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Journal of Clinical Microbiology, February 2007, p. 676-677, Vol. 45, No. 2
0095-1137/07/$08.00+0     doi:10.1128/JCM.01940-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.

LETTER TO THE EDITOR

Plasmalyte as a Cause of False-Positive Results for Aspergillus Galactomannan in Bronchoalveolar Lavage Fluid{triangledown}


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LETTER
 
The detection of galactomannan (GM) in the serum of immunocompromised patients is widely used for the early diagnosis of invasive aspergillosis (6). The test may also be useful when applied to bronchoalveolar lavage (BAL) fluid specimens for clinical diagnosis (5), though not FDA approved for this use. One important limiting factor for GM testing is the potential for false-positive results. Most notably, concomitant administration of piperacillin-tazobactam (1, 8) or amoxicillin clavulanate (4) antibiotics can cause false-positive results. This confounder is clinically important as many patients at risk for invasive aspergillosis receive these antibiotics.

Applying antigen detection strategies to BAL fluid diagnostics can be a potentially powerful tool (3, 5). However, it was unclear if a BAL specimen would have inherent problems with measurement of GM as bronchoscopy is not a sterile technique and contaminating fungal elements are often captured as the bronchoscope passes through the upper airway.

As part of an off-label investigation, we recently noted highly positive Aspergillus galactomannan (Platelia aspergillus kit; Bio-Rad) antigen results in 19 consecutive BAL specimens from a single institution from 19 different patients who were treated at a single institution (Table 1). Samples were collected and banked according to institutional review board guidelines for research. The galactomannan index (GMI) was uniformly high (4.1 to 8.2) in these specimens. The BAL fluids were collected for posttransplant surveillance from lung transplant recipients with no evidence of infection, mostly to monitor for allograft rejection. Serum specimens were not tested, however. Fungal cultures yielded no fungal growth in 17 specimens, 1+ Aspergillus fumigatus growth from one specimen, and 2+ Paecilomyces sp. growth from another. This pattern of positivity was not seen with BAL samples from other institutions tested at this laboratory (MiraVista Diagnostics, Indianapolis, IN); about 10% of these specimens are positive, and GMIs are evenly distributed over the positive range from 0.5 to 5.0. Upon further investigation we learned that Plasmalyte (Baxter) was the solution used to perform bronchoalveolar lavage at that institution. Multiple lots of Plasmalyte were subsequently tested and were highly positive for GM (Table 1). We subsequently tested BAL fluids from procedures that were performed using normal saline, and all samples tested negative for Aspergillus galactomannan, as was the saline solution used for lavage.


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  		TABLE 1. Samples tested for GM

False-positive tests can lead to improper medical decision making. In the case of Aspergillus galactomannan testing, false-positive tests are associated with use of antibiotics produced by fermentation in Penicillium (4, 8, 9). Penicillium produces a galactomannan that is recognized by the monoclonal antibody used in the Platelia assay (7).

Plasmalyte contains sodium gluconate, 503 mg/100 ml, which is produced by fermentation in Aspergillus niger (communication with the manufacturer). The false-positive galactomannan antigen results seen with Plasmalyte resemble those observed with piperacillin-tazobactam. In both cases, the false-positive results result from carryover of small amounts of galactomannan during the production of fermentation product, estimated to be about 2 parts/million for sodium gluconate (1 µg galactomannan/503 mg Na gluconate).

We estimated Plasmalyte to contain about 10 ng/ml galactomannan, based upon demonstration that a 1:10 dilution of Plasmalyte yielded a result comparable to the cutoff control (1 ng/ml) provided in the Platelia kit. Thus, 100 ml of Plasmalyte contains about 1 µg of galactomannan. It is unlikely that bronchoalveolar lavage using 100 ml of Plasmalyte (1 µg of galactomannan) causes false-positive antigenemia, especially since more than half of the instilled fluid is recovered during the lavage and the remaining fluid is unlikely to be totally absorbed into the serum.

Whether intravenous administration of Plasmalyte would cause false-positive antigenemia requires further study. One liter of Plasmalyte contains about 10 µg of galactomannan, which would be diluted into the total plasma volume. Assuming that the 10 µg of galactomannan is diluted into 3 to 4 liters of plasma volume (average 70-kg patient), this would yield a concentration greater than 2.5 ng/ml, which is above the sensitivity (0.5 ng/ml) of the galactomannan assay. Furthermore, with repeated infusion, as occurs in fluid replacement therapy, sufficient galactomannan may accumulate to cause false antigenemia, as with piperacillin-tazobactam (2). Furthermore, the mechanism for elimination of galactomannan is unknown, and conditions affecting elimination could facilitate accumulation following repeated administration. Studies with patients are required to address these issues.

In conclusion, Plasmalyte contains small amounts of Aspergillus galactomannan and can cause false-positive results in BAL specimens. Although not demonstrated, intravenous administration of Plasmalyte should also be considered a potential cause for false antigenemia.


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FOOTNOTES
 
{triangledown} Published ahead of print on 13 December 2006. Back


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REFERENCES
 
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Chadi A. Hage*
Indiana University School of Medicine and
Roudebush VA Medical Center
1481 W. 10th St., 111P-IU
Indianapolis, Indiana 46202,1

John M. Reynolds
Methodist Hospital
Indianapolis, Indiana,2

Michelle Durkin
L. Joseph Wheat
MiraVista Diagnostics
Indianapolis, Indiana,3

Kenneth S. Knox
Indiana University School of Medicine and
Roudebush VA Medical Center
Indianapolis, Indiana,4

* Phone: (317) 988-3811
Fax: (317) 988-3976
E-mail: chage{at}iupui.edu

Journal of Clinical Microbiology, February 2007, p. 676-677, Vol. 45, No. 2
0095-1137/07/$08.00+0     doi:10.1128/JCM.01940-06
Copyright © 2007, American Society for Microbiology. All Rights Reserved.



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