Pneumococcal disease is caused by the bacterium, Streptococcus pneumoniae (pneumococcus). Infection usually starts with a colonising event in the nose and throat, which is asymptomatic, and most infections do not amount to anything beyond colonisation. Some, however, spread locally or invasively to cause disease. Certain pneumococcal diseases are non-invasive, such as middle-ear infections (otitis media), sinusitis or bronchitis.4 Others are invasive, involve the blood or a major organ and are potentially life-threatening. Examples of invasive pneumococcal diseases (IPDs) include septicaemia (sepsis), meningitis or bacteraemic pneumonia. Pneumococci usually possess a polysaccharide capsule, which occurs as more than 90 serotypes, and immunity to the organism is capsule typespecific. Although many serotypes cause disease, only a few cause most infections. The predominant serotypes vary with age, time and geography.
Pneumococcal disease is mainly treated using β-lactam antibiotics, though pneumococci bacteria are increasingly developing antibiotic resistance. Strains have variably become resistant to penicillin, cephalosporins, macrolides, tetracycline, clindamycin and the quinolones.
Transmission occurs through respiratory droplets from people with pneumococcal disease or healthy carriers. If the infected person coughs or sneezes in close proximity of others, infection may spread. Following acquisition, the bacterium becomes established in the nasopharynx of the host with asymptomatic colonisation. It may then spread to other parts of the body where it causes disease. The bacteria’s polysaccharide capsule helps it to resist phagocytosis. If no anti-capsular antibody pre-exists, alveolar macrophages cannot kill the pneumococci.
The major clinical syndromes of IPD are pneumonia, septicaemia and meningitis.2,8 Symptoms of pneumonia include fever, chills, coughing, rapid or difficult breathing, chest pain, rigors, tachycardia, rusty-coloured sputum, cough productive of mucopurulent, dyspnea, tachypnea, hypoxia, or, in older patients, confusion or low alertness. Meningitis, although least common, is the most severe category of IPD and is often fatal.2,3 Symptoms include a stiff neck, fever, lethargy, nuchal rigidity, cranial nerve signs, seizures, coma, headache, pain when looking into bright lights, confusion, or, in babies, poor eating and drinking, low alertness or vomiting. Septicaemia is the most common IPD among young children. Symptoms include fever, chills and low alertness. By 12 months, most children have also experienced otitis media. Pneumococcus is detected in 28 to 55% of middle ear aspirates from children with otitis media. Symptoms include ear pain, a red, swollen eardrum, fever, and sleepiness. Complications of otitis media may include mastoiditis and meningitis.
Who is most at risk?
Anyone can contract IPD though some groups are at heightened risk. These include people younger than two years of age or older than 65; children in group childcare; children in developing countries; nursing homes residents; smokers; people suffering from chronic conditions such as lung, heart, liver or kidney disease, asthma, diabetes or alcoholism; people with cochlear ear implants, cerebrospinal fluid (CSF) leaks or impaired immunity for any reason, including those arising from conditions such as HIV/AIDS, cancer or a damaged or absent spleen; and Aboriginal and Torres Strait Islander people.
Immunocompromised persons who are unable to mount an adequate immune response to pneumococcal capsular antigens, including those with asplenia, have the highest risk of IPD.1,2,4 Aboriginal and Torres Strait Islander people have a disproportionately high burden of IPD.1,12,13
Vaccination is strongly recommended for groups at risk.
IPD still causes serious illness and occasional deaths.
By 2011 this had become much less common than it was before the widespread introduction of infant pneumococcal vaccine in 2005. However, several harmful strains of the pneumococcal germ continue to circulate and cause illness.
The introduction of Prevenar 13® in 2011 is expected to provide protection against the most important of these remaining strains. Routine vaccination of children under the age of three is recommended.
People aged over 65 years
Pneumococcal disease is an important cause of pneumonia in adults aged 65 years or older. The elderly are especially at risk of serious illness and death from this disease. The vaccine for adults, Pneumovax 23® is different from the infant vaccine.
People with underlying medical risk conditions
Adults and children with the following serious medical conditions are at a greater risk of life threatening infection and hospitalisation from pneumococcal disease:
– people with chronic illnesses such as diabetes, heart, lung or kidney disease
– people without a spleen or whose spleen does not work properly
– people with serious problems with their immune system
– Aboriginal and Torres Strait Islander people
All Aboriginal and Torres Strait Islander people over the age of 50 should be offered pneumococcal vaccine.
There are two different types of pneumococcal vaccines – pneumococcal conjugate vaccine (PCV) and pneumococcal polysaccharide vaccine (PPV).
Pneumococcal polysaccharide vaccine (PPV)
23-valent pneumococcal polysaccharide vaccine (23vPPV)
23vPPV contains capsular polysaccharides derived from the 23 most frequent or most virulent types of S. pneumonia. PPV induces significant immune responses in immunocompetent adults, including the elderly, with no substantial differences in immune response between older and younger subjects, but poor responses in the immunocompromised.15 23vPPV is poorly immunogenic for most serotypes in children aged <2 years and does not induce immune memory.
Pneumococcal conjugate vaccines (PCV)
The immunogenicity of capsular polysaccharides can be enhanced by conjugation to carrier proteins.
PCV formulations vary in the number of pneumococcal serotypes included and the conjugating proteins used. Pneumococcal conjugate vaccines are immunogenic in young infants and can induce an immune memory response.
10-valent pneumococcal conjugate vaccine (10vPCV) – registered for use in Australia since 2009 and is included under the NIP.
13-valent pneumococcal conjugate vaccine (13vPCV) – registered in Australia since 2010, and used in the NIP since July 2011.
Who should receive pneumococcal vaccination
Pneumococcal vaccination is recommended for all children < 5 years of age and is funded by the National Immunisation Program. Children > 5 years and adults with medical conditions associated with an increased risk of invasive pneumococcal disease should receive pneumococcal vaccinations. Non-indigenous adults ≥ 65 years and Indigenous adults ≥ 50 years should routinely be offered pneumococcal vaccination. The type and number of doses of pneumococcal vaccination vary in different age groups and risk groups. See the Australian Immunisation Handbook for further details.
Dosage and administration
The dose of pneumococcal conjugate vaccines (10vPCV, 13vPCV) is 0.5 mL, to be given by IM injection, in the opposite limb to other injectable vaccines, if possible.
The dose of pneumococcal polysaccharide vaccine (23vPPV) is 0.5 mL, to be given by either IM or SC injection, in the opposite limb to other injectable vaccines, if possible. The IM route is preferred, as a 3-fold greater rate of injection site reactions is found following administration of 23vPPV by the SC route.15 A vaccine dose administered subcutaneously does not need to be repeated.
– 10vPCV (Synflorix) is registered for use in infants and children aged 6 weeks up to 5 years.
– 13vPCV (Prevenar 13) is registered for use in infants and children aged 6 weeks up to 17 years and adults aged ≥50 years.
– 23vPPV (Pneumovax 23) is registered for use in children aged ≥2 years and in adults.
Pregnancy and breastfeeding
23vPPV is not routinely recommended for pregnant or breastfeeding women – deferral of vaccination with 23vPPV until after delivery is recommended unless there is an increased risk of IPD. 23vPPV may be given to breastfeeding women.
Data on use the use of 10vPCV and 13vPCV during pregnancy or lactation are not available.
Co-administration with other vaccines
Pneumococcal polysaccharide vaccine can be concurrently administered with Zostavax using separate syringes and injection sites (Refer also to 4.24.6 Zoster of the Australian Immunisation Handbook).
Access the 2017 Pneumococcal Webinar here.
A printable GP guide is available here.
Download printable information on pneumococcal vaccination here.
Access the PneumoTool here.
National Immunisation Program Schedule:
1. Black S, Eskola J, Whitney C, Shinefield H. Pneumococcal conjugate vaccine and pneumococcal command protein vaccines. In: Plotkin SA, Orenstein WA, Offit PA, eds. Vaccines. 5th ed. Philadelphia, PA: Saunders Elsevier, 2008.
2. Centers for Disease Control and Prevention (CDC). Pneumococcal disease. In: Atkinson W, Wolfe C, Hamborsky J, eds. Epidemiology and prevention of vaccine-preventable diseases. 12th ed. Washington, D.C.: Public Health Foundation, 2011.
3. Kadioglu A, Weiser JN, Paton JC, Andrew PW. The role of Streptococcus pneumonia virulence factors in host respiratory colonisation and disease. Nature Reviews Microbiology 2008;6:288-301.
4. Weinberger DM, Harboe ZB, Sanders EA, et al. Association of serotype with risk of death due to pneumococcal pneumonia: a meta-analysis. Clinical Infectious Diseases 2010;51:692-9.
5. World Health Organisation(WHO). 23-valent pneumococcal polysaccharide vaccine: WHO position paper. Weekly Epidemiological Record 2008;83:373-84.
6. Hausdorff WP, Feikin DR, Klugman KP. Epidemiological differences among pneumococcal serotypes. The Lancet Infectious Diseases 2005;5:83-93.
7. Roche PW, Krause V, Cook H, et al. Invasive pneumococcal disease in Australia, 2006. Communicable Diseases Intelligence 2008;32:18-30.
8. File TM, Jr., Marrie TJ. Burden of community-acquired pneumonia in North American adults. Postgraduate Medicine 2010;122:130-41.
9. Eskola J, Kilpi T, Palmu A, et al. Efficacy of a pneumococcal conjugate vaccine against acute otitis media. New England Journal of Medicine 2001;344:403-9.
10. Musher DM. Streptococcus pneumoniae. In: Mandell GL, Bennett JE, Dolin R, eds. Mandell, Douglas, and Bennett’s principles and practice of infectious diseases. 7th ed. Philadelphia: Churchill Livingstone, 2010.
11. Pilishvili T, Zell ER, Farley MM, et al. Risk factors for invasive pneumococcal disease in children in the era of conjugate vaccine use. Pediatrics 2010;126:e9-17.
12. Menzies R, Turnour C, Chiu C, McIntyre P. Vaccine preventable diseases and vaccination coverage in Aboriginal and Torres Strait Islander people, Australia, 2003 to 2006. Communicable Diseases Intelligence 2008;32 Suppl:S2-67.
13. van der Poll T, Opal SM. Pathogenesis, treatment and prevention of pneumococcal pneumonia. The Lancet 2009;374:1543-56.
14. Jackson LA, Neuzil KM. Pneumococcal polysaccharide vaccines. In: Plotkin SA, Orenstein WA, Offit PA, eds. Vaccines. 5th ed. Philadelphia, PA: Saunders Elsevier. 2008.
15. Cook IF, Pond D, Hartel G. Comparative reatogenicixy and immunogenicity of 23 valent pneumococcal vaccine administered by intramuscular or subcutaneous injection in elderly adults. Vaccine 2007;25:4767-74.
Page published: 8 March 2017
Page updated: 28 August 2017