Cargando…

567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients

BACKGROUND: Bartonella henselae infection causes Cat Scratch Disease (CSD). Lymphadenopathy is the most common symptom and a small percentage of patients have systemic impairment. CSD can mimic malignancy and manifest atypically, therefore reliable serological testing has clinical importance. CSD is...

Descripción completa

Detalles Bibliográficos
Autores principales: Caratozzolo, Ana M, Toledano, Analía, Praino, María Laura, Ferolla, Fausto Martín, Neyro, Silvina, Cazes, Claudia Inés, López, Eduardo L
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677976/
http://dx.doi.org/10.1093/ofid/ofad500.636
_version_ 1785150256660348928
author Caratozzolo, Ana M
Toledano, Analía
Praino, María Laura
Ferolla, Fausto Martín
Neyro, Silvina
Cazes, Claudia Inés
López, Eduardo L
author_facet Caratozzolo, Ana M
Toledano, Analía
Praino, María Laura
Ferolla, Fausto Martín
Neyro, Silvina
Cazes, Claudia Inés
López, Eduardo L
author_sort Caratozzolo, Ana M
collection PubMed
description BACKGROUND: Bartonella henselae infection causes Cat Scratch Disease (CSD). Lymphadenopathy is the most common symptom and a small percentage of patients have systemic impairment. CSD can mimic malignancy and manifest atypically, therefore reliable serological testing has clinical importance. CSD is diagnosed if two of the following criteria are met: 1) the presence of clinical symptoms consistent with CSD; 2) the existence of antibodies against B. henselae IgM and/or IgG (1:256) (Fig.1). We aim to assess the accuracy and diagnostic utility of IgM and IgG in pediatric patients with suspected CSD. [Figure: see text] METHODS: A retrospective, observational and analytical study was carried out from April 2022 through April 2023. Medical and laboratory records of patients with follow-up in the Infectious Diseases Department of a Children's Hospital in Buenos Aires (Argentina) were evaluated. RESULTS: We included 244 serum samples from patients with clinical suspicion of CSD using Immunofluorescent assay (IFA). Median age: 84 (IQR 48-132) months, 137 were female, 95% (233/244) had cat interaction. Twenty eight percent (70/244) were diagnosed with CSD based on serological evidence: 83,9% (58/70) had IgM +/IgG + (group 1); 10% (7/70), IgM-/IgG+ >1/64 (group 2) and 7,15% (5/70), IgM+/IgG – (group 3). The average time of symptom onset was 22,8 (6-90) days for group 1, 29,4 (11-90) days for group 2, and 11,4 (5-15) days for group 3. Lymphadenopathy was found in 87,1% (61/70) with or without systemic involvement and 6 % (4/70) had systemic involvement without lymphadenopathy. IgM had Sensitivity: 89%, Specificity: 97%, Positive Predictive Value (PPV): 92% and Negative Predictive Value (NPV) : 96%. CONCLUSION: Between 5-15 days after the onset of symptoms, IgM allowed us to diagnose 5 patients with CSD. The identification of IgM antibodies in CSD patients with systemic impairment has a great diagnostic performance. IgM remained positive after 90 days . We were able to diagnose CSD in 7 patients between 11 and 28 days following the onset of symptoms due to the presence of IgG 1:256 or higher. Combination of different methods (e.g., clinical and serological) and a correct time of sampling, greater than 5 days, should be considered for rapid and accurate CSD diagnosis. DISCLOSURES: All Authors: No reported disclosures
format Online
Article
Text
id pubmed-10677976
institution National Center for Biotechnology Information
language English
publishDate 2023
publisher Oxford University Press
record_format MEDLINE/PubMed
spelling pubmed-106779762023-11-27 567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients Caratozzolo, Ana M Toledano, Analía Praino, María Laura Ferolla, Fausto Martín Neyro, Silvina Cazes, Claudia Inés López, Eduardo L Open Forum Infect Dis Abstract BACKGROUND: Bartonella henselae infection causes Cat Scratch Disease (CSD). Lymphadenopathy is the most common symptom and a small percentage of patients have systemic impairment. CSD can mimic malignancy and manifest atypically, therefore reliable serological testing has clinical importance. CSD is diagnosed if two of the following criteria are met: 1) the presence of clinical symptoms consistent with CSD; 2) the existence of antibodies against B. henselae IgM and/or IgG (1:256) (Fig.1). We aim to assess the accuracy and diagnostic utility of IgM and IgG in pediatric patients with suspected CSD. [Figure: see text] METHODS: A retrospective, observational and analytical study was carried out from April 2022 through April 2023. Medical and laboratory records of patients with follow-up in the Infectious Diseases Department of a Children's Hospital in Buenos Aires (Argentina) were evaluated. RESULTS: We included 244 serum samples from patients with clinical suspicion of CSD using Immunofluorescent assay (IFA). Median age: 84 (IQR 48-132) months, 137 were female, 95% (233/244) had cat interaction. Twenty eight percent (70/244) were diagnosed with CSD based on serological evidence: 83,9% (58/70) had IgM +/IgG + (group 1); 10% (7/70), IgM-/IgG+ >1/64 (group 2) and 7,15% (5/70), IgM+/IgG – (group 3). The average time of symptom onset was 22,8 (6-90) days for group 1, 29,4 (11-90) days for group 2, and 11,4 (5-15) days for group 3. Lymphadenopathy was found in 87,1% (61/70) with or without systemic involvement and 6 % (4/70) had systemic involvement without lymphadenopathy. IgM had Sensitivity: 89%, Specificity: 97%, Positive Predictive Value (PPV): 92% and Negative Predictive Value (NPV) : 96%. CONCLUSION: Between 5-15 days after the onset of symptoms, IgM allowed us to diagnose 5 patients with CSD. The identification of IgM antibodies in CSD patients with systemic impairment has a great diagnostic performance. IgM remained positive after 90 days . We were able to diagnose CSD in 7 patients between 11 and 28 days following the onset of symptoms due to the presence of IgG 1:256 or higher. Combination of different methods (e.g., clinical and serological) and a correct time of sampling, greater than 5 days, should be considered for rapid and accurate CSD diagnosis. DISCLOSURES: All Authors: No reported disclosures Oxford University Press 2023-11-27 /pmc/articles/PMC10677976/ http://dx.doi.org/10.1093/ofid/ofad500.636 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of Infectious Diseases Society of America. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Abstract
Caratozzolo, Ana M
Toledano, Analía
Praino, María Laura
Ferolla, Fausto Martín
Neyro, Silvina
Cazes, Claudia Inés
López, Eduardo L
567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients
title 567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients
title_full 567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients
title_fullStr 567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients
title_full_unstemmed 567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients
title_short 567. Performance of IgM and IgG antibodies against Bartonella henselae for diagnosis of Cat Scratch Disease in pediatric patients
title_sort 567. performance of igm and igg antibodies against bartonella henselae for diagnosis of cat scratch disease in pediatric patients
topic Abstract
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10677976/
http://dx.doi.org/10.1093/ofid/ofad500.636
work_keys_str_mv AT caratozzoloanam 567performanceofigmandiggantibodiesagainstbartonellahenselaefordiagnosisofcatscratchdiseaseinpediatricpatients
AT toledanoanalia 567performanceofigmandiggantibodiesagainstbartonellahenselaefordiagnosisofcatscratchdiseaseinpediatricpatients
AT prainomarialaura 567performanceofigmandiggantibodiesagainstbartonellahenselaefordiagnosisofcatscratchdiseaseinpediatricpatients
AT ferollafaustomartin 567performanceofigmandiggantibodiesagainstbartonellahenselaefordiagnosisofcatscratchdiseaseinpediatricpatients
AT neyrosilvina 567performanceofigmandiggantibodiesagainstbartonellahenselaefordiagnosisofcatscratchdiseaseinpediatricpatients
AT cazesclaudiaines 567performanceofigmandiggantibodiesagainstbartonellahenselaefordiagnosisofcatscratchdiseaseinpediatricpatients
AT lopezeduardol 567performanceofigmandiggantibodiesagainstbartonellahenselaefordiagnosisofcatscratchdiseaseinpediatricpatients