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Cutaneous lupus concerns from the patient perspective: a qualitative study

OBJECTIVE: There is a need to identify concerns unique to patients with cutaneous lupus erythematosus (CLE), which may not be captured by current common-practice dermatological quality-of-life tools. This study formally characterises what bothers patients with CLE about their disease by conducting s...

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Autores principales: Yan, Daisy, Zamalin, Danielle, Chakka, Srita, Krain, Rebecca, Concha, Josef, Feng, Rui, Ahmed, Sarah, Okawa, Joyce, Werth, Victoria P
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Publishing Group 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404455/
https://www.ncbi.nlm.nih.gov/pubmed/34452954
http://dx.doi.org/10.1136/lupus-2020-000444
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author Yan, Daisy
Zamalin, Danielle
Chakka, Srita
Krain, Rebecca
Concha, Josef
Feng, Rui
Ahmed, Sarah
Okawa, Joyce
Werth, Victoria P
author_facet Yan, Daisy
Zamalin, Danielle
Chakka, Srita
Krain, Rebecca
Concha, Josef
Feng, Rui
Ahmed, Sarah
Okawa, Joyce
Werth, Victoria P
author_sort Yan, Daisy
collection PubMed
description OBJECTIVE: There is a need to identify concerns unique to patients with cutaneous lupus erythematosus (CLE), which may not be captured by current common-practice dermatological quality-of-life tools. This study formally characterises what bothers patients with CLE about their disease by conducting semistructured, qualitative interviews. METHODS: Sixteen patients with CLE were interviewed about how their cutaneous findings impact their daily life. Each interview was transcribed, coded and categorised for recurrent themes. Current CLE activity and damage were also assessed by the Cutaneous Lupus Activity and Severity Index tool. RESULTS: Responses were categorised into six themes, including Fear of Disease Progression, Unwanted Attention, Self-Consciousness, Physical Signs/Symptoms, Emotional Symptoms and Functional Decline. The most commonly reported themes were Self-Consciousness, mentioned by 13 of 16 (81.3%) patients, Physical Symptoms, mentioned by 12 of 16 (75%), and then Fear of Disease Progression, by 11 of 16 (68.8%). Frequently mentioned physical signs/symptoms included erythema, itch, dyspigmentation, scar and alopecia. The physical signs/symptoms were categorised as activity signs/symptoms, damage signs and other. For activity signs, erythema was mentioned most frequently (5 of 16), then scale (2 of 16). For activity symptoms, itch was mentioned most frequently (6 of 16), then pain (5 of 16). For damage signs, dyspigmentation was mentioned most frequently (4 of 16), followed by scarring (3 of 16). Patients less than 60 years old were more likely to report emotional symptoms than older patients (p<0.05), but there was no significant variation in frequency of reported themes between race, sex or subtype of CLE. CONCLUSIONS: These patient experiences and resultant themes elucidated by this study are worth noting in future standardised estimations of the quality of life of patients with CLE. Additionally, the concerns shown by these interviews are important topics for providers to discuss when evaluating patient disease progression.
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spelling pubmed-84044552021-09-14 Cutaneous lupus concerns from the patient perspective: a qualitative study Yan, Daisy Zamalin, Danielle Chakka, Srita Krain, Rebecca Concha, Josef Feng, Rui Ahmed, Sarah Okawa, Joyce Werth, Victoria P Lupus Sci Med Cutaneous Lupus OBJECTIVE: There is a need to identify concerns unique to patients with cutaneous lupus erythematosus (CLE), which may not be captured by current common-practice dermatological quality-of-life tools. This study formally characterises what bothers patients with CLE about their disease by conducting semistructured, qualitative interviews. METHODS: Sixteen patients with CLE were interviewed about how their cutaneous findings impact their daily life. Each interview was transcribed, coded and categorised for recurrent themes. Current CLE activity and damage were also assessed by the Cutaneous Lupus Activity and Severity Index tool. RESULTS: Responses were categorised into six themes, including Fear of Disease Progression, Unwanted Attention, Self-Consciousness, Physical Signs/Symptoms, Emotional Symptoms and Functional Decline. The most commonly reported themes were Self-Consciousness, mentioned by 13 of 16 (81.3%) patients, Physical Symptoms, mentioned by 12 of 16 (75%), and then Fear of Disease Progression, by 11 of 16 (68.8%). Frequently mentioned physical signs/symptoms included erythema, itch, dyspigmentation, scar and alopecia. The physical signs/symptoms were categorised as activity signs/symptoms, damage signs and other. For activity signs, erythema was mentioned most frequently (5 of 16), then scale (2 of 16). For activity symptoms, itch was mentioned most frequently (6 of 16), then pain (5 of 16). For damage signs, dyspigmentation was mentioned most frequently (4 of 16), followed by scarring (3 of 16). Patients less than 60 years old were more likely to report emotional symptoms than older patients (p<0.05), but there was no significant variation in frequency of reported themes between race, sex or subtype of CLE. CONCLUSIONS: These patient experiences and resultant themes elucidated by this study are worth noting in future standardised estimations of the quality of life of patients with CLE. Additionally, the concerns shown by these interviews are important topics for providers to discuss when evaluating patient disease progression. BMJ Publishing Group 2021-08-27 /pmc/articles/PMC8404455/ /pubmed/34452954 http://dx.doi.org/10.1136/lupus-2020-000444 Text en © Author(s) (or their employer(s)) 2021. Re-use permitted under CC BY-NC. No commercial re-use. See rights and permissions. Published by BMJ. https://creativecommons.org/licenses/by-nc/4.0/This is an open access article distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited, appropriate credit is given, any changes made indicated, and the use is non-commercial. See: http://creativecommons.org/licenses/by-nc/4.0/ (https://creativecommons.org/licenses/by-nc/4.0/) .
spellingShingle Cutaneous Lupus
Yan, Daisy
Zamalin, Danielle
Chakka, Srita
Krain, Rebecca
Concha, Josef
Feng, Rui
Ahmed, Sarah
Okawa, Joyce
Werth, Victoria P
Cutaneous lupus concerns from the patient perspective: a qualitative study
title Cutaneous lupus concerns from the patient perspective: a qualitative study
title_full Cutaneous lupus concerns from the patient perspective: a qualitative study
title_fullStr Cutaneous lupus concerns from the patient perspective: a qualitative study
title_full_unstemmed Cutaneous lupus concerns from the patient perspective: a qualitative study
title_short Cutaneous lupus concerns from the patient perspective: a qualitative study
title_sort cutaneous lupus concerns from the patient perspective: a qualitative study
topic Cutaneous Lupus
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8404455/
https://www.ncbi.nlm.nih.gov/pubmed/34452954
http://dx.doi.org/10.1136/lupus-2020-000444
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