CMV in pregnancy: Difference between revisions
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β | == |
+ | ==Background== |
β | * |
+ | *Infection with [[cytomegalovirus]] during pregnancy |
β | * |
+ | *Infection can be primary infection, non-primary reinfection with another strain, or non-primary reactivation of latent virus |
β | * |
+ | *Mainly of concern because of the risk of causing [[congenital CMV]] |
β | === |
+ | ===Epidemiology=== |
β | * |
+ | *Maternal seroconversion in about 2% of pregnancies |
β | ** |
+ | **Higher in childcare workers |
⚫ | |||
β | * Risk of transmission to fetus |
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+ | *Risk of transmission to fetus is highest with maternal primary infection, and much lower for non-primary infection |
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⚫ | |||
β | ** |
+ | **'''Primary infection''': 30% risk of congenital CMV |
β | ** |
+ | **Non-primary: |
β | *** |
+ | ***'''Reinfection''': 5% risk |
β | *** |
+ | ***'''Reactivation''': 1% risk |
+ | *Risk of transmission to fetus following primary infection increases with gestational age, but risk of neurological sequelae decreases substantially[[CiteRef::enders2011in]] |
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+ | {| class="wikitable" |
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⚫ | |||
+ | ! rowspan="2" |Trimester |
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+ | ! rowspan="2" |Transmission to Fetus |
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+ | ! colspan="3" |Severity of Neurological Disease |
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+ | |- |
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+ | !Severe |
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+ | !Mild/Transient |
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+ | !None |
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+ | |- |
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+ | |First |
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+ | |30% |
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+ | |5% |
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+ | |30% |
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+ | |65% |
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+ | |- |
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+ | |Second |
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+ | |40% |
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+ | |0% |
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+ | |15% |
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+ | |85% |
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+ | |- |
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+ | |Third |
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+ | |70% |
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+ | |0% |
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+ | |0% |
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+ | |100% |
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+ | |} |
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+ | |||
⚫ | |||
β | * |
+ | *Serology with IgM and IgG |
β | ** |
+ | **IgM usually positive for 6 weeks after primary infection, but can remain positive for as long as 12 months |
β | ** |
+ | **IgM has false positives, including from rheumatoid factor, [[EBV]] infection, [[lupus]] |
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β | * |
+ | *Fetal infection is confirmed by amniocentesis sent for PCR |
β | ** |
+ | **To minimized the risk of a false-negative result, it should be be done after 17 weeks gestation and at least 7 weeks after maternal infection |
β | == |
+ | ==Management== |
β | * |
+ | *Counsel mother on risk of fetal infection and subsequent development of congenital CMV |
β | * |
+ | *If they would terminate if CMV-positive due to those risks, then proceed with amniocentesis to diagnose |
[[Category:Infectious diseases]] |
[[Category:Infectious diseases]] |
Revision as of 13:45, 15 August 2020
Background
- Infection with cytomegalovirus during pregnancy
- Infection can be primary infection, non-primary reinfection with another strain, or non-primary reactivation of latent virus
- Mainly of concern because of the risk of causing congenital CMV
Epidemiology
- Maternal seroconversion in about 2% of pregnancies
- Higher in childcare workers
- Affects about 1 in 200 live births in US
- Risk of transmission to fetus is highest with maternal primary infection, and much lower for non-primary infection
- Primary infection: 30% risk of congenital CMV
- Non-primary:
- Reinfection: 5% risk
- Reactivation: 1% risk
- Risk of transmission to fetus following primary infection increases with gestational age, but risk of neurological sequelae decreases substantially1
Trimester | Transmission to Fetus | Severity of Neurological Disease | ||
---|---|---|---|---|
Severe | Mild/Transient | None | ||
First | 30% | 5% | 30% | 65% |
Second | 40% | 0% | 15% | 85% |
Third | 70% | 0% | 0% | 100% |
Diagnosis
- Serology with IgM and IgG
IgG | IgM | Avidity | Interpretation |
---|---|---|---|
+ | β | N/A | past infection, low risk for congenital infection |
+ | + | high | past infection, low risk for congenital infection |
+ | + | low | primary maternal infection within the past 3 months |
β | β | N/A | either no infection, or repeat in 4 weeks |
- Fetal infection is confirmed by amniocentesis sent for PCR
- To minimized the risk of a false-negative result, it should be be done after 17 weeks gestation and at least 7 weeks after maternal infection
Management
- Counsel mother on risk of fetal infection and subsequent development of congenital CMV
- If they would terminate if CMV-positive due to those risks, then proceed with amniocentesis to diagnose
References
- ^ 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.