Pulmonary function abnormalities in Nigerian children with sickle cell anaemia: Prevalence, pattern and predictive factors

B. Kuti, S. Adegoke
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引用次数: 1

Abstract

Background: Advances in care of children with sickle cell anaemia (SCA) have increased their chances of survival to adolescence and adulthood though this is often associated with multi-organ system pathologies including lung dysfunctions. This study aimed to determine the prevalence, pattern and factors associated with pulmonary function abnormalities in Nigerian children with SCA. Methods: Pulmonary functions of 104 children with SCA in steady state and 104 age- and sex-matched haemoglobin AA controls aged 6 to 16 years at the Wesley Guild Hospital, Ilesa Nigeria, were assessed using Spirolab III (Medical International Research, Italy) spirometer following standard protocol. Socio-demographic characteristics, nutritional status and pulmonary function parameters of these children were compared, and the predictive factors of pulmonary function abnormalities in SCA children were determined using binary logistic regression. Results: SCA children had lower lung volumes and capacities and higher prevalence of pulmonary function abnormalities compared to controls, and a restrictive ventilatory pattern (22.1%) was the most predominant form. Adolescent age, previous acute chest syndrome (ACS), repeated painful crises and multiple hospitalisations in the previous year were significantly associated with pulmonary function abnormalities (P < 0.05). Only adolescent age group (odds ratio [OR] = 3.738; 95% confidence interval [CI] = 1.480–9.440; P = 0.005) and previous ACS (OR = 8.500; 95% CI = 2.044–12.959; P = 0.044) independently predicted pulmonary function impairments among the SCA children. Conclusion: SCA predisposes children to pulmonary dysfunction, particularly during adolescent years and in those with ACS, multiple crises and hospitalisations. Routine pulmonary function assessment in these children will facilitate early recognition and prompt management.
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尼日利亚镰状细胞性贫血儿童肺功能异常:患病率、模式和预测因素
背景:镰状细胞性贫血儿童(SCA)的护理进展增加了他们存活到青春期和成年期的机会,尽管这通常与包括肺功能障碍在内的多器官系统病变有关。本研究旨在确定尼日利亚SCA患儿肺功能异常的患病率、模式和相关因素。方法:采用Spirolab III(医学国际研究,意大利)肺活量计,按照标准方案,对尼日利亚Ilesa Wesley Guild医院104例稳定状态SCA患儿和104例年龄和性别匹配的血红蛋白AA对照者进行肺功能评估。比较这些儿童的社会人口学特征、营养状况和肺功能参数,并采用二元logistic回归确定SCA儿童肺功能异常的预测因素。结果:与对照组相比,SCA患儿肺容量和容量更小,肺功能异常患病率更高,限制性通气模式(22.1%)是最主要的形式。青少年年龄、既往急性胸综合征(ACS)、反复疼痛危像和前一年多次住院与肺功能异常显著相关(P < 0.05)。仅青少年年龄组(优势比[OR] = 3.738;95%置信区间[CI] = 1.480-9.440;P = 0.005)和既往ACS (OR = 8.500;95% ci = 2.044-12.959;P = 0.044)独立预测SCA患儿的肺功能损害。结论:SCA易使儿童发生肺功能障碍,特别是在青少年时期和ACS患者,多次危重和住院。对这些患儿进行常规肺功能评估有助于早期识别和及时处理。
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