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Refined risk stratification, current treatment, and new therapeutic approaches in pulmonary arterial hypertension
The 2022 European Society of Cardiology/European Respiratory Society (ESC/ERS) guidelines for pulmonary hypertension have introduced a refined risk...
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Management of the peri-intubation period in patients with pulmonary arterial hypertension and respiratory failure
Purpose of ReviewThe endotracheal intubation of patients with pulmonary arterial hypertension (PAH) in respiratory distress is a highly morbid...
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Novel Drugs for the Treatment of Pulmonary Arterial Hypertension: Where Are We Going?
Pulmonary arterial hypertension (PAH) is a progressive disease that despite advances in therapy is associated with a 7-year survival of approximately...
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A Systematic Review of Novel Therapies of Pulmonary Arterial Hypertension
BackgroundPulmonary arterial hypertension (PAH) is a progressive, cureless disease, characterized by increased pulmonary vascular resistance and...
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Notch ratio in pulmonary flow predicts long-term survival after pulmonary endarterectomy for chronic thromboembolic pulmonary hypertension
BackgroundAssessment of the pattern of the RV outflow tract Doppler provides insights into the hemodynamics of chronic thromboembolic pulmonary...
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Resistin predicts disease severity and survival in patients with pulmonary arterial hypertension
BackgroundAbnormal remodeling of distal pulmonary arteries in patients with pulmonary arterial hypertension (PAH) leads to progressively increased...
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Clinical characteristics and predictors of pulmonary hypertension in chronic obstructive pulmonary disease at different altitudes
BackgroundPulmonary hypertension (PH) is a common complication in patients with chronic obstructive pulmonary disease (COPD) and is closely...
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Spontaneous hemodynamic improvement after balloon pulmonary angioplasty in patients with chronic thromboembolic pulmonary hypertension is observed within a short term after balloon pulmonary angioplasty
Natural hemodynamic changes after balloon pulmonary artery angioplasty (BPA) in a unified state without oxygen administration in patients with...
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Inhibition of PCSK9 Improves the Development of Pulmonary Arterial Hypertension Via Down-Regulating Notch3 Expression
BackgroundPulmonary arterial hypertension (PAH) is a fatal disease characterized by continuous constriction and occlusion of small pulmonary...
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The Role of Lung Ventilation/Perfusion Scan in the Management of Chronic Thromboembolic Pulmonary Hypertension
Chronic thromboembolic pulmonary hypertension (CTEPH), which is classified as a group 4 pulmonary hypertension (PH), is a life-threatening...
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Economic Burden of Delayed Diagnosis in Patients with Pulmonary Arterial Hypertension (PAH)
BackgroundThe aim of this study was to assess health care resource utilization (HRU) and costs associated with delayed pulmonary arterial...
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Chronic Thromboembolic Pulmonary Hypertension
Chronic thromboembolic pulmonary hypertension (CTEPH), defined as precapillary pulmonary hypertension (PH) by right heart catheterization and imaging...
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Ralinepag Phase II Open-Label Extension Study in Patients with Pulmonary Arterial Hypertension
IntroductionRalinepag is a potent, titratable, orally administered prostacyclin (IP) receptor agonist to treat pulmonary arterial hypertension. A...
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The Prevalence of Pulmonary Arterial Hypertension in Patients with Beta Thalassemia Major
Pulmonary arterial hypertension (PAH) remains a concern in patients with Beta thalassemia major (TM). However, this study aims to investigate the...
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Semi-Quantitative Analysis of Lung Perfusion SPECT/CT for Evaluation of Response to Balloon Pulmonary Angioplasty in Chronic Thromboembolic Pulmonary Hypertension
PurposeWe aimed to investigate the response to balloon pulmonary angioplasty (BPA) in chronic thromboembolic pulmonary hypertension (CTEPH) using...
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The management pattern and outcomes of chronic thromboembolic pulmonary hypertension: rationale and design for a Chinese real-world study
BackgroundChronic thromboembolic pulmonary hypertension (CTEPH) is a progressive pulmonary vascular disorder with substantial morbidity and...
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Even non-expert radiologists report chronic thromboembolic pulmonary hypertension (CTEPH) on CT pulmonary angiography with high sensitivity and almost perfect agreement
ObjectivesTo assess the diagnostic performance and interobserver agreement of CT pulmonary angiography (CTPA) in the detection of chronic...
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Hughes-Stovin syndrome—An important differential diagnosis in patients with suspected chronic thromboembolic pulmonary hypertension
Hughes-Stovin syndrome (HSS) is a rare vasculitis of unknown etiology. The disease is characterized by pronounced inflammation and damage to the...
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Patient and Therapeutic Profiles of Pulmonary Hypertension in Chronic Lung Diseases in Japan: A Cohort Study Using a Claims Database
IntroductionPulmonary hypertension (PH) is often complicated by chronic lung diseases (CLDs) such as chronic obstructive pulmonary disease (COPD) and...
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Prognostic and diagnostic utility of interleukin-6 in pediatric pulmonary arterial hypertension — a case-control study
Pulmonary arterial hypertension (PAH) in pediatrics is a progressive disease with significant vascular remodeling, right sided heart failure, and...