All cases of measles seen in New Zealand are the result of non-immune people bringing the virus into the country from overseas. Very high coverage of this vaccine is necessary to prevent the spread of measles, in particular, and no vaccination opportunity should be missed.
After a single dose of MMR vaccine 90–95 out of 100 people will be protected from measles, 69–81 protected from mumps and 90–97 from rubella. After a second dose of MMR vaccine the number of people protected from these diseases increases, almost everyone will be protected from measles and rubella, and around 85% protected from mumps.
MMR vaccine is funded for children and adults, born on/after 1 January1969, who have not completed a two dose course of MMR vaccine.
Other brands: M-M-R® II
Priorix® and M-M-R II vaccines are fully interchangeable, a person who receives one M-M-R II can complete their course of vaccines with Priorix. MMR vaccine is funded as part of the National Immunisation Schedule at 12 months and 15 months of age.
MMR vaccine is also recommended for some occupations: staff in early childhood services, healthcare assistant and long-term facility carers, laboratory staff, medical, nursing and other health professionals, and students in training for these occupations.
MMR vaccine is funded for (re)-immunisation following immunosuppression. MMR vaccine is contraindicated in immunosuppressed individuals.
MMR vaccine is recommended for all HIV-positive children, whether symptomatic or asymptomatic, if the CD4+ lymphocyte percentage is 15 percent or greater. Asymptomatic children who are not severely immunocompromised are recommended to receive MMR vaccine from age 12 months to provide early protection against the three diseases.
Susceptible HIV-positive children and adults aged 14 years and older may receive MMR vaccine if the CD4+ lymphocyte count is 200 cells/mm3 or greater. Administration of MMR with CD4+ counts below these recommended levels has been associated with related pneumonitis (from the measles component).
This vaccine is funded for children aged under 18 years and adults born 1 January 1969 or later who do not have not two documented doses of MMR vaccine given from 12 months of age and a miniumum of 4 weeks apart.
Store vaccine and diluent as per cold chain between 2°C to 8°C.
The Ministry of Health recommends that MMR vaccine is administered via the IM route. However, administration of MMR vaccine by either the IM or SC injection route delivers a valid dose of vaccine. In the original clinical trials, MMR vaccine was given by SC injection and this became the recommended route of injection. Since then, data have shown that administration of MMR vaccine by IM injection generates an immune response equal to the response when the vaccine is given via the SC route, and the vaccine is also well-tolerated.
The second MMR dose is a revaccination intended for those who may not be fully protected following the first dose. It is not a booster dose.
Due to limits of detection levels of assays two documented doses of MMR are adequate presumptive evidence of immunity, even when serology is negative or equivocal for one or more of the diseases covered by the vaccine.
Priorix can be administered concurrently with other vaccines, including varicella and all the National Immunisation Schedule vaccines. Separate syringes and different injection sites should be used. If not given at the same visit as varicella vaccine, a 4 week interval between the two live virus vaccines should be observed.
In the case of a measles outbreak, the Ministry of Health may provide advice that the vaccine may be prescribed for an infant aged 6–11 months who has been in direct contact with a measles case. This dose is called ‘dose zero’ or MMR0. A two further doses are required from 12 months of age as per the Schedule.
Immunisation should be postponed in individuals suffering from a fever over 38°C. However, the presence of a minor infection is not a reason to delay immunisation.
Tuberculin skin testing (Mantoux test) should be avoided for 4–6 weeks following vaccination with Priorix. The measles vaccine component may temporarily suppress tuberculin skin sensitivity.
Infants under 12 months of age may fail to respond to the measles component of MMR vaccine due to persisting transplacental maternal measles antibodies. The younger the infant the less likely it is they will develop protection against measles.
In children aged 12 months and over and adults 90-95% of vaccinees are protected from measles, 69-81% from mumps and 90-97% from rubella after a single MMR vaccination. After a second dose of MMR vaccine the number of people protected from these diseases increases, almost everyone will be protected from measles and rubella, and up to 88% protected from mumps.
Secondary vaccine failure, waned immunity without an anamnestic (memory) response to the presence of wild or vaccine virus, occurs rarely for rubella and in only about 5% recipients for measles, but about 26% of MMR vaccine recipients will become susceptible to mumps around 10–20 years after vaccination.
A single MMR vaccination, administered to a measles non-immune individual within 72 hours of contact with a confirmed measles case, may prevent the development of measles disease in the vacicne recipient. Receipt of an MMR vaccine will not make incubating disease worse.