TY - JOUR
T1 - Standardised Outcomes in Nephrology-Polycystic Kidney Disease (SONG-PKD)
T2 - Study protocol for establishing a core outcome set in polycystic kidney disease
AU - Cho, Yeoungjee
AU - Sautenet, Benedicte
AU - Rangan, Gopala
AU - Craig, Jonathan C.
AU - Ong, Albert C.M.
AU - Chapman, Arlene
AU - Ahn, Curie
AU - Chen, Dongping
AU - Coolican, Helen
AU - Kao, Juliana Tze Wah
AU - Gansevoort, Ron
AU - Perrone, Ronald
AU - Harris, Tess
AU - Torres, Vicente
AU - Pei, York
AU - Kerr, Peter G.
AU - Ryan, Jessica
AU - Gutman, Talia
AU - Howell, Martin
AU - Ju, Angela
AU - Manera, Karine E.
AU - Teixeira-Pinto, Armando
AU - Hamiwka, Lorraine A.
AU - Tong, Allison
N1 - Funding Information:
YC is supported by the National Health and Medical Research Council (NHMRC) Early Career Fellowship (1126256). AT is supported by the NHMRC Career Development Fellowship (1106716). ATP is partially supported by the NHMRC Program Grant BEAT CKD (APP1092957). This project is supported by the NHMRC Program Grant 1092597 and the Polycystic Kidney Disease (PKD) Foundation of Australia. The funding bodies do not have a role in the design, collection, analysis, or interpretation of data; in the writing of the manuscript; or in the decision to submit the manuscript for publication.
Publisher Copyright:
© 2017 The Author(s).
PY - 2017/11/23
Y1 - 2017/11/23
N2 - Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common potentially life threatening inherited kidney disease and is responsible for 5-10% of cases of end-stage kidney disease (ESKD). Cystic kidneys may enlarge up to 20 times the weight of a normal kidney due to the growth of renal cysts, and patients with ADPKD have an increased risk of morbidity, premature mortality, and other life-time complications including renal and hepatic cyst and urinary tract infection, intracranial aneurysm, diverticulosis, and kidney pain which impair quality of life. Despite some therapeutic advances and the growing number of clinical trials in ADPKD, the outcomes that are relevant to patients and clinicians, such as symptoms and quality of life, are infrequently and inconsistently reported. This potentially limits the contribution of trials to inform evidence-based decision-making. The Standardised Outcomes in Nephrology-Polycystic Kidney Disease (SONG-PKD) project aims to establish a consensus-based set of core outcomes for trials in PKD (with an initial focus on ADPKD but inclusive of all stages) that patients and health professionals identify as critically important. Methods: The five phases of SONG-PKD are: a systematic review to identify outcomes that have been reported in existing PKD trials; focus groups with nominal group technique with patients and caregivers to identify, rank, and describe reasons for their choices; qualitative stakeholder interviews with health professionals to elicit individual values and perspectives on outcomes for trials involving patients with PKD; an international three-round Delphi survey with all stakeholder groups (including patients, caregivers, healthcare providers, policy makers, researchers, and industry) to gain consensus on critically important core outcome domains; and a consensus workshop to review and establish a set of core outcome domains and measures for trials in PKD. Discussion: The SONG-PKD core outcome set is aimed at improving the consistency and completeness of outcome reporting across ADPKD trials, leading to improvements in the reliability and relevance of trial-based evidence to inform decisions about treatment and ultimately improve the care and outcomes for people with ADPKD.
AB - Background: Autosomal dominant polycystic kidney disease (ADPKD) is the most common potentially life threatening inherited kidney disease and is responsible for 5-10% of cases of end-stage kidney disease (ESKD). Cystic kidneys may enlarge up to 20 times the weight of a normal kidney due to the growth of renal cysts, and patients with ADPKD have an increased risk of morbidity, premature mortality, and other life-time complications including renal and hepatic cyst and urinary tract infection, intracranial aneurysm, diverticulosis, and kidney pain which impair quality of life. Despite some therapeutic advances and the growing number of clinical trials in ADPKD, the outcomes that are relevant to patients and clinicians, such as symptoms and quality of life, are infrequently and inconsistently reported. This potentially limits the contribution of trials to inform evidence-based decision-making. The Standardised Outcomes in Nephrology-Polycystic Kidney Disease (SONG-PKD) project aims to establish a consensus-based set of core outcomes for trials in PKD (with an initial focus on ADPKD but inclusive of all stages) that patients and health professionals identify as critically important. Methods: The five phases of SONG-PKD are: a systematic review to identify outcomes that have been reported in existing PKD trials; focus groups with nominal group technique with patients and caregivers to identify, rank, and describe reasons for their choices; qualitative stakeholder interviews with health professionals to elicit individual values and perspectives on outcomes for trials involving patients with PKD; an international three-round Delphi survey with all stakeholder groups (including patients, caregivers, healthcare providers, policy makers, researchers, and industry) to gain consensus on critically important core outcome domains; and a consensus workshop to review and establish a set of core outcome domains and measures for trials in PKD. Discussion: The SONG-PKD core outcome set is aimed at improving the consistency and completeness of outcome reporting across ADPKD trials, leading to improvements in the reliability and relevance of trial-based evidence to inform decisions about treatment and ultimately improve the care and outcomes for people with ADPKD.
KW - Autosomal dominant polycystic kidney disease
KW - Chronic kidney disease
KW - Core outcome set
KW - Outcomes research
KW - Patient-centred outcomes clinical trials
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U2 - 10.1186/s13063-017-2298-4
DO - 10.1186/s13063-017-2298-4
M3 - Article
C2 - 29169385
AN - SCOPUS:85035218174
SN - 1745-6215
VL - 18
JO - Trials
JF - Trials
IS - 1
M1 - 560
ER -