𝔖 Bobbio Scriptorium
✦   LIBER   ✦

Acyclovir in chronic hepatitis B virus infection

✍ Scribed by Geoffrey M. Dusheiko


Publisher
John Wiley and Sons
Year
1988
Tongue
English
Weight
273 KB
Volume
8
Category
Article
ISSN
0270-9139

No coin nor oath required. For personal study only.

✦ Synopsis


In a previous study a partial inhibition of viral replication was observed in HBeAg-positive patients after acyclovir (ACV) treatment.

To assess those results and to evaluate different treatment regimens, a randomized controlled trial with ACV given at 45 mg/kg/day by continuous infusion (in 5 patients) or by intermittent 8-hourly infusion (in 6 patients) for 28 days versus placebo has been performed in 20 patients affected by chronic hepatitis positive for both HBsAg and HBeAg for at least 6 months.

Patients were stratified for sex, presence of cirrhosis and homosexual activity.

Modest inhibition of serum DNA polymerase activity was observed after intermittent ACV treatment but not with the continuous infusion. After a 8-12 months follow-up, 2 of 10 of the ACV-treated patients and 3 of the controls had become HBe-Agnegative, with 1 and 2 seroconversions to anti-HBe in the treated and placebo group respectively. No adverse effects were observed in ACV-treated patients after continuous infusion, but 2 of 6 patients who received intermittent therapy had to stop treatment, because of abdominal colics and elevation of the serum creatinine.

Our data confirm that ACV partially inhibits viral replication in HBeAg-positive patients but without significantly affecting the rate of seroconversion to anti-HBe.


πŸ“œ SIMILAR VOLUMES


Controlled clinical trial of acyclovir i
✍ Dr. Graeme J. M. Alexander; Elizabeth A. Fagan; John E. Hegarty; Adrian L. W. F. πŸ“‚ Article πŸ“… 1987 πŸ› John Wiley and Sons 🌐 English βš– 470 KB

A randomised, controlled trial comparing acyclovir, 45 mg/kg/day as a continuous IV infusion for 28 days, with no other therapy, was carried out in 30 stable HBsAg carriers seropositive for HBeAg for more than 6 months. Twenty-eight had hepatitis B virus DNA-polymerase activity and/or hepatitis B vi

AFP in chronic hepatitis B virus infecti
✍ Yun-Fan Liaw; Anna Lok πŸ“‚ Article πŸ“… 1989 πŸ› John Wiley and Sons 🌐 English βš– 151 KB πŸ‘ 2 views

to be controlled for in comparing immunoprophylactic approaches. At present, DNA polymerase activity or HBV DNA is useful for estimating the level of exposure. In an editorial in this issue, Dr. Dienstag pointed out difficulties in comparing the results of two immunoprophylactic regimens conducted a

Leucocyte hepatitis B virus DNA in acute
✍ F. Davison; G. J. M. Alexander; Ch. Anastassakos; E. A. Fagan; Roger Williams πŸ“‚ Article πŸ“… 1987 πŸ› John Wiley and Sons 🌐 English βš– 444 KB πŸ‘ 1 views

In the present study we have investigated 53 patients with a spectrum of acute and chronic hepatitis B virus (HBV) infection for the presence of leucocyte HBV-DNA with the aid of molecular techniques. HBV-DNA was detected in peripheral blood mononuclear cells of 31 of 45 (69%) of chronic HBsAg carri

Hepatitis A Infection in Chronic Carrier
✍ Reinhart Zachoval; Michael Roggendorf; Friedrich Deinhardt πŸ“‚ Article πŸ“… 2007 πŸ› John Wiley and Sons 🌐 English βš– 441 KB πŸ‘ 2 views

By routine screening for serologic markers of hepatitis A and B in patients with acute hepatitis, 30 chronic carriers of hepatitis B virus with serologic evidence of acute hepatitis A and two patients with simultaneous acute infection with hepatitis A virus and hepatitis B virus were detected. For