Surgical Technique of Supine Percutaneous Nephrolithotomy in Children / Técnica quirúrgica de la nefrolitotomía percutánea en supino en niños

Percutaneous nephrolithotomy (PCNL) in children has becomemore widely used due to its high efficacy and safety and to the development of miniaturized instruments. A supine approach is promising due to advantages such as better ventilation, reproducibility, and ergonomics. The purpose of the present study is to describe our surgical technique with special considerations in the pediatric population. We used an oblique supine position supported by one silicone gel positioning pad under the hip and another under the ipsilateral flank. The anatomical landmarks used to guide the puncture were the 11th and 12th ribs, the posterior axillary line, and the iliac crest. Initially, a ureteral catheter was introduced endoscopically. A retrograde pyelography was performed to guide the puncture, which was performed using a biplanar technique. A hydrophilic guide wire was then advanced through the needle. Dilation was performed with Alken telescopic dilators until 14 Ch. Fragmentation was performed either with a 13 Ch semirigid cystoscope or a flexible ureteroscope using a holmium: yttrium aluminum garnet (Ho:Yag) laser.We left a double J catheter. Supine PCNL in the pediatric population has comparable efficacy in terms of stone free rate to that of the prone approach as well as less complications. Certain considerations in children are careful padding and placement of the patient close to the edge of the table. Puncture should be guided by ultrasound to reduce radiation exposure. Miniaturized equipment is not widely available, so adaptation of adult equipment for the pediatric population is sometimes necessary.

La nefrolitotomía percutánea en niños se ha vuelto ampliamente utilizada por su alta efectividad, seguridad, y por la miniaturización de los instrumentos endoscópicos. El abordaje en supino es prometedor por sus ventajas, como mejor ventilación, reproducibilidad, y ergonomía. El propósito es describir nuestra técnica quirúrgica con las consideraciones especiales a tener en cuenta en la población pediátrica. Todos nuestros pacientes han sido intervenidos bajo la siguiente técnica quirúrgica: en una posición oblicua en supino, utilizando soportes de silicona ubicados debajo de la cadera y del flanco ipsilateral, se marcan los reparos anatómicos: las costillas once y doce, la línea axilar posterior y la cresta ilíaca. Inicialmente se introduce un cateter ureteral por vía endoscópica, con el cual se realiza una pielografía retrógrada para guiar la punción con una técnica biplanar. Se avanza una guía hidrofílica y, sobre esta, los dilatadores telescopados de Alken hasta un tracto de 14 Ch. Se realiza la fragmentación con un cistoscopio semirígido de 13 Ch o con un ureteroscopio flexible utilizando el láser Ho:Yag. Se deja un cateter JJ. La nefrolitotomía percutánea en la población pediátrica es comparable en términos de tasa libre de cálculos al abordaje en prono, con menos complicaciones. Una consideración importante en niños es una adecuada posición, cerca al eje de la mesa. La punción debe ser guiada por ultrasonido para disminuir la exposición a radiación. La disponibilidad de equipos miniaturizados es limitada, por lo cual usualmente es necesario adaptar los equipos de adultos.

A new miniature species of Odontocharacidium (Characiformes: Crenuchidae) from the Río Orinoco basin, Venezuela

A new species of Odontocharacidium is described from the upper Río Orinoco basin, in Venezuela. The new species is distinguished from its only congener, Odontocharacidium aphanes, by the presence of: the antorbital, the parietal branch of the supraorbital laterosensory canal, the postcleithrum 1, the conspicuous bars extending ventrally below the middle portion of the body posteriorly, and two dark round blotches at the tip of the caudal peduncle. With the recognition of an additional species of Odontocharacidium the diagnostic characters of the genus and the variability in the number of maxillary teeth in specimens are discussed.(AU)

Uma nova espécie de Odontocharacidium é descrita para a bacia do alto rio Orinoco, na Venezuela. A nova espécie se distingue da sua única congênere, Odontocharacidium aphanes, pela presença: do antorbital, do ramo parietal do canal látero-sensorial supraorbital, do pós-cleitro 1, de barras conspícuas estendendo-se ventralmente à porção média do corpo e de duas manchas escuras e arredondadas na margem distal do pedúnculo caudal. Com o reconhecimento de uma espécie adicional de Odontocharacidium, são discutidos os caracteres diagnósticos do gênero e a variação no número de dentes maxilares nos espécimes.(AU)

Clinco-pathologic Features of Alopecia in a Patient of Cronkhite-Canada Syndrome / 대한피부과학회지

Although hair loss in Cronkhite-Canada syndrome (CCS) developed frequently, its exact mechanism has not been elucidated. Thus, we attempted to investigate the histopathologic features of hair loss with scalp biopsy in one case of CSS. The patient complained of persistent diarrhea and diffuse hair loss of the scalp 1 month prior to the hospital visit. CCS has been already diagnosed through colonoscopy and medical examination. Scalp biopsy was performed to evaluate hair loss of the patient, and pathologic examination showed increased telogen hairs (anagen to telogen is 7:8) without specific dermal inflammation and miniaturization of hair follicles. The patient was treated with topical and systemic steroids, and hair loss has almost completely recovered in 5 months. In this case, we investigated the clinical and pathological features of hair loss through scalp biopsy in one case of CCS and reported them with a review of the literature.

Use of miniplates as a method for orthodontic anchorage: a case report

ABSTRACT Introduction: Temporary anchorage devices (TADs) have been developed to be used as direct adjuncts in orthodontic treatment and have facilitated treatment of more complex orthodontic cases, including patients with dental impaction. Objectives: This clinical case reports the applicability of TADs in the orthodontic treatment of a patient with impacted mandibular second molars. Surgical and orthodontic procedures related to the use of miniplates were also discussed in this study. Conclusions: The use of temporary anchorage devices, such as miniplates, can be suggested as an alternative to treat patients with impacted mandibular second molars.

RESUMO Introdução: os dispositivos de ancoragem temporária vêm sendo desenvolvidos para uso como coadjuvantes no tratamento ortodôntico. Esses dispositivos facilitam o tratamento ortodôntico de casos mais complexos, incluindo pacientes com dentes impactados. Objetivos: o presente relato de caso reporta a aplicabilidade dos dispositivos de ancoragem temporária no tratamento ortodôntico de um paciente com segundos molares inferiores impactados. Os procedimentos cirúrgicos e ortodônticos relacionados ao uso das miniplacas também são discutidos nesse estudo. Conclusões: o uso de dispositivos de ancoragem temporária, tais como as miniplacas, pode ser sugerido como uma alternativa no tratamento de pacientes com segundos molares inferiores impactados.

Current Status and Research into Overcoming Limitations of Capsule Endoscopy

Endoscopic investigation has a critical role in the diagnosis and treatment of gastrointestinal (GI) diseases. Since 2001, capsule endoscopy (CE) has been available for small-bowel exploration and is under continuous development. During the past decade, CE has achieved impressive improvements in areas such as miniaturization, resolution, and battery life. As a result, CE is currently a first-line tool for the investigation of the small bowel in obscure gastrointestinal bleeding and is a useful alternative to wired enteroscopy. Nevertheless, CE still has several limitations, such as incomplete examination and limited diagnostic and therapeutic capabilities. To resolve these problems, many groups have suggested several models (e.g., controlled CO2 insufflation system, magnetic navigation system, mobile robotic platform, tagging and biopsy equipment, and targeted drug-delivery system), which are in development. In the near future, new technological advances will improve the capabilities of CE and broaden its spectrum of applications not only for the small bowel but also for the colon, stomach, and esophagus. The purpose of this review is to introduce the current status of CE and to review the ongoing development of solutions to address its limitations.

New Technology for Type 1 Diabetes / 임상당뇨병

Type 1 diabetes is an autoimmune disease with insulin deficiency which causes microvascular complications such as retinopathy, nephropathy and neuropathy. There have been some trials to simulate the pancreatic endocrine function of insulin and glucagon for homeostatic equilibration of blood glucose, developing artificial pancreas. There are three major functional components of the modern artificial pancreas, a continuous glucose-monitoring system, an insulin-infusion pump and a control algorithm. There are commercially available continuous glucose monitoring systems with subcutaneous glucose measuring, however, there have been many attempts to develop more efficient glucose monitoring systems, including noninvasive systems. Thanks to technological advances and the miniaturization of electronics, recent advances in the accuracy and performance of these systems have placed research on the threshold of prototype commercial devices and large-scale outpatient feasibility studies. In addition, smartphone technology has created the opportunity for caregivers to receive push notification alerts and makes it possible to provide patients with advisory or decision-support systems. Even though there are still some remaining challenges to develop a successful artificial pancreas, glucose control in type 1 diabetes will be more efficient with its advent.

Insertion torque versus mechanical resistance of mini- implants inserted in different cortical thickness

OBJECTIVE: This study aimed to measure insertion torque, tip mechanical resistance to fracture and transmucosal neck of mini-implants (MI) (Conexão Sistemas de PróteseT), as well as to analyze surface morphology. METHODS: Mechanical tests were carried out to measure the insertion torque of MIs in different cortical thicknesses, and tip mechanical resistance to fracture as well as transmucosal neck of MIs. Surface morphology was assessed by scanning electron microscopy (SEM) before and after the mechanical tests. RESULTS: Values of mechanical resistance to fracture (22.14 N.cm and 54.95 N.cm) were higher and statistically different (P < 0.05) from values of insertion torque for 1-mm (7.60 N.cm) and 2-mm (13.27 N.cm) cortical thicknesses. Insertion torque was statistically similar (P > 0.05) to torsional fracture in the tip of MI (22.14 N.cm) when 3 mm cortical thickness (16.11 N.cm) and dense bone (23.95 N.cm) were used. Torsional fracture of the transmucosal neck (54.95 N.cm) was higher and statistically different (P < 0.05) from insertion torsional strength in all tested situations. SEM analysis showed that the MIs had the same smooth surface when received from the manufacturer and after the mechanical tests were performed. Additionally, no significant marks resulting from the manufacturing process were observed. CONCLUSION: All mini-implants tested presented adequate surface morphology. The resistance of mini-implants to fracture safely allows placement in 1 and 2-mm cortical thickness. However, in 3-mm cortical thickness and dense bones, pre-drilling with a bur is recommended before insertion. .

OBJETIVOS: os objetivos foram determinar os torques de inserção, a resistência mecânica à fratura da ponta e do perfil transmucoso de mini-implantes (MI) de uma marca comercial (Conexão Sistemas de Prótese), e analisar sua morfologia de superfície. MÉTODOS: foram realizados testes mecânicos para medir o torque de inserção dos MI em corticais de diferentes espessuras, também foi avaliada a resistência à fratura da ponta e do perfil transmucoso. Antes e após os ensaios mecânicos, foi avaliada a superfície dos MI no microscópio eletrônico de varredura (MEV). RESULTADOS: os valores de resistência à fratura dos MI (22,14N.cm2 e 54,95N.cm2) foram maiores e estatisticamente diferentes (p < 0,05) dos torques de inserção nas corticais de 1mm (7,60N.cm2) e de 2mm (13,27N.cm2). Entretanto, o valor do torque de inserção na cortical de 3mm (16,11N.cm2) e no osso denso (23,95N.cm2) foi estatisticamente semelhante (p > 0,05) ao torque de fratura da ponta do MI (22,14N.cm2). O torque de fratura do perfil transmucoso (54,95N.cm2) foi maior e estatisticamente diferente (p < 0,05) dos torques de inserção em qualquer uma das situações testadas. A análise em MEV mostrou que os MI, como recebidos e após os testes mecânicos, possuem superfícies lisas e sem marcas significativas oriundas do processo de fabricação. CONCLUSÃO: os MI avaliados apresentaram adequada morfologia da superfície. A resistência do MI foi compatível com a instalação em corticais de 1 e 2mm, porém, em cortical de 3mm e em ossos densos recomenda-se prévia perfuração com broca. .

Mini-implants and miniplates generate sub-absolute and absolute anchorage

The functional demand imposed on bone promotes changes in the spatial properties of osteocytes as well as in their extensions uniformly distributed throughout the mineralized surface. Once spatial deformation is established, osteocytes create the need for structural adaptations that result in bone formation and resorption that happen to meet the functional demands. The endosteum and the periosteum are the effectors responsible for stimulating adaptive osteocytes in the inner and outer surfaces.Changes in shape, volume and position of the jaws as a result of skeletal correction of the maxilla and mandible require anchorage to allow bone remodeling to redefine morphology, esthetics and function as a result of spatial deformation conducted by orthodontic appliances. Examining the degree of changes in shape, volume and structural relationship of areas where mini-implants and miniplates are placed allows us to classify mini-implants as devices of subabsolute anchorage and miniplates as devices of absolute anchorage.

Uma demanda funcional sobre o osso promove alterações na forma espacial da rede de osteócitos e seus prolongamentos, distribuídos uniformemente na estrutura mineralizada. A partir da deformação espacial captada, os osteócitos comandam a necessidade de adaptações estruturais, formando osso em novas áreas e reabsorvendo em outras, para que sejam atendidas as demandas funcionais. O endósteo e o periósteo são os verdadeiros efetores desses estímulos osteocíticos adaptativos, nas superfícies internas e externas. As alterações de forma, volume e posição dos ossos maxilares, nas correções esqueléticas da maxila e mandíbula, requerem uma ancoragem para que a remodelação óssea redefina a morfologia, a estética e as funções, a partir de deformações espaciais dirigidas por aparelhos. Verificar o grau de alterações na forma, volume e relações estruturais das áreas onde se fixaram os mini-implantes e as miniplacas poderá levar à classificação dos mini-implantes como dispositivos de ancoragem subabsoluta e as miniplacas, como de ancoragem absoluta.

Comparison of topical and infiltration anesthesia for orthodontic mini-implant placement

Objective: To compare the acceptability and effectiveness of topical and infiltration anesthesia for placement of mini-implants used as temporary anchorage devices. Methods: The sample comprised 40 patients, 17 males and 23 females, whose mean age was 26 years old and who were all undergoing orthodontic treatment and in need for anchorage reinforcement. Mini-implants were bilaterally placed in the maxilla of all individuals, with infiltration anesthesia on one side and topical anesthesia on the other. These 40 patients completed two questionnaires, one before and another after mini-implant placement and pain was measured through a visual analog scale (VAS). The data collected were analyzed using descriptive statistics and the measurements of pain were compared by means of the non-parametric test of Mann-Whitney. Results: It was found that 60% of patients felt more comfortable with the use of topical anesthesia for mini-implant placement; 72.5% of patients described the occurrence of pressure during placement of the anchorage device as the most unpleasant sensation of the entire process; 62.5% of patients felt more pain with the use of topical anesthesia. Conclusion: It was concluded that patients had less pain with the use of infiltration anesthesia, and also preferred this type of anesthetic. .

Objetivo: comparar a aceitabilidade e a efetividade do uso de anestésico tópico e anestésico infiltrativo para inserção de mini-implantes ortodônticos, utilizados como dispositivos de ancoragem temporária. Métodos: foram selecionados 40 pacientes, sendo 17 do sexo masculino e 23 do sexo feminino, com idade média de 26 anos, todos em tratamento ortodôntico e necessitando de reforço de ancoragem. Em todos os indivíduos foram instalados mini-implantes bilateralmente em maxila, sendo em um dos lados com anestesia infiltrativa e do lado oposto com anestesia tópica. Esses 40 pacientes responderam dois questionários, sendo um pré- e outro pós-operatório, e foram obtidos índices de dor por meio da escala visual análoga (VAS). Os dados coletados foram analisados por meio de estatística descritiva e os índices de dor foram comparados por meio do teste não-paramétrico de Mann-Whitney. Resultados: verificou-se que 60% dos pacientes se sentiram mais confortáveis com a utilização de anestesia tópica para a inserção dos mini-implantes; 72,5% dos pacientes apontaram a pressão durante a inserção do dispositivo de ancoragem como a sensação mais desagradável de todo o processo; 62,5% dos pacientes sentiram mais dor com o uso de anestesia tópica. Conclusão: concluiu-se que os pacientes apresentaram menor índice de dor com o uso de anestesia infiltrativa e que, também, preferiram esse tipo de anestésico. .

Reasons for mini-implants failure: choosing installation site should be valued!

Mini-implant loss is often associated with physical and mechanical aspects that result from choosing an inappropriate placement site. It is worth highlighting that: a) Interdental alveolar bone crests are flexible and deformable. For this reason, they may not offer the ideal absolute anchorage. The more cervical the structures, the more delicate they are, thus offering less physical support for mini-implant placement; b) Alveolar bone crests of triangular shape are more deformable, whereas those of rectangular shape are more flexible; c) The bases of the alveolar processes of the maxilla and the mandible are not flexible, for this reason, they are more likely to receive mini-implants; d) The more cervical a mini-implant is placed, the higher the risk of loss; the more apical a mini-implant is placed, the better its prognosis will be; e) 3D evaluations play a major role in planning the use of mini-implants. Based on the aforementioned considerations, the hypotheses about mini-implant loss are as follows: 1) Deflection of maxillary and mandibular alveolar processes when mini-implants are more cervically placed; 2) Mini-implants placed too near the periodontal ligament, with normal intra-alveolar tooth movement; 3) Low bone density, low thickness and low alveolar bone volume; 4) Low alveolar cortical bone thickness; 5) Excessive pressure inducing trabecular bone microfracture; 6) Sites of higher anatomical weakness in the mandible and the maxilla; 7) Thicker gingival tissue not considered when choosing the mini-implant.

As perdas de mini-implantes estão quase sempre relacionadas aos aspectos físicos e mecânicos decorrentes de uma escolha inadequada do local de inserção. Deve se destacar que: a) As cristas ósseas alveolares interdentárias têm flexão e se deformam, e podem não oferecer ancoragem tão absoluta. Quanto mais cervicais, as estruturas são mais delicadas e oferecem menos suporte físico para os mini-implantes; b) as cristas ósseas alveolares triangulares se deformam mais, e as retangulares são menos flexíveis; c) as bases do processo alveolar nos corpos da maxila e mandíbula não têm capacidade flexiva, e seu volume e estruturas são maiores, logo, são mais receptivas para mini-implantes; d) quanto mais próximo da cervical se coloca um mini-implante, maior é o risco de se perdê-lo; quanto mais apical se coloca o mini-implante, melhor é o seu prognóstico; e) avaliar a região tridimensionalmente representa um passo fundamental no planejamento do uso de mini-implantes. Com base nessas considerações, as hipóteses para a perda de mini-implantes são: 1) Deflexão do processo alveolar da maxila e mandíbula, quando fixados em posições mais cervicais; 2) proximidade com o ligamento periodontal e o movimento dentário intra-alveolar normal; 3) densidade óssea menor, pouca espessura e menor volume ósseo alveolar; 4) espessura menor da cortical óssea alveolar; 5) pressão excessiva, induzindo microfraturas ósseas trabeculares; 6) locais de maior fragilidade anatômica mandibular e maxilar; 7) espessura maior do tecido gengival não considerada na escolha do mini-implante.

Systematic review of mini-implant displacement under orthodontic loading / 国际口腔科学杂志·英文版

A growing number of studies have reported that mini-implants do not remain in exactly the same position during treatment, although they remain stable. The aim of this review was to collect data regarding primary displacement immediately straight after loading and secondary displacement over time. A systematic review was performed to investigate primary and secondary displacement. The amount and type of displacement were recorded. A total of 27 studies were included. Sixteen in vitro studies or studies using finite element analysis addressed primary displacement, and nine clinical studies and two animal studies addressed secondary displacement. Significant primary displacement was detected (6.4-24.4 µm) for relevant orthodontic forces (0.5-2.5 N). The mean secondary displacement ranged from 0 to 2.7 mm for entire mini-implants. The maximum values for each clinical study ranged from 1.0 to 4.1 mm for the head, 1.0 to 1.5 for the body and 1.0 to 1.92 mm for the tail part. The most frequent type of movement was controlled tipping or bodily movement. Primary displacement did not reach a clinically significant level. However, clinicians can expect relevant secondary displacement in the direction of force. Consequently, decentralized insertion within the inter-radicular space, away from force direction, might be favourable. More evidence is needed to provide quantitative recommendations.

Flexural strength of mini-implants developed for Herbst appliance skeletal anchorage: a study in Minipigs br1 cadavers

OBJECTIVE: The present study was designed to verify if mini-implant prototypes (MIP) developed for Herbst appliance anchorage are capable of withstanding orthopedic forces, and to determine whether the flexural strength of these MIP varies depending on the site of insertion (maxilla and mandible). METHODS: Thirteen MIP were inserted in three minipig cadavers (six in the maxilla and seven in the mandible). The specimens were prepared and submitted to mechanical testing. The mean and standard deviation were calculated for each region. A two-way Student's t test was used to compare the strength between the sites. A one-way Student's t test was performed to test the hypothesis. Orthopedic forces above 1.0 kgf were considered. RESULTS: The MIP supported flexural strength higher than 1.0 kgf (13.8 ± 2.3 Kg, in the posterior region of the maxilla and 20.5 ± 5.2 Kg in the anterior region of the mandible) with a significantly lower flexural strength in the anterior region of the mandible (P < 0.05). CONCLUSION: The MIP are capable of withstanding orthopedic forces, and are more resistant in the anterior region of the mandible than in the posterior region of the maxilla in Minipigs br1 cadavers.

OBJETIVO: o presente estudo foi delineado para verificar se protótipos de mini-implantes (PMI) desenvolvidos para a ancoragem esquelética do aparelho de Herbst são capazes de suportar forças ortopédicas e, também, determinar a variação da força de flexão desses PMI de acordo com o local de inserção (maxila ou mandíbula). MÉTODOS: após o cálculo do tamanho da amostra, 13 PMI foram colocados em três cadáveres de Minipigs br1 (seis na maxila e sete na mandíbula). Os corpos de prova foram preparados e submetidos a um teste mecânico. Cálculos da média e o do desvio-padrão foram realizados para cada região. O teste t de Student para duas amostras não pareadas foi utilizado para comparar a resistência dos PMI entre as regiões de inserção. O teste t de Student para uma amostra foi realizado para o teste de hipótese. Foram consideradas forças ortopédicas aquelas acima de 1,0kgf. RESULTADOS: os PMI foram capazes de suportar forças de flexão maiores que 1,0kgf (13,8 ± 2,3Kg na região posterior da maxila, e 20,5 ± 5,2Kg na região anterior da mandíbula), apresentando significativa menor força de flexão na região anterior da mandíbula (p < 0,05). CONCLUSÃO: os PMI são capazes de suportar forças ortopédicas, sendo mais resistentes quando utilizados na região anterior da mandíbula do que na posterior da maxila, em cadáveres de Minipigs br1.

Stent farmacológico autoexpansível miniaturizado em coronárias de pequeno calibre: eficácia tardia / Miniaturized self-expanding drug-eluting stent in small coronary arteries: late effectiveness

FUNDAMENTO: Na angioplastia coronária percutânea (ACP), os vasos de fino calibre representam um fator de risco para reestenose. O stent farmacológico (SF) autoexpansível Sparrow®, de perfil menor que os sistemas atuais, nunca foi testado nesse cenário. OBJETIVOS: Avaliar a eficácia tardia do SF Sparrow®, com relação à perda luminal tardia intrastent (PLT intrastent) aos oito meses. MÉTODOS: Estudo prospectivo, randomizado, em P com doença arterial coronária (DAC) sintomática ou com isquemia documentada, submetido à ACP em vasos de calibre < 2,75 mm, dividido em dois grupos quanto ao tipo de stent Sparrow®: grupo 1, SF; grupo 2, stent não farmacológico (SNF). O seguimento clínico foi de 12 meses. De imediato e aos oito meses, avaliação pela angiografia coronária quantitativa (ACQ). Para o cálculo da amostra estimou-se diminuição de mais de 65% de PLT intrastent com o SF. Para análise estatística utilizou-se o programa IBM SPSS Statistics® versão 19 (Chicago, Illinois, EUA). RESULTADOS: Foram incluídos 24 p, 12 em cada grupo. Os grupos SF e SNF foram semelhantes quanto à idade (63,25 ± 10,01 versus 64,58 ± 11,54, p = 0,765), sexo masculino (58,3% versus 33,3%, p = 0,412), fatores de risco e todos os aspectos angiográficos. Os resultados imediatos foram satisfatórios em ambos os grupos. Aos oito meses, a PLT intrastent foi significativamente menor no SF do que no SNF (SF 0,25 ± 0,16 versus SNF 0,97 ± 0,76, p = 0,008). CONCLUSÃO: Em ACP de vasos de calibre < 2,75 mm, o SF Sparrow® determinou significativa redução da PLT intrastent, em comparação ao SNF Sparrow®.

BACKGROUND: Small vessels represent a risk factor for restenosis in percutaneous coronary angioplasty (PCA). The Sparrow® self-expanding drug-eluting stent, which has a lower profile than the current systems, has never been tested in this scenario. OBJECTIVES: To evaluate the late effectiveness of the Sparrow® drug-eluting stent, regarding in-stent late lumen loss (LLL). METHODS: Patients with ischemia, symptomatic or documented, were submitted to PCA in vessels with reference diameter < 2.75 mm, divided into two groups regarding Sparrow® stent type: group 1: Sparrow® drug-eluting stent (DES), group 2: Sparrow® bare metal stent (BMS). Clinical follow-up duration was 12 months. Evaluation using quantitative coronary angiography (QCA) was performed immediately and at 8 months. A decrease of over 65% of in-stent LLL with DES was estimated to calculate sample size. IBM® SPSS software, release 19 (Chicago, Illinois, USA) was used for the statistical analysis. RESULTS: A total of 24 patients were randomized, 12 in each group. The DES and BMS groups were similar in age (63.25 ± 10.01 vs. 64.58 ± 11.54, p = 0.765), male gender (58.3% vs. 33.3%, p = 0.412), risk factors and all angiographs aspects. Immediate results were satisfactory in both groups. At 8 months in-stent late lumen loss was significantly lower in DES than in BMS group (DES vs. BMS 0.25 ± 0.16 0.97 ± 0.76, p = 0.008). CONCLUSION: In small-vessel PCA, the Sparrow® DES determined significant reduction in in-stent LLL, when compared to Sparrow® BMS.

Recent Progress in Lab-on-a-Chip Technology and Its Potential Application to Clinical Diagnoses / 대한배뇨장애요실금학회지

We present the construction of the lab-on-a-chip (LOC) system, a state-of-the-art technology that uses polymer materials (i.e., poly[dimethylsiloxane]) for the miniaturization of conventional laboratory apparatuses, and show the potential use of these microfluidic devices in clinical applications. In particular, we introduce the independent unit components of the LOC system and demonstrate how each component can be functionally integrated into one monolithic system for the realization of a LOC system. In specific, we demonstrate microscale polymerase chain reaction with the use of a single heater, a microscale sample injection device with a disposable plastic syringe and a strategy for device assembly under environmentally mild conditions assisted by surface modification techniques. In this way, we endeavor to construct a totally integrated, disposable microfluidic system operated by a single mode, the pressure, which can be applied on-site with enhanced device portability and disposability and with simple and rapid operation for medical and clinical diagnoses, potentially extending its application to urodynamic studies in molecular level.

The present and future state of minimized extracorporeal circulation / 中国医疗器械杂志

Minimized extracorporeal circulation improved in the postoperative side effects of conventional extracorporeal circulation is a kind of new extracorporeal circulation. This paper introduces the principle, characteristics, applications and related research of minimized extracorporeal circulation. For the problems of systemic inflammatory response syndrome and limited assist time, the article proposes three development direction including system miniaturization and integration, pulsatile blood pump and the adaptive control by human parameter identification.

Estudio del espesor de la mucosa del trígono retromolar con el objetivo de facilitar la planificación de instalación de mini implantes en la región / Study of the mucosa thickness of the retromolar triangle to facilitate the installation planning of mini-implants in the region

El trígono retromolar es un área triangular ubicado en la mandíbula, posterior al último molar. Esta región, debido al grosor y densidad ósea que presenta, es utilizada para la instalación de dispositivos que ofrezcan un sistema de anclaje para el movimiento de los molares inferiores. El objetivo de esta investigación es ofrecer datos morfométricos del grosor de la mucosa de región del trígono retromolar. Se utilizaron 25 pacientes de nacionalidad portuguesa, con indicación de exodoncia del tercer molar inferior retenido (derecho y/o izquierdo). En la región del trígono retromolar fueron demarcados 3 puntos correspondientes a los vértices de un triángulo cuya base se quedaba dirigida hacia la cara distal del tercer molar inferior y el largo de las vertientes correspondían a la dimensión vestíbulolingual del mismo diente; luego fue demarcado un cuarto punto correspondiente al centro geométrico del triángulo. Con un espaciador digital puntiagudo con tope de silicona incorporado se hizo la medición del grosor de la mucosa en cada punto. Los datos obtenidos fueron tabulados y analizados. El menor valor promedio encontrado fue 5,5mm en el lado derecho y el mayor fue 7,13mm en el lado izquierdo. Considerando los valores promedios obtenidos en los puntos de la mucosa, concluimos que la región del trígono retromolar presenta una mucosa gruesa, por lo tanto, los mini implantes indicados para esta región deben tener cuello transmucoso largo.

The retromolar triangle is a triangular area located in the mandible, posteriorly to the last molar. This region, due its thickness and bone density, is widely used for the installation of devices that provide an anchorage system for the movement of the lower molars. The aim of this research is to provide morphometric data of the mucosa thickness of the retromolar triangle. Twenty-five patients of portuguese nationality, with indication for extraction of the impacted lower third molar (right and/or left), were studied. In the region of the retromolar triangle were demarcated 3 points corresponding to the vertices of a triangle whose the base was torned for the distal face of the lower third molar and the lenght of the sides corresponded to vestibulolingual dimension of the same tooth, then was demarcated a fourth point corresponding to the geometric center of the triangle. Then, using a finger spreader with silicone stop were measured the mucosal tickness at each point. The data obtained were tabulated and analyzed. The lowest average value found was 5.5mm on the right side and the highest average value found was 7.13mm on the left side. Considering the mean values obtained at the points of the retromolar triangle mucosa measured in this study, we conclude that the retromolar triangle shows thick mucosa, so the mini-implants indicated for this region should have a long transmucosal neck.

Percutaneous nephrolithotomy of staghorn calculi in patients by mini-tract and standard-tract / 中南大学学报(医学版)

OBJECTIVE@#To compare the outcome of mini-tract vs standard-tract percutaneous nephrolithotomy (PCNL) in staghorn calculi.@*METHODS@#Between May 2009 and May 2011, 122 patients with renal staghorn calculi were treated by PCNL. Fifty-six patients underwent mini-PCNL and the others underwent standard-PCNL. The therapeutic effect and complication of the 2 groups were compared.@*RESULTS@#The two groups had comparable demographic conditions. Although the operation time was significantly longer in mini-PCNL group [(126±24.5) min vs (98±18.9) min], there was no striking difference in hospital stay [(5.7±1.3) d vs (5.3±1.1) d], hemoglobin drop [(9.5±3.2) g/L vs (10.5±3.3) g/L], stone-free state before charge (91.1% vs 89.4%) and complications.@*CONCLUSION@#The efficacy and safety of mini-PCNL and standard-PCNL are not significantly different.

Orthodontic mini-implants: are they a good anchorage resource for cases of retraction after extraction? / Mini-implantes en ortodoncia: ¿son un buen recurso de anclaje para los casos de retracción después de la extracción dentaria?

The aim was to seek scientific evidence in the literature that orthodontic mini-implants provide absolute anchorage during the retraction of maxillary anterior teeth after pre-molar extractions. A search was undertaken in the two databases Ovid and Pub Med. The key words "miniscrew", "mini-implants", "orthodontic anchorage procedure", "Anchorage loss", "tooth movement" and "orthodontic space closure" were used. After the initial search, repeated articles in the databases were excluded, then selection was based on the inclusion and exclusion criteria, using a table developed for this purpose. Of the 550 articles initially listed, 4 were found to be potentially eligible, ending with 3 being selected after applying the inclusion and exclusion criteria. According to the quality required, only 3 of these articles attained a high enough score to be evaluated. Two of these articles showed absolute anchorage provided by mini-implants, and the other demonstrated slight loss of anchorage. There are strong scientific evidences that orthodontic mini-implants provide absolute anchorage during the retraction of maxillary teeth...

El objetivo fue buscar en la literatura evidencia científica que los mini-implantes ortodóncicos proporcionan un anclaje absoluto durante la retracción de los dientes anteriores superiores después de la extracción de los premolares. La búsqueda se realizó dos bases de datos: Ovid y PubMed. Fueron utilizadas las palabras clave "mini tornillo", "mini-implantes", "procedimiento de anclaje ortodóntico", "pérdida de anclaje", "movimiento de los dientes" y "cierre ortodóntico de los espacios ". Después de la búsqueda inicial, los artículos repetidos en las bases de datos fueron excluidos, y la selección se basó en los criterios de inclusión y exclusión, usando una tabla desarrollado para este propósito. De los 550 artículos inicialmente enumerados, 4 resultaron ser potencialmente elegibles, y se terminó con la selección de 3 artículos luego de aplicar los criterios de inclusión y exclusión. De acuerdo con la calidad requerida, sólo 3 artículos alcanzaron una puntuación lo suficientemente alta como para ser evaluados. Dos de estos artículos mostraron un anclaje absoluto proporcionado por los mini-implantes, y el otro demostró una ligera pérdida de anclaje. Existen fuertes evidencias científicas que los mini-implantes ortodónticos proporcionan un anclaje absoluto durante la retracción de los dientes maxilares...