Alerta Sensaflex Underlay Foam Mattress, 2-Inch Foam Support for Emergency Situations - CareSupplies.com Medical Equipment
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  • Alerta Sensaflex Underlay Foam Mattress, 2-Inch Foam Support for Emergency Situations - CareSupplies.com Medical Equipment

Alerta Sensaflex Underlay Foam Mattress, 2-Inch Foam Support for Emergency Situations

  • 2-inch foam underlay mattress designed for placement beneath an air mattress system, providing a firm, stable support surface during power failures when the air mattress deflates, and during cardiopulmonary resuscitation where RESUSCITATION COUNCIL UK guidelines require a firm mattress surface beneath the patient for effective chest compressions - without requiring the air mattress system to be removed from the bed under emergency conditions.
  • Multi-stretch, vapour-permeable PU cover with antimicrobial treatment supports ongoing infection control standards when in use beneath an air mattress system, with machine washable fabric rated to 65°C for standard laundering and 95°C for thermal sanitisation between patients, meeting NHS England and CQC Regulation 12 (Safe Care and Treatment) requirements for decontamination of patient contact bedding equipment.
  • Foam autoclavable at 134°C provides the highest level of thermal disinfection for the foam component, enabling the underlay to meet the decontamination requirements for reuse in care environments where standard machine washing is insufficient for the specific infection risk or patient population - the 134°C autoclave temperature meets the EN ISO 17665 standard for steam sterilisation of porous loads.
  • BS7177: Crib 5 compliant meets the fire resistance standard required for all mattresses and bedding products used in healthcare settings, hotels, care homes and other public buildings under UK fire safety regulations, confirming the underlay is safe for permanent installation beneath air mattress systems in all clinical care environments.

Alerta Sensaflex Underlay Foam Mattress: 2-Inch Foam Support for Under Air Mattress Systems During Power Failure and CPR

The Alerta Sensaflex Underlay Foam Mattress is a 2-inch foam mattress designed for permanent placement beneath an air mattress system, providing a firm support surface during power failures when the air mattress deflates and a stable platform for CPR when Resuscitation Council UK guidelines require a firm mattress surface for effective chest compressions. The foam underlay removes the need to deflate or remove the air mattress system under emergency conditions. The multi-stretch vapour-permeable antimicrobial PU cover is machine washable to 65°C standard and 95°C sanitisation. The foam is autoclavable at 134°C and the unit is BS7177: Crib 5 fire compliant.

Product Specifications

SpecificationDetail
Product CodeNCL-ALT-UND
TypeFoam underlay for use beneath air mattress systems
Foam Thickness2 inches
CoverMulti-stretch, vapour-permeable PU
Cover TreatmentAntimicrobial with white underside
Washing Temperature65°C standard | 95°C sanitisation
Foam SterilisationAutoclavable at 134°C
Fire ComplianceBS7177: Crib 5
ApplicationBeneath air mattress systems in hospitals, care homes

Clinical and Regulatory Compliance

Resuscitation Council UK guidelines specify that CPR should be performed on a firm, flat surface beneath the patient to enable effective sternal compressions: a patient lying on an inflated air mattress system without an underlay will sink into the mattress during compressions, absorbing the compression force and reducing the clinical effectiveness of chest compressions. The Sensaflex Underlay resolves this by providing the firm surface beneath the air mattress that Resuscitation Council guidelines require, without the clinical delay of deflating or removing the air mattress system during an emergency. CQC Regulation 12 (Safe Care and Treatment) requires that clinical equipment enables safe emergency response: the absence of an appropriate underlay beneath an air mattress system in a care home or NHS ward where CPR capability is required is a potential care quality concern. NICE Guideline CG179 (Pressure Ulcers) addresses the period of air mattress power failure by noting that patients should not remain unsupported on a deflated air mattress: the foam underlay ensures continuous pressure redistribution support even when the air mattress system is non-operational.

Frequently Asked Questions

Does the 2-inch foam underlay affect the pressure care performance of the air mattress placed on top of it?

A correctly specified 2-inch foam underlay placed beneath an air mattress system should not materially affect the pressure care performance of the air mattress during normal powered operation, as the air mattress itself provides the active pressure redistribution surface in contact with the patient. The underlay functions as a secondary support layer and emergency surface rather than as a primary pressure care intervention. However, the combined height of the underlay plus air mattress should be assessed against the care bed's safe height range for patient transfer, and the mattress system manufacturer's guidance on underlay compatibility should be checked to confirm the underlay does not affect the air mattress's clinical performance or warranty status. In some configurations, a thick underlay may reduce the effective height adjustment range of a profiling bed.

When should the underlay foam be autoclaved versus machine washed, and what does autoclaving achieve that machine washing does not?

Machine washing the cover at 65°C or 95°C achieves thermal disinfection of the cover material at the temperatures required by NHS laundry guidance for patient contact linen (71°C for 3 minutes, or 65°C for 10 minutes, for standard disinfection). The foam itself is not machine washable and is cleaned separately. Autoclaving the foam at 134°C achieves steam sterilisation of the foam core, destroying bacterial spores and prions that thermal disinfection at lower temperatures does not eliminate. Autoclaving is required between patients in infection risk categories where standard thermal disinfection is insufficient - for example, patients with Clostridium difficile, prion disease, or other high-risk infections where the care home's infection control policy specifies sterilisation rather than disinfection for patient contact equipment. Confirm the required decontamination level with the infection control lead for the specific patient and setting before use.

NCL-ALT-UND