Literature DB >> 16386621

Preemptive therapy with intravenous ganciclovir for the prevention of cytomegalovirus disease in lung transplant recipients.

V Monforte1, A Román, J Gavaldà, C Bravo, P Gispert, A Pahissa, F Morell.   

Abstract

The most effective strategy for the prevention of cytomegalovirus (CMV) disease in lung transplantation has not been conclusively established. The aim of this study was to determine the efficacy of preemptive ganciclovir therapy for this purpose. Twenty-five consecutive adult patients positive for CMV before transplantation and surviving more than 30 days after the procedure were studied. Mean follow-up was 732.2 days (range, 210-1125). All patients received intravenous (IV) ganciclovir prophylaxis for the first 21 days and subsequently underwent frequent CMV antigenemia monitoring: weekly for the first 3 months, every 15 days between 3 and 6 months, and monthly thereafter. IV ganciclovir was given when antigenemia results were greater than 10 infected cells per 100,000 polymorphonuclears. The study group was compared with a historical group of 30 consecutive patients who had received IV ganciclovir prophylaxis and continued on oral ganciclovir up to day 120 posttransplantation. Eighteen of the 25 patients (72.0%) presented episodes of CMV infection. Six of the 25 patients (24.0%) had CMV disease, including 3 viral syndromes and 3 cases of pneumonitis. Four patients debuted with CMV disease, 1 of them with pneumonitis. CMV resistance to ganciclovir was observed in 2 patients. The incidence of infection was higher than in the historical group (72.0% vs 46.7%; P < .05), but there were no significant differences in the incidence of CMV disease (24.0% vs 40.0%; P = not significant [NS]). Mean time before onset of the first episode of disease was lower in the preemptive therapy group than in the comparison patients (82.8 days; range, 42-240 vs 175 days; range, 90-243; P < .05). In conclusion, preemptive therapy for CMV disease is as effective a prevention strategy as oral ganciclovir prophylaxis. However, the early appearance of CMV disease with preemptive therapy can make this approach inadvisable.

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Year:  2005        PMID: 16386621     DOI: 10.1016/j.transproceed.2005.09.141

Source DB:  PubMed          Journal:  Transplant Proc        ISSN: 0041-1345            Impact factor:   1.066


  4 in total

Review 1.  Viral infections in lung transplant recipients.

Authors:  Pali Dedhiya Shah; John F McDyer
Journal:  Semin Respir Crit Care Med       Date:  2010-03-30       Impact factor: 3.119

2.  Risk factors for cytomegalovirus infection in patients with antineutrophil cytoplasmic antibody-associated vasculitis.

Authors:  Michiko Morishita; Ken-Ei Sada; Yoshinori Matsumoto; Keigo Hayashi; Yosuke Asano; Sumie Hiramatsu Asano; Keiji Ohashi; Yoshia Miyawaki; Eri Katsuyama; Haruki Watanabe; Tomoko Kawabata; Jun Wada
Journal:  PLoS One       Date:  2019-07-10       Impact factor: 3.240

Review 3.  Common infections in the lung transplant recipient.

Authors:  Karen D Sims; Emily A Blumberg
Journal:  Clin Chest Med       Date:  2011-06       Impact factor: 2.878

4.  Clinical correlates of pp65 antigenemia monitoring in the first months of post kidney transplant in patients undergoing universal prophylaxis or preemptive therapy.

Authors:  Fabiana Rabe Carvalho; Rachel Ingrid Juliboni Cosendey; Cintia Fernandes Souza; Thalia Medeiros; Paulo Alexandre Menezes; Andrea Alice Silva; Jorge Reis Almeida; Jocemir Ronaldo Lugon
Journal:  Braz J Infect Dis       Date:  2016-11-23       Impact factor: 3.257

  4 in total

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