Cytomegalovirus reactivation following hematopoietic stem cell transplantation

J Infect Dev Ctries. 2013 Dec 15;7(12):1003-7. doi: 10.3855/jidc.2947.

Abstract

Introduction: There is a high prevalence of cytomegalovirus (CMV) seropositivity in developing countries. An apparent risk of CMV reactivation increases following hematopoeitic stem cell transplantation. With effective surveillance and timely treatment using anti-viral therapy, morbidity and mortality associated with CMV reactivation can be reduced.

Objectives: To evaluate the incidence and morbidity associated with CMV reactivation following hematopoeitic stem cell transplantation.

Methodology: We retrospectively analysed 136 hematopoeitic stem cell transplant recipients at our centre for CMV reactivation and their complications. Quantification of CMV-DNA was done by PCR. CMV disease was confirmed histologically via CMV inclusion bodies or immunostaining of biopsy of the affected organ, mainly the gastrointestinal tract.

Results: A total of 13 out of 136 patients (9.56%) had CMV reactivation. 6 out of 13 patients had CMV disease, 3 of which died (23.1% of patients with CMV reactivation). CMV reactivation occurred at a median duration of 52.5 days post transplantation (range 35-178 days). The gastrointestinal tract was the organ most commonly affected by CMV. The median follow-up was 14 months (range 6 - 64 months).

Conclusion: Through a higher rate of sero-prevalance in developing countries, the incidence of CMV infection following hematopoeitic stem cell transplantation is comparable to that reported in Western literature. Oral valganciclovir was an effective pre-emptive therapy for CMV disease.

MeSH terms

  • Adolescent
  • Adult
  • Child
  • Cytomegalovirus / physiology*
  • Cytomegalovirus Infections / drug therapy
  • Cytomegalovirus Infections / epidemiology*
  • Cytomegalovirus Infections / pathology
  • Cytomegalovirus Infections / virology
  • DNA, Viral / blood
  • Female
  • Ganciclovir / analogs & derivatives
  • Ganciclovir / therapeutic use
  • Hematopoietic Stem Cell Transplantation / adverse effects*
  • Histocytochemistry
  • Humans
  • Immunohistochemistry
  • Male
  • Microscopy
  • Middle Aged
  • Polymerase Chain Reaction
  • Retrospective Studies
  • Treatment Outcome
  • Valganciclovir
  • Viral Load
  • Virus Activation*
  • Young Adult

Substances

  • DNA, Viral
  • Valganciclovir
  • Ganciclovir