Define health care–associated infections (HAIs) and recognize their frequency in modern clinical practice.
Roughly 4\% of hospitalized patients develop an HAI.
Understand the importance of infection prevention in respiratory care.
Identify the three elements that must be present for transmission of infection in a health-care setting.
List patient-related risk factors that increase the probability of hospital-acquired infection.
State the three major routes through which pathogens spread from human sources in the health-care environment.
Describe aerosol transmission and the continuum between droplets and droplet nuclei.
Summarize practical strategies for curbing infection spread in hospitals.
Select and apply chemical disinfectants appropriately when processing respiratory-care equipment.
Outline equipment-handling procedures that limit pathogen dissemination.
Recognize situations that demand special infection-control measures.
Determine when and how to use personal protective equipment (PPE).
Explain how infection-control surveillance programs function.
Definition
Any infection that develops during the course of medical treatment.
Sub-categories by point of origin:
Community-onset: develops outside the hospital.
Hospital-onset / nosocomial: originates \ge 48 hours after admission.
Incidence & Impact
Occur in about 4\% of admitted patients.
Lead to prolonged stays, increased costs, higher morbidity/mortality, and reputational harm.
Institutional Response
Infection Prevention (IP) programs are tasked with lowering HAI risk for patients, staff, and visitors by “breaking the chain of infection.”
Multidisciplinary approach: clinicians, nurses, respiratory therapists, environmental services, administration.
Source (reservoir) of pathogens.
Susceptible host.
Route (mode) of transmission.
Human Reservoirs
Patients, visitors, health-care workers.
Endogenous flora (e.g., skin, upper airway, GI tract) serve as major donor microbes.
Inanimate Reservoirs
Contaminated medical equipment, linens, medications, surfaces.
Patients quickly contaminate the local environment (bed rails, over-bed tables, call buttons).
Host susceptibility varies according to immune competence, comorbidities, and invasive devices.
High-risk factors:
Poorly controlled diabetes mellitus.
Extremes of age (neonates; elder adults).
Immunodeficiency (e.g., HIV infection, chemotherapy-induced neutropenia).
Invasive lines and tubes: IV catheters, endotracheal tubes, urinary catheters.
Significance: Understanding host factors guides targeted prevention strategies such as vaccination, prophylaxis, and device-bundle implementation.
Contact (direct & indirect) – most common.
Droplet – large-particle respiratory sprays.
Airborne – small droplet nuclei that remain suspended.
Direct contact
Physical person-to-person transfer (e.g., turning or bathing patient without gloves).
Less frequent in hospitals compared with indirect.
Indirect contact
Transfer via contaminated intermediate objects or personnel (fomites).
Examples: stethoscope, blood-pressure cuff, improperly disinfected bronchoscope.
Droplet
Particles > 5 µm travel short distances (≈ 1 m) and settle on surfaces.
Representative agents: Neisseria meningitidis, influenza virus.
Airborne
Droplet nuclei \le 5 µm remain suspended for hours, dispersing over long distances.
Classic pathogens: Mycobacterium tuberculosis, measles virus.
Continuum Concept: Droplets may partially desiccate, shrinking into droplet nuclei capable of airborne behavior—underlines the need for flexible precautions.
Leadership at all levels must foster a shared commitment to patient & worker safety.
Everyone empowered to “stop the line” if best practices are threatened.
Comprehensive Unit-Based Safety Program (CUSP) promotes frontline involvement.
Sick workers jeopardize care delivery & patient safety.
Measures include:
Immunizations (influenza, HepB, MMR, varicella, Tdap).
Chemoprophylaxis (e.g., oseltamivir during flu outbreaks).
OSHA standards govern employee safety & reporting.
Standard measures encompass thorough environmental cleaning & equipment reprocessing.
Two tactical clusters:
General sanitation (routine surface disinfection, waste disposal).
Specialized equipment processing (cleaning, disinfection, sterilization schedules).
Definitions
Bactericidal: kills bacteria.
Bacteriostatic: inhibits bacterial growth.
Sporicidal: destroys spores.
Virocidal: inactivates viruses.
Adherence to guidance from HICPAC & CDC.
Key interventions: hand hygiene, PPE compliance, safe injection practices, environmental controls.
Baseline strategy for all patients regardless of diagnosis.
Components:
Hand hygiene before & after patient/environment contact.
Gloves when touching blood, body fluids, mucous membranes.
Mask, eye protection/face shield during procedures that generate splashes/sprays.
Respiratory hygiene/cough etiquette.
Gowns/aprons for procedures with expected clothing contamination.
Use of source-control masks for coughing patients.
Single room preferred; if unavailable, cohort with same pathogen.
Wear gown & gloves upon room entry.
Dedicated equipment or disinfect between uses.
Surgical mask within 1 m of patient.
Patient wears mask during transport.
Pathogens: M. tuberculosis, varicella, rubeola.
Requirements:
Negative-pressure room with \ge 2 air exchanges/hr.
HEPA filtration of exhaust air.
NIOSH-approved N-95 (or higher) respirators for staff.
For highly immunocompromised (e.g., allogeneic stem-cell transplant).
Engineering controls:
HEPA-filtered supply air.
Positive pressure relative to corridor.
\ge 12 air changes/hr.
Sealed room envelope; dust reduction strategies; ban on flowers/plants.
CF patients prone to recurrent infections, bronchiectasis, and multidrug-resistant organisms.
Universal contact precautions in all settings.
Patients should wear surgical masks outside their rooms.
Limit movement whenever feasible.
During necessary transport:
Patient dons appropriate barrier (mask, gown).
Manual resuscitator must have expiratory-side filter for respiratory-isolation patients.
Common device infections:
Ventilator-Associated Pneumonia (VAP).
Catheter-Related Bloodstream Infection (CRBSI/CLABSI).
Catheter-Associated Urinary Tract Infection (CAUTI).
Prevention Bundles: sets of evidence-based actions implemented together (e.g., head-of-bed elevation 30^{\circ}–45^{\circ} plus daily sedation holidays for VAP).
Demonstrated to significantly lower HAI rates.
Physical removal of soil; prerequisite for all further processing.
Use soaps/detergents compatible with device.
Noncritical items (commodes, IV pumps, ventilator surfaces) must be cleaned & low-level disinfected between patients.
Destroys vegetative pathogens but not spores.
Methods:
Heat: pasteurization (e.g., 70–75 °C for 30 min).
Chemical: immersion in EPA-registered disinfectants for specified dwell time.
Total immersion ensures internal & external surfaces treated.
Manufacturer instructions dictate concentration, temperature, exposure time, and rinsing.
Destroys all microorganisms, including spores.
Physical: steam under pressure (autoclave) — typically 121 °C, 15 psi, 15 min.
Chemical: low-temperature options for heat-sensitive devices (ETO gas, hydrogen-peroxide plasma).
In-use maintenance: periodic changing of ventilator circuits, suction tubing according to policy.
Reusable processing: adherence to Spaulding classification (critical, semi-critical, non-critical).
Single-patient disposables: eliminate reprocessing but raise cost & waste issues.
Nebulizers (large- & small-volume) — can aerosolize bacteria.
Ventilator circuits — condensate fosters growth; HEPA filters on expiratory limb reduce contamination.
Bag-valve-mask & suction equipment — surfaces become colonized; require cleaning/disinfection.
Oxygen therapy & pulmonary-function devices — mouthpieces, humidifiers must be disinfected/changed.
Decision variables:
Manufacturer’s Instructions for Use (IFU).
Infection-risk category.
Device material & geometry.
Available institutional resources.
Cost (labor + supplies).
High contamination risk due to mucosal contact.
Transmission drivers:
Failure to perform meticulous manual cleaning before high-level disinfection.
Malfunctioning automated endoscope reprocessors (AERs).
Instrument design flaws (e.g., narrow lumens that trap debris).
Pros: eliminates cross-contamination risk, saves reprocessing labor.
Cons: increased cost, variable quality, environmental burden.
Re-use of intended single-use items may breach regulations and compromise integrity.
Fluid & medication precautions: single-dose vials when possible; never top-off humidifiers.
Continuous monitoring of patients & staff to detect infection/colonization trends.
Infection-Control Committee crafts policy; IP experts execute data collection and feedback.
Common surveillance targets:
Hand-hygiene compliance.
Device-related infections (CLABSI, CAUTI, VAP/VAE).
Three-tier hierarchical surveillance construct:
VAC – sustained \uparrow in daily minimum PEEP or FiO_2 \ge 2 calendar days after baseline stability.
IVAC – VAC plus fever/hypothermia or leukocytosis/-penia and ≥ 4 days of new antibiotics.
PVAP – IVAC with positive quantitative culture above threshold or purulent secretions plus culture growth below threshold.
Purpose: provides objective, automatable metrics that capture a wider spectrum of ventilator complications than classic VAP alone.
Limitation: may over- or under-detect true pneumonias; must be complemented by clinical judgment.
Meticulous hand hygiene remains the single most effective HAI countermeasure.
AII rooms = negative pressure, whereas protective environments = positive pressure — memorize the difference for exams & clinical practice.
Cleaning failure negates all downstream disinfection/sterilization — “dirty in, dirty out.”
Device bundles succeed because each component targets a different link in the infection chain; partial compliance erodes benefit.
Surveillance data are actionable only when fed back to frontline staff in a timely, comprehensible format.