The Hampton Extra Active Mattress by Harvest Healthcare is an 18-cell bariatric replacement alternating pressure mattress for residents at very high risk requiring a 1200mm wide profiling bed. The 17 alternating nylon-TPU cells and 1 static pillow cell deliver continuous pressure redistribution across the wider surface at a SWL of 317kg (50 stone). The foam surround extends the cushioned surface to the mattress edge to support safer lateral transfers. The 4-way stretch Crib 5 welded PU cover provides NHS IPC and fire safety compliance. Compatible with Harvest 3 pump only. For Community 1200 and Ultimate 1200 bed frames.
| Specification | Detail |
|---|---|
| Type | Alternating pressure replacement mattress - bariatric 1200mm |
| Air Cells | 17 alternating nylon-TPU cells + 1 static pillow cell (18 total) |
| Foam Surround | Perimeter foam to mattress edge for transfer support |
| Dimensions | 2000 x 1200 x 230mm |
| Safe Working Load | 317kg (50 stone) |
| Cover | 4-way stretch welded PU - VP, water resistant, Crib 5 |
| Pump Compatibility | Harvest 3 only |
| Bed Compatibility | Community 1200, Ultimate 1200 profiling beds |
| Reference | NCL-HAMHAMP002 |
| Clinical Standard | NICE CG179 (very high risk, bariatric pressure care) |
The Hampton Extra is a Class IIa active medical device under Medical Devices Regulation 2017/745. Clinical selection requires validated pressure risk assessment per NICE CG179 confirming very high-risk status in a bariatric resident. SWL must be verified against the resident's documented weight before deployment; MHOR 1992 documentation must record this verification. The Harvest 3 pump must be confirmed available and dedicated to this mattress before prescription. Bed frame must be confirmed as Community 1200 or Ultimate 1200 before procurement. The Crib 5 welded PU cover meets BS 5852 institutional bariatric fire safety requirements. Equipment register records and MDR conformity documentation must be maintained for CQC Regulation 12 compliance.
What is the clinical role of the foam surround, and how does it differ from the standard mattress edge?
A standard alternating pressure mattress has an air cell array that extends to or near the mattress edge; when a bariatric resident is positioned near the edge or during a lateral transfer, the outermost cell at the mattress edge is the only cushioning between the resident and the rigid bed frame or rail junction. If that cell is in its deflation phase during the transfer, the resident may contact the bed frame structure with minimal cushioning, creating a pressure point at the hip or thigh at the moment of highest positional load. The foam surround on the Hampton Extra wraps the perimeter of the cell array in a foam border that provides continuous cushioning at the mattress edge regardless of the alternating cycle phase. This is particularly important in bariatric care where the combination of higher body mass and wider lateral spread means the mattress edge is more frequently in contact with the resident during repositioning and where pressure injuries at the lateral thigh and hip are a recognised risk site.
Why is the Hampton Extra limited to the Harvest 3 pump, and can any other pump be used in an emergency?
The Hampton Extra is a 1200mm wide cell array with a SWL of 317kg, which requires higher airflow and pressure output than the Harvest 1, 2, or 250 pumps can deliver to maintain correct cell inflation pressure across the wider array under bariatric load. The Harvest 3 is the only pump in the range rated for the combination of cell count, array width, and maximum user weight that the Hampton Extra specifies. Using an incompatible pump would result in under-inflation of the cells, which would reduce pressure redistribution effectiveness, increase the risk of bottoming out under bariatric load, and operate the mattress outside its validated clinical specification. No alternative pump should be used, including in emergency situations; if the Harvest 3 pump fails, the manufacturer's emergency protocol should be followed and a replacement pump sourced before restarting therapy. The pump-to-mattress pairing must be documented and the Harvest 3 serial number recorded in the equipment register.