Journal of the American Heart Association · 2026
Cohort Study of Initial Diuretic Dosing and Outcomes Among Patients Hospitalized for Congestive Heart Failure: Insights From the Cardiovascular Quality Improvement and Care Innovation Consortium.
СтатьяМногоцентровое исследованиеНаблюдательное исследованиеПоддержка исследования: вне правительства СШАНазвание и аннотация: Перевод в очереди
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Qadri Naureen, Kwok Erica, Stanberry Larissa, Thomas Chelsey, Irausquin Stephanie J, Gupta Divya, Ebinger Joseph E, Gluckman Ty J, Mutharasan R Kannan, Goyal Abhinav, Brownell Nicholas K, Scirica Benjamin M, Ho P Michael, Das Sandeep R, Downey William, Bradley Steven M
Аннотация
BACKGROUND: Little is known about the initial dosing of loop diuretics among patients hospitalized for heart failure and its association with outcomes.
METHODS: We identified patients admitted for heart failure at 24 hospitals across two health systems between January 1, 2017, and December 31, 2020. Initial diuretic dose was categorized relative to home dose in furosemide equivalents. The primary outcomes (length of stay) and secondary outcomes (rates of acute kidney injury, in-hospital mortality, and 30-day readmissions) were compared across categories of initial diuretic dose.
RESULTS: Among 14 332 patients admitted for heart failure, the initial diuretic dose was lower-than-home dose in 1866 (13.0%) patients, equivalent-to-home dose in 3171 (22.1%) patients, and higher-than-home dose in 9295 (64.9%) patients. Compared with patients who received an equivalent or higher initial diuretic dose relative to home dose, risk-adjusted length of stay was longer among patients receiving a lower dose (4.9 days versus 4.0 days versus 4.0 days, P<0.01). Compared with equivalent-to-home dose, a higher initial diuretic dose was associated with a higher risk-adjusted rate of acute kidney injury (incident risk ratio [IRR], 1.17 [95% CI 1.04-1.31]; P=0.009) and a lower risk of 30-day readmission (IRR, 0.85 [95% CI, 0.78-0.93]; P=0.005).
CONCLUSIONS: In a cohort of patients admitted for heart failure, more than 1 in 3 patients received an initial dose of intravenous loop diuretics that was lower than or equivalent to their home diuretic dose, and the initial dose was associated with length of hospital stay and acute kidney injury.
METHODS: We identified patients admitted for heart failure at 24 hospitals across two health systems between January 1, 2017, and December 31, 2020. Initial diuretic dose was categorized relative to home dose in furosemide equivalents. The primary outcomes (length of stay) and secondary outcomes (rates of acute kidney injury, in-hospital mortality, and 30-day readmissions) were compared across categories of initial diuretic dose.
RESULTS: Among 14 332 patients admitted for heart failure, the initial diuretic dose was lower-than-home dose in 1866 (13.0%) patients, equivalent-to-home dose in 3171 (22.1%) patients, and higher-than-home dose in 9295 (64.9%) patients. Compared with patients who received an equivalent or higher initial diuretic dose relative to home dose, risk-adjusted length of stay was longer among patients receiving a lower dose (4.9 days versus 4.0 days versus 4.0 days, P<0.01). Compared with equivalent-to-home dose, a higher initial diuretic dose was associated with a higher risk-adjusted rate of acute kidney injury (incident risk ratio [IRR], 1.17 [95% CI 1.04-1.31]; P=0.009) and a lower risk of 30-day readmission (IRR, 0.85 [95% CI, 0.78-0.93]; P=0.005).
CONCLUSIONS: In a cohort of patients admitted for heart failure, more than 1 in 3 patients received an initial dose of intravenous loop diuretics that was lower than or equivalent to their home diuretic dose, and the initial dose was associated with length of hospital stay and acute kidney injury.
Предметные рубрики MeSH
AgedAged, 80 and overFemaleHumansMaleMiddle AgedAcute Kidney InjuryDose-Response Relationship, DrugFurosemideHeart FailureHospital MortalityHospitalizationLength of StayPatient ReadmissionQuality ImprovementRetrospective StudiesSodium Potassium Chloride Symporter InhibitorsTreatment OutcomeUnited States