Weighting improves the information provided by joint counts on the severity of arthritis and its impact on patients' well-being in juvenile idiopathic arthritis (original) (raw)

Development and initial validation of composite parent- and child-centered disease assessment indices for juvenile idiopathic arthritis

Maria Alessio

Arthritis Care & Research, 2011

View PDFchevron_right

Assessment of disease activity in juvenile idiopathic arthritis. The number and the size of joints matter

Lisa Wernroth

The Journal of Rheumatology

View PDFchevron_right

Relative responsiveness of condition specific and generic health status measures in juvenile idiopathic arthritis

Silvia Magni-manzoni

Annals of the Rheumatic Diseases, 2005

View PDFchevron_right

The Short Arthritis Assessment Scale: a brief assessment questionnaire for rapid evaluation of arthritis severity in research and clinical practice

Fred Wolfe

The Journal of rheumatology, 2004

View PDFchevron_right

Psychometric characteristics of outcome measures in juvenile idiopathic arthritis: A systematic review

Gillian Sanders Schmidler

Arthritis Care & Research, 2012

View PDFchevron_right

Agreement between physicians and parents in rating functional ability of children with juvenile idiopathic arthritis

Elena Palmisani

Pediatric Rheumatology, 2007

View PDFchevron_right

Development and validation of a new short and simple measure of physical function for juvenile idiopathic arthritis

G. Filocamo

Arthritis & Rheumatism, 2007

View PDFchevron_right

Development and testing of reduced joint counts in juvenile idiopathic arthritis

silvia magni manzoni

The Journal of …, 2009

View PDFchevron_right

Drivers of non-zero physician global scores during periods of inactive disease in juvenile idiopathic arthritis

Francesca Ridella

RMD Open, 2022

View PDFchevron_right

The pediatric rheumatology quality of life scale: validation of the English version in a US cohort of juvenile idiopathic arthritis

Chris Feudtner

Pediatric rheumatology online journal, 2013

View PDFchevron_right

Early detection of high disease activity in juvenile idiopathic arthritis by sequential monitoring of patients' health‐related quality of life scores

Peihua Qiu

Biometrical Journal

View PDFchevron_right

Patient self-report RADAI (Rheumatoid Arthritis Disease Activity Index) joint counts on an MDHAQ (Multidimensional Health Assessment Questionnaire) in usual care of consecutive patients with rheumatic diseases other than rheumatoid arthritis

Isabel Castrejón

Arthritis Care & Research, 2013

View PDFchevron_right

Assessment of quality of rheumatoid arthritis care requires joint count and/or patient questionnaire data not found in a usual medical record: examples from studies of premature mortality, changes in clinical status between 1985 and 2000, and a QUEST-RA global perspective

Theodore Pincus

Clinical and experimental rheumatology

View PDFchevron_right

The difference in pain and overall well-being assessment between patients with juvenile idiopathic arthritis, their parents, and physicians in Ukraine

Halyna Pavlyshyn

Pediatria Polska

View PDFchevron_right

Comparative measurement efficiency and sensitivity of five health status instruments for arthritis research

Matthew H Liang

Arthritis and Rheumatism, 1985

View PDFchevron_right

Level of agreement between children, parents, and physicians in rating pain intensity in juvenile idiopathic arthritis

Marcia Bandeira, Silvia Magni-manzoni

Arthritis & Rheumatism, 2006

View PDFchevron_right

Health of children with chronic arthritis: Relationship of different measures and the quality of parent proxy reporting

Murray Passo

Arthritis & Rheumatism, 2004

View PDFchevron_right

Arthritis Impact Measurement Scales in a Community-Based Rheumatoid Arthritis Population

Pentti Nieminen

Clinical Rheumatology, 2000

View PDFchevron_right

AIMS2. The Content and Properties of a Revised and Expanded Arthritis Impact Measurement Scales Health Status Questionnaire

Lewis Kazis

Arthritis & Rheumatism, 1992

View PDFchevron_right

Most visits of most patients with rheumatoid arthritis to most rheumatologists do not include a formal quantitative joint count

Oscar Segurado

Annals of the Rheumatic Diseases, 2006

View PDFchevron_right

A comparison of the measurement properties of the Juvenile Arthritis Functional Assessment Scale with the childhood health assessment questionnaire in daily practice

Peter Bekkering, Marion Rossum

Clinical Rheumatology, 2007

View PDFchevron_right

RAPID3 (Routine Assessment of Patient Index Data 3), a rheumatoid arthritis index without formal joint counts for routine care: proposed severity categories compared to disease activity score and clinical disease activity index categories

Martin Bergman

2008

View PDFchevron_right

Evidence for Updating the Core Domain Set of Outcome Measures for Juvenile Idiopathic Arthritis: Report from a Special Interest Group at OMERACT 2016

Julia Harris

The Journal of rheumatology, 2017

View PDFchevron_right

Validation of the Brazilian version of the pediatric outcomes data collection instrument: a cross-sectional evaluation in children and adolescents with juvenile idiopathic arthritis

MARIA JAN CORINNE MARIANO

BMC Pediatrics, 2013

View PDFchevron_right

Validity and reliability of self-reported arthritis

Charles Helmick

American Journal of Preventive Medicine, 2005

View PDFchevron_right

Development of a disability measurement tool for juvenile rheumatoid arthritis. The juvenile arthritis functional assessment report for children and their parents

Steven Howe

Arthritis and Rheumatism, 1991

View PDFchevron_right

PReS-FINAL-2116: Assessment of disease activity by patients with juvenile idiopathic arthritis and the parents compared to the assessment by pediatric rheumatologists

Jelte Bouma

Pediatric Rheumatology, 2013

View PDFchevron_right

Health-related quality of life assessment in a group of children with juvenile idiopathic arthritis

Elham Hossny

2020

View PDFchevron_right

Adding patient-reported outcomes to a multisite registry to quantify quality of life and experiences of disease and treatment for youth with juvenile idiopathic arthritis

Parissa K Salimian, Fatma Dedeoglu

Journal of Patient-Reported Outcomes, 2018

View PDFchevron_right

Patient perceptions of foot disability in Juvenile Idiopathic Arthritis: a comparison of the juvenile arthritis foot disability index and the Oxford ankle foot questionnaire for children

Jill Ferrari

Journal of Foot and Ankle Research, 2015

View PDFchevron_right