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A Practical Guide to Immunisation Clinical features The characteristic symptoms of mumps is swelling of one of more of the salivary glands most commonly the parotid gland. Early symptoms also include headache and fever. Photohobia and neck stiffness (meningism) can also develop. At least 30% of cases in children have no symptoms. Most severe in adults. Photo courtesy of CDC The complications of mumps include • Pancreatitis (affects 1 in 25) • Oophoritis (ovarian inflammation) (affects 1 in 20 ) • Orchitis (Testicular inflammation) (affects 25%-40% of post pubertal men) • Meningitis (affects up to 15% of cases) • Encephalitis (0.02-0.3% of the cases) • Deafness (affects 1 in 20,000 patients) • Nephritis, cardiac abnormalities and (rarely) death have been reported. Vaccine schedule in Ireland Mumps immunisation with the combined MMR vaccine is recommended for all children at 12 months as part of the primary childhood immunisation programme. A booster dose MMR is recommended at 4-5 years. Single vaccines are not recommended. 4.2.7 Pertussis Epidemiology of disease and impact of vaccination Pertussis, also known as whooping cough, is a highly infectious bacterial disease involving the respiratory tract caused by the bacterium Bordetella pertussis, which is found in the mouth, nose and throat of an infected person. Pertussis can occur at any age. Although most reported cases occur in children less than five years, cases are reported amongst adolescents and adults every year. It is most dangerous in children under one and most severe in young infants. In Ireland, as in most European countries, the number of pertussis cases reported each year has decreased because of childhood immunisation (Figure 4.7). Cases when they do occur are usually amongst non-vaccinated or incompletely vaccinated children. Transmission Pertussis is spread from person-to-person by droplet infection produced by coughing or sneezing. Incubation period The average incubation period is 7-10 days with a range of 4-21 days. Chapter 4: Vaccine Preventable Diseases Page 37 A Practical Guide to Immunisation 6000 DT P introduced, 1952/53 Number of Notifications 5000 4000 3000 P ertus s is va ccine s ca re mid 1970s 2000 1000 2006 2004 2002 2000 1998 1996 1994 1992 1990 1988 1986 1984 1982 1980 1978 1976 1974 1972 1970 1968 1966 1964 1962 1960 1958 1956 1954 1952 1950 1948 0 Year Figure 4.7: Pertussis cases notified in Ireland 1948-2006. Source: Health Protection Surveillance Centre Period of infectivity An individual can be infectious from six days after exposure (before they even realise that they are sdfsdfsfdsfdsdfsdfsfds ill) to three weeks after onset of cough. Clinical features The illness progresses through three stages: 1. The catarrhal stage (characterized by mild symptoms such as runny nose, sneezing and mild temperature) typically lasts for 1-2 weeks. 2. The paroxysmal stage (paroxysms of coughing followed by an inspiratory whoop), lasts 1 to 6 weeks 3. The convalescent stage with gradual recovery, over 2-3 weeks. The duration of illness can be from two weeks to longer than three months Photo courtesy of CDC Up to 20% of cases may require hospitalisation for complications of the illness. These include pneumonia (1 in 20), middle ear infection, loss of appetite, dehydration, seizures and encephalopathy (approximately 1% and 0.1% respectively), apnoeic episodes (brief cessation of breathing) and death (0.2%). Vaccine schedule in Ireland Pertussis vaccine is administered at 2 , 4 and 6 months with diphtheria, tetanus, hepatitis B, Hib and IPV vaccines (referred to as the “6-in-1” vaccine). Booster vaccine doses are given at 4-5 years of age and again between 11-14 years of age. Page 38 Chapter 4: Vaccine Preventable Diseases A Practical Guide to Immunisation Whole cell pertussis vaccines were used in Ireland and were associated with the development of local side effects. Vaccine development led to the production of acellular Pertussis vaccines which are less immunogenic and produce fewer side effects. All pertussis containing vaccines currently used in Ireland are acellular pertussis vaccines. 4.2.8 Pneumococcal infection Epidemiology of disease and impact of vaccination Pneumococcal infection is a bacterial infection caused by members the Streptococcus Pneumoniae family of which there are more than 90 serotypes. The organism is frequently found in the upper respiratory tract of healthy individuals world-wide. Carriage of the bacteria may range from 10% of adults to 50% of children attending day care facilities. Invasive pneumococcal disease became notifiable on 1st January 2004 in Ireland (Figure 4.8). The very young, the elderly and those in “at risk” groups as laid down in the National Immunisation Guidelines are at increased risk of infection. Age-specific incidence Invasive Pneumococcal Disease (IPD), 2004-2006, by age group Age specific incidence rates (/100,000) 50.0 45.0 40.0 35.0 30.0 25.0 20.0 15.0 10.0 85+ 80-84 75-79 70-74 65-69 60-64 55-59 50-54 45-49 40-44 35-39 30-34 25-29 20-24 15-19 10-14 5-9 3-4 1-2 0.0 <1 5.0 Age group (years) 2004 2005 2006 Figure 4.8: Age-specific incidence of Invasive Pneumococcal disease 2004-2006. Source: Health Protection Surveillance Centre Transmission Transmission requires close contact with cases or carriers and is via droplet infection. Person-to-person transmission of the organism is common, but illness among casual contacts and attendants is infrequent. Incubation period The incubation period is difficult to determine but can be as short as 1-3 days. Period of infectivity The patient is infectious as long as viable pneumoccal organisms are present in nasal, oral or respiratory secretions. Treatment with antibiotics such as penicillin renders patients with susceptible organisms non-infectious within 48 hours. Chapter 4: Vaccine Preventable Diseases Page 39