2G important infectious diseases Flashcards

1
Q

Pertussis

A

ORGANISM
Bordetella Pertussis

CLINICAL FEATURES
-Whooping cough
-cough, cold and fever progressing to coughing paroxysms ending with a whoop or vomiting
- 100 day cough
- can be fatal in infants < 6 months
- milder in adults but causes chronic cough

EPIDEMIOLOGY
- epidemics 3-4 yearly
- large epidemic in England in 2012 prompting vaccination of pregnant women

DIAGNOSIS
- culture of nasal swab but low sensitivity
- PCR
- Enzyme immunoassay

RESEVIOIR
- human

TRANSMISSION
- droplet spread

SURVEILLANCE
- statutory notification
- vaccine coverage

PREVENT
- Prevent: vaccinate in primary childhood immunisations and pregnant women

CONTROL
cases: Abx (but not thought to be beneficial after 21 days), exclude for 48 hours after abx started or for 21 days from symptoms starting, vaccinate if unvaccinated or pregnant
Contacts: abx and vaccination (primary/booster) for close contact if someone is in a vulnerable group and less than 21 days since case had symptoms.
If no vulnerable contacts, no prophylaxis required

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1
Q

Vaccine preventable diseases: Diphtheria

A

ORGANISM
Toxigenic Corynebacterium diphtheria
Corynebacterium Ulcerans

CLINICAL FEATURES
-Acute upper respiratory tract infection
-enlarged lymph nodes with ‘bull neck’ appearance
- may cause respiratory obstruction, paralysis and cardiac failure
- fatal if untreated
- also milder cutaneous form

EPIDEMIOLOGY
- Rare in countries with routine immunisation
- Outbreak in former USSR states in 1990s
- mortality greatest in children and >40 years

DIAGNOSIS
- throat/ nasal/ skin/ulcer swab- identify C.diptheriae (toxigenic)
- Reference lab PCR can confirm toxigenicity within few hours

RESEVIOIR
C. diphtheriae - human reseviour
C. ulcerans - cattle

TRANSMISSION
- C. diphtheriae: direct contact or airborne droplets
- C. Ulcerans: animal contact or consumption of unpasteurised dairy products

SURVEILLANCE
- statutory notification
- vaccine coverage

PREVENT
- Primary vaccinatiion in children’s immunisation schedule.

CONTROL
-cases: barrier nursed, abx, antitoxin, vaccination (booster/primary)
-Contacts (any close contacts with previous 10 days considered at risk): swab, give prophylatic abx, exclude health and social care workers and those working with unvaccinated children, give booster (unless had within last year) or primary vaccination course

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2
Q

Tetanus

A

ORGANISM
clostridium Tetani

CLINICAL FEATURES
-Painful muscular contractions especially of neck and jaw
- often history of tetanus prone wound
- seizures
- respiratory compromise
-can be fatal

EPIDEMIOLOGY
- decreasing in UK since immunisation in 1960s
- occasional cases in IVDU from contaminated needles
- neonatal tetanus from umbilical stump remains major concern in Africa and Asia

DIAGNOSIS
- toxin in serum sample

RESEVIOIR
- Animal and human intestines
- spores in soil contaminated with animal faeces

TRANSMISSION
- dirty wounds
- Contaminated needles
- Abdominal surgery

SURVEILLANCE
- statutory notifications
- vaccine coverage

PREVENTION
- Vaccine in UK primary immunisation schedule

CONTROL
- Tetanus immunoglobulin
- vaccine (booster/primary course)

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3
Q

Polio

A

ORGANISM
poliovirus (3 serotypes, type 2 most virulent)

CLINICAL FEATURES
-normally asymptomatic
- may have mild pyrexia and headache or GI symptoms
- rarely paralysis

EPIDEMIOLOGY
Wild polio types 2 and 3 have been eradicated but wild polio type 2 is still endemic in Pakistan and Afghanistan

DIAGNOSIS
- viral culture
- antibodies

RESEVIOIR
Human

TRANSMISSION
Mainly faeco-oral

SURVEILLANCE
- Statutory notification
- vaccine coverage

PREVENT/ CONTROL
-Primary immunisation in childhood immunisation schedule

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4
Q

Haemophilus

A

ORGANISM
HiB

CLINICAL FEATURES
- Can cause invasive disease
- commonest presentation is meningitis
- can cause pneumonia, epiglottitis, bone and joint infections

EPIDEMIOLOGY
- Prior to vaccine introduction used to be a major cause of UK meningitis
- it is now rare

DIAGNOSIS
- blood/CSF culture
-PCR
- Reference lab for confirmation and typing

RESEVIOIR
Humans

TRANSMISSION
Droplet
Direct contact

SURVEILLANCE
- Enhanced surveillance questionnaire in England
- lab reports
- acute meningitis is notifiable
- Vaccine coverage data

PREVENTION
- vaccination given in primary immunisations. Vaccination prevents carriage

CONTROL
Case: antibiotics, vaccinate (if indicated)

Contacts: household contacts given chemoprophylaxis if vulnerable member in household, vaccinate if indicated

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5
Q

Pneumococcus

A

ORGANISM
Streptococcus Pneumoniae

CLINICAL FEATURES
- can cause pneumonia, meningitis or sepsis

EPIDEMIOLOGY
- mainly effects infants and the elderly
- winter peaks
- reduction in seorotypes covered by vaccine in UK since vaccine introduction (but serotype switching has been seen)

DIAGNOSIS
- culture of sputum/ blood/ CSF
- urinary antigen
- Reference lab for serotyping

RESEVIOIR
- Human

TRANSMISSION
- Direct contact with respiratory secretions

SURVEILLANCE
- Enhanced surveillance in England (all samples sent to reference lab)
- vaccine coverage data

PREVENTION
- Primary immunisation in childhood schedule (PCV)
- PPV recommended for all age >65 years

CONTROL
- case : antibiotics
- Contacts: chemoprophylaxis/ vaccination consider if outbreak in an institution

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6
Q

Mumps

A

ORGANISM
Paramyxovirus

CLINICAL FEATURES
-tenderness and parotid swelling
- orchitis
- pancreatitis
- meningitis

EPIDEMIOLOGY
- incidence in UK decreased with introduction of MMR
- occasional outbreaks/ increases in cases seen likely associated with poor vaccine uptake

DIAGNOSIS
- Serology
- viral culture on saliva/ CSF

RESEVIOIR
- Humans

TRANSMISSION
- direct contact with saliva or droplets of an infected person

SURVEILLANCE
- notifiable
- vaccine coverage

PREVENTION
- included in childhood immunisations

CONTROL
- case: exclude for 5 days after initial parotitis. Check vaccine status
- Contact: consider MMR if not immunised

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6
Q

Menigococcal disease

A

ORGANISM
Neisseria Meningitidis (6 serotypes cause disease A, B, C, W-135, X and Y)

CLINICAL FEATURES
- can cause meningitis or sepsis

EPIDEMIOLOGY
-Endemic worldwide
- highly seasonal- Europe = Winter peak, Africa = dry season peak
- Associated with mass gatherings eg Hajj pilgrimage
- implementation of meningococcal vaccinations in the UK has seen large declines in incidence

DIAGNOSIS
- blood/ CSF culture
- PCR
- reference lab for confirmation and typing

RESEVIOIR
- humans

TRANSMISSION
- direct or indirect person to person spread

SURVEILLANCE
- acute meningitis or meningococcal sepsis are notifiable
- vaccine coverage

PREVENTION
- Given in infant immunisations and at teenage (different serotypes)

CONTROL
- Chemoprophylaxis for close contacts. Vaccination considered depending on serotype.

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7
Q

Tuberculosis

A

ORGANISM
Mycobacterium Tuberculosis
M. Bovis (occasionally)
M. africanum (occasionally)

CLINICAL FEATURES
- long incubation period produces chronic disease with risk of reactivation and fatal without treatment
- cough, weight loss, night sweats

EPIDEMIOLOGY
- In the UK common in immigrant and ethnic groups with the highest rates found in London
- globally in 2022 TB cause 1.3 million deaths
- rate of global TB deaths is declining but not sufficiently to reach WHO targets

DIAGNOSIS
- CXR
- Sputum smear and culture for Acid fast bacilli
- sensitivity testing for multidrug resistant TB
- molecular typing for identifying clusters

RESEVIOIR
- animals and humans

TRANSMISSION
- direct spread from infected case
- bovine tb from ingesting raw milk for infected cows

SURVEILLANCE
- notifiable
- enhanced surveillance
- vaccine coverage

PREVENT
- vaccination offered to selected higher risk infants and immigrants from countries with high incidence of TB (>40 per 100 000)

CONTROL
- cases need to receive adequate treatment, directly observed therapy can be used to ensure course completed
- contacts screened and given prophylaxis if necessary

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8
Q

Measles

A

ORGANISM
A paramyxovirus

CLINICAL FEATURES
- prodromal flu like symptoms
- Kopliks spots
- rash on day 3-4 over trunk, face and limbs
- not itchy
- cough and conjunctivitis
- can cause pneumonitis, pneumonia, encephalitis, miscarriage

EPIDEMIOLOGY
- endemic in developing countries
- levels in UK feel with introduction of MMR however outbreaks occur, particularly in areas of low vaccine coverage
- current outbreak in 2023/24

DIAGNOSIS
- salivary test kit for measles IgM
- serology

RESEVIOIR
Human

TRANSMISSION
Direct contact with salvia or droplets of saliva from infected person
- person to person
- measles is highly infectious

SURVEILLANCE
- notifiable
- vaccine coverage data

CONTROL
- case: exclude for 4 days following rash onset
- Contacts: depending on contact and vulnerability may be considered for IVIG/HNIG or MMR vaccine

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9
Q

Rubella

A

ORGANISM
Rubella virus

CLINICAL FEATURES
-fever, rash, conjunctivitis, pharyngitis
- congenital rubella syndrome

EPIDEMIOLOGY
-declined in UK since introduction of MMR and now UK cases are rare

DIAGNOSIS
- serum or salvia detection of IgM
- viral culture from serum or urine

RESEVIOIR
Human

TRANSMISSION
direct person to person

SURVEILLANCE
Notifiable
Vaccine coverage

PREVENTION
- vaccination in childhood programme

CONTROL
- cases: exclude for 5 days after rash onset
- contacts should avoid pregnant women
- pregnant contacts should be tested and, if susceptible, offered MMR post partum (cannot give during pregnancy)

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10
Q

HPV

A

ORGANISM
human papilloma virus (>100 types, 13 types associated with cervical cancer)

CLINICAL FEATURES
- cervical cancer (mostly types 16 and 18)
- genital warts (mostly types 6 and 11)

EPIDEMIOLOGY
- changing epidemiology since the introduction of the HPV vaccine
- 3.2% of women in UK are estimated to be infected with HPV 16/18

DIAGNOSIS
- PCR test on cells from smear

RESEVIOIR
- Human

TRANSMISSION
- hand warts- close contact
- genital warts/ cervical infection - STI

SURVEILLANCE
- cancer registries
- GUMCAD returns (national STI surveillance system UK)
- vaccine coverage

PREVENTION
- UK early teens immunisation of childhood immunisation schedule
- cervical cancer screening
CONTROL

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11
Q

MRSA

A

ORGANISM
methicillin resistant staphylococcus aureus

CLINICAL FEATURES
- wound infections, pneumonia, conjunctivitis, sepsis

EPIDEMIOLOGY
- incidence of MRSA bacteraemia in the UK has fallen since enhanced surveillance in 2007, it fell quickly until around 2013 and incidence has fluctuated at lower levels since then

DIAGNOSIS
- Microscopy, culture and sensitivity on appropriate specimen

RESEVIOIR
- humans, rarely animals

TRANSMISSION
- direct contact

SURVEILLANCE
- mandatory surveillance scheme for hospital trusts in England

PREVENTION
-Hand hygiene
- compliance with infection control measures
- aseptic technique
- decontamination can prevent colonisation leading to infection

CONTROL
- mandatory surveillance scheme in Uk hospitals

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12
Q

C. diff

A

ORGANISM
clostridium difficile

CLINICAL FEATURES
- diarrhoea post abx
- fever
-pseudomembranous colitis

EPIDEMIOLOGY
- c.diff rates in the UK fell sharply from 2007 and stabilised at a lower level, however incidence has been slowly climbing the last few years
- hospital outbreaks occur
- elderly at greater risk

DIAGNOSIS
- C.diff toxin in stool
- culture and sensitivity

RESEVIOIR
- human (only causes disease when competing gut bacteria killed by abx)

TRANSMISSION
Direct contact
Fomites (eg commodes)

SURVEILLANCE
- mandatory surveillance by NHS trusts

CONTROL
- infection control procedures
- hand hygiene
- isolation of patients
- appropriate abx use

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13
Q

Camplylobacter

A

ORGANISM
mainly campylobacter jejuni

CLINICAL FEATURES
-Ranges from asymptomatic to severe diarrhoea
- about 50% have bloody diarrhoea

EPIDEMIOLOGY
Most common bacterial GI infection in the UK

DIAGNOSIS
Stool microscopy, culture and sensitivity

RESEVIOIR
- GI tract of birds (particularly poultry), and cattle and domestic pets

TRANSMISSION
Animal –> person (water or food contaminated with animal faeces)
Person –> person ( direct contact with faeces of index case)
Raw or undercooked meat, non-pasteurised milk

SURVEILLANCE
- notifiable
-lab reports

PREVENTION
- chlorination of drinking water
- milk pasteurisation
-kitchen hygiene
- cooking meats appropriately
- hand hygiene
- exclusion of symptomatic cases

CONTROL
Cases: enteric precautions

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14
Q

Cholera

A

ORGANISM
Toxin producing vibrio cholerae (bacteria)

CLINICAL FEATURES
watery diarrhoea
vomiting
50% fatality

EPIDEMIOLOGY
- endemic in many developing countries
- rare in the UK - all travel associated

DIAGNOSIS
Stool MC&S
PCR

RESEVIOIR
Untreated/ polluted water

TRANSMISSION
- consumption of untreated water
- contaminated shellfish and foods eaten raw or washed in contaminated water
- person to person spread only likely if hygiene very poor and sanitary facilities inadequate

SURVEILLANCE
- notifiable

PREVENTION
- advice for travellers (boil it, peel it, cook it or forget it)
- vaccination gives short cover and is of little value
- safe drinking water supplies

CONTROL
cases: exclude for 48 hours after first normal stool, enteric precautions. Ensure adequate rehydration and appropriate abx

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15
Q

What is a nosocomial infection

A
  • healthcare related infection
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16
Q

Effects of nosocomial infections on patients (5)

A
  • increased morbidity (pain, anxiety)
  • increased mortality
  • longer stay in hospital
  • increased loss of earnings
  • reduced quality of life
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17
Q

Impact of nosocomial infections on the health service

A
  • increased bed occupancy
  • extended length of stay
  • increased cost associated with treating the infection
  • cost of infection control measures (ie barrier nursing, PPE, cleaning)
  • bed/ward closures
  • require provision of isolation rooms
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18
Q

How are people identified at being at increased risk of spreading GI infection classified

A

Groups A, B , C and D

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19
Q

Increased risk of spreading GI infection: who is in each group

A

GROUP A
People of doubtful personal hygiene or people whose toilet or handwashing/drying facilities are inadequate either at home, work or school

GROUP B
Children who attend preschools or nurseries

GROUP C
People involved in preparing or serving unwrapped food which is not subject to further heating

GROUP D
Clinical and social care staff who have direct contact with highly susceptible people in whom a GI infection would have particularly serious consequences

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20
Q

Cryptosporidoisis

A

ORGANISM
cryptosporidium parvum

CLINICAL FEATURES
- self limiting in healthy individuals
- diarrhoea that may be bloody
- severe illness in immunocompromised that may lead to death

EPIDEMIOLOGY
- seasonal (autumn peak in UK)
- commonest in children

DIAGNOSIS
Stool microscopy
Intestinal biopsy
Serology

RESEVIOIR
-GI tract of humans and animals (particularly farm and domesticated animals)
-Water contaminated with faeces

TRANSMISSION
Person to person
Animal to person
Swimming pool outbreaks

SURVEILLANCE
lab reports

PREVENTION
- hand hygiene
- adequate water treatment
immunocompromised- avoid contact with farm animals, drink boiled water, avoid contact with cases

CONTROL
cases: exclude for 48 hours after first normal stool, avoid swimming for 2 weeks, enteric precautions

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21
Q

Shigellae

A

ORGANISM
Shigella Sonnei (common in UK and mild)
S.dysenteriae, s. flexneri, S.boydii (imported and more severe)

CLINICAL FEATURES
S.Sonnei- mild diarrhoea

Other shigellas:
- watery diarrhoea
- vomiting
- 50% bloody stools

Shigella dysenteriae:
- produces shiga toxin
- toxic megacolon
- HUS
-death

EPIDEMIOLOGY
- Shigella was the second-leading cause of diarrhoeal mortality in 2016 among all ages

DIAGNOSIS
- stool culture
- serotyping
- phage typing

RESEVIOIR
-humans

TRANSMISSION
Person to person
contaminated water/ food
Faeco-oral route

SURVEILLANCE
- infectious bloody diarrhoea and HUS are notifiable
- enhanced surveillance of non-sonnei shigella in the UK

PREVENTION
- hand hygiene
- treatment of drinking and swimming water
- traveller advice

CONTROL
Cases:
-S. sonnei = 48 hours exclusion after first normal stool.
- Other shigella species, case not in at risk group = 48 hours exclusion after first normal stool.
- other shigella species, case in group A-D= microbiological clearances needed (2 negative stools taken 48 hours apart)

Contacts: Contacts of non -sonnei shigella in groups A-D need microbiological clearance before exclusion ends

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22
Q

Verotoxin producing E.coli

A

ORGANISM
- most common in UK is E.coli 0157

CLINICAL FEATURES
- asymptomatic
- diarrhoea
- HUS
- death

EPIDEMIOLOGY
- food borne outbreaks
- greatest in spring/ summer
- highest rates in children

DIAGNOSIS
- Stool MC&S
- biochemical and serological testing
- reference labs for VTEC

RESEVIOIR
GI tract of cattle, goats and other domesticated animals

TRANSMISSION
contaminated food/water
Person to person
Animal to person

SURVEILLANCE
Food poisoning and HUS notifiable

PREVENTION
-Hand hygiene
- adequate cleaning (kitchen)
- precautions during farm visits
- cook food appropriately

CONTROL
Cases: enteric precautions, if not in high risk group exclude for 48 hours following first normal stool, if at risk exclude until microbiological clearance
Contacts: consider exclusion and mircobiological screening based on guidelines

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23
Q

Salmonellosis

A

ORGANISM
Salmonella enteritidis PT4 (associated with eggs and poultry)

Salmonella typhimurium DT104 (increased antibiotic resistance)

CLINICAL FEATURES
- diarrhoea
-rarely abscess, sepsis or meningitis

EPIDEMIOLOGY
- endemic worldwide
- large outbreaks may occur

DIAGNOSIS
- stool culture
- Blood culture
- serotyping
- phage typing

RESEVIOIR
GI tracts of wild and domestic animals, birds (esp poultry), iguanas and occasionally humans

TRANSMISSION
Animal –> person (contaminated food)
Person–> person (faeco-oral)

SURVEILLANCE
Food poisoning is notifiable
Lab reports

PREVENTION
- vaccination of poultry flock
personal/ food hygiene

CONTROL
- case: enteric precautions, exclude for 48 hours after first normal stool

24
Q

Enteric fever (typhoid and paratyphoid fever)

A

Typhoid fever is a disease caused by the bacteria Salmonella Typhi. Paratyphoid fever is a disease caused by the bacteria Salmonella Paratyphi. These diseases cause a similar illness. Paratyphoid infections tend to be less severe and less common than typhoid.

ORGANISM
Salmonella Typhi and paratyphi A (80% in UK), salmonella Typhi and paratyphi B (20% in UK) and salmonella typhi and paratyphi C

CLINICAL FEATURES
- gastroenteritis, fever, headache, malaise, diarrhoea/ constipation, vomiting
- even after treatment a small number of people continue to be colonised with the bacteria, these people can relapse

EPIDEMIOLOGY
- endemic in many developing countries
- mainly travel associated in UK

DIAGNOSIS
- blood, urine, faeces

RESEVIOIR
Humans

TRANSMISSION
-Ingestion of food or water contaminated by faeces or urine of patients or carriers.
- human to human in poor hygiene conditions

SURVEILLANCE
- enteric fever is notifiable
- lab reports
- enhanced surveillance

PREVENTION
- sanitation
-clean water
- hygiene

CONTROL
Cases:
- high risk group= exclude until 3 clear samples, 48 hours apart, taken at least 1 week after abx started
- not high risk group: 48 hours after first normal stool
Contacts: Scene stool

25
Q

Hepatitis A

A

ORGANISM
Hepatitis A

CLINICAL FEATURES
- ranges from asymptomatic to fulminant hepatitis
- young children are commonly asymptomatic, adults are more likely to be symptomatic
- infectious from 2 weeks before jaundice begins

EPIDEMIOLOGY
- endemic in developing countries

DIAGNOSIS
- IgM in blood = acute infection
-IgG in blood = prev infection/immunisation

RESEVIOIR
- Human GI tract

TRANSMISSION
- person to person spread via faeco-oral route and contaminated food
- consumption of food grown or washed in contaminated water (ie shellfish, fruit, vegetable)

SURVEILLANCE
- acute infectious hepatitis is notifiable

PREVENTION
- Advice and immunisation for those travelling

CONTROL
-case: enteric precautions, exclude for 7 days after jaundice (or symptoms if no jaundice)
- contacts: depends on age, risk factors and prev immunisation/ infection. ranges from no action to vaccination and/or HNIG

26
Q

Norovirus

A

ORGANISM
Norovirus

CLINICAL FEATURES
- D and V, normally only lasting a few days
- self limiting in healthy individuals

EPIDEMIOLOGY
-seasonal with winter epidemics in UK
- institutional outbreaks common

DIAGNOSIS
- stool PCR

RESEVIOIR
- humans

TRANSMISSION
- faeco -oral, fomites and contaminated food (esp molluscs)
- transmission high as virus survives in environment for several days and immunity is short lived

SURVEILLANCE
lab reports

PREVENTION
-infection control precautions
- food hygiene
- cleaning and disinfection

CONTROL
Cases: exclude for 48 hours after first normal stool

27
Q

Hepatitis B

A

ORGANISM
Hepatitis B virus

CLINICAL FEATURES
- non specific prodromal illness
- jaundice (often after fever)
- can lead to chronic carriage (90% if infected at birth but 10% if infected as adult)
- chronic carriage confers risk of cirrhosis and HCC
EPIDEMIOLOGY
- endemic in parts of Asia and sub-saharan Africa
- more common in IVDU and Men who have sex with men

DIAGNOSIS
- Viral serology

RESEVIOIR
- Humans

TRANSMISSION
- person to person b y blood borne route- IVDU, Sex, Perinatal

SURVEILLANCE
- infectious hepatitis notifiable

PREVENTION
- HBV vaccine in primary immunisation schedule now
- high risk groups also vaccinated as often not vaccinated as child and serological response checked
- antenatal screening of pregnant mothers

28
Q

What are standard enteric precautions?

A
  • hand hygiene
  • appropriate disposal of excretion
  • appropriate disposal/ cleaning of soiled materials
  • appropriate cleaning of spillages
  • appropriate decontamination of equipment/ facilities
  • education in personal hygiene and hygienic food preparation
29
Q

Hepatitis C

A

ORGANISM
Hepatitis C

CLINICAL FEATURES
- Asymptomatic/ mild infection
- jaundice is unusual
- 80% become carriers, of which 80% develop chronic hepatitis, of which 20% progress to cirrhosis, of which 1% develop HCC each year

EPIDEMIOLOGY
- Endemic worldwide
-HCV is a major cause of liver disease worldwide
- many infected are unaware of their diagnosis

DIAGNOSIS
- anti Hep C antibodies (to confirm prev/ current infection
- if positive PCR for HCV RNA to confirm chronic infection

RESEVIOIR
- humans

TRANSMISSION
- historically transmitted in blood products
- now 80% in IVDU
- body piercing and tattoos
- vertical transmission is rare

SURVEILLANCE
- notifiable as acute hepatitis
- Hepatitis C National Register est in 1998 and ongoing

PREVENTION
- no vaccine
- needle exchange
- safe blood transfusion

CONTROL
- treatment of cases with Direct Acting Antiviral tablets

30
Q

What is dysentery?

A

Dysentery is an infection of the intestines that causes diarrhoea containing blood or mucus.

31
Q

Hepatitis D

A

ORGANISM
Hepatitis D virus

CLINICAL FEATURES
-Exists only in conjunction with Hep B virus
-increases the risk of cirrhosis

DIAGNOSIS
- Serology

RESEVIOIR
- humans

TRANSMISSION
- As for HepB virus
- IVDU and men who have sex with men, perinatal

SURVEILLANCE
PREVENTION
CONTROL

32
Q

Legionella

A

ORGANISM
legionella pneumophilia

CLINICAL FEATURES
- atypical pneumonia resistant to usual abx
- 10-15% mortality

EPIDEMIOLOGY
- About 300 cases a year in the UK

DIAGNOSIS
- sputum culture
- urinary antigen

RESEVIOIR
- environmental water

TRANSMISSION
-airborne droplets/ aerosols (eg cooling towers, air con, hot tubs)

SURVEILLANCE
- notifiable

PREVENTION
- regular maintenance and inspection of water systems
- heat hot water tanks in homes appropriately

32
Q

Gonorrhoea

A

ORGANISM
Neisseria Gonorrhoea

CLINICAL FEATURES
- men more likely to have symptoms than women
- discharge, dysuria, bleeding between periods

EPIDEMIOLOGY
- second most common bacterial STI diagnosed in UK GUM clinics
- highest in those aged 16-24 years
- highest rates in urban areas (esp london)

DIAGNOSIS
- MCand S of urethral or cervical swabs
- PCR of vulvovaginal swabs

RESEVIOIR
Human

TRANSMISSION
Sexual

SURVEILLANCE
GUMCAD
GRASP (gonococcal resistance to antimicrobial surveillance programme)

PREVENTION
- condoms
- testing
-education
- contact tracing

CONTROL
case: Abx
Contacts: test +/- treat

32
Q

Hepatitis E

A

ORGANISM
Hepatitis E

CLINICAL FEATURES
-Illness similar to Hepatitis A
- no chronic carriage or sequel
- most case young/middle aged adults

EPIDEMIOLOGY

DIAGNOSIS
- serology

RESEVIOIR
Humans

TRANSMISSION
faeco-oral
Person to person (low spread)

SURVEILLANCE
- notifiable as acute infectious hepatitis

PREVENTION
- provision of safe water supplies
- no vaccination

33
Q

Influenza

A

ORGANISM
- influenza virus
( 3 types A, B and C)
- type A and B cause most human disease
- Type A is more severe and causes most outbreaks/epidemics

CLINICAL FEATURES
- mild upper resp tract infection
- sometimes diarrhoea and vomiting
- fever, cough
- can lead to severe disease especially in the elderly and be complicated by pneumonitis and bacterial pneumonia

EPIDEMIOLOGY 3 distinct types

  1. seasonal flu: In the northern hemisphere influenza occurs during the winter months
  2. pandemic flu: major flu pandemics can cause morbidity and mortality worldwide, most recently swine flu in 2009

3 Avian influenza (H5N1): associated with close contact with birds. Mainly seen in SE Asia. Concerns this could lead to a pandemic if human to human transmission was to occur

DIAGNOSIS
-PCR
- Antibody testing

RESEVIOIR
Humans for most human infections
New subtypes from birds/mammals (eg swine)

TRANSMISSION
Airborne (droplet)

SURVEILLANCE
- RCGP weekly return service reports on flu like illnesses (syndromic surveillance)
-lab reports
- COVER vaccine coverage data

PREVENTION
- annual flu vaccine

CONTROL
- Cases: tamiflu can be considered in certain circumstances

34
Q

Chlamydia

A

ORGANISM
Chlamydia Trachomatis

CLINICAL FEATURES
- commonest bacterial STI in UK
- highest rates in 16-24 years
- majority asymptomatic
- untreated may lead to pelvic inflammatory disease, ectopic pregnancy and opthalmia neonatorum

EPIDEMIOLOGY
- most commonly diagnosed bacterial STI in GUM clinics in UK
- highest in 16-24 years

DIAGNOSIS
- PCR or culture of urethral, vulvovaginal or cervical swabs

RESEVIOIR
Human

TRANSMISSION
- sexual
- mother to baby

SURVEILLANCE
- GUMCAD
- national chlamydia screening programme

PREVENTION
- national chlamydia screening programme
- condom distribution
-education

CONTROL
- cases: abx
- contacts: test and treat

35
Q

Syphilis

A

ORGANISM
Treponema Pallidum

CLINICAL FEATURES
- primary ulcer
- third of cases develop secondary skin eruption with rash/sores and general malaise/ flu like illness
- tertiary syphilis can present with lesions in skin, bone, organs, CNS (can be 30 years after initial infection)

EPIDEMIOLOGY
- more common in large cities and sea ports
- risk groups include men who have sex with men and young adults

DIAGNOSIS
-Serology

RESEVIOIR
Human

TRANSMISSION
- sex
- mother to baby
- blood transfusion

SURVEILLANCE
-GUMCAD
- enhanced surveillance

PREVENTION
- routine antenatal screening of mothers
-education
- condoms

CONTROL
- cases: antibiotic treamtent
- contact tracing and treatment

36
Q

Hep B serology: significance of HepsAg

A
  • Person is infectious
  • presence for more than 6 months indicates chronic carrier status
37
Q

Hep B serology: Anti-HBs

A

-Antibody to HepBsAg
- Person is immune either through previous infection or vaccination

38
Q

Hep B serology: Total anti-HBc

A
  • total hepatitis core antibody
  • person is immune either from prev infection or vaccination
39
Q

Hep B serology: IgM anti-HBc

A

Acute or recent infection

40
Q

HBeAg

A

-Marker present soon after exposure and then absent within 3 months
-indicates high infectivity

41
Q

Hep B serology: Anti- HBeAg

A

-Develops after HBeAg (except in chronic carriers who may not raise antibody)
- low infectivity

42
Q

malaria

A

ORGANISM
- caused by the protozoa Plasomodium falciparum, p. vivax, p. malariae

CLINICAL FEATURES
- temperature, headache, abdominal pain, jaundice (flu like symptoms)

EPIDEMIOLOGY
- only associated with travel in the UK
- highest burden in Africa
- high risk groups are children and pregnant women
-sickle trait is protective

DIAGNOSIS
- microscopy of blood smears
- rapid diagnostic PCR test

RESEVIOIR
Humans

TRANSMISSION
Vector - anopheles mosquito

SURVEILLANCE
- notifiable in UK
- lab reports

PREVENTION
- travel advice
- Bite prevetion (DEET, nets)
- chemoprophylaxis (anti-malarials)

43
Q

Dengue fever

A

ORGANISM
- caused by a flavivirus (DEN-1, DEN-2, DEN-3, DEN-4)

CLINICAL FEATURES
- fever, headache, myalgia, vomiting, rash
- usually non severe
- can cause haemorrhagic fever in children

EPIDEMIOLOGY
- endemic in tropics
- prevalence increasing markedly
- outbreaks occur 3-4 yearly
- more severe in children

DIAGNOSIS
- PCR

RESEVIOIR
- Humans

TRANSMISSION
- vector -aedes mosquito

SURVEILLANCE
- viral haemorrhagic fever is notifiable
- lab reports

PREVENTION
- avoid bites (DEET)
- aedes aegypti is a day biting mosquito so additional precaution needed in day
- one dengue fever vaccine is licenced in the UK
CONTROL

44
Q

Lyme disease

A

ORGANISM
Borrelia burgdorferi

CLINICAL FEATURES
- early: fever, headache, erythema migrans
- late: arthritis, neurological symptoms, CV symptoms

EPIDEMIOLOGY
- higher risk in some areas of UK ie new forest
- at risk groups include walkers and forestry workers

DIAGNOSIS
- serology

RESEVIOIR
- mice and other rodents

TRANSMISSION
- vector- Ixodes tick

SURVEILLANCE
- lab reports
- enhanced surveillance

PREVENTION
- tick awareness and early removal
- keeping to footpaths

CONTROL
- cases: abx

45
Q

Chicken pox

A

ORGANISM
- varicella zoster

CLINICAL FEATURES
- fever
- vesicular rash
- can cause encephalitis, congenital varicella syndrome
- severe in neonates

EPIDEMIOLOGY
- endemic worldwide
- chickenpox mainly effects young children
- shingles mainly effects elderly

DIAGNOSIS
- clinical

RESEVIOIR
- humans

TRANSMISSION
- direct contact/ airborne droplets
- very infectious until lesions crusted

PREVENTION
- vaccine is available for healthcare staff or immunocompromised if no previous exposure
- routine immunisation being considered in UK
- exclude until lesions have all scabbed

CONTROL
- in some cases VZIg indicated for cases/ exposed

46
Q

CJD

A

ORGANISM
caused by a prion protein

CLINICAL FEATURES
- one of the transmissable spongiform encephalopathies
- neurological symptoms, dementia
- fatal within 1-2 years of diagnosis

EPIDEMIOLOGY
- different types including classical, iatrogenic and variant
- classical is the most common, most cases are sporadic, or may be due to a mutation in the prion protein gene
- iatrogenic cases occur due to contaminated surgical incidents or contaminated blood
- variant CJD was an outbreak in the UK and Europe due to ingestion of meat from bovine spongiform encephalopathy infected cattle

DIAGNOSIS
- clinical
- brain biopsy

RESEVIOIR
- in vCJD infected cattle are the reservoir

TRANSMISSION
- consumption of meat from infected cattle
- contaminated surgical instruments
(but most CJD cases are sporadic)

SURVEILLANCE
- CJD research and surveillance unit

PREVENTION
CJD: disposal of surgical instruments (difficult to destroy prions with decontamination)
vCJD: slaughter of infected cattle and ending the use of meat and bone meat feed
CONTROL

47
Q

Scabies

A

ORGANISM
- mite sarcoptes scabiei

CLINICAL FEATURES
- itchy rash esp between fingers and toes
- itching most intense at night

EPIDEMIOLOGY
- children and young adults most at risk
- winter outbreaks are seen (ie nursing homes)

DIAGNOSIS
- microscopy of skin scrapings

RESEVIOIR
-humans

TRANSMISSION
- close contact

SURVEILLANCE
PREVENTION
- treatment of whole household with permethrin/ malathion
- washing clothes and sheets

48
Q
A

ORGANISM
CLINICAL FEATURES
EPIDEMIOLOGY
DIAGNOSIS
RESEVIOIR
TRANSMISSION
SURVEILLANCE
PREVENTION
CONTROL

49
Q
A

ORGANISM
CLINICAL FEATURES
EPIDEMIOLOGY
DIAGNOSIS
RESEVIOIR
TRANSMISSION
SURVEILLANCE
PREVENTION
CONTROL

50
Q
A

ORGANISM
CLINICAL FEATURES
EPIDEMIOLOGY
DIAGNOSIS
RESEVIOIR
TRANSMISSION
SURVEILLANCE
PREVENTION
CONTROL

51
Q

HIV

A

ORGANISM
Human Immunodeficiency virus

CLINICAL FEATURES
- early symptoms: Asymptomatic/flu like illness
- leads to immunosuppression (loss of CD4 cells)
- reduced CD4 count associated with a higher risk of a range of morbidities

EPIDEMIOLOGY
- emerged in 1980s
- 1 in 16 in the UK now do not know they have a diagnosis of HIV
- globally both incidence of HIV and HIV associated mortality are falling
- prevelance increasing as people are living longer

DIAGNOSIS
- HIV antigen tests
- Viral load/ CD4 count

RESEVIOIR
Human

TRANSMISSION
-Person to person spread
- sex
- blood borne transmission
- vertical transmission

SURVEILLANCE
- HIV and AIDS reporting system (HARS) returns
- lab reports

PREVENTION
- routine antenatal screening
-education
- condoms
- needle exchange
- post exposure prophylaxis

CONTROL
- cases: anti retroviral treatment to reduce viral load, makes infectivity very low and HIV becomes a chronic diease

52
Q

Leptospirosis

A
  • aka weils disease
  • zoonotic infection (transferred from animals to humans) following exposure to urine from infected animals
  • important occupational disease for farmers and abbatoir workers in New Zealand
  • outbreaks are common in developing countries
53
Q

Rheumatic fever

A
  • acute rheumatic fever may occur following a streptococcal throat infection
  • may result in serious damage to heart valves
  • important cause of morbidity and mortality for the indigenous people of new Zealand and Australia
54
Q

Q fever

A
  • caused by coxiella burnetii (bacteria)
  • Acutely: severe flu like illness sometimes associated with hepatitis and pneumonia
  • may progress to a chronic form with endocarditis
  • main carriers are farm animals (cattle, sheep and goats)
  • infection usually occurs through aerosol or dust inhalation when working with infected animals
55
Q

Murray Valley Encephalitis

A
  • Murray Valley encephalitis virus
    -most infections are subclinical
  • symptoms may include fever, rash, confusion, paralysis and seizures
  • permanent neurological disease/ death can occur
  • birds are the natural reservoir
  • mosquitoes infected with the virus transfer it to humans
  • endemic in northern australia
56
Q

Name some important infections in South Africa

A
  • HIV and TB
  • tick bite fever
  • Rabies