武汉地区350例百日咳儿童临床特征及混合感染分析

Analysis on clinical characteristics and mixed infections in 350 children with pertussis in Wuhan

  • 摘要:
    目的 分析百日咳儿童临床特征、混合感染病原体情况, 为临床诊疗提供参考。
    方法 回顾性分析2022年1月-2023年12月武汉儿童医院确诊百日咳住院患儿350例的临床资料。比较不同年龄组患儿、单纯感染组与混合感染组患儿的临床特征、白细胞计数峰值、淋巴细胞比例峰值、超敏C-反应蛋白或C-反应蛋白、降钙素原及并发症情况。
    结果 291例(83.14%)患儿存在混合感染, 以病毒为主(63.43%, 222/350), 人鼻病毒/肠道病毒(32.57%, 114/350)最为常见。 < 6月龄、6月龄~ < 1岁和1~ < 3岁患儿咳嗽家属接触史、喘息、气促、呼吸衰竭发生率、白细胞计数峰值、淋巴细胞比例峰值均高于3~ < 6岁和≥6岁患儿(均P<0.05), 6月龄~ < 1岁和1~ < 3岁患儿咳嗽后呕吐发生率高于其他年龄组患儿(P<0.05), 住院天数随患儿年龄增长呈缩短趋势(P<0.05), 患儿伴阵发性痉挛性咳嗽、咳嗽后紫绀、咳嗽后涨红、咳憋、吸气性三凹征、肺炎和肺部痰鸣音比例均随年龄增长基本呈下降趋势(均P<0.05)。仅 < 1岁患儿出现点头呼吸(P<0.05)。6月龄~ < 1岁组、1~ < 3岁组、3岁~ < 6岁组、≥6岁组患儿发热、合并细菌和肺炎支原体感染发生率均高于 < 6月龄组(均P<0.05)。混合感染组发热发生率高于单纯感染组(P<0.05);单纯感染组患儿住院时间更长、阵发性痉挛性咳嗽、咳嗽夜间为著、咳嗽后涨红、咳憋、肺部痰鸣音的发生率和淋巴细胞比例峰值均更高(均P<0.05); < 3月龄患儿单纯感染组阵发性痉挛性咳嗽发生率更高(P<0.05)。
    结论 百日咳患儿年龄越小, 咳嗽家属接触史占比越高, 越易出现阵发性痉挛性咳嗽、咳嗽后呕吐、咳嗽后紫绀、肺炎等临床表现, 白细胞计数、淋巴细胞比例峰值也越高, 住院时间越长;患儿年龄越大, 越易出现发热、细菌和支原体感染;混合感染病原体种类也因患儿年龄不同而有所差异, 百日咳混合感染可能会掩盖其典型临床症状。

     

    Abstract:
    OBJECTIVE To analyze the clinical characteristics and pathogens for mixed infections in children with pertussis, so as to references for clinical diagnosis and treatment.
    METHODS A retrospective analysis was conducted on the clinical data of 350 children diagnosed with pertussis and hospitalized in Wuhan Children′s Hospital from Jan. 2022 to Dec. 2023. The clinical characteristics, peak white blood cell count, peak lymphocyte ratio, high-sensitivity C-reactive protein or C-reactive protein, procalcitonin and complications were compared between different age groups, as well as between the single infection group and the mixed infection group.
    RESULTS Mixed infections were observed in 291 children (83.14%), predominantly viral (63.43%, 222/350), with human rhinovirus/enterovirus being the most common (32.57%, 114/350). For children aged < 6 months, 6 months to < 1 year and 1 to < 3 years, the incidence of family contact history of cough, panting, hasty breathing, respiratory failure, peak white blood cell count and peak lymphocyte ratio were all higher than those aged 3 to < 6 years and ≥6 years (all P < 0.05). The incidence of post-cough vomiting was higher in children aged 6 months to < 1 year and 1 to < 3 years compared to other age groups (P < 0.05). The length of hospital stay decreased with increasing age (P < 0.05). The proportions of children with paroxysmal spasmodic cough, post-cough cyanosis, post-cough flushing, coughing spells, inspiratory three concave sign, pneumonia and pulmonary phlegm rales all generally decreased with age (all P < 0.05). Nodding respiration was only observed in children aged < 1 year (P < 0.05). The incidence of fever, co-infection with bacteria and Mycoplasma pneumoniae infection was higher in children aged 6 months to < 1 year, 1 to < 3 years, 3 to < 6 years and ≥6 years compared to those aged < 6 months (all P < 0.05). The incidence of fever was higher in the mixed infection group than that in the single infection group (P < 0.05). Children in the single infection group had longer hospital stays, higher incidence of paroxysmal spasmodic cough, nocturnal cough, post-cough flushing, coughing spells, pulmonary phlegm rales and higher peak lymphocyte ratio (all P < 0.05). The incidence of paroxysmal spasmodic cough was higher in the single infection group for children aged < 3 months (P < 0.05).
    CONCLUSIONS The younger children with pertussis have a higher proportion of family contact history of cough and are more prone to clinical manifestations such as paroxysmal spasmodic cough, post-cough vomiting, post-cough cyanosis, and pneumonia. They also have higher peak white blood cell counts, peak lymphocyte ratios and longer hospital stays. As children′ age increased, the incidence of fever, bacterial, and mycoplasma infections also increased. The types of pathogens in mixed infections varies with patients′ age and pertussis mixed infections may mask typical clinical symptoms.

     

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