Perinatal and infant outcomes after assisted reproductive technology treatment for endometriosis alone compared with other causes of infertility: a data linkage cohort study

被引:1
作者
Zhang, Xian [1 ,2 ]
Chambers, Georgina M. [1 ,2 ]
Venetis, Christos [1 ,2 ,3 ]
Choi, Stephanie K. Y. [1 ,2 ]
Gerstl, Brigitte [2 ,4 ,5 ]
Ng, Cecilia H. M. [2 ,4 ,5 ]
Abbott, Jason A. [2 ,4 ,5 ]
机构
[1] Univ New South Wales, Fac Med, Ctr Big Data Res Hlth, Natl Perinatal Epidemiol & Stat Unit, Sydney, Australia
[2] Univ New South Wales, Fac Med & Hlth, Sch Clin Med, Sydney, Australia
[3] Aristotle Univ Thessaloniki, Med Sch, Dept Ob Gyn 1, Unit Human Reprod,Fac Hlth Sci, Thessaloniki, Greece
[4] Royal Hosp Women, Gynaecol Res & Clin Evaluat GRACE Grp, Sydney, NSW, Australia
[5] Univ New South Wales, Sydney, Australia
基金
英国医学研究理事会;
关键词
Assisted reproductive technology; endometriosis; perinatal outcomes; infant outcomes; data linkage study; PREGNANCY OUTCOMES; ADVERSE PREGNANCY; WOMEN; DIAGNOSIS; IMPACT; ART;
D O I
10.1016/j.fertnstert.2024.12.007
中图分类号
R71 [妇产科学];
学科分类号
100211 ;
摘要
Objective: To evaluate whether perinatal and infant outcomes differ between singleton births after assisted reproductive technology (ART) in women with endometriosis alone and those with other causes of infertility. Design: Population-based data linkage cohort study. Subjects: A total of 29,152 ART-conceived singleton births from 24,116 mothers, 2010-2017, New South Wales, Australia. Exposure: Endometriosis, identified from the Australian and New Zealand Assisted Reproduction Database, hospital admissions, and dispensed medication records. The causes of infertility were categorized as follows: endometriosis alone; endometriosis plus other cause(s) of infertility; infertility other than endometriosis; and unstated cause of infertility. The endometriosis alone group was further classified using International Classification of Diseases, Tenth Revision, codes (N80.0-N80.9) into superficial, ovarian, deep, and other endometriosis. Main outcome measures: Perinatal and infant outcomes, included preterm birth (<37 weeks), very preterm birth (<32 weeks), small for gestational age (SGA), large for gestational age, admission to neonatal intensive care unit, perinatal death, and infant hospitalization up to 2 years of age. Generalized estimating equations were used to investigate independent associations between endometriosis and study outcomes. Results: Of the 29,152 ART-conceived singleton births, 19.9% (5,806/29,152) were from mothers with a diagnosis of endometriosis. Among these, 23.8% (1,379/5,806) were from mothers with an endometriosis alone diagnosis, and 76.2% (4,427/5,806) were from mothers with endometriosis plus other cause(s) of infertility. Three quarters (21,795/29,152) of births were from mothers without endometriosis and 5.3% (1,551/29,152) were from mothers with an unstated cause of infertility. After adjusting for maternal age at the time of birth, parity, ART treatment characteristics, gestational hypertension and diabetes, smoking, and socioeconomic status, there was no overall association between endometriosis and perinatal and infant outcomes. However, compared with women without endometriosis, those with deep endometriosis had a higher risk of preterm birth (adjusted relative risk, 1.75; 95% confidence interval, 1.12-2.75) and SGA (adjusted relative risk, 1.58; 95% confidence interval, 1.05-2.37). Conclusion: Reassuringly, perinatal and infant outcomes are generally comparable for ART-conceived infants born to mothers with endometriosis alone and those with other causes of infertility when considered as a singular disease entity. Larger studies are needed to confirm the differential risk associated with endometriosis phenotypes; however, for patients with deep endometriosis undergoing ART, the risks of preterm birth and SGA may be increased. Clinicians should be aware of these potential risks.
引用
收藏
页码:846 / 855
页数:10
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