期刊文献+

支气管肺发育不良早产儿2周岁内呼吸道感染再入院分析 被引量:8

Premature infants with bronchopulmonary dysplasia:rehospitalization for respiratory infections within 2 years of life
原文传递
导出
摘要 目的探讨支气管肺发育不良(bronchoplumnary dysplasia,BPD)早产儿2周岁内因呼吸道感染再入院情况及危险因素。方法选择2016年1月至2017年12月温州医科大学附属第二医院收治的胎龄≤32周早产儿进行回顾性分析,根据是否发生BPD及BPD程度分为轻中度BPD组、重度BPD组和非BPD组,比较3组患儿生后2年内因呼吸道感染再入院率及再入院时的临床资料,采用Logistic回归进行再入院危险因素分析。结果共收治566例胎龄≤32周早产儿,BPD发生率为30.2%(171/566),其中轻中度BPD占81.9%(140/171),重度BPD占18.1%(31/171)。BPD早产儿2周岁内因呼吸道感染再入院率为45.0%(77/171),其中重度BPD组再入院率为71.0%(22/31),分别是非BPD组和轻中度BPD组的2.6和1.8倍。81.8%(63/77)BPD早产儿首次再入院发生在1周岁内,轻中度BPD和重度BPD组分别为83.6%(46/55)和77.3%(17/22)。重度BPD组住院次数>1次的比例较另两组显著升高(P<0.01)。对142例在本院随访的BPD早产儿进行再入院分析,发现呼吸道合胞病毒感染是再入院的主要病因,轻中度和重度BPD患儿2周岁内因呼吸道合胞病毒感染再住院率分别为6.8%(8/118)和16.7%(4/24)。轻中度和重度BPD组再住院后需呼吸支持比例高于非BPD组(P<0.05),重度BPD组入住重症监护室时间长于非BPD组和轻中度BPD组(P<0.05)。颅内出血、新生儿期住院时间长和家族性过敏体质是BPD患儿再入院的独立危险因素。结论BPD尤其重度BPD早产儿2周岁内呼吸道感染再入院率高,再入院后病情重。颅内出血、新生儿期住院时间长和家族性过敏体质是BPD患儿呼吸道感染再入院的危险因素。 Objective To study the load and risk factors of rehospitalization for respiratory infections of premature infants with bronchopulmonary dysplasia(BPD),within the first 2 years of life.Method This was a retrospective study of infants born less than 32 weeks gestational age for the year of 2016 and 2017.Based on the diagnosis and severity of BPD,the infants were classified as non-BPD,mild/moderate BPD and severe BPD group.The rate of rehospitalization for respiratory infections and clinical data during rehospitalization among the three groups were compared.Multiple logistic regression analysis were used to determine risk factors associated with respiratory infections requiring rehospitalization.Result Among the 566 premature infants,171(30.2%)had BPD and of these,140(81.9%)and 31(18.1%)were discharged with the diagnosis of mild/moderate BPD and severe BPD respectively.Within the first 2 years of life,45.0%infants with BPD had one or more rehospitalizations for respiratory infections,among them 71.0%was diagnosed with severe BPD.Compared with non-BPD group and mild/moderate group,severe BPD group had 2.6 and 1.8 times rate of rehospitalization.63 of 77(81.8%)BPD infants were rehospitalized during the first year of life,the rate of rehospitalization of mild/moderate and severe BPD infants were 83.6%(46/55)and 77.3%(17/22)respectively.The severe BPD group had higher rate of multiple rehospitalizations,which had statistically difference(P<0.01).Respiratory syncytial virus infection is the main reason for rehospitalization.Among 142 BPD infants which were followed up at our hospital,8 of 118(6.8%)mild/moderate BPD and 4 of 24(16.7%)severe BPD infants had respiratory syncytial virus related hospitalizations.The rate of respiratory support was lower in non-BPD group compared with the other two groups,and the mean length stay in intensive care unit was higher in severe BPD cases than that of the other two groups(P<0.05).In multivariable logistic analyses,intracranial hemorrhage,duration of neonatal hospitalization and family history of atopy were independently associated with rehospitalization for respiratory infections.Conclusion BPD infants have a very high risk of rehospitalization for respiratory infections in the first 2 years,especially severe BPD.And they tend to have more severe complications.Intracranial hemorrhage,duration of neonatal hospitalization and family history of atopy are the risk factors of rehospitalization for respiratory infections.
作者 潘冰婷 戴媛媛 俞彬媛 梁忠杰 麦菁芸 陈尚勤 Pan Bingting;Dai Yuanyuan;Yu Binyuan;Liang Zhongjie;Mai Jingyun;Chen Shangqin(Department of Neonatology,The Second Affiliated Hospital of Wenzhou Medical University,Yuying Children's Hospital,Wenzhou 325027,China)
出处 《中华新生儿科杂志(中英文)》 CAS 2020年第6期415-419,共5页 Chinese Journal of Neonatology
关键词 支气管肺发育不良 病人再入院 危险因素 呼吸道合胞病毒 Bronchopulmonary dysplasia Patient readmission Risk factors Respiratory syncytial viruses
  • 相关文献

参考文献4

二级参考文献48

  • 1董永绥.婴儿巨细胞病毒性肝炎(上)[J].临床儿科杂志,2006,24(1):74-77. 被引量:69
  • 2Hentschel J, Berger TM, Tschopp A, et al. Population-based study of bronchopulmonary dysplasia in very low birth weight infants in Switzerland. Eur J Pediatr, 2005, 164:292-297.
  • 3Korhonen P, Tammela O, Koivisto AM, et al. Frequency and risk factors in bronchopulmonary dysplasia in a cohort of very low birth weight infants. Early Hum Dev, 1999, 54:245-258.
  • 4Sullivan JL. Iron, plasma antioxidants and the 'oxygen radical disease of prematurity'. Am J Dis Child, 1988, 142 : 1341-1344.
  • 5Williamson P, Griffiths G, Norfolk D, et al. Blood transfusions and human recombinant erythropoietin in premature newborn infants. Arch Dis Child, 1996, 75 :F65-68.
  • 6Demirel N, Bas AY, Zenciroglu A. Bronchopulmonary Dysplasia in Very Low Birth Weight Infants. Indian J Pediatr, 2009, 76: 695-698.
  • 7Jonsson B, Li YH, Noaek G, et al. Downregulatory cytokines in tracheobronchial aspirate fluid from infants with chronic lung disease of prematurity. Acta Paediatr, 2000, 89 : 1375-1380.
  • 8Sche|onka RL, Katz B, Waites KB, et al. Critical appraisal of the role of Ureaplasma in the development of bronchopulmonary dysplasia with metaanalytic techniques. Pediatr Infect Dis J, 2005, 24 : 1033-1039.
  • 9Speer CP. Inflammation and bronchopulmonary dysplasia. Se-min Neonatol, 2003, 8:29-38.
  • 10Tapia JL, Agost D, Alegria A, et al. Bronchopulmonary dysplasia, very low birth weight, risk factors, resource utilization, neonates. J Pediatr, 2006, 82:15-20.

共引文献242

同被引文献83

引证文献8

二级引证文献31

相关作者

内容加载中请稍等...

相关机构

内容加载中请稍等...

相关主题

内容加载中请稍等...

浏览历史

内容加载中请稍等...
;
使用帮助 返回顶部