| Objective:To observe the change of complement in peripheral blood in children withsepsis, discuss the influence of Complement3(C3) depletion on pathogeneticcondition and prognosis and C3’s relationship with coagulation function.Methods:1to12years children with sepsis admitted in pediatric intensive careunit(PICU) of Hunan Children’s Hospital from May,2012to Jan,2013were reviewed andanalyzed. Children with the following conditions were excluded:congenitalimmunodeficiency, autoimmune diseases, immunodeficiency diseases, hematologicaldiseases, cancer, primary liver disease, chronic viral infections (HIV, hepatitis B or C),hypersensitivity disorders, diabetes, immune complex-induced chronic glomerulonephritis(MPGN), acute glomerulonephritis, streptococcal infection (AGN), lupus nephritis,malnutrition, a history of the use of immunosuppressants, the recent use of heparin, pre-hospital use of hormones and/or infusion blood products, blood purification beforemeasurement, radiation-induced neutropenia, chemotherapy-induced malignant lymphomaand those younger than1year old. All the children were given the PCIS scroes within24hafter admission. C3〠C4〠coagulation parameters and other biochemical indicatorswere measured and detected.Results1.IgGã€IgM in C3depletion group were significantly lower than the control group andCD3+Tã€CD4+Tã€CD8+T percent were higher than the control group(P <0.05).2. PCT in C3depletion group were significantly higher than the control group(P <0.05).3. PCIS in C3depletion group were significantly lower than the control group(P <0.05).According to the different level of PCIS score,all cases were divied into more than90points,71to90points and70points or less three groups. The results show: With the PCISscore lower, C3, C4gradually reduced, the difference was statistically significant (P<0.05).The proportion PCIS equal to70points or less in C3depletion group weresignificantly higher than the control group(P <0.01). 4. Serum C3, C4levels in severe sepsis group was signifcantly lower than the sepsis group(P <0.01), the proportion of children with severe sepsis in C3depletion group weresignificantly higher than the control group (P <0.01).5. All the cases were divided into three group according to the number of organ failure onadmission: no organ failure group, two organ failure group, multiple organ failure or shockgroup.We found that the more the number of multiple organ failure, the lower of the serumC3levels were (P <0.01).The proportion of multiple organ failure or shock in C3depletiongroup were significantly higher than the control group (P <0.01).6. Serum C3, C4levels in non survival group was signifcantly lower than the survivalgroup (P <0.01). The mortality rate in C3depletion group were significantly higher thanthe control group (P <0.01).7.18of160cases occurred clinical coagulation dysfunction, of which C3depletionincidence reached66.67%;8of18cases was diagnosed with DIC, of which C3depletionincidence reached75.00%; The proportion of coagulation dysfunction in C3depletiongroup were significantly higher than the control group (P <0.01).PT and APTT in C3depletion group were significantly higher than the control group (P<0.01); D-dimer positive rate in C3depletion group were significantly higher than thecontrol group (P <0.05); complement C3and PT, FIB, Plt were related with each other (P<0.01).Conclusions1.Children with sepsis presented complement C3depletion.2. Septic children with C3depletion appeared coagulation dysfunction.C3depletion inchildren with sepsis was associated with D-dimer.3. C3depletion in septic children prompted a serious condition, the prognosis is poor. |