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Treatment of de novo femoro-popliteal lesions with a new Drug Coated Balloon: early experience of a single Center in the first 50 patients. 新型药物包覆球囊治疗新发股腘窝病变:前50例单中心患者的早期经验
IF 1.5 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-20 eCollection Date: 2018-11-01
U M Bracale, M Di Filippo, A De Capua, L Vanni, D Narese, F Pecoraro, A M Giribono, R Bracale

Angioplasty with drug-coated balloon (DCB) is an emerging and reliable method for the treatment of femoro-popliteal lesions. We report our experience with the Stellarex™ DCB in the first 50 patients.

Methods: From July 2015 to November 2017, 50 patients (41 M, 9F), medium age (64 ± 7.4 year) were subject to 33 angioplasties (PTAs) for femoro-popliteal lesions with a paclitaxel-coated balloon (Stellarex™). Based upon clinical data sixteen patients had severe claudication (56% - Rutherford class 3); ten patients suffered from ischemic rest pain (34% - Rutherford class 4); and five presented minor tissue loss (10% - Rutherford class 5). 42% of patients showed femoro-popliteal lesion TASC-II B, and 58% presented lesions pertaining to TASC-II C.

Results: Immediate technical success was 100% without perioperative complications. Primary patency rate was 94% at twelve months. In three cases restenosis (6%) was detected within a year from procedure, and a further PTA DCB was performed with primary assisted patency rates of 100% at twelve months. Two patients underwent major lower limb amputation. Three patients died during follow-up and one patient was lost at follow-up.

Conclusion: DCB angioplasty with Stellarex™ is a viable alternative to traditional endovascular procedures proving satisfactory primary patency rates at twelve months. Based on our experience, treatment with DCB is a first choice technique for non-complex de novo lesions of the femoro - popliteal tract.

药物包被球囊血管成形术(DCB)是一种新兴的、可靠的治疗股腘窝病变的方法。我们报告了我们在前50名患者中使用Stellarex™DCB的经验。方法:2015年7月至2017年11月,采用紫杉醇包被球囊(Stellarex™)对50例(41 M, 9F)中年龄(64±7.4岁)患者行33例股骨-腘动脉病变血管成形术(pta)。根据临床资料,16例患者有严重跛行(56% - Rutherford分类3);10例患者出现缺血性休息痛(34% - Rutherford分类4);42%的患者表现为股腘窝TASC-II B型病变,58%的患者表现为TASC-II c型病变。结果:立即技术成功率为100%,无围手术期并发症。12个月时原发性通畅率为94%。其中3例(6%)在手术后一年内发现再狭窄,并在12个月时进行了PTA DCB,主要辅助通畅率为100%。2例患者行下肢大截肢。3例患者在随访中死亡,1例患者在随访中丢失。结论:采用Stellarex™的DCB血管成形术是传统血管内手术的可行替代方案,在12个月时具有令人满意的初级通畅率。根据我们的经验,DCB治疗是非复杂的股腘束新发病变的首选技术。
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引用次数: 0
Errata corrige. 勘误表。
IF 1.5 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-20 eCollection Date: 2018-11-01

[This corrects the article on p. 25 in vol. 17, PMID: 30083520.].

[这是对第17卷第25页文章的更正,PMID: 30083520]。
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引用次数: 0
Pediatric Anesthesia. 小儿麻醉。
IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 eCollection Date: 2019-07-01
S Tesoro, L Marchesini, E De Robertis
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引用次数: 0
Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification 当前Espaghan儿科年龄腹腔疾病指南,三级护理中心经验:进一步简化的建议
IF 1.5 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 DOI: 10.14273/UNISA-2794
M. Malamisura, R. Colantuono, V. Salvati, R. Croce, G. D’Adamo, T. Passaro, E. D’Angelo, M. Boffardi, A. Garzi, B. Malamisura
According to the 2012 ESPGHAN criteria for diagnosis of celiac disease (CD), duodenal biopsy (DB) can be avoided in children with a clear malabsorption syndrome, anti-tissue transglutaminase IgA (tTG2) ≥ 10x the cut-off, anti-endomysium IgA (EMA) and HLA DQ2/DQ8 genes. The aim of this study is to report our experience and evaluate the accuracy of the actual guidelines. Patients and methods This is a retrospective study conducted on all patients diagnosed CD from 2012 to 2018 in our Center. For all patients enrolled were analyzed: data of family history, symptoms, serology, genetics, Marsh grade and follow-up. Results A total of 481 children [mean age 6,4 yrs; F:M= 1.8:1] were included in the study. The mean age of patients who were not subject to DB was lower (4.51 yrs) comparing with patients that received DB (6.48 yrs). Out of the 256 patients with anti-tTG2 ≥ 10 fold, 121 underwent DB because of mild symptoms (84/121) or no symptoms (37/121). In all cases Marsh type 3 was found and HLA haplotypes was compatible with CD diagnosis. Conclusions Our study confirms that the serology has a primary importance to diagnose CD, regardless of the symptoms. These data suggest that biopsy and HLA haplotypes search, in presence of anti-tTG2 IgA ≥ 10x the cut-off, are wasteful and unhelpful for the patients.
根据2012年ESPGHAN乳糜泻(CD)诊断标准,患有明显吸收不良综合征、抗组织谷氨酰胺转胺酶IgA(tTG2)≥10倍截止值、抗肌内膜IgA(EMA)和HLA DQ2/DQ8基因的儿童可以避免十二指肠活检(DB)。本研究的目的是报告我们的经验,并评估实际指南的准确性。患者和方法这是一项对我中心2012年至2018年所有诊断为CD的患者进行的回顾性研究。对所有入选患者进行分析:家族史、症状、血清学、遗传学、Marsh分级和随访数据。结果481名儿童[平均年龄6.4岁;F:M=1.8:1]被纳入研究。未接受DB治疗的患者的平均年龄(4.51岁)低于接受DB治疗(6.48岁)。在256名抗tTG2≥10倍的患者中,121名患者因症状轻微(84/121)或无症状(37/121)而接受DB治疗。在所有病例中均发现Marsh 3型,HLA单倍型与CD诊断一致。结论我们的研究证实,无论症状如何,血清学对CD的诊断都具有重要意义。这些数据表明,在抗tTG2 IgA≥10倍临界值的情况下,活检和HLA单倍型搜索对患者来说是浪费和无益的。
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引用次数: 5
Auditory-Verbal Processing Disorder and Dyslexia in Adulthood. 听觉语言处理障碍和成年期阅读障碍。
IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 eCollection Date: 2019-07-01
C Cassandro, A Manassero, A Scarpa, V Landi, G Aschero, S Lovallo, P Velardo, P De Luca, A Albera, R Albera, E Cassandro
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引用次数: 0
Current Espghan Guidelines for Celiac Disease in Pediatric Age, Tertiary Care Center Experience: A Proposal for Further Simplification. 当前的Espaghan小儿腹腔疾病指南,三级护理中心经验:进一步简化的建议。
IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 eCollection Date: 2019-07-01
M Malamisura, R Colantuono, V M Salvati, R Croce, G D'Adamo, T Passaro, E D'Angelo, M Boffardi, A Garzi, B Malamisura

According to the 2012 ESPGHAN criteria for diagnosis of celiac disease (CD), duodenal biopsy (DB) can be avoided in children with a clear malabsorption syndrome, anti-tissue transglutaminase IgA (tTG2) ≥ 10x the cut-off, anti-endomysium IgA (EMA) and HLA DQ2/DQ8 genes. The aim of this study is to report our experience and evaluate the accuracy of the actual guidelines.

Patients and methods: This is a retrospective study conducted on all patients diagnosed CD from 2012 to 2018 in our Center. For all patients enrolled were analyzed: data of family history, symptoms, serology, genetics, Marsh grade and follow-up.

Results: A total of 481 children [mean age 6,4 yrs; F:M= 1.8:1] were included in the study. The mean age of patients who were not subject to DB was lower (4.51 yrs) comparing with patients that received DB (6.48 yrs). Out of the 256 patients with anti-tTG2 ≥ 10 fold, 121 underwent DB because of mild symptoms (84/121) or no symptoms (37/121). In all cases Marsh type 3 was found and HLA haplotypes was compatible with CD diagnosis.

Conclusions: Our study confirms that the serology has a primary importance to diagnose CD, regardless of the symptoms. These data suggest that biopsy and HLA haplotypes search, in presence of anti-tTG2 IgA ≥ 10x the cut-off, are wasteful and unhelpful for the patients.

根据2012年ESPGHAN乳糜泻(CD)诊断标准,患有明显吸收不良综合征、抗组织谷氨酰胺转胺酶IgA(tTG2)≥10倍截止值、抗肌内膜IgA(EMA)和HLA DQ2/DQ8基因的儿童可以避免十二指肠活检(DB)。本研究的目的是报告我们的经验,并评估实际指南的准确性。患者和方法:这是对我中心2012年至2018年所有诊断为CD的患者进行的回顾性研究。对所有入选患者的家族史、症状、血清学、遗传学、Marsh分级和随访数据进行分析。结果:共有481名儿童[平均年龄6.4岁;F:M=1.8:1]被纳入研究。未接受DB治疗的患者的平均年龄(4.51岁)低于接受DB治疗(6.48岁)。在256名抗tTG2≥10倍的患者中,121名患者因症状轻微(84/121)或无症状(37/121)而接受DB治疗。在所有病例中均发现Marsh 3型,HLA单倍型与CD诊断一致。结论:我们的研究证实,无论症状如何,血清学对CD的诊断都具有首要意义。这些数据表明,在抗tTG2 IgA≥10倍临界值的情况下,活检和HLA单倍型搜索对患者来说是浪费和无益的。
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引用次数: 0
Pre and Post-Operative Ph-Metry in Videolaparoscopic Surgery for Gastro Oesophageal Reflux Disease. 胃食管反流病电视腹腔镜手术的术前和术后Ph-Metry。
IF 1.1 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 eCollection Date: 2019-07-01
A Garzi, G Ardimento, U Ferrentino, S Brongo, R M Di Crescenzo, E Calabrò, M S Rubino, B Malamisura, E Clemente

Gastro-oesophageal reflux is common in children, especially in the first year of life, and it may be regarded as physiological. Good functioning of the lower oesophageal sphincter depends largely on the anatomical relationships between oesophagus, stomach and diaphragm hiatus. Relative immaturity of these structures in newborn babies and young children is a risk factor in reflux disease, which may result in a wide variety of typical and/or atypical symptoms and, sometimes, serious complications such as oesophagitis and stenosis. Reflux disease may be diagnosed and studied, basing on morphological and functional aspects and, since the advent of pH-metry, it is possible to personalise the therapeutic approach to children with reflux. Surgical treatment of reflux disease in children has recently been improved due to a mini-invasive surgical approach. Absolute indications are recurrent pneumonia, intractable pain due to oesophagitis and retarded growth, often in association with neurological impairment. In the last three years, 18 children with reflux disease underwent videolaparoscopic surgery in our department, 14 by the Nissen and 4 by the Toupet technique. Post-operative pH-metry always showed a reduction in exposure of the distal oesophagus to acid (integral of H+) and an improvement in oesophageal clearance (short refluxes percentage) indicative of good functioning of the gastro-oesophageal junction. PH-metry proved to be an invaluable technique for planning therapeutic strategy. In follow-up evaluations, it enabled us to monitor functioning of the gastro-oesophageal junction and to avoid other more difficult and invasive tests in patients with severe neurological impairment.

胃食管反流在儿童中很常见,尤其是在出生的第一年,它可能被认为是生理性的。食管下括约肌的良好功能在很大程度上取决于食管、胃和膈肌裂孔之间的解剖关系。新生儿和幼儿的这些结构相对不成熟是反流病的一个危险因素,反流病可能会导致各种典型和/或非典型症状,有时还会导致食道炎和狭窄等严重并发症。反流性疾病可以根据形态学和功能方面进行诊断和研究,并且由于pH测量的出现,有可能对反流性儿童的治疗方法进行个性化。儿童反流性疾病的外科治疗最近由于一种微创手术方法而有所改进。绝对适应症是复发性肺炎、食道炎引起的顽固性疼痛和生长迟缓,通常与神经损伤有关。在过去的三年里,我科有18名患有反流疾病的儿童接受了视频腹腔镜手术,其中14名接受了Nissen手术,4名接受了Toupet技术。术后pH测量始终显示,食管远端暴露于酸的程度减少(H+积分),食管清除率提高(短回流百分比),表明胃-食管交界处功能良好。PH测定被证明是制定治疗策略的一项宝贵技术。在后续评估中,它使我们能够监测胃食管交界处的功能,并避免对严重神经损伤患者进行其他更困难和更具侵入性的测试。
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引用次数: 0
Errata corrige. 勘误表。
IF 1.5 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 eCollection Date: 2019-07-01

[This corrects the article on p. 27 in vol. 19, PMID: 31360664.].

[这是对第19卷第27页文章的更正,PMID: 31360664]。
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引用次数: 0
Auditory-Verbal Processing Disorder and Dyslexia in Adulthood 听觉言语加工障碍与成人阅读障碍
IF 1.5 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 DOI: 10.14273/UNISA-2791
C. Cassandro, A. Manassero, A. Scarpa, V. Landi, G. Aschero, S. Lovallo, P. Velardo, P. De Luca, A. Albera, R. Albera, E. Cassandro
28 Università degli Studi di Salerno Introduction According to the Diagnostic and Statistic Manual of Mental Disorders (DSM-V), the neurodevelopment disorders are characterised by an atypical development of some cognitive domains, with a dysfunctional behavioural correlation supported by phenotypes with a genetic connection. Among these are the specific learning disabilities, which are united by a single condition characterised by difficulty in learning and using academic skills in the presence of an adequate IQ; these include dyslexia, dyscalculia and dysorthography. The clinical features are an inaccurate or slow and laborious reading of the words, difficulty in understanding the meaning of what is read, difficulty in spelling, in written expression, in mastering the concept of number, numerical data ora calculation, and in arithmetic reasoning. Recently, thanks to the better understanding of the neurobiological mechanisms underlying these disorders and thanks to the improvement of neuroimaging and genetic analysis, we better understood the evolution of these pathologies and consequently we have refined the diagnosis and treatment. Studies focused particularly more on dyslexia, both due to its high frequency in general population and to the better understanding of its pathogenesis. Various cognitive models are developed to explain the nature of the processes underlying the recognition of written words; the models explained partially the cause of dyslexia, tracing it back to a phonological deficit of consciousness. Today none of these models seems to prevail, but we believe that, in the context of a general reading disorder, there are several difficulties that can be either phonological or about phonological, motor or visual consciousness, due to the failure of magnocellular/auditory neurons development, because of an altered central processing. Already in the 80s, Tallal et al. recognised the phonological deficit as a symptom of a deficit of sound processing presented in rapid sequence (proper of verbal oral language) and therefore a deficit of elaboration at the auditory temporal cortex. This difficulty in the sounds analysis could lead to a wrong categorization and to a failure to recognise the phoneme as the acoustic characteristics change. From studies carried out on children with dyslexia, deficient performances emerged in conditions of short auditory stimuli presented in rapid sequence, while the performance improved with a longer stimulus interval. These difficulties lead to a need for longer times to discriminate short sounds in rapid sequence. Tallal deduced that children with dyslexia presented not a linguistic deficit but a deficit of temporal elaboration of the variation of the auditory patterns, which then translated into a difficulty in the perception of isolated language. In auditory perception of sounds, both when proposed in rapid sequences and with a longer time intervals, a primary role is played by auditory attention, expeci
28萨莱诺大学简介根据《精神障碍诊断和统计手册》(DSM-V),神经发育障碍的特征是一些认知领域的非典型发展,具有由具有遗传联系的表型支持的功能失调的行为相关性。其中包括特定的学习障碍,这些障碍由一种单一的条件结合在一起,其特征是在智商足够的情况下难以学习和使用学术技能;其中包括阅读障碍、计算障碍和拼写障碍。临床特征是单词阅读不准确或缓慢而费力,难以理解所读内容的含义,拼写、书面表达、掌握数字概念、数字数据或计算以及算术推理困难。最近,由于对这些疾病背后的神经生物学机制的更好理解,以及神经成像和基因分析的改进,我们更好地了解了这些病理的演变,因此我们改进了诊断和治疗。研究尤其集中在阅读障碍上,这既是因为它在普通人群中的频率很高,也是为了更好地了解它的发病机制。开发了各种认知模型来解释书面单词识别过程的本质;这些模型部分解释了阅读障碍的原因,将其追溯到意识的语音缺陷。如今,这些模型似乎都不占上风,但我们认为,在一般阅读障碍的背景下,由于中央处理的改变,大细胞/听觉神经元发育失败,存在一些语音或语音、运动或视觉意识方面的困难。早在80年代,Tallal等人就认识到语音缺陷是声音处理缺陷的一种症状,这种缺陷以快速序列出现(口头语言的固有特征),因此是听觉颞皮层的精细化缺陷。声音分析中的这种困难可能导致错误的分类,并导致在声学特征变化时无法识别音素。根据对阅读障碍儿童进行的研究,在以快速顺序呈现的短听觉刺激条件下,表现会出现缺陷,而刺激间隔越长,表现就会改善。这些困难导致需要更长的时间来区分快速序列中的短音。Tallal推断,患有阅读障碍的儿童表现出的不是语言缺陷,而是听觉模式变化的时间阐述缺陷,这转化为孤立语言感知的困难。在声音的听觉感知中,无论是在快速序列中还是在较长的时间间隔中,主要作用都是听觉注意力,特别是集中的听觉注意力。这项工作的目的是呈现具有特定阅读学习障碍的成年患者的特征,并评估其与语音意识缺陷(因此分析和操纵单词语言结构的能力)以及听觉语言处理障碍的可能相关性。
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引用次数: 2
Recurrence of Non-Hydropic Sudden Sensorineural Hearing Loss (SSNHL): A Literature Review. 非水性突发性感觉神经性听力损失(SSNHL)的复发:文献综述。
IF 1.5 Q4 MEDICINE, RESEARCH & EXPERIMENTAL Pub Date : 2019-01-12 eCollection Date: 2019-07-01
C Cassandro, P De Luca, M Ralli, F Gioacchini, F Di Berardino, A Albera, R Albera, E Cassandro, A Scarpa
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引用次数: 0
期刊
Translational Medicine at UniSa
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