High dose-short duration ribavirin aerosol treatment--a review.

Bull Int Union Tuberc Lung Dis

Center for Biotechnology, Baylor College of Medicine, Houston, Texas 77381.

Published: February 1992

A high-dose, short-duration treatment with ribavirin aerosol consisting of a three-fold increase in concentration of drug (60 mg versus 20 mg of ribavirin per mL in the liquid reservoir of the generator administered for about one-third the time of the standard treatment) was as effective as the standard dosage in the treatment of experimental influenza A and B infections in mice and in the treatment of experimental respiratory syncytial virus infection in cotton rats. Despite some minor pulmonary intolerance, it was considered to be suitable for use in treatment of patients with severe chronic pulmonary disease, and it was well-tolerated and apparently effective in the treatment (by face mask and endotracheal tube) of infants with bronchiolitis principally caused by respiratory syncytial virus infection. Pharmacokinetic studies in mice revealed very high concentrations of drug in the lungs, about triple the level with the standard dose, with similar blood and brain concentrations. Ribavirin concentrations were similarly high in respiratory secretions of infants given the triple dose.

Download full-text PDF

Source

Publication Analysis

Top Keywords

ribavirin aerosol
8
treatment experimental
8
respiratory syncytial
8
syncytial virus
8
virus infection
8
treatment
6
high dose-short
4
dose-short duration
4
ribavirin
4
duration ribavirin
4

Similar Publications

Intranasal antivirals against respiratory syncytial virus: the current therapeutic development landscape.

Expert Rev Anti Infect Ther

August 2024

Menzies Health Institute Queensland, Griffith University, Southport, Queensland, Australia.

Article Synopsis
  • Respiratory syncytial virus (RSV) primarily impacts vulnerable populations, leading to bronchiolitis and respiratory problems, yet effective antivirals have been challenging to develop despite recent RSV vaccine approvals.
  • The newly approved nirsevimab shows promise for use as a prophylactic treatment, while current therapeutics are often delivered via IV or IM rather than more convenient IN methods.
  • Research is increasingly focusing on intranasal (IN) antiviral therapies to target RSV directly in the respiratory tract, aiming to lessen illness severity and halt the spread of the virus more effectively.
View Article and Find Full Text PDF

The emergence of new SARS-CoV-2 variants can affect vaccine efficacy, laboratory diagnosis and the therapies already available, triggering interest in the search for antiviral agents for SARS-CoV-2 infections. Ribavirin (RBV) is a broad-spectrum antiviral with demonstrated in vitro activity against multiple viruses, including SARS-CoV-2. This retrospective study evaluated the dynamics and viral clearance of SARS-CoV-2 in hospitalised adult participants (PTs) with COVID-19 pneumonia who received an RBV aerosol within a compassionate use study.

View Article and Find Full Text PDF

Acute pneumonia (AP), triggered primarily by pathogens like bacteria and viruses, is a leading cause of human mortality. Ribavirin, a broad-spectrum antiviral agent, plays a pivotal role in the treatment of AP. However, its therapeutic use is hindered by the need for high dosages and the associated cardiac and hepatic toxicities.

View Article and Find Full Text PDF

This study systematically combed the existing evidence of Houyanqing Oral Liquid in the treatment of acute pharyngitis from the "6+1" dimensions of safety, effectiveness, economy, innovation, suitability, accessibility, and characteristics of traditional Chinese medicine(TCM) and carried out qualitative and quantitative analysis of the data from each dimension. The multi-criteria decision analysis(MCDA) model and CSC v2.0 were used to evaluate the clinical value of this drug, so as to provide evidence for the selection of essential drugs in the department of otolaryngology and for medical and health decision-making.

View Article and Find Full Text PDF

Background: Human adenovirus (HAdV) infections in children can lead to profound pulmonary injury and are frequently associated with severe complications, particularly in cases concomitant with plastic bronchitis. Managing this condition presents significant challenges and carries an exceptionally high fatality rate. Regrettably, there are currently no specific antiviral agents that have demonstrated efficacy in treating severe adenovirus pneumonia in children.

View Article and Find Full Text PDF

Want AI Summaries of new PubMed Abstracts delivered to your In-box?

Enter search terms and have AI summaries delivered each week - change queries or unsubscribe any time!