Evidence map›Paper›PMID 26967919›Full record

ArticleJournal of visualized experiments : JoVE2016

Heterotopic Renal Autotransplantation in a Porcine Model: A Step-by-Step Protocol.

J Moritz Kaths, Juan Echeverri, Nicolas Goldaracena, Kristine S Louis, Paul Yip, Rohan John, Istvan Mucsi, Anand Ghanekar, Darius Bagli, Markus Selzner and 1 more

Open access · greenAbstract readVideo-Audio Media
In one paragraph

Article in Journal of visualized experiments : JoVE, 2016. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 12 papers.

0numbers the graph read from it
0cells of the map it votes in
12citing papers in PubMed
2.4field-weighted citation impact, top 11% 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

12 citing papers in PubMed, 24 citations in OpenAlex.

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  7. Normothermic ex situ pancreas perfusion for the preservation of porcine pancreas grafts.American journal of transplantation : official journal of the American Society of Transplantation and the American Society of Transplant Surgeons · 2022
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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

11 authors at 2 institutions in 2 countries.

J Moritz KathsMulti Organ Transplant Program, Department of Surgery, Toronto General Hospital; Division of Nephrology, The Hospital for Sick Children; moritz.kaths@gmail.com.
Juan EcheverriMulti Organ Transplant Program, Department of Surgery, Toronto General Hospital; Programa de Doctorat en Medicina, La Universitat Autónoma de Barcelona.
Nicolas GoldaracenaMulti Organ Transplant Program, Department of Surgery, Toronto General Hospital.
Kristine S LouisMulti Organ Transplant Program, Department of Surgery, Toronto General Hospital.
Paul YipLaboratory Medicine and Pathobiology, Toronto General Hospital.
Rohan JohnLaboratory Medicine and Pathobiology, Toronto General Hospital.
Istvan MucsiDepartment of Medicine, Toronto General Hospital.
Anand GhanekarMulti Organ Transplant Program, Department of Surgery, Toronto General Hospital.
Darius BagliDepartments of Surgery (Urology) & Physiology, Developmental & Stem Cell Biology, The Hospital for Sick Children.
Markus SelznerMulti Organ Transplant Program, Department of Surgery, Toronto General Hospital.
Lisa A RobinsonDivision of Nephrology, The Hospital for Sick Children.
Toronto General Hospital · CAHospital for Sick Children · CA

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Kidney transplantation is the treatment of choice for patients suffering from end-stage renal disease. It offers better life expectancy and higher quality of life when compared to dialysis. Although the last few decades have seen major improvements in patient outcomes following kidney transplantation, the increasing shortage of available organs represents a severe problem worldwide. To expand the donor pool, marginal kidney grafts recovered from extended criteria donors (ECD) or donated after circulatory death (DCD) are now accepted for transplantation. To further improve the postoperative outcome of these marginal grafts, research must focus on new therapeutic approaches such as alternative preservation techniques, immunomodulation, gene transfer, and stem cell administration. Experimental studies in animal models are the final step before newly developed techniques can be translated into clinical practice. Porcine kidney transplantation is an excellent model of human transplantation and allows investigation of novel approaches. The major advantage of the porcine model is its anatomical and physiological similarity to the human body, which facilitates the rapid translation of new findings to clinical trials. This article offers a surgical step-by-step protocol for an autotransplantation model and highlights key factors to ensure experimental success. Adequate pre- and postoperative housing, attentive anesthesia, and consistent surgical techniques result in favorable postoperative outcomes. Resection of the contralateral native kidney provides the opportunity to assess post-transplant graft function. The placement of venous and urinary catheters and the use of metabolic cages allow further detailed evaluation. For long-term follow-up studies and investigation of alternative graft preservation techniques, autotransplantation models are superior to allotransplantation models, as they avoid the confounding bias posed by rejection and immunosuppressive medication.

Indexed as

Tissue DonorsAnimalsDisease Models, AnimalKidney Failure, ChronicKidney TransplantationMaleSwineTransplantation, Autologous

Identifiers

PMID26967919
PMCPMC4828178
OpenAlexW2280832603

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.