This first edition of this text was the first book to comprehensively survey the challenges in understanding and working with families whose loved ones are critically ill. The comprehensive nature of that book served as a state-of-the-art reference in this sphere for a broad spectrum of researchers and clinicians. All chapters were authored by established experts in the respective fields, providing an overview that has been used both in theory and practice.
Since the first edition's publication, the public recognition of the importance of families has increased dramatically as a consequence of the COVID-19 pandemic. Most major decisions in the intensive care unit (ICU) are shared by clinicians and someone other than the patient. Improving communication between clinicians and these surrogate decision-makers has proven hard in multiple clinical trials. Families suffer, too, when their loved ones are critically ill. Anxiety,stress, and depression are common, and post-traumatic stress disorder may occur while their loved ones are still in the ICU. Families struggle to understand prognoses, and conflicts with the care team occur frequently. These conflicts not only injure families but also contribute to health care provider burnout. Now in its fully revised and expanded second edition, Families in the Intensive Care Unit reflects lessons learned during the COVID pandemic response, as well as knowledge gained about family support when families cannot be at the bedside.
The chapter subjects again reflect a combination of breadth and depth. Physical and psychological morbidity are explored as barriers to effective decision-making, as are cognitive challenges. The full array of the interdisciplinary and interprofessional team is represented, emphasizing the multimodal approach. This edition includes administrative considerations for health care management and approaches for training members of the health care team. Similarly, family voices are also represented. The complete trajectory of needs of care are addressed, including survivorship and end-of-life care.
Auflage
Sprache
Verlagsort
Verlagsgruppe
Springer International Publishing
Zielgruppe
Editions-Typ
Illustrationen
12
21 farbige Abbildungen, 12 s/w Abbildungen
XIV, 357 p. 33 illus., 21 illus. in color.
Maße
Höhe: 241 mm
Breite: 160 mm
Dicke: 25 mm
Gewicht
ISBN-13
978-3-031-83785-2 (9783031837852)
DOI
10.1007/978-3-031-83786-9
Schweitzer Klassifikation
Ashlee Vance
Henry Ford Health System
Health Policy and Health Services
Detroit, USA
Deena Costa
Yale University School of Nursing
New Haven, USA
Giora Netzer
University of Maryland Medical System
Baltimore, USA
Dr. Ashlee Vance's focus has been parental wellbeing and infant health and developmental outcomes during and after intensive care, specifically focusing on those with medically complex conditions. Dr. Vance conducts research in health services, health equity and economic outcomes associated with having a medically complex infant. Additionally, she concentrates on work to align healthcare system practices with family-focused values to increase parent engagement and self-efficacy in caring for vulnerable infants during and after NICU hospitalization. She has worked as a bedside nurse in many Level 4 and regional NICUs across the US and continues to consult with neonatal providers in the areas of parent engagement, care coordination, discharge preparedness and dismantling of racism in care practices.
Deena Kelly Costa PhD, RN, FAAN is a trained health services researcher with clinical expertise in adult critical care nursing. Her research examines the dynamics of ICU interprofessional teams and how team dynamics impact the implementation of evidence-based care in the ICU. Notably, her research has focused on if, how and in what ways patients and families are included as part of the ICU team. She uses qualitative and quantitative methods to explore ICU teams and patient and family engagement. Her work care has been published in leading journals such as JAMA, American Journal of Respiratory and Critical Care Medicine, and Chest. She is an Assistant Professor at the University of Michigan and Co-Director of the National Clinican Scholar's Program at UM in the Institute for Healthcare Policy and Innovation.
Giora Netzer, MD, MSCE is a critical care physician, clinical epidemiologist, and patient experience leader. Throughout his career, he was worked to better support patients and families through the trajectories of illness and care. His research seeks to better understand morbidity among family members in the ICU and its potential effect on decision-making; as well as better understanding long-term trajectories among survivors of critical illness and their families. Dr. Netzer has published extensively in the peer-reviewed literature, and has co-authored international guidelines for the support of families in the ICU. He continues to attend in the ICU while spearheading organizational efforts to improve patient- and family-centric care.
