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Purple Urine Bag Syndrome: A Rare Spot Diagnosis

Purple urine bag syndrome (PUBS) is a complication of urinary tract infections (UTIs) where catheter bags and tubing turn purple. It is alarming for patients, families, and clinicians; however, it is in itself a benign phenomenon. PUBS is the result of UTIs with specific bacteria that produce sulpha...

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Autores principales: Kalsi, Dilraj S., Ward, Joel, Lee, Regent, Handa, Ashok
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727662/
https://www.ncbi.nlm.nih.gov/pubmed/29317791
http://dx.doi.org/10.1155/2017/9131872
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author Kalsi, Dilraj S.
Ward, Joel
Lee, Regent
Handa, Ashok
author_facet Kalsi, Dilraj S.
Ward, Joel
Lee, Regent
Handa, Ashok
author_sort Kalsi, Dilraj S.
collection PubMed
description Purple urine bag syndrome (PUBS) is a complication of urinary tract infections (UTIs) where catheter bags and tubing turn purple. It is alarming for patients, families, and clinicians; however, it is in itself a benign phenomenon. PUBS is the result of UTIs with specific bacteria that produce sulphatases and phosphatases which lead tryptophan metabolism to produce indigo (blue) and indirubin (red) pigments, a mixture of which becomes purple. Risk factors include female gender, immobility, constipation, chronic catheterisation, and renal disease. Management involves reassurance, antibiotics, and regular changing of catheters, although there are debates regarding how aggressively to treat and no official guidelines. Prognosis is good, but PUBS is associated with high morbidity and mortality due to the backgrounds of patients. Here, we review the literature available on PUBS, present a summary of case studies from the last five years, and propose the Oxford Urine Chart as a tool to aid such diagnoses.
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spelling pubmed-57276622018-01-09 Purple Urine Bag Syndrome: A Rare Spot Diagnosis Kalsi, Dilraj S. Ward, Joel Lee, Regent Handa, Ashok Dis Markers Review Article Purple urine bag syndrome (PUBS) is a complication of urinary tract infections (UTIs) where catheter bags and tubing turn purple. It is alarming for patients, families, and clinicians; however, it is in itself a benign phenomenon. PUBS is the result of UTIs with specific bacteria that produce sulphatases and phosphatases which lead tryptophan metabolism to produce indigo (blue) and indirubin (red) pigments, a mixture of which becomes purple. Risk factors include female gender, immobility, constipation, chronic catheterisation, and renal disease. Management involves reassurance, antibiotics, and regular changing of catheters, although there are debates regarding how aggressively to treat and no official guidelines. Prognosis is good, but PUBS is associated with high morbidity and mortality due to the backgrounds of patients. Here, we review the literature available on PUBS, present a summary of case studies from the last five years, and propose the Oxford Urine Chart as a tool to aid such diagnoses. Hindawi 2017 2017-11-29 /pmc/articles/PMC5727662/ /pubmed/29317791 http://dx.doi.org/10.1155/2017/9131872 Text en Copyright © 2017 Dilraj S. Kalsi et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Review Article
Kalsi, Dilraj S.
Ward, Joel
Lee, Regent
Handa, Ashok
Purple Urine Bag Syndrome: A Rare Spot Diagnosis
title Purple Urine Bag Syndrome: A Rare Spot Diagnosis
title_full Purple Urine Bag Syndrome: A Rare Spot Diagnosis
title_fullStr Purple Urine Bag Syndrome: A Rare Spot Diagnosis
title_full_unstemmed Purple Urine Bag Syndrome: A Rare Spot Diagnosis
title_short Purple Urine Bag Syndrome: A Rare Spot Diagnosis
title_sort purple urine bag syndrome: a rare spot diagnosis
topic Review Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5727662/
https://www.ncbi.nlm.nih.gov/pubmed/29317791
http://dx.doi.org/10.1155/2017/9131872
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