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Clinical Trial
. 1990 Jul-Sep;36(3):M497-500.

A prospective randomized evaluation of chronic peritoneal catheters. Insertion site and intraperitoneal segment

Affiliations
  • PMID: 2252732
Clinical Trial

A prospective randomized evaluation of chronic peritoneal catheters. Insertion site and intraperitoneal segment

J Rubin et al. ASAIO Trans. 1990 Jul-Sep.

Abstract

The insertion site (midline or through the lateral rectus muscle) and type of chronic dialysis catheter (straight or spiral intraperitoneal segment) were evaluated in a prospective randomized trial. Dialysis catheter complications and catheter survival were the endpoints of evaluation. Eighty-five first catheters were evaluated. Neither race, gender, renal diagnosis, type of catheter, nor insertion site was a determinant of dialysis catheter survival. Overall median catheter survival was 308 days. There were 40 catheter complications (70%, n = 28) that occurred during the first 61 days following insertion. Median time to the first complication occurring within the first 61 days was 3 days. Late catheter removals were due to peritonitis episodes that failed to resolve. Complications are frequent with peritoneal dialysis catheters, and care of the peritoneal dialysis catheters requires constant vigilance.

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