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Br J Haematol ; 160(5): 680-7, 2013 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-23278768

RESUMO

Pain is not a symptom generally associated with thalassaemia. However, providers have noted increasing patient reports of pain, creating an impetus for this prospective, observational assessment of pain in thalassaemia patients. The primary study goals were to assess pain prevalence, severity, location, and potential risk factors. This was a multicentre, prospective study of thalassaemia patients receiving care at 12 Thalassaemia Clinical Research Network sites. Pain was assessed using the Brief Pain Inventory. Two hundred and fifty-two thalassaemia patients ranging in age from 12 to 71 years (mean 28.8) were enrolled. Sixty-four per cent reported experiencing pain during the last 4 weeks, 22% of whom reported pain on a daily basis. Ordinal regression analysis of pain ratings demonstrated significant (P < 0.001) correlation of increased age with increased pain, irrespective of diagnosis, transfusion status, gender, bone density, chelator type or iron overload. Eighty-one per cent reported having pain for 1 year or longer and 31% reported pain for five or more years. Pain is a major cause of morbidity and an unrecognized problem for patients with thalassaemia. Age is the strongest predictor of frequency and severity. Little else is known about the aetiology and predictors of this pain syndrome.


Assuntos
Fatores Etários , Dor/epidemiologia , Talassemia/epidemiologia , Adolescente , Adulto , Idoso , Analgésicos/uso terapêutico , Doenças Ósseas Metabólicas/epidemiologia , Criança , Dor Crônica/tratamento farmacológico , Dor Crônica/epidemiologia , Feminino , Fraturas Espontâneas/epidemiologia , Hemoglobinas/análise , Humanos , Ferro/sangue , Quelantes de Ferro/uso terapêutico , Sobrecarga de Ferro/tratamento farmacológico , Sobrecarga de Ferro/etiologia , Masculino , Pessoa de Meia-Idade , Dor/tratamento farmacológico , Medição da Dor , Estudos Prospectivos , Qualidade de Vida , Fatores de Risco , Talassemia/sangue , Talassemia/terapia , Reação Transfusional , Adulto Jovem , Talassemia alfa/epidemiologia
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