Table 2.
Summary of the most important RCTs evaluating effects of levothyroxine replacement in women who are euthyroid with raised TPO antibodies before and during pregnancy.
Trial | Country | Population | Intervention | Control | Primary outcome | Events intervention group | Events control group | Results |
---|---|---|---|---|---|---|---|---|
Wang 201719 | China | N=600 women (N=300 intervention and N=300 control) undergoing IVF-ET. TPO raised and biochemically euthyroid |
Levothyroxine to titrate TSH: 0.1–2.5 mIU/L in first trimester 0.2–3.0 mIU/L in second trimester 0.3–3.0mIU/L in third trimester |
No treatment | Miscarriage before 28 weeks’ gestation in women becoming pregnant | 10.3% | 10.6% |
Absolute RD = -0.34% 95% CI= -8.65– 8.12% |
Dhillon-Smith 201918 | UK | N=940 women with history of miscarriage or infertility (N=476 intervention and N=476 control). TPO raised and biochemically euthyroid |
Levothyroxine 50 µg OD | Placebo | Live birth after 34 weeks’ gestation | 37.4% | 37.9% |
P value=0.74 RR=0.97 95% CI= 0.83–1.14 Absolute RD= -0.4% [-6.6–5.8] |
Van Dijk 202317 | The Netherlands, Belgium, Denmark | N=187 women with two or more pregnancy losses (N=94 intervention and N=93 control). TPO raised and biochemically euthyroid |
Levothyroxine 0.5–1.0 µg/kg depending on pre-conception TSH | Placebo | Live birth after 24 weeks’ gestation | 50% | 48% |
RR=1.03 95% CI= 0.77–1.38 |
RD, Rate difference, RR, Relative risk, CI, Confidence interval.