Compared Performance of the 2023 Duke-International Society for Cardiovascular Infectious Diseases, the 2000 Modified Duke, and the 2015 ESC Criteria for the Diagnosis of Infective Endocarditis in a French Multicenter Prospective Cohort.

2023 Duke-ISCVID criteria Diagnosis classification Infective endocarditis accuracy sensitivity specificity

Journal

Clinical infectious diseases : an official publication of the Infectious Diseases Society of America
ISSN: 1537-6591
Titre abrégé: Clin Infect Dis
Pays: United States
ID NLM: 9203213

Informations de publication

Date de publication:
08 Feb 2024
Historique:
received: 02 06 2023
revised: 03 09 2023
accepted: 26 01 2024
medline: 8 2 2024
pubmed: 8 2 2024
entrez: 8 2 2024
Statut: aheadofprint

Résumé

The 2023 Duke-ISCVID Criteria for infective endocarditis (IE) were proposed as an updated diagnostic classification of IE. Using an open prospective multicenter cohort of patients treated for IE, we compared the performance of these new criteria to that of the 2000 Modified Duke and 2015 ESC criteria. Cases of patients treated for IE between January 2017 and October 2022 were adjudicated as certain IE or not. Each case was also categorized as either definite or possible/rejected within each classification. Sensitivity, specificity, and accuracy were estimated, with 95% confidence intervals. Of the 1194 patients analyzed (mean age 66.1 years, 71.2% men), 414 (34.7%) had a prosthetic valve and 284 (23.8%) had a cardiac implanted electronic device (CIED); 946 (79.2%) were adjudicated as certain IE; 978 (81.9%), 997 (83.5%), and 1057 (88.5%) were classified as definite IE in the 2000 modified Duke, 2015 ESC, and 2023 Duke-ISCVID criteria, respectively. The sensitivity of each set of criteria was 93.2% [91.6-94.8], 95.0% [93.7-96.4], and 97.6% [96.6-98.6], respectively (p<.001 for all 2-by-2 comparisons). Corresponding specificity rates were 61.3% [55.2-67.4), 60.5% [54.4-66.6], and 46.0% [39.8-52.2], respectively. In patients without CIED, sensitivity rates were 94.8% [93.2-96.4], 96.5% [95.1-97.8], and 97.7% [96.6-98.8] and specificity rates were 59.0% [51.6-66.3], 56.6% [49.3-64.0], and 53.8% [46.3-61.2], respectively. Overall, the 2023 Duke-ISCVID criteria had a significantly higher sensitivity but a significantly lower specificity, compared to older criteria. This decreased specificity was mainly attributable to patients with CIED.

Sections du résumé

BACKGROUND BACKGROUND
The 2023 Duke-ISCVID Criteria for infective endocarditis (IE) were proposed as an updated diagnostic classification of IE. Using an open prospective multicenter cohort of patients treated for IE, we compared the performance of these new criteria to that of the 2000 Modified Duke and 2015 ESC criteria.
METHODS METHODS
Cases of patients treated for IE between January 2017 and October 2022 were adjudicated as certain IE or not. Each case was also categorized as either definite or possible/rejected within each classification. Sensitivity, specificity, and accuracy were estimated, with 95% confidence intervals.
RESULTS RESULTS
Of the 1194 patients analyzed (mean age 66.1 years, 71.2% men), 414 (34.7%) had a prosthetic valve and 284 (23.8%) had a cardiac implanted electronic device (CIED); 946 (79.2%) were adjudicated as certain IE; 978 (81.9%), 997 (83.5%), and 1057 (88.5%) were classified as definite IE in the 2000 modified Duke, 2015 ESC, and 2023 Duke-ISCVID criteria, respectively. The sensitivity of each set of criteria was 93.2% [91.6-94.8], 95.0% [93.7-96.4], and 97.6% [96.6-98.6], respectively (p<.001 for all 2-by-2 comparisons). Corresponding specificity rates were 61.3% [55.2-67.4), 60.5% [54.4-66.6], and 46.0% [39.8-52.2], respectively. In patients without CIED, sensitivity rates were 94.8% [93.2-96.4], 96.5% [95.1-97.8], and 97.7% [96.6-98.8] and specificity rates were 59.0% [51.6-66.3], 56.6% [49.3-64.0], and 53.8% [46.3-61.2], respectively.
CONCLUSION CONCLUSIONS
Overall, the 2023 Duke-ISCVID criteria had a significantly higher sensitivity but a significantly lower specificity, compared to older criteria. This decreased specificity was mainly attributable to patients with CIED.

Identifiants

pubmed: 38330171
pii: 7603542
doi: 10.1093/cid/ciae035
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Investigateurs

Nelly Agrinier (N)
François Alla (F)
Guillaume Béraud (G)
Elisabeth Botelho-Nevers (E)
Catherine Chirouze (C)
François Delahaye (F)
Xavier Duval (X)
François Goehringer (F)
Bruno Hoen (B)
Bernard Iung (B)
Christine Selton Suty (CS)
Christophe Strady (C)
Pierre Tattevin (P)
Corentine Alauzet (C)
Patrick Assayag (P)
Kasra Azarnoush (K)
Mathieu Blot (M)
Yohann Bohbot (Y)
Kevin Bouiller (K)
Marielle Buisson (M)
Elodie Curlier (E)
Enrica Dorigo (E)
Michel Duong (M)
Mazen Elfarra (M)
Clémentine Esteve (C)
Laura Filippetti (L)
Damien Fournier (D)
Nathalie Grand (N)
Raphaëlle Huguet (R)
Emila Ilic-Habensus (E)
Audrey Le Bot (A)
Benjamin Lefèvre (B)
Raphaël Lepeule (R)
Sophie Mahy (S)
Charles Monnin (C)
Basile Mouhat (B)
Franck Noël (F)
Nathalie Pansu (N)
Lucas Perez (L)
Andranik Petrosyan (A)
Romain Pierrard (R)
Matthieu Revest (M)
Thibault Sixt (T)
Anne Suzat (A)
Charles Tassigny (C)
Noémie Tissot (N)
Dehbia Aboudaoud (D)
Hassina Bouguerra (H)
Catherine Campagnac (C)
Carole Charles (C)
Giulia Corradi (G)
Sandra Dupuy (S)
Eola Francius (E)
Sandrine Gerset (S)
Sandrine Gohier (S)
Mesut Gun (M)
Maryse André (M)
Véronique Ronat (V)
Tubanur Unal Albayrak (TU)
Marie-Line Erpelding (ML)
Nadine Juge (N)
Benoit Lalloué (B)
Willy Ngueyon Sime (WN)
Marie Sponga (M)
Jean-Marc Virion (JM)

Informations de copyright

© The Author(s) 2024. Published by Oxford University Press on behalf of Infectious Diseases Society of America. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.

Auteurs

Francois Goehringer (F)

Service de maladies infectieuses et tropicales, CHRU Nancy, F-54000, Nancy, France.

Benoit Lalloué (B)

CHRU-Nancy, INSERM, Université de Lorraine, CIC, Epidémiologie Clinique, F-54000 Nancy, France.

Christine Selton-Suty (C)

Département de cardiologie médicale, CHRU-Nancy, CIC-EC, F-54000 Nancy, France.

François Alla (F)

Univ. Bordeaux, INSERM, BPH, U1219, I-prev/PHARES, CIC 1401, F-33000 Bordeaux, France.
CHU de Bordeaux, Service de prévention, F-33000 Bordeaux, France.

Elisabeth Botelho-Nevers (E)

Service de maladies infectieuses, CHU de Saint-Etienne, 42055 Saint-Etienne France.
CIRI - Centre International de Recherche en Infectiologie, Team GIMAP, Université Jean Monnet, Université de Lyon, Inserm, U1111, CNRS, UMR530, F-42023 Saint-Etienne, France.

Catherine Chirouze (C)

Chrono-environnement UMR6249, CNRS, Université Bourgogne Franche-Comté, F-25000, Besançon, France.
Service de maladies infectieuses et tropicales, CHU Jean Minjoz, F-25000, Besançon, France.

Elodie Curlier (E)

Service de maladies infectieuses, CHU de Guadeloupe, Pointe-à-Pitre, Guadeloupe, France.

Safwane El Hatimi (S)

CHU Bicêtre, Université Paris Saclay, Le Kremlin Bicêtre, France.

Amandine Gagneux-Brunon (A)

Service de maladies infectieuses, CHU de Saint-Etienne, 42055 Saint-Etienne France.
CIRI - Centre International de Recherche en Infectiologie, Team GIMAP, Université Jean Monnet, Université de Lyon, Inserm, U1111, CNRS, UMR530, F-42023 Saint-Etienne, France.

Vincent le Moing (V)

Maladies Infectieuses et Tropicales, CHU de Montpellier, Montpellier, France.
Université de Montpellier, Montpellier, France.

Pascal Lim (P)

Assistance Publique-Hôpitaux de Paris (AP-HP), Hôpitaux Universitaires Henri Mondor, Faculté de Santé, Univ. Paris Est Créteil, F-94010 Créteil, France.

Lionel Piroth (L)

Service de maladies infectieuses, CHU de Dijon, 21000 Dijon, France.
CHU Dijon-Bourgogne, INSERM, Université de Bourgogne, CIC 1432, Module Épidémiologie Clinique, Dijon, France.

Christophe Strady (C)

Cabinet d'infectiologie, Groupe Courlancy, 51100 Reims, France.

Christophe Tribouilloy (C)

UR UPJV 7517, Université Jules Verne, Amiens, France.
CHU Amiens-Picardie, Amiens, France.

Jean-Marc Virion (JM)

CHRU-Nancy, INSERM, Université de Lorraine, CIC, Epidémiologie Clinique, F-54000 Nancy, France.

Nelly Agrinier (N)

CHRU-Nancy, INSERM, Université de Lorraine, CIC, Epidémiologie Clinique, F-54000 Nancy, France.

Xavier Duval (X)

Inserm CIC 1425, Paris, France.
AP-HP, Hôpital Bichat Claude-Bernard, Paris, France.
Inserm UMR-1137 IAME, Paris, France.
Université Paris Cité, UFR de Médecine-Bichat, Paris, France.

Bruno Hoen (B)

Université de Lorraine, Ecole de santé publique - UR 4360 Apemac, Nancy, France.

Classifications MeSH