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1.
Perit Dial Int ; 11(3): 213-6, 1991.
Article in English | MEDLINE | ID: mdl-1912015

ABSTRACT

Pseudomonas species infections in the peritoneal dialysis population consist primarily of peritonitis or exit site infections. These organisms have traditionally proven difficult to eradicate, and the standard antibiotic regimen has carried the potential for nephrotoxicity. At our institution, all peritoneal dialysis patients with Pseudomonas exit site infections or peritonitis were treated with an antibiotic combination of intraperitoneal ceftazidime and oral ciprofloxacin. Treatment duration was dependent upon the site of infection. Recurrent exit site infections were treated with a repeated course of the antibiotics, and with surgical debridement and subsequent shaving of the external cuff of double-cuffed catheters. We saw a total of 11 Pseudomonas aeruginosa exit site infections in 7 patients (4 recurrent). Patients with recurrent infections were subsequently cured with the regimen as outlined above. Of 7 patients with Pseudomonas species peritonitis (aeruginosa, fluorescens, stutszeri, and maltophilia), 5 were cured with the initial antibiotic regimen. The 2 failures were both infected with Pseudomonas maltophilia, which is consistent with observed organism sensitivity data. The combination of ceftazidime and ciprofloxacin with the option for surgical debridement of the external cuff (in exit site infections) appears effective in the treatment of Pseudomonas species infections in the peritoneal dialysis population. Sensitivity data should be used to adjust the antibiotic regimen when appropriate.


Subject(s)
Peritoneal Dialysis, Continuous Ambulatory/adverse effects , Peritonitis/drug therapy , Pseudomonas Infections/drug therapy , Ceftazidime/administration & dosage , Ceftazidime/pharmacokinetics , Ceftazidime/therapeutic use , Ciprofloxacin/administration & dosage , Ciprofloxacin/pharmacokinetics , Ciprofloxacin/therapeutic use , Drug Therapy, Combination/therapeutic use , Humans , Microbial Sensitivity Tests , Peritonitis/etiology , Peritonitis/microbiology , Pseudomonas/drug effects , Pseudomonas Infections/etiology
2.
ASAIO Trans ; 35(3): 322-4, 1989.
Article in English | MEDLINE | ID: mdl-2597473

ABSTRACT

With increasing recognition of problems regarding the use of aluminum hydroxide as a phosphate binder, calcium carbonate has become the medication of choice. Use of calcium has, however, frequently been associated with development of hypercalcemia. At this institution, calcium carbonate powder as a phosphate binder, examination of its efficacy, and the frequency of hypercalcemia with its use were of great interest. Calcium carbonate powder (CalCarb-HD, 2.4 gms elemental calcium/packet) (CalCarb-HD, Lafayette Pharmacal Inc., Fort Worth, TX) was used in the study. Twenty-one end-stage renal disease (ESRD) patients (17 hemodialysis and 4 chronic ambulatory peritoneal dialysis) were chosen and converted from their previous binder (primarily, calcium carbonate tablets) to calcium powder. The dosage was adjusted to keep phosphorus levels at 3.5 to 5.5 mg/dl and calcium less than 11.5 mg/dl. At 2 months, the average calcium level in the 16 patients remaining in the study was 9.2 mg/dl, and the average phosphorus level was 5.2 mg/dl with an average calcium dose of 1.4 packets/day. By 7 months, the 8 patients remaining in the study had an average calcium level of 9.9 mg/dl with an average phosphorus level of 5.5 mg/dl; average calcium dose was 1.8 packets/day. Total episodes of hypercalcemia (calcium greater than 11.5 mg/dl) were two. Calcium carbonate powder appears to be an effective phosphate binder in the ESRD population. The relatively few episodes of hypercalcemia may be related to possible enhanced bioavailability of the compound secondary to its powdered form.


Subject(s)
Calcium Carbonate/administration & dosage , Kidney Failure, Chronic/therapy , Peritoneal Dialysis, Continuous Ambulatory , Phosphates/blood , Renal Dialysis , Adult , Aged , Calcium/blood , Humans , Kidney Failure, Chronic/blood , Middle Aged , Powders
3.
Adv Perit Dial ; 5: 227-8, 1989.
Article in English | MEDLINE | ID: mdl-2577418

ABSTRACT

Intraluminal transmission of bacteria remains a significant factor in the morbidity and procedural success of CAPD. A worsening rate of peritonitis in a longstanding CAPD program (first patients 1978) led to a search for a system which might allow a lesser rate of peritonitis. Simplicity in the procedure was a requirement. For this reason disconnect systems were not considered. The Travenol spike system was prospectively compared with Delmed leur lock in terms of rate of peritonitis and difficulty in training. The former had been used by the center since inception of the CAPD program. 28 patients new to CAPD were alternately assigned to each system without other bias, including diagnosis, age, sex, or race. The study, while ongoing, was analyzed at 12 months. 66 patient months were involved with each system. The peritonitis rates were: 2.2 episodes: patient year with the Travenol; 0.9 episode:patient year for the Delmed systems. The Delmed system appears to provide a lower rate of peritonitis. In addition, less manual dexterity, steadiness, and hand eye coordination are necessary.


Subject(s)
Peritoneal Dialysis, Continuous Ambulatory/instrumentation , Adult , Aged , Humans , Middle Aged , Patient Dropouts , Peritoneal Dialysis, Continuous Ambulatory/adverse effects , Peritonitis/etiology
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