Hendry R Sawe, Teri A Reynolds, Juma A Mfinanga, Michael S Runyon, Brittany L Murray, Lee A Wallis, Julie Makani
{"title":"向坦桑尼亚一家三级医院城市急诊科就诊的镰状细胞贫血症患者的临床表现、利用和结果。","authors":"Hendry R Sawe, Teri A Reynolds, Juma A Mfinanga, Michael S Runyon, Brittany L Murray, Lee A Wallis, Julie Makani","doi":"10.1186/s12878-018-0122-3","DOIUrl":null,"url":null,"abstract":"<p><strong>Background: </strong>Sickle cell anaemia (SCA) is prevalent in sub-Saharan Africa, with high risk of complications requiring emergency care. There is limited information about presentation of patients with SCA to hospitals for emergency care. We describe the clinical presentation, resource utilization, and outcomes of SCA patients presenting to the emergency department (ED) at Muhimbili National Hospital (MNH) in Dar es Salaam, Tanzania.</p><p><strong>Methods: </strong>This was a prospective cohort study of consecutive patients with SCA presenting to ED between December 2014 and July 2015. Informed consent was obtained from all patients or patients' proxies prior to being enrolled in the study. A standardized case report form was used to record study information, including demographics, relevant clinical characteristics and overall patients outcomes. Categorical variables were compared with chi-square test or Fisher's exact test; continuous variables were compared with two-sample t-test or Mann-Whitney U-test.</p><p><strong>Results: </strong>We enrolled 752 (2.7%) people with SCA from 28,322 patients who presented to the MNH-ED. The median age was 14 years (Interquartile range [IQR]: 6-23 years), and 395 (52.8%) were female. Pain 614 (81.6%), fever 289 (38.4%) were the most frequent presenting complaint. Patients with fever, hypoxia, altered mental status and bradycardia had statistically significant relative risk of mortality of 10.4, 153, 50 and 12.1 (<i>p</i> < 0.0001) respectively, compared to patients with normal vitals. Overall, 656 (87.2%) patients received Complete Blood Cell counts test, of these 342 (52.1%) had severe anaemia (haemoglobin < 7 g/dl), and a 30.3 (<i>p</i> = 0.02) relative risk of relative risk of mortality compare to patients with higher haemoglobin. Patients who had malaria, elevated renal function test and hypoglycemia, had relative risk of mortality of 22.9, 10.4 and 45.2 (<i>p</i> < 0.0001) respectively, compared to patient with normal values. Most 534 (71.0%) patients were hospitalized for in patients care, and the overall morality rate was 16 (2.1%).</p><p><strong>Conclusions: </strong>We described the clinical presentation, management, and outcomes of patients with SCA presenting to the largest public ED in Tanzania, as well as information on resource utilization. This information can inform development of treatment guidelines, clinical staff education, and clinical research aimed at optimizing care for SCA patients.</p>","PeriodicalId":37740,"journal":{"name":"BMC Hematology","volume":"18 ","pages":"25"},"PeriodicalIF":0.0000,"publicationDate":"2018-09-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://sci-hub-pdf.com/10.1186/s12878-018-0122-3","citationCount":"5","resultStr":"{\"title\":\"The clinical presentation, utilization, and outcome of individuals with sickle cell anaemia presenting to urban emergency department of a tertiary hospital in Tanzania.\",\"authors\":\"Hendry R Sawe, Teri A Reynolds, Juma A Mfinanga, Michael S Runyon, Brittany L Murray, Lee A Wallis, Julie Makani\",\"doi\":\"10.1186/s12878-018-0122-3\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><strong>Background: </strong>Sickle cell anaemia (SCA) is prevalent in sub-Saharan Africa, with high risk of complications requiring emergency care. There is limited information about presentation of patients with SCA to hospitals for emergency care. We describe the clinical presentation, resource utilization, and outcomes of SCA patients presenting to the emergency department (ED) at Muhimbili National Hospital (MNH) in Dar es Salaam, Tanzania.</p><p><strong>Methods: </strong>This was a prospective cohort study of consecutive patients with SCA presenting to ED between December 2014 and July 2015. Informed consent was obtained from all patients or patients' proxies prior to being enrolled in the study. A standardized case report form was used to record study information, including demographics, relevant clinical characteristics and overall patients outcomes. Categorical variables were compared with chi-square test or Fisher's exact test; continuous variables were compared with two-sample t-test or Mann-Whitney U-test.</p><p><strong>Results: </strong>We enrolled 752 (2.7%) people with SCA from 28,322 patients who presented to the MNH-ED. The median age was 14 years (Interquartile range [IQR]: 6-23 years), and 395 (52.8%) were female. Pain 614 (81.6%), fever 289 (38.4%) were the most frequent presenting complaint. Patients with fever, hypoxia, altered mental status and bradycardia had statistically significant relative risk of mortality of 10.4, 153, 50 and 12.1 (<i>p</i> < 0.0001) respectively, compared to patients with normal vitals. Overall, 656 (87.2%) patients received Complete Blood Cell counts test, of these 342 (52.1%) had severe anaemia (haemoglobin < 7 g/dl), and a 30.3 (<i>p</i> = 0.02) relative risk of relative risk of mortality compare to patients with higher haemoglobin. 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引用次数: 5
摘要
背景:镰状细胞贫血(SCA)在撒哈拉以南非洲很普遍,并发症的风险很高,需要紧急护理。关于SCA患者到医院接受急救的信息有限。我们描述了在坦桑尼亚达累斯萨拉姆Muhimbili国立医院(MNH)急诊科就诊的SCA患者的临床表现、资源利用和结果。方法:这是一项前瞻性队列研究,对2014年12月至2015年7月期间连续就诊的SCA患者进行了研究。在纳入研究之前,获得所有患者或患者代理人的知情同意书。使用标准化病例报告表记录研究信息,包括人口统计学、相关临床特征和患者总体结果。将分类变量与卡方检验或Fisher精确检验进行比较;将连续变量与两样本t检验或Mann-Whitney U检验进行比较。结果:我们从28322名接受MN-ED的患者中招募了752名SCA患者(2.7%)。中位年龄为14岁(四分位间距[IQR]:6-23岁),395人(52.8%)为女性。疼痛614例(81.6%),发烧289例(38.4%)是最常见的主诉。发热、缺氧、精神状态改变和心动过缓的患者死亡率的相对风险分别为10.4、153、50和12.1,具有统计学意义(p p = 0.02)相对死亡风险的相对风险。患有疟疾、肾功能测试升高和低血糖症的患者的相对死亡率分别为22.9、10.4和45.2(p 结论:我们描述了SCA患者在坦桑尼亚最大的公共ED中的临床表现、管理和结果,以及资源利用信息。这些信息可以为制定治疗指南、临床工作人员教育和旨在优化SCA患者护理的临床研究提供信息。
The clinical presentation, utilization, and outcome of individuals with sickle cell anaemia presenting to urban emergency department of a tertiary hospital in Tanzania.
Background: Sickle cell anaemia (SCA) is prevalent in sub-Saharan Africa, with high risk of complications requiring emergency care. There is limited information about presentation of patients with SCA to hospitals for emergency care. We describe the clinical presentation, resource utilization, and outcomes of SCA patients presenting to the emergency department (ED) at Muhimbili National Hospital (MNH) in Dar es Salaam, Tanzania.
Methods: This was a prospective cohort study of consecutive patients with SCA presenting to ED between December 2014 and July 2015. Informed consent was obtained from all patients or patients' proxies prior to being enrolled in the study. A standardized case report form was used to record study information, including demographics, relevant clinical characteristics and overall patients outcomes. Categorical variables were compared with chi-square test or Fisher's exact test; continuous variables were compared with two-sample t-test or Mann-Whitney U-test.
Results: We enrolled 752 (2.7%) people with SCA from 28,322 patients who presented to the MNH-ED. The median age was 14 years (Interquartile range [IQR]: 6-23 years), and 395 (52.8%) were female. Pain 614 (81.6%), fever 289 (38.4%) were the most frequent presenting complaint. Patients with fever, hypoxia, altered mental status and bradycardia had statistically significant relative risk of mortality of 10.4, 153, 50 and 12.1 (p < 0.0001) respectively, compared to patients with normal vitals. Overall, 656 (87.2%) patients received Complete Blood Cell counts test, of these 342 (52.1%) had severe anaemia (haemoglobin < 7 g/dl), and a 30.3 (p = 0.02) relative risk of relative risk of mortality compare to patients with higher haemoglobin. Patients who had malaria, elevated renal function test and hypoglycemia, had relative risk of mortality of 22.9, 10.4 and 45.2 (p < 0.0001) respectively, compared to patient with normal values. Most 534 (71.0%) patients were hospitalized for in patients care, and the overall morality rate was 16 (2.1%).
Conclusions: We described the clinical presentation, management, and outcomes of patients with SCA presenting to the largest public ED in Tanzania, as well as information on resource utilization. This information can inform development of treatment guidelines, clinical staff education, and clinical research aimed at optimizing care for SCA patients.
期刊介绍:
BMC Hematology is an open access, peer-reviewed journal that considers articles on basic, experimental and clinical research related to hematology. The journal welcomes submissions on non-malignant and malignant hematological diseases, hemostasis and thrombosis, hematopoiesis, stem cells and transplantation.