Department of Endocrinology, Post Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.
Department of General Surgery, Post Graduate Institute of Medical Education and Research, Chandigarh, 160012, India.
J Endocrinol Invest. 2021 Jul;44(7):1425-1435. doi: 10.1007/s40618-020-01441-z. Epub 2020 Oct 9.
To present the data on primary hyperparathyroidism (PHPT) in pregnancy from India obtained from a large database maintained over 15 years.
We retrieved data of all women with gestational PHPT from the Indian PHPT registry between July 2005 and January 2020, and compared their clinical, biochemical, and other characteristics with age-matched non-pregnant women with PHPT.
Out of 386 women, eight had gestational PHPT (2.1%). The common presenting manifestations were acute pancreatitis (50%) and renal stone disease (50%); two were asymptomatic. Five women (62.5%) had a history of prior miscarriages. Seven patients (88%) had preeclampsia during the present gestation. Serum calcium and intact parathyroid hormone (iPTH) were not statistically different from the age-matched non-pregnant PHPT group. Six patients with mild-to-moderate hypercalcemia were medically managed with hydration with/without cinacalcet while one patient underwent percutaneous ethanol ablation of the parathyroid adenoma; none underwent surgery during pregnancy. Mean serum calcium maintained from treatment initiation till delivery was 10.5 ± 0.4 mg/dl. One patient had spontaneous preterm delivery at 36 weeks; the remaining patients had normal vaginal delivery at term. None had severe preeclampsia/eclampsia. Fetal outcomes included low birth weight in three newborns (37.5%); two of them had hypocalcemic seizures.
The prevalence of gestational PHPT was 2.1% in this largest Indian PHPT cohort, which is higher than that reported from the West (< 1%). Gestational PHPT can lead to preeclampsia and miscarriage. Pregnant PHPT patients with mild-to-moderate hypercalcemia can be managed with hydration/cinacalcet; however, long-term safety data and large-scale randomized controlled trials are required.
从一个超过 15 年的大型数据库中呈现印度原发性甲状旁腺功能亢进症(PHPT)的妊娠数据。
我们从 2005 年 7 月至 2020 年 1 月的印度 PHPT 登记处中检索了所有患有妊娠 PHPT 的女性的数据,并将其临床、生化和其他特征与年龄匹配的非妊娠 PHPT 女性进行了比较。
在 386 名女性中,有 8 名患有妊娠 PHPT(2.1%)。常见的表现为急性胰腺炎(50%)和肾结石病(50%);两名无症状。五名女性(62.5%)有先前流产史。在本次妊娠期间,有 7 名患者(88%)患有子痫前期。血清钙和完整甲状旁腺激素(iPTH)与年龄匹配的非妊娠 PHPT 组无统计学差异。六名轻度至中度高钙血症患者接受水化治疗,联合/不联合西那卡塞治疗,一名患者接受甲状旁腺腺瘤经皮乙醇消融治疗;怀孕期间均未行手术。从开始治疗到分娩时的平均血清钙维持在 10.5±0.4mg/dl。一名患者在 36 周时自发性早产;其余患者足月正常阴道分娩。均无严重子痫前期/子痫。胎儿结局包括 3 名新生儿(37.5%)低出生体重;其中两名有低钙血症抽搐。
在这个最大的印度 PHPT 队列中,妊娠 PHPT 的患病率为 2.1%,高于西方报告的患病率(<1%)。妊娠 PHPT 可导致子痫前期和流产。轻度至中度高钙血症的妊娠 PHPT 患者可以通过水化/cinacalcet 治疗;然而,需要长期安全性数据和大规模随机对照试验。