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Title: Adherence to biochemical monitoring recommendations in patients starting with renin angiotensin system inhibitors: a retrospective cohort study in the Netherlands
Author(s): Bootsma, J.E.
Warle-van Herwaarden, M.F. (32159682X)
Verbeek, A.L.M. (070533687)
Fussenich, P.
Smet, P.A. de (071321144)
Olde Rikkert, M.G.M. (167212737)
Kramers, C. (142708208)
Publication year: 2011
Document type: Article / Letter to editor
Journal: Drug Safety
ISSN: 0114-5916
Volume: vol. 34
Issue: iss. 7
Start page: p. 605
End page: p. 614
Annotation: Bootsma, Janet E M Warle-van Herwaarden, Margreet F Verbeek, Andre L M Fussenich, Peter De Smet, Peter A G M Olde Rikkert, Marcel G Kramers, Cornelis New Zealand Drug Saf. 2011 Jul 1;34(7):605-14. doi: 10.2165/11587250-000000000-00000.
Abstract: Background: Renin angiotensin system inhibitors (RASIs) are frequently involved in serious adverse events. These events principally occur in high-risk patients and often arise within the first days after treatment initiation; therefore, guidelines recommend biochemical monitoring within 3 weeks after the start of therapy with RASIs. Objective: The purpose of this study was to examine the level of biochemical monitoring directly after treatment initiation with RASIs in patients with different risk profiles and to study the attitudes of the physicians involved towards biochemical monitoring. Methods: We carried out a retrospective analysis of 202 patients who started RASI therapy in 2006 in Groesbeek, the Netherlands. We determined the rate of serum creatinine and potassium monitoring within 3 weeks after the start of therapy. In addition, we studied the intentions and attitudes towards biochemical monitoring during RASI therapy among 68 general practitioners and medical specialists by way of a brief questionnaire. Results: Serum creatinine and potassium monitoring after treatment initiation was performed in 34% and 28% of patients, respectively. Of all the patients, 29% had two or more additional risk factors for renal function deterioration. In these high-risk patients, creatinine was significantly less often monitored compared with low-risk patients (22% vs 39%). In contrast to these findings, the prescribing physicians claimed to check serum creatinine within 2 weeks after treatment initiation in 85% of their patients. Most of the prescribing physicians (88%) rated this monitoring as (very) important. Conclusions: We demonstrated that, despite positive intentions of physicians, the biochemical monitoring recommendation in patients treated with RASIs is poorly met. In addition, serum creatinine monitoring was significantly less often performed in high-risk patients compared with low-risk patients.
Subject: IGMD 5: Health aging / healthy living
N4i 2: Invasive mycoses and compromised host
N4i 3: Poverty-related infectious diseases NCEBP 13: Infectious diseases and international health
NCEBP 11: Alzheimer Centre
NCEBP 14: Cardiovascular diseases
NCEBP 1: Molecular epidemiology ONCOL 5: Aetiology, screening and detection
NCEBP 2: Evaluation of complex medical interventions
NCEBP 3: Implementation Science
Subject: NCEBP 2: Evaluation of complex medical interventions ONCOL 5: Aetiology, screening and detection
NCEBP 3: Implementation Science
Organization: UMCN Extern
IQ Healthcare
Epidemiology, Biostatistics & HTA
Clinical Pharmacy
Geriatrics
General Internal Medicine
Pharmacology-Toxicology
Appears in Collections:Academic bibliography

Please use this identifier to cite or link to this item: http://hdl.handle.net/2066/97609

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