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First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review
INTRODUCTION: NF is a life-threatening infection and progressive disease resulting in widespread fulminant tissue destruction. It is rarely caused by Group B Streptococcus pneumonia. Early management with surgical removal of devitalized tissue and urgent antibiotic administration are key therapies....
Autores principales: | , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9216318/ https://www.ncbi.nlm.nih.gov/pubmed/35757071 http://dx.doi.org/10.1016/j.ijregi.2022.01.005 |
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author | Gaber, Nouran Kandasamy, Shalini Thomas, Alasdair Chimunda, Timothy |
author_facet | Gaber, Nouran Kandasamy, Shalini Thomas, Alasdair Chimunda, Timothy |
author_sort | Gaber, Nouran |
collection | PubMed |
description | INTRODUCTION: NF is a life-threatening infection and progressive disease resulting in widespread fulminant tissue destruction. It is rarely caused by Group B Streptococcus pneumonia. Early management with surgical removal of devitalized tissue and urgent antibiotic administration are key therapies. AIM: The aim of this report is to highlight the importance of atypical microorganisms seen in NF. METHOD: A case presentation and cohort summary of reported NF cases secondary to SPN from the year 2011 to 2020. RESULTS: We report the case of a 67-year-old male, not on immune-suppressive medications, admitted to our intensive care unit with septic shock and multiorgan failure secondary to left leg NF following a 3-week history of cactus prick with an SPN bacteraemia and LRINEC score of 5 on admission. He required multiple surgical debridements and was commenced on appropriate antibiotics. Despite continuous vasopressor supportive therapy, high flux CRRT, and IVIG, our patient died after an 8-day inpatient stay. A 10-year review showed only 5 reported GBSPn NF cases with an associated mortality rate of 40%. CONCLUSION: A high clinical suspicion of SPN infections in NF is required to avoid high mortality with early diagnosis and targeted anti-microbial therapy. Severity scores may not align with clinical severity. |
format | Online Article Text |
id | pubmed-9216318 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-92163182022-06-24 First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review Gaber, Nouran Kandasamy, Shalini Thomas, Alasdair Chimunda, Timothy IJID Reg Case Report INTRODUCTION: NF is a life-threatening infection and progressive disease resulting in widespread fulminant tissue destruction. It is rarely caused by Group B Streptococcus pneumonia. Early management with surgical removal of devitalized tissue and urgent antibiotic administration are key therapies. AIM: The aim of this report is to highlight the importance of atypical microorganisms seen in NF. METHOD: A case presentation and cohort summary of reported NF cases secondary to SPN from the year 2011 to 2020. RESULTS: We report the case of a 67-year-old male, not on immune-suppressive medications, admitted to our intensive care unit with septic shock and multiorgan failure secondary to left leg NF following a 3-week history of cactus prick with an SPN bacteraemia and LRINEC score of 5 on admission. He required multiple surgical debridements and was commenced on appropriate antibiotics. Despite continuous vasopressor supportive therapy, high flux CRRT, and IVIG, our patient died after an 8-day inpatient stay. A 10-year review showed only 5 reported GBSPn NF cases with an associated mortality rate of 40%. CONCLUSION: A high clinical suspicion of SPN infections in NF is required to avoid high mortality with early diagnosis and targeted anti-microbial therapy. Severity scores may not align with clinical severity. Elsevier 2022-01-13 /pmc/articles/PMC9216318/ /pubmed/35757071 http://dx.doi.org/10.1016/j.ijregi.2022.01.005 Text en Crown Copyright © 2022 Published by Elsevier Ltd on behalf of International Society for Infectious Diseases. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Case Report Gaber, Nouran Kandasamy, Shalini Thomas, Alasdair Chimunda, Timothy First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review |
title | First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review |
title_full | First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review |
title_fullStr | First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review |
title_full_unstemmed | First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review |
title_short | First Reported Australian case of Fatal Streptococcal Group B Pneumonia (serotype 21) Necrotising fasciitis complicated by Toxic Shock Like Syndrome – A Case report and review |
title_sort | first reported australian case of fatal streptococcal group b pneumonia (serotype 21) necrotising fasciitis complicated by toxic shock like syndrome – a case report and review |
topic | Case Report |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9216318/ https://www.ncbi.nlm.nih.gov/pubmed/35757071 http://dx.doi.org/10.1016/j.ijregi.2022.01.005 |
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