Hereditary pancreatitis epidemiology and demographics: Difference between revisions

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==Overview==
==Overview==
The incidence of hereditary pancreatitis is approximately 3.5–10 per 100,000 individuals in Europe and the USA. In Western countries, the prevalence was found to be 0.3/100 000. Hereditary pancreatitis commonly affects younger age group. The median age at which first diagnosis is made is 19 years. The median age at which the symptoms develop is 10 years.


==Epidemiology and Demographics==
==Epidemiology and Demographics==
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===Prevalence===
===Prevalence===
*The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
*In Western countries, the prevalence was found to be 0.3/100 000.
*In [year], the incidence/prevalence of [disease name] was estimated to be [number range] cases per 100,000 individuals worldwide.
*The prevalence of [disease/malignancy] is estimated to be [number] cases annually.
 
===Case-fatality rate/Mortality rate===
*In [year], the incidence of [disease name] is approximately [number range] per 100,000 individuals with a case-fatality rate/mortality rate of [number range]%.
*The case-fatality rate/mortality rate of [disease name] is approximately [number range].


===Age===
===Age===
*Patients of all age groups may develop [disease name].
*Hereditary pancreatitis commonly affects younger age group.
*The incidence of [disease name] increases with age; the median age at diagnosis is [#] years.
*The median age at which first diagnosis is made is 19 years.<ref name="pmid15017610">{{cite journal |vauthors=Howes N, Lerch MM, Greenhalf W, Stocken DD, Ellis I, Simon P, Truninger K, Ammann R, Cavallini G, Charnley RM, Uomo G, Delhaye M, Spicak J, Drumm B, Jansen J, Mountford R, Whitcomb DC, Neoptolemos JP |title=Clinical and genetic characteristics of hereditary pancreatitis in Europe |journal=Clin. Gastroenterol. Hepatol. |volume=2 |issue=3 |pages=252–61 |year=2004 |pmid=15017610 |doi= |url=}}</ref><ref name="pmid18755888">{{cite journal |vauthors=Rebours V, Boutron-Ruault MC, Schnee M, Férec C, Le Maréchal C, Hentic O, Maire F, Hammel P, Ruszniewski P, Lévy P |title=The natural history of hereditary pancreatitis: a national series |journal=Gut |volume=58 |issue=1 |pages=97–103 |year=2009 |pmid=18755888 |doi=10.1136/gut.2008.149179 |url=}}</ref>
*[Disease name] commonly affects individuals younger than/older than [number of years] years of age.  
*The median age at which the symptoms develop is 10 years.<ref name="pmid15017610">{{cite journal |vauthors=Howes N, Lerch MM, Greenhalf W, Stocken DD, Ellis I, Simon P, Truninger K, Ammann R, Cavallini G, Charnley RM, Uomo G, Delhaye M, Spicak J, Drumm B, Jansen J, Mountford R, Whitcomb DC, Neoptolemos JP |title=Clinical and genetic characteristics of hereditary pancreatitis in Europe |journal=Clin. Gastroenterol. Hepatol. |volume=2 |issue=3 |pages=252–61 |year=2004 |pmid=15017610 |doi= |url=}}</ref><ref name="pmid18755888">{{cite journal |vauthors=Rebours V, Boutron-Ruault MC, Schnee M, Férec C, Le Maréchal C, Hentic O, Maire F, Hammel P, Ruszniewski P, Lévy P |title=The natural history of hereditary pancreatitis: a national series |journal=Gut |volume=58 |issue=1 |pages=97–103 |year=2009 |pmid=18755888 |doi=10.1136/gut.2008.149179 |url=}}</ref>
*[Chronic disease name] is usually first diagnosed among [age group].
*In some patients, the disease may develop before 5 years of age.<ref name="pmid9219780">{{cite journal |vauthors=Sossenheimer MJ, Aston CE, Preston RA, Gates LK, Ulrich CD, Martin SP, Zhang Y, Gorry MC, Ehrlich GD, Whitcomb DC |title=Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG) |journal=Am. J. Gastroenterol. |volume=92 |issue=7 |pages=1113–6 |year=1997 |pmid=9219780 |doi= |url=}}</ref><ref name="pmid11755505">{{cite journal |vauthors=Keim V, Bauer N, Teich N, Simon P, Lerch MM, Mössner J |title=Clinical characterization of patients with hereditary pancreatitis and mutations in the cationic trypsinogen gene |journal=Am. J. Med. |volume=111 |issue=8 |pages=622–6 |year=2001 |pmid=11755505 |doi= |url=}}</ref>
*[Acute disease name] commonly affects [age group].


===Race===
===Race===
*There is no racial predilection to [disease name].
*There is no racial predilection to Hereditary pancreatitis.
*[Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].
===Gender===
===Gender===
*[Disease name] affects men and women equally.
*Hereditary pancreatitis affects men and women equally.<br>
*[Gender 1] are more commonly affected by [disease name] than [gender 2]. The [gender 1] to [gender 2] ratio is approximately [number > 1] to 1.
===Region===
*The majority of [disease name] cases are reported in [geographical region].
 
*[Disease name] is a common/rare disease that tends to affect [patient population 1] and [patient population 2].
 
===Developed Countries===
 
===Developing Countries===
 
 
 
==References==
==References==
{{Reflist|2}}
{{Reflist|2}}

Latest revision as of 20:56, 23 January 2018

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Iqra Qamar M.D.[2]

Overview

The incidence of hereditary pancreatitis is approximately 3.5–10 per 100,000 individuals in Europe and the USA. In Western countries, the prevalence was found to be 0.3/100 000. Hereditary pancreatitis commonly affects younger age group. The median age at which first diagnosis is made is 19 years. The median age at which the symptoms develop is 10 years.

Epidemiology and Demographics

Incidence

  • The incidence of hereditary pancreatitis is approximately 3.5–10 per 100,000 individuals in Europe and the USA.[1][2]

Prevalence

  • In Western countries, the prevalence was found to be 0.3/100 000.

Age

  • Hereditary pancreatitis commonly affects younger age group.
  • The median age at which first diagnosis is made is 19 years.[3][4]
  • The median age at which the symptoms develop is 10 years.[3][4]
  • In some patients, the disease may develop before 5 years of age.[5][6]

Race

  • There is no racial predilection to Hereditary pancreatitis.

Gender

  • Hereditary pancreatitis affects men and women equally.

References

  1. ↑ Andersen BN, Pedersen NT, Scheel J, Worning H (1982). "Incidence of alcoholic chronic pancreatitis in Copenhagen". Scand. J. Gastroenterol. 17 (2): 247–52. PMID 7134849.
  2. ↑ Barkin JS, Fayne SD (1986). "Chronic pancreatitis: update 1986". Mt. Sinai J. Med. 53 (5): 404–8. PMID 3489182.
  3. ↑ 3.0 3.1 Howes N, Lerch MM, Greenhalf W, Stocken DD, Ellis I, Simon P, Truninger K, Ammann R, Cavallini G, Charnley RM, Uomo G, Delhaye M, Spicak J, Drumm B, Jansen J, Mountford R, Whitcomb DC, Neoptolemos JP (2004). "Clinical and genetic characteristics of hereditary pancreatitis in Europe". Clin. Gastroenterol. Hepatol. 2 (3): 252–61. PMID 15017610.
  4. ↑ 4.0 4.1 Rebours V, Boutron-Ruault MC, Schnee M, Férec C, Le Maréchal C, Hentic O, Maire F, Hammel P, Ruszniewski P, Lévy P (2009). "The natural history of hereditary pancreatitis: a national series". Gut. 58 (1): 97–103. doi:10.1136/gut.2008.149179. PMID 18755888.
  5. ↑ Sossenheimer MJ, Aston CE, Preston RA, Gates LK, Ulrich CD, Martin SP, Zhang Y, Gorry MC, Ehrlich GD, Whitcomb DC (1997). "Clinical characteristics of hereditary pancreatitis in a large family, based on high-risk haplotype. The Midwest Multicenter Pancreatic Study Group (MMPSG)". Am. J. Gastroenterol. 92 (7): 1113–6. PMID 9219780.
  6. ↑ Keim V, Bauer N, Teich N, Simon P, Lerch MM, Mössner J (2001). "Clinical characterization of patients with hereditary pancreatitis and mutations in the cationic trypsinogen gene". Am. J. Med. 111 (8): 622–6. PMID 11755505.

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