4 research outputs found
Weil Hastalığı: Aseptik Menenjit, Akut Böbrek Yetmezliği ve Şiddetli Üst Gastrointestinal Sistem Kanaması ile Seyreden Bir Olgu Sunumu
Intravitreal triamcinolone acetonide injection in CRVO associated with Wegener's granulomatosis
A 33-year-old man developed unilateral nonischemic central retinal vein occlusion associated with systemic Wegener's granulomatosis. Four milligrams of triamcinolone acetonide was injected intravitreally twice 6 months apart in conjunction with ongoing systemic immunosuppressive therapy. No change was made in the systemic immunosuppressive regimen. Wegener's granulomatosis should be considered in the differential diagnosis of central retinal vein occlusion in the young age group and intravitreal triamcinolone acetonide is a good adjunct to systemic immunosuppressive therapy that eliminates the need for modifying the systemic treatment regimen
Intravitreal Triamcinolone Acetonide Injection in CRVO Associated With Wegener’s Granulomatosis
Accelerated versus classical hepatitis B virus vaccination programs in healthcare workers accelerated vs. classical HBV vaccination
WOS: 000242137900010PubMed ID: 17072271The aim of this study was to compare the efficacy of a standard hepatitis B virus vaccination program (day 0-30-60) with an accelerated vaccination program (day 0-10-21) in healthy healthcare workers. Participants were randomly assigned to a classical (group 1, days 0, 30, and 60) or an accelerated vaccination program (group 2, days 0, 10, and 21). The vaccine used was 20 mu g recombinant hepatitis B vaccine (recombinant hepatitis B vaccine derived from yeast cells, Engerix B, Smith Cline Beachum). HBV markers were re-examined for the emergence of anti-HBsAg and also to detect the development of a possible acute HBV infection one, two, and three months after the last dose of vaccine. Anti-HBsAg titers > 10 mIU/1 were accepted as protective. The seroprotection rates were similar one, two, and three months after the last dose of vaccine in both groups. Anti-HBsAg titers in group 1 were higher than in group 2 two and three months after the last dose of vaccination (p < 0.05). Our data indicate that the accelerated HBV vaccination program was as effective as the classical vaccination program