A. Toffolo et al., NON-FUROSEMIDE-RELATED RENAL CALCIFICATIONS IN PREMATURE-INFANTS WITHBRONCHOPULMONARY DYSPLASIA, Acta Paediatrica Japonica Overseas Edition, 39(4), 1997, pp. 433-436
Renal calcification is a known complication of long-term furosemide th
erapy in infants with bronchopulmonary dysplasia (BPD). In a prospecti
ve study the clinical course and long-term renal sequelae of renal cal
cifications of 19 consecutive premature neonates (birthweight < 1250 g
) with bronchopulmonary dysplasia who did not receive furosemide were
examined. Infants were divided into two different groups on the basis
of ultrasound evidence of renal calcifications (RC group) or absence o
f renal calcifications (NRC group). Serial examinations, performed at
the age of 1, 2, 3, 6, 9 and 12 months, showed that 12 infants at the
mean age of 68.5 +/- 12.8 days of life had renal calcifications (63%),
and 3 of them had nephrolithiasis; 8 had bilateral renal calcificatio
ns. Among the 9 survivors, 2 had chronic renal calcifications at the a
ge of 9 months; however, all normalized at the age of 12 months. Twelv
e infants received hydrochlorothiazide and spironolactone (63%), 17 ha
d prolonged courses of xanthines and dexamethasone (89.5%), while furo
semide was not part of the routine pharmacological administration. Sta
tistical analysis showed that birthweight, gestational age, Apgar scor
e and length of parenteral nutrition were comparable in the RC and NRC
group infants. Mean serum creatinine, creatinine clearance, fractiona
l sodium excretion and urinary calcium excretion values during the 12-
month study period were comparable in the RC and NRC groups. Mechanica
l ventilation and hospital stay length were instead associated with re
nal calcification occurrence. The strongest indicator of renal calcifi
cation risk for this high-risk population is the severity of the unres
olved acute lung disease, where different facets of respiratory manage
ment, other than the addition of furosemide, represent sufficient stim
uli and renal injury to potentiate stone formation.