Page 65 - rp-may-2020
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CPD ACTIVITY  
63 
RET AIL PHARMA C Y • MA Y 2020 
cause disease.  The faecal-oral route  
12 
is the main mechanism of transmission.  
However, rotavirus can survive on dry  
inanimate surfaces for up to 60 days.   
12 
Typical symptoms and signs among  
children with rotavirus infection include  
vomiting, watery non-bloody diarrhoea,  
and fever, which can last for up to eight  
days. Mild symptoms last for shorter  
duration.  The contraindications and  
13 
adverse effects are reported in Table 1.  
Pneumonia and the pneumococcal vaccine 
There are two types of pneumococcal  
vaccine: 
•  13-valent pneumococcal conjugate  
vaccine (13vPCV). 
•  23-valent pneumococcal polysaccharide  
vaccine (23vPPV). 
The 13vPCV vaccine is composed of  
protein-polysaccharide conjugates derived  
from 13 serotypes. This replaced the  
1 
7vPCV vaccine, which was first introduced  
for infants in 2000/2001.   
4 
13vPCV is recommended for the routine  
immunisation of infants as per the NIP.  
A total of three doses is administered to  
healthy infants in their first year of life at  
two months, four months and 12 months.  
An extra dose is recommended at six  
months for medically at-risk infants and  
Aboriginal and Torres Strait Islander infants  
in certain states and territories. 
1 
Streptococcus pneumoniae 
,  
an encapsulated bacterium, is a major  
cause of pneumonia, bacteraemia and  
meningitis worldwide. The incidence is  
greatest in children aged over two years  
and adults over 65, with associated  
mortality rates ranging from about five to  
20 per cent overall.     
14 
A Cochrane Review revealed invasive  
pneumococcal disease (IPD) was  
prevented in 80 per cent (P <0.0001) of  
cases specifically for serotypes covered  
with the 13vPCV. The overall efficacy for  
IPD prevention caused by any serotype  
was 58 per cent (P = 0.001). 13vPCV was  
effective at reducing all-cause mortality by  
11 per cent (P = 0.08). Analysis involving  
HIV-1 positive children had similar  
findings.  Hence, routine vaccination has  
15 
had a statistically significant impact on  
reducing the incidence of IPD, although  
reductions in mortality wasn’t statistically  
significant, likely due to the large  
number of serotypes which precludes  
widespread eradication. 
However, children vaccinated with  
13vPCV may also be protected from less  
severe forms of the disease, such as acute  
otitis media. In addition, there is good  
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bacterium  
Bordetella pertussis 
. It is  
transmitted via airborne droplets and is  
highly infectious.   
6 
Pertussis affects nearly 24 million  
children aged under five each year and  
causes 160,000 deaths in this age group  
worldwide.  A higher incidence and  
6,7 
hospitalisation rate is observed in those  
under six months old and those not fully  
immunised, compared with older infants.   
6,7 
Mortality is high in this group, possibly  
due to an immature immune system  
and incomplete primary immunisation.   
6,7 
Australia has an accelerated primary  
vaccination schedule at two, four and  
six months to minimise the risks of early  
disease. Pertussis can last up to three  
1 
months and is colloquially termed ‘the 100  
day cough’.  The typical symptoms and  
6,7 
time course are described in Figure 1. 
Antibiotics effectively eliminate  
B. pertussis 
 from the nasopharynx.  
Therefore, treatment of established  
disease minimises transmission to  
susceptible contacts.  In patients of any  
5 
age, antibiotic treatment is recommended  
if the diagnosis of pertussis is made within  
three weeks of cough or other symptom  
onset. Patients should be advised to  
avoid contact with others, especially  
young children and infants, until antibiotic  
therapy has been taken for at least five  
days.   After three weeks of cough or  
5 
other symptom onset, patients are rarely  
infectious and antibiotic therapy is not  
indicated. The antibiotics indicated for  
pertussis are macrolides or trimethoprim  
plus sulfamethoxazole.       
8 
Rotavirus and the live attenuated  
oral vaccine 
The rotavirus vaccine was introduced to  
the NIP in 2006.  It’s a live oral vaccine  
4 
containing sucrose.  It’s recommended  
9 
to be given before injected vaccines as  
the sucrose solution helps to mitigate  
any pain caused by these injections.   
10 
It’s administered at two and four months of  
age. Since the introduction of the rotavirus  
vaccine, rotavirus-coded hospitalisations  
of children aged under five years have  
declined by 71 per cent (from 261 down to  
75 per 100,000).     
11 
Rotavirus is still the leading cause of  
viral gastroenteritis worldwide. It’s highly  
contagious, with a high stool viral burden  
and low infectious dose required to  
Live attenuated vaccine 
•  Weakened form of the bacteria or virus that causes the disease. 
•  Creates long lasting immune response. 
•  Contra-indicated in immunosuppressed patients. 
Inactivated vaccine 
•  Killed bacteria/virus. 
•  Immunity not long lasting and hence booster doses are required. 
Subunit, recombinant, polysaccharide and conjugate vaccines 
•  Specific sections of the bacteria/virus that produces an immune response. 
•  Although strong immune response is evoked, booster doses are often needed later in life. 
Toxoid vaccine 
•  Exotoxin produced by bacteria that causes the symptoms is heat/chemically treated. 
•  The treatment doesn’t affect immunogenicity. 
Table 1. 
 Vaccine types available in Australia. 
3 
Figure 1. 
 The typical course of pertussis.   
5 
Time 
Cough 
1 - 2 weeks 
3 - 4 weeks 
1 - 12 weeks 
Daily cough paroxysms 
20 
15 
10 
5 
Catarrhal phase 
  inspiratory whoop, worsening at night  
Cough,   
Rhinorrhea 
Paroxysmal phase 
Cough paroxysms followed by  
Post-tussive vomiting, Cyanosis,  
Lymphocytosis, No fever 
Convalescent phase
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