# Healthcare utilization and costs in the first two years after heart failure diagnosis: an observational study by phenotype in southwestern Sweden

**Authors:** Jason Davidge, Anders Halling, Björn Agvall

PMC · DOI: 10.1186/s12913-026-14020-4 · BMC Health Services Research · 2026-01-13

## TL;DR

This study examines healthcare use and costs in heart failure patients over two years, finding that hospitalizations are costly and HFpEF patients have the highest sustained burden.

## Contribution

The study provides subgroup-specific healthcare cost analysis for heart failure phenotypes using electronic medical records in a real-world population.

## Key findings

- Hospitalizations accounted for 68% of first-year costs, with HFrEF having the highest initial costs.
- HFpEF patients had the highest costs in year two, indicating a sustained healthcare burden.
- Higher NT-proBNP levels and cardiovascular comorbidities were linked to longer hospital stays across subgroups.

## Abstract

Assess healthcare utilization and direct costs for heart failure (HF) during the first two years post-diagnosis across HF subgroups.

This retrospective population-based study included patients with HF aged 40–90 years in Region Halland. HF subgroups were defined based on echocardiographic ejection fraction, including HF with reduced ejection fraction (HFrEF), mildly reduced ejection fraction (HFmrEF), preserved ejection fraction (HFpEF), and no defined phenotype (HF-NDP). NT-proBNP and comorbidities were analyzed as clinical features. HF phenotypes were identified via algorithmic electronic medical records analysis. Data included primary and hospital care (inpatient and outpatient) healthcare utilization and costs during a two-year post-diagnosis during 2015–2017. Utilization covered visits to physicians, nurses, paramedical staff, and inpatient days. Costs were estimated using the Patient Encounter Costing model. HF phenotypes, differentiated by ejection fraction, were identified via algorithmic analysis of electronic medical records. ANOVA with Bonferroni correction compared subgroups; Poisson regression assessed factors associated with longer hospital stays.

A total of 1769 patients were included: 472 (27%) with HFrEF, 318 (18%) HFmrEF, 505 (28%) HFpEF, and 474 (27%) HF-NDP. Hospitalizations represented the largest cost component, accounting for 68% of first-year expenditures. Average total costs per patient were €15,771 in year one and €7,459 in year two. Subgroup-specific costs declined over time: HFrEF (€18,682 to €7,083), HFpEF (€17,052 to €9,289), HFmrEF (€16,513 to €7,946), and HF-NDP (€11,009 to €5,556). HFpEF patients incurred the highest costs in the second year, indicating a sustained burden. Higher NT-proBNP levels and cardiovascular comorbidities were associated with longer lengths of stay (LoS) in both years. In year one, HFrEF served as reference, while HFmrEF had IRR 0.89 (95% CI:0.88–0.93), HFpEF IRR 0.98 (95% CI:0.94–1.01), and HF-NDP IRR 0.75 (95% CI:0.72–0.79). By year two, LoS risk increased for all other subgroups compared to HFrEF, most notably HFpEF (IRR 1.81; 95% CI:1.70–1.94; p < 0.001).

Hospitalizations drove first-year costs, especially for HFrEF. Costs declined in year two for all subgroups, but HFpEF remained highest. Continuous care should target HFpEF and other high-risk phenotypes to reduce long-term burden.

The online version contains supplementary material available at 10.1186/s12913-026-14020-4.

## Linked entities

- **Diseases:** heart failure (MONDO:0005252)

## Full-text entities

- **Genes:** SLC5A2 (solute carrier family 5 member 2) [NCBI Gene 6524] {aka SGLT2}
- **Diseases:** Impaired kidney function (MESH:D007674), RH (MESH:D020918), HF-NDP (MESH:C537393), ischemic heart disease (MESH:D017202), chronic kidney disease (MESH:D051436), myocardial infarction (MESH:D009203), HF (MESH:D006333), ASCVD (MESH:D002318), deaths (MESH:D003643), peripheral artery disease (MESH:D058729), HFmrEF (MESH:D054143), COPD (MESH:D029424), atrial fibrillation (MESH:D001281), diabetes (MESH:D003920), atherosclerotic cardiovascular diseases (MESH:D050197), HFpEF (MESH:D054144), cancer (MESH:D009369), psychiatric (MESH:D001523), hypertension (MESH:D006973), stroke (MESH:D020521)
- **Chemicals:** 1HF (-)
- **Species:** Homo sapiens (human, species) [taxon 9606], HF [taxon 2008765]

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## References

2 references — full list in the complete paper: https://tomesphere.com/paper/PMC12849546/full.md

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Source: https://tomesphere.com/paper/PMC12849546