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Sökning: L773:1353 8020 OR L773:1873 5126 > (2000-2004)

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1.
  • Hariz, Gun-Marie, et al. (författare)
  • Gender distribution in surgery for Parkinson's disease.
  • 2000
  • Ingår i: Parkinsonism & Related Disorders. - 1353-8020 .- 1873-5126. ; 6:3, s. 155-157
  • Tidskriftsartikel (refereegranskat)abstract
    • Parkinson's disease (PD) affects both women and men. The surgical treatment of this disease has experienced a worldwide increase since the mid-eighties. In order to document eventual differences in gender distribution of patients undergoing various stereotactic surgical procedures for PD, we reviewed scientific papers published during the last 14years.A literature search provided 145 clinical papers, published between January 1985 and February 1999, and dealing with pallidotomy, thalamotomy and deep brain stimulation procedures. These papers were scrutinised with respect to redundancies or other overlap of reported patients. The resulting numbers of patients were compiled according to gender, to surgical procedure, and to geographic area of origin of the publishing centers.In one third of the reviewed publications the gender of the patients was not specified. In the remaining papers, the overall sex distribution of patients who underwent surgery was 35% females and 65% males. These proportions between sexes were relatively consistent regardless of surgical procedure, and regardless of geographic origin of the publications.Male preponderance in patients undergoing surgery for PD cannot be explained by a corresponding difference in gender-prevalence of the disease. The criteria of selection, and patterns of referral, of patients for surgery, as well as the respective attitude of female and male patients toward surgery, may account for the uneven gender distribution in surgical PD patients.
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  • Quittenbam, B H, et al. (författare)
  • Quality of life and pain in Parkinson's disease: a controlled cross-sectional study
  • 2004
  • Ingår i: Parkinsonism & Related Disorders. - : Elsevier BV. - 1873-5126 .- 1353-8020. ; 10:3, s. 129-136
  • Tidskriftsartikel (refereegranskat)abstract
    • Purpose. To compare health-related quality of life (HRQL) and-pain symptoms in patients with PD with a matched control group. To our knowledge, controlled studies of Parkinson's disease (PD) patients within this area are rare. Scope. Fifty-seven patients and 95 controls took part in a self-administered questionnaire study. The instruments were the SF-36, visual analogue scales, pain drawing and pain-specific questions. Conclusions. Pain problems are common in PD patients but also to a large extent in the normal population. HRQL was reduced (p less than or equal to 0.001) for the PD patients on all the scales on the SF-36 and consequently also in the pain dimension. The study indicates that even PD patients, who are optimally diagnosed and treated by a neurologist, might require additional rehabilitation treatment to improve their HRQL and pain problems. (C) 2004 Elsevier Ltd. All rights reserved.
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  • Aquilonius, SM, et al. (författare)
  • Introduction
  • 2004
  • Ingår i: PARKINSONISM & RELATED DISORDERS. - : Elsevier BV. - 1353-8020. ; 10:5, s. 257-258
  • Tidskriftsartikel (övrigt vetenskapligt/konstnärligt)
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  • Hagell, Peter, et al. (författare)
  • International use of health status questionnaires in Parkinson's disease: translation is not enough.
  • 2003
  • Ingår i: Parkinsonism & Related Disorders. - 1873-5126. ; 10:2, s. 89-92
  • Tidskriftsartikel (refereegranskat)abstract
    • The present study assessed the linguistic and content validity of the Swedish version of the 39-item Parkinson's disease questionnaire (PDQ-39). The frame question, response alternatives and two of the 39 items yielded substantial linguistic and stylistic problems. Such shortcomings would be expected to influence responses to, and the quality of, the whole questionnaire. Data support content validity of the PDQ-39 as a functional health status questionnaire, although some shortcomings were identified. This preliminary study illustrates the need for documented linguistic validity before new language adaptations of patient-reported outcome measures can be considered suitable for use in clinical trials, research, and practice.
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