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1.
J Cyst Fibros ; 18(2): 227-232, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30297214

RESUMO

Cystic fibrosis (CF) is characterised by chronic airway infection with bacteria and fungi. Infections caused by Scedosporium/Lomentospora species can occur and are difficult to treat. Moulds belonging to the genus Scedosporium/Lomentospora are detected most frequently in respiratory samples of patients with CF, next to Aspergillus spp. Our aim was to define pulmonary fungal infections due to Scedosporium/Lomentospora in CF and to study the antimycotic treatment. In this multicentre study (12 centres; duration January 2008 to December 2014) 31 patients with a lung infection caused by moulds of the genus Scedosporium/Lomentospora were included. 36 courses of antifungal treatment were documented. Scedosporium apiospermum sensu stricto accounted for 48.4% of cases. In 20/31 patients a therapeutic response under antimycotics (median duration 3.9 months) was achieved. Triple and double therapy was significantly more effective compared to monotherapy regarding FEV1, radiology, and symptoms. This data suggests that combined treatment is superior to monotherapy in patients with CF.


Assuntos
Antifúngicos , Fibrose Cística , Quimioterapia Combinada/métodos , Infecções Fúngicas Invasivas , Pneumopatias Fúngicas , Scedosporium , Adulto , Antifúngicos/administração & dosagem , Antifúngicos/classificação , Fibrose Cística/complicações , Fibrose Cística/microbiologia , Fibrose Cística/terapia , Monitoramento de Medicamentos/métodos , Monitoramento de Medicamentos/estatística & dados numéricos , Feminino , Alemanha , Humanos , Infecções Fúngicas Invasivas/diagnóstico , Infecções Fúngicas Invasivas/tratamento farmacológico , Pulmão/diagnóstico por imagem , Pulmão/fisiopatologia , Pneumopatias Fúngicas/diagnóstico , Pneumopatias Fúngicas/tratamento farmacológico , Pneumopatias Fúngicas/microbiologia , Masculino , Avaliação de Processos e Resultados em Cuidados de Saúde , Testes de Função Respiratória/métodos , Scedosporium/efeitos dos fármacos , Scedosporium/isolamento & purificação , Tomografia Computadorizada por Raios X/métodos
2.
Arch Dis Child ; 104(4): 354-359, 2019 04.
Artigo em Inglês | MEDLINE | ID: mdl-30327331

RESUMO

OBJECTIVES: To investigate the frequency of coeliac disease (CD)-specific human leucocyte antigen (HLA) genotypes in paediatric patients with type 1 diabetes (T1D), who are known to have a higher prevalence of CD than the general population, and to evaluate whether HLA genotyping is a suitable first-line screening method for CD. STUDY DESIGN: The study was a multicentre observational analysis of patients with T1D aged <20 years of whom a subgroup had undergone HLA genotyping. Patient data were retrieved from the Diabetes Prospective Follow-up database, a large diabetes follow-up registry. The present analysis included data from 439 centres throughout Germany, Austria, Switzerland and Luxembourg. RESULTS: In March 2017, the database contained 75 202 patients with T1D (53% male, mean age (SD) 14.6 (4.1) years, mean age at diagnosis 8.8 (4.3) years and mean diabetes duration 5.8 (4.3) years). 1624 patients had undergone coeliac-specific HLA genotyping, of whom 1344 (82.8%) were positive for HLA-DQ2, HLA-DQ8 or both, while 17.2% had no coeliac-specific HLA-markers. 26.6% of at-risk patients had a clinical suspected diagnosis of CD, and 3.6% had biopsy-proven CD. CONCLUSIONS: Genotyping for HLA-DQ2, HLA-DQ8 or both is positive in the vast majority (>80%) of patients with T1D. Therefore, screening for coeliac-specific HLA genotypes as a first-line test is not a suitable method to exclude CD in T1D. Regular screening for coeliac-specific antibodies in T1D is still recommended.


Assuntos
Doença Celíaca/diagnóstico , Diabetes Mellitus Tipo 1/complicações , Adolescente , Áustria , Doença Celíaca/complicações , Doença Celíaca/imunologia , Criança , Diabetes Mellitus Tipo 1/imunologia , Diagnóstico Precoce , Feminino , Genótipo , Alemanha , Antígenos HLA-DQ/genética , Teste de Histocompatibilidade , Humanos , Luxemburgo , Masculino , Suíça
3.
Mycopathologia ; 183(1): 33-43, 2018 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-28864921

RESUMO

Invasive pulmonary mycosis is after allergic bronchopulmonary aspergillosis (ABPA) a frequent and severe complication of CF lung disease. Among CF caregivers, there is an insecurity when and how to treat infections of the lung parenchyma caused by different fungi in patients with CF. This case series provides a multicenter experience on diagnostic, manifestation, and treatment of non-ABPA cases of pulmonary. Non-ABPA cases of pulmonary mycoses in patients with CF have been collected from the CF Centers in Berlin, Essen, Worms, Frankfurt (Germany), Leeds (UK), and Barcelona (Spain). Non-ABPA was defined as total serum IgE level <500 kU/L. Scedosporium and Lomentospora species seem to be more virulent in patients with CF and have been successfully treated with triple antifungal drug regimens in several cases. Rare fungi including yeasts can have pathogenic potential in CF. In this series, antibiotic treatment failure was the main indicator for the initiation of antifungal treatment. For an early and effective treatment of pulmonary mycoses in CF, the identification of biomarkers and of risk factors beyond antibiotic treatment failure is crucial and urgently needed. Furthermore, treatment efficacy studies are necessary for the different causative agents of these infections.


Assuntos
Antifúngicos/administração & dosagem , Fibrose Cística/complicações , Fungos/isolamento & purificação , Infecções Fúngicas Invasivas/diagnóstico , Infecções Fúngicas Invasivas/tratamento farmacológico , Pneumopatias Fúngicas/diagnóstico , Pneumopatias Fúngicas/tratamento farmacológico , Adulto , Criança , Quimioterapia Combinada/métodos , Feminino , Fungos/classificação , Alemanha , Humanos , Masculino , Pessoa de Meia-Idade , Espanha , Reino Unido , Adulto Jovem
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