Evidence map›Paper›PMID 41816435›Full record

ArticleJournal of thoracic disease2026

3D-printing on human acellular dermis for chest wall reconstructions-an

Till Grandjean, Niklas Heumüller, Christian Galata, Alicia Emrich, Maximilian Martin, Nadine Wiesmann-Imilowski, Daniela Nickel, Erol Gercek, Philipp Drees, Eric Dominic Roessner and 1 more

Abstract read
In one paragraph

Article in Journal of thoracic disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

No citing paper in PubMed yet.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

11 authors.

Till GrandjeanDepartment of Orthopedics and Traumatology, BiomaTiCS, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
Niklas HeumüllerDepartment of Orthopedics and Traumatology, BiomaTiCS, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
Christian GalataDepartment of Thoracic Surgery, University Medical Center Mainz, Johannes Gutenberg University Mainz, Mainz, Germany.
Alicia EmrichDepartment of Orthopedics and Traumatology, BiomaTiCS, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
Maximilian MartinDepartment of Orthopedics and Traumatology, BiomaTiCS, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
Nadine Wiesmann-ImilowskiDepartment of Otorhinolaryngology, University Medical Center Mainz, Johannes Gutenberg University Mainz, Mainz, Germany.
Daniela NickelDuale Hochschule Sachsen - Staatliche Studienakademie Glauchau, University of Cooperative Education, Glauchau, Germany.
Erol GercekDepartment of Orthopedics and Traumatology, BiomaTiCS, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
Philipp DreesDepartment of Orthopedics and Traumatology, BiomaTiCS, University Medical Center, Johannes Gutenberg University, Mainz, Germany.
Eric Dominic Roessner *Department of Thoracic Surgery, University Medical Center Mainz, Johannes Gutenberg University Mainz, Mainz, Germany.
Ulrike Ritz *Department of Orthopedics and Traumatology, BiomaTiCS, University Medical Center, Johannes Gutenberg University, Mainz, Germany.ORCID https://orcid.org/0000-0001-8936-3227

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: Massive bone or tissue defects caused by trauma, tumors or infections are a frequently occurring clinical problem. Novel biomaterials combined with new technologies offer new treatment options especially regarding reconstruction of bone and tissue. Aim of this study was to establish the stable and biocompatible combination of decellularized human dermis with a stable polymer via three-dimensional (3D) printing. Methods: Polylactide (PLA) models were 3D-printed onto human acellular dermis (hAD) membranes using FreeCAD (computer-aided design) software for modeling and Ultimaker 2+ for printing. Cytotoxicity was assessed using L929 fibroblast cells in an 3-(4,5-dimethylthiazol-2-yl)-2,5-diphenyltetrazoliumbromid (MTT) assay analogue to DIN EN ISO 10993-5 guidelines. Laser microtome sectioning was performed to enable histological analysis involving hematoxylin-eosin (HE) staining for tissue morphology assessment. The chorioallantoic membrane (CAM) assay was conducted on fertilized chicken eggs to evaluate cytotoxic effects and vascular ingrowth, by microscopic imaging. Results: PLA was successfully 3D-printed onto hAD, forming a stable bond. After 72 hours of incubation in PBS, the printed structure remained securely attached. Histological analysis confirmed the integrity of the collagen structure after printing with high temperatures, with only slight compression in the top layer of the hAD. Cytotoxicity testing according to ISO 10993-5 showed no significant reduction in cell viability (83%), thereby demonstrating biocompatibility. The CAM assay demonstrated vascular integration, with vessels forming around and connecting to the hybrid material. Conclusions: The successful 3D printing of PLA onto hAD resulted in a stable hybrid material with preserved structural integrity and good fluid resistance. Histological and cytotoxicity analyses confirmed biocompatibility, while the CAM assay demonstrated vascular integration. These findings suggest that the hAD-PLA composite holds potential for biomedical applications, particularly in tissue engineering.

Indexed as

biocompatibilitychest wall reconstructionchorioallantoic membrane-assay (CAM-assay)human acellular dermis (hAD)Three-dimensional-printing (3D-printing)

Identifiers

PMID41816435
PMCPMC12972918

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
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Registered trials

None linked

Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the Socratic graph.