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Clinical and psychological phenomenology of pain in autoinflammatory diseases
BACKGROUND: Pain is the clinical hallmark of patients in patients with autoinflammatory diseases (AID) caused by variants of the NLRP3-, MEFV- or TNFRSF1A gene. However, no systematical analysis of the clinical and psychological presentation of pain has been performed to date. METHODS: Twenty-one sy...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
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BioMed Central
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747389/ https://www.ncbi.nlm.nih.gov/pubmed/33334368 http://dx.doi.org/10.1186/s41927-020-00168-x |
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author | Mulazzani, Elisabeth Zolyniak, Nicole Noe, Elisabeth Mulazzani, Matthias Azad, Shahnaz Christina Kümpfel, Tania Kraft, Eduard |
author_facet | Mulazzani, Elisabeth Zolyniak, Nicole Noe, Elisabeth Mulazzani, Matthias Azad, Shahnaz Christina Kümpfel, Tania Kraft, Eduard |
author_sort | Mulazzani, Elisabeth |
collection | PubMed |
description | BACKGROUND: Pain is the clinical hallmark of patients in patients with autoinflammatory diseases (AID) caused by variants of the NLRP3-, MEFV- or TNFRSF1A gene. However, no systematical analysis of the clinical and psychological presentation of pain has been performed to date. METHODS: Twenty-one symptomatic patients with variants in the NLRP3-, MEFV- and TNFRSF1A gene and clinical signs suggestive of an AID were retrospectively included in this monocentric cross-sectional case-series study. Patients were examined and interviewed using the German pain questionnaire. The hospital anxiety and depression scale (HADS) was applied to screen patients for anxiety and depression. RESULTS: Twenty out of 21 AID patients (95%) reported pain at the time of examination. Mean current pain intensity in all AID patients comprised 3.6 ± 1.3 and mean maximum pain intensity was 7.0 ± 1.6 on a 11-point numeric ranging scale (NRS). In 15 patients (71%), pain was present for more than 60 months. Ten patients (48%) experienced recurrent attacks with asymptomatic intervals and 7 patients (33%) suffered from constant pain, while 4 patients (19%) experienced both. Nociceptive pain including musculoskeletal and visceral affection was the most prominent type of pain (n = 20; 95%). Pain symptoms were treated continuously with analgesic or co-analgesic drugs in 10 patients (48%). Five patients (24%) have been positively screened for concomitant depression or anxiety. CONCLUSIONS: Early and prompt diagnosis is necessary to provide multimodal pain treatment and to avoid the development of chronic pain in patients with AID. |
format | Online Article Text |
id | pubmed-7747389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-77473892020-12-21 Clinical and psychological phenomenology of pain in autoinflammatory diseases Mulazzani, Elisabeth Zolyniak, Nicole Noe, Elisabeth Mulazzani, Matthias Azad, Shahnaz Christina Kümpfel, Tania Kraft, Eduard BMC Rheumatol Research Article BACKGROUND: Pain is the clinical hallmark of patients in patients with autoinflammatory diseases (AID) caused by variants of the NLRP3-, MEFV- or TNFRSF1A gene. However, no systematical analysis of the clinical and psychological presentation of pain has been performed to date. METHODS: Twenty-one symptomatic patients with variants in the NLRP3-, MEFV- and TNFRSF1A gene and clinical signs suggestive of an AID were retrospectively included in this monocentric cross-sectional case-series study. Patients were examined and interviewed using the German pain questionnaire. The hospital anxiety and depression scale (HADS) was applied to screen patients for anxiety and depression. RESULTS: Twenty out of 21 AID patients (95%) reported pain at the time of examination. Mean current pain intensity in all AID patients comprised 3.6 ± 1.3 and mean maximum pain intensity was 7.0 ± 1.6 on a 11-point numeric ranging scale (NRS). In 15 patients (71%), pain was present for more than 60 months. Ten patients (48%) experienced recurrent attacks with asymptomatic intervals and 7 patients (33%) suffered from constant pain, while 4 patients (19%) experienced both. Nociceptive pain including musculoskeletal and visceral affection was the most prominent type of pain (n = 20; 95%). Pain symptoms were treated continuously with analgesic or co-analgesic drugs in 10 patients (48%). Five patients (24%) have been positively screened for concomitant depression or anxiety. CONCLUSIONS: Early and prompt diagnosis is necessary to provide multimodal pain treatment and to avoid the development of chronic pain in patients with AID. BioMed Central 2020-12-18 /pmc/articles/PMC7747389/ /pubmed/33334368 http://dx.doi.org/10.1186/s41927-020-00168-x Text en © The Author(s) 2020 Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data. |
spellingShingle | Research Article Mulazzani, Elisabeth Zolyniak, Nicole Noe, Elisabeth Mulazzani, Matthias Azad, Shahnaz Christina Kümpfel, Tania Kraft, Eduard Clinical and psychological phenomenology of pain in autoinflammatory diseases |
title | Clinical and psychological phenomenology of pain in autoinflammatory diseases |
title_full | Clinical and psychological phenomenology of pain in autoinflammatory diseases |
title_fullStr | Clinical and psychological phenomenology of pain in autoinflammatory diseases |
title_full_unstemmed | Clinical and psychological phenomenology of pain in autoinflammatory diseases |
title_short | Clinical and psychological phenomenology of pain in autoinflammatory diseases |
title_sort | clinical and psychological phenomenology of pain in autoinflammatory diseases |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7747389/ https://www.ncbi.nlm.nih.gov/pubmed/33334368 http://dx.doi.org/10.1186/s41927-020-00168-x |
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