# The scientific basis of vascularized bone grafts: Models and perfusion assessments, a systematic review

**Authors:** Marcus Wölffer, Radu Olariu, Alex Woollard, Cédric Zubler

PMC · DOI: 10.1016/j.jpra.2026.01.034 · JPRAS Open · 2026-01-30

## TL;DR

This systematic review explores perfusion assessment techniques for vascularized bone grafts in animal and cadaver models to better understand their viability and effectiveness.

## Contribution

The paper systematically evaluates perfusion assessment methods for vascularized bone grafts and highlights the need for multimodal approaches and standardized research protocols.

## Key findings

- Several perfusion assessment techniques like histology, CT, MRI, and scintigraphy were reviewed for their use in vascularized bone graft studies.
- NIRFI is accurate intraoperatively but limited postoperatively, while scintigraphy and MRI have high false-positive rates.
- A multimodal approach is recommended for reliable perfusion assessment in vascularized bone graft research.

## Abstract

Vascularized bone grafts (VBGs) are assumed to have advantages over non-VBGs, including preservation of cell viability and accelerated osteogenesis. Indications include the reconstruction of large bone defects, poor vascularity and previous radiation. However, clinical evidence supporting their superiority is limited. A return to the basic science of animal and cadaver models seems appropriate. This systematic review focuses on perfusion assessment in studies on VBGs. Only by understanding the vascular anatomy and ensuring bone perfusion is truly maintained in VBGs, can we expect to find differences to non-VBGs in subsequent experiments.

A systematic review was performed according to the PRISMA checklist. In February 2025, MEDLINE via PubMed, Embase, and the Cochrane Library databases were systematically searched for studies presenting animal or cadaver anatomical models of VBGs. Exclusion criteria were: language other than English, missing full-text publication, systematic reviews, prefabrication and tissue engineering, anatomical descriptions of bone grafts without perfusion assessments. Inclusion criteria were: original research on VBGs in animals or cadavers assessed by contrast agents, bone graft perfusion models. Out of 520 initially identified publications, 25 studies were included. Disagreements on the eligibility of articles were resolved by discussion with a senior author.

Pedicled and free VBGs from various anatomical sites were examined, covering indications, contraindications, benefits, and limitations. Several perfusion assessment techniques were employed, including histology, CT, MRI, technetium-based scintigraphy, near-infrared fluorescence imaging (NIRFI), angiography, radioactive microspheres, and fluorochrome bone labeling (FBL). Histology helps confirm viable osteocytes, while FBL and conventional as well as CT-angiography provide insight into vascular integrity. Meanwhile, scintigraphy and MRI offer indirect perfusion markers but demonstrate high false-positive rates. NIRFI seems accurate intraoperatively but is of limited use postoperatively. Advantages and disadvantages of each method are explored.

Reliable perfusion assessment is crucial in research on VBGs and requires a multimodal approach. Future research should standardize models and timing of perfusion assessment while accounting for confounding factors such as spontaneous neoangiogenesis and considering pitfalls of each modality.

## Full-text entities

- **Diseases:** oncologic (MESH:D000072716), necrosis (MESH:D009336), osteomyelitis (MESH:D010019), creep (MESH:D007815), hypertrophy (MESH:D006984), infection (MESH:D007239), VBGs (MESH:D006083), bone defects (MESH:D001847), vein thrombosis (MESH:D012170), osteoid (MESH:D010017), ischemia (MESH:D007511), CLSM (MESH:D004401), ischemic (MESH:D002545), avascular necrosis (MESH:D010020), osteoradionecrosis (MESH:D010025), fibrosis (MESH:D005355), trauma (MESH:D014947), inflammation (MESH:D007249), fractures (MESH:D050723)
- **Chemicals:** calcium (MESH:D002118), Gadolinium (MESH:D005682), ICG (MESH:D007208), Cerium-141 (MESH:C000615004), 1,2-dihydroxyanthracinon-e-methylene-iminodiacetic acid (-), Microfil (MESH:D012826), tetracycline (MESH:D013752), xylenol orange (MESH:C016833), Ce (MESH:D002563), Oxytetracycline (MESH:D010118), methylene blue (MESH:D008751), polymethyl methacrylate (MESH:D019904), Tetracyclines (MESH:D013754), Latex (MESH:D007840), alizarin complexone (MESH:C070804), cyanoacrylate (MESH:D003487), DCAF (MESH:C039244), barium sulfate (MESH:D001466), Tc (MESH:D013667)
- **Species:** Homo sapiens (human, species) [taxon 9606], Canis lupus familiaris (dog, subspecies) [taxon 9615]

## Full text

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## Figures

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12926591/full.md

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Source: https://tomesphere.com/paper/PMC12926591