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1.
J Pediatric Infect Dis Soc ; 9(1): 96-99, 2020 Feb 28.
Artigo em Inglês | MEDLINE | ID: mdl-31183500

RESUMO

Little information on the efficacy and pharmacokinetics of letermovir among immunocompromised children is currently available. We describe here the use of letermovir in a 2-year-old immunocompromised child with ganciclovir-resistant cytomegalovirus disease who required extracorporeal membrane oxygenation. Detailed information on therapeutic-drug-monitoring measures and dosage adjustments for letermovir is provided.


Assuntos
Acetatos/administração & dosagem , Antivirais/administração & dosagem , Infecções por Citomegalovirus/tratamento farmacológico , Citomegalovirus , Monitoramento de Medicamentos/métodos , Hospedeiro Imunocomprometido , Pneumonia Viral/tratamento farmacológico , Quinazolinas/administração & dosagem , Acetatos/farmacocinética , Acetatos/uso terapêutico , Antivirais/farmacocinética , Antivirais/uso terapêutico , Pré-Escolar , Ensaios de Uso Compassivo , Citomegalovirus/genética , Citomegalovirus/isolamento & purificação , Infecções por Citomegalovirus/imunologia , Infecções por Citomegalovirus/virologia , DNA Viral/sangue , Relação Dose-Resposta a Droga , Oxigenação por Membrana Extracorpórea/efeitos adversos , Evolução Fatal , Feminino , Ganciclovir/uso terapêutico , Hepatite Viral Humana/tratamento farmacológico , Hepatite Viral Humana/imunologia , Humanos , Infecções Oportunistas/tratamento farmacológico , Pneumonia Viral/imunologia , Pneumonia Viral/virologia , Reação em Cadeia da Polimerase , Quinazolinas/farmacocinética , Quinazolinas/uso terapêutico , Falha de Tratamento , Carga Viral
2.
Int J Legal Med ; 129(4): 861-7, 2015 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-25381195

RESUMO

Despite the undeniable advantages of postmortem angiography, numerous questions have arisen concerning the influence that the injected contrast media may exercise on biological fluids and tissues collected for toxicological and biochemical investigations. Moreover, cardiac blood for microbiological investigations cannot be obtained post-angiography. In this study, we examined whether the peripheral blood collected prior to postmortem angiography, using percutaneous access to femoral vessels after skin surface disinfection, could be suitable for microbiological investigations when postmortem angiography with femoral vessel cannulation is also performed. A total of 66 cases were included in the study and were divided into two subgroups (angiography and bacteriology group, 33 cases and control group, 33 cases). Autopsies, histology, toxicology, bacteriology, and biochemical investigations (procalcitonin, C-reactive protein, interleukin-6, and soluble triggering receptors expressed on myeloid cells type 1) were performed in all cases. No statistically significant differences between the two groups were noted, and identified category distribution (death unrelated to infection, true infection, false positive, and undetermined) was rather similar in both studied populations. These preliminary results suggest that postmortem angiography using a femoral approach does not constitute an impediment to the collection of peripheral blood for microbiology and vice versa. Moreover, the use of femoral blood for microbiology does not lead to an increased risk of doubtful results.


Assuntos
Angiografia , Sangue/microbiologia , Cateterismo , Artéria Femoral , Veia Femoral , Adulto , Idoso , Translocação Bacteriana , Proteína C-Reativa/análise , Calcitonina/sangue , Peptídeo Relacionado com Gene de Calcitonina , Estudos de Casos e Controles , Feminino , Patologia Legal , Humanos , Interleucina-6/sangue , Masculino , Glicoproteínas de Membrana/sangue , Pessoa de Meia-Idade , Estudos Prospectivos , Precursores de Proteínas/sangue , Receptores Imunológicos/sangue , Receptor Gatilho 1 Expresso em Células Mieloides , Adulto Jovem
4.
Clin Infect Dis ; 49(10): 1532-5, 2009 Nov 15.
Artigo em Inglês | MEDLINE | ID: mdl-19848599

RESUMO

Human immunodeficiency virus (HIV)-infected men who have sex with men (MSM) were enrolled in an anorectal Chlamydia trachomatis screening study. Anorectal Chlamydia DNA was detected in 16 (10.9%) of 147 men, mainly among asymptomatic patients and patients having >20 sexual partners. These results support routine anorectal Chlamydia screening in HIV-infected MSM who report unprotected anal intercourse.


Assuntos
Doenças do Ânus/epidemiologia , Doenças do Ânus/microbiologia , Infecções por Chlamydia/epidemiologia , Doenças Retais/epidemiologia , Doenças Retais/microbiologia , Adulto , Idoso , Infecções por Chlamydia/microbiologia , Chlamydia trachomatis/isolamento & purificação , DNA Bacteriano/isolamento & purificação , Infecções por HIV/complicações , Homossexualidade Masculina , Humanos , Masculino , Pessoa de Meia-Idade , Reação em Cadeia da Polimerase , Prevalência , Suíça/epidemiologia , Adulto Jovem
5.
Diagn Microbiol Infect Dis ; 64(1): 85-9, 2009 May.
Artigo em Inglês | MEDLINE | ID: mdl-19304436

RESUMO

We describe an original case of disseminated infection with Histoplasma capsulatum (Hc) var. duboisii in an African patient with AIDS who migrated to Switzerland. The diagnosis of histoplasmosis was suggested using direct examination of tissues and confirmed in 24 h with a panfungal polymerase chain reaction assay. The variety duboisii of Hc was established using DNA sequencing of the polymorphic genomic region OLE. Molecular tools allow diagnosis of histoplasmosis in 24 h, which is drastically shorter than culture procedures.


Assuntos
Síndrome da Imunodeficiência Adquirida/complicações , Histoplasma/isolamento & purificação , Histoplasmose/diagnóstico , Adulto , DNA Fúngico/química , DNA Fúngico/genética , Emigrantes e Imigrantes , Histoplasma/genética , Humanos , Microscopia/métodos , Dados de Sequência Molecular , Filogenia , Reação em Cadeia da Polimerase/métodos , Análise de Sequência de DNA , Suíça
6.
Rev Med Suisse ; 5(226): 2344-6, 2348-50, 2009 Nov 18.
Artigo em Francês | MEDLINE | ID: mdl-20052867

RESUMO

The incidence of NTM (non tuberculous mycobacteria) pulmonary disease is increasing. The diagnosis must be established in the presence of clinical, radiological and microbiological findings. Groups at risk to contract pulmonary disease due to NTM are patients with underlying structural lung disease. Treatment of NTM is long and requires multiple drugs combinations. Relapses and re-infection are not rare. Our understanding in many matters of NTM pulmonary disease is incomplete. Further research is necessary in order to understand the host's defense mechanisms against NTM, and the factors that influence the evolution to lung disease.


Assuntos
Infecções por Mycobacterium não Tuberculosas/diagnóstico , Infecções por Mycobacterium não Tuberculosas/tratamento farmacológico , Micobactérias não Tuberculosas , Antituberculosos/uso terapêutico , Quimioterapia Combinada , Humanos , Incidência , Macrolídeos/uso terapêutico , Testes de Sensibilidade Microbiana , Infecções por Mycobacterium não Tuberculosas/epidemiologia , Infecções por Mycobacterium não Tuberculosas/microbiologia , Micobactérias não Tuberculosas/classificação , Micobactérias não Tuberculosas/patogenicidade , Recidiva , Fatores de Risco , Escarro/microbiologia , Suíça/epidemiologia , Fatores de Tempo , Resultado do Tratamento , Tuberculose Pulmonar/diagnóstico , Tuberculose Pulmonar/tratamento farmacológico
7.
Expert Opin Med Diagn ; 2(8): 947-61, 2008 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-23495868

RESUMO

BACKGROUND: Microbiological diagnostic procedures have changed significantly over the last decade. Initially the implementation of the polymerase chain reaction (PCR) resulted in improved detection tests for microbes that were difficult or even impossible to detect by conventional methods such as culture and serology, especially in community-acquired respiratory tract infections (CA-RTI). A further improvement was the development of real-time PCR, which allows end point detection and quantification, and many diagnostic laboratories have now implemented this powerful method. OBJECTIVE: At present, new performant and convenient molecular tests have emerged targeting in parallel many viruses and bacteria responsible for lower and/or upper respiratory tract infections. The range of test formats and microbial agents detected is evolving very quickly and the added value of these new tests needs to be studied in terms of better use of antibiotics, better patient management, duration of hospitalization and overall costs. CONCLUSIONS: Molecular tools for a better microbial documentation of CA-RTI are now available. Controlled studies are now required to address the relevance issue of these new methods, such as, for example, the role of some newly detected respiratory viruses or of the microbial DNA load in a particular patient at a particular time. The future challenge for molecular diagnosis will be to become easy to handle, highly efficient and cost-effective, delivering rapid results with a direct impact on clinical management.

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