Eur J Pediatr Surg 2001; 11(S1): S18-S20
DOI: 10.1055/s-2001-19738
Original Article

Georg Thieme Verlag Stuttart, New York · Masson Editeur Paris

Clinical Outcomes that Fetal Surgery for Myelomeningocele Needs to Achieve

D. D. Cochrane1 , B. Irwin2 , K. Chambers3
  • 1 Division of Pediatric Neurosurgery, University of British Columbia, Vancouver BC, Canada
  • 2 Children's and Women's Health Center of British Columbia, University of British Columbia, Vancouver BC, Canada
  • 3 Division of Neurosurgery, Department of Surgery, University of British Columbia, Vancouver BC, Canada
Further Information

Publication History

Publication Date:
24 January 2002 (online)

Summary

Introduction: The development of techniques to close open neural tube malformations prior to birth has generated great interest and hope for fetal interventions and their outcomes. To plan a randomized trial, as is being discussed at three centres in the United States, the determination of what constitutes a clinically significant improvement in outcome is critical. To date, preliminary observations from two centres suggest that improvements may occur, not in spinal cord function as originally postulated, but in the extent of the hindbrain hernia and the frequency that shunting is required to control hydrocephalus.

Purpose: The determination of what outcome would constitute an important and clinically significant difference in outcome to be achieved by fetal intervention for myelomeningocele.

Method: Parents of patients and patients treated in our myelomeningocele clinic were surveyed using a structured and validated tool. From the perspective of a recommendation to a close friend or family member, the interviewees were asked to quantify on a scale from 0 to 100 the chance of specific outcomes (need for a shunt, need for a wheelchair, change of urinary incontinence) that a fetal operation would need to predictably achieve.

Results: Responses were obtained from 77 patients/families. The fifty percentile response in each study dimension was as follows: the chance of needing a shunt was 12 % (range 0 - 50 %), the chance of needing a wheelchair was 8 % and the chance of being incontinent was 5 % (range 0 - 25 %).

Conclusions: Fetal interventions will have to achieve significant improvements in the control of hydrocephalus, mobilization and continence over postnatal treatment to be justified.

References

  • 1 Bannister C M. Suggested goals for intrauterine surgery for the repair of myelomeningoceles.  Eur J Pediatr Surg. 2000;  10 (Suppl I) 42
  • 2 Bruner J P, Tulipan N, Paschall R L. et al . Fetal surgery for myelomeningocele and the incidence of shunt-dependent hydrocephalus.  JAMA. 1999;  282 1819-1825
  • 3 Cochrane D D, Wilson R D, Steinbok P. et al . Prenatal spinal evaluation and functional outcome of patients born with myelomeningocele: information for improved prenatal counselling and outcome prediction.  Fetal Diagn Ther. 1996;  11 159-168
  • 4 Heffez D S, Aryanpur J, Hutchins G M. et al . The paralysis associated with myelomeningocele: clinical and experimental data implicating a preventable spinal cord injury.  Neurosurgery. 1990;  26 987-992
  • 5 Hirose S, Farmer D L, Albanese C T. Fetal surgery for myelomeningocele.  Curr Opin Obstet Gynecol. 2001;  13 215-222
  • 6 Meuli M, Meuli-Simmen C, Hutchins G M. et al . The spinal cord lesion in human fetuses with myelomeningocele: implications for fetal surgery.  J Pediatr Surg. 1997;  32 448-452
  • 7 Meuli M, Meuli-Simmen C, Yingling C D. et al . Creation of myelomeningocele in utero: a model of functional damage from spinal cord exposure in fetal sheep.  J Pediatr Surg. 1995;  30 1028-1032
  • 8 Meuli M, Meuli-Simmen C, Yingling C D. et al . In utero repair of experimental myelomeningocele saves neurological function at birth.  J Pediatr Surg. 1996;  31 397-402
  • 9 Olutoye O O, Adzick N S. Fetal surgery for myelomeningocele.  Semin Perinatol. 1999;  23 462-473
  • 10 Simpson J L. Fetal surgery for myelomeningocele: promise, progress, and problems.  JAMA. 1999;  282 1873-1874
  • 11 Sutton L N, Adzick N S, Bilaniuk L T. et al . Improvement in hindbrain herniation demonstrated by serial fetal magnetic resonance imaging following fetal surgery for myelomeningocele.  JAMA. 1999;  282 1826-1831

M. D., F. R. C. S (C) D. D. Cochrane D. D. Cochrane

Division of Pediatric Neurosurgery University of British Columbia

4480 Oak Street

Vancouver BC, V6 H 3V4

Canada

Email: dcochrane@cw.bc.ca

    >