Key result
Polypharmacy over 12 drugs is linked to ~16.5-fold higher odds of multiple drug interactions in heart failure.
Why the study?
Hospitalized patients with left ventricular failure are at high risk for potential drug-drug interactions due to advanced age, comorbidities, and polypharmacy.
What are the prevalence, severity levels, predictors, and clinical outcomes of potential drug-drug interactions in hospitalized patients with left ventricular failure?
Cross-Sectional (n=385)
Yes
What are the prevalence, severity levels, predictors, and clinical outcomes of potential drug-drug interactions in hospitalized patients with left ventricular failure?
Answers are grounded in this paper and cite their sources.
Hospitalized patients with left ventricular failure experience a very high prevalence (96.4%) of potential drug-drug interactions—predominantly of major and moderate severity—driven strongly by polypharmacy (>12 drugs) and male sex, highlighting the need for routine medication screening and close clinical monitoring.
Hospitalized patients with left ventricular failure (LVF) are at high risk for potential drug-drug interactions (pDDIs) and its related adverse effects owing to multiple risk factors such as old age, comorbidities and polypharmacy. This cross-sectional study conducted in two tertiary care hospitals aim to identify frequency, levels and predictors of pDDIs in LVF patients. Data about patients’ demographic, hospital stay, medication therapy, sign/symptoms and laboratory test results were collected for 385 patients with LVF. Micromedex Drug-Reax® was used to screen patients’ medication profiles for pDDIs. Overall prevalence and severity-wise prevalence of pDDIs were identified. Chi-square test was performed for comparative analysis of various variables. Logistic regression was applied to determine the odds-ratios (OR) for predictors of pDDIs. The prevalence of pDDIs was 96.4% (n=371). Overall 335 drug-interacting pairs were detected, which were presented in a total of 2870 pDDIs. Majority of pDDIs were of major- (48.9%) and moderate-severity (47.5%). Logistic regression analysis shows significant association of >6 all types of pDDIs with >12 drugs as compared with <8 drugs (OR=16.5; p=<0.001). Likewise, there was a significant association of >4 major-pDDIs with men as compared with female (OR=1.9; p=0.007) and >12 drugs as compared with <8 drugs (OR=10.9; p=<0.001). Hypotension (n=57), impaired renal function (23) and increased blood pressure (22) were the most frequent adverse outcomes associated with pDDIs. This study shows high prevalence of pDDIs in LVF patients. Majority of pDDIs were of major- and moderate-severity. Male patients and those prescribed greater number of medicines were more exposed to major-pDDIs.
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Haq et al. (2020) conducted a cross-sectional in Hospitalized left ventricular failure (n=385). Polypharmacy (>12 prescribed drugs) vs. ≤8 prescribed drugs was evaluated on Exposure to >6 potential drug-drug interactions (pDDIs) of all types (OR 16.5, 95% CI 7.8-34.8, p=<0.001). Polypharmacy (>12 drugs vs ≤8 drugs) significantly increased the odds of >6 potential drug-drug interactions (OR 16.5, 95% CI 7.8-34.8, p<0.001) in patients with left ventricular failure.
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