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Efficacy of treat-and-repair strategy for atrial septal defect with pulmonary arterial hypertension
by
Tada, Norio
, Nakazawa, Gaku
, Nanasato, Mamoru
, Hosokawa, Shinobu
, Kanazawa, Hideaki
, Akagi, Teiji
, Ito, Hiroshi
, Fuku, Yasushi
, Takaya, Yoichi
, Murakami, Tsutomu
, Imai, Masao
, Saji, Mike
, Sakamoto, Ichiro
, Yao, Atsushi
, Matsumoto, Kensuke
, Nakagawa, Koji
, Hirokami, Mitsugu
in
atrial septal defect
/ Cardiac Catheterization - adverse effects
/ Clinical outcomes
/ Congenital Heart Disease
/ Familial Primary Pulmonary Hypertension
/ Heart failure
/ Heart Failure - etiology
/ Heart Septal Defects, Atrial - complications
/ Heart Septal Defects, Atrial - therapy
/ Hospitalization
/ Humans
/ Hypertension, Pulmonary - diagnosis
/ Hypertension, Pulmonary - etiology
/ Hypertension, Pulmonary - therapy
/ Patients
/ Peptides
/ pulmonary arterial hypertension
/ Pulmonary Arterial Hypertension - diagnosis
/ Pulmonary Arterial Hypertension - etiology
/ Pulmonary Arterial Hypertension - therapy
/ Pulmonary arteries
/ Pulmonary hypertension
/ Statistical analysis
/ Treatment Outcome
/ Veins & arteries
2022
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Efficacy of treat-and-repair strategy for atrial septal defect with pulmonary arterial hypertension
by
Tada, Norio
, Nakazawa, Gaku
, Nanasato, Mamoru
, Hosokawa, Shinobu
, Kanazawa, Hideaki
, Akagi, Teiji
, Ito, Hiroshi
, Fuku, Yasushi
, Takaya, Yoichi
, Murakami, Tsutomu
, Imai, Masao
, Saji, Mike
, Sakamoto, Ichiro
, Yao, Atsushi
, Matsumoto, Kensuke
, Nakagawa, Koji
, Hirokami, Mitsugu
in
atrial septal defect
/ Cardiac Catheterization - adverse effects
/ Clinical outcomes
/ Congenital Heart Disease
/ Familial Primary Pulmonary Hypertension
/ Heart failure
/ Heart Failure - etiology
/ Heart Septal Defects, Atrial - complications
/ Heart Septal Defects, Atrial - therapy
/ Hospitalization
/ Humans
/ Hypertension, Pulmonary - diagnosis
/ Hypertension, Pulmonary - etiology
/ Hypertension, Pulmonary - therapy
/ Patients
/ Peptides
/ pulmonary arterial hypertension
/ Pulmonary Arterial Hypertension - diagnosis
/ Pulmonary Arterial Hypertension - etiology
/ Pulmonary Arterial Hypertension - therapy
/ Pulmonary arteries
/ Pulmonary hypertension
/ Statistical analysis
/ Treatment Outcome
/ Veins & arteries
2022
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Efficacy of treat-and-repair strategy for atrial septal defect with pulmonary arterial hypertension
by
Tada, Norio
, Nakazawa, Gaku
, Nanasato, Mamoru
, Hosokawa, Shinobu
, Kanazawa, Hideaki
, Akagi, Teiji
, Ito, Hiroshi
, Fuku, Yasushi
, Takaya, Yoichi
, Murakami, Tsutomu
, Imai, Masao
, Saji, Mike
, Sakamoto, Ichiro
, Yao, Atsushi
, Matsumoto, Kensuke
, Nakagawa, Koji
, Hirokami, Mitsugu
in
atrial septal defect
/ Cardiac Catheterization - adverse effects
/ Clinical outcomes
/ Congenital Heart Disease
/ Familial Primary Pulmonary Hypertension
/ Heart failure
/ Heart Failure - etiology
/ Heart Septal Defects, Atrial - complications
/ Heart Septal Defects, Atrial - therapy
/ Hospitalization
/ Humans
/ Hypertension, Pulmonary - diagnosis
/ Hypertension, Pulmonary - etiology
/ Hypertension, Pulmonary - therapy
/ Patients
/ Peptides
/ pulmonary arterial hypertension
/ Pulmonary Arterial Hypertension - diagnosis
/ Pulmonary Arterial Hypertension - etiology
/ Pulmonary Arterial Hypertension - therapy
/ Pulmonary arteries
/ Pulmonary hypertension
/ Statistical analysis
/ Treatment Outcome
/ Veins & arteries
2022
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Efficacy of treat-and-repair strategy for atrial septal defect with pulmonary arterial hypertension
Journal Article
Efficacy of treat-and-repair strategy for atrial septal defect with pulmonary arterial hypertension
2022
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Overview
ObjectiveTherapeutic strategies for atrial septal defect (ASD) with severe pulmonary arterial hypertension (PAH) are controversial. This study aimed to evaluate the efficacy of PAH-specific medications and subsequent transcatheter closure (ie, treat-and-repair strategy) on clinical outcomes.MethodsWe enrolled 42 patients who were referred to 13 institutions for consideration of ASD closure with concomitant PAH and underwent the treat-and-repair strategy. The endpoint was cardiovascular death or hospitalisation due to heart failure or exacerbated PAH.ResultsAt baseline prior to PAH-specific medications, pulmonary to systemic blood flow ratio (Qp:Qs), pulmonary vascular resistance (PVR), and mean pulmonary artery pressure (PAP) were 1.9±0.8, 6.9±3.2 Wood units and 45±15 mm Hg. Qp:Qs was increased to 2.4±1.2, and PVR and mean PAP were decreased to 4.0±1.5 Wood units and 35±9 mm Hg at the time of transcatheter ASD closure after PAH-specific medications. Transcatheter ASD closure was performed without any complications. During a median follow-up period of 33 months (1–126 months) after transcatheter ASD closure, one older patient died and one patient was hospitalised due to heart failure, but the other patients survived with an improvement in WHO functional class. PAP was further decreased after transcatheter ASD closure.ConclusionsThe treat-and-repair strategy results in low complication and mortality rates with a reduction in PAP in selected patients with ASD complicated with PAH who have a favourable response of medical therapy.
Publisher
BMJ Publishing Group Ltd and British Cardiovascular Society,BMJ Publishing Group LTD,BMJ Publishing Group
Subject
/ Cardiac Catheterization - adverse effects
/ Familial Primary Pulmonary Hypertension
/ Heart Septal Defects, Atrial - complications
/ Heart Septal Defects, Atrial - therapy
/ Humans
/ Hypertension, Pulmonary - diagnosis
/ Hypertension, Pulmonary - etiology
/ Hypertension, Pulmonary - therapy
/ Patients
/ Peptides
/ pulmonary arterial hypertension
/ Pulmonary Arterial Hypertension - diagnosis
/ Pulmonary Arterial Hypertension - etiology
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