Yuan Yin, Peng Hua. Recombinant Human Interferon α-2b in the Treatment of Infants with Bronchiolitis by Different Routes of Administration. [J]. 26(9):19-22(2020)
DOI:
Yuan Yin, Peng Hua. Recombinant Human Interferon α-2b in the Treatment of Infants with Bronchiolitis by Different Routes of Administration. [J]. 26(9):19-22(2020) DOI: 10.13407/j.cnki.jpp.1672-108X.2020.09.006.
Recombinant Human Interferon α-2b in the Treatment of Infants with Bronchiolitis by Different Routes of Administration
Objective: To investigate the efficacy and safety of recombinant human interferon α-2b in the treatment of infants with bronchiolitis by different routes of administration. Methods: A total of 150 children with bronchiolitis admitted to our hospital from Jan. 2017 to Mar. 2018 were retrospectively extracted to be divided into the control group
atomization group and intramuscular injection group via the random number table
with 50 cases in each group. Three groups were given conventional treatment. Recombinant human interferon α-2b (100
000 U/kg) by ultrasonic atomizing inhalation was added to atomization group. Recombinant human interferon α-2b (100
000 U/kg) by intramuscular injection was added to intramuscular injection group. The levels of interleukin-4 (IL-4)
interferon-γ (IFN-γ) in the atomization group and intramuscular injection group were collected and analyzed before and after treatment. Clinical efficacy
disappearance time of clinical symptoms and adverse drug reactions of the atomization group and intramuscular injection group were observed. Results: After treatment
the total effective rate of the atomization group and the intramuscular injection group was higher than that of the control group (P<0.05)
the total effective rate of the atomization group and the intramuscular injection group was not statistically different (P>0.05). The levels of IL-4 and IFN-γ of three groups decreased after treatment
and the differences were statistically significant (P<0.05). There was no significant difference in IL-4 and IFN-γ in three groups before treatment (P>0.05). After treatment
the levels of IL-4 and IFN-γ in the atomization group and the intramuscular injection group were lower than those in the control group (P<0.05)
the levels of IL-4 and IFN-γ in the atomization group were lower than those in the intramuscular injection group (P<0.05). The total course of disease
the disappearance time of cough and lung rales
the length of stay
and the disappearance time of wheezing in the atomization group were all shorter than those in the intramuscular injection group
and the difference was statistically significant (P<0.05). In the atomization group
there were 1 case of loss of appetite
1 case of liver dysfunction
and 1 case of thrombocytopenia. While the intramuscular injection group had 2 cases of fever
3 cases of loss of appetite
1 case of liver dysfunction
3 cases of thrombocytopenia
and 3 cases of local erythema at the injection site. The incidence of adverse drug reactions in the atomization group was lower than that in the intramuscular injection group (P<0.05). Conclusion: Recombinant human interferon α-2b has significant curative effects in the treatment of infants with bronchiolitis and can effectively improve the level of inflammatory factors. Aerosol inhalation is beneficial to shorten the course of the disease and is safer than intramuscular injection.
关键词
重组干扰素α-2b毛细支气管炎给药途径婴幼儿
Keywords
recombinant interferon α-2bbronchiolitisroute of administrationnfants
Clinical Characteristics of Neonatal Pertussis: Comparison with Infant Pertussis
Comparison of Efficacy of Budesonide and Salbutamol Aerosol Inhalation at Different Temperatures in Adjuvant Treatment of Children with Bronchiolitis
Effects of Antibiotics on Intestinal Flora in Infants of Mongolian and Han Nationality
Application of Budesonide Suspension for Inhalation in Pediatric Outpatient and Emergency Department of Our Hospital
Related Author
Zhong Qin
Feng Hui
Lu Qi
Wu Lunhui
Wei Yonggang
Liu Puxian
Xiao Daizhou
Wu Shuli
Related Institution
Children’s Hospital of Chongqing Medical University, Ministry of Education Key Laboratory of Child Development and Disorders, National Clinical Research Center for Child Health and Disorders, China International Science and Technology Cooperation Base of Child Development and Critical Disorders, Chongqing Key Laboratory of Pediatrics
Chongqing Qianjiang Ethnic Hospital
Inner Mongolia People’s Hospital
Shenzhen Hospital of Integrated Chinese and Western Medicine