Budd-Chiari syndrome epidemiology and demographics: Difference between revisions
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== | == Overview == | ||
In 2009-2013, the [[prevalence]] of Budd-Chiari syndrome was estimated to be 8 patients cases per 100,000 individuals in South Korea. Budd-Chiari syndrome is a [[Rare diseases|rare disease]]. The annual [[incidence]] of Budd-Chiari syndrome was estimated to be about 11 cases per 100,000 individuals in Sweden. The [[Case fatality rate|annual case fatality rate]] of Budd-Chiari syndrome is approximately 2800 per 100,000 patients. Budd-Chiari syndrome commonly presents in the third or fourth decade of life. The median age at diagnosis is 51 years. Budd-Chiari syndrome is [[rare]] in [[children]]. [[Females]] are more commonly affected with Budd-Chiari syndrome than [[males]]. The female-to-male ratio is approximately 1.8 to 1. Budd-Chiari syndrome in the [[United States]] is predominantly seen in [[women]] and is commonly associated with [[hematologic]] disorders. [[Congenital]] membranous form is the most common cause of [[Budd-Chiari syndrome]] worldwide and particularly in Asia. | |||
==Epidemiology and Demographics== | |||
The [[epidemiology]] and [[demographics]] of Budd-Chiari syndrome are as follows:<ref name="pmid26558363">{{cite journal |vauthors=Ki M, Choi HY, Kim KA, Kim BH, Jang ES, Jeong SH |title=Incidence, prevalence and complications of Budd-Chiari syndrome in South Korea: a nationwide, population-based study |journal=Liver Int. |volume=36 |issue=7 |pages=1067–73 |year=2016 |pmid=26558363 |doi=10.1111/liv.13008 |url=}}</ref><ref name="pmid18694401">{{cite journal |vauthors=Rajani R, Melin T, Björnsson E, Broomé U, Sangfelt P, Danielsson A, Gustavsson A, Grip O, Svensson H, Lööf L, Wallerstedt S, Almer SH |title=Budd-Chiari syndrome in Sweden: epidemiology, clinical characteristics and survival - an 18-year experience |journal=Liver Int. |volume=29 |issue=2 |pages=253–9 |year=2009 |pmid=18694401 |doi=10.1111/j.1478-3231.2008.01838.x |url=}}</ref> | |||
===Prevalence=== | |||
*In 2009-2013, the [[prevalence]] of Budd-Chiari syndrome was estimated to be 8 cases per 100,000 individuals in South Korea. | |||
===Incidence=== | |||
*Budd-Chiari syndrome is a [[rare disease]]. | |||
*The annual [[incidence]] of Budd-Chiari syndrome was estimated to be about 11 cases per 100,000 individuals in Sweden. | |||
===Case Fatality Rate=== | |||
*The annual [[case fatality rate]] of Budd-Chiari syndrome is approximately 2800 per 100,000 individuals. | |||
===Age=== | |||
*Budd-Chiari syndrome commonly presents in the third or fourth decade of life. | |||
*The median age at [[diagnosis]] is 51 years. | |||
*Budd-Chiari syndrome is rare in [[children]]. | |||
===Gender=== | |||
*[[Females]] are more commonly affected with Budd-Chiari syndrome than [[males]]. The female-to-male ratio is approximately 1.8 to 1. | |||
===Developed Countries=== | |||
*Budd-Chiari syndrome in the [[United States]] is predominantly seen in [[women]] and is commonly associated with [[hematologic]] disorders. | |||
===Developing Countries=== | |||
*[[Congenital]] membranous forms is the most common cause of Budd-Chiari syndrome worldwide and particularly in Asia. | |||
==References== | ==References== | ||
{{Reflist|2}} | |||
[[Category:Gastroenterology]] | [[Category:Gastroenterology]] | ||
[[Category:Needs | [[Category:Hepatology]] | ||
[[Category:Needs content]] | |||
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mazia Fatima, MBBS [2]
Overview
In 2009-2013, the prevalence of Budd-Chiari syndrome was estimated to be 8 patients cases per 100,000 individuals in South Korea. Budd-Chiari syndrome is a rare disease. The annual incidence of Budd-Chiari syndrome was estimated to be about 11 cases per 100,000 individuals in Sweden. The annual case fatality rate of Budd-Chiari syndrome is approximately 2800 per 100,000 patients. Budd-Chiari syndrome commonly presents in the third or fourth decade of life. The median age at diagnosis is 51 years. Budd-Chiari syndrome is rare in children. Females are more commonly affected with Budd-Chiari syndrome than males. The female-to-male ratio is approximately 1.8 to 1. Budd-Chiari syndrome in the United States is predominantly seen in women and is commonly associated with hematologic disorders. Congenital membranous form is the most common cause of Budd-Chiari syndrome worldwide and particularly in Asia.
Epidemiology and Demographics
The epidemiology and demographics of Budd-Chiari syndrome are as follows:[1][2]
Prevalence
- In 2009-2013, the prevalence of Budd-Chiari syndrome was estimated to be 8 cases per 100,000 individuals in South Korea.
Incidence
- Budd-Chiari syndrome is a rare disease.
- The annual incidence of Budd-Chiari syndrome was estimated to be about 11 cases per 100,000 individuals in Sweden.
Case Fatality Rate
- The annual case fatality rate of Budd-Chiari syndrome is approximately 2800 per 100,000 individuals.
Age
- Budd-Chiari syndrome commonly presents in the third or fourth decade of life.
- The median age at diagnosis is 51 years.
- Budd-Chiari syndrome is rare in children.
Gender
- Females are more commonly affected with Budd-Chiari syndrome than males. The female-to-male ratio is approximately 1.8 to 1.
Developed Countries
- Budd-Chiari syndrome in the United States is predominantly seen in women and is commonly associated with hematologic disorders.
Developing Countries
- Congenital membranous forms is the most common cause of Budd-Chiari syndrome worldwide and particularly in Asia.
References
- ↑ Ki M, Choi HY, Kim KA, Kim BH, Jang ES, Jeong SH (2016). "Incidence, prevalence and complications of Budd-Chiari syndrome in South Korea: a nationwide, population-based study". Liver Int. 36 (7): 1067–73. doi:10.1111/liv.13008. PMID 26558363.
- ↑ Rajani R, Melin T, Björnsson E, Broomé U, Sangfelt P, Danielsson A, Gustavsson A, Grip O, Svensson H, Lööf L, Wallerstedt S, Almer SH (2009). "Budd-Chiari syndrome in Sweden: epidemiology, clinical characteristics and survival - an 18-year experience". Liver Int. 29 (2): 253–9. doi:10.1111/j.1478-3231.2008.01838.x. PMID 18694401.