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Impact of systemic lupus erythematosus on health, family, and work: The patient perspective

✍ Scribed by Don Robinson Jr.; Daniel Aguilar; Melissa Schoenwetter; Robert Dubois; Simcha Russak; Rosalind Ramsey-Goldman; Sandra Navarra; Benjamin Hsu; Dennis Revicki; David Cella; Mark Hyman Rapaport; Kevin Renahan; Richard Ress; Daniel Wallace; Michael Weisman


Publisher
Wiley (John Wiley & Sons)
Year
2010
Tongue
English
Weight
95 KB
Volume
62
Category
Article
ISSN
2151-464X

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## Abstract ## Objective To compare health care utilization in people with systemic lupus erythematosus (SLE) in health maintenance organizations (HMOs) and fee‐for‐service (FFS). ## Methods A structured survey was administered to a cohort of 982 people with SLE who were assembled between 2002 a

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## Abstract ## Objective To identify coping strategies used by patients with systemic lupus erythematosus (SLE), and to assess the influence of main clinical and coping variables on health‐related quality of life (HRQOL). ## Methods We administered the Coping Orientation to Problems Experienced