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Pneumococcal Vaccine

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Pneumococcal infection

Infection with Streptococcus pneumoniae (pneumococcus) is common and may produce a range of illnesses - some more serious than others e.g. otitis media, meningitis, septicaemia and pneumonia.

Serious or life threatening infection is seen more commonly in children, the elderly, patients who have had their spleen removed and in immunocompromised patients.1

Pneumococcal infection is the most common serious infection seen in the USA and pneumococcal pneumonia is the commonest community acquired pneumonia - a condition which has a mortality of 10-20%.

Pneumococci are spread by person to person contact, commonly by sneezing, coughing or close personal contact. Although antibiotics may be used to treat pneumococcal infections, resistance is becoming increasingly common, and it is likely that vaccination against pneumococcus will have an increasingly large role to play in the fight against the infection in the future.

Pneumococcal vaccine

The vaccine most commonly used in the UK is a polyvalent vaccine containing purified capsular polysaccharide from each of the 23 types of pneumococcus which are responsible for the vast majority of serious pneumococcal infections seen in this country.

Children under the age of 2 are unlikely to develop an immune response to the polysaccharide form of vaccination and those who are considered to be at risk of serious pneumococcal infection should receive a conjugate vaccine containing 7 types of pneumococcus.2 The vaccines are both inactivated and do not contain live organisms.

Pneumococcal vaccination schedule

A single dose of 23 polyvalent vaccine, with no repeat vaccination, is normally all that is required for individuals over the age of 5 with the following exceptions:

  • Patients with no spleen
  • Patients with splenic dysfunction
  • Patients with renal disease including nephrotic syndrome

Antibody levels are more likely to decline rapidly in these individuals and they should receive further vaccinations at 5 yearly intervals. Routine checks of antibody levels prior to re-vaccination in these individuals is not required.3

Childhood immunisation schedule

Since September 2006:4

  • Children aged 2 months will receive the conjugate vaccine (PCV) - Prevenar®.
  • This will be at 2 months, 4 months and 13 months.5
  • All children aged over 2 months and under 2 years of age will be offered PCV as part of the catch-up campaign.
  • Children at special risk of infection, who have received the conjugate vaccine should also have the 23 polyvalent vaccine following their 2nd birthday to protect them from other forms of the organism. This should be given at least two months after the last dose of conjugate vaccine.3
  • At-risk children who present late for immunisation should be offered 2 doses of PCV1 before the age of 12 months, and a further dose at 13 months of age.
  • At-risk children aged over 12 months and under 5 years of age should be offered a single dose of PCV. Please note that children in this age group who have asplenia or splenic dysfunction, or who are immunocompromised, require a second dose of PCV because this group may have a sub-optimal immunological response to the first dose of vaccine.
Indications for pneumoccocal vaccination

Pneumococcal vaccination is recommended for all those in whom pneumococcal infection is likely to be more common or more dangerous. It is currently recommended in the following circumstances:3

  • All adults over the age of 65 years old4,6

Consider all patients over the age of 2 months with increased risk (base decision to immunise on clinical judgment):

  • Asplenia or severe dysfunction of the spleen (e.g. homozygous sickle cell disease or coeliac disease).7 Immunise 2 weeks prior to splenectomy or delay until 2 weeks after if possible.
  • Chronic renal disease, e.g. nephrotic or chronic renal failure or renal transplantation.
  • Patients with immunodeficiency or immunosuppression (6 weeks prior to treatment with chemotherapy/radiotherapy or 3 months after completion of treatment).
  • Chronic lung disease e.g. COPD, cystic fibrosis, lung fibrosis etc. Asthma is NOT an indication, unless requires continuous or frequently repeated use of systemic steroids. Children with respiratory conditions caused by aspiration, or a neuromuscular disease (e.g. cerebral palsy) with a risk of aspiration should be immunised.
  • Chronic heart disease needing regular medication ±follow-up: (IHD, congenital HD, hypertension with cardiac complications).
  • Chronic liver disease - including cirrhosis.
  • Diabetes mellitus - requiring oral or insulin therapy, but not diet-controlled.
  • Patients with cochlear implants, or about to receive cochlear implants.
  • Patients with CSF shunts in-situ.
  • Children under the age of 5 who have previously had invasive pneumococcal disease.
Pneumococcal clinical risk groups those aged two months and over3
Clinical risk group Examples (base decision on clinical judgement)
Asplenia or dysfunction of the spleen e.g. homozygous sickle cell disease and coeliac disease
Chronic respiratory disease e.g. chronic obstructive pulmonary disease (COPD), including chronic bronchitis and emphysema; bronchiectasis, cystic fibrosis, interstitial lung fibrosis, pneumoconiosis and bronchopulmonary dysplasia (BPD). Patients with respiratory conditions caused by aspiration, or a neuromuscular disease (e.g. cerebral palsy) with a risk of aspiration.
Asthma is not an indication, unless continuous or frequently repeated use of systemic steroids (as defined in Immunosuppression below) is needed.
Chronic heart disease Patients requiring regular medication and/or follow-up for ischaemic heart disease, congenital heart disease, hypertension with cardiac complications, and chronic heart failure.
Chronic renal disease Includes nephrotic syndrome, chronic renal failure, renal transplantation.
Chronic liver disease Includes cirrhosis, biliary atresia, chronic hepatitis
Diabetes (requiring insulin or oral hypoglycaemic drugs) Includes type I diabetes requiring insulin or type 2 diabetes requiring oral hypoglycaemic drugs.
It does not include diabetes that is diet controlled.
Immunosuppression Due to disease or treatment, including asplenia or splenic dysfunction and HIV infection at all stages.
Patients undergoing chemotherapy leading to immunosuppression. Individuals treated with or likely to be treated with systemic steroids for more than a month at a dose equivalent to prednisolone 20 mg or more per day (any age), or for children under 20 kg, a dose of ≥1 mg/kg/day.
Some immunocompromised patients may have a suboptimal immunological response to the vaccine.
Individuals with cochlear implants It is important that immunisation does not delay the cochlear implantation. Where possible, pneumococcal vaccination should be completed at least 2 weeks prior to surgery to allow a protective immune response to develop. In some cases it will not be possible to complete the course prior to surgery. In this instance, the course should be started at any time prior to or following surgery and completed according to the immunisation schedule.
Individuals with
cerebrospinal fluid leaks
This includes leakage of cerebrospinal fluid such as following trauma or major skull surgery.
Contraindications to pneumococcal vaccine

There are very few contraindications to the giving of pneumococcal vaccine. The vaccine should not be given to individuals who have had:

  • A confirmed anaphylactic reaction to a previous dose of the vaccine.
  • A confirmed anaphylactic reaction to any component of the vaccine.
  • Although the safety of the vaccine has not been formally assessed during pregnancy, the vaccine may be given if clinically indicated.3
Adverse reactions

The only adverse reactions likely to be encountered with either vaccine are:

  • Mild soreness and induration at the injection site
  • ± a low grade fever


Document references
  1. CDC; Prevention of Pneumococcal Disease. Advisory Committee on Immunization Practices. April 1997.
  2. Immunizations - pneumococcal, Clinical Knowledge Summaries (2007)
  3. Immunisation against infectious disease - 'The Green Book', Department of Health (various dates)
  4. DOH (UK); PL CMO (2006) 1: Important changes to the childhood immunisation programme. Department of Health.
  5. NHS Immunisation Website; Patient information
  6. DOH; Adult Immunisation Update (Pneumococcus/Flu). Department of Health, 2003.
  7. Guidelines for the prevention and treatment of infections in patients with an absent or dysfunctional spleen, British Committee for Standards in Haematology (2002)

Internet and further reading Acknowledgements EMIS is grateful to Dr Hayley Willacy for writing this article. The final copy has passed scrutiny by the independent Mentor GP reviewing team. ©EMIS 2009.
Document ID: 540
Document Version: 3
Document Reference: bgp2062
Last Updated: 15 Jul 2008
Planned Review: 15 Jul 2010

The authors and editors of this article are employed to create accurate and up to date content reflecting reliable research evidence, guidance and best clinical practice. They are free from any commercial conflicts of interest. Find out more about updating.

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