Objective: To compare endoscopic coverage of myelomeningocele with a matern
al split-thickness skin graft in utero to definitive neurosurgical closure
through a hysterotomy. Methods: Four fetuses with isolated myelomeningocele
underwent endoscopic coverage of the defect with a maternal split-thicknes
s skin graft in a CO2 environment at 22-24 weeks' gestation, Subsequently,
4 fetuses underwent standard neurosurgical closure of their myelomeningocel
es at 28-29 weeks' gestation. Results: The mean operating time for the endo
scopic procedures was 297 +/- 69 min. Two fetal losses occurred as a result
of chorioamnionitis and placental abruption, respectively. A third baby de
livered at 28 weeks' gestation after prolonged disruption of the membranes.
The 2 survivors required standard closure of the myelomeningocele after de
livery. The mean operating time for the hysterotomy procedures was 125 +/-
8 min. No mortality occurred, and all the infants delivered between 33 and
36 weeks with well-healed myelomeningocele scars. At present, the functiona
l levels of all infants approximate the anatomical levels of the lesions. C
onclusion: With current technology, in utero repair of congenital myelomeni
ngocele through a hysterotomy appears to be technically superior to procedu
res performed endoscopically, Copyright (C) 2000 S. Karger AG, Basel.