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Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population

BACKGROUND: Sepsis is a life-threatening complication of infection. The incidence of sepsis is thought to be on the increase, but estimates making use of administrative data in the United States may be affected by administrative bias. METHODS: We studied the population-based incidence of sepsis in t...

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Autores principales: Huggan, Paul J, Bell, Anita, Waetford, James, Obertova, Zuzanna, Lawrenson, Ross
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597865/
https://www.ncbi.nlm.nih.gov/pubmed/28948175
http://dx.doi.org/10.1093/ofid/ofx106
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author Huggan, Paul J
Bell, Anita
Waetford, James
Obertova, Zuzanna
Lawrenson, Ross
author_facet Huggan, Paul J
Bell, Anita
Waetford, James
Obertova, Zuzanna
Lawrenson, Ross
author_sort Huggan, Paul J
collection PubMed
description BACKGROUND: Sepsis is a life-threatening complication of infection. The incidence of sepsis is thought to be on the increase, but estimates making use of administrative data in the United States may be affected by administrative bias. METHODS: We studied the population-based incidence of sepsis in the Waikato region of New Zealand from 2007 to 2012 using International Classification of Diseases, Tenth Revision, Australian Modification, which lacks a specific code for sepsis. RESULTS: Between 2007 and 2012, 1643 patients met coding criteria for sepsis in our hospitals. Sixty-three percent of patients were 65 or over, 17% of cases were admitted to an intensive care unit, and the in-hospital and 1-year mortality with sepsis was 19% and 38%, respectively. Age-standardized rate ratios (ASRRs) demonstrated that sepsis was associated with male sex (ASRR 1.4; 95% confidence interval [CI], 1.23–1.59), Maori ethnicity (ASRR 3.22 compared with non-Maori; 95% CI, 2.85–3.65), study year (ASRR 1.62 comparing 2012 with 2008; 95% CI, 1.18–2.24), and socioeconomic deprivation (ASRR 1.72 comparing the highest with the lowest quintile of socioeconomic deprivation; 95% CI, 1.5–1.97). Multiorgan failure was present in approximately 20% of cases in all age groups. Intensive care unit admission rate fell from 30% amongst 25- to 34-year-olds to less than 10% amongst those aged 75 and over. CONCLUSIONS: In a 9% sample of the New Zealand population, the incidence of sepsis increased by 62% over a 5-year period. Maori, elderly, and disadvantaged populations were most affected.
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spelling pubmed-55978652017-09-25 Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population Huggan, Paul J Bell, Anita Waetford, James Obertova, Zuzanna Lawrenson, Ross Open Forum Infect Dis Major Article BACKGROUND: Sepsis is a life-threatening complication of infection. The incidence of sepsis is thought to be on the increase, but estimates making use of administrative data in the United States may be affected by administrative bias. METHODS: We studied the population-based incidence of sepsis in the Waikato region of New Zealand from 2007 to 2012 using International Classification of Diseases, Tenth Revision, Australian Modification, which lacks a specific code for sepsis. RESULTS: Between 2007 and 2012, 1643 patients met coding criteria for sepsis in our hospitals. Sixty-three percent of patients were 65 or over, 17% of cases were admitted to an intensive care unit, and the in-hospital and 1-year mortality with sepsis was 19% and 38%, respectively. Age-standardized rate ratios (ASRRs) demonstrated that sepsis was associated with male sex (ASRR 1.4; 95% confidence interval [CI], 1.23–1.59), Maori ethnicity (ASRR 3.22 compared with non-Maori; 95% CI, 2.85–3.65), study year (ASRR 1.62 comparing 2012 with 2008; 95% CI, 1.18–2.24), and socioeconomic deprivation (ASRR 1.72 comparing the highest with the lowest quintile of socioeconomic deprivation; 95% CI, 1.5–1.97). Multiorgan failure was present in approximately 20% of cases in all age groups. Intensive care unit admission rate fell from 30% amongst 25- to 34-year-olds to less than 10% amongst those aged 75 and over. CONCLUSIONS: In a 9% sample of the New Zealand population, the incidence of sepsis increased by 62% over a 5-year period. Maori, elderly, and disadvantaged populations were most affected. Oxford University Press 2017-08-24 /pmc/articles/PMC5597865/ /pubmed/28948175 http://dx.doi.org/10.1093/ofid/ofx106 Text en © The Author 2017. Published by Oxford University Press on behalf of Infectious Diseases Society of America. http://creativecommons.org/licenses/by-nc-nd/4.0/ 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
spellingShingle Major Article
Huggan, Paul J
Bell, Anita
Waetford, James
Obertova, Zuzanna
Lawrenson, Ross
Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population
title Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population
title_full Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population
title_fullStr Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population
title_full_unstemmed Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population
title_short Evidence of High Mortality and Increasing Burden of Sepsis in a Regional Sample of the New Zealand Population
title_sort evidence of high mortality and increasing burden of sepsis in a regional sample of the new zealand population
topic Major Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5597865/
https://www.ncbi.nlm.nih.gov/pubmed/28948175
http://dx.doi.org/10.1093/ofid/ofx106
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