Ferric carboxymaltose use in pediatric kidney transplant recipients with iron deficiency

Diletta Domenica Torres1, Luigi Antonio Moscogiuri2, Giulia Fontò3

  • 1Pediatric Nephrology and Dialysis Unit, "Giovanni XXIII" Hospital, Via Amendola 207, Bari, 70124, Italy.

Insights

Ferric carboxymaltose (FCM) effectively treats iron deficiency anemia in pediatric kidney transplant patients. This intravenous iron therapy improved hemoglobin and iron levels with no adverse effects observed.

Area of Science:

  • Pediatric Nephrology
  • Transplantation Medicine
  • Hematology

Background:

  • Anemia is a frequent complication in pediatric kidney transplant recipients.
  • Iron deficiency is a common cause of post-transplantation anemia, often poorly responsive to oral iron.
  • The safety and efficacy of intravenous ferric carboxymaltose (FCM) in this population were not previously established.

Purpose of the Study:

  • To evaluate the safety and efficacy of ferric carboxymaltose (FCM) in pediatric kidney transplant recipients with iron deficiency (ID) and/or iron deficiency anemia (IDA).

Main Methods:

  • Single-center, retrospective cohort study.
  • Included pediatric kidney transplant patients diagnosed with ID/IDA (KDIGO guidelines) who received FCM between December 2016 and November 2022.
  • Assessed hemoglobin, ferritin, transferrin saturation (TSat), and phosphate levels at baseline and follow-up points up to 12 months.

Main Results:

  • Fifteen patients with ID (10 with IDA) received FCM.
  • Significant increases in hemoglobin (1.2-1.4 g/dL) and ferritin levels were observed up to six months.
  • Transferrin saturation improved by 30 days post-treatment.
  • No significant decrease in phosphate levels or adverse reactions were noted.

Conclusions:

  • Ferric carboxymaltose (FCM) appears to be an effective and well-tolerated treatment for ID/IDA in pediatric kidney transplant recipients.
  • Larger, powered trials are needed to confirm these findings.
Abstract

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