Idiopathic pulmonary fibrosis epidemiology and demographics: Difference between revisions
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=== Developed countries === | === Developed countries === | ||
* In the United States:<ref name="pmid232041242">{{cite journal| author=Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D| title=Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. | journal=Eur Respir Rev | year= 2012 | volume= 21 | issue= 126 | pages= 355-61 | pmid=23204124 | doi=10.1183/09059180.00002512 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23204124 }}</ref> | |||
** The incidence of idiopathic pulmonary fibrosis ranges from low of 6.8 per 100.000 to 8.8 per 100.000. | |||
* In Europe:<ref name="pmid23204124">{{cite journal| author=Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D| title=Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. | journal=Eur Respir Rev | year= 2012 | volume= 21 | issue= 126 | pages= 355-61 | pmid=23204124 | doi=10.1183/09059180.00002512 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23204124 }}</ref> | * In Europe:<ref name="pmid23204124">{{cite journal| author=Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D| title=Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature. | journal=Eur Respir Rev | year= 2012 | volume= 21 | issue= 126 | pages= 355-61 | pmid=23204124 | doi=10.1183/09059180.00002512 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23204124 }}</ref> | ||
** The prevalence of idiopathic pulmonary fibrosis ranges from a low of 1.25 per 100.000 persons to high of 23.4 per 100.000. | ** The prevalence of idiopathic pulmonary fibrosis ranges from a low of 1.25 per 100.000 persons to high of 23.4 per 100.000. | ||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Ahmed Elsaiey, MBBCH [2]
Overview
Epidemiology and Demographics
Prevalence
- Worldwide, the prevalence of idiopathic pulmonary fibrosis ranges from a low of _____ per 100,000 persons to a high of _____ per 100,000 persons with an average prevalence of _____ per 100,000 persons.
Incidence
- Worldwide, the incidence of idiopathic pulmonary fibrosis ranges from a low of 3 per 100,000 persons to a high of 9 per 100,000 persons.
Age
- The prevalence of idiopathic pulmonary fibrosis increases with age.[1]
- The incidence of idiopathic pulmonary fibrosis is estimated to be 1.2 per 100.000 persons of age 18 to 34 years.
- The incidence of idiopathic pulmonary fibrosis is estimated to be 76.4 per 100.000 persons of 75 years old and older.
Gender
- Idiopathic pulmonary fibrosis is more prevalent in men more than women.[2][3][4]
- The incidence of idiopathic pulmlonary fibrosis is estimated to be 10.7 per 100,000 man annually.
- The incidence of idiopathic pulmlonary fibrosis is estimated to be 7.4 per 100,000 woman annually.
Race
- There is no racial predilection for idiopathic pulmonary fibrosis.
Developed countries
- In the United States:[5]
- The incidence of idiopathic pulmonary fibrosis ranges from low of 6.8 per 100.000 to 8.8 per 100.000.
- In Europe:[6]
- The prevalence of idiopathic pulmonary fibrosis ranges from a low of 1.25 per 100.000 persons to high of 23.4 per 100.000.
- The incidence of idiopathic pulmonary fibrosis ranges from a low of 0.22 per 100.000 persons to high of 7.4 per 100.000.
Developing countries
References
- ↑ Raghu, Ganesh; Weycker, Derek; Edelsberg, John; Bradford, Williamson Z.; Oster, Gerry (2006). "Incidence and Prevalence of Idiopathic Pulmonary Fibrosis". American Journal of Respiratory and Critical Care Medicine. 174 (7): 810–816. doi:10.1164/rccm.200602-163OC. ISSN 1073-449X.
- ↑ Raghu, Ganesh; Weycker, Derek; Edelsberg, John; Bradford, Williamson Z.; Oster, Gerry (2006). "Incidence and Prevalence of Idiopathic Pulmonary Fibrosis". American Journal of Respiratory and Critical Care Medicine. 174 (7): 810–816. doi:10.1164/rccm.200602-163OC. ISSN 1073-449X.
- ↑ Kim, D. S. (2006). "Classification and Natural History of the Idiopathic Interstitial Pneumonias". Proceedings of the American Thoracic Society. 3 (4): 285–292. doi:10.1513/pats.200601-005TK. ISSN 1546-3222.
- ↑ Coultas DB, Zumwalt RE, Black WC, Sobonya RE (1994). "The epidemiology of interstitial lung diseases". Am J Respir Crit Care Med. 150 (4): 967–72. doi:10.1164/ajrccm.150.4.7921471. PMID 7921471.
- ↑ Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D (2012). "Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature". Eur Respir Rev. 21 (126): 355–61. doi:10.1183/09059180.00002512. PMID 23204124.
- ↑ Nalysnyk L, Cid-Ruzafa J, Rotella P, Esser D (2012). "Incidence and prevalence of idiopathic pulmonary fibrosis: review of the literature". Eur Respir Rev. 21 (126): 355–61. doi:10.1183/09059180.00002512. PMID 23204124.