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Gallstone dissolution in methyl tert-butyl ether after mechanical fragmentation: in vitro study
AJR. American Journal of Roentgenology
|July 1, 1990
Summary
Mechanical fragmentation speeds up gallstone dissolution with methyl tert-butyl ether (MTBE) for noncalcified and partially calcified stones. Heavily calcified stones showed no significant improvement, indicating fragmentation effectiveness depends on calcification levels.
Area of Science:
- Gastroenterology
- Surgical Technology
- Biochemistry
Background:
- Gallstones are common, and current treatments like cholecystectomy have risks.
- Chemolysis using methyl tert-butyl ether (MTBE) is an alternative but can be slow.
- Improving dissolution rates for gallstone chemolysis is a clinical need.
Purpose of the Study:
- To evaluate the efficacy of intracorporeal mechanical fragmentation in accelerating gallstone dissolution with MTBE.
- To determine if stone calcification affects the benefit of mechanical fragmentation.
Main Methods:
- Human gallstones were matched and divided into three groups: fragmented then treated with MTBE, intact control treated with MTBE, and analyzed for density and composition.
- Gallstones were classified as noncalcified, partially calcified, or heavily calcified using CT scans.
- Dissolution times were compared between fragmented and intact stones.
Main Results:
- Mechanical fragmentation significantly reduced MTBE dissolution time by 25-69% for noncalcified and 20-42% for partially calcified gallstones.
- No significant reduction in dissolution time was observed for heavily calcified gallstones.
- The reduction in dissolution time was inversely correlated with maximal stone density (r = -0.72).
Conclusions:
- Intracorporeal mechanical fragmentation enhances gallstone chemolysis with MTBE for noncalcified and partially calcified stones.
- Heavily calcified gallstones do not benefit from mechanical fragmentation prior to MTBE treatment.
- Stone density, rather than calcification pattern, is the key factor determining the effectiveness of fragmentation in accelerating gallstone dissolution.