Recurrent event analyses in patients receiving maintenance dialysis and the effect of higher‐ versus lower‐dose chronic intravenous iron therapy: A report focusing on heart failure events from the PIVOTAL trial DOI

Stefan D. Anker,

Michele Robertson, John J.V. McMurray

и другие.

European Journal of Heart Failure, Год журнала: 2025, Номер unknown

Опубликована: Май 20, 2025

Язык: Английский

Intravenous Ferric Carboxymaltose in Heart Failure With Iron Deficiency DOI
Stefan D. Anker, Tim Friede, Javed Butler

и другие.

JAMA, Год журнала: 2025, Номер unknown

Опубликована: Март 30, 2025

Uncertainty remains about the efficacy of intravenous iron in patients with heart failure and deficiency. To assess safety ferric carboxymaltose This multicenter, randomized clinical trial enrolled 1105 (defined as having a left ventricular ejection fraction ≤45%) deficiency (serum ferritin level <100 ng/mL; or if transferrin saturation was <20%, serum between 100 ng/mL 299 ng/mL) at 70 clinic sites 6 European countries from March 2017 to November 2023. The median follow-up 16.6 months (IQR, 7.9-29.9 months). Administration (n = 558) initially given an dose up 2000 mg that followed by 500 every 4 (unless stopping criteria were met) vs saline placebo 547). primary end point events (1) time cardiovascular death first hospitalization, (2) total hospitalizations, (3) hospitalization less than 20%. All measured through follow-up. points would be considered statistically significant they fulfilled least 1 following conditions: P ≤ .05 for all 3 comparisons, .025 2 .0167 any comparisons (Hochberg procedure). Of participants (mean age, years [SD, 12 years]; 33% women), (first outcome) occurred 141 group 166 (hazard ratio, 0.79 [95% CI, 0.63-0.99]; .04). second outcome (total hospitalizations) 264 times 320 (rate 0.80 0.60-1.06]; .12). third (cardiovascular <20%) 103 128 0.61-1.02], .07). A similar amount had serious adverse event (269; 48.2%) (273; 49.9%) (P .61). In deficiency, did not significantly reduce overall cohort 20%, number hospitalizations placebo. ClinicalTrials.gov Identifier: NCT03036462.

Язык: Английский

Процитировано

2

Iron Deficiency Treatment in Heart Failure—Challenges and Therapeutic Solutions DOI Open Access
Lucreția Anghel, Ciprian Dinu,

Diana Pătraș

и другие.

Journal of Clinical Medicine, Год журнала: 2025, Номер 14(9), С. 2934 - 2934

Опубликована: Апрель 24, 2025

Iron deficiency (ID) is a common comorbidity in heart failure (HF), affecting nearly 50% of patients and worsening symptoms, exercise capacity, prognosis. This review summarizes recent evidence from meta-analyses, clinical trials, guidelines on the pathophysiology, diagnosis, treatment ID HF. HF results chronic inflammation, intestinal congestion, impaired iron metabolism. Diagnosis based serum ferritin transferrin saturation (TSAT) levels. While oral therapy has limited efficacy, intravenous iron, particularly ferric carboxymaltose derisomaltose, improves symptoms tolerance reduces hospitalizations. Timely diagnosis are essential. Intravenous preferred therapeutic approach, but further research needed to optimize long-term management.

Язык: Английский

Процитировано

0

Ferric carboxymaltose assessment of morbidity and mortality in patients with iron deficiency and chronic heart failure (FAIRHF2DZHK05) trial: Baseline characteristics and comparison to other relevant clinical trials DOI Creative Commons

Stefan D. Anker,

Tim Friede, Javed Butler

и другие.

European Journal of Heart Failure, Год журнала: 2025, Номер unknown

Опубликована: Апрель 29, 2025

Aims Prior randomized trials have reported conflicting evidence regarding the efficacy of intravenous (IV) iron in patients with heart failure reduced ejection fraction (HFrEF) and deficiency (ID). Methods results FAIR‐HF2 is a double‐blind, randomized, controlled trial evaluating IV ferric carboxymaltose HFrEF ID. We report baseline characteristics enrolled compare them other major (FAIR‐HF, CONFIRM‐HF, AFFIRM‐AHF, IRONMAN, HEART‐FID). A total 1105 were between March 2017 November 2023. Most men (67%) median age was 72 (interquartile range [IQR] 63–79) years. More than one‐third had hospitalization within preceding 12 months (36%), 53% hospitalized at randomization. Common comorbidities included hypertension (79%), coronary artery disease (74%), dyslipidaemia (67%), diabetes (46%). The left ventricular 58% (IQR 42–77) mean estimated glomerular filtration rate 58 ml/min/1.73 m 2 . 1064 (96%) on renin–angiotensin system inhibitors (angiotensin receptor–neprilysin [ARNI] 38%), 1016 (92%) beta‐blockers, 779 (71%) mineralocorticoid receptor antagonists; 261 (24%) sodium–glucose cotransporter (SGLT2) inhibitors, which much higher prior trials. proportion ischaemic (78%) compared to haemoglobin (g/dl) 12.7 11.8–13.4), serum ferritin (μg/dl) 63 36–90), transferrin saturation (%) 16.5 11.8–22.9), resembling that 6‐min walk distance enrolment 314 ± 118 m. Conclusion represents contemporary cohort mostly similar populations. Use SGLT2 ARNI Clinical Trial Registration: ClinicalTrials.gov ID NCT03036462.

Язык: Английский

Процитировано

0

Recurrent event analyses in patients receiving maintenance dialysis and the effect of higher‐ versus lower‐dose chronic intravenous iron therapy: A report focusing on heart failure events from the PIVOTAL trial DOI

Stefan D. Anker,

Michele Robertson, John J.V. McMurray

и другие.

European Journal of Heart Failure, Год журнала: 2025, Номер unknown

Опубликована: Май 20, 2025

Язык: Английский

Процитировано

0