Introduction: Cyanotic congenital heart diseases includes congenital structural anomalies of the heart with shunting resulted in mixing systemic venous blood into the arterial circulation. Two types of surgical therapies are available for the treatment of this anomalies: corrective and palliative. The goal of palliative surgery is to increase the pulmonary blood flow via systemic-to-pulmonary arterial shunting as the conclusive treatment or as a bridge to corrective surgery. Objective: Obstruction of palliative systemic artery-to-pulmonary artery shunts is one of the causes of deterioration in the clinical status, mortality, and morbidity of patients with cyanotic heart disease. For patients contraindicated for the Fontan surgery, a solution is a new shunt insertion or interventional procedures on stenotic shunts. Redo surgery is associated with higher risks of mortality and complications. Method: Herein, we describe 23 patients with obstructed or stenotic systemic artery-to-pulmonary artery shunts who underwent transcatheter stenting at Rajaie Cardiovascular Medical and Research Center between 2011 and 2019. Result: Pulmonary blood flow increased in all the patients, and there were no significant complications or periprocedural deaths. Blalock–Taussig shunt stenting was successful in the early and late stages in all the patients with recorded data. Hematocrit was decreased by a median of 4 units (2–8 units). During the follow-up, 12 patients were rehospitalized, 4 underwent new procedures, and 4 died. Conclusion: Stenting an obstructed or stenotic systemic artery-to-pulmonary artery shunt is a safe and promising alternative to redo surgery with higher success rates and fewer complications compared with balloon angioplasty.
Published in | International Journal of Medical Case Reports (Volume 1, Issue 3) |
DOI | 10.11648/j.ijmcr.20220103.15 |
Page(s) | 29-35 |
Creative Commons |
This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
Copyright |
Copyright © The Author(s), 2022. Published by Science Publishing Group |
Cyanotic Congenital Heart Disease, Palliative Systemic-to-Pulmonary Artery Shunt, Blalock–Taussig Shunt, Central Shunt, Shunt Occlusion
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APA Style
Ata Firouzi, Ehsan Khalilipur, Zahra Khajali, Zahra Hoseini, Sedighe Saedi, et al. (2022). Success Rate and Outcome of Stenting for the Treatment of Stenosis of Palliative Systemic-to-Pulmonary Arterial Shunts: A Case Series. International Journal of Medical Case Reports, 1(3), 29-35. https://doi.org/10.11648/j.ijmcr.20220103.15
ACS Style
Ata Firouzi; Ehsan Khalilipur; Zahra Khajali; Zahra Hoseini; Sedighe Saedi, et al. Success Rate and Outcome of Stenting for the Treatment of Stenosis of Palliative Systemic-to-Pulmonary Arterial Shunts: A Case Series. Int. J. Med. Case Rep. 2022, 1(3), 29-35. doi: 10.11648/j.ijmcr.20220103.15
AMA Style
Ata Firouzi, Ehsan Khalilipur, Zahra Khajali, Zahra Hoseini, Sedighe Saedi, et al. Success Rate and Outcome of Stenting for the Treatment of Stenosis of Palliative Systemic-to-Pulmonary Arterial Shunts: A Case Series. Int J Med Case Rep. 2022;1(3):29-35. doi: 10.11648/j.ijmcr.20220103.15
@article{10.11648/j.ijmcr.20220103.15, author = {Ata Firouzi and Ehsan Khalilipur and Zahra Khajali and Zahra Hoseini and Sedighe Saedi and Somaye Ahmadi and Atefe Shafiee and Amir Abdi}, title = {Success Rate and Outcome of Stenting for the Treatment of Stenosis of Palliative Systemic-to-Pulmonary Arterial Shunts: A Case Series}, journal = {International Journal of Medical Case Reports}, volume = {1}, number = {3}, pages = {29-35}, doi = {10.11648/j.ijmcr.20220103.15}, url = {https://doi.org/10.11648/j.ijmcr.20220103.15}, eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ijmcr.20220103.15}, abstract = {Introduction: Cyanotic congenital heart diseases includes congenital structural anomalies of the heart with shunting resulted in mixing systemic venous blood into the arterial circulation. Two types of surgical therapies are available for the treatment of this anomalies: corrective and palliative. The goal of palliative surgery is to increase the pulmonary blood flow via systemic-to-pulmonary arterial shunting as the conclusive treatment or as a bridge to corrective surgery. Objective: Obstruction of palliative systemic artery-to-pulmonary artery shunts is one of the causes of deterioration in the clinical status, mortality, and morbidity of patients with cyanotic heart disease. For patients contraindicated for the Fontan surgery, a solution is a new shunt insertion or interventional procedures on stenotic shunts. Redo surgery is associated with higher risks of mortality and complications. Method: Herein, we describe 23 patients with obstructed or stenotic systemic artery-to-pulmonary artery shunts who underwent transcatheter stenting at Rajaie Cardiovascular Medical and Research Center between 2011 and 2019. Result: Pulmonary blood flow increased in all the patients, and there were no significant complications or periprocedural deaths. Blalock–Taussig shunt stenting was successful in the early and late stages in all the patients with recorded data. Hematocrit was decreased by a median of 4 units (2–8 units). During the follow-up, 12 patients were rehospitalized, 4 underwent new procedures, and 4 died. Conclusion: Stenting an obstructed or stenotic systemic artery-to-pulmonary artery shunt is a safe and promising alternative to redo surgery with higher success rates and fewer complications compared with balloon angioplasty.}, year = {2022} }
TY - JOUR T1 - Success Rate and Outcome of Stenting for the Treatment of Stenosis of Palliative Systemic-to-Pulmonary Arterial Shunts: A Case Series AU - Ata Firouzi AU - Ehsan Khalilipur AU - Zahra Khajali AU - Zahra Hoseini AU - Sedighe Saedi AU - Somaye Ahmadi AU - Atefe Shafiee AU - Amir Abdi Y1 - 2022/09/29 PY - 2022 N1 - https://doi.org/10.11648/j.ijmcr.20220103.15 DO - 10.11648/j.ijmcr.20220103.15 T2 - International Journal of Medical Case Reports JF - International Journal of Medical Case Reports JO - International Journal of Medical Case Reports SP - 29 EP - 35 PB - Science Publishing Group SN - 2994-7049 UR - https://doi.org/10.11648/j.ijmcr.20220103.15 AB - Introduction: Cyanotic congenital heart diseases includes congenital structural anomalies of the heart with shunting resulted in mixing systemic venous blood into the arterial circulation. Two types of surgical therapies are available for the treatment of this anomalies: corrective and palliative. The goal of palliative surgery is to increase the pulmonary blood flow via systemic-to-pulmonary arterial shunting as the conclusive treatment or as a bridge to corrective surgery. Objective: Obstruction of palliative systemic artery-to-pulmonary artery shunts is one of the causes of deterioration in the clinical status, mortality, and morbidity of patients with cyanotic heart disease. For patients contraindicated for the Fontan surgery, a solution is a new shunt insertion or interventional procedures on stenotic shunts. Redo surgery is associated with higher risks of mortality and complications. Method: Herein, we describe 23 patients with obstructed or stenotic systemic artery-to-pulmonary artery shunts who underwent transcatheter stenting at Rajaie Cardiovascular Medical and Research Center between 2011 and 2019. Result: Pulmonary blood flow increased in all the patients, and there were no significant complications or periprocedural deaths. Blalock–Taussig shunt stenting was successful in the early and late stages in all the patients with recorded data. Hematocrit was decreased by a median of 4 units (2–8 units). During the follow-up, 12 patients were rehospitalized, 4 underwent new procedures, and 4 died. Conclusion: Stenting an obstructed or stenotic systemic artery-to-pulmonary artery shunt is a safe and promising alternative to redo surgery with higher success rates and fewer complications compared with balloon angioplasty. VL - 1 IS - 3 ER -