Paladugu Vinya, Teja Nikhil, Menon Rajashree, Ramachandran Riju
Obstetrics and Gynaecology, Amrita Institute of Medical Sciences and Hospital, Kochi, IND.
Internal Medicine, Amrita Institute of Medical Sciences and Hospital, Kochi, IND.
Cureus. 2024 Aug 15;16(8):e66926. doi: 10.7759/cureus.66926. eCollection 2024 Aug.
Background Pregnant women with primary Sjogren's syndrome (PSS) have a high incidence of maternal and fetal complications due to immunological variations caused by maternal antibodies (anti-Sjogren's-syndrome-related antigen A (SSA) and anti-anti-Sjogren's-syndrome-related antigen B (SSB) crossing the placenta from the 12th week of gestation, mediating the tissue damage. A multidisciplinary approach is required in the management of such patients. Data regarding the effects of PSS on pregnancy are deficient in the Indian context. Methods This was a retrospective observational study on the maternal and fetal outcomes of PSS on a cohort of pregnant women treated at our tertiary care center between 2011 and 2020. Patients who satisfied the criteria for PSS were included, and patients with other associated autoimmune disorders were excluded. Maternal age, number of miscarriages, prior obstetric history, and maternal and fetal complications were recorded and statistically analyzed. Results There were 16 pregnancies in 10 women with PSS (incidence: 1/1,000 pregnancies/year) in our study. The mean gestational age of the mother at presentation was 31 ± 9.0 weeks. Oligohydramnios in five (11.8), intrauterine fetal demise (IUFD) in two (11.8), and first-trimester medical termination of pregnancy (MTP) in four (23.5) were noted. The weight of neonates was 2.3 ± 0.8 kg, and the mean duration of neonatal intensive care (NICU) stay was seven days. Fetal echo revealed congenital heart block (CHB), with six (50.0%) complete and one (8.3%) incomplete (p = 0.004). One baby needed a permanent pacemaker. Conclusion Maternal and fetal complications are high in our set of mothers with PSS. Early detection, regular follow-up, and a multidisciplinary approach may improve the outcome.
患有原发性干燥综合征(PSS)的孕妇由于母体抗体(抗干燥综合征相关抗原A(SSA)和抗干燥综合征相关抗原B(SSB))引起的免疫变化,在妊娠第12周起穿过胎盘,介导组织损伤,导致母婴并发症发生率较高。对此类患者的管理需要多学科方法。在印度背景下,关于PSS对妊娠影响的数据不足。
这是一项对2011年至2020年在我们三级护理中心接受治疗的一组孕妇中PSS的母婴结局进行的回顾性观察研究。纳入符合PSS标准的患者,排除患有其他相关自身免疫性疾病的患者。记录产妇年龄、流产次数、既往产科病史以及母婴并发症,并进行统计分析。
我们的研究中有10名患有PSS的女性发生了16次妊娠(发病率:1/1000次妊娠/年)。母亲就诊时的平均孕周为31±9.0周。观察到5例(11.8%)羊水过少、2例(11.8%)宫内胎儿死亡(IUFD)和4例(23.5%)孕早期人工流产(MTP)。新生儿体重为2.3±0.8千克,新生儿重症监护(NICU)平均住院时间为7天。胎儿超声心动图显示先天性心脏传导阻滞(CHB),其中6例(50.0%)为完全性,1例(8.3%)为不完全性(p = 0.004)。1名婴儿需要永久性起搏器。
在我们这组患有PSS的母亲中,母婴并发症发生率较高。早期检测、定期随访和多学科方法可能会改善结局。