2015
DOI: 10.1161/circinterventions.115.003332
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Catheter-Based Therapies for Patients With Medication-Refractory Pulmonary Arterial Hypertension

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Cited by 13 publications
(5 citation statements)
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“…Similar results were reported at the 1-year follow-up for 66 patients with PH of varied etiology in the Phase-II PADN-1 study 4 . Even though these results were promising, they were taken with caution by the PH community given the limitations of the study design (reduced number of patients, lack of randomization, absence of control group, withdrawal of targeted therapies in PADN patients, unusual baseline characteristics of the patient population not matching most idiopathic PH series and short-term follow-up) 8,17 and the need for a controlled trial was internationally recognized 13 . Finally, in the very recent study by Zhang et al 12 , a series of 10 cases with PH secondary to HF treated with percutaneous PADN was reported.…”
Section: Discussionmentioning
confidence: 99%
“…Similar results were reported at the 1-year follow-up for 66 patients with PH of varied etiology in the Phase-II PADN-1 study 4 . Even though these results were promising, they were taken with caution by the PH community given the limitations of the study design (reduced number of patients, lack of randomization, absence of control group, withdrawal of targeted therapies in PADN patients, unusual baseline characteristics of the patient population not matching most idiopathic PH series and short-term follow-up) 8,17 and the need for a controlled trial was internationally recognized 13 . Finally, in the very recent study by Zhang et al 12 , a series of 10 cases with PH secondary to HF treated with percutaneous PADN was reported.…”
Section: Discussionmentioning
confidence: 99%
“…Эти факты, а также развитие в последнее время ренальной денервации в лечении резистентной ЛГ стали ключевыми для начала исследований легочной денервации у пациентов с ЛАГ [9].…”
Section: экспериментальные исследованияunclassified
“…Pulmonary arterial hypertension (PAH), characterized by mean pulmonary artery pressure (mPAP) ≥ 25 mmHg at rest, pulmonary artery wedge pressure (PAWP) ≤ 15 mmHg and pulmonary vascular resistance (PVR) > 3 Wood units [ 1 ], is a disease induced by a wide range of causes, which makes it difficult to formulate an appropriate therapeutic plan and receive great responses for PAH patients [ 2 ]. Up till the present, most patients can only rely on combined targeted medicine, however, not all patients can be relieved [ 2 , 3 ]. Besides, the 1-year, 3-year and 5-year survival rate of medium to high-risk patients treated by target therapy are 90%, 61%, 43% [ 4 ], and side effects of targeted medicine are not tolerable in a considerable number of patients.…”
Section: Introductionmentioning
confidence: 99%