New medical device coating mouth gel for temporary relief of teething symptoms: a pilot randomized, open-label, controlled study.

BACKGROUND: This study verified the feasibility of the monthly recruitment rate, tested the Face, Legs, Activity, Cry and Consolability Pain Assessment Tool (FLACC) for pain in infants and collected preliminary efficacy and safety data of a new proprietary oral gel formulation of high-molecular-weight hyaluronan (HMWHA) for the relief of teething. Results will support the design a future main trial vs. local anesthetic, that is currently the only clinically proven pain reliever. METHODS: This was a pilot, randomized, controlled, multicenter, open-label, and parallel-group trial. It was performed in two Romanian clinics recruiting infants from 3 to 36 months. Teething diagnosis was based on a minimum of three symptoms such as: local pain, swelling, erythema, hyper-salivation, and depth characteristics of unerupted tooth. Absence of subcutaneous mucosal laceration was also required. The children were assigned either to HMWHA (HABPX V 3.3, Bioplax Ltd, Wallington, UK), or to standard drug (Dentinox®-Gel N; Dentinox, Berlin, Germany) and treated for 7 consecutive days. Investigators recorded the primary endpoints: swelling, redness and pain (by FLACC method), on days 0, 3 and 7. Changes in crying, mouth spasms, salivation, local pain, swelling, and redness were the secondary endpoints, recorded daily by the parents, on diary cards. Tolerability was assessed on day 14, too. RESULTS: Twenty-seven Infants were allocated in HMWHA, and 30 in standard drug. Enrolment rate was 9 patients/month/site. A significant reduction for HMWHA group was evidenced in pain, swelling (from day 0 to 7, P=0.034 between groups), redness (from day 0 to 3, P=0.045 and from day 0 to 7, P<0.001 between groups) and confirmed by the parents' diary records. Pain measurements obtained by FLACC method are consistent with the data belonging to other parameters. Investigator's global assessment of performance was in favor of the HMWHA (P<0.005). Only two patients, both belonging to standard drug group, experienced adverse events (fever, not related to treatment) and dropped out of the study. CONCLUSIONS: The results solve the feasibility questions and clearly evidence the performance of HABPX V 3.3 in teething symptoms, exceeding the objectives of a simple pilot trial to some extent. Coating oral gels containing HMWHA could be a therapeutic solution for both parents and physicians in managing the irritation and pain resulting from tooth eruption in children.

Consensus on early detection of disease progression in patients with multiple sclerosis.

Background: Early identification of the transition from relapsing-remitting multiple sclerosis (RRMS) to secondary progressive MS (SPMS) can be challenging for clinicians, as diagnostic criteria for SPMS are primarily based on physical disability and a holistic interpretation. Objective: To establish a consensus on patient monitoring to identify promptly disease progression and the most useful clinical and paraclinical variables for early identification of disease progression in MS. Methods: A RAND/UCLA Appropriateness Method was used to establish the level of agreement among a panel of 15 medical experts in MS. Eighty-three items were circulated to the experts for confidential rating of the grade of agreement and recommendation. Consensus was defined when ≥66% agreement or disagreement was achieved. Results: Consensus was reached in 72 out of 83 items (86.7%). The items addressed frequency of follow-up visits, definition of progression, identification of clinical, cognitive, and radiological assessments as variables of suspected or confirmed SPMS diagnosis, the need for more accurate assessment tools, and the use of promising molecular and imaging biomarkers to predict disease progression and/or diagnose SPMS. Conclusion: Consensus achieved on these topics could guide neurologists to identify earlier disease progression and to plan targeted clinical and therapeutic interventions during the earliest stages of SPMS.

Angioplastia de tronco de la coronaria izquierda no protegido: evolución clínica al año y a los 3 años. Predictores de eventos / Unprotected Left Main Percutaneous Coronary Intervention: One and 3-Year Evolution. Event Prediction

RESUMEN Introducción: La angioplastia de Tronco de la Coronaria Izquierda es una opción terapéutica en pacientes con anatomía favorable. Objetivos: Reportar nuestra experiencia en el tratamiento de estos pacientes, así como su evolución clínica y evaluar los predictores de eventos clínicos durante el seguimiento. Material y Métodos: Análisis retrospectivo de pacientes intervenidos entre 2011 y 2017 por obstrucción significativa del Tronco de la Coronaria Izquierda (Clínica Bazterrica y Clínica Santa Isabel). Se registró la incidencia de eventos clínicos al año y alejados (3 años como mínimo). Se realizó un análisis univariado y multivariado (modelo de riesgos proporcionales de Cox) para identificar aquellas variables asociadas a la ocurrencia de eventos (muerte e infarto). Resultados: Se incluyeron consecutivamente 95 pacientes, de los cuales en 39 el procedimiento fue no electivo (41,1%). La mortalidad global fue 9,3 % a los 12 meses y 13,6% alejada. La tasa de infarto de miocardio no fatal fue 7,2% al año y 14,5% alejada. La tasa de accidente cerebrovascular fue 2,1% y la de revascularización fue 10,4% a los 12 meses. El único predictor multivariado de eventos a 12 meses fue la indicación no electiva del procedimiento (p = 0,003). Cuando consideramos los eventos ocurridos luego del primer año, el único predictor multivariado fue la edad >70 años (p <0,0001). Conclusiones: Nuestros resultados de la angioplastia del Tronco de la Coronaria Izquierda corresponden a los reportados por otros autores. La ocurrencia de eventos al año y eventos alejados se relacionó con condiciones identificables como la indicación del procedimiento y la edad de los pacientes.

ABSTRACT Background: Left main percutaneous coronary intervention is a therapeutic option for patients with favorable anatomy. Objectives: The aim of this study was to report our experience in the treatment of these patients, their clinical evolution and the variables associated with clinical events during follow-up. Methods: This was a retrospective analysis of patients that underwent percutaneous coronary artery intervention for left main obstructive disease between 2011 and 2017 at Clínica Bazterrica and Clínica Santa Isabel. The incidence of clinical events was evaluated at one year and at long-term follow-up (at least 3 years after the intervention). An univariate and multivariate analysis (Cox proportional risk model) was performed to identify event-associated variables (death and infarction). Results: Among a total of 95 patients included in the study, 39 (41.1%) underwent a non-elective procedure. The rate of overall mortality was 9.3% at 12 months and 13.6% at long-term follow-up, and that of non-fatal myocardial infarction 7.2% and 14.5%, respectively. On the other hand, the rate of stroke and revascularization was 2.1% and 10.4% at 12 months, respectively. On multivariate analysis, the only independent predictors of adverse clinical events were non-elective intervention at 12 months (p = 0.003) and age >70 years after the first year (p <0.0001). Conclusions: Our results of left main percutaneous coronary intervention correspond with those reported by other authors. The incidence of one-year and long-term clinical events was associated with identifiable conditions, as procedure indication and age of the patients at the time of intervention

Falta de rigor científico de dos investigaciones de series de casos sobre diplomáticos estadounidenses en La Habana / Lack of scientific consistency in two investigations of case series of United States diplomats in Havana

Introducción: Con el propósito de justificar la decisión diplomática de los Estados Unidos, se publicaron dos artículos científicos en revistas médicas que intentan sostener la idea de que en La Habana hubo un ataque dirigido a personal de la embajada estadounidense. Objetivo: Demostrar la falta de rigor científico en dos investigaciones de series de casos no independientes sobre los síntomas de salud de diplomáticos de los Estados Unidos en La Habana. Método: Se realiza un análisis documental de dos publicaciones de series de casos. Se evalúan hipótesis diagnósticas. Resultados: Existe superposición amplia entre las dos series en cuanto a pacientes compartidos y en contraste se presentan algunas diferencias en los datos clínicos que superan lo esperado. Conclusiones: En ambas publicaciones se desaprovecha la riqueza semiográfica de síntomas y la información psicosocial. Se enfatiza más en argumentos asociados al fetichismo de la tecnología expresado en la interpretación de hallazgos inespecíficos. El análisis de datos clínicos permitió ver que se trata de un grupo heterogéneo de personas cuyas quejas de salud han sido reunidas por la interacción de otros factores psicosociales contextuales(AU)

Introduction: In order to justify the diplomatic decision of the United States, two scientific articles were published in medical journals that attempt to support the idea that, in Havana, there was an attack aimed at US embassy personnel. Objective: To prove the lack of scientific consistency in two investigations of non-independent case series on the health symptoms of United States diplomats in Havana. Method: A documentary analysis of two publications of case series is carried out. Diagnostic hypotheses are evaluated. Results: There is wide overlap between the two series in terms of shared patients and in contrast there are some differences in the clinical data that exceed what was expected. Conclusions: In both publications the semiographic wealth of symptoms and psychosocial information are wasted. More emphasis is placed on arguments associated with the fetishism of technology expressed in the interpretation of nonspecific findings. The analysis of clinical data allowed us to see that it is a heterogeneous group of people whose health complaints have been brought together by the interaction of other contextual psychosocial factors(AU)

Efficacy and safety of a novel vaginal medical device in recurrent bacterial vaginosis: a multicenter clinical trial.

BACKGROUND: The effectiveness of a new vaginal medical device, which contains polycarbophil, 0.04% lauryl glucoside and glycerides (Polybactum®, Effik Italia Spa, Cinisello Balsamo, Milan, Italy), in reducing BV recurrence rate was investigated. METHODS: This was a multicenter, open label, not comparative study. Women over 18 years old affected by recurrent BV were included. The latest episode was diagnosed by Amsel criteria 6-9 days before the start of the study and treated with vaginal metronidazole (gel 0.75% mg for 5 days or ovules 500 mg for 7 days). The recurrence was defined by at least 2 episodes in the previous 12 months. Polybactum® vaginal ovules, day 1-4-7, were started within the 12th and the 24th hour after the end of metronidazole therapy and repeated monthly for 3 cycles. RESULTS: The first 41 patients enrolled were evaluated for an interim analysis 6 months after the study started; 2 patients interrupted the trial, leaving 39 evaluable subjects. The recurrence rate was significantly reduced compared to previous published data (10.26% vs. 40% P<0.001). In 35 patients without recurrence, the assessment of Lactobacillus vaginal flora performed by phase contrast microscopy evidenced a significant improvement form baseline (P=0.022) The investigator global assessment of tolerability was excellent in 38 out of 39 cases. CONCLUSIONS: Our research showed that 3 monthly cycles of Polybactum® ovules administered after one course of metronidazole vaginal therapy can reduce the rate of Bacterial vaginosis recurrence and improve the vaginal milieu, favoring the growth of vaginal lactobacillus species.

Influencia del desnivel en la carga física del corredor de montaña: un estudio de caso / Slope Influence on the Trail Runner Physical Load: A Case Study

Este estudio analizó las exigencias de carga interna (Frecuencia cardíaca, FC) y externa (Velocidad; Player Load, PL; Power Metabolic, PM; Stiffness Vertical, KVERT; entropía aproximada, ApEn) producidas en función del desnivel del terreno en una carrera de montaña. Un atleta de nivel nacional (edad: 25.3 años; altura: 172 cm; peso: 67 kg; VO2MAX: 70.2 ml/kg/min) participó en una prueba oficial (Distancia: 27.6 km; Desnivel acumulado: 973 m), siendo analizado en 6 segmentos respecto al desnivel (sin desnivel, positivo y negativo). El registro de datos se realizó mediante un dispositivo inercial WIMU PROTM (RealTrack Systems, Almería, España). Los resultados muestran un aumento de PL/min y PM/min en desnivel negativo y de FCAVG en desnivel positivo. KVERT y ApEn fueron más bajos en desnivel positivo, mientras que la velocidad fue mayor sin desnivel. Se encuentra gran variabilidad en las exigencias en función de la orografía del terreno, siendo importante su análisis para el diseño específico del entrenamiento y la planificación del evento

This study analysed the internal (heart rate, HR) and external load demands (Speed; Player Load, PL; Power Metabolic, PM; Vertical stiffness, KVERT; approximated entropy, ApEn) during a trail running race in relation to the slope. A national-level athlete (age: 25.3 years; height: 172 cm; weight: 67 kg; VO2MAX: 70.2 ml/kg/min) participated in an official race (Distance: 27.6 km; Accumulated slope: 973 m), analysed in 6 segments related to the slope (without, positive and negative slope). Data was registered through an inertial device WIMU PROTM (RealTrack Systems, Almería, Spain). The results show an increase of PL/min and PM/min in negative slope and an increase of HRAVG in positive slope. KVERT and ApEn were lower in positive slope, while velocity was faster without slope. It is found a great variability in the trail runner demands related to terrain orography, being important its analysis to design specific training sessions and race planning

Manual and semiautomatic segmentation of bone sarcomas on MRI have high similarity.

The aims of this study were to evaluate the intra- and interobserver reproducibility of manual segmentation of bone sarcomas in magnetic resonance imaging (MRI) studies and to compare manual and semiautomatic segmentation methods. This retrospective study included twelve osteosarcoma and eight Ewing sarcoma MRI studies performed prior to any therapeutic intervention. All cases were histopathologically confirmed. Three radiologists used 3D-Slicer software to perform manual segmentation of bone sarcomas in a blinded and independent manner. One radiologist segmented manually and also performed semiautomatic segmentation with the GrowCut tool. Segmentation exercises were timed for comparison. The dice similarity coefficient (DSC) and Hausdorff distance (HD) were used to evaluate similarity between the segmentation results and further statistical analyses were performed to compare DSC, HD, and volumetric results. Manual segmentation was reproducible with intraobserver DSC varying from 0.83 to 0.97 and HD from 3.37 to 28.73 mm. Interobserver DSC of manual segmentation showed variation from 0.73 to 0.97 and HD from 3.93 to 33.40 mm. Semiautomatic segmentation compared to manual segmentation resulted in DSCs of 0.71-0.96 and HDs of 5.38-31.54 mm. Semiautomatic segmentation required significantly less time compared to manual segmentation (P value ≤0.05). Among all situations compared, tumor volumetry did not show significant statistical differences (P value >0.05). We found excellent intra- and interobserver agreement for manual segmentation of osteosarcoma and Ewing sarcoma. There was high similarity between manual and semiautomatic segmentation, with a significant reduction of segmentation time using the semiautomatic method.

Manual and semiautomatic segmentation of bone sarcomas on MRI have high similarity

The aims of this study were to evaluate the intra- and interobserver reproducibility of manual segmentation of bone sarcomas in magnetic resonance imaging (MRI) studies and to compare manual and semiautomatic segmentation methods. This retrospective study included twelve osteosarcoma and eight Ewing sarcoma MRI studies performed prior to any therapeutic intervention. All cases were histopathologically confirmed. Three radiologists used 3D-Slicer software to perform manual segmentation of bone sarcomas in a blinded and independent manner. One radiologist segmented manually and also performed semiautomatic segmentation with the GrowCut tool. Segmentation exercises were timed for comparison. The dice similarity coefficient (DSC) and Hausdorff distance (HD) were used to evaluate similarity between the segmentation results and further statistical analyses were performed to compare DSC, HD, and volumetric results. Manual segmentation was reproducible with intraobserver DSC varying from 0.83 to 0.97 and HD from 3.37 to 28.73 mm. Interobserver DSC of manual segmentation showed variation from 0.73 to 0.97 and HD from 3.93 to 33.40 mm. Semiautomatic segmentation compared to manual segmentation resulted in DSCs of 0.71−0.96 and HDs of 5.38−31.54 mm. Semiautomatic segmentation required significantly less time compared to manual segmentation (P value ≤0.05). Among all situations compared, tumor volumetry did not show significant statistical differences (P value >0.05). We found excellent intra- and interobserver agreement for manual segmentation of osteosarcoma and Ewing sarcoma. There was high similarity between manual and semiautomatic segmentation, with a significant reduction of segmentation time using the semiautomatic method.

Characterization of ruminal acidosis and initial phase of laminitis inducted by oligofructose in crossbred calves / Caracterização da acidose ruminal e da fase inicial da laminite induzidas por oligofrutose em bezerros mestiços

One of the ways to study cattle laminitis is its experimental induction by supplying a large amount of high fermentation carbohydrate. The most effective protocol until now has been the use of oligofructose. The objective of this study was to evaluate clinical and histological aspects of the hoof in experimental induction of ruminal acidosis and laminitis in calves using oligofructose. Six crossbred (Bos taurus x Bos indicus) yearling calves divided into Group I (GI) and Group II (GII) were used. Animals in GI and GII received intraruminal oligofructose in doses of 13 and 17g/kg, respectively. During 28 hours the calves were clinically evaluated and 30 hours after induction, samples were taken from coronary and abaxial wall of the hoof for histologic evaluation. Were noticed signs of ruminal and metabolic acidosis like rumen distension with fluid, diarrhea, ruminal pH reduction and, at blood gas analysis, pH and bicarbonate below reference range. Lameness was not observed however, some animals had a slower gait and apathy, possibly due to metabolic acidosis, though. Histologically, typical lesions of laminitis like circulatory changes and inflammatory infiltrate in the dermis, irregularities and areas of detachment at basement membrane and morphologic changes in cells from basal epidermis were found. The protocol induced, in the first 30 hours, clinical signs of ruminal and metabolic acidosis and low grade histologic lesions in the digits. Lameness and digit pain were not observed, characterizing the prodromic phase of the disease.(AU)

Uma das formas de se estudar a laminite bovina é sua indução experimental por meio do fornecimento de grande quantidade de carboidrato de alta fermentação. O protocolo mais eficaz até o momento foi o uso de oligofrutose. Objetivou-se avaliar aspectos clínicos e histológicos dos dígitos de bovinos na indução experimental de acidose ruminal e laminite usando oligofrutose. Utilizaram-se seis bezerros mestiços (Bos taurus x Bos indicus) de um ano, divididos em Grupo I (GI) e Grupo II (GII). Os animais em GI e GII receberam oligofrutose por via intrarruminal nas doses de 13 e 17g/kg respectivamente. Os bovinos foram avaliados clinicamente por 28 horas e fragmentos de coroa e muralha abaxial dos dígitos foram colhidos para histologia 30 horas após a indução. Foram identificados sinais de acidose ruminal e metabólica como distensão ruminal com líquido, diarreia e baixo pH ruminal. Os resultados de hemogasometria indicaram baixos pH e nível plasmático de bicarbonato. Os animais não apresentaram claudicação, entretanto, observaram-se apatia e marcha mais lenta, atribuídas à acidose metabólica. Histologicamente foram observadas lesões indicativas de laminite como alterações circulatórias e infiltrado inflamatório na derme, irregularidades e áreas de destacamento da membrana basal e alterações morfológicas de células da epiderme basal. O protocolo induziu, nas primeiras 30 horas, sinais de acidose ruminal e metabólica e lesões histológicas de baixa intensidade nos dígitos. Não foi observada claudicação ou sensibilidade nos dígitos, caracterizando a fase prodrômica da enfermidade.(AU)

Cold crystalloid versus warm blood cardioplegia in patients undergoing aortic valve replacement.

BACKGROUND: Myocardial protection techniques during cardiac arrest have been extensively investigated in the clinical setting of coronary revascularization. Fewer studies have been carried out of patients affected by left ventricular hypertrophy, where the choice of type and temperature of cardioplegia remain controversial. We have retrospectively investigated myocardial injury and short-term outcome in patients undergoing aortic valve replacement plus or minus coronary artery bypass grafting with using cold crystalloid cardioplegia (CCC) or warm blood cardioplegia (WBC). METHODS: From January 2015 to October 2016, 191 consecutive patients underwent aortic valve replacement plus or minus coronary artery bypass grafting in normothermic cardiopulmonary bypass. Cardiac arrest was obtained with use of intermittent antegrade CCC group (n=32) or WBC group (n=159), according with the choice of the surgeon. RESULTS: As compared with WBC group, in CCC group creatine-kinase-MB (CK-MB), cardiac troponin I (cTnI), aspartate aminotransferase (AST) release, and their peak levels, were lower during each time points of evaluation, with the greater statistically significant difference at time 0 (P<0.05, for all comparisons). A time 0, CK-MB/CK ratio >10% was 5.9% in CCC group versus 7.8% in WBC group (P<0.0001). At time 0 CK-MB/CK ratio >10% in patients undergoing isolated aortic valve replacement was 6.0% in CCC group versus 8.0% in WBC group (P<0.01). No any difference was found in perioperative myocardial infarction (0% versus 3.8%), postoperative (PO) major complications (15.6% versus 16.4%), in-hospital mortality (3.1% versus 1.3%). CONCLUSIONS: In aortic valve surgery a significant decrease of myocardial enzymes release is observed in favor of CCC, but this difference does not translate into different clinical outcome. However, this study suggests that in presence of cardiac surgical conditions associated with significant left ventricular hypertrophy, i.e., the aortic valve disease, a better myocardial protection can be achieved with the use of a cold rather than a warm cardioplegia. Therefore, CCC can be still safely used.

Therapeutic approach to pediatric oral disorders.

The promotion of oral health in pediatrics stands as an institutional requirement in countries such as Italy where children's dental disorders still register a high incidence despite high levels of general health. Guidelines indicate the need to target a large age group and stress the relevance of parental education, whom pediatricians and dentists should address to. In this respect, teething is paradigmatic, due to the interactions between inflammation of the gingival mucosa, the possible associations with systemic symptoms as well as the psychological parental component. Teething products include: remedies used in folk medicine (chamomile and rose honey), whose clinical efficacy has not been proved; local anesthetics (lidocaine and benzocaine), easily absorbed by the oral mucosa and able to provide for a rapid, though short-lived relief; salicylates, prescribed by pediatricians in selected cases where the pain and inflammatory component is very high; systemic anti-inflammatory (paracetamol in elixir formulation), prescribed only in particularly serious cases, whereas they are sold over the counter in numerous countries; and - last but not least - film-forming devices containing hyaluronic acid, whose efficacy has been clinically tested in various children disorders of the oral cavity, including teething.

An Unexpected Risk Factor for Early Structural Deterioration of Biological Aortic Valve Prostheses.

BACKGROUND: An alarming rate of early failure has been recently reported for the LivaNova (previously Sorin) Mitroflow (LivaNova, London, UK) bioprosthesis. Here, we aimed at verifying if this possible underperformance is confirmed in a large, single-center experience and identifying the risk factors associated with early deterioration. METHODS: In all, 459 Mitroflow valves have been implanted from July 2009 to December 2013 (patients' mean age 73 years; 204 women). Surviving patients have undergone yearly clinic and echocardiographic follow-up. Dysfunction was defined as moderate if the mean gradient was more than 30 mm Hg or severe if it exceeded 40 mm Hg. The population was divided on the basis of a dimensional mismatch, the model of the prosthesis (LX or DL: follow-up to 4 years), and patient's age at the time of implantation. RESULTS: Cumulative freedom from moderate valve dysfunction was 81% ± 3% at 60 months. It was lower with patient-prosthesis mismatch (71% ± 5% versus 92% ± 3%; p = 0.0065) and with the more recent DL model (at 42 months: 78% ± 6% versus 96% ± 2%; p < 0.0001). Cumulative freedom from severe dysfunction was 93% ± 2% at 5 years. Again, it was inferior among patients with a mismatch (86% ± 4% versus 100%; p = 0.0013) and for the DL model (42 months: 92.5% ± 3% versus 98.5% ± 1%; p = 0.0309). Smaller prostheses showed higher rates of early degeneration. CONCLUSIONS: The LivaNova Mitroflow valve appears to be prone to early deterioration. Smaller size prostheses should be used cautiously and avoided with patient-prosthesis mismatch. The DL model anticalcification treatment seems unable to prevent early degeneration, and possibly contributes to even earlier failure.

Social behaviour involving drug resistance: the role of initial density, initial frequency and population structure in shaping the effect of antibiotic resistance as a public good.

Bacteria sometimes cooperate with co-inhabiting cells. Pathogenic bacteria, for example, often produce and excrete virulence factors, eventually benefitting both producer and non-producer cells. The role of social interactions involving antibiotic resistance, however, has been more elusive. Enzymes that inactivate ß-lactam antibiotics such as ampicillin or penicillin (ß-lactamases) are good candidates as public goods. Nonetheless, it has been claimed that bacteria harbouring plasmids of natural origin coding for ß-lactamase almost do not protect sensitive bacteria. This does not fit with the fact that ampicillin-sensitive bacteria can be isolated from subjects undergoing ampicillin treatment. We hypothesised that there are two non-exclusive explanations for the discrepancy between previous works: (1) the range of values of demographic conditions (such as initial strain frequency, initial total cell density or habitat structure) has not been broad enough to include most scenarios, or (2) there are interactions between some of these factors. We performed experiments with Escherichia coli bacterial cells to measure the degree of protection of sensitive cells when co-cultured with cells harbouring RP4, R16a or the R1 plasmids, all of natural origin and coding for ß-lactamases, and in presence of ampicillin. In these co-cultures, performed in structured and non-structured environments, both the initial total cell density and the initial frequency of sensitive cells spanned four orders of magnitude. We found protection of sensitive cells in 63% of tested conditions. All factors (plasmid, structure, frequency and density) significantly affect levels of protection. Moreover, all factors interact, with interactions revealing large or very large effect sizes.

Fingolimod: efectividad y seguridad en la práctica clínica habitual. Estudio observacional, retrospectivo y multicéntrico en Asturias y Cantabria / Fingolimod: effectiveness and safety in routine clinical practice. An observational, retrospective, multi-centre study in Asturias and Cantabria

Objetivo. Evaluar la efectividad y seguridad del fingolimod en la práctica clínica habitual en la región de Asturias y Cantabria (España). Pacientes y métodos. Estudio retrospectivo y multicéntrico de pacientes con esclerosis múltiple recurrente remitente tratados con fingolimod, según la ficha técnica. La efectividad se evaluó en los pacientes con al menos un año de tratamiento. Se calculó la tasa anualizada de brotes (TAB), el porcentaje de pacientes libres de brotes y libres de lesiones captantes de gadolinio, y los que mejoraron/mantuvieron la puntuación en la escala expandida del estado de discapacidad (EDSS). Se analizó la población total y según el tratamiento previo: inmunomodulador (interferón beta-1 o acetato de glatiramero) o natalizumab. Resultados. Un total de 138 pacientes iniciaron tratamiento con fingolimod; el 60% recibió previamente inmunomodulador; el 28%, natalizumab; y el 9%, ningún tratamiento. Noventa y nueve pacientes estuvieron al menos un año en tratamiento con fingolimod. Después de un año de tratamiento, el fingolimod disminuyó la TAB en un 67% (1,26 a 0,42; p < 0,0001), aumentó el porcentaje de pacientes libres de brotes de un 24% a un 69% (p < 0,0001), y el porcentaje de pacientes libres de lesiones captantes de gadolinio de un 70% a un 85% (p < 0,0106). El 77% de los pacientes mejoró/mantuvo la puntuación en la EDSS. Resultados similares se observaron en pacientes tratados previamente con inmunomodulador. La efectividad de los pacientes tratados previamente con natalizumab se mantuvo tras el tratamiento con fingolimod. Conclusiones. La práctica clínica habitual en las regiones de Asturias y Cantabria muestra que el fingolimod tiene resultados similares a los observados en los ensayos clínicos, al comparar las variables clinicorradiológicas utilizadas en estos últimos (AU)

Aim. To evaluate the effectiveness and safety of fingolimod in routine clinical practice in the region of Asturias and Cantabria (Spain). Patients and methods. We conducted a retrospective multicentre study of patients with relapsing-remitting multiple sclerosis treated with fingolimod, in accordance with the product data sheet. Effectiveness was evaluated in patients with at least one year’s treatment. The following were calculated: annualised relapse rate (ARR), the percentage of patients free from relapses and free from gadolinium-enhancing lesions, and those who improved/maintained their score on the Expanded Disability Status Scale (EDSS). Both total population and according to previous treatment: immunomodulator (interferon beta-1 or glatiramer acetate) or natalizumab, were analysed. Results. A total of 138 patients started treatment with fingolimod; 60% previously received an immunomodulator; 28% were given natalizumab; and 9% had no treatment. Ninety-nine patients were treated with fingolimod for at least one year. After one year of treatment, fingolimod decreased the ARR by 67% (1.26 to 0.42; p < 0.0001), increased the percentage of patients free from relapses from 24% to 69% (p < 0.0001) and the percentage of patients free from gadoliniumenhancing lesions from 70% to 85% (p < 0.0106). Altogether, 77% of the patients improved/maintained their score on the EDSS. Similar results were observed in patients previously treated with an immunomodulator. The effectiveness of the patients previously treated with natalizumab remained the same following treatment with fingolimod. Conclusions. Routine clinical practice in the regions of Asturias and Cantabria shows that fingolimod yields similar results to those observed in clinical trials, on comparing the clinicoradiological variables used in them (AU)

Análise comparativa da morfometria do casco de bovinos das raças Nelore, Curraleira e Pantaneira e de bubalinos e sua relação com a etiopatogenia das enfermidades digitais / Morfometric comparative analysis of the hoof of Nelore, Pantaneira and Curraleira breeds of cattle and buffaloes and their relationship with the pathogenesis of digital diseases

O estudo morfométrico dos dígitos de bovinos e bubalinos pode colaborar para o entendimento da etiopatogenia das enfermidades podais. Este estudo objetivou descrever as características morfométricas dos dígitos de bovinos das raças Curraleira (Bos taurus), Pantaneira (Bos taurus), Nelore (Bos indicus) e de bubalinos (Bubalus bubalis) da raça Murrah e estabelecer possível relação entre tais medidas e a ocorrência de enfermidades digitais. Na pesquisa foram utilizados dez animais, saudáveis, de cada raça e espécie. Foram avaliados dois membros de cada animal, sendo um torácico e outro pélvico, totalizando 80 extremidades distais. As medidas morfométricas foram obtidas com auxílio de um paquímetro mecânico graduado e os ângulos das pinças conferidos por meio de transferidor metálico. Os principais parâmetros digitais avaliados foram o ângulo dorsal do casco (A), comprimento da parede dorsal (B), altura do talão (C), altura da pinça (D), comprimento do casco (E), comprimento diagonal do casco (F), largura do dígito lateral (G), largura do dígito medial (H), comprimento do dígito lateral (I) e comprimento do dígito medial (J). Para a comparação de médias dos resultados obtidos entre as raças foi utilizado o teste de Tukey (p<0,05). A análise multivariada para as representações gráficas das variáveis canônicas foi empregada para expressar a similaridade das medidas estudadas entre os grupos, no qual se utilizou o software R. Os resultados revelaram que os bubalinos apresentam as maiores medidas morfométricas para as variáveis B, C, D, E, F, G, H, I e J e apenas na variável A apresentaram medidas inferiores entre as diferentes raças de bovinos estudadas. Existe similaridade entre as três raças de bovinos estudadas em relação às variáveis, altura da pinça (D), largura do dígito lateral (G) e largura do dígito medial (H) as quais se distanciam dos valores encontrados para essas variáveis nos bubalinos, Concluiu que a morfometria digital pode influenciar na ocorrência de enfermidades digitais, mas não age como fator isolado, necessitando da interação com outros fatores estruturais, ambientais e de manejo para a manifestação dessas doenças.(AU)

Morfometric studies of bovine and buffalo digits can help to understand the etiopathogeny of digital diseases. This study described morphometric characteristics of digits of Curraleira (Bos taurus), Pantaneira (Bos taurus) Nelore (Bos indicus) breeds of cattle and Murrah buffalo (Bubalus bubalis) and stablish possible relation among the parameters and digital infirmities. Were used ten animals of each breed and specie. Two limbs were evaluated, a toracic and a pelvic, in a total of 80 distal limbs. Morphometric measurements were obtained using a graduated paquimeter and angles using a metallic protactor. The main parameters evaluated were hoof dorsal angle (A), dorsal wall length (B), heel height (C), toe height (D), hoof length (E), hoof diagonal hoof (F), lateral digit width (H), medial digit width (I) and medial digit length (J). For results averages comparison among breeds were used Tukey test (p<0,05). Multivariate analysys for graphic representations of canonic variables was used to express similarity of measures studied among groups, using R software. Results shows tha bubaline present higher morphometric measures for the variables B, C, D, E, F, G, H, I and J, only for variable A presented lower measures comparing the bovine breeds studied. There is similarity between the three breeds of cattle studied about toe height (D), lateral digit width (G) and medial digit width (H), which differed of values observed in buffalo. It was concluded that digital morphometry can influence the occurence of digital infirmities, but doesn´t act as an isolated factor, needing interaction of other structural, environmental and management factors for its occurence.(AU)

Shedding of clinical-grade lentiviral vectors is not detected in a gene therapy setting.

Gene therapy using viral vectors that stably integrate into ex vivo cultured cells holds great promises for the treatment of monogenic diseases as well as cancer. However, carry-over of infectious vector particles has been described to occur upon ex vivo transduction of target cells. This, in turn, may lead to inadvertent spreading of viral particles to off-target cells in vivo, raising concerns for potential adverse effects, such as toxicity of ectopic transgene expression, immunogenicity from in vivo transduced antigen-presenting cells and, possibly, gene transfer to germline cells. Here, we have investigated factors influencing the extent of lentiviral vector (LV) shedding upon ex vivo transduction of human hematopoietic stem and progenitor cells. Our results indicate that, although vector carry-over is detectable when using laboratory-grade vector stocks, the use of clinical-grade vector stocks strongly decreases the extent of inadvertent transduction of secondary targets, likely because of the higher degree of purification. These data provide supportive evidence for the safe use of the LV platform in clinical settings.

Trombosis venosa cerebral como complicación tras una punción lumbar diagnóstica / Cerebral venous thrombosis as a complication following a diagnostic lumbar puncture

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