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These studies suggest that losartan exposure during pregnancy may cause fetal toxic effects, including malformations, renal abnormalities, and increased mortality, and should be avoided.
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Losartan, an angiotensin II receptor blocker (ARB), is commonly used to manage hypertension. However, its use during pregnancy is associated with significant risks to fetal development. This article synthesizes research findings on the effects of losartan exposure during pregnancy, highlighting the potential fetal toxicities and the implications for clinical practice.
Several studies have documented the adverse effects of losartan on fetal development. One of the most common and severe outcomes is oligohydramnios, a condition characterized by decreased amniotic fluid, which can lead to further complications such as fetal pulmonary hypoplasia and hypoplastic skull bones . These conditions often result in severe outcomes, including fetal death .
Exposure to losartan in utero has also been linked to incomplete ossification of skull bones and transient oliguria in newborns. Additionally, losartan can cause irreversible renal abnormalities, as evidenced by studies showing renal tubular dysgenesis and other nephropathies in fetuses exposed to the drug .
Case reports further illustrate the dangers of losartan during pregnancy. For instance, a 32-year-old woman with nephrotic syndrome who continued losartan therapy during pregnancy experienced persistent oligohydramnios, which resolved after discontinuation of the drug. Another case involved a 37-year-old woman whose fetus developed severe malformations and died shortly after birth due to complications associated with losartan exposure.
Research on the pharmacokinetics of losartan indicates that the drug and its active metabolites can transfer to the fetus and accumulate in fetal tissues, particularly during late gestation . This transfer is slow but significant enough to cause developmental issues, especially affecting the renal system .
Losartan's mechanism of action involves blocking the angiotensin II receptor, which plays a crucial role in fetal development. Disruption of this system can lead to severe developmental abnormalities, particularly in the kidneys and skeletal system .
Given the substantial evidence of fetal harm, losartan and other ARBs are contraindicated during pregnancy. Healthcare providers should replace these medications with safer alternatives, such as nifedipine, to manage hypertension in pregnant women.
For women who have been exposed to losartan during pregnancy, close monitoring is essential. Regular ultrasound examinations to assess amniotic fluid levels and fetal development can help manage and mitigate potential risks . In cases where losartan exposure has occurred, discontinuation of the drug and appropriate medical interventions can improve outcomes for both the mother and the fetus .
The use of losartan during pregnancy poses significant risks to fetal development, including oligohydramnios, incomplete ossification, and renal abnormalities. These findings underscore the importance of avoiding ARBs in pregnant women and highlight the need for careful monitoring and alternative treatment strategies to ensure maternal and fetal health.
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