Skip to main content Accessibility help
×
Hostname: page-component-cd9895bd7-hc48f Total loading time: 0 Render date: 2024-12-27T15:01:34.707Z Has data issue: false hasContentIssue false

3.6.7 - Pulmonary Hypertension

from Section 3.6 - Acute Respiratory Failure

Published online by Cambridge University Press:  27 July 2023

Ned Gilbert-Kawai
Affiliation:
The Royal Liverpool Hospital
Debashish Dutta
Affiliation:
Princess Alexandra Hospital NHS Trust, Harlow
Carl Waldmann
Affiliation:
Royal Berkshire Hospital, Reading
Get access

Summary

Key Learning Points

  1. 1. Pulmonary hypertension (PH) is present when the mean pulmonary arterial pressure is ≥25 mmHg at rest.

  2. 2. The World Health Organization classifies PH into five groups.

  3. 3. Clinical features of PH may be non-specific, and thus challenging to recognise.

  4. 4. Identification and treatment of any potential reversible causes are fundamental to the management of PH.

  5. 5. PH is progressive and can be fatal if untreated.

Type
Chapter
Information
Intensive Care Medicine
The Essential Guide
, pp. 242 - 244
Publisher: Cambridge University Press
Print publication year: 2021

Access options

Get access to the full version of this content by using one of the access options below. (Log in options will check for institutional or personal access. Content may require purchase if you do not have access.)

References

References and Further Reading

Hoeper, MM, Galie, N, Murali, S, et al. Outcome after cardiopulmonary resuscitation in patients with pulmonary arterial hypertension. Am J Respir Crit Care Med 2002;165:341–4.CrossRefGoogle ScholarPubMed
Hoeper, MM, Granton, J. Intensive care unit management of patients with severe pulmonary hypertension and right heart failure. Am J Respir Crit Care Med 2011;184:1114–24.CrossRefGoogle ScholarPubMed
Ishikawa, S, Miyauchi, T, Sakai, S, et al. Elevated levels of plasma endothelin-1 in young patients with pulmonary hypertension caused by congenital heart disease are decreased after successful surgical repair. J Thorac Cardiovasc Surg 1995;110:271–3.CrossRefGoogle ScholarPubMed
Rubin, LJ, Hopkins, W. Clinical features and diagnosis of pulmonary hypertension of unclear etiology in adults. UpToDate. Waltham, MA: Wolters Kluwer Health. www.uptodate.com/contents/8249Google Scholar
Simonneau, G, Gatzoulis, MA, Adatia, I, et al. Updated clinical classification of pulmonary hypertension. J Am Coll Cardiol 2013;62(25 Suppl):D3441.CrossRefGoogle ScholarPubMed
Zamanian, RT, Haddad, F, Doyle, RL, Weinacker, AB. Management strategies for patients with pulmonary hypertension in the intensive care unit. Crit Care Med 2007;35:2037–50.CrossRefGoogle ScholarPubMed

Save book to Kindle

To save this book to your Kindle, first ensure no-reply@cambridge.org is added to your Approved Personal Document E-mail List under your Personal Document Settings on the Manage Your Content and Devices page of your Amazon account. Then enter the ‘name’ part of your Kindle email address below. Find out more about saving to your Kindle.

Note you can select to save to either the @free.kindle.com or @kindle.com variations. ‘@free.kindle.com’ emails are free but can only be saved to your device when it is connected to wi-fi. ‘@kindle.com’ emails can be delivered even when you are not connected to wi-fi, but note that service fees apply.

Find out more about the Kindle Personal Document Service.

Available formats
×

Save book to Dropbox

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Dropbox.

Available formats
×

Save book to Google Drive

To save content items to your account, please confirm that you agree to abide by our usage policies. If this is the first time you use this feature, you will be asked to authorise Cambridge Core to connect with your account. Find out more about saving content to Google Drive.

Available formats
×