1990
DOI: 10.1177/089686089001000113
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Comparison of Large Volume Culture to Other Methods for Isolation of Microorganisms from Dialysate

Abstract: Patients on continuous ambulatory peritoneal dialysis (CAPD) who reside long distances from a CAPD center often use community medical laboratories to document and manage episodes of peritonitis. We examined the feasibility of using large volume cultures as an alternative to more costly and labor intensive methods and to enhance earlier recovery of microorganisms from these patients. Three methods of processing dialysate from patients on CAPD were compared: (a) inoculation of 400 mL dialysate into a transfer b… Show more

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Cited by 58 publications
(36 citation statements)
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“…is due to another cause (e.g., lipopolysaccharide [8,15,17]). Elevated leukocyte counts in the dialysates of patients just starting CAPD has been described (15).…”
Section: Discussionmentioning
confidence: 99%
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“…is due to another cause (e.g., lipopolysaccharide [8,15,17]). Elevated leukocyte counts in the dialysates of patients just starting CAPD has been described (15).…”
Section: Discussionmentioning
confidence: 99%
“…is due to another cause (e.g., lipopolysaccharide [8,15,17]). Elevated leukocyte counts in the dialysates of patients just starting CAPD has been described (15). Differentiating inflammation due to other causes from true microbial infection is an important issue, since antimicrobial therapy may have little value in these patients and indeed may be detrimental, because it could contribute to the development of increased resistance by the normal flora of patients on CAPD.…”
Section: Discussionmentioning
confidence: 99%
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“…5,16 These problems are, at least, partly obviated by culturing at least 10 mL of dialysate effluent 17 following dwells of at least 4 h, and sending the cultures to the laboratory for processing within 12 h. 16 Culture yields in the microbiology laboratory may also be augmented by using enrichment broth with antiphagocytic and lytic properties, 5 and semiautomated blood culture systems. 18 Subcultures of the enrichment should at least be performed on aerobic chocolate agar and anaerobic blood agar for a period of at least 7 days. One medium should also be incubated at 30 ° C to avoid missing peritonitis caused by psychrophilic microorganisms (such as Rhodotorula glutiris and certain Pseudomonas species).…”
Section: Associate Professor David Johnsonmentioning
confidence: 99%