Salaam, Tanzania.
Africa Academy for Public Health, CM Plaza Building, Mwai Kibaki Road, Mikocheni, P.O.Box 79810, Dar es Salaam, Tanzania.
BMC Pregnancy Childbirth. 2016 May 17;16:110. doi: 10.1186/s12884-016-0900-5.
Few studies have differentiated risk factors for term-small for gestational age (SGA), preterm-appropriate for gestational age (AGA), and preterm-SGA, despite evidence of varying risk of child mortality and poor developmental outcomes.
We analyzed birth outcome data from singleton infants, who were enrolled in a large randomized, double-blind, placebo-controlled trial of neonatal vitamin A supplementation conducted in Tanzania. SGA was defined as birth weight <10th percentile for gestation age and sex using INTERGROWTH standards and preterm birth as delivery at <37 complete weeks of gestation. Risk factors for term-SGA, preterm-AGA, and preterm-SGA were examined independently using log-binomial regression.
Among 19,269 singleton Tanzanian newborns included in this analysis, 68.3 % were term-AGA, 15.8 % term-SGA, 15.5 % preterm-AGA, and 0.3 % preterm-SGA. In multivariate analyses, significant risk factors for term-SGA included maternal age <20 years, starting antenatal care (ANC) in the 3(rd) trimester, short maternal stature, being firstborn, and male sex (all p < 0.05). Independent risk factors for preterm-AGA were maternal age <25 years, short maternal stature, firstborns, and decreased wealth (all p < 0.05). In addition, receiving ANC services in the 1(st) trimester significantly reduced the risk of preterm-AGA (p = 0.01). Significant risk factors for preterm-SGA included maternal age >30 years, being firstborn, and short maternal stature which appeared to carry a particularly strong risk (all p < 0.05).
Over 30 % of newborns in this large urban and rural cohort of Tanzanian newborns were born preterm and/or SGA. Interventions to promote early attendance to ANC services, reduce unintended young pregnancies, increased maternal height, and reduce poverty may significantly decrease the burden of SGA and preterm birth in sub-Saharan Africa.
Australian New Zealand Clinical Trials Registry (ANZCTR) - ACTRN12610000636055 , registered on 3(rd) August 2010.
尽管有证据表明足月小样儿(SGA)、早产适于胎龄儿(AGA)和早产小样儿的儿童死亡风险及发育不良结局存在差异,但很少有研究区分这些情况的危险因素。
我们分析了来自坦桑尼亚一项大型新生儿维生素A补充剂随机、双盲、安慰剂对照试验中纳入的单胎婴儿的出生结局数据。使用INTERGROWTH标准将SGA定义为出生体重低于胎龄和性别的第10百分位数,早产定义为妊娠<37整周分娩。使用对数二项回归独立检验足月小样儿、早产适于胎龄儿和早产小样儿的危险因素。
在本分析纳入的19269名单胎坦桑尼亚新生儿中,68.3%为足月适于胎龄儿,15.8%为足月小样儿,15.5%为早产适于胎龄儿,0.3%为早产小样儿。在多变量分析中,足月小样儿的显著危险因素包括母亲年龄<20岁、在孕晚期开始产前检查(ANC)、母亲身材矮小、初产和男性(均p<0.05)。早产适于胎龄儿的独立危险因素为母亲年龄<25岁、母亲身材矮小、初产和财富减少(均p<0.05)。此外,在孕早期接受ANC服务显著降低了早产适于胎龄儿的风险(p=0.01)。早产小样儿的显著危险因素包括母亲年龄>30岁、初产和母亲身材矮小,后者似乎具有特别高的风险(均p<0.05)。
在这个坦桑尼亚城乡新生儿大样本队列中,超过30%的新生儿早产和/或为小样儿。促进早期接受ANC服务、减少意外早孕、增加母亲身高和减少贫困的干预措施可能会显著减轻撒哈拉以南非洲小样儿和早产的负担。
澳大利亚新西兰临床试验注册中心(ANZCTR)-ACTRN12610000636055,于2010年8月3日注册。