The FDA issued a public health notification regarding use of surgical mesh for the repair of pelvic organ prolapsed and stress urinary incontinence. Surgical mesh has caused severe complications in some patients.
The FDA has issued a public health notification regarding use of surgical mesh for the repair of pelvic organ prolapsed and stress urinary incontinence. Surgical mesh has caused severe complications in some patients. While a lawsuit is pending, surgical mesh is still being used. The FDA recommends physicians obtain specialized training and be aware of the potential risks, thoroughly inform patients of adverse risks, and monitor patients closely for complications.
Maternal sFLT1 and EDN1 linked to late-onset preeclampsia
November 25th 2024A new study highlights the association of maternal soluble Fms-like tyrosine kinase 1 and endothelin 1 with preeclampsia severity, offering insights into the pathogenesis of early- and late-onset forms of the condition.
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