Christina M Abrams, Caroline B Foster, Natalia Davila, Marcelaine Reneau, Earleisha Felder, Martina Mueller, Caroline Davila
{"title":"Maternal and Infant Outcomes in a Subset of Patients with Sickle Cell Disease in South Carolina.","authors":"Christina M Abrams, Caroline B Foster, Natalia Davila, Marcelaine Reneau, Earleisha Felder, Martina Mueller, Caroline Davila","doi":"10.14423/SMJ.0000000000001784","DOIUrl":null,"url":null,"abstract":"<p><strong>Objectives: </strong>Sickle cell disease (SCD), which disproportionately affects minorities, increases complications during pregnancy. Severe maternal mortality is increased in women with SCD, including morbidity related to the disease and other nondisease-related complications. It also can have devastating complications for fetuses, with increases in premature birth and low birth weight. This study aimed to describe the characteristics of women with SCD in South Carolina, with a specific focus on fetal and maternal outcomes and complications. The secondary aim of this study was to identify the effect of maternal characteristics on birth outcomes, including social determinants of health.</p><p><strong>Methods: </strong>A secondary analysis of women from a single institution, the Medical University of South Carolina, which was part of the registry from the multi-institutional Sickle Cell Disease Implementation Consortium, was conducted. Patient demographics, self-reported pregnancy history, hydroxyurea use, and maternal and fetal outcomes were collected from patient-reported survey data. In addition, the number of vaso-occlusive episodes surrounding their pregnancies was collected for analysis.</p><p><strong>Results: </strong>Fifty-nine percent (116/195) of the female participants reported ever being pregnant. Seventy-two percent had live births, 15.8% had miscarriages, 1.8% had stillbirths, and 6.1% had an abortion. The mean age was 22.3 ± 4 years, with no difference in markers of severity between the groups. Most women were HbSS genotype with high rates of pain in the last year. No difference was found in age, education, employment, or income between these groups of women. Women in the nonlive birth cohort had higher body weights (78.7 versus 72.1 kg, <i>P</i> = 0.045). The Distressed Community Index was used as a marker for social determinants of health and was similar between the two groups, with a majority of both cohorts (61.7% and 52%) living in \"at risk\" and \"distressed\" communities. Complications related to SCD were high, including 43% of women experiencing pain during pregnancy, 5.2% developing acute chest syndrome, and 22.4% requiring transfusion. An additional 11% experienced preeclampsia. Unfavorable infant outcomes included 49% of the infants being premature and 40% having babies weighing less than 5.5 lb at birth.</p><p><strong>Conclusions: </strong>High rates of complications to both mother and infant were found in the women with SCD. Although few statistically significant predictors were found, by identifying and addressing specific needs of pregnant women with SCD, we can work toward reducing fetal and maternal mortality in an already vulnerable population.</p>","PeriodicalId":22043,"journal":{"name":"Southern Medical Journal","volume":"118 2","pages":"91-96"},"PeriodicalIF":1.0000,"publicationDate":"2025-02-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":null,"platform":"Semanticscholar","paperid":null,"PeriodicalName":"Southern Medical Journal","FirstCategoryId":"3","ListUrlMain":"https://doi.org/10.14423/SMJ.0000000000001784","RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"Q3","JCRName":"MEDICINE, GENERAL & INTERNAL","Score":null,"Total":0}
引用次数: 0
Abstract
Objectives: Sickle cell disease (SCD), which disproportionately affects minorities, increases complications during pregnancy. Severe maternal mortality is increased in women with SCD, including morbidity related to the disease and other nondisease-related complications. It also can have devastating complications for fetuses, with increases in premature birth and low birth weight. This study aimed to describe the characteristics of women with SCD in South Carolina, with a specific focus on fetal and maternal outcomes and complications. The secondary aim of this study was to identify the effect of maternal characteristics on birth outcomes, including social determinants of health.
Methods: A secondary analysis of women from a single institution, the Medical University of South Carolina, which was part of the registry from the multi-institutional Sickle Cell Disease Implementation Consortium, was conducted. Patient demographics, self-reported pregnancy history, hydroxyurea use, and maternal and fetal outcomes were collected from patient-reported survey data. In addition, the number of vaso-occlusive episodes surrounding their pregnancies was collected for analysis.
Results: Fifty-nine percent (116/195) of the female participants reported ever being pregnant. Seventy-two percent had live births, 15.8% had miscarriages, 1.8% had stillbirths, and 6.1% had an abortion. The mean age was 22.3 ± 4 years, with no difference in markers of severity between the groups. Most women were HbSS genotype with high rates of pain in the last year. No difference was found in age, education, employment, or income between these groups of women. Women in the nonlive birth cohort had higher body weights (78.7 versus 72.1 kg, P = 0.045). The Distressed Community Index was used as a marker for social determinants of health and was similar between the two groups, with a majority of both cohorts (61.7% and 52%) living in "at risk" and "distressed" communities. Complications related to SCD were high, including 43% of women experiencing pain during pregnancy, 5.2% developing acute chest syndrome, and 22.4% requiring transfusion. An additional 11% experienced preeclampsia. Unfavorable infant outcomes included 49% of the infants being premature and 40% having babies weighing less than 5.5 lb at birth.
Conclusions: High rates of complications to both mother and infant were found in the women with SCD. Although few statistically significant predictors were found, by identifying and addressing specific needs of pregnant women with SCD, we can work toward reducing fetal and maternal mortality in an already vulnerable population.
目的:镰状细胞病(SCD)对少数民族的影响不成比例,增加了妊娠期间的并发症。严重的孕产妇死亡率在患有SCD的妇女中增加,包括与疾病和其他非疾病相关的并发症有关的发病率。它也会给胎儿带来毁灭性的并发症,增加早产和低出生体重。本研究旨在描述南卡罗来纳州SCD妇女的特征,特别关注胎儿和母亲的结局和并发症。本研究的第二个目的是确定产妇特征对出生结果的影响,包括健康的社会决定因素。方法:对来自南卡罗来纳医科大学这一单一机构的妇女进行了二次分析,该机构是多机构镰状细胞病实施联盟登记的一部分。从患者报告的调查数据中收集患者人口统计数据、自我报告的妊娠史、羟基脲使用情况以及母婴结局。此外,收集她们怀孕期间血管闭塞发作的次数进行分析。结果:59%(116/195)的女性参与者报告曾经怀孕过。72%的人活产,15.8%的人流产,1.8%的人死产,6.1%的人堕胎。平均年龄为22.3±4岁,两组间严重程度指标无差异。大多数女性为HbSS基因型,去年疼痛发生率高。这些女性在年龄、教育、就业或收入方面没有发现差异。非活产组的女性体重更高(78.7 vs 72.1 kg, P = 0.045)。贫困社区指数被用作健康的社会决定因素的标志,在两组之间是相似的,两组的大多数人(61.7%和52%)都生活在“危险”和“贫困”社区。与SCD相关的并发症很高,包括43%的妇女在怀孕期间经历疼痛,5.2%的妇女出现急性胸部综合征,22.4%的妇女需要输血。另有11%的人经历过先兆子痫。不利的婴儿结果包括49%的婴儿早产,40%的婴儿出生时体重低于5.5磅。结论:SCD患者母婴并发症发生率高。虽然没有发现有统计学意义的预测因素,但通过识别和解决SCD孕妇的特殊需求,我们可以在已经脆弱的人群中努力降低胎儿和孕产妇死亡率。
期刊介绍:
As the official journal of the Birmingham, Alabama-based Southern Medical Association (SMA), the Southern Medical Journal (SMJ) has for more than 100 years provided the latest clinical information in areas that affect patients'' daily lives. Now delivered to individuals exclusively online, the SMJ has a multidisciplinary focus that covers a broad range of topics relevant to physicians and other healthcare specialists in all relevant aspects of the profession, including medicine and medical specialties, surgery and surgery specialties; child and maternal health; mental health; emergency and disaster medicine; public health and environmental medicine; bioethics and medical education; and quality health care, patient safety, and best practices. Each month, articles span the spectrum of medical topics, providing timely, up-to-the-minute information for both primary care physicians and specialists. Contributors include leaders in the healthcare field from across the country and around the world. The SMJ enables physicians to provide the best possible care to patients in this age of rapidly changing modern medicine.