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1.
Mem. Inst. Oswaldo Cruz ; 112(6): 452-455, June 2017. tab
Article Dans Anglais | LILACS | ID: biblio-1040569

Résumé

ABSTRACT Diagnosis of schistosomiasis in migrants coming from endemic areas can be difficult, especially in asymptomatic subjects. Light-intensity disease, in fact, may be missed due to the low sensitivity of the stool microscopy and serologic testing cannot distinguish between a resolved infection and an active infection in patients who have been infected and treated in the past, because specific antibodies can persist despite cure. We describe a cross-sectional study conducted on 82 migrants tested for Schistosoma mansoni on single blood (anti-schistosome antibodies, total IgE) and urine [point-of-care (POC) circulating-cathodic-antigen (CCA) test] samples. A positive POC-CCA test (active infection) resulted in two untreated patients with a positive serology while all patients (n = 66) with a past infection showed a negative POC-CCA test. POC-CCA urine test in combination with serology may be helpful in rapidly differentiate active from past S. mansoni infection in migrants coming from endemic areas.


Sujets)
Humains , Animaux , Mâle , Femelle , Adulte , Schistosoma mansoni/immunologie , Population de passage et migrants/statistiques et données numériques , Schistosomiase à Schistosoma mansoni/diagnostic , Antigènes d'helminthe/analyse , Études transversales , Reproductibilité des résultats , Sensibilité et spécificité , Italie , Adulte d'âge moyen
2.
Braz. j. infect. dis ; 18(2): 164-169, Mar-Apr/2014. tab
Article Dans Anglais | LILACS | ID: lil-709411

Résumé

AIM: To evaluate changes in liver histology in patients with human immunodeficiency virus/hepatitis C virus coinfection non-responders to a suboptimal Interferon+Ribavirine regimen. MATERIALS AND METHODS: We investigated 49 patients with two sequential liver biopsies: 18 were non-responders to Interferon+Ribavirine treatment (Group hepatitis C virus Rx) administered after the 1st liver biopsy who underwent a 2nd liver biopsy after a median period of 3.92 year and 31 were patients who remained untreated for hepatitis C virus disease (Group hepatitis C virus untreated) after the 1st liver biopsy because of refusal and underwent a 2nd liver biopsy after a median period of 5.05-years. Most patients in both groups were under highly active antiretroviral therapy. At the time of 1st liver biopsy similar degrees of necro-inflammation, fibrosis and steatosis were observed in both groups. Changes in liver lesions between 1st and 2nd liver biopsys were adjusted for different intervals between liver biopsys by a mathematic formula. RESULTS: Liver fibrosis did not change in 88.9% of patients in Group hepatitis C virus Rx and in 77.4% in Group hepatitis C virus untreated. A marked deterioration in liver fibrosis was observed in 5 (16%) patients in Group hepatitis C virus untreated and in none in Group hepatitis C virus treated. Necro-inflammation and steatosis remained substantially unchanged in both groups. CONCLUSION: Liver histology remained substantially unchanged in human immunodeficiency virus/hepatitis C virus patients non-responder to anti-hepatitis C virus therapy over 4 years observation, suggesting an effective anti-hepatitis C virus early treatment for all hepatitis C virus/human immunodeficiency virus coinfected patients who can reasonably tolerate therapy. .


Sujets)
Adulte , Femelle , Humains , Mâle , Antiviraux/usage thérapeutique , Co-infection , Infections à VIH/anatomopathologie , Hépatite C/anatomopathologie , Interféron alpha/usage thérapeutique , Cirrhose du foie/virologie , Foie/anatomopathologie , Ribavirine/usage thérapeutique , Antiviraux/effets indésirables , Biopsie , Co-infection/anatomopathologie , Co-infection/virologie , Évolution de la maladie , Infections à VIH/complications , Infections à VIH/traitement médicamenteux , Hépatite C/complications , Hépatite C/traitement médicamenteux , Interféron alpha/effets indésirables , Cirrhose du foie/anatomopathologie , Foie/virologie , Ribavirine/effets indésirables , Indice de gravité de la maladie
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