Literature DB >> 27082377

Fanconi Syndrome Secondary to Deferasirox in Diamond-Blackfan Anemia: Case Series and Recommendations for Early Diagnosis.

Koyelle Papneja1, Mihir D Bhatt1, Melanie Kirby-Allen2, Steven Arora3, John T Wiernikowski1, Uma H Athale1.   

Abstract

Deferasirox is an oral iron chelator used to treat patients with transfusion-related iron overload. We report, from two institutions, two children with Diamond-Blackfan anemia who developed Fanconi syndrome secondary to deferasirox administration, along with a review of the literature. The current recommendation for the laboratory monitoring of patients receiving deferasirox does not include serum electrolytes or urine analysis. Thus, despite routine clinic visits and bloodwork, these two patients presented with life-threatening electrolyte abnormalities requiring hospitalization. Hence, we propose the inclusion of serum electrolytes and urine analysis as part of routine monitoring to facilitate the early diagnosis of Fanconi syndrome in the context of high doses of deferasirox therapy.
© 2016 Wiley Periodicals, Inc.

Entities:  

Keywords:  Diamond-Blackfan anemia; Fanconi syndrome; chronic transfusion therapy; deferasirox; iron chelation

Mesh:

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Year:  2016        PMID: 27082377     DOI: 10.1002/pbc.25995

Source DB:  PubMed          Journal:  Pediatr Blood Cancer        ISSN: 1545-5009            Impact factor:   3.167


  2 in total

Review 1.  Acute kidney injury: emerging pharmacotherapies in current clinical trials.

Authors:  Stefanie Woolridge Benoit; Prasad Devarajan
Journal:  Pediatr Nephrol       Date:  2017-06-10       Impact factor: 3.714

Review 2.  Kidney Tubular Damage Secondary to Deferasirox: Systematic Literature Review.

Authors:  Martin Scoglio; Maria Domenica Cappellini; Emanuela D'Angelo; Mario G Bianchetti; Sebastiano A G Lava; Carlo Agostoni; Gregorio P Milani
Journal:  Children (Basel)       Date:  2021-12-01
  2 in total

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