K. Yoshimoto et al., DIHYDROPYRIDINE TYPE CALCIUM-CHANNEL BLOCKER-INDUCED TURBID DIALYSATEIN PATIENTS UNDERGOING PERITONEAL-DIALYSIS, Clinical nephrology, 50(2), 1998, pp. 90-93
We previously reported that manidipine, a new dihydropyridine type cal
cium channel blocker, produced chylous peritoneal dialysate being visu
ally indistinguishable from infective peritonitis in 5 patients underg
oing continuous ambulatory peritoneal dialysis (CAPD) [Yoshimoto et al
. 1993]. To study whether such an adverse drug reaction would also be
elicited by other commonly prescribed calcium channel blockers in CARD
patients, we have conducted postal inquiry to 15 collaborating hospit
als and an institutional survey in International Medical Center of Jap
an as to the possible occurrence of calcium channel blocker-associated
non-infective, turbid peritoneal dialysate in CAPD patients. Our diag
nostic criteria for drug-induced turbidity of dialysate as a) it devel
oped within 48 h after the administration of a newly introduced calciu
m channel blocker to the therapeutic regimen, b) absence of clinical s
ymptoms of peritoneal inflammation (i. e., pyrexia, abdominal pain, na
usea or vomiting), c) the fluid containing normal leukocyte counts and
being negative for bacterial and fungal culture of the fluid, and d)
it disappeared shortly after the withdrawal of the assumed causative a
gent. Results showed that 19 out of 251 CAPD patients given one of the
calcium channel blockers developed non-infective turbid peritoneal di
alysis that fulfilled all the above criteria. Four calcium channel blo
ckers were suspected to be associated with the events: benidipine [2 o
ut of 2 (100%) patients given the drug], manidipine [15 out of 36 (42%
) patients], nisoldipine [1 out of 11 (9%) patients] and nifedipine [1
out of 159 (0.6%)] in descending order of frequency. None of the pati
ents who received nicardipine, nilvadipine, nitrendipine, barnidipine
and diltiazem (25, 7, 2, 1 and 8 patients, respectively) exhibited tur
bid dialysate. In conclusion, we consider that certain dihydropyridine
type calcium channel blockers would cause turbid peritoneal dialysate
being similar to that observed in patients developing infective perit
onitis. To avoid unnecessary antibiotic therapy the possibility of thi
s adverse reaction should be ruled out whenever a CAPD patient receivi
ng a dihydropyridine type calcium channel blocker develops turbid dial
ysate.