Literature DB >> 32741118

Impact of Limited Health Literacy on Patient-Reported Outcomes in Systemic Lupus Erythematosus.

Patricia Katz1, Maria Dall'Era1, Laura Trupin1, Stephanie Rush1, Louise B Murphy2, Cristina Lanata1, Lindsey A Criswell1, Jinoos Yazdany1.   

Abstract

OBJECTIVE: Health disparities in patient-reported outcomes by income and education are well documented; however, the impact of health literacy on patient-reported outcomes has received less attention. We examined independent effects of income, education, and health literacy on patient-reported outcomes in systemic lupus erythematosus (SLE).
METHODS: Data from the California Lupus Epidemiology Study (n = 323 participants) were used. Health literacy was assessed with a validated 3-item measure (ability to understand written information, reliance on others to understand written information, confidence in completing written forms). Patient-reported outcomes were administered by interview in English, Spanish, Cantonese, or Mandarin. Generic and disease-specific patient-reported outcomes were examined using the following: 10 Patient-Reported Outcomes Measurement Information System (PROMIS) short forms; the 8 Short Form 36 (SF-36) health survey subscales; and 3 patient-reported SLE disease activity and damage measures. We conducted 2 sets of multivariable analyses: the first examined education, income, or health literacy individually; the second included all 3 simultaneously. All multivariable models included age, sex, race/ethnicity, language, disease duration, and physician-assessed disease activity and damage.
RESULTS: More than one-third of participants (38%) had limited health literacy (LHL), including >25% with greater than high school education. In multivariable analyses simultaneously considering education, income, and health literacy, LHL was associated with significantly worse scores on all patient-reported outcomes except disease damage. In contrast, disparities by income were seen in only 3 PROMIS scales, 3 SF-36 subscales, and 1 disease activity measure. No disparities by education level were noted.
CONCLUSION: We found significantly worse patient-reported outcome scores among individuals with LHL, even after controlling for disease activity and damage. Whether disparities are due to actual differences in health or measurement issues requires further study.
© 2020, American College of Rheumatology.

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Year:  2021        PMID: 32741118      PMCID: PMC7775267          DOI: 10.1002/acr.24361

Source DB:  PubMed          Journal:  Arthritis Care Res (Hoboken)        ISSN: 2151-464X            Impact factor:   5.178


  32 in total

1.  A Prospective Study of the Impact of Current Poverty, History of Poverty, and Exiting Poverty on Accumulation of Disease Damage in Systemic Lupus Erythematosus.

Authors:  Edward Yelin; Laura Trupin; Jinoos Yazdany
Journal:  Arthritis Rheumatol       Date:  2017-07-05       Impact factor: 10.995

2.  Health literacy predicts the discrepancy between patient and provider global assessments of rheumatoid arthritis activity at a public urban rheumatology clinic.

Authors:  Joel M Hirsh; Dennis J Boyle; David H Collier; Abbey J Oxenfeld; Liron Caplan
Journal:  J Rheumatol       Date:  2010-03-15       Impact factor: 4.666

3.  Brief index of lupus damage: a patient-reported measure of damage in systemic lupus erythematosus.

Authors:  Jinoos Yazdany; Laura Trupin; Stuart A Gansky; Maria Dall'era; Edward H Yelin; Lindsey A Criswell; Patricia P Katz
Journal:  Arthritis Care Res (Hoboken)       Date:  2011-08       Impact factor: 4.794

4.  Validation of the systemic lupus erythematosus activity questionnaire in a large observational cohort.

Authors:  Jinoos Yazdany; Edward H Yelin; Pantelis Panopalis; Laura Trupin; Laura Julian; Patricia P Katz
Journal:  Arthritis Rheum       Date:  2008-01-15

5.  Readability and suitability assessment of patient education materials in rheumatic diseases.

Authors:  Rennie L Rhee; Joan M Von Feldt; H Ralph Schumacher; Peter A Merkel
Journal:  Arthritis Care Res (Hoboken)       Date:  2013-10       Impact factor: 4.794

6.  Use of Low-Literacy Decision Aid to Enhance Knowledge and Reduce Decisional Conflict Among a Diverse Population of Adults With Rheumatoid Arthritis: Results of a Pilot Study.

Authors:  Jennifer L Barton; Laura Trupin; Dean Schillinger; Gina Evans-Young; John Imboden; Victor M Montori; Edward Yelin
Journal:  Arthritis Care Res (Hoboken)       Date:  2016-07       Impact factor: 4.794

7.  Adherence and health literacy as related to outcome of patients treated for rheumatoid arthritis : Analyses of a large-scale observational study.

Authors:  J G Kuipers; M Koller; F Zeman; K Müller; J U Rüffer
Journal:  Z Rheumatol       Date:  2019-02       Impact factor: 1.372

8.  Limited Health Literacy Is Associated With Worse Patient-Reported Outcomes in Inflammatory Bowel Disease.

Authors:  Lauren K Tormey; Jason Reich; Yu Sarah Chen; Arush Singh; Zachary Lipkin-Moore; Anzhu Yu; Janice Weinberg; Francis A Farraye; Michael K Paasche-Orlow
Journal:  Inflamm Bowel Dis       Date:  2019-01-01       Impact factor: 5.325

Review 9.  The Relationship between Health Literacy and Health Disparities: A Systematic Review.

Authors:  Sarah Mantwill; Silvia Monestel-Umaña; Peter J Schulz
Journal:  PLoS One       Date:  2015-12-23       Impact factor: 3.240

10.  Interview Administration of PROMIS Depression and Anxiety Short Forms.

Authors:  Bayley J Taple; James W Griffith; Michael S Wolf
Journal:  Health Lit Res Pract       Date:  2019-09-06
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  8 in total

1.  Comprehension, utility, and preferences of prostate cancer survivors for visual timelines of patient-reported outcomes co-designed for limited graph literacy: meters and emojis over comics.

Authors:  Lauren E Snyder; Daniel F Phan; Kristen C Williams; Eduardo Piqueiras; Sarah E Connor; Sheba George; Lorna Kwan; Jefersson Villatoro Chavez; Megha D Tandel; Stanley K Frencher; Mark S Litwin; John L Gore; Andrea L Hartzler
Journal:  J Am Med Inform Assoc       Date:  2022-10-07       Impact factor: 7.942

2.  Patient and healthcare professional eHealth literacy and needs for systemic sclerosis support: a mixed methods study.

Authors:  Agnes Kocher; Michael Simon; Andrew A Dwyer; Catherine Blatter; Jasmina Bogdanovic; Patrizia Künzler-Heule; Peter M Villiger; Diana Dan; Oliver Distler; Ulrich A Walker; Dunja Nicca
Journal:  RMD Open       Date:  2021-09

3.  Patient-Reported Outcome Information Collected from Lupus Patients Using a Mobile Application: Compliance and Validation.

Authors:  Kristy Bell; Claire Dykas; Bridget Muckian; Brooke Williams; Hope Rainey; Maggy Comberg; Mary Mora; Katherine A Owen; Peter E Lipsky
Journal:  ACR Open Rheumatol       Date:  2021-11-10

Review 4.  Health Literacy in Patients' Clinical Records of Hospital Settings: A Systematic Review.

Authors:  Elena Cristofori; Valentina Zeffiro; Rosaria Alvaro; Fabio D'Agostino; Maurizio Zega; Antonello Cocchieri
Journal:  SAGE Open Nurs       Date:  2022-03-07

Review 5.  Health disparities in systemic lupus erythematosus-a narrative review.

Authors:  Bilal Hasan; Alice Fike; Sarfaraz Hasni
Journal:  Clin Rheumatol       Date:  2022-07-31       Impact factor: 3.650

6.  A Prospective Follow-Up Study on the Disease Course and Predictors of Poor Outcomes in a Random Population-Based Cohort of Newly Diagnosed Lupus Patients.

Authors:  Saadat Ullah; Muhammad Haroon; Farzana Hashmi; Zaid Tayyab; Saba Javed
Journal:  Cureus       Date:  2022-07-29

7.  COVID-19 vaccine literacy in patients with systemic autoimmune diseases.

Authors:  María Correa-Rodríguez; Blanca Rueda-Medina; José-Luis Callejas-Rubio; Raquel Ríos-Fernández; Javier de la Hera-Fernández; Norberto Ortego-Centeno
Journal:  Curr Psychol       Date:  2022-01-18

Review 8.  Patient-Reported Outcomes in Systemic Lupus Erythematosus. Can Lupus Patients Take the Driver's Seat in Their Disease Monitoring?

Authors:  Ioannis Parodis; Paul Studenic
Journal:  J Clin Med       Date:  2022-01-11       Impact factor: 4.241

  8 in total

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