# Patient-Specific Lattice Implants for Segmental Femoral and Tibial Reconstruction (Part 2): CT-Based Personalization, Design Workflows and Validation—A Review

**Authors:** Mansoureh Rezapourian, Anooshe Sadat Mirhakimi, Tatevik Minasyan, Mahan Nematollahi, Irina Hussainova

PMC · DOI: 10.3390/biomimetics11020145 · Biomimetics · 2026-02-13

## TL;DR

This review outlines how CT scans are used to design and validate patient-specific lattice implants for femoral and tibial bone defects, highlighting current methods and gaps.

## Contribution

The paper introduces a structured workflow for CT-based implant design and identifies key gaps in current methodologies for patient-specific lattice implants.

## Key findings

- Current methods for transforming CT data into lattice implants involve imaging pipelines and material-specific fabrication techniques.
- Studies are categorized into simulation, mechanical, biological, and validation pathways to assess implant performance.
- Common gaps include insufficient reporting of imaging details and limited clinical data on fatigue and remodeling.

## Abstract

Patient-specific lattice implants (PSLIs) and modular porous scaffolds have emerged as promising solutions for treating diaphyseal segmental defects of the femur and tibia, particularly where conventional reconstruction methods fall short. This second part of our two-part review focuses on how current studies transform computed tomography (CT) and μCT datasets into architected lattice implants, as well as how these constructs are fabricated and numerically, mechanically, biologically, and clinically verified. We outline imaging pipelines, including Digital Imaging and Communications in Medicine (DICOM) acquisition, segmentation, contralateral mirroring, and Hounsfield Units (HU)–density–elasticity mapping, and show how these choices impact finite element (FE) models and print-ready geometries. Next, lattice design strategies and mixed-material concepts are compared and linked to specific additive manufacturing routes in metals, polymers, and bioceramics, such as laser powder bed fusion (LPBF), electron beam melting (EBM), fused deposition modeling (FDM), material jetting, and extrusion-based bioprinting. Methodological overviews of linear–elastic models and homogenized finite element (FE) models, along with bench-top mechanical tests, in vitro cell assays, in vivo animal studies, and early clinical series, are utilized to categorize the studies into four pathways: simulation (S), mechanical (E_mech), biological (E_bio), and validation (V). Based on the reviewed literature, we establish a general workflow for CT implants. We identify common gaps in the process, observe insufficient reporting of imaging and modeling details, note a lack of data on fatigue and remodeling, and recognize the limited size of clinical cohorts. Additionally, we provide practical recommendations for developing more standardized and scalable planning pipelines. Part 1 of this two-part review studied defect patterns, anatomical location, and fixation strategies for patient-specific lattice implants used in femoral and tibial segmental reconstruction, with emphasis on how defect morphology and subregional anatomy influence construct selection and mechanical behavior. It established a defect- and fixation-centered review that provides the clinical and anatomical context for the workflow and validation analysis presented in Part 2.

## Full-text entities

- **Genes:** RUNX2 (RUNX family transcription factor 2) [NCBI Gene 860] {aka AML3, CBF-alpha-1, CBFA1, CCD, CCD1, CLCD}, ALPP (alkaline phosphatase, placental) [NCBI Gene 250] {aka ALP, PALP, PLAP, PLAP-1}, BMP2 (bone morphogenetic protein 2) [NCBI Gene 650] {aka BDA2, BMP2A, SSFSC, SSFSC1}, TGFB1 (transforming growth factor beta 1) [NCBI Gene 7040] {aka CAEND1, CED, DPD1, IBDIMDE, LAP, TGF-beta1}, BGLAP (bone gamma-carboxyglutamate protein) [NCBI Gene 632] {aka BGP, OC, OCN}, BMP1 (bone morphogenetic protein 1) [NCBI Gene 649] {aka OI13, PCOLC, PCP, TLD}
- **Diseases:** tumor (MESH:D009369), osteoporotic (MESH:D058866), femur (MESH:D000092524), defect (MESH:D000013), injury to (MESH:D014947), tibia (MESH:C535563), Fatigue (MESH:D005221), long-bone defect (MESH:D050398), Infection (MESH:D007239), femoral and tibial defects (MESH:D013978), bone (MESH:D001847), aseptic loosening (MESH:D011475), diaphyseal femoral segmental defect (MESH:C537538), femoral and (MESH:D005266), nonunion (MESH:C538144), PSLIs (MESH:D057873)
- **Chemicals:** PEEK (MESH:C063834), polymer (MESH:D011108), metal (MESH:D008670), ATS (MESH:D001246), yttrium aluminum garnet (MESH:C503779), Ti (MESH:D014025), beta-glycerophosphate (MESH:C031463), HA (MESH:D017886), Ti6Al4V (MESH:C031462), ABS (-), As (MESH:D001151), CPP (MESH:C014896), ARS (MESH:D001128), alizarin red S (MESH:C004468), TCP (MESH:C049563), calcium pyrophosphate (MESH:D002131), PLA (MESH:C033616)
- **Species:** Sus scrofa (pig, species) [taxon 9823], Ovis aries (domestic sheep, species) [taxon 9940], Rattus norvegicus (brown rat, species) [taxon 10116], Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12938023/full.md

## References

79 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938023/full.md

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Source: https://tomesphere.com/paper/PMC12938023