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Clinical |
Department of Internal Medicine,1 Taoyuan General Hospital, Taoyuan County; Department of Internal Medicine2 and Department of Nursing,3 National Taiwan University Hospital Taipei, Taiwan
Correspondence to: K.D. Wu, Department of Internal Medicine, National Taiwan University Hospital, No. 7, Chung-Shan South Road, Taipei, Taiwan. kdwu{at}ntuh.gov.tw
Objective: Lercanidipine is a lipophilic calcium
channel blocker and a widely used antihypertensive agent. However, it can
cause chyloperitoneum in patients receiving peritoneal dialysis (PD). The
incidence, pathophysiology, and clinical impact of these adverse events are
not known.
Design: Retrospective study.
Method: Patients were screened for use of
antihypertensive agents. Those that had taken lercanidipine were identified
and dialysate cholesterol (Chol) and triglyceride (TG) levels were checked.
Serum levels were taken from the routine biochemistry record closest to the
time of the dialysate levels. Dialysate Chol and TG from patients on other
antihypertensives and with matched serum lipid profiles were compared.
Patients: 14 of 222 patients had taken lercanidipine
during February 2005 to January 2006, accounting for 12% of all patients on
calcium channel blockers in our PD center.
Results: Of 14 patients prescribed lercanidipine, 8
(57%) developed chyloperitoneum. None had peritonitis and the dialysate was
clear under microscopic examination. Mean dialysate TG was 128.4 ±
133.0 mg/dL and mean dialysate Chol was 18.2 ± 24.9 mg/dL in patients
that developed chyloperitoneum. These patients were also noted to have higher
blood TG and Chol than patients that did not develop chyloperitoneum. In
contrast, patients on other antihypertensive agents with matched blood TG and
Chol levels had low dialysate TG levels and zero dialysate Chol.
Conclusion: Lercanidipine frequently causes
chyloperitoneum in Taiwanese PD patients. The risk of developing this adverse
event seems to be related to the blood lipid profile. The mechanism of this
phenomenon is worthy of further investigation.
KEY WORDS: Chyloperitoneum; hyperlipidemia; lercanidipine.
Received 18 January 2008; accepted 1 April 2008.
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