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Clinical Practice Guidelines by the Infectious Diseases Society of America (IDSA), American Academy of Neurology (AAN), and American College of Rheumatology (ACR): 2020 Guidelines for the Prevention, Diagnosis, and Treatment of Lyme Disease
Paul M. Lantos Jeffrey Rumbaugh Linda K. Bockenstedt Yngve T. Falck?Ytter Maria E. Aguero?Rosenfeld Paul G. Auwaerter Kelly Baldwin Raveendhara R. Bannuru Kiran K. Belani William R. Bowie John A. Branda David B. Clifford Francis J. DiMario Jr. John J. Halperin Peter J. Krause Valery Lavergne Matthew H. Liang H. Cody Meissner Lise E. Nigrovic James (Jay) J. Nocton Mikala C. Osani Amy A. Pruitt Jane Rips Lynda E. Rosenfeld Margot L. Savoy Sunil K. Sood Allen C. Steere Franc Strle Robert Sundel Jean Tsao Elizaveta E. Vaysbrot Gary P. Wormser Lawrence S. Zemel
doi : 10.1002/acr.24495
Volume73, Issue1,Pages 1-9
Introduction to the Special Theme Section: Psychosocial Issues in the Rheumatic Diseases
Marian T. Hannan
doi : 10.1002/acr.24518
Volume73, Issue1,Pages 10-10
Cumulative Disadvantage and Disparities in Depression and Pain Among Veterans With Osteoarthritis: The Role of Perceived Discrimination
Juliette McClendon Utibe R. Essien Ada Youk Said A. Ibrahim Ernest Vina C. Kent Kwoh Leslie R. M. Hausmann
doi : 10.1002/acr.24481
Volume73, Issue1,Pages 11-17
Perceived discrimination is associated with chronic pain and depression and contributes to racial health disparities. In a cohort of older adult veterans with osteoarthritis (OA), our objective was to examine how membership in multiple socially disadvantaged groups (cumulative disadvantage) was associated with perceived discrimination, pain, and depression. We also tested whether perceived discrimination mediated the association of cumulative disadvantage with depression and pain.
Parent Perspectives on Addressing Emotional Health for Children and Young Adults With Juvenile Myositis
Kaveh Ardalan Oluwatosin Adeyemi Dawn M. Wahezi Anne E. Caliendo Megan L. Curran Jessica Neely Susan Kim Colleen K. Correll Emily J. Brunner Andrea M. Knight
doi : 10.1002/acr.24466
Volume73, Issue1,Pages 18-29
To assess parent perspectives regarding the emotional health impact of juvenile myositis (JM) on patients and families, and to assess preferences for emotional health screening and interventions.
Impact of Psychiatric Diagnosis and Treatment on Medication Adherence in Youth With Systemic Lupus Erythematosus
Joyce C. Chang Alaina M. Davis Marisa S. Klein?Gitelman Zuleyha Cidav David S. Mandell Andrea M. Knight
doi : 10.1002/acr.24450
Volume73, Issue1,Pages 30-38
Youth with systemic lupus erythematosus (SLE) experience high rates of psychiatric comorbidities, which may affect medication adherence. We undertook this study to examine the association between psychiatric disorders and hydroxychloroquine adherence and to determine whether psychiatric treatment modifies this association.
Clinical Team Perspectives on the Psychosocial Aspects of Transition to Adult Care for Patients With Childhood?Onset Systemic Lupus Erythematosus
Nicole Bitencourt Justin Kramer Bonnie L. Bermas E. Blair Solow Tracey Wright Una E. Makris
doi : 10.1002/acr.24463
Volume73, Issue1,Pages 39-47
The transition from pediatric to adult care for youth with childhood?onset systemic lupus erythematosus (SLE) is a vulnerable period. Adverse outcomes during this transition include gaps in care, unscheduled health care utilization, loss of insurance, and high disease activity. The objective of this study was to examine the clinical care teams’ perspective on the psychosocial factors associated with transition outcomes, which are poorly understood in this population.
Major Depression and Adverse Patient?Reported Outcomes in Systemic Lupus Erythematosus: Results From a Prospective Longitudinal Cohort
Brett Dietz Patricia Katz Maria Dall’Era Louise B. Murphy Cristina Lanata Laura Trupin Lindsey A. Criswell Jinoos Yazdany
doi : 10.1002/acr.24398
Volume73, Issue1,Pages 48-54
Health?related quality of life (HRQoL) is reduced in systemic lupus erythematosus (SLE), partly driven by comorbid depression. Among patients with SLE, the association between major depression and HRQoL, measured using the NIH’s Patient?Reported Outcomes Measurement Information System (PROMIS), is not well characterized. The objective was to determine an association between major depression and HRQoL as measured by PROMIS.
Positive Psychological Factors and Impairment in Rheumatic and Musculoskeletal Disease: Do Psychopathology and Sleep Quality Explain the Linkage?
Jameson K. Hirsch Heather R. Altier Martin Offenb?cher Loren Toussaint Niko Kohls Fuschia M. Sirois
doi : 10.1002/acr.24440
Volume73, Issue1,Pages 55-64
Little is known about potential mechanisms of action linking protective positive psychological variables and functional disability in patients with rheumatic and musculoskeletal disease. The present study was undertaken to examine symptoms of psychopathology, including stress, depression, anxiety, and sleep quality, as serial mediators of the association between gratitude, self?compassion, self?forgiveness, and functional impairment.
Depressive Symptoms and the Arthritis–Employment Interface: A Population?Level Study
Arif Jetha Kristina A. Theis Michael A. Boring Louise B. Murphy Dana Guglielmo
doi : 10.1002/acr.24381
Volume73, Issue1,Pages 65-77
To examine the relationship between depressive symptoms, arthritis, and employment, and to determine whether this relationship differs across young, middle?age, and older working?age adults with arthritis.
Depression and Subsequent Risk for Incident Rheumatoid Arthritis Among Women
Jeffrey A. Sparks Susan Malspeis Jill Hahn Jiaqi Wang Andrea L. Roberts Laura D. Kubzansky Karen H. Costenbader
doi : 10.1002/acr.24441
Volume73, Issue1,Pages 78-89
To investigate the association of depression with subsequent risk of rheumatoid arthritis (RA) by serologic phenotype.
Impact of Psychiatric Comorbidity on Health Care Use in Rheumatoid Arthritis: A Population?Based Study
Carol A. Hitchon Randy Walld Christine A. Peschken Charles N. Bernstein James M. Bolton Renée El?Gabalawy John D. Fisk Alan Katz Lisa M. Lix James Marriott Scott B. Patten Jitender Sareen Alexander Singer Ruth Ann Marrie
doi : 10.1002/acr.24386
Volume73, Issue1,Pages 90-99
Psychiatric comorbidity is frequent in rheumatoid arthritis (RA) and complicates treatment. The present study was undertaken to describe the impact of psychiatric comorbidity on health care use (utilization) in RA.
Addressing Health Literacy Needs in Rheumatology: Which Patient Health Literacy Profiles Need the Attention of Health Professionals?
Mark M. Bakker Polina Putrik Jany Rademakers Mart van de Laar Harald Vonkeman Marc R. Kok Hanneke Voorneveld?Nieuwenhuis Sofia Ramiro Maarten de Wit Rachelle Buchbinder Roy Batterham Richard H. Osborne Annelies Boonen
doi : 10.1002/acr.24480
Volume73, Issue1,Pages 100-109
To identify and describe health literacy profiles of patients with rheumatic diseases and explore whether the identified health literacy profiles can be generalized to a broader rheumatology context.
Impact of Limited Health Literacy on Patient?Reported Outcomes in Systemic Lupus Erythematosus
Patricia Katz Maria Dall’Era Laura Trupin Stephanie Rush Louise B. Murphy Cristina Lanata Lindsey A. Criswell Jinoos Yazdany
doi : 10.1002/acr.24361
Volume73, Issue1,Pages 110-119
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).
Multidimensional Health Assessment Questionnaire as an Effective Tool to Screen for Depression in Routine Rheumatology Care
Rosa M. Morlà Tengfei Li Isabel Castrejon George Luta Theodore Pincus
doi : 10.1002/acr.24467
Volume73, Issue1,Pages 120-129
To analyze the use of the Multidimensional Health Assessment Questionnaire (MDHAQ) to screen for depression, as compared to 2 reference standards, the Patient Health Questionnaire 9 (PHQ?9) and the Hospital Anxiety and Depression Scale depression domain (HADS?D).
Rheumatic Conditions as Risk Factors for Self?Harm: A Retrospective Cohort Study
James A. Prior Zoe Paskins Rebecca Whittle Alyshah Abdul?Sultan Carolyn A. Chew?Graham Sara Muller Ram Bajpai Tom A. Shepherd Athula Sumathipala Christian D. Mallen
doi : 10.1002/acr.24345
Volume73, Issue1,Pages 130-137
To examine the risk of self?harm in rheumatic conditions.
Physical and Psychosocial Burden of Psoriatic Arthritis: Longitudinal Data From a Population?Based Study in Norway
Glenn Haugeberg Tom Ivar Lund Nilsen Arthur Kavanaugh Ruth Stoklund Thomsen Agnete Malm Gulati Mari Hoff
doi : 10.1002/acr.24412
Volume73, Issue1,Pages 138-145
Psoriatic arthritis (PsA) can have a significant impact on health?related quality of life (HRQoL). Data on the timing of changes in the HRQoL of patients with PsA are limited. The present study was undertaken to explore associations between sleep disturbance, fatigue, pain, anxiety, depression, general health status, and satisfaction with life before and after a diagnosis of PsA compared to the general population.
Development of a Set of Lupus?Specific, Ambulatory Care–Sensitive, Potentially Preventable Adverse Conditions: A Delphi Consensus Study
Candace H. Feldman Cameron Speyer Rachel Ashby Bonnie L. Bermas Shamik Bhattacharyya Eliza Chakravarty Brendan Everett Elizabeth Ferucci Aimee O. Hersh Francisco M. Marty Joseph F. Merola Rosalind Ramsey?Goldman Brad H. Rovin Mary Beth Son Laura Tarter Sushrut Waikar Jinoos Yazdany Joel S. Weissman Karen H. Costenbader
doi : 10.1002/acr.24095
Volume73, Issue1,Pages 146-157
Individuals with systemic lupus erythematosus (SLE) are at high risk for infections and SLE? and medication?related complications. The present study was undertaken to define a set of SLE?specific adverse outcomes that could be prevented, or their complications minimized, if timely, effective ambulatory care had been received.
