Resources Category: Exam and Surgical Gloves

What are the recommendations related to glove use during chemotherapy drug clean up and general handling?

Wear chemotherapy-approved gloves when dealing with blood, vomitus, excreta and other bodily fluids from chemotherapy treated patients. Wash hands before and immediately after glove use. Discard gloves after each use. Laundry personnel encountering linen possibly contaminated with chemotherapy or bodily fluids from a patient undergoing chemo treatment should wear chemotherapy-approved gloves. Spills should only be …

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What is breakthrough time?

Breakthrough time is defined as the elapsed time between the initial contact of a chemotherapy drug with the outer surface of the glove and the point in time at which the permeation rate reaches 0.01 µg/cm2/min. When breakthrough occurs, the glove is no longer providing adequate protection against the tested chemotherapy drug. The longer the …

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How are gloves sterilised?

The most common method is using gamma irradiation, whereby products are exposed to gamma radiation which penetrates the packaging and kills all microorganisms. Gamma processing does not cause any significant rise in temperature or leave behind any chemical residue.

What is bioburden?

Bioburden is the total number of viable (live) microbes on a packaged item prior to sterilisation. This includes bacteria, yeasts and fungi.

What is a Sterilisation Assurance Level or SAL?

SAL is the expected probability of an item being non-sterile after exposure to a valid sterilisation process. The normal SAL for medical devices is 10-3 (one in a thousand) for less critical devices and 10-6 (one in a million) for more critical and invasive devices. Surgical gloves are sterilised at 10-6 SAL.

What does SAL 10⁻⁶ mean?

A Sterility Assurance Level of 10-6 means that for every 1,000,000 items sterilised, there may be one that contains viable microorganism that have survived the sterilisation process. The SAL is a statistical probability that is used because it is impossible to prove that all viable microorganism have been killed during the sterilisation process. In practice …

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What is dose setting?

Dose setting is the process undertaken to establish the level of radiation exposure (dose) required to destroy microorganisms (bioburden) on a product within a specified safety level (Sterilisation Assurance Level—SAL). The process includes a determination of the number of organisms on the packaged, unsterilised product, followed by irradiation at a dose calculated to kill 90% …

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What are endotoxins?

Endotoxins are potent inflammatory agents produced by the cell walls of gram-negative bacteria. They are capable of causing multiple local and systemic reactions including irritation, fever, tissue inflammation, diarrhoea, respiratory distress, and endotoxic shock. They are not destroyed by steam, ethylene oxide or irradiation sterilisation. Endotoxins are also adjuvants, a term applied to substances that …

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