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Effectiveness and safety of ferric carboxymaltose therapy in peritoneal dialysis patients: an observational study.
Portolés-Pérez, Jose; Durá-Gúrpide, Beatriz; Merino-Rivas, José Luis; Martín-Rodriguez, Leyre; Hevia-Ojanguren, Covadonga; Burguera-Vion, Victor; Yuste-Lozano, Claudia; Sánchez-García, Luisa; Rodriguez-Palomares, Jose Ramon; Paraiso, Vicente.
Afiliación
  • Portolés-Pérez J; Nephrology Department, University Hospital Puerta de Hierro, Madrid, Spain.
  • Durá-Gúrpide B; RedInRen ISCiii 016/009 Public Research Net, Madrid, Spain.
  • Merino-Rivas JL; Nephrology Department, University Hospital Puerta de Hierro, Madrid, Spain.
  • Martín-Rodriguez L; RedInRen ISCiii 016/009 Public Research Net, Madrid, Spain.
  • Hevia-Ojanguren C; Nephrology Department, University Hospital del Henares, Coslada, Madrid, Spain.
  • Burguera-Vion V; Nephrology Department, University Hospital Puerta de Hierro, Madrid, Spain.
  • Yuste-Lozano C; RedInRen ISCiii 016/009 Public Research Net, Madrid, Spain.
  • Sánchez-García L; Nephrology Department, University Hospital Infanta Sofía, San Sebastián de los Reyes, Madrid, Spain.
  • Rodriguez-Palomares JR; RedInRen ISCiii 016/009 Public Research Net, Madrid, Spain.
  • Paraiso V; Nephrology Department, University Hospital Ramón y Cajal, Madrid, Spain.
Clin Kidney J ; 14(1): 174-180, 2021 Jan.
Article en En | MEDLINE | ID: mdl-33564416
ABSTRACT

BACKGROUND:

The efficacy of intravenous (IV) ferric carboxymaltose (FCM) has been demonstrated in haemodialysis and non-dialysis studies, but evidence is lacking in patients undergoing peritoneal dialysis (PD).

METHODS:

This multicentre, retrospective study evaluated the effectiveness and safety of FCM in patients on PD over 12 months. We retrospectively reviewed the electronic medical records of PD patients who initiated FCM treatment between 2014 and 2017 across seven Spanish centres.

RESULTS:

Ninety-one patients were included in the safety population (mean ± SD age 57.7 ± 15.0 years) and 70 in the efficacy population (mean age 50.9 ± 14.5 years). No hypersensitivity reaction, FCM discontinuation or dose adjustment due to a serious adverse event (SAE) was registered in the safety population. The most common non-SAEs reported were headache (four events), mild hypotension (three events) and hypertension (two events), among others. In the efficacy population (n = 70), 68.6% of patients achieved ferritin levels of 200-800 ng/mL, 78.4% achieved transferrin saturation (TSAT) >20%, and 62.8% achieved TSAT >20% and ferritin >200 ng/mL after 12 months of FCM initiation (P < 0.01). Haemoglobin (Hb) levels were maintained at >11 g/dL with a lower dose of darbepoetin throughout the follow-up. The sub-analysis of patients naïve to IV iron and with absolute or relative iron deficiency (n = 51) showed that 76.5% reached ferritin >200 ng/mL, 80.4% TSAT >20% and Hb increased (1.2 g/dL) after 4 months of FCM treatment (P < 0.01).

CONCLUSION:

In this multicentre, retrospective, real-world study conducted in the PD population, FCM was effective, safe and easy to administer during routine clinical visits.
Palabras clave

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: Clin Kidney J Año: 2021 Tipo del documento: Article País de afiliación: España

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Observational_studies Idioma: En Revista: Clin Kidney J Año: 2021 Tipo del documento: Article País de afiliación: España