Objective. Students will correctly perform and interpret a Bowie-Dick test and an air-removal/leak test on a prevacuum steam sterilizer, and document results on an equipment qualification log.
This lesson, its worked examples and its practice questions has not yet been verified by a licensed clinician in the field or by a certification or approval body. It is a study draft and may contain errors. Do not use it to make decisions about any patient or medication. Always follow your instructor, your supervising professional, and current official references and regulations.
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Prevacuum (pre-vac) steam sterilizers use one or more vacuum pulses before the sterilization phase to pull air out of the chamber and the load. This matters because air is a poor conductor of heat and, if trapped inside a pack or against a surface, it acts as an insulating barrier that prevents steam from reaching the item. An instrument wrapped inside an air pocket may never reach the required sterilization temperature, even though the sterilizer's printout shows a normal cycle. The result is a potentially non-sterile item delivered to a patient — a direct safety risk.
The Bowie-Dick test and the air-removal (leak) test are the two standard tools used every operating day to confirm that a prevacuum sterilizer is evacuating air correctly before any patient-care loads are processed.
The Bowie-Dick test was developed to detect air entrapment and air leaks in prevacuum steam sterilizers. It is not a biological indicator test and it does not assess lethality; its sole purpose is to evaluate the sterilizer's air-removal system.
What it consists of. A commercial Bowie-Dick test pack contains a chemical indicator sheet surrounded by a standardized mass of absorbent material (or a single-use equivalent). The chemical sheet changes color when exposed to steam uniformly.
How to run the test.
1. The test is run on an empty chamber — no other load items are present.
2. Place the test pack on the lowest shelf (or the shelf specified by the sterilizer and pack manufacturer), near the drain, in the front of the chamber. This is typically the most challenging location for air removal.
3. Select the specific Bowie-Dick test cycle on the sterilizer — usually a short prevacuum cycle at 134 °C (273 °F) for approximately 3.5 minutes; always follow the manufacturer's instructions for both the sterilizer and the test pack.
4. After the cycle completes, retrieve the pack and open it. Allow the sheet to cool briefly before reading.
Interpreting the sheet. A pass result shows a uniform color change across the entire indicator sheet with no light areas, streaks, or uneven patterns. A fail result may appear as:
Some facilities run a separate air-removal or leak test (sometimes called a vacuum leak test) in addition to the Bowie-Dick test. This test verifies that the chamber door gaskets and plumbing are not allowing air to re-enter during the vacuum phase. The sterilizer draws down to a defined vacuum level, the pump is shut off, and the rate of pressure rise over a set time period is measured. The manufacturer specifies the acceptable leak rate. If the chamber pressure rises faster than allowed, air is infiltrating the system, and the sterilizer must be taken out of service. Follow your specific sterilizer manufacturer's instructions and your department policy for conducting and passing this test.
According to widely accepted industry standards (including AAMI and HSPA guidance), a Bowie-Dick test should be performed each day the sterilizer is used, before the first processed load. This ensures that any malfunction is detected before patient-care items enter the sterilizer.
Documentation is not optional — it is a patient safety and regulatory requirement. Every Bowie-Dick test run must be logged immediately. A standard equipment qualification log entry includes:
Keep the used Bowie-Dick test sheet attached to or filed with the log entry for that cycle. Many facilities retain these records for a period defined by department policy or accreditation requirements.
A failed Bowie-Dick result means the sterilizer must not be used for patient-care loads until the problem is identified and corrected. The correct sequence is:
1. Do not process any loads in that sterilizer.
2. Affix an out-of-service tag to the sterilizer door so no one inadvertently uses it.
3. Notify your supervisor immediately. You are not expected to diagnose or repair the sterilizer — that is outside your scope of practice.
4. Document the failure in the equipment qualification log, including the time, result, and that the supervisor was notified.
5. The sterilizer should not be returned to service until it has been inspected, repaired if necessary, and passes a requalification Bowie-Dick test (often three consecutive passing tests, per department policy).
Never attempt to override a failed result or quietly run a patient load anyway. A single non-sterile instrument can cause a serious surgical site infection.
Answer each question, then check it. Nothing is recorded; this is your own practice.
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