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EUROPEAN PRESSURE ULCER ADVISORY PANEL

Ninth EPUAP Meeting in Berlin, August 2006

POSTER WINNERS' ABSTRACTS

Poster presentations, Berlin Poster Presentations, Berlin:

First Prize awarded to Alexander Heyneman, Gent, Belgium (centre),

Second Prize awarded to Anne Ballard-Wilson, Dunfermiline, Scotland (left),

Third Prize awarded to Anna-Karin Westerlund, Uppsala, Sweden (right).

Pressure ulcer treatment with dressings: a systematic review of published randomized controlled trials
A. Heyneman, RN, MA; H. Beele, MD, PhD; T. Defloor, RN, PhD

Nursing Science, Department of Public Health, Ghent University, UZ 2 Blok A, De Pintelaan 185, B 9000 Gent, Belgium (Contact: alexander.heyneman@ugent.be)

Introduction:
Pressure ulcers are a common problem in nursing practice and entail great expenses for the patients as well as for the Health Care Services. Financial resources are limited, an optimal use is thus recommended. The aim of the study is to identify and review the published literature on the use of dressings as treatment of pressure ulcers.

Methods:
A Cochrane based search strategy was used in three databases (PubMed, Embase and CENTRAL), manuals, reference lists and conference proceedings. Used keywords were ‘randomized controlled trial’, ‘random allocation’, ‘decubitus ulcer’, ‘therapeutics’ and ‘therapy’. Studies in which pressure ulcers were treated with dressings, as defined by The British National Formulary, were systematically included and analysed. An additional search was performed to identify validated instruments for assessment of the quality and cost-effectiveness analysis. No sufficiently validated instrument could be identified.

Results:
54 publications, dealing with 52 different studies, met the inclusion criteria. Grouping, based on The British National Formulary, resulted in 31 different categories. Based on the available evidence, none of the dressing categories was proven to be more effective than others. There was marginal evidence that dressings which needed to be changed less frequently were better rated by patients and caregivers. The same was true for pain during wearing and changing.

Summary:
A clear recommendation about the most effective dressing category could not be made. Identification and analysis of additional studies is recommended. Additionally, the development of an instrument to validate the quality and the cost-effectiveness is needed.


Pressure Ulcer Prevalence in a District General Division: What are the benefits of doing it?
Anne Ballard Wilson, Tissue Viability Nurse Specialist

Fife Acute Operational Division, Queen Margaret Hospital, Whitefield Road, Dunfermline, KY12 0SU

Introduction:
Pressure ulcers continue to pose serious clinical and economic challenges within the National Health Service. Point Prevalence Studies assist our decision-making by giving valuable information, which can help with identification of the type of care and equipment required within an organisation.

Methodology:
A Point Prevalence Survey was carried out in February 2006 in a 600-bedded Hospital. The Tissue Viability (TV) Service in conjunction with Pegasus Ltd, who compiled the data, conducted it. The audit itself was carried out by the TVN with a team of tissue viability link nurses, working to a predetermined protocol. The survey included age, sex, number of established pressure ulcers, the likelihood of developing a pressure ulcer, and current provision of pressure distributing surfaces. In addition, the ability of patients’ to turn unassisted in bed, and care planning provision.

Results:
Data was collected for 591 patients, 15% having established pressure ulcers. The age, sex and severity of pressure ulcers will be discussed, with particular emphasis on the type of surface patients were nursed on. A comparison will also be made with two studies carried out two and five years ago.

Summary:
This study showed that although the age of patients is steadily increasing, there is no significant change in the overall number or severity of pressure damage. Within this Trust there has been a shift away from nursing patients on the more ‘high tech’ dynamic surfaces, with no apparent detriment to the patient.


Do nutritional supplements for patients with hip fracture reduce postoperative complications?
Anna-Karin Westerlund, RN1,2, Katarina Lönn, MD2, Lena Gunningberg, RN, PhD3,4

1. Department of Public Health and Caring Sciences, Section of Caring Science, Uppsala University, Uppsala, Sweden.
2. Department of Orthopaedics, University Hospital, Uppsala, Sweden.
3. Department of Surgical Sciences, Uppsala University, Uppsala Sweden.
4. Department of Surgery, University Hospital, Uppsala, Sweden.


Introduction:
Malnutrition is common in Swedish hospitals; the incidence of malnutrition in 25 Swedish studies (n = 5120) was 28%. Patients with hip fracture constitute a group at particular risk for malnutrition. British research has shown that these patients do not receive all the energy and calories they need after surgery, which can lead to postoperative complications. Previous research at the University Hospital in Uppsala has showed that 29% of patients with hip fracture developed pressure ulcers during their hospital stay. Pressure ulcers increase the overall cost of care to society and can cause both physical and psychological suffering for patients. Nutritional supplements can delay both the onset and progression of pressure ulcers. However, as 57% of patients develop pressure ulcers within two days after surgery and 76% within four days after, it is important that the supplements be given as early as possible postoperatively.

Aim:
The aim of the present study is to investigate whether nutritional supplements reduce postoperative complications – specifically, pressure ulcers – in patients with hip fracture.

Methods:
The design was quasi-experimental, with both intervention and control groups; 100 patients with hip fracture admitted to the University Hospital in Uppsala are included consecutively (50 patients in each group). Data collection started in September 2005 and will continue until June 2006. The intervention group received a glucose infusion starting the night before surgery and ending the morning the day after surgery, complemented with a carbohydrate-supplement drink. For five days postoperatively, patients also receive nutritional supplements, three times a day. The need of energy was calculated for each patient, nutritional and liquid intake was assessed daily, and interventions according to clinical guidelines were implemented if needed. Outcome measures used were the Modified Norton Scale, pressure ulcer classification according to EPUAP recommendations, weight, Insulin-like Growth Factor-1, Short Portable Mental Square Questionnaire and the Katz index. All of the assessments were collected preoperatively and five days postoperatively. Every patient’s nutrient and liquid intake was assessed daily for five days.

Results:
Data will be analysed in July 2006.

 

 
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