Objective To analyze the correlation between liver pathology and clinical characteristics in a large series of patients with chronic HBV infections , so as to provide the data base for non-invasive medical diagnosis .Methods Liver pathology and clinical characteristics of 1 397 patients with chronic HBV infections were retrospectively analyzed . Ridit analysis and Spearman correlation analysis were performed to investigate the correlations of clinical characteristics with liver pathology of patients .Results In 1 397 patients, there were 604 patients (43.24%) with liver inflammation grading ≥G2 and 504 patients (36.08%) with fibrosis stage ≥S2.Inflammation grade and fibrosis stage of liver tissues were both higher in male patients than those in females (u=3.093 and 2.854, P<0.01).Inflammation grade and fibrosis stage of liver tissues in patients aged ≤30 years were lower than those in patients aged >30-40 years and >40 years (r=0.259 and 0.303, P<0.01;F=4.199 and 12.226,11.610 and 24.359, P<0.05 and <0.01).Patients with HBeAg( -) and HBV DNA≥103 copies/mL were of higher degrees in liver tissue inflammation compared with those with HBeAg ( +) and those with HBeAg ( -) but HBV DNA <103 copies/mL (F=8.788 and 5.635, all P<0.01);while the fibrosis stage in patients with HBeAg (-) and HBV DNA≥103 copies/mL was only higher than that in HBeAg ( +) patients (F=12.886, P<0.01). Liver tissue inflammation and liver fibrosis aggravated with the increase of ALT ( r=0.537 and 0.517, P<0.01).There was no significant difference in liver tissue inflammation among different age groups of patients with ALT (1-<2) ×ULN and HBV DNA≥103 copies/mL (χ2 =4.365, P >0.05),but there was significant difference in liver fibrosis in patients between aged >40 years and ≤30 years ( F=3.177,P<0.05).Conclusions Liver biopsy and antiviral therapy should be considered in chronic HBV infected patients with age of >30 years, lightly elevated ALT levels , HBeAg(-) and detectable HBV DNA levels , especially in male patients .Screening for liver fibrosis should be considered in patients with HBeAg ( -) and low HBV DNA levels .

Objective To analyze the vaccination status of National Immunization Program Vaccines (NIPV) and the occurrence of febrile seizures in children with febrile seizures (FS), and to provide a basis for improving the NIPV vaccination rate and preventing vaccine related disease outbreaks in these children. Methods A total of 416 cases of febrile seizure children who were admitted to the pediatric intensive care unit (PICU) of Guangxi Maternity and Child Health Hospital from January 2021 to January 2023 were selected as the case group. According to 1:1 matching，416 healthy children were randomly selected from the National Immunization Program Information System as the control group. The National Immunization Program Information System was used to inquire about the NIPV vaccination status of the two groups of study subjects. The children in the two groups were asked by phone whether they had febrile seizures after NIPV inoculation. Results The vaccination rates of NIPV (including basic and enhanced NIPV) were lower in the case group than those in the control group, and the differences were statistically significant (all P<0.05). Except for the boosted polio vaccine (PV) and adsorbed diphtheria (DT) vaccine case groups, the overdue vaccination rates were lower than those in the control group, and the overdue vaccination rates in all vaccine case groups were higher than those in the control group (all P<0.05). Conclusion There is no statistically significant difference in adverse reactions between children with a history of febrile seizures and healthy children after NIPV inoculation. The vaccination rate of children with a history of febrile seizures is generally low. All NIPV vaccination rates in children with febrile seizures are lower than those in healthy children, and the vaccines are not vaccinated on time.