Why the study?
The relationship between outpatient oral loop diuretic dose intensification trajectories and the prognosis of patients with chronic heart failure remains unclear.
Does outpatient oral loop diuretic dose intensification trajectory predict all-cause mortality in patients with chronic heart failure?
Does outpatient oral loop diuretic dose intensification trajectory predict all-cause mortality in patients with chronic heart failure?
Irreversible loop diuretic dose intensification over 1 year is associated with worse prognosis in CHF patients, whereas reversible intensification has a prognosis similar to no intensification.
Answers are grounded in this paper and cite their sources.
May flag higher-risk CHF patients via LD trajectories; hypothesis-generating and should not yet change practice.
• The link between loop diuretic (LD) dose intensification trajectories and patients with CHF prognosis is unclear. • LD dose intensification trajectories for 1 year in 832 patients with CHF were consecutively investigated. • These trajetories were categorized into the irreversible, reverssible, and no intensification. • Irreversible LD dose intensification had worse prognoses in patients with CHF than no intensification. • Patients with CHF with reversible LD dose intensification had prognoses similar to those with no intensification. The relationship between outpatient oral loop diuretic (OLD) dose intensification trajectories and the prognosis of patients with chronic heart failure (CHF) remains unclear. In 832 patients with CHF, OLD dose trajectories for 1 year were consecutively investigated. OLD dose intensification was defined as the first occurrence of OLD dose increase from the baseline within the first year. Patients were classified into three groups of OLD dose intensification trajectories: irreversible, reversible, and no intensification. Irreversible intensification was defined as an OLD dose intensification wherein the dose remained above the baseline during the first year of follow-up. Reversible intensification referred to an OLD dose intensification wherein the dose returned to or dropped below the baseline within the first year of follow-up. No intensification was defined as no OLD dose intensification throughout the first year of follow-up. The primary outcome was all-cause mortality. Secondary outcomes were cardiovascular death (CVD), heart failure hospitalisation (HFH), a composite of CVD or HFH, and a composite of all-cause mortality or HFH after 1 year. During the median follow-up (57 [range, 13–102] months), 146 patients died. Irreversible intensification was associated with higher risks of all outcomes than no intensification (e.g., all-cause mortality: hazard ratio [HR], 1.63; 95% confidence interval [CI], 1.08–2.44; HFH: HR, 2.16; 95% CI, 1.65–2.98; CVD or HFH: HR, 2.17; 95% CI, 1.59–2.96). Conversely, reversible intensification had comparable prognoses for all outcomes to no intensification. OLD dose intensification trajectories could stratify the prognosis of CHF patients.
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Koike et al. (2025) studied this question.
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