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Cardiovascular assessment in Noncardiovascular surgery: what evidences say? 非心血管手术中的心血管评估:证据表明什么?
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66097
A. Maskey
Annually more than 300 million patients (about 5% of the world population) undergo major surgery worldwide. Nearly 85% of major operations are noncardiac surgical procedures. Proper preoperative evaluation is important to reduce cardiovascular morbidity and mortality in patients undergoing noncardiac surgery. Cardiac risk is determined by two main factors: patient-related risk and surgical risk. Timing of surgery (Immediate, Urgent, time-sensitive, elective), type of surgical approach ( laparoscopy, vascular and endovascular procedure, open surgeries) , risk of surgery ( Low, intermediate, high surgical risk) determine surgical risk. Patient-related risk is assessed by patient’s age, the presence of cardiovascular risk factors (e.g. smoking, hypertension, diabetes, dyslipidaemia,) or established cardiovascular disease, and comorbidities (heart failure, arrhythmia etc.).In emergency surgery preoperative evaluation is limited as saving life is more important. In elective surgery patient related risk factors, comorbidity, associated cardiovascular diseases, timing and risk of surgery , functional capacity determine further preoperative evaluation with necessary investigations like ECG, Echo, laboratory investigations, biomarkers, stress test, coronary angiogram etc.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 179
全世界每年有超过3亿患者(约占世界人口的5%)接受大手术。近85%的大手术是非心脏外科手术。正确的术前评估对于降低非心脏手术患者的心血管发病率和死亡率非常重要。心脏风险主要由两个因素决定:患者相关风险和手术风险。手术时机(立即,紧急,时间敏感,选择性),手术方式类型(腹腔镜,血管和血管内手术,开放手术),手术风险(低,中,高手术风险)决定手术风险。与患者相关的风险是通过患者的年龄、是否存在心血管危险因素(如吸烟、高血压、糖尿病、血脂异常)或已确诊的心血管疾病以及合并症(心力衰竭、心律失常等)来评估的。在急诊手术中,术前评估是有限的,因为挽救生命更重要。在择期手术中,患者相关危险因素、合并症、相关心血管疾病、手术时机和风险、功能能力确定进一步的术前评估,并进行必要的检查,如ECG、Echo、实验室检查、生物标志物、压力测试、冠状动脉造影等。bangladesh J Medicine 2023;第34卷,第2(1)号补编:179
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引用次数: 0
Prevention of Acute Respiratory Failure Due to Administration of Polymyxins by Intravenous Calcium Gluconate in Critically Ill Patients for Treating Carbapenem Resistant Infections in Acute Medicine Unit: A Quality Improvement Project (Qip) 急性内科重症患者静脉注射葡萄糖酸钙多粘菌素治疗耐碳青霉烯类感染后急性呼吸衰竭的预防:质量改进工程(Qip)
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66171
Bornali Chowdhury, Ahmed Mursel Anam, S. Huq, Adnan Shareef, Mymuna Binte Mukarrom
Background: Polymyxin B and colistin are most potent antibiotics for treating carbapenem resistant infections due tomultidrugs resistant organisms that are currently rising remarkably and alarm signs for global health. These are last resorts options for bacteremia during crisis time when pathogens are only sensitive to polymyxins. Most common life threatening complication is respiratory muscle paralysis due to neuromuscular blockage that lead to apnea, acute type 2 respiratory failure and death. Main aim of this quality Improvement project (QIP)was to demonstrate therapeutic effectiveness and outcomes of I/V calcium gluconate during administration of polymyxins.Methods: This QIP was conducted at acute medicine and HDU of a tertiary care hospital for 2 months in Bangladesh. Patients who got I/V calcium gluconate with polymyxins in January and February, 2023 were compared with similar data without calcium gluconate for prior 4 months. Data analysis and interpretation done by unpaired t test.Results: Primary outcome shows statistically significant decrease dintubation and mechanical ventilation due to sudden respiratory failure and ICU transfer after getting I/V calcium gluconate during polymyxins(30.8%,n=13 and 88.9% ,n=9 and p= <0.005).Conclusion: This study showsstrongly visible positive outcome in prevention of acute respiratory failure by polymyxins in critically ill patients. We feel that all physicians may practice this study in acute medicine and critical care setup.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 216 
背景:多粘菌素B和粘菌素是治疗由多药耐药菌引起的碳青霉烯耐药感染的最有效抗生素,目前这种感染正在显著上升,是全球卫生的警报信号。当病原体只对多粘菌素敏感时,这些是危机时期菌血症的最后选择。最常见的危及生命的并发症是由神经肌肉阻塞引起的呼吸肌肉麻痹,导致呼吸暂停、急性2型呼吸衰竭和死亡。本质量改进项目(QIP)的主要目的是证明I/V葡萄糖酸钙在多粘菌素治疗期间的治疗效果和结果。方法:在孟加拉国某三级医院急诊科和HDU进行为期2个月的QIP研究。将2023年1月和2月接受I/V葡萄糖酸钙多粘菌素治疗的患者与此前4个月未接受葡萄糖酸钙治疗的患者进行比较。数据分析和解释采用非配对t检验。结果:主要终点显示,多粘菌素治疗期间给予I/V葡萄糖酸钙治疗后因突发性呼吸衰竭和转ICU而插管和机械通气减少(30.8%,n=13; 88.9%,n=9, p= <0.005)。结论:本研究显示多粘菌素在预防危重患者急性呼吸衰竭方面具有明显的积极效果。我们认为所有的医生都可以在急症医学和重症监护机构中实践这项研究。孟加拉国J医学2023;第34卷,第2(1)号补编:216
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引用次数: 0
Naphthalene Poisoning in a Young Glucose 6 Phosphate Dehydrogenase Deficient Patient 1例年轻葡萄糖-磷酸脱氢酶缺乏患者的萘中毒
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66179
A. Begum
Naphthalene poisoning is a rare form of toxicity that may occur after ingestion, inhalation, or dermal exposure to naphthalene-containing compounds. It is a volatile polycyclic hydrocarbon used as a household deodorizer and moth repellent.Ingestional naphthalene poisoning can leadto methaemo-globulinaemia and intravascular haemolysis with diagnostic and therapeutic challenge. Associated G6PD deficiency may make it more complicated. A 20-year-old man presented with low-grade fever, lethargy and dark urine for 4 days.His vitals showed normal temperature, tachycardia with normal blood pressure and low oxygen saturation(76%) despite having high flow oxygen (15L/min).On repeated queries, he gave a history of ingesting a few naphthalene balls after a heated conversation with his friends. Laboratory workup showed features of haemolysis, methaemoglobinaemia, haemoglobinuria and low glucose 6 phosphate dehydrogenase level. The patient was treated conservatively with intravenous fluid, packed red blood cells transfusion, N acetylcysteine andascorbic acid with full recovery.J Medicine 2023; Vol. 34, No. 2(1) Supplement: 218
萘中毒是一种罕见的毒性形式,可在摄入、吸入或皮肤接触含萘化合物后发生。它是一种挥发性多环烃,用作家用除臭剂和驱虫剂。摄入萘中毒可导致甲基血球血症和血管内溶血,具有诊断和治疗上的挑战。相关的G6PD缺乏可能使其更加复杂。20岁男性,表现为低烧、嗜睡、尿色深4天。他的生命体征显示体温正常,心动过速,血压正常,低氧饱和度(76%),尽管有高流量氧(15L/min)。在反复询问下,他讲述了自己在与朋友激烈交谈后吞下了几个萘球的历史。实验室检查显示溶血、血红蛋白血症、血红蛋白尿和低葡萄糖-磷酸脱氢酶水平。患者经静脉输液、充血性红细胞输注、N -乙酰半胱氨酸和抗坏血酸治疗后完全恢复。中华医学杂志2023;第34卷,第2(1)号补编:218
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引用次数: 0
Precision Medicine: An Emerging Approach for Patient Care 精准医学:一种新兴的病人护理方法
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66150
M Amir Hossain
The philosophy behind contemporary healthcare is that one size fits all. Unfortunately, the outcomes of a standardized treatment regimen are not always uniform. That’s where the concept of precision medicine comes in. According to the Precision Medicine Initiative, precision medicine is “an emerging approach for disease treatment and prevention that takes into account individual variability in genes, environment, and lifestyle for each person.” This approach allow doctors and researchers to predict more accurately which treatment and prevention strategies for a particular disease will work in which groups of people and is in contrast to a one-size-fits-all approach, in which disease treatment and prevention strategies are developed for the average person, with less consideration for the differences between individuals. Although the term “precision medicine” is relatively new, the concept has been a part of healthcare for many years. For example, a person who needs a blood transfusion is not given blood from a randomly selected donor; instead, the donor’s blood type is matched to the recipient to reduce the risk of complications. The adoption of precision medicine will grow because its benefits to healthcare providers and patients are numerous. The highlighting ones are to shift the emphasis in medicine from reaction to prevention, predict susceptibility to disease, improve disease detection, preempt disease progression, customize disease-prevention strategies, prescribe more effective drugs, avoid prescribing drugs with predictable side effects and so on.The goal of precision medicine is to target the right treatments to the right patients at the right time. The short-term goals involve expanding precision medicine in the area of cancer research. Researchers at the National Cancer Institute (NCI) hope to use an increased knowledge of the genetics and biology of cancer to find new, more effective treatments for various forms of this disease. The long-term goals of the Precision Medicine Initiative focus on bringing precision medicine to all areas of health and healthcare on a large scale. Insufficient technologies, limited knowledge, and gaps in research are major obstacles to adding precision medicine to routine clinical care. Advances in precision medicine have already led to powerful new discoveries and FDA-approved treatments that are tailored to specific characteristics of individuals. Patients with a variety of cancers routinely undergo molecular testing as part of patient care, enabling physicians to select treatments that improve chances of survival and reduce exposure to adverse effects. Precision medicine will timely enable clinicians to integrate healthcare data with targeted assays and tests to identify and assess disease biomarkers and risks, determine actionable genetic variants in patients, obtain the entire picture of the metabolome, and map metabolites to disease pathways. Implementof precision medicine as a holistic approach, req
现代医疗保健背后的理念是一刀切。不幸的是,标准化治疗方案的结果并不总是一致的。这就是精准医疗概念的由来。根据精准医学倡议,精准医学是“一种新兴的疾病治疗和预防方法,它考虑到每个人在基因、环境和生活方式方面的个体差异。”这种方法使医生和研究人员能够更准确地预测针对特定疾病的治疗和预防策略将适用于哪些人群,这与“一刀切”的方法形成了对比。“一刀切”的方法是为普通人制定疾病治疗和预防策略,而较少考虑个体之间的差异。尽管“精准医疗”这个术语相对较新,但这个概念多年来一直是医疗保健的一部分。例如,需要输血的人的血液不是随机选择的献血者提供的;相反,献血者的血型与接受者相匹配,以减少并发症的风险。精准医疗的采用将会增加,因为它对医疗保健提供者和患者的好处很多。重点是将医学的重点从反应转向预防,预测疾病易感性,提高疾病检测,预防疾病进展,定制疾病预防策略,开具更有效的药物,避免开具可预测副作用的药物等。精准医疗的目标是在正确的时间为正确的病人提供正确的治疗。短期目标包括在癌症研究领域扩大精准医疗。美国国家癌症研究所(NCI)的研究人员希望利用对癌症遗传学和生物学的进一步了解,为各种形式的癌症找到新的、更有效的治疗方法。精准医疗计划的长期目标是将精准医疗大规模应用于健康和医疗保健的所有领域。技术不足、知识有限和研究差距是将精准医疗纳入常规临床护理的主要障碍。精准医疗的进步已经带来了强大的新发现和fda批准的针对个人特定特征的治疗方法。作为患者护理的一部分,患有各种癌症的患者经常进行分子检测,使医生能够选择提高生存机会和减少不良反应的治疗方法。精准医疗将及时使临床医生能够将医疗保健数据与有针对性的分析和测试相结合,以识别和评估疾病生物标志物和风险,确定患者可操作的遗传变异,获得代谢组的全图,并将代谢物映射到疾病途径。精准医疗作为一种整体方法的实施,需要使用复杂的机制模型整合基因、基因组、临床、环境和生活方式数据,必须从头开始构建。科学的方法将是对个体基因组进行分析,从而在医疗保健领域产生一种新的预防和个性化医疗形式。基于基因的设计药物的可用性、疾病分子指纹的精确靶向、适当的药物治疗、预测个体对疾病的易感性、疾病的诊断和治疗,这些都是未来十年预计将发生的许多变化中的一小部分。孟加拉国J医学2023;第34卷,第2(1)号增编:201
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引用次数: 0
Approach to multidrug resistant bacterial infections 多重耐药细菌感染的处理方法
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66143
A. Basher
Several bacterial pathogens have evolved into multidrug resistant (MDR) forms both in developed and developing countries at an expanding rate. The World Health Organization has identified antimicrobial resistance as one of the three most important problems facing human health. It was estimated that 4·95 million deaths were associated with bacterial AMR globally in 2019.1 Three infectious syndromes dominated the global burdens attributable to AMR: lower respiratory and thorax infections, bloodstream infections, and intra-abdominal infections. Some of the most important MDR pathogens that currently cause infection in hospital and in the community are the so-called “ESKAPE” pathogens (Enterococcus faecium, Staphylococcus aureus, Klebsiella pneumoniae, Acinetobacter baumanii, Pseudomonas aeruginosa, and Enterobacter species), emphasizing their capacity to “escape” the effects of routine antibiotics. Most of the MDR studies were heterogeneous in terms of study design, patient population, site of infection, choice of antibiotic treatment, duration of followup period, and the outcome definitions, making it difficult to compare the different treatments and combinations of antibiotics used. Current recommendations in Europe and USA are based on systematic reviews that suggest different methods to prevent and control MDR infections, but provide little data on new and alternative antibiotic treatment options and therefore provide little firm guidance on specific treatment choices and algorithms. Attempts are ongoing to overcome antibacterial resistance by using new agents and combinations of new plus old agents. For example, both old (clavulanic acid, tazobactam) and new (avibactam, vaborbactam, relebactam) BLIs are being used in treatment algorithm for critically ill patients in the ICU according to MDR pathogen. There were still controversies regarding microbiological success for single agent compared with combinations of multiple agents. Many bacteria have the ability to produce biofilms, comprising organized congregations of bacteria adhering to each other making complex condition where antibiotic failed to wipe out bacteria despite of retaining in vitro susceptibility. It is also not always possible to conduct randomized controlled studies involving the required number of patients in a timely manner. So a requirement with the increasing choice of highly effective antimicrobial drugs, with dosages based on pharmacokinetic analysis of drug disposition, selection of the appropriate drug based on clinical microbiological data and pharmacodynamic indices. Rational antimicrobial therapy is more applicable today than in the history of antimicrobial therapy. Exploring newer modalities such as phage therapy and lytic antibiotics as well as obtaining a deeper understanding of the pathways involved in MDR mechanisms in order to engineer targeted drugs. Besides, rapid and comprehensive diagnostics are the key factor for the future management of antimicrobial resis
在发达国家和发展中国家,一些细菌病原体已经以越来越快的速度进化成耐多药(MDR)形式。世界卫生组织已将抗菌素耐药性确定为人类健康面临的三大最重要问题之一。据估计,2019年全球有49.5万人死亡与细菌性抗菌素耐药性有关。1三种感染综合征主导了由抗菌素耐药性引起的全球负担:下呼吸道和胸腔感染、血液感染和腹腔内感染。目前在医院和社区引起感染的一些最重要的耐多药病原体是所谓的“ESKAPE”病原体(粪肠球菌、金黄色葡萄球菌、肺炎克雷伯菌、鲍曼不动杆菌、铜绿假单胞菌和肠杆菌),强调它们“逃避”常规抗生素作用的能力。大多数耐多药研究在研究设计、患者人群、感染部位、抗生素治疗选择、随访时间和结局定义等方面存在异质性,因此难以比较不同治疗方法和抗生素联合使用。欧洲和美国目前的建议是基于系统评价,提出了预防和控制耐多药感染的不同方法,但很少提供新的和替代抗生素治疗方案的数据,因此很少提供具体治疗选择和算法的坚定指导。目前正在尝试通过使用新药物和新加旧药物的组合来克服抗菌药物耐药性。例如,旧的(克拉维酸、他唑巴坦)和新的(阿维巴坦、瓦博巴坦、瑞乐巴坦)BLIs都被用于ICU重症患者根据耐多药病原体的治疗算法中。与多种药物联合使用相比,单药在微生物学方面的成功仍然存在争议。许多细菌具有产生生物膜的能力,这些生物膜由有组织的细菌聚集在一起,相互粘附,这使得抗生素尽管保留了体外敏感性,但却无法消灭细菌。也不可能总是及时进行涉及所需数量患者的随机对照研究。因此,随着高效抗菌药物的选择越来越多,需要根据药物处置的药代动力学分析来给药,根据临床微生物学数据和药效学指标来选择合适的药物。合理的抗菌治疗在今天比在抗菌治疗的历史上更适用。探索新的模式,如噬菌体治疗和溶解性抗生素,以及更深入地了解耐多药机制所涉及的途径,以便设计靶向药物。此外,快速和全面的诊断是未来管理抗菌素耐药性的关键因素。孟加拉国J医学2023;第34卷,第2号(1)补编:195-196
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引用次数: 0
Evaluation of the Efficacy and Tolerability of a Fixed Dose Combination of Amlodipine And Indapamide in Patients Older Than 55 Years 55岁以上患者固定剂量氨氯地平与吲达帕胺联合应用的疗效和耐受性评价
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66148
Q. Islam, K. Haque, Kaniz Moula, H. Ahasan, Md. Ismail Patwary, K. A. Azad, Mujibur Rahman, Md Zakir Hossain, M. Miah, A. Azad
Background: There is very limited real-life data on hypertension management in Bangladeshi population. Considering this fact, this study evaluated the effectiveness of treatment with an indapamide/amlodipine single-pill combination (SPC) in Bangladeshi patients over the age of 55 years, in an OPD setting with uncontrolledsystolic hypertension in real-life clinical practice.Methods: This was a 3-month, multicenter, observational, open-label study conducted in 3 divisional cities of Bangladesh among patients with grade I or II hypertensions who were either uncontrolled on previous antihypertensive treatment or treatment-naïve. The effectiveness of indapamide/amlodipine SPC was assessed by the change in office systolic blood pressure (SBP) and the rate of target SBP (< 140 mmHg)achievement at 2 weeks, 1 month and 3 months, in four age groups: 55–59 years, 60–69 years, 70–79 years, and80 years or older.Results: The COMBINE study recruited 213 patients, of whom 185 took indapamide/amlodipine 1.5/5 mg SPC forafull three-month course of therapy.Mean age was 62.4±7.4 years, 76 men [41.1%] and 109 women [58.9%]. The absolute decrease of SBP during 3 months of taking indapamide/amlodipine single-pill combination (SPC) was 27.7 mm Hg, DBP - 10.2 mm Hg.After 3 months of treatment significant SBPdecreases from baseline were observed in each age group:”29.9 mmHg (from 156.7 to 126.8),”25.1 mmHg (from 152.7 to 127.6),”26.1 mmHg (from 152.8 to 126.7),and “ 24.5 mmHg (from 151.8 to 127.3)in the 55–59, 60–69, 70–79, and 80 years and older age groups, respectively.Conclusion: This COMBINE study results showed that indapamide/amlodipine SPC was associated with significant and rapid reductions in BP even in a different age range of Bangladeshi patients in routine clinical practice. This study result is consistent with already achieved data of this SPC globally.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 200
背景:孟加拉国人群高血压管理的实际数据非常有限。考虑到这一事实,本研究评估了indapamide/氨氯地平单片联合用药(SPC)在孟加拉国55岁以上门诊患者中治疗不可控收缩期高血压的有效性。方法:这是一项为期3个月、多中心、观察性、开放标签的研究,在孟加拉国的3个城市进行,研究对象是I级或II级高血压患者,这些患者在既往抗高血压治疗中未得到控制或treatment-naïve。在55-59岁、60-69岁、70-79岁和80岁以上四个年龄组中,通过2周、1个月和3个月时办公室收缩压(SBP)变化和目标收缩压(< 140 mmHg)达到率来评估吲达帕胺/氨氯地平SPC的有效性。结果:联合研究招募了213名患者,其中185名患者接受了吲达帕胺/氨氯地平1.5/5 mg SPC的三个月疗程。平均年龄62.4±7.4岁,男性76人(41.1%),女性109人(58.9%)。在服用吲达帕胺/氨氯地平单丸联合(SPC) 3个月期间,收缩压绝对下降27.7 mmHg,舒张压- 10.2 mmHg。治疗3个月后,各年龄组的收缩压均较基线显著下降:55-59岁、60-69岁、70-79岁和80岁及以上年龄组的收缩压分别为29.9 mmHg(从156.7到126.8)、25.1 mmHg(从152.7到127.6)、26.1 mmHg(从152.8到126.7)和24.5 mmHg(从151.8到127.3)。结论:这项联合研究结果显示,在孟加拉国的常规临床实践中,即使在不同年龄范围的患者中,吲达帕胺/氨氯地平SPC也与显著且快速的血压降低相关。该研究结果与该SPC在全球范围内已获得的数据一致。孟加拉国J医学2023;第34卷,第2(1)增编:200
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引用次数: 0
Treatment of Tuberculosis in special situations 在特殊情况下治疗肺结核
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66145
M. D. Hossain, A. Mahmud, Md Ali Hossain, Mohammad Abdus Shakur Khan, K. Bennoor, Md Ferdous Wahid
Treatment of Tuberculosis in special situations implies overcoming special challenges in patients with diabetes, pregnant women, people aged over 65 years, and those with chronic kidney or liver disease.Rifampicin is a potent hepatic enzyme inducer, may lower plasma levels of sulphonyl urea and can increase the hypoglycemic effect of metformin. Since insulin is not metabolized, no pharmacokinetic interactions with anti-TB drugs occur. Gastrointestinal upset and hepatitis are reported as the most frequent adverse events in older people. In patients >80 years,pyrazinamide may be omitted. In TB patients with chronic kidney disease (CKD), an inappropriate dosage of anti-TB drugs can result in unsuccessful treatment or side effects. Current guidelines for first-line anti-TB drugs therefore recommend that dosages of ethambutol (EMB) and pyrazinamide (PZA) be adjusted according to patient renal function and body weight, although no change in dosage is necessary for patients with mild renal insufficiency . However, it remains unknown how the renal function-based dosage adjustments recommended by the guidelines affect efficacy outcomes for TB patients with CKD. In chronic liver disease (CLD) patients, The Child–Turcotte–Pugh (CTP) score can be used as a guide for designing appropriate regimens. In stable CLD (CTP d”7), a treatment regimen including isoniazid, rifampicin, and ethambutol is recommended, a 2-month intensive phase with the three drugs, followed by isoniazid and rifampicin continuation phase for 7 months partially liver-sparing regimen consisting of Ethambutol, Rifampicin, and a quinolone for 9 months is advisable in case of more severe CLD (CTP 8–10).If CLD is very advanced (CTP £11), a total liver-sparing regimen consisting of Ethambutol and a quinolone (Levofloxacin or Moxifloxacin) for 12 months.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 196-197
在特殊情况下治疗结核病意味着克服糖尿病患者、孕妇、65岁以上的人以及慢性肾病或肝病患者的特殊挑战。利福平是一种有效的肝酶诱导剂,可降低血浆中磺酰脲的水平,并可增强二甲双胍的降糖作用。由于胰岛素不被代谢,因此不会与抗结核药物发生药代动力学相互作用。胃肠不适和肝炎是老年人最常见的不良事件。在>80岁的患者中,吡嗪酰胺可以省略。在伴有慢性肾脏疾病(CKD)的结核病患者中,抗结核药物剂量不适当可能导致治疗失败或产生副作用。因此,目前的一线抗结核药物指南建议根据患者的肾功能和体重调整乙胺丁醇(EMB)和吡嗪酰胺(PZA)的剂量,尽管轻度肾功能不全患者无需改变剂量。然而,目前尚不清楚指南推荐的基于肾功能的剂量调整如何影响结核合并CKD患者的疗效结果。在慢性肝病(CLD)患者中,child - turcote - pugh (CTP)评分可作为设计合适方案的指导。对于稳定型CLD (CTP d”7),建议采用包括异烟肼、利福平和乙胺丁醇在内的治疗方案,3种药物治疗2个月的强化期,如果更严重的CLD (CTP 8-10),建议采用异烟肼和利福平持续7个月的部分保肝方案,包括乙胺丁醇、利福平和喹诺酮治疗9个月。如果CLD非常晚期(CTP为11英镑),则采用乙胺丁醇和喹诺酮类药物(左氧氟沙星或莫西沙星)共12个月的保肝方案。孟加拉国J医学2023;第34卷,第2(1)号补编:196-197
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引用次数: 0
Kidney Disease – Bangladesh Perspective 肾脏疾病-孟加拉国视角
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66098
M. R. Alam
In Bangladesh, most patients with Chronic Kidney Disease (CKD) are diagnosed in the advanced stages of the disease, which leads to a high demand for kidney transplantation and dialysis services.Several studies suggest prevalence rate of CKD 6–18%; of them 11% were in stage III–V.Every year 35,000-40,000 new cases of kidney failure.Every year >20,000 chronic kidney failure patients die as they cannot afford dialysis or kidney transplant.73% treatment cost is out of pocket in Bangladesh.The cost of hemodialysis per session varies from 400- 4500 BDT (USD 4-45) depending on institute.Even the ultra-poor patients who take dialysis at the rate of BDT 500 (USD 5) per session have to spend a minimum of BDT 20,000 (USD 200) per month only for the treatment cost. 40% patients discontinue dialysis after 3-4 months due to financial constraint. The existing facilities can hardly accommodate 9000–10,000 new patients, which means RRT isnot available for 70–75% of ESRD patients.Annually dialysis is done on >18,000 kidney patients across the country.80% of the total kidney-related deaths are caused due to insolvency to continue treatment.Currently >90% of dialysis patients are receiving Hemodialysis.Initiatives are taken to make CAPD more accessible, but high cost of PD fluid & lack of trained personnel remains as major barriers. Challenges are there in providing Nephrocare.There is insufficient number and uneven distribution of trained medical & allied health professionals, lack of proper referral system & follow-up & lack of laboratory facility in many areas, particularly in rural setup.Absence of insurance coverage for kidney dialysis & transplant treatment.Absence of patient support group & their participation in policy making process. To overcome the challenges we have to ensure affordable & equitable access to kidney care for people living with CKD through Public & Public Private Partnerships. Protection from out-of-pocket healthcare expenditure through universal health coverage to provide insurance coverage for CKD patients and Subsidized treatment for dialysis & kidney transplant.Expansion of Fellowship program to develop more Nephrologists & training facility/ centers to develop more allied health professionals.Facilitating research for kidney disease with technical and financial support.Improve screening to ensure timely diagnosis and prevent CKD related complications.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 179-180
在孟加拉国,大多数慢性肾脏疾病(CKD)患者被诊断为疾病晚期,这导致对肾脏移植和透析服务的高需求。多项研究表明CKD患病率为6-18%;其中11%为III-V期。每年有三万五千到四万例新的肾衰竭病例。每年有2万名慢性肾衰竭患者因无法负担透析或肾脏移植而死亡。在孟加拉国,73%的治疗费用是自费的。每次血液透析的费用从400- 4500 BDT(4-45美元)不等,具体取决于研究所。即使是每次透析500泰铢(5美元)的赤贫患者,每月也要花费至少20,000泰铢(200美元)的治疗费用。40%的患者在3-4个月后因经济拮据而停止透析。现有的设施几乎不能容纳9000 - 10000名新患者,这意味着70-75%的ESRD患者无法获得RRT。全国每年约有1.8万名肾病患者接受透析治疗。肾脏相关死亡总数的80%是由于无力继续治疗造成的。目前,90%的透析患者正在接受血液透析。采取措施使CAPD更容易获得,但PD液的高成本和缺乏训练有素的人员仍然是主要障碍。在提供肾脏护理方面存在挑战。在许多地区,特别是农村地区,训练有素的医疗和联合卫生专业人员数量不足且分布不均,缺乏适当的转诊系统和随访以及缺乏实验室设施。没有肾脏透析和移植治疗的保险。缺乏患者支持小组和他们在政策制定过程中的参与。为了克服这些挑战,我们必须通过公私合作伙伴关系,确保CKD患者能够负担得起且公平地获得肾脏护理。通过全民健康保险,为慢性肾病患者提供保险,并为透析和肾移植治疗提供补贴,保护患者免受自费医疗费用的影响。扩大奖学金计划,发展更多的肾病专家和培训设施/中心,培养更多的专职医疗人员。通过技术和资金支持促进肾脏疾病的研究。改善筛查,确保及时诊断,预防CKD相关并发症。孟加拉国J医学2023;第34卷,第2(1)增编:179-180
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引用次数: 0
Modern Insulin, Device, and Technology: Tips For Clinicians 现代胰岛素,设备和技术:给临床医生的提示
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66135
Abm Kamrul Hasan
Insulin has been a lifesaving treatment for people with diabetes since its discovery in 1921. However, the way insulin is delivered evolved over time. Modern insulin, devices, and technology have transformed the management of diabetes and improved the quality of life for millions of people worldwide.Modern insulins are designed to match the needs of people with diabetes better. Traditional insulins, such as regular and NPH insulin, have a delayed onset and peak, making it difficult to manage blood sugar levels. Newer insulins, such as rapid-acting insulin analogs like aspart, glulisine, and lispro, have a faster onset and shorter duration of action, allowing for greater dosing and timing flexibility. Long-acting insulin analogs, like glargine and detemir, provide more consistent blood sugar control and less hypoglycemia risk.Insulin delivery devices have also advanced significantly. The most common device is the insulin pen, which looks like a large pen and uses disposable insulin cartridges. The pen has replaced traditional syringes and vials for many people with diabetes, offering greater convenience and ease of use. Insulin pumps are also becoming more popular, especially among people with type 1 diabetes. A pump delivers insulin through a catheter inserted under the skin, which can be programmed to provide a continuous infusion of insulin or a bolus dose before meals.Technological advancements have also revolutionized diabetes management. Continuous glucose monitoring (CGM) systems use a small sensor inserted under the skin to measure glucose levels every few minutes, providing real-time data to help people make more informed decisions about insulin dosing and food choices. Some CGM systems also offer alerts for high and low blood sugar levels, making it easier to avoid dangerous fluctuations. Automated insulin delivery systems, also known as closed-loop systems or artificial pancreas systems, use CGM data to automatically adjust insulin delivery, reducing the burden of constant monitoring and decision-making for people with diabetes.In summary, modern insulin, devices, and technology have greatly improved the management of diabetes, allowing for better blood sugar control and a better quality of life for people with diabetes. As technology continues to advance, the future of diabetes management looks promising.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 191
自1921年发现胰岛素以来,它一直是糖尿病患者的救命良药。然而,胰岛素的输送方式随着时间的推移而进化。现代胰岛素、设备和技术已经改变了糖尿病的管理,改善了全世界数百万人的生活质量。现代胰岛素的设计是为了更好地满足糖尿病患者的需要。传统的胰岛素,如常规胰岛素和NPH胰岛素,起效较晚,达到峰值,因此很难控制血糖水平。较新的胰岛素,如速效胰岛素类似物,如天冬氨酸、葡氨酸和利斯普罗,起效更快,作用时间更短,允许更大的剂量和时间灵活性。长效胰岛素类似物,如甘精氨酸和地特米,提供更稳定的血糖控制和更低的低血糖风险。胰岛素输送装置也有了显著的进步。最常见的设备是胰岛素笔,它看起来像一支大笔,使用一次性胰岛素盒。对于许多糖尿病患者来说,这种笔已经取代了传统的注射器和小瓶,提供了更大的方便和易用性。胰岛素泵也越来越受欢迎,尤其是在1型糖尿病患者中。胰岛素泵通过插入皮下的导管输送胰岛素,该导管可被设定为连续输注胰岛素或饭前注射胰岛素。技术进步也使糖尿病的管理发生了革命性的变化。连续血糖监测(CGM)系统使用一个插入皮下的小传感器,每隔几分钟测量一次血糖水平,提供实时数据,帮助人们在胰岛素剂量和食物选择方面做出更明智的决定。一些CGM系统还提供高血糖和低血糖警报,使其更容易避免危险的波动。自动胰岛素输送系统,也被称为闭环系统或人工胰腺系统,使用CGM数据自动调整胰岛素输送,减轻糖尿病患者持续监测和决策的负担。总之,现代胰岛素、设备和技术极大地改善了糖尿病的管理,使糖尿病患者能够更好地控制血糖,提高生活质量。随着技术的不断进步,糖尿病管理的未来看起来很有希望。孟加拉国J医学2023;第34卷,第2(1)号补编:191
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引用次数: 0
Challenging Thyroid Cases in Clinical Practice 临床实践中具有挑战性的甲状腺病例
Pub Date : 2023-05-24 DOI: 10.3329/bjm.v34i20.66132
M. Saifuddin
Thyroid disorders are prevalent, and their manifestations are divergent and sometimes it is very challenging to diagnose and deal with some Thyroid cases in clinical practice. Here seven different challenging cases will be discussed that will help clinicians to diagnose and treat such cases in dayto- day clinical practice. First case enlightened us that Thyroid function should not be assessed in seriously ill patients unless there is a strong suspicion of thyroid dysfunction, since there are many other factors in acutely or chronically ill euthyroid patients that influence thyroid function tests. The second case taught us that there is assay interference with Biotin ingestion and patients taking Biotin should hold the supplement for two days prior to assessing thyroid function. Subacute thyroiditis is a self-limiting inflammatory condition of the thyroid gland and COVID-19 virus infection may be associated with subacute thyroiditis as a complication that may occur in patients without any previous thyroid disorder that is revealed in third case. In Secondary hypothyroidism/Hypopituitarism, TSH may be low, normal, or even slightly elevated due to inactive TSH isoform in blood. The fourth case shows us that only TSH testing in clinical practice leads to missing Secondary hypothyroidism/Hypopituitarism. Learning from fifth case is that during monitoring of thyrotoxic patients taking ATDs, serum TSH may remain suppressed for several months after starting therapy and it is therefore not a good parameter for monitoring therapy early during treatment, rather we should rely on FT4 and FT3. The sixth case enlightened us that in case of low TSH in early pregnancy, Gestational transient Thyrotoxicosis should be excluded which is commonly associated with hyperemesis gravidarum with no prior history of thyroid disease, no stigmata of Graves’ disease (Goiter, ophthalmopathy) and a self-limited mild disorder. In poorly compliant patients, there may be a combination of high FT4 and high TSH that is revealed in the seventh case.Bangladesh J Medicine 2023; Vol. 34, No. 2(1) Supplement: 189
甲状腺疾病是一种常见的疾病,其表现形式多种多样,有时在临床实践中诊断和处理一些甲状腺病例非常具有挑战性。这里将讨论七种不同的具有挑战性的病例,这将有助于临床医生在日常临床实践中诊断和治疗此类病例。第一个病例告诉我们,除非强烈怀疑患有甲状腺功能障碍,否则不应对重症患者进行甲状腺功能评估,因为在急性或慢性甲状腺功能正常的患者中,还有许多其他因素会影响甲状腺功能检查。第二个案例告诉我们,生物素的摄入存在检测干扰,服用生物素的患者应在评估甲状腺功能前两天服用补充剂。亚急性甲状腺炎是甲状腺的一种自限性炎症,COVID-19病毒感染可能与亚急性甲状腺炎相关,作为一种并发症,可能发生在没有任何甲状腺疾病的患者中,第三例病例显示。在继发性甲状腺功能减退/垂体功能减退症中,由于血液中TSH异构体失活,TSH可能低、正常或甚至轻微升高。第四个病例告诉我们,在临床实践中,只有TSH检测会导致继发性甲状腺功能减退/垂体功能减退症的遗漏。从第5例中我们了解到,在对服用ATDs的甲状腺毒患者进行监测时,血清TSH可能在开始治疗后几个月仍处于抑制状态,因此它不是治疗早期监测治疗的好参数,而应依靠FT4和FT3。第六例提示,妊娠早期TSH低时应排除妊娠期短暂性甲状腺毒症,该疾病常伴有妊娠剧吐,无甲状腺病史,无Graves病(甲状腺肿、眼病)征,为自限性轻度疾病。在依从性差的患者中,第七例病例显示可能存在高FT4和高TSH的组合。孟加拉国J医学2023;第34卷,第2(1)号补编:189
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引用次数: 0
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Bangladesh Journal of Veterinary Medicine
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