刚果民主共和国卢本巴希儿科急诊室镰状细胞患者的临床特征和治疗结果

Stéphanie Ngimbi Luntadila, Joly Nsele Mwanet, A. Natuhoyila, Daniel Mwamba Balonga, Antoinette Yaba Antoniki, Joséphine Monga Kalenga, Tina Katamea, Dapa A. Diallo, Paul Boma Muteb, Stanis Wembonyama Okitotsho
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引用次数: 0

摘要

目的:描述儿科急诊室收治的镰状细胞患者的流行病学、临床结果和治疗方面的情况,并确定与临床结果相关的风险因素:描述性横断面研究:研究地点和时间:卢本巴希大学教学医院、儿科急诊室和Jason Sendwe转诊医院,时间为2020年2月10日至2022年4月30日。研究方法:研究招募了105名镰状细胞病患儿,年龄在6个月至16岁之间。采用 Kaplan-Meier 法分析至 D22 的存活率,用 log-rank 检验比较存活率曲线,用 Cox 回归确定死亡风险因素,显著性水平为 p ˂ 0.05:入院的主要原因是感染(83.8%)、高痛性血管闭塞危象(73.3%)和严重贫血(36.2%)。根据 Adegoke 严重程度评分,60% 的患儿临床表现为重度,32.4% 为中度,7.6% 为轻度。中位生存期为 5.9 天。存活率从第 2 天的 80% 降至第 22 天的 67.6%。中度和重度临床特征(P = 0.001)、从外围医院转院(P = 0.006)和感染综合征诊断(P = 0.002)的存活期明显缩短。住院头两天是关键时期,死亡率为 20%,而全因死亡率为 12.4%。在调整后的多变量分析中,死亡风险因素为转院(P=0.04)、严重临床特征(P=0.033)、住院时间超过2天(P=0.04)、感染综合征(P=0.01)和疑似肝细胞衰竭(P=0.009):结论:卢本巴希地区镰状细胞病的发病率和死亡率都很高,主要与可控的风险因素有关。通过对医务工作者进行镰状细胞病方面的培训,并在健康金字塔的各个层面更好地组织特定护理,镰状细胞病的预后可以得到改善。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Clinical Features and Outcome of Sickle Cell Patients in Pediatric Emergency Departments in Lubumbashi, Democratic Republic of Congo
Aims: To describe the epidemiology clinical outcome, and therapeutic aspects of sickle cell patients admitted to pediatric emergency departments, and to identify the risk factors associated with the clinical outcome. Study Design: Descriptive cross-sectional study. Place and Duration of Study: University of Lubumbashi teaching hospital, pediatric emergency departments and Jason Sendwe Referral Hospital from 10 February 2020 to 30 April 2022. Methodology: 105 children with sickle cell disease aged 6 months to 16 years were admitted and recruited in the study. The Kaplan-Meier method was used to analyze survival to D22, the log-rank test to compare survival curves, and Cox regression to identify mortality risk factors, at a significance level of p ˂ 0.05. Results: The main reasons for admission were infection (83.8%), hyperalgesic vasoocclusive crisis (73.3%) and severe anemia (36.2%). According to the Adegoke severity score, 60% of the children had a severe clinical profile, 32.4% were moderate and 7.6% were mild. Median survival was 5.9 days. Survival decreased from 80% on day 2 to 67.6% on day 22. Survival was significantly shorter for moderate and severe clinical profiles (P = 0.001), transfer from a peripheral hospital (P = 0.006), and diagnosis of an infectious syndrome (P = 0.002). The critical period was the first 2 days of hospitalization, with a mortality rate at 20% compared with an all-cause mortality rate at 12.4%. In the adjusted multivariate analyses, death risk factors were transfer (P=0.04), severe clinical profile (P=0.033), hospital stay >2 days (P=0.04), infectious syndrome (P=0.01) and suspected hepatocellular failure (P=0.009). Conclusion: Sickle cell morbidity and mortality in Lubumbashi are high and associated with mostly controllable risk factors. The prognosis for sickle cell disease can be improved by training health workers in sickle cell disease and by better organizing specific care at all levels of the health pyramid.
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