scholarly journals Risk Factors for Long-Term Brain Dysfunction after Chronic Critical Illness

2013 ◽  
Vol 10 (4) ◽  
pp. 315-323 ◽  
Author(s):  
Aluko A. Hope ◽  
R. Sean Morrison ◽  
Qingling Du ◽  
Sylvan Wallenstein ◽  
Judith E. Nelson
2017 ◽  
Vol 42 ◽  
pp. 405-406
Author(s):  
Paola Tonin Carpeggiani ◽  
Júlia Bertholdo Bossardi ◽  
Fabricio Piccoli Fortuna ◽  
Vanessa Piccoli ◽  
Nicole Elen Lira ◽  
...  

2021 ◽  
pp. 101-121
Author(s):  
O. Joseph Bienvenu ◽  
Megan M Hosey

Patients with critical illnesses face a number of severe psychic and physical stressors. Survivors often have long-term cognitive and physical impairments, as well as family, financial, and other stressors. These potential stressors increase the risk of psychiatric disturbances substantially. This chapter describes the burden of distress-related psychiatric morbidity in patients who survive critical illnesses, as well as risk factors for this morbidity. This knowledge serves as the motivation to develop new approaches that can ameliorate, or even prevent, long-term distress in survivors. The chapter also presents information about early attempts to reduce, prevent, and manage long-term psychological morbidity.


Author(s):  
Max L. Gunther ◽  
James C. Jackson ◽  
Pratik Pandharipande ◽  
Alessandro Morandi ◽  
Maureen Hahn ◽  
...  

2019 ◽  
Vol 47 (4) ◽  
pp. 566-573 ◽  
Author(s):  
Anna K. Gardner ◽  
Gabriela L. Ghita ◽  
Zhongkai Wang ◽  
Tezcan Ozrazgat-Baslanti ◽  
Steven L. Raymond ◽  
...  

2018 ◽  
Vol 93 (1) ◽  
pp. 68-82 ◽  
Author(s):  
Amra Sakusic ◽  
John C. O'Horo ◽  
Mikhail Dziadzko ◽  
Dziadzko Volha ◽  
Rashid Ali ◽  
...  

2020 ◽  
pp. 104973232097637
Author(s):  
A. Fuchsia Howard ◽  
Sarah Crowe ◽  
Laura Choroszewski ◽  
Joe Kovatch ◽  
Adrianne J. Haynes ◽  
...  

Limited understanding of the psychological challenges experienced by individuals with chronic critical illness hampers efforts to deliver quality care. We used an interpretive description approach to explore sources of distress for individuals with chronic critical illness in residential care, wherein we interviewed six residents, 11 family members, and 21 staff. Rather than discuss physical symptoms, sources of distress for residents were connected to feeling as though they were a patient receiving medical care as opposed to an individual living in their home. The tension between medical care and the unmet need for a sense of home was related to care beyond the physical being overlooked, being dependent on others but feeling neglected, frustration with limited choice and participation in decision making, and feeling sad and alone. Efforts to refine health care for individuals with chronic critical illness must foster a sense of home while ensuring individuals feel safe and supported to make decisions.


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