Incidence of gallstone disease and complications

被引:119
|
作者
Shabanzadeh, Daniel Monsted [1 ,2 ]
机构
[1] Bispebjerg Hosp, Digest Dis Ctr, Bispebjerg Bakke 23, DK-2400 Copenhagen, Denmark
[2] Res Ctr Prevent & Hlth, Capital Region Of Denmar, Denmark
关键词
cholecystolithiasis; cholelithiasis; gallbladder diseases; gallstones; ultrasonography; NATURAL-HISTORY; FOLLOW-UP; ELDERLY-PATIENTS; RISK-FACTORS; PERFORM CHOLECYSTECTOMY; ASYMPTOMATIC GALLSTONES; EXPECTANT MANAGEMENT; GALLBLADDER-DISEASE; ACUTE CHOLECYSTITIS; INCREASED MORBIDITY;
D O I
10.1097/MOG.0000000000000418
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
Purpose of review The purpose of this review was to describe the epidemiology of gallstone disease in the era of ultrasound screening and laparoscopic cholecystectomy. Recent findings Recent general population cohorts, including ultrasound screenings, have contributed to our understanding of formation and clinical course of gallstone disease. Cohorts of symptomatic gallstone disease have been informative about symptom recurrence and need of treatment. Preventive targets for gallstone formation may include obesity and the associated metabolic changes. The presence of gallstone disease is best described as a continuum from asymptomatic to symptomatic disease, with the latter including both pain attacks and complicated disease. Symptomatic disease causes a persistent high risk of symptom recurrence and need of cholecystectomy. The majority of gallstone carriers will remain asymptomatic and about one in five will develop symptoms. Determinants of disease progression from asymptomatic to symptomatic disease include sex, age, body mass index, and gallstone ultrasound characteristics. Summary Because of the absence of effective gallstone formation prevention, targets against the metabolic changes in obesity should be further explored in randomized controlled trials. To optimize patient selection for cholecystectomy, treatment algorithms including identified determinants of symptomatic disease in gallstone carriers should be explored in prospective clinical trials.
引用
收藏
页码:81 / 89
页数:9
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