Pressure Relieving Support Surfaces

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Pressure Relieving Support Surfaces for Pressure Ulcer ...

    https://www.sciencedirect.com/science/article/pii/S2589537019301385
    Pressure Relieving Support Surfaces for Pressure Ulcer Prevention (PRESSURE 2): Clinical and Health Economic Results of a Randomised Controlled Trial Author links open overlay panel Jane Nixon a Isabelle L. Smith a Sarah Brown a Elizabeth McGinnis a b Armando Vargas-Palacios i E. Andrea Nelson d Susanne Coleman a Howard Collier a Catherine ...Cited by: 3

Pressure relieving support surfaces: a randomised evaluation.

    https://www.ncbi.nlm.nih.gov/pubmed/16750060/
    In addition, a focus group interview was carried out with clinical research nurses, who participated in the PRESSURE (Pressure RElieving Support SUrfaces: a Randomised Evaluation) Trial, to explore the experiences of their role and observations of pressure area care.Cited by: 84

Pressure RElieving Support SUrfaces: a Randomised ...

    https://trialsjournal.biomedcentral.com/articles/10.1186/s13063-016-1703-8
    Dec 20, 2016 · Pressure ulcers represent a major burden to patients, carers and the healthcare system, affecting approximately 1 in 17 hospital and 1 in 20 community patients. They impact greatly on an individual’s functional status and health-related quality of life. The mainstay of pressure ulcer prevention practice is the provision of pressure redistribution support surfaces and patient repositioning ...Cited by: 9

Pressure relieving support surfaces (PRESSURE) trial: cost ...

    https://www.bmj.com/content/332/7555/1416
    Jun 15, 2006 · Objective To assess the cost effectiveness of alternating pressure mattresses compared with alternating pressure overlays for the prevention of pressure ulcers in patients admitted to hospital. Design Cost effectiveness analysis carried out alongside the pressure relieving support surfaces (PRESSURE) trial; a multicentre UK based pragmatic randomised controlled trial. Setting 11 hospitals …Cited by: 83

Medicare Policy Regarding Pressure Reducing Support ...

    https://www.cms.gov/Medicare/Medicare-Contracting/ContractorLearningResources/downloads/JA1014.pdf
    Pressure reducing support surfaces are a type of DME used for the care of pressure sores, also known as pressure ulcers. • Pressure ulcers are lesions caused by unrelieved pressure resulting in damage of underlying tissue. • Support surfaces are coded under one of 16 different Healthcare Common Procedure Coding System codes. •

Pressure relieving support surfaces (PRESSURE) trial: cost ...

    https://www.ncbi.nlm.nih.gov/pmc/articles/PMC1479635/
    Jun 17, 2006 · Objective To assess the cost effectiveness of alternating pressure mattresses compared with alternating pressure overlays for the prevention of pressure ulcers in patients admitted to hospital.. Design Cost effectiveness analysis carried out alongside the pressure relieving support surfaces (PRESSURE) trial; a multicentre UK based pragmatic randomised controlled trial.Cited by: 83

CG-DME-16 Pressure Reducing Support Surfaces – Groups 1, 2 …

    https://medicalpolicies.amerigroup.com/medicalpolicies/guidelines/gl_pw_a053642.htm
    Pressure Reducing Support Surfaces-Group 1 Pressure Reducing Support Surfaces-Group 2 Pressure Reducing Support Surfaces-Group 3. The use of specific product names is illustrative only. It is not intended to be a recommendation of one product over another, and is not intended to represent a complete listing of all products available.

Support surfaces for treating pressure injury: A Cochrane ...

    https://www.sciencedirect.com/science/article/pii/S0020748912001794
    The use of pressure-relieving support surfaces for healing pressure injuries are generally used in conjunction with other wound management strategies such as positioning and use of dressings. Support surfaces include overlays, mattresses, cushions, sheepskins and beds. These can be classified either as ‘low-tech’ or ‘high-tech’ devices.

Pressure Relieving Support Surfaces for Pressure Ulcer ...

    https://www.thelancet.com/journals/eclinm/article/PIIS2589-5370(19)30138-5/fulltext
    In high risk (acutely ill, bedfast/chairfast/Category 1 PU/ pain on a PU site) in-patients, we found insufficient evidence of a difference in time to PU development at 30-day final follow-up, which may be related to a low event rate affecting trial power. APMs conferred a small treatment phase benefit. Patient preference, low PU incidence and small group differences suggests the need for ...Cited by: 3



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