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Tight glycemic control in critically ill pediatric patients: a systematic review and meta-analysis.
Crit Care. 2018 03 04; 22(1):57.CC

Abstract

BACKGROUND

Hyperglycemia is prevalent in patients in the pediatric intensive care unit. The purpose of this study was to describe the benefits and risks of tight glucose control (TGC) in critically ill children.

METHODS

A systemic review and meta-analysis of the literature was carried out on randomized controlled trials of TGC in critically ill children admitted to the pediatric intensive care unit. The databases searched were Medline, Embase, and CENTRAL databases until May 1, 2017. Paired reviewers independently screened citations, assessed risk of bias of included studies, and extracted data. A random-effects model was used to report all outcomes. The Grading of Recommendations Assessment, Development and Evaluation system was used to quantify absolute effects and quality of evidence. The primary outcome was hospital mortality. The secondary outcomes were hypoglycemia (any, severe), sepsis, new need for dialysis, and seizures.

RESULTS

A total of 4030 patients were included from six studies. All six studies were rated as at low risk of bias. Our meta-analysis showed that TGC did not result in a decrease in risk of hospital mortality (odds ratio (OR), 0.95; 95% confidence interval (CI), 0.62-1.45; I2 = 40%; moderate quality), sepsis (OR, 0.82; 95% CI, 0.63-1.08), or seizures (OR, 0.98; 95% CI, 0.59-1.63). TGC was associated with a decrease in new need for dialysis (OR, 0.63; 95% CI, 0.45-0.86). However, TGC was associated with a significant increase in any hypoglycemia (OR, 4.39; 95% CI, 2.39-8.06) and severe hypoglycemia (OR, 4.11; 95% CI, 2.67-6.32).

CONCLUSIONS

Among critically ill children with hyperglycemia, TGC does not result in a decrease in hospital mortality, but appears to reduce a new need for dialysis. However, TGC is associated with higher incidence of hypoglycemia.

SYSTEMATIC REVIEW REGISTRATION

PROSPERO registration number CRD42017074039 .

Authors+Show Affiliations

Department of Critical Care Medicine, Affiliated Hospital of Chengdu University, No.82, North Section 2, 2nd Ring Road, Jinniu District, Chengdu, Sichuan, 610081, China.Longquanyi Hospital, Chengdu, Sichuan, China.West China Hospital, Sichuan University, Chengdu, Sichuan, China.Department of Critical Care Medicine, Affiliated Hospital of Chengdu University, No.82, North Section 2, 2nd Ring Road, Jinniu District, Chengdu, Sichuan, 610081, China. tnt1057@gmail.com.University of Pittsburgh Medical Center, Pittsburgh, PA, USA.

Pub Type(s)

Journal Article
Meta-Analysis
Review
Systematic Review

Language

eng

PubMed ID

29501063

Citation

Chen, Lvlin, et al. "Tight Glycemic Control in Critically Ill Pediatric Patients: a Systematic Review and Meta-analysis." Critical Care (London, England), vol. 22, no. 1, 2018, p. 57.
Chen L, Li T, Fang F, et al. Tight glycemic control in critically ill pediatric patients: a systematic review and meta-analysis. Crit Care. 2018;22(1):57.
Chen, L., Li, T., Fang, F., Zhang, Y., & Faramand, A. (2018). Tight glycemic control in critically ill pediatric patients: a systematic review and meta-analysis. Critical Care (London, England), 22(1), 57. https://doi.org/10.1186/s13054-018-1976-2
Chen L, et al. Tight Glycemic Control in Critically Ill Pediatric Patients: a Systematic Review and Meta-analysis. Crit Care. 2018 03 4;22(1):57. PubMed PMID: 29501063.
* Article titles in AMA citation format should be in sentence-case
TY - JOUR T1 - Tight glycemic control in critically ill pediatric patients: a systematic review and meta-analysis. AU - Chen,Lvlin, AU - Li,Tiangui, AU - Fang,Fang, AU - Zhang,Yu, AU - Faramand,Andrew, Y1 - 2018/03/04/ PY - 2017/10/20/received PY - 2018/02/05/accepted PY - 2018/3/5/entrez PY - 2018/3/5/pubmed PY - 2018/10/3/medline KW - Children KW - Hyperglycemia KW - Mortality KW - Randomized controlled trial KW - Tight glycemic control SP - 57 EP - 57 JF - Critical care (London, England) JO - Crit Care VL - 22 IS - 1 N2 - BACKGROUND: Hyperglycemia is prevalent in patients in the pediatric intensive care unit. The purpose of this study was to describe the benefits and risks of tight glucose control (TGC) in critically ill children. METHODS: A systemic review and meta-analysis of the literature was carried out on randomized controlled trials of TGC in critically ill children admitted to the pediatric intensive care unit. The databases searched were Medline, Embase, and CENTRAL databases until May 1, 2017. Paired reviewers independently screened citations, assessed risk of bias of included studies, and extracted data. A random-effects model was used to report all outcomes. The Grading of Recommendations Assessment, Development and Evaluation system was used to quantify absolute effects and quality of evidence. The primary outcome was hospital mortality. The secondary outcomes were hypoglycemia (any, severe), sepsis, new need for dialysis, and seizures. RESULTS: A total of 4030 patients were included from six studies. All six studies were rated as at low risk of bias. Our meta-analysis showed that TGC did not result in a decrease in risk of hospital mortality (odds ratio (OR), 0.95; 95% confidence interval (CI), 0.62-1.45; I2 = 40%; moderate quality), sepsis (OR, 0.82; 95% CI, 0.63-1.08), or seizures (OR, 0.98; 95% CI, 0.59-1.63). TGC was associated with a decrease in new need for dialysis (OR, 0.63; 95% CI, 0.45-0.86). However, TGC was associated with a significant increase in any hypoglycemia (OR, 4.39; 95% CI, 2.39-8.06) and severe hypoglycemia (OR, 4.11; 95% CI, 2.67-6.32). CONCLUSIONS: Among critically ill children with hyperglycemia, TGC does not result in a decrease in hospital mortality, but appears to reduce a new need for dialysis. However, TGC is associated with higher incidence of hypoglycemia. SYSTEMATIC REVIEW REGISTRATION: PROSPERO registration number CRD42017074039 . SN - 1466-609X UR - https://www.unboundmedicine.com/medline/citation/29501063/Tight_glycemic_control_in_critically_ill_pediatric_patients:_a_systematic_review_and_meta_analysis_ L2 - https://ccforum.biomedcentral.com/articles/10.1186/s13054-018-1976-2 DB - PRIME DP - Unbound Medicine ER -