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马的床边和实验室主要交叉配血试验与参考标准方法的一致性。

Agreement of stall-side and laboratory major crossmatch tests with the reference standard method in horses.

机构信息

Cornell University, Department of Clinical Sciences, College of Veterinary Medicine, Ithaca, New York.

Cornell University, Department of Population Medicine and Diagnostic Sciences, College of Veterinary Medicine, Ithaca, New York.

出版信息

J Vet Intern Med. 2020 Mar;34(2):941-948. doi: 10.1111/jvim.15710. Epub 2020 Feb 4.

Abstract

BACKGROUND

Crossmatching is used to prevent life-threatening transfusion reactions in horses. Laboratory methods are laborious and technically challenging, which is impractical during emergencies.

HYPOTHESIS/OBJECTIVES: Evaluate agreement between a stall-side crossmatch kit (KIT) and a laboratory method (LAB) in horses with known and unknown blood types.

ANIMALS

Twenty-four blood-typed and alloantibody-screened healthy adult horses (Aim 1) and 156 adult horses of unknown blood type (Aim 2).

METHODS

Prospective, blinded study. Expected positive (n = 35) and negative (n = 36) crossmatches among 24 antibody and blood-typed horses were used to determine sensitivity and specificity of KIT and LAB against the reference method. Agreement in 156 untyped horses was evaluated by reciprocal crossmatch (n = 156).

RESULTS

Sensitivity (95% confidence interval [CI]) for LAB and KIT compared with expected reactions was 77.1% (59.9%-90.0%) and 91.4% (77.0%-98.2%), and specificity 77.8% (60.9%-89.9%) and 73.5% (55.6%-87.1%), respectively. The KIT was 100% sensitive for Aa reactions; LAB was 100% sensitive for Qab; and both were 100% sensitive for Ca. Cohen's κ agreement for LAB and KIT with expected positive and negative reactions (n = 71) was moderate (0.55 [0.36-0.74]) and substantial (0.65 [0.47-0.82]), respectively. Agreement was fair comparing LAB with KIT in Aim 1 (0.30 [0.08-0.52]) and in untyped horses in Aim 2 (0.26 [0.11-0.41]).

CONCLUSIONS AND CLINICAL IMPORTANCE

Agreement between KIT and LAB with expected reactions was blood type dependent. Performance of both methods depends on blood type prevalence.

摘要

背景

配血用于预防马的危及生命的输血反应。实验室方法既繁琐又具有技术挑战性,在紧急情况下不切实际。

假设/目的:评估已知和未知血型的马中,床边配血试剂盒(KIT)和实验室方法(LAB)之间的一致性。

动物

24 匹经过血型和同种抗体筛查的健康成年马(目的 1)和 156 匹未知血型的成年马(目的 2)。

方法

前瞻性、盲法研究。使用 24 匹抗体和血型马中预期的阳性(n = 35)和阴性(n = 36)配血来确定 KIT 和 LAB 相对于参考方法的灵敏度和特异性。通过相互配血(n = 156)评估 156 匹未分型马的一致性。

结果

与预期反应相比,LAB 和 KIT 的灵敏度(95%置信区间[CI])分别为 77.1%(59.9%-90.0%)和 91.4%(77.0%-98.2%),特异性分别为 77.8%(60.9%-89.9%)和 73.5%(55.6%-87.1%)。KIT 对 Aa 反应的灵敏度为 100%;LAB 对 Qab 的灵敏度为 100%;两者对 Ca 的灵敏度均为 100%。LAB 和 KIT 与预期的阳性和阴性反应(n = 71)的 Cohen's κ 一致性为中度(0.55 [0.36-0.74])和高度(0.65 [0.47-0.82])。在目的 1 中,LAB 与 KIT 之间的一致性为适度(0.30 [0.08-0.52]),在目的 2 中,未分型马之间的一致性为适度(0.26 [0.11-0.41])。

结论和临床意义

KIT 和 LAB 与预期反应的一致性取决于血型。两种方法的性能都取决于血型的流行程度。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/61bd/7096648/0b3fabc71c12/JVIM-34-941-g001.jpg

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