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IMMUNISATIONS Janet Anderson

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Page 1: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

IMMUNISATIONS

Janet Anderson

Page 2: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Immunisations The immunisation programme in the UK

evolves to meet the demand of controlling infection through vaccination

Population immunity if high enough enables the unimmunised to be protected (herd immunity)

Vaccination enabled smallpox to be eradicated from the world in 1980

WHO is working towards global polio eradication

Page 3: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Acquired immunity

Acquired immunity is generally specific to a single or a group of closely related organisms.

Active immunity can be acquired by natural disease or immunisation which provides immunity without the risk of the disease or is complications.

Acquired immunity is either antibody or cell mediated

Page 4: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Passive Immunity Passive immunity is the transfer of active humeral

immunity in the form of ready made antibody from one individual to another .

Passive transfer occurs when antibody passes from mother to child

Artificially acquired transfer occurs when antibody or antitoxin from an immune individual (or animal) is given to an individual at risk.

Used when there is a high risk of infection where there is insufficient time for the body to produce its own response or where the individual is immunodeficient.

Page 5: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 6: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

MEASLES

Viral, droplet spread, incubation 10 days Coryza, conjunctivitis, fever, rash Complications, pneumonia,encephalitis,death Notifiable Catch up programme offered to those with

incomplete immunization because of increasing notifications

Page 7: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

MUMPS

Viral,droplet spread, incubation 14-21 days Parotid swelling Complications

oophritis,orchitis,pancreatitis,and meningitis Notifiable

Page 8: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 9: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

RUBELLA

Viral, droplet spread incubation 14-21 days Mild illness with rash and lymphadenopathy Maternal rubella, 1st trimester 90% foetal

damage ( microcephaly, deafness, cataracts, PDA etc)

History needs confirmation with saliva or serology

Page 10: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Chicken pox vaccine

Given routinely elsewhere, not in UK

Cost?

Possible increase in Herpes Zoster if immunity is not gained by natural infection??

Available for children at risk

Page 11: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 12: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

DIPHTHERIA

Corynebacteria diphtheriae Incubation 2-5 days Infectious for four weeks Inflammatory exudate causing grey

membrane in resp tract. Potential obstruction Toxin mediated damage to myocardium,

nervous system and adrenals

Page 13: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

TETANUS

Toxin mediated from tetanus bacillus Incubation 4-21 days Spore spread Muscular rigidity with spasms ---(lock jaw)

Page 14: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 15: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

POLIO

Polio virus Faecal/oral spread, Incubation 3-21 days Virus may be shed for 6 weeks Range of severity--- asymptomatic to

paralysis

Page 16: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 17: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

PERTUSSIS

Bordetella pertussis Incubation 7-10 days Infectious until 3 weeks after onset of

paroxysms Paroxysmal cough can be associated with

apnoea and /or vomiting ‘The 6 month cough’ Complications--- SIDS, bronchopneumonia

and cerebral hypoxia

Page 18: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 19: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

HAEMOPHILUS INFLUENZAEType B Hib Meningitis with high incidence of

complications +/- bacteraemia Epiglottitis Osteomyelitis

Page 20: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 21: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

MENINGOCOCCAL DISEASE

Neisseria meningitidis Type C vaccine, Type B vaccine being

developed— (also available Type A for travelers) Incubation 2-3 days Onset can be fulminant Meningitis / septicaemia Fever, vomiting, purpuric rash

Page 22: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Routine Immunisation schedule 2 months Diphtheria Pertussis Tetanus

Hib Polio and Pneumococcal (PCV) +Rotavirus

3 months Diphtheria Pertussis Tetanus Hib Polio and Men C + Rotavirus

4 months Diphtheria Pertussis Tetanus Hib Polio and Pneumococcal and Men C

Page 23: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Routine Immunisation schedule 12 months Men C and Hib

13 months MMR and Pneumococcal

3 to 5 yrs Diphtheria Pertussis Tetanus

Polio and MMR 12-13yrs Human papilloma virus vaccine

3 doses ( girls only) 15 yrs Diphtheria Tetanus Polio

Page 24: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Active Immunity

Live Attenuated Vaccines eg BCG, MMR, yellow fever, oral polio, oral Rotavirus, nasal inflenza (from September 2013)

Inactivated Vaccines eg influenza

Extracts of or Detoxified Endotoxins eg tetanus

Page 25: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Passive Immunity

Normal Immunoglobulin eg for replacement therapy of agammaglobulinaemia

Specific Immunoglobulin eg tetanus, VZV rabies, HepB and palivizumab for RSV protection

Page 26: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Contraindications To Vaccination General – Febrile illness Anaphylaxis to previous dose or to components of

vaccine Severe local reaction Inconsolable unexplained crying >3 hrs within 72hrs Encephalopathic illness (hypotonic-hyporesponsive

episode (HHE)) within 72 hours Intramuscular route should not be used for children with

bleeding disorders—use s.c. route

Live Vaccines – Immunosuppressed, e.g. prednisolone therapy, chemotherapy, HIV (note MMR can be if not severely imunocompromised), BMT within 6 months. Pregnancy

Page 27: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

DTaP/IPV/Hib and MenC Diptheria, Tetanus, acellular pertussis,

Inactivated polio , Haemophilus influenzae and Meningitis C

Recent changes are inactivated polio (im) and acellular pertussis

Well tolerated, minimal side effects

For children over 10 years adsorbed diphtheria (low dose),Tetanus and inactivated polio vaccine only if have received primary immunisations

Page 28: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

MMR

Measles, Mumps and Rubella Serious illnesses associated with significant

mortality Fever common 6 to 10 days post vaccination 1:1000 febrile convulsion Can be given to egg allergic children NOT associated with Autism and IBD

Page 29: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 30: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination
Page 31: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Current measles prevelence

First 6 months 2011------497 cases in UK

First 6 months 2012------964

Significant increase in South Wales 2013

Most in the 10-12 age group

Page 32: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

BCG Administered to at risk babies in neonatal period

( where incidence is greater than 40 per 100,000)

Given intradermally Since 2006 risk-based programme for other

children as well Local Side effects common--- ulceration or

abscess Do not give to HIV + or immunocompromised Mantoux induration > 6mm Previous BCG or past/ present TB.

Page 33: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

PNEUMOCOCCAL VACCINES Prevenar < 2yrs previously 7 now 13-valent

polysaccharide

Since 2010 13-valent available—against the most invasive serotypes of pneumococcal bacteria. Part of the routine schedule.

Pneumovax > 2years 23- valent polysaccharide

Indications for Pneumovax--- those not previously immunised ---asplenia, SS disease, Chronic lung or heart disease

Page 34: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Rotavirus Vaccine

Rotavirus is responsible for 1 in 10 hospital admissions in children

Immunisation in UK introduced September 2012, to be routine from July 2013

Live attenuated oral vaccine Two doses four weeks apart Effective after 6 weeks of age To be offered at 2 and 3 months in the

vaccination Schedule

Page 35: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Influenza vaccine Current vaccine trivalent inactivated influenza

vaccine(TIV) licenced form 6 months of age. Live attenuated influenza vaccine given as a nasal

spray (LAIV), licenced in Europe for 2-17s now available.

LAIV contains 3 strains. Not licenced for <2s 2 doses one month apart, unless previously

immunised when one is sufficient. To be piloted this year, role out to <5s next and all

children 2015

Page 36: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

OTHERS RSV - passive immunisation—Palivizumab-

(Synargis) –given during RSV season to high risk groups. Monoclonal antibody given monthly.

HepBV – at risk groups (at present) HPV – Human Papilloma Virus vaccine -3 doses

Given to 12-13 year olds –due to increase coverage to 17-18 year olds in September 2008

Cervarix—effective against Type 16 &18 HPV Protects against 75% of cervical cancers

Gardasil introduced Sept 2012—effective against Type 6,11, 16 &18 –hence against 90% genital warts as well

Page 37: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Others (cont)

Chicken pox routine in USA at 12-15 months/top up at 5/6years. Available but not routine in UK.

Meningococcal B vaccine available from January 2013, but not in immunisation schedule yet.

Pertussis vaccine now advised for every pregnant woman between 28 and 38 weeks ( new recommendation)

Page 38: IMMUNISATIONS Janet Anderson. Immunisations The immunisation programme in the UK evolves to meet the demand of controlling infection through vaccination

Vaccine ANAPHYLAXIS

ABC Adrenaline 10 mcg/Kg (0.01ml/Kg 1:1000) Hydrocortisone 4mg/Kg Chlorphenamine

Beware neomycin and gelatin anaphylaxis – omit MMR