Churg-Strauss syndrome epidemiology and demographics: Difference between revisions
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{{CMG}}{{APM}}{{AE}}{{KW}} | {{CMG}}{{APM}}{{AE}}{{KW}} | ||
==Overview== | ==Overview== | ||
The prevalence of Eosinophilic granulomatosis with polyangiitis | The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million person a year, with higher prevalence's seen in Europeans. <ref name="pmid148724612">{{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> | ||
==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.<ref name="pmid148724613">{{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 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== |
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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 person a year, with higher prevalence's seen in Europeans. [1]
Epidemiology and Demographics
Prevalence
The prevalence of Eosinophilic granulomatosis with polyangiitis ranges from 2 to 13 per million persons.[2]
Incidence
The incidence of Eosinophilic granulomatosis with polyangiitis ranges from 0.5 to 6.8 per million 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
- ↑ 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.
- ↑ 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.