U. Bechtel et al., LIMITATIONS OF PULSE ORAL CALCITRIOL THERAPY IN CONTINUOUS AMBULATORYPERITONEAL-DIALYSIS PATIENTS, American journal of kidney diseases, 25(2), 1995, pp. 291-296
Calcitriol is increasingly used for therapy of secondary hyperparathyr
oidism in patients with end-stage renal disease. Its therapeutic effic
acy, however, often has been limited by the associated increase in int
estinal calcium and phosphorus absorption. Previous studies reported t
hat these side effects could be avoided by intermittent administration
of calcitriol in high doses, subsequently referred to as pulse therap
y. The present study was designed to investigate pulse oral calcitriol
therapy in a patient subgroup especially susceptible to the developme
nt of hypercalcemia and hyperphosphatemia under standard continuous ca
lcitriol treatment. We examined 15 peritoneal dialysis patients with m
oderate degrees of hyperparathyroidism (intact parathyroid hormone [iP
TH] levels, 150 to 903 pg/mL) ingesting between 1.5 and 6 g of calcium
salts as the sole phosphate binders. Treatment consisted of 0.5 mu g
calcitriol twice weekly. Eight of these patients had been previously c
onverted to low calcium dialysate to tolerate the necessary doses of p
hosphate-binding calcium salts. During the study period, comprising 8
pretreatment weeks and 8 weeks of therapy, dialysates and doses of cal
cium salts were not changed, so that only calcitriol influenced the de
termined parameters. As expected, iPTH levels decreased rapidly in all
patients (P < 0.0001). However, within 4 weeks of treatment a marked
increase in calcium phosphorus products was observed (P < 0.0001). Ove
rt hypercalcemia developed in five patients. We concluded that pulse o
ral calcitriol has to be carefully monitored in peritoneal dialysis pa
tients receiving high doses of calcium salts because of the increased
risk for hypercalcemia and hyperphosphatemia. (C) 1995 by the National
Kidney Foundation, Inc.