Management of dyspnea in advanced pulmonary arterial hypertension

Dimitar Sajkov; Nikolai Petrovsky; Paolo Palange

doi:10.1097/SPC.0b013e328338c1e0

Management of dyspnea in advanced pulmonary arterial hypertension

Dimitar Sajkov, Nikolai Petrovsky, Paolo Palange

Research output: Contribution to journal › Review article › peer-review

12 Citations (Scopus)

Abstract

Establishing the cause and clinical severity of pulmonary hypertension is critical for management. The pathophysiology of dyspnea in PAH is complex and related to pulmonary vascular resistance. Although disease-specific treatments are now available, a cure for PAH remains elusive and trials of combination treatments to improve symptoms and outcomes are ongoing.

Original language	English
Pages (from-to)	76-84
Number of pages	9
Journal	Current Opinion in Supportive and Palliative Care
Volume	4
Issue number	2
DOIs	https://doi.org/10.1097/SPC.0b013e328338c1e0
Publication status	Published - Jun 2010

Keywords

Dyspnea
Exercise tolerance
Palliative care
Pulmonary arteries
Pulmonary hypertension

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10.1097/SPC.0b013e328338c1e0

Cite this

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title = "Management of dyspnea in advanced pulmonary arterial hypertension",

abstract = "Establishing the cause and clinical severity of pulmonary hypertension is critical for management. The pathophysiology of dyspnea in PAH is complex and related to pulmonary vascular resistance. Although disease-specific treatments are now available, a cure for PAH remains elusive and trials of combination treatments to improve symptoms and outcomes are ongoing.",

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AU - Sajkov, Dimitar

AU - Petrovsky, Nikolai

AU - Palange, Paolo

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N2 - Establishing the cause and clinical severity of pulmonary hypertension is critical for management. The pathophysiology of dyspnea in PAH is complex and related to pulmonary vascular resistance. Although disease-specific treatments are now available, a cure for PAH remains elusive and trials of combination treatments to improve symptoms and outcomes are ongoing.

AB - Establishing the cause and clinical severity of pulmonary hypertension is critical for management. The pathophysiology of dyspnea in PAH is complex and related to pulmonary vascular resistance. Although disease-specific treatments are now available, a cure for PAH remains elusive and trials of combination treatments to improve symptoms and outcomes are ongoing.

KW - Dyspnea

KW - Exercise tolerance

KW - Palliative care

KW - Pulmonary arteries

KW - Pulmonary hypertension

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DO - 10.1097/SPC.0b013e328338c1e0

M3 - Review article

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EP - 84

JO - Current Opinion in Supportive and Palliative Care

JF - Current Opinion in Supportive and Palliative Care

SN - 1751-4258

IS - 2

ER -

Management of dyspnea in advanced pulmonary arterial hypertension

Abstract

Keywords

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