Pulmonary hypertension is a rare, incurable and life threatening illness. In short, PH is high blood pressure in the pulmonary artery (the blood vessel that leads from your heart to your lungs). PH symptoms include shortness of breath with minimal exertion, fatigue, chest pain, dizzy spells and fainting. PH most often strikes women in the prime of their lives however, it is found in young children, elderly and men.
This is a short and simply article that explains what Pulmonary Hypertention is and has a nice graphic.http://jama.ama-assn.org/cgi/content/full/299/3/372
Filed under: Pulmonary Hypertension | Tagged: Pulmonary Hypertension
High blood pressure in the arteries that supply the lungs is called pulmonary hypertension (PHT). The blood pressure measured by cuff on your arm isn’t directly related to the pressure in your lungs. The blood vessels that supply the lungs constrict and their walls thicken, so they can’t carry as much blood. As in a kinked garden hose, pressure builds up and backs up. The heart works harder, trying to force the blood through. If the pressure is high enough, eventually the heart can’t keep up, and less blood can circulate through the lungs to pick up oxygen. Patients then become tired, dizzy and short of breath.
If a pre-existing disease triggered the PHT, doctors call it secondary PHT. That’s because it’s secondary to another problem, such as a heart or lung disorder. Congenital heart disease can cause PHT.
It’s important to repair congenital heart problems (when possible) before permanent pulmonary hypertensive changes develop. Intracardiac left-to-right shunts (such as a ventricular or atrial septal defect, a hole in the wall between the two ventricles or atria) can cause too much blood flow through the lungs. This situation is sometimes called Eisenmenger complex. Heart valve conditions, such as mitral stenosis (a narrowing of the mitral valve), can also cause PHT. Fixing the valve usually reverses the PHT.