School of Public Health and Community Medicine, University of New South Wales, Sydney NSW 2052, Australia.
Australian Centre for Public and Population Health Research, Faculty of Health, University of Technology Sydney, 235 Jones St, Ultimo NSW 2007, Australia.
Hum Reprod. 2018 Feb 1;33(2):320-327. doi: 10.1093/humrep/dex340.
Is perinatal mortality rate higher among births born following assisted reproductive technology (ART) compared to non-ART births?
Overall perinatal mortality rates in ART births was higher compared to non-ART births, but gestational age-specific perinatal mortality rate of ART births was lower for very preterm and moderate to late preterm births.
Births born following ART are reported to have higher risk of adverse perinatal outcomes compared to non-ART births.
STUDY DESIGN, SIZE, DURATION: This population-based retrospective cohort study included 407 368 babies (391 952 non-ART and 15 416 ART)-393 491 singletons and 10 877 twins or high order multiples.
PARTICIPANTS/MATERIALS, SETTING, METHODS: All births (≥20 weeks of gestation and/or ≥400 g of birthweight) in five states and territories in Australia during the period 2007-2009 were included in the study, using National Perinatal Data Collection (NPDC). Primary outcome measures were rates of stillbirth, neonatal and perinatal deaths. Adjusted odds ratio (AOR) and 95% confidence interval (CI) were used to estimate the likelihood of perinatal death.
Rates of multiple birth and low birthweight were significantly higher in ART group compared to the non-ART group (P < 0.01). Overall perinatal mortality rate was significantly higher for ART births (16.5 per 1000 births, 95% CI 14.5-18.6), compared to non-ART births (11.3 per 1000 births, 95% CI 11.0-11.6) (AOR 1.45, 95% CI 1.26-1.68). However, gestational age-specific perinatal mortality rate of ART births (including both singletons and multiples) was lower for very preterm (<32 weeks' gestation) and moderate to late preterm births (32-36 weeks' gestation) (AOR 0.61, 95% CI 0.53-0.70 and AOR 0.61, 95% CI 0.53-0.70, respectively) compared to non-ART births. Congenital abnormality and spontaneous preterm were the most common causes of neonatal deaths in both ART and non-ART group.
LIMITATIONS, REASONS FOR CAUTION: Due to different cut-off limit for perinatal period in Australia, the results of this study should be interpreted with cautions for other countries. Australian definition of perinatal period commences at 20 completed weeks (140 days) of gestation and ends 27 completed days after birth which is different from the definition by World Health Organisation (commences at 22 completed weeks (154 days) of gestation and ends seven completed days after birth) and by Centers for Disease Control and Prevention (includes infant deaths under age 7 days and fetal deaths at 28 weeks of gestation or more).
Preterm birth is the single most important contributing factor to increased risk of perinatal mortality among ART singletons compared to non-ART singletons. Further research on reducing early preterm delivery, with the aim of reducing the perinatal mortality among ART births is needed. Couples who access ART treatment should be fully informed regarding the risk of preterm birth and subsequent risk of perinatal death.
STUDY FUNDING/COMPETING INTEREST(S): There was no funding associated with this study. No conflict of interest was declared.
与非辅助生殖技术(ART)出生相比,围产儿死亡率在接受辅助生殖技术的出生中是否更高?
与非 ART 出生相比,ART 出生的总体围产儿死亡率更高,但极早产儿和中晚期早产儿的 ART 出生的特定胎龄围产儿死亡率较低。
与非 ART 出生相比,报告称接受辅助生殖技术的出生具有更高的不良围产儿结局风险。
研究设计、规模、持续时间:本基于人群的回顾性队列研究包括澳大利亚五个州和地区的 407368 名婴儿(391952 名非 ART 和 15416 名 ART)-393491 名单胎和 10877 名双胞胎或多胎。
参与者/材料、设置、方法:使用国家围产期数据收集(NPDC),研究纳入了澳大利亚五个州和地区 2007-2009 年期间所有(≥20 孕周和/或≥400g 出生体重)的分娩,纳入标准为活产、新生儿和围产儿死亡。采用调整后的优势比(AOR)和 95%置信区间(CI)来估计围产儿死亡的可能性。
ART 组的多胎和低出生体重率明显高于非 ART 组(P<0.01)。与非 ART 出生相比,ART 出生的总体围产儿死亡率明显更高(16.5/1000 活产,95%CI 14.5-18.6),(AOR 1.45,95%CI 1.26-1.68)。然而,ART 出生(包括单胎和多胎)的特定胎龄围产儿死亡率对于极早产儿(<32 孕周)和中晚期早产儿(32-36 孕周)较低(AOR 0.61,95%CI 0.53-0.70 和 AOR 0.61,95%CI 0.53-0.70)与非 ART 出生相比。先天性异常和自发性早产是 ART 和非 ART 组新生儿死亡的最常见原因。
局限性、谨慎的原因:由于澳大利亚围产期的截止时间不同,因此应谨慎解释本研究的结果。本研究的结果应谨慎解释,以便适用于其他国家。澳大利亚的围产期定义始于 20 周(140 天)的完整妊娠,结束于出生后 27 天,与世界卫生组织(始于 22 周(154 天)的完整妊娠,结束于出生后 7 天)和疾病控制和预防中心(包括 7 天内的婴儿死亡和 28 周胎龄或以上的胎儿死亡)的定义不同。
与非 ART 单胎相比,ART 单胎中早产是导致围产儿死亡率增加的最重要单一因素。需要进一步研究减少早期早产,以降低 ART 出生的围产儿死亡率。接受辅助生殖技术治疗的夫妇应充分了解早产的风险以及随后围产儿死亡的风险。
研究资助/利益冲突:本研究无资金支持。没有申报利益冲突。