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Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis

Infective endocarditis (IE) can cause multiorgan dysfunction and chronic kidney disease, in addition to cardiac sequelae. The presentation may be vague and can manifest as acute glomerulonephritis. While the most common pathogens of infective endocarditis are Staphylococcus and Streptococcus species...

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Autores principales: Gavcovich, Tara, Al Barbandi, Malek, Millan, Pamela, Isner, Elizabeth, Defreitas, Marissa J., Glaberson, Wendy, Katsoufis, Chryso P., Chandar, Jayanthi, Sigurjonsdottir, Vaka, Gonzalez, Ivan A., Swaminathan, Sethuraman, Zuo, Yiqin, Abitbol, Carolyn L., Seeherunvong, Wacharee
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884818/
https://www.ncbi.nlm.nih.gov/pubmed/36727008
http://dx.doi.org/10.3389/fped.2022.1093300
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author Gavcovich, Tara
Al Barbandi, Malek
Millan, Pamela
Isner, Elizabeth
Defreitas, Marissa J.
Glaberson, Wendy
Katsoufis, Chryso P.
Chandar, Jayanthi
Sigurjonsdottir, Vaka
Gonzalez, Ivan A.
Swaminathan, Sethuraman
Zuo, Yiqin
Abitbol, Carolyn L.
Seeherunvong, Wacharee
author_facet Gavcovich, Tara
Al Barbandi, Malek
Millan, Pamela
Isner, Elizabeth
Defreitas, Marissa J.
Glaberson, Wendy
Katsoufis, Chryso P.
Chandar, Jayanthi
Sigurjonsdottir, Vaka
Gonzalez, Ivan A.
Swaminathan, Sethuraman
Zuo, Yiqin
Abitbol, Carolyn L.
Seeherunvong, Wacharee
author_sort Gavcovich, Tara
collection PubMed
description Infective endocarditis (IE) can cause multiorgan dysfunction and chronic kidney disease, in addition to cardiac sequelae. The presentation may be vague and can manifest as acute glomerulonephritis. While the most common pathogens of infective endocarditis are Staphylococcus and Streptococcus species, we report a rare pathogen Bordetella holmesii causing infective endocarditis associated glomerulonephritis. A 20-year-old male patient with tetralogy of Fallot with pulmonary atresia and aortopulmonary collaterals underwent several cardiac surgeries including prosthetic pulmonary valve replacement in the past. He was admitted for 3 days at an outside hospital for fever, cough, and hemoptysis, and diagnosed with streptococcal pharyngitis, for which he received antibiotics. Five weeks later, he presented to our institution with lower extremity edema and gross hematuria. On examination, he was afebrile, normotensive, had a 7-kg weight gain with anasarca, and a systolic murmur, without rash. Investigations revealed elevated serum creatinine, nephrotic range proteinuria, hematuria, and hypocomplementemia, consistent with acute glomerulonephritis. Given his cardiac history, blood cultures were collected from three sites. Broad-spectrum antibiotics were initiated when he subsequently developed fever. Renal pathology on biopsy showed diffuse proliferative immune complex-mediated glomerulonephritis. Transesophageal echocardiogram visualized a vegetation on the pulmonary valve. Bordetella holmesii was ultimately cultured from the prior and current hospitalization. A serum sample detecting microbial cell-free DNA sequencing confirmed Bordetella holmesii at very high levels. After completing 6 weeks of intravenous antibiotics with concurrent angiotensin receptor blockade, his kidney function recovered with improvement in hypocomplementemia and proteinuria. This case report highlights the early recognition and comprehensive evaluation of a rare organism causing IE-associated GN, which allowed for renal recovery and preserved cardiac function.
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spelling pubmed-98848182023-01-31 Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis Gavcovich, Tara Al Barbandi, Malek Millan, Pamela Isner, Elizabeth Defreitas, Marissa J. Glaberson, Wendy Katsoufis, Chryso P. Chandar, Jayanthi Sigurjonsdottir, Vaka Gonzalez, Ivan A. Swaminathan, Sethuraman Zuo, Yiqin Abitbol, Carolyn L. Seeherunvong, Wacharee Front Pediatr Pediatrics Infective endocarditis (IE) can cause multiorgan dysfunction and chronic kidney disease, in addition to cardiac sequelae. The presentation may be vague and can manifest as acute glomerulonephritis. While the most common pathogens of infective endocarditis are Staphylococcus and Streptococcus species, we report a rare pathogen Bordetella holmesii causing infective endocarditis associated glomerulonephritis. A 20-year-old male patient with tetralogy of Fallot with pulmonary atresia and aortopulmonary collaterals underwent several cardiac surgeries including prosthetic pulmonary valve replacement in the past. He was admitted for 3 days at an outside hospital for fever, cough, and hemoptysis, and diagnosed with streptococcal pharyngitis, for which he received antibiotics. Five weeks later, he presented to our institution with lower extremity edema and gross hematuria. On examination, he was afebrile, normotensive, had a 7-kg weight gain with anasarca, and a systolic murmur, without rash. Investigations revealed elevated serum creatinine, nephrotic range proteinuria, hematuria, and hypocomplementemia, consistent with acute glomerulonephritis. Given his cardiac history, blood cultures were collected from three sites. Broad-spectrum antibiotics were initiated when he subsequently developed fever. Renal pathology on biopsy showed diffuse proliferative immune complex-mediated glomerulonephritis. Transesophageal echocardiogram visualized a vegetation on the pulmonary valve. Bordetella holmesii was ultimately cultured from the prior and current hospitalization. A serum sample detecting microbial cell-free DNA sequencing confirmed Bordetella holmesii at very high levels. After completing 6 weeks of intravenous antibiotics with concurrent angiotensin receptor blockade, his kidney function recovered with improvement in hypocomplementemia and proteinuria. This case report highlights the early recognition and comprehensive evaluation of a rare organism causing IE-associated GN, which allowed for renal recovery and preserved cardiac function. Frontiers Media S.A. 2023-01-16 /pmc/articles/PMC9884818/ /pubmed/36727008 http://dx.doi.org/10.3389/fped.2022.1093300 Text en © 2023 Gavcovich, Al Barbandi, Millan, Isner, DeFreitas, Glaberson, Katsoufis, Chandar, Sigurjonsdottir, Gonzalez, Swaminathan, Zuo, Abitbol and Seeherunvong. https://creativecommons.org/licenses/by/4.0/This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY) (https://creativecommons.org/licenses/by/4.0/) . The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Pediatrics
Gavcovich, Tara
Al Barbandi, Malek
Millan, Pamela
Isner, Elizabeth
Defreitas, Marissa J.
Glaberson, Wendy
Katsoufis, Chryso P.
Chandar, Jayanthi
Sigurjonsdottir, Vaka
Gonzalez, Ivan A.
Swaminathan, Sethuraman
Zuo, Yiqin
Abitbol, Carolyn L.
Seeherunvong, Wacharee
Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis
title Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis
title_full Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis
title_fullStr Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis
title_full_unstemmed Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis
title_short Case report: Bordetella holmesii: A rare pathogen causing infective endocarditis associated glomerulonephritis
title_sort case report: bordetella holmesii: a rare pathogen causing infective endocarditis associated glomerulonephritis
topic Pediatrics
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9884818/
https://www.ncbi.nlm.nih.gov/pubmed/36727008
http://dx.doi.org/10.3389/fped.2022.1093300
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