Invasive Bacterial Infections in Children With Sickle Cell Disease: 2014–2019

Author:

Gaschignard Jean12,Koehl Bérengère345,Rees David C.6,Rincón-López Elena78,Vanderfaeillie Anna9,Pascault Alice3,Allali Slimane410,Cela Elena11,Odièvre Marie-Hélène412,Hau Isabelle13,Oliveira Marisa14,Guillaumat Cécile15,Brousse Valentine345,de Montalembert Mariane104,Navarro Gómez Maria Luisa78,Beldjoudi Naima16,Bardon-Cancho Eduardo Jesus11,Epalza Cristina171819,Epalza Cristina,Benkerrou Malika,Gaschignard Jean,Koehl Berengère,Pascault Alice,Brousse Valentine,Allali Slimane,de Montalembert Marianne,Odièvre Marie-Hélène,Hau Isabelle,Guillaumat Cécile,Blais Sophie,Runel-Belliard Camille,Pellegrino Béatrice,Malric Aurore,Guitton Corinne,Gouraud François,Petras Marie,Bensaid Philippe,Basmaci Romain,Eyssette-Guereau Stéphanie,Pham Luu-Ly,Bardon-Cancho Eduardo J.,Cela Elena,Gómez Maria Luisa Navarro,Rincon-Lopez Elena,Ruiz-Llobet Anna,Adan Rosa,Puyo Pablo Velasco,Recasens Valle,Epalza Cristina,Perez-Alonso Vanesa,Torrent Montserrat,Gomez Amanda Bermejo,Vázquez Angeles,Rodríguez Raquel Portugal,Alfaridi Huda,Almaghrabi Rana,Hoyoux Marie,Vanderfaeillie Anna,Oliveira Marisa,Ferreira Teresa,Rees David,

Affiliation:

1. aDepartment of Pediatrics, Groupe Hospitalier Nord Essonne, Longjumeau, France

2. bIAME, INSERM 1137, Hôpital Bichat, Paris, France

3. Departments of cSickle Cell Disease, Hôpital Robert Debré

4. dUniversité de Paris-Cité, Paris, France

5. eINSERM U1134, Integrated Red Globule Biology, Paris, France

6. fRed Cell Haematology Laboratory, School of Cancer and Pharmaceutical Sciences, King’s College London and King’s College Hospital, London, United Kingdom

7. Departments of gPediatrics

8. hBiomedical Research Networking Center on Infectious Diseases (CIBERINFEC), Instituto de Salud Carlos III, Madrid, Spain

9. iDepartment of Pediatrics, UMC Saint Pierre, Brussels, Belgium

10. jGeneral Pediatrics and Pediatric Infectious Diseases, Sickle Cell Center, Necker-Enfants Malades Hospital, Université Paris Cité

11. kPediatric Hematology and Oncology Unit, Universidad Complutense de Madrid, Hospital General Universitario Gregorio Marañón, Madrid, Spain

12. lPediatrics, Hôpital Trousseau

13. mDepartment of Pediatrics, Centre Hospitalier Intercommunal, Créteil, France

14. nPediatric Hematology Unit, Hospital D. Estefânia, Centro Hospitalar Universitário de Lisboa Central, Lisbon, Portugal

15. oDepartment of Pediatrics, Centre Hospitalier Sud Francilien, Corbeil-Essonne, France

16. pEpidemiology and Clinical Research Department, GH Paris Nord Val de Seine, Assistance Publique – Hôpitaux de Paris, Paris, France

17. qPaediatric Infectious Diseases Unit, Department of Paediatrics, Hospital Universitario 12 de Octubre, Madrid, Spain

18. rPaediatric Research and Clinical Trials Unit (UPIC), Instituto de Investigación Sanitaria Hospital 12 de Octubre (imas12), Madrid, Spain

19. sTranslational Research Network in Paediatric Infectious Diseases (RITIP), Madrid, Spain

Abstract

BACKGROUND Children with sickle cell disease (SCD) are at a high risk of invasive bacterial infections (IBI). Universal penicillin prophylaxis and vaccination, especially against Streptococcus pneumoniae, have deeply changed its epidemiology. Analysis of IBI in children with SCD in a post-13-valent pneumococcal vaccine era is limited. METHODS Twenty-eight pediatric hospitals from 5 European countries retrospectively collected IBI episodes in SCD children aged 1 month to 18 years between 2014 and 2019. IBI was defined as a positive bacterial culture or polymerase chain reaction from a normally sterile fluid: blood, cerebrospinal, joint, or pleural fluid and deep surgical specimen. RESULTS We recorded 169 IBI episodes. Salmonella spp. was the main isolated bacteria (n = 44, 26%), followed by Streptococcus pneumonia (Sp; n = 31, 18%) and Staphylococcus aureus (n = 20, 12%). Salmonella prevailed in osteoarticular infections and in primary bacteremia (45% and 23% of episodes, respectively) and Sp in meningitis and acute chest syndrome (88% and 50%, respectively). All Sp IBI occurred in children ≤10 years old, including 35% in children 5 to 10 years old. Twenty-seven (17%) children had complications of infection and 3 died: 2 because of Sp, and 1 because of Salmonella. The main risk factors for a severe IBI were a previous IBI and pneumococcal infection (17 Sp/51 cases). CONCLUSIONS In a post-13-valent pneumococcal vaccine era, Salmonella was the leading cause of bacteremia in IBI in children with SCD in Europe. Sp came second, was isolated in children ≤10 years old, and was more likely to cause severe and fatal cases.

Publisher

American Academy of Pediatrics (AAP)

Subject

Pediatrics, Perinatology and Child Health

Reference41 articles.

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