3D printing for congenital heart disease: a single site’s initial three-yearexperience

Abstract Background 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 describ...

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Main Authors: Justin Ryan, Jonathan Plasencia, Randy Richardson, Daniel Velez, John J. Nigro, Stephen Pophal, David Frakes
Format: Article
Language:English
Published: BMC 2018-11-01
Series:3D Printing in Medicine
Subjects:
Online Access:http://link.springer.com/article/10.1186/s41205-018-0033-8
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spelling doaj-3e9d764c6d0243ccb49969ae62e6f3b52020-11-25T02:27:49ZengBMC3D Printing in Medicine2365-62712018-11-01411910.1186/s41205-018-0033-83D printing for congenital heart disease: a single site’s initial three-yearexperienceJustin Ryan0Jonathan Plasencia1Randy Richardson2Daniel Velez3John J. Nigro4Stephen Pophal5David Frakes6Rady Children’s Hospital–San DiegoPhoenix Children’s HospitalSt. Joseph’s Hospital and Medical CenterPhoenix Children’s HospitalRady Children’s Hospital–San DiegoPhoenix Children’s HospitalArizona State UniversityAbstract Background 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. Methods 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. Results 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. Discussion & conclusion 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.http://link.springer.com/article/10.1186/s41205-018-0033-8Congenital heart disease3D printingRetrospective chart reviewPatient outcomes
collection DOAJ
language English
format Article
sources DOAJ
author Justin Ryan
Jonathan Plasencia
Randy Richardson
Daniel Velez
John J. Nigro
Stephen Pophal
David Frakes
spellingShingle Justin Ryan
Jonathan Plasencia
Randy Richardson
Daniel Velez
John J. Nigro
Stephen Pophal
David Frakes
3D printing for congenital heart disease: a single site’s initial three-yearexperience
3D Printing in Medicine
Congenital heart disease
3D printing
Retrospective chart review
Patient outcomes
author_facet Justin Ryan
Jonathan Plasencia
Randy Richardson
Daniel Velez
John J. Nigro
Stephen Pophal
David Frakes
author_sort Justin Ryan
title 3D printing for congenital heart disease: a single site’s initial three-yearexperience
title_short 3D printing for congenital heart disease: a single site’s initial three-yearexperience
title_full 3D printing for congenital heart disease: a single site’s initial three-yearexperience
title_fullStr 3D printing for congenital heart disease: a single site’s initial three-yearexperience
title_full_unstemmed 3D printing for congenital heart disease: a single site’s initial three-yearexperience
title_sort 3d printing for congenital heart disease: a single site’s initial three-yearexperience
publisher BMC
series 3D Printing in Medicine
issn 2365-6271
publishDate 2018-11-01
description Abstract Background 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. Methods 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. Results 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. Discussion & conclusion 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.
topic Congenital heart disease
3D printing
Retrospective chart review
Patient outcomes
url http://link.springer.com/article/10.1186/s41205-018-0033-8
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