Haemophilus Influenzae type b (Hib) meningitis

Hib meningitis is caused by bacteria called Haemophilus influenzae type b.

Until the introduction of the Hib vaccine in 1992, this was the main form of meningitis in young children in the UK. It mainly affects children under 4 years of age1. Nowadays, Hib is rare in all age groups. In the UK, cases in adults tend to occur in people at the ages most likely to mix with children, both as parents and as grandparents2 .

Hib can cause a range of serious illness, most frequently meningitis3. Hib meningitis is an inflammation of the lining of the brain and spinal cord, and it has the same symptoms as other kinds of bacterial meningitis.

  • In the early stages, a person usually feels unwell, with fever, headache and vomiting, just like many mild illnesses.
  • Typical meningitis symptoms - stiff neck and dislike of bright light normally happen later.
  • As the disease gets worse the person affected may become very sleepy and difficult to wake, confused or delirious, and may have seizures (fits).

Babies and young children often do not get a stiff neck or dislike of bright lights.

  • They may refuse to feed and be irritable with a high-pitched or moaning cry, especially when you pick them up.
  • They may have blotchy, pale or bluish skin.
  • Their body may be stiff, with jerky movements or go floppy and lifeless.
  • The soft spot on a baby’s head may be tense or bulging.

People with Hib meningitis do not normally get a rash. A meningitis rash is more typical of meningococcal infection, which is now the most frequent cause of meningitis in the UK, and often occurs together with septicaemia (blood-poisoning).

Nowadays in the UK, at least 95% of people with Hib meningitis recover4, but it can be fatal.

As many as one survivor in eight may be left with disabilities, that may be as severe as deafness, problems with co-ordination and epilepsy5. In many cases, after effects are temporary or improve over time. In the early stages of recovery, and especially with young children, it can be difficult to tell if problems will be long-lasting.

Other severe Hib diseases include septicaemia, epiglottitis (inflammation of the back of the throat), pneumonia, cellulitis (inflammation of tissue), osteomyelitis (bone infection), arthritis, and pericarditis (inflammation of the heart lining) 4.

Hib can also cause milder ailments like ear infections and minor respiratory illness.

How do you get Hib?

Hib bacteria are found only in humans, and live temporarily in the back of the nose and throat4.

Hib infection is spread through close contact with mucus or droplets from the throat of someone who carries the bacteria. Hib bacteria are too fragile to live outside the human body. Although we don’t know exactly how long they can survive outside, we do know that in general, prolonged close contact is necessary to pick up Hib bacteria. The majority of people who carry Hib do not become ill, which means that we are most likely to meet the bacteria through contact with perfectly healthy carriers. Before Hib vaccine was introduced, young children quite commonly carried Hib bacteria.

The incubation period for Hib is uncertain, however it is generally agreed that when Hib disease occurs, it develops within days of exposure to the bacteria1.

Who is at risk?

Only a small fraction of the people who acquire Hib bacteria fall ill with the disease and the reasons for this are not entirely understood. People with a deficient immune system, such as those without a spleen, are at higher risk. Although the disease is now rare, doctors report all cases to the Public Health doctor. Depending on their age and whether they have been vaccinated, some household contacts of a case may be more at risk than the general public. The Public Health doctor decides what action to take in these cases.

Is there a Hib vaccine?

A conjugate vaccine against Hib was introduced in the UK in 1992. Since the introduction of the Hib vaccine, meningitis caused by Haemophilus influenzae has been reduced by over 90% across the UK6. Introduction of the conjugate Hib vaccine has also dramatically reduced carriage of the bacteria7. Before the vaccine was introduced, a large proportion of children under age 5 carried the bacteria. Now that vaccination is routine, carriage of the bacteria is much less common, and as a result protection is extended to the rest of the population, even those not immunised. This is called ‘herd immunity’.

Conjugate vaccines

Conjugate vaccines are made by linking a tiny fragment from the bacteria’s sugar coat, (which a child’s immune system cannot respond to), to a protein (which a child can respond to). In this way, the immune system is able to recognise the bacteria that cause serious diseases like meningitis. These conjugate vaccines are effective in babies as young as 2 months of age and trigger a long-lasting immune response.

Is the vaccine safe?

Millions of doses given to children worldwide over more than a decade have established an excellent safety record8. Adverse reactions are no more common than for other vaccines routinely given to babies and children.

Who gets the vaccine?

The Hib vaccine is routinely offered to babies at 2, 3, and 4 months of age as part of the 5-in1 vaccine that also protects against diphtheria, tetanus, whooping cough and polio. A Hib booster, as combined Hib/MenC vaccine, is then offered at 12 months of age4 .

In addition, Hib vaccine is recommended for anyone with certain immune deficiencies such as people without a functioning spleen (asplenics and hyposplenics) including people who have sickle cell disorder4.

A.

Meningitis vaccines in the routine immunisation schedule for children in the UK

2 months 3 months 4 months 12 to 13 months  13/14 years*
Hib & diptheria, tetanus, 
whooping cough, polio
(DTaP/IPV/Hib)
Hib & diptheria, tetanus, 
whooping cough, polio
(DTaP/IPV/Hib)
Hib & diptheria, tetanus, 
whooping cough, polio
(DTaP/IPV/Hib)
   
Pneumococcal(PCV13)   Pneumococcal(PCV13) Pneumococcal(PCV13)  
        Meningococcal ACWY*
      Hib & Meningococcal C (Hib/MenC)  
Meningococcal B (MenB)+   Meningococcal B (MenB)+ Meningococcal B (MenB)  
      MeaslesMumps, Rubella (MMR)  

* The routine MenACWY immunisation for teenagers started in August 2015. 

+ Liquid paracetamol should be given to babies who are being vaccinated with MenB as part of the routine schedule at 2 and 4 months of age. You should make sure you have a supply of liquid paracetamol at home in readiness for your baby’s immunisations.

Current schedule for children in Ireland

2 months 4 months 6 months 12 months 13 months
Diptheria/ Tetanus/ Pertussis/ Polio / Hib/ Hepatitis B
('6-in-one')
Diptheria/ Tetanus/ Pertussis/ Polio / Hib/ Hepatitis B
('6-in-one')
Diptheria/ Tetanus/ Pertussis/ Polio / Hib/ Hepatitis B
('6-in-one')
   
  Meningococcal Group C (MenC)     Meningococcal Group C (MenC)
Pneumococcal   Pneumococcal Pneumococcal  
      MMR  
        Hib

Schedule for babies in Ireland born on or after 1st October 2016

2 months 4 months 6 months 12 months 13 months
Diptheria/ Tetanus/ Pertussis/ Polio /Hib/ Hepatitis B
('6-in-one')
Diptheria/ Tetanus/ Pertussis/ Polio / Hib/ Hepatitis B
('6-in-one')
Diptheria/ Tetanus/ Pertussis/ Polio / Hib/ Hepatitis B
('6-in-one')
   
    Meningococcal Group C (MenC)    
Pneumococcal   Pneumococcal   Pneumococcal
      MMR  
        Hib/Meningococcal Group C (MenC)
Meningococcal B(MenB) Meningococcal B (MenB)   Meningococcal B (MenB)  
Rotavirus Rotavirus      

Is Hib still an important cause of meningitis?

The Hib vaccine is very effective10, but no vaccine is 100% effective. It does not work as well in children with certain immune problems. In addition, a very small proportion of perfectly healthy children do not respond to the vaccine well enough to be protected against Hib meningitis. Illness caused by non-b types of Haemophilus influenzae is also being monitored.

Immunisation has dramatically reduced cases of Hib meningitis, but in countries that have not introduced the vaccine, Hib is still a major cause of serious disease in children.

Download the MRF Hib Meningitis factsheet

A.
  1. Davies EG, Elliman DAC, Hart AC, Nicoll A, Rudd P for the RCPCH. Manual of Childhood Infections. 2nd Edition, 2001; WB Saunders, London.
  2. McVernon J, Trotter CL, Slack MPE, Ramsay ME. Trends in Haemophilus influenzae type b infections in adults in England and Wales: surveillance study. 2004. BMJ 329: 655-658.
  3. Anderson EC, Begg NT, Crawshaw SC et al. Epidemiology of invasive Haemophilus influenzae infections in England and Wales in the pre-vaccination era (1990-2). Epidemiol Infect 1995; 115: 89-100.
  4. Department of Health. Immunisation against infectious diseases. Chapter 16: Haemophilus influenzae type B (Hib) pages 127-135. Ed Salisbury D, Ramsay M and Noakes K. 2006. Third edition. TSO. http://www.dh.gov.uk/en/Policyandguidance/Healthandsocialcaretopics/Greenbook/D H_4097254 (accessed 17 March 2008).
  5. Sell S. Haemophilus influenzae type b meningitis: manifestations and long term sequelae. Paediatric Infectious Disease Journal 1987;6:775-8.
  6. JCVI Statement: Haemophilus influenzae type b (Hib) Disease and Hib Vaccine. Executive Summary. http://www.advisorybodies.doh.gov.uk/jcvi/hib.pdf (accessed 17 March 2008).
  7. McVernon J, Howard AJ, Slack MPE, Ramsay ME. Short Report: Long-term impact of vaccination on Haemophilus influenzae type b (Hib) carriage in the United Kingdom. 2004. Epidemiol.Infect. 132: 765-767.
  8. Black SB, Shinefield H, Lampert D et al. Safety and immunogenicity of oligosaccharide conjugate Haemophilus influenzae type b (HbOC) vaccine in infancy. Paediatric Infectious Disease Journal 1991;10:2.
  9. Professional Letter - Chief Medical Officer (2007)5: Haemophilus influenzae type b (Hib) vaccine for young children: catch-up programme. http://www.dh.gov.uk/en/Publicationsandstatistics/Lettersandcirculars/Professionallett ers/Chiefmedicalofficerletters/DH_076964 (accessed March 2008)
  10. Booy R, Hodgson S, Carpenter L, et al. Efficacy of Haemophilus influenzae type b conjugate vaccine PRP-T. Lancet 1994; 344(8919):362-6.
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Dr Fiona McGill answers one of our most frequently asked questions.
Connect families affected by meningitis so they don’t feel alone
Connect families affected by meningitis so they don’t feel alone
£58 funds one support worker to attend our ‘Meningitis Meet-Ups’ – a chance for families affected by meningitis to meet each other for informal peer support.
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The MRF Membership and Support team are here for you for any questions you might have about meningitis and septicaemia and their effects on you, or your family and friends.

Tel: Helpline UK 080 8800 3344 Ireland 1800 41 33 44