Rubella Flashcards
Routine rubella screening test and cut-offs
IgG only
-ve –> immunise post-partum
+ve 10-15IU/mL –> consider re-immunising post-partum
+ve >15 IU/mL immune
When to test for rubella (IgG and IgM)
- contact with rubella
- rubella-like illnes (fever, erythematous rash, arthralgia), obtain serum 7-10 days after onset of rash
When to repeat rubella serological testing
- IgG +ve and IgM +ve (repeat in 2-3 weeks to confirm)
- IgG -ve and IgM -ve but <3wks since contact, <7 days since onset of illness
- IgG -ve and IgM +ve (could be false positive or not yet seroconverted)
Risks with primary rubella at 1-12 weeks
- 80% fetal infection
- 85% congenital defects
Risks with primary rubella at 13-16 weeks
- 54% fetal infection
- 35% congenital defects
Risks with primary rubella at 17-22 weeks
- 36% fetal infection
- congenital defects rare
Risks with primary rubella at 23-30 weeks
- 30% fetal infection
- congenital defects rare
Risks with fetal rubella at 31-36 weeks
- 60% fetal infection
- congenital defects rare
Risks with fetal rubella at >36 weeks
- 100% fetal infection
- congenital defects rare
Rate of fetal infection with re-infection (Rubella)
<10%
CRS rare especially after 12 weeks
Prenatal fetal diagnosis / testing for rubella
Rubella virus PCR or culture on CVS or amnio at least 6 weeks after known maternal infection. OR cordocentesis for rubella IgM.
BUT
- CVS can produce false positive PCR if contaminated
- PCR not widely avaiable and sensitivity not well validated
- False neg fetal IgM common until late in pregnancy
Rubella period of infectivity
One week before until 7 days after rash
Early manifestations of congenital rubella syndrome
1- Deafness (SNHL 60-75%)
2 - CNS dysfunction (10-25%, e.g. intellectual disability, DD, microcephaly)
3 - Cardiovascular defects (10-20%, PD, pulm a stenosis)
4 - Ophthalmological abnormalities (10-25%, cataracts, microophthalmos, retinopathy etc)
5 - Other (FGR, haem abn., GIT, pneumonitis, osteitis)
Late manifestations of congenital rubella syndrome
- Deafness (SNHL)
- Neuro deficiencies, epilepsy
- Retinopathy, cataracts
- Tooth defects
- Growth retardation
- T1DM (50x risk), thyroid dysfunction
- Panencephalitis