Alerta Sensaflex 1000 Foam Mattress, Castellated Foam Design for High-Risk Pressure Relief - CareSupplies.com Medical Equipment
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  • Alerta Sensaflex 1000 Foam Mattress, Castellated Foam Design for High-Risk Pressure Relief - CareSupplies.com Medical Equipment

Alerta Sensaflex 1000 Foam Mattress, Castellated Foam Design for High-Risk Pressure Relief

  • High-risk profiling mattress with castellated foam delivering superior pressure redistribution for patients assessed at high risk on the Waterlow Risk Assessment Scale, where the increased foam density and castellated structure of the 1000 specification provides greater interface pressure reduction than the medium-risk 500 at the same bony prominence locations, matched to the clinical requirement for patients where medium-risk specification static surfaces are insufficient.
  • Multi-stretch, vapour-permeable PU cover reduces shear and friction during repositioning, supporting the EPUAP/NPIAP guideline that patient repositioning for high-risk patients should be facilitated by low-shear cover surfaces that reduce the tissue damage risk during the turn - particularly relevant for high-risk patients who require frequent repositioning schedules and where cumulative shear exposure across multiple daily turns contributes to tissue damage risk.
  • Antimicrobial cover washable to 95°C with foam autoclavable at 134°C, providing thermal sanitisation and steam sterilisation capability to meet the decontamination standards required for high-risk patient contact equipment across the range of infection scenarios encountered in NHS ward and care home environments where high-risk pressure care patients are managed.
  • BS7177: Crib 5 fire compliant profiling mattress for permanent installation on profiling care beds in NHS wards and care homes, maintaining full pressure redistribution performance across all bed profiling positions including head elevation, knee break and Trendelenburg positioning used in high-dependency clinical care.

Alerta Sensaflex 1000 Foam Mattress: Castellated Foam Pressure Relief for High-Risk Users

The Alerta Sensaflex 1000 Foam Mattress is a high-risk profiling mattress with castellated foam for patients assessed at high risk on the Waterlow Risk Assessment Scale, providing superior pressure redistribution to the medium-risk Sensaflex 500 through increased foam density and castellated construction. The multi-stretch vapour-permeable PU cover reduces shear and friction during repositioning, the antimicrobial cover is machine washable to 95°C, and the foam is autoclavable at 134°C for high-level decontamination between patients. BS7177: Crib 5 fire compliant for use across all NHS and care home profiling bed environments.

Product Specifications

SpecificationDetail
Product CodeNCL-ALT-1000
TypeStatic foam profiling mattress
Risk LevelHigh risk (Waterlow 20+)
Foam ConstructionCastellated foam - high-risk specification
CoverMulti-stretch, vapour-permeable PU
Cover TreatmentAntimicrobial with white underside
Washing TemperatureUp to 95°C for thermal sanitisation
Foam SterilisationAutoclavable at 134°C
Fire ComplianceBS7177: Crib 5
ApplicationHigh-risk patients on profiling beds in care homes and NHS wards

Clinical and Regulatory Compliance

NICE Guideline CG179 (Pressure Ulcers: Prevention and Management) specifies that high-risk patients should receive a higher-specification pressure redistribution surface than medium-risk patients, and that surface specification decisions should be based on the individual's risk assessment using a validated tool such as the Waterlow Scale. The Sensaflex 1000 is the high-risk specification within the Sensaflex static foam mattress range, providing the greater interface pressure reduction required for patients whose Waterlow score places them in the high-risk category. CQC Regulation 12 (Safe Care and Treatment) requires that the pressure care surface specification matches the documented risk assessment: using a medium-risk mattress for a patient assessed at high risk is a documented care quality shortfall. The repositioning guidance in NICE CG179 recognises that even with a high-specification static mattress, repositioning schedules remain required for high-risk patients - the Sensaflex 1000's low-shear vapour-permeable cover supports the clinical safety of repositioning by reducing the tissue damage contribution from the cover-to-skin shear during turning.

Frequently Asked Questions

What is the difference between the Sensaflex 500 and the Sensaflex 1000, and when should each be selected?

The Sensaflex 500 is specified for medium-risk patients (Waterlow 15-19 or equivalent) and the Sensaflex 1000 for high-risk patients (Waterlow 20+ or equivalent). The principal difference is foam density and castellated construction specification: the 1000 provides greater interface pressure redistribution than the 500 at the same bony prominence locations, matched to the higher clinical requirement of the high-risk patient category. The Waterlow risk category determines the selection: a patient at medium risk receives the 500, a patient at high risk receives the 1000. When a patient's risk assessment changes - for example, following deterioration in clinical condition, skin status or mobility - the mattress specification should be upgraded to match the new risk assessment rather than continuing with the previous specification.

For a high-risk patient, when would the Sensaflex 1000 be appropriate rather than an alternating pressure mattress?

NICE CG179 recommends that the decision between a high-specification static surface and an alternating pressure system for a high-risk patient is based on clinical assessment of the individual's skin status, mobility, comfort and care needs, not solely on risk score. A high-specification static mattress such as the Sensaflex 1000 is appropriate for high-risk patients who can be repositioned on a regular schedule, whose skin integrity is currently maintained and who have no existing pressure damage, and for whom the alternating pressure system's mechanical complexity or noise would be clinically or practically inappropriate. An alternating pressure mattress is typically indicated when static surface repositioning alone is insufficient for the individual - for example, for patients who cannot be repositioned safely or frequently enough, or for patients with existing pressure damage at Stage 2 or above where NICE CG179 recommends consideration of higher-specification active surfaces.

NCL-ALT-1000