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This Week in the Journal

August 21, 2003

Original Articles
Coronary Angioplasty versus Fibrinolytic Therapy for Myocardial Infarction

In hospitals with angioplasty facilities, coronary angioplasty is the preferred approach to revascularization in patients with acute myocardial infarction. In this Danish study, patients initially admitted to hospitals without angioplasty facilities were randomly assigned to receive on-site fibrinolytic therapy or to be transferred to an invasive-treatment center for angioplasty. Despite the time required for transfer, patients assigned to angioplasty had a better outcome than those assigned to fibrinolytic therapy.

Angioplasty should be considered the standard method of revascularization for patients with myocardial infarction.

Related Editorial

 Original Articles
Effect of Granulocyte Colony-Stimulating Factor on Chemotherapy for Acute Myeloid Leukemia

This trial of concurrent chemotherapy and granulocyte colony-stimulating factor (G-CSF) for acute myeloid leukemia was based on the ability of G-CSF to heighten the sensitivity of cultured leukemia cells to chemotherapeutic agents. Patients who received the dual treatment ("G-CSF priming") fared better than patients given chemotherapy alone.

G-CSF priming is a novel approach to augmenting the cytotoxicity of chemotherapy without incurring additional myelotoxicity.

Related Perspective


Original Articles
Brief Report: A Mutation in the FSH Receptor as a Cause of Gestational Spontaneous Ovarian Hyperstimulation Syndrome

This Brief Report describes recurrent gestational spontaneous ovarian hyperstimulation syndrome in a family with a heterozygous mutation in the transmembrane domain of the receptor for follicle-stimulating hormone (FSH). The mutant receptor responded to human chorionic gonadotropin as well as to follicle-stimulating hormone. A second Brief Report describes another FSH receptor mutation that also leads to gestational ovarian hyperstimulation syndrome.

When the follicle-stimulating hormone receptor responds to more than one ligand, ovarian hyperstimulation syndrome may result.

Related Perspective

 Original Articles
Brief Report: Ovarian Hyperstimulation Syndrome Due to a Mutation in the FSH Receptor

The overproduction of endogenous chorionic gonadotropin during pregnancy has been associated with spontaneous ovarian hyperstimulation syndrome. Yet the syndrome has been observed in women with normal levels of chorionic gonadotropin. This Brief Report defines a mutation in the follicle-stimulating hormone (FSH) receptor that is associated with recurrent, spontaneous ovarian hyperstimulation syndrome. In this instance, the mutant receptor responded both to chorionic gonadotropin and to thyrotropin.

Inappropriate stimulation of the follicle-stimulating hormone receptor is a key element in the development of the ovarian hyperstimulation syndrome.

Related Perspective


Special Article
Costs of Health Care Administration in the United States and Canada

The authors estimate that the costs of health care administration in the United States are about $1,000 per capita and represent 31 percent of all health care expenditures. Administrative costs in Canada are lower, at roughly $300 per capita and 17 percent of all health care expenditures.

This article updates the estimates of the costs of health care administration made in 1991 by the same authors. Administrative costs in the United States account for almost one third of all health care expenditures and remain substantially higher than those in Canada.

Related Editorial

 Health Policy Reports
Canada's Health Care System

In this review of recent developments in Canadian health care policy, Detsky and Naylor describe the strains on the system in the 1990s that led to declining satisfaction on the part of the public and providers and to national debate about health care reform. A 2003 agreement between the federal and provincial governments called for a substantial increase in federal funds for health care but no major changes in organization, delivery, or financing.


Review Article
Medical Progress: Congenital Adrenal Hyperplasia
 

Congenital adrenal hyperplasia is a group of autosomal recessive disorders resulting from the deficiency of one of the enzymes required for cortisol synthesis in the adrenal cortex. The most frequent is steroid 21-hydroxylase deficiency, accounting for more than 90 percent of cases. This article discusses the molecular mechanisms, diagnosis, and management of this disease and highlights new developments, including genotype–phenotype correlations, gene-specific prenatal diagnosis, and prenatal therapy.

   

Correspondence
Nitroprusside in Critically Ill Patients with Aortic Stenosis
Full Text

Folate Supplementation in Sickle Cell Anemia
Full Text

The AIDS Pandemic
Full Text

  Restless Legs Syndrome
Full Text

Enfuvirtide for Prophylaxis against HIV Infection
Full Text

Treatment of Primary Erythromelalgia with Cyclosporine
Full Text

Severe Pseudohypocalcemia after Gadolinium-Enhanced Magnetic Resonance Angiography
Full Text


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