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Kikuchi Disease "A Lupus Mimicker": A Case Report. 菊池病 "狼疮的模仿者":病例报告
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.21
Aliya Juma Alsaadi, Saud Al Hashmi, Nabila Al-Julandani

Kikuchi disease, also called, Kikuchi-Fujimoto disease or histiocytic necrotizing lymphadenitis, is a rare self-limiting illness with an unknown etiology and pathogenesis. It is predominantly seen among young females. The cardinal clinical features include fever and cervical lymphadenopathy. Skin eruptions have also been reported. In Oman, two cases have been reported to date, in 2005 and 2020, with only one case exhibiting skin manifestations. There is a paucity of disease in our country and worldwide. In this case report, we discuss the diagnosis of Kikuchi disease in a previously healthy 17-year-old Omani female who presented with fever, cervical lymphadenopathy, and malar rash. The clinical picture in this case resembled that of systemic lupus erythematosus. Due to the rarity of Kikuchi disease, particularly in our region, it is crucial to consider it as a differential diagnosis when a patient exhibits the aforementioned symptoms to prevent misdiagnosis and inappropriate treatment, as it can easily be misdiagnosed as systemic lupus erythematosus.

菊池病又称菊池-藤本病或组织细胞坏死性淋巴结炎,是一种罕见的自限性疾病,病因和发病机制不明。它主要见于年轻女性。主要临床特征包括发热和颈淋巴结病变。皮肤糜烂也有报道。迄今为止,阿曼分别于 2005 年和 2020 年报告了两例病例,其中只有一例有皮肤表现。这种疾病在我国和全世界都很少见。在本病例报告中,我们讨论了对一名以前健康的 17 岁阿曼女性菊地病的诊断,该患者表现为发热、颈部淋巴结肿大和颊部皮疹。该病例的临床表现与系统性红斑狼疮相似。由于菊池病非常罕见,尤其是在我国地区,当患者出现上述症状时,必须将其作为鉴别诊断,以防误诊和治疗不当,因为菊池病很容易被误诊为系统性红斑狼疮。
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引用次数: 0
Translated Perinatal Grief Scale-Persian Version Requires Modified Analysis. 翻译后的围产期悲伤量表-波斯语版需要修改分析。
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.64
Elham Khoori, Tayebe Ziaei, Judith N Lasker
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引用次数: 0
Influential Factors in the Selection of Subspecialty Fellowship Training Among Surgical Trainees in Oman. 阿曼外科学员选择亚专科奖学金培训的影响因素。
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.66
Ghassan Al Habsi, Ahmed Al Ghaithi, Yousef Al Weshahi, Ahmed Jahwari

Objectives: Surgical training has evolved over the past few decades, with an increasing number of surgeons pursuing subspecialty training through fellowship programs across various surgical specialties. While published reports confirm this trend, few studies explored the factors that determine which fellowship training surgical residents would pursue. This cross-sectional study aims to investigate the factors influencing fellowship choices made by surgical trainees in Oman.

Methods: An online questionnaire, developed based on previously validated instruments, included 14 factors considered crucial for choosing a future career. Statistical analysis was performed to determine item-level validity, scale-level validity, and reliability. The survey was distributed via email and closed after six weeks for data analysis.

Results: The survey achieved a response rate of 60.9%. The analysis revealed that the most influential factor among surveyed surgeons in selecting a subspecialty was prestige, with an average score of 2.7. The least reported influential factors were variety of cases (average score of 1.8) and personal interest (average score of 1.4). Only 57.7% of respondents received career choice guidance.

Conclusions: Factors influencing the choice of surgical subspecialties vary among the different groups. This information can be valuable in designing programs and structuring professional career guidance and counseling.

目的:过去几十年来,外科培训不断发展,越来越多的外科医生通过各种外科专业的研究金项目接受亚专业培训。虽然已发表的报告证实了这一趋势,但很少有研究探讨决定外科住院医生接受哪种研究金培训的因素。本横断面研究旨在调查影响阿曼外科学员选择奖学金的因素:方法:根据以前验证过的工具编制了一份在线问卷,其中包括 14 个被认为对选择未来职业至关重要的因素。对问卷进行了统计分析,以确定项目有效性、量表有效性和可靠性。调查通过电子邮件发送,并在六周后结束,以便进行数据分析:调查的回复率为 60.9%。分析显示,受访外科医生在选择亚专科时最有影响力的因素是声望,平均得分为 2.7 分。影响最小的因素是病例的多样性(平均分为 1.8 分)和个人兴趣(平均分为 1.4 分)。只有 57.7% 的受访者接受过职业选择指导:结论:不同群体选择外科亚专业的影响因素各不相同。这些信息对于设计计划和构建专业职业指导与咨询很有价值。
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引用次数: 0
A Rare Case of Familial Methemoglobinemia with Congenital Heart Disease. 家族性高铁血红蛋白血症伴先天性心脏病的罕见病例
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.16
Jhasaketan Nayak, Karthik Kumar, Sashi Kant Singh, Gaurav Dhingra, Uttam Kumar Nath

Methemoglobinemia is a rare dyshemoglobin disorder which can either be congenital or acquired. Dyshemoglobin disorders can be asymptomatic or symptomatic. We narrate the case of a 12-year-old girl who presented with a fever, cough, and oxygen saturation of 85%. She was diagnosed with COVID-19, along with a large atrial septal defect and pulmonary arterial hypertension. Arterial blood gas analysis revealed normal partial pressure of oxygen and on 100% exposure to oxygen, blood color turned chocolate brown. After the resolution of COVID-19 in 10 days, the patient was treated with oral ascorbic acid and successful atrial septal defect repair. It is important to suspect dyshemoglobin disorder in a patient who presents with hypoxia/hypoxemia.

高铁血红蛋白症是一种罕见的血红蛋白异常疾病,可以是先天性的,也可以是后天获得的。血红蛋白异常症可以是无症状的,也可以是有症状的。我们讲述了一个 12 岁女孩的病例,她出现发烧、咳嗽和血氧饱和度 85%。她被诊断为 COVID-19,同时伴有房间隔缺损和肺动脉高压。动脉血气分析显示氧分压正常,100%接触氧气时,血液颜色变成巧克力色。COVID-19 在 10 天内缓解后,患者接受了口服抗坏血酸治疗,并成功修复了房间隔缺损。对于出现缺氧/低氧血症的患者,怀疑血红蛋白异常非常重要。
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引用次数: 0
Idiopathic Capillary Leak Syndrome (Clarkson's Disease): First Reported Case in Oman. 特发性毛细血管渗漏综合征(克拉克森病):阿曼首例报告病例
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.17
Fatma Al-Zaabi, Hatem Al-Farhan, Ali Al-Lawati, Mujahid Al-Busaidi

Idiopathic capillary leak syndrome, also known as Clarkson's Disease, is a rare cause of hypovolemic shock that physicians should be aware of. It is characterized by a state of hypovolemia with features of widespread fluid third spacing and poses diagnostic and therapeutic challenges. Here, we present a challenging case of a 36-year-old woman who experienced recurrent episodes of widespread edema and hypovolemic shock symptoms suggestive of capillary leak syndrome. The resuscitative and therapeutic measures employed in managing this disease are described in this case report.

特发性毛细血管渗漏综合征又称克拉克森氏病,是导致低血容量性休克的一种罕见病因,医生应该对此有所了解。它的特点是低血容量状态,并伴有广泛的液体三分之一间隔,给诊断和治疗带来了挑战。在此,我们介绍一例具有挑战性的病例,患者是一名 36 岁女性,反复出现广泛水肿和低血容量休克症状,提示为毛细血管渗漏综合征。本病例报告介绍了治疗该病的抢救和治疗措施。
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引用次数: 0
Evaluating the Impact of Pulmonary Arterial Hypertension Therapies on Pericardial Effusion and Patient Survival. 评估肺动脉高压疗法对心包积液和患者存活率的影响。
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.82
Arif Albulushi, Shabib Al-Asmi, Moosa Al-Abri, Hatem Al-Farhan

Objectives: To evaluate the impact of Pulmonary Arterial Hypertension (PAH) therapies on the incidence of pericardial effusion and its prognostic implications for patient survival.

Methods: This retrospective cohort study included 60 patients diagnosed with PAH at a high-volume tertiary care center, treated with intravenous or subcutaneous prostanoids. Data were collected from 2015 to 2019, including echocardiographic assessments, right heart catheterization, World Health Organization functional class evaluations, six-minute walk distance tests, and biomarkers such as brain natriuretic peptide and N-terminal prohormone of brain natriuretic peptide. Follow-up was conducted at least 90 days post-treatment initiation.

Results: Pericardial effusion was observed in 31.7% of patients before therapy. Patients with moderate to large effusions had a significantly higher mortality risk (HR = 1.92; 95% CI 1.1-44.78; p =0.0044), while small effusions appeared protective (HR = 0.27; 95% CI 0.15-0.48; p =0.006). Survival rates declined from 89% at one year to 71% at three years post-therapy, with effusion presence correlating with more severe PAH manifestations.

Conclusions: Initial pericardial effusion severity is a critical predictor of mortality in PAH patients. Early assessment and stratified management of pericardial effusion are essential for optimizing therapeutic outcomes in PAH management. Future research should explore targeted interventions for managing pericardial effusion to improve patient prognosis.

目的评估肺动脉高压(PAH)疗法对心包积液发生率的影响及其对患者生存预后的影响:这项回顾性队列研究纳入了在一家高容量三级医疗中心确诊的60名PAH患者,这些患者接受了静脉或皮下前列腺素治疗。数据收集时间为 2015 年至 2019 年,包括超声心动图评估、右心导管检查、世界卫生组织功能分级评估、六分钟步行距离测试以及脑钠肽和脑钠肽 N 端前体等生物标志物。治疗开始后至少 90 天进行随访:结果:31.7%的患者在治疗前出现心包积液。中度至大量积液患者的死亡风险明显较高(HR = 1.92;95% CI 1.1-44.78;P =0.0044),而少量积液似乎具有保护作用(HR = 0.27;95% CI 0.15-0.48;P =0.006)。治疗后的存活率从一年的89%下降到三年的71%,积液的存在与更严重的PAH表现相关:结论:最初的心包积液严重程度是预测 PAH 患者死亡率的关键因素。心包积液的早期评估和分层管理对于优化 PAH 治疗效果至关重要。未来的研究应探索管理心包积液的针对性干预措施,以改善患者的预后。
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引用次数: 0
Complementary and Alternative Medicine for People with Epilepsy: Opinions of Physicians in Oman. 癫痫患者的补充和替代医学:阿曼医生的观点。
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.70
Abdullah Al-Asmi, Fatema Al Sabahi, Samir Al-Adawi, Intisar Al-Yaqoubi, Sanjay Jaju, Moon Fai Chan, Haifa Al-Abri, Zahir Al-Anqoodi, Ali A Asadi-Pooya

Objectives: Several studies have explored the opinions of healthcare workers on the use of complementary and alternative medicine (CAM) in epilepsy treatment. We sought to survey the views of non-neurologist and non-psychiatrist physicians in Oman on the use of CAM for epilepsy.

Methods: We used convenience sampling to recruit physicians (except neurologists and psychiatrists) from all 11 governorates of Oman. The online questionnaire was open to physicians from 5 January 2022 to 15 February 2023. This study collected anonymous data on their demographics, discipline, work settings, geographical area, and years of practice. Additionally, participants were asked to answer questions about their perception of CAM use and its effectiveness in treating epilepsy.

Results: A total of 190 physicians participated, of whom 69.5% were men. Respondents were mostly 36 to 45 years old (51.1%). The majority (52.1%) were general practitioners, 21.1% were internists, 17.9% were pediatricians, and 8.9% were family physicians. Most participants (n = 144; 75.8%) believed that CAM may help treat patients with epilepsy (PWE). The most common therapies that participants considered helpful were meditation (46.0%), prayers (44.7%), yoga (32.6%), and exercise (31.1%).

Conclusions: While the evidence supporting the use of CAM for the treatment of epilepsy is scarce, this survey showed that most physicians (non-neurologists and non-psychiatrists), who manage PWE in Oman, believed that some CAM modalities would help treat epilepsy. Well-designed controlled trials are needed to provide reliable evidence on the usefulness of CAM options in PWE.

目的:有几项研究探讨了医护人员对在癫痫治疗中使用补充和替代医学(CAM)的看法。我们试图调查阿曼非神经科和非精神病科医生对使用 CAM 治疗癫痫的看法:我们采用方便抽样的方法,从阿曼的所有 11 个省招募医生(神经科医生和精神科医生除外)。在线问卷从 2022 年 1 月 5 日至 2023 年 2 月 15 日向医生开放。本研究收集了有关人口统计学、学科、工作环境、地理区域和从业年限的匿名数据。此外,还要求参与者回答有关他们对使用 CAM 及其治疗癫痫有效性的看法的问题:共有 190 名医生参加了调查,其中 69.5% 为男性。受访者的年龄大多在 36 至 45 岁之间(51.1%)。大多数(52.1%)是全科医生,21.1%是内科医生,17.9%是儿科医生,8.9%是家庭医生。大多数参与者(n = 144;75.8%)认为 CAM 可以帮助治疗癫痫患者(PWE)。参与者认为最常见的疗法是冥想(46.0%)、祈祷(44.7%)、瑜伽(32.6%)和运动(31.1%):虽然支持使用 CAM 治疗癫痫的证据很少,但这项调查显示,阿曼大多数管理病患的医生(非神经病学家和非精神病学家)都认为某些 CAM 方式有助于治疗癫痫。需要进行设计良好的对照试验,以提供可靠的证据,说明治疗癫痫病的 CAM 方案对病患是否有用。
{"title":"Complementary and Alternative Medicine for People with Epilepsy: Opinions of Physicians in Oman.","authors":"Abdullah Al-Asmi, Fatema Al Sabahi, Samir Al-Adawi, Intisar Al-Yaqoubi, Sanjay Jaju, Moon Fai Chan, Haifa Al-Abri, Zahir Al-Anqoodi, Ali A Asadi-Pooya","doi":"10.5001/omj.2024.70","DOIUrl":"https://doi.org/10.5001/omj.2024.70","url":null,"abstract":"<p><strong>Objectives: </strong>Several studies have explored the opinions of healthcare workers on the use of complementary and alternative medicine (CAM) in epilepsy treatment. We sought to survey the views of non-neurologist and non-psychiatrist physicians in Oman on the use of CAM for epilepsy.</p><p><strong>Methods: </strong>We used convenience sampling to recruit physicians (except neurologists and psychiatrists) from all 11 governorates of Oman. The online questionnaire was open to physicians from 5 January 2022 to 15 February 2023. This study collected anonymous data on their demographics, discipline, work settings, geographical area, and years of practice. Additionally, participants were asked to answer questions about their perception of CAM use and its effectiveness in treating epilepsy.</p><p><strong>Results: </strong>A total of 190 physicians participated, of whom 69.5% were men. Respondents were mostly 36 to 45 years old (51.1%). The majority (52.1%) were general practitioners, 21.1% were internists, 17.9% were pediatricians, and 8.9% were family physicians. Most participants (n = 144; 75.8%) believed that CAM may help treat patients with epilepsy (PWE). The most common therapies that participants considered helpful were meditation (46.0%), prayers (44.7%), yoga (32.6%), and exercise (31.1%).</p><p><strong>Conclusions: </strong>While the evidence supporting the use of CAM for the treatment of epilepsy is scarce, this survey showed that most physicians (non-neurologists and non-psychiatrists), who manage PWE in Oman, believed that some CAM modalities would help treat epilepsy. Well-designed controlled trials are needed to provide reliable evidence on the usefulness of CAM options in PWE.</p>","PeriodicalId":19667,"journal":{"name":"Oman Medical Journal","volume":"39 3","pages":"e629"},"PeriodicalIF":0.0,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11422801/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142351426","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Simultaneous Pancreatic and Kidney Transplant in Adult with Autosomal Dominant Polycystic Kidney Disease and Type I Diabetes Mellitus: Post Surgical Events and Genetic Review. 常染色体显性多囊肾和 I 型糖尿病成人的胰肾同时移植:手术后事件和遗传学回顾。
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.18
Intisar Al Alawi, Ehab Mohammed, Fatma Al Rahbi, AbdelMasieh Metry, Suad Hannawi, Issa Al Salmi

Autosomal dominant polycystic kidney disease (ADPKD) is a common inherited condition characterized by the growth of multiple bilateral cysts in the kidneys. We describe the case of a 35-year-old male with combined ADPKD and type 1 diabetes mellitus with a strong family history of both. At the age of 32, he developed end-stage kidney disease for which he underwent preemptive simultaneous pancreatic and kidney transplant, which in turn led to multiple perioperative complications. Evaluation of familial clustering of genetic disease is critical in genetic epidemiology and precision medicine as it enables estimation of lifetime disease risk and early assessment as well as detection of the disease among one's siblings.

常染色体显性多囊肾病(ADPKD)是一种常见的遗传性疾病,其特征是肾脏中长出多个双侧囊肿。我们描述了一例 35 岁男性患者的病例,他同时患有 ADPKD 和 1 型糖尿病,并有家族遗传史。32 岁时,他患上了终末期肾病,为此他接受了先期同时进行的胰腺和肾脏移植手术,而这又导致了多种围手术期并发症。评估遗传病的家族聚集性在遗传流行病学和精准医疗中至关重要,因为它可以估算终生患病风险,并在兄弟姐妹中进行早期评估和疾病检测。
{"title":"Simultaneous Pancreatic and Kidney Transplant in Adult with Autosomal Dominant Polycystic Kidney Disease and Type I Diabetes Mellitus: Post Surgical Events and Genetic Review.","authors":"Intisar Al Alawi, Ehab Mohammed, Fatma Al Rahbi, AbdelMasieh Metry, Suad Hannawi, Issa Al Salmi","doi":"10.5001/omj.2024.18","DOIUrl":"10.5001/omj.2024.18","url":null,"abstract":"<p><p>Autosomal dominant polycystic kidney disease (ADPKD) is a common inherited condition characterized by the growth of multiple bilateral cysts in the kidneys. We describe the case of a 35-year-old male with combined ADPKD and type 1 diabetes mellitus with a strong family history of both. At the age of 32, he developed end-stage kidney disease for which he underwent preemptive simultaneous pancreatic and kidney transplant, which in turn led to multiple perioperative complications. Evaluation of familial clustering of genetic disease is critical in genetic epidemiology and precision medicine as it enables estimation of lifetime disease risk and early assessment as well as detection of the disease among one's siblings.</p>","PeriodicalId":19667,"journal":{"name":"Oman Medical Journal","volume":"1 1","pages":"e636"},"PeriodicalIF":0.0,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11263795/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"70684595","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Role of Serum and Urine Neutrophil Gelatinase-associated Lipocalin as Biomarkers for Assessing Graft Function in Kidney Transplant Recipients. 血清和尿液中性粒细胞明胶酶相关脂质体作为评估肾移植受者移植物功能的生物标记物的作用
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.71
Shankar Prasad Nagaraju, Shilna Muttickal Swaminathan, Shruti Bhattacharya, Ravindra Prabhu Attur, Dharshan Rangaswamy, Indu Ramachandra Rao, Srinivas Vinayak Shenoy, Mohan Varadanayakanahalli Bhojaraja

Objectives: The existing biomarkers used to promptly identify graft dysfunction after kidney transplantation lack consistency. Neutrophil gelatinase-associated lipocalin (NGAL) appears to be a promising biomarker but its levels measured from serum and urine have demonstrated varying predictive values. Our study aimed to explore the potential of NGAL as a biomarker in predicting graft dysfunction in kidney transplant patients, including live and deceased donor recipients.

Methods: A single-centered observational cohort study with live and deceased kidney recipients as participants was conducted between 2018 and 2022 at a tertiary care hospital in Southern India. Serum creatinine levels were monitored daily; creatinine reduction on day two and day seven were calculated. The recipients were categorized based on graft recovery into three groups: delayed graft function (DGF), slow graft function (SGF), or immediate graft function (IGF). Analysis of serum and urine NGAL was conducted two hours after the transplant and their predictive values were evaluated by the area under the curves (AUC) method.

Results: Of the 40 participants, 34 (85.0%) received their transplant from live-related donors, while six (15.0%) received kidneys from deceased donors. DGF occurred in four (10.0%) patients, SGF in 12 (30.0%), and 24 (60.0%) patients achieved IGF. Serum NGAL demonstrated higher sensitivity compared to urine NGAL. At a cut-off value of 678 ng/mL (AUC = 0.77), serum NGAL showed 90.0% sensitivity and 53.0% specificity. Urine NGAL had 70.0% sensitivity and 74.0% specificity at a cut-off value of 489 ng/mL (AUC = 0.72).

Conclusions: Kidney recipients in SGF and DGF categories had elevated levels of serum and urine NGAL compared to those without IGF. Although serum NGAL showed higher sensitivity than urine NGAL in predicting graft dysfunction, both markers lacked the specificity needed for accurate predictions.

目的:现有用于及时识别肾移植后移植物功能障碍的生物标志物缺乏一致性。中性粒细胞明胶酶相关脂联素(NGAL)似乎是一种很有前景的生物标志物,但其在血清和尿液中的水平却显示出不同的预测价值。我们的研究旨在探索 NGAL 作为生物标记物预测肾移植患者(包括活体和死亡供体受者)移植物功能障碍的潜力:2018 年至 2022 年期间,印度南部一家三级医院开展了一项以活体和已故肾脏受者为参与者的单中心观察性队列研究。每天监测血清肌酐水平;计算第二天和第七天的肌酐降幅。受者根据移植物恢复情况分为三组:延迟移植物功能组(DGF)、缓慢移植物功能组(SGF)或即时移植物功能组(IGF)。移植两小时后进行血清和尿液 NGAL 分析,并用曲线下面积(AUC)法评估其预测值:结果:在 40 名参与者中,34 人(85.0%)的移植肾来自活体捐献者,6 人(15.0%)的移植肾来自已故捐献者。4名患者(10.0%)出现 DGF,12 名患者(30.0%)出现 SGF,24 名患者(60.0%)出现 IGF。与尿液 NGAL 相比,血清 NGAL 的灵敏度更高。截断值为 678 ng/mL(AUC = 0.77)时,血清 NGAL 的灵敏度为 90.0%,特异度为 53.0%。尿液 NGAL 的灵敏度为 70.0%,特异性为 74.0%,临界值为 489 ng/mL(AUC = 0.72):结论:与没有IGF的肾脏受者相比,SGF和DGF类别的肾脏受者血清和尿液NGAL水平升高。虽然在预测移植物功能障碍方面,血清 NGAL 的灵敏度高于尿液 NGAL,但这两种标记物都缺乏准确预测所需的特异性。
{"title":"Role of Serum and Urine Neutrophil Gelatinase-associated Lipocalin as Biomarkers for Assessing Graft Function in Kidney Transplant Recipients.","authors":"Shankar Prasad Nagaraju, Shilna Muttickal Swaminathan, Shruti Bhattacharya, Ravindra Prabhu Attur, Dharshan Rangaswamy, Indu Ramachandra Rao, Srinivas Vinayak Shenoy, Mohan Varadanayakanahalli Bhojaraja","doi":"10.5001/omj.2024.71","DOIUrl":"10.5001/omj.2024.71","url":null,"abstract":"<p><strong>Objectives: </strong>The existing biomarkers used to promptly identify graft dysfunction after kidney transplantation lack consistency. Neutrophil gelatinase-associated lipocalin (NGAL) appears to be a promising biomarker but its levels measured from serum and urine have demonstrated varying predictive values. Our study aimed to explore the potential of NGAL as a biomarker in predicting graft dysfunction in kidney transplant patients, including live and deceased donor recipients.</p><p><strong>Methods: </strong>A single-centered observational cohort study with live and deceased kidney recipients as participants was conducted between 2018 and 2022 at a tertiary care hospital in Southern India. Serum creatinine levels were monitored daily; creatinine reduction on day two and day seven were calculated. The recipients were categorized based on graft recovery into three groups: delayed graft function (DGF), slow graft function (SGF), or immediate graft function (IGF). Analysis of serum and urine NGAL was conducted two hours after the transplant and their predictive values were evaluated by the area under the curves (AUC) method.</p><p><strong>Results: </strong>Of the 40 participants, 34 (85.0%) received their transplant from live-related donors, while six (15.0%) received kidneys from deceased donors. DGF occurred in four (10.0%) patients, SGF in 12 (30.0%), and 24 (60.0%) patients achieved IGF. Serum NGAL demonstrated higher sensitivity compared to urine NGAL. At a cut-off value of 678 ng/mL (AUC = 0.77), serum NGAL showed 90.0% sensitivity and 53.0% specificity. Urine NGAL had 70.0% sensitivity and 74.0% specificity at a cut-off value of 489 ng/mL (AUC = 0.72).</p><p><strong>Conclusions: </strong>Kidney recipients in SGF and DGF categories had elevated levels of serum and urine NGAL compared to those without IGF. Although serum NGAL showed higher sensitivity than urine NGAL in predicting graft dysfunction, both markers lacked the specificity needed for accurate predictions.</p>","PeriodicalId":19667,"journal":{"name":"Oman Medical Journal","volume":"39 3","pages":"e630"},"PeriodicalIF":0.0,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11512701/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142505340","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Medical Tourism and Neurological Diseases: Omani Patients' Experience Seeking Treatment Abroad. 医疗旅游与神经系统疾病:阿曼患者在国外就医的经历。
Q2 Medicine Pub Date : 2024-05-30 eCollection Date: 2024-05-01 DOI: 10.5001/omj.2024.69
Abdullah Al-Asmi, Fatma Sultan Al-Jabri, Sara Abdullah Al-Amrani, Yahya Al Farsi, Fatema Al Sabahi, Amna Al-Futaisi, Samir Al-Adawi

Objectives: There is a dearth of research regarding the motivations and experiences of Omani nationals who travel abroad for medical treatment, especially for neurological diseases. The primary objective was to examine and draw comparisons between Omani adults and children with neurological disorders who pursued medical treatment abroad after being evaluated by local specialists. The study also aimed to gain insights into these patients' motivations and experiences. A related objective was to explore the sociocultural factors and family dynamics that shape the attitudes towards illness and treatment seeking.

Methods: In this cross-sectional study, Omani patients treated at a major tertiary hospital in Muscat for neurological disorders and subsequently traveled overseas for treatment were identified and administered a structured questionnaire.

Results: The participants were 116 Omani nationals (62 children and 54 adults) with neurological disorders, diagnosed predominantly with epilepsy (71.6%) followed by developmental delay, muscular dystrophy, and encephalopathy. Only 19.8% of patients received government sponsorship. The majority (69.8%) followed the recommendations of family members. Most (63.8%) participants reported positive outcomes after treatment abroad, though 4.3% developed complications and 5.2% acquired nosocomial infections. Most (83.6%) participants opined that the treatment they received overseas was comparable to what they would have received in Oman. There were no significant differences between children and adults in most of these aspects.

Conclusions: Public awareness should be increased regarding the pros and cons of medical tourism. Patients must be made aware of the advanced treatment facilities available locally. Efforts should be made to enhance patient outcomes and satisfaction by adopting more efficient and patient-friendly processes.

目的:有关阿曼国民出国就医(尤其是治疗神经系统疾病)的动机和经历的研究十分匮乏。本研究的主要目的是对患有神经系统疾病的阿曼成人和儿童在接受当地专家评估后到国外就医的情况进行研究和比较。研究还旨在深入了解这些患者的动机和经历。与此相关的一个目标是探索影响人们对疾病和寻求治疗的态度的社会文化因素和家庭动态:在这项横断面研究中,确定了在马斯喀特一家大型三级医院接受神经系统疾病治疗、随后前往海外接受治疗的阿曼患者,并对他们进行了结构化问卷调查:结果:116 名阿曼国民(62 名儿童和 54 名成人)患有神经系统疾病,主要诊断为癫痫(71.6%),其次是发育迟缓、肌肉萎缩症和脑病。只有 19.8% 的患者获得了政府资助。大多数患者(69.8%)听从家人的建议。大多数参与者(63.8%)在国外接受治疗后取得了积极的疗效,但也有 4.3% 的患者出现了并发症,5.2% 的患者出现了院内感染。大多数参与者(83.6%)认为,他们在国外接受的治疗与在阿曼接受的治疗效果相当。在这些方面,儿童和成人之间没有明显差异:应提高公众对医疗旅游利弊的认识。必须让患者了解当地先进的治疗设施。应通过采用更高效、更方便患者的流程,努力提高患者的治疗效果和满意度。
{"title":"Medical Tourism and Neurological Diseases: Omani Patients' Experience Seeking Treatment Abroad.","authors":"Abdullah Al-Asmi, Fatma Sultan Al-Jabri, Sara Abdullah Al-Amrani, Yahya Al Farsi, Fatema Al Sabahi, Amna Al-Futaisi, Samir Al-Adawi","doi":"10.5001/omj.2024.69","DOIUrl":"10.5001/omj.2024.69","url":null,"abstract":"<p><strong>Objectives: </strong>There is a dearth of research regarding the motivations and experiences of Omani nationals who travel abroad for medical treatment, especially for neurological diseases. The primary objective was to examine and draw comparisons between Omani adults and children with neurological disorders who pursued medical treatment abroad after being evaluated by local specialists. The study also aimed to gain insights into these patients' motivations and experiences. A related objective was to explore the sociocultural factors and family dynamics that shape the attitudes towards illness and treatment seeking.</p><p><strong>Methods: </strong>In this cross-sectional study, Omani patients treated at a major tertiary hospital in Muscat for neurological disorders and subsequently traveled overseas for treatment were identified and administered a structured questionnaire.</p><p><strong>Results: </strong>The participants were 116 Omani nationals (62 children and 54 adults) with neurological disorders, diagnosed predominantly with epilepsy (71.6%) followed by developmental delay, muscular dystrophy, and encephalopathy. Only 19.8% of patients received government sponsorship. The majority (69.8%) followed the recommendations of family members. Most (63.8%) participants reported positive outcomes after treatment abroad, though 4.3% developed complications and 5.2% acquired nosocomial infections. Most (83.6%) participants opined that the treatment they received overseas was comparable to what they would have received in Oman. There were no significant differences between children and adults in most of these aspects.</p><p><strong>Conclusions: </strong>Public awareness should be increased regarding the pros and cons of medical tourism. Patients must be made aware of the advanced treatment facilities available locally. Efforts should be made to enhance patient outcomes and satisfaction by adopting more efficient and patient-friendly processes.</p>","PeriodicalId":19667,"journal":{"name":"Oman Medical Journal","volume":"39 3","pages":"e628"},"PeriodicalIF":0.0,"publicationDate":"2024-05-30","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11491769/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"142471743","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":0,"RegionCategory":"","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"OA","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
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