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1.
Del Med J ; 87(8): 238-43, 2015 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-26402926

RESUMEN

INTRODUCTION: The familial hypercholesterolemias (FH) are a group of undertreated genetically inherited disorders of lipid metabolism that lead to severely elevated cholesterol levels and early onset cardiovascular disease. Aggressive lifestyle modifications and lipid-lowering medications such as statins and bile acid sequestrants are the backbone of current treatment. Despite these interventions, homozygous FH (HoFH) patients are unable to reach LDL-C targets and remain at significantly increased risk of cardiovascular disease. Recently, two novel lipid-lowering medications, lomitapide and mipomersen, have been approved for the treatment of HoFH. CASE DESCRIPTIONS: We present two patients with HoFH who have been unable to reach target LDL-C goals on standard therapy. Patient A is a 41-year-old male and patient B is a 64-year-old female, both of whom have complex histories of multi-vessel coronary artery disease. In attempt to improve their LDL-C levels and lower their cardiovascular risk, lomitapide and mipomersen were initiated in patient A and B, respectively. DISCUSSION/CONCLUSION: Through inhibition of the microsomal triglyceride transfer protein, lomitapide prevents the formation of triglyceride rich lipoproteins. Mipomersen is an antisense oligonucleotide that inhibits the translation of apolipoprotein B-100. Both medications employ novel mechanisms developed through advances in pharmacogenetic technology and achieve unprecedented LDL-C reductions.


Asunto(s)
Anticolesterolemiantes/uso terapéutico , Bencimidazoles/uso terapéutico , Hiperlipoproteinemia Tipo II/tratamiento farmacológico , Hiperlipoproteinemia Tipo II/genética , Oligonucleótidos/uso terapéutico , Farmacogenética , Adulto , LDL-Colesterol/sangre , Femenino , Humanos , Hiperlipoproteinemia Tipo II/diagnóstico , Masculino , Persona de Mediana Edad
2.
Del Med J ; 87(6): 176-9, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-26189274

RESUMEN

The left internal mammary artery (LIMA) is the preferred arterial graft to be used for the left anterior descending (LAD) artery for coronary artery bypass graft (CABG) due to high graft patency rate. LIMA dissection is a rare, but dreadful complication of graft angiography and may lead to serious complications including death, myocardial infarction (MI), and re-do CABG. Transcatheter management of LIMA dissection involves multiple stenting. However, this may leave a dissection flap at the ostium of the LIMA that may extend to the left subclavian artery jeopardizing flow to the left arm and vertebral artery. We present a case of LIMA dissection where a dual balloon angioplasty was used for the first time offering better "sealing" of the dissection flap at the level of the ostium of the LIMA graft/subclavian artery.


Asunto(s)
Angioplastia de Balón/métodos , Angiografía Coronaria/efectos adversos , Puente de Arteria Coronaria/efectos adversos , Arterias Mamarias/lesiones , Complicaciones Posoperatorias/terapia , Arteria Subclavia/cirugía , Anciano , Humanos , Masculino , Arterias Mamarias/diagnóstico por imagen
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