ID - Hospital Acquired Infections Flashcards

1
Q

Define nosocomial infection.

A

Infection that is diagnosed 48-72 hours after hospital admission (not evident on presentation).

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2
Q

Why is nosocomial infection particularly problematic in ICU patients?

A
EPIC and EPIC II trials identified around 1 in 5 ICU patients will develop nosocomial infection.Most common sites include:- Respiratory- Abdominal- Bacteraemia- Urinary tract

Particularly problematic in ICU due to patient factors and treatment/environmental factors.

Patient factors:
- vulnerable patients
- multiple co-morbidities
- often immunosuppressed or immunodeficient from critical illness
- malnutrition
- unable to tell us of symptoms

Treatment factors:
- invasive devices breach normal barriers to infection
- broad-spectrum antibiotics can damage normal microbiome
- antibiotic resistance organisms and risk of transmission to/contamination of other patients
- loss of cough reflex or clearance of respiratory secretions- recent abdominal contamination or surgery

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3
Q

When would you treat bacteriuria in ICU patients?

A

Commensal bacteriuria in catheterised patients is common as is asymptomatic bacteriuria in elderly patients.Asymptomatic bacteriuria should not be treated.Treatment should be initiated when:
- the patient is symptomatic (LUTS)
- evidence of same organism cultured in blood
- unexplained pyrexia with no other source identified

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4
Q

What is CRBSI?

A

Catheter-related bloodstream infection is a nosocomial infection related to an indwelling vascular device.They account for 10-20% of nosocomial infections in the UK.For diagnosis:- peripheral blood culture positive- no other source of bacteraemia identified- clinical manifestations of infectionPLUS:- Quantitative parameter: culture ratio 5:1 (line to peripheral)AND/OR - Non-quantitative parameter: Time to positivity of catheter sample >2hrs earlier for simultaneous samples.AND/OR - catheter tip sample positive for same organism as peripheral sample

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5
Q

What are the risk factors for CRBSI?

A

Insertion factors
- ANTT- 2% chlorhexadine and 70% alcohol prepCare/Use factors:
- Frequency of access
- TPN

Site factors:
- Subclavian < jugular < femoral
- contiguous infection

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6
Q

What is a CLABSI?

A

Central line associated blood stream infection is a bacteraemia with features of infection that develops with 48 hours of central line insertion that isn’t related to infection at another site.

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7
Q

How can we prevent catheter related blood stream infections.

A

Reduction in risk factors.
The Matching Michigan initiative developed a set of evidence based measures to reduce risk, which have largely become standard practice.Five elements:
1. Aseptic hand washing
2. Strict ANTT with full barrier precautions
3. Use of 2% chlorhexadine and 70% alcohol skin prep
4. Avoidance of femoral route
5. Daily line review and removal if not needed.

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8
Q

What is ventilator associated pneumonia?

A

VAP is the development of pneumonia in a ventilated patient after 48hrs after starting ventilation.It can be classified as early onset (within first 4 days) or late onset (after 4 days).Associated organisms vary;
Early:- Staph- haemophilus- MSSA- ABx sensitive gram -ve
Late:- MRSA- ESBL- pseudomonas

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9
Q

What are the risk factors for ventilator associated pneumonia?

A
  1. Duration of mechanical ventilation
  2. Muscle paralysis/deep sedation
  3. Burns
  4. Trauma
  5. Supine body position
  6. Enteral nutrition
  7. Pulmonary pathology
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10
Q

What can be done to prevent VAP?

A

3 main approaches:1. Reduce colonisation of gastrointestinal tract and oropharynx2. Prevent aspiration3. Limit duration of mechanical ventilationCare bundles:- daily sedation holds- spontaneous ventilation- selective decontamination of digestive tract- Head of bed at 30-45 degrees- regular and frequent physio- chlorhexadine mouth care- subglottic suction

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11
Q

How is VAP diagnosed?

A

Clinical pulmonary infection score (CPIS):TWOCCC
- temperature
- white cell count elevated
- oxygen requirements increased/ P/F ratio decreased
- CXR changes
- chest secretions
- culture of aspirate

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12
Q

What is the management of VAP?

A

Patient should be managed in an ABCDE approach, correcting abnormalities as you find them.
Specific interventions include:
- Antimicrobials based on timing of VAP, previous cultures and known colonisation, then based on positive cultures and sensitivities.
- BAL
- Lung protective ventilation

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13
Q

What is the definition of diarrhoea?

A

WHO definition is of 3 or more loose or liquid stools per day.

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14
Q

What is the incidence of diarrhoea on ICU?

A

25-50%

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15
Q

What is the pathophysiology of diarrhoea?

A

Imbalance between water and solute transport in the GI tract.
4 main causes:
- Osmotic (osmotically active substances in GI which are struggled to absorb e.g enteral feed-associated diarrhoea)
- Inflammatory (inflammed GI mucosa impairs absorption e.g. IBD)
- Secretory (increased secretion or reduced absorption across gut mucosa e.g. enterotoxin production or laxative use).
- Dysmotility (rapid transit time through small bowel which overwhelms the colon e.g. recovery from ileus).

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16
Q

What are the causes of diarrhoea on ICU?

A

Infective and non-infective.
Infective:
- bacterial
- viral
- fungal
- protozoal

Non-infective:
- neoplastic
- mesenteric ischaemia
- IBD
- laxatives
- constipation with overflow
- enteral feed-associated
- antibiotic associated
- short bowel follow surgery

17
Q

What is Clostridium difficile?

A

Spore forming, Toxin-producing gram positive bacillus.
It causes infective diarrhoea which can be a major problem in health-care settings.
It produces Enterotoxin A and cytotoxin B which cause diarrhoea and colonic mucosal inflammation.
Its diagnosis is confirmed by analysis of stool for c.diff culture, galactose-dehydrogenase presence and presence of enterotoxin positive PCR.
Its management is by:
- infection control and isolation and hand washing
- elimination of precipitants (e.g. PPI, broad-spectrum ABx)
- PO/IV Metronidazole- enteral vancomycin
- IV fidaxomicin

18
Q

What are the risk factors for C.difficile

A
  1. Older age
  2. Poor nutritional intake
  3. PPI
  4. Broad-spectrum abx
  5. underlying malignancy
  6. low albumin
  7. renal and pulmonary disease