Am. J. Respir. Crit. Care Med., Vol 150, No. 1, Jul 1994, 146-152.
A comparison of ganciclovir and acyclovir to prevent cytomegalovirus after lung transplantation
SR Duncan, WF Grgurich, AT Iacono, GJ Burckart, SA Yousem, IL Paradis, PA Williams, BA Johnson and BP Griffith
Department of Medicine, University of Pittsburgh, Pennsylvania.
In an attempt to modify the sequelae of cytomegalovirus (CMV) infections
after lung transplantation, 25 allograft recipients were randomized to
either ganciclovir 5 mg/kg once a day 5 d/wk (Group G) or acyclovir 800 mg
four times a day (Group A). All subjects received ganciclovir during
postoperative Weeks 1 through 3, and they were then given either A or G
regimens until Day 90. At termination of study enrollment, the cumulative
incidence of all CMV infections (including seroconversions) was increased
in Group A compared with that in Group G (75% versus 15%, p < 0.01), as
was the incidence of overt CMV shedding and/or pneumonitis (50% versus 15%,
p < 0.043). In comparison with those in Group G, subjects in Group A
were also afflicted with an increased prevalence of obliterative
bronchiolitis (OB) during the first year after transplantation (54% versus
17%, p < 0.033). Intravenous catheters for ganciclovir administration
resulted in four complications among three of the subjects in Group G
(23%). The short- term benefits of ganciclovir were ultimately limited,
moreover, in that cumulative rates of CMV and prevalence of OB are now
similar in both treatment groups after approximately 2 yr of observation.
We conclude that prolonged ganciclovir prophylaxis decreases the early
incidence of CMV and OB among lung transplant recipients, but these effects
are of finite duration. Although CMV prevention appears to have
considerable potential value in this population, definitive viral
prophylaxis will require development of protracted or repeated treatment
regimens, or longer-acting agents.
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Copyright © 1994 American Thoracic Society
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