Evidence map›Paper›PMID 41507241›Full record

Observational studyScientific reports2026

Effect of high-dose baclofen on post-traumatic stress disorder symptoms five years after hospitalization among critically ill patients with unhealthy alcohol use.

Marwan Bouras, Karim Asehnoune, Yann Robert-Valli, Pierre-Joachim Mahe, Jean Reignier, Adel Maamar, Jean-Claude Lacherade, Maud Jonas, Boris Jung, Martine Ferrandiere and 11 more

Registry-linked trialAbstract readObservational Study
In one paragraph

Observational study in Scientific reports, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05877807 (Effect of Baclofen to Prevent Post-Traumatic Stress Disorder), which is not on this map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

NCT05877807 completednot on this map

Effect of Baclofen to Prevent Post-Traumatic Stress Disorder: 5 Years Follow-up of the BACLOREA Randomized Trial

TypeobservationalSponsorNantes University HospitalRan2023 to 2024Enrolled94ConditionsAlcoholism, Post Traumatic Stress DisorderArmsBaclofen, Placebo
3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

21 authors.

Marwan BourasDepartment of Anesthesiology and Critical Care Medicine, Centre Hospitalier Régional Universitaire de Brest, Brest, France.
Karim AsehnouneNantes Université, INSERM, CHU Nantes, Center for Research in Transplantation and Translational Immunology, UMR 1064, 44000, Nantes, France.
Yann Robert-ValliService d'Anesthésie Réanimation, Hopital Laennec, CHU de Nantes, Bd du Professeur Jacques Monod, 44800, Saint-Herblain, France.
Pierre-Joachim MaheService d'Anesthésie Réanimation, Hotel Dieu, Nantes Université, CHU Nantes, 44000, Nantes, France.
Jean ReignierService de Médecine Intensive Réanimation, Centre Hospitalo-Universitaire de Nantes, Nantes, France.
Adel MaamarService de Médecine Intensive Réanimation, Centre Hospitalo-Universitaire de Rennes, Rennes, France.
Jean-Claude LacheradeService de Médecine Intensive Réanimation, Centre Hospitalier Départemental Vendée, La Roche-Sur-Yon, France.
Maud JonasService de Médecine Intensive Réanimation, Centre Hospitalier Général de Saint-Nazaire, Saint-Nazaire, France.
Boris JungService de Médecine-Intensive Réanimation, Centre Hospitalo-Universitaire de Montpellier, Montpellier, France.
Martine FerrandiereService d'Anesthésie-Réanimation, Centre Hospitalo-Universitaire de Tours, Tours, France.
Samir JaberService d'Anesthésie-Réanimation, Centre Hospitalo-Universitaire de Montpellier, Montpellier, France.
Laurent FletService Pharmacie, Centre Hospitalo-Universitaire de Nantes, Nantes, France.
Mikael MoriconiService de Médecine Intensive Réanimation, Centre Hospitalier de Quimper, Quimper, France.
Sigismond LasockiService d'Anesthésie-Réanimation, Centre Hospitalo-Universitaire de Angers, Angers, France.
Roland SmonigService de Médecine Intensive Réanimation, Centre Hospitalier de Lorient, Lorient, France.
Christophe GuittonService de Médecine Intensive Réanimation, Centre Hospitalier de Le Mans, Le Mans, France.
Stephan EhrmannService de Médecine Intensive Réanimation, Centre Hospitalier Universitaire de Tours, Tours, France.
Bertrand RozecService d'Anesthésie Réanimation, Hopital Laennec, CHU de Nantes, Bd du Professeur Jacques Monod, 44800, Saint-Herblain, France.
Christelle VolteauPlateforme de Méthodologie Et Biostatistique, Centre Hospitalo-Universitaire de Nantes, Nantes, France.
Mickael Vourc'hService d'Anesthésie Réanimation, Hopital Laennec, CHU de Nantes, Bd du Professeur Jacques Monod, 44800, Saint-Herblain, France. mickael.vourch@chu-nantes.fr.
BACLOREA study group

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Patients in the intensive care unit (ICU) with unhealthy alcohol use often experience agitation during mechanical ventilation, which can contribute to post-traumatic stress disorder (PTSD). The BACLOREA trial investigated whether high-dose baclofen could reduce agitation in these patients, but its long-term effects on PTSD symptoms remained unclear. This study aimed to assess whether baclofen administered during ICU stay to reduce the incidence of agitation could reduce the 5-year PTSD symptoms in adult patients with unhealthy alcohol use and improve long-term quality of life and psychological status. This observational follow-up study was conducted between September 2021 and February 2024 and included patients alive five years after participation in the BACLOREA trial, a randomized, placebo-controlled trial evaluating high-dose baclofen for the prevention of agitation-related events during mechanical ventilation in critically ill patients with unhealthy alcohol use. The primary outcome was the prevalence of PTSD symptoms measured using the Impact of Event Scale-Revised (IES-R), with a score ≥ 33 indicating PTSD symptoms. Secondary outcomes included the prevalence of PTSD symptoms using the PTSD Checklist Scale (PCL-S), the quality of life assessed through the SF-36, EQ-5D, and HADS scales. Among the 152 patients who survived five years after ICU admission, 94 (61.8%) completed the follow-up and were included in the BACLO-PTSD study. In this cohort, the 5-year prevalence of PTSD symptoms was 14.9%. For the primary outcome assessed with the IES-R, PTSD symptom prevalence was similar in the baclofen and placebo groups (13.0% vs. 16.7%, p = 0.62). Mean IES-R scores were 10.4 ± 12.5 in the baclofen group and 12.2 ± 13.5 in the placebo group (p = 0.49), while mean PCL-S scores were 25.4 ± 8.6 and 25.5 ± 7.0, respectively (p = 0.94). Quality of life and psychological status, assessed using the SF-36, EQ-5D, and HADS, were also comparable between groups. High-dose baclofen administered during mechanical ventilation did not reduce the 5-year prevalence of PTSD symptoms, nor did it impact quality of life or symptoms of anxiety and depression. Further research is needed to explore alternative strategies for preventing long-term psychological consequences in this population.Trial registration : NCT05877807, 03 april 2023, retrospectively registered.

Indexed as

AlcoholismBaclofenStress Disorders, Post-TraumaticAdultAgedCritical IllnessFemaleFollow-Up StudiesHospitalizationHumansIntensive Care UnitsMaleMiddle AgedQuality of LifeRandomized Controlled Trials as TopicRespiration, ArtificialBaclofenAlcohol-related disordersBaclofenDeliriumPosttraumatic stress disorderQuality of life

Identifiers

PMID41507241
PMCPMC12789491

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.