Vitamin A deficiency in critically ill children with sepsis

Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically il...

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Published inCritical care (London, England) Vol. 23; no. 1; pp. 267 - 9
Main Authors Zhang, Xuepeng, Yang, Kaiying, Chen, Linwen, Liao, Xuelian, Deng, Liping, Chen, Siyuan, Ji, Yi
Format Journal Article
LanguageEnglish
Published London BioMed Central 01.08.2019
BioMed Central Ltd
BMC
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ISSN1364-8535
1466-609X
1364-8535
1466-609X
DOI10.1186/s13054-019-2548-9

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Abstract Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes. Methods Critically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock. Results One hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group ( P  < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency ( P  > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD ( r  = − 0.260, P  = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P  = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027–20.866; P  = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009–1.048; P  = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009–1.228; P  = 0.003) were independently associated with septic shock. Conclusion The prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis. Trial registration Clinicaltrials.gov , NCT03598127
AbstractList Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes. Critically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock. One hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group (P < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency (P > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD (r = - 0.260, P = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027-20.866; P = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009-1.048; P = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009-1.228; P = 0.003) were independently associated with septic shock. The prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis.
Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes.BACKGROUNDData that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes.Critically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock.METHODSCritically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock.One hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group (P < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency (P > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD (r = - 0.260, P = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027-20.866; P = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009-1.048; P = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009-1.228; P = 0.003) were independently associated with septic shock.RESULTSOne hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group (P < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency (P > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD (r = - 0.260, P = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027-20.866; P = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009-1.048; P = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009-1.228; P = 0.003) were independently associated with septic shock.The prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis.CONCLUSIONThe prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis.Clinicaltrials.gov , NCT03598127.TRIAL REGISTRATIONClinicaltrials.gov , NCT03598127.
Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes. Critically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock. One hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group (P < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency (P > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD (r = - 0.260, P = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027-20.866; P = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009-1.048; P = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009-1.228; P = 0.003) were independently associated with septic shock. The prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis. Clinicaltrials.gov , NCT03598127.
Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes. Methods Critically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock. Results One hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group (P < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency (P > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD (r = - 0.260, P = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027-20.866; P = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009-1.048; P = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009-1.228; P = 0.003) were independently associated with septic shock. Conclusion The prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis. Trial registration Clinicaltrials.gov, NCT03598127 Keywords: Sepsis, Pediatrics, Vitamin A, Vitamin A deficiency
Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes. Methods Critically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock. Results One hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group ( P  < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency ( P  > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD ( r  = − 0.260, P  = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P  = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027–20.866; P  = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009–1.048; P  = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009–1.228; P  = 0.003) were independently associated with septic shock. Conclusion The prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis. Trial registration Clinicaltrials.gov , NCT03598127
Abstract Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes of sepsis has not been well assessed. The aim of this study was to assess the prevalence of vitamin A deficiency in critically ill children with sepsis and its association with clinical outcomes. Methods Critically ill children with sepsis admitted to the pediatric intensive care unit were engaged in this prospective study. Sex- and age-matched approximate-health children from the Department of Pediatric Surgery were enrolled as the control group. Blood samples were collected from all patients in the first 24 h of admission for the measurement of serum vitamin A status. We compared vitamin A status between the sepsis group and the control group. In addition, we compared the clinical characteristics of the two subgroups of septic patients with vitamin A deficiency and those without vitamin A deficiency. Univariate and multivariable methods were used to evaluate the association between vitamin A deficiency and septic shock. Results One hundred sixty septic children and 49 approximate-health children were enrolled in this study. Vitamin A deficiency was found in 94 (58.8%) subjects in the study group and 6 (12.2%) subjects in the control group (P < 0.001). In septic patients, 28-day mortality and hospital mortality in patients with vitamin A deficiency were not significantly higher than that in patients without vitamin A deficiency (P > 0.05). However, vitamin A levels were inversely associated with higher PRISM scores in septic children with VAD (r = − 0.260, P = 0.012). Vitamin A deficiency was associated with septic shock with an unadjusted odds ratio (OR) of 3.297 (95% confidence interval (CI), 1.169 to 9.300; P = 0.024). In a logistic model, vitamin A deficiency (OR, 4.630; 95% CI, 1.027–20.866; P = 0.046), procalcitonin (OR, 1.029; 95% CI, 1.009–1.048; P = 0.003), and the Pediatric Risk of Mortality scores (OR, 1.132; 95% CI, 1.009–1.228; P = 0.003) were independently associated with septic shock. Conclusion The prevalence of vitamin A deficiency was high in children with sepsis. Vitamin A deficiency may be a marker of mortality in critically ill children with sepsis. Trial registration Clinicaltrials.gov, NCT03598127
ArticleNumber 267
Audience Academic
Author Ji, Yi
Deng, Liping
Chen, Siyuan
Yang, Kaiying
Zhang, Xuepeng
Liao, Xuelian
Chen, Linwen
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  organization: Division of Oncology, Department of Pediatric Surgery, West China Hospital of Sichuan University
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Cites_doi 10.2217/imt-2016-0020
10.1056/NEJMra021333
10.3945/jn.113.185876
10.1097/01.PCC.0000149131.72248.E6
10.1038/nrg2340
10.1093/ajcn/40.5.1090
10.1164/rccm.200207-682OC
10.1093/oxfordjournals.aje.a115502
10.4049/jimmunol.181.4.2277
10.1016/S0140-6736(12)60560-1
10.1146/annurev-pathol-011110-130327
10.1016/j.jnutbio.2008.01.002
10.1097/PCC.0000000000000247
10.1093/ajcn/26.1.77
10.1017/S003118200007548X
10.1097/PCC.0b013e3182917fad
10.1189/jlb.0109006
10.1182/blood-2015-11-680744
10.1128/IAI.63.8.3062-3068.1995
10.1016/j.clnu.2011.12.005
10.1093/ajcn/60.3.388
10.1017/S0007114513004133
10.1093/jn/127.4.558
10.1016/S0140-6736(86)91157-8
10.1096/fasebj.10.9.8801180
10.1097/ALN.0000000000001882
10.1097/CCM.0000000000001520
10.1093/ajcn/68.5.1095
10.1007/s00134-012-2713-y
10.1146/annurev.nutr.22.010402.102745E
10.4269/ajtmh.1992.47.16
10.1177/0310057X0903700510
10.1046/j.1365-3083.1996.d01-351.x
10.1128/IAI.64.1.209-214.1996
10.1016/S1473-3099(13)70001-X
10.1146/annurev.nutr.21.1.167
10.1093/jn/137.5.1328
10.1086/315912
10.1126/science.1145697
10.1093/ajcn/45.5.977
10.3181/00379727-178-41999
10.1111/jth.13861
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Issue 1
Keywords Pediatrics
Vitamin A
Sepsis
Vitamin A deficiency
Language English
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References T Tanaka (2548_CR27) 2016; 88
RS Hotchkiss (2548_CR15) 2013; 133
A Imdad (2548_CR40) 2017; 3
M Ongsakul (2548_CR37) 1985; 1782
E Amit-Romach (2548_CR7) 2009; 201
RS Watson (2548_CR19) 2003; 1675
K Niederreither (2548_CR3) 2008; 97
KA Thornton (2548_CR25) 2014; 1444
B Goldstein (2548_CR17) 2005; 61
ME Hartman (2548_CR12) 2013; 147
D Mucida (2548_CR4) 2007; 3175835
M Clagett-Dame (2548_CR2) 2002; 22
L Liu (2548_CR11) 2012; 3799832
AC Ross (2548_CR5) 1996; 109
SS Twining (2548_CR6) 1997; 1274
A Bai (2548_CR29) 2009; 864
S Chen (2548_CR8) 2012; 314
DJ Stearns-Kurosawa (2548_CR14) 2011; 6
Y Wang (2548_CR10) 2014; 159
A Sommer (2548_CR21) 1984; 405
S Chen (2548_CR9) 2014; 1119
U Wiedermann (2548_CR38) 1996; 641
U Wiedermann (2548_CR28) 1996; 446
N Thiery-Antier (2548_CR31) 2016; 444
CB Stephensen (2548_CR44) 1994; 603
A Sommer (2548_CR39) 1986; 18491
C Keane (2548_CR16) 2017; 1276
P Nair (2548_CR46) 2013; 392
RS Hotchkiss (2548_CR13) 2003; 3482
A Sommer (2548_CR23) 1987; 455
DI Thurnham (2548_CR35) 2000; 182
U Wiedermann (2548_CR36) 1995; 638
S Xiao (2548_CR26) 2008; 1814
MW Bloem (2548_CR22) 1990; 1312
SG Berger (2548_CR24) 2007; 1375
TA Claushuis (2548_CR32) 2016; 12724
H Schwertz (2548_CR34) 2017; 1512
L Mata (2548_CR42) 1992; 471
Z Tan (2548_CR20) 2002; 363
V Herbert (2548_CR41) 1973; 261
CB Stephensen (2548_CR1) 2001; 21
AK Mitra (2548_CR45) 1998; 685
WHO (2548_CR18) 2009
TB Corcoran (2548_CR30) 2009; 375
NW Solomons (2548_CR43) 1993; 107
SF de Stoppelaar (2548_CR33) 2014; 1124
References_xml – volume: 88
  start-page: 959
  year: 2016
  ident: 2548_CR27
  publication-title: Immunotherapy
  doi: 10.2217/imt-2016-0020
– volume: 3482
  start-page: 138
  year: 2003
  ident: 2548_CR13
  publication-title: N Engl J Med
  doi: 10.1056/NEJMra021333
– volume: 1444
  start-page: 496
  year: 2014
  ident: 2548_CR25
  publication-title: J Nutr
  doi: 10.3945/jn.113.185876
– volume: 61
  start-page: 2
  year: 2005
  ident: 2548_CR17
  publication-title: Pediatr Crit Care Med
  doi: 10.1097/01.PCC.0000149131.72248.E6
– volume: 97
  start-page: 541
  year: 2008
  ident: 2548_CR3
  publication-title: Nat Rev Genet
  doi: 10.1038/nrg2340
– volume: 405
  start-page: 1090
  year: 1984
  ident: 2548_CR21
  publication-title: Am J Clin Nutr
  doi: 10.1093/ajcn/40.5.1090
– volume: 1124
  start-page: 666
  year: 2014
  ident: 2548_CR33
  publication-title: Thromb Haemost
– volume: 1675
  start-page: 695
  year: 2003
  ident: 2548_CR19
  publication-title: Am J Respir Crit Care Med
  doi: 10.1164/rccm.200207-682OC
– volume: 1312
  start-page: 332
  year: 1990
  ident: 2548_CR22
  publication-title: Am J Epidemiol
  doi: 10.1093/oxfordjournals.aje.a115502
– volume: 1814
  start-page: 2277
  year: 2008
  ident: 2548_CR26
  publication-title: J Immunol
  doi: 10.4049/jimmunol.181.4.2277
– volume: 3799832
  start-page: 2151
  year: 2012
  ident: 2548_CR11
  publication-title: Lancet.
  doi: 10.1016/S0140-6736(12)60560-1
– volume: 6
  start-page: 19
  year: 2011
  ident: 2548_CR14
  publication-title: Annu Rev Pathol
  doi: 10.1146/annurev-pathol-011110-130327
– volume: 201
  start-page: 70
  year: 2009
  ident: 2548_CR7
  publication-title: J Nutr Biochem
  doi: 10.1016/j.jnutbio.2008.01.002
– volume: 159
  start-page: 814
  year: 2014
  ident: 2548_CR10
  publication-title: Pediatr Crit Care Med
  doi: 10.1097/PCC.0000000000000247
– volume: 261
  start-page: 77
  year: 1973
  ident: 2548_CR41
  publication-title: Am J Clin Nutr
  doi: 10.1093/ajcn/26.1.77
– volume: 107
  start-page: S19
  issue: Suppl
  year: 1993
  ident: 2548_CR43
  publication-title: Parasitology.
  doi: 10.1017/S003118200007548X
– volume: 147
  start-page: 686
  year: 2013
  ident: 2548_CR12
  publication-title: Pediatr Crit Care Med
  doi: 10.1097/PCC.0b013e3182917fad
– volume: 864
  start-page: 959
  year: 2009
  ident: 2548_CR29
  publication-title: J Leukoc Biol
  doi: 10.1189/jlb.0109006
– volume: 12724
  start-page: 3062
  year: 2016
  ident: 2548_CR32
  publication-title: Blood.
  doi: 10.1182/blood-2015-11-680744
– volume: 638
  start-page: 3062
  year: 1995
  ident: 2548_CR36
  publication-title: Infect Immun
  doi: 10.1128/IAI.63.8.3062-3068.1995
– volume: 314
  start-page: 543
  year: 2012
  ident: 2548_CR8
  publication-title: Clin Nutr
  doi: 10.1016/j.clnu.2011.12.005
– volume: 603
  start-page: 388
  year: 1994
  ident: 2548_CR44
  publication-title: Am J Clin Nutr
  doi: 10.1093/ajcn/60.3.388
– volume: 1119
  start-page: 1586
  year: 2014
  ident: 2548_CR9
  publication-title: Br J Nutr
  doi: 10.1017/S0007114513004133
– volume: 363
  start-page: 161
  year: 2002
  ident: 2548_CR20
  publication-title: Zhonghua Yu Fang Yi Xue Za Zhi
– volume: 1274
  start-page: 558
  year: 1997
  ident: 2548_CR6
  publication-title: J Nutr
  doi: 10.1093/jn/127.4.558
– volume: 18491
  start-page: 1169
  year: 1986
  ident: 2548_CR39
  publication-title: Lancet
  doi: 10.1016/S0140-6736(86)91157-8
– volume: 109
  start-page: 979
  year: 1996
  ident: 2548_CR5
  publication-title: FASEB J
  doi: 10.1096/fasebj.10.9.8801180
– volume: 1276
  start-page: 1017
  year: 2017
  ident: 2548_CR16
  publication-title: Anesthesiology.
  doi: 10.1097/ALN.0000000000001882
– volume-title: Global prevalence of vitamin A deficiency in populations at risk 1995–2005: WHO global database on vitamin A deficiency
  year: 2009
  ident: 2548_CR18
– volume: 444
  start-page: 764
  year: 2016
  ident: 2548_CR31
  publication-title: Crit Care Med
  doi: 10.1097/CCM.0000000000001520
– volume: 685
  start-page: 1095
  year: 1998
  ident: 2548_CR45
  publication-title: Am J Clin Nutr
  doi: 10.1093/ajcn/68.5.1095
– volume: 392
  start-page: 267
  year: 2013
  ident: 2548_CR46
  publication-title: Intensive Care Med
  doi: 10.1007/s00134-012-2713-y
– volume: 22
  start-page: 347
  year: 2002
  ident: 2548_CR2
  publication-title: Annu Rev Nutr
  doi: 10.1146/annurev.nutr.22.010402.102745E
– volume: 471
  start-page: 16
  year: 1992
  ident: 2548_CR42
  publication-title: Am J Trop Med Hyg
  doi: 10.4269/ajtmh.1992.47.16
– volume: 3
  start-page: Cd008524
  year: 2017
  ident: 2548_CR40
  publication-title: Cochrane Database Syst Rev
– volume: 375
  start-page: 740
  year: 2009
  ident: 2548_CR30
  publication-title: Anaesth Intensive Care
  doi: 10.1177/0310057X0903700510
– volume: 446
  start-page: 578
  year: 1996
  ident: 2548_CR28
  publication-title: Scand J Immunol
  doi: 10.1046/j.1365-3083.1996.d01-351.x
– volume: 641
  start-page: 209
  year: 1996
  ident: 2548_CR38
  publication-title: Infect Immun
  doi: 10.1128/IAI.64.1.209-214.1996
– volume: 133
  start-page: 260
  year: 2013
  ident: 2548_CR15
  publication-title: Lancet Infect Dis
  doi: 10.1016/S1473-3099(13)70001-X
– volume: 21
  start-page: 167
  year: 2001
  ident: 2548_CR1
  publication-title: Annu Rev Nutr
  doi: 10.1146/annurev.nutr.21.1.167
– volume: 1375
  start-page: 1328
  year: 2007
  ident: 2548_CR24
  publication-title: J Nutr
  doi: 10.1093/jn/137.5.1328
– volume: 182
  start-page: S23
  issue: Suppl 1
  year: 2000
  ident: 2548_CR35
  publication-title: J Infect Dis
  doi: 10.1086/315912
– volume: 3175835
  start-page: 256
  year: 2007
  ident: 2548_CR4
  publication-title: Science.
  doi: 10.1126/science.1145697
– volume: 455
  start-page: 977
  year: 1987
  ident: 2548_CR23
  publication-title: Am J Clin Nutr
  doi: 10.1093/ajcn/45.5.977
– volume: 1782
  start-page: 204
  year: 1985
  ident: 2548_CR37
  publication-title: Proc Soc Exp Biol Med
  doi: 10.3181/00379727-178-41999
– volume: 1512
  start-page: 2408
  year: 2017
  ident: 2548_CR34
  publication-title: J Thromb Haemost
  doi: 10.1111/jth.13861
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Snippet Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the...
Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the clinical outcomes...
Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and the...
Abstract Background Data that indicate vitamin A status in critically ill children with sepsis are sparse. The association between serum vitamin A levels and...
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StartPage 267
SubjectTerms Adolescent
Biomarkers - analysis
Biomarkers - blood
Care and treatment
Child
Child health
Child, Preschool
Children
China - epidemiology
Critical Care Medicine
Critical Illness - epidemiology
Critically ill children
Diagnosis
Emergency Medicine
Female
Health
Humans
Infant
Infection
Intensive
Male
Medicine
Medicine & Public Health
Mortality
Pediatric intensive care
Pediatric surgery
Pediatrics
Prospective Studies
Sepsis
Sepsis - blood
Sepsis - complications
Sepsis - physiopathology
Septic shock
Shock
Surgery
Vitamin A
Vitamin A - analysis
Vitamin A - blood
Vitamin A deficiency
Vitamin A Deficiency - physiopathology
Vitamins
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Title Vitamin A deficiency in critically ill children with sepsis
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