Evidence map›Paper›PMID 29181557›Full record

Trial reportIntensive care medicine2017

A tailored multicomponent program to reduce discomfort in critically ill patients: a cluster-randomized controlled trial.

Pierre Kalfon, Karine Baumstarck, Philippe Estagnasie, Marie-Agnès Geantot, Audrey Berric, Georges Simon, Bernard Floccard, Thomas Signouret, Mohamed Boucekine, Mélanie Fromentin and 20 more

2 registry-linked trialsAbstract readRandomized Controlled Trial
PubMed Publisher
In one paragraph

Trial report in Intensive care medicine, 2017. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to 2 registered trials, which are not on this map. Cited by 13 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
13citing papers in PubMed, 1 pooled it
2.5field-weighted citation impact, top 10% of its field
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.

NCT02442934 nacompletednot on this map

A Multicomponent Intervention to Reduce Perceived Discomforts in Critically Ill Patients: a Randomized Controlled Trial

TypeinterventionalSponsorDr Pierre KALFONRan2014 to 2015Enrolled5,411ConditionsCritical IllnessArmsAdministration of the IPREA3 questionnaire, Immediate feedback through electronic reminder messages, Targeted interventions in each ICU to reduce discomforts
NCT03991611 naunknown statusnot on this mapstarted 2019, after this paper: background citation

Tailored Multicomponent Program for Discomfort Reduction in Critically il Patients May Decrease Post-traumatic Stress Disorder in General ICU Survivors at One Year

TypeinterventionalSponsorCentre Hospitalier of ChartresRan2019 to 2023Enrolled3,312ConditionsCritical IllnessArmsAdministration of the IPREA3 questionnaire, Immediate feedback through electronic reminder messages, Targeted interventions in each ICU to reduce discomforts, 6 months follow-up to assess the prevalence of PTSD symptoms, 1 year follow-up to assess psychiatric morbidity
3 · Its place in the literature

Who cites it

13 citing papers in PubMed, 1 synthesis or guideline pooled it, 35 citations in OpenAlex.

  1. Guideline
  2. Article
  3. Critical care in hematologic emergencies.Intensive care medicine · 2026
    Article
  4. Article
  5. Article
  6. Observational
  7. Review
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  12. Observational
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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

30 authors at 20 institutions in 4 countries.

Pierre KalfonRéanimation Polyvalente, Hôpital Louis Pasteur, CH de Chartres, Le Coudray, France. pkalfon@ch-chartres.fr.ORCID http://orcid.org/0000-0002-0095-8759
Karine BaumstarckUnité de Recherche EA3279, Aix-Marseille Université, Marseille, France.
Philippe EstagnasieRéanimation, Clinique Ambroise Paré, Neuilly/Seine, France.
Marie-Agnès GeantotDépartement d'Anesthésie Réanimation, CHU Dijon Bourgogne, Dijon, France.
Audrey BerricRéanimation Polyvalente, Centre Hospitalier Intercommunal Toulon/La Seyne Sur Mer, Toulon, France.
Georges SimonRéanimation, CH Troyes, Troyes, France.
Bernard FloccardRéanimation Polyvalente, CHU Edouard Herriot, Hospices Civils de Lyon, Lyon, France.
Thomas SignouretRéanimation, Hôpital Européen de Marseille, Marseille, France.
Mohamed BoucekineUnité de Recherche EA3279, Aix-Marseille Université, Marseille, France.
Mélanie FromentinRéanimation Chirurgicale, CHU Cochin, Assistance Publique-Hôpitaux de Paris (AP-HP), Paris, France.
Martine NyungaRéanimation Polyvalente, CH Victor Provo, Roubaix, France.
Achille SossouRéanimation, CH Emile Roux, Le Puy-En-Velay, France.
Marion VenotRéanimation Médicale, CHU Saint-Louis, AP-HP, Paris, France.
René RobertRéanimation Médicale, CHU La Milétrie, Poitiers, France.
Arnaud FollinRéanimation Chirurgicale, Hôpital Européen Georges Pompidou, AP-HP, Paris, France.
Juliette AudibertRéanimation Polyvalente, Hôpital Louis Pasteur, CH de Chartres, Le Coudray, France.
Anne RenaultRéanimation Médicale, CHU Brest, Brest, France.
Maïté Garrouste-OrgeasMédecine Intensive et Réanimation, Groupe Hospitalier Paris Saint-Joseph, Paris, France.
Olivier CollangeRéanimation Chirurgicale Polyvalente, Hôpital Civil, CHU Strasbourg, Strasbourg, France.
Quentin LevratRéanimation, Groupe Hospitalier de La Rochelle-Ré-Aunis, La Rochelle, France.
Isabelle VillardAnesthésie Réanimation, CHU Beaujon, AP-HP, Clichy, France.
Didier TheveninRéanimation, CH Lens, Lens, France.
Julien PottecherRéanimation Chirurgicale, Hôpital Hautepierre, CHU Strasbourg, Strasbourg, France.
René-Gilles PatrigeonRéanimation, CH Auxerre, Auxerre, France.
Nathalie RevelRéanimation Médico-chirurgicale, Hôpital Pasteur, CHU Nice, Nice, France.
Coralie VigneRéanimation Chirurgicale, CHU Hôpital Nord, Assistance Publique-Hôpitaux de Marseille, Marseille, France.
Elie AzoulayRéanimation Médicale, CHU Saint-Louis, AP-HP, Paris, France.
Olivier MimozRéanimation chirugicale, CHU La Milétrie, Poitiers, France.
Pascal AuquierUnité de Recherche EA3279, Aix-Marseille Université, Marseille, France.
IPREA Study group
Aix-Marseille Université · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Poitiers · FRLes Hôpitaux de Chartres · FRClinique Ambroise Paré · FRHôpital Beaujon · FRHôpital Pasteur · FRCentre Hospitalier de La Rochelle · FRCentre Hospitalier de Lens · FRCentre Hospitalier de Roubaix · FRCentre Hospitalier de Troyes · FRCentre Hospitalier de Vitré · FRCentre hospitalier Emile Roux · FRCentre Hospitalier Intercommunal Toulon-La Seyne-sur-Mer · FRCentre Hospitalier Régional Universitaire de Brest · FRCHU Dijon Bourgogne · FRHôpital Civil, Strasbourg · FRHôpital Cochin · FRHôpital d'Hautepierre · FRHôpital Européen · FR

Funding

French Ministry of Health, Programme Hospitalier de Recherche Clinique National 12-010-0554
6 · The paper itself

Abstract

purposeCritically ill patients are exposed to stressful conditions and experience several discomforts. The primary objective was to assess whether a tailored multicomponent program is effective for reducing self-perceived discomfort.

methodsIn a cluster-randomized two-arm parallel trial, 34 French adult intensive care units (ICUs) without planned interventions to reduce discomfort were randomized, 17 to the arm including a 6-month period of program implementation followed by a 6-month period without the program (experimental group), and 17 to the arm with an inversed sequence (control group). The tailored multicomponent program consisted of assessment of ICU-related self-perceived discomforts, immediate and monthly feedback to healthcare teams, and site-specific tailored interventions. The primary outcome was the overall discomfort score derived from the 16-item IPREA questionnaire (0, minimal, 100, maximal overall discomfort) and the secondary outcomes were the discomfort scores of each IPREA item. IPREA was administered on the day of ICU discharge with a considered timeframe from the ICU admission until ICU discharge.

resultsDuring a 1-month assessment period, 398 and 360 patients were included in the experimental group and the control group, respectively. The difference (experimental minus control) of the overall discomfort score between groups was - 7.00 (95% CI - 9.89 to - 4.11, p < 0.001). After adjustment (age, gender, ICU duration, mechanical ventilation duration, and type of admission), the program effect was still positive for the overall discomfort score (difference - 6.35, SE 1.23, p < 0.001) and for 12 out of 16 items.

conclusionsThis tailored multicomponent program decreased self-perceived discomfort in adult critically ill patients.

trial registrationClinicaltrials.gov Identifier NCT02442934.

Indexed as

Pain MeasurementQuality of LifeAgedAged, 80 and overCritical CareCritical IllnessFemaleHumansIntensive Care UnitsMaleMiddle AgedPerceptionSelf ReportCluster-randomized controlled trialCritical careDiscomfortICUPatient-reported outcomeTailored program

Identifiers

PMID29181557
OpenAlexW2770351821

What OpenQuestion holds

Textmetadata
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 OpenQuestion graph.