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A retrospective analysis of the impact of treatments and blood counts on survival and the risk of vascular events during the course of polycythaemia vera.
Enblom-Larsson, Anneli; Girodon, Francois; Bak, Marie; Hersby, Ditte; Jooste, Valérie; Hasselbalch, Hans; Johansson, Peter; Andreasson, Björn.
Afiliação
  • Enblom-Larsson A; Department of Internal Medicine, Sunderby hospital, Luleå, Sweden.
  • Girodon F; Service d'hématologie Biologique, CHU de Dijon, Dijon, France.
  • Bak M; Department of Hematology, Roskilde hospital, Roskilde, Denmark.
  • Hersby D; Department of Hematology, Roskilde hospital, Roskilde, Denmark.
  • Jooste V; Registre Bourguignon des Cancers Digestifs, INSERM UMR 866 - CHU Dijon Bourgogne - Université Bourgogne Franche-Comté, Dijon, France.
  • Hasselbalch H; Department of Hematology, Roskilde hospital, Roskilde, Denmark.
  • Johansson P; Hematology and Coagulation section, Department of Medicine, Sahlgrenska University Hospital, Gothenburg, Sweden.
  • Andreasson B; NU hospital group, Uddevalla Hospital, Uddevalla, Sweden.
Br J Haematol ; 177(5): 800-805, 2017 06.
Article em En | MEDLINE | ID: mdl-28474342
ABSTRACT
Vascular and non-vascular complications are common in patients with polycythaemia vera. This retrospective study of 217 patients with polycythaemia vera aimed to determine whether blood counts with respect to different treatments influenced the complication rate and survival. We found that 78 (36%) patients suffered from at least one complication during follow-up. Older age and elevated lactate dehydrogenase at diagnosis were found to be risk factors for vascular complications. When the vascular complication occurred, 41% of the patients with a complication had elevated white blood cells (WBC) compared with 20% of patients without a complication (P = 0·042). Patients treated with hydroxycarbamide (HC; also termed hydroxyurea) experienced significantly fewer vascular complications (11%) than patients treated with phlebotomy only (27%) (P = 0·013). We also found a survival advantage for patients treated with HC, when adjusted for age, gender and time period of diagnosis (Hazard ratio for phlebotomy-treated patients compared to HC-treated patients at 5 years was 2·42, 95% confidence interval 1·03-5·72, P = 0·043). Concerning survival and vascular complications, HC-treated patients who needed at least one phlebotomy per year were not significantly different from HC-treated patients with a low phlebotomy requirement. We conclude that complementary phlebotomy in HC-treated patients in order to maintain the haematocrit, is safe.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Policitemia Vera / Doenças Vasculares Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Policitemia Vera / Doenças Vasculares Tipo de estudo: Etiology_studies / Observational_studies / Risk_factors_studies Limite: Aged / Female / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article