US2017258074A1PendingUtilityA1
Repaired organ and method for making the same
Est. expiryJun 22, 2031(~4.9 yrs left)· nominal 20-yr term from priority
A01N 1/0247A01N 1/021A01N 1/0226A01N 1/0215A01N 1/143A01N 1/126A01N 1/124A01N 1/122
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Claims
Abstract
A repaired ex vivo organ suitable for transplantation in a human, said repaired ex vivo organ having undergone ex vivo organ perfusion for a maintenance period, wherein said organ had been assessed as being unsuitable for transplantation into a human before the maintenance period and was determined to be suitable for transplantation after the maintenance period.
Claims
exact text as granted — not AI-modified1 - 16 . (canceled)
17 . A method of improving an ex vivo organ, said method comprising the steps of:
(i) determining the status of the organ by evaluating pre-selected criteria; (ii) subjecting the organ to an acellular perfusate at normothermic temperatures for a maintenance period; and (iii) determining improvement of the organ by re-evaluating the pre-selected criteria.
18 . The method according to claim 17 , wherein the organ is a lung, liver, heart, kidney, or pancreas.
19 . The method according to claim 17 , wherein the ex vivo organ is a lung and the pre-selected criteria include the ratio of partial pressure of arterial oxygen to the fraction of inspired oxygen.
20 . The method according to claim 19 , where the pre-selected criteria shows an improvement of at least 10%, at least 20%, or at least 40% between steps (i) and (iii).
21 . A method of repairing a donor organ so that the donor organ is suitable for transplantation into a human, said method comprising the steps of
(i) determining the status of the organ by evaluating pre-selected criteria; (ii) subjecting the organ to an acellular perfusate at normothermic temperatures for a maintenance period; and (iii) determining repair of the perfused organ by re-evaluating the pre-selected criteria.
22 . The method according to claim 21 , wherein the maintenance period is within the range of 1 to 10 hours, 1 to 7 hours, or 1 to 3 hours.
23 . The method according to claim 21 , the steps (i) and (ii) are performed concurrently.
24 . The method according to claim 21 , further comprising a step of treating the organ with a suitable medical treatment for a treatment period after step (ii).
25 . The method according to claim 24 , wherein the suitable medical treatment is one or more of antibiotics, hyperperfusion techniques, beta-agonists, anti-inflammatory agents, flow techniques, gene therapy, stem cell treatments, and anti-coagulants.
26 . The method according to claim 24 , wherein the treatment period is within the range of 1 to 10 hours, 1 to 7 hours, or 1 to 3 hours.
27 . The method according to claim 21 , wherein the organ is a lung, liver, heart, kidney, or pancreas.
28 . The method according to claim 27 , wherein the organ is a lung.
29 . The method according to claim 28 , wherein the lung is a donation after cardiocirculatory death (DCD) lung.
30 . The method according to claim 28 , wherein the acellular perfusate replaces substantially all blood in the lung.
31 . A method of conditioning an ex vivo donation after cardiocirculatory death (DCD) lung for transplantation into a human, the method comprising subjecting the DCD lung to ex vivo perfusion with an acellular perfusate at normothermic temperatures for a maintenance period, thereby conditioning the DCD lung such that it is suitable for transplantation into a human.
32 . The method according to claim 31 , further comprising determining suitability for transplantation into a human of the perfused lung by evaluating pre-selected criteria.
33 . The method according to claim 32 , wherein the pre-selected criteria include an atrial pressure in the left atrium in a range of 3 mmHg to 5 mmHg
34 . The method according to claim 31 , further comprising treating the organ with a suitable medical treatment for a treatment period.
35 . The method according to claim 34 , wherein the suitable medical treatment is one or more of antibiotics, hyperperfusion techniques, beta-agonists, anti-inflammatory agents, flow techniques, gene therapy, stem cell treatments, and anti-coagulants.
36 . The method according to claim 31 , wherein the DCD lung is a Maastricht category III or IV lung.Cited by (0)
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