测试ID:l你pn

羽扇豆,Ige,血清

对...有用
建议临床疾病或测试可能有帮助的临床疾病或设置

establishing the diagnosis of an allergy to lupin

定义负责引起体征和症状的过敏原

我dentifying allergens:

- 负责过敏性疾病和/或过敏性发作

- 在开始免疫疗法之前确认敏化

- 研究对昆虫毒液,药物或化学过敏原的过敏反应的特异性

对IgE抗体的测试是没有用在先前接受免疫疗法治疗的患者中,以确定是否存在残留的临床敏感性,或者医疗管理不依赖过敏原特异性的患者。

特别说明
library of PDFs including pertinent information and forms related to the test

方法名称
Ashort description of the method used to perform the test

荧光enzyme免疫测定(FEIA)

纽约州可用
我ndicates the status of NY State approval and if the test is orderable for NY State clients.

是的

报告名称
列出了测试的已发表名称的简短或缩写版本

lupin, IgE

别名
lists additional common names for a test, as an aid in searching

蓝色羽扇豆(lupinus angustifolius)

lupin

羽扇豆

lupinus albus

Lupinus sativus

Lupinus termis

sweet Lupin

白色羽扇豆(羽扇豆)

yellow Lupin (Lupinus luteus)

specimen Type
描述了测试验证的样品类型

血清

ordering Guidance

需要标本
定义执行测试所需的最佳标本和首选卷以完成测试

Container/Tube:

首选:红色上衣

Acceptable:血清凝胶

specimen Volume:每5个过敏原的每50毫升

特别说明
library of PDFs including pertinent information and forms related to the test

形式

标本最小体积
定义由测试实验室确定的提供临床相关结果所需的样本数量

对于1个过敏原:0.3 ml

more than 1 allergen: (0.05 mL x number of allergens) + 0.25 mL dead space

reject Due To
标识可能导致样品被拒绝的样本类型和条件

严重的溶血 好的
高脂肪血症 好的

标本稳定性信息
提供了将样品运输到表演实验室所需的温度的描述,还包括可接受的温度

specimen Type 温度 时间 特殊容器
血清 冷藏(首选) 14天
Frozen 90天

对...有用
建议临床疾病或测试可能有帮助的临床疾病或设置

establishing the diagnosis of an allergy to lupin

定义负责引起体征和症状的过敏原

我dentifying allergens:

- 负责过敏性疾病和/或过敏性发作

- 在开始免疫疗法之前确认敏化

- 研究对昆虫毒液,药物或化学过敏原的过敏反应的特异性

对IgE抗体的测试是没有用在先前接受免疫疗法治疗的患者中,以确定是否存在残留的临床敏感性,或者医疗管理不依赖过敏原特异性的患者。

Clinical Information
discusses physiology, pathophysiology, and general clinical aspects, as they relate to a laboratory test

直接过敏性(过敏性)的临床表现疾病是由促炎介质的释放引起的(组胺,白细胞和前列腺素)来自免疫球蛋白E(IgE)敏感性效应细胞(肥大细胞和嗜碱性粒细胞)bound IgE antibodies interact with allergen.

IgE抗体的体外血清测试提供了表明immune response to allergen that may be associated with allergic疾病。

选择进行测试的过敏原通常取决于患者,过敏原暴露史,一年中的季节和临床manifestations. In individuals predisposed to develop allergic disease,随着敏化和临床表现的顺序,随着follows: eczema and respiratory disease (rhinitis and bronchospasm)由于食物敏感性,婴儿和儿童<5岁(牛奶,egg, soy, and wheat proteins) followed by respiratory disease (rhinitis由于对吸入剂的敏感性,在大龄儿童和成人中)allergens (dust mite, mold, and pollen inhalants).

reference Values
describes reference intervals and additional information for interpretation of test results. May include intervals based on age and sex when appropriate. Intervals are Mayo-derived, unless otherwise designated. If an interpretive report is provided, the reference value field will state this.

班级

我gE kU/L

解释

0

<0.35

消极的

1

0.35-0.69

模棱两可

2

0.70-3.49

积极的

3

3。50-17.4

积极的

4

17.5-49.9

strongly positive

5

50。0-99.9

strongly positive

6

>或= 100

strongly positive

参考值适用于所有年龄段。

解释
提供信息以帮助解释测试结果

警告
讨论可能导致诊断混乱的条件,包括标本收集和处理不当,不适当的测试选择以及干扰物质

一些对过敏原临床敏感性微不足道的个体可能具有可测量的血清中IgE抗体水平,并且必须在临床背景下解释结果。

False-positive results for IgE antibodies may occur in patients with markedly elevated serum IgE (>2500 kU/L) due to nonspecific binding to allergen solid phases.

Clinical Reference
深入阅读临床性质的建议

Homburger HA, Hamilton RG: Allergic diseases. In: McPherson RA, Pincus MR, eds. Henry's Clinical Diagnosis and Management by Laboratory Methods. 23rd ed.Elsevier;2017:1057-1070

特别说明
library of PDFs including pertinent information and forms related to the test

方法描述
describes how the test is performed and provides a method-specific reference

pdFreport
指示该报告是否包含带有图表,图像或其他丰富信息的其他文档

day(s) Performed
概述了进行测试的日子。该领域反映了样品必须在测试实验室中才能开始测试过程的一天,并包括进行测试之前的任何标本准备和处理时间。一些测试被列为连续执行的,这意味着测定在白天多次进行。

从星期一到星期五

report Available
the interval of time (receipt of sample at Mayo Clinic Laboratories to results available) taking into account standard setup days and weekends. The first day is the time that it typically takes for a result to be available. The last day is the time it might take, accounting for any necessary repeated testing.

same day/1 to 3 days

标本保留时间
概述了测试样品在丢弃之前将标本保存在实验室中的时间长度

14天

performing Laboratory Location
指示执行测试的实验室的位置

罗切斯特

费用
几个因素决定了进行测试的费用。请与您的美国或国际区域经理联系,以获取有关建立费用时间表的信息,或了解有关资源以优化测试选择的更多信息。

  • Authorized users can sign in totest Prices有关详细的费用信息。
  • Clients without access to Test Prices can contact亚搏24hours a day, seven days a week.
  • prospective clients should contact their Regional Manager. For assistance, contact亚搏

test Classification
provides information regarding the medical device classification for laboratory test kits and reagents. Tests may be classified as cleared or approved by the US Food and Drug Administration (FDA) and used per manufacturer instructions, or as products that do not undergo full FDA review and approval, and are then labeled as an Analyte Specific Reagent (ASR) product.

this test was developed using an analyte specific reagent. Its performance characteristics were determined by Mayo Clinic in a manner consistent with CLIA requirements. This test has not been cleared or approved by the US Food and Drug Administration.

CPT代码信息
为确定每个测试或配置文件的适当当前程序术语(CPT)代码提供指导。列出的CPT代码反映了梅奥诊所实验室的CPT编码要求解释。yabo208每个实验室的责任是确定用于计费的正确CPT代码。

CPT代码由表演实验室提供。

86003

loinc® Information
provides guidance in determining the Logical Observation Identifiers Names and Codes (LOINC) values for the order and results codes of this test. LOINC values are provided by the performing laboratory.

测试ID 测试订单名称 订单loinc值
l你pn lupin, IgE 11180-7
结果ID 测试结果名称 结果lainc值
仅适用于最初由表演实验室报告的度量单位表达的结果。这些值不适用于转换为其他度量单位的结果。
l你pn lupin, IgE 11180-7

测试设置资源

设置文件
test setup information contains test file definition details to support order and result interfacing between Mayo Clinic Laboratories and your Laboratory Information System.

Excel|PDF

样本报告
不rmal and Abnormal sample reports are provided as references for report appearance.

不rmal Reports|异常报告

SI样本报告
国际的system (SI) of Unit reports are provided for a limited number of tests. These reports are intended for international account use and are only available through MayoLINK accounts that have been defined to receive them.

SI正常报告|s我异常报告