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  Vol. 104 No. 6, June 1972 TABLE OF CONTENTS
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  PAPERS READ BEFORE THE ANNUAL MEETING OF THE SOUTHERN CALIFORNIA CHAPTER OF THE AMERICAN COLLEGE OF SURGEONS, SANTA BARBARA, CALIF, JAN 14-16, 1972
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Surgery in Patients With Sickle Cell Disease

Auri Spigelman, MD; M. James Warden, MD

AMA Arch Surg. 1972;104(6):761-764.


Abstract

Between 1962 and 1971, a total of 12 children and adolescents underwent 29 surgical procedures without operative mortality, but with significant postoperative morbidity. Biliary tract disease was the most frequent indication for surgery. Infections and pulmonary problems were common and often difficult to control. Severe complications were prevented by preoperative transfusion, adequate hydration, and the avoidance of hypoxia, acidosis, hyperosmolality, and capillary erythrostasis. A sickle cell preparation or hemoglobin electrophoresis is advised for every black child and adolescent prior to contemplated, elective surgery.



Author Affiliations

Los Angeles

From the Department of Surgery, Kaiser Foundation Hospital, Los Angeles.


Footnotes

Accepted for publication Feb 15, 1972.

Read before the annual meeting of the Southern California Chapter of the American College of Surgeons, Santa Barbara, Calif, Jan 14, 1972.

Reprint requests to 1526 N Edgemont St, Los Angeles 90027 (Dr. Warden).



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Partial Exchange Transfusion in Sickle Cell Anemia: Use in Children With Serious Complications
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