Kebede Fassikaw, Tarekegn Habtamu, Molla Mulugeta, Jara Dube, Abate Abebe
Woldia University, College of Health Sciences, School Public Health, Department of Epidemiology & Biostatics, Woldia, Ethiopia.
Pawe Health Science College, Department of Pharmacy, Pawe Metekel, Ethiopia.
J Trop Med. 2022 Jan 29;2022:9925693. doi: 10.1155/2022/9925693. eCollection 2022.
The human immune deficiency virus (HIV) is the strongest risk factor for endogenous reactivation of pulmonary tuberculosis (PTB) through target reduction of CD4, T-lymphocytes, and cellular immune function. Almost one-third of deaths among people living with HIV are attributed to tuberculosis. Despite this evidence, in Ethiopia, information is scarce and meager regarding PTB incidence after ART initiated for seropositive children. . Facility-based multicenter historical cohort was conducted among 721 seropositive children after initiating ART from January 1, 2009, to December 31, 2019. Data from the records of children were extracted using a standardized checklist. The collected data were entered using Epi-Data version 4.2 and exported to STATA (SE) R-14 version statistical soft wares for further analysis. Bivariable and multivariable Cox regression analyses were conducted to identify predictors of PTB incidence. . Seven hundred twenty-one ( = 721) seropositive children were included with a mean (±SD) age of 118.4 ± 38.24 months. During the follow-up periods, 63 (15.2%) participants developed new cases of TB; majority (61/63, 96.8%) of them were PTB. The overall incidence rate and the median (±IQR) time of PTB reported were determined as 5.86 per 100 child years (95% CI: 4.58, 7.5) and 17.8 (±11) months, respectively. At baseline, children being severely stunted (AHR = 2.9 : 95% CI, 1.2-7.8, =0.03), with Hgb ≤10 mg/dl (AHR = 4.0; 95% CI, 2.1-8.1, =0.001), and not given isoniazid and cotrimoxazole preventive therapy (AHR = 2.4; 95% CI: 1.2; 5.1, =0.001) (AHR = 2.5; 95% CI, 1.4-4.7, =0.021) were significantly associated with PTB incidence. . A high incidence rate of PTB was observed in our study as compared with the previous finding in Ethiopia. Cases at baseline not taking IPT and CPT, being severely stunted, and having low hemoglobin (≤10 mg/dl) levels were found to be at higher risk of developing PTB.
人类免疫缺陷病毒(HIV)是导致肺结核(PTB)内源性再激活的最强风险因素,它会使CD4、T淋巴细胞数量减少,并损害细胞免疫功能。在感染HIV的人群中,几乎三分之一的死亡归因于结核病。尽管有这些证据,但在埃塞俄比亚,关于血清反应阳性儿童开始抗逆转录病毒治疗(ART)后PTB发病率的信息却很少且不全面。在2009年1月1日至2019年12月31日期间,对721名开始接受ART治疗的血清反应阳性儿童进行了基于医疗机构的多中心历史队列研究。使用标准化清单从儿童记录中提取数据。收集到的数据使用Epi-Data 4.2版本录入,并导出到STATA(SE)R-14版本的统计软件中进行进一步分析。进行双变量和多变量Cox回归分析以确定PTB发病率的预测因素。纳入了721名血清反应阳性儿童,平均(±标准差)年龄为118.4±38.24个月。在随访期间,63名(15.2%)参与者出现了新的结核病病例;其中大多数(61/63,96.8%)为PTB。报告的PTB总体发病率和中位数(±四分位间距)时间分别确定为每100儿童年5.86例(95%置信区间:4.58,7.5)和17.8(±11)个月。在基线时,严重发育迟缓的儿童(调整后风险比[AHR]=2.9:95%置信区间,1.2 - 7.8,P = 0.03)、血红蛋白(Hgb)≤10mg/dl的儿童(AHR = 4.0;95%置信区间,2.1 - 8.1,P = 0.001)以及未接受异烟肼和复方新诺明预防性治疗的儿童(AHR = 2.4;95%置信区间:1.2;5.1,P = 0.001)(AHR = 2.5;95%置信区间,1.4 - 4.7,P = 0.021)与PTB发病率显著相关。与埃塞俄比亚之前的研究结果相比,我们的研究中观察到PTB的发病率较高。发现基线时未接受IPT和CPT、严重发育迟缓以及血红蛋白水平低(≤10mg/dl)的儿童发生PTB的风险更高。