Cited by 822

The DOI matches its Crossref record; 6 of the 6 references it cites were found in a registry or an index.

Gallstones

Lammert, Frank, Gurusamy, Kurinchi, Ko, Cynthia W., Miquel, Juan-Francisco, Méndez-Sánchez, Nahum, Portincasa, Piero, van Erpecum, Karel J., van Laarhoven, Cees J., Wang, David Q.-H.·2016·Nature Reviews Disease Primers

Abstract

Gallstones grow inside the gallbladder or biliary tract. These stones can be asymptomatic or symptomatic; only gallstones with symptoms or complications are defined as gallstone disease. Based on their composition, gallstones are classified into cholesterol gallstones, which represent the predominant entity, and bilirubin ('pigment') stones. Black pigment stones can be caused by chronic haemolysis; brown pigment stones typically develop in obstructed and infected bile ducts. For treatment, localization of the gallstones in the biliary tract is more relevant than composition. Overall, up to 20% of adults develop gallstones and >20% of those develop symptoms or complications. Risk factors for gallstones are female sex, age, pregnancy, physical inactivity, obesity and overnutrition. Factors involved in metabolic syndrome increase the risk of developing gallstones and form the basis of primary prevention by lifestyle changes. Common mutations in the hepatic cholesterol transporter ABCG8 confer most of the genetic risk of developing gallstones, which accounts for ∼25% of the total risk. Diagnosis is mainly based on clinical symptoms, abdominal ultrasonography and liver biochemistry tests. Symptoms often precede the onset of the three common and potentially life-threatening complications of gallstones (acute cholecystitis, acute cholangitis and biliary pancreatitis). Although our knowledge on the genetics and pathophysiology of gallstones has expanded recently, current treatment al…

Overview

Integrity signals

Registry

Crossref · 10.1038/nrdp.2016.24

Cites

6 of 6 references verified0 citation errors · 0 not checkable

Statistics

Recomputing p-values needs the paper’s full text.

Verification

Claims the paper makes

This paper’s full text isn’t openly available, so its claims and self-check weren’t run. The registry and citation checks still apply.

Claims other papers make about this one

Each is checked against this paper’s own text: does it say what the citing paper says it does?

Citations

Cites

Flagged first, then by citations

Research works printed but not linked: 212

  1. Everhart, J. E. & Ruhl, C. E. Burden of digestive diseases in the United States Part III: liver, biliary tract, and pancreas. Gastroenterology 136, 1134–1144 (2009). · DOI · Paper page
  2. Schafmayer, C. et al. Predictors of gallstone composition in 1025 symptomatic gallstones from Northern Germany. BMC Gastroenterol. 6, 36 (2006). · DOI
  3. Shoda, J. et al. Etiologic significance of defects in cholesterol, phospholipid, and bile acid metabolism in the liver of patients with intrahepatic calculi. Hepatology 33, 1194–1205 (2001). · DOI
  4. Aerts, R. & Penninckx, F. The burden of gallstone disease in Europe. Aliment. Pharmacol. Ther. 18 (Suppl. 3), 49–53 (2003). · DOI
  5. Völzke, H. et al. Independent risk factors for gallstone formation in a region with high cholelithiasis prevalence. Digestion 71, 97–105 (2005). · DOI · Paper page
  6. Miquel, J. F. et al. Genetic epidemiology of cholesterol cholelithiasis among Chilean Hispanics, Amerindians, and Maoris. Gastroenterology 115, 937–946 (1998). This is a unique epidemiological study on gallstone disease in a multi-ethnic setting. · DOI
  7. Everhart, J. E. et al. Prevalence of gallbladder disease in American Indian populations: findings from the Strong Heart Study. Hepatology 35, 1507–1512 (2002). · DOI
  8. Sampliner, R. E., Bennett, P. H., Comess, L. J., Rose, F. A. & Burch, T. A. Gallbladder disease in Pima Indians. Demonstration of high prevalence and early onset by cholecystography. N. Engl. J. Med. 283, 1358–1364 (1970). · DOI
  9. Carey, M. C. & Paigen, B. Epidemiology of the American Indians' burden and its likely genetic origins. Hepatology 36, 781–791 (2002). · DOI
  10. Nervi, F., Miquel, J. F. & Marshall, G. The Amerindian epidemics of cholesterol gallstones: the North and South connection. Hepatology 37, 947–948; author reply 948–949 (2003). · DOI
  11. Tsai, C. J., Leitzmann, M. F., Willett, W. C. & Giovannucci, E. L. Macronutrients and insulin resistance in cholesterol gallstone disease. Am. J. Gastroenterol. 103, 2932–2939 (2008). · DOI
  12. Perez-Ayuso, R. M. et al. [Natural history of cholelithiasis and incidence of cholecystectomy in an urban and a Mapuche rural area]. Rev. Med. Chil. 130, 723–730 (in Spanish) (2002). · DOI
  13. Stokes, C. S., Krawczyk, M. & Lammert, F. Gallstones: environment, lifestyle and genes. Dig. Dis. 29, 191–201 (2011). · DOI
  14. Paigen, B. & Carey, M. C. in The Genetic Basis of Common Diseases (eds King, R. A., Rotter, J. I. & Motulsky, A. G. ) 298–335 (Oxford Univ. Press, 2002).
  15. Portincasa, P., Moschetta, A. & Palasciano, G. Cholesterol gallstone disease. Lancet 368, 230–239 (2006). · DOI · Paper page
  16. Méndez-Sánchez, N. et al. Metabolic syndrome as a risk factor for gallstone disease. World J. Gastroenterol. 11, 1653–1657 (2005). · DOI
  17. Tsai, C. J., Leitzmann, M. F., Willett, W. C. & Giovannucci, E. L. Central adiposity, regional fat distribution, and the risk of cholecystectomy in women. Gut 55, 708–714 (2006). · DOI · Paper page
  18. Chait, A., Bierman, E. L. & Albers, J. J. Low-density lipoprotein receptor activity in cultured human skin fibroblasts. Mechanism of insulin-induced stimulation. J. Clin. Invest. 64, 1309–1319 (1979). · DOI
  19. Nepokroeff, C. M., Lakshmanan, M. R., Ness, G. C., Dugan, R. E. & Porter, J. W. Regulation of the diurnal rhythm of rat liver β-hydroxy-β-methylglutaryl coenzmye A reductase activity by insulin, glucagon, cyclic AMP and hydrocortisone. Arch. Biochem. Biophys. 160, 387–396 (1974). · DOI
  20. Subbiah, M. T. & Yunker, R. L. Cholesterol 7α-hydroxylase of rat liver: an insulin sensitive enzyme. Biochem. Biophys. Res. Commun. 124, 896–902 (1984). · DOI
  21. Weikert, C. et al. Presence of gallstones or kidney stones and risk of type 2 diabetes. Am. J. Epidemiol. 171, 447–454 (2010). · DOI
  22. Nervi, F. et al. Gallbladder disease is associated with insulin resistance in a high risk Hispanic population. J. Hepatol 45, 299–305 (2006). · DOI
  23. Aune, D., Leitzmann, M. & Vatten, L. J. Physical activity and the risk of gallbladder disease: a systematic review and meta-analysis of cohort studies. J. Phys. Act. Healthhttp://dx.doi.org/10.1123/jpah.2015-0456 (2016). · DOI
  24. Aune, D., Norat, T. & Vatten, L. J. Body mass index, abdominal fatness and the risk of gallbladder disease. Eur. J. Epidemiol. 30, 1009–1019 (2015). · DOI
  25. Aune, D. & Vatten, L. J. Diabetes mellitus and the risk of gallbladder disease: a systematic review and meta-analysis of prospective studies. J. Diabetes Complications 30, 368–373 (2016). · DOI
  26. Everhart, J. E. Contributions of obesity and weight loss to gallstone disease. Ann. Intern. Med. 119, 1029–1035 (1993). · DOI · Paper page
  27. Moon, R. C., Teixeira, A. F., DuCoin, C., Varnadore, S. & Jawad, M. A. Comparison of cholecystectomy cases after Roux-en-Y gastric bypass, sleeve gastrectomy, and gastric banding. Surg. Obes. Relat. Dis. 10, 64–68 (2014). · DOI
  28. Tsirline, V. B. et al. How frequently and when do patients undergo cholecystectomy after bariatric surgery? Surg. Obes. Relat. Dis. 10, 313–321 (2014). · DOI · Paper page
  29. Amaral, J. F. & Thompson, W. R. Gallbladder disease in the morbidly obese. Am. J. Surg. 149, 551–557 (1985). · DOI · Paper page
  30. Shiffman, M. L., Sugerman, H. J., Kellum, J. M., Brewer, W. H. & Moore, E. W. Gallstone formation after rapid weight loss: a prospective study in patients undergoing gastric bypass surgery for treatment of morbid obesity. Am. J. Gastroenterol. 86, 1000–1005 (1991).
  31. Sugerman, H. J. et al. A multicenter, placebo-controlled, randomized, double-blind, prospective trial of prophylactic ursodiol for the prevention of gallstone formation following gastric-bypass-induced rapid weight loss. Am. J. Surg. 169, 91–96 (1995). · DOI · Paper page
  32. Festi, D., Villanova, N. & Colecchia, A. Risk factors for gallstone formation during weight loss. Clin. Gastroenterol. Hepatol. 13, 613 (2015). · DOI
  33. Valdivieso, V., Covarrubias, C., Siegel, F. & Cruz, F. Pregnancy and cholelithiasis: pathogenesis and natural course of gallstones diagnosed in early puerperium. Hepatology 17, 1–4 (1993).
  34. Ko, C. W., Beresford, S. A., Schulte, S. J. & Lee, S. P. Insulin resistance and incident gallbladder disease in pregnancy. Clin. Gastroenterol. Hepatol 6, 76–81 (2008). · DOI
  35. Katsika, D. et al. Genetic and environmental influences on symptomatic gallstone disease: a Swedish study of 43,141 twin pairs. Hepatology 41, 1138–1143 (2005). This is a large twin study establishing the role of genetic risk factors in gallstone disease. · DOI
  36. Méndez-Sánchez, N., King-Martínez, A. C., Ramos, M. H., Pichardo-Bahena, R. & Uribe, M. The Amerindian's genes in the Mexican population are associated with development of gallstone disease. Am. J. Gastroenterol. 99, 2166–2170 (2004). · DOI
  37. Wang, D. Q., Cohen, D. E. & Carey, M. C. Biliary lipids and cholesterol gallstone disease. J. Lipid Res. 50, S406–S411 (2009). · DOI
  38. Lammert, F. & Sauerbruch, T. Mechanisms of disease: the genetic epidemiology of gallbladder stones. Nat. Clin. Pract. Gastroenterol. Hepatol 2, 423–433 (2005). · DOI
  39. Khanuja, B. et al. Lith1, a major gene affecting cholesterol gallstone formation among inbred strains of mice. Proc. Natl Acad. Sci. USA 92, 7729–7733 (1995). This study in mice introduces the concept of lithogenic genes. · DOI
  40. Paigen, B. et al. Quantitative trait loci mapping for cholesterol gallstones in AKR/J and C57L/J strains of mice. Physiol. Genomics 4, 59–65 (2000). · DOI
  41. Wang, D. Q., Paigen, B. & Carey, M. C. Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice: physical-chemistry of gallbladder bile. J. Lipid Res. 38, 1395–1411 (1997). · DOI
  42. Wang, D. Q., Lammert, F., Paigen, B. & Carey, M. C. Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice. Pathophysiology of biliary lipid secretion. J. Lipid Res. 40, 2066–2079 (1999). · DOI
  43. Lammert, F., Wang, D. Q., Paigen, B. & Carey, M. C. Phenotypic characterization of Lith genes that determine susceptibility to cholesterol cholelithiasis in inbred mice: integrated activities of hepatic lipid regulatory enzymes. J. Lipid Res. 40, 2080–2090 (1999). · DOI
  44. Lyons, M. A. & Wittenburg, H. Cholesterol gallstone susceptibility loci: a mouse map, candidate gene evaluation, and guide to human LITH genes. Gastroenterology 131, 1943–1970 (2006). · DOI
  45. Buch, S. et al. A genome-wide association scan identifies the hepatic cholesterol transporter ABCG8 as a susceptibility factor for human gallstone disease. Nat. Genet. 39, 995–999 (2007). This is the first genome-wide association study in hepatology that established ABCG8 as the most important genetic risk factor in humans. · DOI
  46. Buch, S. et al. Loci from a genome-wide analysis of bilirubin levels are associated with gallstone risk and composition. Gastroenterology 139, 1942–1951 (2010). · DOI
  47. Wang, D. Q. & Afdhal, N. H. in Sleisenger and Fordtran's Gastrointestinal and Liver Disease (eds Feldman, M., Friedman, L. S. & Brandt, L. ) 1100–1133 (Elsevier Saunders, 2014).
  48. Poupon, R. et al. Genotype–phenotype relationships in the low-phospholipid-associated cholelithiasis syndrome: a study of 156 consecutive patients. Hepatology 58, 1105–1110 (2013). This is a recent summary on this peculiar subtype (LPAC syndrome) of genetic gallstone disease. · DOI
  49. Hirschfield, G. M. et al. The genetics of complex cholestatic disorders. Gastroenterology 144, 1357–1374 (2013). · DOI
  50. Vitek, L. & Carey, M. C. New pathophysiological concepts underlying pathogenesis of pigment gallstones. Clin. Res. Hepatol. Gastroenterol. 36, 122–129 (2012). · DOI
  51. Biddinger, S. B. et al. Hepatic insulin resistance directly promotes formation of cholesterol gallstones. Nat. Med. 14, 778–782 (2008). · DOI
  52. de Bari, O., Wang, T. Y., Liu, M., Portincasa, P. & Wang, D. Q. Estrogen induces two distinct cholesterol crystallization pathways by activating ERα and GPR30 in female mice. J. Lipid Res. 56, 1691–1700 (2015). · DOI
  53. Moschetta, A., Bookout, A. L. & Mangelsdorf, D. J. Prevention of cholesterol gallstone disease by FXR agonists in a mouse model. Nat. Med. 10, 1352–1358 (2004). · DOI
  54. Uppal, H. et al. Activation of liver X receptor sensitizes mice to gallbladder cholesterol crystallization. Hepatology 47, 1331–1342 (2008). · DOI
  55. Krawczyk, M., Acalovschi, M. & Lammert, F. Genetic study of FGF19 receptor variants in gallstone disease. Hepatology 56, 2424 (2012). · DOI
  56. Carey, M. C. & Small, D. M. The physical chemistry of cholesterol solubility in bile. Relationship to gallstone formation and dissolution in man. J. Clin. Invest. 61, 998–1026 (1978). This is a seminal paper on the physical chemistry of gallstone formation. · DOI
  57. Wang, D. Q. & Carey, M. C. Complete mapping of crystallization pathways during cholesterol precipitation from model bile: influence of physical–chemical variables of pathophysiologic relevance and identification of a stable liquid crystalline state in cold, dilute and hydrophilic bile salt-containing systems. J. Lipid Res. 37, 606–630 (1996). · DOI
  58. Holzbach, R. T. et al. Biliary proteins. Unique inhibitors of cholesterol crystal nucleation in human gallbladder bile. J. Clin. Invest. 73, 35–45 (1984). · DOI
  59. Levy, P. F., Smith, B. F. & LaMont, J. T. Human gallbladder mucin accelerates nucleation of cholesterol in artificial bile. Gastroenterology 87, 270–275 (1984). · DOI
  60. Holzbach, R. T., Marsh, M., Olszewski, M. & Holan, K. Cholesterol solubility in bile. Evidence that supersaturated bile is frequent in healthy man. J. Clin. Invest. 52, 1467–1479 (1973). · DOI
  61. Holan, K. R., Holzbach, R. T., Hermann, R. E., Cooperman, A. M. & Claffey, W. J. Nucleation time: a key factor in the pathogenesis of cholesterol gallstone disease. Gastroenterology 77, 611–617 (1979). · DOI
  62. Lee, S. P., LaMont, J. T. & Carey, M. C. Role of gallbladder mucus hypersecretion in the evolution of cholesterol gallstones. J. Clin. Invest. 67, 1712–1723 (1981). · DOI
  63. Wang, D. Q., Schmitz, F., Kopin, A. S. & Carey, M. C. Targeted disruption of the murine cholecystokinin-1 receptor promotes intestinal cholesterol absorption and susceptibility to cholesterol cholelithiasis. J. Clin. Invest. 114, 521–528 (2004). · DOI
  64. Wang, D. Q., Zhang, L. & Wang, H. H. High cholesterol absorption efficiency and rapid biliary secretion of chylomicron remnant cholesterol enhance cholelithogenesis in gallstone-susceptible mice. Biochim. Biophys. Acta 1733, 90–99 (2005). · DOI
  65. Wang, D. Q., Lammert, F., Cohen, D. E., Paigen, B. & Carey, M. C. Cholic acid aids absorption, biliary secretion, and phase transitions of cholesterol in murine cholelithogenesis. Am. J. Physiol. 276, G751–G760 (1999). · DOI
  66. Wang, H. H., Portincasa, P., Mendez-Sanchez, N., Uribe, M. & Wang, D. Q. Effect of ezetimibe on the prevention and dissolution of cholesterol gallstones. Gastroenterology 134, 2101–2110 (2008). · DOI
  67. Maurer, K. J. et al. T-cell function is critical for murine cholesterol gallstone formation. Gastroenterology 133, 1304–1315 (2007). · DOI
  68. Soloway, R. D., Trotman, B. W., Maddrey, W. C. & Nakayama, F. Pigment gallstone composition in patients with hemolysis or infection/stasis. Dig. Dis. Sci. 31, 454–460 (1986). · DOI
  69. Wasmuth, H. E. et al. Coinheritance of Gilbert syndrome-associated UGT1A1 mutation increases gallstone risk in cystic fibrosis. Hepatology 43, 738–741 (2006). · DOI
  70. Portincasa, P. et al. Gallstone disease: symptoms and diagnosis of gallbladder stones. Best Pract. Res. Clin. Gastroenterol. 20, 1017–1029 (2006). · DOI
  71. Lamberts, M. P. et al. Prospective multicentre cohort study of patient-reported outcomes after cholecystectomy for uncomplicated symptomatic cholecystolithiasis. Br. J. Surg. 102, 1402–1409 (2015). · DOI
  72. Shea, J. A. et al. Revised estimates of diagnostic test sensitivity and specificity in suspected biliary tract disease. Arch. Intern. Med. 154, 2573–2581 (1994). · DOI
  73. Mayumi, T. et al. Results of the Tokyo Consensus Meeting Tokyo Guidelines. J. Hepatobiliary Pancreat. Surg. 14, 114–121 (2007). · DOI
  74. Trowbridge, R. L., Rutkowski, N. K. & Shojania, K. G. Does this patient have acute cholecystitis? JAMA 289, 80–86 (2003). · DOI
  75. Kiewiet, J. J. et al. A systematic review and meta-analysis of diagnostic performance of imaging in acute cholecystitis. Radiology 264, 708–720 (2012). · DOI
  76. Nathwani, R. A., Kumar, S. R., Reynolds, T. B. & Kaplowitz, N. Marked elevation in serum transaminases: an atypical presentation of choledocholithiasis. Am. J. Gastroenterol. 100, 295–298 (2005). · DOI
  77. Sharara, A. I., Mansour, N. M., El-Hakam, M., Ghaith, O. & El Halabi, M. Duration of pain is correlated with elevation in liver function tests in patients with symptomatic choledocholithiasis. Clin. Gastroenterol. Hepatol. 8, 1077–1082 (2010). · DOI
  78. Abboud, P. A. et al. Predictors of common bile duct stones prior to cholecystectomy: a meta-analysis. Gastrointest. Endosc. 44, 450–455 (1996). · DOI
  79. Giljaca, V. et al. Endoscopic ultrasound versus magnetic resonance cholangiopancreatography for common bile duct stones. Cochrane Database Syst. Rev. 2, CD011549 (2015).
  80. Maple, J. T. et al. The role of endoscopy in the management of choledocholithiasis. Gastrointest. Endosc. 74, 731–744 (2011). · DOI
  81. Iranmanesh, P. et al. Initial cholecystectomy versus sequential common duct endoscopic assessment and subsequent cholecystectomy for suspected gallstone migration: a randomized clinical trial. JAMA 312, 137–144 (2014). · DOI
  82. Mori, T., Sugiyama, M. & Atomi, Y. Gallstone disease: management of intrahepatic stones. Best Pract. Res. Clin. Gastroenterol. 20, 1117–1137 (2006). · DOI
  83. Di Ciaula, A. et al. Therapeutic reflections in cholesterol homeostasis and gallstone disease: a review. Curr. Med. Chem. 21, 1435–1447 (2014). · DOI
  84. Erichsen, R., Frøslev, T., Lash, T. L., Pedersen, L. & Sørensen, H. T. Long-term statin use and the risk of gallstone disease: a population-based case–control study. Am. J. Epidemiol. 173, 162–170 (2011). · DOI
  85. Wang, H. H. et al. Prevention of cholesterol gallstones by inhibiting hepatic biosynthesis and intestinal absorption of cholesterol. Eur. J. Clin. Invest. 43, 413–426 (2013). · DOI
  86. Stender, S., Nordestgaard, B. G. & Tybjaerg-Hansen, A. Elevated body mass index as a causal risk factor for symptomatic gallstone disease: a Mendelian randomization study. Hepatology 58, 2133–2141 (2013). · DOI · Paper page
  87. Leitzmann, M. F. et al. The relation of physical activity to risk for symptomatic gallstone disease in men. Ann. Intern. Med. 128, 417–425 (1998). · DOI · Paper page
  88. Leitzmann, M. F. et al. Recreational physical activity and the risk of cholecystectomy in women. N. Engl. J. Med. 341, 777–784 (1999). · DOI · Paper page
  89. Banim, P. J. et al. Physical activity reduces the risk of symptomatic gallstones: a prospective cohort study. Eur. J. Gastroenterol. Hepatol. 22, 983–988 (2010). · DOI
  90. Philipp, E., Wilckens, T., Friess, E., Platte, P. & Pirke, K. M. Cholecystokinin, gastrin and stress hormone responses in marathon runners. Peptides 13, 125–128 (1992). · DOI
  91. Capron, J. P. et al. Meal frequency and duration of overnight fast: a role in gall-stone formation? Br. Med. J. (Clin. Res. Ed.) 283, 1435 (1981). · DOI
  92. Ortega, R. M., Fernandez-Azuela, M., Encinas-Sotillos, A., Andres, P. & Lopez-Sobaler, A. M. Differences in diet and food habits between patients with gallstones and controls. J. Am. Coll. Nutr. 16, 88–95 (1997). · DOI · Paper page
  93. Tsunoda, K., Shirai, Y. & Hatakeyama, K. Prevalence of cholesterol gallstones positively correlates with per capita daily calorie intake. Hepatogastroenterology 51, 1271–1274 (2004).
  94. Pixley, F., Wilson, D., McPherson, K. & Mann, J. Effect of vegetarianism on development of gall stones in women. Br. Med. J. (Clin. Res. Ed.) 291, 11–12 (1985). · DOI
  95. Simon, J. A. & Hudes, E. S. Serum ascorbic acid and gallbladder disease prevalence among US adults: the Third National Health and Nutrition Examination Survey (NHANES III). Arch. Intern. Med. 160, 931–936 (2000). · DOI
  96. Festi, D. et al. Gallbladder motility and gallstone formation in obese patients following very low calorie diets. Use it (fat) to lose it (well). Int. J. Obes. Relat. Metab. Disord. 22, 592–600 (1998). · DOI · Paper page
  97. Broomfield, P. H. et al. Effects of ursodeoxycholic acid and aspirin on the formation of lithogenic bile and gallstones during loss of weight. N. Engl. J. Med. 319, 1567–1572 (1988). · DOI · Paper page
  98. Uy, M. C., Talingdan-Te, M. C., Espinosa, W. Z., Daez, M. L. & Ong, J. P. Ursodeoxycholic acid in the prevention of gallstone formation after bariatric surgery: a meta-analysis. Obes. Surg. 18, 1532–1538 (2008). · DOI · Paper page
  99. Shoheiber, O., Biskupiak, J. E. & Nash, D. B. Estimation of the cost savings resulting from the use of ursodiol for the prevention of gallstones in obese patients undergoing rapid weight reduction. Int. J. Obes. Relat. Metab. Disord. 21, 1038–1045 (1997). · DOI
  100. Stokes, C. S. & Lammert, F. Reply: To PMID 24321208. Clin. Gastroenterol. Hepatol. 13, 614 (2015). · DOI
  101. Mendez-Sanchez, N. et al. Fish oil (n-3) polyunsaturated fatty acids beneficially affect biliary cholesterol nucleation time in obese women losing weight. J. Nutr. 131, 2300–2303 (2001). · DOI · Paper page
  102. Plecka Ostlund, M. et al. Population-based study of the need for cholecystectomy after obesity surgery. Br. J. Surg. 99, 864–869 (2012). · DOI
  103. Papasavas, P. K., Gagne, D. J., Ceppa, F. A. & Caushaj, P. F. Routine gallbladder screening not necessary in patients undergoing laparoscopic Roux-en-Y gastric bypass. Surg. Obes. Relat. Dis. 2, 41–46; discussion 46–47 (2006). · DOI
  104. Ellner, S. J., Myers, T. T., Piorkowski, J. R., Mavanur, A. A. & Barba, C. A. Routine cholecystectomy is not mandatory during morbid obesity surgery. Surg. Obes. Relat. Dis. 3, 456–460 (2007). · DOI · Paper page
  105. Patel, J. A. et al. Perioperative management of cholelithiasis in patients presenting for laparoscopic Roux-en-Y gastric bypass: have we reached a consensus? Am. Surg. 75, 470–476; discussion 476 (2009). · DOI
  106. Tarantino, I. et al. Is routine cholecystectomy justified in severely obese patients undergoing a laparoscopic Roux-en-Y gastric bypass procedure? A comparative cohort study. Obes. Surg. 21, 1870–1878 (2011). · DOI
  107. van Liessum, P. A. et al. Postprandial gallbladder motility during long term treatment with the long-acting somatostatin analog SMS 201–995 in acromegaly. J. Clin. Endocrinol. Metab. 69, 557–562 (1989). · DOI
  108. Roti, E. et al. Chronic treatment with a long-acting somatostatin analogue in a patient with intestinal carcinoid tumor: occurrence of cholelithiasis. J. Endocrinol. Invest. 13, 69–72 (1990). · DOI
  109. Venneman, N. G. & van Erpecum, K. J. Gallstone disease: primary and secondary prevention. Best Pract. Res. Clin. Gastroenterol. 20, 1063–1073 (2006). · DOI
  110. McSherry, C. K., Ferstenberg, H., Calhoun, W. F., Lahman, E. & Virshup, M. The natural history of diagnosed gallstone disease in symptomatic and asymptomatic patients. Ann. Surg. 202, 59–63 (1985). · DOI
  111. Friedman, G. D., Raviola, C. A. & Fireman, B. Prognosis of gallstones with mild or no symptoms: 25 years of follow-up in a health maintenance organization. J. Clin. Epidemiol. 42, 127–136 (1989). · DOI
  112. Attili, A. F., De Santis, A., Capri, R., Repice, A. M. & Maselli, S. The natural history of gallstones: the GREPCO experience. The GREPCO group. Hepatology 21, 655–660 (1995). · DOI
  113. Halldestam, I., Enell, E. L., Kullman, E. & Borch, K. Development of symptoms and complications in individuals with asymptomatic gallstones. Br. J. Surg. 91, 734–738 (2004). · DOI
  114. Festi, D. et al. Natural history of gallstone disease: expectant management or active treatment? Results from a population-based cohort study. J. Gastroenterol. Hepatol. 25, 719–724 (2010). · DOI
  115. Schmidt, M. et al. A 24-year controlled follow-up of patients with silent gallstones showed no long-term risk of symptoms or adverse events leading to cholecystectomy. Scand. J. Gastroenterol. 46, 949–954 (2011). · DOI
  116. May, G. R., Sutherland, L. R. & Shaffer, E. A. Efficacy of bile acid therapy for gallstone dissolution: a meta-analysis of randomized trials. Aliment. Pharmacol. Ther. 7, 139–148 (1993). · DOI
  117. Rabenstein, T. et al. Ten years experience with piezoelectric extracorporeal shockwave lithotripsy of gallbladder stones. Eur. J. Gastroenterol. Hepatol. 17, 629–639 (2005). · DOI
  118. Carrilho-Ribeiro, L., Pinto-Correia, A., Velosa, J. & Carneiro De Moura, M. A ten-year prospective study on gallbladder stone recurrence after successful extracorporeal shock-wave lithotripsy. Scand. J. Gastroenterol. 41, 338–342 (2006). · DOI
  119. Venneman, N. G. et al. Ursodeoxycholic acid exerts no beneficial effect in patients with symptomatic gallstones awaiting cholecystectomy. Hepatology 43, 1276–1283 (2006). · DOI
  120. Stephen, A. E. & Berger, D. L. Carcinoma in the porcelain gallbladder: a relationship revisited. Surgery 129, 699–703 (2001). · DOI
  121. Schmidt, M., Sondenaa, K., Vetrhus, M., Berhane, T. & Eide, G. E. A randomized controlled study of uncomplicated gallstone disease with a 14-year follow-up showed that operation was the preferred treatment. Dig. Surg. 28, 270–276 (2011). · DOI
  122. Schmidt, M., Sondenaa, K., Vetrhus, M., Berhane, T. & Eide, G. E. Long-term follow-up of a randomized controlled trial of observation versus surgery for acute cholecystitis: non-operative management is an option in some patients. Scand. J. Gastroenterol. 46, 1257–1262 (2011). · DOI
  123. Nicholl, J. P. et al. Randomised controlled trial of cost-effectiveness of lithotripsy and open cholecystectomy as treatments for gallbladder stones. Lancet 340, 801–807 (1992). · DOI
  124. Barkun, A. N. et al. Costs and effectiveness of extracorporeal gallbladder stone shock wave lithotripsy versus laparoscopic cholecystectomy. A randomized clinical trial. McGill Gallstone Treatment Group. Int. J. Technol. Assess. Health Care 13, 589–601 (1997). · DOI
  125. Plaisier, P. W. et al. The course of biliary and gastrointestinal symptoms after treatment of uncomplicated symptomatic gallstones: results of a randomized study comparing extracorporeal shock wave lithotripsy with conventional cholecystectomy. Am. J. Gastroenterol. 89, 739–744 (1994).
  126. Fort, J. M., Azpiroz, F., Casellas, F., Andreu, J. & Malagelada, J. R. Bowel habit after cholecystectomy: physiological changes and clinical implications. Gastroenterology 111, 617–622 (1996). · DOI
  127. Huntington, C. R. et al. Nationwide variation in outcomes and cost of laparoscopic procedures. Surg. Endosc. 30, 934–946 (2016). · DOI
  128. Keus, F., de Jong, J. A., Gooszen, H. G. & van Laarhoven, C. J. Laparoscopic versus open cholecystectomy for patients with symptomatic cholecystolithiasis. Cochrane Database Syst. Rev. 4, CD006231 (2006).
  129. Keus, F., de Jong, J. A., Gooszen, H. G. & van Laarhoven, C. J. Laparoscopic versus small-incision cholecystectomy for patients with symptomatic cholecystolithiasis.Cochrane Database Syst. Rev. 4, CD006229 (2006).
  130. Keus, F., de Jonge, T., Gooszen, H. G., Buskens, E. & van Laarhoven, C. J. Cost-minimization analysis in a blind randomized trial on small-incision versus laparoscopic cholecystectomy from a societal perspective: sick leave outweighs efforts in hospital savings. Trials 10, 80 (2009). · DOI
  131. Coccolini, F. et al. Open versus laparoscopic cholecystectomy in acute cholecystitis. Systematic review and meta-analysis. Int. J. Surg. 18, 196–204 (2015). · DOI
  132. de Goede, B. et al. Meta-analysis of laparoscopic versus open cholecystectomy for patients with liver cirrhosis and symptomatic cholecystolithiasis. Br. J. Surg. 100, 209–216 (2013). · DOI
  133. Gurusamy, K. S., Vaughan, J., Ramamoorthy, R., Fusai, G. & Davidson, B. R. Miniports versus standard ports for laparoscopic cholecystectomy. Cochrane Database Syst. Rev. 8, CD006804 (2013).
  134. Gurusamy, K. S., Vaughan, J., Rossi, M. & Davidson, B. R. Fewer-than-four ports versus four ports for laparoscopic cholecystectomy. Cochrane Database Syst. Rev. 2, CD007109 (2014).
  135. Sanabria, A., Dominguez, L. C., Valdivieso, E. & Gomez, G. Antibiotic prophylaxis for patients undergoing elective laparoscopic cholecystectomy. Cochrane Database Syst. Rev. 12, CD005265 (2010).
  136. Ford, J. A., Soop, M., Du, J., Loveday, B. P. & Rodgers, M. Systematic review of intraoperative cholangiography in cholecystectomy. Br. J. Surg. 99, 160–167 (2012). · DOI
  137. Gurusamy, K. S., Koti, R. & Davidson, B. R. Routine abdominal drainage versus no abdominal drainage for uncomplicated laparoscopic cholecystectomy. Cochrane Database Syst. Rev. 9, CD006004 (2013).
  138. Vaughan, J., Gurusamy, K. S. & Davidson, B. R. Day-surgery versus overnight stay surgery for laparoscopic cholecystectomy. Cochrane Database Syst. Rev. 7, CD006798 (2013).
  139. Gurusamy, K. S., Koti, R., Fusai, G. & Davidson, B. R. Early versus delayed laparoscopic cholecystectomy for uncomplicated biliary colic. Cochrane Database Syst. Rev. 6, CD007196 (2013).
  140. Gurusamy, K. S., Davidson, C., Gluud, C. & Davidson, B. R. Early versus delayed laparoscopic cholecystectomy for people with acute cholecystitis. Cochrane Database Syst. Rev. 6, CD005440 (2013).
  141. Gutt, C. N. et al. Acute cholecystitis: early versus delayed cholecystectomy, a multicenter randomized trial (ACDC study, NCT00447304). Ann. Surg. 258, 385–393 (2013). This is a multicentre RCT on the timing of cholecystectomy in acute cholecystitis. · DOI
  142. Aboulian, A. et al. Early cholecystectomy safely decreases hospital stay in patients with mild gallstone pancreatitis: a randomized prospective study. Ann. Surg. 251, 615–619 (2010). · DOI
  143. Gurusamy, K. S., Nagendran, M. & Davidson, B. R. Early versus delayed laparoscopic cholecystectomy for acute gallstone pancreatitis. Cochrane Database Syst. Rev. 9, CD010326 (2013).
  144. da Costa, D. W. et al. Same-admission versus interval cholecystectomy for mild gallstone pancreatitis (PONCHO): a multicentre randomised controlled trial. Lancet 386, 1261–1268 (2015). This is a large RCT on the timing of cholecystectomy after mild biliary pancreatitis. · DOI
  145. Lill, S. et al. Elective laparoscopic cholecystectomy without routine intraoperative cholangiography: a retrospective analysis of 1101 consecutive cases. Scand. J. Surg. 99, 197–200 (2010). · DOI
  146. Hamad, M. A., Nada, A. A., Abdel-Atty, M. Y. & Kawashti, A. S. Major biliary complications in 2,714 cases of laparoscopic cholecystectomy without intraoperative cholangiography: a multicenter retrospective study. Surg. Endosc. 25, 3747–3751 (2011). · DOI
  147. Tornqvist, B., Stromberg, C., Persson, G. & Nilsson, M. Effect of intended intraoperative cholangiography and early detection of bile duct injury on survival after cholecystectomy: population based cohort study. BMJ 345, e6457 (2012). · DOI
  148. Enochsson, L., Lindberg, B., Swahn, F. & Arnelo, U. Intraoperative endoscopic retrograde cholangiopancreatography (ERCP) to remove common bile duct stones during routine laparoscopic cholecystectomy does not prolong hospitalization: a 2-year experience. Surg. Endosc. 18, 367–371 (2004). · DOI
  149. Alvarez, F. A. et al. Impact of routine intraoperative cholangiography during laparoscopic cholecystectomy on bile duct injury. Br. J. Surg. 101, 677–684 (2014). · DOI
  150. Gurusamy, K. S., Rossi, M. & Davidson, B. R. Percutaneous cholecystostomy for high-risk surgical patients with acute calculous cholecystitis. Cochrane Database Syst. Rev. 8, CD007088 (2013).
  151. Hatzidakis, A. A. et al. Acute cholecystitis in high-risk patients: percutaneous cholecystostomy versus conservative treatment. Eur. Radiol. 12, 1778–1784 (2002). · DOI
  152. Caddy, G. R. & Tham, T. C. Gallstone disease: symptoms, diagnosis and endoscopic management of common bile duct stones. Best Pract. Res. Clin. Gastroenterol. 20, 1085–1101 (2006). · DOI
  153. Collins, C., Maguire, D., Ireland, A., Fitzgerald, E. & O'Sullivan, G. C. A prospective study of common bile duct calculi in patients undergoing laparoscopic cholecystectomy: natural history of choledocholithiasis revisited. Ann. Surg. 239, 28–33 (2004). · DOI
  154. Rosseland, A. R. & Glomsaker, T. B. Asymptomatic common bile duct stones. Eur. J. Gastroenterol. Hepatol. 12, 1171–1173 (2000). · DOI
  155. Murison, M. S., Gartell, P. C. & McGinn, F. P. Does selective peroperative cholangiography result in missed common bile duct stones? J. R. Coll. Surg. Edinb. 38, 220–224 (1993).
  156. Caddy, G. R. et al. Natural history of asymptomatic bile duct stones at time of cholecystectomy. Ulster Med. J. 74, 108–112 (2005).
  157. Möller, M., Gustafsson, U., Rasmussen, F., Persson, G. & Thorell, A. Natural course versus interventions to clear common bile duct stones: data from the Swedish Registry for Gallstone Surgery and Endoscopic Retrograde Cholangiopancreatography (GallRiks). JAMA Surg. 149, 1008–1013 (2014). · DOI
  158. Johnson, A. G. & Hosking, S. W. Appraisal of the management of bile duct stones. Br. J. Surg. 74, 555–560 (1987). · DOI
  159. Freeman, M. L. et al. Complications of endoscopic biliary sphincterotomy. N. Engl. J. Med. 335, 909–918 (1996). · DOI
  160. McAlister, V. C., Davenport, E. & Renouf, E. Cholecystectomy deferral in patients with endoscopic sphincterotomy. Cochrane Database Syst. Rev. 4, CD006233 (2007).
  161. Reinders, J. S. et al. Early laparoscopic cholecystectomy improves outcomes after endoscopic sphincterotomy for choledochocystolithiasis. Gastroenterology 138, 2315–2320 (2010). This is a RCT on the timing of cholecystectomy after bile duct clearance. · DOI
  162. Baron, T. H. & Harewood, G. C. Endoscopic balloon dilation of the biliary sphincter compared to endoscopic biliary sphincterotomy for removal of common bile duct stones during ERCP: a metaanalysis of randomized, controlled trials. Am. J. Gastroenterol. 99, 1455–1460 (2004). · DOI
  163. Weinberg, B. M., Shindy, W. & Lo, S. Endoscopic balloon sphincter dilation (sphincteroplasty) versus sphincterotomy for common bile duct stones. Cochrane Database Syst. Rev. 4, CD004890 (2006).
  164. Dasari, B. V. et al. Surgical versus endoscopic treatment of bile duct stones. Cochrane Database Syst. Rev. 12, CD003327 (2013).
  165. Swahn, F. et al. Rendezvous cannulation technique reduces post-ERCP pancreatitis: a prospective nationwide study of 12,718 ERCP procedures. Am. J. Gastroenterol. 108, 552–559 (2013). · DOI
  166. Katsinelos, P., Kountouras, J., Paroutoglou, G., Chatzimavroudis, G. & Zavos, C. Combination of endoprostheses and oral ursodeoxycholic acid or placebo in the treatment of difficult to extract common bile duct stones. Dig. Liver Dis. 40, 453–459 (2008). · DOI
  167. Besselink, M. G. et al. Is complicated gallstone disease preceded by biliary colic? J. Gastrointest. Surg. 13, 312–317 (2009). · DOI
  168. Hui, C. K. et al. Outcome of emergency ERCP for acute cholangitis in patients 90 years of age and older. Aliment. Pharmacol. Ther. 19, 1153–1158 (2004). · DOI
  169. Leung, J. W. et al. Antibiotics, biliary sepsis, and bile duct stones. Gastrointest. Endosc. 40, 716–721 (1994). · DOI
  170. Dhalluin-Venier, V. et al. Effects of biliary obstruction on the penetration of ciprofloxacin and cefotaxime. Eur. J. Gastroenterol. Hepatol. 20, 127–130 (2008). · DOI
  171. van Erpecum, K. J. Gallstone disease. Complications of bile-duct stones: acute cholangitis and pancreatitis. Best Pract. Res. Clin. Gastroenterol. 20, 1139–1152 (2006). · DOI
  172. Lai, E. C. et al. Endoscopic biliary drainage for severe acute cholangitis. N. Engl. J. Med. 326, 1582–1586 (1992). · DOI
  173. Leese, T., Neoptolemos, J. P., Baker, A. R. & Carr-Locke, D. L. Management of acute cholangitis and the impact of endoscopic sphincterotomy. Br. J. Surg. 73, 988–992 (1986). · DOI
  174. Sugiyama, M. & Atomi, Y. Treatment of acute cholangitis due to choledocholithiasis in elderly and younger patients. Arch. Surg. 132, 1129–1133 (1997). · DOI
  175. Sharma, B. C., Kumar, R., Agarwal, N. & Sarin, S. K. Endoscopic biliary drainage by nasobiliary drain or by stent placement in patients with acute cholangitis. Endoscopy 37, 439–443 (2005). · DOI
  176. Venneman, N. G. et al. Small gallstones, preserved gallbladder motility, and fast crystallization are associated with pancreatitis. Hepatology 41, 738–746 (2005). · DOI
  177. Venneman, N. G. et al. Small gallstones are associated with increased risk of acute pancreatitis: potential benefits of prophylactic cholecystectomy? Am. J. Gastroenterol. 100, 2540–2550 (2005). · DOI
  178. Cohen, M. E., Slezak, L., Wells, C. K., Andersen, D. K. & Topazian, M. Prediction of bile duct stones and complications in gallstone pancreatitis using early laboratory trends. Am. J. Gastroenterol. 96, 3305–3311 (2001). · DOI
  179. Tenner, S., Dubner, H. & Steinberg, W. Predicting gallstone pancreatitis with laboratory parameters: a meta-analysis. Am. J. Gastroenterol. 89, 1863–1866 (1994).
  180. van Santvoort, H. C. et al. Prediction of common bile duct stones in the earliest stages of acute biliary pancreatitis. Endoscopy 43, 8–13 (2011). · DOI
  181. Working Group IAP/APA Acute Pancreatitis Guidelines. IAP/APA evidence-based guidelines for the management of acute pancreatitis. Pancreatology 13, e1–e15 (2013). · DOI
  182. Higuchi, R. et al. TG13 miscellaneous etiology of cholangitis and cholecystitis. J. Hepatobiliary Pancreat. Sci. 20, 97–105 (2013). · DOI
  183. Kusano, T., Isa, T., Ohtsubo, M., Yasaka, T. & Furukawa, M. Natural progression of untreated hepatolithiasis that shows no clinical signs at its initial presentation. J. Clin. Gastroenterol. 33, 114–117 (2001). · DOI
  184. Okugawa, T. et al. Peroral cholangioscopic treatment of hepatolithiasis: long-term results. Gastrointest. Endosc. 56, 366–371 (2002). · DOI
  185. Lee, S. K. et al. Percutaneous transhepatic cholangioscopic treatment for hepatolithiasis: an evaluation of long-term results and risk factors for recurrence. Gastrointest. Endosc. 53, 318–323 (2001). · DOI
  186. Huang, M. H. et al. Long-term outcome of percutaneous transhepatic cholangioscopic lithotomy for hepatolithiasis. Am. J. Gastroenterol. 98, 2655–2662 (2003). · DOI
  187. Othman, M. O., Stone, E., Hashimi, M. & Parasher, G. Conservative management of cholelithiasis and its complications in pregnancy is associated with recurrent symptoms and more emergency department visits. Gastrointest. Endosc. 76, 564–569 (2012). · DOI
  188. Jorge, A. M., Keswani, R. N., Veerappan, A., Soper, N. J. & Gawron, A. J. Non-operative management of symptomatic cholelithiasis in pregnancy is associated with frequent hospitalizations. J. Gastrointest. Surg. 19, 598–603 (2015). · DOI
  189. Strasberg, S. M. Clinical practice. Acute calculous cholecystitis. N. Engl. J. Med. 358, 2804–2811 (2008). · DOI
  190. Lu, E. J., Curet, M. J., El-Sayed, Y. Y. & Kirkwood, K. S. Medical versus surgical management of biliary tract disease in pregnancy. Am. J. Surg. 188, 755–759 (2004). · DOI
  191. Swisher, S. G. et al. Biliary disease during pregnancy. Am. J. Surg. 168, 576–579; discussion 580–581 (1994). · DOI
  192. Kuy, S., Roman, S. A., Desai, R. & Sosa, J. A. Outcomes following cholecystectomy in pregnant and nonpregnant women. Surgery 146, 358–366 (2009). · DOI
  193. Silvestri, M. T. et al. Morbidity of appendectomy and cholecystectomy in pregnant and nonpregnant women. Obstet. Gynecol. 118, 1261–1270 (2011). · DOI
  194. Kahaleh, M. et al. Safety and efficacy of ERCP in pregnancy. Gastrointest. Endosc. 60, 287–292 (2004). · DOI
  195. Tang, S. J. et al. Safety and utility of ERCP during pregnancy. Gastrointest. Endosc. 69, 453–461 (2009). · DOI
  196. Ainslie, W. G. et al. Micropuncture cholecystectomy versus conventional laparoscopic cholecystectomy: a randomized controlled trial. Surg. Endosc. 17, 766–772 (2003). · DOI
  197. Nilsson, E., Ros, A., Rahmqvist, M., Backman, K. & Carlsson, P. Cholecystectomy: costs and health-related quality of life: a comparison of two techniques. Int. J. Qual. Health Care 16, 473–482 (2004). · DOI
  198. Abd Ellatif, M. E. et al. Quality-of-life measures after single-access versus conventional laparoscopic cholecystectomy: a prospective randomized study. Surg. Endosc. 27, 1896–1906 (2013). · DOI
  199. Keus, F., de Vries, J., Gooszen, H. G. & van Laarhoven, C. J. Laparoscopic versus small-incision cholecystectomy: health status in a blind randomised trial. Surg. Endosc. 22, 1649–1659 (2008). · DOI
  200. Ma, J. et al. Randomized controlled trial comparing single-port laparoscopic cholecystectomy and four-port laparoscopic cholecystectomy. Ann. Surg. 254, 22–27 (2011). · DOI

200 of 212 shown

Cited by

Sorted by citations

Metadata

Authors
Lammert, F., Gurusamy, K., Ko, C. W., Miquel, J.-F., Méndez-Sánchez, N., Portincasa, P., van Erpecum, K. J., van Laarhoven, C. J., & Wang, D. Q.-H.
Venue
Nature Reviews Disease Primers
Published
2016-04-28
Volume
2
Issue
1
ISSN
2056-676X
Cited by
822
References
6
Language
en

About these checks

Registry, retraction, Cites and statistics results are computed, not judged, with one exception: a printed reference that no index lists is read once by a model before it counts as a citation error. Claims are extracted by a model and kept only when their quote appears verbatim in the text; each cited source is then checked, with a model’s help, for whether it says what the claim relies on. Those verdicts can be wrong — read the claim’s quote and the cited source before relying on one.

Statistics and arithmetic are recomputed, not judged.

Confidence bands are shown only for fields calibrated on our annotated test set. None is calibrated yet, so no band is shown.

What counts as a claim ›How we measure confidence ›How we check this ›

Are you an author, or do you see a problem with this page? Request a review