Hereditary pancreatitis epidemiology and demographics: Difference between revisions
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===Age=== | ===Age=== | ||
*Hereditary pancreatitis commonly affects younger age group. | *Hereditary pancreatitis commonly affects younger age group. | ||
*The median age at which first diagnosis is made is 19 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> | ||
*The median age at which the symptoms develop is 10 years. | *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> | ||
*In some patients, the disease may develop before 5 years of age. | *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> | ||
===Race=== | ===Race=== |
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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
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
- The incidence/prevalence of [disease name] is approximately [number range] per 100,000 individuals worldwide.
- 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
- 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 [disease name].
- [Disease name] usually affects individuals of the [race 1] race. [Race 2] individuals are less likely to develop [disease name].
Gender
- [Disease name] affects men and women equally.
- [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
- ↑ 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.
- ↑ Barkin JS, Fayne SD (1986). "Chronic pancreatitis: update 1986". Mt. Sinai J. Med. 53 (5): 404–8. PMID 3489182.
- ↑ 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.
- ↑ 4.0 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.
- ↑ 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.
- ↑ 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.