The effect of analyst training on fecal egg counting variability.
Analyst
Automated
Fecal egg count
Horse
McMaster
Wisconsin
Journal
Parasitology research
ISSN: 1432-1955
Titre abrégé: Parasitol Res
Pays: Germany
ID NLM: 8703571
Informations de publication
Date de publication:
Apr 2021
Apr 2021
Historique:
received:
08
12
2020
accepted:
27
01
2021
pubmed:
3
2
2021
medline:
15
5
2021
entrez:
2
2
2021
Statut:
ppublish
Résumé
Fecal egg counts (FECs) are essential for veterinary parasite control programs. Recent advances led to the creation of an automated FEC system that performs with increased precision and reduces the need for training of analysts. However, the variability contributed by analysts has not been quantified for FEC methods, nor has the impact of training on analyst performance been quantified. In this study, three untrained analysts performed FECs on the same slides using the modified McMaster (MM), modified Wisconsin (MW), and the automated system with two different algorithms: particle shape analysis (PSA) and machine learning (ML). Samples were screened and separated into negative (no strongylid eggs seen), 1-200 eggs per gram of feces (EPG), 201-500 EPG, 501-1000 EPG, and 1001+ EPG levels, and ten repeated counts were performed for each level and method. Analysts were then formally trained and repeated the study protocol. Between analyst variability (BV), analyst precision (AP), and the proportion of variance contributed by analysts were calculated. Total BV was significantly lower for MM post-training (p = 0.0105). Additionally, AP variability and analyst variance both tended to decrease for the manual MM and MW methods. Overall, MM had the lowest BV both pre- and post-training, although PSA and ML were minimally affected by analyst training. This research illustrates not only how the automated methods could be useful when formal training is unavailable but also how impactful formal training is for traditional manual FEC methods.
Identifiants
pubmed: 33527172
doi: 10.1007/s00436-021-07074-2
pii: 10.1007/s00436-021-07074-2
doi:
Types de publication
Journal Article
Langues
eng
Sous-ensembles de citation
IM
Pagination
1363-1370Références
Auger J, Eustache F, Ducot B, Blandin T, Daudin M, Diaz I, El Matribi S, Gony B, Keskes L, Kolbezen M, Lamarte A, Lornage J, Nomal N, Pitaval G, Simon O, Virant-Klun I, Spira A, Jouannet P (2000) Intra- and inter-individual variability in human sperm concentration, motility, and vitality assessment during a workshop involving ten laboratories. Hum Reprod 15(11):2360-2368
Cain JL, Slusarewicz P, Rutledge MH, McVey MR, Wielgus KM, Zynda HM, Wehling LM, Scare JA, Steuer AE, Nielsen MK (2020) Diagnostic performance of McMaster, Wisconsin, and automated egg counting techniques for enumeration of equine strongyle eggs in fecal samples. Vet Parasitol 284:109199
doi: 10.1016/j.vetpar.2020.109199
Calvete C, Uriarte J (2013) Improving the detection of anthelmintic resistance: evaluation of faecal egg count reduction test procedures suitable for farm routines. Vet Parasitol 196:438–452
doi: 10.1016/j.vetpar.2013.02.027
Carstensen H, Larsen L, Ritz C, Nielsen MK (2013) Daily variability of strongyle fecal egg counts in horses. J Equine Vet Sci 33(3):161–164
doi: 10.1016/j.jevs.2012.06.001
Coles GC, Bauer C, Borgsteede FHM, Geerts S, Klei TR, Taylor A, Waller PJ (1992) World Association for the Advancement of Veterinary Parasitology (W.A.A.V.P.) methods for the detection of anthelmintic resistance in nematodes of veterinary importance. Vet Parasitol 44:35–44
doi: 10.1016/0304-4017(92)90141-U
ESCCAP (2019) A guide to the treatment and control of equine gastrointestinal parasite infections. 2nd edition. European Scientific Counsel Companion Animal Parasites. https://www.esccap.org/uploads/docs/rtjqmu6t_0796_ESCCAP_Guideline_GL8_v7_1p.pdf . Accessed 5 October 2020
Kaplan R (2013) Recommendations for control of gastrointestinal nematode parasites in small ruminants: these ain’t your father’s parasites. Bovine Pr 47(2):97–109
Kaplan RM, Nielsen MK (2010) An evidence-based approach to equine parasite control: it ain’t the 60s anymore. Equine Vet Educ 22:306–316
doi: 10.1111/j.2042-3292.2010.00084.x
Kaplan R, Vidyashankar A (2012) An inconvenient truth: global worming and anthelmintic resistance. Vet Parasitol 186(1-2):70–78
doi: 10.1016/j.vetpar.2011.11.048
Kenyon F, Jackson F (2012) Targeted flock/herd and individual ruminant treatment approaches. Vet Parasitol 186(1-2):10–17
doi: 10.1016/j.vetpar.2011.11.041
Li Y, Zheng R, Wu Y, Chu K, Xu Q, Sun M, Smith ZJ (2019) A low-cost, automated parasite diagnostic system via a portable, robotic microscope and deep learning. J Biophotonics 12(9):e201800410
pubmed: 31081258
Mariee N, Tuckrman E, Ali A, Li W, Laird S, Li TC (2012) The observer and cycle-to-cycle variability in the measurement of uterine natural killer cells by immunohistochemistry. J Reprod Imm 95:93–100
doi: 10.1016/j.jri.2012.05.001
Mes THM, Eysker M, Ploeger HW (2007) A simple, robust and semi-automated parasite egg isolation protocol. Nat Prot 2:486–489
doi: 10.1038/nprot.2007.56
Nielsen MK, Mittel L, Grice A, Erskine M, Graves E, Vaala W, Tully RC, French D D, Bowman R, Kaplan RM (2019) AAEP parasite control guidelines. https://aaep.org/sites/default/files/Guidelines/AAEPParasiteControlGuidelines_0.pdf . Accessed 5 October 2020
Noel ML, Scare JA, Bellaw JL, Nielsen MK (2017) Accuracy and precision of mini-FLOTAC and McMaster techniques for determining equine strongyle egg counts. J Equine Vet Sci 48:1–6
doi: 10.1016/j.jevs.2016.09.006
O’Brien D (2018) Managing dewormer resistance. American Consortium for Small Ruminant Parasite Control. https://60f7303d-ac52-4cac-b7fb-6050f500b0b6.filesusr.com/ugd/6ef604_3981789ca4d34d74913834b1ea1b0b16.pdf . Accessed 12 October 2020
Peregrine AS, Molento MB, Kaplan RM, Nielsen MK (2014) Anthelmintic resistance in important parasites of horses: does it really matter? Vet Parasitol 201:1–8
doi: 10.1016/j.vetpar.2014.01.004
Popović ZB, Thomas JD (2017) Assessing observer variability: a user’s guide. Cardiovasc Diagn Ther 7(3):317–324
doi: 10.21037/cdt.2017.03.12
Powell K, Kwee E, Nutter B, Herderick E, Paul P, Thut D, Boehm C, Muschler G (2016) Variability in subjective review of umbilical cord blood colony forming unit assay. Cytometry B Clin Cytom 90(6):517–524
doi: 10.1002/cyto.b.21376
R Core Team (2019) R: a language and environment for statistical computing. R Foundation for Statistical Computing. Vienna, Austria. https://www.R-project.org/ . Accessed 5 October 2020
Rendle D, Austin C, Bowen M, Cameron I, Furtado T, Hodgkinson J, McGorum B, Matthews J (2019) Equine de-worming: a consensus on current best practice. UK-Vet Equine 3:1):1–1)14
Slusarewicz M, Slusarewicz P, Nielsen MK (2019) The effect of counting duration on quantitative fecal egg count test performance. Vet Par: X 2:100020
Slusarewicz P, Pagano S, Mills C, Popa G, Chow KM, Mendenhall M, Rodgers DW, Nielsen MK (2016) Automated parasite faecal egg counting using fluorescence labelling, smartphone image capture and computational image analysis. Int J Parasitol 46:485–493
doi: 10.1016/j.ijpara.2016.02.004
Suzuki CTN, Gomes JF, Falcão AX, Papa JP, Hoshino-Shimizu S (2013) Automatic segmentation and classification of human intestinal parasites from microscopy images. IEEE Trans Bio-med Eng 60:803–812
doi: 10.1109/TBME.2012.2187204
Vidyashankar AN, Hanlon BM, Kaplan RM (2012) Statistical and biological considerations in evaluating drug efficacy in equine strongyle parasites using fecal egg count data. Vet Parasitol 185:45–56
doi: 10.1016/j.vetpar.2011.10.011
Yang YS, Park DK, Kim HC (2001) Automatic identification of human helminth eggs on microscopic fecal specimens using digital image processing and an artificial neural network. IEEE Trans Bio-med Eng 48:718–730
doi: 10.1109/10.923789