Impact of Systematic Whole-body 18F-Fluorodeoxyglucose PET/CT on the Management of Patients Suspected of Infective Endocarditis: The Prospective Multicenter TEPvENDO Study
Author:
Duval Xavier1234, Le Moing Vincent5, Tubiana Sarah123, Esposito-Farèse Marina126, Ilic-Habensus Emila12, Leclercq Florence7, Bourdon Aurélie8, Goehringer François9, Selton-Suty Christine10, Chevalier Elodie11, Boutoille David12, Piriou Nicolas1314, Le Tourneau Thierry13, Chirouze Catherine15, Seronde Marie-France16, Morel Olivier17, Piroth Lionel18, Eicher Jean-Christophe19, Humbert Olivier20, Revest Matthieu2122, Thébault Elise22, Devillers Anne23, Delahaye François24, Boibieux André25, Grégoire Bastien26, Hoen Bruno9, Laouenan Cédric12346, Iung Bernard1234, Rouzet François123427, Duval Xavier, Hoen Bruno, Iung Bernard, Rouzet Francois, Tubiana Sarah, Albayrak Tubanur, Bernard Yvette, Boulahdour Hatem, Briand Florent, Chirouze Catherine, Faucher Jean-François, Guignier Alexandre, Hustache-Mathieu Laurent, Illes-Hajnal Gabriela, Moreau Joséphine, Morel Olivier, Seronde Marie-France, Behechti Niloufar, Blot Mathieu, Buisson Marielle, Cochet Alexandre, Eicher Jean-Christophe, Humbert Olivier, Lecluse-Barth Julien, Mahy Sophie, Piroth Lionel, Andre Philippe, Delahaye François, Delahaye Armelle, Grégoire Bastien, Bourdon Aurélie, Cade Stéphane, Casanova Marie-Laure, Cerutti Diane, De Verbizier Delphine, Le Moing Vincent, Martinez Angelina, Morquin David, Solecki Kamila, Bonay Stéphanie, Chevalier Elodie, Claudin Marine, Djaballah Wassila, Goehringer François, Huttin Olivier, Jeanmaire Eliette, Marie Pierre-Yves, Roch Véronique, Selton-Suty Christine, Vauthier Sandrine, Venner Clément, Asseray Nathalie, Biron Charlotte, Boutoille David, Brochard-Libois Julia, Cavellec Morgane, Cueff Caroline, Delarue Sandrine, Di Prizio Catherine, Dinc Levent, Fellah Imen, Guijarro Damien, Lachaud Mathias, Le Gloan Laurianne, Le Tourneau Thierry, Lecompte Anne-Sophie, Lefebvre Maeva, Luçon Adrien, Mathieu Cédric, Orain Jérémie, Pallardy Amandine, Piriou Nicolas, Poilane Maxime, Sassier Jérôme, Ben Ali Khadija, Brochet Eric, Burdet Charles, Celestin Bettia, Cimadevilla Claire, Duval Xavier, Hiafyl Fabien, Ilic-Habensus Emila, Iung Bernard, Lachatre Marie, Lepage Laurent, Lescure Xavier, Rouzet François, Vindrios William, Wolff Michel, Yazdanpanah Yazdan, Devillers Anne, Donal Erwan, Lacroix Adèle, Lelong Bernard, Revest Matthieu, Tattevin Pierre, Thebault Elise, Couffignal Camille, Esposito-Farese Marina, Laouenan Cédric, Maklouf Sonia, Mentre France, Prevault Margot, Rogier Ophélie,
Affiliation:
1. INSERM CIC 1425, Paris, France 2. AP-HP, University Hospital of Bichat, Paris, France 3. INSERM UMR-1137 IAME, Paris, France 4. University Paris Diderot, Paris 7, UFR de Médecine-Bichat, Paris, France 5. Department of Infectious Diseases, University Hospital of Montpellier, Montpellier, France 6. Unité de Recherche Clinique, AP-HP, HUPNVS, Hôpital Universitaire Paris Nord-Val de Seine, Paris, France 7. Department of Cardiology, University Hospital of Montpellier, Montpellier, France 8. Department of Nuclear Medicine, University Hospital of Montpellier, Montpellier, France 9. Department of Infectious Diseases, University Hospital of Nancy, Nancy, France 10. Department of Cardiology, University Hospital of Nancy, Nancy, France 11. Department of Nuclear Medicine, University Hospital of Nancy, Nancy, France 12. Department of Infectious Diseases, CIC UIC 1413 INSERM, University Hospital of Nantes, Nantes, France 13. Thorax Institute, INSERM, UMR 1087, University Hospital of Nantes, Nantes, France 14. Department of Nuclear Medicine, Nantes University Hospital, G. et R. Laennec Hospital, Nantes, France 15. University Hospital of Besançon, France, UMR CNRS 6249 Chrono-Environnement, Bourgogne University, Franche-Comté, Dijon, France 16. Department of Cardiology, University Hospital of Besançon, Besançon, France 17. Department of Nuclear Medicine, University Hospital of Besançon, Besançon, France 18. Department of Infectious Diseases, University Hospital of Dijon, INSERM CIC 1432, CHU Dijon, France 19. Department of Cardiology, University Hospital of Dijon, Dijon, France 20. Department of Nuclear Medicine, University Hospital of Dijon, Dijon, France 21. Infectious Diseases and Intensive Care Unit, University Hospital of Rennes France, INSERM U1230 CHU Rennes, France 22. INSERM CIC 1414, University Hospital of Rennes, France 23. Department of Nuclear Medicine, University Hospital of Rennes, France 24. Department of Cardiology, University Hospital of Lyon, Lyon, France 25. Department of Nuclear Medicine, University Hospital of Lyon, Lyon, France 26. Department of Infectious Diseases, University Hospital of Lyon, Lyon, France 27. Department of Nuclear Medicine, AP-HP, University Hospital of Bichat, Paris, France
Abstract
Abstract
Background
Diagnostic and patients’ management modifications induced by whole-body 18F-FDG-PET/CT had not been evaluated so far in prosthetic valve (PV) or native valve (NV) infective endocarditis (IE)-suspected patients.
Methods
In sum, 140 consecutive patients in 8 tertiary care hospitals underwent 18F-FDG-PET/CT. ESC-2015-modified Duke criteria and patients’ management plan were established jointly by 2 experts before 18F-FDG-PET/CT. The same experts reestablished Duke classification and patients’ management plan immediately after qualitative interpretation of 18F-FDG-PET/CT. A 6-month final Duke classification was established.
Results
Among the 70 PV and 70 NV patients, 34 and 46 were classified as definite IE before 18F-FDG-PET/CT. Abnormal perivalvular 18F-FDG uptake was recorded in 67.2% PV and 24.3% NV patients respectively (P < .001) and extracardiac uptake in 44.3% PV and 51.4% NV patients. IE classification was modified in 24.3% and 5.7% patients (P = .005) (net reclassification index 20% and 4.3%). Patients’ managements were modified in 21.4% PV and 31.4% NV patients (P = .25). It was mainly due to perivalvular uptake in PV patients and to extra-cardiac uptake in NV patients and consisted in surgery plan modifications in 7 patients, antibiotic plan modifications in 22 patients and both in 5 patients. Altogether, 18F-FDG-PET/CT modified classification and/or care in 40% of the patients (95% confidence interval: 32–48), which was most likely to occur in those with a noncontributing echocardiography (P < .001) or IE classified as possible at baseline (P = .04), while there was no difference between NV and PV.
Conclusions
Systematic 18F-FDG-PET/CT did significantly and appropriately impact diagnostic classification and/or IE management in PV and NV-IE suspected patients.
Clinical Trials Registration
NCT02287792.
Funder
French Ministry of Health
Publisher
Oxford University Press (OUP)
Subject
Infectious Diseases,Microbiology (medical)
Cited by
48 articles.
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