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Measles 30-40 million cases a year worldwide 750,000 deaths (WHO 2002) – half in Africa Accounts for about half of all vaccine preventable deaths.

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Presentation on theme: "Measles 30-40 million cases a year worldwide 750,000 deaths (WHO 2002) – half in Africa Accounts for about half of all vaccine preventable deaths."— Presentation transcript:

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2 Measles 30-40 million cases a year worldwide 750,000 deaths (WHO 2002) – half in Africa Accounts for about half of all vaccine preventable deaths

3 Measles Morbillivirus of Paramyxovirus family Transmission through fine and large droplets Incubation 7-18 days Early symptoms: fever,coryza, conjunctivitis, cough, malaise Koplik’s spots

4 Measles Rash – erythematous, maculopapular

5 Measles Infectious from start of symptoms until 4 days after the rash appears, very highly infectious R = 17 Common complications of Measles are otitis media, pneumonia, diarrhoea and convulsions Rare complications are encephalitis and SSPE

6 2 dose MMR About 90% children develop immunity to Measles after 1 vaccination In order to maintain high enough levels of herd immunity to prevent transmission need 2 doses of MMR Finland introduced a 2 dose strategy in 1982, the US introduced one in 1989

7 Measles UK

8 Measles British Isles In UK, from 1940 to 1968, Measles in 2 yearly cycles with between 160,000 and 800,000 cases/yr Single Measles introduced in 1968 MMR introduced in 1988 No deaths since 1992 1994 MR campaign, 8 million vaccinated aged 5 -16 1996 2 nd dose MMR introduced

9 Measles/MMR uptake by year in England 1980-2005

10 MMR uptake and adverse publicity

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12 At risk groups Immunocompromised individuals Infants under 1 yr of age Pregnant women at any stage of gestation

13 Interventions Proactive immunisation, coverage needs to be 95% or more to prevent outbreaks as population immunity of 90% is required and vaccine is about 90% effective Lower levels of population immunity will limit spread

14 Reactive interventions Immunisation with MMR, if given within 72 hrs of first exposure, currently recommended in children over the age of 6 months HNIG, for immunosuppressed, younger infants and pregnant women School exclusion

15 Case definitions Confirmed case, compatible rash illness with either serological evidence of recent Measles infection or PCR identification of Measles virus Probable case, compatible illness and epidemiological link to confirmed case Possible case, compatible illness but no epidemiological link to confirmed case

16 What is significant exposure in this context? EITHER 15 mins in same room as probable or confirmed case OR face to face contact with probable or confirmed case WITHIN 4/5 days before and 4 days after, rash appeared

17 School/Nursery Exclusion Any child with Measles-like rash for 5 days after rash appeared Any unvaccinated child with significant contact who develops symptoms suggestive of Measles prodrome Unvaccinated siblings of probable/confirmed case

18 What constitutes vaccinated? MMR vaccine failure is not rare, so MMRx2 needed to be confident that rash illness is not Measles

19 Measles in Camborne Imported via family visit to London, unvaccinated child Spread within school – rel low uptake area Also to associated pre-school groups Only 2 generations of spread

20 Joint working Essential for DPH to be on board Most important intervention is vaccinating around cases Strategy was to start by encouraging GPs to vaccinate then to target schools affected, then those in the next ring outside

21 Vaccination strategy Vaccination strategy was informed by availability of MMR cover data for children on school roll, enabled targeted approach to schools Can also target schools with low uptake and pupils who are immunocompromised

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24 Measles In Newquay Case is adult teacher at secondary school Waiting on results of 2 probable cases, 2 have already tested negative

25 Other case Adult who had been to public venue in London ( War room) Admitted to hospital No other associated cases

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27 What to learn from this? Can’t be complacent about Measles with current MMR uptake levels and consequent population immunity However, levels of immunity in SW are unlikely to support prolonged outbreaks, except where there are communities of low uptake individuals

28 Important preparations Communications, ensure that public, primary care and secondary care know about the outbreak and what they need to do Ensure that salivary kits are available in primary care – predistributed is best Ensure that there is a system for obtaining HNIG promptly

29 Resources Resources used in o/b to be combined into SW Measles pack through development group Only problem, some represent draft documents not yet consulted on.

30 DRAFT Managing Individual Contacts of Measles. Chart 2 - for infants contacts of cases confirmed or where there is a high index of suspicion (note 1) IMPORTANT The table below applies to healthy infants. If there is a particular reason to avoid measles (such as a recent severe illness) obtain further advice. Maternal history Age of exposed infant (completed months) 0-34-66-89+ Index case HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) MMR vaccine (within 72 hours of exposure) MMR vaccine (within 72 hours of exposure) Known antibody negative HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) MMR vaccine (within 72 hours of exposure) MMR vaccine (within 72 hours of exposure) Natural measles or born < 1970 Nothing HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) MMR vaccine (within 72 hours of exposure) Measles vaccinati on HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) MMR vaccine (within 72 hours of exposure) MMR vaccine (within 72 hours of exposure) Unsure of status and born >1969 HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) MMR vaccine (within 72 hours of exposure) Preterm infant (born before 28 weeks) HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) HNIG (within 6 days of exposure) MMR vaccine (within 72 hours of exposure) Note: If MMR is not given within 72 hours of exposure it may still be worthwhile as there may be further exposure at a later date (See note 4).

31 Has the contact: -Been fully vaccinated (2 doses of MMR) or -Had measles in the past (less likely to have had measles if born after 1970)? Is the contact immunosuppressed? (see note 2) Advise vigilance for prodromal symptoms and investigate if symptoms develop Likely to need HNIG as soon as possible but refer to Immunoglobulin Handbook and seek advice from HPA or supervising hospital consultant. Is the contact an infant aged 12 months or under See separate chart 2 No Yes No Is the contact an unvaccinated sibling of the case Yes Offer MMR as soon as possible (see note 4 AND Exclude from school, nursery, playgroup etc until beyond the incubation period or it is clear they don’t have measles or for the infectious period if become symptomatic. No Is the contact pregnant?See note 3 and separate flow chart Yes No Offer MMR as soon as possible (see note 4). Any dose should be at least a month after any previous dose. Is the contact unvaccinated or partially vaccinated?

32 Does the pregnant contact have a well documented history of either 2 doses of MMR / measles vaccine? See Note 3 Where time allows Serum should be taken for urgent measles specific IgG (where possible use antenatal booking specimens) Reassure as to low likelihood of infection Offer HNIG as soon as possible. Take follow-up serum 3 weeks after contact with case Blood results: IgG detected within 10 days of contact with case? NY Advise vigilance for prodromal symptoms and investigate if rash develops Result received within 6 days of contact with case? Probably immune – reassure as to low likelihood of infection YN YN If no time for IgG testing. i.e. result would not be available within 6 days of exposure If antenatal serum not available collect and store serum. Advise vigilance for prodromal symptoms and investigate if rash develops Within 6 days of contact Beyond 6 days of contact

33 Immunisation It is relatively easy to target areas of low uptake successfully where this is due to access problems However, dealing with parental refusal is much more difficult and long-term


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