Churg-Strauss syndrome epidemiology and demographics: Difference between revisions
No edit summary |
|||
Line 4: | Line 4: | ||
{{CMG}}{{APM}}{{AE}}{{KW}} | {{CMG}}{{APM}}{{AE}}{{KW}} | ||
==Overview== | ==Overview== | ||
The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million | The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million persons per year, with higher prevalences seen in Europeans.<ref name="pmid14872461" /> | ||
==Epidemiology and Demographics== | ==Epidemiology and Demographics== | ||
===Prevalence=== | ===Prevalence=== | ||
The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million | The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million persons per year.<ref name="pmid14872461">{{cite journal| author=Mahr A, Guillevin L, Poissonnet M, Aymé S| title=Prevalences of polyarteritis nodosa, microscopic polyangiitis, Wegener's granulomatosis, and Churg-Strauss syndrome in a French urban multiethnic population in 2000: a capture-recapture estimate. | journal=Arthritis Rheum | year= 2004 | volume= 51 | issue= 1 | pages= 92-9 | pmid=14872461 | doi=10.1002/art.20077 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=14872461 }} </ref> | ||
===Incidence=== | |||
The incidence of Eosinophilic granulomatosis with polyangiitis ranges from 0.5 to 6.8 per million persons per year. | |||
==Demographics== | |||
The rate distribution of Eosinophilic granulomatosis with polyangiitis varies upon age, sex, and race. | |||
===Age=== | ===Age=== | ||
The mean age at diagnosis is 50. The initial onset of symptoms may be 10-20 years earlier. | The mean age at diagnosis is 50. The initial onset of symptoms may be 10-20 years earlier. | ||
===Gender=== | ===Gender=== | ||
There is no gender predominance. | There is no gender predominance. | ||
===Race=== | |||
==References== | ==References== |
Revision as of 14:44, 21 November 2016
Churg-Strauss syndrome Microchapters |
Diagnosis |
---|
Treatment |
Case Studies |
Churg-Strauss syndrome epidemiology and demographics On the Web |
American Roentgen Ray Society Images of Churg-Strauss syndrome epidemiology and demographics |
Churg-Strauss syndrome epidemiology and demographics in the news |
Blogs on Churg-Strauss syndrome epidemiology and demographics |
Risk calculators and risk factors for Churg-Strauss syndrome epidemiology and demographics |
Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]Ali Poyan Mehr, M.D. [2]Associate Editor(s)-in-Chief: Krzysztof Wierzbicki M.D. [3]
Overview
The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million persons per year, with higher prevalences seen in Europeans.[1]
Epidemiology and Demographics
Prevalence
The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million persons per year.[1]
Incidence
The incidence of Eosinophilic granulomatosis with polyangiitis ranges from 0.5 to 6.8 per million persons per year.
Demographics
The rate distribution of Eosinophilic granulomatosis with polyangiitis varies upon age, sex, and race.
Age
The mean age at diagnosis is 50. The initial onset of symptoms may be 10-20 years earlier.
Gender
There is no gender predominance.
Race
References
- ↑ 1.0 1.1 Mahr A, Guillevin L, Poissonnet M, Aymé S (2004). "Prevalences of polyarteritis nodosa, microscopic polyangiitis, Wegener's granulomatosis, and Churg-Strauss syndrome in a French urban multiethnic population in 2000: a capture-recapture estimate". Arthritis Rheum. 51 (1): 92–9. doi:10.1002/art.20077. PMID 14872461.