Health-related quality of life after heart and lung transplantation with prolonged intensive medical care

2010 ◽  
Vol 58 (S 01) ◽  
Author(s):  
P Azhari ◽  
G Marggraf ◽  
Y Erim ◽  
M Beckmann ◽  
M Pennewiß ◽  
...  
2001 ◽  
Vol 89 (3) ◽  
pp. 707-717 ◽  
Author(s):  
E. M. TenVergert ◽  
K. M. Vermeulen ◽  
A. Geertsma ◽  
P. J. van Enckevort ◽  
W. J. de Boer ◽  
...  

Whether lung transplantation improves Health-related Quality of Life in patients with emphysema and other end-stage lung diseases before and after lung transplantation was examined. Berween 1992 and 1999, 23 patients with emphysema and 19 patients with other indications completed self-administered questionnaires before lung transplantation, and at 4, 7, 13, and 25 mo. after transplantation. The questionnaire included the Nottingham Health Profile, the State-Trait Anxiety Inventory, the Self-rating Depression Scale, the Index of Well-being, the self-report Karnofsky Index, and four respiratory-specific questions. Neither before nor after transplantation were significant differences found on most dimensions of Health-related Quality of Life between patients with emphysema and other indications. Before transplantation, both groups report major restrictions on the dimensions Energy and Mobility of the Nottingham Health Profile, low experienced well-being, depressive symptoms, and high dyspnea. About 4 mo. after transplantation, most Health-related Quality of Life measures improved significantly in both groups. These improvements were maintained in the following 21 mo.


CHEST Journal ◽  
2005 ◽  
Vol 128 (3) ◽  
pp. 1371-1378 ◽  
Author(s):  
Margaret W. Gerbase ◽  
Anastase Spiliopoulos ◽  
Thierry Rochat ◽  
Marc Archinard ◽  
Laurent P. Nicod

2015 ◽  
Vol 192 (8) ◽  
pp. 965-973 ◽  
Author(s):  
Lianne G. Singer ◽  
Noori A. Chowdhury ◽  
Marie E. Faughnan ◽  
John Granton ◽  
Shaf Keshavjee ◽  
...  

Medical Care ◽  
1998 ◽  
Vol 36 (3) ◽  
pp. 295-306 ◽  
Author(s):  
William E. Cunningham ◽  
Ron D. Hays ◽  
Margo K. Ettl ◽  
Wilfrid J. Dixon ◽  
Rebecca Ching-Chi Liu ◽  
...  

2000 ◽  
Vol 161 (6) ◽  
pp. 1937-1941 ◽  
Author(s):  
JAN W. K. van den BERG ◽  
ALBERT GEERTSMA ◽  
WIM van der BIJ ◽  
GERARD H. KOËTER ◽  
WILLEM J. de BOER ◽  
...  

2017 ◽  
Vol 62 (5) ◽  
pp. 588-594 ◽  
Author(s):  
Annemieke Oude Lansink-Hartgring ◽  
Wim van der Bij ◽  
Erik A Verschuuren ◽  
Michiel E Erasmus ◽  
Adrianus J de Vries ◽  
...  

Folia Medica ◽  
2019 ◽  
Vol 61 (2) ◽  
pp. 213-222 ◽  
Author(s):  
Zoran Nikola Nakov ◽  
Stojka Naceva Fushtikj ◽  
Jasmina Tonikj-Ribarska ◽  
Suzana Trajkovikj Jolevska

Abstract Background: : Health-related quality of life (HRQoL) is a parameter that is examined in the area of clinical effectiveness. Like other chronic health conditions, paediatric cystic fibrosis (CF) impacts not only children but also their families. Aim: The present study investigates for the first time the HRQoL of children and parents in the Republic of North Macedonia. Materials and methods: The survey included 22 children (6 to 13 years of age) and their parents and 7 parents of children under 6 years of age by using the CFQ Revised and questions for current medical treatment. Results: Children (6-13 years) reported the highest score for the digestive condition (84.85), while the lowest score was given for social activity (59.74). The highest score for digestive condition was also obtained from the parents of children from 6-13 years and under age of 6. The parents of children (6-13 years) reported the lowest score (60.56) for treatment burden activity, while the lowest score (50.0) for eating condition was obtained from the parents of children under 6 years. Conclusion: Nationality and gender have no significant impact on the HRQoL parameters. The highest scores for the digestive condition, respiratory function and physical condition are in a positive correlation with the fact that enzyme, antibiotic and physical therapy are given as a standard medical care. The lowest scores of the social aspect of the CF patients indicate the need for including a psychological support and support of social workers as a part of the standard medical care of these patients.


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