Pregnancy Outcomes in Women With Thalassemia Trait: A Multicenter Cohort Study.

IF 3.7 Q3 HEMATOLOGY
Anemia Pub Date : 2025-12-29 eCollection Date: 2025-01-01 DOI:10.1155/anem/8899690
Daria Chelysheva, Ameera Syed, Hannah Ruby, Anna Homeniuk, Anas Atrash, Feras Al Moussally
{"title":"Pregnancy Outcomes in Women With Thalassemia Trait: A Multicenter Cohort Study.","authors":"Daria Chelysheva, Ameera Syed, Hannah Ruby, Anna Homeniuk, Anas Atrash, Feras Al Moussally","doi":"10.1155/anem/8899690","DOIUrl":null,"url":null,"abstract":"<p><strong>Introduction: </strong>Thalassemia trait generally has minimal clinical impact, but physiologic changes during pregnancy may increase the risk of anemia, transfusion requirements, and hypertensive disorders. Existing evidence on pregnancy outcomes in this population is limited, with some conflicting data. This study aims to evaluate pregnancy-related outcomes in patients with thalassemia trait using a large, multicenter database.</p><p><strong>Methods: </strong>For this retrospective cohort study, we used data from the TriNetX US Collaborative Network. Females aged 18-45 with ICD-10 codes indicating pregnancy (Z33.1, O00-O9A, Z34, or Z3A) were included. Patients with pregnancy and coexisting thalassemia trait (D56.3) were assigned to the thalassemia cohort (<i>n</i> = 22,913), while those without any thalassemia diagnosis comprised the nonthalassemia cohort (<i>n</i> = 5,611,147). Propensity score matching was performed to balance age, race/ethnicity, obesity, smoking status, essential hypertension, and Type 2 diabetes mellitus. After 1:1 matching, 22,770 patients remained in each cohort (total <i>N</i> = 45,540). Outcomes were assessed within 1 year of the index date, including anemia during pregnancy, blood transfusion, preeclampsia/eclampsia, cesarean delivery, venous thromboembolism (VTE), heart failure/cardiomyopathy, preterm delivery, intrauterine growth restriction (IUGR), and intrauterine fetal demise (IUFD). Risk ratios (RRs) with 95% confidence intervals (CIs) were calculated.</p><p><strong>Results: </strong>Thalassemia trait was associated with higher risks of anemia during pregnancy (RR: 3.00 and 95% CI: 2.87-3.13), needing blood transfusion (RR: 1.90 and 95% CI: 1.69-2.20), preeclampsia/eclampsia (RR: 1.54 and 95% CI: 1.47-1.61), cesarean delivery (RR: 1.43 and 95% CI: 1.36-1.51), preterm delivery < 37 weeks (RR: 1.40 and 95% CI: 1.31-1.65), and IUGR (RR: 1.96 and 95% CI: 1.72-2.23), all were statistically significant with a <i>p</i> < 0.001. Increased risk was also observed for VTE (RR: 1.57 and 95% CI: 1.12-2.20, <i>p</i> < 0.001) and IUFD (RR: 1.37 and 95% CI: 1.087-1.75, <i>p</i> < 0.001). No significant association was found with heart failure/cardiomyopathy (RR: 1.28 and 95% CI: 0.93-1.76, <i>p</i> = 0.124).</p><p><strong>Conclusion: </strong>Thalassemia trait in pregnancy was associated with increased rates of anemia, transfusion, and adverse maternal and fetal outcomes. Such adverse outcomes include pre-eclampsia/eclampsia, cesarean delivery, preterm birth and IUGR. These findings underscore the need for tailored peripartum care strategies in this high-risk population.</p>","PeriodicalId":46055,"journal":{"name":"Anemia","volume":"2025 ","pages":"8899690"},"PeriodicalIF":3.7000,"publicationDate":"2025-12-29","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12748928/pdf/","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Anemia","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.1155/anem/8899690","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"2025/1/1 0:00:00","PubModel":"eCollection","JCR":"Q3","JCRName":"HEMATOLOGY","Score":null,"Total":0}
引用次数: 0

Abstract

Introduction: Thalassemia trait generally has minimal clinical impact, but physiologic changes during pregnancy may increase the risk of anemia, transfusion requirements, and hypertensive disorders. Existing evidence on pregnancy outcomes in this population is limited, with some conflicting data. This study aims to evaluate pregnancy-related outcomes in patients with thalassemia trait using a large, multicenter database.

Methods: For this retrospective cohort study, we used data from the TriNetX US Collaborative Network. Females aged 18-45 with ICD-10 codes indicating pregnancy (Z33.1, O00-O9A, Z34, or Z3A) were included. Patients with pregnancy and coexisting thalassemia trait (D56.3) were assigned to the thalassemia cohort (n = 22,913), while those without any thalassemia diagnosis comprised the nonthalassemia cohort (n = 5,611,147). Propensity score matching was performed to balance age, race/ethnicity, obesity, smoking status, essential hypertension, and Type 2 diabetes mellitus. After 1:1 matching, 22,770 patients remained in each cohort (total N = 45,540). Outcomes were assessed within 1 year of the index date, including anemia during pregnancy, blood transfusion, preeclampsia/eclampsia, cesarean delivery, venous thromboembolism (VTE), heart failure/cardiomyopathy, preterm delivery, intrauterine growth restriction (IUGR), and intrauterine fetal demise (IUFD). Risk ratios (RRs) with 95% confidence intervals (CIs) were calculated.

Results: Thalassemia trait was associated with higher risks of anemia during pregnancy (RR: 3.00 and 95% CI: 2.87-3.13), needing blood transfusion (RR: 1.90 and 95% CI: 1.69-2.20), preeclampsia/eclampsia (RR: 1.54 and 95% CI: 1.47-1.61), cesarean delivery (RR: 1.43 and 95% CI: 1.36-1.51), preterm delivery < 37 weeks (RR: 1.40 and 95% CI: 1.31-1.65), and IUGR (RR: 1.96 and 95% CI: 1.72-2.23), all were statistically significant with a p < 0.001. Increased risk was also observed for VTE (RR: 1.57 and 95% CI: 1.12-2.20, p < 0.001) and IUFD (RR: 1.37 and 95% CI: 1.087-1.75, p < 0.001). No significant association was found with heart failure/cardiomyopathy (RR: 1.28 and 95% CI: 0.93-1.76, p = 0.124).

Conclusion: Thalassemia trait in pregnancy was associated with increased rates of anemia, transfusion, and adverse maternal and fetal outcomes. Such adverse outcomes include pre-eclampsia/eclampsia, cesarean delivery, preterm birth and IUGR. These findings underscore the need for tailored peripartum care strategies in this high-risk population.

Abstract Image

Abstract Image

地中海贫血女性的妊娠结局:一项多中心队列研究
地中海贫血的特点通常对临床影响很小,但妊娠期间的生理变化可能增加贫血、输血需求和高血压疾病的风险。该人群妊娠结局的现有证据有限,有一些相互矛盾的数据。本研究旨在利用大型多中心数据库评估地中海贫血患者妊娠相关结局。方法:在这项回顾性队列研究中,我们使用了来自TriNetX美国合作网络的数据。纳入年龄在18-45岁,ICD-10编码显示怀孕的女性(Z33.1、00- o9a、Z34或Z3A)。怀孕并伴有地中海贫血特征(D56.3)的患者被分配到地中海贫血队列(n = 22,913),而没有任何地中海贫血诊断的患者组成非地中海贫血队列(n = 5,611147)。进行倾向评分匹配,以平衡年龄、种族/民族、肥胖、吸烟状况、原发性高血压和2型糖尿病。1:1匹配后,每个队列中仍有22,770例患者(总N = 45,540例)。指标日期后1年内评估结局,包括妊娠期贫血、输血、先兆子痫/子痫、剖宫产、静脉血栓栓塞(VTE)、心力衰竭/心肌病、早产、宫内生长受限(IUGR)和宫内胎儿死亡(IUFD)。计算95%置信区间(ci)的风险比(rr)。结果:地中海贫血性状与妊娠期贫血(RR: 3.00, 95% CI: 2.87-3.13)、需要输血(RR: 1.90, 95% CI: 1.69-2.20)、先兆子痫/子痫(RR: 1.54, 95% CI: 1.47-1.61)、剖宫产(RR: 1.43, 95% CI: 1.36-1.51)、早产< 37周(RR: 1.40, 95% CI: 1.31-1.65)、IUGR (RR: 1.96, 95% CI: 1.72-2.23)的高风险相关,均有统计学意义,p < 0.001。VTE (RR: 1.57, 95% CI: 1.12-2.20, p < 0.001)和IUFD (RR: 1.37, 95% CI: 1.087-1.75, p < 0.001)的风险也增加。与心力衰竭/心肌病无显著相关性(RR: 1.28, 95% CI: 0.93-1.76, p = 0.124)。结论:妊娠期地中海贫血与贫血、输血和不良母婴结局的发生率增加有关。这些不良后果包括先兆子痫/子痫、剖宫产、早产和IUGR。这些发现强调了在高危人群中定制围产期护理策略的必要性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
求助全文
约1分钟内获得全文 求助全文
来源期刊
Anemia
Anemia HEMATOLOGY-
CiteScore
4.80
自引率
3.40%
发文量
11
审稿时长
18 weeks
期刊介绍: Anemia is a peer-reviewed, Open Access journal that publishes original research articles, review articles, and clinical studies on all types of anemia. Articles focusing on patient care, health systems, epidemiology, and animal models will be considered, among other relevant topics. Affecting roughly one third of the world’s population, anemia is a major public health concern. The journal aims to facilitate the exchange of research addressing global health and mortality relating to anemia and associated diseases.
×
引用
GB/T 7714-2015
复制
MLA
复制
APA
复制
导出至
BibTeX EndNote RefMan NoteFirst NoteExpress
×
提示
您的信息不完整,为了账户安全,请先补充。
现在去补充
×
提示
您因"违规操作"
具体请查看互助需知
我知道了
×
提示
确定
请完成安全验证×
copy
已复制链接
快去分享给好友吧!
我知道了
右上角分享
点击右上角分享
0
联系我们:info@booksci.cn Book学术提供免费学术资源搜索服务,方便国内外学者检索中英文文献。致力于提供最便捷和优质的服务体验。 Copyright © 2023 布克学术 All rights reserved.
京ICP备2023020795号-1
ghs 京公网安备 11010802042870号
Book学术文献互助
Book学术文献互助群
群 号:604180095
Book学术官方微信
小红书