Imaging of pulmonary hypertension: pictorial essay
Type de document :
Article dans une revue scientifique: Article original
PMID :
URL permanente :
Titre :
Imaging of pulmonary hypertension: pictorial essay
Auteur(s) :
Altschul, Erica [Auteur]
Remy, Martine [Auteur]
Hôpital Albert Calmette
Machnicki, Stephen [Auteur]
Sulica, Roxana [Auteur]
Moore, Jonathan A. [Auteur]
Singh, Anup [Auteur]
Raoof, Suhail [Auteur]
Remy, Martine [Auteur]
Hôpital Albert Calmette
Machnicki, Stephen [Auteur]
Sulica, Roxana [Auteur]
Moore, Jonathan A. [Auteur]
Singh, Anup [Auteur]
Raoof, Suhail [Auteur]
Titre de la revue :
Chest
Nom court de la revue :
Chest
Numéro :
156
Pagination :
211-227
Date de publication :
2019-04-11
ISSN :
1931-3543
Discipline(s) HAL :
Sciences du Vivant [q-bio]
Résumé en anglais : [en]
Pulmonary hypertension (PH) is an end result of a diverse array of complex clinical conditions that invoke hemodynamic and pathophysiological changes in the pulmonary vasculature. Many patients' symptoms begin with dyspnea ...
Lire la suite >Pulmonary hypertension (PH) is an end result of a diverse array of complex clinical conditions that invoke hemodynamic and pathophysiological changes in the pulmonary vasculature. Many patients' symptoms begin with dyspnea on exertion for which screening tests such as chest roentgenograms and more definitive noninvasive tests such as CT scans are ordered initially. It is imperative that clinicians are cognizant of subtle clues on these imaging modalities that alert them to the possibility of PH. These clues may serve as a stepping stone towards more advanced noninvasive (echocardiogram) and invasive (right heart catheterization) testing. On the CT scan, the signs are classified into mediastinal and lung parenchymal abnormalities. In addition to suspecting the diagnosis of PH, this paper provides a pictorial essay to guide health care professionals in identifying the etiology of PH. This paper also provides concrete definitions, wherever possible, of what constitutes abnormalities in PH, such as dilated pulmonary arteries, pruning of vessels, and increased thickness of free wall of the right ventricle. The sensitivities and specificities of each sign are enumerated. The common radiographic and clinical features of many different etiologies of PH are tabulated for the convenience of the readers. Some newer imaging modalities such as dual-energy CT of the chest that hold promise for the future are also described.Lire moins >
Lire la suite >Pulmonary hypertension (PH) is an end result of a diverse array of complex clinical conditions that invoke hemodynamic and pathophysiological changes in the pulmonary vasculature. Many patients' symptoms begin with dyspnea on exertion for which screening tests such as chest roentgenograms and more definitive noninvasive tests such as CT scans are ordered initially. It is imperative that clinicians are cognizant of subtle clues on these imaging modalities that alert them to the possibility of PH. These clues may serve as a stepping stone towards more advanced noninvasive (echocardiogram) and invasive (right heart catheterization) testing. On the CT scan, the signs are classified into mediastinal and lung parenchymal abnormalities. In addition to suspecting the diagnosis of PH, this paper provides a pictorial essay to guide health care professionals in identifying the etiology of PH. This paper also provides concrete definitions, wherever possible, of what constitutes abnormalities in PH, such as dilated pulmonary arteries, pruning of vessels, and increased thickness of free wall of the right ventricle. The sensitivities and specificities of each sign are enumerated. The common radiographic and clinical features of many different etiologies of PH are tabulated for the convenience of the readers. Some newer imaging modalities such as dual-energy CT of the chest that hold promise for the future are also described.Lire moins >
Langue :
Anglais
Audience :
Internationale
Vulgarisation :
Non
Établissement(s) :
CHU Lille
Université de Lille
Université de Lille
Date de dépôt :
2019-12-09T16:48:15Z
2024-04-16T13:32:04Z
2024-04-16T13:32:04Z