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1.
J Stroke Cerebrovasc Dis ; 29(9): 105095, 2020 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-32807489
2.
Am J Emerg Med ; 32(4): 293-6, 2014 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-24480311

RESUMO

BACKGROUND: High-sensitivity troponin (HS-TnT) combined with copeptin have been proposed to expedite the diagnostic exclusion of acute myocardial infarction. The Global Registry of Acute Coronary Events (GRACE) has been validated and recommended by the European Society of Cardiology as a prognostic score in the management of acute coronary syndrome (ACS) without ST-segment elevation (non-ST+) on the electrocardiogram. Our study examined whether a low GRACE score (<108) combined with negative HS-TnT (<14 ng/L) and copeptin (<14 pmol/L) reliably exclude the diagnosis of non-ST+ ACS, including non-ST-segment elevation myocardial infarction and unstable angina. METHODS: This observational, prospective study included patients presenting with chest pain lasting <6 hours, consistent with non-ST+ ACS. Blood was collected early for measurements of copeptin and HS-TnT. The negative predictive value of combined copeptin, HS-TnT, and GRACE score was calculated in the diagnosis of non-ST+ ACS. The thresholds of positivity were 14 ng/L for HS-TnT, 14 pmol/L for copeptin and 108 for the GRACE score. RESULTS: Among 247 patients retained in the analysis, the diagnosis of ACS was made in 50 (20.4%), including 39 non-ST-segment elevation myocardial infarction and 11 unstable angina. The negative predictive value of combined HS-TnT, copeptin and GRACE score was 99%. CONCLUSION: A negative copeptin associated with a negative HS-TnT in a patient presenting with a low GRACE score expedited the diagnostic exclusion of non-ST+ ACS.


Assuntos
Síndrome Coronariana Aguda/diagnóstico , Medicina de Emergência/normas , Glicopeptídeos/sangue , Índice de Gravidade de Doença , Troponina/sangue , Síndrome Coronariana Aguda/sangue , Biomarcadores/sangue , Diagnóstico Diferencial , Eletrocardiografia , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Valor Preditivo dos Testes , Estudos Prospectivos , Sensibilidade e Especificidade , Fatores de Tempo
4.
Ann Biol Clin (Paris) ; 79(2): 143-150, 2021 Apr 01.
Artigo em Francês | MEDLINE | ID: mdl-33875412

RESUMO

High-sensitivity troponin has become an essential emergency biomarker for diagnosing or ruling out an ACS. The establishment of a point of care biology related to the reorganization and fusion of laboratories raise a question about transferability of results between techniques. In this study, we propose to compare the bioclinical performances of high-sensitivity troponin measured by two different techniques on laboratory immunoanalyzer (Siemens Advia Centaur XPT) and on point of care device (Mitsubishi Pathfast). The assay of high-sensitivity troponin (n = 90 patients), according to our study, show consistent clinical results with both method.


Assuntos
Bioensaio , Troponina I , Biomarcadores , Humanos , Laboratórios , Sistemas Automatizados de Assistência Junto ao Leito , Sensibilidade e Especificidade
6.
Ann Biol Clin (Paris) ; 75(1): 87-91, 2017 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-28132947

RESUMO

We present the case of an Addison's disease revealed by a serious hyponatremia. The serum concentration of ACTH and 21-hydroxylase antibodies were increased and lead to the diagnosis. The cortisol blood level was lowered but required to take into account the stress induced by the hospitalisation of the patient. Addison's disease is characterized by the destruction of the adrenal cortex. Autoimmune adrenalitis is the main cause of adrenal insufficiency. Treatment involves normalisation of sodium concentration and corticosteroids replacement. With a good patient compliance, the survival rate of Addisonian patient is similar to that of the normal population. Management of patient requires vigilance because of the occurrence of others autoimmunes diseases during patient life.


Assuntos
Doença de Addison/diagnóstico , Hiponatremia/diagnóstico , Doença de Addison/sangue , Doença de Addison/complicações , Hormônio Adrenocorticotrópico/análise , Hormônio Adrenocorticotrópico/sangue , Autoanticorpos/sangue , Coma/sangue , Coma/diagnóstico , Coma/etiologia , Diagnóstico Diferencial , Humanos , Hidrocortisona/análise , Hidrocortisona/sangue , Hiponatremia/sangue , Hiponatremia/complicações , Masculino , Pessoa de Meia-Idade , Índice de Gravidade de Doença , Esteroide 21-Hidroxilase/imunologia
7.
Nephrol Ther ; 1(1): 52-61, 2005 Mar.
Artigo em Francês | MEDLINE | ID: mdl-16895668

RESUMO

A 29 year-old female patient developed severe arterial hypertension in the beginning of her second pregnancy. Investigations performed at 16 weeks of amenorrhea showed hypokaliemia in relation to severe hyperreninism: plasma active renin was 25 fold normal value, 94% as prorenin (prorenin representing 94% of total renin). Radiological investigations including ultrasonography and MRI disclosed an homogenous and avascular tumor in the right kidney. Its ablation confirmed renin tumor, and allowed recovery from HTA and continuation of pregnancy. This is the 75th reported case in the literature, enabling to make a new statement about diagnostic and therapeutic procedures, which are modified during pregnancy by contra-indication to X-rays and renin-angiotensin-aldosteron axis inhibitors.


Assuntos
Neoplasias Renais/diagnóstico , Complicações Cardiovasculares na Gravidez/etiologia , Complicações Neoplásicas na Gravidez/diagnóstico , Renina/metabolismo , Adulto , Feminino , Humanos , Neoplasias Renais/diagnóstico por imagem , Neoplasias Renais/enzimologia , Neoplasias Renais/patologia , Neoplasias Renais/cirurgia , Gravidez , Complicações Neoplásicas na Gravidez/diagnóstico por imagem , Complicações Neoplásicas na Gravidez/patologia , Complicações Neoplásicas na Gravidez/cirurgia , Radiografia , Resultado do Tratamento
8.
Ann Biol Clin (Paris) ; 71(2): 235-9, 2013.
Artigo em Francês | MEDLINE | ID: mdl-23587595

RESUMO

We described a case of Gitelman syndrome. A 56-year-old healthy man presented with facial paralysis. Initial laboratory tests revealed hypokalemia. Despite potassium supplements, kaliemia remains at low levels. Further investigations showed urinary potassium wasting, hypomagnesemia and hypocalciuria. Diagnosis of Gitelman syndrome has been confirmed by molecular diagnosis with identification of a composite heterozygote mutation on SLC12A3 gene. One of the mutations on exon 1 SCL12A3 gene wasn't yet known. In the patient family, the same genetic disorder has been found in the sister. Treatment and follow up schedule were proposed to patient.


Assuntos
Síndrome de Gitelman/diagnóstico , Receptores de Droga/genética , Simportadores/genética , Algoritmos , Análise Mutacional de DNA , Paralisia Facial/diagnóstico , Paralisia Facial/etiologia , Paralisia Facial/genética , Síndrome de Gitelman/complicações , Síndrome de Gitelman/genética , Humanos , Masculino , Pessoa de Meia-Idade , Membro 3 da Família 12 de Carreador de Soluto
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