TY - JOUR
T1 - Developing a disease-specific patient reported outcome measure to enhance understanding of the lived experiences of ANCA associated vasculitis
T2 - A protocol paper
AU - Floyd, Lauren
AU - Dhaygude, Ajay
AU - Mitra, Sandip
AU - Rowland, Christine
N1 - Publisher Copyright:
© 2024 Floyd et al. This is an open access article distributed under the terms of the Creative Commons Attribution License,
PY - 2024/3/7
Y1 - 2024/3/7
N2 - Anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) is a chronic, relapsing-remitting condition associated with increased morbidity. Previous research has shown patients with AAV report high levels of fatigue, pain, depression and anxiety. Over recent years successful work has been carried out to improve clinical outcomes, resulting in reduced mortality and end stage kidney disease (ESKD). Despite this, little work has been done to better understand the role of the patient within this condition. The prevalence of AAV is increasing and to date, there is a shortage of specific tools that assess and measure key features relating to patient reported outcomes (PROs). This protocol details how we can better understand the lived experiences of those with AAV through the development of a disease specific, patient reported outcome measure (PROM), to be used in clinic practice. This will allow us to recognise and validate PROs and the impact the disease and its treatment has on patients’ health related quality of life (HRQoL). In addition, we aim to identify potential differences in PRO’s between demographics, organ involvement and treatment subgroups in AAV as well as outcomes relating to the patient experience. Patients from a single centre in the UK will be recruited to take part in the exploratory qualitative study which will include focus groups and semi-structured interviews. The inclusion criteria comprise anyone with a diagnosis of AAV and willing to participate, including those who have active or relapsing disease, those are economically active, unemployed, retired and patients receiving renal replacement therapy. The aim of the project is to identify key issues patients experience in relation to their disease and its management and how these can be better assessed in a new PROM developed for use in the clinic setting. This will enable better delivery of individualised care and inform shared decision making, while also serving as a platform for future research looking at PROs in other glomerulonephritides.
AB - Anti-neutrophil cytoplasmic antibody (ANCA) associated vasculitis (AAV) is a chronic, relapsing-remitting condition associated with increased morbidity. Previous research has shown patients with AAV report high levels of fatigue, pain, depression and anxiety. Over recent years successful work has been carried out to improve clinical outcomes, resulting in reduced mortality and end stage kidney disease (ESKD). Despite this, little work has been done to better understand the role of the patient within this condition. The prevalence of AAV is increasing and to date, there is a shortage of specific tools that assess and measure key features relating to patient reported outcomes (PROs). This protocol details how we can better understand the lived experiences of those with AAV through the development of a disease specific, patient reported outcome measure (PROM), to be used in clinic practice. This will allow us to recognise and validate PROs and the impact the disease and its treatment has on patients’ health related quality of life (HRQoL). In addition, we aim to identify potential differences in PRO’s between demographics, organ involvement and treatment subgroups in AAV as well as outcomes relating to the patient experience. Patients from a single centre in the UK will be recruited to take part in the exploratory qualitative study which will include focus groups and semi-structured interviews. The inclusion criteria comprise anyone with a diagnosis of AAV and willing to participate, including those who have active or relapsing disease, those are economically active, unemployed, retired and patients receiving renal replacement therapy. The aim of the project is to identify key issues patients experience in relation to their disease and its management and how these can be better assessed in a new PROM developed for use in the clinic setting. This will enable better delivery of individualised care and inform shared decision making, while also serving as a platform for future research looking at PROs in other glomerulonephritides.
KW - Humans
KW - Quality of Life
KW - Anti-Neutrophil Cytoplasmic Antibody-Associated Vasculitis
KW - Glomerulonephritis/complications
KW - Antibodies, Antineutrophil Cytoplasmic
KW - Patient Reported Outcome Measures
UR - http://www.scopus.com/inward/record.url?scp=85186972304&partnerID=8YFLogxK
UR - https://www.mendeley.com/catalogue/53cba7fd-c47c-3f84-b73b-2d088639d0cd/
U2 - 10.1371/journal.pone.0298796
DO - 10.1371/journal.pone.0298796
M3 - Article
C2 - 38451929
AN - SCOPUS:85186972304
SN - 1932-6203
VL - 19
JO - PLoS ONE
JF - PLoS ONE
IS - 3
M1 - e0298796
ER -