Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension
In some subjects, high-altitude hypobaric hypoxia leads to high-altitude pulmonary hypertension. The threshold for the diagnosis of high-altitude pulmonary hypertension is a mean pulmonary artery pressure of 30 mmHg, even though for general pulmonary hypertension is ≥25 mmHg. High-altitude pulmonary...
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Series: | Pulmonary Circulation |
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doaj-17afbbef2ccc405fb44cc12d937453f42020-11-25T03:41:26ZengSAGE PublishingPulmonary Circulation2045-89402020-09-011010.1177/2045894020934625Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertensionJulio Brito0Patricia Siques1Eduardo Pena2Institute DECIPHER, German-Chilean Institute for Research on Pulmonary Hypoxia and Its Health Sequelae, Hamburg, GermanyInstitute DECIPHER, German-Chilean Institute for Research on Pulmonary Hypoxia and Its Health Sequelae, Hamburg, GermanyInstitute DECIPHER, German-Chilean Institute for Research on Pulmonary Hypoxia and Its Health Sequelae, Hamburg, GermanyIn some subjects, high-altitude hypobaric hypoxia leads to high-altitude pulmonary hypertension. The threshold for the diagnosis of high-altitude pulmonary hypertension is a mean pulmonary artery pressure of 30 mmHg, even though for general pulmonary hypertension is ≥25 mmHg. High-altitude pulmonary hypertension has been associated with high hematocrit findings (chronic mountain sickness), and although these are two separate entities, they have a synergistic effect that should be considered. In recent years, a new condition associated with high altitude was described in South America named long-term chronic intermittent hypoxia and has appeared in individuals who commute to work at high altitude but live and rest at sea level. In this review, we discuss the initial epidemiological pattern from the early studies done in Chile, the clinical presentation and possible molecular mechanism and a discussion of the potential management of this condition.https://doi.org/10.1177/2045894020934625 |
collection |
DOAJ |
language |
English |
format |
Article |
sources |
DOAJ |
author |
Julio Brito Patricia Siques Eduardo Pena |
spellingShingle |
Julio Brito Patricia Siques Eduardo Pena Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension Pulmonary Circulation |
author_facet |
Julio Brito Patricia Siques Eduardo Pena |
author_sort |
Julio Brito |
title |
Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension |
title_short |
Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension |
title_full |
Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension |
title_fullStr |
Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension |
title_full_unstemmed |
Long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension |
title_sort |
long-term chronic intermittent hypoxia: a particular form of chronic high-altitude pulmonary hypertension |
publisher |
SAGE Publishing |
series |
Pulmonary Circulation |
issn |
2045-8940 |
publishDate |
2020-09-01 |
description |
In some subjects, high-altitude hypobaric hypoxia leads to high-altitude pulmonary hypertension. The threshold for the diagnosis of high-altitude pulmonary hypertension is a mean pulmonary artery pressure of 30 mmHg, even though for general pulmonary hypertension is ≥25 mmHg. High-altitude pulmonary hypertension has been associated with high hematocrit findings (chronic mountain sickness), and although these are two separate entities, they have a synergistic effect that should be considered. In recent years, a new condition associated with high altitude was described in South America named long-term chronic intermittent hypoxia and has appeared in individuals who commute to work at high altitude but live and rest at sea level. In this review, we discuss the initial epidemiological pattern from the early studies done in Chile, the clinical presentation and possible molecular mechanism and a discussion of the potential management of this condition. |
url |
https://doi.org/10.1177/2045894020934625 |
work_keys_str_mv |
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