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Diagnostic value of serum adenosine deaminase in tuberculous lymphadenitis 血清腺苷脱氨酶对结核性淋巴结炎的诊断价值
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i2.57773
M. Adhikari, S. M. Arafat, M. Ananna, Md. Atikur Rahman, H. Imam, Shah Mohammad Mohaimenul Haq
Background: Extra-pulmonary tuberculosis often requires FNAC or biopsy of lymph node to reach a final diagnosis of tuberculous lymphadenitis, which is invasive, expensive, and needs an advanced setting. Estimation of adenosine deaminase (ADA) in different body fluid and serum has been suggested as a quick, cheap, and reliable test for tuberculosis.Objective: The study was intended to assess the usefulness of serum ADA in the diagnosis of tuberculous lymphadenitis.Methods: This was a cross-sectional observational study, conducted in BSMMU over a two year period and included 68 participants, divided equally into two group e.g. tuberculous lymphadenitis and a healthy comparison group. As tuberculous lymphadenitis, only newly diagnosed cases, labeled on the basis of histopathological findings of epithelioid granuloma with caseation necrosis were included. Serum ADA concentrations were estimated by enzymatic method and compared between groups.Results: The mean serum ADA concentration was found to be 25.52±7.11 U/L in tuberculous lymphadenitis group, which was significantly higher (p=0.000) than that of the healthy comparison group (14.82±3.85 U/L). Three different cut-off values of serum ADA (18.25 U/L, 20.45 U/L, 22.15 U/L) were used to determine the best predictive value for the diagnosis of tuberculous lymphadenitis. Sensitivity and specificity of these cut off values were 91.2% and 82.4%, 79.4% and 88.2%, 67.6% and 97.1% respectively.Conclusion: It is clearly denoted by the study that, tuberculous lymphadenitis patients has significant higher serum ADA then the healthy comparison group. This result indicates that serum ADA can be used as a useful adjunct in the diagnosis of tuberculous lymphadenitis with conventional investigations.Bangladesh Med Res Counc Bull 2021; 47(2): 151-155
背景:肺外结核通常需要FNAC或淋巴结活检才能最终诊断为结核性淋巴结炎,这是侵入性的,昂贵的,需要先进的设置。不同体液和血清中腺苷脱氨酶(ADA)的测定被认为是一种快速、廉价和可靠的结核病检测方法。目的:本研究旨在评估血清ADA在结核性淋巴结炎诊断中的价值。方法:这是一项横断面观察性研究,在BSMMU进行了为期两年的研究,包括68名参与者,平均分为两组,如结核性淋巴结炎组和健康对照组。作为结核性淋巴结炎,仅包括新诊断的病例,根据组织病理学结果标记为上皮样肉芽肿伴干酪样坏死。酶法测定血清ADA浓度并比较各组间差异。结果:结核性淋巴结炎组血清ADA平均浓度为25.52±7.11 U/L,显著高于健康对照组(14.82±3.85 U/L) (p=0.000)。采用血清ADA的3个不同临界值(18.25 U/L、20.45 U/L、22.15 U/L)确定诊断结核性淋巴结炎的最佳预测值。这些截断值的敏感性和特异性分别为91.2%和82.4%、79.4%和88.2%、67.6%和97.1%。结论:本研究明确表明,结核性淋巴结炎患者血清ADA明显高于健康对照组。提示血清ADA可作为常规检查诊断结核性淋巴结炎的辅助手段。孟加拉国地中海理事会2021年公报;47 (2): 151 - 155
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引用次数: 0
Intra-articular Injection of Hyaluronic Acid (HA) and Plateletrich Plasma (PRP) in the Treatment of Mild and Moderate Osteoarthritis of Knee 关节内注射透明质酸和富血小板血浆治疗轻中度膝关节骨性关节炎
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i1.55800
Farzana Khan Shoma, Z. Chowdhury, F. Hossain, Abul Khair Mohammad Salek, M. Khasru, Md. Nuruzzaman Khandaker
Background: Osteoarthritis (OA) is the most prevalent chronic joint disorder worldwide and is associated with significant pain and disability. Introduction of platelet-rich plasma (PRP) injection has been viewed as an advance in the management of OA knee.Objective: To compare the effectiveness of PRP and Hyaluronic Acid (HA) in the treatment of mild and moderate OA kneeMethods: The present randomized clinical trial had been conducted in the Department of Physical Medicine and Rehabilitation, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka from 2018 to 2019. A total of 154 patients with mild and moderate OA knee were randomly allocated into two groups: group A (received PRP injection) and group B (received HA injection) where 133 patients completed the follow-up schedule. Outcomes were measured by OA specific translated and validated Bengali instrument- Western Ontario and McMaster Universities Osteoarthritis Index (WOMAC) questionnaire and visual analogue scale (VAS 0-10). They were followed-up for 6 months.Results: There was no significant statistical difference at the baseline between the groups regarding age, sex, grading of OA knee, side involvement, mean duration of the disease, VAS scores and WOMAC scores. After one month, VAS score significantly decreased in PRP group compared to HA group (p<0.001). However, there was no statistical difference regarding total WOMAC scores between two groups (p=0.063). In third and sixth month, VAS score significantly decreased in PRP group compared to HA group (p<0.001). Though the stiffness and physical activity scores of WOMAC did not reduce significantly, the pain score reduced significantly in PRP group compared to HA group. In both groups, significant reduction of VAS and WOMAC total scores was observed after six months follow-up compared to baseline values (p<0.001).Conclusion: Intra-articular platelet-rich plasma improves pain and function of the knee in patients with osteoarthritis. Though intra-articular hyaluronic acid also improves pain and function in the foot, PRP is more effective than hyaluronic acid. Multi-centered clinical trial with long term follow-up should be conducted to see the effects of PRP and HA.Bangladesh Med Res Counc Bull 2021; 47(1): 62-69
背景:骨关节炎(OA)是世界上最常见的慢性关节疾病,与严重的疼痛和残疾有关。富血小板血浆(PRP)注射被认为是膝关节骨性关节炎治疗的一个进步。目的:比较PRP和透明质酸(HA)治疗轻度和中度OA膝关节的有效性方法:本随机临床试验于2018年至2019年在达卡Bangabandhu Sheikh Mujib医科大学(BSMMU)物理医学与康复系进行。共有154名轻度和中度膝关节骨性关节炎患者被随机分为两组:A组(接受PRP注射)和B组(接受HA注射),其中133名患者完成了随访计划。通过OA特异性翻译和验证的孟加拉语仪器-西安大略大学和麦克马斯特大学骨关节炎指数(WOMAC)问卷和视觉模拟量表(VAS 0-10)测量结果。随访6个月。结果:在基线时,两组在年龄、性别、OA膝关节分级、侧面受累、疾病平均持续时间、VAS评分和WOMAC评分方面没有显著的统计学差异。一个月后,与HA组相比,PRP组的VAS评分显著降低(p<0.001)。然而,两组之间的WOMAC总分没有统计学差异(p=0.063)。在第三个月和第六个月,PRP小组的VAS评分与HA组比较显著降低(p<0.001),尽管WOMAC的僵硬和体力活动评分没有显著降低,与HA组相比,PRP组的疼痛评分显著降低。与基线值相比,两组患者在随访6个月后VAS和WOMAC总分均显著降低(p<0.001)。结论:关节内富含血小板的血浆可改善骨关节炎患者的膝盖疼痛和功能。尽管关节内透明质酸也能改善足部疼痛和功能,但PRP比透明质酸更有效。应进行长期随访的多中心临床试验,以观察PRP和HA的效果。Bangladesh Med Res Counc Bull 2021;47(1):62-69
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引用次数: 1
Insulin Resistance in Obese Adolescents at a Tertiary care hospital in Bangladesh 孟加拉国一家三级护理医院肥胖青少年的胰岛素抵抗
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i2.57782
Roksana Parvin, Suraiya Begum, Abul Basher Md. Osman Hayder Mazumder, I. Jahan, K. J. Shyamaly
Background: Insulin resistance has evolved as an important metabolic alteration in obese children especially during adolescence. Emerging data suggest that insulin resistance in obesity play the key role in the pathogenesis of hypertension, dyslipidemia, impaired glucose tolerance, type 2 diabetes mellitus, non-alcoholic fatty liver disease and metabolic syndrome. Objective: The aim of this study was to assess the insulin resistance status of Bangladeshi obese adolescents in hospital settings. Methods: It was a cross sectional study done in children, aged 10 to 16 years, attending the paediatric endocrine clinic, paediatric outpatient and paediatric inpatient department, Bangabandhu Sheikh Mujib Medical University (BSMMU), Dhaka over a period of 15 months. Homeostasis Model Assessment of Insulin Resistance (HOMA- IR) value was obtained from fasting insulin & fasting blood glucose level to assess insulin resistance in obese and normal weight children. Results: Among obese adolescents, 78.8% were insulin resistant in comparison to16% in non-obese adolescent. Mean HOMA-IR level of obese group were significantly higher than non-obese group (4.46±1.82 Vs 1.98±1.26, p<0.001). Insulin resistance was observed in 73.8% and 84.2% among grade 1 obese and grade 2 obese adolescents respectively. HOMA-IR showed positive correlation with BMI and waist circumference. Insulin resistance showed significant association with central obesity, puberty and acanthosis nigricans (AN). Conclusion: In this study, insulin resistance was observed in higher frequency among obese adolescents than normal weight adolescents. Obese adolescents with central obesity, acanthosis nigricans and puberty are at increased risk of insulin resistance. Bangladesh Med Res Counc Bull 2021; 47(2): 212-218
背景:胰岛素抵抗是肥胖儿童尤其是青春期肥胖儿童重要的代谢改变。新的数据表明,肥胖症中的胰岛素抵抗在高血压、血脂异常、糖耐量受损、2型糖尿病、非酒精性脂肪性肝病和代谢综合征的发病机制中起关键作用。目的:本研究的目的是评估孟加拉国肥胖青少年在医院环境中的胰岛素抵抗状况。方法:这是一项横断面研究,在达卡班班杜谢赫穆吉布医科大学(BSMMU)儿科内分泌门诊、儿科门诊和儿科住院科室就诊的10至16岁儿童中进行,为期15个月。通过空腹胰岛素和空腹血糖水平获得胰岛素抵抗稳态模型评估(HOMA- IR)值,评估肥胖和正常体重儿童的胰岛素抵抗。结果:在肥胖青少年中,78.8%的人有胰岛素抵抗,而在非肥胖青少年中,这一比例为16%。肥胖组平均HOMA-IR水平显著高于非肥胖组(4.46±1.82 Vs 1.98±1.26,p<0.001)。1级肥胖青少年胰岛素抵抗率为73.8%,2级肥胖青少年胰岛素抵抗率为84.2%。HOMA-IR与BMI、腰围呈正相关。胰岛素抵抗与中枢性肥胖、青春期和黑棘皮病(AN)有显著关联。结论:在本研究中,肥胖青少年胰岛素抵抗的发生率高于正常体重青少年。伴有中枢性肥胖、黑棘皮病和青春期的肥胖青少年发生胰岛素抵抗的风险增加。孟加拉国地中海理事会2021年公报;47 (2): 212 - 218
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引用次数: 1
Under-five Nutritional Status and its Relationship with Household Dietary Diversity and Food Security among the Dayak Communities in Sarawak, Malaysia 马来西亚砂拉越达亚克社区五岁以下儿童营养状况及其与家庭饮食多样性和粮食安全的关系
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i2.57770
Md. Mizanur Rahman, Neilson Richard Seling, A. Kiyu
Background: Malnutrition among under-five children is one of the paramount public health concerns in the country.Objectives: This study aimed to determine the relationship between under-five nutritional status and household dietary diversity (HDD) and household food security (HFS).Methods: In this cross-sectional study analysed 808 under-five children’s data from 50 villages in five divisions of Sarawak using a multistage cluster sampling technique. Data were collected by face-to-face interview using interviewer-administered questionnaires. WHO Anthro version 3.2.2 was used for anthropometric, and IBM SPSS version 22.0 was used for multivariate data analysis.Results: Multivariate analysis showed that children with low HDD were 1.68 times more likely to be stunted than those with high HDD. Children from households with food insecurity but without hunger were 3.86 times and with hunger were 4.02 times likely to be wasted in the last three months and were almost six times more likely to stunted at the same time. The likelihood of being underweight was 2.86 times more likely to occur in households with food insecurity without hunger and 4.89 times in food insecurity with hunger households. In the past 12 months, children from households with food insecurity with hunger were 8.56 times and four times more likely to be stunted with food insecurity without hunger. Underweight children had twice the odds of occurring in households with food insecurity without hunger compared with food secured households. HFS in the last three months had a significant association with wasting, stunting and underweight of the children, while HFS in the last 12 months was associated with stunting and underweight children.Conclusion: Low HDD had resulted in stunting, and food insecurity had resulted in wasting, stunting and underweight in under-five Dayak children in rural areas of Sarawak. A food-based intervention programme should be undertaken for malnourished children.Bangladesh Med Res Counc Bull 2021; 47(2): 127-135
背景:五岁以下儿童营养不良是该国最重要的公共卫生问题之一。目的:本研究旨在确定五岁以下儿童营养状况与家庭饮食多样性(HDD)和家庭粮食安全(HFS)之间的关系。数据是通过面对面访谈收集的,使用访谈者管理的问卷。世界卫生组织Anthro 3.2.2版用于人体测量,IBM SPSS 22.0版用于多变量数据分析。结果:多因素分析显示,低HDD儿童发育迟缓的可能性是高HDD儿童的1.68倍。在过去三个月里,来自粮食不安全但没有饥饿的家庭的儿童被浪费的可能性是其他家庭的3.86倍,有饥饿的儿童被消耗的可能性是这些家庭的4.02倍,同时发育迟缓的可能性几乎是其他家庭中的6倍。在没有饥饿的粮食不安全家庭中,体重不足的可能性高出2.86倍,在有饥饿的粮食无安全家庭中是4.89倍。在过去的12个月里,来自粮食不安全家庭的儿童在没有饥饿的情况下因粮食不安全而发育迟缓的可能性是其他家庭的8.56倍和4倍。与有粮食保障的家庭相比,八岁以下儿童在没有饥饿的粮食不安全家庭中发生的几率是有粮食保障家庭的两倍。过去三个月的HFS与儿童的消瘦、发育迟缓和体重不足有显著关联,而过去12个月的高频S与发育迟缓和重量不足的儿童有关。结论:在砂拉越农村地区,低HDD导致发育迟缓,粮食不安全导致5岁以下的Dayak儿童消瘦、发育迟缓和体重不足。应当为营养不良的儿童实施以粮食为基础的干预方案。2021年孟加拉医学研究会;47(2):127-135
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引用次数: 0
Mind-set of Recent Medical Graduates: A Channel for Teaching Medical Ethics and Professionalism in Bangladesh 最近医学毕业生的思维定式:孟加拉国教授医学道德和专业精神的渠道
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i1.55801
S. Jahan, M. Flora
Background: The medical ethics and professionalism teaching have an influence on knowledge, attitude and skills of physicians. The scope of learning medical ethics and professionalism is limited in Curriculum for Medical Education in Bangladesh. There is an unhealthy situation in physician-patient relationship as a consequence of this limitation.Objectives: This study was aimed to assess attitude of recent medical graduates towards medical ethics and professionalism. The findings of this study might be helpful to strengthen medical ethics and professionalism in the medical education.Methods: This descriptive study was conducted on recent medical graduates of seven medical colleges under four universities in Bangladesh from January 2018 to June 2019. Data were collected using a pretested self administered semi-structured questionnaire, based on attitude measuring scale regarding medical ethics and professionalism.Results: Attitude scores of 308 recent medical graduates were in ethical conduct, autonomy, information of wrong doing during treatment, confidentiality, informed consent, sharing the condition of patient to close relatives, paternalism, treating of violent patient, abortion, euthanasia, religious beliefs influencing the choice of treatment, physician-patient relationship, informed decision making, continued medical education and role of pharmaceutical representative were assessed. The average scores were ranging from 2.1 to 4.2; with maximum clustering around score ‘3’ or “not sure”. Majority of the study population thought that the current standard of ethics practice was lower than expectation (59.1%) and should give more attention (76.6%) than the present. Furthermore, most of them (85.4%) felt a need for a separate module on medical ethics and professionalism in undergraduate medical curriculum.Conclusion: The recent medical graduates showed a positive attitude towards medical ethics and professionalism. So, a favourable environment was observed for learning medical ethics and professionalism. Thus, to strengthening of medical ethics and professionalism in medical education curricula is suggested.Bangladesh Med Res Counc Bull 2021; 47(1): 57-61
背景:医学伦理学和专业化教学对医生的知识、态度和技能都有影响。孟加拉国的医学教育课程限制了学习医学伦理和专业精神的范围。由于这种限制,医患关系出现了不健康的状况。目的:本研究旨在评估应届医学毕业生对医学伦理和专业精神的态度。本研究的发现可能有助于加强医学教育中的医德和专业精神。方法:本描述性研究于2018年1月至2019年6月对孟加拉国四所大学下属七所医学院的应届医学毕业生进行。数据是使用预先测试的自我管理半结构化问卷收集的,该问卷基于对医学伦理和专业精神的态度测量量表。结果:308名应届医学生的态度得分分别为:伦理行为、自主性、治疗过程中的错误信息、保密性、知情同意、与近亲分享患者状况、家长作风、暴力患者治疗、堕胎、安乐死、影响治疗选择的宗教信仰、医患关系、,对知情决策、继续医学教育和药物代表的作用进行了评估。平均得分在2.1到4.2之间;最大聚类围绕得分“3”或“不确定”。大多数研究人群认为,目前的道德实践标准低于预期(59.1%),应该给予比现在更多的关注(76.6%)。此外,他们中的大多数人(85.4%)认为有必要在本科医学课程中设立一个单独的医学伦理和专业模块。结论:应届医学生对医德医风和专业精神有积极的态度。因此,为学习医学伦理和专业精神创造了有利的环境。因此,建议在医学教育课程中加强医德医风和专业素养的培养。2021年孟加拉医学研究会;47(1):57-61
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引用次数: 0
Assessing the diagnosis Delay Among Breast Cancer Patients Attending in a Tertiary Care Hospital in Dhaka 评估在达卡三级医院就诊的乳腺癌患者的诊断延迟
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i2.57771
K. Akhtar, K. Hossain, S. Nahar, K. Akhtar
Background: Diagnosis is a key determinant for any disease outcome. For that, we want to find out in which stage a breast cancer patient got admitted in hospital including various methods of laboratory investigations were done at different visits.Objectives: This study was aimed to generate information on the stages that a breast cancer patient got admitted including various methods of laboratory investigations were done at different visits.Methodology:   We conducted a cross sectional study at the National Institute of Cancer Research and Hospital, Dhaka, Bangladesh from July 2017-June 2018. We randomly selected a total of 200 patients who came to that hospital through face-to-face interview by using pretested semi-structured questionnaire.Results: A total 77.0% (154) patients investigated Fine Needle Aspiration Cytology (FNAC) at first visit and mean duration for diagnosis was 11 months. Maximum patients came for diagnosis at stage II, III or IV; nobody came at stage I. As consequences, we found that stage of cancer had 7 times more likely to cause diagnostic delay (OR=7.957; 95% CI 3.206-19.749) p <0.0001. Number of consultations was one of the cause for diagnostic delay (c2= 12.825, p <0.0001). Diagnostic delay had strong association between first consultation with physician versus other health care providers (c2= 17.645, p <0.0001). Excluding physicians, first consultation with health care providers also had 3 times more likely to cause delay in diagnosis (OR-3.862; 95% CI1.877-7.944) p<0.0001.Conclusion: Breast cancer patients attended to health care provider at advanced stage. Knowledge, negative perception, social support were the contributing factor for delay in breast cancer diagnosis.Bangladesh Med Res Counc Bull 2021; 47(2): 136-142
背景:诊断是任何疾病结果的关键决定因素。为此,我们想了解癌症患者是在哪个阶段入院的,包括在不同的就诊时进行的各种实验室调查方法。目的:本研究旨在获得癌症患者入院的分期信息,包括在不同就诊时进行的各种实验室调查方法。方法:我们于2017年7月至2018年6月在孟加拉国达卡癌症研究和医院国家研究所进行了一项横断面研究。我们使用预测试的半结构化问卷,通过面对面访谈随机选择了200名来该医院的患者。结果:共有77.0%(154)的患者在第一次就诊时进行了细针抽吸细胞学(FNAC)检查,平均诊断时间为11个月。大多数患者在II、III或IV期进行诊断;结果,我们发现癌症分期导致诊断延迟的可能性高出7倍(OR=7.957;95%CI 3.206-19.749),p<0.0001。咨询次数是诊断延迟的原因之一(c2=12.825,p<0.0001)。首次咨询医生与其他医疗服务提供者之间的诊断延迟有很强的相关性(c2=17.645,p<.0001)。不包括医生,第一次咨询医疗服务提供者也有3倍的可能性导致诊断延迟(OR-3.862;95%CI1.877-7.944)p<0.0001。结论:癌症患者在晚期就诊于医疗服务提供者。知识、负面认知、社会支持是延迟癌症诊断的因素。2021年孟加拉医学研究会;47(2):136-142
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引用次数: 0
Frequency of G-Globin Promoter -158(C>T) Xmnl polymorphism and its correlation with Beta thalassaemia mutations in Bangladeshi population 孟加拉国人群g -珠蛋白启动子-158(C bbbbt) xml多态性频率及其与β地中海贫血突变的相关性
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i2.57783
Waqar A Khan, B. Banu, Md. Abdul Aziz, S. Sadiya, Md. Belayet Hossain, M. Selimuzzaman
Background: In Bangladesh, more than 14000 children on are born annually with in thalassaemia – a common congenital disease Hb E trait is 6.1%. Hb E beta thalassaemia is the most common type of thalassaemia, followed by Beta thalassaemia major.Objectives: To determine the frequency of Xmn1 polymorphism and its association with Beta thalassaemia mutations.Methods: A total of one hundred and four Bangladeshi thalassaemia patients were analysed. Amplification Refractory Mutation System (ARMS) was utilized for Beta thalassaemia mutations and digestion of the PCR product using Xmn1 restriction enzyme Pdml for Xmn1 polymorphism.Results: Xmn1 polymorphism was detected in seventy patients of which 60(57.69%) were heterozygous for Xmn1 polymorphism and seventeen (16.35%) were homozygous. The most common genotype found was heterozygous Xmn1(-/+)seen in 57.70%. The age of presentation of thalassaemic patients was delayed in those who had Xm1 polymorphism.The mean age of presentation of Hb E beta thalassaemia was 13.35 years having homozygous Xm1 polymorphism,7.21 years in heterozygous and 6.25 years without Xmn 1 polymorphism. The most common mutation detected was Cd26 (G-A) +IVS 1-5(G-C) in fifty eight patients in which thirty nine (67.24%) were heterozygous for Xmn 1 polymorphism and 8 (13.79%) were homozygous (+/+).The second most common mutation observed was Cd26(G-A)+30(G-C) seen in fourteen patients where 57.14% were homozygous for Xmn 1 polymorphism and 35.71% were heterozygous. In thalassaemia major 9 (90%) were negative for Xmn1 polymorphism. Allele frequency of Xmn 1 polymorphism was 0.45.Conclusion: The association of Xmn1 polymorphism with two common mutations seen in Hb E beta thalassemia patients may be utilized for hydroxyurea therapy to reduce the requirement of blood transfusion.Bangladesh Med Res Counc Bull 2021; 47(2): 219-224
背景:在孟加拉国,每年有14000多名儿童出生时患有地中海贫血,这是一种常见的先天性疾病,Hb E特征为6.1%。乙型地中海贫血是最常见的地中海贫血类型,其次是乙型地中海贫血。目的:确定Xmn1多态性的频率及其与β地中海贫血突变的关系。方法:对104例孟加拉地中海贫血患者的临床资料进行分析。采用扩增难解突变系统(ARMS)进行β地中海贫血突变,用Xmn1限制性内切酶Pdml对PCR产物进行酶切,分析Xmn1多态性。结果:70例患者检出Xmn1多态性,其中杂合60例(57.69%),纯合17例(16.35%)。最常见的基因型为杂合型Xmn1(-/+),占57.70%。具有Xm1多态性的地中海贫血患者的出现年龄延迟。伴有纯合子Xm1多态性的Hb E β地中海贫血平均发病年龄为13.35岁,杂合子为7.21岁,无Xm1多态性的平均发病年龄为6.25岁。58例患者中最常见的突变为Cd26 (G-A) +IVS 1-5(G-C),其中39例(67.24%)为Xmn 1多态性杂合,8例(13.79%)为纯合(+/+)。第二常见的突变是Cd26(G-A)+30(G-C), 14例患者中有57.14%为纯合子,35.71%为杂合子。地中海贫血9例(90%)Xmn1多态性阴性。xmn1多态性等位基因频率为0.45。结论:hmn1多态性与hbe β地中海贫血患者两种常见突变的相关性可用于羟脲治疗以减少输血需求。孟加拉国地中海理事会2021年公报;47 (2): 219 - 224
{"title":"Frequency of G-Globin Promoter -158(C>T) Xmnl polymorphism and its correlation with Beta thalassaemia mutations in Bangladeshi population","authors":"Waqar A Khan, B. Banu, Md. Abdul Aziz, S. Sadiya, Md. Belayet Hossain, M. Selimuzzaman","doi":"10.3329/bmrcb.v47i2.57783","DOIUrl":"https://doi.org/10.3329/bmrcb.v47i2.57783","url":null,"abstract":"Background: In Bangladesh, more than 14000 children on are born annually with in thalassaemia – a common congenital disease Hb E trait is 6.1%. Hb E beta thalassaemia is the most common type of thalassaemia, followed by Beta thalassaemia major.\u0000Objectives: To determine the frequency of Xmn1 polymorphism and its association with Beta thalassaemia mutations.\u0000Methods: A total of one hundred and four Bangladeshi thalassaemia patients were analysed. Amplification Refractory Mutation System (ARMS) was utilized for Beta thalassaemia mutations and digestion of the PCR product using Xmn1 restriction enzyme Pdml for Xmn1 polymorphism.\u0000Results: Xmn1 polymorphism was detected in seventy patients of which 60(57.69%) were heterozygous for Xmn1 polymorphism and seventeen (16.35%) were homozygous. The most common genotype found was heterozygous Xmn1(-/+)seen in 57.70%. The age of presentation of thalassaemic patients was delayed in those who had Xm1 polymorphism.The mean age of presentation of Hb E beta thalassaemia was 13.35 years having homozygous Xm1 polymorphism,7.21 years in heterozygous and 6.25 years without Xmn 1 polymorphism. The most common mutation detected was Cd26 (G-A) +IVS 1-5(G-C) in fifty eight patients in which thirty nine (67.24%) were heterozygous for Xmn 1 polymorphism and 8 (13.79%) were homozygous (+/+).The second most common mutation observed was Cd26(G-A)+30(G-C) seen in fourteen patients where 57.14% were homozygous for Xmn 1 polymorphism and 35.71% were heterozygous. In thalassaemia major 9 (90%) were negative for Xmn1 polymorphism. Allele frequency of Xmn 1 polymorphism was 0.45.\u0000Conclusion: The association of Xmn1 polymorphism with two common mutations seen in Hb E beta thalassemia patients may be utilized for hydroxyurea therapy to reduce the requirement of blood transfusion.\u0000Bangladesh Med Res Counc Bull 2021; 47(2): 219-224","PeriodicalId":8704,"journal":{"name":"Bangladesh Medical Research Council Bulletin","volume":" ","pages":""},"PeriodicalIF":0.0,"publicationDate":"2022-05-17","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"46100267","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
Low Birth Weight Baby and Its Associated Factors among Rural Women in Bangladesh: A Decision Curve Analysis 孟加拉国农村妇女低出生体重儿及其相关因素:决策曲线分析
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i1.55798
M. G. Uddin, M. S. Islam, M. I. H. Methun
Background: Low birth weight is considered to be one of the main risk factors for infant mortality and morbidity. It is associated with a range of both short- and long-term consequences.Objectives: The study examined the factors contributing to low birth weight of the baby in Bangladesh. This study also attempted with the objective of ensuing a prediction of low birth weight.Methods: The study was a case-control quantitative survey. A three-stage cluster sample design was used to conduct the survey. A total of 674 (337 cases and 337 control) mothers/care givers of under 1 year children were selected from 2 districts of Bangladesh. Binary logistic regression and decision curve analysis were used to investigate the factors which attribute to low birth weight baby born.Results: The findings of the study revealed that mean birth weight was 2.1±0.4 kg among low birth weight children whereas it was 3.0±0.5 kg for normal birth weight children. The mean age of sampled mothers was 25.2±5.4 years. Every 2 in 3 mage got married before 18 years. The prevalence of low birth weight baby among the women with secondary or higher education was lower (47.4%) compared to the women no formal education (65.4%). Analysis revealed that several socio-demographic factors like parental education level, maternal age at first marriage, working status were significantly associated with low birth weight of the baby (p<0.05). Some biological and medical factors like multiple births, maturity of the birth, prenatal care and taking iron and folic acid during pregnancy were also significantly associated with low birth weight baby born. Finally, decision curve analysis technique predicted a net benefit of 0.3907 for the profitable model with highest number of factors. This result implies that the fitted model can predict 39% low birth weight based on independent factors.Conclusion: Prediction model indicates that parental and biological factors are caused for low birth weight baby born in rural areas. Maternal and child health program should focus behavioural change regarding create awareness of disadvantage of early marriage, intake IFA supplementation, at least 4 ANC visit to reduce low birth weight baby born.Bangladesh Med Res Counc Bull 2021; 47(1): 42-49
背景:低出生体重被认为是婴儿死亡和发病的主要危险因素之一。它与一系列短期和长期的后果有关。目的:本研究探讨了导致孟加拉国婴儿出生体重过低的因素。本研究还试图对低出生体重进行预测。方法:采用病例-对照定量调查法。采用三阶段整群样本设计进行调查。从孟加拉国的两个县共选择了674名1岁以下儿童的母亲/照料者(337例病例和337例对照)。采用二元logistic回归和决策曲线分析对新生儿低出生体重的影响因素进行分析。结果:低出生体重儿平均出生体重为2.1±0.4 kg,正常出生体重儿平均出生体重为3.0±0.5 kg。母亲的平均年龄为25.2±5.4岁。每3个法师中就有2个在18岁之前结婚。受过中等或高等教育的妇女的低出生体重儿患病率(47.4%)低于未受过正规教育的妇女(65.4%)。分析发现,父母受教育程度、母亲初婚年龄、工作状态等社会人口因素与婴儿低出生体重有显著相关(p<0.05)。一些生物和医学因素,如多胎、出生成熟度、产前护理和怀孕期间服用铁和叶酸,也与出生体重低的婴儿显著相关。最后,决策曲线分析技术预测因子数量最多的盈利模型的净效益为0.3907。这一结果表明,拟合的模型可以在独立因素的基础上预测39%的低出生体重。结论:预测模型表明,父母因素和生物学因素是农村低出生体重儿的主要原因。妇幼保健方案应注重行为改变,提高对早婚不利因素的认识,摄入IFA补充剂,至少4次产前检查以减少低出生体重婴儿的出生。孟加拉国地中海理事会2021年公报;(1): 47 42-49
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引用次数: 0
ESBL Genes, blaTEM, blaOXA, and blaSHV in Poultry Gut Bacteria: An Endemic Public Health Burden in Bangladesh 家禽肠道细菌中的ESBL基因、blaTEM、blaOXA和blaSHV:孟加拉国的一种地方性公共卫生负担
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i2.57775
S. Nahar, U. Urmi, T. Ali, Adity Rumnaz, T. A. Haque, B. Ara, Mohammed Shah Alam, Abu Syed Md. Mosaddek, Salequl Islam
Background: In Bangladesh, the poultry industry contributes a significant role in the food sector. A vast amount of antibiotic is used as prophylaxis and growth promotion factors in farms. These unconcerned uses of antibiotics ultimately generate resistant bacteria affecting substantial adverse consequences on human health. Extended-spectrum b-lactamase (ESBL) genes are responsible for inactivation of antibiotics containing b-lactam ring, namely, penicillin, cephalosporins, monobactams, and carbapenems.Objectives: This study was designed to analyse the distribution of three ESBL genes and associated antimicrobial susceptibility profile of poultry gut bacteria.Methods: This study was designed to analsze the distribution of three ESBL genes and associated antimicrobial susceptibility profile of poultry gut bacteria. Poultry feces were collected and cultured on cysteine lactose electrolyte deficient (CLED) agar and Salmonella-Shigella (SS) agar to differentiate various isolates based on colony characteristics. Identification of the isolates was made by convention biochemical tests, analytical profile index (API-20E), and 16S rRNA sequence analysis. Antibiotic susceptibility test was done by disc diffusion method using 17 antibiotics from seven groups. Subsequently, polymerase chain reaction (PCR) was employed with a specific primer to identify respective ESBL genes (blaTEM, blaSHV, blaOXA). All data were analysed by SPSS.Results: A total of 113 isolates were identified from 85 poultry feces tested. Most of the bacteria belonged to Enterobacteriaceae family, notably Proteus spp., E. coli, Klebsiella spp., Salmonella spp., and Enterobacter spp. Different bacteria were detected, namely, Kurthia populi, Cronobactersp, and Eikenella corrodens.   Most of the poultry isolates were resistant against more than one group of antibiotics. ESBL gene, blaTEM gene was identified most frequently (53.9%), followed by blaOXA (52.2%), and blaSHV (23%). Higher phenotypic resistance was observed in isolates carrying ESBL genes.Conclusion: This study revealed a very high frequency of three ESBL genes with their phenotypic resistance- capacities in Bangladeshi poultry gut microbiota. Excess uses of antibiotics in local poultry farms may result in the emergence of antibiotic resistance that is imposing public health threatening in Bangladesh.Bangladesh Med Res Counc Bull 2021; 47(2): 165-174
背景:在孟加拉国,家禽业在食品部门发挥着重要作用。大量的抗生素被用作农场的预防和生长促进因子。这些不受关注的抗生素使用最终会产生耐药细菌,对人类健康造成重大不利后果。广谱b-内酰胺酶(ESBL)基因负责含有b-内酰胺环的抗生素失活,即青霉素、头孢菌素、单巴菌素和碳青霉烯类抗生素。目的:本研究旨在分析3个ESBL基因在家禽肠道菌群中的分布及相关的抗菌药物敏感性。方法:分析3个ESBL基因在家禽肠道菌群中的分布及相关的抗菌药物敏感性。收集家禽粪便,在半胱氨酸乳糖电解质缺乏(半胱氨酸乳糖电解质缺乏)琼脂和沙门氏菌-志贺菌(沙门氏菌-志贺菌)琼脂上培养,根据菌落特征区分不同的分离株。采用常规生化试验、分析谱指数(API-20E)和16S rRNA序列分析对分离株进行鉴定。采用圆盘扩散法对7组17种抗生素进行药敏试验。随后,采用特异性引物聚合酶链反应(PCR)鉴定ESBL基因(blaTEM, blaSHV, blaOXA)。所有数据均采用SPSS进行分析。结果:从85株家禽粪便中分离出113株。大部分细菌属于肠杆菌科,以变形杆菌、大肠杆菌、克雷伯氏菌、沙门氏菌和肠杆菌为主,检出不同的细菌,分别为克氏菌、克氏菌和艾肯氏菌。大多数禽类分离株对一组以上抗生素具有耐药性。ESBL基因、blaTEM基因检出频率最高(53.9%),其次是blaOXA(52.2%)和blaSHV(23%)。在携带ESBL基因的菌株中观察到更高的表型抗性。结论:本研究揭示了孟加拉国家禽肠道菌群中三个ESBL基因及其表型耐药能力的高频率。当地家禽养殖场过度使用抗生素可能导致抗生素耐药性的出现,对孟加拉国的公共卫生构成威胁。孟加拉国地中海理事会2021年公报;47 (2): 165 - 174
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引用次数: 1
Ultrasonographic assessment of dengue fever and its correlation with platelet count 登革热的超声评估及其与血小板计数的相关性
Q4 Medicine Pub Date : 2022-05-17 DOI: 10.3329/bmrcb.v47i1.55794
K. Nahar, M. Jahan, S. Akhter, Saikat Barua, D. Begum, M. Hasan
Background: Dengue virus infections are a significant threat to human populations particularly in the tropical and subtropical regions. This is mainly transmitted by Aedes aegypti mosquito from humans to humans. The main pathological mechanisms associated include thrombocytopenia, haemorrhagic diathesis with haemoconcentration. Ultrasonography is used because of its ability to detect plasma leakage signs and prediction of disease severity. Objective: To evaluate the usefulness of ultrasonographic findings of dengue fever and its correlation with platelet count. Methods: It was a prospective observational study, carried out in Bangladesh Medical College Hospital, Dhaka from May 2019 to August 2019. A total of 213 patients of suspected dengue fever during the epidemic were included in this study. All the cases were serologically diagnosed and evaluated with ultrasonographic findings. Platelet counts were estimated in all the cases and compared with findings recorded on ultrasonographic findings. Results: The mean age of the study population was 28.7 years. The male female ratio was 1.7:1. The common features on ultrasonography were thickened and oedematous gall bladder wall, mild to moderate ascites, pleural effusion (unilateral and bilateral), and hepatosplenomegaly. Thickened and oedematous gall bladder wall were observed in 68.8%, mild to moderate ascites 65.3%, bilateral pleural effusion 58.2 %, unilateral pleural effusion 40.4%, hepatomegaly 34.3 % and splenomegaly 13.6 % Platelet counts were significantly lower in abnormal ultrasonographic findings (p=0.001). Conclusion: In a febrile patient with thrombocytopenia and positive dengue serology, ultrasonography of the abdomen is a useful tool to evaluate the severity of illness. Ultrasound findings of gall bladder wall oedema, ascites, and pleural effusion were correlated with the severity of thrombocytopenia. In epidemic scenarios, Ultrasonographic features may help in roughly estimating the platelet count even before serology and platelet results are available. Thus, it helps in treatment planning without waiting for the laboratory results. Bangladesh Med Res Counc Bull 2021; 47(1): 23-28
背景:登革热病毒感染对人类构成重大威胁,特别是在热带和亚热带地区。这主要是由埃及伊蚊从人类传播给人类的。相关的主要病理机制包括血小板减少、出血素质和血液浓度。使用超声检查是因为它能够检测血浆渗漏迹象和预测疾病严重程度。目的:评价登革热的超声表现及其与血小板计数的相关性。方法:这是一项前瞻性观察性研究,于2019年5月至2019年8月在达卡孟加拉国医学院医院进行。本研究共纳入213名疫情期间疑似登革热患者。所有病例均经血清学诊断和超声检查。对所有病例的血小板计数进行了评估,并与超声检查结果进行了比较。结果:研究人群的平均年龄为28.7岁。男女比例为1.7:1。超声检查的常见特征是胆囊壁增厚和水肿、轻度至中度腹水、胸腔积液(单侧和双侧)和肝脾肿大。胆囊壁增厚和水肿的发生率为68.8%,轻度至中度腹水为65.3%,双侧胸腔积液为58.2%,单侧胸腔积液为40.4%,肝肿大为34.3%,脾肿大为13.6%,腹部超声检查是评估疾病严重程度的有用工具。胆囊壁水肿、腹水和胸腔积液的超声检查结果与血小板减少症的严重程度相关。在流行情况下,即使在血清学和血小板结果可用之前,超声特征也可能有助于粗略估计血小板计数。因此,它有助于制定治疗计划,而无需等待实验室结果。2021年孟加拉医学研究会;47(1):23-28
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引用次数: 0
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Bangladesh Medical Research Council Bulletin
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