Related Experiment Video
Updated: Aug 17, 2026

Design of Cecal Ligation and Puncture and Intranasal Infection Dual Model of Sepsis-Induced Immunosuppression
Published on: June 15, 2019
Intravenous polyclonal immunoglobulin administration to sepsis syndrome patients: a prospective study in a pediatric
Ahmed El-Nawawy1, Hassan El-Kinany, Mona Hamdy El-Sayed
1Pediatric Department, Faculty of Medicine, Alexandria University, Egypt. dr_anawawy@yahoo.com
Insights
Polyclonal intravenous immunoglobulin (IVIG) significantly reduced mortality and complications in pediatric intensive care unit (PICU) sepsis patients. This adjuvant therapy shortened hospital stays and improved survival rates in young children with severe infections.
Area of Science:
- Pediatric Intensive Care
- Infectious Diseases
- Immunology
Background:
- Sepsis is a leading cause of PICU admissions, with high mortality.
- The efficacy of polyclonal intravenous immunoglobulins (IVIG) as an adjuvant therapy for pediatric sepsis remains debated.
Purpose of the Study:
- To evaluate the impact of polyclonal IVIG on outcomes in pediatric sepsis patients admitted to the PICU.
Main Methods:
- A prospective study of 100 pediatric sepsis patients (1-24 months) in two groups: standard PICU care and standard care plus IVIG.
- Patients received daily laboratory tests, tumor necrosis factor-alpha (TNF-alpha) measurements, and outcome assessments for 5 days.
Main Results:
- The IVIG group showed significantly higher discharge rates (72% vs. 44%), shorter PICU length of stay (LOS) (6.1 vs. 9.1 days), and fewer complications (8% vs. 32%).
- Tumor necrosis factor-alpha levels were significantly reduced in the IVIG group upon discharge.
- IVIG treatment, LOS, sepsis severity, and lymphocyte percentage predicted survival.
Conclusions:
- Polyclonal IVIG as an adjuvant therapy significantly reduces mortality, LOS, and complications in pediatric sepsis.
- Further multicenter studies are recommended to validate these findings.
Abstract:
Life-threatening infections account for about 25 per cent of children requiring admission to pediatric intensive care units (PICU). The results of the use of polyclonal intravenous immunoglobulins as an adjuvant in pediatric sepsis syndrome therapy are conflicting. A prospective study of 100 sepsis syndrome PICU patients aged 1-24 months and divided into two matching groups (septic cases and control, 50 patients each) was performed. All patients were treated according to the routine protocol PICU therapy. Only the cases group received, in addition, polyclonal IVIG (Pentaglobin, Biotest) in a dose of 400 mg/kg for 3 days. All cases were evaluated for PRISM III score 8 h after admission; routine blood, urine, stool and cerebrospinal fluid (whenever appropriate) culture. Daily laboratory examination (blood gases, electrolytes, liver and renal functions, complete blood picture and C-reactive protein) were performed for the first 5 days. Blood samples were obtained for evaluation of tumor necrosis factor-alpha (TNF-alpha) daily for the first 5 days. Referral site (ward or casuality), length of PICU stay (LOS) and outcome (discharged or deceased), the number and percentage of cases who progressed to complications were recorded. Results showed that group I had a significantly higher percentage of discharged cases (72 per cent vs. 44 per cent), significantly shorter LOS (6.1 days vs. 9.1 days), and a significantly lower percentage of progress to complications (8 per cent vs. 32 per cent) especially disseminated intravascular coagulation (4 per cent vs. 24 per cent). TNF-alpha was significantly reduced among septic cases on discharge (2.24 vs. 3.6 mg/dl, p<0.001). A multiple logistic regression model revealed that treatment with IVIG, LOS, severity of sepsis and lymphocyte percentage (L per cent) on admission were significant predictors for survival. In summary the study revealed that the use of polyclonal IVIG among PICU sepsis syndrome showed a significant reduction in mortality, LOS and less progress to complications. A multicenter study is recommended to confirm these results.
Related Concept Videos
Acute Pyelonephritis II: Diagnostic Studies and Management
Pneumonia IV: Management
Bacterial Pneumonia Treatment
For bacterial pneumonia, antibiotics serve as the cornerstone of therapy. Initial treatment often begins with empirical antibiotics, tailored to the anticipated causative organism and adjusted based on culture results. Key antibiotic choices include:
Acute Kidney Injury IV: Diagnostic Studies and Prevention
Acute Pyelonephritis I: Introduction