Pub Date : 2025-11-01Epub Date: 2025-10-12DOI: 10.4103/ijp.ijp_979_25
Sandhya Rajaram, Bikash Medhi
{"title":"Orphan drugs: The final frontier in the fight against rare diseases.","authors":"Sandhya Rajaram, Bikash Medhi","doi":"10.4103/ijp.ijp_979_25","DOIUrl":"10.4103/ijp.ijp_979_25","url":null,"abstract":"","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"367-370"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662615/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495313","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}
Pub Date : 2025-11-01Epub Date: 2025-10-12DOI: 10.4103/ijp.ijp_365_25
Sumit Mehndiratta
{"title":"Anaphylactic shock due to mefenamic acid.","authors":"Sumit Mehndiratta","doi":"10.4103/ijp.ijp_365_25","DOIUrl":"10.4103/ijp.ijp_365_25","url":null,"abstract":"","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"417-418"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662608/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495206","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}
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.
{"title":"Assessment of knowledge, attitude, and practice regarding reporting of adverse events due to medical devices among healthcare workers in Gujarat.","authors":"Jonsi Tavethia, Samidh Shah, Anshul Bhadania, Shubh Mehta, Prahar Himanshubhai Darji, Kavya Darji, Kinjal Mulubhai Solanki","doi":"10.4103/ijp.ijp_754_24","DOIUrl":"10.4103/ijp.ijp_754_24","url":null,"abstract":"<p><strong>Objective: </strong>To assess the knowledge, attitude, and practice (KAP) regarding reporting adverse events due to medical devices among healthcare workers in our hospital.</p><p><strong>Materials and methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"409-413"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662616/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495215","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}
Pub Date : 2025-11-01Epub Date: 2025-10-12DOI: 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。
{"title":"Efficacy and safety of tranexamic acid nebulization to control bleeding of hemoptysis: The TXA-NEB randomized controlled clinical trial.","authors":"Aman Agrawal, Deba Prasad Dhibar, Ajay Prakash, B C Sreedhara, Valliappan Muthu, Ashok Kumar Pannu","doi":"10.4103/ijp.ijp_824_25","DOIUrl":"10.4103/ijp.ijp_824_25","url":null,"abstract":"<p><strong>Objectives: </strong>The objective of this study was to evaluate the efficacy and safety of tranexamic acid (TXA) nebulization to control bleeding in hemoptysis.</p><p><strong>Materials and methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusion: </strong>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.</p>","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"392-400"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662606/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495187","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}
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。
{"title":"Efficacy of epigallocatechin-3-gallate against oleic acid-induced acute respiratory distress syndrome.","authors":"Subham Kumar Panda, Vadlamani Girish Shankar Sharma, Vishal L Sorathiya, Pratap Kumar Sahu","doi":"10.4103/ijp.ijp_518_24","DOIUrl":"10.4103/ijp.ijp_518_24","url":null,"abstract":"<p><strong>Objective: </strong>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.</p><p><strong>Background: </strong>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.</p><p><strong>Materials and methods: </strong>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.</p><p><strong>Results: </strong>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.</p><p><strong>Conclusions: </strong>EGCG has both prophylactic and therapeutic effectiveness against ARDS.</p>","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"380-384"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662607/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495334","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}
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.
{"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}
Pub Date : 2025-11-01Epub Date: 2025-10-12DOI: 10.4103/ijp.ijp_347_25
Elisha Paikray, Anima Rout, Ratikanta Tripathy
{"title":"Ponsegromab: The new miracle drug for cancer cachexia.","authors":"Elisha Paikray, Anima Rout, Ratikanta Tripathy","doi":"10.4103/ijp.ijp_347_25","DOIUrl":"10.4103/ijp.ijp_347_25","url":null,"abstract":"","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"419-420"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662614/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495347","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}
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.
{"title":"Follicle fiasco - Unraveling the cause of sudden hair loss!","authors":"Sanyam Mehta, Kailash Bhatia, Chaitanya Namdeo, Lavin Bhatia","doi":"10.4103/ijp.ijp_919_24","DOIUrl":"10.4103/ijp.ijp_919_24","url":null,"abstract":"<p><strong>Abstract: </strong>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.</p>","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"414-416"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12663763/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495331","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}
Pub Date : 2025-11-01Epub Date: 2025-10-12DOI: 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.
{"title":"A comprehensive review on cardiovascular and chronic kidney disease interplay, exploring biomarkers and algorithmic approaches in unraveling organ crosstalk.","authors":"Prashant Kumar, Yogendra Pal, Shiv Dev Singh, Shashi Bhooshan Tiwari","doi":"10.4103/ijp.ijp_66_24","DOIUrl":"10.4103/ijp.ijp_66_24","url":null,"abstract":"<p><strong>Abstract: </strong>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.</p>","PeriodicalId":13490,"journal":{"name":"Indian Journal of Pharmacology","volume":"57 6","pages":"371-379"},"PeriodicalIF":1.5,"publicationDate":"2025-11-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC12662617/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"145495098","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}