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1.
Br J Cardiol ; 30(1): 5, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-37705836

RESUMO

Low high-density lipoprotein-cholesterol (HDL-C) concentration is among the strongest independent risk factors for cardiovascular disease, however, studies to assess the cardioprotective effect of normal or high HDL-C level are lacking. To determine the prognostic impact of initial serum HDL-C level on in-hospital major adverse cardiovascular and cerebrovascular events (MACCE) and the one-year all-cause mortality in patients presenting with ST-elevation myocardial infarction (STEMI) we performed a retrospective analysis of the data from 1,415 patients presenting with STEMI in a tertiary-care centre equipped with a 24-hour-ready catheterisation laboratory. The period from June 2014 to June 2017 was reviewed with a follow-up as regards one-year all-cause mortality. Patients were divided into two groups according to HDL-C level. HDL-C <40 mg/dL (2.22 mmol/L) was considered low, while HDL-C ≥40 mg/dL was considered normal. There were 1,109 patients with low HDL-C, while 306 had normal HDL-C levels, which was statistically significant (p<0.001). Total MACCE and all-cause mortality were significantly lower in patients with normal HDL-C (p=0.03 and p=0.01, respectively). In conclusion, this retrospective study to assess the prognostic effect of HDL-C in patients presenting with STEMI, found normal HDL-C level was associated with lower in-hospital MACCE and all-cause mortality at one-year follow-up.

2.
BMJ Case Rep ; 15(3)2022 Mar 02.
Artigo em Inglês | MEDLINE | ID: mdl-35236681

RESUMO

Granulomatosis with polyangiitis (GPA) is a rare small-vessel vasculitis associated with high mortality without appropriate treatment. Acute ST-elevation myocardial infarction (STEMI) has been reported as an atypical presentation of GPA. We report a case of STEMI, shortly followed by subacute in-stent thrombosis with extensive thrombus burden in a 53-year-old male patient with undiagnosed GPA. After aggressive treatment with triple therapy consisting of aspirin, clopidogrel and rivaroxaban, He started to have haemoptysis. Despite the discontinuation of aspirin, he ended up with massive haemoptysis and acute respiratory failure necessitating endotracheal intubation. CT of the chest revealed bilateral ground-glass opacities consistent with diffuse alveolar haemorrhage. Extensive workup revealed positive antiproteinase 3 antibodies; hence, a diagnosis of GPA was made. He was treated with induction therapy consisting of methylprednisolone, mycophenolate mofetil, cyclophosphamide and rituximab, leading to a gradual improvement in his clinical conditions and subsequent extubation.


Assuntos
Granulomatose com Poliangiite , Infarto do Miocárdio com Supradesnível do Segmento ST , Anticorpos Anticitoplasma de Neutrófilos , Granulomatose com Poliangiite/complicações , Granulomatose com Poliangiite/diagnóstico , Granulomatose com Poliangiite/tratamento farmacológico , Hemoptise/etiologia , Humanos , Masculino , Pessoa de Meia-Idade , Mieloblastina , Infarto do Miocárdio com Supradesnível do Segmento ST/complicações , Infarto do Miocárdio com Supradesnível do Segmento ST/diagnóstico
4.
Echocardiography ; 36(8): 1590-1593, 2019 08.
Artigo em Inglês | MEDLINE | ID: mdl-31246322

RESUMO

Cogan's syndrome is a rare disorder characterized by the coexistence of ocular and audio-vestibular manifestations. Systemic manifestations are quite unusual with pan-vasculitis and cardiac involvement reported in the form of aortitis with aortic aneurysm, dissection, or extremely rare aortic valve perforation. Hereby, we report a case of a 56-year-old woman presented with ocular, audio-vestibular, and systemic manifestations with medium-sized vasculitis in the form of multiple splenic artery aneurysms, superior mesenteric artery thrombosis, and cardiovascular involvement in the form of aortic regurgitation due to noncoronary cusp perforation. To the best of our knowledge, this is the second case to report aortic perforation in the setting of Cogan's syndrome.


Assuntos
Insuficiência da Valva Aórtica/etiologia , Valva Aórtica , Síndrome de Cogan/complicações , Ruptura Cardíaca/complicações , Insuficiência da Valva Aórtica/diagnóstico , Síndrome de Cogan/diagnóstico , Diagnóstico Diferencial , Ecocardiografia , Feminino , Seguimentos , Ruptura Cardíaca/diagnóstico , Humanos , Pessoa de Meia-Idade , Tomografia Computadorizada por Raios X
5.
Echocardiography ; 36(3): 615-617, 2019 03.
Artigo em Inglês | MEDLINE | ID: mdl-30738004

RESUMO

Unguarded tricuspid orifice is the most extreme of tricuspid valve dysplasia with a very variable natural history. They can tolerate tricuspid regurgitation well, and they become symptomatic only if significant right ventricular dysfunction or atrial fibrillation occurs. Patients with a mild degree of right ventricular dysfunction can survive to adulthood and even reach old age. Surgical treatment is a difficult option due to variable natural history, and surgical results are not too encouraging.


Assuntos
Ecocardiografia , Achados Incidentais , Valva Tricúspide/anormalidades , Valva Tricúspide/diagnóstico por imagem , Adulto , Anticoagulantes/uso terapêutico , Diuréticos/uso terapêutico , Ecocardiografia Tridimensional , Humanos , Masculino
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