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Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany
Background and Objective: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a severe illness with the hallmark symptom of Post-Exertional Malaise (PEM). Currently, no biomarkers or established diagnostic tests for ME/CFS exist. In Germany, it is estimated that over 300,000 people are af...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306083/ https://www.ncbi.nlm.nih.gov/pubmed/34201825 http://dx.doi.org/10.3390/medicina57070646 |
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author | Froehlich, Laura Hattesohl, Daniel B. R. Jason, Leonard A. Scheibenbogen, Carmen Behrends, Uta Thoma, Manuel |
author_facet | Froehlich, Laura Hattesohl, Daniel B. R. Jason, Leonard A. Scheibenbogen, Carmen Behrends, Uta Thoma, Manuel |
author_sort | Froehlich, Laura |
collection | PubMed |
description | Background and Objective: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a severe illness with the hallmark symptom of Post-Exertional Malaise (PEM). Currently, no biomarkers or established diagnostic tests for ME/CFS exist. In Germany, it is estimated that over 300,000 people are affected by ME/CFS. Research from the United States and the UK shows that patients with ME/CFS are medically underserved, as they face barriers to medical care access and are dissatisfied with medical care. The first aim of the current research was to investigate whether patients with ME/CFS are medically underserved in Germany in terms of access to and satisfaction with medical care. Second, we aimed at providing a German-language version of the DePaul Symptom Questionnaire Short Form (DSQ-SF) as a tool for ME/CFS diagnostics and research in German-speaking countries. Materials and Methods: The current research conducted an online questionnaire study in Germany investigating the medical care situation of patients with ME/CFS. The questionnaire was completed by 499 participants who fulfilled the Canadian Consensus Criteria and reported PEM of 14 h or longer. Results: Participants frequently reported geographic and financial reasons for not using the available medical services. Furthermore, they reported low satisfaction with medical care by the physician they most frequently visited due to ME/CFS. The German version of the DSQ-SF showed good reliability, a one-factorial structure and construct validity, demonstrated by correlations with the SF-36 as a measure of functional status. Conclusions: Findings provide evidence that patients with ME/CFS in Germany are medically underserved. The German-language translation of the DSQ-SF provides a brief, reliable and valid instrument to assess ME/CFS symptoms to be used for research and clinical practice in German-speaking countries. Pathways to improve the medical care of patients with ME/CFS are discussed. |
format | Online Article Text |
id | pubmed-8306083 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-83060832021-07-25 Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany Froehlich, Laura Hattesohl, Daniel B. R. Jason, Leonard A. Scheibenbogen, Carmen Behrends, Uta Thoma, Manuel Medicina (Kaunas) Article Background and Objective: Myalgic Encephalomyelitis/Chronic Fatigue Syndrome (ME/CFS) is a severe illness with the hallmark symptom of Post-Exertional Malaise (PEM). Currently, no biomarkers or established diagnostic tests for ME/CFS exist. In Germany, it is estimated that over 300,000 people are affected by ME/CFS. Research from the United States and the UK shows that patients with ME/CFS are medically underserved, as they face barriers to medical care access and are dissatisfied with medical care. The first aim of the current research was to investigate whether patients with ME/CFS are medically underserved in Germany in terms of access to and satisfaction with medical care. Second, we aimed at providing a German-language version of the DePaul Symptom Questionnaire Short Form (DSQ-SF) as a tool for ME/CFS diagnostics and research in German-speaking countries. Materials and Methods: The current research conducted an online questionnaire study in Germany investigating the medical care situation of patients with ME/CFS. The questionnaire was completed by 499 participants who fulfilled the Canadian Consensus Criteria and reported PEM of 14 h or longer. Results: Participants frequently reported geographic and financial reasons for not using the available medical services. Furthermore, they reported low satisfaction with medical care by the physician they most frequently visited due to ME/CFS. The German version of the DSQ-SF showed good reliability, a one-factorial structure and construct validity, demonstrated by correlations with the SF-36 as a measure of functional status. Conclusions: Findings provide evidence that patients with ME/CFS in Germany are medically underserved. The German-language translation of the DSQ-SF provides a brief, reliable and valid instrument to assess ME/CFS symptoms to be used for research and clinical practice in German-speaking countries. Pathways to improve the medical care of patients with ME/CFS are discussed. MDPI 2021-06-23 /pmc/articles/PMC8306083/ /pubmed/34201825 http://dx.doi.org/10.3390/medicina57070646 Text en © 2021 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Froehlich, Laura Hattesohl, Daniel B. R. Jason, Leonard A. Scheibenbogen, Carmen Behrends, Uta Thoma, Manuel Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany |
title | Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany |
title_full | Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany |
title_fullStr | Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany |
title_full_unstemmed | Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany |
title_short | Medical Care Situation of People with Myalgic Encephalomyelitis/Chronic Fatigue Syndrome in Germany |
title_sort | medical care situation of people with myalgic encephalomyelitis/chronic fatigue syndrome in germany |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8306083/ https://www.ncbi.nlm.nih.gov/pubmed/34201825 http://dx.doi.org/10.3390/medicina57070646 |
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