URN zum Zitieren der Version auf EPub Bayreuth: urn:nbn:de:bvb:703-epub-7529-9
Titelangaben
Senn, Katja ; Thiele, Simone ; Gumbert, Laura ; Krause, Sabine ; Walter, Maggie C. ; Nagels, Klaus:
Inclusion body myositis : health‑related quality of life and care situation during phases of the "patience journey" in Germany: results from a qualitative study.
In: Health and Quality of Life Outcomes.
Bd. 21
(2023)
.
- 111.
ISSN 1477-7525
DOI der Verlagsversion: https://doi.org/10.1186/s12955-023-02196-w
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Angaben zu Projekten
Projekttitel: |
Offizieller Projekttitel Projekt-ID Open Access Publizieren Ohne Angabe |
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Projektfinanzierung: |
Deutsche Forschungsgemeinschaft Friedrich-Baur Public Trust, Burgkunstadt within the ‘Oberfranken Förderprogramm’ (Upper Frankonia Program) Open Access Publishing Fund of the University of Bayreuth |
Abstract
Background To understand the health-related quality of life (HRQoL) in inclusion body myositis (IBM) from a holistic perspective on the background of a complex care situation. The focus was on how the patient journey may be structured over the course of this rare disease. Methods An exploratory qualitative study was performed via in-depth semi-structured interviews. Seven patients (males n = 5) with 2011 European Neuromuscular Centre (ENMC) IBM criteria from the German IBM patient registry were interviewed for this study. The dynamic network approach of resilience and the throughput-model of health services research were used to structure the qualitative analysis. Results Our results suggest that IBM patients experience the holistic HRQoL and care situation typically in four phases: (1) uncertainty about physical vulnerability until diagnosis, (2) promising treatment approaches, (3) selfmanagement and dyadic coping, (4) weak body, busy mind and caregiver burden. The homophonous in-vivo code “patience journey” describes the frequently reported emotional perspective of the patient journey. Although the overarching theme of perceived social support varied throughout these phases, a reliable patient-partner-dyad may lead to improved HRQoL in the long-term. Conclusions New hypotheses for future quantitative research were generated to better understand the IBM patients’ burden in the long term. The identified relevance of social support emphasizes the patients’ need to handle IBM as manageable in medical settings. During exhausting phases of IBM progression, more effective care elements for patients and their partners could disclose varying needs. Strengthening multi-professional healthcare services via individualised informational, practical, or emotional support could improve HRQoL, especially since there is no curative treatment available so far.
Weitere Angaben
Publikationsform: | Artikel in einer Zeitschrift |
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Keywords: | Health-related quality of life; Inclusion body myositis; Social support; Qualitative research; Health services research |
Themengebiete aus DDC: | 600 Technik, Medizin, angewandte Wissenschaften > 610 Medizin und Gesundheit |
Institutionen der Universität: | Fakultäten > Rechts- und Wirtschaftswissenschaftliche Fakultät > Lehrstuhl Medizinmanagement und Versorgungsforschung Fakultäten Fakultäten > Rechts- und Wirtschaftswissenschaftliche Fakultät |
Sprache: | Englisch |
Titel an der UBT entstanden: | Ja |
URN: | urn:nbn:de:bvb:703-epub-7529-9 |
Eingestellt am: | 12 Mrz 2024 09:24 |
Letzte Änderung: | 12 Mrz 2024 09:25 |
URI: | https://epub.uni-bayreuth.de/id/eprint/7529 |