Why the study?
Due to a lack of prospective multicenter randomized clinical trials, there is no universally accepted prenatal treatment regimen for fetal tachyarrhythmias, and drug treatments carry potential risks.
The management of fetal tachyarrhythmias relies on observational data, highlighting a critical need for prospective randomized trials to establish safe and effective prenatal drug regimens.
No universal fetal tachyarrhythmia regimen exists; leaves open the need for multicenter RCTs to define safe regimens.
It is estimated that 1%-2% of pregnancies are complicated by fetal arrhythmias, with most arrhythmias considered benign and not requiring further treatment or intervention. However, persistent tachyarrhythmias can lead to fetal heart failure, preterm birth, stillbirth, and increased risks during the perinatal period. Therefore, timely treatment during pregnancy is often necessary. Currently, prenatal treatment for fetal tachyarrhythmias (FTs) is primarily drug based, aiming to restore normal fetal heart rate, prevent or reverse fetal heart failure, and avoid adverse outcomes such as preterm birth and stillbirth. Despite decades of clinical experience, the lack of prospective, multicenter randomized clinical trials on the safety and efficacy of drugs means that there is still no universally accepted prenatal treatment regimen for FTs, and treatment relies on series of observational studies or clinical cases. Moreover, all drug treatments carry potential risks to the mother, fetus, and pregnancy, hence the need for more clinical diagnostic and therapeutic experience to provide more clinical evidence for prenatal treatment of FTs.
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Tang et al. (2024) studied this question.
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