ID Epidemiology Flashcards

1
Q

what is an epidemic?

when does it become a pandemic?

A

epidemic:

an outbreak; an increase in numbers of cases of an infection over and above expected levels

OR
a single case, or small number of cases of an unusual organism

pandemic: epidemic that travels (epidemic with passport)

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2
Q

whats the difference between epidemic and endemic?

A

An endemic is a disease outbreak that is consistently present but limited to a particular region. This makes the disease spread and rates predictable. e.g. malaria in SSA

epidemic: an unexpected increase in the number of disease cases in a specific geographical area.

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3
Q

what is

a) incidence (& incidence rate)
b) prevalence?

A

a) incidence: measure of probability of infection. infection rate is no. of new cases per pop. at risk in given time
b) prevalence: proportion of infection found to be affecting a particular pop.

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4
Q

X conveys information about the risk of contracting the disease, Y indicates how widespread disease is:

what are X and Y?

A

incidence conveys information about the risk of contracting the disease, prevalence indicates how widespread disease is:

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5
Q

what are different modes of transmission? for ID

A
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6
Q

what is the first case called of transmission?

what is a primary case?

what is a clinica and sub-clinical case

A
  • *index:** first case identified
  • *primary case:** the case that brings infection into population (also get 2/3 cases)
  • *sub-clinical case:** transfer virus to cases
  • *clinical:** where symptoms and virus spread (could be 1/2/3 people)
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7
Q

what are factors that influence disease transmission?

A
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8
Q

what are 6 e.g. of resp. tract infections (viruses)

A
  1. resp. syncytial virus
  2. influenza
  3. COVID
  4. adenovirus
  5. rhinovirus
  6. nipah
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9
Q

which resp. viruses stay in upper resp tract? (4)

which resp. viruses go to low resp tract? (3)

A

infections of upper resp. tract

  1. rhinitis: inflammation of the nose
  2. pharyngitis: inflammation of the pharynx
  3. laryngitis: inflammation of the larynx
  4. conjunctivitis: inflammation of the mucus membrane of the eye

infections of lower resp. tract:

  1. croup: swelling of trachea (causes barking cough)
  2. bronchilotis
  3. pneumonia
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10
Q

how does a bacterial superinfection occur?

A

viral resp tract infections followed by bacterial superinfection:

  • *-mucociliary escalator** (moves mucous out of lungs to be expelled by coughing) **damaged
  • **viral infection OR inflammation can damaeg mucociliary escalator
  • mucous not expelled
  • followed by bacterial superinfection
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11
Q

how u diagnose resp. tract infections? (2)

what is a ct value / high or low ct value?

A

PCR - using a nasal pharyngeal swab:

  • nucleic acids from virus is picked by virus panel -> recognise the viruses
  • (can also check for bacterial panel to d/c if pneumonia is bacterial)
  • ct value: no. of rounds of replication required to ID virus on swab
  • high ct value: need lots of rounds of replication (low virus no.)
  • low ct value: need few rounds to detect to virus
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12
Q

what is order, family, subfamily and genus of COVID?

how are coronaviruses diviied?

what were the intermediate hosts for SARs CoV-1, MERS, SARs CoV-2?

A
  • *order:** Nidovirales
  • *family:** Coronaviridae
  • *subfamily:** Coronaviridae
  • *genus:
  • alpha coronavirus:**common colds (HCoC-NL63, HCoV-229E
  • *- beta coronavirus:** common colds (HCov-HKU1/0), worse: (SARs CoV-1, MERS, SARs CoV-2)
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13
Q
A
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14
Q

(what could have been the intermediate host for covid?)

A

unsure atm, could be:

  • fish market
  • civet cat
  • racoon dog
  • snake
  • pangolin
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15
Q

whats the difference between droplet and airbourne transmission?

A
  • *droplet t:** larger, coughs and sneezes can spread droplets of saliva and mucus.
  • *airborne t:** tiny particles (e.g. produced by talking), are suspended for longer. travel further
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16
Q

what is difference between SARS-CoV-2 and COVID 19?

A

SARS-CoV-2: virus
COVID 19: disease

17
Q

what are symptoms of COVID-19?

A
  • resp. distress
  • fever
  • dry cough
  • GI symptoms
  • dyspnea (Shortness of breath)
  • MSK symptoms (fatigue, joint pain)
  • altered mental status
  • anosmia (loss of smell), dysgeusia (loss taste)
  • alveoli infected: pneumonia
18
Q

differences between SARS-CoV-1/ MERS / COV-2 in :

a) setting
b) infected pop
c) transmission (symptomatic?)
d) death / infections?

A
  • *SARS CoV-1:** Hospital setting, 100% infected had disease, transmission = 24-36hrs after contact, 8098 infections, 774 deaths
  • *MERS:** Hospital setting, most had disease, few asymptomic transmissions, camel reservoir, 866 deaths (34% death rate) , 2521 infections
  • *SARs CoV-2:** public domain, >65 with co-morbid, many asymptomatic transmissions, only 30% have severe disease

first two: disease was obvious - so could be contained

19
Q

what does ebola virus cause?
spread by?
(named after?)
when was big outbreak?

A

ebola virus caueses: haemorrhagic fever
spread: zoonotic disease, then spreads by: transmission of infected blood / bodily fluids (sex, contaminated needles, among family members
infects: primary spread - into blood, secondary spread: lungs, spleen liver
named: after river in Congo
big out break: 2013-15 - 39.5% death rate

20
Q

describe the initiation of Zaire Ebola Virus Outbreak

A

Zaire Ebola Virus Outbreak:

  • Patient Zero: Dec 2013 in Guinea
  • Grandmother infected (who was a nurse), spread different hospital settings: 28 000 people infected
21
Q
A
22
Q

what are clinical features / symptoms of ebola?

A
23
Q

why were ebola outbreaks not controlled in 2014?

A
  • poor countries with fragile healthcare systems
  • hight rate of infection of healthcare workers
  • lack of PPE
  • movement across porous borders
24
Q

how does surveillance and and ring vaccination occur (with ebola?)

A
  • *contact tracing:** sick individuals asked to ID contacts -> traced
  • *community monitoring:** communities w/ infected individuals monitored daily
  • *ring vaccination:** all those near to patient 0, neighbours etc - given vaccine

= reduced infection to zero by 28 june 2018 (in DRC)

25
Q

why not vaccinate everyone for ebola?

A
  • huge population: 81m in DRC.
  • manufacturer (Merck) doesnt have manfacturing capacity to do this many
26
Q

what % of world is infected by influenza (yearly?)
- how many severe cases / deaths/

symptoms? whats a major difference between COVID?

A
  • yearly infections: 15-20% of world pop
  • 3-5m severe cases = 250 - 500 000 deaths a year

symptoms: (see pic)

- vs COVID: v. similar, but instead of total loss of taste and smell in covid, influenza is more stuffy.
-

27
Q

influenza history?

who can catch influenza?

A
  • 1918 (H1N1) pandemic: 20-40 million deaths
  • 1957 (H2N2) - 1 m deaths
  • 1968 (H3N2) - 1m deaths
  • 2009 (H1N1) - 200 000 deaths
  • influena viruses infect lots & lots of animals (e.g. bird flu)
28
Q

describe the genome of influenza / how this influences transmission?
what is transmission cycle like?

A

genome: segmented - many different parts are expressed on individual nucleic acid pieces: if two viruses infecting the same cell -> pieces swap around (reassortment) and get new varients

29
Q

what is influenza virus structure like?

what is influenza virus serology like?

A
  • *- Orthomyxovirus (family)**
  • enveloped
  • surface spikes: Hemagglutinin protein (HA) (16 types), Neuraminidae protein (NA) (9 types)
  • SS(-)RNA
  • 8 segmented genes
  • *- serology:**
  • A = humans, animals and birds
  • B = humans only (more chill)
  • C = humans only (more more chill - mild resp. tract infections)
30
Q

How are virus subtypes named?

A

Subtypes named:

  • differentiated by HA (16 types) and NA (9 types)
  • SO, named by specific HA / NA: e.g H1N1
31
Q

how does influenza change / involve?

A
  • *point mutations**
  • single point mutations only genome - change antigen
  • most meaningful mutations occur in HA1 protein
  • *antigenic shifts:**
  • mixing of genomes: genetic reassortment between circulating human and animal strains. creates novel H/N combinations
  • accounts for emergence of new strains of virus
  • only in type A
32
Q

which type of influenza has the point mutation rate?

A

type A = highest, type C = lowest

33
Q

what faciliates antigenic shift of influenza virus?

A

segemented genomes facilates the genetic reassortment

34
Q

what do u know about zika virus?
vector?
initial disease profile?
when were there outbreaks?

A
  • serological detection through Africa and Asia, but no outbreaks < 20 cases in over 50 yrs
  • vector: mosquito
35
Q

clinical presentation of zika virus?
what % is asymptomatic?
onsset of symptoms takes how long?
symtpms?
spread?

A
  • most (80%) asymptomatic
  • onset of symptoms: 3-12 days
  • fever, rash, headache, conjunctivitis
  • microcephaly (birth defect where a baby’s head is smaller than expected when compared to babies of the same sex and age)
  • spread by mosquito bites. (found in bodily fluids but so far cant see if spread that way)
36
Q

how can u control mosquito spread of diseases?

A
  • vaccines
  • pop. control: insecticides
  • vector compentacy
37
Q

how do u do public health in practise?

A
  • *- surveillance
  • diagnostitcs (**pop-screening)
  • *- immunisation / prevention
  • outbreak management**