Frontiers in Pediatrics (Oct 2021)
Diagnostic Accuracy of Routinely Available Biomarkers to Predict Bacteremia in Children With Community-Acquired Pneumonia: A Secondary Analysis of the GPIP/ACTIV Pneumonia Study in France, 2009–2018
- Danaé Dudognon,
- Corinne Levy,
- Corinne Levy,
- Corinne Levy,
- Corinne Levy,
- Martin Chalumeau,
- Martin Chalumeau,
- Sandra Biscardi,
- Sandra Biscardi,
- Marie-Aliette Dommergues,
- Marie-Aliette Dommergues,
- François Dubos,
- François Dubos,
- Karine Levieux,
- Karine Levieux,
- Marie Aurel,
- Marie Aurel,
- Philippe Minodier,
- Philippe Minodier,
- Ferielle Zenkhri,
- Ferielle Zenkhri,
- Ellia Mezgueldi,
- Ellia Mezgueldi,
- Irina Craiu,
- Irina Craiu,
- Laurence Morin,
- Laurence Morin,
- Stéphane Béchet,
- Emmanuelle Varon,
- Robert Cohen,
- Robert Cohen,
- Robert Cohen,
- Robert Cohen,
- Robert Cohen,
- Jérémie F. Cohen,
- Jérémie F. Cohen,
- The Pneumonia Study Group,
- François Angoulvant,
- Yves Gillet,
- Christèle Gras-Le Guen,
- Isabelle Hau,
- Laure Hees,
- Elise Launay,
- Mathie Lorrot,
- Fouad Madhi,
- Alain Martinot,
- Naim Ouldali
Affiliations
- Danaé Dudognon
- Department of General Pediatrics and Pediatric Infectious Diseases, AP-HP, Hôpital Necker-Enfants Malades, Université de Paris, Paris, France
- Corinne Levy
- Association Clinique et Thérapeutique Infantile du Val de Marne (ACTIV), Créteil, France
- Corinne Levy
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Corinne Levy
- Clinical Research Centre, Centre Hospitalier Intercommunal de Créteil, Créteil, France
- Corinne Levy
- Paris Est University, IMRB-GRC GEMINI, Créteil, France
- Martin Chalumeau
- Department of General Pediatrics and Pediatric Infectious Diseases, AP-HP, Hôpital Necker-Enfants Malades, Université de Paris, Paris, France
- Martin Chalumeau
- Epidemiology and Statistics Research Centre - CRESS, INSERM, Obstetrical, Perinatal and Pediatric Epidemiology Research Team, Université de Paris, Paris, France
- Sandra Biscardi
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Sandra Biscardi
- Pediatric Emergency Department, Centre Hospitalier Intercommunal de Créteil, Créteil, France
- Marie-Aliette Dommergues
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Marie-Aliette Dommergues
- Department of General Pediatrics, Centre Hospitalier de Versailles-Le Chesnay, Versailles, France
- François Dubos
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- François Dubos
- Pediatric Emergency Unit and Infectious Diseases, Univ. Lille, CHU Lille, Lille, France
- Karine Levieux
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Karine Levieux
- 0Department of Pediatrics, Centre Hospitalier Universitaire de Nantes, Nantes, France
- Marie Aurel
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Marie Aurel
- 1Department of General Pediatrics, AP-HP, Hôpital Robert Debré, Université de Paris, Paris, France
- Philippe Minodier
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Philippe Minodier
- 2Pediatric Emergency Department, Centre Hospitalier Universitaire Nord, Marseille, France
- Ferielle Zenkhri
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Ferielle Zenkhri
- 3Pediatric Emergency Department, AP-HP, Hôpital Le Kremlin-Bicêtre, Université Paris Sud, Bicêtre, France
- Ellia Mezgueldi
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Ellia Mezgueldi
- 4Pediatric Emergency Department, Hospices Civils de Lyon, Hôpital Femme-Mère-Enfant, Lyon, France
- Irina Craiu
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Irina Craiu
- 3Pediatric Emergency Department, AP-HP, Hôpital Le Kremlin-Bicêtre, Université Paris Sud, Bicêtre, France
- Laurence Morin
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Laurence Morin
- 5Pediatric Emergency Department, AP-HP, Hôpital Robert Debré, Université de Paris, Paris, France
- Stéphane Béchet
- Association Clinique et Thérapeutique Infantile du Val de Marne (ACTIV), Créteil, France
- Emmanuelle Varon
- 6Centre National de Référence des Pneumocoques, Centre Hospitalier Intercommunal de Créteil, Créteil, France
- Robert Cohen
- Association Clinique et Thérapeutique Infantile du Val de Marne (ACTIV), Créteil, France
- Robert Cohen
- Groupe de Pathologie Infectieuse Pédiatrique (GPIP), Paris, France
- Robert Cohen
- Clinical Research Centre, Centre Hospitalier Intercommunal de Créteil, Créteil, France
- Robert Cohen
- Paris Est University, IMRB-GRC GEMINI, Créteil, France
- Robert Cohen
- 7Service des Petits Nourrissons, Centre Hospitalier Intercommunal de Créteil, Créteil, France
- Jérémie F. Cohen
- Department of General Pediatrics and Pediatric Infectious Diseases, AP-HP, Hôpital Necker-Enfants Malades, Université de Paris, Paris, France
- Jérémie F. Cohen
- Epidemiology and Statistics Research Centre - CRESS, INSERM, Obstetrical, Perinatal and Pediatric Epidemiology Research Team, Université de Paris, Paris, France
- The Pneumonia Study Group
- François Angoulvant
- Yves Gillet
- Christèle Gras-Le Guen
- Isabelle Hau
- Laure Hees
- Elise Launay
- Mathie Lorrot
- Fouad Madhi
- Alain Martinot
- Naim Ouldali
- DOI
- https://doi.org/10.3389/fped.2021.684628
- Journal volume & issue
-
Vol. 9
Abstract
Objective(s): Blood cultures (BC), when performed in children seen in the emergency department with community-acquired pneumonia (CAP), are most of the time sterile. We described the diagnostic accuracy of white blood cells (WBC), absolute neutrophils count (ANC), C-reactive protein (CRP), and procalcitonin (PCT) to predict blood culture (BC) result in childhood CAP.Study Design: Secondary analysis of a prospective study carried out in eight pediatric emergency departments (France, 2009–2018), including children (≤15 years) with CAP. Analyses involved univariate comparisons and ROC curves.Results: We included 13,752 children with CAP. BC was positive in 137 (3.6%) of the 3,829 children (mean age 3.7 years) in whom it was performed, mostly with Streptococcus pneumoniae (n = 107). In children with bacteremia, ANC, CRP and PCT levels were higher (median 12,256 vs. 9,251/mm3, 223 vs. 72 mg/L and 8.6 vs. 1.0 ng/mL, respectively; p ≤ 0.002), but WBC levels were not. The area under the ROC curve of PCT (0.73 [95%CI 0.64–0.82]) was significantly higher (p ≤ 0.01) than that of WBC (0.51 [0.43–0.60]) and of ANC (0.55 [0.46–0.64]), but not than that of CRP (0.66 [0.56–0.76]; p = 0.21). CRP and PCT thresholds that provided a sensitivity of at least 90% were 30 mg/L and 0.25 ng/mL, respectively, for a specificity of 25.4 and 23.4%, respectively. CRP and PCT thresholds that provided a specificity of at least 90% were 300 mg/L and 20 ng/mL, respectively, for a sensitivity of 31.3 and 28.9%, respectively.Conclusions: PCT and CRP are the best routinely available predictive biomarkers of bacteremia in childhood CAP.
Keywords
- pneumonia
- bacteremia
- biomarkers
- procalcitonin (PCT)
- pneumococcus (Streptococcus pneumoniae)
- diagnostic test