hypercholesterolemia/تقيؤ

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Iomitapide (Lojuxta). Use only in homozygous familial hypercholesterolaemia, with caution.

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Patients with rare homozygous familial hypercholesterolaemia are at risk of dying at a very young age. When liver transplantation is not feasible, treatment is based on regular LDL apheresis sessions, a burdensome and inconvenient procedure, and on high-dose statins in combination with ezetimibe.

The use of high-resolution MRI to detect thrombosis and lipid-rich carotid artery plaques in a patient with homozygous familial hypercholesterolemia.

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Homozygous familial hypercholesterolemia is a rarely agentic disorder of the lipoprotein metabolism intimately related to premature atherosclerotic cardiovascular disease that can lead to high disability and mortality. Homozygous familial hypercholesterolemia typically affects not only the aortic

Juvenile acute intermittent porphyria with hypercholesterolemia and epilepsy: a case report and review of the literature.

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A case of acute intermittent porphyria in a 10-year-old boy with seizures and hypercholesterolemia is presented. The problems of management when seizures and porphyria coincide and discussion of hypercholesterolemia are included. A comprehensive review of the world literature reveals that

A case of montelukast induced hypercholesterolemia, severe hypertriglyceridemia and pancreatitis.

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Montelukast sodium is a leukotriene inhibitor, and competitively antagonizes cys-LT1 receptor and used widely and effectively in treating allergic rhinitis, bronchial asthma and allied respiratory conditions. This case report outlines a rare case of montelukast induced hypercholesterolemia, severe

A comparative study of policosanol Versus acipimox in patients with type II hypercholesterolemia.

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An 8-week, randomized, double-blind study comparing the efficacy and tolerability of policosanol and acipimox was conducted in patients with type II hypercholesterolemia. Prior to entry into active treatment, all patients followed a standard cholesterol-lowering diet for 12 weeks. Sixty-three

[Pravastatin vs. probucol in the treatment of hypercholesterolemia. A double-blind study].

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This 16-week, double-blind study compared the efficacy and safety of pravastatin, a new HMG-CoA reductase inhibitor, with probucol in the treatment of hyperlipidemia in 26 patients at the Instituto Nacional de Cardiología "Ignacio Chávez" in Mexico City. Patients had to have a low-density

[Safety and efficacy of pitavastatin in patients with hypercholesterolemia: a multicenter study].

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OBJECTIVE To evaluate the safety and efficacy of pitavastatin in patients with hypercholesterolemia in China under conditions of extensive usage. METHODS This was a 12-week, multicenter, open-label, without parallel-group comparison, phase IV clinical trial. RESULTS There were 427 subjects in the

Anorexia nervosa manifesting as massive ascites, hypercholesterolemia, and sequential binge eating in an 11-year-old girl: A case report

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Rationale: Anorexia nervosa (AN) is a serious eating disorder associated with a distorted body image. Hypercholesterolemia has been found in patients with AN but the mechanism of hyperlipidemia in AN remains little known. Ascites in

Niacin treatment of hypercholesterolemia in children.

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OBJECTIVE To determine the efficacy and adverse effects of niacin treatment of hypercholesterolemia in children. METHODS Retrospective review. METHODS Two university hospital referral clinics. METHODS All children who received single-drug niacin treatment for severe hypercholesterolemia between 1980

Defining the role of lipoprotein apheresis in the management of familial hypercholesterolemia.

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Familial hypercholesterolemia (FH) is an autosomal co-dominant disorder characterized by a marked elevation of serum low-density lipoprotein (LDL) cholesterol (LDL-C) concentration, which in turn is associated with a greatly increased risk of premature cardiovascular disease. International consensus

Successful treatment of homozygous familial hypercholesterolemia using cascade filtration plasmapheresis.

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OBJECTIVE The aim of this study was to report the efficacy of low-density lipoprotein cholesterol (LDL-C) apheresisusing a cascade filtration system in pediatric patients with homozygous familial hypercholesterolemia (FH), and toclarify the associated adverse effects and difficulties. METHODS LDL-C

Low density lipoprotein apheresis in pediatric patients with homozygous familial hypercholesterolemia.

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The aim of the present study is to clarify the low density lipoprotein apheresis procedure for pediatric patients with homozygous familial hypercholesterolemia (FH) in terms of efficacy, adverse effects and difficulties. The follow-up was carried out using an open, prospective uncontrolled clinical

Effect of simvastatin in CAPD patients with hypercholesterolemia.

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The effect of simvastatin on serum total and HDL cholesterol and total triglyceride levels in 20 hypercholesterolemic patients on CAPD treatment was studied. The drug was given at the initial dose of 10 mg/day which was doubled up to 40 mg/day. Two non-compliant patients stopped the drug in the

Isolated Subarachnoidal Hemorrhage following Carotid Endarterectomy.

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Cerebral hyperperfusion syndrome is a rare but well-described complication following carotid endarterectomy or stenting. Clinical signs are ipsilateral, throbbing, unilateral headache with nausea or vomiting, seizures, and neurological deficits, with or without intracerebral abnormalities on CT

A case of acute pancreatitis possibly associated with combined salicylate and simvastatin treatment.

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BACKGROUND Drug-induced acute pancreatitis is a rather rare clinical entity. From time to time, several cases have been reported in which statins or salicylates have been associated with the development of acute pancreatitis. There is only one report which implies the involvement of both drugs in

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