Patient profile and outcomes associated with follow-up in specialty vs. primary care in heart failure
- PMID: 35170237
- PMCID: PMC8934918
- DOI: 10.1002/ehf2.13848
Patient profile and outcomes associated with follow-up in specialty vs. primary care in heart failure
Erratum in
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Correction to: "Heart failure: an update from the last years and a look at the near future" and articles listed below.ESC Heart Fail. 2023 Jun;10(3):2143. doi: 10.1002/ehf2.14323. Epub 2023 Mar 23. ESC Heart Fail. 2023. PMID: 36959126 Free PMC article. No abstract available.
Abstract
Aims: Factors influencing follow-up referral decisions and their prognostic implications are poorly investigated in patients with heart failure (HF) with reduced (HFrEF), mildly reduced (HFmrEF), and preserved (HFpEF) ejection fraction (EF). We assessed (i) the proportion of, (ii) independent predictors of, and (iii) outcomes associated with follow-up in specialty vs. primary care across the EF spectrum.
Methods and results: We analysed 75 518 patients from the large and nationwide Swedish HF registry between 2000-2018. Multivariable logistic regression models were fitted to identify the independent predictors of planned follow-up in specialty vs. primary care, and multivariable Cox models to assess the association between follow-up type and outcomes. In this nationwide registry, 48 115 (64%) patients were planned for follow-up in specialty and 27 403 (36%) in primary care. The median age was 76 [interquartile range (IQR) 67-83] years and 27 546 (36.5%) patients were female. Key independent predictors of planned follow-up in specialty care included optimized HF care, that is follow-up in a nurse-led HF clinic [odds ratio (OR) 4.60, 95% confidence interval (95% CI) 4.41-4.79], use of HF devices (OR 3.99, 95% CI 3.62-4.40), beta-blockers (OR 1.39, 95% CI 1.32-1.47), renin-angiotensin system/angiotensin-receptor-neprilysin inhibitors (OR 1.21, 95% CI 1.15-1.27), and mineralocorticoid receptor antagonists (OR 1.31, 95% CI 1.26-1.37); and more severe HF, that is higher NT-proBNP (OR 1.13, 95% CI 1.06-1.20) and NYHA class (OR 1.13, 95% CI 1.08-1.19). Factors associated with lower likelihood of follow-up in specialty care included older age (OR 0.29, 95% CI 0.28-0.30), female sex (OR 0.89, 95% CI 0.86-0.93), lower income (OR 0.79, 95% CI 0.76-0.82) and educational level (OR 0.77, 95% CI 0.73-0.81), higher EF [HFmrEF (OR 0.65, 95% CI 0.62-0.68) and HFpEF (OR 0.56, 95% CI 0.53-0.58) vs. HFrEF], and higher comorbidity burden, such as presence of kidney disease (OR 0.91, 95% CI 0.87-0.95), atrial fibrillation (OR 0.85, 95% CI 0.81-0.89), and diabetes mellitus (OR 0.92, 95% CI 0.88-0.96). A planned follow-up in specialty care was independently associated with lower risk of all-cause [hazard ratio (HR) 0.78, 95% CI 0.76-0.80] and cardiovascular death (HR 0.76, 95% CI 0.73-0.78) across the EF spectrum, but not of HF hospitalization (HR 1.06, 95% CI 1.03-1.10).
Conclusions: In a large nationwide HF population, referral to specialty care was linked with male sex, younger age, lower EF, lower comorbidity burden, better socioeconomic environment and optimized HF care, and associated with better survival across the EF spectrum. Our findings highlight the need for greater and more equal access to HF specialty care and improved quality of primary care.
Keywords: Disparaties; Follow-up referrals; Heart failure; Quality and outcomes; Risk factors.
© 2022 The Authors. ESC Heart Failure published by John Wiley & Sons Ltd on behalf of European Society of Cardiology.
Conflict of interest statement
G. S. reports grants and personal fees from Vifor, grants and non‐financial support from Boehringer Ingelheim, personal fees from Società Prodotti Antibiotici, grants and personal fees from AstraZeneca, personal fees from Roche, personal fees from Servier, grants from Novartis, personal fees from GENESIS, personal fees from Cytokinetics, personal fees from Medtronic, grants from Boston Scientific, grants from PHARMACOSMOS, grants from Merck, outside the submitted work.
F. L. has nothing to disclose.
M. E. has nothing to disclose.
L. H. L reports research grants from AstraZeneca, Novartis, Boerhinger Ingelheim, Vifor‐Fresenius, and Boston Scientific, and consulting or speaker's honoraria from AstraZeneca, Novartis, Boehringer Ingelheim, Vifor‐Fresenius, Bayer, Sanofi, Merck, Myokardia, Orion Pharma, MedScape, Radcliffe Cardiology, Lexicon, and Respicardia, and stock ownership in AnaCardio, outside the submitted work.
C. L. reports consulting fees from AstraZeneca, Roche diagnostics and speaker Honoria from Novartis, Astra, Bayer, Medtronic, Impulse Dynamics and Vifor.
U. D. reports grants from AstraZeneca, Pfizer, Vifor, Boston Scientific, Boehringer Ingelheim and Roche Diagnostics and consultancies from Amgen, AstraZeneca and Novartis, outside the submitted work.
B. S. reports grants from the German Research Foundaten and the Else Kröner‐Fresenius‐Stiftung and personal fees from AstraZeneca and Abiomed, outside of the submitted work.
G. R. has no conflict of interest related to the current work.
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