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1.
Am Fam Physician ; 96(11): 709-715, 2017 Dec 01.
Artigo em Inglês | MEDLINE | ID: mdl-29431403

RESUMO

Mild, asymptomatic elevations (less than five times the upper limit of normal) of alanine transaminase and aspartate transaminase levels are common in primary care. It is estimated that approximately 10% of the U.S. population has elevated transaminase levels. An approach based on the prevalence of diseases that cause asymptomatic transaminase elevations can help clinicians efficiently identify common and serious liver disease. The most common causes of elevated transaminase levels are nonalcoholic fatty liver disease and alcoholic liver disease. Uncommon causes include drug-induced liver injury, hepatitis B and C, and hereditary hemochromatosis. Rare causes include alpha1-antitrypsin deficiency, autoimmune hepatitis, and Wilson disease. Extrahepatic sources, such as thyroid disorders, celiac sprue, hemolysis, and muscle disorders, are also associated with mildly elevated transaminase levels. The initial evaluation should include an assessment for metabolic syndrome and insulin resistance (i.e., waist circumference, blood pressure, fasting lipid level, and fasting glucose or A1C level); a complete blood count with platelets; measurement of serum albumin, iron, total iron-binding capacity, and ferritin; and hepatitis C antibody and hepatitis B surface antigen testing. The nonalcoholic fatty liver disease fibrosis score and the alcoholic liver disease/nonalcoholic fatty liver disease index can be helpful in the evaluation of mildly elevated transaminase levels. If testing for common causes is consistent with nonalcoholic fatty liver disease and is otherwise unremarkable, a trial of lifestyle modification is appropriate. If the elevation persists, hepatic ultrasonography and further testing for uncommon causes should be considered.


Assuntos
Alanina Transaminase/sangue , Aspartato Aminotransferases/sangue , Hemocromatose/diagnóstico , Hepatopatias Alcoólicas/diagnóstico , Hepatopatia Gordurosa não Alcoólica/diagnóstico , Doença Celíaca/sangue , Doença Celíaca/diagnóstico , Doença Hepática Induzida por Substâncias e Drogas/sangue , Doença Hepática Induzida por Substâncias e Drogas/diagnóstico , Hemocromatose/sangue , Hepatite B/sangue , Hepatite B/diagnóstico , Antígenos de Superfície da Hepatite B/sangue , Hepatite C/sangue , Hepatite C/diagnóstico , Anticorpos Anti-Hepatite C/sangue , Hepatite Autoimune/sangue , Hepatite Autoimune/diagnóstico , Degeneração Hepatolenticular/sangue , Degeneração Hepatolenticular/diagnóstico , Humanos , Resistência à Insulina , Estilo de Vida , Hepatopatias Alcoólicas/sangue , Síndrome Metabólica/sangue , Síndrome Metabólica/diagnóstico , Hepatopatia Gordurosa não Alcoólica/sangue , Hepatopatia Gordurosa não Alcoólica/terapia , Doenças da Glândula Tireoide/sangue , Doenças da Glândula Tireoide/diagnóstico , Deficiência de alfa 1-Antitripsina/sangue , Deficiência de alfa 1-Antitripsina/diagnóstico
2.
Am Fam Physician ; 84(9): 1003-8, 2011 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-22046940

RESUMO

Mild elevations in levels of the liver enzymes alanine transaminase and aspartate transaminase are commonly discovered in asymptomatic patients in primary care. Evidence to guide the diagnostic workup is limited. If the history and physical examination do not suggest a cause, a stepwise evaluation should be initiated based on the prevalence of diseases that cause mild elevations in transaminase levels. The most common cause is nonalcoholic fatty liver disease, which can affect up to 30 percent of the population. Other common causes include alcoholic liver disease, medication-associated liver injury, viral hepatitis (hepatitis B and C), and hemochromatosis. Less common causes include α(1)-antitrypsin deficiency, autoimmune hepatitis, and Wilson disease. Extrahepatic conditions (e.g., thyroid disorders, celiac disease, hemolysis, muscle disorders) can also cause elevated liver transaminase levels. Initial testing should include a fasting lipid profile; measurement of glucose, serum iron, and ferritin; total iron-binding capacity; and hepatitis B surface antigen and hepatitis C virus antibody testing. If test results are normal, a trial of lifestyle modification with observation or further testing for less common causes is appropriate. Additional testing may include ultrasonography; measurement of α(1)-antitrypsin and ceruloplasmin; serum protein electrophoresis; and antinuclear antibody, smooth muscle antibody, and liver/kidney microsomal antibody type 1 testing. Referral for further evaluation and possible liver biopsy is recommended if transaminase levels remain elevated for six months or more.


Assuntos
Alanina Transaminase/metabolismo , Hepatopatias/diagnóstico , Hepatopatias/enzimologia , Diagnóstico Diferencial , Fígado Gorduroso/diagnóstico , Fígado Gorduroso/enzimologia , Hepatite C Crônica/diagnóstico , Hepatite C Crônica/enzimologia , Hepatite Alcoólica/diagnóstico , Hepatite Alcoólica/enzimologia , Humanos , Cirrose Hepática/diagnóstico , Cirrose Hepática/enzimologia , Cirrose Hepática Biliar/diagnóstico , Cirrose Hepática Biliar/enzimologia
3.
J Am Board Fam Med ; 19(5): 521-3, 2006.
Artigo em Inglês | MEDLINE | ID: mdl-16951303

RESUMO

Epidural analgesia is a widely used method of pain control in the labor and delivery setting but is not without risks. We present a case of Horner's syndrome and trigeminal nerve palsy as a rare complication of epidural analgesia in an obstetric patient. Although reported in few instances in the anesthesia literature, awareness among providers in obstetrics is critical because this could be the first sign of a high sympathetic blockade resulting in potential maternal-fetal morbidity.


Assuntos
Anestesia Epidural/efeitos adversos , Síndrome de Horner/etiologia , Dor do Parto/terapia , Doenças do Nervo Trigêmeo/etiologia , Adulto , Feminino , Humanos , Recém-Nascido , Masculino , Gravidez , Resultado da Gravidez
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