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Virtue of methotrexate in ectopic pregnancy 甲氨蝶呤治疗宫外孕的优点
Pub Date : 2024-01-28 DOI: 10.26452/fjphs.v4i1.563
Salma Shaik, Lakshmi Manasa Venkata Sai, Kavya Rachamsetty, Dhachinamoorthi Duraiswamy, Rama Chandra Reddy L
In recent times there is a shortfall of care about ectopic pregnancy among everyone, inciting conceded finding and potentially non -violent results. Ectopic pregnancy is a very dangerous medical disorder. This occurs when a fertilised egg implants outside of the uterus, generally in the fallopian tube. Making up 5%–10% of all pregnancy-related deaths, ectopic pregnancies are the leading cause of maternal death in the first trimester. Methotrexate is a folic acid inhibitor. It interferes with DNA synthesis and cell multiplication by inhibiting the spontaneous synthesis of purines and pyrimidines. Methotrexate will be used in the middle of six and eight weeks of pregnancy. The likelihood of a future pregnancy succeeding after using methotrexate is generally positive, according to studies. However, a few things could have an impact on these odds. As per to research, ectopic pregnancies are more common among women of reproductive age, usually between the ages of 20 and 35. Given that they are more likely to be sexually active and trying to get pregnant, women in this age range are at their most fertile. Additionally, the prevalence of sexually transmitted diseases (STIs) is higher in this age group, which can mark up the chance of an ectopic pregnancy. Factors affecting ectopic pregnancy risk include previous pelvic surgeries, infections, in vitro fertilization [IVF], endometriosis, smoking, assisted reproductive technologies, and tubal sterilization or previous pregnancies. This review of the literature attempts to shed insight on how methotrexate is currently used to treat ectopic pregnancies
近来,每个人都对宫外孕缺乏关注,从而导致了误诊和潜在的非暴力结果。宫外孕是一种非常危险的疾病。当受精卵着床于子宫以外的地方,通常是输卵管时,就会发生宫外孕。宫外孕占所有妊娠相关死亡的 5%-10%,是妊娠头三个月孕产妇死亡的主要原因。甲氨蝶呤是一种叶酸抑制剂。它通过抑制嘌呤和嘧啶的自发合成来干扰 DNA 合成和细胞繁殖。甲氨蝶呤将在怀孕六周和八周中期使用。根据研究,使用甲氨蝶呤后未来成功怀孕的可能性一般是积极的。不过,有几种情况可能会对这种可能性产生影响。根据研究,宫外孕在育龄妇女中更为常见,通常在 20 至 35 岁之间。鉴于她们更有可能性生活活跃并试图怀孕,这个年龄段的女性正处于生育能力最强的时期。此外,这个年龄段的女性性传播疾病(STI)发病率较高,这也会增加宫外孕的几率。影响宫外孕风险的因素包括既往盆腔手术、感染、体外受精(IVF)、子宫内膜异位症、吸烟、辅助生殖技术、输卵管绝育或既往妊娠。本文献综述试图深入探讨目前如何使用甲氨蝶呤治疗异位妊娠
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引用次数: 0
A review on osteoarthritis 骨关节炎综述
Pub Date : 2023-11-29 DOI: 10.26452/fjphs.v3i4.526
Rabbani Shaik, Surya Sritaja Podila, Ijaz Sheik
Degenerative joint disease, or osteoarthritis (OA), is a prevalent chronic synovial joint condition characterized by non-inflammatory degeneration, leading to pain and restricted joint movement. OA patients navigate a spectrum of therapeutic options, from social media advice to prescriptions from primary care physicians. This article critically assesses evidence-based treatments for generalized or monoarticular OA, advocating multidisciplinary and multimodal therapy. Evaluation covers patient education, pharmaceuticals, complementary and alternative medicine, surgery, manual techniques, acupuncture, bracing, assistive devices, physical therapy, modalities, and interventional procedures (corticosteroid injection, viscosupplementation, pulsed radiofrequency). Optimal benefits emerge from early diagnosis and prevention combined with multidisciplinary and multimodal treatments. The review highlights the synergy of complementary therapies. Healthcare professionals should be well-versed in diverse OA management resources, emphasizing tailored treatment plans aligned with individual needs and encouraging healthier lifestyle choices for optimal patient outcomes.Top of Form
退行性关节病或骨关节炎(OA)是一种普遍存在的慢性滑膜关节疾病,其特点是非炎症性退化,导致疼痛和关节活动受限。从社交媒体上的建议到初级保健医生开出的处方,OA 患者可选择的治疗方法多种多样。本文对全身性或单关节 OA 的循证疗法进行了严格评估,提倡多学科和多模式疗法。评估内容包括患者教育、药物、补充和替代医学、手术、手法、针灸、支具、辅助设备、理疗、模式和介入治疗(皮质类固醇注射、粘液补充、脉冲射频)。早期诊断和预防结合多学科和多模式治疗可带来最佳疗效。综述强调了辅助疗法的协同作用。医疗保健专业人员应精通各种 OA 管理资源,强调符合个人需求的定制治疗计划,并鼓励选择更健康的生活方式,以获得最佳的患者疗效。
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引用次数: 0
The prescription pattern for coronary artery disease in tertiary care hospitals 三级医院冠心病处方模式
Pub Date : 2023-11-24 DOI: 10.26452/fjphs.v3i4.525
Gautham Chakra R, Chandana Sai Y, Jyoshna V, Likhitha K, Tejeswini N, Iswarya N, Naga Lakshmi N
The study aims to assess the current prescribing patterns for drugs managing Coronary Heart Disease (CHD) at the designated site to promote rational drug use in a specialized population. Conducted in the Medicine ward over six months, this observational retrospective study focused on patients consulting cardiologists for cardiac issues. Among lipid-lowering agents, rosuvastatin was the most prescribed (52.84%), followed by atorvastatin (43.15%). Anti-hypertensive agents were widely used, with beta-blockers, ACE inhibitors, and diuretics being popular choices. Adrenergic receptor blockers were common for hypertension, with metoprolol (55.7%) and bisoprolol (10.8%) frequently prescribed. ACE inhibitors, particularly Enalapril (65.6%), dominated prescriptions. Diuretics, including eplerenone (37.2%) and furosemide (33.3%), ranked third. The majority of patients were male, potentially linked to smoking and alcohol habits. Analysis revealed the prevalence of statins and anti-atherogenic agents in cardiovascular prescriptions. Beta-blockers, ACE inhibitors, and diuretics were prominent in managing hypertension.Top of Form
这项研究旨在评估目前在指定地点治疗冠心病(CHD)的药物处方模式,以促进专业人群的合理用药。这项观察性回顾研究在内科病房进行,历时六个月,主要针对因心脏问题向心脏病专家咨询的患者。在降血脂药物中,处方最多的是罗伐他汀(52.84%),其次是阿托伐他汀(43.15%)。抗高血压药物被广泛使用,β-受体阻滞剂、血管紧张素转换酶抑制剂和利尿剂是常用药物。肾上腺素能受体阻滞剂是治疗高血压的常用药物,其中美托洛尔(55.7%)和比索洛尔(10.8%)是常用药物。ACE 抑制剂,尤其是依那普利(65.6%),在处方中占主导地位。利尿剂,包括依普利酮(37.2%)和呋塞米(33.3%),排在第三位。大多数患者为男性,这可能与吸烟和酗酒习惯有关。分析显示,他汀类药物和抗动脉粥样硬化药物在心血管处方中很普遍。β-受体阻滞剂、血管紧张素转换酶抑制剂和利尿剂在高血压治疗中占有突出地位。
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引用次数: 0
Background, Trends, Applications and Therapeutic Approaches of Nanoparticles: A Review 纳米粒子的背景、趋势、应用和治疗方法:综述
Pub Date : 2023-11-19 DOI: 10.26452/fjphs.v3i4.523
Saravanakumar Kasimedu, Hemalatha Palavuri, Swathi Puchakayala, Dhanalakshmi Rayavarapu, Akash Govindan, Harshitha Debbati, Niranjan Babu Mudduluru
The development of nanoscience and nanotechnology in practically every field of science has simplified modern life. Since the arrangement of atoms in structures, electronics and systems produce their distinctive properties and functionalities on the scale of 1-100 nm. Beginning in the early 2000s, there was a rise in public discussion and understanding of the field which prompted the first commercial applications of nanotechnology. Nanotechnologies have a positive impact on almost all fields of study including physics, materials science, chemistry, biology, computer science and engineering. Notably, nanotechnologies have recently been employed with hopeful results to enhance human health, particularly in the field of cancer therapy. Understanding the nature of nanotechnology requires an understanding of the history of scientific discoveries that led to our current understanding of the field.
纳米科学和纳米技术在几乎所有科学领域的发展都简化了现代生活。由于原子在结构、电子和系统中的排列在 1-100 纳米的尺度上产生其独特的性质和功能。从 2000 年代初开始,公众对这一领域的讨论和了解不断增加,促使纳米技术首次得到商业应用。纳米技术对物理学、材料科学、化学、生物学、计算机科学和工程学等几乎所有研究领域都产生了积极影响。值得注意的是,纳米技术最近已被用于改善人类健康,特别是在癌症治疗领域,并取得了可喜的成果。要了解纳米技术的本质,就必须了解科学发现的历史,正是这些科学发现促成了我们目前对该领域的了解。
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引用次数: 0
An Overview of Contemporary Phenotypes, Present Challenges, and Novel Implications for Medical Services in the Diagnosis of Spinal Muscular Atrophy 脊髓肌肉萎缩症诊断中的当代表型、当前挑战和对医疗服务的新影响概述
Pub Date : 2023-11-19 DOI: 10.26452/fjphs.v3i4.524
Sujana A, Durga Prasad K, Divya E, Kalyani G
Spinal muscular atrophy (SMA) is a form of muscle disease induced by SMN1 gene mutations. It can cause motor neurons and muscle strength to weaken. The intensity of the disease’s progression varies depending on the stage of development. Over the past ten years, new ways to help people with SMA have been found. These include the use of gene therapy and the modification of the SMN2 and SMN1 genes. First drugs approved for this condition were able to significantly alter the course of the disease. However, the evidence that is now available for these novel therapies is frequently constrained to a small range of individuals in terms of age and illness stage. To better understand the impact of treatment on people with all SMA subtypes and to build a platform for clinical decision-making in SMA, it will be necessary to gather real-world data with standardized outcome markers.
脊髓性肌萎缩症(SMA)是一种由 SMN1 基因突变诱发的肌肉疾病。它会导致运动神经元和肌肉力量减弱。该病的发展程度因发展阶段而异。过去十年间,人们发现了帮助 SMA 患者的新方法。其中包括使用基因疗法以及修改 SMN2 和 SMN1 基因。首批获批的药物能够显著改变疾病的进程。然而,就年龄和疾病阶段而言,这些新型疗法的现有证据往往局限于小范围的个体。为了更好地了解治疗对所有 SMA 亚型患者的影响,并为 SMA 的临床决策建立一个平台,有必要收集具有标准化结果标记的真实世界数据。
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引用次数: 0
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Future Journal of Pharmaceuticals and Health Sciences
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