Health‐related quality of life trajectories in critical illness: Protocol for a Monte Carlo simulation study

Author:

Kaas‐Hansen Benjamin Skov12ORCID,Kjær Maj‐Brit Nørregaard1ORCID,Møller Morten Hylander1ORCID,Jensen Aksel Karl Georg2,Larsen Mia Esta1,Cuthbertson Brian H.3ORCID,Perner Anders1,Granholm Anders1ORCID

Affiliation:

1. Department of Intensive Care Copenhagen University Hospital—Rigshospitalet Copenhagen Denmark

2. Section of Biostatistics, Deparment of Public Health University of Copenhagen Copenhagen Denmark

3. Department of Critical Care Sunnybrook Health Sciences Centre Toronto Canada

Abstract

AbstractBackgroundHealth‐related quality of life (HRQoL) is a patient‐centred outcome increasingly used as a secondary outcome in critical care research. It may cover several important dimensions of clinical status in intensive care unit (ICU) patients that arguably elude other more easily quantified outcomes such as mortality. Poor associations with harder outcomes, conflicting data on HRQoL in critically ill compared to the background population, and paradoxical effects on HRQoL and mortality complicate the current operationalisation in critical care trials. This protocol outlines a simulation study that will gauge if the areas under the HRQoL trajectories could be a viable alternative.MethodsWe will gauge the behaviour of the proposed HRQoL operationalisation through Monte Carlo simulations, under clinical scenarios that reflect a broad critical care population eligible for inclusion in a large pragmatic trial. We will simulate 15,360 clinical scenarios based on a full factorial design with the following seven simulation parameters: number of patients per arm, relative mortality reduction in the interventional arm, acceleration of HRQoL improvement in the interventional arm, the relative improvement in final HRQoL in the interventional arm, dampening effect of mortality on HRQoL values at discharge from the ICU, proportion of so‐called mortality benefiters in the interventional arm and mortality trajectory shape. For each clinical scenario, we will simulate 100,000 two‐arm trials with 1:1 randomisation. HRQoL will be sampled fortnightly after ICU discharge. Outcomes will include HRQoL in survivors and all patients at the end of follow‐up; mean areas under the HRQoL trajectories in both arms; and mean difference between areas under the HRQoL trajectories and single‐sampled HRQoLs at the end of follow‐up.DiscussionIn the outlined simulation study, we aim to assess whether the area under the HRQoL trajectory curve could be a candidate for reconciling the seemingly paradoxical effects on improved mortality and reduced HRQoL while remaining sensitive to early or accelerated improvement in patient outcomes. The resultant insights will inform subsequent methodological work on prudent collection and statistical analysis of such data from real critically ill patients.

Funder

Novo Nordisk Fonden

Publisher

Wiley

Subject

Anesthesiology and Pain Medicine,General Medicine

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