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HAIs are the most frequently occurring medical adverse event worldwide, with a prevalence of around 7-10%.3, 4
There can be serious physical and emotional impacts to patients that acquire an HAI.2
Facilities and practitioners may also suffer financial as well as reputational damage as a result of HAIs associated with their facility.
The Australian Commission on Safety and Quality in Health Care (ACSQHC) estimates 11,142 fewer HAIs would result in a possible value capture of $459,984,691.5
In the first of its kind, a UK study revealed an "unacceptable risk" of patient infection following ultrasound. The study revealed an increased infection risk in the 30 days following endocavitary ultrasound. Commissioned by a national health authority, the study revealed an increased infection risk in the 30 days following endocavitary ultrasound.11
90.5% of facilities were not performing high level disinfection (HLD) of these probes at the time of the study.
Of the 982,911 patients followed, 330,500 were gynaecological patients.
60,698 of these patients had undergone transvaginal ultrasound.

The national health authority now recommends HLD for endocavitary ultrasound probes.

The Spaulding Classification identifies the level of disinfection or sterilisation required for medical devices based on the expected patient tissue the device will contact.
The Spaulding Classification forms the basis of international ultrasound probe reprocessing guidelines.
Internationally, Federal authorities and professional societies provide guidance on the proper reprocessing of ultrasound probes, to help keep patients safe from HAIs.
These guidelines are based on The Spaulding Classification.
Learn when to HLD ultrasound probes
Learn about the clinical risks from improper ultrasound probe reprocessing