Medicina-buenos Aires最新文献

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[Falls in hospitalized elderly people: characterization and incumbency of polypharmacy and inappropriate prescription of medications]. [住院老年人跌倒:多药和不当用药的特征和现状]。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Ana Fajreldines, Marcelo Pellizzari
{"title":"[Falls in hospitalized elderly people: characterization and incumbency of polypharmacy and inappropriate prescription of medications].","authors":"Ana Fajreldines, Marcelo Pellizzari","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>Falls in the elderly are a frequent phenomenon during hospitalization and are preventable adverse events. Falls could cause serious injuries in this vulnerable patient population and also lead to poor health outcomes such as increased morbidity, mortality and healthcare costs. The objective of this study is to characterize falls in hospitalized elderly people and analyze the implication of polypharmacy and inappropriate prescription of medications in a University Hospital in Argentina.</p><p><strong>Materials and methods: </strong>Descriptive, observational, retrospective study.</p><p><strong>Results: </strong>A sampling 226 patients was taken, the mean age was 74.7 SD: 12.9, range 69-91. The total number of falls was 237 (9 patients suffered more than one fall). Falls are associated with several factors including polypharmacy, cognitive status, advanced age, female sex, and inappropriate prescription of medications.</p><p><strong>Discussion: </strong>Incidents of falls are frequent, preventable and multi-causal. Some factors such as polypharmacy, cognitive impairment, among others, would be associated with its occurrence; the published literature confirms these concepts.</p>","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 3","pages":"543-549"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144512130","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Are patient registries necessary? The example of the Argentine Bronchiectasis Registry]. 病人登记是必要的吗?阿根廷支气管扩张登记的例子]。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Miguel Penizzotto, Carlos S Wustten, Ana M López, Vanesa Abrate, Sergio Arias, Miguel Ángel Martínez-García
{"title":"[Are patient registries necessary? The example of the Argentine Bronchiectasis Registry].","authors":"Miguel Penizzotto, Carlos S Wustten, Ana M López, Vanesa Abrate, Sergio Arias, Miguel Ángel Martínez-García","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 4","pages":"885-887"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144821960","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Can narrative medicine help us?] 叙事医学能帮助我们吗?]
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Carlos Tajer, Gustavo Kusminsky
{"title":"[Can narrative medicine help us?]","authors":"Carlos Tajer, Gustavo Kusminsky","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 1","pages":"260"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143123210","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Lesch-Nyhan syndrome in dizygotic twins]. [异卵双胞胎的Lesch-Nyhan综合征]。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Rocío V García, Norma Specola, Paula Ivarola, Roberto Caraballo
{"title":"[Lesch-Nyhan syndrome in dizygotic twins].","authors":"Rocío V García, Norma Specola, Paula Ivarola, Roberto Caraballo","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Lesch-Nyhan syndrome is an inborn error of purine metabolism caused by deficiency of the enzyme hypoxanthine-guanine phosphoribosyl transferase, with X-linked inheritance. At present, there are a few cases available in the international literature of twins with this condition. The object of this publication is to report the case of two twins with Lesch-Nyhan syndrome and to describe the clinical and therapeutic management. We present two dizygotic 10-year-old twins, with global developmental delay and nephrolithiasis, who developed dystonia and self-mutilation. The diagnosis was suspected due to the developmental delay associated with dystonia and hyperuricemia in two male patients, as in most of these patients. It was confirmed with the measurement of enzymatic activity, being undetectable. They required multiple therapeutic schemes, including extraction of teeth and restraint measures to avoid major injuries.</p>","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 2","pages":"445-448"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143803197","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Malaria and paludism: a necessary clarification]. [疟疾和疟疾:必要的澄清]。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Mario O Melcon, Celeste Garcías
{"title":"[Malaria and paludism: a necessary clarification].","authors":"Mario O Melcon, Celeste Garcías","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 2","pages":"482"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143803200","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Mechanisms of tricuspid insufficiency in the follow-up of patients post orthotopic heart transplantation]. [原位心脏移植术后随访中三尖瓣功能不全的机制]。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Pilar Domenech, Estefanía Mestrallet, Ricardo Posatini, César Belziti, Rodolfo Pizarro
{"title":"[Mechanisms of tricuspid insufficiency in the follow-up of patients post orthotopic heart transplantation].","authors":"Pilar Domenech, Estefanía Mestrallet, Ricardo Posatini, César Belziti, Rodolfo Pizarro","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>Tricuspid regurgitation (TR) is the most frequent valvulopathy after cardiac transplantation, with an incidence ranging from 19% to 84%. Severity increases with follow-up. The objectives were to describe the mechanisms involved in the development of post-transplantation TR.</p><p><strong>Materials and methods: </strong>Single-center, retrospective cohort study including patients who received orthotopic heart transplantation between 2012 and 2022. Echocardiograms were performed at 6, 12 and 18 months' post-transplantation. The mechanisms of tricuspid regurgitation described were atrial dilatation or bi-atrial technique, multiple endomyocardial biopsies, right ventricular dilatation and dysfunction, previous pulmonary hypertension and mismatch of the recipient cavity with the transplanted organ.</p><p><strong>Results: </strong>A total of 234 patients were included. The incidence of significant tricuspid regurgitation from 6 months post-transplantation was 12.8%. Right ventricular dilatation and dysfunction was the most prevalent mechanism in 67%, mismatch 17%, organic valve lesion and previous pulmonary hypertension 7% and atrial dilatation 3%. The 40% of patients who had right ventricular dysfunction also presented left ventricular dysfunction.</p><p><strong>Discussion: </strong>The incidence of tricuspid regurgitation in heart transplant patients was 12.8% during the follow-up. The main mechanism observed was the right ventricular dilatation and dysfunction.</p>","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 2","pages":"331-336"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143803431","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Acromegaly as a differential diagnosis of hyperphosphatemia]. 肢端肥大症作为高磷血症的鉴别诊断。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Mariela Varsavsky, Mariela Glerean, Mirena Buttazzoni
{"title":"[Acromegaly as a differential diagnosis of hyperphosphatemia].","authors":"Mariela Varsavsky, Mariela Glerean, Mirena Buttazzoni","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Acromegaly is characterized by hypersecretion of growth hormone (GH) caused by a pituitary adenoma in 99% of cases. Increased serum phosphate is a rare finding in this pathology. This hyperphosphatemia results from increased phosphate reabsorption in the proximal renal tubule via sodium-phosphate cotransporter type IIa: an effect mediated by insulin-like factor 1 (IGF-1) consequent to excess GH. We present the clinical case of a 66-year-old woman with persistent hyperphosphatemia 4.8 ng/dl (VN: 2.5-4.5) with elevated tubular phosphorus reabsorption (TPR) 95% (VN: 85-94) with subtle features of acromegaly. Acromegaly was diagnosed by IGF1 measurements and oral glucose tolerance test with GH measurement (OGTT/GH). In search of the source of GH hypersecretion, a pituitary MRI was requested, and the pituitary microadenoma was evident only in the third year of follow-up. Achieving remission of the disease (IGF-1 in normal range) after transsphenoidal endoscopic surgery and observing normalization of previous hyperphosphatemia. No evidence of recurrence was found in the 18 years of follow-up. In cases of hyperphosphatemia to review the signs and symptoms of acromegaly to diagnose and treat in early stages, when the probability of remission is high.</p>","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 2","pages":"434-438"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143803648","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
Fabry disease in Argentina: clinical, biochemical and molecular correlation in all reported GLA variants. 阿根廷法布里病:所有报告的GLA变异的临床、生化和分子相关性
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Juan Politei, Romina Ceci, Domingo Procopio, Lucas Silvestroff, Rita Valdez, Paula A Rozenfeld
{"title":"Fabry disease in Argentina: clinical, biochemical and molecular correlation in all reported GLA variants.","authors":"Juan Politei, Romina Ceci, Domingo Procopio, Lucas Silvestroff, Rita Valdez, Paula A Rozenfeld","doi":"","DOIUrl":"","url":null,"abstract":"<p><strong>Introduction: </strong>Fabry disease is an X-linked trait due to pathogenic variants in the GLA gene, causing deficient GLA enzyme activity, and producing a chronic accumulation of globotriaosylceramide and its derivative globotriaosylsphingosine (LysoGb3) in tissues and fluids. Conflicting or discordant results of interpretation of multiple variants in GLA were reported in literature. The aim of this article is to report the spectrum of GLA variants in Argentine population, as well as the revised interpretation of variants classification. Moreover, we intend to find a possible correlation between biochemical parameters, clinical manifestations and genetic variants of adult male Fabry patients that could be of help for interpretation of variants.</p><p><strong>Materials and methods: </strong>Blood samples from patients with clinical suspicion of Fabry disease were evaluated for specific laboratory tests: alfa-galactosidase A enzyme activity, LysoGb3 and GLA genetic test.</p><p><strong>Results: </strong>There are 44 males with pathogenic GLA variants which showed deficient enzyme activity. Among them, thirty-two presented the classic phenotype (72%) and twelve the late onset clinical features (28%). Mean percentage of enzyme activity was 0.9% for classical patients and 3.2% for later onset ones. LysoGb3 values were increased in all males, with classic patients showing considerable higher values than that of late onset.</p><p><strong>Discussion: </strong>Our results showed that the combined analysis of the clinical picture, leukocyte enzyme activity, globotriaosylsphingosine concentration and a detailed exhaustive study of the genetic variant lead to a definite diagnosis in those cases previously interpreted as of unknown significance, together with a revised interpretation of the phenotype.</p>","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 2","pages":"322-330"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143803734","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Breastfeeding in people with HIV, from taboo to reality]. 艾滋病毒感染者的母乳喂养,从禁忌到现实。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Leda Guzzi, Silvana Lauro, Gloria Amborosioni, Pilar Cancela, Mónica Castells, Claudio Comparato, Rocío López, Natalia Laufer, Isabel Casetti
{"title":"[Breastfeeding in people with HIV, from taboo to reality].","authors":"Leda Guzzi, Silvana Lauro, Gloria Amborosioni, Pilar Cancela, Mónica Castells, Claudio Comparato, Rocío López, Natalia Laufer, Isabel Casetti","doi":"","DOIUrl":"","url":null,"abstract":"<p><p>Breastfeeding in newborn infants born to people living with HIV continues to be a controversial issue. However, there is numerous evidence that reveals that in the context of sustained virological suppression, the risk of postnatal HIV transmission through breast milk is less than 1%. From the activism of people with HIV, civil society and the medical and scientific community, there is a demand for reopening the issue, with the purpose of defining new guidelines for the feeding of children born to people with HIV. This review analyzes the available scientific evidence and the current knowledge gaps regarding breastfeeding in HIV situations and proposes an institutional approach and shared decision-making modality for HIV-positive pregnant people who wish to breastfeed.</p>","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 1","pages":"182-196"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"143123208","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","ArticlePicture":[],"TitleCN":null,"AbstractTextCN":null,"PMCID":"","EPubDate":null,"PubModel":null,"JCR":null,"JCRName":null,"Score":null,"Total":0}
引用次数: 0
[Lights, shadows, and lessons learned five years after the start of COVID: the relevance of the World Health Organization]. [疫情爆发五年后的光明、阴影和经验教训:世界卫生组织的重要性]。
IF 0.6 4区 医学
Medicina-buenos Aires Pub Date : 2025-01-01
Manuel E Cortés, Eduardo A Herrera-Aliaga
{"title":"[Lights, shadows, and lessons learned five years after the start of COVID: the relevance of the World Health Organization].","authors":"Manuel E Cortés, Eduardo A Herrera-Aliaga","doi":"","DOIUrl":"","url":null,"abstract":"","PeriodicalId":18419,"journal":{"name":"Medicina-buenos Aires","volume":"85 3","pages":"646-647"},"PeriodicalIF":0.6,"publicationDate":"2025-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"144512133","PeriodicalName":null,"FirstCategoryId":null,"ListUrlMain":null,"RegionNum":4,"RegionCategory":"医学","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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