Air Readiness: Why Emergency Preparedness Must Include Indoor Air Quality and Disinfection
J. Hudson Garrett Jr., Ph.D., MSN, MPH, MBA, IP-BC, PLNC, CFER, AS-BC, VA-BC, CMRP, HACP, HACP-IC, HACP-PE, LTC-CIP, CIC, AL-CIP, CAIP, DICO-C, CPPS, CCHR-S, CPHQ, CVAHP, CPXP, CDIPC, CPHRM, CHIPP-B, FACDONA, FAAPM, eFACHDM, FAPIC, FAOM, FRSPH, FNAP, FAHVAP, FACHE, FSHEA, FIDSA

When the next pandemic wave, wildfire season, or mass-casualty event hits, the quality of the air inside our healthcare facilities will either slow the crisis—or accelerate it. Emergency preparedness plans that focus only on beds, PPE, and staffing overlook a critical, controllable variable: air. Viruses, bacteria, smoke, dust, and chemical irritants all move through it; staff and patients breathe it thousands of times a day. Building “air readiness” into emergency operations is no longer optional—it’s core resilience.
The Multi-Hazard Case for “Air Readiness”
Preparedness must anticipate multiple airborne threats. Respiratory pathogens spread via aerosols in crowded triage areas and waiting rooms. Wildfire smoke can infiltrate buildings hundreds of miles away, raising fine particulate levels that worsen respiratory and cardiac conditions. After storms or infrastructure failures, humidity spikes and power interruptions can degrade filtration and pressurization, allowing contaminants to travel between zones. A single strategy won’t address all of it; a layered approach will.
From Ventilation to Verification
Traditional plans often stop at “meet code.” In emergencies, proof of performance matters more than prescriptive checklists. A robust program includes:
- Ventilation: Ensure outdoor air and air-change targets can be met in surge modes without compromising temperature or humidity. Pre-plan “airflow ladders” for triage tents, PACUs converted to ICUs, and overflow wards.
- Filtration: Match filter efficiency to risk (e.g., MERV 13+ for general areas; HEPA for high-risk spaces). Stockpile filters, not just masks.
- Air Disinfection: Add active technologies—in-room, autonomous HEPA units that are portable—to reduce viable airborne pathogens between people, especially where ventilation cannot be upgraded quickly or is not functional.
- Pressurization: Maintain negative pressure in isolation zones and positive pressure in ORs; instrument these rooms so facilities can see drift early.
- Monitoring: Use continuous sensing (e.g., differential pressure, CO₂ as a ventilation proxy, particles) and alarm thresholds. In a crisis, you can only manage what you measure.
Design for Surge—Not Just Steady State
Crises demand rapid reconfiguration. Pre-engineer surge playbooks that specify how to convert spaces within hours:
- Zoning: Pre-label electrical, duct, and data access for quick deployment of portable HEPA or UV devices. Map clean/dirty corridors and don/doff areas.
- Mobile Solutions: Maintain a fleet of portable air cleaners sized to room volumes, with casters, spare filters, and power redundancy. Keep a cache for ambulances, triage tents, and long-term care affiliates.
- Temporary Structures: For tents and pop-up clinics, specify airflow rates, UVGI placement, and generator loads in advance. Practice setup during drills.
The People Side of Air
Preparedness succeeds when clinical leaders, facilities, infection prevention, and supply chain work from one script.
- Governance: Add an “Air Operations” branch to your Incident Command structure. Define roles for monitoring, deployment, documentation, and vendor coordination.
- Training & Drills: Competency-based training for placing portable HEPA units, verifying airflows, replacing filters, and reading dashboards should be part of annual exercises—just like fit testing.
- Communication: Post real-time air-quality status boards in high-traffic areas (ED, waiting rooms). Transparency builds trust with staff and families and reduces anxiety during prolonged events.
Evidence First: Buying Outcomes, Not Boxes
In an emergency, rushed purchasing can lock organizations into costly, ineffective solutions. Apply the same evidence-based rigor you use for clinical products:
- Define endpoints: Particle reduction, equivalent air changes, time to target, impact on SSI or respiratory infections, noise levels, and power draw.
- Pilot with data: Test in representative rooms; measure before/after performance and interference with workflow.
- Total cost of ownership: Include filters, maintenance, staff time, service response, and decontamination. Prefer devices with validated performance and straightforward upkeep.
- Contract for resilience: Stipulate delivery timeframes, spare parts, and loaner pools in disasters. Consider shared-risk terms tied to verified performance.
Infection Prevention & Surgical Safety
Air strategy intersects directly with surgical outcomes. Operating rooms rely on stable airflow, positive pressure, and low particle counts. During outbreaks or construction, layering portable HEPA or UV with existing HVAC infrastructure can add a safety margin that supports surgical site infection (SSI) mitigation. Pre-define protocols for adding supplemental air disinfection during high-risk periods (e.g., surge intubations, aerosol-generating procedures, or when ceiling work compromises laminar flow). Measure and document the effect on particulates and environmental bioburden—your risk and quality teams will need that evidence.
Don’t Forget the Edges of the System
Preparedness extends beyond tertiary hospitals. Alternate sites—urgent care, dialysis centers, ambulatory surgery, long-term care, and shelters—often operate with lower air-handling capability and higher crowding. Include them in planning:
- Train local leaders on room sizing, placement, and maintenance.
- Share remote support and dashboards so the enterprise can see and manage risk in real time.
Finance: The ROI of Breathing Better
Air interventions pay for themselves through avoided infections, reduced staff sick days, fewer cancelled procedures, and better patient flow when smoke or smog blows in. Build a business case that quantifies:
- Cost per avoided infection or procedure cancellation
- Impact on throughput and length of stay during poor air events
- Labor saved by quicker room turnover and fewer terminal cleans
- Avoided revenue loss from downtime of critical rooms
Tie capital plans to these outcomes and include maintenance and monitoring in operating budgets so readiness doesn’t erode between crises.
A Practical Checklist to Start Tomorrow
- Baseline: Audit ventilation, filtration, pressure, and monitoring in priority spaces; fix obvious gaps.
- Prioritize: Stratify by risk—ED triage, ORs, PACUs, ICUs, oncology infusion, and waiting rooms.
- Equip: Pre-purchase portable air disinfection units where needed, with spare filters and maintain them according to the manufacturer’s instructions for use.
- Instrument: Add pressure and air-quality sensors with alarms and dashboards.
- Plan: Write surge playbooks for room conversions and temporary structures.
- Drill: Run a twice-yearly “air readiness” exercise with facilities, IP, and clinical leaders.
- Communicate: Publish an air-quality status page for staff and create simple tip sheets for unit leaders.
- Review: After every activation, do a short after-action review and update the playbook.
The Bottom Line
Emergencies expose the invisible systems we take for granted. Air is one of them, and it is a risk that is shared by both patients and healthcare providers. By embedding air quality and air disinfection into emergency preparedness—backed by monitoring, training, and evidence-based procurement—healthcare organizations can protect people, preserve capacity, and perform with confidence when conditions are at their worst. The next crisis is not a question of if, but when. Air readiness ensures we’re prepared to meet it—safely, reliably, and at speed.

Aerobiotix’s Illuvia Sense is uniquely positioned to help healthcare facilities exceed guidelines and reduce risk. This FDA-registered Class II medical device delivers continuous air decontamination and real-time monitoring, ensuring optimal air quality.
About the Author
J. Hudson Garrett Jr., Ph.D., MSN, MPH, MBA, IP-BC, PLNC, CFER, AS-BC, VA-BC, CMRP, HACP, HACP-IC, HACP-PE, LTC-CIP, CIC, AL-CIP, CAIP, DICO-C, CPPS, CCHR-S, CPHQ, CVAHP, CPXP, CDIPC, CPHRM, CHIPP-B, FACDONA, FAAPM, eFACHDM, FAPIC, FAOM, FRSPH, FNAP, FAHVAP, FACHE, FSHEA, FIDSA
Dr. Garrett is an Adjunct Assistant Professor of Medicine in the Division of Infectious Diseases at the University of Louisville School of Medicine. He is Board Certified in Infection Prevention and Control, Advanced Leadership in Infection Control, Patient Safety, Healthcare Risk Management, and Healthcare Management and Leadership. Dr. Garrett is a Liaison to the AORN Guidelines Advisory Board.








