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Implications of prescribing a fixed-dose combination in clinical cardiology practice: a retrospective observational
Hyungseop Kim1, Hyuck-Jun Yoon1, Hyoung-Seob Park1
1Division of Cardiology, Department of Internal Medicine, Keimyung University Dongsan Medical Center, Daegu, Republic of Korea.
Insights
Fixed-dose combination (FDC) drug discontinuation was common, especially in lower-risk patients. Discontinuing FDC medications in high atherosclerotic cardiovascular disease (ASCVD) risk individuals may increase cardiovascular event rates.
Area of Science:
- Cardiology
- Pharmacology
- Public Health
Background:
- Fixed-dose combination (FDC) prescribing improves medication adherence.
- Limited data exist on FDC usefulness across diverse patient risk groups.
- Understanding FDC discontinuation's impact on clinical outcomes is crucial.
Purpose of the Study:
- To investigate the association between FDC discontinuation and cardiovascular (CV) events.
- To explore FDC discontinuation patterns in relation to patient risk stratification.
Main Methods:
- Retrospective analysis of 502 patients with FDC prescriptions from cardiology outpatient clinics (2008-2014).
- Assessment of 10-year atherosclerotic cardiovascular disease (ASCVD) risk scores and 20 CV risk factors.
- Classification of patients by FDC continuation status and ASCVD risk tertiles. CV events defined as composite of specific adverse outcomes.
Main Results:
- 40.4% of patients discontinued FDC therapy during follow-up (mean 2.8 years).
- FDC discontinuation was more frequent in patients with lower ASCVD risk scores (<6 risk factors).
- FDC discontinuation (p<0.001) and high ASCVD risk (p=0.017) were independently associated with increased CV events.
Conclusions:
- FDC discontinuation is a frequent occurrence in cardiology outpatient settings.
- Discontinuation of FDC therapy in high ASCVD risk patients may elevate CV event rates.
- Further research is needed to optimize FDC use in various cardiovascular risk strata.
Objective:
Fixed-dose combination (FDC) prescribing enhances adherence to medication. However, there are limited data regarding the usefulness of FDC drugs across different risk groups. The aim of this study was to explore the relationship between FDC discontinuation and clinical outcomes.
Methods:
From January 2008 to December 2014, patients with FDC prescriptions who visited a cardiology outpatient clinic at a tertiary university hospital in Daegu, Republic of Korea were retrospectively identified. The 10-year atherosclerotic cardiovascular disease (ASCVD) risk score and 20 conventional cardiovascular (CV) risk factors were assessed. Patients were classified according to FDC continuation, together with a tertile of 20 risks. CV events were defined as the composite of admission for worsening heart failure or diabetes, stroke, ischaemic heart disease, and CV death.
Results:
502 patients were prescribed with one of the following FDC products: calcium channel blocker (CCB) plus angiotensin receptor blockers (ARB), CCB plus statins, and ARB plus diuretics. During follow-up (mean 2.8±2.4 years), 203 discontinuations (40.4%) occurred. FDC-discontinued patients had lower ASCVD risk scores (24.8% vs. 28.8%, p<0.001), and patients with <6 risk factors discontinued FDC frequently. During follow-up, 57 events (11.4%) were reported: 30 (14.8%) in FDC-discontinued patients and 27 (9.1%) in FDC-continued patients (p=0.062). In multivariate models accounting for events, FDC discontinuation (p<0.001) and high ASCVD risk score (p=0.017) were associated with CV events.
Conclusions:
FDC discontinuation was common among patients attending the cardiology outpatient clinic. Our analyses suggest that FDC discontinuation in patients at high ASCVD risk may have an impact on CV event rates.
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