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Pulmonary hypertension

Potts Anastomosis: Transthoracic Echocardiographic Features – Tetralogy of Fallot, Doubly Committed Sub-arterial Ventricular Septal Defect, Anomalous Left Anterior Descending Coronary Artery Crossing Right Ventricular Outflow Tract

Issue: 
DOI: 
10.7727/wimj.2017.049
Pages: 
274-8

ABSTRACT

Accepted: 
13 Mar, 2017
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Journal Authors: 
e-Published: 21 Mar, 2017

Recent Advances of Diagnosis and Treatment of Pulmonary Arterial Hypertension

DOI: 
10.7727/wimj.2016.460
Synopsis: 
The mechanisms of pulmonary arterial hypertension remain uncertain, and the diagnosis of pulmonary arterial hypertension is challenging. The major advances of the diagnostic modalities and management strategies include new uses of routine biomarkers including antinuclear antibody, B-type natriuretic peptide, circulating endothelial cells and microRNA in diagnosis; and microRNA, mesenchymal stem cells and remote postconditioning for pulmonary protection in treatment. Understanding the progress in terms of the mechanisms and concepts of pulmonary hypertension implicates significant improvement of the management protocols of this disorder. In this article, the advances of the diagnostic modalities and management strategies of PAH are discussed.

ABSTRACT

Accepted: 
27 Sep, 2016
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Journal Authors: 
e-Published: 27 Oct, 2016

Disclaimer

Manuscripts that are Published Ahead of Print have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear in their original format and may not be copy edited or formatted in the style guide of this Journal. While accepted manuscripts are not yet assigned a volume, issue or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. The contents of the manuscript may change before it is published in its final form. Manuscripts in this section will be removed once they have been issued to a volume and issue, but will still retain the DOI and date of e-publication.

Rapamycin Improves Vascular Remodelling in a Controlled Rat Model of Monocrotaline-Induced Pulmonary Hypertension

Issue: 
DOI: 
10.7727/wimj.2015.222
Pages: 
638-44
Synopsis: 
We evaluated the effect of rapamycin on pulmonary arterial hypertension. Rapamycin provided improvements in exercise capacity, right ventricular systolic pressure and hypertrophy, but those were not significant. There were significant recoveries in the pulmonary artery muscular layer thickness and in the median life span of rats.

ABSTRACT

Background: Pulmonary arterial hypertension (PAH) is a serious disease characterized by the progressive elevation of the pulmonary arterial resistance, leading to the right ventricular failure and death. Objective: To evaluate the effect of rapamycin (RAPA), a potent cell-cycle inhibitor, on exercise capacity, right ventricular hypertrophy and pulmonary vascular remodelling on rats.

Accepted: 
18 May, 2015
PDF Attachment: 
Journal Sections: 
e-Published: 13 Aug, 2015

Truncus Arteriosus in Adolescents and Adult Afro-Caribbeans with no Intervention: Echocardiographic Findings

DOI: 
10.7727/wimj.2015.301

ABSTRACT

Accepted: 
12 Jun, 2015
Journal Sections: 
Journal Authors: 
e-Published: 12 Jun, 2015

Disclaimer

Manuscripts that are Published Ahead of Print have been peer reviewed and accepted for publication by the Editorial Board of the West Indian Medical Journal. They may appear in their original format and may not be copy edited or formatted in the style guide of this Journal. While accepted manuscripts are not yet assigned a volume, issue or page numbers, they can be cited using the DOI and date of e-publication. See our Instructions for Authors on how to properly cite manuscripts at this stage. The contents of the manuscript may change before it is published in its final form. Manuscripts in this section will be removed once they have been issued to a volume and issue, but will still retain the DOI and date of e-publication.

Pulmonary Hypertension: A Review of the Aetiology, Pathophysiology and Management

Issue: 
Pages: 
153–9
Synopsis: 
This paper gives an update on pulmonary hypertensive diseases which are a challenge to treat.

ABSTRACT

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e-Published: 18 Sep, 2013

Anomalous Origin of Left Coronary Artery with Left Anterior Descending Artery Connected to Left Pulmonary Artery from Single Right Coronary Artery

Issue: 
DOI: 
10.7727/wimj.2013.076
Pages: 
277–80

ABSTRACT

Accepted: 
25 Mar, 2013
PDF Attachment: 
Journal Sections: 
Journal Authors: 
e-Published: 24 Apr, 2013

Truncus Arteriosus: Surviving at 46 Years without Intervention

Issue: 
DOI: 
10.7727/wimj.2013.082
Pages: 
273–6

 

ABSTRACT

The median survival of patients with truncus arteriosus is five weeks of age with rare cases reaching adulthood. The longest reported survivor with balanced ventricles, as the index case has, is 38 years of age. The index case is a 46-year old male with Type 3 truncus arteriosus. His case has never been documented in the English Literature as far as the author is aware.

Accepted: 
02 Apr, 2013
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Journal Sections: 
Journal Authors: 
e-Published: 23 Apr, 2013
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