TY - JOUR
T1 - Hypothermic machine perfusion can safely prolong cold ischemia time in deceased donor kidney transplantation. A retrospective analysis on postoperative morbidity and graft function
AU - Adani, Gian Luigi
AU - Pravisani, Riccardo
AU - Tulissi, Patrizia
AU - Isola, Miriam
AU - Calini, Giacomo
AU - Terrosu, Giovanni
AU - Boscutti, Giuliano
AU - Avital, Itzhak
AU - Ekser, Burcin
AU - Baccarani, Umberto
N1 - Publisher Copyright:
© 2020 International Center for Artificial Organs and Transplantation and Wiley Periodicals LLC.
PY - 2021/5/1
Y1 - 2021/5/1
N2 - In deceased donor kidney transplantation (KT), a prolonged cold ischemia time (CIT) is a negative prognostic factor for KT outcome, and the efficacy of hypothermic machine perfusion (HMP) in prolonging CIT without any additional hazard is highly debated. We conducted a retrospective study on a cohort of 154 single graft deceased donor KTs, in which a delayed HMP, after a preliminary period of static cold storage (SCS), was used to prolong CIT for logistic reasons. Primary outcomes were postoperative complications as well as 1 year graft survival and function. 73 cases (47.4%) were managed with HMP and planned KT, while 81 (52.6%) with SCS and urgent KT. The median CIT in HMP group and SCS group was 29 hour:57 minutes [27-31 hour:45 minutes] and 11 hour:25 minutes [9-14 hour:30 minutes], respectively (P <.001). The period of SCS in the HMP group was significantly shorter than in the SCS group (10 vs. 11 hour:25 minutes, P =.02) as well as the prevalence of expanded criteria donors was significantly higher (43.8% vs. 18.5%, P <.01). After propensity score matching for these two baseline characteristics, the HMP and SCS groups showed comparable outcomes in terms of delayed graft function, vascular, and urologic complications, infections, and episodes of graft rejection. At 1 year follow-up, serum creatinine levels were comparable between the groups. Therefore, the use of HMP to prolong the CIT and convert KT into a planned procedure seemed to have an adequate safety profile, with outcomes comparable to KT managed as an urgent procedure and a CIT nearly three time shorter.
AB - In deceased donor kidney transplantation (KT), a prolonged cold ischemia time (CIT) is a negative prognostic factor for KT outcome, and the efficacy of hypothermic machine perfusion (HMP) in prolonging CIT without any additional hazard is highly debated. We conducted a retrospective study on a cohort of 154 single graft deceased donor KTs, in which a delayed HMP, after a preliminary period of static cold storage (SCS), was used to prolong CIT for logistic reasons. Primary outcomes were postoperative complications as well as 1 year graft survival and function. 73 cases (47.4%) were managed with HMP and planned KT, while 81 (52.6%) with SCS and urgent KT. The median CIT in HMP group and SCS group was 29 hour:57 minutes [27-31 hour:45 minutes] and 11 hour:25 minutes [9-14 hour:30 minutes], respectively (P <.001). The period of SCS in the HMP group was significantly shorter than in the SCS group (10 vs. 11 hour:25 minutes, P =.02) as well as the prevalence of expanded criteria donors was significantly higher (43.8% vs. 18.5%, P <.01). After propensity score matching for these two baseline characteristics, the HMP and SCS groups showed comparable outcomes in terms of delayed graft function, vascular, and urologic complications, infections, and episodes of graft rejection. At 1 year follow-up, serum creatinine levels were comparable between the groups. Therefore, the use of HMP to prolong the CIT and convert KT into a planned procedure seemed to have an adequate safety profile, with outcomes comparable to KT managed as an urgent procedure and a CIT nearly three time shorter.
KW - cold ischemia time
KW - delayed graft function
KW - hypothermic machine perfusion
KW - kidney transplant morbidity
KW - kidney transplantation
UR - http://www.scopus.com/inward/record.url?scp=85099088267&partnerID=8YFLogxK
U2 - 10.1111/aor.13858
DO - 10.1111/aor.13858
M3 - Article
C2 - 33210745
AN - SCOPUS:85099088267
SN - 0160-564X
VL - 45
SP - 516
EP - 523
JO - Artificial Organs
JF - Artificial Organs
IS - 5
ER -