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Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016

BACKGROUND: The clinical spectrum of the acute disease varies in different locations around the world. Israel is endemic for Q fever, and our hospital is located in a hyper-endemic area. The aim of our study was to describe the clinical characteristic of acute Q fever in our area. METHODS: A histori...

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Autores principales: Reisfeld, Sharon, Mhamed, Shayma Hasadia, Stein, Michal, Chowers, Michal
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631814/
http://dx.doi.org/10.1093/ofid/ofx163.163
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author Reisfeld, Sharon
Mhamed, Shayma Hasadia
Stein, Michal
Chowers, Michal
author_facet Reisfeld, Sharon
Mhamed, Shayma Hasadia
Stein, Michal
Chowers, Michal
author_sort Reisfeld, Sharon
collection PubMed
description BACKGROUND: The clinical spectrum of the acute disease varies in different locations around the world. Israel is endemic for Q fever, and our hospital is located in a hyper-endemic area. The aim of our study was to describe the clinical characteristic of acute Q fever in our area. METHODS: A historical cohort, including adult patients with a serologic diagnosis of Q fever. Demographic, clinical, laboratory, and imaging data were collected and analyzed. Serologic definitions for an acute disease were IgM phase 2 ≥50 and/or IgG phase 2 ≥100, and chronic disease was defined as IgG phase 1≥800. RESULTS: During 2006–2016, 3352 blood samples were sent for serology to the reference laboratory, 205 (6.1%) were positive for Q fever. We observed an increase in positive results from 1.3 to 3.7% in 2007–2011 to 3.9–7.3% during 2012–2015, and up to 41% in 2016. Full data was available for 153 patients. Ninety-nine patients (65%) were male, median age was 50 years, and half of the patients had no comorbidities. The patients presented with fever in 85% of the cases, a respiratory symptom in 58%, rash was present in 7%. Anemia was present in 46 patients (30%), but leukopenia and thrombocytopenia were less common (6 and 16%, respectively). Liver enzymes were elevated in 29 patients (19%), and 49 patients (32%) had pneumonia according to chest X-ray. Seventeen patients had risk factors for a chronic disease: three of those had chronic infection at presentation, four patients had an appropriate follow-up; one patient developed a chronic disease shortly after the acute infection. Three patients died from other severe medical conditions and seven patients were not followed up. Although only 46 patients (30%) were discharged with a diagnosis of either Q fever or unspecified rickettsial disease, 74 (48%) were treated with doxycycline. CONCLUSION: Most of our patients had an unspecified febrile illness, 81% of them had normal liver tests, as oppose to published data from Israel and Europe, where elevated liver enzymes were reported in the vast majority of patients. Although there is a high index of suspicion and the acute disease is diagnosed frequently, only four out of 11 high-risk patients had an appropriate follow-up. Education about the management of high-risk patients is warranted. DISCLOSURES: All authors: No reported disclosures.
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spelling pubmed-56318142017-11-07 Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016 Reisfeld, Sharon Mhamed, Shayma Hasadia Stein, Michal Chowers, Michal Open Forum Infect Dis Abstracts BACKGROUND: The clinical spectrum of the acute disease varies in different locations around the world. Israel is endemic for Q fever, and our hospital is located in a hyper-endemic area. The aim of our study was to describe the clinical characteristic of acute Q fever in our area. METHODS: A historical cohort, including adult patients with a serologic diagnosis of Q fever. Demographic, clinical, laboratory, and imaging data were collected and analyzed. Serologic definitions for an acute disease were IgM phase 2 ≥50 and/or IgG phase 2 ≥100, and chronic disease was defined as IgG phase 1≥800. RESULTS: During 2006–2016, 3352 blood samples were sent for serology to the reference laboratory, 205 (6.1%) were positive for Q fever. We observed an increase in positive results from 1.3 to 3.7% in 2007–2011 to 3.9–7.3% during 2012–2015, and up to 41% in 2016. Full data was available for 153 patients. Ninety-nine patients (65%) were male, median age was 50 years, and half of the patients had no comorbidities. The patients presented with fever in 85% of the cases, a respiratory symptom in 58%, rash was present in 7%. Anemia was present in 46 patients (30%), but leukopenia and thrombocytopenia were less common (6 and 16%, respectively). Liver enzymes were elevated in 29 patients (19%), and 49 patients (32%) had pneumonia according to chest X-ray. Seventeen patients had risk factors for a chronic disease: three of those had chronic infection at presentation, four patients had an appropriate follow-up; one patient developed a chronic disease shortly after the acute infection. Three patients died from other severe medical conditions and seven patients were not followed up. Although only 46 patients (30%) were discharged with a diagnosis of either Q fever or unspecified rickettsial disease, 74 (48%) were treated with doxycycline. CONCLUSION: Most of our patients had an unspecified febrile illness, 81% of them had normal liver tests, as oppose to published data from Israel and Europe, where elevated liver enzymes were reported in the vast majority of patients. Although there is a high index of suspicion and the acute disease is diagnosed frequently, only four out of 11 high-risk patients had an appropriate follow-up. Education about the management of high-risk patients is warranted. DISCLOSURES: All authors: No reported disclosures. Oxford University Press 2017-10-04 /pmc/articles/PMC5631814/ http://dx.doi.org/10.1093/ofid/ofx163.163 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 Abstracts
Reisfeld, Sharon
Mhamed, Shayma Hasadia
Stein, Michal
Chowers, Michal
Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016
title Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016
title_full Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016
title_fullStr Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016
title_full_unstemmed Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016
title_short Acute Q Fever in Israel: Clinical and Demographic Data 2006–2016
title_sort acute q fever in israel: clinical and demographic data 2006–2016
topic Abstracts
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5631814/
http://dx.doi.org/10.1093/ofid/ofx163.163
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