1995
DOI: 10.1128/jcm.33.7.1912-1914.1995
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Sandwich enzyme-linked immunosorbent assay compared with Pastorex latex agglutination test for diagnosing invasive aspergillosis in immunocompromised patients

Abstract: The performance of a direct sandwich enzyme-linked immunosorbent assay (ELISA) for detecting Aspergillus galactomannan was compared with that of the Pastorex Aspergillus antigen latex agglutination (LA) test by using 532 serum samples from 61 patients at risk for invasive aspergillosis. The ELISA gave positive results earlier in the course of infection than did the LA test. A sensitivity of 70% and a specificity of 86% were obtained for the LA test and corresponding values of 90 and 84% were obtained for the E… Show more

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Cited by 175 publications
(66 citation statements)
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“…In our study, 11 of 74 episodes (14AE9%) from the control patient population had an index value of ‡0AE5. The resulting specificity of 85AE1% for a single positive result was significantly lower compared with previously reported specificities using higher cut-off values (Verweij et al, 1995;Sulahian et al, 1996Sulahian et al, , 2001Maertens et al, 1999Maertens et al, , 2001; a similar drop in specificity (from 99AE4% to 88AE7%) has also been reported when the cut-off was reduced from 1AE5 to 0AE6 (Herbrecht et al, 2002b). In addition, accepting a single positive assay of ‡0AE5 as a diagnostic criterion also had a markedly negative impact on PPV and clinical efficiency when compared with a cut-off value of 0AE8, 0AE9 or 1AE0.…”
Section: Static Dynamiccontrasting
confidence: 77%
“…In our study, 11 of 74 episodes (14AE9%) from the control patient population had an index value of ‡0AE5. The resulting specificity of 85AE1% for a single positive result was significantly lower compared with previously reported specificities using higher cut-off values (Verweij et al, 1995;Sulahian et al, 1996Sulahian et al, , 2001Maertens et al, 1999Maertens et al, , 2001; a similar drop in specificity (from 99AE4% to 88AE7%) has also been reported when the cut-off was reduced from 1AE5 to 0AE6 (Herbrecht et al, 2002b). In addition, accepting a single positive assay of ‡0AE5 as a diagnostic criterion also had a markedly negative impact on PPV and clinical efficiency when compared with a cut-off value of 0AE8, 0AE9 or 1AE0.…”
Section: Static Dynamiccontrasting
confidence: 77%
“…10 Introducing a sandwich ELISA technique that incorporates the b 1-5 galactofuranosespecific EBA2 monoclonal antibody as detector for GM, Stynen et al showed considerably improved sensitivity rates due to a significantly lower GM detection limit in vitro (1.0 ng ml )1 serum). 11,12 Using this technique to evaluate the test clinically, Maertens et al prospectively screened 2172 serial blood samples from 186 patients with haematological malig-nancies and found, based on histologically and culturally proven invasive infections, sensitivity and specificity rates of 92.6% and 95.4%, respectively; PPV and NPV were 93% and 95%, respectively. False-positive findings occured in 8%.…”
Section: Serological Assays To Diagnose Invasive Aspergillosismentioning
confidence: 99%
“…8 Methods like enzyme immunoassay, radioimmunoassay and latex agglutination have been used to identify GM in different specimens. 9,10 Commercial kits (Platelia Ò Aspergillus; Bio-Rad Laboratories, Marnes-la-Coquette, France) that use the monoclonal anti-GM antibody EB-A2 as both capture and peroxidase-linked antibodies in sandwich enzyme-linked immunosorbent assay (ELISA) are available. 10,11 While the specificity of the test is quite high, reported sensitivities in different studies display wide variations.…”
Section: Introductionmentioning
confidence: 99%