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Sökning: id:"swepub:oai:research.chalmers.se:7e271462-4683-4f1c-ab34-8719fda38581" > Long-term Transplan...

Long-term Transplant Function After Thrombolytic Treatment Ex Vivo of Donated Kidneys Retrieved 4 to 5 Hours After Circulatory Death

Olausson, Michael (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Antony, Deepti (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Johansson, Martin (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
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Travnikova, Galina (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Nayakawde, Nikhil (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Banerjee, Debashish (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Söfteland, John M (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Ognissanti, Damiano, 1990 (författare)
Chalmers tekniska högskola,Chalmers University of Technology
Andresen Bergstrom, Moa (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Hammarsten, Ola (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
Premaratne, Goditha U. (författare)
Sahlgrenska universitetssjukhuset,Sahlgrenska University Hospital
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 (creator_code:org_t)
2022
2022
Engelska.
Ingår i: Transplantation. - 0041-1337. ; 106:12, s. 2348-2359
  • Tidskriftsartikel (refereegranskat)
Abstract Ämnesord
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  • Background.  Using a novel thrombolytic technique, we present long-term transplant function, measured by creatinine and iohexol clearance, after utilizing kidneys from porcine donors with uncontrolled donation after circulatory deaths, with 4.5–5 h of warm ischemia. Methods.  Pigs in the study group were subjected to simulated circulatory death. After 2 h, ice slush was inserted into the abdomen and 4.5 h after death, the kidneys were retrieved. Lys-plasminogen, antithrombin-III, and alteplase were injected through the renal arteries on the back table. Subsequent ex vivo perfusion was continued for 3 h at 15°C, followed by 3 h with red blood cells at 32°C, and then transplanted into pigs as an autologous graft as only renal support. Living-donor recipient pigs that did not receive ex vivo perfusion, and unilateral nephrectomized pigs served as the controls. Results.  Pigs in the study group (n = 13), surviving 10 d or more were included, of which 7 survived for 3 mo. Four animals in the living-donor group (n = 6) and all 5 nephrectomized animals survived for 3 mo. Creatinine levels in the plasma and urine, neutrophil gelatinase-associated lipocalin levels, Kidney Injury Marker-1 expression, and iohexol clearance at 3 mo did not differ significantly between the study and living-donor groups. Histology and transmission electron microscopy after 3 mo showed negligible fibrosis and no other damage. Conclusions.  The present method salvages kidneys from extended unontrolled donation after circulatory death using thrombolytic treatment while preserving histology and enabling transplantation after ex vivo reconditioning, with clinically acceptable late function after 3 mo, as measured by creatinine and iohexol clearance.

Ämnesord

MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine (hsv//eng)
MEDICIN OCH HÄLSOVETENSKAP  -- Klinisk medicin -- Urologi och njurmedicin (hsv//swe)
MEDICAL AND HEALTH SCIENCES  -- Clinical Medicine -- Urology and Nephrology (hsv//eng)

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