A prospective, randomized, controlled study was conducted to identify patients with end-stage renal disease who required open peritoneal dialysis catheterization, preoperative enema or no enema was used to evaluate the efficacy and safety of reducing catheter dysfunction.
A prospective, randomized, controlled study was conducted to identify patients with end-stage renal disease who required open peritoneal dialysis catheterization, preoperative enema or no enema was used to evaluate the efficacy and safety of reducing catheter dysfunction. All the patients were divided into two groups: preoperative enema group and no intervention group. The peritoneal dialysis malfuction were observed.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
PREVENTION
Masking
NONE
Enrollment
136
preoperative enema
Incidence of Catheter dysfunction requiring intervention within 3 months of peritoneal dialysis catheterization
Time frame: 3 months
Time of first peritoneal dialysis catheter dysfunction
Time frame: 6 months
Incidence of Catheter dysfunction requiring intervention within 6 months of peritoneal dialysis catheterization
Time frame: 6 months
Catheter survival time
Time frame: 6 months
Incidence of peritoneal dialysis-associated Peritonitis
Time frame: 6 months
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