Cytomegalovirus: Difference between revisions

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** Donor+/Recipient+ intermediate risk
** Donor+/Recipient+ intermediate risk
** Donorā€“/Recipientā€“ lowest risk
** Donorā€“/Recipientā€“ lowest risk
** High and intermediate risk patients get '''prophylaxis''' with valganciclovir for some amount of duration...
** High and intermediate risk patients get '''prophylaxis''' with valganciclovir 900 mg po bid for some amount of duration...
* '''Hematologic stem cell transplant'''
* '''Hematologic stem cell transplant'''
** Donor+/Recipient+ high risk for reactivation
** Donor+/Recipient+ high risk for reactivation

Revision as of 21:11, 10 September 2019

Definition

  • Human herpesvirus (DNA virus) transferred by respiratory droplets and blood transfusions that lies dormant in white blood cells

Epidemiology

  • 80% of people are CMV-IgG positive

Risk Factors

  • Crowding

Clinical Presentation

  • Asymptomatic when young
  • Mono-like or influenza-like illness when older

Stem cell transplantation

  • Low risk until day 21 post-transplantation, when cell lines begin to return
  • May presents as asymptomatic viremia
  • Most common symptomatic presentation is pneumonitis
    • Can also present with GI involvement

Solid-organ transplantation

  • Tends to reactivate within the transplanted organ
  • However, all can have GI involvement

Investigations

  • CBC showing leukopenia or pancytopenia
  • Mild elevation in liver enzymes
  • CMV-IgG positive
  • Detectable CMV DNA in peripheral blood, though it can rise during intercurrent illness

Management

  • First-line: valganciclovir or ganciclovir
    • Measure baseline CBC first
  • Second-line, if cytopenias: foscarnet
  • Third-line: cidofovir, maribavir, letermovir
  • At McMaster, expect 1-log drop within 2 weeks (lab-dependent)
  • Continue treatment until PCR is negative

Prophylaxis

  • Solid-organ transplant
    • Donor+/Recipientā€“ high risk for reactivation, the the donor organ infecting the recipient
    • Donorā€“/Recipient+ intermediate risk
    • Donor+/Recipient+ intermediate risk
    • Donorā€“/Recipientā€“ lowest risk
    • High and intermediate risk patients get prophylaxis with valganciclovir 900 mg po bid for some amount of duration...
  • Hematologic stem cell transplant
    • Donor+/Recipient+ high risk for reactivation
    • Donorā€“/Recipient+ high risk
    • Donor+/Recipientā€“ intermediate risk
    • Donorā€“/Recipientā€“ lowest risk
    • Preemptive monitoring with weekly CMV DNA PCR starting week 2
  • Treat if greater than threshold (1425 at McMaster) or if rising titre with symptoms

Complications

  • Even when dormant, can cause mild immunosuppression that predisposes to fungal infections
  • Asymptomatic shedding in lungs during intercurrent illness
  • Viremia with influenza-like illness
  • End-orgam damage
    • CMV colitis
    • Retinitis in AIDS patient (CD4 < 50-100)
    • Organ inflammation of solid-organ transplants
    • Pneumonitis in stem cell transplants

Resistance

  • Inherent acyclovir resistance
  • Tyrosine kinase mutation UL97? confers resistance to (val)ganciclovir
  • Polymerase mutation U54? confers resistance to (val)ganciclovir and foscarnet
  • Consider resistance if CMV DNA titres not decreasing despite appropriate treatment
  • Resistance genotyping available

References

  1. ^  Michael J. Cannon, D. Scott Schmid, Terri B. Hyde. Review of cytomegalovirus seroprevalence and demographic characteristics associated with infection. Reviews in Medical Virology. 2010;20(4):202-213. doi:10.1002/rmv.655.
  2. ^  Jutta K. Preiksaitis, R. P. Bryce Larke, Glory J. Froese. Comparative seroepidemiology of cytomegalovirus infection in the Canadian Arctic and an Urban center. Journal of Medical Virology. 1988;24(3):299-307. doi:10.1002/jmv.1890240307.