Drug-drug interactions in pediatric oncology patients

被引:19
|
作者
Balk, T. E. [1 ,2 ]
van der Sijs, I. H. [1 ]
van Gelder, T. [1 ]
Janssen, J. J. B. [3 ]
van der Sluis, I. M. [4 ]
van Leeuwen, R. W. F. [1 ,3 ]
Engels, F. K. [1 ]
机构
[1] Erasmus MC, Dept Pharm, Postbus 2040, NL-3000 CA Rotterdam, Netherlands
[2] Univ Utrecht, Fac Pharm, Utrecht, Netherlands
[3] Erasmus MC, Dept Med Oncol, Canc Inst, Rotterdam, Netherlands
[4] Erasmus MC Sophia, Dept Pediat Hematol Oncol, Rotterdam, Netherlands
关键词
cancer pharmacology; chemotherapy; drug-drug interactions; pediatric hematology; oncology; support care; TRIMETHOPRIM-SULFAMETHOXAZOLE; METHOTREXATE; APREPITANT; CHILDREN; THERAPY;
D O I
10.1002/pbc.26410
中图分类号
R73 [肿瘤学];
学科分类号
100214 ;
摘要
BackgroundDrug-drug interactions (DDIs) can negatively affect pharmacotherapy. However, pediatric DDI studies are scarce. We undertook an exploratory study to investigate prevalence and clinical relevance of DDIs between cytostatic and noncytostatic drugs in outpatient pediatric oncology patients. ProcedureAfter informed consent and inclusion, the following information was collected: currently prescribed noncytostatic and cytostatic drugs, comorbidities, and use of over-the-counter (OTC) drugs, complementary and alternative medicines (CAMs), and dietary supplements. All medication was screened for DDIs according to two databases: Micromedex((R)) Solutions and the Dutch drug database G-Standard. The researcher presented DDIs with an associated potential for adverse outcome and a proposal for intervention to three independent experts. If the experts considered a DDI to be potentially clinically relevant and requiring intervention, the physician was notified. ResultsSeventy-three patients were included (median age 8.9 years). A total of 67 different DDIs were counted (66 in Micromedex((R)) Solutions, 14 in G-Standard, and 13 DDIs in both databases). The medication reviews resulted in 35 interventions related to 11 different DDIs. The majority of DDIs concerned noncytostatic drugs (25/35) and one third occurred between cytostatic and noncytostatic drugs (10/35). The use of QTc-interval-prolonging drugs resulted in one intervention. The use of OTC drugs, CAM, or dietary supplements did not lead to DDIs. ConclusionsThis study resulted in a selection of 11 potentially clinically relevant DDIs for 73 outpatients in our pediatric oncology department. Interventions were formulated in close collaboration between physicians and clinical pharmacists. Future research should focus on assessing DDIs concerning QTc-interval prolongation.
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页数:7
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