Other bits Flashcards

1
Q

what is IRIS

A

immune reconstitution inflammatory syndrome

Seen in some cases of immunosuppression
when the immune system begins to recover e.g. when ARVs initiated
The immune system then responds to a previously acquired opportunistic infection with an overwhelming inflammatory response
This paradoxically makes the symptoms worse

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2
Q

What are the notifiable diseases

A
Acute encephalitis
Acute infectious hepatitis
Acute meningitis
Acute poliomyelitis
Anthrax
Botulism
Brucellosis
Cholera
Diphtheria
Enteric fever (typhoid or paratyphoid fever)
Food poisoning
Haemolytic uraemic syndrome (HUS)
Infectious bloody diarrhoea
Invasive group A streptococcal disease
Legionnaires’ disease
Leprosy
Malaria
Measles
Meningococcal septicaemia
Mumps
Plague
Rabies
Rubella
Severe Acute Respiratory Syndrome (SARS)
Scarlet fever
Smallpox
Tetanus
Tuberculosis
Typhus
Viral haemorrhagic fever (VHF)
Whooping cough
Yellow fever
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3
Q

Who should be offered the HPV vaccine

A

males <45yrs if MSM or HIV +ve or immunocompromised

Trans-men or trans-women who has / is likely to have receptive anal sex if ≤45 years

Consider in F aged 9 - 26 if a victim of sexual assault and have not started or completed the course

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4
Q

Vaccination schedule for HPV

A

0, 1 and 3- 6 months - if aged 1 5 - 26 = 3 dose schedule

0, 6 - 12 months if 9 - 14 years = 2 dose schedule

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5
Q

types of observational study.

A

2 types of observational study:

descriptive observational studies

analytical observational studies

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6
Q

different types of descriptive observational studies

A

Case report
Case series
Cross-sectional

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7
Q

advantages and disadvantages of case reports

A

Definition - A case report is a profile of an individual patient that has experienced a particular outcome which is reported in detail.

Advantage = useful to document rare outcomes.

Disadvantages = not possible to draw any inference from a case report as it refers to only one observation

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8
Q

advantages and disadvantages of case series

A

Definition = includes a number of patients who have all experienced the same, particular outcome.

Advantage = may suggest a possible hypothesis to investigate with an analytical, observational study or an experimental study

Disadvantage = Although more than one observation - it is not sufficient numbers to draw any robust conclusions.

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9
Q

advantages and disadvantages of cross sectional descriptive studies

A

Definition = A cross-sectional study involves observing a subset of the population at a single point in time - in terms of the frequency and characteristics of an outcome of interest

Advantage = Robust relationships can be identified if a sufficiently large number of people are studied.

Disadvantage = cannot establish causality with a cross-sectional study. No information about the sequence of events is gained. Association only

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10
Q

Types of analytical observational study

A

4 types of analytical observational study:
Ecological studies
Cohort studies (also known as longitudinal studies)
Case-control studies
Cross-sectional studies

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11
Q

advantages and disadvantages of an ecological study

A

An ecological study is one in which the unit of analysis is a population rather than an individual

Advantages = economical / quick / tend to use existing, aggregate data.

Disadvantages = regarded as inferior to individual-level study designs as they only provide indicative rather than compelling evidence of causal relationships because they are susceptible to ecological fallacy

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12
Q

what is a cohort study

A

individuals with a particular characteristic are followed over time + compared with a group who do not have the characteristic, for the occurrence of an outcome of interest.

usually prospective (can be retrospective)
involve collecting data on at least two time points over the study period
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13
Q

advantages and disadvantages of a cohort study

A

Advantages = useful to study relatively rare outcomes
Recall error can be minimised - due to collection of data at regular intervals

Disadvantages = Expensive
Time-consuming
Sensitive to attrition

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14
Q

What is a case-control study

A

case-control study = comparing a group of people who experience the outcome with a group of individuals who do not experience this outcome

Risk factors preceding the outcome are compared between groups

Often selecting matched controls

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15
Q

advantages and disadvantages of a case-control study

A
Advantages = 
Relatively economical
Relatively quick
Can investigate a wide range of factors
Useful for studying rare diseases

Disadvantages =
Prone to ‘selection bias’ of cases and controls
Prone to ‘observer bias’
Difficult to determine sequence of events
Cannot obtain estimates of disease incidence

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16
Q

what is the CONSORT statement

A

an evidence-based, minimum set of recommendations for reporting RCTs.

A standard way for researchers to prepare reports of their trial findings
Facilitating complete and transparent reporting
Aiding critical appraisal and interpretation

17
Q

define prevalence

A

Prevalence is used to measure how commonly a disease or condition occurs in a population.

Calculated as the number of cases in a population at one point in time divided by the total number of persons in the population at that time

aka ‘point prevalence’

prevalence is a proportion

18
Q

Factors influencing prevalence

A

The frequency with which the cases occur and are identified

The average duration of the condition (i.e. time to either recover or die from the condition)

19
Q

Define incidence

A

Incidence = used to measure the number of new cases of a condition that develop in a population at risk during a specified time interval.

Where the denominator is person-time at risk then it is referred to as the ‘incidence rate’

Incidence rate = the number of new cases during a specified time interval divided by the person-time at risk (and so free from the disease) during the study period.

20
Q

How can the relationship between incidence and prevalence be approximated

A

Prevalence = incidence x average duration

21
Q

what is risk ratio

A

The ratio of the risk of having the outcome of interest if in the exposed group
compared to the risk of having the outcome of interest if in the unexposed group

A/(A+C) / B/(B+D)

22
Q

what is the odds ratio

A

The ratio of the odds of having the outcome of interest if in the exposed group
compared to the odds of having the outcome of interest if in the unexposed group

(A/C) / (B/D)

23
Q

what does a relative risk of <1 mean

A

Relative risk value of less than 1.0

= an inverse association

= a decreased risk among the exposed group

i.e. the exposure is protective

24
Q

what does a relative risk of 1 mean

A

Relative risk = 1.0
indicates the incidence of disease in the exposed and non-exposed groups are the same

No association between the exposure and the disease

25
Q

what does a relative risk of >1 mean

A

Relative risk > 1.0

Indicates a positive association

An increased risk among the exposed group

26
Q

what is the difference between register based and opportunistic screening programmes

A

Register-based = where eligible individuals in a defined population are identified and proactively invited for screening using a register

Opportunistic = individuals that come into contact with services are assessed for their eligibility for screening and then invited to be tested.

27
Q

Pros and cons of opportunistic screening

A

Pros - avoids cost of register
avoids potential breach of confidentiality

cons - unlikely to reach all those at risk
the hardest to reach may be most at risk

28
Q

define sensitivity

A

Sensitivity = A fraction

Those with the disease correctly identified by a positive test.

29
Q

define specificity

A

specificity = A fraction

Those without the disease correctly identified by a negative test.

30
Q

Define positive predictive value

A

those with a positive test

who actually have the disease

31
Q

Define negative predictive value

A

those with a negative test

who do not have the disease