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1.
Transplant Proc ; 35(5): 1978-80, 2003 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-12962868

RESUMO

Sirolimus (SRL) is a potent non-nephrotoxic immunosuppressant. In our unit, SRL was administered to 17 heart transplant (HT) recipients at 1770+/-1234 days' posttransplant surgery, for the following reasons: (1) calcineurin inhibitor (CI) withdrawal due to renal insufficiency (RI; n=6); (2) neurotoxicity (n=1) and pancytopenia (n=1); (3) vascular graft disease (VGD) treatment (n=5); (4) immunosuppression optimization due to lung cancer (n=2); (5) CI use was delayed due to postsurgery RI (n=2). The mean follow-up was 190+/-165 days. Mean SRL doses (mg)/concentrations (ng/mL) at 7 (n=17), 30 (n=14), and 180 (n=8) days were: 1.2+/-0.6/5.9+/-6; 1.6+/-0.8/4.8+/-3.1; and 1.7+/-1.0/5.2+/-3.7. Among group 1, CI patients were discontinued without favorable functional impact. Neurotoxicity and pancytopenia improved, but there were no major clinical events in the VGD group. One "bridge" to CI was successfully performed (postsurgery RI). Total leukocyte count fell while hemoglobin, platelet, and cholesterol profiles were not affected. Ten of 15 patients (67%) were discontinued from CI without rejection and with a dose reduction of mycophenolate mofetil. There were 8 episodes (47%) of SRL-related toxicity, leading to 4 discontinuations (23%); 8 patients (47%) have died during follow-up. This retrospective analysis of outcomes in the context of severe complicated patients suggests that more premature introduction SRL is preferable, particularly in a large patient cohort.


Assuntos
Transplante de Coração/imunologia , Imunossupressores/uso terapêutico , Sirolimo/uso terapêutico , Humanos , Estudos Retrospectivos , Resultado do Tratamento
4.
Eur Respir J ; 16(6): 1202-4, 2000 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-11292127

RESUMO

Two cases of primary pulmonary artery sarcoma resembling chronic thromboembolic disease features are presented. Tumour identification was achieved after pulmonarv thromboendarterectomy, which was indicated by documentation of a prothrombotic state in both patients. A doubtful history of pulmonary emboli or deep venous thrombosis should alert medical personnel to the possible presence of a primary pulmonary artery sarcoma. Advanced imaging methods such as gadolinium-enhanced magnetic resonance imaging could be useful in considering pulmonary thromboendarterectomy. If a tumour is detected, its surgical resection should be considered with caution, taking into account the poor survival results. Invasion of the adventitia or the right ventricle, as documented in the present cases, is unusual. As far as the present authors know, this is the first report of this kind of tumour and its coexistence with an activated protein C resistance state and type II heparin-induced thrombocytopenia.


Assuntos
Histiocitoma Fibroso Benigno/diagnóstico , Artéria Pulmonar , Embolia Pulmonar/diagnóstico , Sarcoma/diagnóstico , Neoplasias Vasculares/diagnóstico , Adulto , Diagnóstico Diferencial , Embolectomia , Feminino , Histiocitoma Fibroso Benigno/patologia , Histiocitoma Fibroso Benigno/cirurgia , Humanos , Masculino , Artéria Pulmonar/patologia , Artéria Pulmonar/cirurgia , Embolia Pulmonar/patologia , Embolia Pulmonar/cirurgia , Sarcoma/patologia , Sarcoma/cirurgia , Trombectomia , Neoplasias Vasculares/patologia , Neoplasias Vasculares/cirurgia
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