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The Need to Vaccinate Against COVID-19 接种COVID-19疫苗的必要性
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2022-0058
T. Sim
Globally, now in the third year of the pandemic, COVID-19 deaths have exceeded more than 6 million. As new subvariants emerge and spread, vaccines work to limit the worst of COVID-19 and continue to be important. Restraints are lifted, and COVID-19 may be seen as done for some, but COVID-19 is not yet done with others, no matter how badly everyone wants it to end. The SARS-CoV-2 pandemic has caused considerable morbidity and mortality worldwide. The protection provided by vaccines and booster doses offer a method of mitigating severe clinical outcomes and mortality. As debates over additional booster shots for COVID-19 intensify, many researchers are looking to the universal coronavirus vaccine model as a guide for managing future variants of SARS-CoV-2 and preempt the next COVID-19 surge.
在全球范围内,2019冠状病毒病大流行已进入第三年,死亡人数已超过600万。随着新的亚变体的出现和传播,疫苗可以限制COVID-19的最坏情况,并继续发挥重要作用。限制解除了,对一些人来说,COVID-19可能已经结束,但对另一些人来说,COVID-19还没有结束,无论每个人都多么希望它结束。SARS-CoV-2大流行在全球造成了相当大的发病率和死亡率。疫苗和加强剂提供的保护提供了一种减轻严重临床结果和死亡率的方法。随着关于COVID-19额外加强注射的争论愈演愈烈,许多研究人员正在寻求通用冠状病毒疫苗模型,作为管理未来SARS-CoV-2变体的指南,并预防下一次COVID-19激增。
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引用次数: 0
Telemedicine Screening of the Prevalence of Diabetic Retinopathy Among Type 2 Diabetic Filipinos in the Community 菲律宾社区2型糖尿病患者糖尿病视网膜病变患病率的远程医疗筛查
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2022-0024
Jessica Daza, Jocelyn Sy, M. V. Rondaris, John Philip Uy
Purpose: To determine the feasibility of telemedicine screening for diabetic retinopathy in a community setting and to determine the prevalence of diabetic retinopathy among Filipino patients with type 2 diabetes in the community. Study Design: Cross-sectional study among patients with type 2 diabetes in six community health centers in an urban city in the Philippines. Materials and methods: Subjects were examined from November 2018 to December 2018. A three-field non-mydriatic 45’ fundus photographs were taken for each patient and photographs were uploaded in cloud storage and read by a retina specialist in a tertiary hospital for assessment of diabetic retinopathy and grading of the fundus photographs. The results were sent back to local health centers. Results: A total of 387 eyes of 195 persons were examined. Overall, 288 out of 387 eyes (95.36%) had gradable quality fundus photo (grade 3 and higher) and did not need eye dilation. Prevalence of diabetic retinopathy among the respondents was 25.26% - 3.16% had mild diabetic retinopathy, 15.79% had moderate diabetic retinopathy, 3.68% had severe diabetic retinopathy, and 3.68% had proliferative diabetic retinopathy. Other fundus findings noted include hypertensive retinopathy glaucomatous optic nerve, age-related macular degeneration, posterior vitreous detachment, clinically significant macular edema, and epiretinal membrane. Conclusion: Due to the significant number of patients with diabetic retinopathy among type 2 diabetics in the community, telemedicine screening was a feasible alternative to dilated fundus examination and may be considered as part of the local health program to prevent blindness due to diabetes.
目的:确定远程医疗筛查社区糖尿病视网膜病变的可行性,并确定菲律宾社区2型糖尿病患者糖尿病视网膜病变的患病率。研究设计:在菲律宾一个城市的六个社区卫生中心对2型糖尿病患者进行横断面研究。材料与方法:研究时间为2018年11月至2018年12月。为每位患者拍摄三场无散瞳的45 '眼底照片,并将照片上传到云存储中,由三级医院的视网膜专家阅读,以评估糖尿病视网膜病变和眼底照片的分级。检测结果被送回当地的医疗中心。结果:共检查195人387只眼。总体而言,387只眼睛中有288只(95.36%)的眼底照片质量可分级(3级及以上),不需要扩眼。受访人群糖尿病视网膜病变患病率为:轻度糖尿病视网膜病变25.26% ~ 3.16%,中度糖尿病视网膜病变15.79%,重度糖尿病视网膜病变3.68%,增殖性糖尿病视网膜病变3.68%。其他眼底表现包括高血压性视网膜病变、青光眼视神经、年龄相关性黄斑变性、玻璃体后脱离、临床显著的黄斑水肿和视网膜前膜。结论:由于社区2型糖尿病患者中糖尿病视网膜病变患者数量较多,远程医疗筛查是一种可行的替代眼底扩张检查的方法,可以考虑作为当地卫生计划的一部分,以预防糖尿病致盲。
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引用次数: 1
Effects of Aeroallergen Sensitization on Symptom Severity, Pulmonary Function, and Bronchodilator Response in Children With Bronchial Asthma 空气过敏原致敏对支气管哮喘患儿症状严重程度、肺功能和支气管扩张剂反应的影响
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2019-0003
Glaiza M Madulara, Agnes G. Andaya
Background: Allergen sensitization, symptom severity, pulmonary function test, and bronchodilator response are important in the diagnosis and treatment of asthma. However, the relationship between these factors remains unclear. Objective: The objective of this study was to investigate the relationship between aeroallergen sensitization and asthma severity, pulmonary function, and bronchodilator response among pediatric patients with bronchial asthma. Methods: This was a prospective study where 155 pediatric patients aged 7–18 years old with bronchial asthma were recruited from Outpatient Clinics. Patients who met the inclusion criteria proceeded with spirometry and aeroallergen skin prick test. Results: There was a significant degree of sensitization, wherein 100% of the patients had sensitization to one or more aeroallergens. Among these children, 106 (68%) were polysensitized. The polysensitized group had more severe and persistent asthma severity profile (p<0.001) and worse pulmonary function (p<0.001). The frequency of abnormal pre-bronchodilator lung function of the polysensitized group was higher than the monosensitized group (p<0.001). A positive bronchodilator response was higher among polysensitized children as compared to monosensitized children (p<0.001). Sensitization to Dermatophagoides farinae, Dermatophagoides pteronyssinus and dog correlated with impairment of both the large airways and distal small airways while sensitization to cat, cockroach, and horse correlated only with impairment of the large airways (p<0.05). Patients sensitized to D. farinae, D. pteronyssinus, cat and dog had significant bronchodilator response (p<0.05). Conclusion: Polysensitized asthmatic children had a more persistent and severe asthma profile, worse pulmonary function, and higher bronchodilator reversibility compared to the monosensitized group.
背景:过敏原致敏性、症状严重程度、肺功能检查和支气管扩张剂反应是哮喘诊断和治疗的重要指标。然而,这些因素之间的关系尚不清楚。目的:探讨小儿支气管哮喘患者气致过敏原致敏与哮喘严重程度、肺功能和支气管扩张剂反应的关系。方法:这是一项前瞻性研究,从门诊诊所招募了155名7-18岁的支气管哮喘患儿。符合纳入标准的患者进行肺活量测定和空气过敏原皮肤点刺试验。结果:有明显程度的致敏,其中100%的患者对一种或多种空气过敏原过敏。这些儿童中,106例(68%)为多敏化。多致敏组哮喘严重程度和持续性更严重(p<0.001),肺功能更差(p<0.001)。多致敏组支气管扩张前肺功能异常频次高于单致敏组(p<0.001)。与单致敏儿童相比,多致敏儿童的支气管扩张剂阳性反应更高(p<0.001)。对粉棘棘球螨、翼状棘球螨和狗致敏与大气道和远端小气道损伤均相关,而对猫、蟑螂和马致敏仅与大气道损伤相关(p<0.05)。粉蝶、蝶窦、猫、狗致敏患者支气管扩张剂反应显著(p<0.05)。结论:与单致敏组相比,多致敏哮喘患儿具有更持久和更严重的哮喘特征,更差的肺功能和更高的支气管扩张剂可逆性。
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引用次数: 0
Dextrose Prolotherapy for Supraspinatus Partial Tear: A Case Report 葡萄糖前体治疗冈上肌部分撕裂1例
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2022-0054
Teinny Suryadi, A. Suhaimi, Frandy Susatia, Wahida Ratnawati, Winny Winaldy, Lin Chia-Hung
Introduction: Rotator cuff (RC) tears account for about 20% of RC disorders and presents with severe shoulder pain that can significantly impact activities of daily life. Case report: A 34-year-old male with a history of chronic right shoulder pain presents with tenderness at the lateral shoulder, positive subacromial impingement tests, painful end range of motion and pain score of 6. Ultrasound shows a partial supraspinatus tear at the bursal side. The patient was treated with 15% dextrose to the supraspinatus tendon intrasubstance 3 times, for 4 weeks. Result: Significant pain improvement after the first treatment (VAS 1), with pain-free full range of motion until 4 weeks after treatment and sonographic evidence of supraspinatus tendon healing. Discussion: Dextrose concentrations higher than 12.5% produce an osmotic gradient which stimulates the accumulation of growth factors and inflammatory cells, which in turn can initiate the wound healing process. In this case we can find that the healing process translates to good clinical outcome by ultrasound imaging. Conclusion: Dextrose prolotherapy can be used as an option for supraspinatus tendon partial tear with good results.
简介:肩袖撕裂约占肩袖疾病的20%,并伴有严重的肩部疼痛,严重影响日常生活活动。病例报告:34岁男性,有右肩慢性疼痛史,表现为肩外侧压痛,肩峰下撞击试验阳性,运动末端疼痛,疼痛评分6分。超声显示滑囊一侧冈上肌部分撕裂。患者给予冈上肌腱实质内15%葡萄糖治疗3次,共4周。结果:首次治疗后疼痛明显改善(VAS 1),治疗后4周无疼痛全活动,超声显示冈上肌腱愈合。讨论:葡萄糖浓度高于12.5%会产生渗透梯度,刺激生长因子和炎症细胞的积累,从而启动伤口愈合过程。在这种情况下,我们可以发现愈合过程转化为良好的临床结果超声成像。结论:葡萄糖前体疗法可作为冈上肌腱部分撕裂的治疗方法,效果良好。
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引用次数: 0
Dupuytren’s Contracture in a Filipino Male: a Case Report and Review of the Literature 菲律宾男性Dupuytren挛缩:个案报告及文献回顾
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2020-0080
T. M. P. Evangelista, J. Pua
Dupuytren’s disease (DD) is a heritable, benign, chronic fibroproliferative process which affects the connective tissue of the palmar fascia. DD is rare among Asians with a prevalence of 0.004 to 0.032 percent. There are only 74 cases of DD among Asians identified in literature, and there are no published cases from the Philippines. We discuss a rare case of DD in a 60-year-old male Filipino presenting with bilateral loss of range of motion of the middle, ring, and little finger of both hands.
Dupuytren病(DD)是一种遗传性、良性、慢性纤维增生性疾病,影响掌筋膜结缔组织。DD在亚洲人中很少见,患病率为0.004%至0.032%。在文献中发现的亚洲人只有74例DD,菲律宾没有发表的病例。我们讨论一个罕见的DD病例在60岁的菲律宾男性表现为双侧失去活动范围的中,无名指,和双手的小指。
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引用次数: 0
Leigh Syndrome in a Filipino Child: A Case Report 菲律宾儿童Leigh综合征一例报告
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2021-0015
M. Sy, M. Moral-Valencia
Introduction: Leigh disease and Leigh-like syndrome are a heterogenous group of neurodegenerative disorders involving any level of the neuraxis and may present with a variety of clinical presentations, prominent among them is psychomotor regression. Despite the remarkable number of established disease genes and novel mutations being discovered, many cases of Leigh syndrome remain without a genetic diagnosis, indicating that there are still more disease genes to be identified. Case: Here we present a case of a two and a half-year-old girl who presented with delayed acquisition of developmental milestones with subsequent regression, ataxia, and dyskinesia. Her work-up showed raised blood lactate levels and lactate peak in MR spectroscopy. Mitochondria genome showed absence of mitochondrial DNA mutation, while whole exome sequence analysis revealed a novel dynein gene variant, p.A1577S. Her parents underwent genetic testing as well, and her father also had the same dynein mutation, however, is non-symptomatic. She had an older brother who initially presented with ophthalmoplegia and eventually developed psychomotor regression. He subsequently expired from respiratory failure after almost 2 years from initial presentation. Both siblings were diagnosed with Leigh syndrome. Conclusion: The diagnosis of Leigh syndrome remains based on characteristic clinical and radiologic findings. However, a specific defect must be identified if reliable genetic counseling is to be provided.
Leigh病和Leigh样综合征是一种异质性的神经退行性疾病,涉及任何水平的神经轴,可能表现为多种临床表现,其中突出的是精神运动性退行。尽管发现了大量已确定的疾病基因和新的突变,但许多Leigh综合征病例仍未得到遗传诊断,这表明仍有更多的疾病基因有待鉴定。病例:这里我们报告一个两岁半的女孩,她表现出发育里程碑的获得延迟,随后出现倒退,共济失调和运动障碍。她的检查显示血乳酸水平升高,MR光谱显示乳酸峰值。线粒体基因组显示没有线粒体DNA突变,而全外显子组序列分析显示一个新的动力蛋白基因变异p.A1577S。她的父母也接受了基因检测,她的父亲也有同样的动力蛋白突变,但没有症状。她有一个哥哥,最初表现为眼麻痹,最终发展为精神运动性退化。他随后因呼吸衰竭而死亡,离最初的表现大约2年。兄妹俩都被诊断出患有利氏综合症。结论:利氏综合征的诊断应以临床和影像学表现为基础。然而,如果要提供可靠的遗传咨询,必须确定特定的缺陷。
{"title":"Leigh Syndrome in a Filipino Child: A Case Report","authors":"M. Sy, M. Moral-Valencia","doi":"10.35460/2546-1621.2021-0015","DOIUrl":"https://doi.org/10.35460/2546-1621.2021-0015","url":null,"abstract":"Introduction: Leigh disease and Leigh-like syndrome are a heterogenous group of neurodegenerative disorders involving any level of the neuraxis and may present with a variety of clinical presentations, prominent among them is psychomotor regression. Despite the remarkable number of established disease genes and novel mutations being discovered, many cases of Leigh syndrome remain without a genetic diagnosis, indicating that there are still more disease genes to be identified. Case: Here we present a case of a two and a half-year-old girl who presented with delayed acquisition of developmental milestones with subsequent regression, ataxia, and dyskinesia. Her work-up showed raised blood lactate levels and lactate peak in MR spectroscopy. Mitochondria genome showed absence of mitochondrial DNA mutation, while whole exome sequence analysis revealed a novel dynein gene variant, p.A1577S. Her parents underwent genetic testing as well, and her father also had the same dynein mutation, however, is non-symptomatic. She had an older brother who initially presented with ophthalmoplegia and eventually developed psychomotor regression. He subsequently expired from respiratory failure after almost 2 years from initial presentation. Both siblings were diagnosed with Leigh syndrome. Conclusion: The diagnosis of Leigh syndrome remains based on characteristic clinical and radiologic findings. However, a specific defect must be identified if reliable genetic counseling is to be provided.","PeriodicalId":399180,"journal":{"name":"Journal of Medicine, University of Santo Tomas","volume":"79 1","pages":"0"},"PeriodicalIF":0.0,"publicationDate":"2022-10-31","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"125540711","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
Incidence of Urologic Disease Among 95 Consecutive Filipino Patients Presenting With Asymptomatic Microscopic Hematuria 菲律宾连续95例无症状显微镜下血尿患者泌尿系统疾病的发生率
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2022-0036
R. Uy, D. Bolong
Objective: One of the common clinical problems warranting urologic evaluation is asymptomatic microscopic hematuria (AMH). According to some studies, it has prevalence as high as 38% with a possibility of urologic disease or malignancy around 23%. The presence of AMH would be quite a dilemma to a urologist in terms of how aggressive urologic evaluation and follow up is recommended. The present study was to determine the incidence of significant urologic diseases among Filipino patients with AMH on initial evaluation and on follow-up. This study would also determine if there would be a significant difference in terms of incidence of urologic disease among patients less than 35 years old and more than 35 years old with AMH. Methods: A total number of 95 patients (38 male, 57 female) were included in this study. All patients presented with AMH. They were grouped in terms of age, gender, and duration of follow-up. All patients underwent cystoscopy and a diagnostic imaging (ultrasound, CT urogram, or CT stonogram) on initial evaluation. Patients then were followed up. They were divided into two groups, those less than 2 years of follow-up and those more than 2 years of follow-up. Excluded from the study are those patients with gross hematuria, on indwelling catheter, with urinary tract infection, with previous malignancy, history of pelvic irradiation, and those who did not undergo cystoscopy, or any urologic imaging. Results: Out of 95 patients with AMH who underwent urologic evaluation, the incidence of urologic disease was noted to be 12% (11 out of 95). There was no malignancy related cause of AMH discovered. Age and gender failed to show any significant difference in terms of developing urologic disease. Among patients with negative findings on initial urologic evaluation, no urologic disease was noted even on follow-up. Among those with positive findings on initial evaluation, no new urologic disease was discovered on follow-up. Conclusion: AMH has a low incidence of urologic disease or any GUT malignancy. Age and gender alone are not sufficient risk factors warranting an invasive endoscopic procedure. They are recommended only to those patients with high risk of urologic disease and can be avoided in majority of the population. We would recommend a kidney, urinary bladder, and prostate (KUBP) ultrasound as the initial imaging of choice since the only findings noted on evaluation through imaging were just two cases of nephrolithiasis, one via CT stonogram and the other through a CT urogram, which can also be diagnosed with a regular KUBP ultrasound. This would be more cost-effective as well as beneficial in terms of the patient’s risk regarding radiation and contrast-related effects. Clinicians may decrease unnecessary repeated urologic evaluation and follow-ups on patients with AMH, as the results of the study failed to show any significant difference in developing urologic disease for patients with persistent AMH on initial assessment and even
目的:无症状显微镜下血尿(AMH)是泌尿外科评估的常见临床问题之一。根据一些研究,它的患病率高达38%,泌尿系统疾病或恶性肿瘤的可能性约为23%。对于泌尿科医生来说,AMH的存在是一个相当两难的选择,即如何积极地进行泌尿科评估和随访。本研究旨在通过初步评估和随访确定菲律宾AMH患者中重大泌尿系统疾病的发生率。本研究还将确定35岁以下和35岁以上AMH患者的泌尿系统疾病发病率是否存在显著差异。方法:共纳入95例患者,其中男38例,女57例。所有患者均表现为AMH。他们按照年龄、性别和随访时间进行分组。所有患者在初步评估时均行膀胱镜检查和诊断性影像学检查(超声、CT尿路图或CT结石图)。然后对患者进行随访。他们被分为两组,一组少于2年,另一组超过2年。排除有肉眼血尿、留置导尿、尿路感染、既往恶性肿瘤、盆腔照射史以及未行膀胱镜检查或任何泌尿影像学检查的患者。结果:95例AMH患者行泌尿系统评估,发现泌尿系统疾病发生率为12%(11 / 95)。未发现与AMH有关的恶性原因。在发生泌尿系统疾病方面,年龄和性别没有明显差异。在最初泌尿系统评估阴性的患者中,即使在随访中也没有发现泌尿系统疾病。在初步评估阳性的患者中,随访时未发现新的泌尿系统疾病。结论:AMH在泌尿系统疾病及肠道恶性肿瘤中的发病率较低。年龄和性别本身并不是进行侵入性内窥镜手术的充分危险因素。它们只推荐给那些有泌尿系统疾病高风险的患者,在大多数人群中可以避免。我们推荐肾、膀胱和前列腺(KUBP)超声作为首选的初始影像学检查,因为通过影像学评估所发现的仅有两例肾结石,一例通过CT结石图,另一例通过CT尿路图,这也可以通过常规KUBP超声诊断。这将更具成本效益,也有利于降低患者在放疗和对比相关影响方面的风险。临床医生可以减少对AMH患者不必要的重复泌尿系统评估和随访,因为本研究结果在初始评估甚至随访中均未显示持续性AMH患者发生泌尿系统疾病的显著差异。
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引用次数: 0
Case Study: Use of Decentralized Clinical Technologies in Lower Urinary Tract Symptoms 案例研究:分散临床技术在下尿路症状中的应用
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2022-0052
Nadina Jose, Avik Pal
A clinical study with 46 participants was started and completed at the height of the Covid-19 pandemic with the use of decentralized clinical trial (DCT) methodologies. All participants and the study team remained safe and were able to conduct the study efficiently. Patients were able to provide consent electronically, received experimental supplements and were given the option to provide feedback through the system’s telemedicine feature.
一项有46名参与者的临床研究在Covid-19大流行高峰期开始并完成,采用分散式临床试验(DCT)方法。所有参与者和研究小组都是安全的,能够有效地进行研究。患者可以通过电子方式提供同意,接受实验性补充,并可以选择通过系统的远程医疗功能提供反馈。
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引用次数: 0
The Difference in Risk Factors Between Adults With Early-Onset (<40 Years Old) Versus Late-Onset (≥40 Years Old) Type 2 Diabetes in a University Hospital From January 2015-December 2017 2015年1月- 2017年12月某大学医院早发性(<40岁)与晚发性(≥40岁)2型糖尿病成人危险因素差异
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2018-0100
M. Caro, E. Cunanan
Background: Diabetes will remain a threat to global health. No longer just a disorder of mature age, there is now a well-recognized trend towards the young. Early diagnosis leads to early intervention and prevention of complications in this susceptible but vital portion of the population. Objective: To compare the risk factors predisposing adults to early-onset (<40 years old) versus late-onset (≥40 years old) type 2 diabetes at the University of Santo Tomas Hospital from January 2015-December 2017. Methods: This is a retrospective review of medical records. All adult patients who fulfilled the inclusion criteria from January 2015 to December 2017 were included in the study. Data from charts were reviewed and analyzed. Results: The early-onset group had a mean age of 34 years, while the late-onset group had a mean age of 51 years. The early-onset diabetics were mostly obese, had higher HbA1c, worse lipid profiles, and had a positive family history of diabetes. Only a BMI of >27.50 kg/m2 was found to be a significant risk factor contributing to early-onset of diabetes. Myocardial infarction and nephropathy were more frequent in the late-onset group while retinopathy was more common in the early-onset group. Lastly, only retinopathy and neuropathy were significantly associated with longer duration of diabetes. Conclusion: The mean age of Filipinos was at least 5 years younger than the studies done on Caucasians. Most patients in the early-onset group were obese and had worse metabolic profiles. Retinopathy was more common in the early-onset group, while myocardial infarction and neuropathy were more common in the latter.
背景:糖尿病仍将是全球健康的一大威胁。不再仅仅是一种成熟年龄的疾病,现在有一种公认的趋势是向年轻人倾斜。在这一易感但至关重要的人群中,早期诊断可导致早期干预和预防并发症。目的:比较诱发成人早发性糖尿病的危险因素(27.50 kg/m2是导致糖尿病早发性的重要危险因素)。心肌梗死和肾病在晚发组多见,而视网膜病变在早发组多见。最后,只有视网膜病变和神经病变与糖尿病持续时间延长显著相关。结论:菲律宾人的平均年龄比白种人至少年轻5岁。早发组的大多数患者肥胖,代谢谱更差。早发组以视网膜病变多见,而后发组以心肌梗死和神经病变多见。
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引用次数: 0
Geriatric Medicine in the Medical Curriculum: A MUST in the Globally Aging World 医学课程中的老年医学:全球老龄化世界的必修课
Pub Date : 2022-10-31 DOI: 10.35460/2546-1621.2022-0061
L. Mercado-Asis, M. L. Domingo-Maglinao
Geriatrics is a branch of medicine concerned with diagnosing, treating, and preventing diseases in older people and problems specific to aging. The World Health Organization (WHO) has reported that the number of people aged 65 or older is projected to grow from an estimated 524 million in 2010 to nearly 1.5 billion in 2050. The burden of diseases in the aging population will dramatically impact healthcare expenses in low- and middle-income countries and even developed ones. A preventive approach is essential. The role of medical institutions and inclusion of geriatrics in the medical curriculum have become important. However, incorporating geriatrics into the medical curriculum is associated with various issues and challenges: compact pre-existing curriculum, attitudes of teachers and students, and shortage of teaching geriatricians. An individualized institutional approach to curricular integration guided by the American Geriatrics Society’s minimum required competencies for the undergraduate will circumvent these challenges.
老年病学是医学的一个分支,涉及诊断、治疗和预防老年人的疾病和衰老特有的问题。世界卫生组织(世卫组织)报告说,65岁或65岁以上人口的数量预计将从2010年的5.24亿增长到2050年的近15亿。人口老龄化带来的疾病负担将对中低收入国家甚至发达国家的医疗费用产生巨大影响。预防措施是必不可少的。医疗机构的作用和将老年病学纳入医学课程已变得十分重要。然而,将老年病学纳入医学课程涉及各种问题和挑战:紧凑的现有课程,教师和学生的态度,以及教学老年病学专家的短缺。在美国老年医学学会对本科生的最低要求能力的指导下,个性化的课程整合制度方法将规避这些挑战。
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引用次数: 0
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Journal of Medicine, University of Santo Tomas
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