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Aortopulmonary window

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https://www.readbyqxmd.com/read/28198042/transcatheter-closure-of-a-residual-aortopulmonary-window-defect
#1
Mohamad Alkhouli, Abdul Tarabishy, Akram Kawsara, Fahad Alqahtani, Naser Moiduddin
No abstract text is available yet for this article.
February 14, 2017: Journal of Cardiac Surgery
https://www.readbyqxmd.com/read/28163441/transcatheter-closure-of-aortopulmonary-window-with-amplatzer-duct-occluder-ii
#2
Hemant Kumar Nayak, Nurul Islam, Bhanu Kumar Bansal
No abstract text is available yet for this article.
January 2017: Annals of Pediatric Cardiology
https://www.readbyqxmd.com/read/28139013/aortopulmonary-window-morphology-diagnosis-and-long-term-results
#3
Sachin Talwar, Palkesh Agarwal, Shiv Kumar Choudhary, Shyam Sunder Kothari, Rajnish Juneja, Anita Saxena, Balram Airan
OBJECTIVE: Aortopulmonary window (APW) is a rare congenital heart defect. We reviewed our experience with this condition over the last two decades. METHODS: Between September 1993 and December 2013, 62 patients underwent surgery for APW. Depending on the associated lesions, they were divided into two groups: Simple (Group 1) or complex (Group 2). In the complex group, six patients had a ventricular septal defect, five patients had interrupted aortic arch, three patients had tetralogy of Fallot, two patients had double outlet right ventricle, and one patient had the right pulmonary artery arising from the ascending aorta...
January 30, 2017: Journal of Cardiac Surgery
https://www.readbyqxmd.com/read/28109398/evaluation-of-the-mediastinum-differentiating-between-stations-4l-5-and-6-using-ebus-and-eus
#4
Anna Bendzsak, Ricardo Oliveira, Eric Goudie, Vicky Thiffault, Adeline Jouquan, Pasquale Ferraro, Moishe Liberman
Correct identification of mediastinal lymph node stations with endoscopic ultrasound (EUS) and endobronchial ultrasound (EBUS) requires knowledge of their ultrasonic anatomical positions and relations. The ultrasonic positions of the lymph node stations located in and around the aortopulmonary window (stations 4L, 5, and 6) can be more challenging to understand. The aim of this report is to describe the endosonographic anatomic positions of stations 4L, 5, and 6 and to demonstrate their locations using EUS and EBUS...
February 2017: Annals of Thoracic Surgery
https://www.readbyqxmd.com/read/28089641/current-outcomes-of-one-stage-surgical-correction-for-berry-syndrome
#5
Renjie Hu, Wen Zhang, Xinrong Liu, Wei Dong, Hongbin Zhu, Haibo Zhang
OBJECTIVES: Berry syndrome is a combination of distal aortopulmonary window (APW), aortic origin of the right pulmonary artery (RPA), intact ventricular septum, and interrupted aortic arch. We present here our current experience of primary repair of this syndrome with the goal of optimizing treatment for this rare condition. METHODS: From January 2003 through December 2015, 16 infants with Berry syndrome underwent one-stage repair at Shanghai Children's Medical Center...
December 19, 2016: Journal of Thoracic and Cardiovascular Surgery
https://www.readbyqxmd.com/read/28054283/mediastinal-seminoma-associated-with-multilocular-thymic-cyst
#6
Masato Inui, Jun-Ichi Nitadori, Shogo Tajima, Takahusa Yoshioka, Noriko Hiyama, Takeyuki Watadani, Aya Shinozaki-Ushiku, Kazuhiro Nagayama, Masaki Anraku, Masaaki Sato, Masashi Fukayama, Jun Nakajima
An asymptomatic 26-year-old man received an annual medical check-up, and chest X-ray showed a protrusion of the aortopulmonary window. Chest computed tomography (CT) revealed an anterior mediastinal tumor and cysts with thin wall and septum enhancement. The preoperative diagnosis was cystic thymoma or malignant lymphoma. We performed total resection of the tumor through a median sternotomy. The pathological findings revealed seminoma, positive for c-kit stain, and multilocular thymic cysts. Cysts were lined by normal squamous epithelium and no seminoma cells were located on their surface...
December 2017: Surgical Case Reports
https://www.readbyqxmd.com/read/27941485/anesthetic-management-of-a-tracheoesophageal-fistula-in-a-patient-with-a-large-uncorrected-aortopulmonary-window
#7
Adam C Adler, James M Steven, Matthew A Jolley
Aortopulmonary window is a rare form of congenital heart disease that requires significant anesthetic considerations. Cardiac involvement is a well-known comorbidity identified in patients with tracheoesophageal fistula (TEF). Identification of coexisting lesions, specifically congenital heart disease, is crucial before undergoing repair of a TEF. Understanding the complex physiology and expected changes occurring during the anesthetic and surgical intervention for correction of TEF with a significant unrepaired shunting defect is crucial to prevent hemodynamic instability...
December 9, 2016: A & A Case Reports
https://www.readbyqxmd.com/read/27869054/percutaneous-closure-of-an-aortopulmonary-window-using-amplatzer-duct-occluder-ii-additional-sizes-the-first-reported-case
#8
Roland Fiszer, Karol Zbroński, Małgorzata Szkutnik
To date, there are no reported cases of the Amplatzer Duct Occluder II: Additional Sizes' use in percutaneous closure of an aortopulmonary window. We report a case of percutaneous closure of an aortopulmonary window in a 4.5-month-old, 6 kg child. Owing to the patient's low weight, high risk of damage to the pulmonary valve, as well as the possibility of aortic and pulmonary artery obstruction, classic implants were deemed unsuitable and a decision was made to use the Amplatzer Duct Occluder II: Additional Sizes...
November 21, 2016: Cardiology in the Young
https://www.readbyqxmd.com/read/27865679/percutaneous-closure-of-isolated-ostium-secundum-type-atrial-septal-defect-in-a-patient-with-mayer-rokitansky-k%C3%A3-ster-hauser-syndrome
#9
Murat Akcay, Okan Gulel, Korhan Soylu, Murat Meric, Muzaffer Elmali
Mayer-Rokitansky-Küster-Hauser (MRKH) syndrome is a rare congenital anomaly characterized by complete or partial aplasia of the uterus and the upper part of the vagina. It is reported to be associated with cardiovascular disorders including atrial septal defect, anomalous pulmonary venous return, aortopulmonary window, pulmonary valve stenosis, mitral valve prolapse, tetralogy of Fallot, truncus arteriosus, and patent ductus arteriosus. Herein, for the first time in the medical literature, we present percutaneous closure of an isolated ostium secundum atrial septal defect in this syndrome...
December 2016: Portuguese Journal of Cardiology: An Official Journal of the Portuguese Society of Cardiology
https://www.readbyqxmd.com/read/27747035/thick-lung-wedge-resection-for-acute-life-threatening-massive-hemoptysis-due-to-aortobronchial-fistula
#10
Mitsuaki Sakai, Yuichiro Ozawa, Tomomi Nakajima, Akihiko Ikeda, Taisuke Konishi, Kanji Matsuzaki
Massive hemoptysis from an aortobronchial fistula due to thoracic aortic dissection is an extremely rare symptom, but is a potentially life-threatening condition. We report a case of acute massive hemoptysis due to aortobronchial fistula that was successfully controlled by a simple and rapid thick wedge resection of the lung with hematoma by using the black cartilage stapler. A 65-year-old man was admitted to our hospital with acute massive hemoptysis. After tracheal intubation, chest computed tomography revealed hematoma in the left lung and ruptured aortic dissection from the distal arch to the descending aorta...
September 2016: Journal of Thoracic Disease
https://www.readbyqxmd.com/read/27727969/eisenmenger-syndrome-in-an-adult-patient-with-aortopulmonary-window
#11
Nerusu Hari Babu
No abstract text is available yet for this article.
January 2016: Journal of the Association of Physicians of India
https://www.readbyqxmd.com/read/27680574/tricuspid-atresia-associated-with-aortopulmonary-window-diagnostic-and-therapeutic-dilemmas
#12
Vladimir Milovanovic, Igor Stefanovic, Slobodan Ilic
The association of tricuspid atresia with aortopulmonary window is exceptionally rare. We report a patient with tricuspid atresia, normally related great arteries, non-restrictive ventricular septal defect, and no pulmonary stenosis (type IC) with an aortopulmonary window who underwent successful initial surgical palliation. The unique anatomical feature of this case, other than the presence of the aortopulmonary window, was the absence of pulmonary stenosis at the level of either the ventricular septal defect or the pulmonary valve...
September 29, 2016: Cardiology in the Young
https://www.readbyqxmd.com/read/27644773/ep04-01-a-very-rare-congenital-aortic-arch-defect-defined-prenatally-aortopulmonary-window-associated-with-sacral-teratoma
#13
T Sarac Sivrikoz, R Has, A Yuksel, I Kalelioglu, R Eker Omeroglu
No abstract text is available yet for this article.
September 2016: Ultrasound in Obstetrics & Gynecology
https://www.readbyqxmd.com/read/27576371/a-hidden-culprit-for-ventricular-dysfunction-in-aortopulmonary-window-repair-anomalous-origin-of-left-coronary-artery-case-report-and-review-of-literature
#14
Adnan Alhadlaq, Santokh Dhillon, Camille L Hancock-Friesen, Arif Hussain
No abstract text is available yet for this article.
August 5, 2016: Journal of Thoracic and Cardiovascular Surgery
https://www.readbyqxmd.com/read/27503753/prenatal-diagnosis-of-an-aortopulmonary-window-with-an-interrupted-aortic-arch
#15
REVIEW
Cecilia García, Teresa Álvarez, Coral Bravo, Ramón Pérez-Caballero, María Teresa Viadero, Francisco Gámez, Ricardo Pérez, Juan De León-Luis
A prenatal aortopulmonary window with an interrupted aortic arch was detected in a 22-week-old fetus. The 3-vessel and trachea view showed a communication between the ascending aorta and the pulmonary artery. Early postnatal surgery was successful. A PubMed-based search identified all cases of prenatal aortopulmonary windows between 2002 and 2015. Nine articles were identified. The average gestational age at diagnosis was 28 weeks (range, 22-33 weeks). The most frequent aortopulmonary window was type I (40%)...
October 2016: Journal of Ultrasound in Medicine: Official Journal of the American Institute of Ultrasound in Medicine
https://www.readbyqxmd.com/read/27449901/use-of-an-amplatz-canine-ductal-occluder-acdo-device-to-close-an-acquired-aortopulmonary-fistula-with-a-hybrid-approach-in-a-dog
#16
A Zani, E Becchetti, T Chimenti, V Daddi, M Zani, C Miotti, C Bussadori
A 2-year-old recently spayed female Rottweiler was referred as an emergency with cardiac tamponade and the presence of an anomalous retrograde flow in the pulmonary artery. Echocardiography and angiography demonstrated a left-to-right aortopulmonary fistula. Clinical history and data indicated a possible infectious aetiology. Antibiotics and heart failure medications were administered for 30 days before intervention. Initial attempt at insertion of an Amplatz occluder by means of a percutaneous catheterization technique was tried but a safe release of the device was judged to be not possible due to the angle and the fragile and irregular margins of the window...
December 2016: Journal of Veterinary Cardiology: the Official Journal of the European Society of Veterinary Cardiology
https://www.readbyqxmd.com/read/27374635/closure-of-aortopulmonary-window-using-nit-occlud%C3%A2-pda-r-device-in-a-3-month-old-infant
#17
Ender Odemis, Osman Guvenc, Murat Saygi, Ibrahim Halil Demir
Aortopulmonary window (APW) is a rare abnormality in which a pulmonary defect exists between the ascending aorta and the main pulmonary artery. Given that it may result in cardiac failure and pulmonary vascular disease in the early period, treatment needs to be performed without delay. In addition to surgical treatment, transcatheter closure may also be performed for selected patients. This study describes the case of an infant diagnosed with APW and who underwent successful transcatheter closure using a Nit-Occlud® PDA-R device...
August 2016: Pediatrics International: Official Journal of the Japan Pediatric Society
https://www.readbyqxmd.com/read/27372619/aortopulmonary-window-in-adulthood-surviving-at-22-years-without-intervention-or-pulmonary-vascular-disease
#18
İsa Öner Yüksel, Erkan Köklü, Şakir Arslan, Çağın Mustafa Üreyen, Selçuk Küçükseymen
Aortopulmonary window is a rare anomaly, a communication between the ascending aorta and the main pulmonary artery. Prognosis in the absence of correction is poor, with mortality of around 40% in the first year of life. A case of aortopulmonary window without pulmonary vascular disease in adulthood is described in the present report.
June 2016: Türk Kardiyoloji Derneği Arşivi: Türk Kardiyoloji Derneğinin Yayın Organıdır
https://www.readbyqxmd.com/read/27212854/complex-aortopulmonary-window-in-a-single-ventricle-setting-technical-considerations-for-staged-palliation
#19
Gananjay G Salve, Shreepal A Jain, Sandip S Katkade, Krishnanaik Shivaprakash
We report a successful surgical management of a case presented with a combination of aortopulmonary window (APW) with large ventricular septal defect (VSD) amounting to a single ventricle, with a view to highlight technical considerations during staged single-ventricle palliation.
May 2016: Annals of Pediatric Cardiology
https://www.readbyqxmd.com/read/27209612/arterial-switch-operation-with-and-without-coronary-relocation-for-intramural-coronary%C3%A2-arteries
#20
Hiroshi Koshiyama, Mitsugi Nagashima, Goki Matsumura, Takeshi Hiramatsu, Toshio Nakanishi, Kenji Yamazaki
BACKGROUND: The arterial switch operation (ASO) for the transposition of the great arteries (TGA) with intramural coronary arteries has been performed using several techniques to avoid coronary events. We mainly performed ASO without coronary relocation by creating an aortopulmonary fenestration (Imai technique). Coronary circulation was rerouted by covering the aortopulmonary window and coronary orifices with a nonfacing sinus flap. Long-term results have not been reported. We describe our early and late results...
October 2016: Annals of Thoracic Surgery
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