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Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort

OBJECTIVE: Systemic loxoscelism is a rare illness resulting from the bite of the recluse spider and, in its most severe form, can lead to widespread hemolysis, coagulopathy, and death. We aim to describe the clinical features and outcomes of the largest known cohort of individuals with moderate to s...

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Autores principales: Robinson, Jamie R., Kennedy, Vanessa E., Doss, Youssef, Bastarache, Lisa, Denny, Joshua, Warner, Jeremy L.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2017
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396866/
https://www.ncbi.nlm.nih.gov/pubmed/28422977
http://dx.doi.org/10.1371/journal.pone.0174941
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author Robinson, Jamie R.
Kennedy, Vanessa E.
Doss, Youssef
Bastarache, Lisa
Denny, Joshua
Warner, Jeremy L.
author_facet Robinson, Jamie R.
Kennedy, Vanessa E.
Doss, Youssef
Bastarache, Lisa
Denny, Joshua
Warner, Jeremy L.
author_sort Robinson, Jamie R.
collection PubMed
description OBJECTIVE: Systemic loxoscelism is a rare illness resulting from the bite of the recluse spider and, in its most severe form, can lead to widespread hemolysis, coagulopathy, and death. We aim to describe the clinical features and outcomes of the largest known cohort of individuals with moderate to severe loxoscelism. METHODS: We performed a retrospective, cross sectional study from January 1, 1995, to December 31, 2015, at a tertiary-care academic medical center, to determine individuals with clinical records consistent with moderate to severe loxoscelism. Age-, sex-, and race-matched controls were compared. Demographics, clinical characteristics, laboratory measures, and outcomes of individuals with loxoscelism are described. Case and control groups were compared with descriptive statistics and phenome-wide association study (PheWAS). RESULTS: During the time period, 57 individuals were identified as having moderate to severe loxoscelism. Of these, only 33% had an antecedent spider bite documented. Median age of individuals diagnosed with moderate to severe loxoscelism was 14 years old (IQR 9.0–24.0 years). PheWAS confirmed associations of systemic loxoscelism with 29 other phenotypes, e.g., rash, hemolytic anemia, and sepsis. Hemoglobin level dropped an average of 3.1 g/dL over an average of 2.0 days (IQR 2.0–6.0). Lactate dehydrogenase and total bilirubin levels were on average over two times their upper limit of normal values. Eighteen individuals of 32 tested had a positive direct antiglobulin (Coombs’) test. Mortality was 3.5% (2/57 individuals). CONCLUSION: Systemic loxoscelism is a rare but devastating process with only a minority of patients recalling the toxic exposure; hemolysis reaches a peak at 2 days after admission, with some cases taking more than a week before recovery. In endemic areas, suspicion for systemic loxoscelism should be high in individuals, especially children and younger adults, presenting with a cutaneous ulcer and hemolysis or coagulopathy, even in the absence of a bite exposure history.
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spelling pubmed-53968662017-05-04 Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort Robinson, Jamie R. Kennedy, Vanessa E. Doss, Youssef Bastarache, Lisa Denny, Joshua Warner, Jeremy L. PLoS One Research Article OBJECTIVE: Systemic loxoscelism is a rare illness resulting from the bite of the recluse spider and, in its most severe form, can lead to widespread hemolysis, coagulopathy, and death. We aim to describe the clinical features and outcomes of the largest known cohort of individuals with moderate to severe loxoscelism. METHODS: We performed a retrospective, cross sectional study from January 1, 1995, to December 31, 2015, at a tertiary-care academic medical center, to determine individuals with clinical records consistent with moderate to severe loxoscelism. Age-, sex-, and race-matched controls were compared. Demographics, clinical characteristics, laboratory measures, and outcomes of individuals with loxoscelism are described. Case and control groups were compared with descriptive statistics and phenome-wide association study (PheWAS). RESULTS: During the time period, 57 individuals were identified as having moderate to severe loxoscelism. Of these, only 33% had an antecedent spider bite documented. Median age of individuals diagnosed with moderate to severe loxoscelism was 14 years old (IQR 9.0–24.0 years). PheWAS confirmed associations of systemic loxoscelism with 29 other phenotypes, e.g., rash, hemolytic anemia, and sepsis. Hemoglobin level dropped an average of 3.1 g/dL over an average of 2.0 days (IQR 2.0–6.0). Lactate dehydrogenase and total bilirubin levels were on average over two times their upper limit of normal values. Eighteen individuals of 32 tested had a positive direct antiglobulin (Coombs’) test. Mortality was 3.5% (2/57 individuals). CONCLUSION: Systemic loxoscelism is a rare but devastating process with only a minority of patients recalling the toxic exposure; hemolysis reaches a peak at 2 days after admission, with some cases taking more than a week before recovery. In endemic areas, suspicion for systemic loxoscelism should be high in individuals, especially children and younger adults, presenting with a cutaneous ulcer and hemolysis or coagulopathy, even in the absence of a bite exposure history. Public Library of Science 2017-04-19 /pmc/articles/PMC5396866/ /pubmed/28422977 http://dx.doi.org/10.1371/journal.pone.0174941 Text en © 2017 Robinson et al http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0/) , which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited.
spellingShingle Research Article
Robinson, Jamie R.
Kennedy, Vanessa E.
Doss, Youssef
Bastarache, Lisa
Denny, Joshua
Warner, Jeremy L.
Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort
title Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort
title_full Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort
title_fullStr Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort
title_full_unstemmed Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort
title_short Defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort
title_sort defining the complex phenotype of severe systemic loxoscelism using a large electronic health record cohort
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5396866/
https://www.ncbi.nlm.nih.gov/pubmed/28422977
http://dx.doi.org/10.1371/journal.pone.0174941
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