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, Julio Collazos, MD, PhD Infectious Diseases, Hospital De Galdacano, Galdacano, Spain Search for other works by this author on: Oxford Academic Belen De La Fuente, MD, PhD Medicine, Hospital De Cabueñes, Gijon, Spain Search for other works by this author on: Oxford Academic Alicia Garcia, MD Medicine, Hospital Universitario Central De Asturias, Oviedo University School Medicine, Oviedo, Spain Search for other works by this author on: Oxford Academic Helena Gomez, GOMEZ Medicine, Hospital Universitario Central De Asturias, Oviedo University School Medicine, Oviedo, Spain Search for other works by this author on: Oxford Academic Candela Menendez, MD Medicine, Hospital Universitario Central De Asturias, Oviedo University School Medicine, Oviedo, Spain Search for other works by this author on: Oxford Academic Hector Enriquez, MD Medicine, Hospital De Povisa, Vigo, Spain Search for other works by this author on: Oxford Academic Paula Sanchez, MD Hospital De Povisa, Vigo, Spain Search for other works by this author on: Oxford Academic Maria Alonso, MD Medicine, Hospital De Povisa, Vigo, Spain Search for other works by this author on: Oxford Academic Jose Guerra, MD, PhD Medicine, Hospital De Leon, Leon, Spain Search for other works by this author on: Oxford Academic Arturo Artero, MD, PhD Medicine and Infectious Diseases, Hospital Dr Peset, Valencia, Spain Search for other works by this author on: Oxford Academic
, Marino Blanes, MD, PhD Infectious Diseases, Hospital La Fe, Valencia, Spain Search for other works by this author on: Oxford Academic Javier De La Fuente, MD, PhD Medicine, Hospital De Povisa, Vigo, Spain Search for other works by this author on: Oxford Academic Victor Asensi, MD, PhD Medicine and Infectious Diseases, Hospital Universitario Central De Asturias, Oviedo University School Medicine, Oviedo, Spain Search for other works by this author on: Oxford Academic
Open Forum Infectious Diseases, Volume 5, Issue suppl_1, November 2018, Page S703, https://doi.org/10.1093/ofid/ofy210.2014
Published:
26 November 2018
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Julio Collazos, Belen De La Fuente, Alicia Garcia, Helena Gomez, Candela Menendez, Hector Enriquez, Paula Sanchez, Maria Alonso, Jose Guerra, Arturo Artero, Marino Blanes, Javier De La Fuente, Victor Asensi, 2361. Factors Associated With Sepsis Development in Cellulitis. A Prospective Analysis of 606 Episodes in Adult Patients, Open Forum Infectious Diseases, Volume 5, Issue suppl_1, November 2018, Page S703, https://doi.org/10.1093/ofid/ofy210.2014
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Abstract
Background
Cellulitis, a frequent cause of admission of adult patients to medical wards, occasionally evolves to sepsis. In this study, we analyze the factors related to sepsis development.
Methods
Prospective and observational study of 606 adult patients with cellulitis admitted to several Spanish hospitals. Comorbidities, microbiological, clinical, laboratory, diagnostic, and treatment data were analyzed. Sepsis was diagnosed according to the criteria of the 2016 International Sepsis Definitions Conference. Multiple logistic regression modeling was performed to determine the variables independently associated with sepsis development.
Results
Mean age was 63.4 years and 51.8% were men. Overall 65 (10.7%) patients developed sepsis, 7 (10.8%) of whom died, but only 4 (6.2%) due to cellulitis. Drawing of blood (P < 0.0001) or any (P < 0.0001) culture, and identification of the agent (P = 0.005) were more likely among septic patients. Septics had also a longer duration of symptoms (P = 0.04), higher temperature (P = 0.03), more extensive cellulitis (P = 0.02), higher leukocyte (P < 0.0001) and neutrophil (P < 0.0001) counts, serum creatinine (P = 0.001), and CRP (P = 0.008) than non-septics. Regarding therapy, septic patients were more likely to undergo changes in the initial antimicrobial regimen (P < 0.0001), received more antimicrobials (P < 0.0001), were intravenously treated for longer (P = 0.03), and underwent surgery more commonly (P = 0.01) than non-septics. Death (P = 0.002), leukocyte counts (P = 0.002), serum creatinine (P = 0.003), drawing of blood cultures (P = 0.004), change of the initial antimicrobial regimen (P = 0.007) and length of cellulitis (P = 0.009) were independently associated with sepsis development in the multivariate analysis. The area under the ROC curve of a formula derived from blood leukocytes and serum creatinine for predicting sepsis development was 0.732 (95% CI 0.659–0.805), P < 0.0001, and its most discriminant cutoff value had a sensitivity 67.7% and specificity 74.4% for this purpose.
Conclusion
Death, increased blood leukocytes and serum creatinine, blood culture drawn, modification of the initial antimicrobial regimen, and maximum length of cellulitis were associated with sepsis development in cellulitis patients.
Disclosures
All authors: No reported disclosures.
Session: 249. Skin and Skin Structure Infection
Saturday, October 6, 2018: 12:30 PM
© The Author(s) 2018. Published by Oxford University Press on behalf of Infectious Diseases Society of America.
This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial-NoDerivs licence (http://creativecommons.org/licenses/by-nc-nd/4.0/), which permits non-commercial reproduction and distribution of the work, in any medium, provided the original work is not altered or transformed in any way, and that the work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
Topic:
- sepsis
- cellulitis
- adult
- comorbidity
- disclosure
- leukocyte count
- leukocytes
- leukocytosis
- neutrophils
- surgical procedures, operative
- body temperature
- diagnosis
- surgery specialty
- temperature
- antimicrobials
- creatinine tests, serum
- blood culture
- time symptom lasts
- area under the roc curve
Issue Section:
Abstracts > B. Poster Abstracts
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