Reducing the rate of premature births through early diagnosis and pregnancy-adapted treatment of hypothyroidism

• Verfasst von: Torremante, Elio [VerfasserIn]
• Verfasst von: Berge, Nils Kristian [VerfasserIn]
• Verfasst von: Weiß, Christel [VerfasserIn]
• Titel: Reducing the rate of premature births through early diagnosis and pregnancy-adapted treatment of hypothyroidism
• Paralleltitel: Reduktion der Frühgeburtenrate durch frühzeitige Diagnostik und schwangerschaftsadaptierte Therapie der Schilddrüsenunterfunktion
• Verf.angabe: Authors: Pompilio Torremante, Nils Kristian Berge, Christel Weiss
• E-Jahr: 2023
• Jahr: 05. Oktober 2023
• Umfang: 10 S.
• Illustrationen: Illustrationen
• Fussnoten: Artikel online veröffentlicht: 05. Oktober 2023 ; Gesehen am 18.12.2023
• Titel Quelle: Enthalten in: Geburtshilfe und Frauenheilkunde
• Ort Quelle: Stuttgart : Thieme, 1980
• Jahr Quelle: 2023
• Band/Heft Quelle: 83(2023), 11, Seite 1361-1370
• ISSN Quelle: 1438-8804
• DOI: doi:10.1055/a-2103-8143
• Datenträger: Online-Ressource
• Sprache: eng ger
• K10plus-PPN: 1876305428

Abstract

The aim of this study was to determine the extent to which regular monitoring of maternal free thyroxine level and pregnancy-adapted L-thyroxine replacement therapy before and during pregnancy in patients with existing or newly diagnosed latent and manifest hypothyroidism as well as hypothyroxinemia can influence the rate of premature births. This is a retrospective cohort study assessing 1440 pseudonymized survey questionnaires to evaluate the risks of premature birth with two study groups from the same medical practice, and a nationally recruited control group. Study group A (n = 360) had already been taking L-thyroxine prior to conception, study group B (n = 580) started taking it after conception. Both study groups had a maximum gestational age of 12 + 0 GW. In the study groups, TSH and free thyroxine levels were determined regularly for dose adjustment purposes. The aim was to keep the free thyroxine level in the euthyroid hyperthyroxinemic range within the pregnancy adapted reference range. The control group (n = 500) had taken L-thyroxine during pregnancy according to criteria that were not known, as the questionnaire did not include any questions regarding this matter. Taking other risk factors into account, the influence of pregnancy-adapted L-thyroxine replacement therapy on the rate of premature births was determined using logistic regression analysis. Compared with the control group, the premature birth rate was 70% lower (p < 0.0001) in study group A and 42% lower in study group B (p = 0.0086), while the odds ratio, at 3.46, was particularly significant in study group A. High blood pressure (odds ratio 5.21), body mass index per kg/m2 (odds ratio 0.91) and S. p. premature birth were identified as other independent risk factors. The results show an association between more intensive thyroid diagnostics and pregnancy-adapted L-thyroxine replacement therapy and a decrease in premature births. Further studies should be conducted to confirm these results.