Virus
Cytomegalovirus
search
Cytomegalovirus
, CMV-Induced Mononucleosis, CMV
See Also
CMV Chorioretinitis
Epidemiology
Gene
ral Population
Prior exposure in 40-100% of general population
Many cases occur in childhood and adolescence
May account for 2% of febrile adult cases
Wreghitt (2003) Clin Infect Dis 37:1603-6 [PubMed]
HIV patients
Infects 75-100% of HIV positive patients
Active CMV disease occurs in 20% with
CD4 Count
<100
CMV disease rarely occurs at
CD4 Count
> 50 cells
Pathophysiology
Human Herpes Virus
(
Herpesviridae
)
Pathogenesis
CMV remains latent after initial infection
CMV reactivates in
Immunocompromised
patients
Infectivity
Spread by close contact with body fluids
Passed by
Saliva
, urine, blood, semen,
Breast Milk
Also passed by organ tissue transplants
Risk Factors
Pregnant day care workers (see
TORCH Virus
)
Organ transplant recipients
Immunocompromised
patients (e.g.
HIV Infection
)
Findings
Asymptomatic in most immunocompetent patients
CMV-Induced Mononucleosis
Identical to
EBV-Induced Mononucleosis
Accounts for up to 7% of
Mononucleosis
cases
Classic
Ampicillin
rash also occurs with CMV
Intrauterine adverse effects to fetus
CMV is a
TORCH Virus
Risk of
Intrauterine Growth Retardation
CMV
Esophagitis
or colitis (HIV/
AIDS
, organ transplant)
Odynophagia
Abdominal Pain
Diarrhea
CMV Retinitis
(HIV/
AIDS
)
Dilated
Eye Exam
recommended in HIV/
AIDS
with suspected CMV infection
Labs
Complete Blood Count
CMV-Induced Mononucleosis changes
Lymphocyte
s increased >50%
Atypical lymphocyte
s 10% of total
Lymphocyte
s
Uncommon findings
Anemia
Thrombocytopenia
Liver Function Test
abnormalities (in acute infection)
Most common clinical factor to distinguish CMV
Abnormal in 72% of cases
Wreghitt (2003) Clin Infect Dis 37:1603-6 [PubMed]
Aspartate
transaminase increased less than 5x normal
Alanine
Transaminase increased less than 5x normal
Serology
CMV IgM titer
Best diagnostic test for CMV-Induced Mononucleosis
Indicated if
Heterophil Antibody Test
negative
CMV PCR
Indications
Immunocompromised
patients
Suspected CMV
Encephalitis
or polyradiculopathy
Not useful in acute infection
Positive test may be transient reactivation
Histology of tissue biopsy (CMV organ involvement)
Owls-eye inclusion body (highly specific for CMV)
CMV-Induced
False Positive
tests
Rheumatoid Factor
Direct Coombs
Cryoglobulinemia
Speckled pattern of
Antinuclear Antibody
test
Differential Diagnosis
Mononucleosis
(nearly identical presentation)
See
Mononucleosis Differential Diagnosis
Diagnosis
See
Mononucleosis Diagnostic Approach
Complications in Immunocompromised patients
CMV Chorioretinitis
(occurs in 15-20% of HIV patients)
Gastrointestinal Tract
infection (in 5-10% of HIV; also in transplant patients)
Esophagitis
Hepatitis
Pancreatitis
Enteritis or Colitis
Less common or rare effects
Guillain-Barre Syndrome
Neurologic involvement
Encephalitis
Peripheral Neuropathy
Interstitial
Pneumonia
Myocarditis
Epididymitis
Skin changes
Nonspecific rash
Perifollicular papulopustules
Vesiculobullous lesion
s
Management
Gene
ral
No school or work restrictions in acute infection
Children may continue to attend school or daycare
Healthcare workers may continue to work
Management
Immunocompromised
patients (especially HIV, transplant patients)
Highly Active Antiretroviral Therapy
(HAART) in HIV
Critical to prevent CMV organ involvement
Risk in HIV highest when
CD4 Count
<50/mm3
Indications for Viral
DNA Polymerase
inhibitors
CMV Retinitis
(Urgent therapy)
Clinically Significant
colitis or other end-organ
Treatment of asymptomatic CMV not indicated
Preparations
Ganciclovir
Granulocytopenia
and
Anemia
risk (25%)
Foscarnet
(
Foscavir
)
Nephrotoxicity (33%)
Neurotoxicity
Electrolyte
disturbance (
Hypokalemia
,
Hypocalcemia
)
Cidofovir
(
Vistide
)
Nephrotoxicity
Neutropenia
Alopecia
Efficacy
CMV Retinitis
responds to 14-21 day in 75-90% cases
Patients failing one drug should move to the other
Dosing
Acute (until CMV PCR undetectable, clinically resolved and at least 3 week course)
Ganciclovir
5 mg/kg IV every 12 hours (preferred) for 3-6 weeks OR
Foscarnet
90 mg/kg IV every 12 hours for 3-6 weeks OR
Cidofovir
5 mg/kg IV weeky for 3-6 weeks
Secondary Prophylaxis (Follows acute management if high risk of relapse)
Valganaciclovir 900 mg orally every 12-24 hours for 1-3 months
References
(2015) Sanford Guide, accessed in IOS app 4/24/2016
Resources
CDC National Center for Infectious Diseases
http://www.cdc.gov/ncidod/diseases/cmv.htm
References
de Jong (1998) Antiviral Res 39:141-62 [PubMed]
Taylor (2003) Am Fam Physician 67(3):519-26 [PubMed]
Type your search phrase here