Alpha 1-antitrypsin deficiency laboratory findings: Difference between revisions
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==Laboratory Findings== | ==Laboratory Findings== | ||
A reduced concentration of serum alpha1-antitrypsin levels is diagnostic of AATD. | |||
Laboratory findings consistent with the diagnosis of AATD include : | |||
Moderate-to-severe airflow obstruction with an FEV1 in the range of 30-40% of the predicted value | |||
Reduced vital capacity | |||
Increased lung volumes secondary to air trapping (residual volume >120% of predicted value) are usually present | |||
Diffusing capacity values are reduced substantially (<50% of predicted value) in most symptomatic patients. | |||
Alpha1-antitrypsin deficiency (AATD) should be considered on the differential diagnosis in any patient who presents with early onset emphysema or COPD, regardless of their smoking history. | |||
Alpha1-antitrypsin deficiency (AATD) should be considered in patients with unexplained liver disease at any age, including obstructive jaundice of infancy | |||
AATD testing should be considered as a laboratory diagnosis and not as a clinical diagnosis. | |||
Serum alpha1-antitrypsin levels | |||
Serum alpha1-antitrypsin levels are determined by nephelometry. | |||
Serum testing is used for diagnostic testing in those patients with family histories compatible with alpha1-antitrypsin deficiency or with siblings with known alpha1-antitrypsin deficiency. | |||
ATS/ERS AAT Deficiency Task Force does not recommend predispositional fetal testing or population screening unless the prevalence of AATD is high (>1 case per 1500 population), smoking is prevalent, and adequate counseling services are available. | |||
serum alpha1-antitrypsin levels has a normal reference range of 100-300 mg/dL. Levels less than 80 mg/dL suggest a significant risk for lung disease. | |||
Serum alpha1-antitrypsin level alone has a low sensitivity for detecting AATD. | |||
Emphysema is common below 11 mmol/L (80 mg/mL) which represents the threshold level. | |||
Functional assay of alpha1-antiprotease | |||
In patients with clinical features that are highly suggestive of alpha1-antitrypsin deficiency but whose serum levels are within the reference range the next best step is to perform functional assay of alpha1 antiprotease, which measures the ability of the patient's serum to inhibit human leukocyte elastase. | |||
Perform liver function tests in patients with low or borderline levels of alpha1-antitrypsin. Measurement of serum transaminases,bilirubin, albumin, and routine clotting function (activated partial thromboplastin time and international normalized ratio). | |||
==References== | ==References== | ||
Revision as of 11:48, 12 December 2017
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Alpha 1-antitrypsin deficiency Microchapters |
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Differentiating Alpha 1-antitrypsin deficiency from other Diseases |
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Directions to Hospitals Treating Alpha 1-antitrypsin deficiency |
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Risk calculators and risk factors for Alpha 1-antitrypsin deficiency laboratory findings |
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Overview
Laboratory Findings
A reduced concentration of serum alpha1-antitrypsin levels is diagnostic of AATD. Laboratory findings consistent with the diagnosis of AATD include : Moderate-to-severe airflow obstruction with an FEV1 in the range of 30-40% of the predicted value Reduced vital capacity Increased lung volumes secondary to air trapping (residual volume >120% of predicted value) are usually present Diffusing capacity values are reduced substantially (<50% of predicted value) in most symptomatic patients.
Alpha1-antitrypsin deficiency (AATD) should be considered on the differential diagnosis in any patient who presents with early onset emphysema or COPD, regardless of their smoking history. Alpha1-antitrypsin deficiency (AATD) should be considered in patients with unexplained liver disease at any age, including obstructive jaundice of infancy AATD testing should be considered as a laboratory diagnosis and not as a clinical diagnosis. Serum alpha1-antitrypsin levels Serum alpha1-antitrypsin levels are determined by nephelometry. Serum testing is used for diagnostic testing in those patients with family histories compatible with alpha1-antitrypsin deficiency or with siblings with known alpha1-antitrypsin deficiency. ATS/ERS AAT Deficiency Task Force does not recommend predispositional fetal testing or population screening unless the prevalence of AATD is high (>1 case per 1500 population), smoking is prevalent, and adequate counseling services are available. serum alpha1-antitrypsin levels has a normal reference range of 100-300 mg/dL. Levels less than 80 mg/dL suggest a significant risk for lung disease. Serum alpha1-antitrypsin level alone has a low sensitivity for detecting AATD. Emphysema is common below 11 mmol/L (80 mg/mL) which represents the threshold level. Functional assay of alpha1-antiprotease In patients with clinical features that are highly suggestive of alpha1-antitrypsin deficiency but whose serum levels are within the reference range the next best step is to perform functional assay of alpha1 antiprotease, which measures the ability of the patient's serum to inhibit human leukocyte elastase. Perform liver function tests in patients with low or borderline levels of alpha1-antitrypsin. Measurement of serum transaminases,bilirubin, albumin, and routine clotting function (activated partial thromboplastin time and international normalized ratio).