Antimicrobial Stewardship
Antimicrobial Stewardship
Why is antibiotic resistance important?
Poses a big threat to global health.
All germs can develop resistance to antibiotics
The number of new antimicrobials being developed has decreased over time so patients are more likely to be resistant to the ones that have been developed and it is important to manage the use of antibiotics more wisely.
Can increase mortality of patients and the amount of time patients spend in hospital.
There is an increase in antimicrobial resistant organisms globally.
Examples of gram positive and gram negative bacteria that require antibiotic treatment -
How do bacteria become resistant to antibiotics?
Antibiotic resistance happens when bacteria change and become resistant to the antibiotics which used to treat the infections that they cause. Antibiotic resistance can occur in humans and animals.
It is predicted that by 2050, 10 million people will die due to antimicrobial resistance.
Antibiotic consumption correlates with antibiotic resistance
Healthcare Associated multidrug resistant infections
All require patient isolation in side room to prevent infection spreading.
ESBL (extended spectrum beta lactamase) | CPE (carbapenemase producing enterobacteriaceae) | VRE (vancomycin resistant enterococci) |
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| CARB (patient colonised with CPE (tag) | CARC (Contact with patient with CPE) |
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| Patient tag to indicate contact with CARB patient |
Solutions to antimicrobial resistance
Infection, prevention and control
Develop new antimicrobials
Preserve the antibiotics we have got!
Antimicrobial Stewardship
The primary goals of antimicrobial stewardship are to -
Optimise Clinical Outcomes
Minimise consequences of antimicrobial use – toxicity, selection of opportunistic pathogens and emergence of resistance (individual and population)
Culture First – microscopy, culture and sensitivity
Empirical treatment – start immediately if the condition is serious or if a treatable infection is likely.
The choice of antibiotic is based on – the likely infecting organism, the local antimicrobial resistance rates and the severity of disease.
It is important to know which patients are tagged for MRSA/ESBL as they need isolating in side rooms.
Follow up sensitivities from microbiologists and aim to narrow the spectrum if an organism is identified to decrease the risk of resistance and the risk of clostridioides difficil which is associated diarrhoea.
Clostridioides Difficile (c.diff)
An opportunistic infection that occurs through the overuse of antibiotics which disrupt the gut flora
Risk Factors =
Older than 65
Extended healthcare stays in hospitals and care homes
Broad spectrum antibiotics
Gastric acid suppressents e.g PPIS (protein pump inhibitors)
Weakened immune system due to steroids, chemo and diabetes
Previous infection
GI surgery
Underlying conditions e.g IBD, cancer, CKD (chronic kidney damage)
Management of C.Diff
Reduce risk by reviewing and stopping antibiotics when appropriate following guidelines
Review PPIs and H2 antagonists and stop if needed or reduce dose.
Avoid antidiarrhoeals
Minimise duration of antibiotics
40-60% risk of further reoccurrence
Treatment of C.diff is usually 10-14 days and treatment is stopped at 10 days if the patient is asymptomatic
Oral Vancomycin is only used to treat C.Diff as it is not systemically absorbed.
If the C-diff is not responding of is worsening refer to microbiologists for testing.
Missed Doses
Patients must not miss their doses of antibiotics because it can lead to resistance, lack of response to treatment which means broader spectrum antimicrobials are used which can lead to resistance.
IV to oral switch
All IV antibiotics should be reviewed after 48 hours of initiation and daily thereafter if appropriate
Some deep-seated infections will require long durations of IV antibiotics E.g. endocarditis, osteomyelitis
May require a micro review for the most suitable oral step down i.e. meropenem
Ensure documentation of indication and review date on drug chart
When to prompt switch?
★ Inflammatory marks improving - Reducing WCC and Reducing CRP (There can be a 48 hr lag on CRP)
★ Stable observations - BP + RR stable and No unexplained tachycardia
★ Apyrexial (absence of fever) for ≥24 hours
★ Able to take oral meds i.e. no GIT dysfunction
CQUINs (Commissioning for quality and innovation)
A framework within the NHS that supports improvements in the quality of services and creation of new, improved patterns of care.
Covers a wide range of areas with the intention to drive transformational change in the NHS.
Infection, Prevention and Control
Responsibilities -
Abide by the Health and Social Care Act 2008 (updated 2015)
Compliance is assessed by the Care Quality Commission (CQC) and the National Health Service improvements (NHSI)
Everyone's Responsibility!
Transmission of infection -
Direct Contact – physical contact with the infected person
Indirect Contact – on the hands/ contact with contaminated objects and equipment
Faecal-oral – from gut to the mouth of susceptible individual
Airborne/Droplet - respiratory droplets through the air
Inoculation/Splashes - via needle stick injuries and splashes to eyes and mouths
Vectors – insects and rodents
Vertical – via the placenta
HAND HYGIENE EXTREMELY IMPORTANT
Follow uniform policy
Change into uniform when arriving and before leaving work
Bare below elbow
Hair tied back
Wash hands regularly
PPE (personal protective equipment)