Overview
The Accella Therapy Surface is designed to assist in the prevention and treatment of pressure ulcers in low- to high-risk adult patients by addressing external, non-patient-related risk factors for skin breakdown.
The surface offers Continuous Low Pressure (CLP) or Alternating Low Pressure (ALP) modes and provides real I-mmersion therapy, designed to help achieve and maintain low interface pressures.
In both modes, the precise level of pressure redistribution is continuously and automatically controlled by the internal I-mmersion sensor which adjusts internal cell pressures according to each patient’s size, weight and position in bed.
The patented Microclimate Management system is also designed to manage the patient microclimate and help reduce the risk of tissue breakdown as a result of excessive heat and/or moisture.
Features
- Surface is controlled through the Graphical Caregiver Interface (GCI)® in the integrated siderail controls and includes single step CPR
- Boost feature and other therapies
- One-touch deflate designed to support rapid deflation for CPR
- P-MAX feature designed to provide inflation to help support patient repositioning and transfer
- Integrated X-ray cassette sleeve assists in helping to reduce patient repositioning and discomfort during portable X‑ray procedures
- Continuous or alternating low‑pressure therapy modes are designed to provide flexibility with patient therapy
- Real-time pressure adjustment, controlled by the internal I-mmersion sensor, is designed to adjust cushion pressures according to patient size, shape, weight or position in the bed without caregiver intervention
- Microclimate Management limits the effects of temperature and moisture build-up¹
- Five individual low-pressure zones provide pressure redistribution
- Dedicated heel zone with ultra-low pressure and enhanced lower‑leg support delivers protection of the vulnerable heel area
Education & Documents
Please visit our manuals & technical documents center.
Related Products
For safe and proper use of the product mentioned herein, please refer to the appropriate Operator’s Manual or Instructions for Use.
This medical device is a regulated health product which, pursuant to such regulation, bears a CE mark. Baxter recommends that you carefully read the detailed instructions for safe and proper use included in the documents accompanying the medical devices.
The personnel of healthcare establishments are responsible for the proper use and maintenance of this medical device.