I. Mushtaq et al., MECONINM ILEUS SECONDARY TO CYSTIC-FIBROSIS - THE EAST LONDON EXPERIENCE, Pediatric surgery international, 13(5-6), 1998, pp. 365-369
Meconium ileus (MI) affects 15% of neonates with cystic fibrosis (CF).
The authors reviewed the management and outcome of 51 neonates presen
ting to a single institution between 1976 and 1995 with MI secondary t
o CF. Clinical presentation included abdominal distension (96%), bilio
us vomiting (49%), and delayed passage of meconium (36%), A family his
tory of CF was present in 4 cases (8%). Twenty-three neonates presente
d with MI and evidence of volvulus, atresia, or perforation (complicat
ed MI). Of these, 16 underwent stoma formation, 1 appendicectomy, and
6 resection with primary anastomosis. Twenty-eight neonates presented
with uncomplicated MI. Of these, 11 were managed non-operatively by Ga
strografin enema (10) or enteral N-acetylcysteine (1). The remainder r
equired stoma formation (15) or bowel resection with primary anastomos
is (2). Early postoperative complications occurred in 2 neonates (4%).
In this hospital the 1-year survival for this condition has increased
from 49% (1953-1970) to 98% (1976-1995) irrespective of the surgical
procedure performed or the presence of volvulus, atresia, or perforati
on. In our experience, bowel resection with primary anastomosis is as
safe as stoma formation and is associated with a reduced length of ini
tial hospital stay.