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INFECTION
PREVENTION AND
CONTROL
Introduction—Why Infection Control?
Hospital acquired infections are a common
problem—prevalence about 9%
Hospital acquired infections contribute to
AMR
Overuse of antimicrobials (development)
Poor infection control practices (spread)
Introduction—Why Infection Control?
Hospital-acquired infections increase the cost
of health care
 World Bank studies have shown that two-
thirds of developing countries spend more
than 50% of their health care budgets on
hospitals
Effective IC programs are beneficial
They decrease spread of nosocomial
infections, morbidity, mortality, and health
care costs
Introduction—Development of AMR
Poor or absent IC practices, especially in
intensive care units, results in cross-transmission
of antibiotic-resistant bacteria.
Resistant bacteria prompts even greater
antibiotic use by physicians.
Perception of knowledge by physicians of poor
sterilization, disinfection, or patient care
practices prompts increased antibiotic use (e.g.,
broad spectrum and prolonged surgical
prophylaxis in an effort to prevent infections).
Mechanism of action
•Inhibition of bacterial cell wall synthesis
•Inhibition of bacterial cytoplasmic
membrane function
•Inhibition of bacterial nucleic acid
synthesis
•Inhibition of bacterial protein synthesis
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)
6. Infection control (Microbiology)

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6. Infection control (Microbiology)

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  • 10. Introduction—Why Infection Control? Hospital acquired infections are a common problem—prevalence about 9% Hospital acquired infections contribute to AMR Overuse of antimicrobials (development) Poor infection control practices (spread)
  • 11. Introduction—Why Infection Control? Hospital-acquired infections increase the cost of health care  World Bank studies have shown that two- thirds of developing countries spend more than 50% of their health care budgets on hospitals Effective IC programs are beneficial They decrease spread of nosocomial infections, morbidity, mortality, and health care costs
  • 12. Introduction—Development of AMR Poor or absent IC practices, especially in intensive care units, results in cross-transmission of antibiotic-resistant bacteria. Resistant bacteria prompts even greater antibiotic use by physicians. Perception of knowledge by physicians of poor sterilization, disinfection, or patient care practices prompts increased antibiotic use (e.g., broad spectrum and prolonged surgical prophylaxis in an effort to prevent infections).
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  • 121. Mechanism of action •Inhibition of bacterial cell wall synthesis •Inhibition of bacterial cytoplasmic membrane function •Inhibition of bacterial nucleic acid synthesis •Inhibition of bacterial protein synthesis