Literature DB >> 27133488

Patient-Reported Outcomes in Systemic Lupus Erythematosus.

Mary Mahieu1, Susan Yount2, Rosalind Ramsey-Goldman1.   

Abstract

Successful management of complex conditions such as systemic lupus erythematosus (SLE) and comorbid conditions benefit from patient-reported outcomes (PRO). Measuring health-related quality of life with PROs provides SLE patients with an opportunity to participate in their treatment and to facilitate better communication with the multidisciplinary team involved in their care. Health outcomes research has produced well-validated instruments that can be used across diseases; others have been specifically developed for SLE. The use of generic and SLE-specific PROs depends on needs, including population monitoring, treatment decision making, clinical trials research, and for evaluating and comparing the effect of therapies.
Copyright © 2016 Elsevier Inc. All rights reserved.

Entities:  

Keywords:  Patient-reported outcomes (PROs); Quality of life (QoL); Systemic lupus erythematosus (SLE, lupus)

Mesh:

Year:  2016        PMID: 27133488      PMCID: PMC4853651          DOI: 10.1016/j.rdc.2016.01.001

Source DB:  PubMed          Journal:  Rheum Dis Clin North Am        ISSN: 0889-857X            Impact factor:   2.670


  78 in total

1.  Learning from discordance in patient and physician global assessments of systemic lupus erythematosus disease activity.

Authors:  C Neville; A E Clarke; L Joseph; P Belisle; D Ferland; P R Fortin
Journal:  J Rheumatol       Date:  2000-03       Impact factor: 4.666

Review 2.  The epidemiology of systemic lupus erythematosus.

Authors:  M Siegel; S L Lee
Journal:  Semin Arthritis Rheum       Date:  1973       Impact factor: 5.532

3.  Body image intervention to improve health outcomes in lupus: a pilot study.

Authors:  Meenakshi Jolly; Kristin F Peters; Rachel Mikolaitis; Kali Evans-Raoul; Joel A Block
Journal:  J Clin Rheumatol       Date:  2014-12       Impact factor: 3.517

4.  Quality of life of women with systemic lupus erythematosus: a comparison with women with rheumatoid arthritis.

Authors:  C S Burckhardt; B Archenholtz; A Bjelle
Journal:  J Rheumatol       Date:  1993-06       Impact factor: 4.666

5.  Cross-cultural validation of a disease-specific patient-reported outcome measure for lupus in Philippines.

Authors:  S V Navarra; R M D V Tanangunan; R A Mikolaitis-Preuss; M Kosinski; J A Block; M Jolly
Journal:  Lupus       Date:  2013-01-22       Impact factor: 2.911

6.  Predictors of self-reported health-related quality of life in systemic lupus erythematosus.

Authors:  Adnan N Kiani; Vibeke Strand; Hong Fang; Jawali Jaranilla; Michelle Petri
Journal:  Rheumatology (Oxford)       Date:  2013-05-16       Impact factor: 7.580

Review 7.  Understanding the epidemiology and progression of systemic lupus erythematosus.

Authors:  Guillermo J Pons-Estel; Graciela S Alarcón; Lacie Scofield; Leslie Reinlib; Glinda S Cooper
Journal:  Semin Arthritis Rheum       Date:  2009-01-10       Impact factor: 5.532

8.  Morbidity and mortality in systemic lupus erythematosus during a 10-year period: a comparison of early and late manifestations in a cohort of 1,000 patients.

Authors:  Ricard Cervera; Munther A Khamashta; Josep Font; Gian Domenico Sebastiani; Antonio Gil; Paz Lavilla; Juan Carlos Mejía; A Olcay Aydintug; Hanna Chwalinska-Sadowska; Enrique de Ramón; Antonio Fernández-Nebro; Mauro Galeazzi; Merete Valen; Alessandro Mathieu; Frédéric Houssiau; Natividad Caro; Paula Alba; Manuel Ramos-Casals; Miguel Ingelmo; Graham R V Hughes
Journal:  Medicine (Baltimore)       Date:  2003-09       Impact factor: 1.889

9.  Quality of life over time in patients with systemic lupus erythematosus.

Authors:  Bindee Kuriya; Dafna D Gladman; Dominque Ibañez; Murray B Urowitz
Journal:  Arthritis Rheum       Date:  2008-02-15

10.  EQ-5D and SF-36 quality of life measures in systemic lupus erythematosus: comparisons with rheumatoid arthritis, noninflammatory rheumatic disorders, and fibromyalgia.

Authors:  Frederick Wolfe; Kaleb Michaud; Tracy Li; Robert S Katz
Journal:  J Rheumatol       Date:  2009-12-23       Impact factor: 4.666

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  16 in total

1.  Factors influencing implementation of a computerized, individualized, culturally tailored lupus decision aid in lupus clinics: a qualitative semi-structured interview study.

Authors:  Haiyan Qu; Xuejun Hu; Jasvinder A Singh
Journal:  Clin Rheumatol       Date:  2019-06-20       Impact factor: 2.980

Review 2.  Lupus education for physicians and patients in a resource-limited setting.

Authors:  Sandra V Navarra; Leonid D Zamora; Ma Theresa M Collante
Journal:  Clin Rheumatol       Date:  2019-11-05       Impact factor: 2.980

3.  Self-reported disease severity in women with systemic lupus erythematosus.

Authors:  A Dima; S Caraiola; C Delcea; R A Ionescu; C Jurcut; C Badea
Journal:  Rheumatol Int       Date:  2018-11-10       Impact factor: 2.631

Review 4.  Anxiety and Mood Disorders in Systemic Lupus Erythematosus: Current Insights and Future Directions.

Authors:  Annaliese Tisseverasinghe; Christine Peschken; Carol Hitchon
Journal:  Curr Rheumatol Rep       Date:  2018-11-12       Impact factor: 4.592

5.  Chronic Cutaneous Lupus Erythematosus: Depression Burden and Associated Factors.

Authors:  Jennifer Hong; Laura Aspey; Gaobin Bao; Tamara Haynes; S Sam Lim; Cristina Drenkard
Journal:  Am J Clin Dermatol       Date:  2019-06       Impact factor: 7.403

6.  Patient-Reported Outcomes Predict Mortality in Lupus.

Authors:  Desiree R Azizoddin; Meenakshi Jolly; Shilpa Arora; Ed Yelin; Patricia Katz
Journal:  Arthritis Care Res (Hoboken)       Date:  2019-07-13       Impact factor: 4.794

7.  Symptom assessment in hypereosinophilic syndrome: Toward development of a patient-reported outcomes tool.

Authors:  Nicholas Kovacs; Katy Benjamin; Nicole Holland-Thomas; Olga Moshkovich; Linda M Nelsen; Hector Ortega; Ethan J Schwartz; Jonathan Steinfeld; Suyong Yun Kirby; Amy Klion; Paneez Khoury
Journal:  J Allergy Clin Immunol Pract       Date:  2020-05-15

Review 8.  Measuring and monitoring health-related quality of life responsiveness in systemic lupus erythematosus patients: current perspectives.

Authors:  Jamal Mikdashi
Journal:  Patient Relat Outcome Meas       Date:  2018-10-04

9.  Naturopathic approaches to irritable bowel syndrome: protocol for a prospective observational study in academic teaching clinics.

Authors:  Joshua Z Goldenberg; Amie Steel; Andrew Day; Christina Yap; Ryan Bradley; Kieran Cooley
Journal:  Integr Med Res       Date:  2018-06-09

10.  Patient-reported outcome measures for use in clinical trials of SLE: a review.

Authors:  Zara Izadi; Julie Gandrup; Patricia P Katz; Jinoos Yazdany
Journal:  Lupus Sci Med       Date:  2018-08-21
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