RediRoom Mk II: Infection Prevention and Control evaluation

Following on from last week's blog about the functional characteristics
of the RediRoom (a temporary isolation room designed for single patient use), this week's blog reviews a second study that evaluates the infection prevention and control characteristics and potential benefits of the RediRoom.

Whether to favour single rooms or multi-occupany bays is a balance. On the one hand, single rooms provide more privacy, less noise, and better containment of pathogens. On the other hand though, multi-occupancy bays provide more social interaction, reduced cost in terms of staffing levels, and patients who fall or deteriorate will be spotted more quickly. Perhaps as a result of this balancing act, patient opinion is divided on whether single rooms or mutli-occupancy bays are better. Most modern hospitals have decided to provide a mixture of single rooms and multi-occupancy bays, to offer flexibility to staff in finding the best accommodation for patients. The RediRoom occupies the middle ground: providing many of the benefits of single occupancy rooms (in terms of more privacy, less noise, and better containment of pathogens) and multi-occupancy bays (patient visibility, and reduced cost in terms of staffing).

The RediRoom was installed in a simulated clinical environment, and its function was assessed from an IPC viewpoint against key standards or guidelines (Australasian Health Facility Guidelines and the Department of Health (NHS) Infection Control in the Built Environment), and the ease of assembly and dismantling, and the ability to clean the RediRoom as judged by the removal of fluorescent markers were evaluated. The RediRoom was found to be fully compliant with 17/19 relevant guidelines or standards, and partially compliant with the other two. The two guidelines rated as partially compliant were the storage and use of personal protective equipment, and the provision of additional storage capacity. Another limitation was the lack of a sink for hand hygiene inside the RediRoom, but there is provision for alcohol gel to be situated both inside and outside the RediRoom. The review of assembly and dismantling of the RediRoom identified limited infection control risk. Impressively, the RediRoom was installed in less than 5 minutes! Finally, the cleaning assessment found that the UV fluorescent markers were fully removed from 23 (96%) of the 24 surfaces marked, and partially removed from the other surface. Whilst this cleaning assessment was not performed in the business of clinical practice, it demonstrates that the RediRoom does not present a barrier to cleaning in principle.

The RediRoom performed well when compared against standards and guidelines for a safe healthcare environment, it did not introduce infection control risks during assembly and dismantling, and was designed in a way that should not be a barrier to cleaning. Clearly, further assessments of the RediRoom in clinical practice are required, but it is poised to deliver IPC benefits!

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