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Determinants of ineligibility for intravenous iron therapy in patients with heart failure and LVEF <45%: a retrospective cohort study

Identifikátory výsledku

  • Kód výsledku v IS VaVaI

    <a href="https://www.isvavai.cz/riv?ss=detail&h=RIV%2F00843989%3A_____%2F25%3AE0112145" target="_blank" >RIV/00843989:_____/25:E0112145 - isvavai.cz</a>

  • Nalezeny alternativní kódy

    RIV/61988987:17110/25:A2603DG8

  • Výsledek na webu

    <a href="https://www.e-coretvasa.cz/pdfs/cor/2025/06/01.pdf" target="_blank" >https://www.e-coretvasa.cz/pdfs/cor/2025/06/01.pdf</a>

  • DOI - Digital Object Identifier

    <a href="http://dx.doi.org/10.33678/cor.2025.093" target="_blank" >10.33678/cor.2025.093</a>

Alternativní jazyky

  • Jazyk výsledku

    angličtina

  • Název v původním jazyce

    Determinants of ineligibility for intravenous iron therapy in patients with heart failure and LVEF <45%: a retrospective cohort study

  • Popis výsledku v původním jazyce

    Background: Intravenous iron therapy improves symptoms and reduces hospitalizations in patients with heart failure (HF) and iron deficiency (ID). Clinical trials evaluating this therapy have often excluded patients with higher hemoglobin (HGB) levels, although current European Society of Cardiology guidelines do not specify an upper HGB limit. This study aimed to assess how HGB thresholds influence eligibility for intravenous iron among real-world HF patients with left ventricular ejection fraction (LVEF) < 45%. Methods: We retrospectively analyzed consecutive patients attending a specialized HF outpatient clinic in 2024. ID was defined as ferritin < 100 µg/L, or 100-299 µg/L with transferrin saturation (TSAT) < 20%. Eligibility for intravenous iron was simulated using various HGB thresholds ranging from ?150 g/L to ?160 g/L. Clinical and laboratory characteristics of eligible and non-eligible patients were compared. Results: Among 176 patients with LVEF < 45%, 98 (55.7%) fulfilled ID criteria. Using an HGB threshold of ?150 g/L, only 29.5% of patients were eligible for intravenous iron. Increasing the threshold to 155 g/L and 160 g/L would expand eligibility to 38.1% and 46.7%, respectively. Patients excluded based on higher HGB levels often exhibited functional ID and elevated NT-proBNP, indicating advanced HF. All patients who met the eligibility criteria during the study period received intravenous iron. Conclusion: A substantial proportion of HF patients with LVEF < 45% and clinically relevant ID may be excluded from intravenous iron therapy based on HGB levels, despite current guidelines not imposing a strict cutoff. A modest increase in the HGB threshold may allow more symptomatic patients to benefit from guideline-recommended treatment.

  • Název v anglickém jazyce

    Determinants of ineligibility for intravenous iron therapy in patients with heart failure and LVEF <45%: a retrospective cohort study

  • Popis výsledku anglicky

    Background: Intravenous iron therapy improves symptoms and reduces hospitalizations in patients with heart failure (HF) and iron deficiency (ID). Clinical trials evaluating this therapy have often excluded patients with higher hemoglobin (HGB) levels, although current European Society of Cardiology guidelines do not specify an upper HGB limit. This study aimed to assess how HGB thresholds influence eligibility for intravenous iron among real-world HF patients with left ventricular ejection fraction (LVEF) < 45%. Methods: We retrospectively analyzed consecutive patients attending a specialized HF outpatient clinic in 2024. ID was defined as ferritin < 100 µg/L, or 100-299 µg/L with transferrin saturation (TSAT) < 20%. Eligibility for intravenous iron was simulated using various HGB thresholds ranging from ?150 g/L to ?160 g/L. Clinical and laboratory characteristics of eligible and non-eligible patients were compared. Results: Among 176 patients with LVEF < 45%, 98 (55.7%) fulfilled ID criteria. Using an HGB threshold of ?150 g/L, only 29.5% of patients were eligible for intravenous iron. Increasing the threshold to 155 g/L and 160 g/L would expand eligibility to 38.1% and 46.7%, respectively. Patients excluded based on higher HGB levels often exhibited functional ID and elevated NT-proBNP, indicating advanced HF. All patients who met the eligibility criteria during the study period received intravenous iron. Conclusion: A substantial proportion of HF patients with LVEF < 45% and clinically relevant ID may be excluded from intravenous iron therapy based on HGB levels, despite current guidelines not imposing a strict cutoff. A modest increase in the HGB threshold may allow more symptomatic patients to benefit from guideline-recommended treatment.

Klasifikace

  • Druh

    J<sub>imp</sub> - Článek v periodiku v databázi Web of Science

  • CEP obor

  • OECD FORD obor

    30201 - Cardiac and Cardiovascular systems

Návaznosti výsledku

  • Projekt

  • Návaznosti

    V - Vyzkumna aktivita podporovana z jinych verejnych zdroju

Ostatní

  • Rok uplatnění

    2025

  • Kód důvěrnosti údajů

    S - Úplné a pravdivé údaje o projektu nepodléhají ochraně podle zvláštních právních předpisů

Údaje specifické pro druh výsledku

  • Název periodika

    Cor et Vasa

  • ISSN

    0010-8650

  • e-ISSN

    1803-7712

  • Svazek periodika

    67

  • Číslo periodika v rámci svazku

    6

  • Stát vydavatele periodika

    CZ - Česká republika

  • Počet stran výsledku

    6

  • Strana od-do

    671-676

  • Kód UT WoS článku

    001644058600001

  • EID výsledku v databázi Scopus