| 网络： | mayocliniclabs.com |
|---|---|
| 电子邮件： | mcl@mayo.edu |
| Telephone: | 800-533-1710 |
| International: | +1 855-379-3115 |
| Values are valid only on day of printing | |
Test Id :FPTH
PTH Antibody
Method Name
A short description of the method used to perform the test
A short description of the method used to perform the test
Radiobinding Assay
NY State Available
Indicates the status of NY State approval and if the test is orderable for NY State clients.
Indicates the status of NY State approval and if the test is orderable for NY State clients.
Yes
Reporting Name
Lists a shorter or abbreviated version of the Published Name for a test
Lists a shorter or abbreviated version of the Published Name for a test
PTH Ab
Aliases
Lists additional common names for a test, as an aid in searching
Lists additional common names for a test, as an aid in searching
Anti-PTH Ab
Anti-PTH Antibody
Parathyroid
Specimen Type
Describes the specimen type validated for testing
Describes the specimen type validated for testing
Serum
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
定义执行测试所需的最佳标本和首选卷以完成测试
Specimen Type: Serum
Container/Tube：红色或SST
Specimen Volume: 1 mL
在普通的红色管中画血液，血清凝胶管是可以接受的。向下旋转并在塑料小瓶中发送1毫升血清环境。
Specimen Minimum Volume
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory
Defines the amount of sample necessary to provide a clinically relevant result as determined by the Testing Laboratory
0.5 mL
Reject Due To
Identifies specimen types and conditions that may cause the specimen to be rejected
Identifies specimen types and conditions that may cause the specimen to be rejected
| 标本以外 | Serum |
| Anticoagulants other than | NA |
| Hemolysis | NA |
| Lipemia | NA |
| Icteric | NA |
Specimen Stability Information
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
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 | Time | Special Container |
|---|---|---|---|
| Serum | Ambient (preferred) | 14 days | |
| Frozen | 28 days | ||
| 冷藏 | 14 days |
Reference Values
描述参考间隔和其他信息，以解释测试结果。可能会在适当的情况下包括基于年龄和性别的间隔。除非另有指定，否则间隔是梅奥衍生的。如果提供了解释性报告，则参考值字段将陈述。
描述参考间隔和其他信息，以解释测试结果。可能会在适当的情况下包括基于年龄和性别的间隔。除非另有指定，否则间隔是梅奥衍生的。如果提供了解释性报告，则参考值字段将陈述。
Negative
PDF Report
Indicates whether the report includes an additional document with charts, images or other enriched information
Indicates whether the report includes an additional document with charts, images or other enriched information
不
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.
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.
4 to 14 days
Performing Laboratory Location
Indicates the location of the laboratory that performs the test
Indicates the location of the laboratory that performs the test
Quest Diagnostics Nichols Institute
费用
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
Several factors determine the fee charged to perform a test. Contact your U.S. or International Regional Manager for information about establishing a fee schedule or to learn more about resources to optimize test selection.
- Authorized users can sign in toTest Pricesfor detailed fee information.
- Clients without access to Test Prices can contact必威平台官网每周7天，每天24小时。
- 潜在客户应联系其区域经理。寻求帮助，联系必威平台官网。
Test Classification
提供有关实验室测试套件和试剂的医疗设备分类的信息。测试可能被归类为美国食品药品监督管理局（FDA）和每个制造商说明使用的清除或批准，或者用作未经全面FDA审查和批准的产品，然后被标记为Analyte特定试剂（ASR）产品。
提供有关实验室测试套件和试剂的医疗设备分类的信息。测试可能被归类为美国食品药品监督管理局（FDA）和每个制造商说明使用的清除或批准，或者用作未经全面FDA审查和批准的产品，然后被标记为Analyte特定试剂（ASR）产品。
This test was developed and its analytical performance characteristics have been determined by Quest Diagnostics. It has not been cleared or approved by FDA. This assay has been validated pursuant to the CLIA regulations and is used for clinical purposes.
CPT Code Information
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
CPT codes are provided by the performing laboratory.
Provides guidance in determining the appropriate Current Procedural Terminology (CPT) code(s) information for each test or profile. The listed CPT codes reflect Mayo Clinic Laboratories interpretation of CPT coding requirements. It is the responsibility of each laboratory to determine correct CPT codes to use for billing.
CPT codes are provided by the performing laboratory.
CPT codes are provided by the performing laboratory.
83519
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.
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.
| Test Id | Test Order Name | Order LOINC Value |
|---|---|---|
| FPTH | PTH Ab | 13928-7 |
| Result 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。
|
|---|---|---|
| Z1555 | PTH Ab | 13928-7 |
Test Setup Resources
设置文件
测试设置信息包含测试文件定义详细信息，以支持Mayo Clinic Laboratories和您的实验室信息系统之间的订单和结果接口。betway中国版
测试设置信息包含测试文件定义详细信息，以支持Mayo Clinic Laboratories和您的实验室信息系统之间的订单和结果接口。betway中国版
Sample Reports
不rmal and Abnormal sample reports are provided as references for report appearance.
不rmal and Abnormal sample reports are provided as references for report appearance.
SI Sample Reports
为有限数量的测试提供了单位报告的国际系统（SI）。这些报告旨在用于国际帐户使用，只能通过定义为接收它们的Mayolink帐户提供。
为有限数量的测试提供了单位报告的国际系统（SI）。这些报告旨在用于国际帐户使用，只能通过定义为接收它们的Mayolink帐户提供。