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3.
Am J Case Rep ; 19: 1053-1056, 2018 Sep 03.
Artigo em Inglês | MEDLINE | ID: mdl-30174327

RESUMO

BACKGROUND Vancomycin has been used for decades to treat infections by Gram-positive bacteria, particularly those caused by methicillin-resistant staphylococci. Agranulocytosis is an infrequent complication of this antibiotic, postulated in its genesis a mechanism immune-mediated by antineutrophil antibodies and antineutrophil cytoplasm antibodies (ANCA). Treatment includes discontinuing vancomycin, and granulocyte colony-stimulating factor administration. CASE REPORT We present the case of a patient who developed agranulocytosis secondary to vancomycin during the treatment of an infectious endocarditis, which was reversed when the antibiotic was stopped. Concomitantly to neutropenia, he had ANCA positivity, which subsequently became negative. CONCLUSIONS Agranulocytosis induced by vancomycin is infrequent and generally occurs after day 12 of treatment. In most cases, like in our case, it is caused by an immune-mediated mechanism. More studies are needed to determine the pathogenic mechanism and the ANCA role in this adverse effect.


Assuntos
Agranulocitose/induzido quimicamente , Antibacterianos/efeitos adversos , Staphylococcus aureus Resistente à Meticilina/isolamento & purificação , Infecções Estafilocócicas/tratamento farmacológico , Vancomicina/efeitos adversos , Abscesso Abdominal/tratamento farmacológico , Abscesso Abdominal/microbiologia , Adulto , Agranulocitose/sangue , Agranulocitose/terapia , Antibacterianos/uso terapêutico , Anticorpos Anticitoplasma de Neutrófilos/sangue , Endocardite Bacteriana/tratamento farmacológico , Endocardite Bacteriana/microbiologia , Fator Estimulador de Colônias de Granulócitos/uso terapêutico , Humanos , Nefropatias/tratamento farmacológico , Nefropatias/microbiologia , Masculino , Infecções Estafilocócicas/microbiologia , Infecções Urinárias/tratamento farmacológico , Infecções Urinárias/microbiologia , Vancomicina/uso terapêutico
4.
Ther Adv Respir Dis ; 9(3): 121-9, 2015 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-25862013

RESUMO

Idiopathic pulmonary fibrosis (IPF) is a progressive and ultimately fatal lung disease that occurs in older adults. The clinical course of IPF is variable and hard to predict in an individual patient. Nintedanib is a tyrosine kinase inhibitor that has recently been approved in the US and European Union for the treatment of IPF. Preclinical studies have shown that nintedanib interferes with processes active in fibrosis such as fibroblast proliferation, migration and differentiation and the secretion of extracellular matrix. The safety and efficacy of nintedanib have been investigated in the phase II TOMORROW trial and in two replicate 52-week randomized, placebo-controlled phase III trials known as the INPULSIS trials. These trials demonstrated that nintedanib slowed disease progression by reducing the annual rate of decline in forced vital capacity, with a manageable side-effect profile. In this review, we summarize key data supporting nintedanib as a treatment for patients with IPF and address key questions regarding the use of nintedanib in the clinical setting.


Assuntos
Inibidores Enzimáticos/uso terapêutico , Fibrose Pulmonar Idiopática/tratamento farmacológico , Indóis/uso terapêutico , Adulto , Ensaios Clínicos como Assunto , Quimioterapia Combinada , Humanos , Seleção de Pacientes , Receptores Proteína Tirosina Quinases/antagonistas & inibidores
5.
Lung India ; 31(2): 149-51, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24778479

RESUMO

Human immunodeficiency virus (HIV) disease is widespread all over the world, and the neurological and respiratory complications have been described previously. Peripheral neuropathy is one of the commonest neurological complications of the HIV infection. In this report we describe a HIV positive male smoker who was admitted to the hospital because of community acquired pneumonia. Bilateral diaphragmatic paralysis was diagnosed for which no other cause was found and was attributed to the HIV infection. Isolated phrenic neuropathy and diaphragmatic paralysis in an HIV positive patient is extremely rare and only a single such association has been described previously.

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