Krimer Paula M, Haley Allison C, Harvey Stephen B, Schatzberg Scott J
Athens Veterinary Diagnostic Laboratory and Department of Pathology (Krimer), College of Veterinary Medicine, University of Georgia, Athens, GASmall Animal Medicine and Surgery (Haley), College of Veterinary Medicine, University of Georgia, Athens, GAUniversity Research Animal Resources (Harvey), College of Veterinary Medicine, University of Georgia, Athens, GAThe Animal Neurology & Imaging Center, Algodones, NM (Schatzberg)
Athens Veterinary Diagnostic Laboratory and Department of Pathology (Krimer), College of Veterinary Medicine, University of Georgia, Athens, GASmall Animal Medicine and Surgery (Haley), College of Veterinary Medicine, University of Georgia, Athens, GAUniversity Research Animal Resources (Harvey), College of Veterinary Medicine, University of Georgia, Athens, GAThe Animal Neurology & Imaging Center, Algodones, NM (Schatzberg).
J Vet Diagn Invest. 2016 Mar;28(2):158-64. doi: 10.1177/1040638715626960.
The cell count and differential of cerebrospinal fluid (CSF) cytologic examination classify CSF as inflammatory or not. The cytospin cell yield is related to cell count, but to our knowledge a relationship has not been characterized and cytospin precision is undocumented in any species. The objective of our study was to calculate intra-assay precision of cellular yield and differential on cytocentrifuged canine CSF, determine the factors that may affect precision, and predict the number of cytospins necessary to confirm mild neutrophilic pleocytosis. Ten concurrent replicate cytospins were created from nonhemorrhagic CSF, obtained from 60 dogs in other terminal studies, with either a manual or calibrated pipetting technique. Up to 500 cells per cytospin were counted and classified on each slide. Coefficient of variation (CV), multiple regression, and probabilities were calculated for relationships between cell yield and independent factors including technique, total nucleated cell count, cell differential, and total protein. Manual and calibrated pipetting had similar CVs (average 31%) for total cell yield, but the calibrated technique had fewer foamy macrophages. CV for neutrophil percentage among low cellularity samples with any neutrophils was 146%. Probability based on linear regression showed that 1 cytospin is sufficient to identify samples with >3% neutrophils. Occasional neutrophils, eosinophils, mitotic figures, phagocytic cells, and ependymal cells were seen in many low cellularity canine CSF samples. Canine CSF cytospin cell yield and differential evaluations are imprecise. Calibrated rather than manual pipetting is recommended.
脑脊液(CSF)细胞学检查的细胞计数和分类可将CSF分为炎性或非炎性。细胞离心涂片的细胞产量与细胞计数有关,但据我们所知,这种关系尚未得到明确描述,且在任何物种中细胞离心涂片的精密度都没有文献记载。我们研究的目的是计算犬CSF细胞离心涂片的细胞产量和分类的批内精密度,确定可能影响精密度的因素,并预测确认轻度嗜中性粒细胞增多所需的细胞离心涂片数量。从其他终末研究的60只犬获得的非出血性CSF中,采用手动或校准移液技术同时制作10个重复的细胞离心涂片。每张涂片计数并分类多达500个细胞。计算细胞产量与包括技术、总核细胞计数、细胞分类和总蛋白在内的独立因素之间关系的变异系数(CV)、多元回归和概率。手动和校准移液在总细胞产量方面的CV相似(平均31%),但校准技术产生的泡沫巨噬细胞较少。在有任何嗜中性粒细胞的低细胞数样本中,嗜中性粒细胞百分比的CV为146%。基于线性回归的概率表明,1张细胞离心涂片足以识别嗜中性粒细胞>3%的样本。在许多低细胞数的犬CSF样本中可见偶尔的嗜中性粒细胞、嗜酸性粒细胞、有丝分裂图、吞噬细胞和室管膜细胞。犬CSF细胞离心涂片的细胞产量和分类评估不精确。建议采用校准移液而非手动移液。