Long-Term Quality of Life Among Survivors of Severe Sepsis: Analyses of Two International Trials
- PMID: 26992066
- PMCID: PMC4949079
- DOI: 10.1097/CCM.0000000000001658
Long-Term Quality of Life Among Survivors of Severe Sepsis: Analyses of Two International Trials
Abstract
Objectives: To describe the quality of life among sepsis survivors.
Design: Secondary analyses of two international, randomized clinical trials (A Controlled Comparison of Eritoran and placebo in patients with Severe Sepsis [derivation cohort] and PROWESS-SHOCK [validation cohort]).
Setting: ICUs in North and South America, Europe, Africa, Asia, and Australia.
Patients: Adults with severe sepsis. We analyzed only patients who were functional and living at home without help before sepsis hospitalization (n = 1,143 and 987 from A Controlled Comparison of Eritoran and placebo in patients with Severe Sepsis and PROWESS-SHOCK, respectively).
Interventions: None.
Measurements and main results: In A Controlled Comparison of Eritoran and placebo in patients with Severe Sepsis and PROWESS-SHOCK, the average age of patients living at home independently was 63 and 61 years; 400 (34.9%) and 298 (30.2%) died by 6 months. In A Controlled Comparison of Eritoran and placebo in patients with Severe Sepsis, 580 patients had a quality of life measured using EQ-5D at 6 months. Of these, 41.6% could not live independently (22.7% were home but required help, 5.1% were in nursing home or rehabilitation facilities, and 5.3% were in acute care hospitals). Poor quality of life at 6 months, as evidenced by problems in mobility, usual activities, and self-care domains were reported in 37.4%, 43.7%, and 20.5%, respectively, and the high incidence of poor quality of life was also seen in patients in PROWESS-SHOCK. Over 45% of patients with mobility and self-care problems at 6 months in A Controlled Comparison of Eritoran and placebo in patients with Severe Sepsis died or reported persistent problems at 1 year.
Conclusions: Among individuals enrolled in a clinical trial who lived independently prior to severe sepsis, one third had died and of those who survived, a further one third had not returned to independent living by 6 months. Both mortality and quality of life should be considered when designing new interventions and considering endpoints for sepsis trials.
Figures
Comment in
-
Surviving Severe Sepsis: Is That Enough?Crit Care Med. 2016 Aug;44(8):1603-4. doi: 10.1097/CCM.0000000000001764. Crit Care Med. 2016. PMID: 27428119 No abstract available.
-
Functional Limitations Do Not Mean Poor Quality of Life.Crit Care Med. 2017 Jan;45(1):e113. doi: 10.1097/CCM.0000000000002139. Crit Care Med. 2017. PMID: 27984292 No abstract available.
-
The authors reply.Crit Care Med. 2017 Jan;45(1):e113-e114. doi: 10.1097/CCM.0000000000002167. Crit Care Med. 2017. PMID: 27984293 No abstract available.
References
-
- Angus DC, van der Poll T. Severe Sepsis and Septic Shock. N Engl J Med. 2013;369:840–851. - PubMed
-
- Angus DC, Linde-Zwirble WT, Lidicker J, Clermont G, Carcillo J, Pinsky MR. Epidemiology of severe sepsis in the United States: Analysis of incidence, outcome, and associated costs of care. Crit Care Med. 2001;29:1303–1310. - PubMed
-
- National Center for Health Statistics. [Accessed October 2015]; http://www.cdc.gov/nchs/data/databriefs/db118.htm#hospitaldeaths.
Publication types
MeSH terms
Substances
Grants and funding
LinkOut - more resources
Full Text Sources
Other Literature Sources
Medical
