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New Insights on integer-programming models for the kidney exchange problem

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New Insights on integer-programming models for the kidney exchange problem

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© © All Rights Reserved
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European Journal of Operational Research 231 (2013) 57–68

Contents lists available at SciVerse ScienceDirect

European Journal of Operational Research


journal homepage: www.elsevier.com/locate/ejor

Discrete Optimization

New insights on integer-programming models for the kidney exchange


problem
Miguel Constantino b,⇑,1,2, Xenia Klimentova a,1, Ana Viana a,c,1, Abdur Rais d,1
a
INESC TEC (formerly INESC Porto), Campus da FEUP, Rua Dr. Roberto Frias, 378, 4200-465 Porto, Portugal
b
Centro de Investigação Operacional, Departamento de Estatística e Investigação Operacional, Faculdade de Ciências da Universidade de Lisboa, Campo Grande, 1749-016
Lisboa, Portugal
c
ISEP – School of Engineering, Polytechnic of Porto, Rua Dr. António Bernardino de Almeida, 431, 4200-072 Porto, Portugal
d
Centro Algoritmi, Universidade do Minho, Campus de Gualtar, 4710-057 Braga, Portugal

a r t i c l e i n f o a b s t r a c t

Article history: In recent years several countries have set up policies that allow exchange of kidneys between two or
Received 3 August 2012 more incompatible patient–donor pairs. These policies lead to what is commonly known as kidney
Accepted 15 May 2013 exchange programs.
Available online 30 May 2013
The underlying optimization problems can be formulated as integer programming models. Previously
proposed models for kidney exchange programs have exponential numbers of constraints or variables,
Keywords: which makes them fairly difficult to solve when the problem size is large. In this work we propose
Kidney exchange program
two compact formulations for the problem, explain how these formulations can be adapted to address
Integer programming
Combinatorial optimization
some problem variants, and provide results on the dominance of some models over others. Finally we
Healthcare present a systematic comparison between our models and two previously proposed ones via thorough
computational analysis. Results show that compact formulations have advantages over non-compact
ones when the problem size is large.
 2013 Elsevier B.V. All rights reserved.

1. Introduction physiologically compatible, then transplantation could not be


performed.
Kidney transplants are essential for the survival of many pa- In recent years kidney exchange programs brought new hope
tients suffering from kidney failure, but finding suitable kidneys for many kidney patients. These programs involve patient–donor
can be difficult because of their scarcity as well as blood or tissue pairs in which donors are incompatible with their recipients. The
incompatibility between donors and patients. For a long time, de- key aspect is to organize exchanges between a number of such
ceased donors were typically the most acceptable source of kid- pairs so that patient P in one pair receives a kidney from donor D
neys for transplantation. However, they only met a tiny fraction in the other pair. Fig. 1 (left) illustrates the simplest case with only
of the demand and alternative transplantation policies considering two pairs (P1, D1) and (P2, D2), where patient and donor in each pair
living donors progressively stepped forward. Within these policies, are incompatible (dotted lines represent incompatibilities). How-
if a patient had someone willing to donate a kidney and the pa- ever, P1 is compatible with D2 and P2 is compatible with D1. Previ-
tient–donor pair was compatible, then the transplant could be ously, when exchanges between pairs were not allowed, no
done. However, if a patient and the prospective donor were not transplants could be performed in this situation. Within the evolv-
ing frameworks of new programs, exchanges between such pairs
are allowed and the two transplants can be performed (arrows rep-
⇑ Corresponding author. Tel.: +351 214500402; fax: +351 217500022. resent the exchange in the figure).
E-mail addresses: [email protected] (M. Constantino), xenia.klimentova@i- Kidney exchange programs have already been introduced in
nescporto.pt (X. Klimentova), [email protected] (A. Viana), [email protected] many countries, including South Korea [20], Switzerland [37], Tur-
minho.pt (A. Rais).
1
key [15], Romania [21], The Netherlands [8,9,19], UK [7,17,23] and
This work is financed by the ERDF – European Regional Development Fund
through the COMPETE Programme (operational programm for competitiveness) and
the US [35,36,2,39]. Very recently, similar programs have also been
by National Funds through the FCT – Fundação para a Ciência e a Tecnologia set up in other countries: in 2010, Canada, Portugal, Australia, and
(Portuguese Foundation for Science and Technology) within project ‘‘KEP – New New Zealand kicked-off their own programs while Spain initiated
models for enhancing the kidney transplantation process./FCT ref: PTDC/EGE-GES/ its program in 2011.
110940/2009’’.
2 The objective for optimization in a kidney exchange program is
FCT – Fundação para a Ciência e a Tecnologia, under the project PEst-OE/MAT/
UI0152. generally to maximize the collective benefit for a given pool of

0377-2217/$ - see front matter  2013 Elsevier B.V. All rights reserved.
http://dx.doi.org/10.1016/j.ejor.2013.05.025
58 M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68

open: the cycle formulation presents an exponential number of


variables, while the edge formulation has an exponential number
of constraints.
This paper focuses on mathematical modeling aspects of the
KEP: we propose two new compact formulations for the problem.
Moreover we investigate the relationships between different for-
mulations and provide some proofs of dominance of one formula-
tion over the other in the sense of values of upper bounds for
optimal solutions obtained with the linear relaxations (LP relax-
ations) of each formulation. Finally, a systematic comparison of
these formulations with the two previously reported ones is pre-
Fig. 1. A 2-way exchange (left) and a 3-way exchange (right). sented by thorough computational analysis.
The paper is organized as follows. Following this introduction
incompatible pairs, usually measured by the number of possible we review in Section 2 relevant literature with respect to variants
kidney exchanges [36,8] — in the entirety of the paper we will refer of the KEP and solution methods. In Section 3 the problem state-
to this optimization problem as the Kidney Exchange Problem (KEP). ment and the known IP models are presented. The new compact
Although such an optimal solution is typically desirable, there are formulations for the KEP are introduced in Section 4. In Section 5
other factors which may also be considered in some situations; e.g. the adaptation of formulations for variants of the KEP is discussed.
maximize the weighted sum of kidney exchanges [23] and/or the The interrelations of upper bounds of linear relaxations for the pre-
quality-adjusted life expectancy of transplant candidates [42]. sented IP models are investigated in Section 6. Section 7 reports
One of the crucial questions for the KEP is the definition of a the computational analysis and conclusions on the effectiveness
bound on the number of pairs that can be involved in an exchange. of each formulation. Finally Section 8 provides conclusions and
When a kidney exchange involves only two donor–recipient pairs directions for future work.
as illustrated in Fig. 1 (left) it is commonly known as a 2-way or
2-cycle exchange. Basically this is an alternating directed cycle of
two donors and two recipients in which the donor from one incom- 2. Literature review
patible pair gives one kidney to the recipient in the other pair and
vice versa. One can note that the size of the exchange cycle can be The concept of kidney exchange program for incompatible pa-
increased. For example, the 3-way exchange presented in Fig. 1 tient–donor pairs was first promoted in 1986 in [27] as an alterna-
(right) allows three patients to get transplants instead of two; solid tive to deceased donor programs. Since then, several models for the
lines here represent compatibilities and arrows represent the ac- KEP have been proposed that differ mostly on type of exchanges al-
tual exchanges that derive maximum collective benefit. lowed, matching requirements and optimization objectives. For
Generally k-cycle exchanges with k P 3 can be better for opti- ethical issues concerning the programs, readers may see [30,31];
mization as they have the potential for increasing the options for an overview of contemporary ideas and challenges can be found
involving more incompatible pairs in an ‘‘exchange cycle’’. If there in [40,12]. In this section we survey KEP variants as well as optimi-
is no bound on the number of pairs in an exchange cycle, i.e., k is zation solution methods used to attack the problem.
not fixed, the problem turns into an assignment problem and can
be solved in polynomial time [2]. Ideally all operations involved 2.1. Problem variants
in a cycle should be performed simultaneously so that donors re-
main committed when the incompatible partners receive other do- The basic variant of the KEP is a 2-exchange mechanism involv-
nors’ kidneys. Therefore for a solution to be practical and ing two patients in two distinct pairs such that each patient is
manageable, the length of the cycles should be restricted for at incompatible with the associated donor [22,18,36] (see Fig. 1
least two main reasons. First, the number of personnel and facili- (left)). The notion can be generalized to a k-exchange (k P 3) in
ties needed for simultaneous operations of donors and patients which up to k pairs can be involved in the exchange cycle [8,2,7].
raise several logistic issues that can make it prohibitively inconve- Variants of the k-exchange problem can include altruistic donors;
nient to handle too many operations simultaneously [2]. Second, i.e., donors that are not associated to any patient, but willing to do-
because last-minute tests on donors and patients can bring out nate a kidney to someone in need. Non-directed (ND) exchanges oc-
new incompatibility issues that can cause a kidney donation and cur when an altruistic donor gives a kidney to a patient in a kidney
related exchanges in the cycle to be canceled, it is preferable for exchange program and the recipient’s donor is ‘‘dominoed’’ to the
the cycles to be shorter. next compatible patient on the deceased donor waiting list, or is
For a given pool of donor–recipient pairs, a 2-cycle exchange used to add another incompatible pair to the chain [25,13,32].
can be seen as a task of pairwise compatibility matching, and Ed- The maximum size of a chain is determined by national or regional
mond’s maximum cardinality matching algorithm [11] can provide programs.
an optimal solution in polynomial time. The problem with k-cycle Contrary to the above mentioned problems where simultaneity
exchange certainly is a generalized model and much more interest- of exchanges is considered, Non-simultaneous Extended Altruistic
ing for practical applications. However, the associated problem is Donor (NEAD) chains allow non-simultaneity of exchanges
known to be NP-complete for k P 3 and difficult to solve efficiently [10,28,4,12]. Unlike the conventional form of non-direct donation,
when a problem instance is large [2]. where the size of the chain is limited, the cascade in NEAD may
Current work on solving the KEP focuses mostly on Integer Pro- theoretically never end. The first donor who is incompatible, and
gramming (IP) formulations. Two IP models, referred to in this pa- whose related patient receives a kidney from the altruistic donor,
per as the ‘‘edge formulation’’ and the ‘‘cycle formulation’’, were gives his kidney to someone else with whom he is compatible.
proposed in [34]. Despite the very good results reported for the cy- The recipient’s incompatible donor can then do the same, and so
cle formulation in [2], the question of finding a compact formula- on. By not assigning a kidney to a patient in the deceased donor list
tion that has a number of variables and constraints bounded by a the cascading donor chain may continue indefinitely, unless a do-
polynomial in the size of the problem (i.e., on the total number nor whose related recipient has already been transplanted drops
of pairs in a donor–recipient pool), has, up until now, remained out of the program.
M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68 59

The inclusion of compatible pairs in kidney exchange programs Some results on the dynamic variant of KEP are reported in
defines one more variant of the KEP [14]. In this variant the com- [38,5,42]. In [38] the author study how exchanges should be con-
patible pair can be involved in an exchange only in the case that ducted through a centralized mechanism in a dynamically evolving
the patient of this pair benefits from being in the pool (e.g. receive agent pool with time and compatibility based preferences. They
a ‘‘better’’ kidney than he/she would have received from his/her derive dynamically efficient 2-way and multi-way exchange mech-
compatible donor). anisms that maximize total discounted exchange surplus. In [5],
Another variant is the multiple donors case, when one or more KEP is considered an online problem in which patient–donor pairs
patients have multiple donors associated. For such patients only and altruistic donors appear and expire over time. The authors
one of their multiple donors can be selected to create an exchange studied trajectory-based online stochastic optimization algorithms
cycle [2]. The donor selected is the one that would lead to maxi- for this problem. They identified tradeoffs between different
mum collective benefit. parameters and developed an experimental methodology for set-
All variants of KEP outlined above consider the problem as a sta- ting them. The work in [42] considers KEP as a dynamic resource
tic or offline problem. But the problem can also be dynamic (online) allocation problem with three objectives: maximize the quality-
when isolated patients, patient–donor pairs, and altruistic donors adjusted life expectancy of transplant candidates (clinical effi-
appear and expire over time [38,5,42,41,3]. ciency), and minimize two measures of inequity – the first measure
is a linear function of the likelihood of transplantation of the vari-
2.2. Solution methods ous types of patients and the second is a quadratic function that
quantifies the differences in mean waiting times across patient
The complexity of the k-exchange problem was investigated types. The dynamic status of patients is modeled by a set of linear
in [1,2,7]. In [1,2] it is shown that for a given graph G and differential equations.
k P 3 the problem of deciding if G admits a perfect cycle cover
containing cycles of length at most k is NP-complete. The proof 3. Problem definition and formulation
uses a reduction from the 3D–matching problem which is NP-
complete. In [7] the authors proved the APX-completeness of Graph theory can provide a natural framework for representing
the problem of finding a maximum size exchange involving only the KEP models. Let G(V, A) be a directed graph with the set of ver-
2- and 3-cycles. In other words they claim that the 3-exchange tices V = {1, . . . , jVj} consisting of all incompatible patient–donor
KEP do not admit any polynomial-time approximation scheme, pairs and the set of arcs A designating compatibilities between
unless P = NP. the vertices. Two vertices i, j 2 V are connected by arc (i, j) if the pa-
Edmonds’ algorithm [11] for maximum cardinality matching tient in pair j is compatible with the donor in pair i. To each arc is
was followed by [36] and [33] for the 2-exchange problem. When associated a weight wij, (i, j) 2 A. If the objective is to maximize the
k P 3 a natural and perspective way for attacking the KEP is total number of transplants wij = 1, "(i, j) 2 A.
through IP models. Two different integer programs were used in Fig. 2 illustrates an example where four incompatible pairs are
[2] and [34]: the edge and the cycle formulations. In [2] a sketch considered, the compatibility between pairs being represented by
of a proof is presented showing that the cycle formulation provides weighted arcs. An exchange is defined by a set of disjoint cycles
a better upper bound of the optimal solution with LP relaxation in the whole graph and it is feasible if every cycle length does
than the edge formulation. In the same work a cutting plane meth- not exceed a given limit k. In Fig. 2 for k = 3 the possible cycles
od was implemented for the edge formulation while a column gen- are 1–2–3–1 and 3–4–3. However these cycles are not vertex-dis-
eration method with branch-and-bound was designed for the cycle joint as they have vertex 3 in common.
formulation. The cycle formulation is used in [23] to solve the KEP If only 2-way exchanges can be considered, the maximum num-
in UK. The program in UK allows direct and altruistic exchanges ber of transplants in this pool will be two (between pairs 3 and 4).
and considers a set of criteria that should be pursued in a hierarchi- However, if up to three pairs can be involved in an exchange cycle
cal way. the optimal matching for this example will be three (donor 1 gives
Results related to the potential for developing NEAD strategy a kidney to patient 2, donor 2 to patient 3, and donor 3 to patient
were presented in [28]. In [13] the authors created a pool of incom- 1).
patible pairs based on the statistical data for blood-type, positive
cross-matching probabilities, and others, and looked for 2-ex- Definition 1. The Kidney Exchange Problem can be defined as
changes. They implemented Monte Carlo simulations and calcu- follows:
lated the maximum number of transplants under different Find a maximum weight set of vertex-disjoint cycles having length
scenarios when including ND donors and NEAD chains and con- at most k.
cluded that NEAD chains are not clearly superior in terms of the
number of transplants achieved. The authors of [4] presented some One of the most effective ways to deal with it is using Integer
simulations similar to [13], but allowing long chain segments. With Programming. Below we introduce the two formulations previ-
this additional flexibility they concluded that NEAD chains lead to ously proposed in the literature for this problem: the edge and cy-
more transplants. Some theoretical and computational analysis of cle formulations.
the efficacy of chains initiated by altruistic donation are provided
by [10].
The possibility of opening the pool of kidney exchange pro-
grams to compatible pairs has been addressed by, e.g. [29] and
[14]. A mixed pool of compatible and incompatible pairs was sim-
ulated in [14], the results show the benefits of such policy in terms
of the increase in probability of matching incompatible patients
that might otherwise not get a compatible donor. But the inclusion
of compatible pairs in a pool of incompatible pairs is a controver-
sial topic. Some of the ethical aspects associated with it are pointed
out in [29,32].
Fig. 2. KEP graph.
60 M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68

3.1. Edge formulation ‘‘compact’’ ones [26] but computationally the size of the problem
may become a bottleneck as solution procedures can take long
In the edge formulation, a variable xij is associated with each arc time for solving large problem instances.
(i, j) 2 A in the graph G(V, A), defined as follows: We present two new formulations for the problem: the edge-
 assignment formulation and the extended edge formulation. Each of
1 if patient of pair j gets a kidney from donor of pair i;
xij ¼ these formulations is compact, i.e., both the number of variables
0 otherwise: and constraints are bounded by a polynomial in the size of the
problem, given by the number of pairs. In the edge-assignment for-
The edge formulation is given by:
mulation the path constraints represented by (1d) are reformu-
X
Maximize wij xij ð1aÞ lated using additional assignment variables. In the extended edge
ði;jÞ2A formulation an extra index will be introduced in the variables xij
X X for allowing the cycle cardinality constraints to be created in a sim-
Subject to xji ¼ xij 8i 2 V ð1bÞ
j:ðj;iÞ2A j:ði;jÞ2A ple way. In the next couple of sections we present the IP models. A
X discussion on their downsizing into ‘‘reduced’’ formulations is also
xij 6 1 8i 2 V ð1cÞ
provided.
j:ði;jÞ2A
X
xip ipþ1 6 k  1 8paths ði1 ; i2 ; . . . ; ik ; ikþ1 Þ ð1dÞ 4.1. Edge-assignment formulation
16p6k

xij 2 f0; 1g 8ði; jÞ 2 A: ð1eÞ Let L be an upper bound on the number of cycles in any solution.
For instance, a simple upper bound is L = jVj as the number of cy-
The objective function (1a) maximizes the weighted sum of the
cles cannot exceed the number of vertices. Let each cycle in the
exchange – in the case of unitary weights, it corresponds to maxi-
solution be indexed by l, 1 6 l 6 L and denote by V(l) # V the set
mizing the total number of transplants. Constraints (1b) assure
of vertices in cycle l. Define the following assignment variables:
that patient i receives a kidney iff donor i donates a kidney. Con-

straints (1c) guarantee that a donor can only donate one kidney 1 if node i belongs to cycle l;
and constraints (1d) enforce the cycle-length: to exclude cycles lar-
yli ¼
0 otherwise:
ger than k, we need to make sure that every path of length k arcs
does not have more than k  1 arcs in a feasible exchange. This With these additional variables, we can write the cycle cardinal-
constraint requires all paths of length k to be considered explicitly ity constraints as:
X
in the model. In general the number of such paths can grow expo- yli 6 k 8l 2 1; . . . ; L: ð3aÞ
nentially with k. i

It is necessary now to ensure that each node i is properly as-


3.2. Cycle formulation
signed to a cycle l, and this is done using the following constraints:
X X
An alternative IP model for the edge formulation is the so called yli ¼ xij 8i 2 V ð4aÞ
cycle formulation. Let CðkÞ be the set of all cycles in G with length l j:ði;jÞ2A
at most k. We assume that a cycle is an ordered set of arcs. Define a yli þ xij 6 1 þ ylj 8ði; jÞ 2 A; 8l 2 1; . . . ; L ð4bÞ
variable zc for each cycle c 2 CðkÞ:
 yli 2 f0; 1g 8i 2 V; 8l 2 1; . . . ; L: ð4cÞ
1 if cycle c is selected for the exchange; P 
zc ¼ Constraints (4a) ensure that node i is in a cycle
0 otherwise: j:ði;jÞ2A xij ¼ 1
P l 
if and only if there is an assignment of i to some l y ¼ 1 . Con-
Denote by V(c) # V the set of vertices which belong to cycle c.  l l i
P straints (4b) state that if node i is in cycle l yi ¼ 1 and donor i
The model can be written as follows (where wc ¼ ði;jÞ2c wij ):
X gives a kidney to recipient j (xij = 1) then node j must also be in cy-
 
Maximize wc zc ð2aÞ cle l ylj ¼ 1 .
c2CðkÞ
X The edge-assignment formulation is composed of constraints
Subject to z c 6 1 8i 2 V ð2bÞ from the edge formulation – (1a), (1b), (1c) and (1e) – together
c:i2VðcÞ
with the constraints (3a), (4a), (4b) and (4c).
zc 2 f0; 1g 8c 2 CðkÞ: ð2cÞ For the formulation above, for a given index l, the set of nodes i
2 V(l) giving yli ¼ 1 could in fact belong to more than one vertex-
In the case of unitary weights, wc equals the number of edges in
disjoint simple cycle (see e.g. Fig. 3), but the number of arcs in
c, i.e., the number of transplants associated with cycle c. The objec-
all of these cycles are guaranteed to have no more than k arcs.
tive function (2a) maximizes the weighted number of transplants.
Furthermore, the edge-assignment formulation allows for mul-
Constraints (2b) ensure that every vertex is in at most one of the
tiple equivalent solutions, i.e. has symmetry. If there is a solution
selected cycles (i.e., each donor may donate, and each patient
having p cycles represented by indices l1, . . . , lp, other orderings
may receive only one kidney). Compared to the edge formulation,
of p indices may correspond to the same solution as exemplified
the difficulty with this formulation is induced by the exponential
in Fig. 4. A solution consisting of cycles between pairs 2, 3 and 4
number of variables. Indeed, the number of cycles can grow expo-
and pairs 1 and 5 can be obtained with different indexing l for cy-
nentially with k.
cles 1 and 2.
The symmetry can be a problem because, as stated in [24],
4. New compact formulations ‘‘Even for relatively modestly sized problems, ILPs with large sym-
metry groups are difficult to solve using traditional branch-and-
As previously noted the number of constraints or variables in bound or branch-and-cut algorithms’’. One way to avoid the sym-
the formulations that had been proposed up to now for the KEP metry of the edge-assignment formulation is by representing each
can grow exponentially with k. It is known that such formulations cycle by its node with the lowest index. In other words, for L = jVj, a
can sometimes provide better bounds with linear relaxation than cycle having nodes i1, . . . , ir is represented by index l = min{i1,
M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68 61

4.2. Extended edge formulation

Consider L copies of the graph G, and let l be the index of a copy.


Recall that L is an upper bound on the number of cycles in a solu-
tion. In each copy l at most k arcs can create a cycle and each node
i 2 V can belong to at most one such cycle. This can be captured by
‘‘cycle cardinality constraints’’ in a new model using the variables
xlij . Let

1 if arc ði; jÞ is selected to be in copy l of the graph;
Fig. 3. Index l can represent more than one cycle. For e.g. l = 1, the solution with xlij ¼
y11 ¼ y15 ¼ y12 ¼ y13 ¼ y14 ¼ 1, x15 ¼ x51 ¼ x23 ¼ x34 ¼ x42 ¼ 1 and all other variables 0 otherwise:
equal to 0 satisfies all the constraints of the edge-assignment formulation for k = 5.
The extended edge formulation is given by:
X X
maximize wij xlij ð7aÞ
. . . , ir}. In this case only variables yli
with i P l are necessary and l2f1;...;Lgði;jÞ2A
this can be enforced by restricting the variables yli to indices X X
subject to xlji ¼ xlij 8i 2 V; 8l 2 f1; . . . Lg ð7bÞ
1 6 l 6 i 6 L and by adding constraints:
j:ðj;iÞ2A j:ði;jÞ2A
XX
yli 6 yll 8i 2 V; l ¼ 1; . . . ; L; i>l ð5aÞ xlij 6 1 8i 2 V ð7cÞ
l j:ði;jÞ2A
Note that here and below we eliminate variables by fixing them to 0 X
(i.e. yli ¼ 0; 8i 2 V; l ¼ 1; . . . ; L; i 6 l). xlij 6 k 8l 2 f1; . . . Lg ð7dÞ
ði;jÞ2A

4.1.1. Reduced edge-assignment formulation xlij 2 f0; 1g: 8ði; jÞ 2 A; 8l 2 f1; . . . Lg ð7eÞ
To tighten the model further, in some situations the variable yli
can be eliminated if l and i cannot be in the same cycle. Let The objective (7a) is to maximize the total weight of the arcs ta-
e l ¼ fi 2 V : i P lg and dl denote the shortest path distance in
V ken from all copies of the graph. Constraints (7b) state that in each
ij
terms of number of arcs in graph G from i to j for i; j 2 V e l such that copy l of the graph, the number of kidneys received by patient i is
the path passes only through vertices of set V e l . Let dl ¼ þ1 if there equal to the number of kidneys given by donor i. To make sure that
ij
l l
is no such path from i to j. For a given i if dli þ dil > k, then there is a donor/patient intervene only once, constraints (7c) ensure that a
no cycle with length k or less containing both nodes l and i. In this node can only be selected in at most one copy of the graph. Con-
case the variables yli need not be considered in the model. More straints (7d) state that at most k edges can be used from each copy
precisely, for each vertex l 2 V,olet us build the set of vertices of the graph. This essentially prevents the cycles from becoming
n
l l
V l ¼ i 2 Vji P l and dli þ dil 6 k . It can happen that for some larger than k as each copy of the graph allows only cycles of length
l
l 2 {1, . . . ,L} V = ;. Denote by L # f1; . . . ; Lg the set of indices l such k or less. There can be more than one cycle in a copy of the graph
that Vl – ;. The reduced edge-assignment formulation can now be but the total number of edges in all the cycles is at most k.
represented by Eqs. 6a, (6b)–(6i). As with the edge-assignment formulation the extended edge
X formulation also has symmetry. To avoid multiplicity of solutions
maximize wij xij ð6aÞ a similar approach can be used here as well. If a copy l of the graph
ði;jÞ2A provides a cycle for some solution, then node l must be in this cycle
X X
subject to xji ¼ xij 8i 2 V ð6bÞ and all other nodes must have indices larger than l. Hence, all vari-
j:ðj;iÞ2A j:ði;jÞ2A ables xlij such that i < l or j < l may be discarded from the model, and
X
xij 6 1 8i 2 V ð6cÞ constraints similar to (5a) can be added to set l as the lowest index
j:ði;jÞ2A of all nodes in the cycle:
X
yli 6 k 8l 2 L ð6dÞ X X
xlij 6 xllj 8i > l: ð8Þ
i2V l
X X j j
yli ¼ xij 8i 2 V ð6eÞ
l2L:i2V l j:ði;jÞ2A
4.2.1. Reduced extended edge formulation
yli þ xij 6 1 þ ylj 8ði; jÞ 2 A; i 2 V l; 8l 2 L ð6fÞ
Along the same lines as the elimination procedures for the vari-
yli 6 yll 8i 2 V l ; l 2 L ð6gÞ ables yli proposed for the edge-assignment formulation (see Sec-
yli 2 f0; 1g 8i 2 V ; 8l 2 L l
ð6hÞ tion 4.1), one may also be able to eliminate variables xlij in the
extended edge formulation. If there is no cycle of size at most k
xij 2 f0; 1g 8ði; jÞ 2 A ð6iÞ

Fig. 4. Symmetry in edge-assignment formulation. The complete solution for k = 3 with x15 = x51 = x23 = x34 = x42 = 1 and all other xij = 0 can be obtained with different
indexing l. For e.g. l = 1 for Cycle 1 and l = 2 for Cycle 2 with y11 ¼ y15 ¼ y22 ¼ y23 ¼ y24 ¼ 1 and vice versa l = 2 for Cycle 1 and l = 1 for Cycle 2 with y21 ¼ y25 ¼ y12 ¼ y13 ¼ y14 ¼ 1, all
other yli ¼ 0.
62 M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68

containing both node l and an arc (i,j) with i P l, j P l, then variable


xlij can be set to zero or simply eliminated from the model.
Summarizing, the application of the elimination procedures
leads to the construction of a subgraph Gl = (Vl, Al) for each index
l
l 2 L, with V l ; L and dij as defined in Section 4.1 and
n o
l l
Al ¼ ði; jÞ 2 Aji; j 2 V l and dli þ 1 þ djl 6 k . With this notation
the reduced extended edge formulation is given as follows.
Fig. 5. Inclusion of altruistic donor with m = 1 and n = 2. Node 1 is the altruistic
XX donor, and dashed arcs (2, 1) and (3, 1) are the arcs to the altruistic donor’s dummy
maximize wij xlij ; ð9aÞ patient.
l2L ði;jÞ2Al
X X
subject to xlji ¼ xlij 8i 2 V l ; 8l 2 L; ð9bÞ
j:ðj;iÞ2Al j:ði;jÞ2Al
X X [ l Similarly, for the edge-assignment formulation in Section 4.1
xlij 6 1 8i 2 V; ð9cÞ we define L = n + m. In addition to variables yli ; l; i ¼ m þ 1; . . . ; L
l2L j:ði;jÞ2Al l2L
X for the incompatible pairs consider variables yll for l = 1, . . . , m
xlij 6 k 8l 2 L ð9dÞ and yli for l = 1, . . . , m, i = m + 1, . . . , L. Then Eq. (3a) limiting the size
ði;jÞ2Al of cycles is divided into the two following inequalities:
X X X
xlij 6 xllj 8i 2 V l ; 8l 2 L ð9eÞ yli 6 k
0
8l 2 1; . . . ; m ð11aÞ
l l
j:ði;jÞ2A j:ðl;jÞ2A i2flg[fmþ1;...;Lg
X
xlij 2 f0; 1g: 8ði; jÞ 2 A; 8l 2 L yli 6 k 8l 2 m þ 1; . . . ; L ð11bÞ
iPmþ1

The same idea is applied to Eq. (7d), resulting in:


5. Adaptation of each model to include problem variants
X 0
xlij 6 k 8l 2 1; . . . ; m ð12aÞ
In the following text we discuss how formulations for the KEP ði;jÞ2A:i;j2flg[fmþ1;...;Lg
can be adapted to three variants: the problem with altruistic do-
X
xlij 6 k 8l 2 m þ 1; . . . ; L ð12bÞ
nors participating, the problem where compatible pairs are in- ði;jÞ2A:i;jPmþ1
cluded into the pool, and the problem with one or more patients
having multiple donors associated.
5.2. Inclusion of compatible pairs

5.1. Inclusion of altruistic donors Opening kidney exchange programs to compatible pairs will re-
quire slight modifications in the IP models discussed in this paper.
The inclusion of altruistic donors in KEP IP formulations is dis- The set of vertices V will now represent both compatible an incom-
cussed in [23]. Exchanges involving altruistic donors are labeled as patible pairs, VC  V denoting the subset of compatible pairs. For
domino paired chains (DPC) and, due to program regulations, the the cycle formulation, one will have to consider the existence of
authors do only consider chains of lengths 1 and 2 (when one or loops ii of size 1 for all vertices of set VC. All the other formulations
two incompatible pairs are involved in the exchange), but their ap- will have to consider that it is now possible that patient i gets a
proach can be used for chains of any size. The problem is again kidney from donor i. Therefore variables xij must be extended to in-
modeled as a weighted directed graph with n + m nodes: clude variables xii"i 2 VC.
V = {1, . . . , n + m}, n being the number of incompatible patient–do-
nor pairs and m the number of altruistic donors. Let the nodes
5.3. Multiple donors
{1, . . . , m} represent the altruistic donors, nodes
{m + 1, . . . , m + n} represent the incompatible pairs, and a dummy
Within kidney exchange programs it is possible that instead of
patient compatible with all donors j 2 {m + 1, . . . , m + n} be associ-
a single donor a patient has multiple donors associated. If that is
ated with each altruistic donor. An example is given in Fig. 5.
the case, and if the patient is selected for kidney transplantation,
Within this description denote by k0 the maximum length of a
a donor that would allow the cycle where the corresponding pa-
chain (in terms of nodes) started by an altruistic donor and let
0 tient appears to be created will be selected. In such cases,
Cðk; k Þ define the set of all cycles in G with length at most k involv-
depending on the scoring system used, two situations can occur:
ing only incompatible pairs, and of all cycles with length at most k0
0 (i) the weight of an arc from a vertex i to a vertex j has a compo-
with one altruistic donor. Replacing CðkÞ by Cðk; k Þ the cycle formu-
nent that depends on which donor is chosen in each pair i and j
lation can be directly used to solve the problem.
(for instance, in the UK system this weight has a component that
For the other formulations the main impact is on the cardinality
relates to the difference in age between the donors in i and j
constraints that define the maximum size of the cycle. They will
[23]): (ii) the weight of arc (i, j) 2 A does not depend on the donor
now have to be separated in two sets: one for cycles including
selected in pair i.
one altruistic donor, and another for cycles that only include
For the first case, a possible way of modeling the problem is by
incompatible pairs.
considering different vertices for  all donors of a patient Pi, each
For the edge formulation in Section 3.1 assume also that k0 6 k.
vertex representing the pair Pi ; Dji ; j ¼ 1 . . . NDi , where NDi is
The following additional set of constraints must be added:
the number of donors of patient Pi. More precisely denote by P
X 0   the set of patients in the pool. For each patient p 2 P let us define
xij ijþ1 6 k  1 8 i1 ; i2 ; . . . ; ik0 ; ik0 þ1 2 Paths a ð10Þ
set DðpÞ as the set of vertices associated with patient p, the set of
16j6k0
sets fDðpÞ; p 2 Pg defines a partition of the set of vertices V.
For the edge formulation (see Section 3.1) the Eq. (1c) need to
where Paths_a is the set of simple paths of length k0 with
be replaced by:
i1 2 {1, . . . , m} and i2 ; . . . ; ik0 þ1 2 fm þ 1; . . . ; n þ mg.
M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68 63

X X  
xkj 6 1 8p 2 P ð13Þ Proof 1. For each l, let Xl be the set of vectors xl ¼ xlij ; ði; jÞ 2 A
k2DðpÞj:ðk;jÞ2A defined by constraints (7b), (7d), (7e), (8) and
P l l
j:ði;jÞ2A xij 6 1; 8i 2 V. Each element of X corresponds either to a
These constraints guarantee that only one of the (possible) mul-
cycle of cardinality at most k, or to a set of disjoint cycles with a
tiple donors associated with a patient will be selected. The same
total number of edges not exceeding k. The extended edge formu-
principle will have to be followed in the edge assignment formula-
lation can be rewritten as:
tion by replacing Eq. (6c) by the ones above. And similarly for the XX
extended edge formulation by replacing Eq. (9c) by equations maximize wij xlij ð16aÞ
XX X l ði;jÞ2A
xlkj 6 1 8i 2 P: ð14Þ XX
l2L k2DðpÞj:ðk;jÞ2A subject to xlij 6 1 8i 2 V ð16bÞ
l j:ði;jÞ2A
Finally, for the cycle formulation two considerations must be
xl 2 X l ð16cÞ
made: all cycles in CðkÞ can contain at most one vertex with patient
p, and Eq. (2b) must be replaced by: l l
Now let U be the set of vectors of X that induce at most one
X X cycle. Ul can replace Xl in the above formulation, although to obtain
zc 6 1 8p 2 P ð15Þ
an explicit formulation in variables xlij constraints preventing mul-
k2DðpÞc:k2VðcÞ
tiple cycles would have to be added. Consider the following relax-
For the second case the IP models discussed do not suffer any ation of the above model:
structural changes and are handled as follows: for all patients i XX
maximize wij xlij ð17aÞ
with multiple donors, an arc (i,j) will exist if there is at least one l ði;jÞ2A
donor in pair i compatible with patient j. If the arcs are weighted
and two or more donors in i are compatible with patient j the larg- XX
subject to xlij 6 1 8i 2 V ð17bÞ
est weight associated to a transplant from i to j is assigned to the l j:ði;jÞ2A
arc between nodes i and j. The associated IP models will be the
same as described in previous sections but a final straightforward
xl 2 conv ðU l Þ 8l 2 K ð17cÞ
procedure will be required, if a multiple donor node appears in the
l l
optimal solution to determine which donor within this node where conv(U ) denotes the convex hull of U . The optimal value of
should be selected. If only one donor is compatible with the asso- the above model is less than or equal to the optimal value of the
ciated recipient, he/she is selected. Otherwise for weighted arcs the LP relaxation of the extended edge model. Indeed, the optimal value
donor associated with the maximum weight is selected; for un- of problem (17a), (17b) and (17c) is less than or equal to the optimal
weighted graphs if more than one donor is compatible with the pa- value of the linear relaxation of the problem (16a) and (16b) with
tient, additional criteria are required for the selection of a donor. xl 2 Ul. But this value is obviously less than or equal to the optimal
value of the linear relaxation of problem (16a), (16b) and (16c) be-
6. Linear relaxations and comparison of the bounds for cause Ul # Xl.
different models One way to write a linear program equivalent to model (17a),
(17b) and (17c) is to replace conv(Ul) by its extreme point
It is well known that the strength of the LP relaxation is one of the representation. An extreme point of Ul is either the null vector or
most important factors for a formulation to be effective when a LP the inducing vector pc of a cycle c in G of cardinality at most k,
based branch-and-bound algorithm is used as a resolution method. containing node l and not containing nodes i < l. Let CðkÞ be the set of
Let IP be some optimization program and A and B be two different all cycles of cardinality at most k and Cl be the set of cycles defined by
integer linear formulations of IP, which define linear relaxation Ul, that is Cl ¼ fc 2 CðkÞ : l 2 VðcÞ # fl; . . . ; ngg (recall that V(c)
upper bounds (for the maximization problem) UB(A) and UB(B). denotes the set of vertices of cycle c). Now observe that fCl ; l 2 Kg
We say that formulation A dominates formulation B if UB(A) 6 UB(B). is a partition of CðkÞ, hence xl 2 conv(Ul) if and only if there exist
In this section we present a comparison, from a theoretical point of P
nonnegative scalars uc, with c 2 Cl , such that xl ¼ c2Cl uc pc and
view, of the strength of the formulations described in the previous P l l
section. A first result on interaction of the upper bounds of optimal c2Cl uc 6 1. So x 2 conv(U ), l 2 K can be rewritten as:
X
solutions provided by linear relaxations of edge and cycle formula- xlij ¼ uc 8ði; jÞ 2 A; 8l 2 K; ð18aÞ
tions (Theorem 1) was presented and proven in [2]. c2Cl :ði;jÞ2c
X
uc 6 1 8l 2 K; ð18bÞ
Theorem 1. The cycle formulation dominates the edge formulation.
c2Cl
As mentioned above the IP formulations with exponential num- uc P 0 8c 2 Cl ; 8l 2 K: ð18cÞ
ber of variables or constraints sometimes provide better bounds P
with linear relaxations than compact formulations. We now show Let wc ¼ ði;jÞ2c wij for c 2 CðkÞ. Using (18a), (18b) and (18c), the
that the cycle formulation also dominates the extended edge for- model (17a), (17b), (17c) can be written as follows.
mulation and that the extended edge formulation dominates the X
maximize wc uc ð19aÞ
edge-assignment formulation. c2CðkÞ
Assume that the extended edge formulation satisfies the follow- X
ing properties: (i) L = jVj, denote by K = {1, . . . , L}; (ii) the non elim- subject to uc 6 1 8i 2 V; ð19bÞ
c2CðkÞ:i2VðcÞ
inated variables are xlij such that i P l or j P l, and (iii) the model X
contains constraints (8). The following results remain true for the uc 6 1 8l 2 K; ð19cÞ
reduced extended edge formulation given in the second half of c2Cl

Section 4.2. u c P 0 8 c 2 C l ; l 2 K: ð19dÞ

Theorem 2. The cycle formulation dominates the extended edge It is straightforward to see that constraints (19c) are always sat-
formulation. isfied with respect to constraints (19b). Thus problem (19a), (19b),
(19c), (19d) is the cycle formulation and from the previous
64 M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68

discussion its optimal value is less than or equal to the value of the
LP relaxation of the extended edge model. h

Theorem 3. The extended edge formulation dominates the edge-


assignment formulation.

xlij ; ði; jÞ 2 A; l 2 K be an optimal solution of the linear


Proof 2. Let 
relaxation of the extended edge model 7a, (7b)–(7e). We build a
Fig. 6. An optimal solution for k = 3 is, for e.g. the cycle 1–4–5–1.
feasible solution for the LP relaxation of the edge-assignment
model with same objective value. The optimal LP solution for the edge formulation is
Define the variables  xij and yli as:
x12 = x23 = x34 = x41 = 0.66(7), x13 = x31 = 0.33(3), and x42 = 0, with
X
xij ¼ xlij 8ði; jÞ 2 A ð20Þ value 3.33(3). An optimal LP solution for the extended edge
l2K formulation is x112 ¼ x123 ¼ x134 ¼ x141 ¼ 0:75, x223 ¼ x234 ¼ x242 ¼ 0:25
X
li ¼
y xlij 8i 2 V; i P l ð21Þ and xlij ¼ 0 for all other variables, with value 3.75. h
j:ði;jÞ2A
Theorem 3 and Remark 2 imply that the edge-assignment for-
The verification that the objective value is the same for both mulation does not dominate the edge formulation. It is an open
solutions uses (20) and it is straightforward. Also, constraints question whether the edge formulation dominates the edge-
(1b) and (1c) follow directly from (7b) and (7c) respectively, and assignment formulation. However, if the reduction procedure is
(20). Similarly, (3a) follows from (7d) and (21), and (4a) is obtained applied (Section 4.1), the edge formulation does not dominate
from summing both sides of (21) over l and both sides of (20) over edge-assignment. The example presented by Fig. 6 can be consid-
j. We show next that (4b) is satisfied. ered. The optimal value of LP solution for the edge formulation is
P P 4, and the reduced edge-assignment formulation has value 3.
By (20) and (21) y li þ  xlip þ l2K 
xij ¼ p:ði;pÞ2A  xlij . Now observe
Despite the results presented in this section, compact formula-
that the only common variable in the two previous sums is  xlij .
P P tions can turn out to be effective computationally because of their
 l  l  l  l
Hence yi þ xij 6 l2K p:ði;pÞ2A xip þ xij 6 1 þ yi , the last inequality polynomial size, as will be shown in the computational study pre-
following from (7c) and from (21) and the nonnegativity of the sented in the next section.
variables.
li 6 1 and 0 6 
Finally, 0 6 y xij 6 1 are a consequence of the 7. Computational analysis
nonnegativity of  xlij and constraints (1c) and (4a), already verified.
Thus there always exists a feasible point for the edge-assignment Computational experiments were carried out to compare the
formulation which provides the same objective value as an optimal proposed and known formulations in terms of time needed to find
solution for the extended edge formulation. Hence we conclude an optimal solution and of the LP gaps with respect to upper
that the value of the LP relaxation of the edge-assignment bounds of linear relaxations of the models. CPU times and bounds
formulation is greater than or equal to the value of the LP were obtained with CPLEX 12.2 on a computer with a Quad-Core
relaxation of the extended edge formulation. h Intel Xeon processor at 2.66 gigahertz, 16 gigabytes of RAM and
Next we show that the extended edge formulation and the edge running Mac OS X 10.6.6. Only one core of the processor was as-
formulation do not dominate each other. signed to these experiments.
Two generators where used to create the instances for the com-
Remark 1. The edge formulation does not dominate the extended putational study:
edge formulation.
(1) the instance generator described in [35], which creates ran-
dom graphs based on probability of blood type and of
Proof 3. We present an example in which the value of the LP relax- donor–patient compatibility. These instances will be
ation of the edge formulation is larger than the one of the extended referred to as blood-type test instances;
edge formulation. Let k = 3, the set of nodes (incompatible pairs) be (2) a random generator implemented by the authors of this
V = {1, 2, 3, 4, 5} and the set of arcs be paper used to generate graphs with three different densities:
A = {(1, 2), (1, 3), (1, 4), (2, 3), (3, 1), (3, 4), (4, 1), (4, 5), (5, 1)}, wij = 1 low, medium and high. To do that different values are set for
"(i, j) 2 A – Fig. 6. The optimal value for this instance is 3, given the probability of having 1 (i.e. compatibility) on each posi-
for e.g. by cycle 1–4–5–1. tion of the adjacency matrix of a graph. Low density graphs
Observe that all cycles contain vertex 1. Hence in the extended are generated with probability 0.2. This value leads to an
edge formulation xlij ¼ 0 for all (i, j) and l P 2, and the optimal LP average density similar to the one obtained for the blood-
value is 3. The optimal LP solution for the edge formulation is type test instances. The probability is set to 0.5 for medium
x12 = x13 = x23 = x41 = x45 = x51 = 0.5, x34 = 1, and x31 = x14 = 0, with density, and to 0.7 for high density graphs.
value 4. h
The computational analysis was performed as follows. First, for
cases with up to 50 nodes and k ranging from 3 to 6, fifty instances
Remark 2. The extended edge formulation does not dominate the
of the same size were generated with both generators for the three
edge formulation.
density levels.3 The performance of all formulations was tested for all
instances. Besides that, for this set of problem instances we compared
Proof 4. Consider the example illustrated by Fig. 7, where k = 3,
the set of nodes is V = {1, 2, 3, 4} and the set of arcs is 3
Currently implemented kidney exchange programs work in general with a
A = {(1, 2), (1, 3), (2, 3), (3, 1), (3, 4), (4, 1), (4, 2)}, wij = 1 "(i, j) 2 A. The maximum value of k = 3. However this value has already been exceeded by large: the
optimal value for this instance is 3. maximum number of simultaneous transplantations performed up to now being 6
[6].
M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68 65

formulation; EA – reduced edge-assignment formulation; EE – re-


duced extended edge formulation. Computational results are pro-
vided in Tables 1 and 3 where:

– n is the number of nodes in the graph;


– k is the maximum length of the cycle;
– tc and tp are the average CPU times (in seconds) to find all cycles
and paths, respectively. The time needed to carry out reduction
procedures for the EA and the EE formulations was less than 1 s
Fig. 7. An optimal solution for k = 3 is the cycle 1–2–3–1. for all small instances and less than 3 seconds for all large
instances, and therefore it is not shown in the tables;
– T is the average CPU time the solver CPLEX [16] needed to reach
optimal solutions for the given set of instances (50 instances for
the average number of constraints and variables for different models
small problems, 10 for large problems); maximum CPU time
and the percentage reduction in size for the edge-assignment and ex-
was set to 1800 seconds for all formulations;
tended edge formulations when reduction procedures are imple-
– #opt is the number of instances from each set which were
mented (see Sections 4.1, 4.2). Afterwards the formulations with
solved to optimality within the time limit (1800 seconds).
generally better performance on ‘‘small’’ instances were selected
Whenever this information is not provided in Table 1 it means
for testing on larger problem instances (n > 50). Ten instances were
that all instances of the set were solved;
generated for different large problem instance sizes.
– gap is the average LP gap associated to a formulation:
In the remainder of this document the following notation will be
gap ¼ UBOpt  100%, where UB is the upper bound provided by
used to refer to each formulation: E – edge formulation; C – cycle Opt

Table 1
Results for small instances.

n k C E EA EE C E EA EE
tc/T gap tp/T #opt gap T #opt gap T gap tc/T #opt gap tp/T #opt gap T #opt gap T gap
Blood-type test instances Medium density test instances
10 3 0/0 0.0 0/0 0.5 0 1.0 0 0.0 0/0 0.6 0/0 0.9 0 1.0 0 0.7
4 0/0 0.0 0/0 0.0 0 0.0 0 0.0 0/0 0.0 0/0 0.2 0 0.2 0 0.0
5 0/0 0.0 0/0 0.0 0 0.0 0 0.0 0/0 0.0 0/0 0.0 0 0.0 0 0.0
6 0/0 0.0 0/0 0.0 0 0.0 0 0.0 0/0 0.0 0/0 0.0 0 0.0 0 0.0
20 3 0/0 0.0 0/1 5.6 0 6.5 0 2.8 0/0 0.0 0/1 0.0 2 0.0 0 0.0
4 0/0 0.0 0/0 1.5 0 1.9 0 1.1 0/0 0.0 0/5 0.0 1 0.0 0 0.0
5 0/0 0.1 1/0 0.7 0 0.9 0 0.8 0/0 0.0 2/55 0.0 1 0.0 0 0.0
6 0/0 0.0 9/1 47(47) 0.2 0 0.2 0 0.2 0/3 0.0 – 0 0.0 0 0.0
30 3 0/0 0.0 0/0 4.0 6 4.9 0 1.2 0/0 0.0 0/15 0.0 162 47 0.0 0 0.0
4 0/0 0.0 1/1 0.6 1 0.7 0 0.5 0/0 0.0 2/138 49 0.0 30 0.0 1 0.0
5 0/0 0.0 10/2 42(42) 0.0 0 0.0 0 0.0 0/5 0.0 – – 4 0.0 0 0.0
6 2/0 0.0 185/0 12(12) 0.0 0 0.0 0 0.0 4/267 49 0.0 – – 2 0.0 0 0.0
40 3 0/0 0.1 0/48 5.6 85 45 6.1 0 2.7 0/0 0.0 1/171 0.0 564 24 0.0 1 0.0
4 0/0 0.0 3/28 0.9 49 1.0 0 0.9 0/1 0.0 6/624 39 0.0 203 40 0.0 2 0.0
5 1/0 0.0 54/4 18(18) 1.5 2 0.6 0 0.6 1/67 0.0 – – 106 49 0.0 2 0.0
6 11/1 0.0 1727/1 4(4) 2.4 3 0.2 0 0.2 – – – – 16 0.0 1 0.0
50 3 0/0 0.0 0/134 49 3.6 112 30 3.9 0 2.0 0/0 0.0 1/440 47 0.0 745 3 0.0 4 0.0
4 0/0 0.0 12/109 47 0.6 42 44 0.7 1 0.3 0/4 0.0 – – 645 18 0.0 5 0.0
5 2/0 0.1 213/7 3(3) 0.0 14 48 0.4 1 0.2 4/385 48 0.0 – – 116 34 0.0 6 0.0
6 45/6 0.0 – – 8 0.1 1 0.0 - - - - 62 46 0.0 3 0.0
Low density test instances High density test instances
10 3 0/0 0.2 0/0 21.8 0 33.2 0 0.3 0/0 0.0 0/0 0.0 0 0.0 0 0.0
4 0/0 0.5 0/0 11.6 0 15.2 0 0.9 0/0 0.0 0/0 0.0 0 0.0 0 0.0
5 0/0 0.0 0/0 7.0 0 8.2 0 0.2 0/0 0.0 0/0 0.0 0 0.0 0 0.0
6 0/0 0.2 0/0 1.1 0 1.7 0 1.1 0/0 0.0 0/1 0.0 0 0.0 0 0.0
20 3 0/0 1.4 0/0 21.5 1 23.7 0 2.6 0/0 0.0 0/1 0.0 2 0.0 0 0.0
4 0/0 0.4 0/0 5.7 1 6.2 0 1.5 0/0 0.0 1/16 0.0 1 0.0 0 0.0
5 0/0 0.6 1/1 1.9 1 1.9 0 1.2 0/2 0.0 – – 0 0.0 0 0.0
6 0/0 0.4 7/1 0.8 0 0.8 0 0.7 1/52 0.0 – – 0 0.0 0 0.0
30 3 0/0 0.5 0/44 4.9 714 33 4.9 0 1.1 0/0 0.0 0/9 0.0 32 0.0 1 0.0
4 0/0 0.1 0/33 0.2 348 42 0.2 1 0.1 0/1 0.0 – – 5 0.0 1 0.0
5 0/0 0.0 8/65 0.0 86 0.0 1 0.0 1/66 0.0 – – 2 0.0 0 0.0
6 2/0 0.0 188/226 0.0 17 0.0 1 0.0 – – – – 1 0.0 0 0.0
40 3 0/0 0.0 0/512 20 0.1 – 0.5 0 0.1 0/0 0.0 1/64 0.0 238 36 0.0 2 0.0
4 0/0 0.0 2/571 30 0.0 851 9 0.0 4 0.0 0/5 0.0 – – 38 49 0.0 2 0.0
5 1/1 0.0 – – 453 30 0.0 5 0.0 4/66 34(41) 0.0 – – 12 0.0 1 0.0
6 10/2 0.0 – – 246 45 0.0 3 0.0 – – – – 4 0.0 1 0.0
50 3 0/0 0.0 0/506 3 0.0 – 0.0 0 0.0 0/0 0.0 3/238 48 0.0 250 15 0.0 10 0.0
4 0/0 0.0 – – – 0.0 20 0.0 – – – – 130 39 0.0 7 0.0
5 2/1 0.0 – – – 0.0 15 0.0 – – – – 25 0.0 5 0.0
6 42/11 0.0 – – 618 20 0.0 7 0.0 – – – – 47 0.0 2 0.0
66 M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68

Table 2
Sizes of formulations and reduction for EA and EE. ‘‘Low’’ and ‘‘high’’ density test instances.

n k C E EA EE
#var #con #var #con #var #con rv% rc% #var #con rv% rc%
Low density test instances
10 3 3 2 17 55 22 53 70.6 76.4 7 16 96.4 86.1
4 5 4 17 62 25 65 66.3 71.2 12 24 93.9 80.0
5 7 4 17 63 27 73 63.3 67.7 16 28 91.8 75.9
6 8 5 17 55 28 75 62.0 66.7 18 30 90.5 74.2
30 3 82 28 174 5215 280 1318 56.2 68.5 169 242 96.8 74.8
4 336 30 174 26,634 401 2354 37.4 43.6 498 484 90.5 49.6
5 1377 30 174 131,770 496 2978 22.5 28.5 1008 674 80.8 29.8
6 5681 30 174 626,695 539 3225 15.6 22.4 1412 761 73.0 20.7
50 3 363 50 491 44,579 851 6782 51.8 62.5 684 770 97.2 70.4
4 2596 50 – >3  106 1342 13,059 24.0 27.8 2672 1752 89.1 32.6
5 19,010 50 – >3  106 1601 15,628 9.3 13.6 6140 2271 75.0 12.7
6 142,190 50 – >3  106 1665 16,332 5.7 9.6 7780 2399 68.3 7.7
High density test instances
10 3 100 10 62 1667 110 488 6.4 10.6 139 105 77.7 12.3
4 384 10 62 6856 114 506 2.8 7.1 211 114 66.1 5.3
5 1331 10 62 23,732 114 507 2.7 7.0 228 114 63.1 5.1
6 4075 10 62 65,993 114 507 2.7 7.0 229 114 63.0 5.1
30 3 2949 30 606 221,941 1026 12,290 4.2 6.0 3341 870 81.6 9.3
4 41,556 30 – >3  106 1066 12,887 0.4 1.4 5731 950 68.5 1.0
5 600,569 30 – >3  106 1066 12,896 0.4 1.4 6251 951 65.6 0.9
6 >3  106 – – >3  106 1066 12,896 0.4 1.4 6252 951 65.6 0.9
50 3 14,157 50 1719 1,911,261 2883 56,974 3.7 5.0 15,272 2377 82.2 8.6
4 >3  106 – – >3  106 2992 59,750 0.1 0.3 26,817 2595 68.8 0.2
5 >3  106 – – >3  106 2992 59,762 0.1 0.3 29,272 2595 66.0 0.2
6 >3  106 – – >3  106 2992 59,764 0.1 0.3 29,273 2595 65.9 0.2

Notations: – #var and #con are the average number of variables and constraints for a given n for different values of k;
– rv% and rc% are the average relative reductions on the number of variables and constraints in the EA and EE formulations after implementing reduction procedures.
Dashes for the formulations C and E mean that no test instance out of 50 was considered due to the bound on number of cycles or paths.

the linear relaxation of the formulation and Opt is the optimal considered, either because the CPU time or the maximum number
value of the problem. of paths were exceeded. The additional difficulty raised up by these
instances may be partially explained by the larger LP gaps obtained
Values 0 in tables related to CPU time mean that the solver took for smaller problems. Again, the C and EE formulations dominate
less than 1 s to solve the instances. the others, both formulations having solved to optimality all
Since the number of paths associated with the edge formulation instances.
increases sharply for larger values of k (k = 5 and k = 6), a bound of The importance of developing compact formulations is reflected
3 million was set on the number of paths to be generated. The for- in the results obtained for medium density test instances, and cor-
mulation was not studied for instances where the number of paths roborated and strengthened by high density test instances. In this
exceeded that value. The same bound was used for the number of cases the EE formulation proved to be extremely efficient at solving
cycles in the cycle formulation. With respect to this limitation in larger problem instances. It was capable of solving to optimality
column #opt we show in parenthesis the number of instances the both complete sets. The EA, although performing worse than
out of 50 (or 10 for larger instances) that were studied, if necessary. the EE, still solved to optimality almost 95% of the high density in-
stances considered.
7.1. Small test instances Furthermore, none of the compact formulations suffered the
‘‘curse of dimensionality’’ that affects both the E and the C formu-
Test instances of 10, 20, 30, 40 and 50 nodes were created with lations, which exceeded either the maximum number of cycles/
the two generators, for the second one for the three graph densi- paths or CPU times for larger instances. In fact, the problems raised
ties. Fifty instances of each size were considered. Computational up by non-compact formulations become more evident for high
results are presented in Table 1. density test instances: the number of cycles for the cycle formula-
The results for blood-type test instances clearly show the domi- tion exceeds the allowed limit for all test instances of size 50, for
nance of the C and EE formulations, both in terms of effectiveness values of k = 4, 5, 6; the edge formulation was not run even for in-
and efficiency: all instances are solved to optimality in general stances with 20 nodes and k = 5, 6 because number of paths exceed
with less CPU time than the E and EA formulations. The consider- the limit of 3 million previously set.
able increase in CPU time for the cycle formulation when k = 6 It is also worth mentioning that although for the blood-type and
and n = 40, 50 is caused by the time needed to enumerate all the low density instances most of the CPU time associated to the C for-
cycles. As shown, the smaller average gap is associated to the C mulation was spent at generating cycles, in this case it was spent in
formulation. the optimization phase.
Although the density of the graphs of low density test instances is Table 2 shows the average number of variables and constraints
of the same order of magnitude of the previously reported ones, for problems of different size for the low and high density test in-
the E and EA formulations performed very poorly for larger in- stances, as well as the percentage of reduction of the number of
stances: in most cases the EA formulation exceeded the maximum variables and constraints for the EA and EE formulations after
CPU time for all test instances of a given size (represented by (–) in implementing reduction routines presented in Sections 4.1 and
Table 1); in several cases the E formulation was not also 4.2. Evidently the impact of the reduction is high, in particular
M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68 67

Table 3 cycles/variables and paths/constraints; whereas decreasing times


Results for large instances. for other models could be explained by smaller gaps. Indeed gaps
n k C EE decrease for EE and EA with k and density, while remaining approx-
tc T #opt gap T #opt gap imately constant for C. This decrease in gaps may be explained as
follows: EE and EA are exact formulations if the problems are unca-
Blood-type test instances
70 3 0 0 10 0.0 2 10 1.8
pacitated, that is, for k sufficiently large there is always an LP solu-
100 0 0 10 0.1 3 10 0.8 tion that is optimal for the integer program. When k increases the
200 1 0 10 0.0 1221 4 0.4 problems become closer to being uncapacitated so the LP solutions
300 3 2 10 0.0 – 0 – are closer to being integral and the LP values are closer to the inte-
500 23 11 10 0.0 – 0 –
ger optima. When the density increases the explanation is not so
800 141 148 10 0.0 – 0 –
900 223 398 9(9) 0.0 – 0 – clear; probably since more feasible cycles are available, it may be
1000 343 479 7(7) 0.0 – 0 – easier for LP solutions to have some entire feasible cycles in their
70 4 0 0 10 0.0 11 10 0.5 composition, i.e. more variables equal to one.
100 2 0 10 0.0 53 10 0.0
200 42 25 10 0.0 – 0 0.0 7.2. Large scale test instances
70 5 10 2 10 0.0 7 10 0.0
100 67 13 10 0.0 72 10 0.0 This section reports the results obtained for the C and EE formu-
70 6 370 25 9(9) 0.0 4 10 0.0 lations, for problems ranging from 70 to 1000 pairs (see Table 3);
100 3255 19 1(1) 0.0 102 10 0.0 10 instances of each size were generated. These formulations were
selected because they were the dominant for at least one set of the
Low density test instances
70 3 0 0 10 0.0 5 10 0.0
previous computational simulations: blood-type, low, medium or
100 0 0 10 0.0 52 10 0.0 high density graphs.
300 3 11 10 0.0 – 0 – Again for blood-type and low density graphs the C formulation
500 26 605 7(7) 0.0 – 0 – dominates over the EE for lower values of k, being able to solve
70 4 0 1 10 0.0 385 10 0.0 some problems with 1000 pairs for k = 3. However, as in the previ-
100 2 5 10 0.0 – 0 – ous analysis results for medium and high density graphs confirm
200 44 341 8(8) 0.0 – 0 –
the effectiveness of the compact formulation on dense graphs with
70 5 10 10 10 0.0 371 10 0.0 large values of k. With the cycle formulation it was possible to
100 64 226 10 0.0 – 0 0.0
solve instances for k = 3 and some instances for k = 4. This formu-
70 6 368 211 10 0.0 90 10 0.0
100 – – 0 – 240 4 0.0 lation was not capable of solving any instance with k > 4 within
the limit on number of cycles considered. For these values of k
Medium density test instances the EE was more efficient being able to solve to optimality some
70 3 0 0 10 0.0 127 10 0.0 instances.
100 0 4 10 0.0 270 5 0.0
300 5 279 10 0.0 – 0 –
To conclude, these results clearly indicate that appropriate
400 13 204 4(4) 0.0 – 0 – methods have to be implemented if one wishes to use any of the
70 4 1 25 10 0.0 138 10 0.0
formulations discussed in larger pools and for bigger size cycles.
100 3 516 9(9) 0.0 460 7 0.0
70 5 – – 0 – 45 10 0.0 8. Conclusions
100 – – 0 – 360 7 0.5a
70 6 – – 0 – 33 10 0.0 This paper presents two new formulations for the Kidney Ex-
100 – – 0 – 177 8 0.5a change Problem – edge-assignment and extended edge formula-
tions – that have the advantage over other formulations
High density test instances
proposed in the literature of having polynomially bounded number
70 3 0 2 10 0.0 161 10 0.0
100 0 5 10 0.0 505 7 0.6 of constraints and variables. A proof of dominance of some formu-
200 2 167 10 0.0 – 0 – lations over others is also given and a discussion on the adaptabil-
70 4 2 301 9 0.0 90 10 0.0 ity of each formulation to different problem variants is provided.
100 – – 0 – 419 7 0.3a Finally, computational results that compare the previous and pro-
70 5 – – 0 – 37 10 0.0 posed formulations in terms of time needed to find an optimal
100 – – 0 – 402 8 0.2 solution and of the gaps of linear relaxations upper bounds of the
70 6 – – 0 – 39 10 0.0 models are provided.
100 – – 0 – 247 10 0.0 Computational results show that the edge formulation has a
a bad performance and that it is not effective at solving instances
For the test instances which were not solved to optimality within the time limit
with any formulation the gap value for the best found lower bound is given by larger than 50 pairs. The non-compact cycle formulation is very
gap ¼ UBLB
LB  100%, where LB is the best found lower bound and UB is the LP upper
efficient for low density graphs with small values of k. However
bound for the optimal value. for larger values of k and especially if graphs are denser this for-
mulation becomes inefficient. In such cases compact formula-
tions provide better results – in particular the extended edge
for the low density test instances. No results are provided for these formulation – and are able to solve larger problems. Therefore,
formulations before reduction as they were clearly worse. although we prove in this paper that linear relaxations of the
The results of the computational study for small instances show compact formulations do not provide better upper bounds for
that in general CPU times increase with increasing k and graph optimal solutions than the cycle formulation, computational re-
density for the cycle formulation; however they decrease with sults reinforce the idea that compact formulations are of practi-
increasing density for the other models and decrease with increas- cal relevance.
ing k for compact formulations. Increasing times for the cycle and As future work an interesting direction is to use decomposition
edge formulations can be justified by the increasing number of methods on the extended edge formulation, in order to solve larger
68 M. Constantino et al. / European Journal of Operational Research 231 (2013) 57–68

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