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Bioarchaeological Notes on the Commingled Human Remains Held in the Church of Saint Francis of Paola, Sant'Angelo di Brolo, Sicily, Italy. 意大利西西里岛圣安杰洛迪布罗洛圣弗朗西斯保拉教堂保存的混合人类遗骸的生物考古学注释。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-07-26 DOI: 10.15388/Amed.2022.29.1.16
Aurelija Kemežytė, Dario Piombino-Mascali

In this study, we examine human skeletal remains from the church of Saint Francis of Paola located in the small town of Sant'Angelo di Brolo, in the Italian region of Sicily. The preserved skeletal remains were temporarily transferred from their permanent resting place in the crypt for a macroscopic examination and evaluation. Various established methods were used to estimate age at death, sex, stature, any evidence of disease(s) as well as the fact that there was a minimum of 15 individuals. The findings were then subdivided into different groups of pathologies and recorded as individual cases. Amongst which, dental issues and cases of trauma were most prevalent. Additional conditions such as joint disease, congenital, metabolic and multifactorial disorders were also identified. The prevalence of dental decay indicates that the group's diet consisted largely of carbohydrates, and that their oral hygiene was poor. Furthermore, evidence of trauma and poor healing suggested that the town was isolated from the main medical centres of the island. Severe complications of traumas linked with a loss of movement and overall independence, as well as physical pain, must have had a significant impact on the lives of those affected.

在这项研究中,我们检查了位于意大利西西里岛地区Sant'Angelo di Brolo小镇的保拉圣弗朗西斯教堂的人类骨骼遗骸。保存下来的骨骼残骸暂时从他们永久的安息地转移到地穴进行宏观检查和评估。使用了各种既定的方法来估计死亡时的年龄、性别、身材、任何疾病证据以及至少有15个人的事实。然后将结果细分为不同的病理组,并作为个案记录。其中,牙齿问题和创伤病例最为普遍。其他情况,如关节疾病、先天性、代谢和多因素疾病也被确定。蛀牙的流行表明这组人的饮食主要由碳水化合物组成,而且他们的口腔卫生很差。此外,创伤和愈合不良的证据表明,该镇与岛上的主要医疗中心隔绝。与丧失行动能力和整体独立性相关的严重创伤并发症,以及身体疼痛,肯定对受影响者的生活产生了重大影响。
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引用次数: 0
An Exploratory Study of the Differences in Attitudes and Motives Regarding COVID-19 Plasma Donation. 新型冠状病毒肺炎献血态度和动机差异的探索性研究
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-07-26 DOI: 10.15388/Amed.2022.29.1.14
Ashish Maheshwari, Mohit Varshney, Meenu Bajpai, Neeraj Raizada, Tarika Sharma

Background: Understanding the attitude and motives and differences between voluntary and replacement blood donation is the key to the sustainable availability of this precious resource. This study aimed to assess the attitude and motives for convalescent plasma (CP) donation in the recovered COVID-19 plasma donors and further understand the differences between voluntary and replacement donation.

Materials and methods: This prospective cross-sectional survey-based study was conducted among500 COVID-19 recovered blood donors who visited for CP donation at a tertiary care super-speciality centre in northern India. Data were collected using a structured questionnaire based on donor attitude, motives, and belief, which was validated by the experts of Psychiatry, Transfusion Medicine, and Epidemiology and was administered by the online medium.

Results: The study's findings depicted that voluntary plasma donors were previously regular blood donors (36.8%) compared to replacement plasma donors (26.4%). Almost all voluntary donors (99.5%) showed altruistic reasons to donate plasma and expressed that donating plasma is a good way to save a life, and it was more than for replacement plasma donors (p=0.004). The motives of most voluntary plasma donors were to contribute to society, and they believed that donating plasma is a good way, while it was not the case for most replacement plasma donors (p=0.02). Voluntary donors were more eagerly willing to donate plasma to help COVID sufferers (40.9%) when compared to replacement donors (33.2%) (p=0.037).

Conclusion: Most voluntary plasma donors were regular whole blood donors and were keen to contribute to society. Convalescent plasma donation during this time of grief and loss was considered a moral responsibility by voluntary donors. The impact of media was more highly perceived in voluntary plasma donors when compared to replacement donors.

背景:了解自愿献血和替代献血的态度、动机和差异是这一宝贵资源可持续利用的关键。本研究旨在评估COVID-19恢复血浆献血者对恢复期血浆(CP)捐献的态度和动机,进一步了解自愿捐献与替代捐献的差异。材料和方法:这项基于前瞻性横断面调查的研究是在印度北部一家三级保健超级专科中心进行CP捐赠的500名COVID-19康复献血者中进行的。数据收集采用基于捐赠者态度、动机和信念的结构化问卷,经精神病学、输血医学和流行病学专家验证,并通过在线媒体进行管理。结果:研究结果显示,自愿献血者以前是定期献血者(36.8%),而替代献血者(26.4%)。几乎所有的自愿献血者(99.5%)都出于利他的原因捐献血浆,并表示捐献血浆是挽救生命的好方法,比替代献血者多(p=0.004)。大多数自愿献血的动机是为社会做贡献,他们认为捐献血浆是一种很好的方式,而大多数替代献血的人则不是这样(p=0.02)。与替代献血者(33.2%)相比,自愿献血者(40.9%)更愿意捐献血浆来帮助COVID患者(p=0.037)。结论:自愿血浆献血者多为定期全血献血者,对社会有积极贡献。在这个悲伤和失去亲人的时刻,自愿捐献血浆被认为是一种道德责任。与替代献血者相比,媒体对自愿血浆献血者的影响更明显。
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引用次数: 0
Caesarean Scar Pregnancy: A Case Report. 瘢痕剖宫产妊娠1例报告。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.1.17
Vilius Rudaitis, Gailė Maldutytė, Jūratė Brazauskienė, Mykolas Pavlauskas, Dileta Valančienė

Caesarean scar pregnancy is a potentially life-threatening gynaecological condition, becoming more common due to steadily increasing rate of caesarean sections worldwide. More than one-third of women presenting with caesarean scar pregnancy are asymptomatic, but over the time if left untreated this condition can lead to the uterine rupture and massive maternal haemorrhage. Therefore it is necessary to diagnose and manage caesarean scar pregnancies properly at the beginning of the first trimester. We present the case of woman with three previous caesarean sections, who was diagnosed with complicated caesarean scar pregnancy and then successfully managed using surgical intervention.

剖宫产瘢痕妊娠是一种潜在的危及生命的妇科疾病,由于世界范围内剖宫产率的稳步上升,瘢痕妊娠变得越来越常见。超过三分之一的剖宫产瘢痕妊娠妇女是无症状的,但随着时间的推移,如果不及时治疗,这种情况可能导致子宫破裂和大量产妇出血。因此,在妊娠早期对瘢痕妊娠进行正确的诊断和处理是十分必要的。我们提出的情况下,妇女有三个以前的剖宫产,谁被诊断为复杂的剖宫产疤痕妊娠,然后成功地管理使用手术干预。
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引用次数: 1
Creutzfeldt-Jakob Disease with Stroke-Like Symptoms: Case report. 克雅氏病伴中风样症状:病例报告。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.3
Bünyamin Tosunoğlu, Sıddıka Sena Dilek, Ümmühanı Emektar, Tahir Kurtuluş Yoldaş

Creutzfeldt-Jakob disease (CJD) is a rare, progressive, and fatal prion disease. Often the first sign of CJD is rapidly progressive dementia, leading to memory loss, personality changes, and hallucinations. Myoclonus typically occurs in 90% of cases, but often may not be an initial symptom. Other frequently occurring psychiatric symptoms include depression, anxiety, paranoia, obsessive-compulsive symptoms, and psychosis. Speech disorder, loss of balance and coordination may also accompany. We present a case of CJD with sudden onset of right hemiparesis.

克雅氏病(CJD)是一种罕见的、进行性的、致命的朊病毒疾病。CJD的第一个症状通常是快速进行性痴呆,导致记忆力丧失、性格变化和幻觉。肌阵挛通常发生在90%的病例中,但通常可能不是最初的症状。其他常见的精神症状包括抑郁、焦虑、偏执、强迫症状和精神病。言语障碍、失去平衡和协调也可能伴随而来。我们报告一例CJD突然发作的右偏瘫。
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引用次数: 0
Experience with Dopamine Agonists in the Treatment of Prolactinomas. 多巴胺激动剂治疗泌乳素瘤的经验。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.15
Nadiya Ye Barabash, Tetiana M Tykhonova

The article is devoted to the conservative treatment of hyperprolactinemia of tumor origin. Cabergoline is considered as an effective treatment not only for microadenomas but also for large pituitary tumors which is illustrated by the clinical case of the patient P. The most important effects of cabergoline demonstrated in this clinical case are reduction in the size of the adenoma from macro to micro, reverse development of chiasmal syndrome with restoration of visual functions, achievement and maintenance of the target level of prolactin. Besides the article focused on the possible development of primary and secondary resistance to dopamine analogues. One of such difficult clinical scenarios is illustrated by the clinical case of patient M., who was treated with different dopamine analogues with the development of secondary dopamine resistance. Along with described in literature possible mechanisms for its development in our patient we also suggest the role of prolonged inadequate therapy with dopamine agonists, when the dose of the drug was not properly adjusted, despite not reaching the target prolactin level. The literature considers several ways of optimization of treatment in resistant patients but despite of this fact it remains one of unresolved problems in the management of patients with hyperprolactinemia.

本文致力于肿瘤源性高泌乳素血症的保守治疗。卡麦角林被认为不仅是治疗微腺瘤的有效方法,而且是治疗大型垂体瘤的有效方法。患者P的临床病例说明了这一点。在该临床病例中证明的卡麦角碱最重要的作用是从宏观到微观缩小腺瘤的大小,逆转交叉综合征的发展并恢复视觉功能,泌乳素目标水平的实现和维持。此外,本文还重点讨论了对多巴胺类似物的一级和二级耐药性的可能发展。患者M的临床案例说明了这种困难的临床场景之一,他接受了不同的多巴胺类似物治疗,并出现了继发性多巴胺耐药性。除了文献中描述的其在我们患者中发展的可能机制外,我们还提出了多巴胺激动剂长期不足治疗的作用,当药物剂量没有得到适当调整时,尽管没有达到目标催乳素水平。文献考虑了几种优化耐药患者治疗的方法,但尽管如此,这仍然是高泌乳素血症患者管理中尚未解决的问题之一。
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引用次数: 0
Clinical Overview of Leber Hereditary Optic Neuropathy. Leber遗传性视神经病变的临床综述。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.1.19
Almina Stramkauskaitė, Ieva Povilaitytė, Brigita Glebauskienė, Rasa Liutkevičienė

Leber hereditary ptic neuropathy (LHON) is a disease of young adults with bilateral, painless, subacute visual loss. The peak age of onset of LHON is in the second and third decades of life. Men are 4 times more likely to be affected than women. In about 25-50% of cases, both eyes are affected simultaneously. In unilateral cases, the other eye is usually affected 2 to 3 months later. Visual acuity deteriorates to counting fingers or worse with a dense central or centrocecal scotoma. In the subacute phase, the optic disc may appear hyperemic with swelling of the peripapillary retinal nerve fibre layer, peripapillary telangiectasias, and increased vascular tortuosity. Ocular coherence tomography of the macula shows marked thinning of the ganglion cell complex even at this stage. The diagnosis of LHON is made in a subject with a consistent clinical history and/or one of three common pathogenic mitochondrial DNA (mtDNA) variants identified by molecular genetic testing. Idebenone was approved by the European Medicines Agency under exceptional circumstances for the treatment of LHON. Current evidence suggests some benefit to vision in a subset of affected individuals treated with idebenone, particularly when treated within the first year of onset of vision loss. In this article, we discuss aetiology, clinical features, diagnosis, differential dignosis, prognosis and treatment.

Leber遗传性视神经病变(LHON)是一种年轻人双侧、无痛、亚急性视力丧失的疾病。LHON发病的高峰年龄是在生命的第二和第三个十年。男性受影响的可能性是女性的4倍。在大约25-50%的病例中,两只眼睛同时受到影响。在单侧病例中,另一只眼睛通常在2至3个月后受到影响。视力恶化到数手指或更糟,有密集的中央或中央暗瘤。在亚急性期,视盘可能出现充血,乳头周围视网膜神经纤维层肿胀,乳头周围毛细血管扩张,血管扭曲增加。黄斑的眼相干断层扫描显示,即使在这个阶段,神经节细胞复合体也明显变薄。LHON的诊断是在具有一致的临床病史和/或通过分子基因检测确定的三种常见致病线粒体DNA (mtDNA)变异之一的受试者中进行的。伊地贝酮在特殊情况下被欧洲药品管理局批准用于治疗LHON。目前的证据表明,使用依地贝酮治疗对一部分受影响个体的视力有一定的好处,特别是在视力丧失发病的第一年内治疗。本文就本病的病因、临床特征、诊断、鉴别诊断、预后及治疗进行讨论。
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引用次数: 5
Embryonal Rhabdomyosarcoma of the Biliary Tree as a Differential in a Paediatric Patient Presenting with Biliary Dilatation: Not Always a Choledochal Cyst. 胆道树胚胎性横纹肌肉瘤在以胆道扩张为表现的儿科患者中的鉴别诊断:并不总是胆道囊肿。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-01-24 DOI: 10.15388/Amed.2021.29.1.2
Tara Prasad Tripathy, Yashwant Patidar, Karamvir Chandel, Annapoorani Varadarajan, Vikrant Sood, Shalini Thapar Laroia
Abstract. Rhabdomyosarcoma is a soft tissue malignant musculoskeletal tumour and is the most prevalent soft-tissue sarcoma in the paediatric population. Although, Embryonal RMS of the biliary tree is a rare entity, however, it is the most common cause of paediatric malignant obstructive jaundice. We present a 4-year-old child who had symptoms of obstructive jaundice and palpable liver. The non-contrast magnetic resonance imaging and magnetic resonance cholangiopancreatography (MRCP) features were consistent with choledochal cyst. However, contrast enhanced computed tomography and PET CT images revealed biliary RMS as the differential diagnosis. Percutaneous biopsy followed by histopathology confirmed the diagnosis of embryonal biliary RMS. Since embryonal rhabdomyosarcoma is uncommonly recorded in the literature and can mimic the appearance of a choledochal cyst, this case report emphasises the necessity of keeping embryonal RMS as a differential in paediatric cases of obstructive jaundice.
横纹肌肉瘤是一种软组织恶性肌肉骨骼肿瘤,是儿科人群中最常见的软组织肉瘤。虽然,胆道树的胚胎性RMS是一种罕见的实体,然而,它是小儿恶性梗阻性黄疸的最常见原因。我们提出一个4岁的儿童谁的症状梗阻性黄疸和可触及的肝脏。非对比磁共振及磁共振胆管造影(MRCP)表现与胆总管囊肿一致。然而,对比增强计算机断层扫描和PET CT图像显示胆道RMS作为鉴别诊断。经皮穿刺活检和组织病理学证实了胚胎性胆道RMS的诊断。由于胚胎性横纹肌肉瘤在文献中很少记录,并且可以模仿胆总管囊肿的外观,本病例报告强调保留胚胎性RMS作为儿科阻塞性黄疸病例的鉴别诊断的必要性。
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引用次数: 1
Gubernaculum and Epididymo-Testicular Descent: Review of the Literature. 引带和附睾睾丸下降:文献综述。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.6
Eleonora Ivanova, Beata Vincel, Gilvydas Verkauskas, Faruk Hadziselimovic

Cryptorchidism is a common disorder in boys that has been widely studied both experimentally and clinically. The role of the gubernaculum, a mesenchymal tissue extending from the fetal testis and epididymis to the developing scrotum, is still unclear. Even the name is debated: 'gubernaculum epididymis' or 'gubernaculum testis'. This review does not aim to provide a global overview of competing theories on testicular descent, but focuses on the role of the gubernaculum in epididymo-testicular descent. We identified four major pitfalls of gubernaculum research: the role of the gubernaculum, of insulin-like peptide 3, anti-Müllerian hormone, and androgens. The major critical issues were that the gubernaculum plays a guiding role for the epididymis, descending prior to the testis and expanding the inguinal canal; insulin-like peptide 3 is not as important for the process of descent in humans as the rate of insulin-like peptide 3 mutations is low; anti-Müllerian hormone plays no significant role in epididymo-testicular descent; androgens and gonadotropins play a crucial role in epididymo-testicular descent. The role of the epididymis in the complex process of gubernaculum, epididymis, and testis migration is underestimated and should be included in future research.

隐睾症是一种常见的男孩疾病,在实验和临床上都得到了广泛的研究。引带是一种从胎儿睾丸和附睾延伸到发育中的阴囊的间充质组织,其作用尚不清楚。甚至这个名字也存在争议:“附睾引带”或“睾丸引带”。这篇综述的目的不是提供关于睾丸下降的竞争理论的全球综述,而是关注引带在附睾-睾丸下降中的作用。我们确定了引带研究的四个主要陷阱:引带的作用、胰岛素样肽3、抗米勒激素和雄激素。主要的关键问题是,引带对附睾起着引导作用,先于睾丸下降并扩张腹股沟管;胰岛素样肽3对人类的下降过程并不重要,因为胰岛素样肽的突变率低;抗苗勒管激素在附睾睾丸下降中没有显著作用;雄激素和促性腺激素在附睾睾丸下降中起着至关重要的作用。附睾在引带、附睾和睾丸迁移的复杂过程中的作用被低估,应纳入未来的研究。
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引用次数: 0
Pediatric Hematopoietic Stem Cell Transplantation in Lithuania - 20 Years of Progress through Collaboration. 立陶宛儿童造血干细胞移植——20年合作进展。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.Supp.2022.292.2
Jelena Rascon, Goda Elizabeta Vaitkevičienė, Sonata Šaulytė Trakymienė, Ramunė Pasaulienė
Hematopoietic stem cell transplantation (HSCT) is a complex procedure that is curative for several fatal pediatric malignancies and non-malignant diseases. Despite its complexity, potential toxicity, and high costs HSCT has become a standard procedure worldwide for several decades. Pediatric HSCT programs encounter several specific challenges. The rarity and heterogeneity of primary diseases, result in an almost 10-fold inferior number of pediatric HSCT as compared to adults. In con-trast to the adult programs, where autologous HSCT is more common, allogeneic HSCT (that is more complex) prevails in pediatric setting which is underpinned by a higher number of inborn disorders transplanted in early childhood. In Here we summarize conference proceedings presented at the scientific event “Pediatric hematopoietic stem cell transplantation in Lithuania – 20 years of progress through collaboration”. The meeting held on September 22-23, 2022, in Vilnius and aimed at commemorating 20 years of the launch of the pediatric transplant program in Lithuania. The event pursued sharing the experience in the field of pediatric HSCT in the Baltic countries. Given a very in all three Baltic countries, and face an additional challenge in maintaining sufficient transplant volume and gaining experience. Several distinguished speakers from USA, Spain, UK and shared their expertise in the field and emphasized the crucial role of national and international collaboration to achieve progress in the management of this very rare and complex procedure that offers for otherwise fatal pediatric conditions. Background: Neuroblastoma (NB) is the most common extracranial solid tumor in childhood. High-risk NB still has a poor prognosis and requires complex aggressive therapy. For a decade, immunotherapy with dinutuximab – anti GD2 chimeric monoclonal antibody – was integrated into treatment protocols as a routine part of the treatment. However, drug administration is related to potentially severe adverse effects. Thus, its administration is recommended in experienced centers. We aim to describe the first Lithuanian experience with dinutuximab. Methods: We performed a retrospective analysis of patients with high-risk NB treated with dinutuximab at our institution in 2020-2022. Toxicity and treatment outcomes were evaluated. The data were retrieved from electronic and paper records. Results: in 2020-2022, four patients were treated with dinutuximab. Totally, 20 cycles were de-livered, 5 cycles in each patient. One patient received dinutuximab as the first-line treatment. In 3 children dinutuximab was administered as second-line therapy with a median of 18 months (range 9-21) after relapse. For the majority of patients, the treatment tolerance was acceptable. The main adverse events were fever (n = 4), vision impairment (n = 1) and capillary leak syndrome (n = 1). The adverse events were 1-2 degrees, so all patients completed the treatment. At the time of analysis, two patients remain
{"title":"Pediatric Hematopoietic Stem Cell Transplantation in Lithuania - 20 Years of Progress through Collaboration.","authors":"Jelena Rascon,&nbsp;Goda Elizabeta Vaitkevičienė,&nbsp;Sonata Šaulytė Trakymienė,&nbsp;Ramunė Pasaulienė","doi":"10.15388/Amed.Supp.2022.292.2","DOIUrl":"https://doi.org/10.15388/Amed.Supp.2022.292.2","url":null,"abstract":"Hematopoietic stem cell transplantation (HSCT) is a complex procedure that is curative for several fatal pediatric malignancies and non-malignant diseases. Despite its complexity, potential toxicity, and high costs HSCT has become a standard procedure worldwide for several decades. Pediatric HSCT programs encounter several specific challenges. The rarity and heterogeneity of primary diseases, result in an almost 10-fold inferior number of pediatric HSCT as compared to adults. In con-trast to the adult programs, where autologous HSCT is more common, allogeneic HSCT (that is more complex) prevails in pediatric setting which is underpinned by a higher number of inborn disorders transplanted in early childhood. In Here we summarize conference proceedings presented at the scientific event “Pediatric hematopoietic stem cell transplantation in Lithuania – 20 years of progress through collaboration”. The meeting held on September 22-23, 2022, in Vilnius and aimed at commemorating 20 years of the launch of the pediatric transplant program in Lithuania. The event pursued sharing the experience in the field of pediatric HSCT in the Baltic countries. Given a very in all three Baltic countries, and face an additional challenge in maintaining sufficient transplant volume and gaining experience. Several distinguished speakers from USA, Spain, UK and shared their expertise in the field and emphasized the crucial role of national and international collaboration to achieve progress in the management of this very rare and complex procedure that offers for otherwise fatal pediatric conditions. Background: Neuroblastoma (NB) is the most common extracranial solid tumor in childhood. High-risk NB still has a poor prognosis and requires complex aggressive therapy. For a decade, immunotherapy with dinutuximab – anti GD2 chimeric monoclonal antibody – was integrated into treatment protocols as a routine part of the treatment. However, drug administration is related to potentially severe adverse effects. Thus, its administration is recommended in experienced centers. We aim to describe the first Lithuanian experience with dinutuximab. Methods: We performed a retrospective analysis of patients with high-risk NB treated with dinutuximab at our institution in 2020-2022. Toxicity and treatment outcomes were evaluated. The data were retrieved from electronic and paper records. Results: in 2020-2022, four patients were treated with dinutuximab. Totally, 20 cycles were de-livered, 5 cycles in each patient. One patient received dinutuximab as the first-line treatment. In 3 children dinutuximab was administered as second-line therapy with a median of 18 months (range 9-21) after relapse. For the majority of patients, the treatment tolerance was acceptable. The main adverse events were fever (n = 4), vision impairment (n = 1) and capillary leak syndrome (n = 1). The adverse events were 1-2 degrees, so all patients completed the treatment. At the time of analysis, two patients remain","PeriodicalId":34365,"journal":{"name":"Acta Medica Lituanica","volume":"29 2","pages":"1-17"},"PeriodicalIF":0.0,"publicationDate":"2022-01-01","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9799012/pdf/","citationCount":null,"resultStr":null,"platform":"Semanticscholar","paperid":"41158248","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
Ultrasound Simulation for Training Trainees when the Luxury Becomes Essential: Opinion and Evidence Obtained during the Latvian Research Council Project Implementation. 当奢侈品变得必不可少时,培训学员的超声波模拟:拉脱维亚研究委员会项目实施期间获得的意见和证据。
Q3 Medicine Pub Date : 2022-01-01 Epub Date: 2022-06-29 DOI: 10.15388/Amed.2022.29.2.16
Natālija Vedmedovska, Anda Ķīvīte-Urtāne, Ija Lisovaja, Laura Rācene, Līva Ķīse, Beāte Sārta, Agnija Vaska, Zane Rostoka, Violeta Bule, Ieva Pitkēviča, Dace Rezeberga

Background: Simulation as a proxy tool for conditional clinical training became a powerful technique for introducing trainees to the ultrasound imaging world, allowing them to become a trained sonographer taking into consideration different rates of progress in completing a specific task against the time and ensuring the long-lasting maintenance of the obtained practical skills. Adding a costly, but effective high-fidelity simulator to the residency program justified the expense, demonstrating efficiency of training for improving the clinical performance and confidence of trainees.

Materials and methods: A pilot study in Riga Maternity Hospital within the framework of the study "Role of metabolome, biomarkers and ultrasound parameters in successful labor induction" (Fundamental and Applied Research Programme lzp-2021/1-0300) was performed between March 1st 2022 and 31st April 2022. A virtual-reality simulator (ScanTrainer, MedaphorTM, Cardiff, UK) was used with the teaching module for assessment of the uterine cervix. Five trainees in obstetrics and two young specialists included in the study. None of them had Fetal Medicine Foundation certificate of competence in the assessment of the uterine cervical lenght before. The time used on the simulator, the number of simulations and a mean confidence in cervical length assessment before and after simulation were recorded.

Results: The study on assesment of uterine cervical lenght demonstrated statistically significant increase in confidence (p=0.008) and statistically significant decrease in time needed to complete correctly the same tasks for the trainees (p=0.008) that shows a positive learning curve over the time of training on ScanTrainer, Medaphor.

Conclusions: The simple task allows to become a certified specialist in uterine cervical assessment in the short period of time. That support the productiveness of the simulation-based education. The training program should be updated taking into consideration simulation curriculum.

背景:模拟作为有条件临床培训的代理工具,成为将受训者介绍到超声成像世界的一项强大技术,使他们能够成为一名训练有素的声谱师,同时考虑到在完成特定任务时不同的进度,并确保长期保持所获得的实用技能。在住院医师项目中添加一个昂贵但有效的高保真度模拟器证明了费用的合理性,证明了培训的效率,可以提高受训人员的临床表现和信心。材料和方法:在2022年3月1日至2022年4月31日期间,里加妇产医院在“代谢组、生物标志物和超声参数在成功引产中的作用”研究(基础和应用研究计划lzp-2021/1-0300)的框架内进行了一项试点研究。虚拟现实模拟器(ScanTrainer,MedaphorTM,英国加的夫)与教学模块一起用于评估子宫颈。五名产科受训人员和两名年轻专家参与了这项研究。他们之前都没有胎儿医学基金会的子宫颈长度评估能力证书。记录模拟器上使用的时间、模拟次数以及模拟前后颈部长度评估的平均置信度。结果:对子宫颈长度评估的研究表明,受训人员的置信度在统计学上显著提高(p=0.008),正确完成相同任务所需的时间在统计学上明显减少(p=0.008,结论:简单的任务可以在短时间内成为子宫颈评估的认证专家。这支持了基于模拟的教育的生产力。培训计划应根据模拟课程进行更新。
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引用次数: 0
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Acta Medica Lituanica
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