Pulmonary arterial hypertension /Clive Handler, Gerry Coghlan.
Material type: TextSeries: Publication details: Oxford ; New York : Oxford University Press, (c)2010.Edition: First editionDescription: 1 online resource (xix, 124 pages) : illustrationsContent type:- text
- computer
- online resource
- 9780191001819
- 9781306260497
- RC776 .P856 2010
- COPYRIGHT NOT covered - Click this link to request copyright permission: https://lib.ciu.edu/copyright-request-form
Item type | Current library | Collection | Call number | URL | Status | Date due | Barcode | |
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Online Book (LOGIN USING YOUR MY CIU LOGIN AND PASSWORD) | G. Allen Fleece Library ONLINE | Non-fiction | RC776.87 (Browse shelf(Opens below)) | Link to resource | Available | ocn867050359 |
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Includes bibliographies and index.
So you've been told you have pulmonary arterial hypertension (PAH) -- The structure of the heart -- The oxygenation and circulation of blood -- Blood pressure -- Palpitation -- What is PAH? -- The difference between PH and PAH -- Your clinic appointments -- Tests for PAH -- Clinical trials and evidence-based medicine -- Supportive treatments for PAH -- Targeted therapy -- When medication is not enough -- Living your life -- Useful contacts and and PH specialist centres.
Pulmonary arterial hypertension (PAH) is a high blood pressure in the arteries that supply the lungs with blood. Patients with mild PAH, particularly young patients, may feel quite well and get breathless or tired only with vigorous exertion. Those with severe PAH may get breathless on minimal exertion and feel tired, exhausted and experience chest pain, forceful heart beats, dizzy turns, loss of appetite, and have swelling of the legs due to fluid retention. This book will help patients and their families understand what PAH is, and advise them on how to cope with their illness. In the UK pat.
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