Pulmonary Hypertension News and Research

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Pulmonary arterial hypertension (PAH) is a condition involving high blood pressure and structural changes in the walls of the pulmonary arteries, which are the blood vessels that connect the right side of the heart to the lungs. Affecting people of all ages and ethnic backgrounds - but most commonly found in young women of child-bearing years - the disease has historically been chronic and incurable, with a poor survival rate. PAH is often not diagnosed in a timely manner because its early symptoms can be confused with those of many other pulmonary and respiratory conditions. Symptoms include shortness of breath, extreme fatigue, dizziness, fainting, swollen ankles and legs and chest pain (especially during physical activity). With proper diagnosis, there are currently several therapies to alleviate symptoms and improve quality of life for PAH patients. The key is to find a PAH specialist and pursue immediate treatment.
Inhalable gene therapy may restore function of crucial enzyme to reverse deadly PAH

Inhalable gene therapy may restore function of crucial enzyme to reverse deadly PAH

Scientists identify new genetic mutations that can cause pulmonary arterial hypertension

Scientists identify new genetic mutations that can cause pulmonary arterial hypertension

MedUni Vienna cardiologist demonstrates effectiveness of substance that makes heart softer

MedUni Vienna cardiologist demonstrates effectiveness of substance that makes heart softer

Eisai submits BELVIQ NDS with Health Canada

Eisai submits BELVIQ NDS with Health Canada

Nutritional supplement may improve survival rates of babies born with heart defects

Nutritional supplement may improve survival rates of babies born with heart defects

ECMO can be used on neonates with severe respiratory failure until lung transplantation, say scientists

ECMO can be used on neonates with severe respiratory failure until lung transplantation, say scientists

Researcher discovers additional mechanical properties of articular cartilage result in osteoarthritis

Researcher discovers additional mechanical properties of articular cartilage result in osteoarthritis

FDA grants priority review for Bayer HealthCare's riociguat for treatment of CTEPH

FDA grants priority review for Bayer HealthCare's riociguat for treatment of CTEPH

GE Healthcare seeks approval to supply Optison to EU market from Oslo manufacturing facility

GE Healthcare seeks approval to supply Optison to EU market from Oslo manufacturing facility

CALHM1 protein controls sense of taste, finds study

CALHM1 protein controls sense of taste, finds study

Feinstein Institute, Merck Serono to develop antibodies for treatment of SLE

Feinstein Institute, Merck Serono to develop antibodies for treatment of SLE

RSAS honors Feinstein Institute scientist with Crafoord Prize for genetic research on arthritis

RSAS honors Feinstein Institute scientist with Crafoord Prize for genetic research on arthritis

Monitor white blood cell count in pertussis infants

Monitor white blood cell count in pertussis infants

Taking early and repeated WBC is critical in determining infants at high risk of pertussis

Taking early and repeated WBC is critical in determining infants at high risk of pertussis

Merck’s resubmission of the NDA for suggammadex sodium injection accepted for review by the FDA

Merck’s resubmission of the NDA for suggammadex sodium injection accepted for review by the FDA

No significant link between SSRI use during pregnancy and risk of stillbirth, neonatal death

No significant link between SSRI use during pregnancy and risk of stillbirth, neonatal death

Early problems in processing knowledge-based information linked to Alzheimer's disease

Early problems in processing knowledge-based information linked to Alzheimer's disease

Tadalafil may offer therapeutic strategy in patients with Becker muscular dystrophy

Tadalafil may offer therapeutic strategy in patients with Becker muscular dystrophy

Tanshinones protect against sepsis: Study

Tanshinones protect against sepsis: Study

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