Fetal repair of myelomeningocele: current status and urologic implications

J Pediatr Urol. 2020 Feb;16(1):3-9. doi: 10.1016/j.jpurol.2019.11.019. Epub 2019 Dec 6.

Abstract

Over the last 40 years, vast changes have occurred in the care of children with open neural tube defects. Not only has newborn survival dramatically improved but survival into adulthood has improved as well. Now, the ability to accurately identify and repair myelomeningocele (MMC) lesions before birth has become a reality. Pioneering efforts at several institutions in the United States paved the way for such advancements in care. Substantial data now exist to support the positive benefits of fetal MMC repair from a neurosurgical standpoint, chiefly the significant reduction in hindbrain herniation, decrease in shunt-dependent hydrocephalus, and improvement in lower-extremity motor function. However, until only recently, the urological impact of fetal repair has not been nearly as positive overall. Multiple retrospective reports of newborn bladder function from the United States suggest that prenatal repair has provided neither short-term nor long-term improvements in bladder function. Yet, the retrospective nature of these data and their focus upon urodynamic studies (UDS) parameters have hampered the ability to draw conclusions. Recently, published data from the landmark Management of Myelomeningocele Study indicate that fetal repair may improve certain aspects of bladder function when compared with conventional repair. This review provides an overview of the history and timeline of fetal repair in the United States and brings the reader quickly up to date on the current impact of repair on both neurosurgical and urological outcomes.

Keywords: Fetal therapy; Hydrocephalus; Myelomeningocele; Neurogenic; Urinary bladder.

Publication types

  • Review

MeSH terms

  • Fetus / surgery*
  • Humans
  • Meningomyelocele / surgery*
  • Treatment Outcome
  • Urinary Bladder / physiopathology*
  • Urology