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Tight glycemic control in critically ill pediatric patients: a systematic review and meta-analysis
Lvlin Chen1, Tiangui Li2, Fang Fang3
1Department of Critical Care Medicine, Affiliated Hospital of Chengdu University, No.82, North Section 2, 2nd Ring Road, Jinniu District, Chengdu, Sichuan, 610081, China.
Insights
Tight glucose control (TGC) in pediatric intensive care units did not lower hospital mortality but reduced the need for dialysis. However, TGC significantly increased hypoglycemia risk in critically ill children.
Area of Science:
- Pediatric Intensive Care
- Endocrinology
- Critical Care Medicine
Background:
- Hyperglycemia is common in pediatric intensive care unit (PICU) patients.
- Understanding the risks and benefits of tight glucose control (TGC) is crucial for this population.
Purpose of the Study:
- To evaluate the benefits and risks of tight glucose control (TGC) in critically ill children.
- To synthesize evidence from randomized controlled trials on TGC in PICU settings.
Main Methods:
- Systematic review and meta-analysis of randomized controlled trials.
- Searched Medline, Embase, and CENTRAL databases up to May 2017.
- Assessed risk of bias and used GRADE for evidence quality.
Main Results:
- Included 4030 patients from six low-risk-of-bias studies.
- TGC did not decrease hospital mortality, sepsis, or seizures.
- TGC reduced the need for dialysis but significantly increased hypoglycemia incidence.
Conclusions:
- TGC in critically ill children does not improve mortality but may reduce dialysis needs.
- Increased risk of hypoglycemia is a significant concern with TGC in this patient group.
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 .
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