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Utility of CHA2DS2-VASc Score in Predicting Contrast-induced Nephropathy in Patients with Acute Myocardial Infarction Following Percutaneous Coronary Angiography: A Cross-sectional Study in South India. CHA2DS2-VASc评分在预测经皮冠状动脉造影后急性心肌梗死患者造影剂肾病中的应用:印度南部的一项横断面研究
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1192
Ramya R Bhat, Ashwin Kulkarni, Anupama V Hegde, Aslam M Shaikh, M K Suhail

Background: Contrast-induced nephropathy (CIN) is an iatrogenic impairment to the kidneys that can occur in susceptible persons after intravascular injections of contrast agents. Individuals undergoing percutaneous coronary intervention (PCI) for acute coronary syndrome (ACS) often bear the risk of developing CIN. The likelihood of CIN can be predicted using several techniques, although none of them are very accurate. CHA2DS2-VASc score is used to predict unfavorable clinical outcomes in patients with ACS and atrial fibrillation. The score comprises preprocedural variables and is simple to calculate and can be used for predicting CIN. This study aims to validate CHA2DS2-VASc score to predict occurrence of CIN among patients undergoing PCI.

Materials and methods: This cross-sectional research has been carried out at a tertiary care hospital. The study comprised a total of 182 patients who were admitted with ACS and underwent PCI. CIN incidence was computed. The study population was divided into two groups (the CIN group and the non-CIN group) based on the incidence of CIN. The CHA2DS2-VASc score was computed for every patient. The best cutoff values of the CHA2DS2-VASc score to predict the development of CIN were found using receiver operating characteristic (ROC) curve analysis. The incidence of CIN was computed both above and below the CHA2DS2-VASc score's optimal cutoff point.

Results: The incidence of CIN among patients undergoing PCI was 14.3%, and the ROC value for the CHA2DS2-VASc score was 0.896. Statistically significant increases in the incidence of CIN were observed in patients undergoing PCI who had a CHA2DS2-VASc score of >2. Additionally, a significant relationship was discovered between CIN and age, diabetes, hypertension, prior coronary artery disease (CAD), and Killip class ≥2.

Conclusion: Patients with CHA2DS2-VASc score of >2 had higher incidence of CIN. CHA2DS2-VASc score was found to be useful in predicting contrast nephropathy among patients with acute myocardial infarction undergoing angiography.

背景:造影剂肾病(CIN)是一种医源性肾脏损害,可发生在易感人群血管内注射造影剂后。急性冠脉综合征(ACS)患者接受经皮冠状动脉介入治疗(PCI)往往有发生CIN的风险。可以使用几种技术预测CIN的可能性,尽管没有一种技术是非常准确的。CHA2DS2-VASc评分用于预测ACS合并心房颤动患者的不良临床结局。该评分包含程序前变量,计算简单,可用于预测CIN。本研究旨在验证CHA2DS2-VASc评分对PCI患者CIN发生的预测作用。材料和方法:本横断面研究在一家三级保健医院进行。该研究共包括182名因ACS入院并接受PCI的患者。计算CIN发生率。研究人群根据CIN的发生率分为两组(CIN组和非CIN组)。计算每位患者的CHA2DS2-VASc评分。采用受试者工作特征(ROC)曲线分析,找到CHA2DS2-VASc评分预测CIN发展的最佳截止值。在CHA2DS2-VASc评分的最佳截止点以上和以下计算CIN的发生率。结果:PCI患者CIN发生率为14.3%,CHA2DS2-VASc评分的ROC值为0.896。在CHA2DS2-VASc评分为bbbb2的PCI患者中,CIN的发生率有统计学意义的增加。此外,CIN与年龄、糖尿病、高血压、既往冠状动脉疾病(CAD)和Killip分级≥2之间存在显著相关性。结论:CHA2DS2-VASc评分为>2的患者CIN发生率较高。CHA2DS2-VASc评分可用于预测急性心肌梗死血管造影患者的造影剂肾病。
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引用次数: 0
The Unexplored Link between Nailfold Capillaroscopy and Acanthosis Nigricans: A Cross-sectional Clinicodermoscopic Study. 甲襞毛细血管镜检查与黑棘皮病之间未被探索的联系:一项横断面临床皮镜研究。
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1187
Aditi P Shete, Bhavana R Doshi, Manjunath Goroshi, Jinisha A Jain, Balachandra S Ankad

Introduction: Acanthosis nigricans (AN), a commonly encountered condition in clinical practice, is linked with numerous systemic disorders. Currently, there is a dearth of literature on the correlation of clinical and dermoscopic features of AN with nailfold capillaroscopy (NFC) changes. This study intended to evaluate patients with AN who have underlying microvascular complications as a consequence of metabolic diseases.

Objectives: Primarily to study the association of clinical and dermoscopic findings of AN with NFC and to elucidate the spectrum of NFC changes in patients of AN.

Materials and methods: This was a cross-sectional, hospital-based study with a sample size of 97. Clinical Burke's grading and dermoscopy were performed in clinically diagnosed AN patients. NFC was performed on all 10 fingernails. The fourth and fifth fingernails of each hand were considered for studying the association.

Results: NFC changes seen were tortuous, dilated, cross-linked, ramified capillaries, and dropouts. There was a positive association of clinical Burke's grading (p-value = 0.002) and duration (p-value = 0.003) of AN with dermoscopic features such as depth of sulci cutis, number of hyperpigmented dots, and shape of papillary projections. Tortuous, cross-linked capillaries showed a significant association with the clinical scale of AN (p-value < 0.05). Ramified and cross-linked capillaries showed a significant association with the duration of AN (p-value < 0.05).

Conclusion: Dermoscopy in AN showed gradation in changes corresponding to the clinical Burke's grading and duration. Ramified and cross-linked capillaries showed a significant association with the duration of AN, while tortuous, cross-linked capillaries showed a significant association with the clinical scale of AN. The present study aids in the early detection of microvascular changes in AN, such as tortuous, ramified, and cross-linked capillaries, and proves helpful in referring the patient for screening of diabetic retinopathy and nephropathy at the earliest.

简介:黑棘皮病(AN)是临床实践中常见的疾病,与许多全身性疾病有关。目前,关于AN的临床和皮肤镜特征与甲襞毛细血管镜(NFC)变化的相关性的文献缺乏。本研究旨在评估因代谢疾病而伴有潜在微血管并发症的AN患者。目的:主要研究AN的临床和皮肤镜表现与NFC的关系,并阐明AN患者NFC变化的谱。材料和方法:这是一项以医院为基础的横断面研究,样本量为97。对临床诊断为AN的患者进行临床Burke分级及皮肤镜检查。所有10个指甲都进行了近距离接触。每只手的第四和第五个指甲被用来研究这种联系。结果:NFC改变表现为毛细血管扭曲、扩张、交联、分叉和脱落。AN的临床Burke分级(p值= 0.002)和持续时间(p值= 0.003)与皮肤镜特征(如皮肤沟深度、色素沉着点数量和乳头突起形状)呈正相关。弯曲、交联的毛细血管与AN的临床评分有显著相关性(p值< 0.05)。分枝和交联毛细血管与AN持续时间显著相关(p值< 0.05)。结论:AN的皮肤镜检查表现出与临床Burke的分级和持续时间相对应的分级变化。分叉和交联的毛细血管与AN持续时间显著相关,而弯曲和交联的毛细血管与AN的临床规模显著相关。本研究有助于早期发现AN的微血管变化,如弯曲、分叉、交联毛细血管,并有助于患者尽早筛查糖尿病视网膜病变和肾病。
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引用次数: 0
Usage of Guideline-directed Medical Therapy in Patients with Heart Failure and Reduced Ejection Fraction in a Tertiary Care Hospital. 三级医院心力衰竭和射血分数降低患者的指导药物治疗的应用
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1188
Sebin George, Raja J Selvaraj, Santhosh Satheesh, Bindhya Karthikeyan

Objective: To assess the prevalence of guideline-directed medical therapy (GDMT) and identify reasons for nonprescription and dose optimization in heart failure patients with reduced ejection fraction (HFrEF) in a tertiary care hospital in southern India.

Methods: A cross-sectional study was conducted in a tertiary care hospital involving HFrEF patients. Patients with heart failure were categorized based on GDMT prescriptions. Reasons for nonprescription and suboptimal dosing were identified.

Results: The study included 102 HFrEF patients with a mean age of 54 ± 11.7 years, predominantly male (89%). Only 10.8% of patients received GDMT at optimal doses. Although 62% were on triple therapy, many had one or more medications at suboptimal doses. Additionally, 26% of patients were not prescribed all recommended drug classes. Notably, the majority of patients with renal impairment fail to receive triple therapy. Barriers identified included hemodynamic issues and renal dysfunction.

Conclusion: GDMT adherence in HFrEF patients is significantly lower than expected, with only 10.8% receiving therapy at recommended doses. Key issues include suboptimal dosing and incomplete prescription of drug classes, influenced by patient-specific factors and systemic barriers.

目的:评估指南导向药物治疗(GDMT)的流行程度,并确定非处方和剂量优化在印度南部三级医院心力衰竭患者降低射血分数(HFrEF)的原因。方法:在一家三级医院对HFrEF患者进行横断面研究。根据GDMT处方对心力衰竭患者进行分类。确定了非处方和次优给药的原因。结果:本研究纳入102例HFrEF患者,平均年龄54±11.7岁,以男性为主(89%)。只有10.8%的患者接受了最佳剂量的GDMT治疗。虽然62%的患者接受了三联疗法,但许多人服用了一种或多种药物,剂量不够理想。此外,26%的患者没有得到所有推荐的药物类别。值得注意的是,大多数肾功能损害患者未能接受三联疗法。确定的障碍包括血流动力学问题和肾功能障碍。结论:HFrEF患者的GDMT依从性明显低于预期,只有10.8%的患者接受了推荐剂量的治疗。关键问题包括次优给药和不完整的药物处方,受患者特异性因素和系统性障碍的影响。
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引用次数: 0
Prediabetes: To Be Treated or Not? 糖尿病前期:该不该治疗?
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1172
Rajesh Agrawal
<p><p>Prediabetes (PD) is a bridge between normoglycemia and hyperglycemia or diabetes mellitus (DM) characterized by higher than normal blood glucose but not fulfilling the criteria for type 2 DM (T2DM). PD is defined by impaired fasting glucose (IFG), impaired glucose tolerance (IGT), and/or hemoglobin A1c (HbA1c) above 5.7% but <6.4%. Individuals with PD are at increased risk of progressing to T2DM at a pace of 5-10% every year and other micro- and macrovascular complications, including cardiovascular diseases. Prevalence of IGT and IFG in 2021 was 9.1% (about 464 million), which is projected to increase to 10.0% (638 million) in 2045; that of IFG was 5.8% (about 298 million), projected to increase to 6.5% (414 million) in 2045 globally. That is why we must seriously take aggressive steps to prevent progression to T2DM and to reduce the morbidity and mortality associated with DM, its complications, and healthcare burden. Why PD is important? Why PD to be treated? Individuals with PD have a 5-10% annual risk of progressing to T2DM and are associated with increased risk of micro- and macrovascular complications like nephropathy, retinopathy, neuropathy, and cardiovascular risks, myocardial infarction, and stroke. To prevent progression or conversion of PD to DM, we must be very aggressive. These are sufficient reasons for treatment of PD by lifestyle intervention or pharmacotherapy, as intensive lifestyle modifications, dietary modification, and enhanced physical activity have been shown to reduce the progression of PD to T2DM by 40-70%. These measures also lead to weight loss and better cardiovascular health. PD develops due to insulin resistance, impaired insulin secretion, and increased hepatic glucose production. Therefore, pharmacotherapy with metformin, pioglitazone, α-glucosidase inhibitors (AGIs), dipeptidyl peptidase IV (DPP IV) inhibitors, sodium-glucose cotransporter 2 (SGLT2) inhibitors, and glucagon-like peptide-1 receptor agonists (GLP1 RA) targeting these defects are efficacious in preventing T2DM in PD. Diabetes Prevention Program (DPP) has shown 31% reduction in DM incidence with metformin. There is increasing evidence for prevention of DM in adults with PD by pharmacotherapy, but options other than metformin have adverse effects, and there is no unanimity for their use in PD. The role of pharmacotherapy is still debatable, and no consensus is made. We recommend that patients who are at high risk, having a strong family history of DM, signs of severe insulin resistance like acanthosis nigricans, severe obesity, or associated comorbidities, must be considered for disease-modifying pharmacotherapy like SGLT2 inhibitors, DPP IV inhibitors, and GLP1 RA. Those who do not have the above risk factors should be followed up at regular intervals, at least every year. Why PD not to be treated? When we treat DM, our "treat to target" is HbA1c of 7% or less, and organizations like the European Association for the Study of Diabetes (EASD) rec
糖尿病前期(PD)是介于正常血糖和高血糖或糖尿病(DM)之间的桥梁,其特征是血糖高于正常水平,但不符合2型糖尿病(T2DM)的标准。PD的定义是空腹血糖(IFG)受损,葡萄糖耐量(IGT)受损,和/或血红蛋白A1c (HbA1c)高于5.7%
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引用次数: 0
Achieving Diabetes Remission: Current Guidelines and Emerging Pharmacotherapies in India. 实现糖尿病缓解:当前指南和新兴药物治疗在印度。
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1184
Arpan, Navrajbir Singh, Kusum Bali, Tarundeep Singh

Type 2 diabetes mellitus (T2DM) remission has emerged as a critical area of research and clinical interest, especially in India, where diabetes prevalence is rising at an alarming rate. Achieving remission through pharmacologic, dietary, and surgical interventions is now an attainable goal for a subset of patients. This systematic review synthesizes evidence from clinical trials, emerging pharmacologic interventions, and current guidelines for diabetes remission. We explore the mechanisms of diabetes reversal, highlighting novel agents such as glucagon-like peptide-1 (GLP-1) receptor agonists, dual glucose-dependent insulinotropic polypeptide (GIP)/GLP-1 agonists, and sodium-glucose cotransporter 2 (SGLT2) inhibitors. This review also addresses the long-term sustainability of remission, epidemiological trends in India, and current treatment recommendations, integrating data from major studies. The findings underscore the need for a patient-centered, evidence-based approach to diabetes management. Additionally, we discuss the role of continuous glucose monitoring (CGM), dietary interventions, and the benefits of millet consumption in diabetes remission.

2型糖尿病(T2DM)缓解已成为研究和临床兴趣的关键领域,特别是在印度,糖尿病患病率正以惊人的速度上升。通过药物、饮食和手术干预实现缓解现在是一部分患者可以达到的目标。本系统综述综合了来自临床试验、新出现的药物干预和当前糖尿病缓解指南的证据。我们探讨了糖尿病逆转的机制,重点介绍了新型药物,如胰高血糖素样肽-1 (GLP-1)受体激动剂、双葡萄糖依赖性胰岛素性多肽(GIP)/GLP-1激动剂和钠-葡萄糖共转运蛋白2 (SGLT2)抑制剂。本综述还综合了来自主要研究的数据,讨论了缓解的长期可持续性、印度的流行病学趋势和当前的治疗建议。研究结果强调了以患者为中心、以证据为基础的糖尿病管理方法的必要性。此外,我们讨论了连续血糖监测(CGM)的作用,饮食干预,以及小米消费在糖尿病缓解中的益处。
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引用次数: 0
Unveiling the Complexities of Rheumatoid Arthritis: A Comprehensive Pathoepidemiological Review. 揭示类风湿关节炎的复杂性:一项全面的病理流行病学综述。
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1183
Nikhil Raj, Apurva Rautela, Ravindra K Gupta, Riddhi Singh, Mridu Singh, Jyotsna Agarwal, Jaya Garg

Rheumatoid arthritis (RA) is a common autoimmune disorder characterized by inflammation in the joints, affecting around 0.24-1% of the population. RA can develop through a variety of paths, resulting in a nonspecific clinical appearance. It progresses from preclinical to chronic disease, with pathogenic mechanisms that may differ across people, confounding therapy efforts. Numerous factors have been found to be associated with RA, including lifestyle-related risk factors like smoking and obesity, which are modifiable, as well as advancing age and female gender, which are nonmodifiable. RA pathophysiology is an intricate interaction between different genetic and immunological variables resulting in disease progression. With a better knowledge of the pathophysiology of RA, new therapeutic approaches are being developed for effective management of RA. This review article summarizes epidemiology, pathogenesis, and diagnostic options for RA.

类风湿关节炎(RA)是一种常见的自身免疫性疾病,以关节炎症为特征,影响约0.24-1%的人口。RA可通过多种途径发展,导致非特异性临床表现。它从临床前发展为慢性疾病,其致病机制可能因人而异,使治疗努力混淆。许多因素与类风湿性关节炎有关,包括与生活方式相关的风险因素,如吸烟和肥胖,这些因素是可以改变的,以及年龄增长和女性性别,这些因素是不可改变的。RA的病理生理是不同遗传和免疫变量之间复杂的相互作用,导致疾病进展。随着对类风湿性关节炎病理生理学的进一步了解,新的治疗方法正在被开发出来,以有效地管理类风湿性关节炎。本文综述了类风湿性关节炎的流行病学、发病机制和诊断方法。
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引用次数: 0
Serum Liver Enzymes in Metabolic Syndrome and Nonmetabolic Syndrome Patients: A Case-Control Study. 代谢综合征和非代谢综合征患者血清肝酶:一项病例-对照研究。
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1106
Anjali B Patel, Archana U Gandhi, Aayushi Rajani, Pathik Patel

Background: Metabolic syndrome (Met-S) is a major threat to human health all over the world due to a rise in obesity and sedentary lifestyle. It is associated with many cardiovascular risk factors, including insulin resistance, obesity, atherogenic dyslipidemia, and hypertension. This study was conducted to determine the correlation of serum liver enzymes, especially serum gamma-glutamyl transferase (GGT), in Met-S and non-Met-S patients.

Objectives: To determine the correlation of serum liver enzymes, especially serum GGT, in Met-S and non-Met-S patients.

Materials and methods: An observational case-control study was carried out on a total of 100 patients-50 cases of Met-S as defined by the International Diabetes Federation (IDF) 2005 and 50 age- and gender-matched controls (non-Met-S patients) aged >18 years-at a tertiary care hospital of Western India. Patients' history taking, general anthropometric, and systemic examination were done. Liver function tests [serum glutamate pyruvate transaminase (SGPT), serum glutamate oxaloacetate transaminase (SGOT), GGT, alkaline phosphatase (ALP)], C-reactive protein (CRP), and ultrasonography (USG) for visualizing liver involvement were done.

Results: The maximum number of patients with Met-S were >50 years of age, with male predominance (78%) and a high prevalence of diabetes, hypertension, and central obesity among them as major components of Met-S. Liver function tests such as GGT, SGPT, SGOT, and CRP were significantly raised in Met-S patients compared to non-Met-S patients. The majority of the Met-S patients with deranged liver function tests had fatty liver on USG abdomen.

Conclusion: This study showed a significant association between elevated levels of GGT, SGPT, SGOT, CRP, and fatty liver in Met-S patients compared to non-Met-S patients.

背景:由于肥胖和久坐不动的生活方式的增加,代谢综合征(Met-S)是全世界人类健康的主要威胁。它与许多心血管危险因素有关,包括胰岛素抵抗、肥胖、动脉粥样硬化性血脂异常和高血压。本研究旨在确定Met-S和非Met-S患者血清肝酶,特别是血清γ -谷氨酰转移酶(GGT)的相关性。目的:探讨Met-S和非Met-S患者血清肝酶,尤其是血清GGT的相关性。材料和方法:一项观察性病例对照研究在印度西部的一家三级医院对总共100例患者进行了研究,其中50例为国际糖尿病联合会(IDF) 2005年定义的Met-S患者,50例年龄和性别匹配的对照组(非Met-S患者),年龄在100 - 18岁之间。对患者进行病史、全身测量和全身检查。进行肝功能检查[血清谷氨酸丙酮酸转氨酶(SGPT)、血清谷氨酸草酰乙酸转氨酶(SGOT)、GGT、碱性磷酸酶(ALP)]、c反应蛋白(CRP)和超声检查(USG)观察肝脏受累情况。结果:Met-S患者最多为50岁,男性居多(78%),其中糖尿病、高血压和中心性肥胖患病率高,是Met-S的主要组成部分。与非Met-S患者相比,Met-S患者的肝功能测试如GGT、SGPT、SGOT和CRP显著升高。Met-S型肝功能紊乱患者以USG腹部脂肪肝为主。结论:本研究显示,与非Met-S患者相比,Met-S患者GGT、SGPT、SGOT、CRP水平升高与脂肪肝存在显著相关性。
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引用次数: 0
The Function of Platelet-to-lymphocyte Ratio and Neutrophil-to-lymphocyte Ratio in Assessing Disease Activity in Rheumatoid Arthritis Patients. 血小板与淋巴细胞比值和中性粒细胞与淋巴细胞比值在类风湿关节炎患者疾病活动性评估中的作用。
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1173
Himanshu Mehta, Pooja Dhaon, Sangita Bohara, Siddharth Tiwari, Dharmendra Uraiya, Ruchi Verma

Aim: To ascertain the function of neutrophil-to-lymphocyte ratio (NLR) and platelet-to-lymphocyte ratio (PLR) as biomarkers in evaluation of disease activity in rheumatoid arthritis (RA) patients.

Materials and methods: This cross-sectional research was performed in a hospital and included 381 patients who met the 2010 ACR/EULAR criteria for RA. The clinical disease activity assessment (CDAI) was used to evaluate activity of disease in addition to demographic and disease-related variables. Based on preestablished CDAI cutoff values, the participants were categorized into four groups. For each patient, laboratory analysis included the following: C-reactive protein (CRP), erythrocyte sedimentation rate (ESR), and complete blood count (CBC). The conventional procedure was followed in the appropriate computation of PLR and NLR. The four patient groups' NLR and PLR values were compared, and the relation among disease activity indices and NLR and PLR was investigated using Pearson correlation analysis.

Results: In patients, the mean PLR was 132.8 ± 127.7 and the mean NLR was 3.66 ± 2.6. Patients with low disease activity had a substantially lower mean PLR (p = 0.021) in comparison to those with higher disease activity. The mean NLR in relation to CDAI was not observed to be statistically significant (p = 0.69) across the four groups. While there was a weak positive association between PLR and the physician visual analog scale (VAS) (r = 0.22), patient VAS (r = 0.12), and CDAI (r = 0.17), there was no correlation among CDAI and specific disease indices with NLR, according to Pearson correlation analysis.

Conclusion: PLR, but not NLR, may be an effective biomarker for evaluating the disease activity level in RA patients, particularly higher disease activity.

目的:探讨中性粒细胞与淋巴细胞比值(NLR)和血小板与淋巴细胞比值(PLR)在类风湿关节炎(RA)患者疾病活动性评价中的作用。材料和方法:本横断面研究在一家医院进行,纳入381例符合2010年ACR/EULAR RA标准的患者。临床疾病活动性评估(CDAI)用于评估疾病活动性以及人口统计学和疾病相关变量。根据预先设定的CDAI截止值,将参与者分为四组。对于每位患者,实验室分析包括以下内容:c反应蛋白(CRP)、红细胞沉降率(ESR)和全血细胞计数(CBC)。按常规程序计算相应的PLR和NLR。比较4组患者NLR和PLR值,采用Pearson相关分析探讨疾病活动性指标与NLR和PLR之间的关系。结果:患者平均PLR为132.8±127.7,平均NLR为3.66±2.6。与疾病活动度较高的患者相比,疾病活动度较低的患者的平均PLR明显较低(p = 0.021)。四组患者与CDAI相关的平均NLR无统计学意义(p = 0.69)。虽然PLR与医生视觉模拟量表(VAS) (r = 0.22)、患者VAS (r = 0.12)和CDAI (r = 0.17)之间存在弱正相关,但根据Pearson相关分析,CDAI和特定疾病指标与NLR之间没有相关性。结论:PLR,而非NLR,可能是评估RA患者疾病活动性水平的有效生物标志物,尤其是疾病活动性较高的患者。
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引用次数: 0
Optimizing Proton-pump Inhibitor Therapy in Patients with Comorbidities Receiving Polypharmacy Treatment: Insights from Clinical Practice in India. 优化质子泵抑制剂治疗接受多种药物治疗的合并症患者:来自印度临床实践的见解。
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1185
Hemant T Juneja, Sanjeev Gambhir, Khizer H Junaidy

Background: The safety and efficacy of proton-pump inhibitors (PPIs) in gastroesophageal reflux disease (GERD) patients on polypharmacy is challenging to manage. Rabeprazole's unique metabolism reduces drug-drug interactions (DDI), making it beneficial for patients with polypharmacy. This study aimed to explore the safety and effectiveness of rabeprazole in Indian comorbid GERD patients on polypharmacy.

Methods: A cross-sectional survey was conducted (November, 2024 and January, 2025), which included healthcare professionals (HCPs) with experience in prescribing PPIs. The survey included 10 questions addressing issues faced in polypharmacy settings.

Results: Around 91.9% preferred prescribing rabeprazole over other PPIs in polypharmacy patients. CYP450 enzyme interactions are considered by 73.3% HCPs when prescribing PPIs, with a strong emphasis on minimizing DDI in polypharmacy contexts. Rabeprazole was chosen by a major share of HCPs for its unique nonenzymatic metabolism and minimal interaction with the cytochrome P450 system, suggesting suitability in polypharmacy patients. Furthermore, 70% HCPs suggested rabeprazole could improve cardiovascular (CV) outcomes by optimizing antiplatelet therapy, and 74.4% supported its safety in patients on antiplatelet therapy.

Conclusion: Rabeprazole appears to be the preferred PPI in managing GERD among patients on polypharmacy, primarily due to its favorable safety profile and minimal DDI, and may be advantageous in clinical practice.

背景:质子泵抑制剂(PPIs)在胃食管反流病(GERD)患者多药治疗中的安全性和有效性是具有挑战性的。雷贝拉唑独特的代谢减少了药物相互作用(DDI),使其对多药患者有益。本研究旨在探讨雷贝拉唑在印度合并症胃食管反流患者多药治疗中的安全性和有效性。方法:于2024年11月和2025年1月进行横断面调查,调查对象包括具有ppi处方经验的医疗保健专业人员(HCPs)。该调查包括10个问题,解决了在综合药房环境中面临的问题。结果:在多药患者中,约91.9%的患者倾向于使用雷贝拉唑而不是其他PPIs。73.3%的HCPs在开PPIs处方时会考虑CYP450酶的相互作用,并强调在多药环境下尽量减少DDI。大部分HCPs选择雷贝拉唑是因为其独特的非酶代谢和与细胞色素P450系统的最小相互作用,这表明雷贝拉唑适用于多药患者。此外,70%的HCPs认为雷贝拉唑可以通过优化抗血小板治疗来改善心血管(CV)结局,74.4%的HCPs支持雷贝拉唑在抗血小板治疗患者中的安全性。结论:雷贝拉唑是治疗多药患者胃食管反流的首选PPI,主要是由于其良好的安全性和最小的DDI,可能在临床实践中具有优势。
{"title":"Optimizing Proton-pump Inhibitor Therapy in Patients with Comorbidities Receiving Polypharmacy Treatment: Insights from Clinical Practice in India.","authors":"Hemant T Juneja, Sanjeev Gambhir, Khizer H Junaidy","doi":"10.59556/japi.73.1185","DOIUrl":"https://doi.org/10.59556/japi.73.1185","url":null,"abstract":"<p><strong>Background: </strong>The safety and efficacy of proton-pump inhibitors (PPIs) in gastroesophageal reflux disease (GERD) patients on polypharmacy is challenging to manage. Rabeprazole's unique metabolism reduces drug-drug interactions (DDI), making it beneficial for patients with polypharmacy. This study aimed to explore the safety and effectiveness of rabeprazole in Indian comorbid GERD patients on polypharmacy.</p><p><strong>Methods: </strong>A cross-sectional survey was conducted (November, 2024 and January, 2025), which included healthcare professionals (HCPs) with experience in prescribing PPIs. The survey included 10 questions addressing issues faced in polypharmacy settings.</p><p><strong>Results: </strong>Around 91.9% preferred prescribing rabeprazole over other PPIs in polypharmacy patients. CYP450 enzyme interactions are considered by 73.3% HCPs when prescribing PPIs, with a strong emphasis on minimizing DDI in polypharmacy contexts. Rabeprazole was chosen by a major share of HCPs for its unique nonenzymatic metabolism and minimal interaction with the cytochrome P450 system, suggesting suitability in polypharmacy patients. Furthermore, 70% HCPs suggested rabeprazole could improve cardiovascular (CV) outcomes by optimizing antiplatelet therapy, and 74.4% supported its safety in patients on antiplatelet therapy.</p><p><strong>Conclusion: </strong>Rabeprazole appears to be the preferred PPI in managing GERD among patients on polypharmacy, primarily due to its favorable safety profile and minimal DDI, and may be advantageous in clinical practice.</p>","PeriodicalId":22693,"journal":{"name":"The Journal of the Association of Physicians of India","volume":"73 10","pages":"e38-e41"},"PeriodicalIF":0.0,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145309241","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
Bedside FibroScan as a Point-of-care Tool for Quantification for Cirrhosis: A Single-center Prospective Observational Study from Western India. 床边纤维扫描作为肝硬化量化的护理点工具:一项来自印度西部的单中心前瞻性观察研究。
Q3 Medicine Pub Date : 2025-10-01 DOI: 10.59556/japi.73.1190
Pranav Ramesh Shelke, Saurabh Vivek Padole, Paulami Deshmukh, Paris Lalge, Supriya Raosaheb Patil, Jitendra Ingole

Background: Cirrhosis, a major cause of global morbidity and mortality, necessitates early detection and accurate staging for optimal management. Traditional reliance on liver biopsy is being challenged by noninvasive techniques such as transient elastography (FibroScan®), which measures liver stiffness to estimate fibrosis severity. The potential for FibroScan® as a point-of-care (POC) tool supports rapid clinical decision-making in multiple clinical settings and scenarios.

Materials and methods: A prospective observational study was conducted from December 2024 to February 2025 at a tertiary center in Western India, enrolling adult patients with suspected liver disease, metabolic risk factors, or excessive alcohol consumption. Liver fibrosis was assessed using the Echosense FibroScan mini+430 device, applying the Metabolic Dysfunction-Associated Steatohepatitis (MASH) scoring system (F0-F4). At least 10 valid liver stiffness measurements (LSM) were obtained per patient. Data analysis included t-tests, analysis of variance (ANOVA), Chi-squared tests, and receiver operating characteristic (ROC) curve analysis for diagnostic accuracy.

Results: Of the 93 patients (mean age 52.3 years; 69.9% male), 41.9% had advanced fibrosis, and 30.1% demonstrated cirrhosis. Alcohol intake and diabetes were significantly associated with fibrosis stage (p = 0.002 and p = 0.008, respectively). FibroScan® showed excellent diagnostic accuracy for cirrhosis (AUROC = 0.91) and good accuracy for significant fibrosis (AUROC = 0.82); the optimal LSM cutoff for F4 was 12.5 kPa. Body mass index (BMI) correlated weakly but significantly with CAP values.

Conclusion: Bedside FibroScan® offers a highly accurate, rapid, and noninvasive method for quantifying liver fibrosis and cirrhosis in clinical practice. Its integration into routine care could substantially improve management for patients at risk of liver disease.

背景:肝硬化是全球发病率和死亡率的主要原因,需要早期发现和准确分期以获得最佳治疗。非侵入性技术如瞬时弹性成像(FibroScan®)正在挑战对肝活检的传统依赖,该技术通过测量肝脏硬度来估计纤维化的严重程度。FibroScan®作为护理点(POC)工具的潜力,支持在多种临床环境和情况下的快速临床决策。材料和方法:一项前瞻性观察性研究于2024年12月至2025年2月在印度西部的一个三级中心进行,纳入了疑似肝病、代谢危险因素或过度饮酒的成年患者。使用Echosense FibroScan mini+430设备评估肝纤维化,应用代谢功能障碍相关脂肪性肝炎(MASH)评分系统(F0-F4)。每位患者至少获得10个有效的肝脏硬度测量(LSM)。数据分析包括t检验、方差分析(ANOVA)、卡方检验和受试者工作特征(ROC)曲线分析。结果:93例患者(平均年龄52.3岁,69.9%为男性)中,41.9%为晚期纤维化,30.1%为肝硬化。酒精摄入和糖尿病与纤维化分期显著相关(p = 0.002和p = 0.008)。FibroScan®对肝硬化的诊断准确率很高(AUROC = 0.91),对显著纤维化的诊断准确率很高(AUROC = 0.82);F4的最佳LSM截止值为12.5 kPa。身体质量指数(BMI)与CAP值呈弱而显著相关。结论:在临床实践中,床边纤维扫描®提供了一种高度准确、快速、无创的方法来量化肝纤维化和肝硬化。将其纳入常规护理可以大大改善对有肝病风险患者的管理。
{"title":"Bedside FibroScan as a Point-of-care Tool for Quantification for Cirrhosis: A Single-center Prospective Observational Study from Western India.","authors":"Pranav Ramesh Shelke, Saurabh Vivek Padole, Paulami Deshmukh, Paris Lalge, Supriya Raosaheb Patil, Jitendra Ingole","doi":"10.59556/japi.73.1190","DOIUrl":"10.59556/japi.73.1190","url":null,"abstract":"<p><strong>Background: </strong>Cirrhosis, a major cause of global morbidity and mortality, necessitates early detection and accurate staging for optimal management. Traditional reliance on liver biopsy is being challenged by noninvasive techniques such as transient elastography (FibroScan<sup>®</sup>), which measures liver stiffness to estimate fibrosis severity. The potential for FibroScan<sup>®</sup> as a point-of-care (POC) tool supports rapid clinical decision-making in multiple clinical settings and scenarios.</p><p><strong>Materials and methods: </strong>A prospective observational study was conducted from December 2024 to February 2025 at a tertiary center in Western India, enrolling adult patients with suspected liver disease, metabolic risk factors, or excessive alcohol consumption. Liver fibrosis was assessed using the Echosense FibroScan mini+430 device, applying the Metabolic Dysfunction-Associated Steatohepatitis (MASH) scoring system (F0-F4). At least 10 valid liver stiffness measurements (LSM) were obtained per patient. Data analysis included <i>t</i>-tests, analysis of variance (ANOVA), Chi-squared tests, and receiver operating characteristic (ROC) curve analysis for diagnostic accuracy.</p><p><strong>Results: </strong>Of the 93 patients (mean age 52.3 years; 69.9% male), 41.9% had advanced fibrosis, and 30.1% demonstrated cirrhosis. Alcohol intake and diabetes were significantly associated with fibrosis stage (<i>p</i> = 0.002 and <i>p</i> = 0.008, respectively). FibroScan<sup>®</sup> showed excellent diagnostic accuracy for cirrhosis (AUROC = 0.91) and good accuracy for significant fibrosis (AUROC = 0.82); the optimal LSM cutoff for F4 was 12.5 kPa. Body mass index (BMI) correlated weakly but significantly with CAP values.</p><p><strong>Conclusion: </strong>Bedside FibroScan® offers a highly accurate, rapid, and noninvasive method for quantifying liver fibrosis and cirrhosis in clinical practice. Its integration into routine care could substantially improve management for patients at risk of liver disease.</p>","PeriodicalId":22693,"journal":{"name":"The Journal of the Association of Physicians of India","volume":"73 10","pages":"e24-e27"},"PeriodicalIF":0.0,"publicationDate":"2025-10-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145309190","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}
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The Journal of the Association of Physicians of India
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