I would like to know if a terrible desease called Pulmonary Hypertension could be solved soon?

December 17th, 2008 | by Pressurized |
josemix1970 asked:


First at all, I apoligize for my mistakes in English. I have a sister who suffers a terrible deseade called Pulmonary Hypertension and I would like to know if could be possible to solve her bad health situation soon? She´s been treated with some pills: bosentan, sildenafil, etc….but unfortunately there is no a easy solution and we can´t wait much more… She needs news pills or mother cells or something like that to cure her emphisea and to down her pulmonary hypertension, so I request information using yahoo answer and I hope some doctor tell me something about this desease and most important: any kind of solution. Thanks in advanced, any information about could be appreciated. From Spain my best wishes to all.

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  1. 3 Responses to “I would like to know if a terrible desease called Pulmonary Hypertension could be solved soon?”

  2. By Trailbalzer on Dec 19, 2008 | Reply

    Cause of PAH

    Collagen vascular disease
    Congenital heart disease
    Portal hypertension
    Human immunodeficiency virus
    Left ventricular diastolic dysfunction
    Mitral valve disease
    Mediastinal fibrosis
    Chronic obstructive lung disease
    Obstructive sleep apnea
    Pulmonary fibrosis
    Interstitial pneumonitis
    Pulmonary thromboembolic disease Spiral CT, Sarcoidosis

    If all these causes have been ruled out
    then it is called Primry pulmonry hypertension

    several pathobiologic processes that result in pulmonary arterial hypertension :These include inhibition of the voltage-regulated potassium channel producing vasoconstriction of the pulmonary artery smooth-muscle cells, reduced expression of nitric oxide synthase in the endothelium of the pulmonary arterial bed, increased expression of endothelin and basic fibroblast growth factor, and thrombin deposition related to a procoagulant stat

    OUTCOME IS POOR
    research is slow

  3. By lalaland...123 on Dec 21, 2008 | Reply

    pulmonary hypertension is merely the side effect of an underlying problem. doctors could try addressing the pulmonary hypertension problem, but if nobody pays attention to the underlying cause, then your sister will remain in that state.

    here i believe is one good explanation as to why pulmonary hypertension occurs.

    when a person has a lung problem, the blood vessels in their lungs constrict (narrows) therefore the blood being pumped by the right heart — creates a back pressure. think of yourself as a water pump for example. you are pumping water through a tube with let’s say 2 cm diameter… try pumping water through a 1cm diameter — it’s harder isn’t it? and most of the fluids stay in that tubing — being pumped back and forth — creating a “back pressure” and this results in an increased blood pressure in the pulmonary artery — thus results in pulmonary hypertension.

    one of the most common cases wherein pulmonary hypertension would occur is among patients with pulmonary edema — if your sister had this condition, wherein there is excess fluids in her blood, then a diuretic therapy would be advisable.

    but if your sister has a lung problem wherein her blood vessels constricts (common case among patients with emphysema) then the doctors would need to address that underlying lung problem. she may be put to a mechanical ventilator so that her breathing will normalize and hopefully everything will be back to normal. otherwise, if the pressure keeps going up — then there is a risk of right heart failure.

    to sum it all up — pulmonary hypertension is not a disease, but merely the side effect of an underlying problem which needs to address as soon as possible.

  4. By sis_ter_di on Dec 24, 2008 | Reply

    First of all, the responder above me is correct only in the case of secondary PAH. In the case of Primary PAH, there is no underlying cause that can be treated to relieve the condition.

    I have secondary pulmonary hypertension. The condition that cause mine is called sarcoidosis. I also take silfenadil and am on oxygen therapy. My sarcoidosis is in remission right now, but that won’t change the fact that I will always have PAH.

    What I have been told is that the only “cure” for this is a heart/lung transplant. The transplants are done together because PAH causes heart failure, for one, and the transplants are more successful when done together.

    For more information, please check out the links below. Good luck to you and your sister.

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