Treatment restrictions after acute stroke across nine European countries and their association with 90-day mortality: a post hoc analysis of the PRECIOUS randomised controlled trial

Background In patients with acute stroke, early withholding or withdrawal of life-sustaining therapies is associated with an increased risk of death. We used practice variation across nine European countries to assess whether this relation may be causal. Methods We performed a post hoc analysis of the PREvention of Complications to Improve OUtcome in elderly patients with acute Stroke (PRECIOUS) trial, a randomised clinical trial of metoclopramide, paracetamol, and/or ceftriaxone started within 24 h of symptom onset in older patients with acute ischaemic stroke or intracerebral haemorrhage (ISRCTN82217627). The frequency of early treatment restrictions, defined as those installed within 24 h after randomisation, was calculated per participating country and their relation with the primary outcome ‘death at 90 days' was estimated through: 1) adjustment for confounders with regression analysis with inverse-propensity score reweighting; and 2) comparing patients enrolled in countries with and without early restrictions, adjusted for confounders with regression analysis. Findings Of 1493 patients enrolled in PRECIOUS between 2016 and 2022, 1451/1493 (97%) were included in this analysis, of whom 276/1451 (19%) had an early treatment restriction. The rate of these restrictions ranged from 0% to 48% across the participating countries. Patients with restrictions were more likely to die within 90 days (inverse propensity-weighted odds ratio (OR) 3.39; 95% CI 2.71–4.25). However, there was no difference in the rate of death at 90 days between countries with and those without restrictions (21.3% vs 23.5%, adjusted OR 1.39; 95% CI 0.8–2.39). Interpretation The use of treatment restrictions early after stroke varied widely across Europe. Although restrictions were independently associated with an increased rate of death, the comparison of death rates between countries with and those without such restrictions provides no indication that this relation is causal. Funding European Union's Horizon 2020 research and innovation programme; grant agreement No. 634809.

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Journal
The Lancet Regional Health - Europe
Published
2026-10-14
DOI
https://doi.org/10.1016/j.lanepe.2026.101894
Primary Topic
Palliative Care and End-of-Life Issues
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article
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article

Treatment restrictions after acute stroke across nine European countries and their association with 90-day mortality: a post hoc analysis of the PRECIOUS randomised controlled trial

Iwona Kurkowska‐Jastrzębska, Anne Hege Aamodt, Wouter A. C. van Amsterdam, László Csiba et al.
The Lancet Regional Health - Europe
Palliative Care and End-of-Life Issues
article

Treatment restrictions after acute stroke across nine European countries and their association with 90-day mortality: a post hoc analysis of the PRECIOUS randomised controlled trial

Iwona Kurkowska‐Jastrzębska, Anne Hege Aamodt, Wouter A. C. van Amsterdam, László Csiba, Alfonso Ciccone, Hendrik Reinink, Diederik W.J. Dippel, Jeroen Christiaan de Jonge, Gary Randall, Philip M. Bath, G. Thomalla, Wouter M. Sluis, Diederik van de Beek, H. Bart van der Worp, Janika Kõrv, H. Bart van der Worp, Eivind Berge, Kennedy R. Lees, George Ntaios, Malcolm R. Macleod, Jacques Demotes
article en

Abstract

Background In patients with acute stroke, early withholding or withdrawal of life-sustaining therapies is associated with an increased risk of death. We used practice variation across nine European countries to assess whether this relation may be causal. Methods We performed a post hoc analysis of the PREvention of Complications to Improve OUtcome in elderly patients with acute Stroke (PRECIOUS) trial, a randomised clinical trial of metoclopramide, paracetamol, and/or ceftriaxone started within 24 h of symptom onset in older patients with acute ischaemic stroke or intracerebral haemorrhage (ISRCTN82217627). The frequency of early treatment restrictions, defined as those installed within 24 h after randomisation, was calculated per participating country and their relation with the primary outcome ‘death at 90 days' was estimated through: 1) adjustment for confounders with regression analysis with inverse-propensity score reweighting; and 2) comparing patients enrolled in countries with and without early restrictions, adjusted for confounders with regression analysis. Findings Of 1493 patients enrolled in PRECIOUS between 2016 and 2022, 1451/1493 (97%) were included in this analysis, of whom 276/1451 (19%) had an early treatment restriction. The rate of these restrictions ranged from 0% to 48% across the participating countries. Patients with restrictions were more likely to die within 90 days (inverse propensity-weighted odds ratio (OR) 3.39; 95% CI 2.71–4.25). However, there was no difference in the rate of death at 90 days between countries with and those without restrictions (21.3% vs 23.5%, adjusted OR 1.39; 95% CI 0.8–2.39). Interpretation The use of treatment restrictions early after stroke varied widely across Europe. Although restrictions were independently associated with an increased rate of death, the comparison of death rates between countries with and those without such restrictions provides no indication that this relation is causal. Funding European Union's Horizon 2020 research and innovation programme; grant agreement No. 634809.

The Lancet Regional Health - EuropeVol. 71
Oslo University Hospital (NO), University of Debrecen (HU), Utrecht University (NL), Aristotle University of Thessaloniki (GR), AHEPA University Hospital (GR), University Medical Center Utrecht (NL), St. Antonius Ziekenhuis (NL), Ospedale Papa Giovanni XXIII (IT), University Medical Center Hamburg-Eppendorf (DE), Queen's Medical Centre (GB), Institute of Psychiatry and Neurology (PL), Spaarne Gasthuis (NL), Azienda Ospedaliera Carlo Poma (IT), University of Tartu (EE), University of Edinburgh (GB)
HORIZON EUROPE Framework Programme
Good health and well-being
Openalex Percentile: Top 11%
Palliative Care and End-of-Life Issues
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