Literature DB >> 11590848

Atrial septostomy for pulmonary hypertension.

J Sandoval1, A Rothman, T Pulido.   

Abstract

Atrial septostomy represents an additional, promising strategy in the treatment of severe PPH. Experience with this procedure still is limited; however, based on analyses of the worldwide experience, several general conclusions and recommendations can be made. 1. Atrial septostomy can be performed successfully in selected patients with advanced pulmonary vascular disease. 2. Patients with primary pulmonary hypertension who have undergone successful AS have shown: a significant clinical improvement beneficial and long-lasting hemodynamic effects at rest a trend toward improved survival 3. The procedure-related mortality of the collective experience is high (16%). Several recommendations can be made to minimize the risk: [figure: see text] Atrial septostomy should be attempted only in institutions with an established track record in the treatment of advanced pulmonary hypertension, where septostomy is performed with low morbidity. Atrial septostomy should not be performed in patients in whom death is impending or who have severe right ventricular failure and are on maximal cardiorespiratory support. An mRAP greater than 20 mm Hg, PVR index greater than 55 u/m2, and a predicted 1-year survival less than 40% are significant predictors of procedure-related death. Before cardiac catheterization, patients should have an acceptable baseline systemic oxygen saturation (> 90% in room air) and optimized cardiac function (adequate right heart filling pressure, additional inotropic support if necessary). During cardiac catheterization, the following are mandatory: Supplemental oxygen Mild sedation to prevent anxiety Careful monitoring of variables (left atrial pressure, SaO2, and mRAP) Step by step procedure After AS, it is important to optimize oxygen delivery. Transfusion of packed red blood cells or erythropoietin (before and following the procedure, if needed) may be necessary to increase oxygen content. 4. Because the disease process in PPH is unaffected by the procedure (late deaths), the long-term effects of an AS must be considered to be palliative. 5. Despite its risk, AS may represent a viable alternative for selected patients with severe PPH. Indications for the procedure may include: Recurrent syncope or right ventricular failure, despite maximal medical therapy, including oral calcium-channel blockers or continuous intravenous prostacyclin (Fig. 11) As a bridge to transplantation When no other option exists.

Entities:  

Mesh:

Year:  2001        PMID: 11590848     DOI: 10.1016/s0272-5231(05)70291-4

Source DB:  PubMed          Journal:  Clin Chest Med        ISSN: 0272-5231            Impact factor:   2.878


  24 in total

1.  Use of Amplatzer fenestrated atrial septal defect device in a child with familial pulmonary hypertension.

Authors:  Alain Fraisse; Philippe Chetaille; Zahid Amin; Francis Rouault; Marc Humbert
Journal:  Pediatr Cardiol       Date:  2006-11-16       Impact factor: 1.655

2.  Interatrial shunt for chronic pulmonary hypertension: differential impact of low-flow vs. high-flow shunting.

Authors:  Andreas Zierer; Spencer J Melby; Rochus K Voeller; Marc R Moon
Journal:  Am J Physiol Heart Circ Physiol       Date:  2009-01-09       Impact factor: 4.733

Review 3.  Pulmonary hypertension-"state of the art" management in 2012.

Authors:  Anita Saxena
Journal:  Indian Heart J       Date:  2012-03-26

Review 4.  Treatment of pulmonary arterial hypertension in children.

Authors:  Heiner Latus; Tammo Delhaas; Dietmar Schranz; Christian Apitz
Journal:  Nat Rev Cardiol       Date:  2015-02-03       Impact factor: 32.419

Review 5.  Current clinical management of pulmonary arterial hypertension.

Authors:  Roham T Zamanian; Kristina T Kudelko; Yon K Sung; Vinicio de Jesus Perez; Juliana Liu; Edda Spiekerkoetter
Journal:  Circ Res       Date:  2014-06-20       Impact factor: 17.367

6.  Consecutive Sessions of Rescue Balloon Atrial Septostomy for an Idiopathic Pulmonary Arterial Hypertension Patient with Refractory Right Heart Failure - Usefulness of Intracardiac Echocardiography Guidance.

Authors:  Yu-Wei Chen; Hung-Chih Pan; Kuo-Yang Wang; Kae-Woei Liang
Journal:  Acta Cardiol Sin       Date:  2017-05       Impact factor: 2.672

7.  Impact of differential right-to-left shunting on systemic perfusion in pulmonary arterial hypertension.

Authors:  Timo Weimar; Yoshiyuki Watanabe; Toshinobu Kazui; Urvi S Lee; Alessandro Montecalvo; Richard B Schuessler; Marc R Moon
Journal:  Catheter Cardiovasc Interv       Date:  2012-11-14       Impact factor: 2.692

8.  2014 Guidelines of Taiwan Society of Cardiology (TSOC) for the Management of Pulmonary Arterial Hypertension.

Authors:  Chih-Hsin Hsu; Wan-Jing Ho; Wei-Chun Huang; Yu-Wei Chiu; Tsu-Shiu Hsu; Ping-Hung Kuo; Hsao-Hsun Hsu; Jia-Kan Chang; Chin-Chang Cheng; Chao-Lun Lai; Kae-Woei Liang; Shoa-Lin Lin; Hsao-Hsun Sung; Wei-Chuan Tsai; Ken-Pen Weng; Kai-Sheng Hsieh; Wei-Hsian Yin; Shing-Jong Lin; Kuo-Yang Wang
Journal:  Acta Cardiol Sin       Date:  2014-09       Impact factor: 2.672

9.  Atrial septostomy in the treatment of severe pulmonary arterial hypertension.

Authors:  F Reichenberger; J Pepke-Zaba; K McNeil; J Parameshwar; L M Shapiro
Journal:  Thorax       Date:  2003-09       Impact factor: 9.139

Review 10.  Updated evidence-based treatment algorithm in pulmonary arterial hypertension.

Authors:  Robyn J Barst; J Simon R Gibbs; Hossein A Ghofrani; Marius M Hoeper; Vallerie V McLaughlin; Lewis J Rubin; Olivier Sitbon; Victor F Tapson; Nazzareno Galiè
Journal:  J Am Coll Cardiol       Date:  2009-06-30       Impact factor: 24.094

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