G. Steinkamp et H. Vonderhardt, IMPROVEMENT OF NUTRITIONAL-STATUS AND LUNG-FUNCTION AFTER LONG-TERM NOCTURNAL GASTROSTOMY FEEDINGS IN CYSTIC-FIBROSIS, The Journal of pediatrics, 124(2), 1994, pp. 244-249
We investigated weight gain and clinical course of 14 patients with cy
stic fibrosis (CF), aged 7 to 23 years, who received long-term nocturn
al supplemental feedings by means of percutaneous endoscopic gastrosto
mies (PEGs). The patients (nine female, five male) were moderately mal
nourished; the weight-for-height value was 77.8% (SD 6.4%) of the pred
icted value. Lung function tests revealed severe airway obstruction; m
ean vital capacity was 46.1% (SD 14.4%), and mean forced expiratory vo
lume in 1 second (FEV(1)) was 30.8% (SD 12.3%) of predicted value. A n
onelemental formula providing 35% of total energy from fat was used fo
r nocturnal feedings. The patients received 800 to 1500 kcal per night
by slow intragastric infusions. Enteric-coated pancreatic microsphere
preparations were taken orally just before bedtime. After 1 year of s
upplemental feedings, body weight had increased by 6.0 kg (SD 3.6 kg)
and weight-for-height value by 9.0% (SD 6.1%) of predicted compared wi
th baseline values. Lung function also improved significantly: vital c
apacity increased by 8.2% (SD 6.3%) and FEV(1) by 3.9% (SD 4.2%) of pr
edicted values (p<0.01). The total duration of nocturnal feedings was
364 months, or 26 months per patient. Nine of the fourteen patients co
ntinue to use the PEG, three patients had the PEG tube removed, and tw
o patients have died 21 end 23 months after PEG insertion. We conclude
that nocturnal PEG feedings of malnourished patients with CF improve
nutritional status and lung function without major side effects.