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首页> 外文期刊>Thyroid: official journal of the American Thyroid Association >The magnitude of increased levothyroxine requirements in hypothyroid pregnant women depends upon the etiology of the hypothyroidism.
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The magnitude of increased levothyroxine requirements in hypothyroid pregnant women depends upon the etiology of the hypothyroidism.

机译:甲状腺功能减退孕妇中左甲状腺素需求量增加的幅度取决于甲状腺功能减退症的病因。

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摘要

BACKGROUND: In the United States, many women with hypothyroidism are on thyroid hormone replacement during pregnancy. The optimal management strategy for thyroid hormone dosing in hypothyroid women during pregnancy is controversial. We hypothesized that dosage requirements during pregnancy might differ depending upon the nature of the underlying hypothyroidism. METHODS: We conducted a retrospective review of 45 pregnancies from 38 women whose hypothyroidism was managed during pregnancy. Thyroid function tests were obtained when pregnancy was confirmed, then every 4-8 weeks. The thyrotropin (TSH) goal was 0.4-4.1 microU/mL (SI unit conversion: multiply TSH by 1.0 for mIU/L). RESULTS: On average, the entire group required a cumulative increase from baseline in levothyroxine (LT(4)) dosage of 13% in the first trimester, 26% in the second trimester, and 26% in the third trimester (p < 0.001, p < 0.001, p < 0.001, respectively). Average baseline LT(4) dose for patients with primary hypothyroidism was 92.5 +/- 32.0 microg daily. These patients required small cumulative dose increases of 11%, 16%, and 16% from baseline in each trimester, respectively (p values = 0.125, 0.016, 0.016). Average baseline LT(4) dose for patients with hypothyroidism resulting from treated Graves' disease or goiter was 140.4 +/- 62.4 microg daily. These patients required the largest cumulative increases in LT(4) dosage (first trimester, 27%; second trimester, 51%; third trimester, 45%; p = 0.063, 0.063, 0.063, respectively). Average baseline LT(4) dose for patients with thyroid cancer was 153.2 +/- 30.3 microg. The cumulative LT(4) dose increases for patients with thyroid cancer were 9%, 21%, and 26% in each trimester, respectively (p = 0.03, p < 0.001, p < 0.001). CONCLUSIONS: The etiology of hypothyroidism plays a pivotal role in determining the timing and magnitude of thyroid hormone adjustments during pregnancy. Patients require vigilant monitoring of thyroid function upon confirmation of conception and anticipatory adjustments to LT(4) dosing based on the etiology of their hypothyroidism.
机译:背景:在美国,许多甲状腺功能低下的妇女在怀孕期间正在服用甲状腺激素。甲状腺功能减退妇女在怀孕期间服用甲状腺激素的最佳管理策略存在争议。我们假设怀孕期间的剂量要求可能会因潜在甲状腺功能减退症的性质而异。方法:我们对38例在妊娠期间甲状腺功能减退的女性进行了45次妊娠的回顾性研究。确认怀孕后进行甲状腺功能检查,然后每4-8周进行一次。促甲状腺素(TSH)的目标是0.4-4.1 microU / mL(SI单位转换:将mSH / L的TSH乘以1.0)。结果:平均而言,整个组在妊娠前三个月的左甲状腺素(LT(4))剂量累计比基线分别增加13%,孕中期26%和孕中期26%(p <0.001, p <0.001,p <0.001)。原发性甲状腺功能减退症患者的平均基线LT(4)剂量为每日92.5 +/- 32.0微克。这些患者在每个孕中期分别需要少量的累积剂量分别较基线增加11%,16%和16%(p值= 0.125、0.016、0.016)。因治疗的格雷夫斯病或甲状腺肿大导致甲状腺功能减退的患者的平均基线LT(4)剂量为每日140.4 +/- 62.4微克。这些患者需要LT(4)剂量的最大累积增加量(孕中期为27%;孕中期为51%;孕晚期为45%; p分别为0.063、0.063、0.063)。甲状腺癌患者的平均基线LT(4)剂量为153.2 +/- 30.3微克。在每个孕中期,甲状腺癌患者的累积LT(4)剂量增加分别为9%,21%和26%(p = 0.03,p <0.001,p <0.001)。结论:甲状腺功能减退的病因在决定怀孕期间甲状腺激素调节的时机和幅度方面起着关键作用。确认构想并根据甲状腺功能减退症的病因对LT(4)剂量进行预期调整后,患者需要对甲状腺功能进行警惕的监测。

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