Abstract

Galactomannan (GM) is widely used for detection of invasive aspergillosis in high-risk haemato-oncology patients. Recent publications have reported a lack of repeatability of GM detection. The objective of this retrospective study was to assess the repeatability of GM levels during storage of clinical samples. In a GM screening strategy, positive sera were repeat tested as per manufacturer’s recommendations. Short-term (ST) storage of samples was at +4 °C while long-term (LT) storage was at −80 °C. Bronchoalveolar (BAL) fluid was also repeating tested after ST storage and LT storage. Wilcoxon Signed Ranks Test was employed to assess the repeatability of GM levels. In a subset of 14 GM positive sera, repeat testing was performed on both the original serum and ethylenediaminetetraacetic acid (EDTA) pre-treated sample. There was a significant reduction in GM signals on repeat testing following ST storage (median GM index: 0.65 vs. 0.19; p < 0.001) and LT storage (median GM index: 0.56 vs. 0.10; p < 0.001) of serum samples. Of samples that were initially GM positive, an average GM index reduction of 50% was seen, with approximately two-thirds becoming GM negative on repeat testing of the same sample. In contrast, GM signal loss was not seen on repeat testing of BAL fluid following ST or LT storage. When GM positive serum samples were repeat tested using EDTA pre-treated serum from the first step of the testing protocol, all samples remained GM positive. In contrast, when the same samples were repeat tested from the original collected serum, 9 samples (64%) became GM negative. The significant reduction in GM signals during ST and LT storage of serum samples has implications for clinical management. Although the reasons for GM decline are unknown, they occur prior to the EDTA pre-treatment stage, indicating that the time from phlebotomy to testing should be minimized. BAL fluid GM index values remain stable.

Highlights

  • Invasive pulmonary aspergillosis (IA) remains a life-threatening opportunistic invasive mycosis in immunocompromised patients [1]

  • Bizzini et al [6] report a similar reduction in reactivity of samples on retesting of positive samples within three days, with lower values in 23/29 (79%) repeats. These observations raise doubts about the interpretation of data from frozen/thawed samples, as well as samples tested in “real-time” for patient management. The aim of this retrospective study was to clarify the effects of sample storage on the repeatability of GM levels using the Platelia Aspergillus enzyme immunoassay (PA-EIA)

  • We have published our rate of invasive fungal disease (IFD) using the EORTC/MSG criteria of probable/proven IFD, which are usually regarded as representing true cases, as only 8/589 episodes (1.4%) by 2008 and 20/589 (3.5%) by 2002 criteria [8]

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Summary

Introduction

Invasive pulmonary aspergillosis (IA) remains a life-threatening opportunistic invasive mycosis in immunocompromised patients [1]. Bizzini et al [6] report a similar reduction in reactivity of samples on retesting of positive samples within three days, with lower values in 23/29 (79%) repeats. These observations raise doubts about the interpretation of data from frozen/thawed samples, as well as samples tested in “real-time” for patient management. The aim of this retrospective study was to clarify the effects of sample storage on the repeatability of GM levels using the PA-EIA

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