David Frakes

Dr. David Frakes


Research Focus & Metrics

Academic Career Length

19Years (2008-Present)

(Calculated once Scilit publication data is synced: current year − year of first publication + 1)

Representative Publications

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8 November 2018 in 3D Printing in Medicine
Verified
Journal Article
Open access
PDF file
JRJustin Ryan
Justin Ryan
JPJonathan Plasencia
Jonathan Plasencia
RRRandy Richardson
Randy Richardson
DVDaniel Velez
Daniel Velez
JNJohn J. Nigro
John J. Nigro
DFDavid Frakes
David Frakes
3D printing is an ideal manufacturing process for creating patient-matched models (anatomical models) for surgical and interventional planning. Cardiac anatomical models have been described in numerous case studies and journal publications. However, few studies attempt to describe wider impact of the novel planning augmentation tool. The work here presents the evolution of an institution’s first 3 full years of 3D prints following consistent integration of the technology into clinical workflow (2012–2014) - a center which produced 79 models for surgical planning (within that time frame). Patient outcomes and technology acceptance following implementation of 3D printing were reviewed. A retrospective analysis was designed to investigate the anatomical model’s impact on time-based surgical metrics. A contemporaneous cohort of standard-of-care pre-procedural planning (no anatomical models) was identified for comparative analysis. A post-surgery technology acceptance assessment was also employed in a smaller subset to measure perceived efficacy of the anatomical models. The data was examined. Within the timeframe of the study, 928 primary-case cardiothoracic surgeries (encompassing both CHD and non-CHD surgeries) took place at the practicing pediatric hospital. One hundred sixty four anatomical models had been generated for various purposes. An inclusion criterion based on lesion type limited those with anatomic models to 33; there were 113 cases matching the same criterion that received no anatomical model. Time-based metrics such as case length-of-time showed a mean reduction in overall time for anatomical models. These reductions were not statistically significant. The technology acceptance survey did demonstrate strong perceived efficacy. Anecdotal vignettes further support the technology acceptance. The anatomical models demonstrate trends for reduced operating room and case length of time when compared with similar surgeries in the same time-period; in turn, these reductions could have significant impact on patient outcomes and operating room economics. While analysis did not yield robust statistical powering, strong Cohen’s d values suggest poor powering may be more related to sample size than non-ideal outcomes. The utility of planning with an anatomical model is further supported by the technology acceptance study which demonstrated that surgeons perceive the anatomical models to be an effective tool in surgical planning for a complex CHD repair. A prospective multi-center trial is currently in progress to further validate or reject these findings.

16 March 2016 in Cardiovascular Engineering and Technology
Verified
Journal Article
Closed access
PDF file
RCRafeed A. Chaudhury
Rafeed A. Chaudhury
VAVictor Atlasman
Victor Atlasman
GPGirish Pathangey
Girish Pathangey
NPNicholas Pracht
Nicholas Pracht
RARonald J. Adrian
Ronald J. Adrian
DFDavid Frakes
David Frakes

1 June 2015 in World Neurosurgery
Verified
Journal Article
Closed access
JRJonathan Russin
Jonathan Russin
HBHaithem Babiker
Haithem Babiker
JRJustin Ryan
Justin Ryan
LRLeonardo Rangel-Castilla
Leonardo Rangel-Castilla
DFDavid Frakes
David Frakes
PNPeter Nakaji
Peter Nakaji

27 January 2016 in Journal of Biomechanical Engineering
Verified
Journal Article
Closed access
PDF file
PNPriya Nair
Priya Nair
BCBrian W. Chong
Brian W. Chong
AIAprinda Indahlastari
Aprinda Indahlastari
JRJustin Ryan
Justin Ryan
CWChristopher Workman
Christopher Workman
DFDavid Frakes
David Frakes
Embolic coiling is one of the most effective treatments for cerebral aneurysms (CAs), largely due to the hemodynamic modifications that the treatment effects in the aneurysmal environment. However, coiling can have very different hemodynamic outcomes in aneurysms with different geometries. Previous work in the field of biofluid mechanics has demonstrated on a general level that geometry is a driving factor behind aneurysmal hemodynamics. The goal of this study was to relate two specific geometric factors that describe CAs (i.e., dome size (DS) and parent-vessel contact-angle (PV-CA)) and one factor that describes treatment (i.e., coil packing density (PD)) to three clinically relevant hemodynamic responses (i.e., aneurysmal root-mean-square velocity (Vrms), aneurysmal wall shear stress (WSS), and cross-neck flow (CNF)). Idealized models of basilar tip aneurysms were created in both virtual and physical forms to satisfy two-level multifactorial experimental designs. Steady and pulsatile flow hemodynamics were then evaluated in the virtual models using computational fluid dynamics (CFD) (before and after virtual treatment with finite element (FE) embolic coil models), and hemodynamics were also evaluated in the physical models using particle image velocimetry (PIV) (before and after treatment with actual embolic coils). Results showed that among the factors considered, PD made the greatest contributions to effects on hemodynamic responses in and around the aneurysmal sac (i.e., Vrms and WSS), while DS made the greatest contributions to effects on hemodynamics at the neck (i.e., CNF). Results also showed that while a geometric factor (e.g., PV-CA) may play a relatively minor role in dictating hemodynamics in the untreated case, the same factor can play a much greater role after coiling. We consider the significance of these findings in the context of aneurysmal recurrence and rupture, and explore potential roles for the proposed methods in endovascular treatment planning.

13 June 2008 in Experiments in Fluids
Verified
Journal Article
Closed access
PDF file
DFDavid Frakes
David Frakes
KPKerem Pekkan
Kerem Pekkan
LDLakshmi P. Dasi
Lakshmi P. Dasi
HKHiroumi D. Kitajima
Hiroumi D. Kitajima
DZDiane de Zelicourt
Diane de Zelicourt
AYAjit P. Yoganathan
Ajit P. Yoganathan

24 April 2013 in Computational and Mathematical Methods in Medicine
Verified
Journal Article
Open access
PDF file
MGMorgan Giers
Morgan Giers
AMAlex C. McLaren
Alex C. McLaren
JPJonathan D. Plasencia
Jonathan D. Plasencia
DFDavid Frakes
David Frakes
RMRyan McLemore
Ryan McLemore
MCMichael R. Caplan
Michael R. Caplan
Controlled release formulations for local, in vivo drug delivery are of growing interest to device manufacturers, research scientists, and clinicians; however, most research characterizing controlled release formulations occurs in vitro because the spatial and temporal distribution of drug delivery is difficult to measure in vivo. In this work, in vivo magnetic resonance imaging (MRI) of local drug delivery was performed to visualize and quantify the time resolved distribution of MRI contrast agents. Three-dimensional maps (generated from -weighted images with varied ) were processed using noise-reducing filtering. A segmented region of contrast, from a thresholded image, was converted to concentration maps using the equation , where and are the precontrast and postcontrast map values, respectively. In this technique, a uniform estimated value for was used. Error estimations were performed for each step. The practical usefulness of this method was assessed using comparisons between devices located in different locations both with and without contrast. The method using a uniform , requiring no registration of pre- and postcontrast image volumes, was compared to a method using either affine or deformation registrations.