Mb. Allen et al., CHANGES IN NOCTURNAL OXIMETRY AFTER TREATMENT OF EXACERBATIONS IN CYSTIC-FIBROSIS, Archives of Disease in Childhood, 69(2), 1993, pp. 197-201
Sleep related arterial oxygen desaturation has been described in clini
cally stable young adults with cystic fibrosis. The incidence and seve
rity of nocturnal oxygen desaturation in children during infective exa
cerbations and the changes that occur with treatment were examined. Fo
rty five children with proved cystic fibrosis, median age 8.9 years, a
dmitted to the Regional Cystic Fibrosis Unit underwent clinical evalua
tion, spirometry, and measurement of peak flow and nocturnal oxygen sa
turation on admission and after 10 days' treatment. There was a signif
icant improvement in all the above measurements, with the averaged ove
rnight saturation changing from a mean (SD) 92.7 (2.7)% to 94.3 (2.0)%
, mean (SE) difference 1.58 (0.37). The time spent with a saturation 4
% or more below their clinic value showed a marked improvement from 12
2 (152) minutes on the first night to 21 (30.7) on the second, mean (S
E) difference 101 (22.4). Eight young children could not perform pulmo
nary function tests, all desaturated on the admission night. Nocturnal
hypoxaemia is a common finding in young cystic fibrosis patients duri
ng infective exacerbations but improves with treatment. Overnight oxim
etry is simple to perform, well tolerated, and identifies patients wit
h marked nocturnal desaturation.