Evidence map›Paper›PMID 27188874›Full record

ArticleStem cell research & therapy2016

Novel skin chamber for rat ischemic flap studies in regenerative wound repair.

Yuan-Yu Hsueh, Duo-Hsiang Wang, Tzu-Chieh Huang, Ya-Ju Chang, Wei-Chi Shao, Tai-Lan Tuan, Michael W Hughes, Chia-Ching Wu

Open access · goldAbstract read
In one paragraph

Article in Stem cell research & therapy, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 8 papers.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed
1.5field-weighted citation impact, top 17% of its field
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

8 citing papers in PubMed, 18 citations in OpenAlex.

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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

8 authors at 2 institutions in 1 country.

Yuan-Yu HsuehDivision of Plastic Surgery, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Duo-Hsiang WangDivision of Plastic Surgery, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Tzu-Chieh HuangDepartment of Cell Biology & Anatomy, National Cheng Kung University, Tainan, Taiwan.
Ya-Ju ChangDepartment of Cell Biology & Anatomy, National Cheng Kung University, Tainan, Taiwan.
Wei-Chi ShaoDepartment of Occupational Therapy, National Cheng Kung University, Tainan, Taiwan.
Tai-Lan TuanInternational Research Center for Wound Repair and Regeneration, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Michael W HughesInstitute of Clinical Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan.
Chia-Ching WuInstitute of Clinical Medicine, National Cheng Kung University Hospital, College of Medicine, National Cheng Kung University, Tainan, Taiwan. joshccwu@mail.ncku.edu.tw.
National Cheng Kung University · TWNational Cheng Kung University Hospital · TW

Funding

siRNA Inhibition of Keloid Fibrosis in Fibrin Matrix Skin Equivalent Mouse ModelsR01GM095821 · NIGMS · CHILDREN'S HOSPITAL OF LOS ANGELES · PI BENYA, PAUL DAVID, TUAN, TAI-LAN · 2012 to 2015
$1.2M
NIGMS NIH HHS R01 GM095821
6 · The paper itself

Abstract

backgroundIn plastic surgery, skin flap is an important approach to reconstructive wound repairs. The rat dorsal skin flap is a clinically relevant and popular animal model to investigate and evaluate flap survival and necrosis. Nonetheless, flap survival is often unstable with unpredictable outcomes, regardless of previous attempts at design modification. METHODS &

resultsIn the present study, we report a novel flap chamber that provides stable and reproducible outcomes by separating the dorsal skin flap from its surrounding skin by in situ immobilization. The flap chamber blocks circulation that disturbs flap ischemia from both basal and lateral sides of the flap tissue. Demarcation of skin necrosis is macroscopically evident on the flap and supported by distinct changes in histological architecture under microscopic examination. The utility of the novel skin flap chamber is further proven by applying it to the examination of flap survival in streptozotocin-induced diabetic rats with an increase in skin necrosis. The flap chamber also affords size modifications where a narrower flap chamber increases ischemia and provides manipulable therapeutic windows for studying cell therapies. Accordingly, intradermal injection of endothelial cells 3 days before flap ischemia significantly increases the survival of skin flaps.

conclusionsThe novel flap chamber not only may stabilize the skin flap and provide reproducible outcomes that overcome the shortfalls of the traditional ischemic flap but also may afford size modifications that support research designs and test therapeutic approaches to regenerative repair.

Indexed as

Wound HealingAnimalsBlood GlucoseDermatologic Surgical ProceduresDiabetes Mellitus, ExperimentalDisease Models, AnimalGraft SurvivalHumansHuman Umbilical Vein Endothelial CellsInjections, IntradermalMaleNecrosisRatsRats, Sprague-DawleyRegenerative MedicineReproducibility of ResultsBlood GlucoseStreptozocinCell therapyDiabetesMcFarlane flapSkin flapSkin flap chamber

Identifiers

PMID27188874
PMCPMC4869367
OpenAlexW2404881923

What OpenQuestion holds

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LicenceCC BY
Read underepoch 390

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 OpenQuestion graph.