Influence of Traditional Cardiovascular Risk Factors in the Recipient on the Development of Cardiac Allograft Vasculopathy After Heart Transplantation

Abstract Background Cardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence of cardiovascular risk factors (CVRFs) in HT recipients on the development of CAV after 1 year of follow-up. Materials and Methods F...

Full description

Saved in:
Bibliographic Details
Published in:Transplantation proceedings Vol. 40; no. 9; pp. 3056 - 3057
Main Authors: Lázaro, I.J.Sánchez, Bonet, L. Almenar, López, J. Moro, Lacuesta, E.Sánchez, Martínez-Dolz, L, Ramón-Llín, J. Agüero, Lalaguna, L. Andrés, Pérez, O. Cano, Martínez, V. Ortiz, Fuentes, F. Buendía, Sanz, A. Salvador
Format: Journal Article Conference Proceeding
Language:English
Published: Amsterdam Elsevier Inc 01-11-2008
Elsevier
Subjects:
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
Abstract Abstract Background Cardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence of cardiovascular risk factors (CVRFs) in HT recipients on the development of CAV after 1 year of follow-up. Materials and Methods From 2001 to 2005, we studied 72 patients who received a HT and survived for at least 1 years. All patients underwent coronary arteriography and intravascular ultrasonography at 1 year after HT. Cardiac allograft vasculopathy was defined as intimal proliferation of 0.5 mm or more. The analyzed CVRFs were age, sex, body mass index, diabetes mellitus, hypertension, dyslipidemia, and smoking. We also considered the heart disease that was the reason for HT. The statistical tests used in the univariate analysis were the t and χ2 tests. Logistic regression was performed with the variables obtained at univariate analysis. Results Mean (SD) recipient age at HT was 51 (9) years. Eighty patients (90.5%) were men. Dyslipidemia was significantly associated with a greater incidence of CAV at 1 year (68.3% vs 41.9%; P = .03). Ischemia, as opposed to all other causes, was also significantly associated with CAV (69.4% vs 44.4%; P = .03). Older age, hypertension, smoking history, and high body mass index were associated with a higher incidence of CAV, albeit without statistical significance. At multivariate analysis, dyslipidemia was the most significant CVRF ( P = .045) for the development of CAV. Conclusions Recipient dyslipidemia is a risk factor for the development of CAV in HT. The remaining traditional CVRFs are more weakly associated with CAV. After HT close monitoring of recipients with pretransplantation CVRFs is essential for early detection of CAV.
AbstractList BACKGROUNDCardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence of cardiovascular risk factors (CVRFs) in HT recipients on the development of CAV after 1 year of follow-up.MATERIALS AND METHODSFrom 2001 to 2005, we studied 72 patients who received a HT and survived for at least 1 years. All patients underwent coronary arteriography and intravascular ultrasonography at 1 year after HT. Cardiac allograft vasculopathy was defined as intimal proliferation of 0.5 mm or more. The analyzed CVRFs were age, sex, body mass index, diabetes mellitus, hypertension, dyslipidemia, and smoking. We also considered the heart disease that was the reason for HT. The statistical tests used in the univariate analysis were the t and chi(2) tests. Logistic regression was performed with the variables obtained at univariate analysis.RESULTSMean (SD) recipient age at HT was 51 (9) years. Eighty patients (90.5%) were men. Dyslipidemia was significantly associated with a greater incidence of CAV at 1 year (68.3% vs 41.9%; P = .03). Ischemia, as opposed to all other causes, was also significantly associated with CAV (69.4% vs 44.4%; P = .03). Older age, hypertension, smoking history, and high body mass index were associated with a higher incidence of CAV, albeit without statistical significance. At multivariate analysis, dyslipidemia was the most significant CVRF (P = .045) for the development of CAV.CONCLUSIONSRecipient dyslipidemia is a risk factor for the development of CAV in HT. The remaining traditional CVRFs are more weakly associated with CAV. After HT close monitoring of recipients with pretransplantation CVRFs is essential for early detection of CAV.
Abstract Background Cardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence of cardiovascular risk factors (CVRFs) in HT recipients on the development of CAV after 1 year of follow-up. Materials and Methods From 2001 to 2005, we studied 72 patients who received a HT and survived for at least 1 years. All patients underwent coronary arteriography and intravascular ultrasonography at 1 year after HT. Cardiac allograft vasculopathy was defined as intimal proliferation of 0.5 mm or more. The analyzed CVRFs were age, sex, body mass index, diabetes mellitus, hypertension, dyslipidemia, and smoking. We also considered the heart disease that was the reason for HT. The statistical tests used in the univariate analysis were the t and χ2 tests. Logistic regression was performed with the variables obtained at univariate analysis. Results Mean (SD) recipient age at HT was 51 (9) years. Eighty patients (90.5%) were men. Dyslipidemia was significantly associated with a greater incidence of CAV at 1 year (68.3% vs 41.9%; P = .03). Ischemia, as opposed to all other causes, was also significantly associated with CAV (69.4% vs 44.4%; P = .03). Older age, hypertension, smoking history, and high body mass index were associated with a higher incidence of CAV, albeit without statistical significance. At multivariate analysis, dyslipidemia was the most significant CVRF ( P = .045) for the development of CAV. Conclusions Recipient dyslipidemia is a risk factor for the development of CAV in HT. The remaining traditional CVRFs are more weakly associated with CAV. After HT close monitoring of recipients with pretransplantation CVRFs is essential for early detection of CAV.
Cardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence of cardiovascular risk factors (CVRFs) in HT recipients on the development of CAV after 1 year of follow-up. From 2001 to 2005, we studied 72 patients who received a HT and survived for at least 1 years. All patients underwent coronary arteriography and intravascular ultrasonography at 1 year after HT. Cardiac allograft vasculopathy was defined as intimal proliferation of 0.5 mm or more. The analyzed CVRFs were age, sex, body mass index, diabetes mellitus, hypertension, dyslipidemia, and smoking. We also considered the heart disease that was the reason for HT. The statistical tests used in the univariate analysis were the t and chi(2) tests. Logistic regression was performed with the variables obtained at univariate analysis. Mean (SD) recipient age at HT was 51 (9) years. Eighty patients (90.5%) were men. Dyslipidemia was significantly associated with a greater incidence of CAV at 1 year (68.3% vs 41.9%; P = .03). Ischemia, as opposed to all other causes, was also significantly associated with CAV (69.4% vs 44.4%; P = .03). Older age, hypertension, smoking history, and high body mass index were associated with a higher incidence of CAV, albeit without statistical significance. At multivariate analysis, dyslipidemia was the most significant CVRF (P = .045) for the development of CAV. Recipient dyslipidemia is a risk factor for the development of CAV in HT. The remaining traditional CVRFs are more weakly associated with CAV. After HT close monitoring of recipients with pretransplantation CVRFs is essential for early detection of CAV.
Cardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence of cardiovascular risk factors (CVRFs) in HT recipients on the development of CAV after 1 year of follow-up. From 2001 to 2005, we studied 72 patients who received a HT and survived for at least 1 years. All patients underwent coronary arteriography and intravascular ultrasonography at 1 year after HT. Cardiac allograft vasculopathy was defined as intimal proliferation of 0.5 mm or more. The analyzed CVRFs were age, sex, body mass index, diabetes mellitus, hypertension, dyslipidemia, and smoking. We also considered the heart disease that was the reason for HT. The statistical tests used in the univariate analysis were the t and χ 2 tests. Logistic regression was performed with the variables obtained at univariate analysis. Mean (SD) recipient age at HT was 51 (9) years. Eighty patients (90.5%) were men. Dyslipidemia was significantly associated with a greater incidence of CAV at 1 year (68.3% vs 41.9%; P = .03). Ischemia, as opposed to all other causes, was also significantly associated with CAV (69.4% vs 44.4%; P = .03). Older age, hypertension, smoking history, and high body mass index were associated with a higher incidence of CAV, albeit without statistical significance. At multivariate analysis, dyslipidemia was the most significant CVRF ( P = .045) for the development of CAV. Recipient dyslipidemia is a risk factor for the development of CAV in HT. The remaining traditional CVRFs are more weakly associated with CAV. After HT close monitoring of recipients with pretransplantation CVRFs is essential for early detection of CAV.
Author Sanz, A. Salvador
Pérez, O. Cano
Ramón-Llín, J. Agüero
Fuentes, F. Buendía
Martínez, V. Ortiz
Martínez-Dolz, L
Lacuesta, E.Sánchez
Lalaguna, L. Andrés
Bonet, L. Almenar
Lázaro, I.J.Sánchez
López, J. Moro
Author_xml – sequence: 1
  fullname: Lázaro, I.J.Sánchez
– sequence: 2
  fullname: Bonet, L. Almenar
– sequence: 3
  fullname: López, J. Moro
– sequence: 4
  fullname: Lacuesta, E.Sánchez
– sequence: 5
  fullname: Martínez-Dolz, L
– sequence: 6
  fullname: Ramón-Llín, J. Agüero
– sequence: 7
  fullname: Lalaguna, L. Andrés
– sequence: 8
  fullname: Pérez, O. Cano
– sequence: 9
  fullname: Martínez, V. Ortiz
– sequence: 10
  fullname: Fuentes, F. Buendía
– sequence: 11
  fullname: Sanz, A. Salvador
BackLink http://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20876149$$DView record in Pascal Francis
https://www.ncbi.nlm.nih.gov/pubmed/19010192$$D View this record in MEDLINE/PubMed
BookMark eNqNUl1rFDEUDVKx2-pfkCDo26y5k_mKD8KytbZQEGr1NWQzd2y22ck0ySzsH_H3muksRXwSLoTcnHvOzT33jJz0rkdC3gFbAoPq43YZverD4J1GbJc5Y80yBUD5giygqXmWVzk_IQvGCsiAF-UpOQthy9I9L_grcgqCJSaRL8jv676zI_YaqevonVeticb1ytK18q1xexX0aJWntyY80Eulo_OBmp7Ge6S3qM1gsI_UzYkL3KN1w-4p1c0UStOVte6XV12kP5_o3KDi_YGuuoieXqHycVJOP7Kqj2rSf01edsoGfHM8z8mPyy9366vs5tvX6_XqJtNFxWOmoeSwKZkQldjwRrei0VBBDh2vCgDWCFEIULiBNtdMIArOapGLUlUKFRb8nHyYedMwH0cMUe5M0GhTI-jGICtRi6IuqwT8NAO1dyF47OTgzU75gwQmJ1fkVv7tipxckSmSK6n47VFl3OzS23Pp0YYEeH8EpPko2yUibcIzLmdNXUEhEu5ixmGayd6gl0GbybzWeNRRts78Xz-f_6HR1vQmKT_gAcPWjT5tQJAgQy6Z_D7t0bRGrGEAgtf8D28syt0
CODEN TRPPA8
CitedBy_id crossref_primary_10_1007_s40472_016_0105_x
crossref_primary_10_1007_s40472_019_0232_2
crossref_primary_10_1016_j_healun_2011_04_008
crossref_primary_10_1016_j_athoracsur_2010_03_043
crossref_primary_10_1111_j_1751_7117_2009_00049_x
crossref_primary_10_1016_j_heliyon_2023_e20230
crossref_primary_10_1017_S1047951121003784
crossref_primary_10_1097_TP_0b013e3182398058
crossref_primary_10_4236_pp_2014_510107
crossref_primary_10_1111_j_1399_0012_2011_01565_x
crossref_primary_10_1097_JCN_0b013e31822ce6c9
crossref_primary_10_1097_CRD_0000000000000437
crossref_primary_10_1007_s00392_024_02477_4
crossref_primary_10_1172_JCI90596
crossref_primary_10_1007_s12265_012_9414_3
crossref_primary_10_1097_MOT_0b013e32833deb03
crossref_primary_10_1016_j_ijcard_2022_06_062
crossref_primary_10_1097_MOT_0000000000000381
crossref_primary_10_1016_j_carpath_2014_05_001
crossref_primary_10_1016_j_ijcard_2021_02_002
crossref_primary_10_1016_j_healun_2016_06_004
crossref_primary_10_1016_j_healun_2018_04_002
crossref_primary_10_1016_j_trim_2011_11_005
crossref_primary_10_1016_j_crvasa_2017_03_002
crossref_primary_10_15825_1995_1191_2017_1_89_102
crossref_primary_10_3892_etm_2014_1714
crossref_primary_10_1097_TP_0000000000000848
crossref_primary_10_1016_j_transproceed_2011_05_015
Cites_doi 10.1016/j.healun.2004.03.009
10.1157/13111790
10.1056/NEJMoa022171
ContentType Journal Article
Conference Proceeding
Copyright Elsevier Inc.
2008 Elsevier Inc.
2009 INIST-CNRS
Copyright_xml – notice: Elsevier Inc.
– notice: 2008 Elsevier Inc.
– notice: 2009 INIST-CNRS
DBID IQODW
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
DOI 10.1016/j.transproceed.2008.08.115
DatabaseName Pascal-Francis
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
CrossRef
MEDLINE - Academic
DatabaseTitle MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
CrossRef
MEDLINE - Academic
DatabaseTitleList MEDLINE - Academic

MEDLINE

Database_xml – sequence: 1
  dbid: ECM
  name: MEDLINE
  url: https://search.ebscohost.com/login.aspx?direct=true&db=cmedm&site=ehost-live
  sourceTypes: Index Database
DeliveryMethod fulltext_linktorsrc
Discipline Anatomy & Physiology
Biology
Pharmacy, Therapeutics, & Pharmacology
EISSN 1873-2623
EndPage 3057
ExternalDocumentID 10_1016_j_transproceed_2008_08_115
19010192
20876149
S0041134508011937
1_s2_0_S0041134508011937
Genre Journal Article
GroupedDBID ---
--K
--M
.1-
.55
.FO
.GJ
.~1
0R~
123
1B1
1P~
1~.
1~5
29Q
3O-
4.4
457
4G.
53G
5RE
5VS
7-5
71M
8P~
AABNK
AACTN
AAEDT
AAEDW
AAIKJ
AAKOC
AALRI
AAOAW
AAQFI
AAQXK
AAXKI
AAXUO
ABBQC
ABFRF
ABJNI
ABLJU
ABMAC
ABMZM
ABOCM
ABXDB
ACDAQ
ACGFO
ACIUM
ACRLP
ADBBV
ADEZE
ADMUD
AEBSH
AEFWE
AEKER
AENEX
AEVXI
AFCTW
AFJKZ
AFKWA
AFRHN
AFTJW
AFXIZ
AGHFR
AGUBO
AGYEJ
AIEXJ
AIKHN
AITUG
AJOXV
AJRQY
AJUYK
AKRWK
ALMA_UNASSIGNED_HOLDINGS
AMFUW
AMRAJ
ANZVX
ASPBG
AVWKF
AXJTR
AZFZN
BKOJK
BLXMC
BNPGV
CS3
DU5
EBS
EFJIC
EJD
EO8
EO9
EP2
EP3
F5P
FDB
FEDTE
FGOYB
FIRID
FNPLU
FYGXN
G-Q
GBLVA
HVGLF
HZ~
IHE
J1W
J5H
K-O
KOM
L7B
M41
MO0
N9A
O-L
O9-
OAUVE
OK-
OW-
OZT
P-8
P-9
P2P
PC.
Q38
R2-
RIG
ROL
RPZ
SCC
SDF
SDG
SDP
SEL
SES
SEW
SPCBC
SSH
SSZ
T5K
UDS
WH7
X7M
XPP
Y6R
Z5R
ZGI
ZXP
~G-
AAIAV
ABLVK
ABYKQ
AHPSJ
AJBFU
EFLBG
LCYCR
ZA5
08R
AAPBV
AAUGY
ABPIF
ABPTK
IQODW
CGR
CUY
CVF
ECM
EIF
NPM
AAYXX
CITATION
7X8
ID FETCH-LOGICAL-c463t-c1531b509969b38cd98c16121f364110899491aeb1d2c09ee93079295a6aeae43
ISSN 0041-1345
IngestDate Fri Oct 25 11:07:31 EDT 2024
Thu Sep 26 17:05:40 EDT 2024
Sat Sep 28 07:54:14 EDT 2024
Sun Oct 22 16:09:37 EDT 2023
Fri Feb 23 02:33:26 EST 2024
Tue Oct 15 22:56:12 EDT 2024
IsPeerReviewed true
IsScholarly true
Issue 9
Keywords Heart
Human
Cardiovascular disease
Recipient
Transplantation
Homotransplantation
Epidemiology
Vascular disease
Medicine
Graft vascular disease
Treatment
Surgery
Atherosclerosis
Risk factor
Cardiovascular risk
Development
Graft
Circulatory system
Influence factor
Language English
License CC BY 4.0
LinkModel OpenURL
MergedId FETCHMERGED-LOGICAL-c463t-c1531b509969b38cd98c16121f364110899491aeb1d2c09ee93079295a6aeae43
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
PMID 19010192
PQID 69794756
PQPubID 23479
PageCount 2
ParticipantIDs proquest_miscellaneous_69794756
crossref_primary_10_1016_j_transproceed_2008_08_115
pubmed_primary_19010192
pascalfrancis_primary_20876149
elsevier_sciencedirect_doi_10_1016_j_transproceed_2008_08_115
elsevier_clinicalkeyesjournals_1_s2_0_S0041134508011937
PublicationCentury 2000
PublicationDate 2008-11-01
PublicationDateYYYYMMDD 2008-11-01
PublicationDate_xml – month: 11
  year: 2008
  text: 2008-11-01
  day: 01
PublicationDecade 2000
PublicationPlace Amsterdam
PublicationPlace_xml – name: Amsterdam
– name: United States
PublicationTitle Transplantation proceedings
PublicationTitleAlternate Transplant Proc
PublicationYear 2008
Publisher Elsevier Inc
Elsevier
Publisher_xml – name: Elsevier Inc
– name: Elsevier
References Almenar-Bonet (bib1) 2007; 60
Eisen, Tuzcu, Dorent (bib3) 2003; 28
Valantine (bib2) 2004; 23
Almenar-Bonet (10.1016/j.transproceed.2008.08.115_bib1) 2007; 60
Valantine (10.1016/j.transproceed.2008.08.115_bib2) 2004; 23
Eisen (10.1016/j.transproceed.2008.08.115_bib3) 2003; 28
References_xml – volume: 23
  start-page: S187
  year: 2004
  ident: bib2
  article-title: Cardiac allograft vasculopathy after heart transplantation: risk factors and management
  publication-title: J Heart Lung Transplant
  contributor:
    fullname: Valantine
– volume: 28
  start-page: 847
  year: 2003
  ident: bib3
  article-title: Everolimus for the prevention of allograft rejection and vasculopathy in cardiac-transplant recipients
  publication-title: N Engl J Med
  contributor:
    fullname: Dorent
– volume: 60
  start-page: 1177
  year: 2007
  ident: bib1
  article-title: Spanish Heart Transplantation Registry: 18th official report of the Spanish Society of Cardiology Working Group on Heart Failure, Heart Transplantation, and Associated Therapies (1984–2006) [in Spanish]
  publication-title: Rev Esp Cardiol
  contributor:
    fullname: Almenar-Bonet
– volume: 23
  start-page: S187
  year: 2004
  ident: 10.1016/j.transproceed.2008.08.115_bib2
  article-title: Cardiac allograft vasculopathy after heart transplantation: risk factors and management
  publication-title: J Heart Lung Transplant
  doi: 10.1016/j.healun.2004.03.009
  contributor:
    fullname: Valantine
– volume: 60
  start-page: 1177
  year: 2007
  ident: 10.1016/j.transproceed.2008.08.115_bib1
  article-title: Spanish Heart Transplantation Registry: 18th official report of the Spanish Society of Cardiology Working Group on Heart Failure, Heart Transplantation, and Associated Therapies (1984–2006) [in Spanish]
  publication-title: Rev Esp Cardiol
  doi: 10.1157/13111790
  contributor:
    fullname: Almenar-Bonet
– volume: 28
  start-page: 847
  year: 2003
  ident: 10.1016/j.transproceed.2008.08.115_bib3
  article-title: Everolimus for the prevention of allograft rejection and vasculopathy in cardiac-transplant recipients
  publication-title: N Engl J Med
  doi: 10.1056/NEJMoa022171
  contributor:
    fullname: Eisen
SSID ssj0004243
Score 2.0503483
Snippet Abstract Background Cardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the...
Cardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence of...
BACKGROUNDCardiac allograft vasculopathy (CAV) is the leading cause of death heart transplant (HT) recipients after the first year. We assessed the influence...
SourceID proquest
crossref
pubmed
pascalfrancis
elsevier
SourceType Aggregation Database
Index Database
Publisher
StartPage 3056
SubjectTerms Analysis of Variance
Atherosclerosis (general aspects, experimental research)
Biological and medical sciences
Blood and lymphatic vessels
Body Mass Index
Cardiology. Vascular system
Cardiovascular Diseases - epidemiology
Dyslipidemias - complications
Female
Follow-Up Studies
Fundamental and applied biological sciences. Psychology
Fundamental immunology
Heart Diseases - classification
Heart Diseases - surgery
Heart Transplantation - adverse effects
Heart Transplantation - mortality
Heart Transplantation - pathology
Humans
Male
Medical sciences
Middle Aged
Retrospective Studies
Risk Factors
Smoking - epidemiology
Surgery
Surgery (general aspects). Transplantations, organ and tissue grafts. Graft diseases
Time Factors
Tissue, organ and graft immunology
Transplantation, Homologous - pathology
Vascular Diseases - epidemiology
Title Influence of Traditional Cardiovascular Risk Factors in the Recipient on the Development of Cardiac Allograft Vasculopathy After Heart Transplantation
URI https://www.clinicalkey.es/playcontent/1-s2.0-S0041134508011937
https://dx.doi.org/10.1016/j.transproceed.2008.08.115
https://www.ncbi.nlm.nih.gov/pubmed/19010192
https://search.proquest.com/docview/69794756
Volume 40
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
link http://sdu.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwtV1Lb9NAEF6lRUhIHKAtNDzKHlAvrqP4Edt74OCmroKUJlEaKpSLtX5EShXsCDuH_BF-L7Mv2wlEwIGL5ay868d82ZnZ_WYGoY9xYkRJN6F6QiMHHJSFqxPCdgpBv0ZeRB2ry-KdB_fu6Kt3E9hBq6UqkNZt_1XS0AayZpGz_yDtalBogHOQORxB6nD8Ve6H1c96RTNJJKwvKpoA-azKkzB7EfokS7ks2N-lqE4Z-fxWluWRrEgwNpfrJacRiIYG90hEfDHcxZq_4imxF6X2wIfLWQHkrebzwuQD-PSltve01YqPP-oPgrk29Of-dMxnsk69heUP74KRP9Wux6NgVsdO8H7DB_9mPNVggPnOWu3deDrWhuNJMK93w9Ryhyfj_qo1OGkwNOd029ANSySl7KRiGvdcSzcdEcms5nmRFkrimTQmbeZFNQwA-On-VrmIdY7HTsk_jJCdZON6oHp6tUpVNII9TVvxH02WCBB80yP0hJemZ3FPvWkdz2sqtqd4M5Usl_MSD939kGH1fA0CpquFqNNy2JHiBtXsBTqrQ03xpALoS9RKsxN06me0zL9t8SXmDGW-9XOCnl6rs8uJyLi-vcKzOoCwuOIdqlzs21P0o0I5zhe4gXK8i3LMUI4lyvEywwBqXKEc56KhgXI2nEQ5rlCOmyjHHOWYoxzvofwMfbkNZv2BLkuR6LHtWKUeg2FgRGBcE4dElhcnxIsNlnxvYTk2i6QhxCYGBcMnMeMuSVMCuhM8jx51aEpT23qFjrM8S88Rtp2E-QieZVm2zao5xCY1YocQai5IjxhtZCk5hmuRcSZUVMzHsCl9WULWAy--10auEnmoYqrBCkgLOTUVoREWZtgN7xmqGKjAVTTAe3Pb6FPVU1rdwpoOAfd_deeLHYRVD61A3kYfFORC0F1sQ5Jmab4pQoeANeD2nDZ6LZBYvzBjjYHz-eZPg79Fz-pZ4h06Lr9v0vfoqEg2F_w_9ROt0Bcx
link.rule.ids 310,311,315,782,786,791,792,23939,23940,25149,27933,27934
linkProvider Elsevier
openUrl ctx_ver=Z39.88-2004&ctx_enc=info%3Aofi%2Fenc%3AUTF-8&rfr_id=info%3Asid%2Fsummon.serialssolutions.com&rft_val_fmt=info%3Aofi%2Ffmt%3Akev%3Amtx%3Ajournal&rft.genre=proceeding&rft.title=Transplantation+proceedings&rft.atitle=Influence+of+Traditional+Cardiovascular+Risk+Factors+in+the+Recipient+on+the+Development+of+Cardiac+Allograft+Vasculopathy+After+Heart+Transplantation&rft.au=SANCHEZ+LAZARO%2C+I.+J&rft.au=ALMENAR+BONET%2C+L&rft.au=SALVADOR+SANZ%2C+A&rft.au=MORO+LOPEZ%2C+J&rft.date=2008-11-01&rft.pub=Elsevier&rft.issn=0041-1345&rft.eissn=1873-2623&rft.volume=40&rft.issue=9&rft.spage=3056&rft.epage=3057&rft_id=info:doi/10.1016%2Fj.transproceed.2008.08.115&rft.externalDBID=n%2Fa&rft.externalDocID=20876149
thumbnail_m http://sdu.summon.serialssolutions.com/2.0.0/image/custom?url=https%3A%2F%2Fcdn.clinicalkey.com%2Fck-thumbnails%2F00411345%2FS0041134508X00107%2Fcov150h.gif