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Robert H. Bartlett

Researcher at University of Michigan

Publications -  569
Citations -  28295

Robert H. Bartlett is an academic researcher from University of Michigan. The author has contributed to research in topics: Extracorporeal membrane oxygenation & Extracorporeal. The author has an hindex of 81, co-authored 550 publications receiving 25619 citations. Previous affiliations of Robert H. Bartlett include University of California, Irvine & NewYork–Presbyterian Hospital.

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Successful Porcine Renal Transplantation After 60 Minutes of Donor Warm Ischemia: Extracorporeal Perfusion and Thrombolytics

TL;DR: Thrombolytics plus ECS precondition organs in situ yielding functional kidneys in a porcine model of uDCD with 60 min of WIT is evaluated to address logistical limitations for uD CD use in the United States and could have a major impact on the organ donor pool.
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Development of an artificial placenta: CO2 elimination and hemodynamics as a function of arteriovenous blood flow.

TL;DR: In this rabbit model, A-V blood flows at 25% to 30% of cardiac output allow full gas exchange without hemodynamic compromise, which raises the possibility of using A-v support and an artificial placenta in newborns with respiratory failure.
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The effect of norepinephrine infusion on oxygen delivery and consumption in the canine model

TL;DR: The effectiveness of NE administration could be most effectively monitored by the mixed venous oxygen saturation (SVO2), rather than by intermittent assessment of BP, CO, or DO2.
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Preliminary In Vivo Testing of a Novel Pump for Short-Term Extracorporeal Life Support

TL;DR: The BioVAD provided adequate flow in an acute in vivo model and may be superior for short-term extracorporeal support and afterload insensitive, and incapable of cavitation or excessive hemolysis.
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Comparison of Diazeniumdiolated Dialkylhexanediamines as Nitric Oxide Release Agents on Nonthrombogenicity in an Extracorporeal Circulation Model

TL;DR: Both DPHDN2O2 and DPHD n-N-di-N'-propyl-1,6-hexanediamine are good candidates as NO donor molecules for creating nonthrombogenic polymer coatings for ECCs and AG was no different than AG in preserving platelet count and function.