Impact on antimicrobial consumption of procalcitonin-guided antibiotic therapy for pneumonia/pneumonitis associated with aspiration in comatose mechanically ventilated patients: a multicenter, randomized controlled study.

Aspiration Coma Intensive care unit Pneumonia Procalcitonin

Journal

Annals of intensive care
ISSN: 2110-5820
Titre abrégé: Ann Intensive Care
Pays: Germany
ID NLM: 101562873

Informations de publication

Date de publication:
12 Oct 2021
Historique:
received: 27 06 2021
accepted: 21 09 2021
entrez: 12 10 2021
pubmed: 13 10 2021
medline: 13 10 2021
Statut: epublish

Résumé

In comatose patients receiving oro-tracheal intubation for mechanical ventilation (MV), the risk of aspiration is increased. Aspiration can lead to chemical pneumonitis (inflammatory reaction to the gastric contents), or aspiration pneumonia (infection caused by inhalation of microorganisms). Distinguishing between the two types is challenging. We tested the interest of using a decisional algorithm based on procalcitonin (PCT) values to guide initiation and discontinuation of antibiotic therapies in intubated patients. The PROPASPI (PROcalcitonin Pneumonia/pneumonitis Associated with ASPIration) trial is a multicenter, prospective, randomized, controlled, single-blind, superiority study comparing two strategies: (1) an intervention group where threshold PCT values were used to guide initiation and discontinuation of antibiotics (PCT group); and (2) a control group, where antibiotic therapy was managed at the physician's discretion. Patients aged 18 years or over, intubated for coma (Glasgow score ≤ 8), with MV initiated within 48 h after admission, were eligible. The primary endpoint was the duration of antibiotic treatment during the first 15 days after admission to the ICU. From 24/2/2015 to 28/8/2019, 1712 patients were intubated for coma in the 5 participating centers, of whom 166 were included in the study. Data from 159 were available for intention-to-treat analysis: 81 in the PCT group, and 78 in the control group. Overall, 67 patients (43%) received antibiotics in the intensive care unit (ICU); there was no significant difference between groups (37 (46%) vs 30 (40%) for PCT vs control, p = 0.432). The mean duration of antibiotic treatment during the first 15 days in the ICU was 2.7 ± 3.8 days; there was no significant difference between groups (3.0 ± 4.1 days vs 2.3 ± 3.4 days for PCT vs control, p = 0.311). The mean number of days under MV was significantly higher in the PCT group (3.7 ± 3.6 days) than in controls (2.7 ± 2.5 days, p = 0.033). The duration of ICU stay was also significantly longer in the PCT group: 6.4 ± 6.5 days vs 4.6 ± 3.5 days in the control group (p = 0.043). After adjustment for SAPS II score, the difference in length of stay and duration of mechanical ventilation between groups was no longer significant. The use of PCT values to guide therapy, in comparison to the use of clinical, biological (apart from PCT) and radiological criteria, does not modify exposure to antibiotics in patients intubated for coma. Trial registration Clinicaltrials.gov Identifier NCT02862314.

Sections du résumé

BACKGROUND BACKGROUND
In comatose patients receiving oro-tracheal intubation for mechanical ventilation (MV), the risk of aspiration is increased. Aspiration can lead to chemical pneumonitis (inflammatory reaction to the gastric contents), or aspiration pneumonia (infection caused by inhalation of microorganisms). Distinguishing between the two types is challenging. We tested the interest of using a decisional algorithm based on procalcitonin (PCT) values to guide initiation and discontinuation of antibiotic therapies in intubated patients.
METHODS METHODS
The PROPASPI (PROcalcitonin Pneumonia/pneumonitis Associated with ASPIration) trial is a multicenter, prospective, randomized, controlled, single-blind, superiority study comparing two strategies: (1) an intervention group where threshold PCT values were used to guide initiation and discontinuation of antibiotics (PCT group); and (2) a control group, where antibiotic therapy was managed at the physician's discretion. Patients aged 18 years or over, intubated for coma (Glasgow score ≤ 8), with MV initiated within 48 h after admission, were eligible. The primary endpoint was the duration of antibiotic treatment during the first 15 days after admission to the ICU.
RESULTS RESULTS
From 24/2/2015 to 28/8/2019, 1712 patients were intubated for coma in the 5 participating centers, of whom 166 were included in the study. Data from 159 were available for intention-to-treat analysis: 81 in the PCT group, and 78 in the control group. Overall, 67 patients (43%) received antibiotics in the intensive care unit (ICU); there was no significant difference between groups (37 (46%) vs 30 (40%) for PCT vs control, p = 0.432). The mean duration of antibiotic treatment during the first 15 days in the ICU was 2.7 ± 3.8 days; there was no significant difference between groups (3.0 ± 4.1 days vs 2.3 ± 3.4 days for PCT vs control, p = 0.311). The mean number of days under MV was significantly higher in the PCT group (3.7 ± 3.6 days) than in controls (2.7 ± 2.5 days, p = 0.033). The duration of ICU stay was also significantly longer in the PCT group: 6.4 ± 6.5 days vs 4.6 ± 3.5 days in the control group (p = 0.043). After adjustment for SAPS II score, the difference in length of stay and duration of mechanical ventilation between groups was no longer significant.
CONCLUSION CONCLUSIONS
The use of PCT values to guide therapy, in comparison to the use of clinical, biological (apart from PCT) and radiological criteria, does not modify exposure to antibiotics in patients intubated for coma. Trial registration Clinicaltrials.gov Identifier NCT02862314.

Identifiants

pubmed: 34636974
doi: 10.1186/s13613-021-00931-4
pii: 10.1186/s13613-021-00931-4
pmc: PMC8505789
doi:

Banques de données

ClinicalTrials.gov
['NCT02862314']

Types de publication

Journal Article

Langues

eng

Pagination

145

Subventions

Organisme : centre hospitalier universitaire de besançon
ID : APICHU 2016

Investigateurs

Jean-Christophe Navellou (JC)
Claire Chaignat (C)
Mathilde Grandperrin (M)
Mélanie Claveau (M)
Nicolas Belin (N)
Cyrille Patry (C)
Frédéric Claude (F)
François Belon (F)
Loïc Barrot (L)
Marion Colnot (M)
Guillaume Besch (G)
Gilles Blasco (G)
Marc Ginet (M)
Yannick Brunin (Y)
Pascal Andreu (P)
Auguste Dargent (A)
Pierre Emmanuel Charles (PE)
Ferhat Meziani (F)
Alexandra Monnier (A)
Antoine Studer (A)
Raphaël Clere-Jehl (R)
Hassene Rahmani (H)
Anne Florence Dureau (AF)
Antoine Poidevin (A)
Joy Mootien (J)
Gokhan Bodur (G)
Carmen Ionescu (C)
Philippe Guiot (P)

Informations de copyright

© 2021. The Author(s).

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Auteurs

Guylaine Labro (G)

Medical Intensive Care Unit, University Hospital, Besançon, France.
Medical Intensive Care Unit, Hospital of Mulhouse, Mulhouse, France.

François Aptel (F)

Department of Intensive Care, François Mitterrand University Hospital, Dijon, France.

Marc Puyraveau (M)

INSERM Clinical Investigation Center 1431, Besançon, France.

Jonathan Paillot (J)

Surgical Intensive Care Unit, University Hospital, Besançon, France.

Sébastien Pili Floury (S)

Surgical Intensive Care Unit, University Hospital, Besançon, France.
EA3920, University of Burgundy Franche-Comté, 25000, Besancon, France.

Hamid Merdji (H)

Service de Médecine Intensive Réanimation, Nouvel Hôpital Civil, Université de Strasbourg, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
UMR 1260, Fédération de Médecine Translationnelle de Strasbourg (FMTS), INSERM, Strasbourg, France.

Julie Helms (J)

Service de Médecine Intensive Réanimation, Nouvel Hôpital Civil, Université de Strasbourg, Hôpitaux Universitaires de Strasbourg, Strasbourg, France.
UMR 1260, Fédération de Médecine Translationnelle de Strasbourg (FMTS), INSERM, Strasbourg, France.

Gaël Piton (G)

Medical Intensive Care Unit, University Hospital, Besançon, France.
EA3920, University of Burgundy Franche-Comté, 25000, Besancon, France.

Fiona Ecarnot (F)

EA3920, University of Burgundy Franche-Comté, 25000, Besancon, France.
Department of Cardiology, University Hospital, Besançon, France.

Khaldoun Kuteifan (K)

Medical Intensive Care Unit, Hospital of Mulhouse, Mulhouse, France.

Jean Pierre Quenot (JP)

Department of Intensive Care, François Mitterrand University Hospital, Dijon, France. jean-pierre.quenot@chu-dijon.fr.
Lipness Team, INSERM Research Center LNC-UMR1231 and LabEx LipSTIC, University of Burgundy, Dijon, France. jean-pierre.quenot@chu-dijon.fr.
INSERM CIC 1432, Clinical Epidemiology, University of Burgundy, Dijon, France. jean-pierre.quenot@chu-dijon.fr.

Gilles Capellier (G)

Medical Intensive Care Unit, University Hospital, Besançon, France.
EA3920, University of Burgundy Franche-Comté, 25000, Besancon, France.
Australian and New Zealand Intensive Care Research Centre, Department of Epidemiology and Preventive Medicine, Monash University, Melbourne, Australia.

Classifications MeSH