Congenital CMV: Difference between revisions

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* Mother may have had asymptomatic infection
 
* Mother may have had asymptomatic infection
 
* At birth
 
* At birth
βˆ’
** Microcephaly
+
** [[Causes::Microcephaly]]
βˆ’
** Periventricular calcifications
+
** [[Causes::Periventricular calcifications]]
βˆ’
** Chorioretinitis
+
** [[Causes::Chorioretinitis]]
βˆ’
** Sensorineural hearing loss
+
** [[Causes::Sensorineural hearing loss]]
βˆ’
** Optic nerve atrophy
+
** [[Causes::Optic nerve atrophy]]
βˆ’
** Hepatosplenomegaly
+
** [[Causes::Hepatosplenomegaly]]
  +
** [[Causes::Cytopenias]]
βˆ’
** Cytopenia
 
 
* Later
 
* Later
βˆ’
** Cognitive deficits (7%)
+
** [[Causes::Cognitive deficits]] (7%)
βˆ’
** Sensorineural hearing loss (20%)
+
** [[Causes::Sensorineural hearing loss]] (20%)
   
 
== Diagnosis ==
 
== Diagnosis ==

Revision as of 11:07, 8 February 2020

Epidemiology

  • Risk of transmission to fetus
    • Primary infection: 30% risk of congenital CMV; higher risk later in pregnancy, but worse outcomes earlier
    • Non-primary
      • Reinfection: 5% risk
      • Reactivation: 1% risk

Clinical Presentation

Diagnosis

  • In mom, IgM antibodies
  • In baby, urine PCR within 2 weeks of birth

Management

  • Treatment is indicated for symptomatic babies
    • Brain
    • Hearing
    • Eye
  • IV ganciclovir or PO valganciclovir, for 6 months
  • Monitor CBC while on therapy

References

  1. ^  Gisela Enders, Anja Daiminger, Ursula BΓ€der, Simone Exler, Martin Enders. Intrauterine transmission and clinical outcome of 248 pregnancies with primary cytomegalovirus infection in relation to gestational age. Journal of Clinical Virology. 2011;52(3):244-246. doi:10.1016/j.jcv.2011.07.005.