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Hereditary Persistence Of Alpha-fetoprotein: A Rare Entity From A Primary Care Center In Bangladesh 甲胎蛋白的遗传持久性:来自孟加拉国初级保健中心的罕见实体
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66172
C. Podder, M. Amin, N. Chowdhury
Hereditary persistence of alpha- fetoprotein (HFAFP) is a rare benign autosomal dominant disorder.Here we report a case of 15 years old boy who was found to have elevated alpha-fetoprotein during her routine evaluation for gynaecomastia. All other common possibilities for raised alpha-fetoprotein were excluded.Subsequently, 2 of his family members were found to have raised alpha-fetoprotein.One is his father and another one is his brother.Raised alpha-fetoprotein has a wide differential diagnosis including, pregnancy, germ cell tumors, hepatocellular carcinoma and others.But after exclusion of other possibilities, persisting elevated alphafetoprotein raises the suspicion for HPAFP.Testing other family members for AFP and specific genetic study aid in diagnosis.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 216-217
遗传性甲胎蛋白(hafp)是一种罕见的良性常染色体显性遗传病。在这里,我们报告一个15岁的男孩谁被发现有升高的甲胎蛋白在她的妇科乳房发育的常规评估。所有其他常见的升高甲胎蛋白的可能性均被排除。其后,他的两名家庭成员被发现有甲胎蛋白升高。一个是他的父亲,另一个是他的兄弟。升高的甲胎蛋白具有广泛的鉴别诊断,包括妊娠、生殖细胞肿瘤、肝细胞癌等。但在排除了其他可能性后,持续升高的甲胎蛋白引起了对hpaf的怀疑。检测其他家庭成员的AFP和特定的基因研究有助于诊断。孟加拉国J医学2023;第34卷,第2(1)增编:216-217
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引用次数: 0
Acute pancreatitis: Early Management 急性胰腺炎:早期治疗
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66131
Md Golam Kibria
Abdominal pain caused by acute pancreatitis (AP) is not uncommon in day to day medical practice worldwide. AP is the sudden inflammation of the pancreas, and it may be confined to the pancreas, or may be more life-threatening, affecting all organs and systems. It progresses mildly in 80% of patients and resolves with treatment, but in cases of severe AP, with mortality of around 30% has been recorded. AP is most often established by clinical symptoms and at least threefold raised enzymes and by imaging (any two of these three).In the management AP, treatment is mainly related to the severity of the disease and approaches are constantly being updated. With early diagnosis and treatment, most of the patients can be discharged, and the development of complications and mortality can be reduced. Hemodynamic status should be assessed immediately upon presentation and resuscitative measures begun as needed. Early targeted fluid therapy within the first 48 h is critical to improve the outcome of severe AP. Patients with organ failure and or SIRS should be admitted to an ICU /HDU whenever possible. Emergency management decision are early fluid management strategy, utility and timing of antibiotics, the timing and type of nutritional support and in relevant cases endoscopic retrograde cholangiopancreatography (ERCP) and cholecystectomy approachescan change the course of the disease and the length of stay in the hospital. Therefore, emergency management is important.Enteral nutrition is recommended to prevent infectious complications, whereas parenteral nutrition should be avoided.Routine use of prophylactic antibiotics in patients with severe AP and or sterile necrosis is not recommended.In patients with infected necrosis, antibiotics known to penetrate pancreatic necrosis may be useful in delaying intervention, thus decreasing morbidity and mortality. Successful clinical management requires close interdisciplinary cooperation and coordination from experienced gastroenterologists, intensive care physicians, surgeons, and radiologists. Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 188-189
急性胰腺炎(AP)引起的腹痛在世界范围内的日常医疗实践中并不罕见。AP是胰腺的突发性炎症,它可能局限于胰腺,也可能更危及生命,影响所有器官和系统。80%的患者病情进展轻微,经治疗后会消退,但在严重AP病例中,死亡率约为30%。AP通常通过临床症状和至少三倍的酶升高以及影像学(这三种中的任意两种)来确定。在AP管理中,治疗主要与疾病的严重程度有关,方法也在不断更新。通过早期诊断和治疗,大多数患者可以出院,并且可以减少并发症的发生和死亡率。入院后应立即评估血流动力学状态,并根据需要开始采取复苏措施。在最初48小时内进行早期靶向液体治疗对于改善严重AP的预后至关重要。器官衰竭和/或SIRS患者应尽可能入住ICU /HDU。急诊管理决策是早期液体管理策略,抗生素的使用和时机,营养支持的时机和类型,在相关病例中,内窥镜逆行胆管胰胆管造影(ERCP)和胆囊切除术方法可以改变疾病的进程和住院时间。因此,应急管理非常重要。建议肠内营养以预防感染并发症,而应避免肠外营养。不建议对严重AP和/或无菌性坏死患者常规使用预防性抗生素。对于感染性坏死患者,已知能穿透胰腺坏死的抗生素可用于延迟干预,从而降低发病率和死亡率。成功的临床管理需要有经验的胃肠病学家、重症监护内科医生、外科医生和放射科医生密切的跨学科合作和协调。孟加拉国J医学2023;第34卷,第2号(1)补编:188-189
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引用次数: 0
Childhood obesity: Sequelae in adult life 儿童肥胖:成年后的后遗症
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66136
Suraiya Begum
Childhood obesity is a growing global health hazard extending to adulthood. The prevalence of obesity in children in developed and developing countries has risen dramatically in the past few decades and is currently at epidemic proportions. Obese children and adolescents were around five times more likely to be obese in adulthood than those who were not obese. Adiposity rebound in early childhood is a risk factor for obesity in adolescence and adulthood. Numerous sequelae are associated with children being overweight or obese, even at a very young age. Obesity in childhood and adolescence is significantly associated with an increased risk of insulin resistance, type 2 diabetes mellitus, dyslipidemia, hypertension, metabolic syndrome, non-alcoholic fatty liver disease, and obstructive sleep apnea. Obese children are more likely to experience psychological morbidity, lower self-esteem, and more behavioral problems than non-obese children. These comorbid conditions may progress to adult life and the development of atherosclerosis, cerebrovascular disorders, and cardiovascular morbidity later in life. Obese children are more likely to become obese adults and suffer lifelong physical and mental problems and risk of premature mortality. The use of infant formula, decreased physical activity, excessive calorie intake, and changes in gut microbiota patterns are associated with the increasing prevalence of childhood obesity. Efforts will be focused on trying to treat obesity itself and, therefore, prevent progression to overt sequelae, either in childhood or later in adult life. The most important strategy for preventing obesity and sequelae is lifestyle modification which includes healthy eating behaviors, regular physical activity, and reduced sedentary activity. Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 191-192
儿童肥胖是一种日益严重的全球健康危害,并延伸至成年期。在过去几十年里,发达国家和发展中国家的儿童肥胖率急剧上升,目前已达到流行病的程度。肥胖儿童和青少年成年后肥胖的可能性是不肥胖儿童和青少年的五倍左右。儿童早期肥胖反弹是青春期和成年期肥胖的危险因素。许多后遗症与儿童超重或肥胖有关,甚至在很小的时候。儿童期和青春期肥胖与胰岛素抵抗、2型糖尿病、血脂异常、高血压、代谢综合征、非酒精性脂肪性肝病和阻塞性睡眠呼吸暂停的风险增加显著相关。与非肥胖儿童相比,肥胖儿童更容易出现心理疾病、自卑和行为问题。这些合并症可能发展到成年,并在以后的生活中发展为动脉粥样硬化、脑血管疾病和心血管疾病。肥胖儿童更有可能成为肥胖的成年人,终生遭受身体和精神问题,并有过早死亡的风险。婴儿配方奶粉的使用、体力活动的减少、卡路里摄入过多以及肠道微生物群模式的变化与儿童肥胖症患病率的增加有关。努力将集中在治疗肥胖本身,从而防止在童年或成年后发展为明显的后遗症。预防肥胖及其后遗症最重要的策略是改变生活方式,包括健康的饮食习惯、规律的体育活动和减少久坐不动的活动。孟加拉国J医学2023;第34卷,第2(1)增编:191-192
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引用次数: 0
Heart failure with preserved ejection fraction (HFpEF): A missed diagnosis 心力衰竭伴保留射血分数(HFpEF):漏诊
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66117
Chaudury Meshkat Ahmed
One of the most common cause for “unexplained shortness of breath” is heart failure with preserved ejection fraction (HFpEF), that is frequently missed by the physician. Untill the wide use of BNP/NT ProBNP the term even remained unfamaliar to many of them. More over the concepts that, to make a diagnosis of HFpEF, a diastolic dysfunction is mandatory accounts for another cause of missing the diagnosis of HFpEF.The reality is Half of the all forms of heart failure is attributed to HFpEF. The diagnosis based on : the symptom of heart failure, the raised BNP/NT Pro BNP and any of the two of the either left venticular hypertrophy (LVH)/ left atrial enlargement (LAE) or features of diastolic dysfunction( as assessed by an echocadiography).The first criteria that is the symptom of heart failure is often non specific and frequently difficult to distinguish from other clinical conditions. The levels of BNP/NT ProBNP also needed to be defined according to various clinical conditions where there may be raised level of this biomarkers in the absence of heart failure.On the other hand the echocardiographic detection of LVH, LAE or left ventricular diastolic dysfunction is either time consuming or inconclusive in many patients. The various clinical phenotypes of HFpEF in the clinical back ground also make it diffcult to “fit one size for all”. Our presentation will focus on the various facets of missed diagnosed HFpEF. Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 181-182
“不明原因的呼吸短促”最常见的原因之一是心力衰竭并保留射血分数(HFpEF),这经常被医生忽略。直到BNP/NT ProBNP的广泛使用,这个术语对他们中的许多人来说仍然是陌生的。更重要的是,要诊断HFpEF,舒张功能障碍是强制性的,这是遗漏HFpEF诊断的另一个原因。事实上,所有形式的心力衰竭中有一半是由HFpEF引起的。诊断依据:心衰症状、BNP/NT Pro BNP升高、左心室肥厚(LVH)/左心房扩大(LAE)或舒张功能障碍(超声心动图评估)中的任意两种。作为心衰症状的第一个标准通常是非特异性的,并且常常难以与其他临床情况区分开来。BNP/NT ProBNP的水平也需要根据不同的临床情况来确定,在没有心力衰竭的情况下,这些生物标志物的水平可能会升高。另一方面,超声心动图检测LVH、LAE或左室舒张功能不全在许多患者中要么耗时,要么不确定。临床背景下HFpEF的各种临床表型也使其难以“一刀切”。我们的演讲将集中在漏诊HFpEF的各个方面。孟加拉国J医学2023;第34卷,第2号(1)补编:181-182
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引用次数: 0
Assessment of Depression and Anxiety Among Adult Patients With Solid Tumours Admitted in National Institute of Cancer Research & Hospital 国立肿瘤研究所住院的成年实体瘤患者抑郁和焦虑的评估
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66170
Salman Bashar Al Ayub, M. H. Rahman, Muhammad Rafiqul Islam, N. Khatun
Background: Cancer is one of the most common causes of mortality & morbidity globally, accounting for an estimated 10 million deaths in 2020. The diagnosis of cancer is a stressful event causing significant psychological distresses, most commonly depression and anxiety, directly interfering with disease outcome and quality of life. The aim of the study is to assess the level of depression and anxiety among adult patients with solid tumours as well as the association of various socio-demographic and clinical factors with them.Methods: This cross-sectional type of descriptive study was conducted at the National Institute of Cancer Research & Hospital (NICRH), Dhaka for a period of 12 months. A total of 405 histologically confirmed adult solid tumour patients were enrolled in the study using purposive sampling after fulfilling inclusion and exclusion criteria. Data were collected from the patients by face-to-face interviews using a semi-structured questionnaire and Bangla version of the DASS-21 scale.Results: In this study, the mean age of the respondents was 47.4 ± 16.5 years, the respondents were predominantly male with the male-tofemale ratio being 3:2 roughly. Gastrointestinal cancers (27.4%) were most prevalent, followed by lung (19.5%), gynaecological (11.4%), breast cancers and sarcomas (both 9.4%). The majority of the patients were undergoing chemotherapy (71.9%) and harbouring stage IV disease (64.4%) with duration of illness for less than twelve months (62% of respondents). The prevalence of depressive and anxious symptomatology among all patients was 38.02% and 42.96%, respectively. More than half (53.3%) of the adult patients with solid tumours were suffering from either of depression and/or anxiety. 19.7% had mild, 13.6% had moderate, 3.7% had severe and 1% had extremely severe levels of depression, while the percentages were 17.3%, 11.6%, 9.4% and 4.7% respectively, for severity of anxiety. In inpatient setting, depressive disorders were significantly higher in females than males (p<0.01) and among the lung cancer patients; in contrast, gastrointestinal cancer and the presence of co-morbidities predisposed more to anxiety (p<0.05). Although mode of treatment and severity of disease showed no significant relationship with the prevalence of depression or anxiety, ECOG performance status was found to have a significant impact on both of the disorders. On analysis of the socio-demographic variables, illiterate and low-income people were seen to suffer more with a severe and extremely severe level of depression, on the other hand, homemakers and lower socio-economic class had higher levels of anxiety.Conclusion: The study findings demonstrated a higher prevalence of depressive and anxious symptomatology in the inpatient setting; therefore, counselling, screening, and timely evaluation of mental health should be a part of the standard protocol of oncology care.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 215-216
背景:癌症是全球最常见的死亡和发病原因之一,2020年估计造成1000万人死亡。癌症的诊断是一个压力事件,会引起严重的心理困扰,最常见的是抑郁和焦虑,直接影响疾病的预后和生活质量。该研究的目的是评估患有实体瘤的成年患者的抑郁和焦虑水平,以及各种社会人口统计学和临床因素与之的关系。方法:在达卡国立癌症研究所和医院(NICRH)进行了为期12个月的横断面描述性研究。在满足纳入和排除标准后,共有405例组织学证实的成人实体瘤患者采用目的抽样纳入研究。采用半结构化问卷和孟加拉语版DASS-21量表对患者进行面对面访谈,收集数据。结果:本组调查对象平均年龄为47.4±16.5岁,以男性为主,男女比例约为3:2。最常见的是胃肠道癌症(27.4%),其次是肺癌(19.5%)、妇科(11.4%)、乳腺癌和肉瘤(均为9.4%)。大多数患者正在接受化疗(71.9%)和IV期疾病(64.4%),病程少于12个月(62%)。抑郁和焦虑症状在所有患者中的患病率分别为38.02%和42.96%。超过一半(53.3%)的成年实体瘤患者患有抑郁和/或焦虑。轻度抑郁占19.7%,中度抑郁占13.6%,重度抑郁占3.7%,极重度抑郁占1%,焦虑严重程度分别为17.3%、11.6%、9.4%和4.7%。住院患者中,女性患者抑郁程度显著高于男性(p<0.01),肺癌患者抑郁程度显著高于男性(p<0.01);相比之下,胃肠道癌症和合并症的存在更容易导致焦虑(p<0.05)。虽然治疗方式和疾病严重程度与抑郁或焦虑的患病率没有显著关系,但ECOG表现状态对这两种疾病都有显著影响。在对社会人口变量的分析中,文盲和低收入的人更容易患严重和极严重的抑郁症,另一方面,家庭主妇和较低的社会经济阶层的焦虑程度更高。结论:研究结果表明,在住院患者中,抑郁和焦虑症状的患病率较高;因此,心理健康的咨询、筛查和及时评估应成为肿瘤治疗标准方案的一部分。孟加拉国J医学2023;第34卷,第2(1)号补编:215-216
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引用次数: 0
HCV Management: Recent Updates HCV管理:最近的更新
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66129
S. Rahman
Background: Hepatitis C virus (HCV) has been a major public health threatboth worldwide and in Bangladesh due to itsconsiderable disease burden, morbidities, and death. An individualized, cost-effective, standard treatment regimen can help combat and eliminate HCV once and for all.Methods: This is an executive summary of the latest EASL (European Association for the Study of the Liver) recommendationsbased on existing literature, and clinical expertise from a panel of specialists chosen by the EASL Governing Board. Additionally, author’s clinical experience is undertaken for considering country level context. Results: HCV infection requires personalized treatment, based on factors such as genotype, liver fibrosis stage, and comorbidities. Direct-acting antiviral (DAA) regimens have replaced interferon, and are recommended as the first-line treatment for all patients with chronic HCV infection, irrespective of genotype. It is recommended to initiate treatment as soon as possible to prevent the progression of liver disease, and associated complications. For patients with decompensated cirrhosis, liver transplantation should be considered as a treatment option after weighing risk-benefit. Additionally, the management of special populations such as children, pregnant women, lactating mother, HCVpatients co-infected with HIV, HBV or SARS-CoV-2, patients with renal impairment, haemoglobin-opathies or bleeding disorders require special attention. Monitoring patients during and after treatment is recommended to ensure sustained virologic response (SVR), to detect any potential complication, and to check potential HCV reinfection.Conclusion: The EASL recommendations provide a comprehensive overview on personalized treatment of HCV, and monitoring for optimal patient outcomes, ushering high hopes for HCV elimination in the future.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 188
背景:丙型肝炎病毒(HCV)由于其巨大的疾病负担、发病率和死亡率,一直是全球和孟加拉国的主要公共卫生威胁。个体化的、具有成本效益的标准治疗方案有助于一劳永逸地对抗和消除丙型肝炎病毒。方法:这是最新的EASL(欧洲肝脏研究协会)建议的执行摘要,该建议基于现有文献和EASL管理委员会选择的专家小组的临床专业知识。此外,作者的临床经验是承担考虑国家层面的情况。结果:HCV感染需要根据基因型、肝纤维化分期和合并症等因素进行个性化治疗。直接作用抗病毒(DAA)方案已取代干扰素,并被推荐为所有慢性丙型肝炎病毒感染患者的一线治疗,无论其基因型如何。建议尽早开始治疗,以防止肝脏疾病的进展和相关并发症。对于失代偿性肝硬化患者,在权衡风险-收益后,应考虑肝移植作为一种治疗选择。此外,需要特别注意特殊人群的管理,如儿童、孕妇、哺乳期母亲、合并感染艾滋病毒、乙型肝炎病毒或SARS-CoV-2的丙型肝炎患者、肾功能损害患者、血红蛋白病变或出血性疾病患者。建议在治疗期间和治疗后监测患者,以确保持续的病毒学反应(SVR),发现任何潜在的并发症,并检查潜在的HCV再感染。结论:EASL建议提供了HCV个性化治疗的全面概述,并监测了最佳患者结果,为未来消除HCV带来了很高的希望。孟加拉国J医学2023;第34卷,第2(1)号补编:188
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引用次数: 0
New Hope in Parkinson’s Disease Management 帕金森病治疗的新希望
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66119
Aminur Rahman
Parkinson’s disease (PD) is the second most common neurodegenerative disorder worldwide, projected to affect at least 12 million people worldwide by 2040. The Hoehn and Yahr Scale stages 4 or 5 are referred to as advanced Parkinson’s disease (PD), which is characterized by significant motor deficits, a high risk of falling, extremely limited independence in terms of mobility, and cognitive and psychotic disorders. Motor fluctuations and dyskinesias frequently affect persons living with advanced PD, in which dyskinesia develops within 5.81 years from diagnosis, and motor fluctuations within 10 years. Continuous monitoring is necessary when motor fluctuations first appear to decide when to start an advanced treatment. Consequently, there is a vast need for improved treatments to address these motor symptoms. Deep brain stimulation, apomorphine subcutaneous infusion, levodopa-carbidopa intestinal gel infusion, and magnetic resonance-guided high-intensity focused ultrasound (FUS) are four device-aided therapies that provide new hope for treating PD in its advanced stages. The selection of device-assisted therapies is now mostly driven by the motor profile of the patient, with non-motor symptoms having a minimal impact on the decision-making process for the delivery and maintenance of successful therapy. In preliminary human trials, passive and active antiprotein á—synuclein vaccinations are being investigated. Monoclonal antibodies (mAbs) like prasinezumab that target the aggregates of á— synuclein can reduce the levels of free á—synuclein in serum by 97% by passive vaccination. The use of á—synuclein fragments or equivalent epitopes in active vaccination to stimulate an immune response is also being investigated. Although cell-based regeneration therapies utilizing fetal brain cells are successful in a small number of cases, this treatment is not practical due to the lack of fetal tissue. A sustainable source of dopamine-producing cells, such as stem cells, dopaminergic progenitors obtained from induced pluripotent stem cells (iPSCs), or cells derived from embryonic stem cells (ESCs), is currently being researched.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 182-183
帕金森病(PD)是全球第二大最常见的神经退行性疾病,预计到2040年全球至少有1200万人受到影响。Hoehn和Yahr量表的第4或第5阶段被称为晚期帕金森病(PD),其特征是严重的运动缺陷,摔倒的风险很高,在行动方面的独立性极其有限,以及认知和精神障碍。运动波动和运动障碍经常影响晚期PD患者,其中运动障碍在诊断后5.81年内出现,运动波动在10年内出现。当运动波动首次出现时,需要持续监测,以决定何时开始进一步治疗。因此,迫切需要改进治疗方法来解决这些运动症状。脑深部电刺激、阿波啡皮下输注、左旋多巴-卡比多巴肠道凝胶输注、磁共振引导下的高强度聚焦超声(FUS)是四种器械辅助治疗PD晚期的新希望。器械辅助疗法的选择现在主要是由患者的运动特征驱动的,非运动症状对成功治疗的交付和维持的决策过程影响最小。在初步的人体试验中,正在研究被动和主动抗蛋白á-synuclein疫苗接种。单克隆抗体(mab),如prasinezumab,靶向 - synuclein聚集体,可通过被动接种将血清中游离á-synuclein水平降低97%。在主动疫苗接种中使用á-synuclein片段或等效表位来刺激免疫反应也正在研究中。尽管利用胎儿脑细胞的细胞再生疗法在少数情况下是成功的,但由于缺乏胎儿组织,这种治疗并不实用。目前正在研究多巴胺产生细胞的可持续来源,如干细胞、从诱导多能干细胞(iPSCs)获得的多巴胺能祖细胞或来自胚胎干细胞(ESCs)的细胞。孟加拉国J医学2023;第34卷,第2(1)号补编:182-183
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引用次数: 0
Prediction of the Need for Niv in Patients With Acute Exacerbation of Chronic Obstructive Pulmonary Disease: A Comparative Study Between Decaf And Modified Decaf Score 预测慢性阻塞性肺疾病急性加重患者对Niv的需求:无咖啡因与改良无咖啡因评分的比较研究
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66162
Mushfiq Newaz Ahmed, Nihar Ranjan Saha, Md. Sayedul Islam
Background: Exacerbation of chronic obstructive pulmonary disease (COPD) leads to multiple hospital admissions, longer hospital stays, increased treatment costs as well as increased morbidity and mortality. Currently, no optimal scoring system exists that can predict need for NIV in patients with acute exacerbation of COPD. Accurate prognostic tool can help physicians to select the appropriate level of care and preparedness.To compare DECAF [(D) dyspnoea, (E) eosinopenia, (C) consolidation, (A) acidemia, (F) atrial fibrillation] and modified DECAF score [(D) dyspnoea, (E) eosinopenia, (C) consolidation, (A) acidemia, (F) frequency of hospital admission] in predicting the need for NIV in patients with acute exacerbation of chronic obstructive pulmonary disease.Methods: This cross-sectional study was conducted in the Department of Respiratory Medicine, NIDCH, Mohakhali, Dhaka from June 2021 to August 2022. A total of 91 patients with acute exacerbation of COPD were enrolled in this study. All patients were subjected to complete medical history taking, chest examination, dyspnoea assessment by extended modified Medical Research Council Dyspnoea (eMRCD), complete blood count, chest radiograph, ECG, and arterial blood gas analysis. Both DECAF and modified DECAF score were calculated and the need for NIV was documented. All collected data were analysed using appropriate statistical formula and SPSS programme.Results: Out of 91 patients, 20 patients (21.97%) required non-invasive ventilation. The area under the ROC curve of DECAF and modified DECAF score was 0.973 and 0.974 respectively in predicting the need for NIV. The sensitivity, specificity, PPV and NPV of DECAF score were 84.21%, 94.44%, 80.00% and 95.77% respectively at a cut off value of 3. The sensitivity, specificity, PPV and NPV of modified DECAF score were 84.52%, 100%, 100% and 96.51% respectively at a cut off value of 4Conclusion: Both DECAF score and the modified DECAF score are practical and can be calculated easily using simple questions and routine investigations available during the initial admission. Both were good predictors, but modified DECAF was superior in predicting need for NIV in patients with acute exacerbation of COPD BangladeshJ Medicine 2023; Vol. 34, No. 2(1) Supplement: 208-209          
背景:慢性阻塞性肺疾病(COPD)的恶化导致多次住院,住院时间延长,治疗费用增加以及发病率和死亡率增加。目前,尚无最优评分系统能够预测COPD急性加重期患者是否需要使用NIV。准确的预后工具可以帮助医生选择适当的护理和准备水平。比较DECAF [(D)呼吸困难,(E)红细胞减少,(C)实变,(A)酸血症,(F)房颤]和改良的DECAF评分[(D)呼吸困难,(E)红细胞减少,(C)实变,(A)酸血症,(F)住院次数]预测慢性阻塞性肺疾病急性加重期患者是否需要使用无创通气。方法:本横断面研究于2021年6月至2022年8月在达卡Mohakhali NIDCH呼吸内科进行。共有91例COPD急性加重患者参加了这项研究。所有患者均接受完整的病史记录、胸部检查、呼吸困难评估(eMRCD)、全血细胞计数、胸片、心电图和动脉血气分析。计算DECAF和改良DECAF评分,记录有无需要使用NIV。所有收集的数据采用相应的统计公式和SPSS程序进行分析。结果:91例患者中有20例(21.97%)需要无创通气。DECAF评分和修正DECAF评分的ROC曲线下面积分别为0.973和0.974。在截断值为3时,DECAF评分的敏感性为84.21%,特异性为94.44%,PPV和NPV分别为80.00%和95.77%。修正后的DECAF评分的敏感性为84.52%,特异性为100%,PPV为100%,NPV为96.51%,临界值为4。结论:修正后的DECAF评分和修正后的DECAF评分均具有实用性,可通过入院时的简单问题和常规调查轻松计算。两者都是良好的预测指标,但改良的DECAF在预测COPD急性加重患者是否需要NIV方面更优[孟加拉国医药2023];第34卷,第2(1)增编:208-209
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引用次数: 0
Cancer pain: way to overcome 癌症疼痛:克服的方法
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66128
Mostofa Kamal Chowdhury
Cancers are among the leading causes of morbidity and mortality worldwide. Cancer itself or cancer treatment often causes pain which can affectthe quality of life. Cancer pain management is an essential part of cancer treatment and palliative care. Cancer patients may require pain management at any stage of their disease, not only at the end. Expert opinion and statistics from country experiences from numerous low-income countries, where treatment coverage is typically inadequate or non-existent, indicate that around 80% of cancer patients feel moderate or severe pain that lasts on average 90 days. As a result, cancer pain is a major source of avoidable unnecessary suffering. Cancer pain management plans often involve pharmacological and nonpharmacological therapies and psycho-social and spiritual support. Palliative care and pain management are critical components of Universal Health Care. The medical use of narcotic drugs is essential for the treatment of pain and suffering. Therefore appropriate provisions must be made to assure their availability for such purposes. Some obstacles exist that limit the appropriate management of cancer-related discomfort. Communication difficulties, lack of pain management training and education, ethnic/cultural/ religious disparities, opiophobia among health professionals and the general public, and restricted availability to opioids are the primary barriers to successful cancer pain treatment. To combat cancer pain and reduce the suffering of these incurable people, education and training of health professionals on cancer pain management, provision of suitable holistic supports, opioids should be made accessible and available, and general awareness development are some examples. All government and nongovernment players must come forward and work together to win this battle. Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 187
癌症是全世界发病率和死亡率的主要原因之一。癌症本身或癌症治疗通常会引起疼痛,从而影响生活质量。癌症疼痛管理是癌症治疗和姑息治疗的重要组成部分。癌症患者可能在疾病的任何阶段都需要疼痛管理,而不仅仅是在晚期。专家意见和来自许多低收入国家经验的统计数据表明,大约80%的癌症患者感到中度或重度疼痛,平均持续90天。在这些国家,治疗覆盖通常不足或根本不存在。因此,癌症疼痛是可避免的不必要痛苦的主要来源。癌症疼痛管理计划通常包括药物和非药物治疗以及心理社会和精神支持。姑息治疗和疼痛管理是全民卫生保健的关键组成部分。麻醉药品的医疗用途对于治疗疼痛和痛苦是必不可少的。因此,必须作出适当的规定,以确保它们可用于这种目的。存在一些障碍,限制了癌症相关不适的适当管理。沟通困难、缺乏疼痛管理培训和教育、种族/文化/宗教差异、卫生专业人员和公众中的阿片类药物恐惧症以及阿片类药物的有限供应是成功治疗癌症疼痛的主要障碍。为防治癌症疼痛和减少这些不治之症患者的痛苦,应对保健专业人员进行癌症疼痛管理教育和培训,提供适当的整体支持,提供阿片类药物,以及提高普遍认识。所有政府和非政府参与者都必须挺身而出,共同努力赢得这场战斗。孟加拉国J医学2023;第34卷,第2(1)号补编:187
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引用次数: 0
Kidney replacement therapy: Pros and Cons 肾脏替代疗法:利弊
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66100
D. K. Roy
Kidney replacement therapy (KRT) is a term used to encompass life-supporting treatments for kidney failure. Kidney replacement therapy except kidney transplantation replaces nonendocrine kidney functions in patients with kidney failure. Researchers have noted that dialysis, which is one of the most common KRT used, cannot compensate for all the tasks performed by a kidney, and thus the term ‘Kidney support therapy’ has been suggested to be a better name. Support of kidney function in modern times encompasses a wide array of methods and clinical scenarios, from the ambulatory patient to the critically ill. The ability to safely and routinely deliver ongoing organ support in the outpatient setting has, until recently, separated kidney replacement therapy from other organ support. Kidney replacement therapy (KRT) can be applied intermittently or continuously using extracorporeal (hemodialysis) or Para corporeal (peritoneal dialysis) methods. All modalities exchange solute and remove fluid from the blood, using dialysis and filtration across permeable membranes. Nearly 4 million people in the world are living on kidney replacement therapy(KRT),and haemodialysis (HD) remains the commonest form of KRT, accounting forapproximately 69% of all KRT and 89% of all dialysis. Continuous therapy although costly is used mainly for hemodynamically unstable patients; benefits over intermittent therapy are improved tolerability as a result of slower removal of solute and water. Kidney transplantation is the ultimate step for end stage kidney failure management, as it replaces native kidney function completely. The main disadvantages of KRT relate to: Catheter related complications – blood loss, disconnection, infection or failure of access, mechanical complications of the extracorporeal circuit, fluctuations in the salt-water balance, activation of the coagulation cascade. Specific complications of peritoneal dialysis include: peritonitis, catheter- associated infections, hyperglycemia, protein loss etc. Current trends in artificial kidney research are ongoing with the lofty goal of a small device, preferably implanted with little or no maintenance required by the wearer that would deliver safe and highly effective renal replacement therapy including metabolic and endocrine functions.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 181
肾脏替代疗法(KRT)是一个术语,用于包括维持生命的治疗肾衰竭。肾移植以外的肾脏替代疗法可替代肾衰竭患者的非内分泌肾功能。研究人员指出,透析是最常用的KRT之一,不能补偿肾脏执行的所有任务,因此“肾脏支持疗法”一词被认为是一个更好的名字。在现代,肾脏功能的支持包含了广泛的方法和临床场景,从门诊病人到危重病人。直到最近,在门诊环境中安全、常规地提供持续器官支持的能力已经将肾脏替代治疗与其他器官支持分开。肾脏替代疗法(KRT)可以间歇或连续使用体外(血液透析)或体外(腹膜透析)方法。所有的模式交换溶质和从血液中清除液体,使用透析和过滤通过渗透膜。世界上有近400万人依靠肾脏替代疗法(KRT)生活,血液透析(HD)仍然是最常见的KRT形式,约占所有KRT的69%和所有透析的89%。持续治疗虽然费用昂贵,但主要用于血流动力学不稳定的患者;间歇性治疗的好处是由于溶质和水的去除较慢,耐受性得到改善。肾移植是终末期肾衰竭治疗的最终步骤,因为它完全取代了天然肾功能。KRT的主要缺点涉及:导管相关并发症——失血、断线、感染或通路失败、体外回路的机械并发症、盐水平衡的波动、凝血级联的激活。腹膜透析的特殊并发症包括:腹膜炎、导管相关性感染、高血糖、蛋白丢失等。目前人工肾脏研究的趋势正在进行中,其崇高目标是制造一种小型装置,最好是在植入时很少或不需要佩戴者进行维护,从而提供安全有效的肾脏替代治疗,包括代谢和内分泌功能。孟加拉国J医学2023;第34卷,第2(1)号补编:181
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引用次数: 0
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Bangladesh Journal of Veterinary Medicine
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