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An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement
BACKGROUND: Peritonitis is a significant cause of morbidity and healthcare cost among pediatric patients undergoing peritoneal dialysis. Culture-negative peritonitis has been associated with an increased risk of technique failure. Known risk factors for culture-negative peritonitis are related to th...
Autores principales: | , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021362/ https://www.ncbi.nlm.nih.gov/pubmed/35445978 http://dx.doi.org/10.1007/s00467-022-05533-1 |
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author | Pangonis, Scott F. Schaffzin, Joshua K. Claes, Donna Mortenson, Joel E. Nehus, Edward |
author_facet | Pangonis, Scott F. Schaffzin, Joshua K. Claes, Donna Mortenson, Joel E. Nehus, Edward |
author_sort | Pangonis, Scott F. |
collection | PubMed |
description | BACKGROUND: Peritonitis is a significant cause of morbidity and healthcare cost among pediatric patients undergoing peritoneal dialysis. Culture-negative peritonitis has been associated with an increased risk of technique failure. Known risk factors for culture-negative peritonitis are related to the process of collection and sample processing for culture, but additional studies are needed. A culture detection rate of 16.7% was identified among our patients undergoing peritoneal dialysis, which is below the national benchmark of ≥ 85%. Our primary objective of this quality improvement project was to improve culture detection rates. METHODS: Interventions were developed aimed at standardizing the process of effluent collection and laboratory processing, timely collection and processing of samples, and addressing other modifying risk factors for lack of bacterial growth from culture. These interventions included direct inoculation of effluent into blood culture bottles at bedside and use of an automated blood culture system. Two Plan-Do-Study-Act cycles were completed prior to moving to the sustain phase. RESULTS: The culture detection rate improved from 16.7% (pre-intervention) to 100% (post-intervention). A decrease in the median process time also occurred from 83 min (pre-intervention) to 53 min (post-intervention). An individual and moving range chart identified a decrease in both the centerline (mean) and upper control limit, indicating that the process became more reliable during the sustain phase. CONCLUSIONS: An improvement in process time and culture positivity rate occurred following standardization of our PD fluid culture process. Future studies should be aimed at the impact of the components of collection and processing methods on the effluent culture yield. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material including a Graphical Abstract available at 10.1007/s00467-022-05533-1. |
format | Online Article Text |
id | pubmed-9021362 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-90213622022-04-21 An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement Pangonis, Scott F. Schaffzin, Joshua K. Claes, Donna Mortenson, Joel E. Nehus, Edward Pediatr Nephrol Original Article BACKGROUND: Peritonitis is a significant cause of morbidity and healthcare cost among pediatric patients undergoing peritoneal dialysis. Culture-negative peritonitis has been associated with an increased risk of technique failure. Known risk factors for culture-negative peritonitis are related to the process of collection and sample processing for culture, but additional studies are needed. A culture detection rate of 16.7% was identified among our patients undergoing peritoneal dialysis, which is below the national benchmark of ≥ 85%. Our primary objective of this quality improvement project was to improve culture detection rates. METHODS: Interventions were developed aimed at standardizing the process of effluent collection and laboratory processing, timely collection and processing of samples, and addressing other modifying risk factors for lack of bacterial growth from culture. These interventions included direct inoculation of effluent into blood culture bottles at bedside and use of an automated blood culture system. Two Plan-Do-Study-Act cycles were completed prior to moving to the sustain phase. RESULTS: The culture detection rate improved from 16.7% (pre-intervention) to 100% (post-intervention). A decrease in the median process time also occurred from 83 min (pre-intervention) to 53 min (post-intervention). An individual and moving range chart identified a decrease in both the centerline (mean) and upper control limit, indicating that the process became more reliable during the sustain phase. CONCLUSIONS: An improvement in process time and culture positivity rate occurred following standardization of our PD fluid culture process. Future studies should be aimed at the impact of the components of collection and processing methods on the effluent culture yield. GRAPHICAL ABSTRACT: A higher resolution version of the Graphical abstract is available as Supplementary information. [Image: see text] SUPPLEMENTARY INFORMATION: The online version contains supplementary material including a Graphical Abstract available at 10.1007/s00467-022-05533-1. Springer Berlin Heidelberg 2022-04-20 2023 /pmc/articles/PMC9021362/ /pubmed/35445978 http://dx.doi.org/10.1007/s00467-022-05533-1 Text en © The Author(s), under exclusive licence to International Pediatric Nephrology Association 2022 This article is made available via the PMC Open Access Subset for unrestricted research re-use and secondary analysis in any form or by any means with acknowledgement of the original source. These permissions are granted for the duration of the World Health Organization (WHO) declaration of COVID-19 as a global pandemic. |
spellingShingle | Original Article Pangonis, Scott F. Schaffzin, Joshua K. Claes, Donna Mortenson, Joel E. Nehus, Edward An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement |
title | An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement |
title_full | An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement |
title_fullStr | An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement |
title_full_unstemmed | An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement |
title_short | An initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement |
title_sort | initiative to improve effluent culture detection among pediatric patients undergoing peritoneal dialysis through process improvement |
topic | Original Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9021362/ https://www.ncbi.nlm.nih.gov/pubmed/35445978 http://dx.doi.org/10.1007/s00467-022-05533-1 |
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