Alkaline phosphatase activity after cardiothoracic surgery in infants and correlation with post-operative support and inflammation: a prospective cohort study

Introduction Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in m...

Full description

Saved in:
Bibliographic Details
Published inCritical care (London, England) Vol. 16; no. 4; p. R160
Main Authors Davidson, Jesse, Tong, Suhong, Hauck, Amanda, Lawson, D Scott, Jaggers, James, Kaufman, Jon, da Cruz, Eduardo
Format Journal Article
LanguageEnglish
Published London BioMed Central 20.08.2012
BioMed Central Ltd
Subjects
Online AccessGet full text
ISSN1364-8535
1466-609X
1364-8535
1466-609X
DOI10.1186/cc11483

Cover

Abstract Introduction Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in multiple settings, including during adult cardiopulmonary bypass. We sought to describe the change in alkaline phosphatase activity after cardiothoracic surgery in infants and to assess for a correlation with intensity and duration of post-operative support, markers of inflammation, and short-term clinical outcomes. Methods Sub-analysis of a prospective observational study on the kinetics of procalcitonin in 70 infants (≤90 days old) undergoing cardiothoracic surgery. Subjects were grouped based on the use of cardiopulmonary bypass and delayed sternal closure. Alkaline phosphatase, procalcitonin, and C-reactive protein (CRP) levels were obtained pre-operation and on post-operative day 1. Mean change in alkaline phosphatase activity was determined in each surgical group. Generalized linear modeling and logistic regression were employed to assess for associations between post-operative alkaline phosphatase activity and post-operative support, inflammation, and short term outcomes. Primary endpoints were vasoactive-inotropic score at 24 hours and length of intubation. Secondary endpoints included procalcitonin/CRP levels on post-operative day 1, length of hospital stay, and cardiac arrest or death. Results Mean decrease in alkaline phosphatase was 30 U/L (p = 0.01) in the non-bypass group, 114 U/L (p<0.0001) in the bypass group, and 94 U/L (p<0.0001) in the delayed sternal closure group. On multivariate analysis, each 10 U/L decrease in alkaline phosphatase activity on post-operative day 1 was independently associated with an increase in vasoactive-inotropic score by 0.7 (p<0.0001), intubation time by 6% (p<0.05), hospital stay by 5% (p<0.05), and procalcitonin by 14% (P<0.01), with a trend towards increased odds of cardiac arrest or death (OR 1.3; p = 0.06). Post-operative alkaline phosphatase activity was not associated with CRP (p = 0.7). Conclusions Alkaline phosphatase activity decreases after cardiothoracic surgery in infants. Low post-operative alkaline phosphatase activity is independently associated with increased procalcitonin, increased vasoactive/inotropic support, prolonged intubation time, and prolonged hospital stay. Alkaline phosphatase may serve as a biomarker and potential modulator of post-operative support and inflammation following cardiothoracic surgery in infants.
AbstractList Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in multiple settings, including during adult cardiopulmonary bypass. We sought to describe the change in alkaline phosphatase activity after cardiothoracic surgery in infants and to assess for a correlation with intensity and duration of post-operative support, markers of inflammation, and short-term clinical outcomes. Sub-analysis of a prospective observational study on the kinetics of procalcitonin in 70 infants (≤ 90 days old) undergoing cardiothoracic surgery. Subjects were grouped based on the use of cardiopulmonary bypass and delayed sternal closure. Alkaline phosphatase, procalcitonin, and C-reactive protein (CRP) levels were obtained pre-operation and on post-operative day 1. Mean change in alkaline phosphatase activity was determined in each surgical group. Generalized linear modeling and logistic regression were employed to assess for associations between post-operative alkaline phosphatase activity and post-operative support, inflammation, and short term outcomes. Primary endpoints were vasoactive-inotropic score at 24 hours and length of intubation. Secondary endpoints included procalcitonin/CRP levels on post-operative day 1, length of hospital stay, and cardiac arrest or death. Mean decrease in alkaline phosphatase was 30 U/L (p = 0.01) in the non-bypass group, 114 U/L (p < 0.0001) in the bypass group, and 94 U/L (p < 0.0001) in the delayed sternal closure group. On multivariate analysis, each 10 U/L decrease in alkaline phosphatase activity on post-operative day 1 was independently associated with an increase in vasoactive-inotropic score by 0.7 (p < 0.0001), intubation time by 6% (p < 0.05), hospital stay by 5% (p < 0.05), and procalcitonin by 14% (P < 0.01), with a trend towards increased odds of cardiac arrest or death (OR 1.3; p = 0.06). Post-operative alkaline phosphatase activity was not associated with CRP (p = 0.7). Alkaline phosphatase activity decreases after cardiothoracic surgery in infants. Low post-operative alkaline phosphatase activity is independently associated with increased procalcitonin, increased vasoactive/inotropic support, prolonged intubation time, and prolonged hospital stay. Alkaline phosphatase may serve as a biomarker and potential modulator of post-operative support and inflammation following cardiothoracic surgery in infants.
Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in multiple settings, including during adult cardiopulmonary bypass. We sought to describe the change in alkaline phosphatase activity after cardiothoracic surgery in infants and to assess for a correlation with intensity and duration of post-operative support, markers of inflammation, and short-term clinical outcomes.INTRODUCTIONLimited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in multiple settings, including during adult cardiopulmonary bypass. We sought to describe the change in alkaline phosphatase activity after cardiothoracic surgery in infants and to assess for a correlation with intensity and duration of post-operative support, markers of inflammation, and short-term clinical outcomes.Sub-analysis of a prospective observational study on the kinetics of procalcitonin in 70 infants (≤ 90 days old) undergoing cardiothoracic surgery. Subjects were grouped based on the use of cardiopulmonary bypass and delayed sternal closure. Alkaline phosphatase, procalcitonin, and C-reactive protein (CRP) levels were obtained pre-operation and on post-operative day 1. Mean change in alkaline phosphatase activity was determined in each surgical group. Generalized linear modeling and logistic regression were employed to assess for associations between post-operative alkaline phosphatase activity and post-operative support, inflammation, and short term outcomes. Primary endpoints were vasoactive-inotropic score at 24 hours and length of intubation. Secondary endpoints included procalcitonin/CRP levels on post-operative day 1, length of hospital stay, and cardiac arrest or death.METHODSSub-analysis of a prospective observational study on the kinetics of procalcitonin in 70 infants (≤ 90 days old) undergoing cardiothoracic surgery. Subjects were grouped based on the use of cardiopulmonary bypass and delayed sternal closure. Alkaline phosphatase, procalcitonin, and C-reactive protein (CRP) levels were obtained pre-operation and on post-operative day 1. Mean change in alkaline phosphatase activity was determined in each surgical group. Generalized linear modeling and logistic regression were employed to assess for associations between post-operative alkaline phosphatase activity and post-operative support, inflammation, and short term outcomes. Primary endpoints were vasoactive-inotropic score at 24 hours and length of intubation. Secondary endpoints included procalcitonin/CRP levels on post-operative day 1, length of hospital stay, and cardiac arrest or death.Mean decrease in alkaline phosphatase was 30 U/L (p = 0.01) in the non-bypass group, 114 U/L (p < 0.0001) in the bypass group, and 94 U/L (p < 0.0001) in the delayed sternal closure group. On multivariate analysis, each 10 U/L decrease in alkaline phosphatase activity on post-operative day 1 was independently associated with an increase in vasoactive-inotropic score by 0.7 (p < 0.0001), intubation time by 6% (p < 0.05), hospital stay by 5% (p < 0.05), and procalcitonin by 14% (P < 0.01), with a trend towards increased odds of cardiac arrest or death (OR 1.3; p = 0.06). Post-operative alkaline phosphatase activity was not associated with CRP (p = 0.7).RESULTSMean decrease in alkaline phosphatase was 30 U/L (p = 0.01) in the non-bypass group, 114 U/L (p < 0.0001) in the bypass group, and 94 U/L (p < 0.0001) in the delayed sternal closure group. On multivariate analysis, each 10 U/L decrease in alkaline phosphatase activity on post-operative day 1 was independently associated with an increase in vasoactive-inotropic score by 0.7 (p < 0.0001), intubation time by 6% (p < 0.05), hospital stay by 5% (p < 0.05), and procalcitonin by 14% (P < 0.01), with a trend towards increased odds of cardiac arrest or death (OR 1.3; p = 0.06). Post-operative alkaline phosphatase activity was not associated with CRP (p = 0.7).Alkaline phosphatase activity decreases after cardiothoracic surgery in infants. Low post-operative alkaline phosphatase activity is independently associated with increased procalcitonin, increased vasoactive/inotropic support, prolonged intubation time, and prolonged hospital stay. Alkaline phosphatase may serve as a biomarker and potential modulator of post-operative support and inflammation following cardiothoracic surgery in infants.CONCLUSIONSAlkaline phosphatase activity decreases after cardiothoracic surgery in infants. Low post-operative alkaline phosphatase activity is independently associated with increased procalcitonin, increased vasoactive/inotropic support, prolonged intubation time, and prolonged hospital stay. Alkaline phosphatase may serve as a biomarker and potential modulator of post-operative support and inflammation following cardiothoracic surgery in infants.
Introduction Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in multiple settings, including during adult cardiopulmonary bypass. We sought to describe the change in alkaline phosphatase activity after cardiothoracic surgery in infants and to assess for a correlation with intensity and duration of post-operative support, markers of inflammation, and short-term clinical outcomes. Methods Sub-analysis of a prospective observational study on the kinetics of procalcitonin in 70 infants (≤90 days old) undergoing cardiothoracic surgery. Subjects were grouped based on the use of cardiopulmonary bypass and delayed sternal closure. Alkaline phosphatase, procalcitonin, and C-reactive protein (CRP) levels were obtained pre-operation and on post-operative day 1. Mean change in alkaline phosphatase activity was determined in each surgical group. Generalized linear modeling and logistic regression were employed to assess for associations between post-operative alkaline phosphatase activity and post-operative support, inflammation, and short term outcomes. Primary endpoints were vasoactive-inotropic score at 24 hours and length of intubation. Secondary endpoints included procalcitonin/CRP levels on post-operative day 1, length of hospital stay, and cardiac arrest or death. Results Mean decrease in alkaline phosphatase was 30 U/L (p = 0.01) in the non-bypass group, 114 U/L (p<0.0001) in the bypass group, and 94 U/L (p<0.0001) in the delayed sternal closure group. On multivariate analysis, each 10 U/L decrease in alkaline phosphatase activity on post-operative day 1 was independently associated with an increase in vasoactive-inotropic score by 0.7 (p<0.0001), intubation time by 6% (p<0.05), hospital stay by 5% (p<0.05), and procalcitonin by 14% (P<0.01), with a trend towards increased odds of cardiac arrest or death (OR 1.3; p = 0.06). Post-operative alkaline phosphatase activity was not associated with CRP (p = 0.7). Conclusions Alkaline phosphatase activity decreases after cardiothoracic surgery in infants. Low post-operative alkaline phosphatase activity is independently associated with increased procalcitonin, increased vasoactive/inotropic support, prolonged intubation time, and prolonged hospital stay. Alkaline phosphatase may serve as a biomarker and potential modulator of post-operative support and inflammation following cardiothoracic surgery in infants.
Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in multiple settings, including during adult cardiopulmonary bypass. We sought to describe the change in alkaline phosphatase activity after cardiothoracic surgery in infants and to assess for a correlation with intensity and duration of post-operative support, markers of inflammation, and short-term clinical outcomes. Sub-analysis of a prospective observational study on the kinetics of procalcitonin in 70 infants ([less than or equai to]90 days old) undergoing cardiothoracic surgery. Subjects were grouped based on the use of cardiopulmonary bypass and delayed sternal closure. Alkaline phosphatase, procalcitonin, and C-reactive protein (CRP) levels were obtained pre-operation and on post-operative day 1. Mean change in alkaline phosphatase activity was determined in each surgical group. Generalized linear modeling and logistic regression were employed to assess for associations between post-operative alkaline phosphatase activity and post-operative support, inflammation, and short term outcomes. Primary endpoints were vasoactive-inotropic score at 24 hours and length of intubation. Secondary endpoints included procalcitonin/CRP levels on post-operative day 1, length of hospital stay, and cardiac arrest or death. Mean decrease in alkaline phosphatase was 30 U/L (p = 0.01) in the non-bypass group, 114 U/L (p<0.0001) in the bypass group, and 94 U/L (p<0.0001) in the delayed sternal closure group. On multivariate analysis, each 10 U/L decrease in alkaline phosphatase activity on post-operative day 1 was independently associated with an increase in vasoactive-inotropic score by 0.7 (p<0.0001), intubation time by 6% (p<0.05), hospital stay by 5% (p<0.05), and procalcitonin by 14% (P<0.01), with a trend towards increased odds of cardiac arrest or death (OR 1.3; p = 0.06). Post-operative alkaline phosphatase activity was not associated with CRP (p = 0.7). Alkaline phosphatase activity decreases after cardiothoracic surgery in infants. Low post-operative alkaline phosphatase activity is independently associated with increased procalcitonin, increased vasoactive/inotropic support, prolonged intubation time, and prolonged hospital stay. Alkaline phosphatase may serve as a biomarker and potential modulator of post-operative support and inflammation following cardiothoracic surgery in infants.
Introduction Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is not known. Recent studies, however, have identified a potential role for alkaline phosphatase as modulator of inflammation in multiple settings, including during adult cardiopulmonary bypass. We sought to describe the change in alkaline phosphatase activity after cardiothoracic surgery in infants and to assess for a correlation with intensity and duration of post-operative support, markers of inflammation, and short-term clinical outcomes. Methods Sub-analysis of a prospective observational study on the kinetics of procalcitonin in 70 infants ([less than or equai to]90 days old) undergoing cardiothoracic surgery. Subjects were grouped based on the use of cardiopulmonary bypass and delayed sternal closure. Alkaline phosphatase, procalcitonin, and C-reactive protein (CRP) levels were obtained pre-operation and on post-operative day 1. Mean change in alkaline phosphatase activity was determined in each surgical group. Generalized linear modeling and logistic regression were employed to assess for associations between post-operative alkaline phosphatase activity and post-operative support, inflammation, and short term outcomes. Primary endpoints were vasoactive-inotropic score at 24 hours and length of intubation. Secondary endpoints included procalcitonin/CRP levels on post-operative day 1, length of hospital stay, and cardiac arrest or death. Results Mean decrease in alkaline phosphatase was 30 U/L (p = 0.01) in the non-bypass group, 114 U/L (p<0.0001) in the bypass group, and 94 U/L (p<0.0001) in the delayed sternal closure group. On multivariate analysis, each 10 U/L decrease in alkaline phosphatase activity on post-operative day 1 was independently associated with an increase in vasoactive-inotropic score by 0.7 (p<0.0001), intubation time by 6% (p<0.05), hospital stay by 5% (p<0.05), and procalcitonin by 14% (P<0.01), with a trend towards increased odds of cardiac arrest or death (OR 1.3; p = 0.06). Post-operative alkaline phosphatase activity was not associated with CRP (p = 0.7). Conclusions Alkaline phosphatase activity decreases after cardiothoracic surgery in infants. Low post-operative alkaline phosphatase activity is independently associated with increased procalcitonin, increased vasoactive/inotropic support, prolonged intubation time, and prolonged hospital stay. Alkaline phosphatase may serve as a biomarker and potential modulator of post-operative support and inflammation following cardiothoracic surgery in infants.
ArticleNumber R160
Audience Academic
Author Tong, Suhong
Jaggers, James
Kaufman, Jon
Lawson, D Scott
Hauck, Amanda
da Cruz, Eduardo
Davidson, Jesse
AuthorAffiliation 1 The Heart Institute, Department of Pediatrics, Children's Hospital Colorado, 13123 East 16th Ave, Box 100 Aurora, CO 80045, USA
2 Department of Biostatistics, University of Colorado Denver, 13001 E 17th Place, Campus Box B119, Aurora, CO 80045, USA
AuthorAffiliation_xml – name: 1 The Heart Institute, Department of Pediatrics, Children's Hospital Colorado, 13123 East 16th Ave, Box 100 Aurora, CO 80045, USA
– name: 2 Department of Biostatistics, University of Colorado Denver, 13001 E 17th Place, Campus Box B119, Aurora, CO 80045, USA
Author_xml – sequence: 1
  givenname: Jesse
  surname: Davidson
  fullname: Davidson, Jesse
  email: jesse.davidson@childrenscolorado.org
  organization: The Heart Institute, Department of Pediatrics, Children's Hospital Colorado
– sequence: 2
  givenname: Suhong
  surname: Tong
  fullname: Tong, Suhong
  organization: Department of Biostatistics, University of Colorado Denver
– sequence: 3
  givenname: Amanda
  surname: Hauck
  fullname: Hauck, Amanda
  organization: The Heart Institute, Department of Pediatrics, Children's Hospital Colorado
– sequence: 4
  givenname: D Scott
  surname: Lawson
  fullname: Lawson, D Scott
  organization: The Heart Institute, Department of Pediatrics, Children's Hospital Colorado
– sequence: 5
  givenname: James
  surname: Jaggers
  fullname: Jaggers, James
  organization: The Heart Institute, Department of Pediatrics, Children's Hospital Colorado
– sequence: 6
  givenname: Jon
  surname: Kaufman
  fullname: Kaufman, Jon
  organization: The Heart Institute, Department of Pediatrics, Children's Hospital Colorado
– sequence: 7
  givenname: Eduardo
  surname: da Cruz
  fullname: da Cruz, Eduardo
  organization: The Heart Institute, Department of Pediatrics, Children's Hospital Colorado
BackLink https://www.ncbi.nlm.nih.gov/pubmed/22906145$$D View this record in MEDLINE/PubMed
BookMark eNp1kltvFSEQxzemxl40fgND4oN92QrsAnt8MDlp6iVp4os-k1mWPUtlYQX2NOfL-FnlXLSt1kACGX4zw_xnTosj550uipcEXxDS8LdKEVI31ZPihFS8LhtWsaN79-PiNMYbjIloePWsOKZ0gTmp2Unxc2m_gzVOo2nwcRogQdQIVDJrkzYI-qQDUhA649PgAyijUJzDSocNMi7vHlyKCFyHlA9BW0jGO3Rr0oAmH1PpJx2yba2z2zT5kHZs9rMwjjv4HQI0hZxcqx2n_LDFYpq7zfPiaQ826heH86z49uHq6-Wn8vrLx8-Xy-tS1XyRSq7bngva60VLadNiWndcCBCEUFLXvG4YZ7TptG5B9Ep0DKClC9aD4IRgwauz4nwfd3YTbG7BWjkFM0LYSILlVmJ5kDij7_foNLej7pR2KcAd7sHIhy_ODHLl17JiDRYM3-XKRf-YdUxyNFFpa8FpP0dJGCMVFRhvc73eoyuwWmbRfI6otrhcsqquakrZlrp4hMqr06NReVB6k-0PHF7dL-HP33-PRQbKPaByX2LQvVQm7ZqVIxv7iCZv_uL_r96h-JgJl8dI3vg5uNzbf9BfXTHm6A
CitedBy_id crossref_primary_10_1371_journal_pone_0158981
crossref_primary_10_1253_circj_CJ_16_1288
crossref_primary_10_3390_biomedicines8090363
crossref_primary_10_1093_nutrit_nuz015
crossref_primary_10_1177_0148607113505326
crossref_primary_10_1097_SHK_0000000000001162
crossref_primary_10_1016_j_cca_2015_04_013
crossref_primary_10_3390_ijerph20043644
crossref_primary_10_1053_j_jvca_2019_10_043
crossref_primary_10_1124_jpet_112_198226
crossref_primary_10_3390_biom11050748
crossref_primary_10_1007_s11011_018_0322_3
crossref_primary_10_1038_s41598_019_50481_w
crossref_primary_10_3390_nu17050775
crossref_primary_10_1093_icvts_ivaa103
crossref_primary_10_1186_s12950_020_00256_2
crossref_primary_10_3390_ijms241411728
crossref_primary_10_1038_pr_2017_325
crossref_primary_10_1590_S0102_86502016001300010
crossref_primary_10_1016_j_jpeds_2017_07_035
crossref_primary_10_1186_s12882_018_1028_9
crossref_primary_10_1177_21501351221100791
Cites_doi 10.1097/01.shk.0000132485.05049.8a
10.1016/j.jss.2010.04.048
10.1016/0002-8703(74)90237-3
10.1186/1471-2431-8-18
10.1073/pnas.0914730107
10.1152/ajpgi.00364.2009
10.1002/ibd.21161
10.1136/gut.2007.128868
10.1186/cc10051
10.1017/S1047951108002904
10.1177/021849230501300422
10.1016/j.anpedi.2010.05.011
10.3109/10408369409084677
10.1017/S1047951103000301
10.1053/j.pcsu.2004.02.011
10.1186/cc11159
10.1007/s11605-010-1405-6
10.1093/clinchem/35.4.664
10.1007/s00228-008-0591-6
10.1093/clinchem/44.8.1621
10.1093/clinchem/33.10.1783
10.1097/PCC.0b013e3181b806fc
10.2174/187221309789257388
10.1097/CCM.0b013e31819598af
10.1016/j.ejcts.2010.06.011
10.1016/j.athoracsur.2005.06.038
ContentType Journal Article
Copyright Davidson et al.; licensee BioMed Central Ltd. 2012
COPYRIGHT 2012 BioMed Central Ltd.
Copyright ©2012 Davidson et al.; licensee BioMed Central Ltd. 2012 Davidson et al.; licensee BioMed Central Ltd.
Copyright_xml – notice: Davidson et al.; licensee BioMed Central Ltd. 2012
– notice: COPYRIGHT 2012 BioMed Central Ltd.
– notice: Copyright ©2012 Davidson et al.; licensee BioMed Central Ltd. 2012 Davidson et al.; licensee BioMed Central Ltd.
DBID C6C
AAYXX
CITATION
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
ADTOC
UNPAY
DOI 10.1186/cc11483
DatabaseName SpringerOpen Free (Free internet resource, activated by CARLI)
CrossRef
Medline
MEDLINE
MEDLINE (Ovid)
MEDLINE
MEDLINE
PubMed
MEDLINE - Academic
PubMed Central (Full Participant titles)
Unpaywall for CDI: Periodical Content
Unpaywall
DatabaseTitle CrossRef
MEDLINE
Medline Complete
MEDLINE with Full Text
PubMed
MEDLINE (Ovid)
MEDLINE - Academic
DatabaseTitleList MEDLINE
MEDLINE - Academic



Database_xml – sequence: 1
  dbid: C6C
  name: Springer Nature OA Free Journals
  url: http://www.springeropen.com/
  sourceTypes: Publisher
– sequence: 2
  dbid: NPM
  name: PubMed
  url: https://proxy.k.utb.cz/login?url=http://www.ncbi.nlm.nih.gov/entrez/query.fcgi?db=PubMed
  sourceTypes: Index Database
– sequence: 3
  dbid: EIF
  name: MEDLINE
  url: https://proxy.k.utb.cz/login?url=https://www.webofscience.com/wos/medline/basic-search
  sourceTypes: Index Database
– sequence: 4
  dbid: UNPAY
  name: Unpaywall
  url: https://proxy.k.utb.cz/login?url=https://unpaywall.org/
  sourceTypes: Open Access Repository
DeliveryMethod fulltext_linktorsrc
Discipline Medicine
EISSN 1364-8535
1466-609X
EndPage R160
ExternalDocumentID 10.1186/cc11483
PMC3580750
A534342253
22906145
10_1186_cc11483
Genre Research Support, Non-U.S. Gov't
Journal Article
Observational Study
Research Support, N.I.H., Extramural
GrantInformation_xml – fundername: NCRR NIH HHS
  grantid: UL1 RR025780
– fundername: NCATS NIH HHS
  grantid: UL1 TR001082
GroupedDBID ---
0R~
29F
2WC
4.4
53G
5GY
5VS
6J9
6PF
AAFWJ
AAJSJ
AASML
AAWTL
ACGFS
ACJQM
ADBBV
ADUKV
AEGXH
AENEX
AFPKN
AHBYD
AHMBA
AHSBF
AHYZX
ALMA_UNASSIGNED_HOLDINGS
AMKLP
AMTXH
AOIAM
AOIJS
BAPOH
BAWUL
BCNDV
BFQNJ
BMC
C6C
CS3
DIK
E3Z
EBD
EBLON
EBS
EJD
EMOBN
F5P
GROUPED_DOAJ
GX1
HYE
IAO
IHR
INH
INR
ITC
KQ8
OK1
PQQKQ
RBZ
ROL
RPM
RSV
SJN
SMD
SOJ
SV3
TR2
U2A
WOQ
YOC
AAYXX
CITATION
-5E
-5G
-BR
ACRMQ
ADINQ
ALIPV
C24
CGR
CUY
CVF
ECM
EIF
NPM
7X8
5PM
7X7
88E
8FI
8FJ
ABUWG
ADTOC
AFKRA
BENPR
BPHCQ
BVXVI
C1A
CCPQU
FYUFA
H13
HMCUK
M1P
O5R
O5S
PHGZM
PHGZT
PIMPY
PJZUB
PPXIY
PROAC
PSQYO
UKHRP
UNPAY
ID FETCH-LOGICAL-c469t-6ebf672fe9b228b024d677a711214464856528deeba7fc7d5aab295fa76110763
IEDL.DBID U2A
ISSN 1364-8535
1466-609X
IngestDate Wed Aug 20 00:17:45 EDT 2025
Thu Aug 21 14:08:52 EDT 2025
Thu Sep 04 19:17:07 EDT 2025
Tue Jun 17 22:05:13 EDT 2025
Tue Jun 10 21:03:45 EDT 2025
Thu Jan 02 22:44:12 EST 2025
Wed Oct 01 04:33:40 EDT 2025
Thu Apr 24 22:53:39 EDT 2025
Sat Sep 06 07:29:35 EDT 2025
IsDoiOpenAccess true
IsOpenAccess true
IsPeerReviewed true
IsScholarly true
Issue 4
Keywords Moderate Inverse Correlation
Total Alkaline Phosphatase Activity
Alkaline Phosphatase Activity
Procalcitonin
Cardiac Intensive Care Unit
Language English
License This is an open access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
cc-by
LinkModel DirectLink
MergedId FETCHMERGED-LOGICAL-c469t-6ebf672fe9b228b024d677a711214464856528deeba7fc7d5aab295fa76110763
Notes ObjectType-Article-1
SourceType-Scholarly Journals-1
ObjectType-Feature-2
content type line 23
ObjectType-Undefined-3
OpenAccessLink https://link.springer.com/10.1186/cc11483
PMID 22906145
PQID 1551327003
PQPubID 23479
ParticipantIDs unpaywall_primary_10_1186_cc11483
pubmedcentral_primary_oai_pubmedcentral_nih_gov_3580750
proquest_miscellaneous_1551327003
gale_infotracmisc_A534342253
gale_infotracacademiconefile_A534342253
pubmed_primary_22906145
crossref_citationtrail_10_1186_cc11483
crossref_primary_10_1186_cc11483
springer_journals_10_1186_cc11483
ProviderPackageCode CITATION
AAYXX
PublicationCentury 2000
PublicationDate 20120820
PublicationDateYYYYMMDD 2012-08-20
PublicationDate_xml – month: 8
  year: 2012
  text: 20120820
  day: 20
PublicationDecade 2010
PublicationPlace London
PublicationPlace_xml – name: London
– name: England
PublicationTitle Critical care (London, England)
PublicationTitleAbbrev Crit Care
PublicationTitleAlternate Crit Care
PublicationYear 2012
Publisher BioMed Central
BioMed Central Ltd
Publisher_xml – name: BioMed Central
– name: BioMed Central Ltd
References VO Van Hoof (933_CR1) 1994; 31
G Lum (933_CR18) 1989; 35
M Lukas (933_CR7) 2010; 16
F Ebrahimi (933_CR14) 2011; 15
PM Crofton (933_CR3) 1987; 33
D Crespo-Marcos (933_CR25) 2010; 73
WR Verweij (933_CR6) 2004; 22
S Heemskerk (933_CR13) 2009; 37
M Beghetti (933_CR24) 2003; 13
F Lacour-Gayet (933_CR21) 2004; 7
A Tuin (933_CR10) 2009; 58
MG Gaies (933_CR22) 2010; 11
P Magnusson (933_CR2) 1998; 44
R Ascione (933_CR17) 2006; 81
S Kats (933_CR8) 2009; 3
DJ Klein (933_CR16) 2011; 15
JS Whitehouse (933_CR11) 2010; 163
ML Jacobs (933_CR20) 2008; 18
P Pickkers (933_CR23) 2012; 16
KT Chen (933_CR4) 2010; 299
EL Campbell (933_CR5) 2010; 107
SG Raja (933_CR15) 2005; 13
M Los Arcos (933_CR26) 2008; 8
S Kats (933_CR9) 2011; 39
P Pickkers (933_CR12) 2009; 65
JM Neutze (933_CR19) 1974; 88
15283368 - Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2004;7:185-91
19063787 - Cardiol Young. 2008 Dec;18 Suppl 2:163-8
19885903 - Inflamm Bowel Dis. 2010 Jul;16(7):1180-6
2702751 - Clin Chem. 1989 Apr;35(4):664-7
4421995 - Am Heart J. 1974 Nov;88(5):553-6
16368344 - Ann Thorac Surg. 2006 Jan;81(1):97-103
19534671 - Recent Pat Inflamm Allergy Drug Discov. 2009 Nov;3(3):214-20
3665030 - Clin Chem. 1987 Oct;33(10):1783-7
21345192 - Crit Care. 2011;15(1):R69
15257092 - Shock. 2004 Aug;22(2):174-9
12887072 - Cardiol Young. 2003 Apr;13(2):161-7
20621577 - An Pediatr (Barc). 2010 Oct;73(4):162-8
19114895 - Crit Care Med. 2009 Feb;37(2):417-23, e1
22269279 - Crit Care. 2012;16(1):R14
20599220 - J Surg Res. 2010 Sep;163(1):79-85
9702948 - Clin Chem. 1998 Aug;44(8 Pt 1):1621-8
16304234 - Asian Cardiovasc Thorac Ann. 2005 Dec;13(4):382-95
20660763 - Proc Natl Acad Sci U S A. 2010 Aug 10;107(32):14298-303
18852260 - Gut. 2009 Mar;58(3):379-87
19048243 - Eur J Clin Pharmacol. 2009 Apr;65(4):393-402
21360208 - J Gastrointest Surg. 2011 May;15(5):860-9
19794327 - Pediatr Crit Care Med. 2010 Mar;11(2):234-8
20663682 - Eur J Cardiothorac Surg. 2011 Apr;39(4):451-8
7818774 - Crit Rev Clin Lab Sci. 1994;31(3):197-293
20489044 - Am J Physiol Gastrointest Liver Physiol. 2010 Aug;299(2):G467-75
18447945 - BMC Pediatr. 2008;8:18
References_xml – volume: 22
  start-page: 174
  year: 2004
  ident: 933_CR6
  publication-title: Shock
  doi: 10.1097/01.shk.0000132485.05049.8a
– volume: 163
  start-page: 79
  year: 2010
  ident: 933_CR11
  publication-title: J Surg Res
  doi: 10.1016/j.jss.2010.04.048
– volume: 88
  start-page: 553
  year: 1974
  ident: 933_CR19
  publication-title: Am Heart J
  doi: 10.1016/0002-8703(74)90237-3
– volume: 8
  start-page: 18
  year: 2008
  ident: 933_CR26
  publication-title: BMC Pediatr
  doi: 10.1186/1471-2431-8-18
– volume: 107
  start-page: 14298
  year: 2010
  ident: 933_CR5
  publication-title: Proc Natl Acad Sci USA
  doi: 10.1073/pnas.0914730107
– volume: 299
  start-page: G467
  year: 2010
  ident: 933_CR4
  publication-title: Am J Physiol Gastrointest Liver Physiol
  doi: 10.1152/ajpgi.00364.2009
– volume: 16
  start-page: 1180
  year: 2010
  ident: 933_CR7
  publication-title: Inflamm Bowel Dis
  doi: 10.1002/ibd.21161
– volume: 58
  start-page: 379
  year: 2009
  ident: 933_CR10
  publication-title: Gut
  doi: 10.1136/gut.2007.128868
– volume: 15
  start-page: R69
  year: 2011
  ident: 933_CR16
  publication-title: Crit Care
  doi: 10.1186/cc10051
– volume: 18
  start-page: 163
  issue: Suppl 2
  year: 2008
  ident: 933_CR20
  publication-title: Cardiol Young
  doi: 10.1017/S1047951108002904
– volume: 13
  start-page: 382
  year: 2005
  ident: 933_CR15
  publication-title: Asian Cardiovasc Thorac Ann
  doi: 10.1177/021849230501300422
– volume: 73
  start-page: 162
  year: 2010
  ident: 933_CR25
  publication-title: An Pediatr (Barc)
  doi: 10.1016/j.anpedi.2010.05.011
– volume: 31
  start-page: 197
  year: 1994
  ident: 933_CR1
  publication-title: Crit Rev Clin Lab Sci
  doi: 10.3109/10408369409084677
– volume: 13
  start-page: 161
  year: 2003
  ident: 933_CR24
  publication-title: Cardiol Young
  doi: 10.1017/S1047951103000301
– volume: 7
  start-page: 185
  year: 2004
  ident: 933_CR21
  publication-title: Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu
  doi: 10.1053/j.pcsu.2004.02.011
– volume: 16
  start-page: R14
  year: 2012
  ident: 933_CR23
  publication-title: Crit Care
  doi: 10.1186/cc11159
– volume: 15
  start-page: 860
  year: 2011
  ident: 933_CR14
  publication-title: J Gastrointest Surg
  doi: 10.1007/s11605-010-1405-6
– volume: 35
  start-page: 664
  year: 1989
  ident: 933_CR18
  publication-title: Clin Chem
  doi: 10.1093/clinchem/35.4.664
– volume: 65
  start-page: 393
  year: 2009
  ident: 933_CR12
  publication-title: Eur J Clin Pharmacol
  doi: 10.1007/s00228-008-0591-6
– volume: 44
  start-page: 1621
  year: 1998
  ident: 933_CR2
  publication-title: Clinical ChemistryI
  doi: 10.1093/clinchem/44.8.1621
– volume: 33
  start-page: 1783
  year: 1987
  ident: 933_CR3
  publication-title: Clin Chem
  doi: 10.1093/clinchem/33.10.1783
– volume: 11
  start-page: 234
  year: 2010
  ident: 933_CR22
  publication-title: Pediatr Crit Care Med
  doi: 10.1097/PCC.0b013e3181b806fc
– volume: 3
  start-page: 214
  year: 2009
  ident: 933_CR8
  publication-title: Recent Pat Inflamm Allergy Drug Discov
  doi: 10.2174/187221309789257388
– volume: 37
  start-page: 417
  year: 2009
  ident: 933_CR13
  publication-title: Crit Care Med
  doi: 10.1097/CCM.0b013e31819598af
– volume: 39
  start-page: 451
  year: 2011
  ident: 933_CR9
  publication-title: Eur J Cardiothorac Surg
  doi: 10.1016/j.ejcts.2010.06.011
– volume: 81
  start-page: 97
  year: 2006
  ident: 933_CR17
  publication-title: Ann Thorac Surg
  doi: 10.1016/j.athoracsur.2005.06.038
– reference: 2702751 - Clin Chem. 1989 Apr;35(4):664-7
– reference: 19794327 - Pediatr Crit Care Med. 2010 Mar;11(2):234-8
– reference: 21360208 - J Gastrointest Surg. 2011 May;15(5):860-9
– reference: 12887072 - Cardiol Young. 2003 Apr;13(2):161-7
– reference: 15257092 - Shock. 2004 Aug;22(2):174-9
– reference: 7818774 - Crit Rev Clin Lab Sci. 1994;31(3):197-293
– reference: 20599220 - J Surg Res. 2010 Sep;163(1):79-85
– reference: 19114895 - Crit Care Med. 2009 Feb;37(2):417-23, e1
– reference: 18852260 - Gut. 2009 Mar;58(3):379-87
– reference: 22269279 - Crit Care. 2012;16(1):R14
– reference: 16368344 - Ann Thorac Surg. 2006 Jan;81(1):97-103
– reference: 20663682 - Eur J Cardiothorac Surg. 2011 Apr;39(4):451-8
– reference: 19534671 - Recent Pat Inflamm Allergy Drug Discov. 2009 Nov;3(3):214-20
– reference: 20621577 - An Pediatr (Barc). 2010 Oct;73(4):162-8
– reference: 19063787 - Cardiol Young. 2008 Dec;18 Suppl 2:163-8
– reference: 15283368 - Semin Thorac Cardiovasc Surg Pediatr Card Surg Annu. 2004;7:185-91
– reference: 18447945 - BMC Pediatr. 2008;8:18
– reference: 20660763 - Proc Natl Acad Sci U S A. 2010 Aug 10;107(32):14298-303
– reference: 16304234 - Asian Cardiovasc Thorac Ann. 2005 Dec;13(4):382-95
– reference: 9702948 - Clin Chem. 1998 Aug;44(8 Pt 1):1621-8
– reference: 20489044 - Am J Physiol Gastrointest Liver Physiol. 2010 Aug;299(2):G467-75
– reference: 21345192 - Crit Care. 2011;15(1):R69
– reference: 3665030 - Clin Chem. 1987 Oct;33(10):1783-7
– reference: 19048243 - Eur J Clin Pharmacol. 2009 Apr;65(4):393-402
– reference: 19885903 - Inflamm Bowel Dis. 2010 Jul;16(7):1180-6
– reference: 4421995 - Am Heart J. 1974 Nov;88(5):553-6
SSID ssj0017863
Score 2.1567492
Snippet Introduction Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of...
Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of this finding is...
Introduction Limited evidence suggests that serum alkaline phosphatase activity may decrease after cardiac surgery in adults and children. The importance of...
SourceID unpaywall
pubmedcentral
proquest
gale
pubmed
crossref
springer
SourceType Open Access Repository
Aggregation Database
Index Database
Enrichment Source
Publisher
StartPage R160
SubjectTerms Alkaline phosphatase
Alkaline Phosphatase - blood
Analysis
Biomarkers - blood
C-reactive protein
C-Reactive Protein - metabolism
Calcitonin - blood
Calcitonin Gene-Related Peptide
Cardiac Surgical Procedures - adverse effects
Cardiotonic Agents - therapeutic use
Coronary artery bypass
Critical Care Medicine
Emergency Medicine
Female
Heart
Humans
Infant
Infant, Newborn
Infants
Inflammation
Inflammation - enzymology
Inflammation - etiology
Intensive
Intubation, Intratracheal
Length of Stay
Male
Medicine
Medicine & Public Health
Patient outcomes
Phosphatases
Postoperative Care
Prospective Studies
Protein Precursors - blood
Surgery
Thoracic Surgical Procedures - adverse effects
SummonAdditionalLinks – databaseName: Unpaywall
  dbid: UNPAY
  link: http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Li9swEBZtFvo49P1Iuy1aKO1JWduRZbu3ULoshV16aCA9GUmWSFhjm7VDaX9Mf2tnJMfEWQql4JtGsa2M5mHN9w0h76y0cIWKGQg3GOdJxrLASqZEIE0SxfPYIhr54lKcL_mXVbzqa3MQC6O1IyGY7YPPS49twN4J5vq0Kazf6qkAaQzn57fJkcDzpQk5Wl5-XXz3WCvOwBXFHl0kmAiylQfN7s8ceaNDm7znlA4LJodT0_vk7rZq5M8fsiz3HNPZQ999tXV8hliPcjXbdmqmfx2wPf73Oz8iD_qQlS68jj0mt0z1hNy56A_ln5Lfi_JKYrRKm3XdNmvZgWekCJjAvhTUdSGn2tW9dmvQOL3RtPVobLqp4LJYi0NlVVCNvUJ8dR7FL8S0qduO1Y3x_OQwrcF8wcnCPNBmj7z8SCWFBdjBRim2_QUxx537jCzPPn_7dM76tg9MQ67eMWGUFUlkTaaiKFUQRBQiSWQCkSEmrzyFGDRKC2OUTKxOilhKFWWxlYnAZFbMn5NJVVfmJaFhxgMVCgmGy3AFmV4chKbIJIRJeI9gSt7v_v5c95zo2JqjzF1ulIq8X-0poYNg42lAbop8QP3J0TDAb2jZ4xvgSZBiK1_Ecz7nYD5B8ngkCRtaj4ZPdhqY4xBWwVWm3ra568aDlQIg88Jr5PA0jrc_5PGUJCNdHQSQR3w8Um3Wjk8cT8JhReC-O63Oe0PW3nzJk0Hd_7YQr_5B5jW5B5FnhB_no-CYTLrrrXkD0V2n3vZ7-A8XyVLd
  priority: 102
  providerName: Unpaywall
Title Alkaline phosphatase activity after cardiothoracic surgery in infants and correlation with post-operative support and inflammation: a prospective cohort study
URI https://link.springer.com/article/10.1186/cc11483
https://www.ncbi.nlm.nih.gov/pubmed/22906145
https://www.proquest.com/docview/1551327003
https://pubmed.ncbi.nlm.nih.gov/PMC3580750
https://ccforum.biomedcentral.com/counter/pdf/10.1186/cc11483
UnpaywallVersion publishedVersion
Volume 16
hasFullText 1
inHoldings 1
isFullTextHit
isPrint
journalDatabaseRights – providerCode: PRVADU
  databaseName: BioMed Central Open Access Free
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: RBZ
  dateStart: 19970101
  isFulltext: true
  titleUrlDefault: https://www.biomedcentral.com/search/
  providerName: BioMedCentral
– providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: KQ8
  dateStart: 19970101
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: KQ8
  dateStart: 19970801
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVAFT
  databaseName: Open Access Digital Library
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: KQ8
  dateStart: 19980101
  isFulltext: true
  titleUrlDefault: http://grweb.coalliance.org/oadl/oadl.html
  providerName: Colorado Alliance of Research Libraries
– providerCode: PRVAON
  databaseName: DOAJ Directory of Open Access Journals
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 20231231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: DOA
  dateStart: 19980101
  isFulltext: true
  titleUrlDefault: https://www.doaj.org/
  providerName: Directory of Open Access Journals
– providerCode: PRVBFR
  databaseName: Free Medical Journals
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: DIK
  dateStart: 19970101
  isFulltext: true
  titleUrlDefault: http://www.freemedicaljournals.com
  providerName: Flying Publisher
– providerCode: PRVFQY
  databaseName: GFMER Free Medical Journals
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: GX1
  dateStart: 0
  isFulltext: true
  titleUrlDefault: http://www.gfmer.ch/Medical_journals/Free_medical.php
  providerName: Geneva Foundation for Medical Education and Research
– providerCode: PRVAQN
  databaseName: PubMed Central (PMC)
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: RPM
  dateStart: 19970101
  isFulltext: true
  titleUrlDefault: https://www.ncbi.nlm.nih.gov/pmc/
  providerName: National Library of Medicine
– providerCode: PRVAVX
  databaseName: HAS SpringerNature Open Access 2022
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: AAJSJ
  dateStart: 19970401
  isFulltext: true
  titleUrlDefault: https://www.springernature.com
  providerName: Springer Nature
– providerCode: PRVAVX
  databaseName: Springer Nature OA Free Journals
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: C6C
  dateStart: 19970401
  isFulltext: true
  titleUrlDefault: http://www.springeropen.com/
  providerName: Springer Nature
– providerCode: PRVAVX
  databaseName: SpringerLink Journals (ICM)
  customDbUrl:
  eissn: 1364-8535
  dateEnd: 99991231
  omitProxy: true
  ssIdentifier: ssj0017863
  issn: 1466-609X
  databaseCode: U2A
  dateStart: 19970401
  isFulltext: true
  titleUrlDefault: http://www.springerlink.com/journals/
  providerName: Springer Nature
link http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1ba9RAFB5sC1ofxGu7tS5TEH0K5jKXxLe4WIrQIuJC9SXMTCbs4pKEJov4Z_ytPWdyYdMiCCEvc3I9Z858Z86NkLeFKuAItGcBbniMycRL_EJ5WvjKypBHvMBs5MsrcbFkX675dV8suhmi3QeXpNPUblrH4oMxCN2jPXLAUWpAdJdhOjoMZCyiLid2l3iy2NxVuTtrzt14yNEp-pg82pa1-vNbbTY76875U_KkB4w07Tj8jDyw5XPy8LJ3ib8gf9PNL4VYkdarqqlXqoV1iWK6AnaFoK4HODUu6rRdAb_N2tCmy4Wm6xKOAiNhqCpzarBTRxcbR3F_ltZV03pVbbvq4HBZjWjd0cJ1IEtd3uNHqih87pC0SbHpLpC5yrUvyfL88_fFhdc3XfAMWMqtJ6wuhAwLm-gwjDUs4bmQUknAZWg6shgQYBjn1molCyNzrpQOE14oKdCUFNErsl9WpT0mNEiYrwOhQG1YpsHO4n5g80QBSMFn-DPybuBOZvqK5NgYY5M5yyQWWc_GGaEjYd0V4bhP8h7Zm-G0hHsY1WcXwJtggass5RGLGCgvoDydUMJ0MpPhs0FAMhzCGLTSVtsmc71w0E8PNEedwIxv46rmB4zPiJyI0kiAVbynI-V65ap5ox8a_gg8dxC6rFcjzf2PPBul8V8_4uQ_7vOaHALuC3FrPPRPyX57s7VvAFu1ek72FmIxdzsTcP726efczbM5OVhefU1_3AKFhStx
linkProvider Springer Nature
linkToHtml http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV1Zi9RAEG50Flx9EO8dXbUXRJ_C5ugj8S2Iyzju7Iu7sG-hu9NhBockbDKIf8bfalXnYLKLIOStK2dVV32Vugj5UKgCjkB7FuCGx5hMvMQvlKeFr6wMecQLrEZeXYjFFVte8-u-WXQzZLsPIUmnqd22jsWpMQjdo_vkIOZcsBk5SNPlj-UYMpCxiLqq2H3yibm5rXT3rM7tjMgxLPqIHO7KWv3-pbbbPctz9oQ87iEjTTsePyX3bPmMPFj1QfHn5E-6_akQLdJ6XTX1WrVgmSgWLOBcCOqmgFPj8k7bNXDcbAxtumpouinhKDAXhqoypwZndXTZcRT_0NK6alqvqm3XHxxOqxGvO1o4D6Spq3z8TBWF1x3KNimO3QUy17v2Bbk6-3r5ZeH1Yxc8A75y6wmrCyHDwiY6DGMNRjwXUioJyAydRxYDBgzj3FqtZGFkzpXSYcILJQU6kyJ6SWZlVdojQoOE-ToQChSHZRo8Le4HNk8UwBS8hz8nHwfuZKbvSY6jMbaZ801ikfVsnBM6EtZdG467JJ-QvRluTLiGUX19ATwJtrjKUh6xiIH6AsrjCSVsKDNZPhkEJMMlzEIrbbVrMjcNByP1QPOqE5jxaVzf_IDxOZETURoJsI_3dKXcrF0_b4xEwxeB-w5Cl_WKpLn7kiejNP7rQ7z-j-u8J4eLy9V5dv7t4vsb8hBQYIg_ykP_mMzam519C0ir1e_6PfYXFikrFA
linkToPdf http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwjV3da9RAEF9qC1Ufil_Vs1W3IPoUmq_dTXwLrUc9bRG00Lewu9nlDo8kmBziP-Pf6kw2CZcWQcjbTnaTzOzObzJfhLy10sIVKM8A3PDiWKRe6lvpKe5LI0IWMYvZyJdX_OI6Xtywmx3ChlyYLtp9cEm6nAas0lS2p3Vh3RZP-KnWCOOje2QvYSkHm2svyxbfFqP7QCQ8chmy2-QT1XP7AN7SQLejI0cX6UNyf1PW8vcvuV5vaaH5I3LQw0eaOX4_JjumfEL2L3sH-VPyJ1v_kIgcab2smnopW9BSFJMXsEcE7TqCU93FoLZL4L5eadq4zGi6KuGyGBdDZVlQjX07XKQcxb-1tK6a1qtq42qFw201YveOFu4DyXJZkB-opPC6QwonxRa8QNbVsX1Grucfv59deH0LBk-D3dx63CjLRWhNqsIwUaDQCy6EFIDS0JCME8CDYVIYo6SwWhRMShWmzErB0bDk0SHZLavSvCA0SGNfBVzCIWJiBVYX8wNTpBIgC67hz8i7gTu57uuTY5uMdd7ZKQnPezbOCB0Ja1eS4y7Je2RvjpsU5tCyzzWAJ8FyV3nGojiK4SgDyuMJJWwuPRk-GQQkxyGMSCtNtWnyrjMOeu2B5rkTmPFpuhr6QcxmRExEaSTAmt7TkXK17Gp7o1cavgisOwhd3h8qzd2XPBml8V8f4uV_zPOG7H89n-dfPl19PiIPABCG-M889I_JbvtzY14B6GrV636L_QVnsi9e
linkToUnpaywall http://utb.summon.serialssolutions.com/2.0.0/link/0/eLvHCXMwnV1Li9swEBZtFvo49P1Iuy1aKO1JWduRZbu3ULoshV16aCA9GUmWSFhjm7VDaX9Mf2tnJMfEWQql4JtGsa2M5mHN9w0h76y0cIWKGQg3GOdJxrLASqZEIE0SxfPYIhr54lKcL_mXVbzqa3MQC6O1IyGY7YPPS49twN4J5vq0Kazf6qkAaQzn57fJkcDzpQk5Wl5-XXz3WCvOwBXFHl0kmAiylQfN7s8ceaNDm7znlA4LJodT0_vk7rZq5M8fsiz3HNPZQ999tXV8hliPcjXbdmqmfx2wPf73Oz8iD_qQlS68jj0mt0z1hNy56A_ln5Lfi_JKYrRKm3XdNmvZgWekCJjAvhTUdSGn2tW9dmvQOL3RtPVobLqp4LJYi0NlVVCNvUJ8dR7FL8S0qduO1Y3x_OQwrcF8wcnCPNBmj7z8SCWFBdjBRim2_QUxx537jCzPPn_7dM76tg9MQ67eMWGUFUlkTaaiKFUQRBQiSWQCkSEmrzyFGDRKC2OUTKxOilhKFWWxlYnAZFbMn5NJVVfmJaFhxgMVCgmGy3AFmV4chKbIJIRJeI9gSt7v_v5c95zo2JqjzF1ulIq8X-0poYNg42lAbop8QP3J0TDAb2jZ4xvgSZBiK1_Ecz7nYD5B8ngkCRtaj4ZPdhqY4xBWwVWm3ra568aDlQIg88Jr5PA0jrc_5PGUJCNdHQSQR3w8Um3Wjk8cT8JhReC-O63Oe0PW3nzJk0Hd_7YQr_5B5jW5B5FnhB_no-CYTLrrrXkD0V2n3vZ7-A8XyVLd
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=article&rft.atitle=Alkaline+phosphatase+activity+after+cardiothoracic+surgery+in+infants+and+correlation+with+post-operative+support+and+inflammation%3A+a+prospective+cohort+study&rft.jtitle=Critical+care+%28London%2C+England%29&rft.au=Davidson%2C+Jesse&rft.au=Tong%2C+Suhong&rft.au=Hauck%2C+Amanda&rft.au=Lawson%2C+D+Scott&rft.date=2012-08-20&rft.eissn=1466-609X&rft.volume=16&rft.issue=4&rft.spage=R160&rft_id=info:doi/10.1186%2Fcc11483&rft_id=info%3Apmid%2F22906145&rft.externalDocID=22906145
thumbnail_l http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/lc.gif&issn=1364-8535&client=summon
thumbnail_m http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/mc.gif&issn=1364-8535&client=summon
thumbnail_s http://covers-cdn.summon.serialssolutions.com/index.aspx?isbn=/sc.gif&issn=1364-8535&client=summon