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==Overview==
==Overview==
Prevalence of idiopathic pulmonary fibrosis ranges from a low of 0.5 per 100.000 persons to a high of 27.9 per 100.000. Incidence of idiopathic pulmonary fibrosis ranges from a low of 3 per 100,000 persons to a high of 9 per 100,000 persons. The prevalence of idiopathic pulmonary fibrosis increases with age. Idiopathic pulmonary fibrosis is more prevalent in men more than women.  
Prevalence of idiopathic pulmonary fibrosis ranges from a low of 0.5 per 100,000 persons to a high of 27.9 per 100,000. [[Incidence]] of idiopathic pulmonary fibrosis ranges from a low of 3 per 100,000 persons to a high of 9 per 100,000 persons. The [[prevalence]] of idiopathic pulmonary fibrosis increases with age. Idiopathic pulmonary fibrosis is more [[Prevalence|prevalent]] in men more than women.  


==Epidemiology and Demographics==
==Epidemiology and Demographics==


=== Prevalence ===
=== Prevalence ===
* Worldwide, the prevalence of idiopathic pulmonary fibrosis ranges from a low of 0.5 per 100.000 persons to a high of 27.9 per 100.000.<ref name="pmid23962167">{{cite journal| author=Kaunisto J, Salomaa ER, Hodgson U, Kaarteenaho R, Myllärniemi M| title=Idiopathic pulmonary fibrosis--a systematic review on methodology for the collection of epidemiological data. | journal=BMC Pulm Med | year= 2013 | volume= 13 | issue=  | pages= 53 | pmid=23962167 | doi=10.1186/1471-2466-13-53 | pmc=3765635 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23962167  }}</ref>
* Worldwide, the [[prevalence]] of idiopathic pulmonary fibrosis ranges from a low of 0.5 per 100,000 persons to a high of 27.9 per 100.000.<ref name="pmid23962167">{{cite journal| author=Kaunisto J, Salomaa ER, Hodgson U, Kaarteenaho R, Myllärniemi M| title=Idiopathic pulmonary fibrosis--a systematic review on methodology for the collection of epidemiological data. | journal=BMC Pulm Med | year= 2013 | volume= 13 | issue=  | pages= 53 | pmid=23962167 | doi=10.1186/1471-2466-13-53 | pmc=3765635 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=23962167  }}</ref>


=== Incidence ===
=== 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.  
* 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 ===
=== Age ===
* The prevalence of idiopathic pulmonary fibrosis increases with age.<ref name="RaghuWeycker20062">{{cite journal|last1=Raghu|first1=Ganesh|last2=Weycker|first2=Derek|last3=Edelsberg|first3=John|last4=Bradford|first4=Williamson Z.|last5=Oster|first5=Gerry|title=Incidence and Prevalence of Idiopathic Pulmonary Fibrosis|journal=American Journal of Respiratory and Critical Care Medicine|volume=174|issue=7|year=2006|pages=810–816|issn=1073-449X|doi=10.1164/rccm.200602-163OC}}</ref>
* The [[prevalence]] of idiopathic pulmonary fibrosis increases with age.<ref name="RaghuWeycker20062">{{cite journal|last1=Raghu|first1=Ganesh|last2=Weycker|first2=Derek|last3=Edelsberg|first3=John|last4=Bradford|first4=Williamson Z.|last5=Oster|first5=Gerry|title=Incidence and Prevalence of Idiopathic Pulmonary Fibrosis|journal=American Journal of Respiratory and Critical Care Medicine|volume=174|issue=7|year=2006|pages=810–816|issn=1073-449X|doi=10.1164/rccm.200602-163OC}}</ref>
* 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 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.   
* The [[incidence]] of idiopathic pulmonary fibrosis is estimated to be 76.4 per 100.000 persons of 75 years old and older.   


=== Gender ===
=== Gender ===
* Idiopathic pulmonary fibrosis is more prevalent in men more than women.<ref name="RaghuWeycker2006">{{cite journal|last1=Raghu|first1=Ganesh|last2=Weycker|first2=Derek|last3=Edelsberg|first3=John|last4=Bradford|first4=Williamson Z.|last5=Oster|first5=Gerry|title=Incidence and Prevalence of Idiopathic Pulmonary Fibrosis|journal=American Journal of Respiratory and Critical Care Medicine|volume=174|issue=7|year=2006|pages=810–816|issn=1073-449X|doi=10.1164/rccm.200602-163OC}}</ref><ref name="Kim2006">{{cite journal|last1=Kim|first1=D. S.|title=Classification and Natural History of the Idiopathic Interstitial Pneumonias|journal=Proceedings of the American Thoracic Society|volume=3|issue=4|year=2006|pages=285–292|issn=1546-3222|doi=10.1513/pats.200601-005TK}}</ref><ref name="pmid7921471">{{cite journal| author=Coultas DB, Zumwalt RE, Black WC, Sobonya RE| title=The epidemiology of interstitial lung diseases. | journal=Am J Respir Crit Care Med | year= 1994 | volume= 150 | issue= 4 | pages= 967-72 | pmid=7921471 | doi=10.1164/ajrccm.150.4.7921471 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7921471  }}</ref>
* Idiopathic pulmonary fibrosis is more [[Prevalence|prevalent]] in men more than women.<ref name="RaghuWeycker2006">{{cite journal|last1=Raghu|first1=Ganesh|last2=Weycker|first2=Derek|last3=Edelsberg|first3=John|last4=Bradford|first4=Williamson Z.|last5=Oster|first5=Gerry|title=Incidence and Prevalence of Idiopathic Pulmonary Fibrosis|journal=American Journal of Respiratory and Critical Care Medicine|volume=174|issue=7|year=2006|pages=810–816|issn=1073-449X|doi=10.1164/rccm.200602-163OC}}</ref><ref name="Kim2006">{{cite journal|last1=Kim|first1=D. S.|title=Classification and Natural History of the Idiopathic Interstitial Pneumonias|journal=Proceedings of the American Thoracic Society|volume=3|issue=4|year=2006|pages=285–292|issn=1546-3222|doi=10.1513/pats.200601-005TK}}</ref><ref name="pmid7921471">{{cite journal| author=Coultas DB, Zumwalt RE, Black WC, Sobonya RE| title=The epidemiology of interstitial lung diseases. | journal=Am J Respir Crit Care Med | year= 1994 | volume= 150 | issue= 4 | pages= 967-72 | pmid=7921471 | doi=10.1164/ajrccm.150.4.7921471 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=7921471  }}</ref>
* The incidence of idiopathic pulmlonary fibrosis is estimated to be 10.7 per 100,000 man annually.  
* The [[incidence]] of idiopathic pulmonary 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.  
* The [[incidence]] of idiopathic pulmonary fibrosis is estimated to be 7.4 per 100,000 woman annually.  


=== Race ===
=== Race ===
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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>
* '''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.  
** 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.  
** 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.   
** 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 ===
=== Developing countries ===
* In Korea, the prevalence of idiopathic pulmonary fibrosis ranges from a low of 39.7 per 100.000 persons to high of 24.3 per 100.000 persons.<ref name="pmid27287654">{{cite journal| author=Lee HE, Myong JP, Kim HR, Rhee CK, Yoon HK, Koo JW| title=Incidence and prevalence of idiopathic interstitial pneumonia and idiopathic pulmonary fibrosis in Korea. | journal=Int J Tuberc Lung Dis | year= 2016 | volume= 20 | issue= 7 | pages= 978-84 | pmid=27287654 | doi=10.5588/ijtld.16.0003 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27287654  }}</ref>  
* In Korea, the [[prevalence]] of idiopathic pulmonary fibrosis ranges from a low of 39.7 per 100,000 persons to high of 24.3 per 100,000 persons.<ref name="pmid27287654">{{cite journal| author=Lee HE, Myong JP, Kim HR, Rhee CK, Yoon HK, Koo JW| title=Incidence and prevalence of idiopathic interstitial pneumonia and idiopathic pulmonary fibrosis in Korea. | journal=Int J Tuberc Lung Dis | year= 2016 | volume= 20 | issue= 7 | pages= 978-84 | pmid=27287654 | doi=10.5588/ijtld.16.0003 | pmc= | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=27287654  }}</ref>  


==References==
==References==

Revision as of 16:08, 2 April 2018

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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

Prevalence of idiopathic pulmonary fibrosis ranges from a low of 0.5 per 100,000 persons to a high of 27.9 per 100,000. Incidence of idiopathic pulmonary fibrosis ranges from a low of 3 per 100,000 persons to a high of 9 per 100,000 persons. The prevalence of idiopathic pulmonary fibrosis increases with age. Idiopathic pulmonary fibrosis is more prevalent in men more than women.

Epidemiology and Demographics

Prevalence

  • Worldwide, the prevalence of idiopathic pulmonary fibrosis ranges from a low of 0.5 per 100,000 persons to a high of 27.9 per 100.000.[1]

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.[2]
  • 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.[3][4][5]
  • The incidence of idiopathic pulmonary fibrosis is estimated to be 10.7 per 100,000 man annually.
  • The incidence of idiopathic pulmonary 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:[6]
    • The incidence of idiopathic pulmonary fibrosis ranges from low of 6.8 per 100,000 to 8.8 per 100,000.
  • In Europe:[7]
    • 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

  • In Korea, the prevalence of idiopathic pulmonary fibrosis ranges from a low of 39.7 per 100,000 persons to high of 24.3 per 100,000 persons.[8]

References

  1. ↑ Kaunisto J, Salomaa ER, Hodgson U, Kaarteenaho R, Myllärniemi M (2013). "Idiopathic pulmonary fibrosis--a systematic review on methodology for the collection of epidemiological data". BMC Pulm Med. 13: 53. doi:10.1186/1471-2466-13-53. PMC 3765635. PMID 23962167.
  2. ↑ 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.
  3. ↑ 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.
  4. ↑ 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.
  5. ↑ 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.
  6. ↑ 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.
  7. ↑ 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.
  8. ↑ Lee HE, Myong JP, Kim HR, Rhee CK, Yoon HK, Koo JW (2016). "Incidence and prevalence of idiopathic interstitial pneumonia and idiopathic pulmonary fibrosis in Korea". Int J Tuberc Lung Dis. 20 (7): 978–84. doi:10.5588/ijtld.16.0003. PMID 27287654.

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