Communicable Diseases, Meningococcal Septicemia, HIV, Influenza, Tuberculosis, SARS Flashcards

1
Q

changes in Medical Thinking:

A

Development of public health strategies
• Quarantine
• sanitation
• urban clean ups
• magic bullets -quinine penicillin, antibiotics
•Concealment: China and SARS – Naples and cholera
Ethical issues of human experimentation

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2
Q

Methicillin – Resistant Staphylococcus Aureus Infections

A

MRSA is a term used to describe a number of strains of bacteria in
particular Staphylococcus aureus that are resistant to a number of
antibiotics including methicillin.
Symptoms most commonly localised to the skin signs of redness, swelling,
pain, pus and area is hot to touch. May progress to become boils,
abscesses , cellulitis.
Patient may also present with signs of sepsis – malaise, febrile, rigors,
SOB, dizziness secondary to hypotension or pneumon

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3
Q

Those at Risk of MRSA:

A
  • People with weak immune systems (HIV/AIDS, cancer patients,
    immunocompromised patients)
  • Young children
  • Elderly people
  • People staying or working in a health care for prolonged time
  • People who spend time in enclosed high population density area
    including occupants of homeless shelters, prison inmates, and any
    common areas i.e.. Leisure centres/gyms et
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4
Q

Why is MRSA important to paramedics?

A

Numerous recent studies have been conducted worldwide in testing for the
presence of MRSA in Ambulances.
Outstandingly one study by Kurt B. Stevenson et al. in Southern Maine (USA)
reported 49% of the ambulances in the study had at least one positive area
for MRSA. Other studies report much lower percentages.
Another study by Merlin et al. highlighted the presence of MRSA on medical
practitioners Stethoscopes.
On placement how many times have you seen paramedics disinfect their
stethoscopes after each patient? Yet their partner has disinfected the entire stretcher with VIRKON and hard surfaces while their partner was completing
their VACIS.

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5
Q

Meningococcal Septicaemia;

A
Bacterial infection leading to sepsis 
Signs & Symptoms:
Neck Stiffness/Joint Pain
Altered Conscious State
Headache
Photophobia
Febrile
Nausea & Vomiting
Tachypnoea
Tachycardia (Bradycardia late sign)
Hypotension
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6
Q

Which rash is which?

A

Meningococcal Septicaemia is recognised for its Blue/Purple Rash that is non blanching. Tumbler Test – If a glass (i.e.. Tumbler) is held against the rash the rash will not blanch or change colour.

VS

Urticaria
– Or hives are pale red, raised, itchy bumps resultant from allergic/anaphylaxis reaction\
Hand, foot & Mouth Disease
– body rash followed by sores with blisters on palms of hand, soles of
feet, and sometimes on the lips. The rash is rarely itchy for children, but can be extremely itchy

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7
Q

Severe sepsis/meningococcal septicaemia or meningitis paramedic management:

A

Is it severe sepsis or is it meningococcal septicaemia or meningitis? Does this
affect our treatment?

PPE! (particularly if advanced airway management is required as it is spread
via airway secretions & droplets. Close contact and breathing in this bacteria
may lead to bacteria penetrating your larynx and nasal passages)
Ceftriaxone
Adult – 1g Ceftriaxone
IM – diluted with 3.5ml lignocaine (1g in 4ml)
IV – diluted with 9.5 ml water for injection (1g in 10ml)
Children – 50mg/kg
IM ONLY! – diluted with 3.5ml lignocaine.
(if >20kg will receive adult dose)
NOTIFY receiving hospital!!
Notify DTM for follow up for possible staff exposure

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8
Q

HIV/AIDS:

A

Member of the retrovirus family that causes acquired immunodeficiency syndrome (AIDS)
• Essentially progressive deficiency of immune cells, activation, and immune response
Transfer of disease via:
• Blood and body fluids i.e.. Semen, vaginal or cervical secretions
Directly transmitted person to person by:
Anal or vaginal sex
Across the placenta/breast milk
Direct contact with infected body fluids or blood on mucous membranes or open wounds
Indirect Transmission via:
Blood transfusion with whole blood or blood products
Transplanted tissues and organs
Needle-stick injuries or contaminated needles/syringes
Can transmit as either:
• Free virus particles
• Infected immune cells

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9
Q

HIV risk factors:

A
  • High Risk Sexual behaviour – sexual intercourse, particularly anal
    sex without use of a condom
  • IV drug use – especially relating to sharing of needles (decreased
    risk through Australian implementation of free needles policies)
  • Blood or Blood product transfusion recipients prior to routine
    screening (1985)
  • Infants born of HIV positive mother – remains a significant issue
    in African countries.
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10
Q

HIV to AIDS:

A

Most of the HIV infected population die of AIDS:

  • Opportunistic infections
  • Malignancies
  • Cardiovascular disease

Most develop AIDS within 10 years depending on:

  • Co-morbidities
  • Environmental
  • Health care access

Treatment with antiretroviral therapy significantly impacts on clinical
prediction

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11
Q

HIV signs and symptoms:

A
  • Elevated viral load
  • Acute infection
  • Fever
  • Rash
  • Malaise+++
  • Oesophageal abrasions and lesions
  • Latency
  • Very few symptoms approx. several years
  • AIDS
  • Various opportunistic infections
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12
Q

Acute HIV infection:

A

Introduction of virus
• Rapid viral replication stage
• Peripheral blood may display approx. 1-10 billion replicated viruses
• Extreme depletion of CD4 cells!!
• CD* T cells destroy the infected CD4 cells
• B cell produces antibodies
• Seroconversion
• Rebound CD4 cell re-population
• At this stage most develop an influenza infection!! &
• Constitutional symptoms

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13
Q

Chronic HIV infection:

A

• Powerful immune response
-Lasts anywhere from approx. 2 weeks -20 years if treated

• Activation of virus within lymph nodes
- Surrounding lymph tissues rich in CD4 population become infect

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14
Q

AIDS:

A
When CD4 cell numbers reach a critically low level and CMI is completely 
depleted:
• Opportunistic infections ensue:
• Respiratory compromise
• Rashes
• Ulcerations
• Tuberculosis
• Pneumonia

Super infections with no immunity!

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15
Q

clinical perspective

A

Opportunistic:
• Infections
• Malignancies

The virus itself supresses the activity of the bone marrow:
• Low WBC
• Low haemoglobins
• Anaemia's
• Constitutional symptoms
• Weight loss
• Anorexia
• Night sweats
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16
Q

Impact on Paramedic Practice:

A

Impact on Paramedic Practice

  • UNIVERSAL PRECAUTIONS (GLOVES/GOGGLES)!!!!
    Increased risk to paramedics if exposure to:
  • Large amount of blood i.e.. Exsanguination
  • Contact with instrument or tool contaminated with blood (needle stick injury)
  • Potential assault in the presence of open wounds.
  • Important to note that these patients should be treated the same as any other
    patient. Do NOT be prejudice or judgemental particularly if you have no idea how the patient was infected
  • Often these patients will not present to you due to HIV infection but rather due
    to complications or secondary infections.
17
Q

Influenza

A
  • In 2009 influenza type A (H1N1 – haemagglutinin neuraminidase glycoprotein)
    emerged from animals:
    Pig to humans
  • Epidemic emerged as a result

• Influenza is a virus that has a segmented genome:
• Has eight segments:
• This means the virus can interact with other influenza viruses when a
single person is co-infected with
both types of viruses:
•Segments can be exchanged between viruses and potentially new
viruses can emerge from the interaction

18
Q

There are two types of genetic changes that can occur with influenza viruses these are..

A

There are two types of genetic changes that can occur with influenza viruses:

Minor changes – referred to as antigenic drift
• Minor changes in any one of the genes that codes for haemagglutinin or neuraminidase
• Result in subtle differences in the surface folds or structure of the virus:
This is why we have updated influenza vaccines!

Infectious disease surveillance is about identifying trends in virus
strains and developing vaccines for use

Antigenic drift promotes the development of seasonal vaccines

19
Q

2013 Influenza Vaccine - As stated on Australian Department of Health and Ageing Website

A

2013 Influenza Vaccine
As stated on Australian Department of Health and Ageing Website

The Australian Influenza Vaccine Committee (AIVC) met on 3 October 2012,
and agreed to adopt the WHO recommendations (Sep 2012).
The Committee decided that the influenza vaccine components for the 2013
season should contain the following:

  • A (H1N1): an A/California/7/2009 (H1N1) - like virus, 15 μg HA per dose
  • A (H3N2): an A/Victoria/361/2011 (H3N2) - like virus, 15 μg HA per dose

The Therapeutic Goods Administration (TGA) considers the viruses… as
suitable vaccine strains for H1N1, H3N2 and B-Yamagata/16/88 lineage viruses.

20
Q

Why the Elderly weren’t affected by

H1N1:

A

Older individuals that did not get infected with H1N1 was due to the fact that
those elderly populations were more likely to be alive anytime from 1918
onwards…

The 1918 pandemic flu that caused catastrophic mortality was a swine flu –
remains in many influenza strains today – remains in our memory

21
Q

influenza - how is it different?

A
  • Sudden onset
    • Begins with chills and fever 38-39
    • Aches and pains predominately to the legs and back
- S&S
• Fever
• Cough
• Congestion
• Aches
• Fatigue ++
• Headache
• +/- nausea/vomiting
Differential from common cold
• SO & extreme fatigue
• Shouldn't be mistaken for ‘Man Flu’ (Male version of the common col
22
Q

influenza:

A

Transmission:
• Transmission from person to person occurs prior to onset of
symptoms!
• Remain highly infective 3-5 days after infection!

Mode of transmission:
Direct transmission
• Sneezing, coughing etc.

Airborne
• Aerosols etc.
Hand to mouth, eye, hand etc.

23
Q

influenza - Paramedic Management

A
  • PPE (gloves/goggles/mask)
  • Treat symptomatically
  • Transportation with patient adopting respective PPE (face mask)
  • Notification of hospital for isolation of patient if necessary
  • VIRCON EVERYTHING!
24
Q

Tuberculosis:

A
  • Tuberculosis has recently re-emerged as a major health concern
  • 2 million persons worldwide die of tuberculosis and 9 million become infected
    United States, approximately 14000 cases of tuberculosis were reported in 2006
  • In contrast National Notifiable Diseases Surveillance System in Australia reported
    1,194 cases in 2008 and 1,322 in 2009 respectively.

-The incidence of TB in Australia was 5.6 cases per 100,000 population in 2008
and 6.0 per 100,000 in 2009, similar to rates since 1986.
In both 2

25
Q

Prevalence of tuberculosis:

A

Prevalence of tuberculosis is continuing to increase because of:

• patients infected with human immunodeficiency virus
• bacterial resistance to medications
• increased international travel and immigration from countries with high
prevalence
• growing numbers of the homeless and drug abuser

26
Q

Aetiology

A
  • Tuberculosis is an infection caused by
    aerobic bacterium Mycobacterium tuberculosis

Have a unique cell wall structure crucial to their adaptive capacity

Cell wall contains
mycolic acid, covalently attached to the underlying peptidoglycan-bound polysaccharide providing an enhanced lipid barrier

An important component of the cell wall architecture is lipoarabinomannan
, a carbohydrate structural antigen on the outside of the organism that is immunogenic and facilitates the
survival of mycobacteria within macrophages

27
Q

Disease transmission

A

Droplet formation - coughing, sneezing, yawning, talking…

Droplets can remain airborne for minutes to hours after
expectoration

Influenza is broken down quickly by heat and UV

Introduction of M tuberculosis into the lungs leads to infection of the respiratory system; however, the organisms can spread to other organs, such as the lymphatics, pleura, bones/joints,
or meninges, and cause extrapulmonary tuberculosis

28
Q

Pathophysiology of TB:

A
  • Infectious droplets reside in the airways.
    The majority of the bacilli are trapped in the upper airways where the mucus-secreting goblet
    cells exist
    M. tuberculosis
    usually enters the alveolar passages of exposed humans in an aerosol droplet,
    where its first contact is thought be with resident macrophages, but it is also possible that
    bacteria can be initially ingested by alveolar epithelial type II pneumocytes.
    TB infection happens in 4 stages: the initial macrophage response, the growth stage, the immune
    control stage, and the lung cavitation stage. These four stages happen over roughly one month.
    In stage 3 the lungs, the TB bacilli and macrophages that swallowed them build a round complex
    – with TB bacilli and infected macrophages in the middle and healthy macrophages surrounding
    them. This is called a Ghon focus, after the Austrian pathologist who first described it. Often TB
    bacilli also infect the surrounding lymph nodes. The combination of a complex in the lung tissue
    and an infected local lymph node is called the primary complex (also Ghon comple
29
Q

Pathophysiology of TB:

A
  • Infectious droplets reside in the airways.
  • The majority of the bacilli are trapped in the upper airways where the mucus-secreting goblet cells exist
  • M. tuberculosis
    usually enters the alveolar passages of exposed humans in an aerosol droplet,
    where its first contact is thought be with resident macrophages, but it is also possible that bacteria can be initially ingested by alveolar epithelial type II pneumocytes.
  • TB infection happens in 4 stages: the initial macrophage response, the growth stage, the immune
    control stage, and the lung cavitation stage. These four stages happen over roughly one month.

In stage 3 the lungs, the TB bacilli and macrophages that swallowed them build a round complex – with TB bacilli and infected macrophages in the middle and healthy macrophages surrounding
them. This is called a Ghon focus, after the Austrian pathologist who first described it. Often TB bacilli also infect the surrounding lymph nodes. The combination of a complex in the lung tissue
and an infected local lymph node is called the primary complex (also Ghon complex)

30
Q

TB symptoms:

A
A cough that lasts for more than three weeks 
• Fevers 
• Unexplained weight loss 
• Night sweats 
• Extreme lethargy
• Loss of appetite 
• Blood stained sputum/cough
31
Q

TB paramedic management:

A
  • PPE (specifically respiratory protection)
  • Treat symptomatically
  • Transportation with patient adopting respective PPE
  • Notification of hospital for isolation of patient +++ (hospitals often only have one isolation room in the ED
32
Q

Severe Acute Respiratory Syndrome

(SARS):

A

Caused by virus SARS associated coronavirus (SARS-CoV)

Global Threat from 2003, first known cases in China in 2002

Transmitted by droplets (airborne) from coughing/sneezing. Also due to
contact with contaminated services (object -hands-mouth/eyes)

Symptoms: 2-7 days
Flu like symptoms (fever often > 38, malaise, headache,
rigors, body aches)

> 7 days
Cough (usually non productive), dyspnoea and diarrhoea

Severe cases, rapid increase in respiratory distress, oxygen desaturation +/- 
ICU admin (20% of cases)

Predominantly lower respiratory tract but may have rhinnohoea, sore thro

33
Q

Paramedic management/history taking:

A

In the presence of SOB and Fever ask patient if:

  • They have had close contact with a person who is a suspect or
    probable case
    of SARS
  • A history of travel to an area with recent local cases of SARS
  • Residing in an area with recent local transmission of SARS

PPE +++ (mask for patient, bystanders/family and paramedics)

Treat symptomatically

Notification of hospital for isolation of patient +++ (hospitals often only have one isolation room in the ED)

Vircon/sanitise all equipment and vehicle once case completed.

Notify DTM of possible exposure

34
Q

What to do if you are exposed to a

possible communicable disease?

A

• Complete Hazard/Injury/Illness form (HII) or incident report form

• Notify Duty Team Manager ASAP who will notify Healthcare provider
and/or University if it occurs on Clinical Placement

• Follow up with review with local GP where required

• If extended period of time off required complete WorkCover
documentation

35
Q

when not to go to work?

A
  • Episode of Gastro in which return to work is less than 48hours after
    resolving of symptoms
    • If you have the flu/contagious infection i.e. Conjunctivitis, tonsillitis,
    chicken pox etc.
36
Q

Reminder regarding Communicable Disease:

A

• Treat all your patients the same – do not be judgmental/prejudicial or treat your patients differently because
there is a possibility of an communicable disease/infection.

• Don’t avoid doing things for your patients if you think they have a
communicable disease such as advance airway/IV cannulation/IM
injections, wound dressing and splinting.