Abstract
Background
Three-dimensional printing (3DP) is increasingly applied in surgical training; however, its effectiveness and reliability in hepatobiliary surgery education remain uncertain.
Objectives
To systematically review the literature on the application and effectiveness of 3DP in hepatobiliary surgical training and anatomical education.
Method
PubMed, Embase and the Cochrane Library were searched for publications dated 1 January 1995, to 19 January 2025. Two investigators independently performed the literature search and screened eligible studies that reported the use of 3DP models for surgical training or anatomical education. Study quality was assessed using the Medical Education Research Study Quality Instrument (MERSQI), and levels of evidence were graded using the Oxford Centre for Evidence-Based Medicine (OCEBM) framework. Extracted data included study design, participant numbers, type of surgical training, type of anatomical education, and reported subjective and objective outcomes.
Results
Twenty-two studies investigated the application of 3DP in clinical surgical training and 12 studies focused on anatomical education. Laparoscopic procedures were the most frequently reported training context (59%). In anatomical education, tumor localization was the most common task (50%). Ten studies reported that 3DP significantly improved operative performance, reducing operation time by 34–54.6% in laparoscopic and choledochoscopic training. In anatomical education, 3DP models improved students’ performance by 57–70% in liver segment memorization.
Conclusion
3DP models demonstrated substantial value in both surgical training and anatomical education for hepatobiliary surgery. Although still developing, 3DP has already achieved broad acceptance among surgeons and medical students as an effective adjunct for skill acquisition and anatomical understanding.
Keywords: 3D printing, hepatobiliary surgery, surgical training, anatomy education
HIGHLIGHTS
3DP models are applied in both surgical training and anatomical education, demonstrating broad educational value in hepatobiliary surgery.
3DP models significantly shorten operation time and improve surgical skills in hepatobiliary training.
In anatomical education, 3DP models enhance tumor localization and outperform CT/VR models.
Introduction
Hepatobiliary surgery is one of the most technically demanding subspecialties within general surgery. Considerable anatomical variability exists in the hepatic artery, portal vein, biliary tract and hepatic veins, all of which complicate surgical approaches. These complexities, coupled with high operative risks, technical difficulty, frequent postoperative complications and prolonged training requirements, make hepatobiliary surgery particularly challenging. Traditional teaching tools – such as atlases, videos and CT imaging – remain widely used. However, due to the intricate liver anatomy and marked interindividual differences, these conventional approaches often fail to provide learners with an adequate understanding of hepatobiliary structures. Consequently, educational outcomes are suboptimal, and the acquisition of surgical skills remains difficult.
Additive manufacturing, commonly referred to as three-dimensional printing (3DP), enables rapid fabrication of high-fidelity anatomical models through specialized printers [1,2]. With ongoing advances in printer hardware, software and material diversity, 3DP has gained broad applicability across medicine. Historically, medical students’ comprehension of radiologic images has been limited to two-dimensional representations in textbooks or on computer screens [3,4]. By contrast, 3DP allows direct conversion of medical imaging data, such as CT scans, into accurate three-dimensional structures [5,6]. This capability makes 3DP a powerful adjunct or alternative to traditional teaching methods in medical education [7,8]. Improvements in resolution, processing speed and material costs have steadily enhanced its accessibility [9,10]. Modern 3DP models not only achieve higher fidelity and anatomical precision but also simulate human tissues with notable realism [11], thereby holding strong potential for surgical simulation and skills training.
Evidence from multiple randomized controlled trials [12–15] across diverse surgical disciplines demonstrates that 3DP models facilitate both early skills acquisition and advanced procedural training. Studies in neurosurgery, otolaryngology, gastrointestinal surgery and neurology have shown measurable improvements in operative efficiency when trainees practiced with 3DP-based simulations [3,16–19]. Within hepatobiliary surgery, 3DP models have been applied in laparoscopy, endoscopy, preoperative planning, anatomical teaching, tumour localization and patient education. High-quality, reproducible simulation is critical for building both decision-making capacity and technical proficiency. Yet, traditional training for surgical residents faces increasing constraints, including restricted work hours and expanding subspecialization. Integration of 3DP models into hepatobiliary training may help address these challenges by providing additional opportunities for safe, hands-on practice [20–23]. By enabling detailed three-dimensional visualization of organ anatomy, 3DP represents a potentially transformative tool in surgical education [24–27]. While surgical training has historically relied on apprenticeship models with direct observation in the operating theatre, contemporary studies highlight the value of simulation in providing safe, effective and transferable procedural training [28–30]. Nonetheless, limitations remain: high-fidelity models are costly, concerns persist regarding accuracy and standardized manufacturing protocols are lacking.
Prior systematic reviews [31,32] have primarily addressed the application of 3DP in anatomical replication and preoperative planning. Christou et al. [33] specifically explored 3DP and 3D bioprinting in hepatocellular carcinoma, while Alkhouri et al. [34] summarized its use in paediatric liver disease and transplantation. However, no systematic review has comprehensively examined the role of 3DP in hepatobiliary surgical education, particularly from the perspective of skill acquisition and anatomical knowledge enhancement aimed at improving both technical performance and cognitive understanding.
The present study systematically reviews published evidence to address two objectives: To evaluate the role of 3DP in improving surgical skills relevant to hepatobiliary surgery and to assess the contribution of 3DP to anatomical education in hepatobiliary surgery.
Materials and methods
The protocol for this review was pre-registered in the PROSPERO database and conducted in strict accordance with the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) [35] guidelines and the Assessing the Methodological Quality of Systematic Reviews (AMSTAR) framework [36].
Search strategy
A systematic literature search was conducted in PubMed (all fields), Embase (all fields) and the Cochrane Library (all text) by J Lin and W Li. The search strategy employed the keywords ‘3D model’, ‘liver/hepatic’ and ‘teaching/education/sim’. The complete strategy is provided in Appendix 1 in Supplemental data. The search was restricted to publications in English from1 January 1995, to 19 January 2025, with the final search executed on 19 January 2025. Additionally, the reference lists of included articles were manually screened to identify further eligible studies.
Study selection
To comprehensively capture empirical investigations on 3DP applications in hepatobiliary surgery education and training, a predefined eligibility framework was established. Studies were included if they (1) constituted primary research with original data; (2) explicitly documented the use of 3DP in surgical education and (3) involved medically trained participants. Exclusion criteria comprised (a) non-empirical publications such as editorials, commentaries and opinion pieces, and (b) secondary literature including systematic reviews and meta-analyses, in order to preserve the integrity of primary data synthesis. This step was completed by J Lin and W Li.
Quality assessment
Two assessors (X Yu and Y Zhang) independently evaluated study quality, resolving discrepancies through consensus. Owing to heterogeneity in study design, multiple appraisal instruments were employed. Levels of evidence and recommendations were classified using a modified Oxford Centre for Evidence-Based Medicine (OCEBM) educational framework, where Grade A represents the highest and Grade D the lowest level of recommendation [37] Methodological rigor was further assessed using the Medical Education Research Study Quality Instrument (MERSQI), which evaluates the quality of quantitative medical education research [38].
Data extraction and analysis
Data extraction was performed by J Lin and W Li with a standardized template to ensure consistency across studies. Extracted parameters included: (1) bibliographic information (authors, year, country); (2) methodological characteristics (design, sample size); (3) technical specifications (materials, costs); (4) educational components (tasks performed with the models) and (5) validation outcomes, both objective (fidelity assessments, performance measures) and subjective (expert/trainee feedback). For studies with incomplete technical details on 3DP hepatobiliary models, missing information was inferred from supplementary materials or cross-referenced with methodological precedents in related surgical education literature.
Results
The initial searches yielded 673 studies and 160 articles were excluded as duplicates; a further 436 were excluded following screening of abstracts and 5 were unable to retrieved. A total of 34 studies met the inclusion criteria: 22 evaluated 3DP applications in clinical surgical training and 12 in anatomical education (Figure 1). Of these, 19 studies originated from China.
Figure 1.
PRISMA statement flow diagram of the search and study selection process. PRISMA, Preferred reporting items for systematic reviews and meta-analyses.
Quality assessment
The included studies spanned OCEBM evidence levels 1–4, with 10 studies [3,39–47] rated Level 1b, 7 studies [22,48–53] Level 2b, 1 study [54] Level 3a, 2 studies [55,56] Level 3b, 9 studies [57–65] Level 4 and 5 studies [21,23, 66–68] Level 5. As detailed in Supplementary Table 1, the mean MERSQI score was 11.6 (range: 7–13.5), with complete inter-rater agreement (100%), reflecting a consistently low risk of bias.
3DP model preparation information
Table 1 summarizes the characteristics of the included 3DP models. Most models were reconstructed from CT scans, and all liver models were segmented from CT-based structures. A few studies also reported the use of MRI [65] or MRCP [46,57,67] as imaging sources. Approximately 38% of models required manual refinement during reconstruction, and 3 studies [57,58,61] specifically described manual segmentation. In terms of fabrication, 56% of models were constructed in-house, while 26% were outsourced.
Table 1.
Preparation information for 3DP models.
| Authors |
Materials |
Data source | Reconstruction software | Modeling approach | Self-made or outsource | 3D printer |
|---|---|---|---|---|---|---|
| Dhir et al. [57], 2015 | Polycarbonate | MRCP | CAD | Manual modeling | Self-made | Viper SI2 stereo-lithography system |
| Holt et al. [58], 2015 | Polymer resin, Silicone | N/A | CAD | Manual modeling | Self-made | Connex 260v |
| Burdall et al. [59], 2016 | Silicone | Digital hepatic anatomy images | CAD | N/A | Outsource | 3D systems project 660pro |
| Li. et al. [3], 2018 | N/A | CT | Hisense computer-assisted surgery system | Software modeling | Self-made | Stratasys Connex3350 |
| Wei et al. [39], 2019 | N/A | CT | N/A | N/A | Outsource | N/A |
| Kwon et al. [23], 2020 | Silicone | CT | MeshLab MeshMixer |
Software modeling | Self-made | 3DM DW-06, 3DMaterials, Zeron2500 |
| Wei et al. [66], 2020 | N/A | CT | N/A | Software modeling Manual polishing |
Outsource | N/A |
| Murillo et al. [67], 2021 | Acrylonitrile butadiene styrene, P53 silicone rubber, Elmer’s slime | MRCP | CADD | Software modeling Manual polishing | Self-made | 3D Zortrax |
| Wang et al. [60], 2022 | N/A | CT | N/A | Software modeling Manual polishing | Outsource | N/A |
| Micallef et al. [61], 2022 | Ecotough™ polylactic acid, Ecoflex™ 00–20 FAST silicone, Ease Release 200, SilcPig™ coloring | N/A | Fusion 360™ | Manual modeling | Self-made | Ultimaker S5 |
| Yu et al. [48], 2022 | Silicone | CT | E3D digital medical modelling | Software modeling Manual polishing | N/A | N/A |
| Yang et al. [22], 2022 | Silicone | CT | E3D digital medical modelling | Software modeling Manual polishing | N/A | N/A |
| Fechner et al. [55], 2023 | Silicone-based soft resin, silicone | CT | Blender Fusion360 |
Software modeling Manual polishing | Self-made | Form 3B Creality CR 10S Pro |
| Xia et al. [49], 2023 | Silicone | CT | Magic 24 Zbush |
Software modeling Manual polishing | Self-made | FDM |
| Shen et al. [50], 2023 | Silicone | CT | N/A | N/A | Outsource | N/A |
| Lu et al. [62], 2023 | ACGE | CT | Yorktal digital medical imaging | Software modeling | Self-made | Prismlab, RP400 |
| Shen et al. [40], 2024 | Silicone | N/A | N/A | N/A | Outsource | N/A |
| Elisei et al. [63], 2024 | FDM/PLA | CT | InVesalius Fusion 360 |
Software modeling Manual polishing | Self-made | Fortus 380 mc |
| Gu et al. [51], 2024 | Silicone | CT | N/A | Software modeling Manual polishing |
Outsource | Silplot-S400 |
| Yang et al. [41], 2024 | Agilus30, Vero Vivid, Vero Ultra | CT | Magics | Software modeling Manual polishing | Self-made | Stratasys J850 |
| Aranovich et al. [64], 2024 | Thermoplastic elastomer TPU-95 | CT | N/A | N/A | N/A | N/A |
| Cao et al. [65], 2024 | Silicone | MRI | E3D digital medical modelling | Software modeling Manual polishing | Self-made | SilplotS400 |
| Kong et al. [42], 2016 | ZP150 | CT | N/A | N/A | N/A | N/A |
| Kong et al. [43], 2016 | ZP150, transparent jelly wax | CT | Geomagic 12 | Software modeling Manual polishing | Self-made | Spectrum ZTM 510 |
| Streba et al. [21], 2018 | nGenN/AFlex black flexible filament | CT MRI |
Meshmixer | Software modeling Manual polishing | Self-made | Tiertime |
| Yang et al. [44], 2019 | VeroClear™, RGD720 | CT | N/A | Software modeling | Self-made | Stratasys J750TM |
| Chedid et al. [45], 2020 | N/A | N/A | N/A | N/A | N/A | N/A |
| Bati et al. [46], 2020 | N/A | MRCP | Analyze 12.0 | Software modeling | Self-made | Mass Portal Pharaoh xd 20 Form Labs2 |
| Huettl et al. [47], 2021 | Polyurethane rubber, acrylonitrile butadiene styrene | CT | Synapse 3D | N/A | Self-made | Cella Medical Solutions |
| Lopez-Lopez et al. [52], 2021 | N/A | N/A | 3D-MSP | N/A | N/A | N/A |
| Song et al. [54], 2023 | Vero Family, photocurable resin | CT | N/A | Software modeling | Outsource | Stratasys J826 |
| Cheng et al. [68], 2023 | Photosensitive resin | CT | E3D digital medical modeling | Software modeling | Self-made | SL600 |
| Shahbaz et al. [56], 2023 | RGD720 | Digital human specimen | N/A | N/A | Outsource | J401Pro |
| Bao et al. [53], 2023 | Photosensitive resin, VeroCyanV, VeroYellowV, VeroMagentaV, VeroPureWhite, VeroUltraClea | CT | N/A | Software modeling | Self-made | Stratasys J850 |
Note: 3D: three-dimensional; 2D: two-dimensional; 3DP: three-dimensional printing; CT: computed tomography; MRI: magnetic resonance imaging; N/A: not available.
Surgical training
A total of 22 studies evaluated the role of 3DP models in surgical training (Table 2). Training tasks most frequently included bilioenteric anastomosis (27%) and pancreaticojejunostomy (18%). Of these studies, half (n = 11) reported fidelity scores ≥4/5, and 18 (81.8%) indicated that participants rated 3DP models as useful for skill acquisition (scores ≥4/5). Quantitative outcomes showed that 3DP training reduced operation time by 34-55% and improved OSATS scores by 33–73%. Comparative studies further highlighted these benefits: Li et al. [3] demonstrated that residents trained with 3DP models achieved higher anatomical recognition scores than those using images (57 vs. 16), while Shen et al. [50] found that residents trained with 3DP models performed better than those using TLCST, with shorter operation times (20.8 vs. 25.8 min) and higher performance scores (28.8 vs. 19.7).
Table 2.
Application of 3DP models in surgical training.
| Authors | Participants | Allocation | Task | Fidelity | Self-evaluation usefulness | Validity | Others |
|---|---|---|---|---|---|---|---|
| Dhir et al. [57], 2015 | 20 endosonographers | No | Endoscopic ultrasonography-guided biliary drainage | Overall realism: 13/15, Puncture sensation: 4/5 | 4/5 | N/A | N/A |
| Holt et al. [58], 2015 | 16 endoscopists | No | Endoscopic ampullectomy | Overall realism: 3.2/5 | N/A | Core procedural steps: 3.1/5 | Self-evaluation self-confidence improvement: 2.2→2.9/5 |
| Burdall et al. [59], 2016 | 20 senior pediatric surgical trainees | No | Laparoscopic choledochal surgery | N/A | 7.4/10 | N/A | Recommendation: 100% |
| Li. et al. [3], 2018 | 20 residents | 3DP group, images group | Choledochoscopy techniques | Anatomical accuracy: 4.5/5 | 4.7/5 | Operation time:3DP 29→12mins Anatomic recognition accuracy: 3DP > Images (57 > 16) |
N/A |
| Wei et al. [39], 2019 | 3 surgeons | 2 rounds 3DP training group, 1 round 3DP training group, 0 round 3DP training | Laparoscopic pancreaticojejunostomy | N/A | N/A | Operation time: 2 rounds < 1 round < 0 round(20 < 30 < 40 mins) Operation level: 2 rounds > 1 round > 0 round |
N/A |
| Kwon et al. [23], 2020 | / | No | Endoscopic retrograde bilioenteric anastomosis | N/A | N/A | N/A | N/A |
| Wei et al. [66], 2020 | 3 residents 3 fellows |
No | Laparoscopic bilioenteric anastomosis | N/A | N/A | N/A | N/A |
| Murillo et al. [67], 2021 | 13 practitioners | No | Laparoscopic cholecystectomy | Overall realism:4.5/5 Texture:4.5/5 |
N/A | N/A | Recommendation: 90% Durability: 4.3/5 |
| Wang et al. [60], 2022 | 1 junior surgeon | No | Laparoscopic pancreaticojejunostomy | N/A | N/A | OSATS score: 15→26, Operation time: 1,734→1,142 s | N/A |
| Micallef et al. [61], 2022 | 6 surgeons 2 residents 1 medical student |
No | Bile duct anastomosis | Anatomical accuracy: 3.56/5 | 4.5/5 | N/A | Feasibility:3/5 |
| Yu et al. [48], 2022 | 5 attendings 5 fellows 5 residents |
Attendings group, fellows group, residents group | Laparoscopic pancreaticojejunostomy | Overall realism: 3.96/5 Elasticity: 3.88/5 Tearability: 3.83/5 |
N/A | Operation time: residents > fellows > attendings (1254.8 > 797.8 > 569.2s) Operation scores: residents < fellows < attendings (14.4 < 17.2 < 18.8) N/ASA-TLX: residents > attendings > fellows (261.6 > 265.4 > 412.8) |
Recommendation: 100% |
| Yang et al. [22], 2022 | 4 attendings 4 fellows 8 residents |
Attendings group, fellows group, residents group | Laparoscopic pancreaticojejunostomy | Overall realism: 4.22/5 Tactile: 4.58/5 Breakthrough sensation: 4.5/5 Tearability: 3.75/5 |
N/A | Operation time: residents > fellows > attendings (106.2 > 62.5 > 37.8) Operation scores: residents < fellows < attendings (19 < 19.5 < 23) |
N/A |
| Fechner et al. [55], 2023 | 20 residents | No | Percutaneous transhepatic cholangial drainage | Overall realism: 3.67/4 Anatomical accuracy: 3.67/4 |
3.55/4 | KAP: 677→262 mGy/cm2 Puncture time: 16:15 → 7:42 min Fluoroscopy time: 175 → 52 s |
Self-evaluation self-confidence improvement: 3.83/4 |
| Xia et al. [49], 2023 | 5 attendings 5 fellows 5 residents |
Attendings group, fellows group, residents group | Laparoscopic bilioenteric anastomosis | Overall realism: 4.17/5 Texture: 4.17/5 Tactile: 4.00/5 |
4.83/5 | Operating time: residents > fellows > attendings (39.84 > 19.92 > 13.32 min) OSATS scores: residents < fellows < attendings (19.8 < 26.8 < 29.2) |
Self-evaluation self-confidence improvement: 4.33/5 Recommendation: 100% |
| Shen et al. [50], 2023 | 5 attendings 5 fellows 5 residents |
Attendings group, fellows group, residents group | Laparoscopic bilioenteric anastomosis | Overall realism: 4.70/5 Tactile: 4.9/5 Breakthrough sensation: 4.60/5 Tearabilty: 4.3/5 |
N/A | Operating time: residents > fellows > attendings OSATS score: residents < fellows < attendings |
N/A |
| Lu et al. [62], 2023 | A novice doctor | No | Laparoscopic liver tumor excision | N/A | N/A | N/A | N/A |
| Shen et al. [40], 2024 | 15 surgeons | 3DP group, simple suture group, video group | Laparoscopic bilioenteric anastomosis | N/A | N/A | Operation time: 3DP < simple suture < video (29.4 < 42.4 < 45.4 min) Operation score: 3DP > simple suture > video (8.2 > 6.8 > 5.2) GOALS score: 3DP > simple suture > video (21.2 > 17.8 > 15.6) |
N/A |
| Elisei et al. [63], 2024 | 33 residents and specialist surgeons | No | Diagnosis, biopsy, drainage | Overall realism: 31/33 | > 4.5/5 | N/A | Durability: >90% |
| Gu et al. [51], 2024 | 4 residents 4 senior surgeons 4 experts |
Experts group, senior surgeon group, residents group | Laparoscopic and robotic bilioenteric anastomosis | Overall realism: 4.5/5 | 4.70/5 | Operation time: residents:59.3→34.8 min, senior surgeons: 38.8→24.5 min, experts: 27.5→17.6 min OSATS score: residents: 2.1→2.8, senior surgeons:3.3→3.8, experts: 4.3→4.6 min |
Operability: 4.43/5 |
| Yang et al. [41], 2024 | 20 residents | 3DP group, TLCST group | Laparoscopic bile duct exploration | Overall realism: 8/10 Tissue pliability: 6/10 Texture: 6/10 |
4.5/5 | Operation time: 3DP < TLCST (20.8 < 25.8 min) Operation scores: 3DP > TLCST (28.8 > 19.7) |
Teaching satisfaction: 3DP > TLCST |
| Aranovich et al. [64], 2024 | 10 residents | No | Hepatic packing | N/A | N/A | Completion rate: 90% | N/A |
| Cao et al. [65], 2024 | 2 experts | No | Complex liver cancer resection | N/A | N/A | N/A | N/A |
Notes:2D: two-dimensional; 3DP: three-dimensional printing; OSATS: objective structured assessment of technical skills; NASA-TLX: NASA Task Load Index; KAP: Kerma Area Product; TLCST: traditional laparoscopic simulation training group; N/A: not available.
Anatomical education
A total of 12 studies involved the application of the 3DP model in anatomy education (Table 3). Most compared 3DP with CT/MRI/atlas-based teaching (58.3%), and 25% compared 3DP with VR models. Medical students trained with 3DP models demonstrated 57–70% improvements in liver segment memorization compared with CT/MRI/atlas. Among residents, 3DP training reduced tumour localization time by 28-67% and improved localization scores by 28–135%. Representative models for surgical training and anatomical education, as well as the preparation workflow, are shown in Figure 2.
Table 3.
Application of 3DP models in anatomy education.
| Authors | Participants | Allocation | Task | Fidelity | Self-evaluation usefulness | Validity | Others |
|---|---|---|---|---|---|---|---|
| Kong et al. [42], 2016 | 61 medical students | 3DP group, digital models group, atlas group | Liver segment memory | Overall realism: 4/5 | N/A | Teaching effect: 3DP > atlas | N/A |
| Kong et al. [43], 2016 | 92 medical students | Type 1 group, Type 2 group, Type 3 group, atlas group | Liver segment memory | Anatomical accuracy: Type 3 > Type 2> Type 1 |
N/A | Examination sores: Type 3 > Type 1 > Type 2 > atlas | Overall satisfaction: Type 3 > Type 2 > Type 1 |
| Streba et al. [21], 2018 | 12 residents 43 medical students |
Residents group, medical students group | Tumor location identification | Overall realism: students: 4.13/5, residents: 4.11/5 Texture: students: 2.84/5, residents: 2.17/5 |
Students: 3.79/5 Residents: 4.17/5 |
Surgical planning improvement: students: 3.98/5, residents: 4.42/5 Knowledge improvement: students: 3.58/5, residents: 4.08/5 |
N/A |
| Yang et al. [44], 2019 | 3 residents | 3DP group, VR group, CT group | Tumor location identification | N/A | N/A | Completion time: 3DP < VR < CT (93.42 < 223.12 < 286.10 s) Completion score: 3DP > VR > CT (80.92 > 55.25 > 34.50) |
N/A |
| Chedid et al. [45], 2020 | 116 physicians | 3DP group, CT group | Liver segment memory | N/A | N/A | Liver segment recognition scores: 3DP: 42→71; CT: 39→69 | Preference: 3DP: 39.6% |
| Bati et al. [46], 2020 | 19 residents | No | Anatomical identification, diagnosis, and preoperative preparation | N/A | N/A | Anatomical positioning: 100% Surgical planning improvement: 100% |
N/A |
| Huettl et al. [47], 2021 | 5 experts 5 fellows 10 residents 10 medical students |
Experts group, fellows group, residents group, medical students group | Tumor location identification | N/A | 3.67/5 | Surgical planning improvement: 90% Completion time: experts < students, 3DP < VR < digital model (509 < 702 < 704 s) Accuracy rates: experts > students 3DP > VR > digital model |
Preference: 3DP: experts: 60%, fellows: 60%, residents: 20%, students: 0 |
| Lopez-Lopez et al. [52], 2021 | 75 medical students | 3DP group, CT/MRI group, digital model group | Tumor location identification | Tumor-vascular branch distance was consistent with CT/MRI. | N/A | The average performance: 3DP > CT/MRI > digital model |
N/A |
| Song et al. [54], 2023 | 3 staffs 3 residents |
Staffs group, resident group | Tumor location identification | T stage was consistent with the pathology report. | Staff: 4.60/5 Resident: 4.33/5 |
Completion scores improvement: 3DP: staffs: 3.96→4.75, residents: 3.84→4.37 | N/A |
| Cheng et al. [68], 2023 | 62 interns | 3DP group, VR group, CT group | Tumor location identification | N/A | 4.03/5 | Completion score: 3DP > VR > CT (89.4 > 75.8 > 69.5) | Satisfaction: 86.2% Interest: 92.1% |
| Shahbaz et al. [56], 2023 | 26 surgeons | No | Anatomy of hepatic blood vessels and biliary tracts | N/A | N/A | Surgical planning improvement: 100% Training young surgeons: 84% |
N/A |
| Bao et al. [53], 2023 | 8 interns 10 standardized training trainees 12 professional training trainees |
Interns group, standardized training trainees group, professional training trainees group | Tumor location identification | N/A | 3.65/5 | Understanding key points: interns < standardized training trainees < professional training trainees (3DP: 23 < 33 < 36; 2D: 17 < 27 < 28) | N/A |
Notes: 2D: two-dimensional; 3DP: three-dimensional printing; CT: computed tomography; MRI: magnetic resonance imaging; VR: visual reality; Type 1: liver segmental vascular models without parenchyma; Type 2: liver segmental vascular models with transparent parenchyma; Type 3: liver segmental vascular models with partitions; N/A: not available.
Figure 2.
Typical 3DP models and process of preparation The DICOM files obtained from CT/MRI will be converted into STL files and imported into modeling software. After modeling, the next step will be carried out according to the production plan: A. the 3D model would be sliced for 3DP and be printed; B. the 3D model would be printed to create a mold, followed by material pouring, ultimately resulting in the final model. CT: computed tomography; MRI: magnetic resonance imaging; DICOM: Digital Imaging and Communication on Medicine. a, b, c, d: Reprinted with permission under the open access [41,47, 49,51]; e, f: Reprinted with permission through Copyright Clearance Center’s RightsLinkⓇ service [43,54].
Discussion
This systematic review critically evaluates the role of 3DP models in hepatobiliary surgical training and anatomical education. Current evidence highlights their extensive use in endoscopic and laparoscopic skill acquisition, with broad consensus among both trainees and experts regarding their pedagogical value. In anatomical teaching, 3DP models surpass conventional atlas-based methods, particularly by enhancing spatial visualization of hepatic segmentation and tumour localization.
Our analysis of the technical workflow reveals that while CT and MRI are the predominant imaging sources, the journey from DICOM data to a functional educational model is non-trivial. Only a few [52,54] validated printed models against the source imaging data, while the majority required manual post-processing (e.g. edge smoothing) to achieve clinical or educational suitability. It highlights a significant challenge in automated segmentation for complex hepatobiliary structures. In general, training objectives dictated model requirements: anatomical precision was essential for tumour localization, whereas tactile fidelity [47] outweighed visual accuracy in basic skills such as suturing [61]. More advanced applications, such as tumour resection training, required not only anatomically precise replication but also the integration of functional features, including simulated blood circulation and fluorescent tumour labelling [65].
Current printing materials provide realistic haptic feedback for cutting and suturing, with self-healing properties enabling repeated practice. However, their mechanical and thermal responses remain inconsistent with those of living tissue, limiting their application in advanced procedures such as intraoperative bleeding control or bile leakage management. Animal models, by contrast, inherently reproduce such complications, underscoring a critical limitation in the translational capacity of current 3DP platforms.
A pivotal strength of 3DP, as evidenced in this review, is its performance relative to established teaching modalities. In anatomical education, 3DP models consistently outperformed CT, MRI, and atlas-based learning, particularly in spatial tasks like liver segment memorization and tumour localization [42,44]. 3DP offers superior retention of spatial knowledge through haptic-visual multisensory integration, enabling students and residents to observe and understand hepatobiliary anatomy from multiple perspectives, thereby deepening their understanding of anatomical structures. 3DP models allow for surgical procedure practice in simulated environments, such as laparoscopic surgery, choledochoscopy and tumour resection, helping residents become familiar with surgical procedures and techniques, thus demonstrating higher proficiency in actual surgeries. Additionally, these models provide a low-stakes platform for identifying and rectifying technical errors, effectively mitigating the risk of intraoperative mishaps and complications in clinical settings. When compared to VR, 3DP offers the distinct advantage of physicality, allowing for authentic instrument-tissue interaction which is crucial for practicing surgical manoeuvres like anastomosis. However, VR may surpass 3DP in visualizing internal structures non-destructively. This suggests that these technologies are not mutually exclusive but potentially complementary, and future research should explore hybrid simulation strategies.
For 3DP to transition from a novel tool to a cornerstone of hepatobiliary training, its integration into standardized curricula is essential. Isolated training sessions, as seen in many included studies, provide proof of concept but may not maximize long-term skill retention. The technology’s greatest potential may lie in structured, progressive training pathways – from basic anatomy recognition on low-fidelity models to advanced resection planning on high-fidelity, patient-specific simulators. A significant barrier to this integration is the current ambiguity surrounding cost-effectiveness. The frequent omission of detailed cost analyses in the literature is a major limitation. While the initial investment in printers and materials is quantifiable, a comprehensive economic evaluation must weigh these against the potential benefits: reduced operative time, decreased error rates in the operating room, diminished reliance on cadavers and animal models, and, ultimately, improved patient outcomes.
Despite encouraging results, our review identifies several translational gaps. Evidence remains constrained by small sample sizes, short training exposures and limited longitudinal data on model durability. Cost analyses are inconsistent, and the frequent omission of economic considerations prevents comprehensive evaluation. Assessments are predominantly based on subjective expert ratings, with limited use of blinded designs or objective outcome measures such as blood loss or iatrogenic injury. To address these limitations, future research must prioritize well-designed, multi-institutional randomized controlled trials (RCTs) with blinding where possible. These trials should employ standardized, objective assessment tools, including AI-driven performance analytics [69]. Beyond validation, the technological frontier is rapidly advancing. The emergence of bioprinting, multi-material composites (e.g. ACEG-x resin) and self-healing hydrogels [62] promises to better replicate parenchymal biomechanics and enhance model durability. Finally, developing standardized manufacturing and validation protocols will be crucial for ensuring consistency and reliability across different training centres.
Limitations
This review has several limitations. The included studies showed methodological heterogeneity, generally low quality, and often lacked blinding. Most trials were small and qualitative, and cost data were frequently omitted. In addition, the included studies varied in design (e.g. RCTs vs. single-group cross-sectional), which may have influenced the interpretation of results. Moreover, differences in objectives and material choices meant that 3DP applications could not be meaningfully compared across studies, further limiting synthesis. Well-designed, adequately powered RCTs with standardized outcomes are needed to establish the effectiveness of 3DP in hepatobiliary surgical education.
Conclusion
This review consolidates compelling evidence for 3DP as a transformative tool in hepatobiliary surgical education, significantly enhancing both anatomical understanding and technical skill acquisition. It provides a safe, reproducible platform for complex procedural rehearsal, bridging a critical gap in contemporary training constrained by work-hour limits and ethical concerns. Further studies should prioritize multi-centre trials with standardized assessment tools and establish high fidelity, cost-effectiveness 3DP models for advanced hepatobiliary surgical procedures curricula development.
Provenance and peer review
Not commissioned, externally peer-reviewed.
Supplementary Material
Funding Statement
This work was supported by hospital-enterprise joint project of Zhujiang Hospital, Southern Medical University (LCYJ240304).
Disclosure statement
This research did not receive any specific grant from funding agencies in the public, commercial, or not-for-profit sectors. The authors report no financial or personal conflicts of interest.
Data availability statement
The data that support the findings of this study are available from the corresponding author, Jing Tian, upon reasonable request.
References
- 1.Vávra P, Roman J, Zonča P, et al. Recent development of augmented reality in surgery: a review. J Healthc Eng. 2017;2017:4574172–4574179. doi: 10.1155/2017/4574172. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 2.Malik HH, Darwood ARJ, Shaunak S, et al. Three-dimensional printing in surgery: a review of current surgical applications. J Surg Res. 2015;199(2):512–522. doi: 10.1016/j.jss.2015.06.051. [DOI] [PubMed] [Google Scholar]
- 3.Li A, Tang R, Rong Z, et al. The use of three-dimensional printing model in the training of choledochoscopy techniques. World J Surg. 2018;42(12):4033–4038. doi: 10.1007/s00268-018-4731-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 4.Park L, Price-Williams S, Jalali A, et al. Increasing access to medical training with three-dimensional printing: creation of an endotracheal intubation model. JMIR Med Educ. 2019;5(1):e12626. doi: 10.2196/12626. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 5.Smillie RW, Williams MA, Richard M, et al. Producing three-dimensional printed models of the hepatobiliary system from computed tomography imaging data. Ann R Coll Surg Engl. 2021;103(1):41–46. doi: 10.1308/rcsann.2020.0191. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 6.Yi Z, He B, Liu Y, et al. Development and evaluation of a craniocerebral model with tactile-realistic feature and intracranial pressure for neurosurgical training. J Neurointerv Surg. 2020;12(1):94–97. doi: 10.1136/neurintsurg-2019-015008. [DOI] [PubMed] [Google Scholar]
- 7.Harb SC, Rodriguez LL, Vukicevic M, et al. Three-dimensional printing applications in percutaneous structural heart interventions. Circ Cardiovasc Imaging. 2019;12(10):e009014. doi: 10.1161/CIRCIMAGING.119.009014. [DOI] [PubMed] [Google Scholar]
- 8.Tsui JKS, Bell S, Cruz L, et al. Applications of three-dimensional printing in ophthalmology. Surv Ophthalmol. 2022;67(4):1287–1310. doi: 10.1016/j.survophthal.2022.01.004. [DOI] [PubMed] [Google Scholar]
- 9.Chen JV, Dang ABC, Dang A.. Comparing cost and print time estimates for six commercially-available 3D printers obtained through slicing software for clinically relevant anatomical models. 3D Print Med. 2021;7(1):1. doi: 10.1186/s41205-020-00091-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 10.Hamabe A, Ishii M, Kamoda R, et al. Artificial intelligence-based technology to make a three-dimensional pelvic model for preoperative simulation of rectal cancer surgery using MRI. Ann Gastroenterol Surg. 2022;6(6):788–794. doi: 10.1002/ags3.12574. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 11.Tack P, Victor J, Gemmel P, et al. 3D-printing techniques in a medical setting: a systematic literature review. Biomed Eng Online. 2016;15(1):115. doi: 10.1186/s12938-016-0236-4. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 12.Ryan JR, Almefty KK, Nakaji P, et al. Cerebral aneurysm clipping surgery simulation using patient-specific 3D printing and silicone casting. World Neurosurg. 2016;88:175–181. doi: 10.1016/j.wneu.2015.12.102. [DOI] [PubMed] [Google Scholar]
- 13.Ryan JR, Chen T, Nakaji P, et al. Ventriculostomy simulation using patient-specific ventricular anatomy, 3D printing, and hydrogel casting. World Neurosurg. 2015;84(5):1333–1339. doi: 10.1016/j.wneu.2015.06.016. [DOI] [PubMed] [Google Scholar]
- 14.Ploch CC, Mansi CSSA, Jayamohan J, et al. Using 3D printing to create personalized brain models for neurosurgical training and preoperative planning. World Neurosurg. 2016;90:668–674. doi: 10.1016/j.wneu.2016.02.081. [DOI] [PubMed] [Google Scholar]
- 15.Mashiko T, Otani K, Kawano R, et al. Development of three-dimensional hollow elastic model for cerebral aneurysm clipping simulation enabling rapid and low cost prototyping. World Neurosurg. 2015;83(3):351–361. doi: 10.1016/j.wneu.2013.10.032. [DOI] [PubMed] [Google Scholar]
- 16.Blohm JE, Salinas PA, Avila MJ, et al. Three-dimensional printing in neurosurgery residency training: a systematic review of the literature. World Neurosurg. 2022;161:111–122. doi: 10.1016/j.wneu.2021.10.069. [DOI] [PubMed] [Google Scholar]
- 17.McGuire LS, Fuentes A, Alaraj A.. Three-dimensional modeling in training, simulation, and surgical planning in open vascular and endovascular neurosurgery: a systematic review of the literature. World Neurosurg. 2021;154:53–63. doi: 10.1016/j.wneu.2021.07.057. [DOI] [PubMed] [Google Scholar]
- 18.Langridge B, Momin S, Coumbe B, et al. Systematic review of the use of 3-dimensional printing in surgical teaching and assessment. J Surg Educ. 2018;75(1):209–221. doi: 10.1016/j.jsurg.2017.06.033. [DOI] [PubMed] [Google Scholar]
- 19.Oxford K, Walsh G, Bungay J, et al. Development, manufacture and initial assessment of validity of a 3-dimensional-printed bowel anastomosis simulation training model. Can J Surg. 2021;64(5):E484–E490. doi: 10.1503/cjs.018719. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 20.Gallo C, Boškoski I, Matteo MV, et al. Training in endoscopic retrograde cholangio-pancreatography: a critical assessment of the broad scenario of training programs and models. Expert Rev Gastroenterol Hepatol. 2021;15(6):675–688. doi: 10.1080/17474124.2021.1886078. [DOI] [PubMed] [Google Scholar]
- 21.Streba CT, Popescu S, Pirici D, et al. Three-dimensional printing of liver tumors using CT data: proof of concept morphological study. Rom J Morphol Embryol. 2018;59(3):885–893. [PubMed] [Google Scholar]
- 22.Yang J, Luo P, Wang Z, et al. Simulation training of laparoscopic pancreaticojejunostomy and stepwise training program on a 3D-printed model. Int J Surg. 2022;107:106958. doi: 10.1016/j.ijsu.2022.106958. [DOI] [PubMed] [Google Scholar]
- 23.Kwon CI, Shin Y, Hong J, et al. Production of ERCP training model using a 3D printing technique (with video). BMC Gastroenterol. 2020;20(1):145. doi: 10.1186/s12876-020-01295-y. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 24.Backhouse S, Taylor D, Armitage JA.. Is this mine to keep? Three‐dimensional printing enables active, personalized learning in anatomy. Anat Sci Educ. 2019;12(5):518–528. doi: 10.1002/ase.1840. [DOI] [PubMed] [Google Scholar]
- 25.Cacciamani GE, Okhunov Z, Meneses AD, et al. Impact of three-dimensional printing in urology: state of the art and future perspectives. a systematic review by ESUT-YAUWP Group. Eur Urol. 2019;76(2):209–221. doi: 10.1016/j.eururo.2019.04.044. [DOI] [PubMed] [Google Scholar]
- 26.Giannopoulos AA, Mitsouras D, Yoo SJ, et al. Applications of 3D printing in cardiovascular diseases. Nat Rev Cardiol. 2016;13(12):701–718. doi: 10.1038/nrcardio.2016.170. [DOI] [PubMed] [Google Scholar]
- 27.Pucci JU, Christophe BR, Sisti JA, et al. Three-dimensional printing: technologies, applications, and limitations in neurosurgery. Biotechnol Adv. 2017;35(5):521–529. doi: 10.1016/j.biotechadv.2017.05.007. [DOI] [PubMed] [Google Scholar]
- 28.Nassar AK, Al-Manaseer F, Knowlton LM, et al. Virtual reality (VR) as a simulation modality for technical skills acquisition. Ann Med Surg (Lond). 2021;71:102945. doi: 10.1016/j.amsu.2021.102945. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 29.Pietersen PI, Bjerrum F, Tolsgaard MG, et al. Standard setting in simulation-based training of surgical procedures: a systematic review. Ann Surg. 2022;275(5):872–882. doi: 10.1097/SLA.0000000000005209. [DOI] [PubMed] [Google Scholar]
- 30.Aydın A, Ahmed K, Abe T, et al. Effect of simulation-based training on surgical proficiency and patient outcomes: a randomised controlled clinical and educational trial. Eur Urol. 2022;81(4):385–393. doi: 10.1016/j.eururo.2021.10.030. [DOI] [PubMed] [Google Scholar]
- 31.Perica ER, Sun Z.. A systematic review of three-dimensional printing in liver disease. J Digit Imaging. 2018;31(5):692–701. doi: 10.1007/s10278-018-0067-x. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 32.Witowski JS, Coles-Black J, Zuzak TZ, et al. 3D printing in liver surgery: a systematic review. Telemed J E Health. 2017;23(12):943–947. doi: 10.1089/tmj.2017.0049. [DOI] [PubMed] [Google Scholar]
- 33.Christou CD, Tsoulfas G.. Role of three-dimensional printing and artificial intelligence in the management of hepatocellular carcinoma: challenges and opportunities. World J Gastrointest Oncol. 2022;14(4):765–793. doi: 10.4251/wjgo.v14.i4.765. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 34.Alkhouri N, Zein NN.. Three-dimensional printing and pediatric liver disease. Curr Opin Pediatr. 2016;28(5):626–630. doi: 10.1097/MOP.0000000000000395. [DOI] [PubMed] [Google Scholar]
- 35.Page MJ, McKenzie JE, Bossuyt PM, et al. The PRISMA 2020 statement: an updated guideline for reporting systematic reviews. BMJ. 2021;372:n71. doi: 10.1136/bmj.n71. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 36.Shea BJ, Reeves BC, Wells G, et al. AMSTAR 2: a critical appraisal tool for systematic reviews that include randomised or non-randomised studies of healthcare interventions, or both. BMJ. 2017;358:j4008. doi: 10.1136/bmj.j4008. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 37.Carter FJ, Schijven MP, Aggarwal R, et al. Consensus guidelines for validation of virtual reality surgical simulators. Surg Endosc. 2005;19(12):1523–1532. doi: 10.1007/s00464-005-0384-2. [DOI] [PubMed] [Google Scholar]
- 38.Reed DA, Cook DA, Beckman TJ, et al. Association between funding and quality of published medical education research. JAMA. 2007;298(9):1002–1009. doi: 10.1001/jama.298.9.1002. [DOI] [PubMed] [Google Scholar]
- 39.Wei F, Xu M, Lai X, et al. Three-dimensional printed dry lab training models to simulate robotic-assisted pancreaticojejunostomy. ANZ J Surg. 2019;89(12):1631–1635. doi: 10.1111/ans.15544. [DOI] [PubMed] [Google Scholar]
- 40.Shen J, Zhang Y, Zhang B, et al. Simulation training of laparoscopic biliary-enteric anastomosis with a 3D-printed model leads to better skill transfer: a randomized controlled trial. Int J Surg. 2024;110(4):2134–2140. Published online January 11,. doi: 10.1097/JS9.0000000000001079. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 41.Yang Z, Tong Y, Duan D, et al. A novel 3D-printed educational model for the training of laparoscopic bile duct Exploration:a pilot study for beginning trainees. Heliyon. 2024;10(17):e36689. doi: 10.1016/j.heliyon.2024.e36689. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 42.Kong X, Nie L, Zhang H, et al. Do three-dimensional visualization and three-dimensional printing improve hepatic segment anatomy teaching? A randomized controlled study. J Surg Educ. 2016;73(2):264–269. doi: 10.1016/j.jsurg.2015.10.002. [DOI] [PubMed] [Google Scholar]
- 43.Kong X, Nie L, Zhang H, et al. Do 3D printing models improve anatomical teaching about hepatic segments to medical students? A randomized controlled study. World J Surg. 2016;40(8):1969–1976. doi: 10.1007/s00268-016-3541-y. [DOI] [PubMed] [Google Scholar]
- 44.Yang T, Lin S, Xie Q, et al. Impact of 3D printing technology on the comprehension of surgical liver anatomy. Surg Endosc. 2019;33(2):411–417. doi: 10.1007/s00464-018-6308-8. [DOI] [PubMed] [Google Scholar]
- 45.Chedid VG, Kamath AA, M Knudsen J, et al. Three-dimensional-printed liver model helps learners identify hepatic subsegments: a randomized-controlled cross-over trial. Am J Gastroenterol. 2020;115(11):1906–1910. doi: 10.14309/ajg.0000000000000958. [DOI] [PubMed] [Google Scholar]
- 46.Bati AH, Guler E, Ozer MA, et al. Surgical planning with patient-specific three-dimensional printed pancreaticobiliary disease models – Cross-sectional study. Int J Surg. 2020;80:175–183. doi: 10.1016/j.ijsu.2020.06.017. [DOI] [PubMed] [Google Scholar]
- 47.Huettl F, Saalfeld P, Hansen C, et al. Virtual reality and 3D printing improve preoperative visualization of 3D liver reconstructions-results from a preclinical comparison of presentation modalities and user’s preference. Ann Transl Med. 2021;9(13):1074–1074. doi: 10.21037/atm-21-512. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 48.Yu H, Yu T, Wang J, et al. Validation of a three-dimensional printed dry lab pancreaticojejunostomy model in surgical assessment: a cross-sectional study. BMJ Open. 2022;12(2):e052295. doi: 10.1136/bmjopen-2021-052295. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 49.Xia J, Mao J, Chen H, et al. Development and evaluation of a portable and soft 3D-printed cast for laparoscopic choledochojejunostomy model in surgical training. BMC Med Educ. 2023;23(1):77. doi: 10.1186/s12909-023-04055-0. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 50.Shen J, Chen M, Jin R, et al. A study of simulation training in laparoscopic bilioenteric anastomosis on a 3D-printed dry lab model. Surg Endosc. 2023;37(1):337–346. doi: 10.1007/s00464-022-09465-7. [DOI] [PubMed] [Google Scholar]
- 51.Gu J, Cao J, Cao W, et al. Optimized reusable modular 3D-printed models of choledochal cyst to simulate laparoscopic and robotic bilioenteric anastomosis. Sci Rep. 2024;14(1):8807. doi: 10.1038/s41598-024-59351-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 52.Lopez-Lopez V, Robles-Campos R, García-Calderon D, et al. Applicability of 3D-printed models in hepatobiliary surgey: results from “LIV3DPRINT” multicenter study. HPB (Oxford). 2021;23(5):675–684. doi: 10.1016/j.hpb.2020.09.020. [DOI] [PubMed] [Google Scholar]
- 53.Bao G, Yang P, Yi J, et al. Full-sized realistic 3D printed models of liver and tumour anatomy: a useful tool for the clinical medicine education of beginning trainees. BMC Med Educ. 2023;23(1):574. doi: 10.1186/s12909-023-04535-3. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 54.Song C, Min JH, Jeong WK, et al. Use of individualized 3D-printed models of pancreatic cancer to improve surgeons’ anatomic understanding and surgical planning. Eur Radiol. 2023;Published online May33(11):7646–7655. doi: 10.1007/s00330-023-09756-0. [DOI] [PubMed] [Google Scholar]
- 55.Fechner C, Reyes Del Castillo T, Roos JE, et al. 3D printed percutaneous transhepatic cholangiography and drainage (PTCD) simulator for interventional radiology. Cardiovasc Intervent Radiol. 2023;46(4):500–507. doi: 10.1007/s00270-022-03347-0. [DOI] [PubMed] [Google Scholar]
- 56.Shahbaz M, Miao H, Farhaj Z, et al. Mixed reality navigation training system for liver surgery based on a high-definition human cross-sectional anatomy data set. Cancer Med. 2023;12(7):7992–8004. doi: 10.1002/cam4.5583. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 57.Dhir V, Itoi T, Fockens P, et al. Novel ex vivo model for hands-on teaching of and training in EUS-guided biliary drainage: creation of “Mumbai EUS” stereolithography/3D printing bile duct prototype (with videos). Gastrointest Endosc. 2015;81(2):440–446. doi: 10.1016/j.gie.2014.09.011. [DOI] [PubMed] [Google Scholar]
- 58.Holt BA, Hearn G, Hawes R, et al. Development and evaluation of a 3D printed endoscopic ampullectomy training model (with video). Gastrointest Endosc. 2015;81(6):1470–1475.e5. doi: 10.1016/j.gie.2015.03.1916. [DOI] [PubMed] [Google Scholar]
- 59.Burdall OC, Makin E, Davenport M, et al. 3D printing to simulate laparoscopic choledochal surgery. J Pediatr Surg. 2016;51(5):828–831. doi: 10.1016/j.jpedsurg.2016.02.093. [DOI] [PubMed] [Google Scholar]
- 60.Wang W, Wang Z, Gong H, et al. 5G-assisted remote guidance in laparoscopic simulation training based on 3D printed dry lab models. Indian J Surg. 2022;24(10):1–5. doi: 10.1007/s12262-022-03590-2. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 61.Micallef J, Sivanathan M, Clarke KM, et al. Development and initial assessment of a novel and customized bile duct simulator for handsewn anastomosis training. Cureus. 2022;14(11):e31749. doi: 10.7759/cureus.31749. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 62.Lu Y, Chen X, Han F, et al. 3D printing of self-healing personalized liver models for surgical training and preoperative planning. Nat Commun. 2023;14(1):8447. doi: 10.1038/s41467-023-44324-6. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 63.Elisei RC, Graur F, Melzer A, et al. Liver phantoms cast in 3D-printed mold for image-guided procedures. Diagnostics (Basel). 2024;14(14):1521. doi: 10.3390/diagnostics14141521. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 64.Aranovich D, Goldman YF, Tchernin N, et al. Specialized educational program for high-grade liver injury management: a three-dimensional printed model approach. Surg Today. 2025. 55(2):283–287. doi: 10.1007/s00595-024-02911-0. [DOI] [PubMed] [Google Scholar]
- 65.Cao W, Pan X, Jin L, et al. Construction of reusable fluorescent assembled 3D-printed hydrogen-based models to simulate minimally invasive resection of complex liver cancer. PLoS One. 2024;19(12):e0316199. doi: 10.1371/journal.pone.0316199. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 66.Wei F, Wang W, Gong H, et al. Reusable modular 3D-printed dry lab training models to simulate minimally invasive choledochojejunostomy. J Gastrointest Surg. 2021;25(7):1899–1901. doi: 10.1007/s11605-020-04888-w. [DOI] [PubMed] [Google Scholar]
- 67.Casas-Murillo C, Zuñiga-Ruiz A, Lopez-Barron RE, et al. 3D-printed anatomical models of the cystic duct and its variants, a low-cost solution for an in-house built simulator for laparoscopic surgery training. Surg Radiol Anat. 2021;43(4):537–544. doi: 10.1007/s00276-020-02631-3. [DOI] [PubMed] [Google Scholar]
- 68.Cheng J, Wang ZF, Yao WF, et al. Comparison of 3D printing model to 3D virtual reconstruction and 2D imaging for the clinical education of interns in hepatocellular carcinoma: a randomized controlled study. J Gastrointest Oncol. 2023;14(1):325–333. doi: 10.21037/jgo-23-28. [DOI] [PMC free article] [PubMed] [Google Scholar]
- 69.Li C, Zheng B, Yu Q, et al. Augmented reality and 3-dimensional printing technologies for guiding complex thoracoscopic surgery. Ann Thorac Surg. 2021;112(5):1624–1631. doi: 10.1016/j.athoracsur.2020.10.037. [DOI] [PubMed] [Google Scholar]
Associated Data
This section collects any data citations, data availability statements, or supplementary materials included in this article.
Supplementary Materials
Data Availability Statement
The data that support the findings of this study are available from the corresponding author, Jing Tian, upon reasonable request.


