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1.
J Viral Hepat ; 10(3): 189-96, 2003 May.
Article de Anglais | MEDLINE | ID: mdl-12753337

RÉSUMÉ

A randomized trial was conducted to assess the efficacy of daily (QD) or thrice weekly (TIW) administration of interferon-alpha (IFN) in high doses in combination with ribavirin (1.0-1.2 g/day) in patients with chronic hepatitis C (CHC) who were nonresponders to previous IFN monotherapy. Interferon was administered as 10 MU IFN (QD or TIW) for 4 weeks, followed by 5 MU IFN (QD or TIW) for 20 weeks, and then by 3 MU IFN (QD or TIW) for 24 weeks. Sustained virological response (SVR) was evaluated in 142 patients who received at least one dose of medication. One-fourth of the patients achieved SVR, 26% of those treated with IFN QD and 25% of those treated with IFN TIW (P = 0.85). For genotype 1 patients, SVR rates were 32.4 and 15.8% for IFN QD and IFN TIW, respectively, whereas for genotype non-1 patients the corresponding SVR rates were 20.6 and 36.4%, respectively (test of homogeneity: P = 0.031). This finding was further confirmed by multivariate logistic regression analysis where a statistically significant interaction (P = 0.012) was found between treatment and HCV genotype indicating that the IFN QD regimen was superior to IFN TIW among genotype 1 patients whereas, among genotype non-1 patients, the two treatments were similar (odds ratio of SVR in IFN QD vs IFN TIW: 3.33 among genotype 1 patients, 95% CI: 1.00-11.14). In conclusion, re-treatment of patients not responding to previous IFN monotherapy with a combination of high daily dose of IFN with ribavirin may be beneficial for genotype 1 infected patients.


Sujet(s)
Antiviraux/usage thérapeutique , Hépatite C chronique/traitement médicamenteux , Interféron alpha/usage thérapeutique , Ribavirine/usage thérapeutique , Adolescent , Adulte , Sujet âgé , Antiviraux/administration et posologie , Association de médicaments , Femelle , Hepacivirus/classification , Hepacivirus/effets des médicaments et des substances chimiques , Hepacivirus/génétique , Hépatite C chronique/virologie , Humains , Interféron alpha-2 , Interféron alpha/administration et posologie , Mâle , Adulte d'âge moyen , ARN viral/sang , Protéines recombinantes , Ribavirine/administration et posologie , Résultat thérapeutique
2.
Scand J Infect Dis ; 33(11): 859-60, 2001.
Article de Anglais | MEDLINE | ID: mdl-11760171

RÉSUMÉ

We report a case of transfusion-mediated Yersinia enterocolitica septicemia in a 43-y-old woman with homozygous beta-thalassemia. Two h after transfusion of 3 units of red blood cells the patient suffered high-grade fever and shaking chills. Y. enterocolitica serotype O3 grew in blood cultures. Prolonged treatment with i.v. ceftriaxone plus ciprofloxacin led to a favorable outcome. Transfusion-associated Y. enterocolitica septicemia has not previously been reported in an adult beta-thalassemic patient from the Mediterranean area. Our report is particularly important, because of the high incidence of chronically transfused thalassemic patients in Mediterranean countries.


Sujet(s)
Réaction transfusionnelle , Yersinioses/étiologie , Yersinia enterocolitica/isolement et purification , bêta-Thalassémie/thérapie , Adulte , Anti-infectieux/usage thérapeutique , Ceftriaxone/usage thérapeutique , Céphalosporines/usage thérapeutique , Ciprofloxacine/usage thérapeutique , Femelle , Humains , Résultat thérapeutique , Yersinioses/traitement médicamenteux , Yersinioses/microbiologie
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