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Canadian Paediatric Society

Position statement

Prevention of congenital rubella syndrome

Posted: Nov 1 2007 | Updated: Mar 24 2016


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Principal author(s)

JL Robinson; Canadian Paediatric Society (CPS), Infectious Diseases and Immunization Committee

Paediatr Child Health 2007; 12(9): 795-77

Rare cases of congenital rubella syndrome (CRS) continue to occur more than 40 years after the introduction of a rubella immunization program in Canada. This position statement updates the information previously published in 1999 [1].

How effective has the rubella vaccination program been?

Before rubella immunization, the majority of Canadians contracted rubella during childhood. The rubella vaccination program has been very effective, with there being fewer than 30 cases of rubella per year reported in Canada between 1998 and 2004 [2] compared with a mean of over 15,000 cases per year between 1941 and 1958. There were over 300 cases of rubella reported in southwestern Ontario in 2005, primarily in communities opposed to immunization – a situation that is likely to recur [2]. There has been enhanced surveillance of rubella through the Canadian Measles Rubella Surveillance System since 2006. There were only one to 13 cases of rubella annually in Canada in 2006-2014 (49 cases in total) (www.healthycanadians.gc.ca/diseases-conditions-maladies-affections/disease-maladie/rubella-rubeole/surveillance-eng.php) and no cases in 2015 (www.phac-aspc.gc.ca/mrwr-rhrr/2015/w52/index-eng.php). Over that ten year period, there were single cases of CRS reported in 2009 and 2011. The incidence of abortions and stillbirths related to rubella in Canada is not known.

Why does CRS continue to occur in Canada?

Rubella virus continues to be introduced into the community by travellers. Because of vaccine failure or failure to be immunized, some pregnant women are susceptible. Women may not be immunized because they are missed, refuse immunization or come from countries where the routine immunization program includes the monovalent measles vaccine rather than the measles-mumps-rubella (MMR) vaccine. A study [3] showed that 8.8% of women in Albertawere seronegative for rubella at the time of routine prenatal screening.

How common is vaccine failure and does vaccine failure contribute to CRS?

Although almost 100% of people immunized with rubella vaccine seroconvert, failure of one dose of rubella vaccine to protect against disease occurs in up to 10% of cases [4]. Vaccine failure is predicted to be less common in the future now that the majority of Canadian children receive two doses of the MMR vaccine. Infection in a previously immune mother (secondary vaccine failure) is rare. A small number of cases of CRS have been described in infants born to women with primary or secondary vaccine failure or rubella reinfection [5].

Can more be done?

Yes, more can be done. There are missed opportunities to prevent CRS. The elimination of CRS not only depends on effective childhood immunization, but also on identification and immunization of susceptible women of childbearing age. Women with no documentation of either previous rubella immunization or rubella seropositivity should be screened during pregnancy and should receive one dose of rubella vaccine postpartum if susceptible. The utility of screening women who have received vaccine but have not had seropositivity documented and the utility of repeat doses of vaccine for women who remain seronegative have not been established, and thus remain controversial [4]. These practices are not recommended in the current Canadian Immunization Guide [6], but are part of some provincial programs. The immunization status of women of child-bearing age who are new to Canada needs to be consistently reviewed [5]. Many will have received monovalent measles vaccine and, thus, remain susceptible to rubella. Unless women are already pregnant, or it is clear they have received a rubella-containing vaccine in the past or have documented immunity, they should be offered the MMR vaccine during their initial encounter with the health care system. Delaying immunization to determine their serostatus may result in a missed opportunity to immunize before pregnancy.

Ongoing surveillance for all cases of rubella and of CRS is a vital component of a prevention program. Patients with illnesses that are compatible with rubella or measles should have a serum rubella and measles immunoglobulin (Ig) M serology requested. In low-prevalence situations as seen for measles and rubella in Canada , in the absence of clear epidemiological links or travel history to endemic areas, IgM serology has a low positive predictive value for both measles and rubella. Thus, additional laboratory testing such as paired acute and convalescent IgG serology (to look for a fourfold or greater rise in titre) and/or virus detection is necessary to confirm measles and rubella infections. This is not only important for surveillance purposes, but is critical for the laboratory investigation of suspected rubella in pregnant women where important patient management decisions must be made. In this situation of suspected rubella in a pregnant woman, rubella IgG avidity testing has been shown to be a very useful laboratory test for differentiating primary infection (with a high risk of CRS) from past infection (low risk of CRS) [7]. Infants with unexplained microcephaly, cataracts, glaucoma, pigmentary retinopathy, hearing impairment, patent ductus arteriosus, hepatosplenomegaly, thrombocytopenia or radiolucent bone densities should be evaluated for CRS with the appropriate investigations depending on the age of the child [4].

Are there any complications of rubella immunization of seronegative individuals, including women in the postpartum period?

The frequency of true vaccine-related transient acute arthritis or arthralgia in nonimmune women is in the order of 5% to 10%, although a higher percentage will complain of arthralgias when warned of this potential adverse event. In contrast, acute and persistent forms of arthritis after natural rubella infection are more common, with up to 30% of naturally infected women experiencing recurrent joint manifestations for up to two years [8]. There is no evidence of any increased risk of new-onset chronic arthropathies or neurological conditions in women receiving the rubella vaccine [9]. No adverse events have been described from inadvertent immunization of women who are already immune to rubella or who are already pregnant, although it is still recommended that pregnancy be delayed for 28 days following immunization. Because rubella vaccine is a live vaccine, it is contraindicated in persons with immunodeficiency.

Recommendations

To prevent CRS, the following recommendations should be followed:

  • Immunizing all nonpregnant immigrant and refugee women at their first encounter with the Canadian health care system without checking serology, unless they have documentation of effective vaccination or natural immunity;
  • Continued universal infant immunization to protect recipients and to decrease circulation of the virus;
  • Use of the MMR vaccine rather than the monovalent measles vaccine as the immunizing agent in all immunization programs for measles worldwide to expedite the elimination of rubella [4];
  • Screening of all pregnant women to determine the need to confirm seropositivity and to enable postpartum immunization of all women found to be susceptible on prenatal screening. Standing orders on the postpartum ward should be implemented (similar to the RhoGam [Ortho-Clinical Diagnostics Inc, USA] standing order in the postpartum period) because they will expedite postpartum immunization. Breastfeeding is not a contraindication to immunization;
  • Screening for immunity and vaccination, if necessary, of all health care personnel, including students in training; and
  • Fully investigating and reporting every case of possible rubella or CRS [4].

INFECTIOUS DISEASES AND IMMUNIZATION COMMITTEE

Members: Robert Bortolussi MD (Chair); Dorothy L Moore MD; Joan L Robinson MD; Élisabeth Rousseau-Harsany MD (Board Representative); Lindy M Samson MD
Consultant: Noni E MacDonald MD
Liaisons: Upton D Allen MD, Canadian Pediatric AIDS Research Group; Scott A Halperin MD, Immunization Program, ACTive; Charles PS Hui MD, Health Canada, Committee to Advise on Tropical Medicine and Travel; Larry Pickering MD, American Academy of Pediatrics, Red Book Editor and ex-officio member of the Committee on Infectious Diseases; Marina I Salvadori MD, Health Canada, National Advisory Committee on Immunization
Principal author: Joan L Robinson MD 


References

  1. Canadian Paediatric Society, Infectious Diseases and Immunization Committee [Principal authors: EL Ford-Jones and T Tam]. Prevention of congenital rubella syndrome. Paediatr Child Health 1999;4:155-7.
  2. Canada Communicable Disease Report, Public Health Agency of Canada. Canadian National Report on Immunization, 2006. http://www.phac-aspc.gc.ca/publicat/ccdr-rmtc/06vol32/32s3/index.html (Version current at September 14, 2007 ).
  3. Lee B, Plitt S, Robinson JL. Population-based study of rubella immunity among pregnant women in Alberta. Can J Infect Dis Med Microbiol 2006;17:365. (Abst)
  4. Robinson JL, Lee BE, Preiksaitis JK, Plitt S, Tipples GA. Prevention of congenital rubella syndrome – what makes sense in 2006? Epidemiol Rev 2006;28:81-7.
  5. Banerji A, Ford-Jones EL, Kelly E, Robinson JL. Congenital rubella syndrome despite maternal antibodies. CMAJ 2005;172:1678-9.
  6. Public Health Agency of Canada. Canadian Immunization Guide. www.phac-aspc.gc.ca/publicat/cig-gci/index-eng.php (Version current at March 21, 2016).
  7. Best JM, O’Shea S, Tipples G, et al. Interpretation of rubella serology in pregnancy – pitfalls and problems. BMJ 2002;325:147-8.
  8. Tingle AJ, Mitchell LA, Grace M, et al. Randomised double-blind placebo-controlled study on adverse effects of rubella immunisation in seronegative women. Lancet 1997;349:1277-81.
  9. Ray P, Black S, Shinefield H, et al. Risk of chronic arthropathy among women after rubella vaccination. Vaccine Safety Datalink Team. JAMA 1997;278:551-6.

Disclaimer: The recommendations in this position statement do not indicate an exclusive course of treatment or procedure to be followed. Variations, taking into account individual circumstances, may be appropriate. Internet addresses are current at time of publication.

Last updated: Mar 29 2016