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Published ahead of print on October 26, 2006, doi:10.1164/rccm.200604-493OC

Am. J. Respir. Crit. Care Med., Volume 175, Number 2, January 2007, 167-173

A more recent version of this article appeared on January 15, 2007
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Submitted on April 7, 2006
Accepted on October 26, 2006

Informal Caregiver Burden Among Survivors of Prolonged Mechanical Ventilation

David C Van Pelt1, Eric B Milbrandt1*, Li Qin2, Lisa A Weissfeld2, Armando J Rotondi3, Richard Schulz4, Lakshmipathi Chelluri5, Derek C Angus1, and Michael R Pinsky5

1 The CRISMA Laboratory (Clinical Research, Investigation, and Systems Modeling of Acute Illness), University of Pittsburgh, Pittsburgh, PA, USA; Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA, 2 The CRISMA Laboratory (Clinical Research, Investigation, and Systems Modeling of Acute Illness), University of Pittsburgh, Pittsburgh, PA, USA; Department of Biostatistics, University of Pittsburgh, Pittsburgh, PA, USA, 3 Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA; Department of Health Policy and Management, University of Pittsburgh, Pittsburgh, PA, USA, 4 Department of Psychiatry, University of Pittsburgh, Pittsburgh, PA, USA; University Center for Social and Urban Research, University of Pittsburgh, Pittsburgh, PA, USA, 5 Department of Critical Care Medicine, University of Pittsburgh, Pittsburgh, PA, USA

* To whom correspondence should be addressed. E-mail: milbeb{at}ccm.upmc.edu.

Rationale: Although caregiver burden is well described in chronic illness, few studies have examined burden in caregivers of survivors of critical illness. In existing studies, it is unclear whether the observed burden is a consequence of critical illness or preexisting patient illness. Objectives: To describe one-year, longitudinal outcomes of caregivers of patients who survived critical illness, and compare depression risk between caregivers of patients with and without pre-intensive care unit (ICU) functional dependency. Methods: Prospective, parallel, cohort study of survivors of prolonged (>48h) mechanical ventilation and their informal caregivers. Caregivers were divided into two cohorts based upon whether patients were functionally independent (n=99, 59%), or dependent (n=70, 41%) prior to admission. Functional dependency was defined as dependency in ≥1 activities of daily living (ADL) or ≥3 instrumental ADLs. Patient and caregiver outcomes were measured 2, 6, 12 months after mechanical ventilation initiation. Measurements and Main Results: We studied three caregiver outcomes: depression risk, lifestyle disruption, employment reduction. Most patients were male (59.8%), with mean (standard deviation[SD]) age 56.6 (19.0) years. Caregivers were mostly female (75.7%), with mean (SD) age 54.6 (14.7) years. Prevalence of caregiver depression risk was high at all time points (33.9%, 30.8%, 22.8%, p=0.83) and did not vary by patient pre-ICU functional status. Lifestyle disruption and employment reduction were also common and persistent. Conclusions: Depression symptoms, lifestyle disruption, and employment reduction were common among informal caregivers of critical illness survivors. Depression risk was high regardless of patient pre-ICU functional status.


Key words: caregivers; depression; mechanical ventilation; outcomes research; quality of life




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