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. 2022 May 12;15:166. doi: 10.1186/s13071-022-05266-y

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© The Author(s) 2022

Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.

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Fig. 3 — Comparison of number of epg obtained with the M-FLOTAC and FECPAK^G2 methods for strongyle (a) and Parascaris spp. (b) nematode eggs. To allow a logarithmic presentation, 0.1 was added to all values. The number of samples negative for strongyle eggs was 19 for the Mini-FLOTAC and 137 for the FECPAK^G2 method, respectively. For Parascaris spp., 1024 and 1047 samples were negative with the Mini-FLOTAC and FECPAK^G2 methods, respectively. Even though more samples were positive with Mini-FLOTAC than with FECPAK^G2, the mean number of strongyle epgs was significantly lower (P = 0.017) for Mini-FLOTAC than for FECPAK^G2 applying a paired Student’s t-test. For Parascaris spp. epgs, higher mean epgs were measured with Mini-FLOTAC than with to FECPAK^G2 (P = 0.0007). Asterisks indicate a significant difference at ***P < 0.001 and *P < 0.05