Cytomegalovirus: Difference between revisions
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== Background == |
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=== Microbiology === |
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* A DNA virus and member of the [[Human herpesviruses]] |
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* 80% of people are CMV-IgG positive |
* 80% of people are CMV-IgG positive |
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== Risk Factors == |
=== Risk Factors === |
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* Crowding |
* Crowding |
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== Clinical Presentation == |
== Clinical Presentation == |
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* Asymptomatic when young |
* Asymptomatic when young |
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* Mono-like or influenza-like illness when older |
* Mono-like or influenza-like illness when older |
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=== Stem cell transplantation === |
=== Stem cell transplantation === |
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* 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 |
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* May presents as asymptomatic viremia |
* May presents as asymptomatic viremia |
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=== Solid-organ transplantation === |
=== Solid-organ transplantation === |
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* Tends to reactivate within the transplanted organ |
* Tends to reactivate within the transplanted organ |
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* However, all can have GI involvement |
* However, all can have GI involvement |
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== Investigations == |
== Investigations == |
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* CBC showing leukopenia or pancytopenia |
* CBC showing leukopenia or pancytopenia |
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* 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 |
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== |
== Diagnosis == |
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* Serology for IgG only useful for prior exposure (suggesting latent infection) |
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* PCR most useful for diagnosis |
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** Can be done on blood and BAL |
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** However, can shed CMV asymptomatically during an acute illness, so must be taken within the clinical context |
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== Management == |
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* Antivirals |
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* At McMaster, expect 1-log drop within 2 weeks (lab-dependent) |
* At McMaster, expect 1-log drop within 2 weeks (lab-dependent) |
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* Continue treatment until PCR is negative |
* Continue treatment until PCR is negative |
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=== Resistance === |
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== Prophylaxis == |
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* '''Solid-organ transplant''' |
* '''Solid-organ transplant''' |
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** 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 == |
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* Even when dormant, can cause mild immunosuppression that predisposes to fungal infections |
* Even when dormant, can cause mild immunosuppression that predisposes to fungal infections |
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* 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 |
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** Pneumonitis in stem cell transplants |
** Pneumonitis in stem cell transplants |
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== Resistance == |
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[[Category:Herpesviridae]] |
[[Category:Herpesviridae]] |
Revision as of 20:10, 23 October 2019
Background
Microbiology
- A DNA virus and member of the Human herpesviruses
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
- Antivirals
- First-line: valganciclovir or ganciclovir
- Measure baseline CBC first due to risk of cytopenias
- Second-line, if cytopenias: foscarnet
- Third-line: cidofovir, maribavir, letermovir
- First-line: valganciclovir or ganciclovir
- At McMaster, expect 1-log drop within 2 weeks (lab-dependent)
- Continue treatment until PCR is negative
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
- ^ 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.
- ^ 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.