Примери за използване на Hbeag на Английски и техните преводи на Български
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HBeAg positive.
Clinical Laboratory HBeAg 17.00.
HBeAg Seroconversion.
Nucleoside Naive HBeAg Positive(study 022).
HBeAg positive(study 026).
Хората също превеждат
Lamivudine-refractory HBeAg positive(study 026) n.
HBeAg Negative(study 027).
Active chronic hepatitis without HBeAg(with mutant HBV particles).
HBeAg negative/ anti-HBe positive Study WV16241.
Blood test for the determination of hepatitis markers(positive HBSAg, HBeAg, anti-HBc-IgM).
Serology HBeAg loss/ seroconversiond.
By 48 weeks of post-treatment follow-up, a substantial number of HBeAg negative patients lost response.
HBeAg Seroconversion*p value vs lamivudine< 0.05 a.
Its also used on clinical trial data in nucleoside inhibitor treatment for the HBeAg positive and HBeAg negative HBV infection.
In HBeAg positive patients without cirrhosis, treatment should be administered for at least.
Serum ALT and HBV DNA levels should be monitored at 3 month intervals andin HBeAg positive patients HBeAg should be assessed every 6 months.
In HBeAg negative patients without cirrhosis, treatment should be administered at least until.
These patients had completed≥ 52 weeks of telbivudine treatment, and had exhibited HBeAg loss for≥ 24 weeks with HBV DNA< 5 log10 copies/ml at the last on-treatment visit.
HBeAg positive and HBeAg negative chronic hepatitis B with compensated liver disease.
Serum ALT levels should be monitored at3 month intervals and HBV DNA and HBeAg should be assessed every 6 months.
Of patients were HBeAg positive, and 35% of patients had LVDr substitutions at baseline.
In the subgroup of patients with baseline ALT levels≥ 2x ULN(320), a significantly higher proportion of telbivudine patients than lamivudine patients achieved HBeAg seroconversions at week 104(36% vs 28%, respectively).
HBeAg seroconversion and loss assessed only in patients with detectable HBeAg at baseline.
After a median off-treatment follow-up period of 120 weeks,the majority of HBeAg-positive telbivudine treated-patients showed sustained HBeAg loss(83.3%; 25/30), and sustained HBeAg seroconversion(79.2%; 19/24).
In HBeAg negative paediatric patients, treatment should be administered until HBs seroconversion or there is evidence of loss of efficacy.
HBV DNA< 50 IU/mL and HBeAg seroconversiona HBV DNA< 50 IU/mLa HBeAg seroconversiona ALT normalizationa.
HBeAg negative, 47.5% were HBeAg positive, mean HBV DNA level was 6.5 log10 copies/ml, and mean ALT was 79 U/l, respectively.
In an extended treatment study in Asian patients(NUCB3018) the HBeAg seroconversion rate and ALT normalisation rate at the end of the 5 year treatment period was 48%(28/58) and 47%(15/32), respectively.
HBeAg seroconversion was increased in patients with elevated ALT levels; 77%(20/26) of patients with pre-treatment ALT> 2 x ULN seroconverted.
In adult patients with loss of HBeAg and HBV-DNA, a significant reduction in morbidity and mortality has been observed.