2020
DOI: 10.1016/j.ekir.2019.12.008
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Serum Galactomannan Index for the Rapid Diagnosis of Fungal Peritonitis in Patients With Peritoneal Dialysis

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Cited by 6 publications
(10 citation statements)
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“…156 For rapid diagnosis of fungal peritonitis, PD effluent and serum galactomannan index might offer a faster turnaround time than the conventional culture method, but with a diagnostic accuracy of 65.2% sensitivity, 85.0% specificity only. 157,158 False-positive galactomannan results 159 leading to unnecessary use of antifungals is a definite concern.…”
Section: Other Novel Diagnostic Techniquesmentioning
confidence: 99%
“…156 For rapid diagnosis of fungal peritonitis, PD effluent and serum galactomannan index might offer a faster turnaround time than the conventional culture method, but with a diagnostic accuracy of 65.2% sensitivity, 85.0% specificity only. 157,158 False-positive galactomannan results 159 leading to unnecessary use of antifungals is a definite concern.…”
Section: Other Novel Diagnostic Techniquesmentioning
confidence: 99%
“…Therefore, the presence of catheter problems was a protective factor on patients’ mortality in our study. Not surprisingly, a positive galactomannan test (a diagnostic marker for invasive fungal infections and PD-related peritonitis [ 24 , 25 ] and a prognostic marker for invasive aspergillosis in critical illness patients [ 26 ]) was detected less frequently in PDE from patients with yeast peritonitis (61%) than those with mold peritonitis (76–81%). Generally, yeasts contain a low amount of galactomannan in their cell walls, and Pneumocystis jiroveci and Candida spp.…”
Section: Resultsmentioning
confidence: 99%
“…The recommended regimens of antifungal agents used in this study were either of the following: (i) voriconazole 200 mg tablet at a dose of 6 mg/kg/dose twice daily on the first day, followed by 4 mg/kg/dose twice daily for 14 days and (ii) amphotericin B at 1 mg/kg/day in combination with 5-fluorocytosine 500 mg tablet twice daily for 14 days. To mitigate the risk of artifactual serum GM results during blood collection and handling, a protocol collection 7 was emphasized to charge nurses as follows: applying the tourniquet during venous puncture for no longer than 1 minute and avoiding fist-clenching, completing air dry after cleaning the puncture area with 70% alcohol (avoiding iodine-containing or chlorhexidine-containing antiseptic agents), using a 20 to 22 gauge needle, placing the bevel of the needle face-up, collecting blood only from the antecubital region of the arm, pulling the syringe plunger gently, drawing the blood into sterile sodium citrate tube and mixing thoroughly by inverting the tube slowly 3 to 4 times, separating the serum by centrifugation at 150 g for 5 minutes, and shipping the separated serum to the local laboratory. Serum samples were stored at −70 °C until analyzed.…”
Section: Methodsmentioning
confidence: 99%
“…For fungal culture, the pellet from another 50 ml of centrifuged PDE was streaked on Sabouraud dextrose agar, blood agar (Oxoid), and specific agar plates (as needed) then incubated at 25 °C and 37 °C for 15 to 30 days. Bacterial pathogens were identified by Gram stain and Vitek MS system (bioMérieux, USA), 7 whereas fungi were identified by API20c AUX kit (bioMérieux, Marcy l’Etoile, France) based on biochemical reactions and stained by Lactophenol Cotton Blue technique to classify mold-form fungi based on the morphology of their sexual spores and conidia. To exclude coincidental infection with Mycobacterium organisms, the pellet from an additional 50 ml PDE was inoculated in Ogawa medium slants and BACTEC MGIT 960 media for 2 months.…”
Section: Methodsmentioning
confidence: 99%
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