Mc. Petersen et al., ABNORMALITIES IN CONTROL OF VENTILATION IN NEWBORN-INFANTS WITH MYELOMENINGOCELE, The Journal of pediatrics, 126(6), 1995, pp. 1011-1015
Objective: The objective of this study was to assess respiratory respo
nses of newborn infants with myelomeningocele through pneumograms and
carbon dioxide challenge, and to evaluate the possibility of predictin
g which patients with myelomeningocele acquired respiratory symptoms r
elated to the Arnold-Chiari deformity and brain-stem dysfunction. Meth
ods: All surviving infants with spina bifida who were born at the Univ
ersity of lowa Hospitals and Clinics (UIHC) or were transferred there
on the first day of life between January 1987 and January 1991 were as
sessed with a pneumogram and CO2 challenge once they were medically st
able, and were followed for a mean of 30 months (10 to 53 months). Res
ults: Thirty patients met the inclusion criteria for this study; four
died before being studied. Of the 26 remaining patients, 12 were born
at the UIHC and 14 were transferred to the UIHC on the first day of li
fe. Of the 26 infants studied, 12 (46%) had abnormalities on the pneum
ogram including 2 with significant periodic breathing and 10 with epis
odes of desaturation below 87%. Of the 26 infants studied, 4 had no de
tectable response to an increasing fraction of CO2 in inspired air on
the CO2 challenge and 12 had an increase in exhaled minute ventilation
per increase in the alveolar fraction of CO2 in exhaled air more than
2 SD below the mean. Only 10 patients (38.5%) had normal ventilatory
responses to the increasing fraction of CO2 in inspired air. On follow
-up, only one study patient had symptoms related to Arnold-Chiari defo
rmity and brain-stem dysfunction (bilateral vocal cord paralysis). His
neonatal CO2 challenge results and his pneumogram were normal. Conclu
sion: We conclude that these two tests are not useful in predicting wh
ich patients wilt have symptoms related to Arnold-Chiari deformity, Sp
ecificity for the pneumogram and the CO2 challenge was 0.52 and 0.36,
respectively. Sensitivity was zero for both tests, although this resul
t is limited by the low incidence of symptomatic Arnold-Chiari deformi
ty in this sample. As previous investigators have found, a significant
number of patients with meningomyelocele had abnormal ventilatory pat
terns. These ventilatory abnormalities indicate that even in the absen
ce of severe symptoms, the control of the ventilatory response is some
what impaired in many patients with meningomyelocele. This alteration
in ventilatory control is probably related to abnormalities in the dev
elopment of the brain stem.