TY - JOUR
T1 - Optimization of Donor-Recipient match and identification of the futile match cutoff. A national italian study on liver transplantation.
AU - Avolio, Alfonso Wolfango
AU - Agnes, Salvatore
AU - Lirosi, Maria Carmen
AU - Salizzoni, Mauro
AU - Pinna, Antonio Daniele
AU - Gridelli, Bruno
AU - De Carlis, Luciano
AU - Colledan, Michele
AU - Gerunda, Giorgio Enrico
AU - Valente, Umberto
AU - Rossi, Giorgio
AU - Ettorre, Giuseppe Maria
AU - Risaliti, Andrea
AU - Mazzaferro, Vincenzo
AU - Bresadola, Francesco
AU - Rossi, Massimo
AU - Tisone, Giuseppe
AU - Zamboni, Fausto
AU - Lupo, Luigi
AU - Cuomo, Oreste
AU - Calise, Fulvio
AU - Donataccio, Matteo
AU - Nicolotti, Nicola
AU - Vitale, Alessandro
AU - Romagnoli, Renato
AU - Lupo, Francesco
AU - Cucchetti, Alessandro
AU - Gruttadauria, Salvo
AU - Mangoni, Iacopo
AU - Pinelli, Domenico
AU - Montalti, Roberto
AU - Gelli, Massimiliano
AU - Caccamo, Lucio
AU - Vennarecci, Giovanni
AU - Nicolini, Daniele
AU - Regalia, Enzo
AU - Baccarani, Umberto
AU - Lai, Quirino
AU - Manzia, Tommaso
AU - Tondolo, Enzo
AU - Rendina, Maria
AU - Barone, Michele
AU - Perrella, Alessandro
AU - Romano, Maria
AU - De Waure, Chiara
AU - Burra, Patrizia
AU - Gasbarrini, Antonio
AU - Cillo, Umberto
PY - 2011
Y1 - 2011
N2 - Intentional matching of liver transplant donor-recipient risk factors,
supported by D-MELD (donor age × biochemical MELD), could offer
a new therapeutic strategy with effects on survival. As yet, an
extensive stratification of cases according to the futile transplant
principle using a continous quantitative parameter has not been
performed.
To stratify the prognosis according to donor-recipient match and
assess the predictive role of D-MELD together with covariates, a
database detailing 5946 liver transplants performed in 21 Italian
Centers (2002–2009) was analyzed. Primary endpoint was to
evaluate the prognostic power of D-MELD and covariates in terms of
3-year patient survival. The futile-transplant cutoff (life-expectancy
<50% at 5 years) was investigated. The database was divided into
a training and a validation set. The adequacy of fit for both sets
was tested using Hosmer-Lemeshow and C-statistics. Cases were
stratified in ten D-MELD deciles.
Significant differences among D-MELD deciles allowed regrouping
them in three D-MELD classes (A <338, B 338–1628, C >1628).
D-MELD classes were used for regression analyses. At 3 years, the
odds ratio (OR) for death is 2.03 (95% CI 1.44–2.85) in D-MELD
class C versus class B (reference). The OR is 0.40 (95% CI 0.24–
0.66) in D-MELD class A versus class B. Other significant covariates
were HCV status (OR = 1.42; 95% CI 1.11–1.81), HBV status (OR = 0.69;
95% CI 0.51–0.93), re-transplant status (OR = 1.82; 95% CI 1.16–
2.67) and low-volume transplant Center (OR = 1.48; 95% CI 1.11–
1.99). Results were confirmed by Cox regressions. The “futilematch
cutoff” was identified only in HCV patients (D-MELD=1750,
p < 0.001).Assuming the same high D-MELD value, an organ from an elderly
donor is likely to fail in an old recipient or in an HCV recipient
but not in an HBV recipient. The identification of predictive factors
(D-MELD class and covariates) and the introduction of the futile
cutoff may lead to formulate new organ-allocation policies. The
futile matches should be proibited by national allocation rules.
Fatal allocation of high-risk organs to high-risk patients should
be avoided. Organs from young donors should not be allocated to
recipients with a low biochemical MELD without additional risk
factors.
AB - Intentional matching of liver transplant donor-recipient risk factors,
supported by D-MELD (donor age × biochemical MELD), could offer
a new therapeutic strategy with effects on survival. As yet, an
extensive stratification of cases according to the futile transplant
principle using a continous quantitative parameter has not been
performed.
To stratify the prognosis according to donor-recipient match and
assess the predictive role of D-MELD together with covariates, a
database detailing 5946 liver transplants performed in 21 Italian
Centers (2002–2009) was analyzed. Primary endpoint was to
evaluate the prognostic power of D-MELD and covariates in terms of
3-year patient survival. The futile-transplant cutoff (life-expectancy
<50% at 5 years) was investigated. The database was divided into
a training and a validation set. The adequacy of fit for both sets
was tested using Hosmer-Lemeshow and C-statistics. Cases were
stratified in ten D-MELD deciles.
Significant differences among D-MELD deciles allowed regrouping
them in three D-MELD classes (A <338, B 338–1628, C >1628).
D-MELD classes were used for regression analyses. At 3 years, the
odds ratio (OR) for death is 2.03 (95% CI 1.44–2.85) in D-MELD
class C versus class B (reference). The OR is 0.40 (95% CI 0.24–
0.66) in D-MELD class A versus class B. Other significant covariates
were HCV status (OR = 1.42; 95% CI 1.11–1.81), HBV status (OR = 0.69;
95% CI 0.51–0.93), re-transplant status (OR = 1.82; 95% CI 1.16–
2.67) and low-volume transplant Center (OR = 1.48; 95% CI 1.11–
1.99). Results were confirmed by Cox regressions. The “futilematch
cutoff” was identified only in HCV patients (D-MELD=1750,
p < 0.001).Assuming the same high D-MELD value, an organ from an elderly
donor is likely to fail in an old recipient or in an HCV recipient
but not in an HBV recipient. The identification of predictive factors
(D-MELD class and covariates) and the introduction of the futile
cutoff may lead to formulate new organ-allocation policies. The
futile matches should be proibited by national allocation rules.
Fatal allocation of high-risk organs to high-risk patients should
be avoided. Organs from young donors should not be allocated to
recipients with a low biochemical MELD without additional risk
factors.
KW - D-MELD
KW - Donor recipient match
KW - Futile match
KW - HCV
KW - Liver Transplantation
KW - MELD
KW - outcome
KW - risk factors
KW - D-MELD
KW - Donor recipient match
KW - Futile match
KW - HCV
KW - Liver Transplantation
KW - MELD
KW - outcome
KW - risk factors
UR - http://hdl.handle.net/10807/18119
UR - http://www.jhep-elsevier.com/rss
M3 - Conference article
SN - 0168-8278
VL - 2011
SP - 17
EP - 17
JO - Journal of Hepatology
JF - Journal of Hepatology
T2 - The International Liver Congress TM 2011 by EASL
Y2 - 30 March 2011 through 3 April 2011
ER -