Glucosuria as an early marker of late-onset sepsis in preterms: a prospective cohort study

被引:6
|
作者
Bekhof, Jolita [1 ]
Kollen, Boudewijn J. [2 ]
Kok, Joke H. [3 ]
Van Straaten, Henrica L. M. [1 ]
机构
[1] Isala, Princess Amalia Childrens Clin, NL-8000 GK Zwolle, Netherlands
[2] Univ Groningen, Univ Med Ctr Groningen, Dept Gen Practice, Groningen, Netherlands
[3] Univ Amsterdam, Acad Med Ctr, Dept Neonatol, NL-1105 AZ Amsterdam, Netherlands
关键词
Premature infant; Infection; Nosocomial sepsis; Signs and symptoms; Diagnosis; Glucose; Hyperglycaemia; C-REACTIVE PROTEIN; NEONATAL SEPSIS; CLINICAL SIGNS; HYPERGLYCEMIA; INFECTION; DIAGNOSIS; PREDICTION; ACCURACY; INFANTS;
D O I
10.1186/s12887-015-0425-5
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Early and accurate diagnosis of late-onset sepsis (LONS) in preterm infants is difficult since presenting signs are subtle and non-specific. Because neonatal sepsis may be accompanied by glucose intolerance and glucosuria, we hypothesized that glucosuria may be associated with LONS in preterms, in an early stage. We aim to evaluate the association of glucosuria and late-onset neonatal sepsis (LONS) in preterm infants, in an attempt to improve early and accurate diagnosis of LONS. Methods: We performed a prospective observational cohort study in 316 preterms (<34 weeks). We daily measured glucosuria and followed patients for occurrence of LONS, defined as clinical and blood culture-proven sepsis occurring after 72 h. Attending physicians were blinded to glucosuria results. We assessed the diagnostic value of glucosuria for clinical and blood culture-proven LONS using logistic regression analysis. Results: Glucosuria was found in 65.8 % of 316 preterm patients, and sepsis was suspected 157 times in 123 patients. LONS was found in 47.1 % of 157 suspected episodes. The presence of glucosuria was associated with LONS (OR 2.59, 95 % CI 1.24-5.43, p = 0.012) with sensitivity 69.0 % and specificity 53.8 % (Likelihoodratio 1.49). After adjustment for gestational age, birth weight, and postnatal age, this association weakened and was no longer significant (adjusted OR 2.16; 95 % CI 0.99-1.85, p = 0.055). An increase in glucosuria 48-24 h before onset of symptoms was not associated with LONS. Conclusion: In preterms glucosuria is associated with LONS within 24 h, however this association is too weak to be of diagnostic value.
引用
收藏
页数:6
相关论文
共 50 条
  • [21] Incidence, aetiology and resistance of late-onset neonatal sepsis: A five-year prospective study
    Hammoud, Majeda S.
    Al-Taiar, Abdullah
    Thalib, Lukman
    Al-Sweih, Noura
    Pathan, Seema
    Isaacs, David
    JOURNAL OF PAEDIATRICS AND CHILD HEALTH, 2012, 48 (07) : 604 - 609
  • [22] Biomarkers for late-onset neonatal sepsis
    Richard A Polin
    Tara M Randis
    Genome Medicine, 2
  • [23] Phagocyte CD11b expression as an early diagnostic marker for late-onset sepsis in preterm infants
    Nupponen, I
    Turunen, R
    Andersson, S
    Repo, H
    PEDIATRIC RESEARCH, 2002, 51 (04) : 265A - 265A
  • [24] YOUNG VERSUS LATE-ONSET RHEUMATOID ARTHRITIS: A PROSPECTIVE 12 MONTH-FOLLOW-UP COHORT STUDY IN AN EARLY ARTHRITIS COHORT
    Prata, A. R.
    Sousa, M.
    Assuncao, H.
    Saraiva, L.
    Brites, L.
    Luis, M.
    Freitas, P.
    Campos Costa, F.
    Santiago, T.
    da Silva, J. A. P.
    Duarte, C.
    ANNALS OF THE RHEUMATIC DISEASES, 2021, 80 : 481 - 481
  • [25] Association between duration of early empiric antibiotics and necrotizing enterocolitis and late-onset sepsis in preterm infants: a multicenter cohort study
    Thomas H. Dierikx
    Nancy Deianova
    Jip Groen
    Daniel C. Vijlbrief
    Christian Hulzebos
    Willem P. de Boode
    Esther J. d’Haens
    Veerle Cossey
    Boris W. Kramer
    Mirjam M. van Weissenbruch
    Wouter J. de Jonge
    Marc A. Benninga
    Chris H. van den Akker
    Anton H. van Kaam
    Nanne K. H. de Boer
    Douwe H. Visser
    Hendrik J. Niemarkt
    Tim G. J. de Meij
    European Journal of Pediatrics, 2022, 181 : 3715 - 3724
  • [26] Association between duration of early empiric antibiotics and necrotizing enterocolitis and late-onset sepsis in preterm infants: a multicenter cohort study
    Dierikx, Thomas H.
    Deianova, Nancy
    Groen, Jip
    Vijlbrief, Daniel C.
    Hulzebos, Christian
    de Boode, Willem P.
    d'Haens, Esther J.
    Cossey, Veerle
    Kramer, Boris W.
    van Weissenbruch, Mirjam M.
    de Jonge, Wouter J.
    Benninga, Marc A.
    van den Akker, Chris H.
    van Kaam, Anton H.
    de Boer, Nanne K. H.
    Visser, Douwe H.
    Niemarkt, Hendrik J.
    de Meij, Tim G. J.
    EUROPEAN JOURNAL OF PEDIATRICS, 2022, 181 (10) : 3715 - 3724
  • [27] Prediction model for early diagnosis of late-onset sepsis in preterm newborns
    Seyhanli, D.
    Yildirim, T. Gokmen
    Kalkanli, O. H.
    Soysal, B.
    Ozdemir, S. Alkan
    Devrim, I.
    Calkavur, S.
    JOURNAL OF NEONATAL-PERINATAL MEDICINE, 2024, 17 (05) : 661 - 671
  • [28] Premature infants respond to early-onset and late-onset sepsis with leukocyte activation
    Weinschenk, NP
    Farina, A
    Bianchi, DW
    JOURNAL OF PEDIATRICS, 2000, 137 (03): : 345 - 350
  • [29] Late-onset Sepsis in Preterm Infants Can Be Detected Preclinically by Fecal Volatile Organic Compound Analysis: A Prospective, Multicenter Cohort Study
    Berkhout, Daniel J. C.
    van Keulen, Britt J.
    Niemarkt, Hendrik J.
    Bessem, Jet R.
    de Boode, Willem P.
    Cossey, Veerle
    Hoogenes, Neil
    Hulzebos, Christiaan V.
    Klaver, Ellen
    Andriessen, Peter
    van Kaam, Anton H.
    Kramer, Boris W.
    van Lingen, Richard A.
    Schouten, Aaron
    van Goudoever, Johannes B.
    Vijlbrief, Daniel C.
    van Weissenbruch, Mirjam M.
    Wicaksono, Alfian N.
    Covington, James A.
    Benninga, Marc A.
    de Boer, Nanne K. H.
    de Meij, Tim G. J.
    CLINICAL INFECTIOUS DISEASES, 2019, 68 (01) : 70 - 77
  • [30] Late-Onset Alopecia Areata: A Retrospective Cohort Study
    Lyakhovitsky, Anna
    Gilboa, Sarit
    Eshkol, Anna
    Barzilai, Aviv
    Baum, Sharon
    DERMATOLOGY, 2017, 233 (04) : 289 - 294