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Right Ventricular Function Assessment in Sickle Cell Anaemia Patients Using Echocardiography 超声心动图评价镰状细胞性贫血患者右心室功能
Pub Date : 1900-01-01 DOI: 10.23880/HIJ-16000136
A. Adebiyi
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引用次数: 2
Prevalence of Transfusion-Transmissible Infections and Associated Risk Factors among Blood Donors in Bamenda, Cameroon 喀麦隆巴门达献血者中输血传播感染的流行及相关危险因素
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000188
A. Le
Introduction: Blood transfusion is considered a life-saving procedure but the presence of transfusion transmitted infections (TTIs) is a major public health concern. TTIs such as hepatitis B virus (HBV), hepatitis C virus (HCV), human immunodeficiency virus (HIV), and Treponema pallidum (syphilis) are among the greatest threats to blood safety. In Cameroon, most of the patients remain undiagnosed as they are asymptomatic. This study aimed at determining the prevalence of TTIs and its associated risk factors in blood donors from the Northwest region of Cameroon. Methodology: A retrospective study of blood donors’ records from a rural and urban towns between 2015 to 2017 was reviewed. The data were analyzed using SPSS vs 23.0 and a p-value <0.05 was considered statistically significant. Results: A total of 4020 (91.5%) blood donors were included in the study. The mean age was 27.8years and the proportion of male was 78.3% (3143). The prevalence of TTIs was 7.3% (292) and showed a significant (P=0.001) decreasing trend from 10.2% to 5.7 %. The prevalence of HBV, HCV, HIV and syphilis were 0.7% (27), 1.8% (73) and 1.9% (77) respectively. Except for HCV, all TTIs showed a decreasing trend. From the results, the positive rate of anyone of the TTIs was significantly (p< 0.05) higher among male 8.1% (255), replacement donors 9.1% (240) and those who had attained only basic education 8.5% (91). Co-infection was detected among 0.5% (19) blood donors and the highest prevalence was between HIV and Syphilis 0.15% (6). Independent predictors of anyone of the TTIs were; living in rural towns, males, age group >20 years replacement donors, civil servants, and those who had attained either basic or secondary education. Conclusion: Our data provides important findings that contribute to a better understanding of TTIs epidemiology in Bamenda. Further investigations are needed to assess the prevalence and determinants of these infections in other communities to support the development of effective prevention and control strategies. There is a need for stringent selection of blood donors. High sensitive and specific screening tests such as Nucleic acid testing enzyme immunoassays should be used to diagnose the high-risk donors.
输血被认为是一种挽救生命的方法,但输血传播感染(tti)的存在是一个主要的公共卫生问题。乙型肝炎病毒(HBV)、丙型肝炎病毒(HCV)、人类免疫缺陷病毒(HIV)和梅毒螺旋体(梅毒)等tti是对血液安全的最大威胁。在喀麦隆,大多数患者仍未得到诊断,因为他们没有症状。本研究旨在确定喀麦隆西北地区献血者中传播性感染的流行情况及其相关危险因素。方法:对2015年至2017年农村和城镇献血者记录进行回顾性研究。使用SPSS vs . 23.0和p值分析20年替代供者、公务员和接受过基础或中等教育的人的数据。结论:我们的数据提供了重要的发现,有助于更好地了解巴门达地区的tti流行病学。需要进一步调查,以评估其他社区中这些感染的流行情况和决定因素,以支持制定有效的预防和控制战略。有必要严格选择献血者。对高危献血者的诊断应采用核酸检测、酶免疫测定等高灵敏度和特异性筛选试验。
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引用次数: 0
The VACD-Thal Protocol in the Treatment of Multiple Myeloma in Abidjan (Côte D’ivoire) VACD-Thal方案在阿比让治疗多发性骨髓瘤(Côte科特迪瓦)
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000144
Packo Dieu-le-Veut Saint-Cyr Sylvestre
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引用次数: 0
Evaluation of Haematoimmunological, Erythropoietic Growth Factor and Virological Status in HIV-Patients hiv患者血液免疫学、红细胞生长因子和病毒学状况的评价
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000193
E. J.
Background: Human Immunodeficiency Virus reduces immune status and diminishes haematological values causing decreased or ineffective haematopoiesis in HIV-infected individuals. Aim: To evaluate haematoimmunological, erythropoietic growth factor and virological status in HIV-patients. Methodology: This study was carried out at Federal Teaching Hospital, Ido-Ekiti. One hundred samples each were collected from HIV positive subjects on ART and ART-naïve, one hundred samples were collected from apparently healthy individuals as control. Six milliliters of whole blood were collected from each subject; 3mls of whole blood was dispensed into K2EDTA bottle for immediate analysis of haematological parameters using haematology analyzer, CD4 and CD8 count were analyzed using flow cytometer. The remaining 3ml of blood was dispensed into plain bottle, serum was extracted for erythropoietin analysis using enzyme-linked immunosorbent assay technique and viral load using polymerase chain reaction. Results: Mean values of RBC indices CD4, CD4/CD8, EPO, TWBC and LYM among ART-naïve were significantly lower (p<0.05) compared to ART and control subjects. Mean values of CD8, VL, NEU, MONO, EOSIN and BASO in ART-naïve were significantly higher (p<0.05) compared to ART and control subjects. Conclusion: HIV infection suppresses erythropoietic growth factor, haematoimmunological, and virological parameters as observed in the study. However, there is an improvement in HIV subjects on ART compared with ART-naïve, this suggested that there is positive response to antiretroviral therapy in HIV patients.
背景:人类免疫缺陷病毒降低免疫状态,降低血液学值,导致hiv感染者造血功能下降或无效。目的:了解hiv患者的血液免疫学、红细胞生长因子及病毒学状况。方法:本研究在Ido-Ekiti联邦教学医院进行。从接受抗逆转录病毒治疗的艾滋病毒阳性受试者和ART-naïve中各收集100个样本,从表面健康的个体中收集100个样本作为对照。每位受试者采集6毫升全血;取全血3ml装于K2EDTA瓶中,血液学分析仪即时分析血液学参数,流式细胞仪分析CD4、CD8计数。取剩余血3ml装于普通瓶中,提取血清,酶联免疫吸附法测定促红细胞生成素,聚合酶链反应测定病毒载量。结果:ART-naïve组患者红细胞指标CD4、CD4/CD8、EPO、TWBC、LYM均值较ART组和对照组显著降低(p<0.05)。ART-naïve组CD8、VL、NEU、MONO、EOSIN、BASO均值较ART组和对照组显著升高(p<0.05)。结论:本研究观察到HIV感染可抑制红细胞生长因子、血液免疫学和病毒学参数。然而,与ART-naïve相比,抗逆转录病毒治疗的艾滋病毒患者有所改善,这表明艾滋病毒患者对抗逆转录病毒治疗有积极反应。
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引用次数: 0
Prevalence of ABO and RhD Antigen in District Nowshera an Experience in Blood Bank of Qazi Hussain Ahmed Medical Complex Nowshera 诺谢拉地区ABO和RhD抗原的流行情况&卡齐侯赛因艾哈迈德医院诺谢拉血库的经验
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000171
Khan H
Objectives: To screen the donors for the frequency of different blood groups, reason for deferral and comparative analysis of the donation in two consecutive years in blood bank of Qazi Hussian Ahmed Medical Complex Nowshera. Methodology: This cross sectional study was carried out in the Blood bank of Qazi Hussain Ahmed Medical Complex, Nowshera from 25th April 2017 to 5th May 2019. A total of 3429 donors were included in the study. From each donor blood was collected in strict sterile environment. ABO and Rh blood grouping were done by agglutination method using antisera A, antisera B and antisera D. The frequency of different blood group was recorded. Data was analyzed for percentage calculation. Results: A total of 3429 donors received in the blood bank for donation. The age range of the donor was from 18 years to 52 years. The mean age was 35 years with standard deviation of 3.24. 3018(88%) of the donors were males and 411(12%) females. The distribution of RhD+ and RhD- blood groups was 89.90% and 10.09% respectively. The frequency of “RhD+ blood groups in target population” was B: 1226(35.75%), O: 807(23.53%), A: 754(22%) and AB:296(8.63%). The frequency of “Rh Negative blood groups” was: B: 139(4.05%), O: 95(2.77%), A:84(2.45%) and AB: 28(0.82%). The packed cell wastage rate in our blood bank was 185 (5.4%). The donor deferral rate was 0.7% (24cases) due to positive virology. In quarter 2 of 2017, 767 bags received for transfusion due to dengue outbreak in District Nowshera. Hepatitis B Virus was major cause of deferral that was reported in 14 cases followed by HCV Virus in 13 cases. Conclusion: The frequency of “Rh-positive blood group” was BOA and AB respectively. Blood Group B was noted in 35% of the donors that counted to be the major prevalent Rh positive blood group in our population. Regarding the Rh Negative blood group again the frequency was B,O,A and AB. Blood group B- was prevalent as a major negative blood group in our population that was recorded in 4.05% cases. AB- Blood group was the rare blood group noted in 0.82% of the donors. The main cause of deferral was Hep B virus that was noted in 14 cases followed by HCV virus in 13 case. The total prevalence of the hepatitis in the donors presented to our blood bank was 0.7%.
目的:对诺谢拉卡齐侯赛因艾哈迈德医疗中心血库的献血者进行不同血型频率、延迟献血原因的筛查,并对连续两年献血者进行对比分析。方法:本横断面研究于2017年4月25日至2019年5月5日在瑙谢拉Qazi Hussain Ahmed医疗中心血库进行。共有3429名捐赠者参与了这项研究。每位献血者的血液均在严格的无菌环境中采集。采用抗血清A、抗血清B、抗血清d凝集法进行ABO、Rh血型的分型,记录不同血型的出现频率。对数据进行分析,计算百分比。结果:共有3429名献血者在血库接受捐献。供体年龄从18岁到52岁不等。平均年龄35岁,标准差为3.24。男性3018例(88%),女性411例(12%)。RhD+和RhD-血型分布分别为89.90%和10.09%。“目标人群中RhD+血型”出现频率分别为B: 1226(35.75%)、O: 807(23.53%)、A: 754(22%)、AB:296(8.63%)。Rh阴性血型出现频率分别为:B: 139(4.05%)、O: 95(2.77%)、A:84(2.45%)、AB: 28(0.82%)。血库中堆积细胞流失率为185(5.4%)。由于病毒学阳性,供体延迟率为0.7%(24例)。2017年第二季度,由于瑙谢拉区爆发登革热疫情,收到了767袋输血。乙型肝炎病毒是延误的主要原因,有14例报告,其次是丙型肝炎病毒,有13例报告。结论:rh阳性血型分别以BOA和AB出现。在35%的献血者中发现了B型血,这被认为是我们人群中主要流行的Rh阳性血型。Rh阴性血型再次以B型、O型、A型和AB型为主。B-型是我国人群中主要的阴性血型,占4.05%。AB血型为罕见血型,占献血者的0.82%。延迟的主要原因是乙肝病毒(14例),其次是丙肝病毒(13例)。献血者肝炎总患病率为0.7%。
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引用次数: 0
Cutaneous Gamma Delta T cell Lymphoma Leading to Hemophagocytic Lymphohistiocytosis that Presented as Posterior Reversible Encephalopathy Syndrome 皮肤γ δ T细胞淋巴瘤导致噬血细胞性淋巴组织细胞增多症,表现为后部可逆性脑病综合征
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000142
K. Kannan
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引用次数: 0
Association of Methylene Tetrahydrofolate Reductase Gene A1298C (Rs1801131) Polymorphism with Myocardial Infarction among Sudanese Patients 亚甲基四氢叶酸还原酶基因A1298C (Rs1801131)多态性与苏丹患者心肌梗死的关系
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000192
H. Tam
Background: Myocardial infarction (MI) is among the leading causes of mortality worldwide. Variations in folate metabolism including genetic polymorphisms in the key metabolic enzymes had showed influences in the MI process. Objectives: To determine whether the C1298A transition in the Methylene Tetrahydrofolate Reductase ( MTHFR ) gene is associated with increased risk for MI among Sudanese patients. Material and methods: This is a hospital based case control study in which a total of 140 Sudanese subjects were enrolled, 70 patients with myocardial infarction and 70 age- and sex matched healthy volunteers as a control group. Genomic DNA was extracted by (QIA gene, Korea) kits and the SNPs genotypes were determined using polymerase chain reaction followed by restriction fragment length polymorphism (PCR- RFLP). Data of this study were collected using a structured interview questionnaire and analyzed by statistical package for social sciences (version 21). Results: The frequency of the AA genotype was higher in the patients group compared with control (96%, 71% respectively); while the AC genotype was higher in the control (20%, 5% respectively), while the CC genotype was not observed in this study population. The frequencies of A and C alleles were 0.68 and 0.02 respectively in MI patients while frequencies were 0.60 and 0.10 respectively in the control group. No statistically significant association was observed between MTHFR genotypes and MI (P. values = 0.4 and 0.1 for AA and AC genotypes respectively). Conclusion: In this study population, the A1298C MTHFR polymorphism is not associated with the risk of MI among the Sudanese population.
背景:心肌梗死(MI)是世界范围内死亡的主要原因之一。叶酸代谢的变化,包括关键代谢酶的遗传多态性,在心肌梗死过程中显示出影响。目的:确定亚甲基四氢叶酸还原酶(MTHFR)基因中的C1298A转换是否与苏丹患者心肌梗死风险增加有关。材料和方法:这是一项基于医院的病例对照研究,共纳入140名苏丹受试者,70名心肌梗死患者和70名年龄和性别匹配的健康志愿者作为对照组。采用(QIA gene, Korea)试剂盒提取基因组DNA,采用聚合酶链反应-限制性片段长度多态性(PCR- RFLP)检测snp基因型。本研究使用结构化访谈问卷收集数据,并使用社会科学统计软件包(第21版)进行分析。结果:患者组AA基因型出现频率高于对照组(分别为96%、71%);而AC基因型在对照组中较高(分别为20%和5%),而CC基因型在本研究人群中未观察到。心肌梗死患者A、C等位基因频率分别为0.68、0.02,对照组为0.60、0.10。MTHFR基因型与心肌梗死无统计学意义(AA和AC基因型p值分别为0.4和0.1)。结论:在本研究人群中,苏丹人群中A1298C MTHFR多态性与心肌梗死风险无关。
{"title":"Association of Methylene Tetrahydrofolate Reductase Gene A1298C (Rs1801131) Polymorphism with Myocardial Infarction among Sudanese Patients","authors":"H. Tam","doi":"10.23880/hij-16000192","DOIUrl":"https://doi.org/10.23880/hij-16000192","url":null,"abstract":"Background: Myocardial infarction (MI) is among the leading causes of mortality worldwide. Variations in folate metabolism including genetic polymorphisms in the key metabolic enzymes had showed influences in the MI process. Objectives: To determine whether the C1298A transition in the Methylene Tetrahydrofolate Reductase ( MTHFR ) gene is associated with increased risk for MI among Sudanese patients. Material and methods: This is a hospital based case control study in which a total of 140 Sudanese subjects were enrolled, 70 patients with myocardial infarction and 70 age- and sex matched healthy volunteers as a control group. Genomic DNA was extracted by (QIA gene, Korea) kits and the SNPs genotypes were determined using polymerase chain reaction followed by restriction fragment length polymorphism (PCR- RFLP). Data of this study were collected using a structured interview questionnaire and analyzed by statistical package for social sciences (version 21). Results: The frequency of the AA genotype was higher in the patients group compared with control (96%, 71% respectively); while the AC genotype was higher in the control (20%, 5% respectively), while the CC genotype was not observed in this study population. The frequencies of A and C alleles were 0.68 and 0.02 respectively in MI patients while frequencies were 0.60 and 0.10 respectively in the control group. No statistically significant association was observed between MTHFR genotypes and MI (P. values = 0.4 and 0.1 for AA and AC genotypes respectively). Conclusion: In this study population, the A1298C MTHFR polymorphism is not associated with the risk of MI among the Sudanese population.","PeriodicalId":245976,"journal":{"name":"Haematology International Journal","volume":"1 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"1900-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"122425272","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Thrombocytosis on Adult Patient with SARS-Cov-2 in Africa 非洲成年SARS-Cov-2患者的血小板增多
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000166
Ngolet Lo
The 2019-2020 pandemic caused by a novel coronavirus, SARS-Cov-2 or COVID-19 is ongoing. The outbreak of a respiratory illness caused by COVID-19 was first identified in Wuhan, Hubei Province, China and declared by the local authorities in December 2019. Since the beginning of the pandemic, Governments and health authorities across the world are striving to limit the widespread of the virus. The African continent registered its first cases about two months ago, and then readily implemented massive preventive measures such as lockdown, confinement and curfew. Like others, African Scientists are learning from and sharing their experiences about the disease. The aim of this article is to present a case of a COVID-19-related moderate pneumonia with unusual laboratory findings. This study has been approved by the local bioethics committee.
由新型冠状病毒SARS-Cov-2或COVID-19引起的2019-2020年大流行正在进行中。2019年12月,中国湖北省武汉市首次发现了由COVID-19引起的呼吸系统疾病疫情,并由当地政府宣布。自大流行开始以来,世界各国政府和卫生当局正在努力限制该病毒的传播。大约两个月前,非洲大陆出现了第一例病例,随后迅速实施了封锁、禁闭和宵禁等大规模预防措施。和其他人一样,非洲科学家正在学习和分享他们对这种疾病的经验。本文的目的是报告一例与covid -19相关的中度肺炎,其实验室结果异常。本研究已获得当地生物伦理委员会的批准。
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引用次数: 0
Treating SARS-CoV-2 Based Upon the Fleming InflammoThrombotic Response (ITR) & Cardiovascular Disease Theory 基于Fleming炎症血栓反应(ITR)和心血管疾病理论治疗SARS-CoV-2
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000209
R. Fleming
This paper discusses the importance of addressing, measuring and treating the infectious, inflammatory and thrombotic tissue effect resulting from the body’s immunologic response to SARS-CoV-2 using methods previously detailed in the medical literature, in an effort to reduce SARS-CoV-2 morbidity and mortality. Successful treatment of SARS-CoV-2 requires addressing each of the four stages of the viral infection including oxygenation, acute cytotoxic immune response, adaptive humoral-antibody response, and viral cellular attachment and replication. Information obtained from the National Clinical Trial NCT04349410 has proven the benefit of treating each of these four factors. A paper detailing the NCT04349410 results has been published elsewhere.
本文讨论了利用先前医学文献中详细介绍的方法解决、测量和治疗由机体对SARS-CoV-2的免疫反应引起的感染、炎症和血栓组织效应的重要性,以降低SARS-CoV-2的发病率和死亡率。成功治疗SARS-CoV-2需要解决病毒感染的四个阶段,包括氧合作用、急性细胞毒性免疫反应、适应性体液抗体反应以及病毒细胞附着和复制。从国家临床试验NCT04349410中获得的信息已经证明了治疗这四个因素的益处。详细介绍NCT04349410结果的论文已在其他地方发表。
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引用次数: 0
Genetic Polymorphism of Endothelial Nitric Oxide Synthase in Sickle Cell Disease Patients in South-Eastern Nigeria 尼日利亚东南部镰状细胞病患者内皮型一氧化氮合酶的遗传多态性
Pub Date : 1900-01-01 DOI: 10.23880/hij-16000187
Okonkwo Co
Background: Sickle cell disease (SCD) is an inherited blood disorder resulting from a point mutation of thymine (T) for adenine (A) at codon 6 of the gene for beta-globin chain of haemoglobin, leading to substitution of Valine for Glutamate at position 6 of the amino acid sequence, thereby shifting the isoelectric point of the protein. The single nucleotide polymorphism (SNP) (T-786C) in the 5’ promoter region which affects the expression of endothelial nitric oxide synthase (ENOS) gene is critical in determining the predisposition of humans to diseases including SCD. This work was therefore aimed at investigating the presence of SNP (T-786C) in the 5’ promoter region of ENOS gene in patients with SCD with respect to controls, visiting the University of Nigeria Teaching Hospital (UNTH) Ituku-Ozalla, Enugu State, south-Eastern Nigeria. Materials and Methods: The study recruited a total of 50 subjects including 20 SCD patients (SS), 15 sickle cell carriers (AS) and 15 healthy non-carriers (AA). DNA was extracted from venous blood samples; PCR amplification was done using specified primers to the region of polymorphism, and finally followed by HpaII restriction enzyme digestion. Results: The results obtained showed only TT genotype across all samples, and so could not establish any relationship between the SNP T-786C ENOS gene region and SCD. There was presence of the same genotype in both test and control groups. Conclusion: This research findings therefore suggest that T-786C ENOS gene polymorphism is not associated with SCD in south-Eastern Nigeria and thus cannot genetically influence the phenotypic outcome of the disease in the clime.
背景:镰状细胞病(SCD)是一种遗传性血液疾病,由血红蛋白β -珠蛋白链基因密码子6处胸腺嘧啶(T)点突变为腺嘌呤(a)引起,导致氨基酸序列第6位缬氨酸取代谷氨酸,从而改变蛋白质的等电点。影响内皮型一氧化氮合酶(ENOS)基因表达的5 '启动子区域的单核苷酸多态性(T-786C)在决定人类对SCD等疾病的易感性中至关重要。因此,这项工作旨在调查SCD患者ENOS基因5 '启动子区域中SNP (T-786C)的存在,与对照组相比,访问了尼日利亚东南部埃努古州的尼日利亚大学教学医院(UNTH) Ituku-Ozalla。材料与方法:本研究共招募50例受试者,其中SCD患者20例(SS),镰状细胞携带者15例(AS),健康非携带者15例(AA)。静脉血样本提取DNA;用指定引物对多态性区域进行PCR扩增,最后进行HpaII酶切。结果:得到的结果在所有样本中仅显示TT基因型,因此不能建立SNP T-786C ENOS基因区域与SCD的关系。试验组和对照组均存在相同的基因型。结论:本研究结果提示T-786C ENOS基因多态性与尼日利亚东南部SCD无关,因此不能从遗传上影响该地区SCD的表型结果。
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引用次数: 1
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Haematology International Journal
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