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Orphan drugs: The final frontier in the fight against rare diseases. 孤儿药:对抗罕见疾病的最后前沿。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_979_25
Sandhya Rajaram, Bikash Medhi
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引用次数: 0
Anaphylactic shock due to mefenamic acid. 甲氧胺酸致过敏性休克。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_365_25
Sumit Mehndiratta
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引用次数: 0
Assessment of knowledge, attitude, and practice regarding reporting of adverse events due to medical devices among healthcare workers in Gujarat. 评估古吉拉特邦卫生保健工作者关于医疗器械不良事件报告的知识、态度和做法。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_754_24
Jonsi Tavethia, Samidh Shah, Anshul Bhadania, Shubh Mehta, Prahar Himanshubhai Darji, Kavya Darji, Kinjal Mulubhai Solanki

Objective: To assess the knowledge, attitude, and practice (KAP) regarding reporting adverse events due to medical devices among healthcare workers in our hospital.

Materials and methods: A cross-sectional, observational, and questionnaire (KAP) study was conducted among healthcare professionals working in the various departments of our hospital. Healthcare professionals from different specialties who volunteered to participate in the study were enrolled. A total of 15 questions were included: 8 based on knowledge (7 scored), 2 on attitude, and 5 on practice. Statistical analysis was performed using Microsoft Excel® worksheet, Chi-square, and unpaired t-test. P < 0.05 was considered statistically significant.

Results: A total of 370 responses were received. The knowledge of healthcare workers was found to be 73.57%. The mean score (out of 7) for doctors and paramedical staff was 5.78 ± 1.21 and 3.76 ± 1.50, respectively, indicating a wide knowledge gap between them (P < 0.05). Most healthcare workers (63%) reported witnessing fewer than 5 MDAEs. The majority (37.30%) mentioned that the cause of underreporting was a lack of knowledge. Out of all healthcare workers, 85.13% responded positively and are willing to report MDAEs in future, and most of them considered it important to report MDAEs.

Conclusion: Despite healthcare professionals having adequate knowledge and a positive attitude toward reporting, very poor reporting of MDAEs is observed. Lack of knowledge is a significant barrier leading to underreporting, and a substantial knowledge gap among healthcare professionals is evident.

目的:了解我院医护人员报告医疗器械不良事件的知识、态度和实践情况。材料和方法:采用横断面、观察性和问卷调查(KAP)对在我院各科室工作的医护人员进行研究。来自不同专业的医疗保健专业人员自愿参加了这项研究。共有15个问题,其中8个是关于知识的(7个计分),2个是关于态度的,5个是关于实践的。统计分析采用Microsoft Excel®工作表、卡方和非配对t检验。P < 0.05为差异有统计学意义。结果:共收到回复370份。卫生保健工作者的知晓率为73.57%。医生和辅助医务人员的平均得分(总分为7分)分别为5.78±1.21分和3.76±1.50分,两者的知识差距较大(P < 0.05)。大多数卫生保健工作者(63%)报告目睹的mdae少于5例。大多数人(37.30%)提到低报的原因是缺乏知识。85.13%的医护人员积极回应并愿意在未来报告MDAEs,其中大多数人认为报告MDAEs很重要。结论:尽管卫生保健专业人员有足够的知识和积极的报告态度,但MDAEs的报告非常少。缺乏知识是导致少报的一个重要障碍,医疗保健专业人员之间的知识差距很大。
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引用次数: 0
Efficacy and safety of tranexamic acid nebulization to control bleeding of hemoptysis: The TXA-NEB randomized controlled clinical trial. 氨甲环酸雾化控制咯血出血的有效性和安全性:TXA-NEB随机对照临床试验。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_824_25
Aman Agrawal, Deba Prasad Dhibar, Ajay Prakash, B C Sreedhara, Valliappan Muthu, Ashok Kumar Pannu

Objectives: The objective of this study was to evaluate the efficacy and safety of tranexamic acid (TXA) nebulization to control bleeding in hemoptysis.

Materials and methods: In this randomized controlled clinical trial, 27 participants with hemoptysis received nebulization with TXA (500 mg/5 mL, q 8 hourly for 2 days), and 29 participants with hemoptysis received nebulization with 0.9% normal saline (5 mL, q 8 hourly for 2 days) along with the standard therapy and followed up for 8 weeks.

Results: The mean percentage decrease in the frequency (63.9% vs. 39.8%, P = 0.012) and quantity (73.4% vs. 51.7%, P = 0.024) of hemoptysis was significantly higher in the TXA group compared to the control group at day 1 but was insignificant at day 2. However, after excluding participants who underwent intervention (N = 11), the improvement in frequency (76.2% vs. 50.3%, P = 0.049) and quantity (85.2% vs. 58.6%, P = 0.021) of hemoptysis was significantly better in the TXA group even at day 2. Out of 56 participants, 24 participants achieved resolution of hemoptysis, which was also significantly (P = 0.003) better in the TXA group (63.0%) compared to the control group (24.1%). No serious adverse drug reaction was observed. Minor cough (37.5%) and throat irritation (33.9%) were observed, which were comparable (P = 0.432) between the groups.

Conclusion: TXA nebulization, an alternative route of administration, was found to be safe. Prompt nebulization with TXA was effective as bridging therapy in hemoptysis to achieve the immediate goal of bleeding control before definitive intervention planned or performed. Further studies are encouraged to evaluate this novel approach of TXA nebulization. Trial registration: clinicaltrials.gov PRS ID: NCT05648656.

目的:评价氨甲环酸(TXA)雾化控制咯血出血的疗效和安全性。材料与方法:在本随机对照临床试验中,27例咯血患者接受TXA雾化治疗(500mg / 5ml, q 8小时,连续2天),29例咯血患者在标准治疗的同时接受0.9%生理盐水雾化治疗(5ml, q 8小时,连续2天),随访8周。结果:在第1天,TXA组咯血频率(63.9% vs. 39.8%, P = 0.012)和咯血量(73.4% vs. 51.7%, P = 0.024)的平均下降百分比显著高于对照组,但在第2天无显著差异。然而,在排除接受干预的参与者(N = 11)后,即使在第2天,TXA组咯血频率(76.2%对50.3%,P = 0.049)和咯血数量(85.2%对58.6%,P = 0.021)的改善也明显更好。在56名参与者中,24名参与者实现了咯血的解决,TXA组(63.0%)与对照组(24.1%)相比也显著(P = 0.003)更好。未见严重药物不良反应。轻度咳嗽(37.5%)和咽喉刺激(33.9%),两组间比较具有可比性(P = 0.432)。结论:TXA雾化是一种安全的给药途径。在明确的干预计划或实施之前,及时雾化TXA作为咯血的桥接治疗是有效的,可以实现出血控制的直接目标。我们鼓励进一步的研究来评估这种新型的TXA雾化方法。试验注册:clinicaltrials.gov PRS ID: NCT05648656。
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引用次数: 0
Efficacy of epigallocatechin-3-gallate against oleic acid-induced acute respiratory distress syndrome. 表没食子儿茶素-3-没食子酸酯对油酸诱导的急性呼吸窘迫综合征的疗效。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_518_24
Subham Kumar Panda, Vadlamani Girish Shankar Sharma, Vishal L Sorathiya, Pratap Kumar Sahu

Objective: The objective is to induce acute respiratory distress syndrome (ARDS) in rats by oleic acid and evaluate the prophylactic and therapeutic effectiveness of epigallocatechin-3-gallate (EGCG) against ARDS.

Background: ARDS is an acute, severe inflammatory lung injury. Clinically used anti-inflammatory medication and corticosteroids have side effects, infection risk, and increased treatment costs. Epigallocatechin-3-gallate (EGCG) from green tea is a flavonoid possessing antioxidant and anti-inflammatory properties. Intravenous injection of pure oleic acid causes respiratory distress in diverse animal species, leading to inflammation in the lungs. Hence, we used oleic acid to induce ARDS in rats to assess the prophylactic and therapeutic effectiveness of EGCG against ARDS.

Materials and methods: A total of four groups were formed, with five animals allocated to each group. The control group (G1) was administered with normal saline 0.2 ml/kg, twice at an interval of 1 h, ARDS group (G2) with oleic acid 0.2 ml/kg intravenously, twice at 1-h interval. The prophylactic group (G3) was administered with EGCG 10 mg/kg i.p. 1 h before the administration of oleic acid, whereas therapeutic group (G4) was administered with same dose of EGCG but, 1 h after the administration of oleic acid.

Results: Assessment of animal body and lungs weight, gross macroscopic and microscopic evaluation of lungs did not produce any significant treatment-related changes when compared with the control group. However, a substantial decrease in tumor necrosis factor-alpha levels was observed in G3 and G4 when compared to the G2 group.

Conclusions: EGCG has both prophylactic and therapeutic effectiveness against ARDS.

目的:探讨油酸诱导大鼠急性呼吸窘迫综合征(ARDS)的作用,评价表没食子儿茶素-3-没食子酸酯(EGCG)对ARDS的预防和治疗作用。背景:ARDS是一种急性、严重的炎性肺损伤。临床使用的抗炎药物和皮质类固醇有副作用、感染风险和增加治疗费用。绿茶中的表没食子儿茶素-3-没食子酸酯(EGCG)是一种具有抗氧化和抗炎特性的类黄酮。静脉注射纯油酸会导致多种动物呼吸窘迫,导致肺部炎症。因此,我们采用油酸诱导大鼠急性呼吸窘迫综合征,以评估EGCG对ARDS的预防和治疗效果。材料与方法:共分为4组,每组5只。对照组(G1)静脉滴注生理盐水0.2 ml/kg,间隔1 h 2次;ARDS组(G2)静脉滴注油酸0.2 ml/kg,间隔1 h 2次。预防组(G3)在油酸给药前1 h ig ig EGCG 10 mg/kg,治疗组(G4)在油酸给药后1 h ig ig相同剂量EGCG。结果:与对照组相比,动物体重、肺重评估、肉眼和显微镜下肺质量评估均未发生明显的治疗相关变化。然而,与G2组相比,G3和G4组的肿瘤坏死因子- α水平明显下降。结论:EGCG对ARDS具有预防和治疗双重作用。
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引用次数: 0
Effect of dexmedetomidine combined with ropivacaine in ultrasound-guided paravertebral nerve block for acute herpes zoster neuralgia patients. 右美托咪定联合罗哌卡因超声引导下椎旁神经阻滞治疗急性带状疱疹神经痛的疗效。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_434_23
Cuicui Liu, Yanting Wang, Pei Wang, Chao Meng, Yanwei Yin

Purpose: Early and effective treatment of acute herpes zoster (AHZ) can relief the pain and prevent the occurrence of postherpetic neuralgia (PHN) in patients. The aim of this study is to investigate the efficacy of dexmedetomidine combined with ropivacaine in ultrasound-guided paravertebral nerve block for patients with AHZ neuralgia.

Materials and methods: Seventy-four patients suffering from acute thoracic herpes zoster neuralgia were divided into two equal groups in a prospective, randomized, double-blind controlled manner. All patients received paravertebral nerve block under ultrasound guidance with different drugs: Group I: 0.2% ropivacaine with 1 μg/kg dexmedetomidine; Group II: 0.2% ropivacaine, all drugs were diluted with normal saline to a total of 20 ml. The patients' Visual Analog Scale (VAS) scores were used for assessing pain level while the quality of sleep (QS) scores were used for assessing sleep levels 1, 4, 8, and 12 weeks after the treatment, as well as the pregabalin consumption. Time to pain resolution and skin eruption, total times of block, complications within 24 h after block, and the incidence of persistent PHN at 3 and 6 months were analyzed.

Results: There were no significant differences in the VAS scores between the two groups at various time points (P > 0.05). At the time point 1, 4, and 8 weeks after treatment, the QS scores in Group I were significantly lower than that in Group II (P < 0.05). The pregabalin consumption and the incidence of PHN between the two groups were not significantly different (P > 0.05). The total times of block in Group I were significantly less than Group II.

Conclusion: Both interventions provided similar efficacy in minimizing the pain intensity and reducing the incidence of PHN in AHZ patients. Compared with ropivacaine only, the addition of dexmedetomidine significantly improved patients' sleep quality and reduced the times of block.

目的:早期有效治疗急性带状疱疹(AHZ)可减轻患者疼痛,预防带状疱疹后神经痛(PHN)的发生。本研究旨在探讨右美托咪定联合罗哌卡因在超声引导下椎旁神经阻滞治疗AHZ神经痛患者的疗效。材料与方法:采用前瞻性、随机、双盲对照方法,将74例急性胸部带状疱疹神经痛患者分为两组。所有患者均在超声引导下采用不同药物进行椎旁神经阻滞:I组:0.2%罗哌卡因加1 μg/kg右美托咪定;II组:0.2%罗哌卡因,所有药物均用生理盐水稀释至共20 ml。采用视觉模拟量表(VAS)评分评估患者疼痛水平,采用睡眠质量(QS)评分评估治疗后1、4、8、12周的睡眠水平及普瑞巴林用量。分析疼痛缓解时间、皮肤出疹时间、阻滞总次数、阻滞后24 h内并发症及3、6个月持续性PHN发生率。结果:两组患者各时间点VAS评分比较,差异均无统计学意义(P < 0.05)。治疗后1、4、8周时,I组QS评分显著低于II组(P < 0.05)。两组患者普瑞巴林用量及PHN发生率比较,差异无统计学意义(P < 0.05)。1组总阻滞次数显著少于2组。结论:两种干预措施在减轻AHZ患者疼痛强度和降低PHN发生率方面效果相似。与单独使用罗哌卡因相比,右美托咪定可显著改善患者的睡眠质量,减少阻滞次数。
{"title":"Effect of dexmedetomidine combined with ropivacaine in ultrasound-guided paravertebral nerve block for acute herpes zoster neuralgia patients.","authors":"Cuicui Liu, Yanting Wang, Pei Wang, Chao Meng, Yanwei Yin","doi":"10.4103/ijp.ijp_434_23","DOIUrl":"10.4103/ijp.ijp_434_23","url":null,"abstract":"<p><strong>Purpose: </strong>Early and effective treatment of acute herpes zoster (AHZ) can relief the pain and prevent the occurrence of postherpetic neuralgia (PHN) in patients. The aim of this study is to investigate the efficacy of dexmedetomidine combined with ropivacaine in ultrasound-guided paravertebral nerve block for patients with AHZ neuralgia.</p><p><strong>Materials and methods: </strong>Seventy-four patients suffering from acute thoracic herpes zoster neuralgia were divided into two equal groups in a prospective, randomized, double-blind controlled manner. All patients received paravertebral nerve block under ultrasound guidance with different drugs: Group I: 0.2% ropivacaine with 1 μg/kg dexmedetomidine; Group II: 0.2% ropivacaine, all drugs were diluted with normal saline to a total of 20 ml. The patients' Visual Analog Scale (VAS) scores were used for assessing pain level while the quality of sleep (QS) scores were used for assessing sleep levels 1, 4, 8, and 12 weeks after the treatment, as well as the pregabalin consumption. Time to pain resolution and skin eruption, total times of block, complications within 24 h after block, and the incidence of persistent PHN at 3 and 6 months were analyzed.</p><p><strong>Results: </strong>There were no significant differences in the VAS scores between the two groups at various time points (P > 0.05). At the time point 1, 4, and 8 weeks after treatment, the QS scores in Group I were significantly lower than that in Group II (P < 0.05). The pregabalin consumption and the incidence of PHN between the two groups were not significantly different (P > 0.05). The total times of block in Group I were significantly less than Group II.</p><p><strong>Conclusion: </strong>Both interventions provided similar efficacy in minimizing the pain intensity and reducing the incidence of PHN in AHZ patients. Compared with ropivacaine only, the addition of dexmedetomidine significantly improved patients' sleep quality and reduced the times of block.</p>","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"385-391"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662612/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495211","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Ponsegromab: The new miracle drug for cancer cachexia. Ponsegromab:治疗癌症恶病质的新神药。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_347_25
Elisha Paikray, Anima Rout, Ratikanta Tripathy
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引用次数: 0
Follicle fiasco - Unraveling the cause of sudden hair loss! 毛囊惨败-解开突然脱发的原因!
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_919_24
Sanyam Mehta, Kailash Bhatia, Chaitanya Namdeo, Lavin Bhatia

Abstract: Sudden excessive hair loss poses a diagnostic challenge when encountered in an otherwise healthy individual. We present a case study of a middle-aged female who presented with unexplained and sudden hair loss. After initial consideration of common causes of sudden hair loss, a dispensing error involving azathioprine was identified as the underlying cause. This case underscores the need for further research to elucidate the specific pathways through which azathioprine induces selective damage to the dermal papillae of the hair follicle. This case also emphasizes the importance of meticulous medication management and pharmacovigilance in clinical practice.

摘要:突发性过度脱发对其他健康个体的诊断提出了挑战。我们提出了一个中年女性谁提出了不明原因和突然脱发的案例研究。在对突发性脱发的常见原因进行初步考虑后,一个涉及硫唑嘌呤的配药错误被确定为潜在原因。该病例强调需要进一步研究,以阐明通过硫唑嘌呤诱导毛囊真皮乳头选择性损伤的具体途径。本病例也强调了在临床实践中细致的用药管理和药物警戒的重要性。
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引用次数: 0
Roflumilast in dermatology: Revolutionizing inflammatory skin treatment. 罗氟司特在皮肤病学:革命性的炎症性皮肤治疗。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_161_25
Sharang Gupta
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引用次数: 0
A comprehensive review on cardiovascular and chronic kidney disease interplay, exploring biomarkers and algorithmic approaches in unraveling organ crosstalk. 心血管和慢性肾脏疾病相互作用的综合综述,探索揭示器官串扰的生物标志物和算法方法。
IF 1.5 4区 医学 Q4 PHARMACOLOGY & PHARMACY Pub Date : 2025-11-01 Epub Date: 2025-10-12 DOI: 10.4103/ijp.ijp_66_24
Prashant Kumar, Yogendra Pal, Shiv Dev Singh, Shashi Bhooshan Tiwari

Abstract: This review article is based upon the findings of the role of different biomarkers in the progression of the diseases. These findings were from past studies and meta-analysis of the biomarker in cardiovascular and chronic kidney diseases (CKDs). It mainly focuses on the organ crosstalk of diseases because of different biomarkers such as proteomics, genomics, metabolomics, and bioinformatics. In this reviewing process, we analyzed some biomarkers responsible for various cardiovascular and CKDs, out of which we found few biomarkers which are responsible for indication and diagnosis of disease relating to both the systems. It was found that the MiR-21, a type of genomic biomarker C-reactive protein, N-terminal pro-B-type natriuretic peptide, high-sensitivity cardiac troponin T, and estimated glomerular filtration rate, types of proteomics biomarkers has shown role in the prediction of diseases. As well as we also reviewed research work from the past to analyze the relation between the disease and its clinical outcomes using machine learning, which can be used to create few models to predict the clinical outcomes. Out of all the algorithms used, they showing most promising results was XGBoost method. In the past, there were studies supporting the statement - algorithms created by the scientists gives variables relating to the disease. These variables can be used to predict the disease based on the levels of biomarkers present in the sample of the patients.

摘要:本文综述了不同生物标志物在疾病进展中的作用。这些发现来自过去的研究和心血管和慢性肾脏疾病(CKDs)生物标志物的荟萃分析。主要关注不同生物标志物如蛋白质组学、基因组学、代谢组学和生物信息学对疾病器官串扰的影响。在回顾过程中,我们分析了一些与各种心血管和ckd相关的生物标志物,其中我们发现很少有生物标志物与这两个系统相关的疾病指征和诊断有关。研究发现,MiR-21、一类基因组生物标志物c反应蛋白、n端前b型利钠肽、高敏感性心肌肌钙蛋白T和估计肾小球滤过率等蛋白质组学生物标志物已显示出预测疾病的作用。此外,我们也回顾了过去的研究工作,利用机器学习来分析疾病与其临床结果之间的关系,这可以用来创建一些模型来预测临床结果。在所有使用的算法中,他们显示出最有希望的结果是XGBoost方法。在过去,有研究支持这一说法——科学家创建的算法给出了与疾病相关的变量。这些变量可用于根据患者样本中存在的生物标志物水平来预测疾病。
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引用次数: 0
期刊
Indian Journal of Pharmacology
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