The use of evidence-based medical therapy in patients with critical limb-threatening ischaemia

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningfagfællebedømt

Dokumenter

  • Fulltext

    Forlagets udgivne version, 657 KB, PDF-dokument

Aims
To describe the practice patterns of evidence-based medical therapy (EBM) and overall mortality in high-risk patients with critical limb-threatening ischaemia (CLTI), compared with patients with myocardial infarction (MI).

Methods and results
Using Danish registries, we identified patients 40–100 years of age with a first-time hospitalization for CLTI or MI from 2008–2018 and grouped them into CLTI, MI, and CLTI and history of MI (CLTI + MI). We examined the likelihood of filling prescriptions with EBM [i.e. antiplatelets (Aps), lipid-lowering agents (LLAs), angiotensin-converting enzyme inhibitor (ACEi), or angiotensin II-receptor blockers (ARBs)] within 3 months after discharge among survivors. Further, we assessed the adjusted 3-year mortality rates. We included 92 845 patients: 14 941 with CLTI (54.7% male), 74 830 with MI (64.6% male) and 3,074 with CLTI + MI (65.2% male). Patients with CLTI and CLTI + MI were older and had more comorbidities than patients with MI. Compared with patients with MI, the unadjusted odds ratios of filling prescriptions were 0.15 [confidence interval (CI): 0.14–0.15] for AP, 0.26 (CI: 0.25–0.27) for LLA, and 0.71 (CI: 0.69–0.74) for ARB/ACEi in patients with CLTI, and 0.22 (CI: 0.20–0.24) for AP, 0.38 (CI: 0.35–0.42) for LLA, and 1.17 (CI: 1.08–1.27) for ARB/ACEi in patients with CLTI + MI. Adjusted analyses showed similar results. Compared with patients with MI, adjusted 3-year hazard ratios for mortality were 1.69 (CI: 1.64–1.74) in patients with CLTI and 1.60 (CI: 1.51–1.69) in patients with CLTI + MI.

Conclusion
Patients with CLTI were undertreated with EBM and carried a more adverse prognosis, as compared with patients with MI, despite similar guidelines.
OriginalsprogEngelsk
TidsskriftEuropean Journal of Preventive Cardiology
Vol/bind30
Udgave nummer11
Sider (fra-til)1092-1100
Antal sider9
ISSN2047-4873
DOI
StatusUdgivet - 2023

Bibliografisk note

Funding Information:
This study received funding from a Borregaard Clinical Ascending Investigator grant from the Novo Nordisk Foundations. This had no impact on the study design, analysis, review, or approval of the manuscript.

Funding Information:
Conflict of interest: L.G.V.B., J.K.P., and E.H.-B.: none. T.R.: Consulting and IP from COOK Medical Inc, Research grant/speakers bureau/Advisory Board Medtronic, Gore (Johnson&Johnson), Artivion, Bentley Innomed Gmbh, Kardiozis, Nexus; K.G.S.: Consultant for: Optum Labs, Happify, Tegum, and Abbott Laboratories. Research grants: Merck & Co., Shockwave Medical, and Janssen Pharmaceutical Companies of Johnson & Johnson, Philips, Abbott, Merck. C.M.-H.: Consultant for: Abbott, Cook, Penumbra, Optum Labs. Research grants: Shockwave, Philips, Abbott Jonas Eiberg: Research grant from Philips, WL GORE and Medtronic. Speakers honorarium from Philips and WL GORE. L.K.: Speakers honorarium from Novo, Novartis, AstraZeneca, and Boehringer. E.L.F.: Independent research grant from Novo Nordisk foundation.

Publisher Copyright:
© The Author(s) 2023.

ID: 396094970