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Laser Photocoagulation for the Treatment of Acute Peptic-Ulcer Bleeding

List of authors.
  • Guenter J. Krejs, M.D.,
  • Katherine H. Little, M.D.,
  • Henrik Westergaard, M.D.,
  • J. Kent Hamilton, M.D.,
  • David K. Spady, M.D.,
  • and Daniel E. Polter, M.D.

Abstract

We tested the hypothesis that therapeutic endoscopy using the Nd:YAG (neodymium:yttrium–aluminum–garnet) laser would benefit patients with acute peptic-ulcer bleeding. Over 43 months, 174 patients with active bleeding (n = 32) or stigmata of recent bleeding (n = 142) due to peptic ulcers were randomly assigned during endoscopy to either standard treatment with laser photocoagulation or therapy without photocoagulation. There were no significant differences in a number of outcomes between the group treated with laser photocoagulation and the control group. Continued bleeding or rebleeding was observed in 22 percent of the laser-treated group and in 20 percent of the control group. Urgent surgery was necessary in 16 percent of the laser-treated patients and in 17 percent of the controls. Laser-treated patients spent a mean of 41 hours in the intensive care unit, and controls spent a mean of 32 hours. The mean hospital stay was 12 days in the laser-treated group and 11 days in the control group. One death occurred in each group. When patients with active bleeding were analyzed separately, there was no significant difference in outcome, even though laser photocoagulation stopped active bleeding in 88 percent of cases. Among patients with visible vessels, rebleeding occurred in 5 of 14 (36 percent) who received laser treatment and 2 of 15 (13 percent) who did not. Laser treatment precipitated bleeding in four patients and duodenal perforation in one.

We conclude that Nd:YAG-laser photocoagulation does not benefit patients with acute upper gastrointestinal bleeding from peptic ulcers. (N Engl J Med 1987; 316: 1618–21.)

Funding and Disclosures

We are indebted to the Ralph B. Rodgers Foundation for donating the laser equipment used at Parkland Memorial Hospital; to Drs. Charles B. Mullins and Ron J. Anderson, Chief Executive Officers at Parkland Memorial Hospital, for their support and assistance; to Dr. William J. Fry, Chairman of the Department of Surgery, and his staff for their cooperation; to Dr. Joan Reisch for statistical analysis; to Dr. David Bilheimer, Medical Director, Parkland Memorial Hospital; and to all fellows in gastroenterology in the Dallas training program between 1981 and 1985 (Drs. Marc L. Berger, Lyman Bilhartz, George W. Bo-Linn, Edward D. Carpenter, Thomas J. Colturi, Maria I. Dueno, Stephen J. Ferney, Mary G. Kane, Gerald J. Lieberman, Jonathan B. Meddings, Roger M. Orth, Irving M. Pike, Arthur L. Poch, Ricardo J. Roman, William C. Santangelo, Paul B. Schwartz, William A. Shaver, Charles L. Spurr, Patrick R. Storms, Dwain L. Thiele, Donald E. Vidican, and Howard J. Weiner).

Author Affiliations

From the Departments of Internal Medicine, University of Texas Health Science Center at Dallas, Southwestern Medical School, and Baylor University Medical Center, Dallas. Address reprint requests to Dr. Krejs at the Department of Internal Medicine, Karl-Franzens-University, Auenbruggerplatz 15, A-8036 Graz, Austria.

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