Evidence map›Paper›PMID 41141702›Full record

ArticleFrontiers in surgery2025

Surgical repair of acute Achilles tendon rupture with and without human amniotic membrane augmentation: a retrospective comparative study.

Ju Chun Chien, Meng Chen Kuo, Yi Jiun Chou, Yi Ping Wei

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Article in Frontiers in surgery, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

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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

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3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

4 authors.

Ju Chun Chien *Department of Radiation Oncology, Kaohsiung Veteran General Hospital, Kaohsiung, Taiwan.
Meng Chen Kuo *Department of Orthopedics, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Yi Jiun ChouDepartment of Orthopedics, Kaohsiung Veterans General Hospital, Kaohsiung, Taiwan.
Yi Ping WeiOffice of R&D with International Affairs, Tajen University, Pingtung City, Taiwan.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Objectives: Achilles tendon ruptures are common, particularly in active individuals; however, optimal healing remains challenging due to limited vascularity, adhesions, and re-rupture risk. Human amniotic membrane (hAM), rich in extracellular matrix and bioactive factors, shows regenerative potential, offering a promising adjunct for tendon repair. Methods: After institutional review board approval, patients aged 20-75 years who underwent end-to-end Achilles tendon repair for acute complete rupture between February 2019 and January 2025 were retrospectively reviewed. Patients were grouped by intraoperative use of hAM allografts. Baseline characteristics, rupture location, operative time, complications (tendon re-rupture, wound infection, dehiscence), American Orthopaedic Foot and Ankle Society (AOFAS) Ankle-Hindfoot score, and follow-up duration were analyzed using Results: In total, 45 repairs were performed in 44 patients. Of these, 13 patients (13 feet) received hAM augmentation, while 31 patients (32 feet) underwent primary repair without hAM. The overall mean follow-up time for the entire cohort was 38.16 ± 21.13 months. Complications occurred in 11 of the 45 feet, including 1 wound dehiscence, 3 re-rupture (2 of which were associated with wound infection), and 7 additional cases of wound infection. Operative time was significantly shorter in the hAM group (94.00 ± 30.12 vs. 116.72 ± 24.46 min, Conclusions: The hAM augmentation reduced operative time without affecting complication rates or functional outcomes. Further prospective studies are needed to confirm its clinical benefits.Level of evidence: IV.

Indexed as

Achilles tendon ruptureamniotic membranebiological augmentationorthopedic surgeryregenerative medicinetendon healing

Identifiers

PMID41141702
PMCPMC12546032

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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 OpenQuestion graph.