Critical illness, disability, and the road home
intensive care unit
World Health Organisation Disability Assessment Schedule
Ability to participate in the community is an important outcome for all patients after a major illness, it signposts reaching the end of the road home. A patient’s ability to return to the priority tasks of daily living impacts their satisfaction with life, their carers, their family and ultimately the health system . A large body of literature has demonstrated that long term impairments of physical, mental health and/or cognitive domains affect most survivors of critical illness [2, 3]. Post-intensive care syndrome (PICS)  was developed in 2011 as a framework in which to describe these sequelae. Additionally, it was suggested that these domains be mapped to the World Health Organization (WHO) International Classification of Functioning Disability and Health (ICF) , in order to understand impacts on biological, functional, and social levels, and on quality of life. Clinicians, researchers, patients and communities are now working together to try and decrease impairment and quicken the journey of recovery. But what should we measure to enable us to best implement supportive and transformational care for our patients after discharge?
It is through this lens that we consider a paper recently published in Intensive Care Medicine. Hodgson and colleagues describe the use of the World Health Organization Disability Assessment Schedule 2 (WHO-DAS) in survivors of critical illness, connecting the dots between measures of impairment and measures of function through assessment of disability . Disability is a complex phenomenon, an overarching concept reflecting the interaction between the environment and the person . It maps across all areas of the ICF and can be measured using the WHO-DAS instrument, a composite tool that encompasses six domains of functioning including cognition, mobility, self -care, interactions with people, life activities and participation in the community. Using this instrument, the authors found that 25% of a critical care population at 6 months suffered moderate to severe disability, associated with inability to return to previous activities such as work and education, and reduced health related quality of life, as assessed by the EQ-5D. They conclude that “disability, measured using the WHO-DAS 2.0 (12 level), is an important outcome following critical illness and should be considered in a core outcome set for ICU research.”
So where does measurement of disability fit within a critical care framework? A plethora of different domains of outcome instruments are currently used to assess long term outcomes across the critical care continuum. Recently a core set of outcome measures was developed using rigorous methodology [8, 9]. The “what” to measure identified eight domains, including HRQoL expressed as satisfaction with life and personal enjoyment. The “how” to measure this domain reached consensus as using the EQ-5D and SF-36v2. The WHO-DAS measure of disability was suggested by participants for rating in the second round of the Delphi, but less than 30% of the panel members (including patients and caregivers) agreed it was critical for inclusion in the resulting core set of measures. Whether this was the result of lack of understanding of the concept of disability, lack of familiarity with the tool, lack of previous exposure in the ICU population or lack of specificity as a composite measure, is unknown. Certainly there are no data that support the clinimetric properties of this measure for use in critical care populations. Furthermore, reliability and validity of using proxy measures during a critical care admission have yet to be established although research in other populations supports this method of administration. These data are particularly pertinent in ICU for acquiring baseline data to enable longitudinal comparison, although Hodgson et al. did not measure disability at baseline which would have been valuable for assessing trajectories .
In order to develop and road-test interventions to reduce disability after critical illness, we must understand which patients are at highest risk and the mechanisms that affect prevention or progression. This investigation thoughtfully identified factors associated with moderate/severe disability—history of anxiety or depression, marital status of separated or divorced, mechanical ventilation duration, and discharge to post-acute care facility rather than home. While interesting, these factors provide little guidance in targeting interventions to those who most need it. Nearly half of those with disability did not have pre-ICU anxiety or depression, nearly three-quarters of disabled patients were not divorced or separated, and the median duration of mechanical ventilation was short and similar between disability groups—3–4 days. Even destination of discharge—a factor closely tied to patients’ ability to care for themselves and engage with their environment—was an imperfect predictor of disability in this cohort. It seems unlikely that this composite measure, which does not differentiate etiologies of disability, is the right tool to identify new targeted therapies; instead, we will need to continue with more granular work as well. At the same time, there may be mechanisms that affect many aspects of disability which transcend simple biologic pathways—such as depression and social support—supporting the approach of using both general and specific measures of disability and functional impairment .
How then do we best map a patient’s progression from ICU into the community? Is assessment of disability status a robust option to further our field? From a patient and family perspective development of new, or worsening of pre-existing, disability after a critical care stay seems intuitive to be of concern/must surely matter. The method we use to measure this may be critical in driving the types of intervention and support patients may need. Importantly, targeting the patients and families who require the most support should be a priority. Hodgson and colleagues provide us with an alternative route for assessing all three domains of the ICF in one measure of disability. The domains of measurement included within the WHO-DAS resonate with patients, family and clinician researchers with agreement that physical and cognitive function, mental health and return to work should be the most important co-ordinates assessed on the road map to recovery . However, we still have more to do to understand the applicability of the WHO-DAS measure. Moving forward on the measurement of disability determining how it is best measured, and if it best reflects a measure of improvement may be a useful side trip for the field of critical care on our journey to improve long-term outcomes.
We are grateful to Jennifer Jones, PhD candidate, Department of Physiotherapy, University of Melbourne for producing the figure.
Compliance with ethical standards
Conflicts of interest
The authors have no relevant conflicts of interest.
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