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Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study
Introduction. Deescalation refers to either discontinuation or a step-down of antimicrobials. Despite strong recommendations in the Surviving Sepsis Guidelines (2012) to deescalate, actual practices can vary. Our objective was to identify variables that are associated with deescalation failure. Meth...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Hindawi Publishing Corporation
2016
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963586/ https://www.ncbi.nlm.nih.gov/pubmed/27493799 http://dx.doi.org/10.1155/2016/6794861 |
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author | Salahuddin, Nawal Amer, Lama Joseph, Mini El Hazmi, Alya Hawa, Hassan Maghrabi, Khalid |
author_facet | Salahuddin, Nawal Amer, Lama Joseph, Mini El Hazmi, Alya Hawa, Hassan Maghrabi, Khalid |
author_sort | Salahuddin, Nawal |
collection | PubMed |
description | Introduction. Deescalation refers to either discontinuation or a step-down of antimicrobials. Despite strong recommendations in the Surviving Sepsis Guidelines (2012) to deescalate, actual practices can vary. Our objective was to identify variables that are associated with deescalation failure. Methods. In this prospective study of patients with sepsis/septic shock, patients were categorized into 4 groups based on antibiotic administration: no change in antibiotics, deescalation, escalation (where antibiotics were changed to those with a broader spectrum of antimicrobial coverage), or mixed changes (where both escalation to a broader spectrum of coverage and discontinuation of antibiotics were carried out). Results. 395 patients were studied; mean APACHE II score was 24 ± 7.8. Antimicrobial deescalation occurred in 189 (48%) patients; no changes were made in 156 (39%) patients. On multivariate regression analysis, failure to deescalate was significantly predicted by hematologic malignancy OR 3.3 (95% CI 1.4–7.4) p < 0.004, fungal sepsis OR 2.7 (95% CI 1.2–5.8) p = 0.011, multidrug resistance OR 2.9 (95% CI 1.4–6.0) p = 0.003, baseline serum procalcitonin OR 1.01 (95% CI 1.003–1.016) p = 0.002, and SAPS II scores OR 1.01 (95% CI 1.004–1.02) p = 0.006. Conclusions. Current deescalation practices reflect physician reluctance when dealing with complicated, sicker patients or with drug-resistance or fungal sepsis. Integrating an antibiotic stewardship program may increase physician confidence and provide support towards increasing deescalation rates. |
format | Online Article Text |
id | pubmed-4963586 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2016 |
publisher | Hindawi Publishing Corporation |
record_format | MEDLINE/PubMed |
spelling | pubmed-49635862016-08-04 Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study Salahuddin, Nawal Amer, Lama Joseph, Mini El Hazmi, Alya Hawa, Hassan Maghrabi, Khalid Crit Care Res Pract Research Article Introduction. Deescalation refers to either discontinuation or a step-down of antimicrobials. Despite strong recommendations in the Surviving Sepsis Guidelines (2012) to deescalate, actual practices can vary. Our objective was to identify variables that are associated with deescalation failure. Methods. In this prospective study of patients with sepsis/septic shock, patients were categorized into 4 groups based on antibiotic administration: no change in antibiotics, deescalation, escalation (where antibiotics were changed to those with a broader spectrum of antimicrobial coverage), or mixed changes (where both escalation to a broader spectrum of coverage and discontinuation of antibiotics were carried out). Results. 395 patients were studied; mean APACHE II score was 24 ± 7.8. Antimicrobial deescalation occurred in 189 (48%) patients; no changes were made in 156 (39%) patients. On multivariate regression analysis, failure to deescalate was significantly predicted by hematologic malignancy OR 3.3 (95% CI 1.4–7.4) p < 0.004, fungal sepsis OR 2.7 (95% CI 1.2–5.8) p = 0.011, multidrug resistance OR 2.9 (95% CI 1.4–6.0) p = 0.003, baseline serum procalcitonin OR 1.01 (95% CI 1.003–1.016) p = 0.002, and SAPS II scores OR 1.01 (95% CI 1.004–1.02) p = 0.006. Conclusions. Current deescalation practices reflect physician reluctance when dealing with complicated, sicker patients or with drug-resistance or fungal sepsis. Integrating an antibiotic stewardship program may increase physician confidence and provide support towards increasing deescalation rates. Hindawi Publishing Corporation 2016 2016-07-14 /pmc/articles/PMC4963586/ /pubmed/27493799 http://dx.doi.org/10.1155/2016/6794861 Text en Copyright © 2016 Nawal Salahuddin et al. https://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 | Research Article Salahuddin, Nawal Amer, Lama Joseph, Mini El Hazmi, Alya Hawa, Hassan Maghrabi, Khalid Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study |
title | Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study |
title_full | Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study |
title_fullStr | Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study |
title_full_unstemmed | Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study |
title_short | Determinants of Deescalation Failure in Critically Ill Patients with Sepsis: A Prospective Cohort Study |
title_sort | determinants of deescalation failure in critically ill patients with sepsis: a prospective cohort study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4963586/ https://www.ncbi.nlm.nih.gov/pubmed/27493799 http://dx.doi.org/10.1155/2016/6794861 |
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