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You are here: Home > Ills & Conditions > What Is Pulmonary Hypertension?


What Is Pulmonary Hypertension? 


By Peter Jaret
CONSUMER HEALTH INTERACTIVE

Below:
 • What's the difference between hypertension and pulmonary hypertension?
 • How does pulmonary hypertension affect the body?
 • New insights, new treatments


First, a few words of reassurance. It's natural to feel confused and anxious after being diagnosed with pulmonary hypertension. The condition is not exactly a household word, and it is a serious illness. Pulmonary hypertension often requires treatment by specialists at large medical centers with specific expertise. Being diagnosed with the condition may also require you to make significant changes in your life.

But keep in mind that many people with pulmonary hypertension can manage the disease and live their lives quite normally. New advances in the understanding of this condition and how to treat it have changed the outlook dramatically in recent years.

What's the difference between hypertension and pulmonary hypertension?

"Pulmonary" is from the Latin root "pulmo," or "the lung." "Hypertension" means high blood pressure. Pulmonary hypertension is a condition caused by abnormally high blood pressure in the arteries that supply the lungs with blood.

Most people are familiar with blood pressure as measured with a cuff that goes around the upper arm. This simple test charts the pressure in blood vessels in the body's extremities. If elevated, this is referred to simply as "hypertension."

Pulmonary hypertension, in contrast, is abnormally high blood pressure in just one part of the body: the vessels that supply blood to the lungs. Normally, the pressure in these vessels is much lower than that in the rest of the body. Typical blood pressure measured with a cuff around your arm is 120/80 mm Hg. Normal pulmonary artery blood pressure is only about 25/14 mm Hg.

How does pulmonary hypertension affect the body?

When pulmonary blood pressure becomes abnormally high, it can seriously damage the heart and lungs. Pulmonary hypertension often occurs when blood vessels become narrowed or blood flow through these vessels is hindered. The pressure of blood moving through the constricted passage increases, just the way water pressure increases if you hold your thumb over the end of a garden hose. Elevated blood pressure can increase the risk of injury to blood vessels. It also puts an extra strain on the heart, which has to work harder to pump blood through narrowed or partially blocked vessels.

In the case of pulmonary hypertension, the right ventricle (the muscle of the right side of the heart that pumps blood to the lungs) has to work harder. The added strain causes the muscle to enlarge and become less efficient.

The extra pressure within the vessels also puts strain on their inner walls, causing them to become stiffer and thicker. Some vessels may gradually become completely blocked. Other complications, such as low oxygen levels, can also ensue. In some people the body begins to produce more red blood cells to make up for lowered levels of oxygen in the blood. This causes blood to become thicker and stickier, further increasing the load on the heart and raising the risk of blood clots.

Under certain conditions, pulmonary hypertension leads to a condition known as cor pulmonale. Cor pulmonale is enlargement of the right ventricle that sometimes occurs when pulmonary hypertension is caused by a disorder of the respiratory system -- for instance, emphysema or fibrotic lung disease. Eventually, if the progress of the disease isn't stopped the right side of the heart may fail completely.

Pulmonary hypertension is divided into two forms. When the condition occurs in people with no other underlying disease that causes it, doctors call it primary pulmonary hypertension. When it is the result of other health problems, such as heart conditions, lung diseases, sickle cell disease, or autoimmune disorders such as scleroderma, it is called secondary pulmonary hypertension. In this case, the underlying cause is the primary condition: Pulmonary hypertension is the secondary result.

New insights, new treatments

Pulmonary hypertension is a challenging illness. But there is much that doctors can do to control the problem and treat the symptoms. Newly developed drugs can lower pulmonary blood pressure and reduce the strain on heart muscles. This can allow people with pulmonary hypertension to lead longer and more active lives. Thanks to these advances, the death rate from pulmonary hypertension has dropped significantly in the last few years. Understanding all you can about pulmonary hypertension is an important part of a comprehensive treatment plan.

-- Peter Jaret is a contributing editor for Health magazine and a winner of the American Medical Association's award for medical reporting. His work has appeared in National Geographic, Newsweek, Hippocrates, and many other national magazines. He is also the author of In Self-Defense (Harcourt Brace Jovanovich), Active Living Every Day, and Heart Healthy for Life.



References


Budev, M.M. et al. Diagnosis and evaluation of pulmonary hypertension. Cleveland Clinic Journal of Medicine, April 2003, pp S9-S27

Nauser, T.D., MD, and Stites, S.W., MD. Diagnosis and treatment of pulmonary hypertension. American Family Physician, May 1, 2001, pp 1789-1798

Primary Pulmonary Hypertension. National Institutes of Health, National Heart, Lung, and Blood Institute, Division of Lung Diseases

Advances in Pulmonary Hypertension. Journal of the Pulmonary Hypertension Association, Autumn 2002

Nauser, T.D., MD, and Stites, S.W., MD. Pulmonary Hypertension: New Perspectives. Medscape, www.medscape.com

Nauser, T.D., and Stites, S.W., MD. Pulmonary Hypertension: new perspectives. Congestive Heart Failure, 2003. May-June; 9 (3):155-62.

Farber, H.W. Pulmonary Hypertension. The Merck Manual, Second Home Edition.

Pulmonary Hypertension. The American Heart Association, www.americanheart.org

Pulmonary Hypertension Association, www.phassociation.org


The Rush Heart Institute Center for Pulmonary Heart Disease, www.rush.edu


National Heart, Lung, and Blood Institute. What Is Pulmonary Arterial Hypertension? August 2006. http://www.nhlbi.nih.gov/health/dci/Diseases/pah/pah_what.html



Reviewed by Trenton D. Nauser, MD, FACP, FCCP, who practices pulmonary and critical care medicine at the Veterans Administration Medical Center in Kansas City, Missouri. He also serves as an assistant professor of medicine at the University of Kansas Medical Center, Kansas City, Kansas.


Our reviewers are members of Consumer Health Interactive's medical advisory board.
To learn more about our writers and editors, click here.

First published October 27, 2003
Last updated November 4, 2008
Copyright © 2003 Consumer Health Interactive


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