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Rubella and Rubella Vaccine Epidemiology and Prevention of Vaccine-Preventable Diseases National Center for Immunization and Respiratory Diseases Centers for Disease Control and Prevention Revised May 2009

Rubella 11

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Page 1: Rubella 11

Rubella and Rubella Vaccine

Epidemiology and Prevention of Vaccine-Preventable Diseases

National Center for Immunization and Respiratory Diseases

Centers for Disease Control and Prevention

Revised May 2009

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Note to presenters:

Images of vaccine-preventable diseases are available from the Immunization Action Coalition website at http://www.vaccineinformation.org/photos/index.asp

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Rubella

• From Latin meaning "little red"

• Discovered in 18th century - thought to be variant of measles

• First described as distinct clinical entity in German literature

• Congenital rubella syndrome (CRS) described by Gregg in 1941

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Rubella Virus

• Togavirus

• RNA virus

• One antigenic type

• Rapidly inactivated by chemical agents, ultraviolet light, low pH, and heat

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Rubella Pathogenesis

• Respiratory transmission of virus

• Replication in nasopharynx and regional lymph nodes

• Viremia 5-7 days after exposure with spread to tissues

• Placenta and fetus infected during viremia

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Rubella Clinical Features

• Incubation period 14 days

(range 12-23 days)

• Prodrome of low-grade fever

• Maculopapular rash 14-17 days after exposure

• Lymphadenopathy in second week

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Rubella Complications

Arthralgia or arthritisadult femalechildren

Thrombocytopenic purpuraEncephalitisNeuritisOrchitis

up to 70% rare

1/3,000 cases1/6,000 casesrarerare

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Epidemic Rubella – United States, 1964-1965

• 12.5 million rubella cases• 2,000 encephalitis cases• 11,250 abortions

(surgical/spontaneous)• 2,100 neonatal deaths• 20,000 CRS cases–deaf - 11,600–blind - 3,580–mentally retarded - 1,800

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Congenital Rubella Syndrome

• Infection may affect all organs

• May lead to fetal death or premature delivery

• Severity of damage to fetus depends on gestational age

• Up to 85% of infants affected if infected during first trimester

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Congenital Rubella Syndrome

• Deafness

• Cataracts

• Heart defects

• Microcephaly

• Mental retardation

• Bone alterations

• Liver and spleen damage

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Rubella Laboratory Diagnosis

• Isolation of rubella virus from clinical specimen (e.g., nasopharynx, urine)

• Positive serologic test for rubella IgM antibody

• Significant rise in rubella IgG by any standard serologic assay (e.g., enzyme immunoassay)

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Rubella Epidemiology

• Reservoir Human

• Transmission RespiratorySubclinical cases may

transmit

• Temporal pattern Peak in late winter and spring

• Communicability 7 days before to 5-7 daysafter rash onset

Infants with CRS may shed virus for a year or more

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0

10000

20000

30000

40000

50000

60000

70000

19661970 1975 1980 1985 1990 1995 2000 2005

Ru

bel

la C

ases

0

10

20

30

40

50

60

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80

CR

S C

ases

Rubella CRS

Rubella - United States, 1966-2007

Year

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0

500

1000

1500

2000

2500

3000

3500

4000

4500

1980 1985 1990 1995 2000 2005

Ru

bel

la C

ases

0

5

10

15

20

25

30

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40

CR

S C

ases

Rubella CRS

Rubella - United States, 1980-2007

Year

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0

10

20

30

40

50

60

70

80

90

100

1980 1985 1990 1995 2000

Per

cen

t

Rubella - United States, 1980-2003Age Distribution of Reported Cases

<5 yrs

15-39 yrs

>40 yrs

5-14 yrs

Year

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Rubella and CRS in the United States

• Most reported rubella in the U.S. since the mid-1990s has occurred among foreign-born Hispanic adult

• Majority of CRS since 1997 occurred in children of unvaccinated women born to Hispanic women, most born in Latin America

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Rubella Case Definition

• Acute onset of generalized maculopapular rash, and

• Temperature of >99°F (37.2 °C), if measured, and

• Arthralgia or arthritis, lymphadenopathy, or conjunctivitis

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Rubella Outbreak Control Guidelines

• Laboratory diagnosis of rubella and CRS

• Step-by-step guidelines on evaluation and management of outbreak

• Rubella prevention and control among women of childbearing age

• Rubella and CRS surveillance

MMWR 2001;50(RR-12)

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VaccineHPV-77:DE5

HPV-77:DK12

GMK-3:RK53

RA 27/3*

Trade Name Meruvax

Rubelogen

Cendevax

Meruvax II

Licensure1969

1969

1969

1979

*Only vaccine currently licensed in U.S.

Rubella Vaccine

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Rubella Vaccine

• Composition Live virus (RA 27/3 strain)

• Efficacy 95% (1 dose)

• Duration ofImmunity Lifelong

• Schedule At least 1 dose

• Should be administered with measles and mumps as MMR or with measles, mumps and varicella as MMRV

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Rubella Vaccine (MMR) Indications

• All infants 12 months of age and older

• Susceptible adolescents and adults without documented evidence of rubella immunity

• Emphasis on nonpregnant women of childbearing age, particularly those born outside the U.S.

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Rubella Immunity

• Documentation of one dose of rubella-containing vaccine on or after the first birthday

• Serologic evidence of immunity

• Birth before 1957 (except women of childbearing age)

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Rubella Immunity

• Birth before 1957 is not acceptable evidence of rubella immunity for women who might become pregnant

• Only serology or documented vaccination should be accepted

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MMR Adverse Reactions

• Fever* 5%-15%

• Rash* 5%

• Joint symptoms* 25%

• Thrombocytopenia <1/30,000 doses

• Parotitis rare

• Deafness rare

• Encephalopathy <1/1,000,000 doses

*reactions that may be attributable to the rubella component

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Rubella Vaccine Arthropathy

• Acute arthralgia in about 25% of vaccinated, susceptible adult women

• Acute arthritis-like signs and symptoms occurs in about 10% of recipients

• Rare reports of chronic or persistent symptoms

• Population-based studies have not confirmed an association with rubella vaccine

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MMR VaccineContraindications and Precautions

• Severe allergic reaction to vaccine component or following a prior dose

• Pregnancy

• Immunosuppression

• Moderate or severe acute illness

• Recent blood product

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Vaccination of Women of Childbearing Age

• Ask if pregnant or likely to become so in next 4 weeks

• Exclude those who say "yes"

• For others

– explain theoretical risks

– vaccinate

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Vaccination in Pregnancy Study 1971-1989

• 321 women received rubella vaccine during pregnancy or near the estimated time of conception

• 324 live births

• No observed CRS

• 95% confidence limits 0%-1.2%

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Vaccine Storage and HandlingMMR Vaccine

• Store 35o - 46oF (2o - 8oC) (may be stored in the freezer)

• Store diluent at room temperature or refrigerate

• Protect vaccine from light

• Discard if not used within 8 hours reconstitution

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Vaccine Storage and HandlingMMRV Vaccine

• Must be stored at an average temperature of 5oF (-15oC ) or colder at all times

• May be stored at refrigerator temperature for up to 72 hours but must then be discarded if not used (do not refreeze)

• Must be administered within 30 minutes of reconstitution or must be discarded

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CDC Vaccines and ImmunizationContact Information

• Telephone 800.CDC.INFO

• Email [email protected]

• Website www.cdc.gov/vaccines