Dergiler / Turkish Journal of Pediatrics / 2018 / Cilt: 60 - Sayı: 2

Association of dysglycemia with mortality in children receiving parenteral nutrition in pediatric intensive care unit

Sayfa
134–141
DOI
—
🏛️Bu makalenin bibliyografik verileri ve tam metin bağlantısı DergiPark üzerinden sağlanmıştır.
DergiPark Kaydı ↗
✨

Yapay Zeka Hızlı Bakış & Çıkarımlar

AI Insight
⚡ TL;DR(1 Cümlede Hızlı Çıkarım)

Results of this study showed that hyperglycemiaand glucose variability are strong predictors of mortality in pediatrics receivingparenteral nutrition.

📌 3 Maddede Bu Makale

🎯
Amaç & Hipotez:One of the most important complications of parenteral nutrition (PN) is ahigh incidence of hyperglycemia.
📊
Temel Bulgular & Veri:Charts of 201 critically illchildren admitted in PICU during 2012-2015 were reviewed retrospectively.We included patients who were <6 years of age and had received at least60% of total energy from PN for a minimum of 5 days in PICU.
💡
Sonuç & Katkı:Results of this study showed that hyperglycemiaand glucose variability are strong predictors of mortality in pediatrics receivingparenteral nutrition.
🔬Tür:Literatür & Derleme Çalışması
📍Kapsam:2012-2015 Verileri
⚙️Değişkenler:Alan Parametreleri

Özet

One of the most important complications of parenteral nutrition (PN) is ahigh incidence of hyperglycemia. The aim of this study was to assess theeffect of parenteral nutrition dysglycemia on clinical outcomes among criticallyill children in pediatric intensive care unit (PICU). Charts of 201 critically illchildren admitted in PICU during 2012-2015 were reviewed retrospectively.We included patients who were <6 years of age and had received at least60% of total energy from PN for a minimum of 5 days in PICU. Theexclusion criteria were patients with diagnosis of diabetes mellitus, primaryhypoglycemia, inborn errors of metabolism and patients who received dialyses.We defined hyperglycemia as blood glucose ≥150 mg/dl, and hypoglycemia asblood glucose ≤60 mg/dl. Based on blood glucose, patients were divided intofour groups: “only hyperglycemia group” (having at least one hyperglycemiaepisode), “only hypoglycemia group” (having at least one hypoglycemiaepisode), “glucose variability” (having both hypoglycemia and hyperglycemiaepisodes), and “normoglycemia” (all glucose measurements were in normalrange). Hyperglycemia and hypoglycemia occurred in 52.8% and 24.9% of allchildren, respectively; glucose variability occurred in 13.9% of all children.Multiple logistic regression analysis showed that glucose variability (OR: 3.1;95% CI: 1.13-8.43) and hyperglycemia (OR: 2.14; 95% CI: 1.1-4.57) wereassociated with mortality independently. In “only hypoglycemia” group (N=22)there were only three deaths. There were no significant differences in thequantities of macronutrients prescribed via parenteral nutrition among thefour blood glucose groups. Results of this study showed that hyperglycemiaand glucose variability are strong predictors of mortality in pediatrics receivingparenteral nutrition.

🔖

Bu Makaleye Atıf Yap

KHAJAVI, L., KHADEMI, G., MEHRAMIZ, M., NOROUZY, A., SAFARIAN, M. (2018). Association of dysglycemia with mortality in children receiving parenteral nutrition in pediatric intensive care unit. Turkish Journal of Pediatrics, Cilt: 60 - Sayı: 2, 134–141. https://ajindex.com/articles/412176

📄 Tam Metin PDF Okuyucu

📄

PDF görüntüleyici hazırlanıyor...

Kaynakça (14)

  1. Kyle UG, Jaimon N, Coss-Bu JA. Nutrition support in critically ill children: Underdelivery of energy and protein compared with current recommendations. J Acad Nutr Diet 2012; 112: 1987-1992
  2. Fivez T, Kerklaan D, Mesotten D, et al. Early versus late parenteral nutrition in critically ill children. N Engl J Med 2016; 374: 1111-1122
  3. Peyret B, Collardeau S, Touzet S, et al. Prevalence of liver complications in children receiving long-term parenteral nutrition. Eur J Clin Nutr 2011; 65: 743- 749
  4. Rosmarin DK, Wardlaw GM, Mirtallo J. Hyperglycemia associated with high, continuous infusion rates of total parenteral nutrition dextrose. Nutr Clin Pract 1996; 11: 151-156
  5. Mitanchez D. Glucose regulation in preterm newborn infants. Horm Res Paediatr 2007; 68: 265-271
  6. Lou S, MacLaren G, Paul E, Best D, Delzoppo C, Butt W. Prevalence of dysglycemia and association with outcomes in pediatric extracorporeal membrane oxygenation. Pediatr Crit Care Med 2015; 16: 270-275
  7. Wu Y, Pei J, Yang X-d, Zhao Y-y, Xiang B. Hyperglycemia and its association with clinical outcomes for patients in the pediatric intensive care unit after abdominal surgery. J Pediatr Surg 2013; 48: 801-805
  8. Yung M, Wilkins B, Norton L, Slater A, Group PS. Glucose control, organ failure, and mortality in pediatric intensive care. Pediatr Crit Care Med 2008; 9: 147-152
  9. Rake AJ, Srinivasan V, Nadkarni V, Kaptan R, Newth CJ. Glucose variability and survival in critically ill children: allostasis or harm? Pediatr Crit Care Med 2010; 11: 707-712
  10. Hirshberg E, Larsen G, Van Duker H. Alterations in glucose homeostasis in the pediatric intensive care unit: Hyperglycemia and glucose variability are associated with increased mortality and morbidity. Pediatr Crit Care Med 2008; 9: 361-366
  11. Srinivasan V. Stress hyperglycemia in pediatric critical illness: the intensive care unit adds to the stress! J Diabetes Sci Technol 2012; 6: 37-47
  12. Risso A, Mercuri F, Quagliaro L, Damante G, Ceriello A. Intermittent high glucose enhances apoptosis in human umbilical vein endothelial cells in culture. Am J Physiol Endocrinol Metab 2001; 281: 924-930
  13. Quagliaro L, Piconi L, Assaloni R, Martinelli L, Motz E, Ceriello A. Intermittent high glucose enhances apoptosis related to oxidative stress in human umbilical vein endothelial cells. Diabetes 2003; 52: 2795-2804
  14. Sperling MA, Menon RK. Differential diagnosis and management of neonatal hypoglycemia. Pediatr Clin North Am 2004; 51: 703