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Poncet's Disease-A Rare Complication of Tuberculosis: A Case Report. 庞塞病——一种罕见的肺结核并发症:1例报告。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1399
Arushi Seth, Surinderpal Singh

Objectives: We present a rare case of Poncet's disease, a sterile reactive arthritis associated with active tuberculosis (TB), mimicking seronegative spondyloarthritis in a young diabetic male. We aim to highlight the diagnostic challenges and emphasize the importance of considering Poncet's disease in patients with inflammatory arthritis, especially in the context of subclinical TB.

Methods: We present a detailed case report of a 28-year-old male with poorly controlled diabetes mellitus type 2 [glycated hemoglobin (HbA1c) 13.9%] who presented with a 3-week history of bilateral ankle pain, swelling, and redness. The pain progressed to involve multiple small joints of the hands, wrists, elbows, and knees, significantly impacting his mobility, with no history of trauma, fever, rash, or urinary symptoms. Physical examination revealed tenderness and swelling in the affected joints with limited range of motion. Laboratory investigations showed an elevated erythrocyte sedimentation rate (ESR) of 74 mm/hour and C-reactive protein (CRP) of 104 mg/L. Chest X-ray revealed bilateral hilar lymphadenopathy, and computed tomography (CT) scan confirmed multiple enlarged lymph nodes in the mediastinum and bilateral hilar regions, suggestive of pulmonary TB. Despite the absence of acid-fast bacilli in bronchoalveolar lavage (BAL), the clinical presentation, imaging findings, exclusion of other causes of reactive arthritis, and a dramatic response to anti-TB therapy within days of initiation strongly supported the diagnosis of Poncet's disease. The patient completed 6 months of anti-TB therapy and achieved complete resolution of joint pain and swelling, regaining his full range of motion.

Results: The patient's symptoms, including joint pain, swelling, and inflammatory markers, significantly improved within weeks of starting anti-TB therapy. Serial CRP and ESR readings showed a downward trend, confirming the response to treatment.

Conclusion: This case report highlights the importance of considering Poncet's disease in the differential diagnosis of seronegative spondyloarthritis, particularly in patients with underlying TB. A high index of suspicion and prompt initiation of anti-TB therapy can lead to rapid improvement in symptoms and prevent unnecessary investigations and potentially harmful immunosuppressive medications.

目的:我们报告一例罕见的Poncet病,无菌反应性关节炎与活动性结核(TB)相关,在一个年轻的糖尿病男性中模拟血清阴性脊柱炎。我们的目的是强调诊断的挑战,并强调在炎症性关节炎患者中考虑Poncet病的重要性,特别是在亚临床结核病的背景下。方法:我们提出了一个详细的病例报告,28岁的男性患有控制不良的2型糖尿病[糖化血红蛋白(HbA1c) 13.9%],他有3周的双侧踝关节疼痛、肿胀和发红的病史。疼痛进展到手、手腕、肘部和膝盖的多个小关节,严重影响其活动能力,无外伤史、发热、皮疹或泌尿系统症状。体格检查显示受累关节有压痛和肿胀,活动范围有限。实验室检查显示红细胞沉降率(ESR)升高74 mm/小时,c反应蛋白(CRP)升高104 mg/L。胸部x线显示双侧肺门淋巴结病变,CT扫描证实纵隔及双侧肺门区多发肿大淋巴结,提示肺结核。尽管支气管肺泡灌洗(BAL)中没有抗酸杆菌,但临床表现、影像学发现、排除其他原因的反应性关节炎,以及在开始治疗几天内对抗结核治疗的显著反应,都有力地支持了Poncet病的诊断。患者完成了6个月的抗结核治疗,完全消除了关节疼痛和肿胀,恢复了全活动能力。结果:患者的症状,包括关节疼痛、肿胀和炎症标志物,在开始抗结核治疗的几周内显著改善。系列CRP和ESR读数呈下降趋势,证实了治疗的反应。结论:本病例报告强调了在血清阴性脊柱炎的鉴别诊断中考虑Poncet病的重要性,特别是在伴有潜在结核病的患者中。高度怀疑和迅速开始抗结核治疗可导致症状迅速改善,并防止不必要的调查和可能有害的免疫抑制药物。
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引用次数: 0
Coexistent Antiphospholipid Syndrome with Polycythemia Vera in a 25-year-old Lady Presented with Splenic Vein Thrombosis. 并存抗磷脂综合征与真性红细胞增多症的25岁女性表现为脾静脉血栓。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1432
C Mohammed Ameen, Bhargavan Pallivalappil

A high risk of thrombosis is linked to myeloproliferative neoplasm (MPN) and antiphospholipid syndrome (APS). The systemic autoimmune disorder known as APS is characterized by persistently positive antiphospholipid antibodies [anticardiolipin (aCL), lupus anticoagulant, and antibeta 2 glycoprotein 1 IgG and IgM antibodies] in conjunction with obstetrical complications or thrombosis (Chayoua et al.). Polycythemia vera (PV) is a MPN that causes too many red blood cells (RBCs) in the blood and proinflammatory cytokines. In this report, we present a case of a 25-year-old lady with a history of second-trimester abortion who presented with abdominal pain and hepatosplenomegaly. Owing to erythrocytosis, thrombocytosis, and moderate hepatosplenomegaly, workup for MPN was done along with prothrombotic workup including APS, and she turned out to be positive for both. Coexistence of MPN and APS is rare in the literature. The optimal management of patients with coexistent APS and MPN has not been defined so far. Immediate anticoagulation with specific treatment for MPN is essential to prevent further thromboembolic episodes and progression to catastrophic APS.

血栓形成的高风险与骨髓增生性肿瘤(MPN)和抗磷脂综合征(APS)有关。被称为APS的系统性自身免疫性疾病的特征是抗磷脂抗体(抗心磷脂(aCL)、狼疮抗凝血剂、抗- 2糖蛋白1 IgG和IgM抗体)持续阳性,并伴有产科并发症或血栓形成(Chayoua等)。真性红细胞增多症(PV)是一种MPN,导致血液中红细胞(rbc)和促炎细胞因子过多。在这个报告中,我们提出了一个25岁的妇女与历史的中期妊娠流产谁提出腹痛和肝脾肿大。由于红细胞增多、血小板增多和中度肝脾肿大,在进行MPN检查的同时进行了包括APS在内的血栓前检查,结果两项检查均呈阳性。在文献中,MPN与APS并存的情况并不多见。APS合并MPN患者的最佳处理至今尚未明确。立即抗凝治疗特异性治疗MPN是必不可少的,以防止进一步血栓栓塞发作和发展为灾难性APS。
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引用次数: 0
Thyrotropin Controversy in Subclinical Thyroid Disorders. 促甲状腺激素在亚临床甲状腺疾病中的争议。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1442
Rajesh Agrawal
<p><strong>Aim: </strong>The thyrotropin controversy in subclinical thyroid disorders (STDs) is among the most common endocrine disorders globally. In India, approximately 42 million people suffer from thyroid disorders, with subclinical hypothyroidism (SCH) affecting about 9.4% of the population. SCH is more prevalent in females (11.4%) compared to males (6.2%).</p><p><strong>Discussion: </strong>The diagnosis and treatment of SCH and subclinical hyperthyroidism (SHT) are controversial. SCH is often diagnosed based on biochemical markers, as patients may be asymptomatic or exhibit vague symptoms. Thyrotropin (TSH) levels may be elevated or decreased, while triiodothyronine (T3) and thyroxine (T4) remain within the normal reference range or near the lower or upper limits. STDs refers to an abnormal TSH with normal thyroxine (FT4) and free triiodothyronine (FT3) levels. It includes STDs and individuals at high risk for disease progression or adverse outcomes, with unclear prognosis. Progression of SCH to overt hypothyroidism depends on initial serum TSH levels, thyroid peroxidase antibodies (TPO), family history of thyroid disorders, previous radiation, and smoking. Controversies surround SCH and its association with cardiovascular diseases (CVD), pregnancy outcomes, neuropsychiatric issues, metabolic syndrome, dyslipidemia, and diabetes. Assay interference is a problem in interpreting thyroid function tests (TFTs), occurring in 1% of cases. The health package investigation systems often overlooks the impact of drug intake and assay interference. Various methods for measuring TFTs, such as radioimmunoassay, immunometric assay, and ELISA, differ in sensitivity, specificity, and standardization, leading to methodological variability. Common causes of assay interference include human antimurine antibodies (HAMA), thyroid hormone autoantibodies (THAAbs), rheumatoid factor, antistreptavidin, and antiruthenium antibodies. When diagnosing SCH, it is crucial to rule out other causes of elevated TSH, such as autoantibodies, goiter, and rare conditions such as thyroid hormone resistance (THR), diagnosed by serum glycoprotein alpha subunit (α-GSU) and family history. Biotin, a common supplement, can affect TFT assays, leading to spurious results. It can cause falsely high T4 and T3 levels and low TSH, leading to misdiagnosis of SCH.</p><p><strong>Conclusion and recommendations: </strong>The timing of TFTs, whether fasting, postprandial, or random, remains a debated issue. Assay interference and biotin intake should be considered when analyzing TFTs. The role of iodine and iodine supplementation during pregnancy and its impact on STDs are not yet fully conceptualized. Large randomized clinical and epidemiological studies are needed to establish a consensus on the diagnostic threshold for TSH. These studies should include diverse populations and medical conditions to improve our understanding of the disease and patient outcomes. In practice, avoid rushing to t
目的:亚临床甲状腺疾病(std)是全球最常见的内分泌疾病之一。在印度,大约有4200万人患有甲状腺疾病,其中亚临床甲状腺功能减退症(SCH)影响了约9.4%的人口。女性(11.4%)比男性(6.2%)更普遍。讨论:SCH和亚临床甲状腺功能亢进(SHT)的诊断和治疗存在争议。SCH通常根据生化指标诊断,因为患者可能无症状或表现出模糊的症状。促甲状腺激素(TSH)水平可能升高或降低,而三碘甲状腺原氨酸(T3)和甲状腺素(T4)保持在正常参考范围内或接近下限或上限。性传播疾病是指TSH异常,甲状腺素(FT4)和游离三碘甲状腺原氨酸(FT3)水平正常。它包括性病患者和疾病进展或不良后果高风险的个体,预后不明确。SCH发展为明显的甲状腺功能减退取决于初始血清TSH水平、甲状腺过氧化物酶抗体(TPO)、甲状腺疾病家族史、既往放疗和吸烟。围绕SCH及其与心血管疾病(CVD)、妊娠结局、神经精神问题、代谢综合征、血脂异常和糖尿病的关系存在争议。分析干扰是解释甲状腺功能检查(TFTs)的一个问题,发生在1%的病例中。卫生一揽子调查系统往往忽略了药物摄入和检测干扰的影响。测量tft的各种方法,如放射免疫测定法、免疫测定法和ELISA,在敏感性、特异性和标准化方面存在差异,导致方法的可变性。检测干扰的常见原因包括人抗尿抗体(HAMA)、甲状腺激素自身抗体(THAAbs)、类风湿因子、抗链霉亲和素和抗钌抗体。在诊断SCH时,排除TSH升高的其他原因是至关重要的,如自身抗体、甲状腺肿和罕见的情况,如甲状腺激素抵抗(THR),通过血清糖蛋白α亚基(α-GSU)和家族史诊断。生物素,一种常见的补充剂,可以影响TFT测定,导致虚假的结果。结论和建议:TFTs的时机,无论是空腹、餐后还是随机,仍然是一个有争议的问题。在分析TFTs时应考虑检测干扰和生物素摄入。在怀孕期间碘和碘补充的作用及其对性传播疾病的影响尚未完全概念化。需要进行大量随机临床和流行病学研究,才能就TSH的诊断阈值达成共识。这些研究应该包括不同的人群和医疗条件,以提高我们对疾病和患者结果的理解。在实践中,避免急于治疗4 - 10 mIU/L之间的TSH升高或0.5 - 0.1 mIU/L之间的TSH低,而没有通过额外的测试(T3, T4, FT4, FT3和TPO)确认诊断。TSH本身不应该是唯一的决策者;考虑其他tft和来自同一实验室的连续测试和时间,以做出更明智的决定。虽然TSH水平会受到时间和膳食状态的影响,但FT3和FT4水平保持稳定,这表明这三种tft可能有助于准确的诊断和治疗决策。
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引用次数: 0
Early LDL-C Lowering Efficacy of High-intensity Atorvastatin and Ezetimibe Combination Compared with High-intensity Atorvastatin Alone in Acute Coronary Syndrome: The LAI EARLY ACS Study. 高强度阿托伐他汀联合依折替米比与单独高强度阿托伐他汀治疗急性冠脉综合征的早期降LDL-C效果:LAI早期ACS研究
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1444
Vimal Mehta, Nikhil Agarwal, Pratishtha Mehra, Navya Mehta, Jamal Yusuf, Pradeep Kumar Dabla, Sana Sukhija, Safal Safal, Mohit Gupta, Surendra Kumar, Sanjeev Kathuria, Akhilesh Kumar, P Barton Duell, K K Pareek, Raman Puri

Background: High-intensity statins are recommended in patients experiencing acute coronary syndrome (ACS) to lower low-density lipoprotein cholesterol (LDL-C) levels, but evidence-based recommended LDL-C goals often remain unmet. We assessed the therapeutic benefit of early LDL-C lowering and the safety of high-intensity atorvastatin and ezetimibe combination versus high-intensity atorvastatin alone in ACS.

Methods: In this investigator-initiated trial, 254 patients admitted with ACS were randomized 1:1 to either atorvastatin 80 mg once daily (group A) or a combination of atorvastatin 80 mg and ezetimibe 10 mg once daily (group B). The first dose was administered orally immediately after diagnosis and then continued daily. The primary and secondary endpoints were percentage reductions in direct LDL-C measurements over the initial 4-week period and at 12 weeks, respectively.

Results: The mean percentage reduction in LDL-C was 8.12% in group A vs 14.43% in group B (p < 0.001) at week 1, 16.62% in group A vs 28.34% in group B at 2 weeks (p < 0.001), 29.43% in group A vs 45.15% in group B at 4 weeks (p < 0.001), and 41.88% in group A vs 60.76% in group B (p < 0.001) at 12 weeks. Adverse events were similar in both groups.

Conclusion: Ezetimibe added to high-intensity statin therapy was well tolerated and resulted in an immediate and robust additional decrease in circulating LDL-C concentrations, with a markedly higher proportion of participants achieving LDL-C goals at 4 and 12 weeks. These promising results show that dual therapy started immediately at the diagnosis of ACS has the potential to improve cardiovascular outcomes in ACS.

背景:高强度他汀类药物被推荐用于急性冠脉综合征(ACS)患者,以降低低密度脂蛋白胆固醇(LDL-C)水平,但循证推荐的LDL-C目标往往无法实现。我们评估了早期降低LDL-C的疗效,以及与单独使用高强度阿托伐他汀相比,高强度阿托伐他汀和依泽替米贝联合使用的安全性。方法:在这项研究者发起的试验中,254例入院的ACS患者以1:1的比例随机分配到阿托伐他汀80 mg每日一次(A组)或阿托伐他汀80 mg与依泽替米贝10 mg每日一次(B组)。第一剂在诊断后立即口服,然后每天继续服用。主要和次要终点分别是在最初的4周和12周期间直接LDL-C测量的百分比下降。结果:第1周时A组LDL-C平均降低率为8.12%,B组为14.43% (p < 0.001), 2周时A组为16.62%,B组为28.34% (p < 0.001), 4周时A组为29.43%,B组为45.15% (p < 0.001), 12周时A组为41.88%,B组为60.76% (p < 0.001)。两组不良事件相似。结论:依zetimibe加入高强度他汀类药物治疗具有良好的耐受性,可立即显著降低循环LDL-C浓度,在第4周和第12周达到LDL-C目标的参与者比例明显更高。这些有希望的结果表明,在ACS诊断时立即开始双重治疗有可能改善ACS的心血管预后。
{"title":"Early LDL-C Lowering Efficacy of High-intensity Atorvastatin and Ezetimibe Combination Compared with High-intensity Atorvastatin Alone in Acute Coronary Syndrome: The LAI EARLY ACS Study.","authors":"Vimal Mehta, Nikhil Agarwal, Pratishtha Mehra, Navya Mehta, Jamal Yusuf, Pradeep Kumar Dabla, Sana Sukhija, Safal Safal, Mohit Gupta, Surendra Kumar, Sanjeev Kathuria, Akhilesh Kumar, P Barton Duell, K K Pareek, Raman Puri","doi":"10.59556/japi.74.1444","DOIUrl":"https://doi.org/10.59556/japi.74.1444","url":null,"abstract":"<p><strong>Background: </strong>High-intensity statins are recommended in patients experiencing acute coronary syndrome (ACS) to lower low-density lipoprotein cholesterol (LDL-C) levels, but evidence-based recommended LDL-C goals often remain unmet. We assessed the therapeutic benefit of early LDL-C lowering and the safety of high-intensity atorvastatin and ezetimibe combination versus high-intensity atorvastatin alone in ACS.</p><p><strong>Methods: </strong>In this investigator-initiated trial, 254 patients admitted with ACS were randomized 1:1 to either atorvastatin 80 mg once daily (group A) or a combination of atorvastatin 80 mg and ezetimibe 10 mg once daily (group B). The first dose was administered orally immediately after diagnosis and then continued daily. The primary and secondary endpoints were percentage reductions in direct LDL-C measurements over the initial 4-week period and at 12 weeks, respectively.</p><p><strong>Results: </strong>The mean percentage reduction in LDL-C was 8.12% in group A vs 14.43% in group B (<i>p</i> < 0.001) at week 1, 16.62% in group A vs 28.34% in group B at 2 weeks (<i>p</i> < 0.001), 29.43% in group A vs 45.15% in group B at 4 weeks (<i>p</i> < 0.001), and 41.88% in group A vs 60.76% in group B (<i>p</i> < 0.001) at 12 weeks. Adverse events were similar in both groups.</p><p><strong>Conclusion: </strong>Ezetimibe added to high-intensity statin therapy was well tolerated and resulted in an immediate and robust additional decrease in circulating LDL-C concentrations, with a markedly higher proportion of participants achieving LDL-C goals at 4 and 12 weeks. These promising results show that dual therapy started immediately at the diagnosis of ACS has the potential to improve cardiovascular outcomes in ACS.</p>","PeriodicalId":22693,"journal":{"name":"The Journal of the Association of Physicians of India","volume":"74 3","pages":"68-74"},"PeriodicalIF":0.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147445212","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
Semaglutide Hype or Hope: Evidence-based Review in Diabesity. 西马鲁肽的炒作还是希望:糖尿病的循证评价。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1439
Sunil Gupta, Brij Mohan Makkar, Jothydev Kesavadev, Ajay Kumar

India is struggling with the twin epidemics of diabetes and weight issues, holding the second position globally in the former and third in the latter. Despite multiple advancements with therapies that offer glycemic control and weight benefits, there has remained a gap for a comprehensive drug for the management of "diabesity." Semaglutide, since its global approval in 2017, has become a blockbuster, owing to the popularity of "Ozempic." While Ozempic has been traditionally approved for glycemic control in type 2 diabetes mellitus (T2DM), it does offer significant other benefits powerful weight loss, cardiovascular benefits, renal protection benefits, and functional improvement in peripheral arterial disease. The drug is approved in India for first-line use in adults with T2DM as an adjunct to diet and exercise. The long use of semaglutide globally and in India has ensured adequate data on efficacy and safety, ensuring confidence and trust. Gastrointestinal side effects are the most common adverse events seen with the molecule, as with other GLP-1 drugs. This review highlights the global clinical data and practicalities of the use of Ozempic in diabesity in the Indian context.

印度正与糖尿病和体重问题这两大流行病作斗争,前者在全球排名第二,后者在全球排名第三。尽管在控制血糖和减轻体重方面取得了多项进展,但在治疗“糖尿病”的综合药物方面仍然存在差距。Semaglutide自2017年在全球获得批准以来,由于“Ozempic”的流行而成为重磅炸弹。虽然Ozempic传统上被批准用于2型糖尿病(T2DM)的血糖控制,但它确实具有显著的其他益处-强大的减肥,心血管益处,肾脏保护益处和外周动脉疾病的功能改善。该药在印度被批准用于成人2型糖尿病的一线治疗,作为饮食和运动的辅助药物。在全球和印度长期使用西马鲁肽确保了关于疗效和安全性的充分数据,确保了信心和信任。与其他GLP-1药物一样,胃肠道副作用是该分子最常见的不良反应。这篇综述强调了Ozempic在印度糖尿病治疗中的全球临床数据和实用性。
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引用次数: 0
A Case of Drowning with Acute Kidney Injury and Raised Intracranial Tension. 溺水并发急性肾损伤颅内压升高1例。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1393
M Yamuna, T Geetha, N K Shiva, S Dinesh

Background: Drowning is the third leading cause of unintentional injury and death worldwide, accounting for 7% of all injury-related deaths. People who are at higher risk include those who have free accessibility to water and younger children lacking supervision. The common complications of drowning are mainly due to hypoxia. It mainly affects the respiratory, cardiac, and central nervous system. Rarely, drowning may cause acute kidney injury (AKI) secondary to rhabdomyolysis. Here, we present a case of near drowning with AKI, rhabdomyolysis, and elevated intracranial tension (ICT) with a false localizing sign (abducent nerve palsy).

Case description: A 21-year-old female patient was brought with a history of alleged drowning for about 3-5 minutes. The patient presented with loss of consciousness; she was gasping and had diffuse subcutaneous emphysema. On examination, the patient had bilateral coarse crepitations. She was started on mechanical ventilation. After 2 days, the patient developed elevated renal parameters and had an episode of ventricular tachycardia. After 10 days, the patient developed diplopia and blurring of vision. Ophthalmological examination revealed bilateral abducent nerve palsy with established papilledema and hemorrhagic retinopathy. The patient was treated with IV antibiotics, IV fluids, DC shock, inotropes, hemodialysis, and acetazolamide. After 15 days, the patient recovered from bilateral lateral rectus palsy and had no blurring of vision.

Conclusion: Drowning is a leading cause of accidental death. This patient had diffuse subcutaneous emphysema, rhabdomyolysis with AKI, ventricular tachycardia, and raised ICT. In drowning, raised ICT often has a poor outcome. However, with constant monitoring and timely intervention this patient survived.

背景:溺水是全世界意外伤害和死亡的第三大原因,占所有伤害相关死亡的7%。风险较高的人群包括那些可以免费获得水的人和缺乏监督的年幼儿童。溺水常见的并发症主要是由于缺氧。它主要影响呼吸、心脏和中枢神经系统。极少情况下,溺水可引起继发于横纹肌溶解的急性肾损伤(AKI)。在这里,我们报告了一例几乎溺水的AKI,横纹肌溶解,颅内压升高(ICT)伴假定位征象(外展神经麻痹)。病例描述:一名21岁女性患者被送来,有溺水史约3-5分钟。患者表现为意识丧失;她在喘气,有弥漫性皮下肺气肿。检查时,患者双侧有粗糙的颤音。她开始使用机械通气。2天后,患者出现肾脏参数升高,并发生室性心动过速。10天后,患者出现复视和视力模糊。眼科检查显示双侧外展神经麻痹,并有乳头水肿和出血性视网膜病变。患者给予静脉抗生素、静脉输液、直流电休克、肌力药物、血液透析和乙酰唑胺治疗。15天后,患者从双侧直肌麻痹中恢复,视力无模糊。结论:溺水是意外死亡的主要原因。该患者有弥漫性皮下肺气肿,横纹肌溶解伴AKI,室性心动过速,ICT升高。在溺水的情况下,提高ICT的效果往往很差。然而,在持续监测和及时干预下,该患者存活了下来。
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引用次数: 0
Chronic Kidney Disease with Risk Factor Diabetes: Need for Change in Nomenclature Reflecting Heterogeneity of Kidney Disease in Diabetes. 慢性肾病伴危险因素糖尿病:需要改变命名法以反映糖尿病肾病的异质性。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1390
Madhurima Basu, Sujoy Ghosh

The International Diabetes Federation estimates that 537 million individuals around the globe currently have diabetes, and this number is anticipated to rise to approximately 783 million by 2045. About 30% or more of individuals diagnosed with diabetes are more prone to developing chronic kidney disease (CKD), and a considerable portion progresses to renal impairment that requires renal replacement therapy.1,2.

国际糖尿病联合会估计,目前全球有5.37亿人患有糖尿病,预计到2045年,这一数字将上升到约7.83亿。大约30%或更多的糖尿病患者更容易发展为慢性肾脏疾病(CKD),其中相当一部分发展为肾脏损害,需要肾脏替代治疗。
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引用次数: 0
The Essential Role of Bedside Training in Undergraduate Medical Education: A Systematic Review. 床边训练在本科医学教育中的重要作用:系统回顾。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1063
Christopher Mathew, John C Mathew, Sumana S Philip

This systematic review examined the role of bedside teaching (BST) in undergraduate medical education, focusing on its impact on clinical competence and professional growth. The review included 15 studies that investigated the effects of BST on physical examination skills, diagnostic abilities, communication skills, and confidence among medical students. The results showed that BST significantly improved physical examination skills, diagnostic abilities, and communication skills, and increased confidence among students. BST was also found to enhance empathy and professionalism among students. However, the review highlighted several challenges in implementing BST, including time constraints, lack of trained faculty, and declining opportunities for BST. To address these challenges, the review recommended integrating BST into the medical curriculum, providing faculty development programs, and utilizing technology-enhanced learning tools. The findings of this systematic review underscore the importance of BST in undergraduate medical education, emphasizing its potential to enhance clinical competence and professional growth among future healthcare professionals.

本系统综述探讨了床边教学(BST)在本科医学教育中的作用,重点关注其对临床能力和专业成长的影响。本综述包括15项研究,调查了BST对医学生体格检查技能、诊断能力、沟通技巧和信心的影响。结果表明,BST显著提高了学生的体检技能、诊断能力和沟通能力,增强了学生的自信心。此外,体恤教学亦有助提高学生的同理心和专业精神。然而,审查强调了实施BST的几个挑战,包括时间限制、缺乏训练有素的教师以及BST的机会减少。为了应对这些挑战,审查建议将BST纳入医学课程,提供教师发展计划,并利用技术增强的学习工具。本系统综述的研究结果强调了BST在本科医学教育中的重要性,强调了它在提高未来医疗专业人员临床能力和专业成长方面的潜力。
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引用次数: 0
Hospital Hyperglycemia is Associated with Adverse Short-term Metabolic and Mortality Outcomes. 医院高血糖与不良的短期代谢和死亡率结果相关
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1391
Apoorv Ojha, Ramesh Aggarwal, Anupam Prakash, L H Ghotekar, Parijat Gogoi, Priya Bansal

Introduction: Stress hyperglycemia has been implicated in acute illnesses, but the risk of future diabetes is seldom studied. Hospital hyperglycemia, as defined by in-hospital random blood glucose (RBG) >140 mg/dL, is much less studied. This study aimed to determine the profile and short-term outcome of hospital hyperglycemia patients.

Methods: A descriptive follow-up study was conducted in 50 patients with hospital hyperglycemia. Based on their HbA1c status, patients were categorized into known cases of diabetes (group A, n = 12, 24%), undiagnosed diabetes (group B, n = 13, 26%), prediabetes (group C, n = 13, 26%), and normoglycemic (group D, n = 12, 24%). Duration of hospital stay and in-hospital mortality were noted. At 4 weeks post-discharge, HbA1c, along with the glucose tolerance test, was performed for groups C and D, and outcomes were recorded.

Results: Half of the hospital hyperglycemia patients were diabetic, although 26% of the patients with hospital hyperglycemia were unaware of their diabetes status. Average age and BMI were found to be higher in diabetes patients (25.63 ± 5.25 kg/m2) than prediabetes (22.98 ± 2.24 kg/m2) and normoglycemic patients (21.38 ± 2.37 kg/m2). Two deaths were encountered during hospital stay in the prediabetes group. At 4 weeks post-discharge, in group C, 2 (8.7%) developed diabetes, 4 (17.4%) had impaired fasting glucose, and 3 (13%) had impaired glucose tolerance. One prediabetes patient became normoglycemic. All 12 patients of group D remained normoglycemic.

Conclusion: Hospital hyperglycemia in diabetics as well as prediabetes subjects is associated with a higher age and BMI compared to normoglycemic individuals. Hospital hyperglycemia in prediabetes subjects is associated with higher mortality and greater propensity to develop diabetes in the short-term, compared to normoglycemic individuals.

简介:应激性高血糖与急性疾病有关,但对未来糖尿病的风险很少研究。医院高血糖,定义为院内随机血糖(RBG) >140 mg/dL,研究较少。本研究旨在确定医院高血糖患者的概况和短期预后。方法:对50例住院高血糖患者进行描述性随访研究。根据患者的HbA1c状态,将患者分为已知糖尿病(A组,n = 12,24%)、未确诊糖尿病(B组,n = 13,26%)、糖尿病前期(C组,n = 13,26%)和血糖正常(D组,n = 12,24%)。记录了住院时间和住院死亡率。出院后4周,C组和D组分别进行糖化血红蛋白和葡萄糖耐量试验,并记录结果。结果:半数医院高血糖患者为糖尿病患者,26%的医院高血糖患者不知道自己的糖尿病状态。糖尿病患者的平均年龄(25.63±5.25 kg/m2)高于糖尿病前期(22.98±2.24 kg/m2)和血糖正常患者(21.38±2.37 kg/m2)。糖尿病前期组住院期间有两人死亡。出院后4周,C组2例(8.7%)发生糖尿病,4例(17.4%)空腹血糖受损,3例(13%)糖耐量受损。一名糖尿病前期患者血糖恢复正常。D组12例患者血糖均保持正常。结论:与血糖正常者相比,糖尿病患者和前驱糖尿病患者的医院高血糖与更高的年龄和BMI相关。与血糖正常者相比,医院糖尿病前期患者的高血糖与更高的死亡率和更大的短期糖尿病发病倾向相关。
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引用次数: 0
E-health Initiatives for Screening and Management of Anemia in Rural Rajasthan. 拉贾斯坦邦农村贫血筛查和管理电子保健倡议。
Q3 Medicine Pub Date : 2026-03-01 DOI: 10.59556/japi.74.1333
Shweta Mangal, Disha Mangal, Ashok Kumar, Raja Babu Panwar

Introduction: Anemia is considered to be a public health issue of serious concern universally. In the current era of advancing technology, electronic health (e-health) initiatives are being employed in various health programs for disease screening and management. This study was planned to screen for anemia and manage it through a multidimensional approach comprising iron folic acid (IFA) supplementation, deworming among children, and dietary guidance and health education through pop-up videos with the aid of e-health initiatives.

Methods: This was a prospective cohort study. An Android e-application (app) was used on tablets to identify anemia after hemoglobin estimation through the Hemoglobin Color Scale. Accredited Social Health Activists (ASHAs) managed anemia by providing health education and dietary guidance through pop-up videos and IFA supplementation. Statistical analysis was done using the Statistical Package for the Social Sciences (SPSS) version 29. Tests of significance in the form of Cochran's Q, McNemar, chi-square, and repeated measures analysis of variance (ANOVA) and independent t-test were applied.

Results: The overall prevalence of anemia significantly declined from 46.08% at baseline to 14.65% at the 9th month. Males had a higher anemia prevalence (52.8%) compared to females (39.16%). An overall improvement of 68.2% was observed in the anemia status, with the maximum being in the 1-5-year age-group and females. Mean hemoglobin levels showed a consistent increase across all age-groups, with the maximum being in the 6-month-1-year age-group and females.

Conclusion: This study demonstrated that community-based, sustained, and targeted strategies through the use of e-health initiatives can effectively combat anemia and achieve significant improvements in hemoglobin levels across all age and gender groups.

贫血被认为是一个普遍关注的公共卫生问题。在当今技术进步的时代,电子健康(e-health)倡议被用于各种疾病筛查和管理的健康计划。该研究计划通过一种多维方法筛查贫血并对其进行管理,该方法包括补充叶酸铁(IFA)、在儿童中驱虫、在电子卫生倡议的帮助下通过弹出式视频进行饮食指导和健康教育。方法:这是一项前瞻性队列研究。通过血红蛋白色度评估血红蛋白后,在平板电脑上使用Android电子应用程序(app)来识别贫血。经认可的社会健康活动家(ASHAs)通过弹出式视频和IFA补充剂提供健康教育和饮食指导来管理贫血。使用社会科学统计软件包(SPSS)第29版进行统计分析。采用Cochran’s Q、McNemar、卡方、重复测量方差分析(ANOVA)和独立t检验进行显著性检验。结果:贫血的总体患病率从基线时的46.08%显著下降到第9个月时的14.65%。男性的贫血患病率(52.8%)高于女性(39.16%)。贫血状况总体改善68.2%,其中1-5岁年龄组和女性改善最大。平均血红蛋白水平在所有年龄组中均显示出一致的增加,最大的是6个月1岁年龄组和女性。结论:本研究表明,通过使用电子卫生倡议,以社区为基础的、持续的和有针对性的战略可以有效地对抗贫血,并在所有年龄和性别群体中显著改善血红蛋白水平。
{"title":"E-health Initiatives for Screening and Management of Anemia in Rural Rajasthan.","authors":"Shweta Mangal, Disha Mangal, Ashok Kumar, Raja Babu Panwar","doi":"10.59556/japi.74.1333","DOIUrl":"https://doi.org/10.59556/japi.74.1333","url":null,"abstract":"<p><strong>Introduction: </strong>Anemia is considered to be a public health issue of serious concern universally. In the current era of advancing technology, electronic health (e-health) initiatives are being employed in various health programs for disease screening and management. This study was planned to screen for anemia and manage it through a multidimensional approach comprising iron folic acid (IFA) supplementation, deworming among children, and dietary guidance and health education through pop-up videos with the aid of e-health initiatives.</p><p><strong>Methods: </strong>This was a prospective cohort study. An Android e-application (app) was used on tablets to identify anemia after hemoglobin estimation through the Hemoglobin Color Scale. Accredited Social Health Activists (ASHAs) managed anemia by providing health education and dietary guidance through pop-up videos and IFA supplementation. Statistical analysis was done using the Statistical Package for the Social Sciences (SPSS) version 29. Tests of significance in the form of Cochran's Q, McNemar, chi-square, and repeated measures analysis of variance (ANOVA) and independent <i>t</i>-test were applied.</p><p><strong>Results: </strong>The overall prevalence of anemia significantly declined from 46.08% at baseline to 14.65% at the 9th month. Males had a higher anemia prevalence (52.8%) compared to females (39.16%). An overall improvement of 68.2% was observed in the anemia status, with the maximum being in the 1-5-year age-group and females. Mean hemoglobin levels showed a consistent increase across all age-groups, with the maximum being in the 6-month-1-year age-group and females.</p><p><strong>Conclusion: </strong>This study demonstrated that community-based, sustained, and targeted strategies through the use of e-health initiatives can effectively combat anemia and achieve significant improvements in hemoglobin levels across all age and gender groups.</p>","PeriodicalId":22693,"journal":{"name":"The Journal of the Association of Physicians of India","volume":"74 3","pages":"26-30"},"PeriodicalIF":0.0,"publicationDate":"2026-03-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"147445251","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
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The Journal of the Association of Physicians of India
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