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Symptom control and survival for people severely ill with COVID: a multicentre cohort study (CovPall-Symptom)

Irene J. Higginson, M. Hocaoglu, L. Fraser, M. Maddocks, K. Sleeman, A. Oluyase, R. Chambers, N. Preston et al.

Journal of Pain and Symptom Management, 2022

572 participants · 8 citations

Abstract

CONTEXT

Evidence of symptom control outcomes in severe COVID is scant.

OBJECTIVE

To determine changes in symptoms among people severely ill or dying with COVID supported by palliative care, and associations with treatments and survival.

METHODS

Multicentre cohort study of people with COVID across England and Wales supported by palliative care services, during the pandemic in 2020 and 2021. We analysed clinical, demographic and survival data, symptom severity at baseline (referral to palliative care, first COVID assessment) and at three follow-up assessments using the Integrated Palliative Outcome Scale - COVID version (IPOS-COV).

RESULTS

We included 572 patients from 25 services, mostly hospital support teams; 496 (87%) were newly referred to palliative care with COVID, 75 (13%) were already supported by palliative care when they contracted COVID. At baseline, patients had a mean of 2.4 co-morbidities, mean age 77 years, a mean of five symptoms, and were often bedfast or semiconscious. The most prevalent symptoms were: breathlessness, weakness/lack of energy, drowsiness, anxiety, agitation, confusion/delirium, and pain. Median time in palliative care was 46 hours; 77% of patients died. During palliative care, breathlessness, agitation, anxiety, delirium, cough, fever, pain, sore/dry mouth and nausea improved; drowsiness became worse. Common treatments were low dose morphine and midazolam. Having moderate to severe breathlessness, agitation and multimorbidity were associated…

How strong is the evidence?

Evidence Hub reads this as a cohort study, done in people. Its evidence level is 3 of 5 (Moderate · trial / cohort / secondary analysis). Trials without a large randomized design, cohorts and secondary analyses give moderate evidence. Reported size: 572 participants or records.

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