The Psychosocial Impact of Rheumatic Conditions - Caring for the Whole Patient

This book focuses on a holistic approach to providing care to patients with rheumatic illnesses that goes beyond the biomedical approach to include the psycho-social and cultural needs of patients. A diagnosis of a chronic rheumatic illness can dramatically affect all aspects of a person s life. These life-altering conditions are characterized by physical pain and inflammation that may reduce or impair functioning of one or more parts of the musculoskeletal system and in some cases impact other organs throughout the body. Often accompanying these physical manifestations of the rheumatic illness are the psychological and social aspects that affect one s overall health and quality of life. Due to the chronicity of many rheumatic illnesses, managing and coping with the illness is often an ever-evolving process that can span throughout the developmental spectrum or lifespan of the patient experience. A strictly biomedical approach to the treatment of rheumatic illnesses often fails to address these key aspects of the patients' overall well-being. A more comprehensive approach, inclusive of the bio-psycho-social-cultural lens, with the patient s voice at its core, is needed to inform and ultimately deliver quality patient care and achieve optimal health outcomes.
This book serves as s a tool for the entire interdisciplinary rheumatology health care team. This comprehensive approach is framed within the context of well-documented health disparities in rheumatology with a focus on psycho, social, emotional and environmental aspects of health that contribute to patient quality of life. It explores the needs of special populations and provide opportunities for clinicians to consider how to treat diverse populations in a more inclusive way.  At the center of this book is the patient s voice utilizing patient stories to provide the reader with real life examples that reflect the life cycle of rheumatology patients and the impact of key interventions or lack thereof that can impact the patient experience. Lastly, offers practical, evidence-based strategies for members of the rheumatology health care team. These tools can be integrated in their assessment and treatment plans for patients and their loved ones. This holistic approach can help to foster effective communication, build trust, enhance partnerships and amplify the patient voice to optimize health outcomes and enhance overall well-being.

List of contents

Introduction: The Rheumatology Patient Journey.- Psychosocial Aspects of Rheumatic Conditions.- Tools for Addressing Psycho-Social-Emotional Aspects of Care.- The Patient-Provider Partnership - It s a Dance!.- Cultural Considerations and Addressing Patient Values.- Special Populations in Rheumatology: LGBTQIA+ Identity.- Compliance/Adherence with Treatment.- Using a Team Approach to Achieve Optimal Outcomes.- Engaging the Family and Support System in Patient Care.- Self-management and Patient Education Interventions.- Health Disparities & Confronting Implicit Bias as a Strategy to Address Them.- Social Determinants of Health.- The Impact of a Global Health Pandemic, Telehealth & the Digital Divide.- Engaging Patients in Research: Incorporating the Patient Perspective.

About the author

Jillian A. Rose, PhD, MPH, LCSW serves as the Vice President and Chief Health Equity Officer at the Hospital for Special Surgery (HSS), a premier institution dedicated to advancing musculoskeletal health. In this pivotal role, Dr. Rose is an integral member of the HSS leadership team, where she spearheads the development and execution of a comprehensive health equity strategy. Her work focuses on promoting a whole health approach addressing physical, behavioral, and social needs aligned with HSS's mission to ensure access for all patients and reduce disparities in care, particularly for those with musculoskeletal conditions.
A passionate advocate for health equity, Dr. Rose has been at the forefront of initiatives aimed at collecting comprehensive demographic data in the electronic medical record. Her leadership extends to guiding quality initiatives that aim to identify and reduce health disparities, ensuring the development of tools and evaluation processes to foster continuous improvement. Dr. Rose also provides operational leadership for HSS’s largest Ambulatory Care Center and the Department of Social Work Programs. Since 2005, Dr. Rose has overseen nationally recognized peer support and psycho-education programs for individuals with lupus and their families, ensuring culturally tailored interventions.
Melissa Flores, MPH, LCSW is the Assistant Director of the Office of Health Equity at the Hospital for Special Surgery (HSS). Ms. Flores collaborates closely with the Chief Health Equity Officer to develop, implement, and monitor the HSS Health Equity Strategic Plan. She plays a central role in tracking, analyzing, and reporting on patient data, including social determinants of health (SDOH), across the institution. She led the interdisciplinary team responsible for designing workflows and launching the collection of SDOH data in both pediatric outpatient and adult inpatient settings. In her position, she works across departments to identify and address health disparities specific to orthopedic and rheumatology care. She is also the leader of the hospital-wide LGBTQIA+ Committee and a key contributor to achieving the hospital’s biennial LGBTQ+ Healthcare Equality Leader designation. She previously served as the Social Work Program Coordinator of the Charla de Lupus (Lupus Chat)® Program for 4+ years, a national program offering people with lupus and their families peer health support and education in both English and Spanish. Ms. Flores holds a Master of Social Work (MSW) and a Master of Public Health (MPH) from Columbia University.
Priscilla Calvache, LCSW, is the Director of the Department of Social Work Programs at the Hospital for Special Surgery (HSS). In her role, she leads a dedicated team focused on supporting and enhancing the quality of life for individuals with rheumatologic and orthopedic conditions, and their families. The department’s innovative national support and education programs are designed to provide essential resources and reduce barriers to access, particularly within culturally diverse communities. Since 2015, Mrs. Calvache has played a pivotal role in managing Rheumatology programs at HSS, specializing in national peer support and education initiatives for individuals living with systemic lupus and their loved ones. Her leadership extends to the HSS Community Health Needs Assessment and the development of the Community Service Plan, which aims to enhance disease self-management and reduce health disparities. Mrs. Calvache also spearheads national training initiatives, with a particular emphasis on the peer health model and the distinctive Lupus Support and Education Programs she oversees, which have an international reach. Mrs. Calvache earned her Master of Social Work degree from Columbia University.

Summary

This book focuses on a holistic approach to providing care to patients with rheumatic illnesses that goes beyond the biomedical approach to include the psycho-social and cultural needs of patients. A diagnosis of a chronic rheumatic illness can dramatically affect all aspects of a person’s life. These life-altering conditions are characterized by physical pain and inflammation that may reduce or impair functioning of one or more parts of the musculoskeletal system and in some cases impact other organs throughout the body. Often accompanying these physical manifestations of the rheumatic illness are the psychological and social aspects that affect one’s overall health and quality of life. Due to the chronicity of many rheumatic illnesses, managing and coping with the illness is often an ever-evolving process that can span throughout the developmental spectrum or lifespan of the patient experience. A strictly biomedical approach to the treatment of rheumatic illnesses often fails to address these key aspects of the patients' overall well-being. A more comprehensive approach, inclusive of the bio-psycho-social-cultural lens, with the patient’s voice at its core, is needed to inform and ultimately deliver quality patient care and achieve optimal health outcomes.
This book serves as s a tool for the entire interdisciplinary rheumatology health care team. This comprehensive approach is framed within the context of well-documented health disparities in rheumatology with a focus on psycho, social, emotional and environmental aspects of health that contribute to patient quality of life. It explores the needs of special populations and provide opportunities for clinicians to consider how to treat diverse populations in a more inclusive way.  At the center of this book is the patient’s voice utilizing patient stories to provide the reader with real life examples that reflect the life cycle of rheumatology patients and the impact of key interventions or lack thereof that can impact the patient experience. Lastly, offers practical, evidence-based strategies for members of the rheumatology health care team. These tools can be integrated in their assessment and treatment plans for patients and their loved ones. This holistic approach can help to foster effective communication, build trust, enhance partnerships and amplify the patient voice to optimize health outcomes and enhance overall well-being.

Product details

• Authors: Pris Calvache, Priscilla Calvache, Melissa Flores, Jillian Rose, Jillian Rose-Smith
• Publisher: Springer, Berlin
• Languages: English
• Product format: Paperback / Softback
• Release: 10.08.2025
• EAN: 9783031953378
• ISBN: 978-3-0-3195337-8
• No. of pages: 170
• Illustrations: XIV, 170 p. 8 illus. in color.
• Subjects: Natural sciences, medicine, IT, technology > Medicine > Clinical medicine; Klinische Psychologie, Depression, Psychology, Clinical psychology, Anxiety, Rheumatology, Chronic Illness, rheumatic diseases, health disparities, Social Determinants