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.