Changing trends of splenectomy in hereditary spherocytosis: The experience of a reference Centre in the last 40 years

Cristina Vercellati, Anna Zaninoni, Anna P. Marcello, Elisa Fermo, Bruno Fattizzo, Juri A. Giannotta, Paola Bianchi, Alberto Zanella, Wilma Barcellini

Research output: Contribution to journalArticlepeer-review

Abstract

We describe the clinical/haematological characteristics of 446 patients with hereditary spherocytosis diagnosed in the last 40 years in a reference centre. The frequency of splenectomy decreased over time (44% before 1990 to 7% in 2011–2020), notwithstanding a confirmed good efficacy. Age at splenectomy progressively increased (63% in children before 1990 to 88% in patients aged ≥20 years in 2011–2020). Our real-life experience showed that even a fraction of patients in the trait/mild categories (19/92, 21%) were splenectomised, whilst 30/78 (38%) in the moderate/severe groups were not. Overall, these data pinpoint to the increasing awareness about post-splenectomy thromboses and infections.

Original languageEnglish
Pages (from-to)912-915
JournalBritish Journal of Haematology
Volume198
Issue number5
DOIs
Publication statusPublished - 2022

Keywords

  • cholecystectomy
  • complications
  • hereditary spherocytosis
  • pregnancy
  • splenectomy

ASJC Scopus subject areas

  • Hematology

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