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Adolescent Health needs - Special attention and a New Subspeciality - Adolescent Medicine 青少年健康需求——特别关注和一个新的亚专科——青少年医学
Pub Date : 2021-06-17 DOI: 10.3329/nimcj.v11i2.54058
B. Yasmeen
Abstract Not Available Northern International Medical College Journal Vol.11 (2) Jan 2020: 443- 446
《北方国际医学院学报》Vol.11 (2) Jan 2020: 443- 446
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引用次数: 0
Apert Syndrome: A Rare Genetic Disorder Apert综合征:一种罕见的遗传疾病
Pub Date : 2021-06-17 DOI: 10.3329/nimcj.v11i2.54066
Mahmuda Hassan, B. Yasmeen, Masuma Khan, A. Mukti
Apert syndrome is a rare type I acrocephalosyndactyly syndrome having autosomal dominant inheritance due to mutations in the fibroblast growth factor receptors gene. New or fresh mutations are also frequent. It is characterized by dysmorphic face, craniosynostosis, severe syndactyly of the hands and feet. Apert syndrome affects the first branchial or pharyngeal arch, the precursor of the maxilla and mandible. Disturbances in the development of branchial arches during fetal period create extensive malformation in different parts of the body. Management of Apert syndrome requires a multidisciplinary approach. We, hereby, report a case of a 45-days old baby with Apert syndrome. Northern International Medical College Journal Vol.11 (2) Jan 2020: 475-477
Apert综合征是一种罕见的I型肢头并指综合征,由于成纤维细胞生长因子受体基因突变而具有常染色体显性遗传。新的或新鲜的突变也很频繁。其特征是面部畸形,颅缝闭合,严重的手和脚并指。Apert综合征影响第一鳃弓或咽弓,即上颌骨和下颌骨的前体。胎儿时期鳃弓发育的紊乱会在身体的不同部位造成广泛的畸形。Apert综合征的治疗需要多学科联合治疗。我们在此报告一例45天大的阿伯特综合征婴儿。北方国际医学院学报Vol.11 (2) Jan 2020: 475-477
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引用次数: 0
Pattern of haematological malignancies among patients attending at the haematology department in a tertiary hospital 某三级医院血液科患者血液系统恶性肿瘤的类型
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50735
Maruf Hasan, Mahbuba Sharmin, A. A. Kabir, J. Ferdous, M. Khan, Md. Kamrul Hassan, Mohammad Farhad, Tamanna Nourin
Background : Hematological malignancies (HM) was comprise approximately 6.5% of all cancer incidences worldwide in 2012. Although prevalence of these malignancies are much lower in Asia and Africa then in Western countries. The incidence of these malignancies is drastically increasing in low-income settings. WHO predicts that the number of bloodrelated cancer cases would be increased about 48% in less developed countries by 2030 as compared to 2012. Objective : In our study we tried to determine the current pattern of haematological malignancies among patients attending at the haematology department in a tertiary hospital. Methods : This cross-sectional observational study was carried out in outpatients and inpatients department of Haematology, Dhaka Medical College Hospital, Dhaka from 13th August 2016 to 12th august 2017 for a duration of 12 months. Detail clinical history, examination findings and investigations of patients were recorded in a pre-designed case record form. All data were converted to tabulated forms to obtain statistical information by Using Microsoft Excel and SPSS 17 program. Results : Out of 400 HM patients, most of them were male (66.75%) and remaining (33.25%) were female and male female ratio was 2.01:1. From rural were (71.25%) and remaining (28.75%) were urban population. Acute lymphoblastic leukaemia (ALL) patients were 87 (21.75%), mean age 25.4 years; Acute myeloid leukaemia (AML) patients were 81 (20.25%), mean age 36.5 years; Chronic myeloid leukaemia (CML) patients were 71 (17.75%), mean age 35.5 years; Non Hodgekin lymphoma (NHL) patients were 56 (14%), mean age 42.9 years; Acute promyelocytic leukaemia (APL) patients were 35 (8.75%), mean age 29.4 years; Multiple myeloma (MM) patients were 33 (8.25%), mean age 55.9 years; Hodgekin lymphoma (HL) patients were 24 (6.00%), mean age 33.8 years; Chronic lymphocytic leukaemia (CLL) patients were 7 (1.75%), mean age 61.9 years; Follicular lymphoma (FL) patients were 4 (1.00%), mean age 56.5 years; Mantle cell lymphoma (MCL) patient was 1 (0.25%), age 70 years and Burkitt lymphoma (BL) patient was 1 (0.25%), age 25 years. Conclusion : Study result showed that acute leukaemias were more common than chronic cases. AML and APL (subtype of AML) were more than ALL. Individually APL was the 5th in position whereas ALL was the 1st and AML was the 2nd highest cases among the 11 types of HM found in this study. Percentage of CML was higher (3rd in position) than CLL (8th in position) among the studied cases. Among the lymphomas NHL was more common (4th in position) than HL (7th in position) and MM (6th in position). FL (subtype of NHL) which is low grade in nature was 9th in position among the eleven. MCL and BL was rare and each was 1 in number in this study. Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 415-418
背景:2012年,血液恶性肿瘤(HM)约占全球所有癌症发病率的6.5%。尽管这些恶性肿瘤的患病率在亚洲和非洲比在西方国家低得多。这些恶性肿瘤的发病率在低收入环境中急剧增加。世卫组织预测,到2030年,较不发达国家与血液有关的癌症病例数将比2012年增加约48%。目的:在我们的研究中,我们试图确定目前在三级医院血液科就诊的患者血液系统恶性肿瘤的模式。方法:本横断面观察性研究于2016年8月13日至2017年8月12日在达卡医学院附属医院血液科门诊和住院患者中进行,为期12个月。详细的临床病史、检查结果和调查记录在预先设计的病例记录表中。使用Microsoft Excel和SPSS 17程序将所有数据转换为表格形式,获得统计信息。结果:400例HM患者中,男性居多(66.75%),女性居多(33.25%),男女比例为2.01:1。农村占71.25%,其余为城镇人口(28.75%)。急性淋巴细胞白血病(ALL) 87例(21.75%),平均年龄25.4岁;急性髓性白血病(AML)患者81例(20.25%),平均年龄36.5岁;慢性髓性白血病(CML) 71例(17.75%),平均年龄35.5岁;非霍奇金淋巴瘤(NHL) 56例(14%),平均年龄42.9岁;急性早幼粒细胞白血病(APL) 35例(8.75%),平均年龄29.4岁;多发性骨髓瘤(MM) 33例(8.25%),平均年龄55.9岁;霍奇金淋巴瘤(HL)患者24例(6.00%),平均年龄33.8岁;慢性淋巴细胞白血病(CLL) 7例(1.75%),平均年龄61.9岁;滤泡性淋巴瘤(FL) 4例(1.00%),平均年龄56.5岁;套细胞淋巴瘤(MCL) 1例(0.25%),年龄70岁;伯基特淋巴瘤(BL) 1例(0.25%),年龄25岁。结论:研究结果表明急性白血病比慢性白血病更常见。AML和APL (AML亚型)多于ALL。在本研究发现的11种HM中,APL排在第5位,ALL排在第1位,AML排在第2位。CML的比例(第3位)高于CLL(第8位)。在淋巴瘤中,NHL(第4位)比HL(第7位)和MM(第6位)更为常见。FL (NHL亚型)在11例中排名第9位,属于低级别。MCL和BL罕见,本研究中各1例。《北方国际医学院学报》2019年7月1日第11卷第415-418页
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引用次数: 0
Serum uric acid level between normotensive and pre-eclamptic patients in third trimester of pregnancy and perinatal outcome 妊娠晚期高血压和先兆子痫患者血清尿酸水平与围产期结局的关系
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50736
F. Nesa, F. Chowdhury, B. Yasmeen, N. Begum, A. Das
Background : Preeclampsia is associated with maternal and neonatal complications. It has been indicated that increased uric acid might have a predictive role on preeclampsia. Several studies have demonstrated a relation between elevated maternal serum uric acid levels and adverse maternal and fetal outcome. The aim of this study was to find out the association of serum uric acid level between normotensive and pre-eclamptic (PE) patients in third trimester of pregnancy and perinatal outcome. Methodology : A case control study was conducted in the department of the Obstetrics and Gynaecology in Dhaka Medical College Hospital from July 2017 to June 2018. A total number of 100 pregnant women in third trimester of pregnancy attending in Obstetrics and Gynaecology department of Dhaka Medical College Hospital were selected purposively as study subjects. Among them 50 diagnosed cases of preeclampsia were selected as cases with age range of 18-35 years and 50 normal healthy age matched pregnant women as controls. Pregnant women with pre-existing hypertension, diabetes mellitus and renal disease were excluded from the study by history, clinical examination and relevant laboratory investigations. Results : The mean serum uric acid level was found 4.49±1.72 mg/dl in normotensive group and 7.03±1.89 mg/dl in preeclampsia group. Serum uric acid was significantly higher (p<0.05) in pre-eclampsia group than normotensive group. Regarding outcome take home as alive neonate was found 48(96.0%) in normotensive group and 41(82.0%) in preeclampsia group. Early neonatal death was 1(2.0%) in normotensive and 4(8.0%) in pre-eclampsia group. Still birth was 1(2.0%) and 5(10.0%) in normotensive and pre-eclampsia group respectively. Conclusion : Hyperuricemia is most basic and reliable observations in pre-eclamptic pregnancies. While elevated concentrations of circulating uric acid are not uniformly increased in every woman with PE. But hyperuricemia is found in a subset of pre-eclamptic women who had higher risk for maternal and fetal complications. Therefore, measurement of serum uric acid concentration seems to be a useful test to predict maternal and fetal complications in a women with preeclampsia. Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 419-422
背景:先兆子痫与产妇和新生儿并发症有关。有研究表明,尿酸升高可能对子痫前期有预测作用。一些研究已经证明了升高的母体血清尿酸水平和不良的母体和胎儿结局之间的关系。本研究旨在探讨妊娠晚期高血压和先兆子痫(PE)患者血清尿酸水平与围产期结局的关系。方法:于2017年7月至2018年6月在达卡医学院附属医院妇产科进行病例对照研究。有目的地选择在达卡医学院附属医院妇产科就诊的100名妊娠晚期孕妇作为研究对象。其中50例诊断为子痫前期患者,年龄18-35岁,50例正常健康年龄匹配的孕妇作为对照。通过病史、临床检查和相关实验室调查排除既往存在高血压、糖尿病和肾脏疾病的孕妇。结果:正常血压组血尿酸均值为4.49±1.72 mg/dl,子痫前期组血尿酸均值为7.03±1.89 mg/dl。子痫前期组血清尿酸显著高于正常血压组(p<0.05)。结果:正常血压组48例(96.0%),子痫前期组41例(82.0%)。高血压组新生儿早期死亡1例(2.0%),先兆子痫组新生儿早期死亡4例(8.0%)。正常血压组死产1例(2.0%),子痫前期组死产5例(10.0%)。结论:高尿酸血症是子痫前期最基本、最可靠的观察指标。而循环尿酸浓度升高在PE患者中并不均匀。但高尿酸血症存在于子痫前期妇女的一个子集中,她们有更高的母胎并发症风险。因此,血清尿酸浓度的测量似乎是一个有用的测试,以预测母体和胎儿并发症的先兆子痫妇女。《北方国际医学院学报》2019年7月1日第11卷第419-422页
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引用次数: 0
Central Diabetes Insipidus in a Child due to Histiocytosis X 组织细胞增多症所致儿童中枢性尿崩症1例
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50739
Habiba Jesmin, S. Afroz, Saenat Haque
Central diabetes insipidus (CDI) occur due to deficiency of vasopressin which is synthesized in supraoptic and paraventricular nuclei of hypothalamus and stored in posterior pituitary. There are many causes of CDI among them histiocytosis X or lymphohistiocytosis (LCH) is a rare cause. Here we are reporting a 2 years old boy with histiocytosis-Xor presented with CDI. The boy presented with polyuria and polydipsia, low urine specific gravity and osmolality with normal blood sugar and osmolality. Positive response to water deprivation test followed by oral DDAVP establish the diagnosis of CDI. X-Ray skull showed osteolytic punched out lesion and T1 weighted MRI of brain showed thickening of pituitary stalk with absence of bright signal of posterior pituitary. Trephine biopsy showed bone marrow was infiltrated by many eosinophil, some macrophage, lymphocyte and plasma cells. On the basis of all these diagnosis was made as CDI due to histiocytosis-X. Due to hypothalamic- pituitary axis infiltration CDI may be the earliest manifestation of LCH, even before it is diagnosed. Therefore, for diagnostic workup of CDI, LCH should be considered. Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 432-434
中枢性尿囊症(CDI)是由下丘脑视上核和室旁核合成并储存于垂体后叶的抗利尿激素缺乏引起的。CDI的病因有很多,其中组织细胞增多症或淋巴组织细胞增多症(LCH)是一种罕见的病因。我们在此报告一2岁男童组织细胞增多症xor表现为CDI。该男孩表现为多尿和烦渴,尿比重和渗透压低,血糖和渗透压正常。缺水试验阳性反应后口服DDAVP确定CDI的诊断。头颅x线示溶骨穿孔病灶,脑T1加权MRI示垂体柄增厚,垂体后叶未见亮信号。骨髓活检显示大量嗜酸性粒细胞、部分巨噬细胞、淋巴细胞和浆细胞浸润。在此基础上诊断为组织细胞增多症- x所致CDI。由于下丘脑-垂体轴浸润,CDI可能是LCH的最早表现,甚至在诊断之前。因此,对于CDI的诊断检查,应考虑LCH。《北方国际医学院学报》2019年7月1日第11卷第432-434页
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引用次数: 0
Short term outcome of epileptic Seizure in children attending at Paediatric Neuroscience Department of Dhaka Shishu Hospital 达卡石树医院儿科神经内科儿童癫痫发作的短期预后
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50734
H. Quaderi, Shaoli Sarker, S. I. Kanta, B. Yasmeen
Background : The optimal response to antiepileptic treatment is the control of seizures. In different studies, it has been shown that childhood epilepsy presents with a variable course, and approximately one-third of epilepsy experience alternating relapse and remission. Some of them do not become seizure-free, despite adequate treatment. Objectives : This study aimed to see the short-term outcome of seizures in children with epilepsy (whether the seizure is controlled or not) and to correlate them with different predictors like socio-demographic factors, associated comorbidities, and adherence with antiepileptic drugs. Methods : This retrospective observational study was conducted in an Epilepsy Clinic of Paediatric Neuroscience Department of Dhaka Shishu Hospital (DSH) over a period of 3 years from January 2013 to December 2015. During this period 1-year follow-up record of each patient was analyzed. Information on bio demographic data, clinical and developmental assessment done by a multidisciplinary team was analyzed. Results : A total of 100 children who had epilepsy were included in this study. Unfavorable outcome (uncontrolled seizure) was found in children <5 years of age, children from the rural area, and those whose parents education were below secondary level (p values were 0.05, 0.03 and 0.04 respectively). Also, the unfavorable outcome was found in children who had H/O perinatal asphyxia (PNA), motor problem, and feeding problem (p-value=0.5, 0.002, 0.05 respectively). After 1 year of regular follow up milestone of development was improved in more than one 1domain in 51children. But there was no improvement found or their condition remained unchanged in 49 children. Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 411-414
背景:抗癫痫治疗的最佳反应是控制癫痫发作。在不同的研究中,已经表明儿童癫痫呈现出一个可变的过程,大约三分之一的癫痫交替复发和缓解。尽管经过适当的治疗,他们中的一些人并没有完全摆脱癫痫。目的:本研究旨在观察癫痫患儿癫痫发作的短期结果(癫痫发作是否得到控制),并将其与社会人口因素、相关合并症和抗癫痫药物依从性等不同预测因素相关联。方法:回顾性观察研究于2013年1月至2015年12月在达卡石树医院(DSH)儿科神经科学癫痫门诊进行,为期3年。在此期间,对每位患者1年的随访记录进行分析。对多学科团队完成的生物人口统计数据、临床和发育评估信息进行了分析。结果:本研究共纳入100例癫痫患儿。5岁以下儿童、农村儿童和父母文化程度为中等以下的儿童出现不良结局(癫痫发作失控)(p值分别为0.05、0.03和0.04)。此外,H/O围产期窒息(PNA)、运动问题和喂养问题患儿的预后较差(p值分别为0.5、0.002和0.05)。经过1年的定期随访,51名儿童的发展里程碑在1个以上领域得到改善。但在49名儿童中,没有发现任何改善,或者他们的状况保持不变。《北方国际医学院学报》2019年7月1日第11卷第411-414页
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引用次数: 0
Recurrent Abdominal Pain: A Rare Presentation of Childhood Intestinal Lymphoma in a Bangladeshi Child 复发性腹痛:孟加拉儿童肠道淋巴瘤的罕见表现
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50741
Md Shafiul Alam, M. Mazumder, M. Begum, -. Md Benzamin, Nadia Haq, Shariful Hasan, A. R. Rahman, Md. Saidul Islam
In children, primary malignant tumors of the gastrointestinal (GI) tract are rare and accounts less than 5% of all pediatric neoplasms.1 Non-Hodgkin’s lymphoma (NHL) remains the most common malignancy of the GI tract in children.2 Moreover small intestine (PLI) is very uncommon. They are different in anatomic distribution and histologic appearance compared to common patterns in adult cases. The disease is rare and having variable clinical presentation that delayed early detection when the possibility of cure exists. The common presentations of PLI are bowel obstruction and intussusception.3,4 NHL of the gastrointestinal tract usually arises in the submucosal lymphoid tissue of the ileocecal region, extendtransmuraly, and involve local mesenteric lymph nodes extensively, forming a bulky abdominal mass. NHL most frequently involved the ileocecal valve (35.8%), followed by the small bowel (31.3%), large bowel (19.4%) and multiple gastrointestinal involvements (13.4%).5 Here we present a case report to show the scenario of a patient suffering from NHL where diagnosis was delayed. The child was suffering from recurrent abdominal pain (RAP) and various treatment was offered but he could not improve. Finally, he was diagnosed as a case of primary non-Hodgkin's lymphoma of the small intestine (PLI). Though PLI is a very uncommon malignancy in childhood. Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 438-439
在儿童中,胃肠道的原发性恶性肿瘤是罕见的,占所有儿科肿瘤的不到5%非霍奇金淋巴瘤(NHL)仍然是儿童消化道最常见的恶性肿瘤此外,小肠(PLI)非常罕见。它们的解剖分布和组织学表现与成人病例的常见模式不同。此病罕见,临床表现多变,在有治愈可能的情况下,早期发现较迟。PLI的常见表现为肠梗阻和肠套叠。3,4胃肠道NHL通常发生于回盲区粘膜下淋巴组织,经粘膜扩展,广泛累及局部肠系膜淋巴结,形成腹部肿物。NHL最常累及回盲瓣(35.8%),其次是小肠(31.3%)、大肠(19.4%)和多发性胃肠道(13.4%)在这里,我们提出了一个病例报告,以显示的情况下,患者患NHL的诊断被推迟。该患儿患有复发性腹痛(RAP),经各种治疗均未能好转。最后,他被诊断为原发性小肠非霍奇金淋巴瘤(PLI)。虽然PLI是一种非常罕见的儿童恶性肿瘤。《北方国际医学院学报》2019年7月1日第11卷第438-439页
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引用次数: 0
Incidental diagnosis of combined deficiency of vitamin C and D in a child admitted with bronchiolitis 偶然诊断合并维生素C和D缺乏症的儿童入院与细支气管炎
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50740
Mahmuda Hassan, K. Chowdhury, B. Yasmeen, H. Rahman, Masuma Khan, A. Mukti, S. Roy
Several cases from developing countries has been reported either on isolated vitamin C or isolated vitamin D deficiency in the recent past. Though nutritional vitamin C deficiency is rare but recently there is re-emergence of vitamin D deficiency found in developed countries. Combined deficiency of vitamin C and D found in the same patient is very rare both in developed and developing countries. Our patient was admitted in Ad Din Women’s Medical College Hospital, Dhaka with bronchiolitis. She had a history of cough and cold for 5 days. She had fever and respiratory difficulty for the last 2 days. On physical examination, she had low grade fever, fast breathing, chest in drawing. She had also widening of the wrist and ankle joints but her parents were unaware of these changes. They thought these could be a normal phenomenon. We suspect Rickets on physical examination findings. The baby was very much irritable and we thought that it was due to cough, cold and difficult breathing (bronchiolitis). Combined vitamin C and D deficiency was an incidental finding in this case. Her X ray of wrist joints, lower limb including knee and ankle joints showed the features of combined deficiency of vitamin C and D. Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 435-437
最近,发展中国家报告了几例孤立的维生素C或孤立的维生素D缺乏症。虽然营养维生素C缺乏症很少见,但最近在发达国家又出现了维生素D缺乏症。在发达国家和发展中国家,同一患者同时缺乏维生素C和D是非常罕见的。本例患者因毛细支气管炎入住达卡阿丁女子医学院医院。她有咳嗽和感冒5天的病史。她最近两天发烧,呼吸困难。体格检查,她有低烧,呼吸急促,胸部下垂。她的手腕和踝关节也变宽了,但她的父母并不知道这些变化。他们认为这是一种正常现象。根据体检结果,我们怀疑是佝偻病。婴儿非常易怒,我们认为这是由于咳嗽,感冒和呼吸困难(细支气管炎)。在这个病例中,复合维生素C和D缺乏症是偶然发现的。她的手腕关节、下肢包括膝盖和踝关节的X光片显示维生素C和d联合缺乏的特征。北方国际医学院杂志2019年7月1日第11卷435-437页
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引用次数: 0
Noninvasive prenatal diagnosis of β-Thalassaemia β-地中海贫血的无创产前诊断
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50732
B. Yasmeen
Abstract not available Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 403-405
《北方国际医学院学报》2019年7月1日第11卷403-405页
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引用次数: 0
Knowledge of Adolescent Girls on Pregnancy and Antenatal care 青春期少女关于怀孕和产前保健的知识
Pub Date : 2020-12-13 DOI: 10.3329/nimcj.v11i1.50737
N. Sultana, Sharmin Sultana, Fakhruddin Ahmed, S. Ullah
Background : Adolescence is particularly a transition period of human development which has profound influence on a person’s future. In Bangladesh adolescents usually gather their knowledge about reproductive health from their family and surroundings and therefore their knowledge remains incorrect and insufficient. Government increases the provision of schooling for girls but there is no provision of sex education. Objective : To assess the knowledge of adolescent girls about pregnancy and antenatal care. Methods : A cross sectional study was done during the period of January ’15 to June ’15 among 143 students of class 1X and X of 2 rural private schools of Rupganj and Narayanganj. Simple random sampling method was applied for enrolling the study population and data was collected by interview method using pretested questionnaire. Finally, data was analyzed by SPSS version 17. Result : Most of the respondents had average knowledge about pregnancy and antenatal care. Nearly three-forth (61.5%) of the respondents had incorrect knowledge about pregnancy period and majority (76.3%) do not know about the correct mother’s organ for developing baby during pregnancy. Maximum respondents (95%) had good knowledge about extra care of a pregnant mother. Although 74.8% mentioned about TT vaccination of a pregnant mother but majority (65%) did not know detail about the vaccines’ dose and schedule. Statistically significant difference found in knowledge on pregnancy and antenatal care among married and unmarried girls. (P=<0.05) Conclusion : Knowledge of adolescent girls about pregnancy and ANC was average in our rural area. Northern International Medical College Journal Vol. 11 No. 1 July 2019, Page 423-426
背景:青春期是人类发展的过渡时期,对一个人的未来有着深远的影响。在孟加拉国,青少年通常从家庭和周围环境获取生殖健康知识,因此他们的知识仍然是不正确和不充分的。政府增加了为女孩提供的学校教育,但没有提供性教育。目的:了解青春期少女对妊娠及产前保健知识的了解情况。方法:于2015年1月至2015年6月对Rupganj和Narayanganj两所农村私立学校1X班和X班143名学生进行横断面调查。采用简单随机抽样方法纳入研究人群,采用预试问卷访谈法收集资料。最后,使用SPSS version 17对数据进行分析。结果:受访妇女对妊娠和产前保健知识的了解程度一般。近四分之三(61.5%)的受访者对怀孕期的认识不正确,大多数(76.3%)的受访者不知道怀孕期间婴儿发育的正确母亲器官。大多数应答者(95%)对孕妇的额外护理有良好的了解。尽管74.8%的人提到怀孕母亲接种过TT疫苗,但大多数(65%)不了解疫苗剂量和接种时间表的细节。已婚女孩和未婚女孩在怀孕和产前保健知识方面存在统计学差异。(P=<0.05)结论:我国农村地区少女对妊娠和ANC的知晓率处于中等水平。《北方国际医学院学报》2019年7月1日第11卷第423-426页
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引用次数: 0
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Northern International Medical College Journal
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