Cytomegalovirus: Difference between revisions

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== Definition ==
== Background ==


=== Microbiology ===
* Human herpesvirus (DNA virus) transferred by respiratory droplets and blood transfusions that lies dormant in white blood cells
* A DNA virus and member of the [[Human herpesviruses]]

== Epidemiology ==


=== Epidemiology ===
* Transferred by respiratory droplets and blood transfusions that lies dormant in white blood cells
* 80% of people are CMV-IgG positive
* 80% of people are CMV-IgG positive


== Risk Factors ==
=== Risk Factors ===

* Crowding
* Crowding


== Clinical Presentation ==
== Clinical Presentation ==

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


=== Stem cell transplantation ===
=== Stem cell transplantation ===

* Low risk until day 21 post-transplantation, when cell lines begin to return
* Low risk until day 21 post-transplantation, when cell lines begin to return
* May presents as asymptomatic viremia
* May presents as asymptomatic viremia
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=== Solid-organ transplantation ===
=== Solid-organ transplantation ===

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


== Investigations ==
== Investigations ==

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


== Management ==
== Diagnosis ==
* Serology for IgG only useful for prior exposure (suggesting latent infection)
* PCR most useful for diagnosis
** Can be done on blood and BAL
** However, can shed CMV asymptomatically during an acute illness, so must be taken within the clinical context


== Management ==
* First-line: valganciclovir or ganciclovir
* Antivirals
** Measure baseline CBC first
** First-line: [[Is treated by::valganciclovir]] or [[Is treated by::ganciclovir]]
* Second-line, if cytopenias: foscarnet
*** Measure baseline CBC first due to risk of cytopenias
* Third-line: cidofovir, maribavir, letermovir
** Second-line, if cytopenias: [[Is treated by::foscarnet]]
** Third-line: [[Is treated by::cidofovir]], [[Is treated by::maribavir]], [[Is treated by::letermovir]]
* At McMaster, expect 1-log drop within 2 weeks (lab-dependent)
* At McMaster, expect 1-log drop within 2 weeks (lab-dependent)
* Continue treatment until PCR is negative
* Continue treatment until PCR is negative


== Prophylaxis ==
=== 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


== Prophylaxis ==
* '''Solid-organ transplant'''
* '''Solid-organ transplant'''
** Donor+/Recipient– high risk for reactivation, the the donor organ infecting the recipient
** Donor+/Recipient– high risk for reactivation, the the donor organ infecting the recipient
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== Complications ==
== Complications ==

* Even when dormant, can cause mild immunosuppression that predisposes to fungal infections
* Even when dormant, can cause mild immunosuppression that predisposes to fungal infections
* Asymptomatic shedding in lungs during intercurrent illness
* Asymptomatic shedding in lungs during intercurrent illness
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** Organ inflammation of solid-organ transplants
** Organ inflammation of solid-organ transplants
** Pneumonitis in stem cell 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


[[Category:Herpesviridae]]
[[Category:Herpesviridae]]

Revision as of 20:10, 23 October 2019

Background

Microbiology

Epidemiology

  • Transferred by respiratory droplets and blood transfusions that lies dormant in white blood cells
  • 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

Diagnosis

  • Serology for IgG only useful for prior exposure (suggesting latent infection)
  • PCR most useful for diagnosis
    • Can be done on blood and BAL
    • However, can shed CMV asymptomatically during an acute illness, so must be taken within the clinical context

Management

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

Prophylaxis

  • Solid-organ transplant
    • Donor+/Recipient– high risk for reactivation, the the donor organ infecting the recipient
    • Donor–/Recipient+ intermediate risk
    • Donor+/Recipient+ intermediate risk
    • Donor–/Recipient– 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
    • Donor–/Recipient+ high risk
    • Donor+/Recipient– intermediate risk
    • Donor–/Recipient– 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

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.