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Negative-Pressure Room Verification

Negative-Pressure Room Verification

Daily AIIR (airborne infection isolation room) negative-pressure verification per CDC + ASHRAE 170. Critical for TB and COVID isolation.

Room Identification and Status

  • AIIR room identifier recorded
    Document the room number, unit, or location being verified.
  • Room designated for airborne isolation use
    Confirm the room is currently assigned to airborne infection isolation use.
  • Current patient isolation indication documented
    Record the reason for isolation, such as TB, COVID-19, or other airborne precaution.

Pressure Differential Verification

  • Negative pressure confirmed at room entry
    Verify airflow is inward from corridor to room using the facility-approved method.
  • Measured pressure differential recorded
    Record the pressure differential between the room and adjacent corridor or anteroom.
  • Pressure monitoring device or indicator functioning
    Confirm the room pressure monitor, gauge, or visual indicator is operating and readable.
  • Pressure reading stable during observation period
    Confirm the negative pressure condition remains stable during the inspection observation period.

Air Handling and Containment

  • Door closed and self-closing function intact
    Verify the isolation room door is closed and the self-closing mechanism operates properly.
  • No obvious air leakage at door, pass-through, or penetrations
    Check for visible gaps, drafts, or other signs of air leakage that could compromise containment.
  • Exhaust and supply air system operating as intended
    Verify the room ventilation system is running and supporting negative-pressure containment.
  • Air changes per hour documented
    Record the current air changes per hour if available from the facility monitoring system or engineering record.

Documentation and Corrective Action

  • Deficiencies documented with immediate notification
    If any critical item failed, confirm the issue was documented and escalated to engineering, infection prevention, or the supervisor on duty.
  • Corrective action recorded for any non-conformance
    Describe the corrective action taken or initiated for any deficiency, including who was notified and when.
  • Inspector signature
    Inspector attestation that the daily verification was completed.
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