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1.
Med Clin (Barc) ; 160(2): 51-59, 2023 01 20.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-35786523

RESUMO

OBJECTIVES: To evaluate the aspects of the basal bone health status in prostate cancer patients. Furthermore, to evaluate in a real-world setting the effect of different schemes (intermittent or continuous) of androgen deprivation therapy (ADT) and the effect of denosumab in bone mass density (BMD). METHODS: Observational, retrospective study of a cohort of prostate cancer patients in treatment with luteinizing hormone-releasing hormone (LH-RH) agonists, evaluated in the rheumatology department of a tertiary center. Demographics, FRAX score, LH-RH treatment scheme, osteoporosis treatment, laboratory data and BMD were collected. Mixed effect regression models to analyze the interaction between LH-RH treatment scheme, denosumab and BMD evolution were used. RESULTS: Eighty-three patients (mean age 71±8years) were included. At the basal evaluation, 16% of patients presented densitometric osteoporosis and 27% of patients presented high fracture risk. Eighty percent of patients had inadequate vitaminD levels. VitaminD >30ng/mL was correlated with higher T-scores. There was no association between LH-RH treatment scheme and BMD evolution, however there was a positive association with denosumab. CONCLUSION: A high proportion of patients presented elevated fracture risk or inadequate vitaminD levels, not previously recognized. Bone health assessment and fracture risk evaluation are convenient in these patients. In a real-world setting, the effect of denosumab in BMD is detected, however the effect of intermittent LH-RH schema treatment is less evident.


Assuntos
Fraturas Ósseas , Osteoporose , Neoplasias da Próstata , Masculino , Humanos , Pessoa de Meia-Idade , Idoso , Neoplasias da Próstata/tratamento farmacológico , Densidade Óssea , Antagonistas de Androgênios/efeitos adversos , Androgênios , Denosumab/uso terapêutico , Denosumab/farmacologia , Estudos Retrospectivos , Osteoporose/induzido quimicamente , Hormônio Liberador de Gonadotropina
3.
Reumatol Clin (Engl Ed) ; 16(1): 38-41, 2020.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-29550251

RESUMO

OBJECTIVE: Polymyalgia rheumatica (PR) can be associated with large vessel vasculitis (LVV). We evaluate the diagnostic role of 18F-fluorodeoxyglucose positron emission tomography/computed tomography (FDG PET/CT) and its impact on the treatment of LVV associated with PR. MATERIALS AND METHODS: Retrospective study of patients diagnosed with PR. Data was collected from health records. Blood analysis included acute-phase reactants (APR), C-reactive protein (CRP) and erythrocyte sedimentation rate. An 18F-FDG PET/CT scan was performed in those patients whose symptoms persisted, in those with elevated APR, those who required higher doses of steroids or those who had atypical features of PR (low-grade fever, weight loss, among others). RESULTS: Twenty-three were eligible; 48% (n = 11) of the patients were diagnosed with LVV associated with PR. The site was heterogeneous, but mostly involved the aorta. In 80% of the patients with LVV, a disease-modifying antirheumatic drug was added to their treatment. Elevated CRP values were associated with the likelihood of presenting LVV. CONCLUSIONS: LVV is not uncommon, clinical features and elevated CRP levels should raise suspicion of LVV associated with PR. 18F-FDG PET/CT is useful in identifying LVV associated with PR.


Assuntos
Fluordesoxiglucose F18 , Polimialgia Reumática/complicações , Tomografia por Emissão de Pósitrons combinada à Tomografia Computadorizada , Compostos Radiofarmacêuticos , Vasculite Reumatoide/diagnóstico por imagem , Proteínas de Fase Aguda/análise , Idoso , Aortite/diagnóstico por imagem , Sedimentação Sanguínea , Proteína C-Reativa/análise , Feminino , Arterite de Células Gigantes/sangue , Arterite de Células Gigantes/complicações , Humanos , Masculino , Polimialgia Reumática/sangue , Polimialgia Reumática/tratamento farmacológico , Estudos Retrospectivos , Vasculite Reumatoide/sangue , Vasculite Reumatoide/tratamento farmacológico , Vasculite Reumatoide/etiologia
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