Wellell Procare Auto G2 | Alternating Pressure & LAL Mattress System

The Procare Auto G2 is a therapeutic mattress system that combines alternating-pressure and low-air-loss functions with automatic firmness adjustment.

It is intended for patients assessed as having a high to very high risk of developing pressure injuries, including individuals with significant mobility limitations.

It is designed for hospitals, post-acute care, skilled nursing facilities, rehabilitation centers, and other appropriate professional care environments.

The control system adjusts the mattress firmness according to the patient’s weight, helping provide personalized immersion and support without repeated manual pressure selection.

Alternating-pressure therapy cycles inflation between groups of air cells to redistribute loading and reduce prolonged pressure on vulnerable areas.

Low air loss circulates air through or beneath the support surface to help manage heat and moisture near the patient’s skin.

It may help manage the skin microclimate by reducing heat and moisture buildup, but it cannot eliminate perspiration or replace moisture-management care.

Common high-risk areas include the sacrum, hips, heels, elbows, and other bony prominences.

The dual-compressor system inflates the mattress in approximately 20 minutes under the manufacturer’s specified conditions.

The dual-compressor design supports faster inflation and efficient therapeutic operation.

The system is designed for quiet operation, although a specific decibel rating was not provided.

It provides a gentler alternating-pressure cycle intended to improve comfort for sensitive or immobile patients.

Additional lower air cells maintain a supportive foundation beneath the adjustable therapeutic cells.

Bottoming out occurs when the patient compresses the surface enough to contact or nearly contact the underlying bed deck, reducing pressure-redistribution performance.

Follow the manufacturer’s hand-check procedure and facility protocol. Never rely only on the pump display or selected pressure setting.

No. No mattress can prevent every pressure injury. The system must be combined with a complete clinician-directed prevention plan.

It may support the management of pressure injuries as part of a professional care plan. Wound stage, patient condition, and treatment suitability must be assessed by a qualified clinician.

The source information discusses early-stage pressure injuries, but exact treatment indications were not supplied. A clinician should determine whether the system is appropriate.

No. Continue all prescribed turning, repositioning, heel offloading, and mobility schedules.

No. It is a support surface and does not replace wound dressings, infection management, nutrition, surgery, or other prescribed care.

A weight capacity was not included in the supplied information. Confirm the minimum and maximum patient weights before use.

Dimensions and size options were not provided. Verify compatibility with the intended bed frame before ordering.

The supplied information describes it as a mattress system but does not specify its exact installation type. Confirm whether it replaces the existing mattress.

Alarm features were not included in the supplied specifications. Confirm whether it provides low-pressure, power-failure, or service alerts.

Power-failure performance was not provided. Follow the manufacturer’s emergency procedure and facility protocol, and assess the patient’s support immediately.

A CPR-release feature was not specified. Confirm emergency deflation and resuscitation procedures before placing the system into service.

Follow the manufacturer’s transfer and edge-support instructions. Therapeutic air surfaces may behave differently from standard foam mattresses.

Contraindications were not included in the supplied information. A clinician must review the patient’s medical condition, stability, and positioning requirements before use.

Use only the manufacturer-approved cleaning and disinfection procedure. Disconnect or protect electrical components as directed and avoid damaging the cover or air cells.

Inspect it before use and according to the facility’s maintenance schedule. Check the cover, cells, hoses, connectors, pump, power cord, and therapy settings.

Monitor skin condition, comfort, alignment, moisture, pressure areas, pump operation, and signs of bottoming out. Document findings according to the care plan.

Use automatic mode and any manual adjustments only as directed by the manufacturer and the patient’s clinical care plan.

A wound-care clinician, nurse, physician, therapist, or other qualified healthcare professional should assess the patient and determine the appropriate support surface.

Continue scheduled repositioning, skin inspection, moisture and incontinence management, nutrition support, heel protection, wound care, and mobility interventions as prescribed.