Retrieval of a detached transseptal sheath tip from a right pulmonary artery branch following catheter ablation

2015 ◽  
Vol 86 (6) ◽  
pp. 1131-1135 ◽  
Author(s):  
Amir A. Schricker ◽  
Gregory K. Feld ◽  
Sotirios Tsimikas
CHEST Journal ◽  
1975 ◽  
Vol 68 (2) ◽  
pp. 258-261 ◽  
Author(s):  
Herbert W.M. Plokker ◽  
Sjoerd Wagenaar ◽  
Albert V.G. Bruschke ◽  
C.A. Wagenvoort

2017 ◽  
Vol 68 (1) ◽  
pp. 47-52 ◽  
Author(s):  
Keishin Sunagawa ◽  
Yoshihito Uchino ◽  
Shinichirou Ishimoto ◽  
Shigeki Nakamura ◽  
Taku Honma ◽  
...  

2021 ◽  
Vol 13 (3) ◽  
pp. 254-257
Author(s):  
İlker Mercan ◽  
Muhammet Akyuz ◽  
Onur Işık

Pulmonary arterial sling (PAS) is a relatively rare congenital anomaly in which left pulmonary artery branch originates abnormally from the right pulmonary artery, eventually resulting with respiratory symptoms, due to airway obstruction. In this report, we present a PAS in a neonate who showed progressive respiratory distress in the second week following delivery. At 25 days of age, the patient underwent total surgical correction of the anomaly, during which left pulmonary artery reimplantation to main pulmonary artery without the use of cardiopulmonary bypass was employed. Following an uneventful recovery, the patient was discharged eighteen days after surgery.


2021 ◽  
Vol 5 (6) ◽  
Author(s):  
Juergen Leick ◽  
Stefan Leinen ◽  
Ivar Friedrich ◽  
Nikos Werner

Abstract Background The use of a pulmonary artery catheter (PAC) continues to be important for the diagnosis and therapeutic control of severe heart failure and in the diagnosis of pulmonary arterial hypertension. One of the most feared complications of this examination is perforation of a pulmonary artery with an estimated incidence of 0.031–0.05% and mortality rates of up to 70%. Case summary We report on an 80-year-old female patient who experienced a perforation of a pulmonary artery branch during the work-up of pulmonary arterial hypertension by PAC. Immediately after the perforation, haemodynamic shock developed rapidly, necessitating cardiopulmonary resuscitation. Occlusion of the pulmonary artery branch with a semicompliant balloon was applied immediately. After 40 min of occlusion, the bleeding persisted, and endovascular coil implantation was performed. Subsequently, the bleeding stopped, and the haemodynamics stabilized. After treatment, the patient was discharged home without any significant sequelae. Discussion Treatment options in pulmonary artery perforation are limited, especially if the patient is inoperable and if balloon occlusion fails. Based on our results, endovascular coil embolization can be considered a therapeutic option.


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