Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term study

Abstract Background Pulmonary arterial hypertension (PAH) is a progressive disease with limited survival. Iron deficiency (ID) correlates with disease severity and mortality. While oral iron supplementation was shown to be insufficient in such patients, the potential impact of parenteral iron on cli...

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Main Authors: Tilmann Kramer, Max Wissmüller, Kristiana Natsina, Felix Gerhardt, Henrik tenFreyhaus, Daniel Dumitrescu, Thomas Viethen, Martin Hellmich, Stephan Baldus, Stephan Rosenkranz
格式: Article
語言:English
出版: Wiley 2021-12-01
叢編:Journal of Cachexia, Sarcopenia and Muscle
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在線閱讀:https://doi.org/10.1002/jcsm.12764
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author Tilmann Kramer
Max Wissmüller
Kristiana Natsina
Felix Gerhardt
Henrik tenFreyhaus
Daniel Dumitrescu
Thomas Viethen
Martin Hellmich
Stephan Baldus
Stephan Rosenkranz
author_facet Tilmann Kramer
Max Wissmüller
Kristiana Natsina
Felix Gerhardt
Henrik tenFreyhaus
Daniel Dumitrescu
Thomas Viethen
Martin Hellmich
Stephan Baldus
Stephan Rosenkranz
author_sort Tilmann Kramer
collection DOAJ
description Abstract Background Pulmonary arterial hypertension (PAH) is a progressive disease with limited survival. Iron deficiency (ID) correlates with disease severity and mortality. While oral iron supplementation was shown to be insufficient in such patients, the potential impact of parenteral iron on clinical measures warrants further investigation. Methods We retrospectively analysed the long‐term effects of intravenous ferric carboxymaltose (FCM) on iron status and clinical measures in patients with PAH and ID [ferritin < 100 μg/L or ferritin 100–300 μg/L and transferrin saturation (TSAT) < 20%] who were on stable targeted PAH therapy, compared with matched controls without ID. Patients with ID received a single infusion of FCM (500 to 1000 mg). Clinical measures monitored included exercise capacity, World Health Organization (WHO) functional class, ESC/ERS risk status, and hospitalizations. The observation period was up to 18 months. Results One hundred and seventeen patients (mean age 60.9 ± 16.1 years; 64.1% females) with confirmed PAH and on stable targeted therapy for ≥3 months were included (58 with and 59 patients without ID who did not receive FCM). In patients with ID, iron supplementation with FCM resulted in an immediate and sustained improvement of iron status for up to 18 months (serum iron, ferritin, TSAT, all P < 0.01). Fourteen patients in the FCM group received a second FCM infusion after 9.6 ± 4.8 months due to recurrent ID. At 6 and 18 months after FCM infusion, 6 min walk distance improved from 377.5 ± 15.9 at baseline to 412.5 ± 15.1 and 400.8 ± 14.5 m, respectively (both P < 0.05). WHO functional class (P < 0.05) and ESC/ERS risk status also improved, and there was a reduction of hospitalizations for worsening PAH in the 12 months post vs. prior to iron repletion (P = 0.029). No significant changes were observed in the control group. FCM was well tolerated in all patients, with no severe adverse events. Conclusions In addition to targeted therapy, correction of ID by parenteral iron supplementation with FCM appears feasible and safe, has sustained effects on iron status, and may improve the clinical status and hospitalization rates in patients with PAH. Larger controlled studies are required to confirm this finding.
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spelling doaj.art-4e91b779634644a49a0e1fdf6e4742a92024-04-26T19:47:53ZengWileyJournal of Cachexia, Sarcopenia and Muscle2190-59912190-60092021-12-011261501151210.1002/jcsm.12764Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term studyTilmann Kramer0Max Wissmüller1Kristiana Natsina2Felix Gerhardt3Henrik tenFreyhaus4Daniel Dumitrescu5Thomas Viethen6Martin Hellmich7Stephan Baldus8Stephan Rosenkranz9Klinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyKlinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyKlinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyKlinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyKlinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyKlinik für Allgemeine und Interventionelle Kardiologie Herz‐ und Diabeteszentrum NRW Bad Oeynhausen GermanyKlinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyInstitut für Medizinische Statistik, Informatik und Epidemiologie (IMSIE) Universität zu Köln Cologne GermanyKlinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyKlinik III für Innere Medizin Herzzentrum der Universität zu Köln Cologne GermanyAbstract Background Pulmonary arterial hypertension (PAH) is a progressive disease with limited survival. Iron deficiency (ID) correlates with disease severity and mortality. While oral iron supplementation was shown to be insufficient in such patients, the potential impact of parenteral iron on clinical measures warrants further investigation. Methods We retrospectively analysed the long‐term effects of intravenous ferric carboxymaltose (FCM) on iron status and clinical measures in patients with PAH and ID [ferritin < 100 μg/L or ferritin 100–300 μg/L and transferrin saturation (TSAT) < 20%] who were on stable targeted PAH therapy, compared with matched controls without ID. Patients with ID received a single infusion of FCM (500 to 1000 mg). Clinical measures monitored included exercise capacity, World Health Organization (WHO) functional class, ESC/ERS risk status, and hospitalizations. The observation period was up to 18 months. Results One hundred and seventeen patients (mean age 60.9 ± 16.1 years; 64.1% females) with confirmed PAH and on stable targeted therapy for ≥3 months were included (58 with and 59 patients without ID who did not receive FCM). In patients with ID, iron supplementation with FCM resulted in an immediate and sustained improvement of iron status for up to 18 months (serum iron, ferritin, TSAT, all P < 0.01). Fourteen patients in the FCM group received a second FCM infusion after 9.6 ± 4.8 months due to recurrent ID. At 6 and 18 months after FCM infusion, 6 min walk distance improved from 377.5 ± 15.9 at baseline to 412.5 ± 15.1 and 400.8 ± 14.5 m, respectively (both P < 0.05). WHO functional class (P < 0.05) and ESC/ERS risk status also improved, and there was a reduction of hospitalizations for worsening PAH in the 12 months post vs. prior to iron repletion (P = 0.029). No significant changes were observed in the control group. FCM was well tolerated in all patients, with no severe adverse events. Conclusions In addition to targeted therapy, correction of ID by parenteral iron supplementation with FCM appears feasible and safe, has sustained effects on iron status, and may improve the clinical status and hospitalization rates in patients with PAH. Larger controlled studies are required to confirm this finding.https://doi.org/10.1002/jcsm.12764Pulmonary arterial hypertension (PAH)Iron deficiencyIronFerric carboxymaltose
spellingShingle Tilmann Kramer
Max Wissmüller
Kristiana Natsina
Felix Gerhardt
Henrik tenFreyhaus
Daniel Dumitrescu
Thomas Viethen
Martin Hellmich
Stephan Baldus
Stephan Rosenkranz
Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term study
Journal of Cachexia, Sarcopenia and Muscle
Pulmonary arterial hypertension (PAH)
Iron deficiency
Iron
Ferric carboxymaltose
title Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term study
title_full Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term study
title_fullStr Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term study
title_full_unstemmed Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term study
title_short Ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency: a long‐term study
title_sort ferric carboxymaltose in patients with pulmonary arterial hypertension and iron deficiency a long term study
topic Pulmonary arterial hypertension (PAH)
Iron deficiency
Iron
Ferric carboxymaltose
url https://doi.org/10.1002/jcsm.12764
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