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. 2013 Dec 10:13:582.
doi: 10.1186/1471-2334-13-582.

Lower incidence of CMV infection and acute rejections with valganciclovir prophylaxis in lung transplant recipients

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Lower incidence of CMV infection and acute rejections with valganciclovir prophylaxis in lung transplant recipients

Inger Johansson et al. BMC Infect Dis. .

Abstract

Background: Cytomegalovirus (CMV) is the most common opportunistic infection following lung transplantation. CMV replication in the lung allograft is described as accelerating the development of bronchiolitis obliterans syndrome (BOS). Finding a strategy to prevent CMV infection is an important issue.

Methods: We performed a retrospective, single-centre study of 114 lung transplant recipients (LTRs) who underwent lung transplantation from January 2001 to December 2006. In a smaller cohort of 88 CMV seropositive (R+) LTRs, three months of valganciclovir prophylaxis (2004-2006) was compared to three months of oral ganciclovir (2001-2003) with respect to the incidence of CMV infection/disease, the severity of CMV disease, acute rejection, BOS-free 4 year survival and 4 year survival. In the whole group of 114 LTRs the impact of CMV infection on long-term survival (BOS free 4 year survival and 6 year survival) was assessed.

Results: For the cohort of 88 CMV seropositive LTRs, the incidence of CMV infection/disease at one year was lower in the valganciclovir group compared to the ganciclovir group (24% vs. 54%, p = 0.003). There was a tendency towards reduced CMV disease, from 33% to 20% and a significant lower incidence of asymptomatic CMV infection (22% vs. 4%, p = 0.005). A lower incidence of acute rejection was observed in the valganciclovir group. However, there was no significant difference between the two groups in BOS free 4 year survival and 4 year survival.For the entire group of 114 LTRs, BOS-free 4 year survival for recipients with CMV disease was (32%, p = 0.005) and among those with asymptomatic CMV infection (36%, p = 0.061) as compared with patients without CMV infection (69%). Six year survival was lower among patients with CMV disease, (64%, p = 0.042) and asymptomatic CMV infection (55%, p = 0.018) than patients without CMV infection (84%).

Conclusions: A lower incidence of CMV infection/disease and acute rejections was observed with valganciclovir (3 months) when compared to oral ganciclovir (3 months). The long-term impact of CMV infection/disease was significant for BOS-free survival and survival.

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Figures

Figure 1
Figure 1
BOS-free survival in 107 lung transplant recipients related to CMV disease. No CMV infection (n = 65), Asymptomatic CMV infection (n = 11), CMV disease (n = 31). BOS-free 4 year survival for patients with CMV disease was 32%, (p = 0.005), for asymptomatic CMV infection 36%, (p = 0.061) as compared with patients without CMV infection (69%).
Figure 2
Figure 2
Survival in 114 lung transplant recipients related to CMV disease. No CMV infection (n = 70), Asymptomatic CMV infection (n = 11), CMV disease (n = 33). Six year survival was lower among patients with CMV disease, (64%, p = 0.042) and asymptomatic CMV infection (55%, p = 0.018) than patients without CMV infection (84%).

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References

    1. Alexander BD, Tapson VF. Infectious complications of lung transplantation. Transpl Infect Dis. 2001;13:128–137. doi: 10.1034/j.1399-3062.2001.003003128.x. - DOI - PubMed
    1. Fishman AJ, Emery V, Freeman R, Pascual M, Rostaing L, Schlitt HJ, Sgarabotto D, Torre-cisneros J, Uknis ME. Cytomegalovirus in transplantation - challenging the status quo. Clin Transplant. 2007;13:149–158. doi: 10.1111/j.1399-0012.2006.00618.x. - DOI - PubMed
    1. Snydman DR, Limaye AP, Potena L, Zamora MR, Weigand K. Update and review: state-of-the-art management of cytomegalovirus infection and disease following thoracic organ transplantation. Transplant Proc. 2011;13:S1–S17. doi: 10.1016/j.transproceed.2011.02.069. - DOI - PubMed
    1. Johanssson I, Mårtensson G, Andersson R. Cytomegalovirus and long-term outcome after lung transplantation in Gothenburg, Sweden. Scand J Infect Dis. 2010;13:129–136. doi: 10.3109/00365540903341828. - DOI - PubMed
    1. Zuk DM, Humar A, Weinkauf JG, Lien DC, Nador RG, Kumar D. An international survey of cytomegalovirus management practices in lung transplantation. Transplantation. 2010;13:672–676. - PubMed

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