Læknablaðið : fylgirit - 01.05.2002, Blaðsíða 48

Læknablaðið : fylgirit - 01.05.2002, Blaðsíða 48
POSTERS / 3 3RD SNC & 2ND SCNN to evaluate the impact of various socio-demographic and medical factor on QoL. Methods: This study is part of the community-bascd Copenhagen Stroke Study, and prospectively included 401 patients with acute stroke. Assessment of QoL was done using the Frenchay Activity Index (FAI). It was performed within the first week of admission, and at the 6-month follow-up. The independent importance of variables on QoL was evaluated in a multiple linear regression model. Results: The following factors were negatively related to QoL before stroke: Male gender (p<0.01), nursing home recidence (p=0.04), living single (p=0.02), diabetes (p=0.01), home help (p<0.01), smoking (p<0.01), previous stroke (p<0.01), other disabling disease (p=0.01), and increasing age (p<0.01). Working prior to stroke was the only positive factor for QoL before stroke (p=0.01). QoL after stroke was negatively related to increasing neurological deficit on the Scandinavian Stroke Scale (p<0.01) and disability in basic activities after stroke (Barthel Index, p=0.02), male gender (p<0.01), nursing home recidence (p<0.01), diabetes (p<0.01), home help (p<0.01), previous stroke (p<0.01), and age (p<0.01), and positively related to QoL before stroke (p<0.01). Conclusion: A good social network is important to life quality. Due to differences in sex roles men performed poorer than women in FAI score. QoL was significantly lower in patients with diabetes both before and after stroke. Smoking was related to a poorer QoL before stroke. Neurological deficit and functional disability after stroke, nursing home recidence, previous stroke and diabetes were the most important negative factors for QoL after stroke. A good life quality before stroke was the most important factor for a good QoL after stroke. Improvement in QoL after stroke should focus on limiting the neurological deficits and basic functional disability after stroke. P34 - Documentation of tacit knowledge. Improving MS nursing Jota PA, Haugstad R, Kornerud U, Wehus R, Klingsheim B, Nortvedt MW Central Hospital in Hedemark HF, Elverum, Norway Background/objective: After the introduction of the interferon-beta therapy in multiple sclerosis (MS), nurses have been given new tasks in the treatment of MS-patients. This includes the development and organisation of information, training and follow-up of patients on treatment. We wish to evaluate how the patients manage their new treatment, and to find elements of our practice related to informa- tion, training and follow-up that might be improved. Method: All patients beginning with interferon treatment (Avonex, Betaferon, Rebif) in four hospitals in Norway are consecutively asked to participate in the study and will be followed-up with individual consultations by MS nurses. The study will include 75 patients. The patients are given a questionnaire including a diary to be filled out during a period ol' three months. In a follow-up after one year the patients will be asked to fill out an equivalent questionnaire. The questionnaire includes questions regarding how the patient evaluates the information, training and the follow-up given by the nurse. It also includes questions regarding side effects and how these are managed. Additionally, a quality of life question- naire (SF-36) is completed at baseline, month three and month 12. Results: The collection of data started in October 2001 and 30 patients are included by the end of February 2002. All 75 patients are expected to be included before the end of 2002. The project has already had a positive effect on the member of the project group during the planning process. We have become more aware of the importance of documenting our clinical experience. Conclusion: As nurses we ought to visualize the importance of what we do. Our challenge is to document our experience and tacit knowledge, and to show that appropriate nursing makes a positive difference for the patients. P35 - Evidence-based nursing to stroke patients. Application of an evidence-based clinical guideline concerning the basic need: Nutrition Zielke S, Christensen D, Muus I H:S Bispebjerg Hospital Copenhagen University Hospital Denmark The aim of the project was to evidence-base nursing care of stroke patients and to monitor the quality of nursing practice concerning the basic needs: nutrition Mcthods: A clinical guideline has been developed. Recommendations for good clinical practice: Identifying the risk patient: Assessment according to screening tool - Drinking test (B) - Nutritional state (C) Nutritional therapy for the risk patient: - Calculating the patient\'s need for energy, protein and fluid (C) Choosing diet: - Adjusting food consistency in relation to dysphagia (C) - nasogastric tube feeding within 72 hrs by transient dysphagia - percutaneous endoscopic gastrostomy tube feeding within 2-4 weeks by expected Persistent dysphagia (B) Evaluating the patient\'s need for specific training Monitoring: Quality indicators: - Daily assessment of energy, protein and fluid - Weekly assessment of body weight - Eating ability according to Barthel Index or other validated instrument - Body Mass Index at admission, after 3 weeks, and at discharge - Events of pneumonia treated with antibiotics during hospitalisation Results/Conclusion: The clinical guideline has been implemented in stroke units at Bispebjerg University Hospital, Árhus University Hospital and Esbpnderup Hospital and results from the database will be present at the congress. P36 - Does rehabilitation improve quality of life in individuals with Parkinson’s disease? Prospective pilot study Gunnbjörnsdóttir H, Bjarnadóttir ÓH Reykjalundur Rehabilitation Center, Mosfellsbær, Iceland Objective: To determine if rehabilitation improves quality of life and secondly, if quality of life measurements can be used for locating hidden nursing problems. Material and inethods: Thirty-five individuals with Parkinson's disease received a five week inpatient group rehabilitation program in small groups (4-6) from November 1999 - September 2001. Mean age was 65 years (49-84). Individuals were selected according to 48 Læknabladið/Fylgirit 43 2002/88
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