Long Term Support for Respiratory Failure: VV ECMO or Oxygenated RVAD?

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Long Term Support for Respiratory Failure: VV ECMO or Oxygenated RVAD? Mechanical Circulatory Support Symposium 2018 (Houston, TX) Charles Hoopes, MD Professor of Surgery University of Alabama (Birmingham) choopes@uabmc.edu

Disclosure: I have no professional or financial relationship with any of the devices or technologies discussed.

THE PARACORPOREAL ARTIFICIAL LUNG: TRANSTHORACIC TOTAL SUPPORT OR PERCUTANEOUS NEAR TOTAL SUPPORT WHICH IS BETTER? Zwischenberger et al (2009), University of Kentucky Ambulatory OxyRVAD for total right heart and respiratory support The OxyRVAD is created by commercially available components consisting of off label use of a compact low resistance gas exchange device coupled with a right ventricular axial flow ventricular assist device central cannulation Percutaneous pump-artificial lung Single site venous cannulation (Wang-Zwische double lumen cannula). Based on double lumen VV ECMO, the DLC is designed to be inserted from the jugular vein traversing the SVC-RA-IVC. The drainage lumen has a wide open end placed in the IVC for the lower body venous drainage and a side opening in SVC for upper body venous drainage. The infusion lumen opens towards the tricuspid valve in the RA. Bi-caval dual lumen venovenous cannula

Requirements for long term support (1) durability (2) normalization of physiology (2) adequate functional performance upright, ambulatory, and socially interactive

VV venovenous ECMO (internal jugular and femoral vein) 42 days VV (DL) venovenous DL (right internal jugular, Avalon dual lumen) 372 days VA (f) venoarterial (femoral vein to femoral artery/retrograde) 35 days RA to Ao walking bypass (right atrium to ascending aorta) 103 days RA to PA oxyrvad (right atrium to pulmonary artery) 91 days PA to LA pulmonary bypass (pulmonary artery to left atrium) 18 days RA to LA pulmonary bypass (right atrium to left atrium) 14 days VV (DL) + BAS venovenous right IJ double lumen catheter + atrial septostomy 5 days VAV (hybrid) RIJ dual lumen catheter with both right subclavian artery 52 days PECLA (central) pumpless extracorporeal lung assist (PA to LA) 11 days PECLA (peripheral) pumpless extracorporeal lung assist (femoral a to femoral v) 3 days ProTek Duo DLC RA to PA 57 days

14 yo cystic fibrosis s/p right completion pneumonectomy VV ECMO DLC Cor pulmonale with PEA to central cannulation ECMO day 103

68 yo scleroderma variant, elevated ANA suprasystemic PA pressures on continuous dobutamine, lasix qtt, high flow O2. Failed vasodilator therapy x 3 non-ambulatory with syncope To cath lab combined atrial septostomy and right IJ dual lumen venovenous ECMO cannulation bridge to transplant (ECMO day 4)

The oxyrvad any blood pump with an in-line oxygenator (by definition) hypoxia with inadequate left ventricular preload (by indication) We define right heart failure as a clinical syndrome due to an alteration of structure and/or function of the right heart circulatory system that leads to sub-optimal delivery of blood flow (high or low) to the pulmonary circulation and/ or elevated venous pressures at rest or with exercise. Mehra et al (2014) J Heart Lung Transplant;33:123 12 Our continued lack of understanding of pulmonary hypertension limitations of a reductionist approach to define a complex clinical syndrome based on end stage pathological observations Chan and Loscalzo (2011),Comp Physiol 1:123-139

Kirklin et al (2015) 7 th INTERMACS annual report JHLT 34:1495-1504

Respiratory failure is not a static process pulmonary hypertension is a common end stage denominator Compensation for pathophysiology is not equivalent to physiological support

15% of ILD cohort associated with IPF decreased performance increased mortality

The final common course in all these patients might be heralded by the onset of PH, which then drives outcomes in a similar fashion, no matter the initial cause or pattern of fibrosis categorizing patients into one of the nine categories or subcategories of IIP might be semantic, because when PH does supervene, invariably there is a component of either UIP or NSIP, no matter the initial clinical or histopathologic presentation.

patients with sclerosis related PAH have relatively depressed RV function during exercise, this results in ventricular-pulmonary vascular uncoupling and acute RV dilation. Hsu et al (2016) Circ 133:2413-2422 RV performance is rarely (if ever) the issue in primary pulmonary hypertension it can be in secondary pulmonary hypertension and hypoxic pulmonary vasoconstriction

JS Haldane arterioles or capillaries may contract or dilate so as to adjust the blood supply. JS Haldane Respiration (1922, p.427)

56 yo idiopathic pulmonary fibrosis uncomplicated bilateral lung tx March 08. Dec 08 Trichosporon pneumonia, progressive SOB secondary to post-infectious obliterative bronchiolitis. Profound hypoxia with effort, non-ambulatory on high flow O2 (ICU) listed for redo lung transplant Stress ECHO (exercise, supine bicycle) Pre VV ECMO Post VV ECMO 6 min 13 sec, max 10 watts 9min, max 50 watts sats 84% on 8L NC with onset exercise sats 87% on RA with onset exercise, 98% on 4L (Stage 3) exercise d/c d secondary SOB (15L O2) exercise d/c d secondary fatigue PASP 60 + RA with peak exercise (PVTI 13) PASP 41 + RA with peak exercise (PVTI 10) R to L shunt via PFO with peak exercise No shunt with peak exercise Non ambulatory secondary to hypoxia Ambulatory on treadmill Subjective recovery time hours Subjective recovery time minutes TV IVC *More fibrinolysis, less thrombocytopenia SVC Efficiency is engineered Efficacy is dependent upon details of deployment IVC RV SVC

OxyRVADs and patient selection Difficult to stratify the appropriate population most likely to benefit from oxyrvad support and develop a communication strategy to convey disease etiology and severity

A TPR > 3 WU predicts poor performance with venovenous ECMO support (n=5)

Idiopathic primary pulmonary hypertension MCS for pre-capillary pulmonary hypertension Hypoxic pulmonary vasoconstriction ( dynamic ) Obstructive (CTEPH, emboli, CWP, PVOD fixed ) congenital heart (Eisenmenger s, Fontan, PA agenesis) Primary PH Secondary PH *PECLA (PA to LA, central) RA to LA (central) **VV ECMO DLC + septostomy RA to PA low flow dynamic (HPV) Peripheral RA to PA (ProTEK Duo) hybrid VV + subclavian Arterial VV ECMO DLC + septostomy OxyRVAD fixed (obstructive) VA ECMO (peripheral salvage ) VA ECMO (central RA to Ao bridge ) * Pumpless Extra Corporeal Lung Assist ** physiological oxyrvad