Evidence map›Paper›PMID 36681325›Full record

Trial reportClinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases2023

Respiratory multiplex PCR and procalcitonin to reduce antibiotic exposure in severe SARS-CoV-2 pneumonia: a multicentre randomized controlled trial.

Muriel Fartoukh, Saad Nseir, Bruno Mégarbane, Yves Cohen, Antoine Lafarge, Damien Contou, Arnaud W Thille, Louis-Marie Galerneau, Florian Reizine, Martin Cour and 8 more

Open access · hybridAbstract readRandomized Controlled TrialMulticenter Study
In one paragraph

Trial report in Clinical microbiology and infection : the official publication of the European Society of Clinical Microbiology and Infectious Diseases, 2023. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 22 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
22citing papers in PubMed, 3 pooled it
7.1field-weighted citation impact, top 2% 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

22 citing papers in PubMed, 3 syntheses or guidelines pooled it, 33 citations in OpenAlex.

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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

18 authors at 11 institutions in 1 country.

Muriel FartoukhSorbonne Université, Assistance Publique-Hôpitaux de Paris (APHP), Hôpital Tenon, Service de Médecine intensive réanimation, Paris, France. Electronic address: muriel.fartoukh@aphp.fr.
Saad NseirCHU de Lille, Médecine Intensive Réanimation, Inserm U1285, CNRS, UMR 8576 - UGSF - Unité de Glycobiologie Structurale et Fonctionnelle, Lille, France.
Bruno MégarbaneDepartment of Medical and Toxicological Critical Care, APHP, Hôpital Lariboisière, Paris Cité University, INSERM UMRS-1144, Paris, France.
Yves CohenRéanimation Médico-Chirurgicale/USC, APHP, Avicenne/Jean Verdier, Hôpitaux Universitaires Paris-Seine-Saint-Denis, Bobigny Cedex, France.
Antoine LafargeService de Médecine Intensive et Réanimation, APHP, Hôpital Saint Louis, Université de Paris, Paris, France.
Damien ContouRéanimation Polyvalente, Centre Hospitalier Victor Dupouy, Argenteuil, France.
Arnaud W ThilleCHU de Poitiers, Médecine Intensive Réanimation, Poitiers, France.
Louis-Marie GalerneauService de Médecine Intensive Réanimation, CHU Grenoble-Alpes, Laboratoire HP2 - Inserm U1042 Hypoxie et Physiopathologies cardiovasculaires et respiratoires, Grenoble, France.
Florian ReizineService des Maladies Infectieuses et Réanimation Médicale, CHU Rennes, Rennes, France.
Martin CourService de Médecine Intensive Réanimation, Hospices Civils de Lyon, Hôpital Edouard Herriot, Lyon, France.
Kada KloucheDepartment of Intensive Care Medicine, Lapeyronie University Hospital, University of Montpellier, PhyMedExp, INSERM (French Institute of Health and Medical Research), CNRS (French National Centre for Scientific Research), School of Medicine, Montpellier, France.
Jean-Christophe NavellouService de réanimation médicale, CHU Jean Minjoz, Université de Bourgogne-Franche Comté, Equipe d'Accueil EA 3920, Besançon, France.
Laurent BitkerService de Médecine Intensive Réanimation. Hôpital de la Croix-Rousse. Hospices Civils de Lyon, Lyon, France.
Alexandra RousseauDepartment of Clinical Pharmacology and Clinical Research Platform Paris-East (URCEST-CRC-CRB), APHP, Hôpital St Antoine, Paris, France.
Sophie TuffetDepartment of Clinical Pharmacology and Clinical Research Platform Paris-East (URCEST-CRC-CRB), APHP, Hôpital St Antoine, Paris, France.
Tabassome SimonDepartment of Clinical Pharmacology and Clinical Research Platform Paris-East (URCEST-CRC-CRB), APHP, Hôpital St Antoine, Paris, France; Sorbonne University, Paris, France.
Guillaume VoiriotSorbonne Université, Assistance Publique-Hôpitaux de Paris (APHP), Hôpital Tenon, Service de Médecine intensive réanimation, Paris, France.
MultiCoV collaborative trial group
Sorbonne Université · FRCentre National de la Recherche Scientifique · FRInserm · FRAssistance Publique – Hôpitaux de Paris · FRCentre Hospitalier Universitaire de Poitiers · FRCentre Hospitalier Universitaire de Rennes · FRCentre Hospitalier Victor Dupouy · FRHôpital de la Croix-Rousse · FRHospices Civils de Lyon · FRUniversité de Bourgogne · FRUniversité Paris Cité · FR

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

objectivesWe aimed at assessing the efficacy and safety on antibiotic exposure of a strategy combining a respiratory multiplex PCR (mPCR) with enlarged panel and daily procalcitonin (PCT) measurements, as compared with a conventional strategy, in adult patients who were critically ill with laboratory-confirmed SARS-CoV-2 pneumonia.

methodsThis multicentre, parallel-group, open-label, randomized controlled trial enrolled patients admitted to 13 intensive care units (ICUs) in France. Patients were assigned (1:1) to the control strategy, in which antibiotic streamlining remained at the discretion of the physicians, or interventional strategy, consisting of using mPCR and daily PCT measurements within the first 7 days of randomization to streamline initial antibiotic therapy, with antibiotic continuation encouraged when PCT was >1 ng/mL and discouraged if < 1 ng/mL or decreased by 80% from baseline. All patients underwent conventional microbiological tests and cultures. The primary end point was antibiotic-free days at day 28.

resultsBetween April 20th and November 23rd 2020, 194 patients were randomized, of whom 191 were retained in the intention-to-treat analysis. Respiratory bacterial co-infection was detected in 48.4% (45/93) and 21.4% (21/98) in the interventional and control group, respectively. The number of antibiotic-free days was 12.0 (0.0; 25.0) and 14.0 (0.0; 24.0) days, respectively (difference, -2.0, (95% CI, -10.6 to 6.6), p=0.89). Superinfection rates were high (51.6% and 48.5%, respectively). Mortality rates and ICU lengths of stay did not differ between groups. DISCUSSION: In severe SARS-CoV-2 pneumonia, the mPCR/PCT algorithm strategy did not affect 28-day antibiotics exposure nor the major clinical outcomes, as compared with routine practice.

Indexed as

Bacterial InfectionsCOVID-19Respiratory Tract InfectionsAdultAnti-Bacterial AgentsCOVID-19 TestingHumansMultiplex Polymerase Chain ReactionProcalcitoninSARS-CoV-2Treatment OutcomeAnti-Bacterial AgentsProcalcitoninAntibiotics useCOVID-19Intensive care unitMultiplex PCRRandomized controlled trial

Identifiers

PMID36681325
PMCPMC9847221
OpenAlexW4317384351

What OpenQuestion holds

Textmetadata
Read underepoch 390

Registered trials

None linked

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.