The effect of inadequate drying of blood spots on newborn screening analyte concentrations.

IF 2.1 4区 医学 Q3 MEDICAL LABORATORY TECHNOLOGY
Stuart J Moat, Melissa Levi, Margaret Birch, Nadia Worlock, Chandra Sundas, Lucy Woodcock, Jude Kay, Sikha de Souza, Annabel Rodham
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Abstract

BackgroundA critical pre-analytical phase of newborn screening (NBS) testing involves the drying of blood applied to the blood collection devices to form the dried blood spots (DBS). Guidance states that blood applied should be air-dried for a minimum of 3 h. A recent survey highlighted that a number of DBS specimens routinely received into laboratories have a 'crinkled' appearance and that DBS specimens collected in a hospital setting are transported to the laboratory in sealed plastic bags. To date no scientific studies have evaluated aspects of blood drying on DBS NBS analyte concentrations.MethodsWe undertook experiments to recreate 'crinkled' DBS specimens in the laboratory and assess the impact on analyte concentrations. We also assessed the impact of storing collection devices following blood application in hermetically sealed plastic bags to impede the drying process. Experiments were performed using whole blood enriched with thyroid stimulating hormone, immunoreactive trypsinogen, phenylalanine, tyrosine, leucine, methionine, octanoyl-carnitine, decanoyl-carnitine, isovaleryl-carnitine and glutaryl-carnitine to pathophysiological concentrations.Results'Crinkled' DBS specimens produced significantly lower results (mean -15.5%, range -25.1 to -4.7%) for all analytes measured versus air-dried DBS specimens (P < .05). Analyte concentrations obtained from DBS specimens following storage in plastic bags before drying were significantly lower (mean -41.6%, range -60.0 to -27.6%) for all analytes measured (P < .05) versus air-dried DBS specimens.ConclusionResults from this study demonstrate that all DBS specimens with a crinkled appearance and those received in plastic specimen bags should be rejected and a repeat specimen collected to prevent erroneous screening results.

血斑干燥不足对新生儿筛查分析物浓度的影响。
新生儿筛查(NBS)检测的关键前分析阶段涉及将血液干燥应用于采血装置以形成干燥血斑(DBS)。指南指出,所使用的血液应至少风干3小时。最近的一项调查强调,常规送到实验室的一些DBS标本有“褶皱”外观,而在医院环境中收集的DBS标本是用密封的塑料袋运送到实验室的。到目前为止,还没有科学研究评估了血液干燥对DBS NBS分析物浓度的影响。方法在实验室中重建“起皱”的DBS标本,并评估其对分析物浓度的影响。我们还评估了在血液应用后将收集装置储存在密封塑料袋中以阻碍干燥过程的影响。实验采用全血富集促甲状腺激素、免疫反应性胰蛋白酶原、苯丙氨酸、酪氨酸、亮氨酸、蛋氨酸、辛酰肉碱、癸酰肉碱、异戊酰肉碱和戊酰肉碱至病理生理浓度。与风干DBS标本相比,“褶皱”DBS标本产生的所有分析物的结果显着降低(平均-15.5%,范围-25.1至-4.7%)(P < 0.05)。与风干DBS标本相比,在干燥前将DBS标本储存在塑料袋中获得的分析物浓度显著降低(平均-41.6%,范围-60.0至-27.6%)(P < 0.05)。结论本研究结果表明,所有外观皱褶的DBS标本和塑料标本袋中收到的DBS标本均应被拒绝,并重复采集标本,以防止错误的筛选结果。
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来源期刊
Annals of Clinical Biochemistry
Annals of Clinical Biochemistry Biochemistry, Genetics and Molecular Biology-Clinical Biochemistry
CiteScore
5.20
自引率
4.50%
发文量
61
期刊介绍: Annals of Clinical Biochemistry is the fully peer reviewed international journal of the Association for Clinical Biochemistry and Laboratory Medicine. Annals of Clinical Biochemistry accepts papers that contribute to knowledge in all fields of laboratory medicine, especially those pertaining to the understanding, diagnosis and treatment of human disease. It publishes papers on clinical biochemistry, clinical audit, metabolic medicine, immunology, genetics, biotechnology, haematology, microbiology, computing and management where they have both biochemical and clinical relevance. Papers describing evaluation or implementation of commercial reagent kits or the performance of new analysers require substantial original information. Unless of exceptional interest and novelty, studies dealing with the redox status in various diseases are not generally considered within the journal''s scope. Studies documenting the association of single nucleotide polymorphisms (SNPs) with particular phenotypes will not normally be considered, given the greater strength of genome wide association studies (GWAS). Research undertaken in non-human animals will not be considered for publication in the Annals. Annals of Clinical Biochemistry is also the official journal of NVKC (de Nederlandse Vereniging voor Klinische Chemie) and JSCC (Japan Society of Clinical Chemistry).
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