犬肾上腺皮质机能亢进专题——垂体-肾上腺皮质轴评估
(2010-08-07 11:52:49)
标签:
犬肾上腺皮质机能亢进库兴氏综合征诊断试验王姜维健康 |
分类: 肾上腺专题 |
检测 |
目的 |
方案 |
结果 |
解释 |
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内源性ACTH |
鉴别PDH和AT |
早晨8点~10点间采集血浆,血样需特殊处理。 |
<10pg/ml |
AT |
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10-45 pg/ml |
无诊断意义 |
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>45 pg/ml |
PDH |
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ACTH刺激后可的松浓度: |
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ACTH刺激试验 |
诊断库兴氏综合征 |
ACTH凝胶*:2.2IU/kg IM,ACTH给予前和之后2小时采集血浆;或合成的ACTH*:0.25mg/犬 IM,ACTH给予前和之后1小时采集血浆 |
>24μg/dl |
强烈暗示存在† |
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19-24μg/dl |
暗示存在‡ |
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8-18μg/dl |
正常 |
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<8μg/dl |
医源性库兴氏综合征 |
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给予地塞米松4小时后 |
给予地塞米松8小时后 |
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低剂量地塞米松抑制试验 |
诊断库兴氏综合征,并鉴别PDH和AT |
地塞米松:0.01mg/kg IV,给药前和之后4小时、8小时采集血浆 |
— |
<1.4μg/dl |
正常 |
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<1.4μg/dl |
>1.4μg/dl |
PDH |
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<50%给药前浓度 |
>1.4μg/dl |
PDH |
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— |
>1.4μg/dl且<50%给药前浓度 |
PDH |
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给药4小时后浓度>1.4μg/dl且>50%给药前浓度 |
>1.4μg/dl |
PDH或AT |
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ACTH给药后 |
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地塞米松抑制试验和ACTH刺激试验结合试验 |
诊断库兴氏综合征 |
地塞米松:0.01mg/kg IV,给药前和给药后2小时采集血浆;然后ACTH凝胶:2.2IU/kg或合成的ACTH:0.25mg/犬 IM,给药后1小时和2小时(ACTH凝胶)或30分钟和60分钟(合成的ACTH)采集血浆 |
<1.5μg/dl |
8-18μg/dl |
正常 |
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>1.5μg/dl |
8-20μg/dl |
暗示 |
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>1.5μg/dl |
>20μg/dl |
强烈暗示存在 |
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<1.5μg/dl |
>20μg/dl |
暗示存在 |
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<1.5μg/dl |
<8μg/dl |
医源性库兴氏综合征 |
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地塞米松给予后可的松浓度 |
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高剂量地塞米松抑制试验 |
鉴别PDH和AT |
地塞米松:0.1mg/kg IV,给药前和之后8小时采集血浆 |
<50%给药前浓度 |
PDH |
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<1.4μg/dl |
PDH |
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≥50%给药前浓度 |
PDH或AT |
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PDH,垂体依赖性肾上腺皮质机能亢进;AT,肾上腺皮质肿瘤。
*ACTH凝胶:Cortigel,Savage实验室;合成的ACTH:替可克肽,米安色林药物制剂。
†强烈暗示存在肾上腺皮质机能亢进。
‡暗示存在肾上腺皮质机能亢进。
Idexx Low-dose Dexamethasone Suppression Test |
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4-hour cortisol level |
8-hour cortisol level |
interpretation |
<1μg/dL |
<1μg/dL |
Normal |
1-1.5μg/dL |
1-1.5μg/dL |
Inconclusive, consider repeating in 6-8weeks |
>1.5μg/dL and >50% of baseline |
>1.5μg/dL and >50% of baseline |
Consistent with Cushing’s syndrome; perform high-dose dexamethasone suppression, endogenous ACTH concentration and/or abdominal ultrasound to discriminate between PDH and ATH |
<1.5μg/dL or <50% of baseline |
>1.5μg/dL and >50% of baseline |
Consistent with PDH |
>1.5μg/dL and >50% of baseline |
>1.5μg/dL and <50% of baseline |
Consistent with PDH |
Idexx ACTH Stimulation Test |
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Pre-ACTH |
Interpretation |
Post-ACTH |
interpretation |
<2μg/dL |
Must evaluate in conjunction with post-ACTH result. If both results are <2μg/dL, results are consistent with hypoadrenocorticism. Begin treatment with mineralocorticoid and/or glucocorticoid as appropriate. |
<2μg/dL |
Ideally, should be evaluated in conjunction with pre-ACTH result. If both results are <2μg/dL, results are consistent with hypoadrenocorticism. Begin treatment with mineralocorticoid and/or glucocorticoid as appropriate. |
2-6μg/dL |
Norml |
2-6μg/dL |
Inconclusive |
>22μg/dL |
Consistent with Cushing’s syndrome; Perform high-dose dexamethasone suppression. |
6-18μg/dL |
Normal |
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18-22μg/dL |
Equivocal; Cushing’s syndrome possible. |
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>22μg/dL |
Consistent with Cushing’s syndrome; perform high-dose dexamethasone suppression to discriminate between PDH and ATH, ACTH level and/or abdominal ultrasound. |