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In vitro cholesterol gallstone dissolution after fragmentation with shock waves.

Abstract
In order to test whether shock wave fragmentation of human gallstones increases their dissolution rates in a bile acid-lecithin solution, we carried out in vitro experiments. Stones comparable in size, weight and cholesterol content (86%) from the same human gallbladder were disintegrated by shock waves. A glycoursodeoxycholic acid (GUDC)-lecithin solution served as solvent. After 10 days incubation in this solvent, intact stones had lost only 4% of their cholesterol. This value increased to 92% after disintegration of the stones by 300 shock wave discharges. Fragments with a size of less than 2 mm had lost 55% of their cholesterol after day 1 and 99% after day 10. A large stone fragment cleaved off by shock waves lost much more cholesterol (42% after 10 days) than an intact untreated stone (4% after 10 days) comparable in size, weight and cholesterol content. These data show that shock wave lithotripsy of cholesterol gallstones considerably accelerates their dissolution rate in a GUDC-lecithin solvent, the desirable fragment size being 2 mm or less. However, even large fragments may lose much more cholesterol than comparable intact stones as a result of changes in surface structure as documented by scanning electron microscopy. The experiments favor the concept of a combined treatment of gallbladder stones by extracorporeally generated shock waves and bile salt therapy.
AuthorsM Neubrand, T Sauerbruch, F Stellaard, G Paumgartner
JournalDigestion (Digestion) Vol. 34 Issue 1 Pg. 51-9 ( 1986) ISSN: 0012-2823 [Print] Switzerland
PMID3710002 (Publication Type: Journal Article, Research Support, Non-U.S. Gov't)
Chemical References
  • Phosphatidylcholines
  • Solutions
  • glycoursodeoxycholic acid
  • Ursodeoxycholic Acid
  • Cholesterol
Topics
  • Cholelithiasis (metabolism, therapy)
  • Cholesterol (metabolism)
  • Humans
  • Lithotripsy
  • Microscopy, Electron, Scanning
  • Phosphatidylcholines
  • Solubility
  • Solutions
  • Ursodeoxycholic Acid (analogs & derivatives)

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