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Diarrhea-associated Hemolytic Uremic Syndrome in Southern Alberta: A Long-term Single-centre Experience

Overview
Specialty Pediatrics
Date 2012 Jun 2
PMID 22654544
Citations 5
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Abstract

Background: Reports of long-term incidence trends of endemic diarrhea-associated hemolytic uremic syndrome (D+HUS) are few and inconclusive.

Objective: To define and analyze the incidence and outcomes of D+HUS over a period of approximately 25 years in a highly endemic region of southern Alberta.

Methods: Annual incidence rates of confirmed cases of D+HUS were compared between two 12-year periods (1980 to 1992 and 1994 to 2006). Differences in therapies used, and some short- and long-term complications observed were also compared between the two periods.

Results: The absolute yearly number of D+HUS cases was highly variable. The comparison between the 1980 to 1992, and 1994 to 2006 periods demonstrated a modest 8.8% decrease in the total number of cases. The population-based average annual incidence rates were not significantly different between the two time periods (3.33 cases versus 2.58 cases per 100,000 population per year, respectively; P=0.30). Only supportive care measures were used in the latter period. A mortality rate of lower than 1% in the latter period was one of the lowest ever reported for a large cohort of D+HUS patients.

Conclusion: The present long-term retrospective study of D+HUS in a highly endemic area documented a modest decrease in the absolute number of cases but no difference in the average annual incidence over an extended period of time.

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Shiga Toxin-Associated Hemolytic Uremic Syndrome: A Narrative Review.

Joseph A, Cointe A, Mariani Kurkdjian P, Rafat C, Hertig A Toxins (Basel). 2020; 12(2).

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Dexamethasone rescues neurovascular unit integrity from cell damage caused by systemic administration of shiga toxin 2 and lipopolysaccharide in mice motor cortex.

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Long-term outcomes of Shiga toxin hemolytic uremic syndrome.

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