Evidence map›Paper›PMID 35382131›Full record

ReviewJournal of clinical and translational research2022

Human stem cells prevent flap necrosis in preclinical animal models: A systematic review.

Francisco R Avila, Ricardo A Torres-Guzman, María T Huayllani, Gunel Guliyeva, Abba C Zubair, Alfredo Quiñones-Hinojosa, Antonio J Forte, Rachel Sarabia-Estrada

Open access · diamondAbstract readReview
In one paragraph

Review in Journal of clinical and translational research, 2022. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
0.6field-weighted citation impact, top 32% 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

4 citing papers in PubMed, 4 citations in OpenAlex.

  1. Article
  2. Article
  3. Article
  4. Review
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 3 institutions in 1 country.

Francisco R AvilaDivision of Plastic Surgery, Mayo Clinic, Jacksonville, Florida, United States.
Ricardo A Torres-GuzmanDivision of Plastic Surgery, Mayo Clinic, Jacksonville, Florida, United States.
María T HuayllaniDivision of Plastic Surgery, Mayo Clinic, Jacksonville, Florida, United States.
Gunel GuliyevaDivision of Plastic Surgery, Mayo Clinic, Jacksonville, Florida, United States.
Abba C ZubairDepartment of Laboratory Medicine and Pathology, Mayo Clinic, Jacksonville, Florida, United States.
Alfredo Quiñones-HinojosaDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, United States.
Antonio J ForteDivision of Plastic Surgery, Mayo Clinic, Jacksonville, Florida, United States.
Rachel Sarabia-EstradaDepartment of Neurosurgery, Mayo Clinic, Jacksonville, Florida, United States.
WinnMed · USJacksonville College · USMayo Clinic in Florida · US

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background and Aim: Adipose-derived mesenchymal stem cells (ADSCs) have been proven effective to prevent distal skin flap necrosis in preclinical models. However, to appropriately translate these findings to clinical trials, the effect of ADSC of human origin (hADSC) needs to be evaluated. We hypothesize that hADSC treatment is as effective as animal ADSC treatment at preventing distal skin flap necrosis in animal flap models. Methods: Three databases were inquired on August 17, 2020, to evaluate the necrotic flap area after using hADSCs in animal models of ischemic flaps. No publication status or dates were considered. Studies were included if they used hADSCs, measured the surviving or necrotic skin area of flaps, used animal models, and were in English. Studies were excluded if they did not use cells of human origin. The flap survival or necrotic area, perfusion, capillary density, vascular endothelial growth factor secretion and HIF-1α expression were extracted. Results: Ten studies met inclusion criteria. The mean absolute risk reduction (ARR) in necrotic skin area was 22.37% (95% confidence interval [CI] 16.98-27.76%, Conclusion: Human ADSCs prevent skin flap necrosis to the same degree as animal ADSCs in rodent and rabbit flap models. Relevance for Patients: This review found that adipose-derived stem cells of human origin are equally effective at reducing the risk of surgical flap necrosis in preclinical models of small animals as autologous animal cells. The findings in this review should encourage researchers to use human adipose-derived stem cells in animal models of ischemic flaps to accelerate their translation into clinical trials and, eventually, surgical practice. The low immunogenicity of these cells should be leveraged to gain insight into the effects of the products that will be ultimately administered to patients. Furthermore, human adipose-derived stem cells' pro-angiogenic mechanism of action sets this therapy as a promising preventive measure for flap necrosis.

Indexed as

adipose-derived stem cellsanimal modelscell- and tissue-based therapynecrosissurgical flap

Identifiers

PMID35382131
PMCPMC8977210
OpenAlexW4214726543

What OpenQuestion holds

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Registered trials

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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.