Literature DB >> 10638772

Haemophilic; arthropathy: assessment of quality of life after total knee arthroplasty.

M Schick1, G Stucki, M Rodriguez, E O Meili, E Huber, B A Michel, P Brühlmann.   

Abstract

The goal of this study was to examine how the known effects of total knee arthroplasty (TKA) on clinical outcome parameters translate into improved quality of life, as measured with validated condition-specific and generic questionnaires (Knee Society Score, WOMAC, SF-12, transition questions), addressing physical, mental and social health. Eleven patients (13 knees) undergoing TKA from 1986 to 1994, with the diagnosis of severe haemophilic arthropathy of the knee, were followed-up over a 4-year period on average. TKA was found to reduce the burden of disease to levels similar to patients with osteoarthritis undergoing hip arthroplasty. Clinical and functional improvement after TKA translated into a substantial and significant increase in quality of life and patient satisfaction, found in objective as well as in patient-perceived measures. However, the physical functional ability did not reach the same level as in the corresponding population not affected by haemophilia, due to residual symptoms and impairment of other joints.

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Year:  1999        PMID: 10638772     DOI: 10.1007/s100670050140

Source DB:  PubMed          Journal:  Clin Rheumatol        ISSN: 0770-3198            Impact factor:   2.980


  5 in total

1.  Longitudinal changes in health-related quality of life for chronic diseases: an example in hemophilia A.

Authors:  Jiat-Ling Poon; Jason N Doctor; Michael B Nichol
Journal:  J Gen Intern Med       Date:  2014-08       Impact factor: 5.128

2.  Successful use of recombinant factor VIIa for hemostasis during total knee replacement in a severe hemophiliac with high-titer factor VIII inhibitor.

Authors:  Marcus E Carr; Thomas P Loughran; John A Cardea; Wade K Smith; Jan G Kuhn; Maribeth V Dottore
Journal:  Int J Hematol       Date:  2002-01       Impact factor: 2.490

3.  Total hip replacement in patients with severe bleeding disorders. A 30 years single center experience.

Authors:  B Habermann; C Eberhardt; L Hovy; L Zichner; I Scharrer; A A Kurth
Journal:  Int Orthop       Date:  2006-05-20       Impact factor: 3.075

4.  Assessing quality of life in individuals with hereditary blood coagulation disorders.

Authors:  S Solovieva; N Santavirta; S Santavirta; Y T Konttinen
Journal:  Qual Life Res       Date:  2004-06       Impact factor: 4.147

5.  Revision arthroplasty in the haemophiliac patient.

Authors:  A P Molloy; B J O'Neill; L Molloy; B White; H Smyth; T Mc Carthy
Journal:  Case Rep Orthop       Date:  2013-05-02
  5 in total

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