Sterilisation of anaesthetic equipment and disinfection of operation theater in MD anaesthesia

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sterilisation anaesthetic equipment disinfection operation theatre MD anaesthesia India guidelines

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https://pmc.ncbi.nlm.nih.gov/articles/PMC3821272

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Sterilisation of Anaesthetic Equipment and Disinfection of the Operation Theatre


1. Key Definitions

Before applying any process, the correct terminology must be understood:
TermMeaning
SterilisationComplete destruction of ALL microbial forms, including bacterial spores
High-level disinfection (HLD)Kills all pathogens except large numbers of bacterial spores
Intermediate-level disinfectionKills all pathogens except bacterial endospores
Low-level disinfectionKills most vegetative bacteria and lipid-enveloped viruses
AntisepsisUse of chemical agents on living tissue to inhibit/eliminate microbes
AsepsisWorking systems that prevent microorganisms from reaching a protected environment
  • Medical Microbiology 9e (Mandell), p. 28

2. Spaulding Classification - Foundation for Anaesthetic Equipment

The Spaulding classification determines the level of decontamination required based on risk:
CategoryDefinitionExamples in AnaesthesiaRequired Process
CriticalEnters sterile tissue or bloodstreamSpinal/epidural needles, IV cannulas, arterial lines, CVP cathetersSterilisation
Semi-criticalContacts mucous membranes or non-intact skinLaryngoscope blades, LMA, ET tubes, bronchoscopes, nasopharyngeal airwaysHLD minimum (sterile preferred)
Non-criticalContacts intact skinBP cuffs, ECG electrodes, pulse oximeter probes, anaesthesia machine exteriorLow-level disinfection
Only items used for invasive procedures require sterilisation; for most others, decontamination or disinfection may suffice. - PMC3821272

3. Methods of Sterilisation

A. Autoclaving (Steam Under Pressure) - Gold Standard

  • Mechanism: Moist heat denatures proteins
  • Standard cycle: 121°C for 15 minutes (gravity displacement) or 132°C for 3-4 minutes (pre-vacuum)
  • A drop of 1.7°C increases required exposure time by 48%
  • Suitable for: Metal instruments, glass, linen, rubber ET tubes, reusable metal laryngoscope handles
  • NOT suitable for: Heat/moisture-sensitive items (fiberoptic scopes, electronic equipment, plastic breathing circuits)

B. Ethylene Oxide (ETO) Gas

  • Mechanism: Alkylates nucleic acids and proteins
  • Conditions: 450-1200 mg/L at 29-65°C for 2-5 hours, followed by aeration for 12 hours to eliminate toxic gas
  • Suitable for: Temperature- or pressure-sensitive items - fiberoptic laryngoscopes, flexible bronchoscopes, ventilator components, plastic circuits
  • Limitations: Flammable, explosive, carcinogenic to animals - use only when alternatives are unavailable

C. Hydrogen Peroxide Plasma Gas (STERRAD)

  • Mechanism: Oxidising free radicals destroy cell membranes and enzymes
  • Conditions: 30% H₂O₂ at 55-60°C; the preferred modern replacement for ETO
  • Cycle time: ~1 hour; no toxic residues remain
  • Suitable for: Heat/moisture-sensitive instruments, metal items, electric and fiberoptic cables, rigid endoscopes
  • NOT suitable for: Cellulosic materials (linen, cotton, paper), items that absorb H₂O₂
  • Advantage: Does not require aeration; equipment can be used immediately

D. Glutaraldehyde 2% (Chemical Sterilant)

  • 2% alkaline glutaraldehyde has better microbicidal properties than acid form
  • Sterilisation requires 10-hour immersion; for HLD, 20-45 minutes suffices
  • Equipment must be rinsed thoroughly in sterile solution after removal
  • Safety concern: Respiratory irritant and sensitiser - use in ventilated areas

E. Peracetic Acid (0.2%)

  • Excellent oxidising activity; end products (acetic acid + oxygen) are non-toxic
  • Used in the Steris system for endoscope reprocessing

F. Dry Heat

  • Requires 160°C for 2 hours or 170°C for 1 hour
  • Damages most instruments; not currently recommended for anaesthetic equipment

G. Pasteurisation

  • Hot water at 70°C for 30 minutes
  • Used for breathing circuits, plastic corrugated tubing, humidifiers, nebulisers, face masks
  • Less damaging than autoclaving; reliable, non-toxic, less expensive
  • After pasteurising: dry equipment in a drying cabinet with HEPA filter

4. Methods of Disinfection

Chemical Disinfectants Summary

AgentLevelConcentrationNotes
GlutaraldehydeHigh2-3.2%Toxic; HLD in 20-45 min
Hydrogen peroxideHigh3-25%Safe end products
Chlorine compoundsHigh100-1000 ppm free chlorineHypochlorite; for surfaces/spillage
Ethyl/isopropyl alcoholIntermediate70-95%Protein denaturant; kills vegetative bacteria; INACTIVE against spores
Phenolic compoundsIntermediate/Low0.4-5%For inanimate surfaces only
Iodophors (povidone-iodine)IntermediateVariableSkin/surface disinfection
Quaternary ammonium compoundsLowVariableNon-critical surfaces only
  • Medical Microbiology 9e, p. 28 (Table 3.2)
Important note on alcohol: 70-95% aqueous solutions are optimal. 100% alcohol dehydrates without killing (lethal process requires water molecules). Inactive against bacterial spores and many viruses. - Sherris & Ryan's Medical Microbiology 8e, p. 109

5. Specific Anaesthetic Equipment - Practical Guide

Airway Equipment

ItemMethod
Metal laryngoscope bladesAutoclave (preferred) or HLD with glutaraldehyde
Fiber-optic laryngoscope bladesHLD (cannot autoclave)
LMA (reusable)Autoclave per manufacturer guidelines (usually up to 40 cycles)
ET tubesSingle-use only; discard after each patient
Oropharyngeal/nasopharyngeal airwaysSingle-use; or autoclave if reusable
Bronchoscope (flexible)HLD with glutaraldehyde or peracetic acid; ETO for sterilisation

Breathing Systems and Circuits

  • Disposable breathing circuits: Single patient use; discard after each case
  • Reusable circuits: Autoclaving or pasteurisation (70°C for 30 min)
  • Bacterial/viral filters (HME filters) placed at the patient end of the circuit greatly reduce circuit contamination and extend reuse interval
  • Soda lime canisters: Routine replacement; the canister itself can be autoclaved when empty

Anaesthesia Machine

  • Internal components (rebreathing valves, CO₂ absorber housing): Dismantle and autoclave periodically
  • External surfaces (control knobs, switches, trolley surface): Wipe with 70% isopropyl alcohol between cases
  • Ventilator bellows and housing: Dismantle and autoclave or HLD
  • Flowmeter knobs and monitor surfaces: Low-level disinfection with alcohol wipes

Invasive Monitoring Equipment

  • Arterial line kits, CVP sets, PA catheters: Sterile, single-use
  • Spinal/epidural needles and kits: Sterile, single-use (commercially gamma-irradiated)
  • Transducer domes: Sterile, disposable

6. Operation Theatre Disinfection

Zones of the OT Complex (Pye's Surgical Handicraft)

The OT is divided into zones to maintain asepsis:
  1. Outer zone (unrestricted) - corridors, changing rooms
  2. Clean zone (semi-restricted) - scrub areas, equipment storage, anaesthetic room
  3. Sterile zone (restricted) - the operating theatre itself
  4. Disposal zone - dirty corridor for soiled materials and waste
Entry protocols:
  • All personnel must change to OT clothing (cotton, freshly laundered) before entering
  • Caps and disposable masks worn at all times (masks become permeable with time - change after long procedures)
  • Antistatic boots or shoes restricted to OT use only
  • OT is positively ventilated - all doors must remain closed to maintain the pressure differential
  • One-way traffic: separate entry and exit doors minimise contamination risk
  • Patients transferred to OT trolley/table before entering; ward beds/trolleys should not enter the OT

Ventilation

  • Ultra-clean ventilation (laminar airflow) for orthopaedic and cardiac surgery: >300 air changes/hour
  • Standard OT: 20-25 air changes per hour with HEPA-filtered air
  • Positive pressure relative to corridors prevents ingress of contaminated air

Surface and Floor Disinfection

  • Between cases: Wipe all surfaces (OT table, anaesthesia machine trolley, IV poles, overhead light handles) with freshly prepared hypochlorite (1000 ppm) or phenolic disinfectant
  • End of day: Thorough mopping of floors with phenolic disinfectant; wipe all horizontal surfaces
  • Fumigation (terminal/weekly): Formaldehyde gas (formalin 40%) or paraformaldehyde pellets. Procedure:
    • Close all doors/windows, seal gaps
    • Calculate volume (length × breadth × height)
    • Formalin: 500 mL/1000 cubic feet; heat to vaporise
    • Exposure time: minimum 24 hours
    • Potassium permanganate (KMnO₄) can be used to neutralise/oxidise formalin vapour after fumigation
    • Aerate thoroughly before allowing entry
  • Modern alternative to formaldehyde: Hydrogen peroxide vapour (HPV) systems - more effective, less toxic, used in infection outbreaks

OT Table and Equipment

  • OT table: Wipe with hypochlorite after each case; detailed disinfection at end of list
  • Equipment packs returning from Central Sterile Supply Department (CSSD): Check for cleanliness, completeness, and sterility indicators (autoclave tape colour change, internal chemical indicator vials)
  • Instrument trays: Autoclave tape changes colour; vial of fluid within the pack changes colour - both confirm sterilisation

7. Infection Control Measures Specific to Anaesthesia Practice

Hand Hygiene

  • Handwashing with soap and water: Standard pre/post patient contact
  • Alcohol hand rub (70% isopropyl): Between procedures and before touching clean areas
  • The WHO 5 Moments of Hand Hygiene apply to anaesthesia practice

Anaesthesia Work Area

  • The anaesthesia work area (the anaesthetic cart and surrounding region) is a documented source of pathogen transmission
  • Use single-use syringes and needles - never re-use
  • Needle-stick protocol: Immediate first aid, report, test donor and recipient, post-exposure prophylaxis if indicated
  • Label all syringes immediately after drawing up
  • Separate clean and contaminated areas on the anaesthesia cart
  • Use alcohol wipes to disinfect injection ports and vial tops before each access

Single-Use vs. Reusable Equipment

Prefer Single-UseReusable with Sterilisation
ET tubes, spinal needles, IV cannulasMetal laryngoscope blades (autoclave)
Gloves, syringes, needlesLMA (up to manufacturer limit)
Breathing circuits (ideally)Rebreathing valves (autoclave)
Arterial/CVP setsMetal airways

8. Resistance Hierarchy of Microorganisms (Sterilisation Challenge)

From most to least resistant (relevant for choosing the correct method):
  1. Prions (most resistant - not inactivated by standard HLD; require 134°C for 18 min in porous-load autoclave, or 1M NaOH)
  2. Bacterial spores (C. difficile, Bacillus)
  3. Mycobacteria (M. tuberculosis)
  4. Non-enveloped viruses (hepatitis A, poliovirus, norovirus)
  5. Fungi
  6. Vegetative bacteria, enveloped viruses (HIV, HBV, HCV)
  7. Enveloped viruses (easiest to kill - killed by intermediate disinfectants)
Prions are not inactivated by high-level disinfection - Sleisenger & Fordtran's Gastroenterology

9. Monitoring of Sterilisation Efficacy

TypeExamplesPurpose
Mechanical indicatorsTemperature/pressure gauges, printoutConfirm cycle parameters were met
Chemical indicatorsAutoclave tape (colour change), Bowie-Dick testConfirm heat/chemical exposure
Biological indicatorsGeobacillus stearothermophilus spores for steam; Bacillus atrophaeus for ETOTrue test of sterilisation efficacy
  • Packs should be checked for indicator colour change on receipt from CSSD before use in theatre - Pye's Surgical Handicraft, p. 121

Summary Points for MD Anaesthesia Exam

  1. Spaulding classification determines the level required (Critical=sterile, Semi-critical=HLD, Non-critical=LLD)
  2. Autoclave (121°C/15 min) is the gold standard for heat-stable items
  3. ETO for heat-sensitive items; must aerate 12 hours post-sterilisation
  4. Plasma gas sterilisation is the modern ETO replacement; no toxic residue
  5. 2% glutaraldehyde - HLD in 20-45 min, sterilisation in 10 hours; must be rinsed in sterile water
  6. Pasteurisation (70°C/30 min) for breathing circuits and plastic equipment
  7. OT fumigation with formalin (500 mL/1000 cu ft) for 24 hours; KMnO₄ used to neutralise
  8. OT uses positive pressure ventilation with 20-25 air changes/hour (laminar flow for ortho/cardiac)
  9. Bacterial/viral circuit filters (HME) at the patient port significantly reduce the need for circuit sterilisation
  10. Prions require special high-temperature protocols; not destroyed by routine HLD
Key references used: Sherris & Ryan's Medical Microbiology 8e; Medical Microbiology 9e (Murray); Pye's Surgical Handicraft 22nd ed; Cleaning and Sterilisation of Anaesthetic Equipment, PMC3821272
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