Potential of Multiplex Polymerase Chain Reaction Performed on Protected Telescope Catheter Samples for Early Adaptation of Antimicrobial Therapy in ARDS Patients.

COVID-19 antibiotic stewardship coinfection multiplex PCR superinfection ventilator-associated pneumonia

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
27 Jul 2022
Historique:
received: 01 06 2022
revised: 20 07 2022
accepted: 23 07 2022
entrez: 12 8 2022
pubmed: 13 8 2022
medline: 13 8 2022
Statut: epublish

Résumé

Diagnosis of co/superinfection in patients with Acute Respiratory Distress Syndrome (ARDS) is challenging. The FilmArray Pneumonia plus Panel (bioMérieux, France), a new rapid multiplex Polymerase Chain Reaction (mPCR), has never been assessed on a blinded protected telescope catheter (PTC) samples, a very common diagnostic tool in patients under mechanical ventilation. We evaluated the performance of mPCR on PTC samples compared with conventional culture and its impact on antibiotic stewardship. Observational study in two intensive care units, conducted between March and July 2020, during the first wave of the COVID-19 pandemic in France. We performed 125 mPCR on blinded PTC samples of 95 ARDS patients, including 73 (77%) SARS-CoV-2 cases and 28 (29%) requiring extracorporeal membrane oxygenation. Respiratory samples were drawn from mechanically ventilated patients either just after intubation ( Rapid mPCR was feasible on blinded PTC with good sensitivity and specificity. New antibiotics were not initiated in more than half of patients and more than one-third of VAP-suspected cases. Further studies are needed to assess mPCR potential in improving antibiotic stewardship.

Sections du résumé

BACKGROUND BACKGROUND
Diagnosis of co/superinfection in patients with Acute Respiratory Distress Syndrome (ARDS) is challenging. The FilmArray Pneumonia plus Panel (bioMérieux, France), a new rapid multiplex Polymerase Chain Reaction (mPCR), has never been assessed on a blinded protected telescope catheter (PTC) samples, a very common diagnostic tool in patients under mechanical ventilation. We evaluated the performance of mPCR on PTC samples compared with conventional culture and its impact on antibiotic stewardship.
METHODS METHODS
Observational study in two intensive care units, conducted between March and July 2020, during the first wave of the COVID-19 pandemic in France.
RESULTS RESULTS
We performed 125 mPCR on blinded PTC samples of 95 ARDS patients, including 73 (77%) SARS-CoV-2 cases and 28 (29%) requiring extracorporeal membrane oxygenation. Respiratory samples were drawn from mechanically ventilated patients either just after intubation (
CONCLUSIONS CONCLUSIONS
Rapid mPCR was feasible on blinded PTC with good sensitivity and specificity. New antibiotics were not initiated in more than half of patients and more than one-third of VAP-suspected cases. Further studies are needed to assess mPCR potential in improving antibiotic stewardship.

Identifiants

pubmed: 35955983
pii: jcm11154366
doi: 10.3390/jcm11154366
pmc: PMC9369416
pii:
doi:

Types de publication

Journal Article

Langues

eng

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Auteurs

Keyvan Razazi (K)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, DMU Médecine, Service de Médecine Intensive Réanimation, CHU Henri Mondor, 51, Av. de Lattre de Tassigny, CEDEX, 94010 Créteil, France.
Faculté de Médecine de Créteil, IMRB, GRC CARMAS, Université Paris Est Créteil, 94010 Créteil, France.

Flora Delamaire (F)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, DMU Médecine, Service de Médecine Intensive Réanimation, CHU Henri Mondor, 51, Av. de Lattre de Tassigny, CEDEX, 94010 Créteil, France.

Vincent Fihman (V)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, Département de Prévention, Diagnostic et Traitement des Infections, Unité de Bactériologie, 94010 Créteil, France.
EA 7380 Dynamyc, UPEC, Ecole Nationale Vétérinaire d'Alfort, USC Anses, 94000 Créteil, France.

Mohamed Ahmed Boujelben (MA)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, DMU Médecine, Service de Médecine Intensive Réanimation, CHU Henri Mondor, 51, Av. de Lattre de Tassigny, CEDEX, 94010 Créteil, France.
Faculté de Médecine de Créteil, IMRB, GRC CARMAS, Université Paris Est Créteil, 94010 Créteil, France.

Nicolas Mongardon (N)

AP-HP Service d'Anesthésie-Réanimation Chirurgicale, DMU CARE, DHU A-TVB, Hôpitaux Universitaires Henri Mondor, 94010 Créteil, France.
U955-IMRB, Equipe 03 "Pharmacologie et Technologies Pour les Maladies Cardiovasculaires (PROTECT)", Inserm, Université Paris Est Créteil (UPEC), Ecole Nationale Vétérinaire d'Alfort (EnVA), 94700 Maisons-Alfort, France.
Faculté de Santé, Université Paris Est Créteil, 94010 Créteil, France.

Ségolène Gendreau (S)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, DMU Médecine, Service de Médecine Intensive Réanimation, CHU Henri Mondor, 51, Av. de Lattre de Tassigny, CEDEX, 94010 Créteil, France.
Faculté de Médecine de Créteil, IMRB, GRC CARMAS, Université Paris Est Créteil, 94010 Créteil, France.

Quentin de Roux (Q)

AP-HP Service d'Anesthésie-Réanimation Chirurgicale, DMU CARE, DHU A-TVB, Hôpitaux Universitaires Henri Mondor, 94010 Créteil, France.
U955-IMRB, Equipe 03 "Pharmacologie et Technologies Pour les Maladies Cardiovasculaires (PROTECT)", Inserm, Université Paris Est Créteil (UPEC), Ecole Nationale Vétérinaire d'Alfort (EnVA), 94700 Maisons-Alfort, France.
Faculté de Santé, Université Paris Est Créteil, 94010 Créteil, France.

Nicolas de Prost (N)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, DMU Médecine, Service de Médecine Intensive Réanimation, CHU Henri Mondor, 51, Av. de Lattre de Tassigny, CEDEX, 94010 Créteil, France.
Faculté de Médecine de Créteil, IMRB, GRC CARMAS, Université Paris Est Créteil, 94010 Créteil, France.
INSERM, Université Paris Est, Unité U955, 94010 Créteil, France.

Guillaume Carteaux (G)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, DMU Médecine, Service de Médecine Intensive Réanimation, CHU Henri Mondor, 51, Av. de Lattre de Tassigny, CEDEX, 94010 Créteil, France.
Faculté de Médecine de Créteil, IMRB, GRC CARMAS, Université Paris Est Créteil, 94010 Créteil, France.
INSERM, Université Paris Est, Unité U955, 94010 Créteil, France.

Paul-Louis Woerther (PL)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, Département de Prévention, Diagnostic et Traitement des Infections, Unité de Bactériologie, 94010 Créteil, France.
EA 7380 Dynamyc, UPEC, Ecole Nationale Vétérinaire d'Alfort, USC Anses, 94000 Créteil, France.

Armand Mekontso Dessap (A)

AP-HP (Assistance Publique-Hôpitaux de Paris), Hôpitaux Universitaires Henri Mondor, DMU Médecine, Service de Médecine Intensive Réanimation, CHU Henri Mondor, 51, Av. de Lattre de Tassigny, CEDEX, 94010 Créteil, France.
Faculté de Médecine de Créteil, IMRB, GRC CARMAS, Université Paris Est Créteil, 94010 Créteil, France.
INSERM, Université Paris Est, Unité U955, 94010 Créteil, France.

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