Zobrazeno 1 - 10
of 101
pro vyhledávání: '"A Y, Finlay"'
Publikováno v:
Acta Dermato-Venereologica, Vol 104 (2024)
This study systematically analysed peer-reviewed publications describing validation aspects of the Dermatology Life Quality Index (DLQI) and used Naicker’s Critically Appraising for Antiracism Tool to assess risk of racial bias. Seven online databa
Externí odkaz:
https://doaj.org/article/2821a8e5ed574cc388f11a330c235cea
Publikováno v:
Medicina, Vol 60, Iss 8, p 1215 (2024)
Background and Objectives: We previously reported on the impact of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on the QoL of persons with ME/CFS and their family members. Here, we present the findings of the impact on the QoL of indiv
Externí odkaz:
https://doaj.org/article/3634884ef0e7490693544b729520e299
Autor:
A. Y. Finlay, J. N. Barker, A. D. Burden, C. E. M. Griffiths, B. Kirby, M. L. Goodman, C. Neill, R. B. Warren
Publikováno v:
JEADV Clinical Practice, Vol 1, Iss 3, Pp 207-218 (2022)
Abstract Background The Family Dermatology Life Quality Index (FDLQI) was developed to meet a need for a dermatology‐specific family member/partner quality‐of‐life (QoL) measure. This paper focuses on the analysis and interpretation of FDLQI da
Externí odkaz:
https://doaj.org/article/885e1faf40d14c64a60a1ef0cf072503
Autor:
Sylvia van Beugen, Christina Schut, Jörg Kupfer, Antony P. Bewley, Andrew Y. Finlay, Uwe Gieler, Andrew R. Thompson, Tamara Grazia-Cazaña, Flora Balieva, Bárbara R. Ferreira, Gregor B. Jemec, Lars Lien, Laurent Misery, Servando E. Marron, Sonja Ständer, Claudia Zeidler, Csanád Szabó, Jacek C. Szepietowski, Adam Reich, Amna Elyas, Ilknur K. Altunay, Franz J. Legat, Vesna Grivcheva-Panovska, Dmitry V. Romanov, Andrey N. Lvov, Géraldine Titeca, Francesca Sampogna, Nienke C. Vulink, Lucia Tomás-Aragones, Andrea W.M. Evers, Florence J. Dalgard
Publikováno v:
Acta Dermato-Venereologica, Vol 103 (2023)
Perceived stigmatization places a large psychosocial burden on patients with some skin conditions. Little is known about the experience of stigmatization across a wide range of skin diseases. This observational cross-sectional study aimed to quantify
Externí odkaz:
https://doaj.org/article/f55d88ecdc9946a5ad95fc492b80fa27
Publikováno v:
Caribbean Medical Journal (2023)
Background & Objectives: Impact of dermatological and other chronic conditions not only affects the quality of life (QoL) of patients but also that of their family members. This pilot study aimed to compare the QoL impact of dermatological and other
Externí odkaz:
https://doaj.org/article/4ff167dd1fe644aeb3910265cafbe8c6
Autor:
Kennedy Otwombe, Andrew Y Finlay, John R Ingram, Rubina Shah, Faraz M Ali, Stuart J Nixon, Sam M Salek
Publikováno v:
BMJ Open, Vol 13, Iss 3 (2023)
Objective To assign clinical meanings to the Family Reported Outcome Measure (FROM-16) scores through the development of score bands using the anchor-based approach.Design and setting A cross-sectional online study recruited participants through UK-b
Externí odkaz:
https://doaj.org/article/e8d004d348fa4afca3e36348f2bc1bd2
Publikováno v:
Health and Quality of Life Outcomes, Vol 19, Iss 1, Pp 1-35 (2021)
Abstract Background A person’s chronic health condition or disability can have a huge impact on the quality of life (QoL) of the whole family, but this important impact is often ignored. This literature review aims to understand the impact of patie
Externí odkaz:
https://doaj.org/article/14c7c60a28fb4a3dbc1464c5b380c027
Autor:
Susanne A. Elsner, Sam S. Salek, Andrew Y. Finlay, Anna Hagemeier, Catherine J. Bottomley, Alexander Katalinic, Annika Waldmann
Publikováno v:
Health and Quality of Life Outcomes, Vol 19, Iss 1, Pp 1-14 (2021)
Abstract Background The Family Reported Outcome Measure (FROM-16) assesses the impact of a patient’s chronic illness on the quality of life (QoL) of the patient’s partner or family members. The aim of the study was to translate, explore the struc
Externí odkaz:
https://doaj.org/article/3a7a5da384c844369f6d2db2c074bc8a
Publikováno v:
BMJ Open, Vol 12, Iss 5 (2022)
Objectives The aim of this study was to assess the impact of myalgic encephalomyelitis/chronic fatigue syndrome (ME/CFS) on the quality of life (QoL) of people with ME/CFS and their relative or partner (family member).Design A patient-partner, multin
Externí odkaz:
https://doaj.org/article/3f08d184dac5475cacf447fbc24271bb
Autor:
Bruce E. Strober, Joelle M. van der Walt, April W. Armstrong, Marc Bourcier, Andre V. E. Carvalho, Edgardo Chouela, Arnon D. Cohen, Claudia de la Cruz, Charles N. Ellis, Andrew Y. Finlay, Alice B. Gottlieb, Johann E. Gudjonsson, Lars Iversen, C. Elise Kleyn, Craig L. Leonardi, Charles W. Lynde, Caitriona Ryan, Colin T. Theng, Fernando Valenzuela, Ronald Vender, Jashin J. Wu, Helen S. Young, Alexa B. Kimball
Publikováno v:
Dermatology and Therapy, Vol 9, Iss 1, Pp 5-18 (2018)
Abstract Engaging global key opinion leaders, the International Psoriasis Council (IPC) held a day-long roundtable discussion with the primary purpose to discuss the treatment goals of psoriasis patients and worldwide barriers to optimal care. Settin
Externí odkaz:
https://doaj.org/article/ee5c476d90bb43d4bc632f02137fee65