Please use this identifier to cite or link to this item: http://cmuir.cmu.ac.th/jspui/handle/6653943832/60674
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dc.contributor.authorKasemsri Srisupunditen_US
dc.contributor.authorSupatra Sirichotiyakulen_US
dc.contributor.authorFuanglada Tongpraserten_US
dc.contributor.authorSuchaya Luewanen_US
dc.contributor.authorTheera Tongsongen_US
dc.date.accessioned2018-09-10T03:47:00Z-
dc.date.available2018-09-10T03:47:00Z-
dc.date.issued2008-02-01en_US
dc.identifier.issn10153837en_US
dc.identifier.other2-s2.0-40049093261en_US
dc.identifier.other10.1159/000111589en_US
dc.identifier.urihttps://www.scopus.com/inward/record.uri?partnerID=HzOxMe3b&scp=40049093261&origin=inwarden_US
dc.identifier.urihttp://cmuir.cmu.ac.th/jspui/handle/6653943832/60674-
dc.description.abstractIntroduction: Fetal thyrotoxicosis, often caused by maternal Grave's disease, can have adverse effects on fetal outcomes, such as growth impairment or fetal hydrops. Therefore, intrauterine treatment is recommended. Objective: To describe the experience of intrauterine medical treatment of fetal thyrotoxicosis. Case: A 19-year-old woman with a history of Grave's disease in a euthyroid clinical status after subtotal thyroidectomy became pregnant 2 months after thyroidectomy. At gestational age 28 weeks, persistent fetal tachycardia was identified and the diagnosis of fetal thyrotoxicosis was established by fetal thyroid function test on umbilical cord blood obtained by cordocentesis. Intrauterine treatment for hyperthyroidism was initiated with antithyroid drugs (150 mg/day of propylthiouracil) via maternal oral administration. Fetal heart rate, size of fetal thyroid gland and umbilical cord blood sampling for thyroid function test were monitored. Fetal heart rate became normal and fetal thyroid function tested on fetal cord blood at 1 month after antithyroid fetal therapy was also normal. Fetal thyrotoxicosis improved but the mother had some degree of hypothyroidism from fetal therapy and needed thyroid hormone replacement. The remaining course of gestation was uneventful. The patient had spontaneous labor and delivery at 38 weeks of gestation resulting in normal female baby, 2,900 g, and had no clinical of neonatal thyrotoxicosis. Maternal thyroid medications were stopped immediately after birth. Conclusion: Intrauterine treatment of fetal thyrotoxicosis with medication via the maternal circulation can possibly improve fetal outcome. Copyright © 2007 S. Karger AG.en_US
dc.subjectMedicineen_US
dc.titleFetal therapy in fetal thyrotoxicosis: A case reporten_US
dc.typeJournalen_US
article.title.sourcetitleFetal Diagnosis and Therapyen_US
article.volume23en_US
article.stream.affiliationsChiang Mai Universityen_US
article.stream.affiliationsFaculty of Medicine, Thammasat Universityen_US
Appears in Collections:CMUL: Journal Articles

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