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Books on the topic 'Pulmonary-arterial'

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Author: Grafiati

Published: 9 March 2023

Last updated: 10 March 2023

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1

Pulmonary arterial hypertension. Oxford: Clinical Pub., 2009.

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2

Barst, Robyn J., ed. Pulmonary Arterial Hypertension. Chichester, UK: John Wiley & Sons, Ltd, 2008. http://dx.doi.org/10.1002/9780470997390.

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3

Gerry, Coghlan, ed. Pulmonary arterial hypertension. Oxford: Oxford University Press, 2010.

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4

Peacock, A. J., and J. A. Barberà. Pulmonary arterial hypertension. Oxford: Clinical Pub., 2009.

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5

Bohnen, Michael S. Potassium Channelopathies in Pulmonary Arterial Hypertension. [New York, N.Y.?]: [publisher not identified], 2017.

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6

Baughman, Robert P., Roberto G. Carbone, and Giovanni Bottino, eds. Pulmonary Arterial Hypertension and Interstitial Lung Diseases. Totowa, NJ: Humana Press, 2009. http://dx.doi.org/10.1007/978-1-60327-074-8.

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7

Maurice, Beghetti, Barst Robyn J, Naeije Robert, and Rubin Lewis J, eds. Pulmonary arterial hypertension related to congenital heart disease. München: Elsevier, Urban & Fischer, 2006.

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8

Robyn, Barst, ed. Pulmonary arterial hypertension: Diagnosis and evidence-based treatment. Chichester, West Sussex, England: John Wiley & Sons, 2008.

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9

Antel, J., M. B. Hesselink, and R. T. Schermuly. Pulmonary arterial hypertension: Focusing on a future : enhancing and extending life. Amsterdam: IOS Press, 2010.

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10

P, Baughman Robert, Carbone Roberto G, and Bottino Giovanni, eds. Pulmonary arterial hypertension and interstitial lung diseases: A clinical guide. Totowa, N.J: Humana, 2009.

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11

Gatzoulis, Professor Michael A., ed. Pulmonary Arterial Hypertension. Oxford University Press, 2011. http://dx.doi.org/10.1093/med/9780199572632.001.0001.

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12

Stewart, Scott. Pulmonary Arterial Hypertension. Taylor & Francis Group, 2008.

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13

Gatzoulis, Michael A. Pulmonary Arterial Hypertension. Oxford University Press, 2012.

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14

Pulmonary Arterial Hypertension. Oxford University Press, Incorporated, 2012.

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15

Pulmonary Arterial Hypertension. Oxford University Press, 2012.

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16

Pulmonary Arterial Hypertension. Oxford University Press, Incorporated, 2010.

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17

Stewart, Simon. Pulmonary Arterial Hypertension: Pocketbook. Taylor & Francis Group, 2008.

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18

Stewart, Simon. Pulmonary Arterial Hypertension: Pocketbook. CRC Press, 2020. http://dx.doi.org/10.3109/9780203640432.

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19

Stewart, Simon. Pulmonary Arterial Hypertension: Pocketbook. Taylor & Francis Group, 2008.

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20

Stewart, Simon. Pulmonary Arterial Hypertension: Pocketbook. Taylor & Francis Group, 2004.

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21

Pulmonary Arterial Hypertension: Pocketbook. Informa Healthcare, 2004.

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22

Stewart, Simon. Pulmonary Arterial Hypertension: Pocketbook. Taylor & Francis Group, 2008.

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23

Stewart, Simon. Pulmonary Arterial Hypertension: Pocketbook. Taylor & Francis Group, 2008.

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24

van den Bosch, Annemien E., Luigi P. Badano, and Julia Grapsa. Right ventricle and pulmonary arterial pressure. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780198726012.003.0023.

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Right ventricular (RV) performance plays an important role in the morbidity and mortality of patients with left ventricular dysfunction, congenital heart disease, and pulmonary hypertension. Assessment of RV size, function, and haemodynamics has been challenging because of its complex geometry. Conventional two-dimensional echocardiography is the modality of choice for assessment of RV function in clinical practice. Recent developments in echocardiography have provided several new techniques for assessment of RV dimensions and function, include tissue Doppler imaging, speckle-tracking imaging, and volumetric three-dimensional imaging. However, specific training, expensive dedicated equipment, and extensive clinical validation are still required. Doppler methods interrogating tricuspid inflow and pulmonary artery flow velocities, which are influenced by changes in pre- and afterload conditions, may not provide robust prognostic information for clinical decision-making. This chapter addresses the role of the various echocardiographic modalities used to assess the RV and pulmonary circulation. Special emphasis has been placed on technical considerations, limitations, and pitfalls of image acquisition and analysis.

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25

Stewart, Simon. Clinician's Guide to Pulmonary Arterial Hypertension. Taylor & Francis Group, 2008.

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26

Stewart, Simon. Clinician's Guide to Pulmonary Arterial Hypertension. Taylor & Francis Group, 2008.

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27

Katritsis, Demosthenes G., Bernard J. Gersh, and A. John Camm. Pulmonary arterial hypertension and hypertension associated with pulmonary venous abnormalities. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199685288.003.1747_update_004.

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Pulmonary arterial hypertension and pulmonary hypertension associated with pulmonary venous or capillary abnormalities, i.e. pulmonary veno-occlusive disease and pulmonary capillary haemangiomatosis, are discussed.

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28

Stewart, Simon. A Clinician's Guide to Pulmonary Arterial Hypertension. CRC Press, 2008. http://dx.doi.org/10.3109/9781439802045.

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29

Southgate, Laura, and Rajiv Machado, eds. Genetics and Genomics of Pulmonary Arterial Hypertension. MDPI, 2022. http://dx.doi.org/10.3390/books978-3-0365-4830-2.

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30

McDonald, T. F., and A. B. Chandler. Connective Tissues in Arterial and Pulmonary Disease. Springer, 2012.

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31

Mcdonald, T. F. Connective Tissues in Arterial and Pulmonary Disease. Springer, 2011.

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32

Pulmonary Arterial Hypertension: Diagnosis and Evidence - Based Treatment. Wiley & Sons, Incorporated, John, 2009.

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33

AACP. Pulmonary Arterial Hypertension: Current Concepts and Clinical Aspects. Karger, 2004.

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34

Barst, Robyn. Pulmonary Arterial Hypertension: Diagnosis and Evidence-Based Treatment. Wiley & Sons, Incorporated, John, 2008.

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35

Barst, Robyn. Pulmonary Arterial Hypertension: Diagnosis and Evidence-Based Treatment. Wiley & Sons, Limited, John, 2008.

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36

Estrada, Victoria. Pulmonary Arterial Hypertension and Nifedipine: Pathogenesis and Management. Nova Science Publishers, Incorporated, 2015.

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37

A Clinician's Guide to Pulmonary Arterial Hypertension: Pocketbook, Second Edition. 2nd ed. Informa Healthcare, 2008.

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38

Baughman, Robert P., Roberto G. Carbone, and Giovanni Bottino. Pulmonary Arterial Hypertension and Interstitial Lung Diseases: A Clinical Guide. Humana Press, 2010.

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39

Pulmonary Arterial Hypertension and Interstitial Lung Diseases: A Clinical Guide. Humana Press, 2008.

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40

Pulmonary Arterial Hypertension, An Issue of Clinics in Chest Medicine. Saunders, 2007.

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41

Trow, Terence K. Pulmonary Arterial Hypertension, an Issue of Clinics in Chest Medicine. Elsevier, 2014.

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42

Daicoff, Barbara Blue. EXAMINATION OF PHYSIOLOGIC RESPONSES TO ENDOTRACHEAL SUCTIONING TECHNIQUES (HYPERTENSION, PULMONARY ARTERIAL PRESSURE). 1993.

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43

Vergnaud, Sophie, David Dobarro, and John Wort. Pulmonary vasculature. Oxford University Press, 2017. http://dx.doi.org/10.1093/med/9780199657742.003.0017.

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A 16-year-old girl with a diagnosis of diffuse cutaneous systemic sclerosis is referred to a specialist pulmonary hypertension centre with a history of progressive breathlessness, reduced exercise tolerance, and raised pulmonary pressures on transthoracic echocardiogram. She is found to have pulmonary arterial hypertension on right cardiac catheterization and is started on sildenafil, a phosphodiesterase-5 inhibitor, which stabilizes her condition. An endothelin receptor antagonist is added, which provides some initial symptomatic improvement. She continues to deteriorate over a period of 5 years, ultimately requiring intravenous prostanoids, the only treatment to provide a real symptomatic and haemodynamic improvement. This chapter explores the physiology and pathophysiology of pulmonary arterial hypertension, its classification, the means of investigation and diagnosis, who to refer to specialist centres, and the concepts behind current and future treatment strategies.

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44

Istaphanous, George K., and Andreas W. Loepke. Pulmonary Hypertension. Oxford University Press, 2013. http://dx.doi.org/10.1093/med/9780199764495.003.0035.

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Pediatric pulmonary arterial hypertension (PAH) is characterized by a pathologically elevated pulmonary artery pressure in children. The etiology of PAH is multifactorial, and while its prognosis is closely related to the reversibility of the underlying disease process, much progress has recently been made in its diagnosis and treatment, significantly decreasing the associated morbidity and mortality.

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45

Hays, Norman. Sїldenafїl: Effective Treatment Erectile Disfunction and Pulmonary Arterial Hypertension. Independently Published, 2019.

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46

Chousterman, Benjamin, and Didier Payen. Pulmonary vasodilators in critical illness. Oxford University Press, 2016. http://dx.doi.org/10.1093/med/9780199600830.003.0039.

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Pulmonary vasodilators (PV) are commonly used in the intensive care unit (ICU) to treat pulmonary hypertension and/or hypoxaemia. The choice of drug is based on its pharmacokinetic and pharmacodynamic properties. The inhaled route of administration is preferred to treat hypoxaemia as it improves the ventilation/perfusion ratio. Systemic administration of PVs can lead to a decrease of mean arterial pressure and a worsening of hypoxaemia. Despite their beneficial effects, PVs have not shown improvement in mortality in acute respiratory distress syndrome patients. Rebound of hypoxaemia and/or pulmonary arterial hypertension should be prevented during PV treatment discontinuation with a slow de-escalation protocol. This chapter reviews the use of the main PV available for use in the ICU.

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47

Carlos, Festus B. Sildenafil Citrate: The Most Powerful Pill for Combating Erectile Dysfunction and Pulmonary Arterial Hypertension. Independently Published, 2018.

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48

Favour. Ultimate and Best: Treats Erectile Dysfunction, Symptoms of Benign Prostatic Hyperplasia, and Pulmonary Arterial Hypertension. Independently Published, 2019.

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49

Zucco, Liana V. Genotypic/phenotypic analysis of endothelial progenitor cells in idiopathic pulmonary arterial hypertension and hereditary hemorrhagic telangiectasia. 2006.

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50

Kugathasan, Lakshmi. Role of the angiopoietin/Tie2 system in a rodent model of hypoxia-induced pulmonary arterial hypertension. 2004.

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