McGowan Institute for Regenerative Medicine
faculty member Michael R. Pinsky, MD (pictured), professor and vice chair for academic affairs, Department of Critical Care Medicine, is the senior author of a study paper finding intensive care unit patients are not the only ones likely to be severely depressed in the aftermath of hospitalization. Family and friends who care for them often suffer emotional and social hardship, too. The prospective study from the University of Pittsburgh School of Medicine is the first to monitor patients and caregivers during a 1-year period for predictors of depression and lifestyle disruption.
The findings, published in Chest, indicate that the informal caregivers of ICU survivors endure even more stress than those caring for Alzheimer’s disease patients, noted Dr. Pinsky.
“Caregiver depression is the collateral damage of these stressful ICU admissions,” he noted. “This research reveals that loved ones of critically ill patients have profound and unmet needs for assistance even after hospital discharge. The emotional and economic burden is enormous, and these issues must be addressed.”
Part of a larger project examining ICU outcomes, this study focused on the survivors of critical illness requiring breathing assistance with a ventilator for at least 48 hours as well as their informal caregivers, meaning family and friends. Caregivers were evaluated for depression symptoms 2, 6, and 12 months after mechanical ventilation was initiated in the patient. At the 2 month mark, more than 40 percent of the patients had died.
Of the 48 caregivers who were interviewed at all three time points, the majority were female and nearly half were wives of the patients. A predictor of depression symptoms at both 2 and 12 months was looking after a male patient. At 12 months, patient tracheostomy, in which a hole is made through the neck directly into the airway to assist breathing, also was a predictor of caregiver symptoms. If patients had at least a high school education, caregivers were more likely to report lifestyle disruption at the 2-month mark. Tracheostomy, functional dependency, and male patient gender were predictive of lifestyle disruption at 12 months.
“Our previous studies indicate that caregivers often change their lives to care for recovering patients, including quitting work, taking lower-paying jobs, or leaving college in order to spend more time at home,” Dr. Pinsky said. “These are highly stressful choices, and it is imperative that we develop interventions to help families cope with the burden of critical illness even after they have left the hospital.”
Studies are now underway to assess approaches designed to mitigate these problems for both patients and caregivers.
Illustration: McGowan Institute for Regenerative Medicine.
University of Pittsburgh Schools of the Health Sciences Media Relations (02/01/10)
Science Daily (02/01/10)
Genetic Engineering & Biotechnology News (02/01/10)
Medical News Today (02/02/10)
Bio: Dr. Michael Pinsky
Abstract (Chest: 2010 Jan;137(1):88-94.)