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A complication risk score to evaluate clinical severity of thalassaemia syndromes.
Vitrano, Angela; Meloni, Antonella; Addario Pollina, Walter; Karimi, Mehran; El-Beshlawy, Amal; Hajipour, Mahmoud; Di Marco, Vito; Hussain Ansari, Saqib; Filosa, Aldo; Ricchi, Paolo; Ceci, Adriana; Daar, Shahina; Titi Singer, Sylvia; Naserullah, Zaki A; Pepe, Alessia; Scondotto, Salvatore; Dardanoni, Gabriella; Bonifazi, Fedele; Vichinsky, Elliott; Maggio, Aurelio.
Afiliação
  • Vitrano A; Campus of Haematology Franco and Piera Cutino, AOOR Villa Sofia-V. Cervello, Palermo, Italy.
  • Meloni A; U.O.C. MRI, Fondazione Toscana G. Monasterio, Pisa, Italy.
  • Addario Pollina W; D.A.S.O.E, Regione Siciliana, Palermo, Italy.
  • Karimi M; Haematology Research Center, Shiraz University of Medical Sciences, Shiraz, Iran.
  • El-Beshlawy A; Cairo University, Giza, Egypt.
  • Hajipour M; Department of Epidemiology, School of Public Health and Safety, Shahid Beheshti University of Medical Sciences, Tehran, Iran.
  • Di Marco V; Sezione di Gastroenterologia e Epatologia, Dipartimento Biomedico di Medicina Interna e Specialistica, University of Palermo, Palermo, Italy.
  • Hussain Ansari S; Department of Paediatric Haematology and Molecular Medicine, National Institute of Blood Diseases and Bone Marrow Transplantation, Karachi, Pakistan.
  • Filosa A; Rare Blood Cell Disease Unit, "Cardarelli" Hospital, Naples, Italy.
  • Ricchi P; Rare Blood Cell Disease Unit, "Cardarelli" Hospital, Naples, Italy.
  • Ceci A; Fondazione per la Ricerca Farmacologica Gianni Benzi Onlus, Valenzano, BA, Italy.
  • Daar S; Department of Haematology, College of Medicine and Health Sciences, Sultan Qaboos University, Muscat, Sultanate of Oman.
  • Titi Singer S; Wallenberg Research Centre, Stellenbosch Institute for Advanced Study, Stellenbosch University, Stellenbosch, South Africa.
  • Naserullah ZA; Haematology/Oncology Department, Oakland, CA, USA.
  • Pepe A; Dammam Maternity and Child Hospital, Dammam, Saudi Arabia.
  • Scondotto S; U.O.C. MRI, Fondazione Toscana G. Monasterio, Pisa, Italy.
  • Dardanoni G; D.A.S.O.E, Regione Siciliana, Palermo, Italy.
  • Bonifazi F; D.A.S.O.E, Regione Siciliana, Palermo, Italy.
  • Vichinsky E; Fondazione per la Ricerca Farmacologica Gianni Benzi Onlus, Valenzano, BA, Italy.
  • Maggio A; Haematology/Oncology Department, Oakland, CA, USA.
Br J Haematol ; 192(3): 626-633, 2021 02.
Article em En | MEDLINE | ID: mdl-33216983
The thalassaemia syndromes (TS) show different phenotype severity. Developing a reliable, practical and global tool to determine disease severity and tailor treatment would be of great value. Overall, 7910 patients were analysed with the aim of constructing a complication risk score (CoRS) to evaluate the probability of developing one or more complications. Nine independent variables were included in the investigation as predictors. Logistic regression models were used for Group A [transfusion-dependent thalassaemia (TDT)], Group B [transfused non-TDT (NTDT)] and Group C (non-transfused NTDT). Statistically significant predictors included age (years), haemoglobin levels, hepatic transaminases [alanine aminotransferase (ALT) and aspartate aminotransferase] and left-ventricular ejection fraction (LVEF) for Group A; age (years), age at first chelation (months), ALT and LVEF for Group B; and age (years), mean serum ferritin (SF) levels and LVEF for Group C. The area under the receiver operating characteristic curve was 84·5%, 82·1% and 80·0% for Groups A, Group B and Group C respectively, suggesting the models had good discrimination. Finally, the CoRS for each group was categorised into four risk classes (low, intermediate, high, and very high) using the centiles of its distribution. In conclusion, we have developed a CoRS for TS that can assist physicians in prospectively tailoring patients' treatment.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Talassemia Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Talassemia Tipo de estudo: Etiology_studies / Prognostic_studies / Risk_factors_studies Limite: Adolescent / Adult / Female / Humans / Male / Middle aged Idioma: En Ano de publicação: 2021 Tipo de documento: Article