S. Kwarteng Owusu, B. A. Baah, J. Sylverken, N. Mensah, Naomi Adjetey, D. Ansong, E. Addo-Yobo
{"title":"在三级医院就诊的肺炎患儿缺氧和死亡率:对记录的回顾性回顾","authors":"S. Kwarteng Owusu, B. A. Baah, J. Sylverken, N. Mensah, Naomi Adjetey, D. Ansong, E. Addo-Yobo","doi":"10.31191/afrijcmr.v5i1.105","DOIUrl":null,"url":null,"abstract":"BackgroundChildhood pneumonia is a leading cause of hospitalisation and death in Low- and Middle-Income Countries (LMIC). Despite remarkable achievements in global mortality trends in children under 5 nearly 700 000 children die annually from pneumonia. In Ghana, an estimated 4,700 children under 5 died from pneumonia in 2017. Hypoxia is a known predictor of death among children hospitalised with pneumonia. Few studies in Ghana have described the predictors of mortality among children with pneumonia. This study aimed to determine the factors associated with mortality among children hospitalized for pneumonia to the Paediatric Emergency Unit (PEU) of Komfo Anokye Teaching Hospital (KATH). \nMethodsMedical records of children admitted to the PEU of KATH from January 2016 to December 2020 were reviewed. Data was cleaned and exported to STATA version 16 for analysis. Outcomes measures of interest were survival and mortality. \nResults Records for 482 children hospitalised with pneumonia to the unit were available of which 55 per cent (n=265) were males, 94 per cent (n= 455) were less than five years and 51 per cent (n=265) were younger than 12 months old. In all, 77 per cent (n=301), had received three doses of the pneumococcal conjugate vaccine. Twenty-one percent (n=89), presented with hypoxia and 15% (n= 77), died from pneumonia. There was a significant association between death as an outcome and hypoxia at presentation [?2 (1)= 13.29, p < .001(OR 2.6, 95% CI 1.42 to 4.75)], axillary temperature of 38oC or more at presentation [?2 (1)= 5.03, p = .025 (OR 2.09 (95% CI 1.08 to 4.02)], fast breathing at presentation [?2 (1) = 5.45, p = .020 (OR 2.12 95% CI 1.11 – 4.01)] and having received all 3 doses of pneumococcal vaccine [?2 (1) = 9.78, p = .002 (OR 0.45 95% CI 0.27 – 0.75). \nConclusion Hypoxia at presentation, axillary temperature of 38oC or greater, fast breathing, are likely predictors of mortality in children under 5 hospitalised for pneumonia. Pneumococcal conjugate vaccine uptake is high among children with pneumonia, receiving all 3 doses likely protects children with pneumonia from death.","PeriodicalId":221258,"journal":{"name":"African Journal of Current Medical Research","volume":"530 1","pages":"0"},"PeriodicalIF":0.0000,"publicationDate":"2022-01-26","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Hypoxia and mortality outcomes in children presenting with pneumonia to a tertiary Hospital: A Retrospective review of records\",\"authors\":\"S. Kwarteng Owusu, B. A. Baah, J. Sylverken, N. Mensah, Naomi Adjetey, D. Ansong, E. Addo-Yobo\",\"doi\":\"10.31191/afrijcmr.v5i1.105\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"BackgroundChildhood pneumonia is a leading cause of hospitalisation and death in Low- and Middle-Income Countries (LMIC). Despite remarkable achievements in global mortality trends in children under 5 nearly 700 000 children die annually from pneumonia. In Ghana, an estimated 4,700 children under 5 died from pneumonia in 2017. Hypoxia is a known predictor of death among children hospitalised with pneumonia. Few studies in Ghana have described the predictors of mortality among children with pneumonia. This study aimed to determine the factors associated with mortality among children hospitalized for pneumonia to the Paediatric Emergency Unit (PEU) of Komfo Anokye Teaching Hospital (KATH). \\nMethodsMedical records of children admitted to the PEU of KATH from January 2016 to December 2020 were reviewed. Data was cleaned and exported to STATA version 16 for analysis. Outcomes measures of interest were survival and mortality. \\nResults Records for 482 children hospitalised with pneumonia to the unit were available of which 55 per cent (n=265) were males, 94 per cent (n= 455) were less than five years and 51 per cent (n=265) were younger than 12 months old. In all, 77 per cent (n=301), had received three doses of the pneumococcal conjugate vaccine. Twenty-one percent (n=89), presented with hypoxia and 15% (n= 77), died from pneumonia. There was a significant association between death as an outcome and hypoxia at presentation [?2 (1)= 13.29, p < .001(OR 2.6, 95% CI 1.42 to 4.75)], axillary temperature of 38oC or more at presentation [?2 (1)= 5.03, p = .025 (OR 2.09 (95% CI 1.08 to 4.02)], fast breathing at presentation [?2 (1) = 5.45, p = .020 (OR 2.12 95% CI 1.11 – 4.01)] and having received all 3 doses of pneumococcal vaccine [?2 (1) = 9.78, p = .002 (OR 0.45 95% CI 0.27 – 0.75). \\nConclusion Hypoxia at presentation, axillary temperature of 38oC or greater, fast breathing, are likely predictors of mortality in children under 5 hospitalised for pneumonia. Pneumococcal conjugate vaccine uptake is high among children with pneumonia, receiving all 3 doses likely protects children with pneumonia from death.\",\"PeriodicalId\":221258,\"journal\":{\"name\":\"African Journal of Current Medical Research\",\"volume\":\"530 1\",\"pages\":\"0\"},\"PeriodicalIF\":0.0000,\"publicationDate\":\"2022-01-26\",\"publicationTypes\":\"Journal Article\",\"fieldsOfStudy\":null,\"isOpenAccess\":false,\"openAccessPdf\":\"\",\"citationCount\":\"0\",\"resultStr\":null,\"platform\":\"Semanticscholar\",\"paperid\":null,\"PeriodicalName\":\"African Journal of Current Medical Research\",\"FirstCategoryId\":\"1085\",\"ListUrlMain\":\"https://doi.org/10.31191/afrijcmr.v5i1.105\",\"RegionNum\":0,\"RegionCategory\":null,\"ArticlePicture\":[],\"TitleCN\":null,\"AbstractTextCN\":null,\"PMCID\":null,\"EPubDate\":\"\",\"PubModel\":\"\",\"JCR\":\"\",\"JCRName\":\"\",\"Score\":null,\"Total\":0}","platform":"Semanticscholar","paperid":null,"PeriodicalName":"African Journal of Current Medical Research","FirstCategoryId":"1085","ListUrlMain":"https://doi.org/10.31191/afrijcmr.v5i1.105","RegionNum":0,"RegionCategory":null,"ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":null,"EPubDate":"","PubModel":"","JCR":"","JCRName":"","Score":null,"Total":0}
引用次数: 0
摘要
背景儿童肺炎是低收入和中等收入国家住院和死亡的主要原因。尽管在全球5岁以下儿童死亡率趋势方面取得了显著成就,但每年仍有近70万儿童死于肺炎。在加纳,2017年估计有4700名5岁以下儿童死于肺炎。缺氧是肺炎住院儿童死亡的已知预测因子。加纳很少有研究描述肺炎儿童死亡率的预测因素。本研究旨在确定在Komfo Anokye教学医院(KATH)儿科急诊科(PEU)因肺炎住院的儿童死亡率相关因素。方法回顾性分析2016年1月至2020年12月我院住院儿童的病历。数据被清理并导出到STATA版本16进行分析。关注的结局指标是生存和死亡率。结果有482名肺炎住院儿童的记录,其中55% (n=265)为男性,94% (n= 455)小于5岁,51% (n=265)小于12个月。总共有77% (n=301)的人接种了三剂肺炎球菌结合疫苗。21% (n=89)表现为缺氧,15% (n= 77)死于肺炎。结果死亡与出现时缺氧之间存在显著关联[?]2 (1)= 13.29, p < .001(OR 2.6, 95% CI 1.42 ~ 4.75)],出现时腋窝温度为38℃或更高[?]2 (1)= 5.03, p = 0.025 (OR 2.09 (95% CI 1.08 ~ 4.02)),就诊时呼吸急促[?]2 (1) = 5.45, p = 0.020 (OR 2.12 95% CI 1.11 - 4.01)],并且接种了全部3剂肺炎球菌疫苗[?]2 (1) = 9.78, p = 0.002 (OR 0.45, 95% CI 0.27 - 0.75)。结论入院时缺氧、腋窝温度38℃或更高、呼吸急促可能是5岁以下肺炎住院儿童死亡的预测因素。肺炎儿童的肺炎球菌结合疫苗接种率很高,接种所有三剂疫苗可能保护肺炎儿童免于死亡。
Hypoxia and mortality outcomes in children presenting with pneumonia to a tertiary Hospital: A Retrospective review of records
BackgroundChildhood pneumonia is a leading cause of hospitalisation and death in Low- and Middle-Income Countries (LMIC). Despite remarkable achievements in global mortality trends in children under 5 nearly 700 000 children die annually from pneumonia. In Ghana, an estimated 4,700 children under 5 died from pneumonia in 2017. Hypoxia is a known predictor of death among children hospitalised with pneumonia. Few studies in Ghana have described the predictors of mortality among children with pneumonia. This study aimed to determine the factors associated with mortality among children hospitalized for pneumonia to the Paediatric Emergency Unit (PEU) of Komfo Anokye Teaching Hospital (KATH).
MethodsMedical records of children admitted to the PEU of KATH from January 2016 to December 2020 were reviewed. Data was cleaned and exported to STATA version 16 for analysis. Outcomes measures of interest were survival and mortality.
Results Records for 482 children hospitalised with pneumonia to the unit were available of which 55 per cent (n=265) were males, 94 per cent (n= 455) were less than five years and 51 per cent (n=265) were younger than 12 months old. In all, 77 per cent (n=301), had received three doses of the pneumococcal conjugate vaccine. Twenty-one percent (n=89), presented with hypoxia and 15% (n= 77), died from pneumonia. There was a significant association between death as an outcome and hypoxia at presentation [?2 (1)= 13.29, p < .001(OR 2.6, 95% CI 1.42 to 4.75)], axillary temperature of 38oC or more at presentation [?2 (1)= 5.03, p = .025 (OR 2.09 (95% CI 1.08 to 4.02)], fast breathing at presentation [?2 (1) = 5.45, p = .020 (OR 2.12 95% CI 1.11 – 4.01)] and having received all 3 doses of pneumococcal vaccine [?2 (1) = 9.78, p = .002 (OR 0.45 95% CI 0.27 – 0.75).
Conclusion Hypoxia at presentation, axillary temperature of 38oC or greater, fast breathing, are likely predictors of mortality in children under 5 hospitalised for pneumonia. Pneumococcal conjugate vaccine uptake is high among children with pneumonia, receiving all 3 doses likely protects children with pneumonia from death.