Hospital isolation rooms rely on airflow to protect people. An airborne infection isolation room (AIIR) keeps an infectious patient's exhaled particles from reaching corridors and other patients. A protective environment (PE) room keeps contaminants away from a severely immunocompromised patient. In both, the HVAC system must deliver the right air change rate and keep air moving in the right direction every hour of every day.
Air valves, particularly pressure-independent venturi valves, are widely used for this job because they hold supply and exhaust flows accurately even when duct pressures change elsewhere in the hospital. This guide covers how they are applied, how the room is controlled, and how to verify it.
Requirements that drive the design
In Canada, health care facility HVAC is governed by CSA Z317.2, Special requirements for heating, ventilation, and air-conditioning (HVAC) systems in health care facilities, as referenced by provincial health authorities and building codes. Many designers also refer to ASHRAE Standard 170. The key isolation room parameters are:
- A minimum total air change rate, typically 12 ACH for AIIR and PE rooms under ASHRAE 170, with CSA Z317.2 values to be confirmed for the edition in force.
- Pressure direction: negative to adjacent spaces for AIIR, positive for PE.
- A minimum pressure differential, with 2.5 Pa (0.01 in. w.c.) commonly cited as a minimum in ASHRAE 170, and owners often designing for more.
- AIIR exhaust ducted directly outdoors, with discharge located away from intakes.
- HEPA filtration of supply air for PE rooms.
- A permanent means of monitoring pressure, usually a continuous monitor with alarm.
Requirements differ by edition and by provincial health authority, so the owner's functional program and the authority having jurisdiction should be confirmed early. See hospital HVAC and CSA Z317.2 for the broader context.
Typical valve arrangement
| Room type | Supply | Exhaust | Pressure relationship |
|---|---|---|---|
| AIIR | Constant volume or two-state valve | Constant volume valve set above supply | Negative to anteroom and corridor |
| PE | Constant volume valve with HEPA supply | Valve set below supply | Positive to anteroom and corridor |
| Anteroom | Valve or transfer air | Valve or transfer air | Intermediate, set by design |
| Convertible room | Two-state valves on supply and exhaust | Two-state valves | Switches between neutral and negative |
Constant volume operation is common because isolation rooms have steady requirements. The valve's mechanical pressure independence holds those flows when other zones change and the main duct pressure moves.
Setting the offset
Most isolation rooms use flow offset control: exhaust exceeds supply by a fixed amount in an AIIR, or supply exceeds exhaust in a PE room. The offset needed to reach the target pressure depends on how tight the room is. A well-sealed room with gasketed doors and sealed ceilings needs a much smaller offset than a room with a lay-in ceiling and gaps at penetrations.
The design process usually runs:
- Specify tight construction: sealed or hard ceilings, sealed penetrations, and doors with appropriate seals and closers.
- Estimate residual leakage, mostly through door undercuts and perimeter gaps.
- Size the offset to produce the target pressure with margin.
- Select valves sized so the required flows fall comfortably within each valve's range.
- Confirm offset and pressure during commissioning, adjusting the offset if construction leakage differs from assumptions.
The comparison of offset and direct pressure methods is in room pressurization control: offset vs direct pressure.
Anterooms
Anterooms add a buffer between the isolation room and the corridor. When one door opens, the other should be closed, so the pressure relationship is preserved. For an AIIR, a common arrangement is corridor to anteroom to patient room, with pressure decreasing at each step. For a PE room, the direction reverses.
Some combined designs serve patients who are both infectious and immunocompromised, using a positive-pressure anteroom with a negative patient room, or similar arrangements defined by the infection control team. These rooms need careful flow design and should follow the specific requirements of CSA Z317.2 and the owner's infection prevention and control program.
Convertible rooms and mode switching
Hospitals often want rooms that can operate as standard patient rooms or as isolation rooms. Two-state air valves allow the room controller to switch flows on command.
Good practice for switchable rooms:
- Limit who can change the mode, typically to facilities staff or nursing leadership with a key switch or BAS permission.
- Display the current mode clearly at the room entrance.
- Sequence changes so the room moves toward the safer pressure first. When entering AIIR mode, raise exhaust before or with supply.
- Alarm if the room is in isolation mode and the pressure monitor shows the wrong direction.
- Record mode changes in the BAS for infection control review.
Some health authorities discourage or restrict switchable rooms because of the risk of being left in the wrong mode. Confirm the owner's policy before designing them.
Monitoring and alarms
A room pressure monitor provides continuous verification independent of the airflow controls. Typical features:
- Differential pressure sensor between the patient room and the corridor or anteroom.
- Local display at the room entrance showing pressure and status.
- Audible and visual alarm after a time delay when pressure falls outside limits.
- Door-open allowance so brief door openings do not cause nuisance alarms.
- Alarm and trend reporting to the BAS and, often, to nursing stations.
Monitor sensors need periodic calibration. A monitor showing a value that does not match a calibrated handheld measurement should be addressed promptly.
Emergency and fire modes
Isolation rooms need a defined response to fire alarm and power failure. Exhaust fans for AIIRs are usually on emergency power so negative pressure is maintained during utility outages. The fire alarm response must be coordinated with the building's fire safety plan and the smoke control strategy. These interactions should be included in integrated testing under CAN/ULC-S1001 where applicable.
Verification
Isolation room verification should be performed at commissioning and repeated periodically, commonly at least annually and after any work affecting the room. Typical checks:
- Measure supply and exhaust airflow at each valve and compare with design and reported values.
- Calculate air change rate from measured supply or exhaust.
- Measure room pressure with a calibrated instrument, doors closed, and compare with the monitor.
- Confirm air direction at door gaps with a smoke visualization.
- Test alarms by opening doors beyond the delay and by simulating a fan failure.
- Verify mode switching and emergency power operation.
An independent air balancing contractor or commissioning provider typically performs these tests and documents results for the facility's records.
Key takeaways
- Isolation rooms need steady, accurate supply and exhaust, which pressure-independent air valves provide even when duct pressure changes.
- Most rooms use flow offset control with a tight envelope; the offset is confirmed by measured pressure.
- Anterooms and careful door design preserve pressure relationships during entry.
- Convertible rooms need strict access control, clear indication and safe switching sequences.
- Continuous pressure monitoring, emergency power on AIIR exhaust and regular verification are essential.
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