Development and Validation of A Frusemide Card to Guide Self-Titration of Oral Frusemide in the Outpatient Setting
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Abstract
Background: Heart failure (HF) causes frequent hospitalisations due to fluid congestion. Patient-friendly self-titration tools are scarce. This study developed and validated a “Frusemide Card” to support safe outpatient dose adjustment.
Methods: This cross-sectional development and validation study was conducted in two phases. Phase 1 involved developing the Frusemide Card through evidence-based content construction and graphical design. Phase 2 included content validation by six experts (four cardiologists, two pharmacists) using the Content Validity Index (CVI) and Content Validity Ratio (CVR), followed by face validation among 20 HF patients in two sequential cohorts using the Face Validity Index (FVI). Content validity included four domains: relevance, clarity, essentiality, and patient instructions. Face validation assessed clarity and comprehension to determine overall acceptance.
Results: Expert validation showed perfect agreement for relevance and essentiality (I-CVI, CVR, and S-CVI/UA = 1.00). Clarity for domains 2–4 was acceptable (I-CVI ≥ 0.83), but domain 1 scored lower (I-CVI = 0.50), reducing the universal agreement (S-CVI/UA = 0.25), though average clarity was acceptable (S-CVI/Ave = 0.79). The first patient cohort reported good average clarity (S-FVI/Ave = 0.90) but low universal agreement (S-FVI/UA = 0.25). Following revisions based on feedback, the second patient cohort confirmed excellent clarity and acceptance, achieving perfect validity across all domains (I-FVI and S-FVI = 1.00).
Conclusion: The Frusemide Card showed strong content and face validity, suggesting that it could be a useful tool for guiding the safe self-titration of oral frusemide in outpatient HF management.
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