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Published on: February 4, 2015
Fetal Therapy for Renal Anhydramnios
Jena L Miller1, Ahmet A Baschat1, Meredith A Atkinson2
1Department of Gynecology and Obstetrics, The Johns Hopkins Center for Fetal Therapy, 600 North Wolfe Street, Nelson 228, Baltimore, MD 21287, USA.
Severe congenital kidney and urinary tract anomalies can be lethal due to pulmonary hypoplasia. Fetal therapy aims to restore amniotic fluid, preventing this lung development issue and addressing the underlying renal disease.
Area of Science:
- Perinatology
- Pediatric Nephrology
- Medical Genetics
Background:
- Congenital anomalies of the kidney and urinary tract (CAKUT) represent a spectrum of developmental abnormalities.
- Severe CAKUT manifesting as renal anhydramnios in fetal life is often lethal due to associated pulmonary hypoplasia.
- Fetal intervention is being explored for select cases, necessitating careful patient stratification.
Purpose of the Study:
- To evaluate the safety and efficacy of fetal therapy for severe CAKUT.
- To assess the role of amnioinfusions in preventing pulmonary hypoplasia.
- To determine appropriate criteria for selecting pregnancies for fetal intervention.
Main Methods:
- The Renal Anhydramnios Fetal Therapy (RAFT) trial is a multi-center study.
- Serial amnioinfusions are administered to restore amniotic fluid volume.
- Detailed anatomic surveys and genetic testing are performed for patient stratification.
Main Results:
- Pulmonary hypoplasia is a primary concern in fetuses with renal anhydramnios.
- Restoration of amniotic fluid is the cornerstone of prenatal treatment.
- Ongoing research aims to establish the efficacy of this therapeutic approach.
Conclusions:
- Fetal intervention, including amnioinfusions, holds potential for managing lethal forms of CAKUT.
- Comprehensive evaluation including genetic testing is crucial for identifying suitable candidates for therapy.
- The RAFT trial will provide critical data on the safety and effectiveness of preventing pulmonary hypoplasia in these high-risk pregnancies.
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