补充叶酸铁对埃塞俄比亚西北部内脏利什曼病患者血红蛋白变化的影响:一项回顾性随访研究

Q2 Medicine BMC Hematology Pub Date : 2018-09-21 eCollection Date: 2018-01-01 DOI:10.1186/s12878-018-0123-2
Tadele Mulaw, Amare Tariku, Adino Tesfahun Tsegaye, Zegeye Abebe
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引用次数: 4

摘要

背景:一个患有内脏利什曼病(VL)的人通常伴有贫血,埃塞俄比亚西北部的一个内脏利什曼病治疗中心建议对这些患者补充叶酸铁。但没有文献证据表明叶酸铁补充剂是否能改善患者的血液学状况。因此,本研究旨在评估埃塞俄比亚西北部补充和未补充叶酸铁的VL患者血红蛋白(Hb)及其决定因素的变化。方法:2015年1月至2016年12月进行回顾性队列研究。数据输入Epi-Data 3.1版本,并转移到SPSS (Statistical Package for Social Science) 20版本进行分析。分别采用独立样本t检验和线性回归来比较Hb的变化,并确定与Hb变化相关的因素。采用95%置信水平和p值小于0.05确定统计学显著性。结果:602例VL患者中,299例(49.7%)来自贡达尔大学医院。从基线到治疗结束,添加和未添加叶酸铁的Hb的平均(±SD)变化分别为0.99(±1.64)和1.61(±1.88)g/dl,平均差异为0.62,95% CI (0.34, 0.90), p值为:结论:补充叶酸铁对Hb的变化有负面影响。SSG-PM联合治疗、年龄、鼻出血、基线白细胞和Hb以及补充铁叶酸是Hb变化的决定因素。因此,为了获得更好的结果,建议避免补充叶酸铁,结合SSG-PM和早期发现并发症,加强VL治疗。
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Effect of iron-folic acid supplementation on change of hemoglobin among visceral Leishmaniasis patients in northwest Ethiopia: a retrospective follow up study.

Background: An individual with visceral Leishmaniasis (VL) commonly present with anemia and one of the VL treatment center in northwest Ethiopia has been recommended iron-folic acid supplementation to these patients. But there is no documented evidence whether iron-folic acid supplementation improves the hematological profile of patients. Therefore, the study aimed to assess change in hemoglobin (Hb) and its determinant factors among VL patients with and without iron-folic acid supplementation in northwest Ethiopia.

Methods: A retrospective cohort study was conducted from January 2015 to December 2016. Data were entered into Epi-Data version 3.1 and transferred to Statistical Package for Social Science (SPSS) version 20 for analysis. Independent sample T-test and linear regression were used to compare the change in Hb and identify factors associated with a change in Hb, respectively. A 95% confidence level and p-values less than 0.05 were used determine statistically significant.

Results: From a total of 602 VL patients, 299 (49.7%) were from University of Gondar hospital. The mean (±SD) change of Hb from baseline to end of treatment was 0.99(±1.64) and 1.61(±1.88) g/dl with and without iron-folate supplementation, respectively, with mean difference 0.62, 95% CI (0.34, 0.90) and a p-value of < 0.0001. In multiple linear regressions, combination therapy of sodium stibogluconate-paramomycin (SSG-PM) was positively associated with a change of Hb (β [SE, p]: 0.710/0.15, < 0.0001). Whereas age (- 0.030/0.009, 0.001), nasal bleeding (- 0.261/0.123, 0.035), baseline white blood cell (- 0.139/0.044, 0.002) and hemoglobin (- 0.513/0.031, < 0.0001), end of treatment spleen size (- 0.059/0.015, < 0.0001) and iron-folic acid supplementation (- 0.574/0.163, < 0.0001) were negatively associated with change of Hb.

Conclusion: Iron-folic acid supplementation had a negative effect on the change of Hb. A combination therapy of SSG-PM, age, nasal bleeding, baseline white blood cells and Hb, and iron-folic acid supplementation were the determinants of change of Hb. Therefore, avoiding iron-folic acid supplementation and strengthening VL treatment with a combination of SSG-PM and, and early identification of complications is recommended for a better outcome.

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来源期刊
BMC Hematology
BMC Hematology Medicine-Hematology
CiteScore
4.10
自引率
0.00%
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0
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.
期刊最新文献
Correction to: Rapid and reliable detection of α-globin copy number variations by quantitative real-time PCR Correction to: Patterns of bone marrow aspiration confirmed hematological malignancies in Eritrean National Health Laboratory. Correction to: The impact of helicobacter pylori eradication on platelet counts of adult patients with idiopathic thrombocytopenic purpura. Assessment of knowledge, attitude and practice and associated factors of blood donation among health care workers in Ethiopia: a cross-sectional study. Health-related quality of life of adolescents with sickle cell disease in sub-Saharan Africa: a cross-sectional study.
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