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Ther Clin Risk Manag. 2008 December; 4(6): 1371–1374.
Published online 2008 December.
PMCID: PMC2643118
Safe and tolerable one-hour pamidronate infusion for multiple myeloma patients
Dimitrios Chantzichristos, Björn Andréasson, and Peter Johansson
Department of Internal Medicine, Uddevalla Hospital, Uddevalla, Sweden
Correspondence: Peter Johansson, Department of Internal Medicine, Uddevalla Hospital, Fjällvägen 7, 45180 Uddevalla, Sweden, Tel +46 522 92000, Fax +46 522 93232, Email peter.l.johansson/at/vgregion.se
Abstract
Background:
Once a month, patients with multiple myeloma received an infusion of bisphosphonates, principally to reduce osteoclastic bone resorption. Recommended infusion time for pamidronate is 2 hours in the US and 4 hours in Europe because of its potential nephrotoxicity. From 2003, a 90 mg infusion of pamidronate was provided over 1 hour to patients with no pre-existing renal impairment, in the Daily Care Unit at Uddevalla Hospital.
Method:
Retrospective analysis of the renal deterioration, serum calcium, and adverse effects in patients with multiple myeloma treated with 1-hour pamidronate 90 mg infusion from January 2003 to April 2007.
Results:
Seventy-nine patients provided valuable data. A total number of 846 infusions were given and the median number of infusion to each patient was 11. Significant creatinine elevation was seen in 7 patients (8.9%), after 19 infusions (2.2%). Renal deterioration occurred in 5 of these 7 patients, which was related to progress of the myeloma or opportunistic infections. Prevalence of infusion-related events was 0.8% and the mean total S-Ca was 0.05 mmol/L lower than the baseline.
Conclusion:
Few events of renal deterioration, hypocalcemia, or other adverse effects resulted from a 1-hour pamidronate 90 mg infusion for multiple myeloma patients with no pre-existing renal impairment.
Keywords: bisphosphonates, pamidronate, multiple myeloma, infusion time