viernes, 7 de enero de 2011

BOLETIN CARDIOLOGICO

BOLETIN CARDIOLOGICO Nº  6

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Asunto: BOLETIN CARDIOLOGICO
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BOLETIN CARDIOLOGICO Nº  6


jueves, 6 de enero de 2011

Síndrome coronario agudo. Conceptos....

Maximo Cuadros Chavez posted in cibermedicos.Maximo Cuadros Chavez10:42pm Jan 6

Síndrome coronario agudo. Conceptos. Epidemiología. Fisiopatología. Nomenclatura
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Síndrome coronario agudo. Conceptos....

Maximo Cuadros Chavez posted in cibermedicos.Maximo Cuadros Chavez10:42pm Jan 6

Síndrome coronario agudo. Conceptos. Epidemiología. Fisiopatología. Nomenclatura
http://www.facebook.com/l/335fbZQuKKaTmRqx_qxiJQ0PA4g;www.elsevier.es/watermark/ctl_servlet?_f=10&pident_articulo=13139207&pident_usuario=0&pident_revista=62&fichero=62v10n37a13139207pdf001.pdf&ty=80&accion=L&origen=medicine&web=www.medicineonline.es&lan=es

 

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tratamiento de caquexia

Manejo de la caquexia en oncología
Treatment of cachexia in oncology
EM Tazi, H Errihani
Indian J Paliative Care 2010:16;136-144.   DOI: 10.4103/0973-1075.73644
 
Background: Cachexia is a complex metabolic syndrome associated with many chronic or end-stage diseases, especially cancer, and is characterized by loss of muscle with or without loss of fat mass. The management of cachexia is a complex challenge that should address the different causes underlying this clinical event with an integrated or multimodal treatment approach targeting the different factors involved in its pathophysiology. Aims and Objectives : The purpose of this article was to review the current medical treatment of cancer-related cachexia, in particular focusing on combination therapy and ongoing research. Results : Among the treatments proposed in the literature for cancer-related cachexia, some proved to be ineffective, namely, cyproheptadine, hydrazine, metoclopramide, and pentoxifylline. Among effective treatments, progestagens are currently considered the best available treatment option for cancer-related cachexia, and they are the only drugs approved in Europe. Drugs with a strong rationale that have failed or have not shown univocal results in clinical trials so far include eicosapentaenoic acid, cannabinoids, bortezomib, and anti-TNF-alpha MoAb. Several emerging drugs have shown promising results but are still under clinical investigation (thalidomide, selective cox-2 inhibitors, ghrelin mimetics, insulin, oxandrolone, and olanzapine). Conclusions : To date, despite several years of coordinated efforts in basic and clinical research, practice guidelines for the prevention and treatment of cancer-related muscle wasting are lacking, mainly because of the multifactorial pathogenesis of the syndrome. From all the data presented, one can speculate that one single therapy may not be completely successful in the treatment of cachexia. From this point of view, treatments involving different combinations are more likely to be successful.
Enlace para leer el artículo completo:
http://www.jpalliativecare.com

: Eplerenone for Mild Heart Failure/Bipolar Depression

conversation.


Teaching Topic
Eplerenone for Mild Heart Failure
Original Article
Eplerenone in Patients with Systolic Heart Failure and Mild Symptoms
F. Zannad and Others
  


In the placebo-controlled Randomized Aldactone Evaluation Study (RALES), adding the mineralocorticoid-receptor antagonist spironolactone to recommended therapy in patients with systolic heart failure and moderate-to-severe symptoms (i.e., New York Heart Association [NYHA] functional class III or IV symptoms) decreased the rate of death from any cause and the risk of hospitalization for cardiovascular reasons.
Clinical Pearls
  What was the aim of this study?
The aim of this study was to investigate the effects of eplerenone, added to evidence-based therapy, on clinical outcomes in patients with systolic heart failure and mild symptoms (i.e., NYHA functional class II symptoms).
  What is the mechanism of action of eplerenone?
Eplerenone is a selective mineralocorticoid-receptor antagonist.
Table 2. Primary Outcome, Component Events, and Key Secondary Outcomes.
Morning Report Questions
Q. Why was this trial stopped prematurely?
A. The trial was stopped prematurely for efficacy, according to prespecified rules, after a median follow-up period of 21 months. The primary outcome occurred in 18.3% of patients in the eplerenone group as compared with 25.9% in the placebo group (hazard ratio, 0.63; 95% confidence interval [CI], 0.54 to 0.74; P<0.001). A total of 12.5% of patients receiving eplerenone and 15.5% of those receiving placebo died (hazard ratio, 0.76; 95% CI, 0.62 to 0.93; P=0.008); 10.8% and 13.5%, respectively, died of cardiovascular causes (hazard ratio, 0.76; 95% CI, 0.61 to 0.94; P=0.01). Hospitalizations for heart failure and for any cause were also reduced with eplerenone.
Q. What adverse effect complicated treatment with eplerenone?
A. A serum potassium level above 5.5 mmol per liter was reported in 158 patients (11.8%) in the eplerenone group and 96 patients (7.2%) in the placebo group (P<0.001). Hypokalemia was significantly less common in the eplerenone- as compared to the placebo-treated group.

sábado, 1 de enero de 2011

Current Cardiology Reviews (1 - 2) 2010

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Current Cardiology Reviews (1 - 2) 2010

Current Cardiology Reviews
Issue: 1, February 2010
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Current Cardiology Reviews
Issue: 2, May 2010
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Murillo Santucci Cesar de Assunção
Unidade de Terapia Intensiva adulto
Disciplina de Anestesiologia, Dor e Terapia Intensiva
Escola Paulista de Medicina
Rua Napoleão de Barros,715
Vila Clementino - São Paulo - CEP: 04024-002
Tel/Fax: +55-11-55757768
Tel/Fax: +55-11- 55764069
m.assuncao@unifesp.br
murilloassuncao@gmail.com