Long-term evaluation of the beneficial effect of subtotal splenectomy for management of hereditary spherocytosis

Author:

Bader-Meunier Brigitte1,Gauthier Frédéric1,Archambaud Frédérique1,Cynober Thérèse1,Miélot Francoise1,Dommergues Jean-Paul1,Warszawski Josiane1,Mohandas Narla1,Tchernia Gil1

Affiliation:

1. From the Département de Pédiatrie, Laboratoire d'Hématologie, Service de médecine nucléaire, Service d'épidémiologie et de statistique, INSERM U 292, Hôpital Bicétre, Le Kremlin Bicétre, France; Assistance Publique des Hôpitaux de Paris, Faculté de Médécine Paris XI, Paris, France; and Lawrence Berkeley National Laboratory, University of California, Berkeley, CA.

Abstract

AbstractClinical manifestations of hereditary spherocytosis (HS) can be abrogated by splenectomy. However, concerns exist regarding exposure of patients to a lifelong risk for overwhelming infections and, to a lesser extent, to vascular complications after total splenectomy. In the search for alternative treatment modalities, we assessed, in a previous pilot study, the potential usefulness of subtotal splenectomy in a small population of patients. During a mean follow-up period of 3.5 years, subtotal splenectomy was shown to be effective in decreasing the hemolytic rate, while maintaining the phagocytic function of the spleen. In the current study, we evaluated the clinical and biologic features of 40 patients with HS who underwent subtotal splenectomy and were monitored for periods ranging from 1 to 14 years. The beneficial effect of subtotal splenectomy included a sustained decrease in hemolytic rate and a continued maintenance of phagocytic function of the splenic remnant. However, mild-to-moderate hemolysis was persistent and accounted for secondary gallstone formation and aplastic crisis in a small subset of patients. Surprisingly, regrowth of the remnant spleen did not seem to have a major impact on the beneficial outcomes of these individuals. Our results suggest that subtotal splenectomy appears to be a reasonable treatment option for management of patients with HS, especially young children.

Publisher

American Society of Hematology

Subject

Cell Biology,Hematology,Immunology,Biochemistry

Reference32 articles.

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