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Anesthesia & ASD Occluder. Presented By R3 顏郁軒 93/8/9. ASD Occluder. The first successful device closure of an ASD was performed in 1974 by King and Mills FDA granted approval two types of ASD occluder : Amplatzer septal occluder & CardioSEAL Septal Occluder. CardioSEAL Septal Occluder.
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Anesthesia & ASD Occluder Presented By R3顏郁軒 93/8/9
ASD Occluder • The first successful device closure of an ASD was performed in 1974 by King and Mills • FDA granted approval two types of ASD occluder : Amplatzer septal occluder & CardioSEAL Septal Occluder
Amplatzer Structure • The AMPLATZER Septal Occluder is a self-expandable, double disc device made from a nickel-titanium (Nitinol) wire mesh • Left atrial disk has a radius only 7 mm greater than the waist of the device (and thus the defect) and the right atrial disk is slightly smaller, being only 5 mm larger than the defect
Patient Selection (1) • secundum ASD measuring less than or equal to 34 mm • Defect should be greater than 5 mm away from the coronary sinus, atrioventricular valves, and right upper pulmonary vein
Patient Selection (2) Exclusion criteria include : • congenital heart disease that requires cardiac surgery • partial anomalous pulmonary venous return • Pulmonary vascular resistance greater than 7 Wood’s U • right-to-left shunting at the atrial level with a systemic saturation of less than 94% • recent myocardial infarction, unstable angina, • and decompensated congestive heart failure or significant right or left ventricular decompensation with an ejection fraction of less than 30%. • The initial lower weight limit was 8 kg
Anesthetic Consideration • Ketamine for initial diagnosiswatch out patient’s hemodynamic status • General anesthesia later and monitored with NIBP , Oximeter , ETCO2 • TEE evaluation
TEE Evaluation • the entire rim of the defect should be visualized • 要看的view : the mid-esophageal 4-chamber view at 0°, the short-axis view at 45° to 60°, and the biatrial long-axis view at 90° to 110°
五個Rim的看法 • ASD 的5個 portion • SPI : bicaval view • PSAI : four chamber view • AS : 和aortic root 的距離
Sizing the defect (1) Two methods can be used • Pull technique • Static technique • The proper device size is selected as the stretched ASD size plus 1 mm
Sizing the defect (2) • As reported in the literature , TEE may underestimate the size of the ASD, as determined by the stretched balloon diameter
Sizing the defect (3) 原因 : 1. ASD形狀不是圓的 2.ASD 的septum 可能不是在同一平面 3. ASD的形狀大小會隨著heart cycle而改 變4.ASD margin 的組織可能是軟或較硬的,所以用sizing balloon 來推向兩邊時會有一些差異
Evaluation, procedure, and postprocedural assessment Preprocedure • Define ASD location • Define ASD size • Define ASD number; look for fenestrations • Delineate ASD rim • Is it firm or pliable? • Is it deficient at any point, eg, inferoposteriorly? • Atrial septal aneurysm? • Look for associated defects (MVP, APVD) • Measure distance from ASD to MV, CS, RUPV
Evaluation, procedure, and postprocedural assessment Intraprocedural • Confirm guide wire in LA • Confirm sizing balloon free in LA before inflation • Confirm inflated balloon closes the defect • Confirm delivery catheter in body of LA • Ensure adequate deployment and positioning of LA disk • Guide positioning during waist and RA disk deployment
Evaluation, procedure, and postprocedural assessment • Watch for deployment difficulties • Cobrahead malformation • Chiari network entanglement • Thrombus on catheters • Assess adequacy of occlusion • Review device relation to MV, CS, RUPV • Check position stability during "Minnesota wiggle" • Document degree of residual shunt through and around device
Evaluation, procedure, and postprocedural assessment Postprocedural • Check device position • Check device structural integrity • Assess residual shunt • Monitor changes in right heart chambers • Check relation to other structures (MV, RUPV) • Look for potential complications: thrombus, infection
Effectiveness of percutaneous device occlusion foratrial septal defect in adult patients withpulmonary hypertension • American Heart Journal November 2002 P877~880 • 29 adult patients • follow up of 21±14 months • Our findings suggest that percutaneous device occlusion of ASD in adult patients with pulmonary hypertension is safe and effective and provides significant and prolonged relief.