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Which RMD to disinfection & which to sterilise?

by Titus

Earle H. Spaulding proposed for an internationally recognised disinfection framework was required since all reusable medical devices (RMDs) cannot be sterilised.

The Spaulding Classification stratifies the risk of infection transmission based on the patient tissue the device will contact during use.

Spaulding Classification

Medical Device Contacts

Risk of Infection Transmission

Disinfection Level

Critical

Sterile tissue or the bloodstream

High

Sterilisation

Semi-critical

Mucous membranes or non-intact skin

Medium

High Level Disinfection (HLD)

Non-critical

Intact skin only

Low

Intermediate level (ILD)

or 

Low level disinfection (LLD)

Understanding & Recognising Disinfection Levels and Sterilisation

Correctly applying Spaulding Classification to medical devices is a key part of keeping patients safe from healthcare-associated infections (HAIs).

Sterilisation

  • Sterilisation destroys all microorganisms.
  • Critical devices must be sterile when used.
  • Heat sterilization, including steam or hot air.

(Refer to manufacturer’s recommendations, steam sterilization processing time from 3-30 minutes)

High Level Disinfection (HLD)

  • HLD destroys all microorganisms except for high numbers of bacterial spores.
  • A high-level disinfectant is therefore bactericidal, virucidal (both lipid and non-lipid viruses), fungicidal and mycobactericidal.
  • Semi-critical ultrasound probes must undergo HLD and be used with a sheath.
  • Critical ultrasound probes that cannot be sterilised can also undergo HLD.
  • They must also be used with a sterile sheath.

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