903 resultados para arterial blood


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Objetivo: Determinar diferencias en las impedancias basales registradas durante los procedimientos de denervación renal por radiofrecuencia de los pacientes sometidos a este procedimiento en la Fundación Cardioinfantil de Bogotá durante los años 2012 a 2015. Materiales y métodos: Estudio observacional, analítico de corte retrospectivo, donde se analizaron todas las impedancias basales medidas durante los procedimientos de denervación renal, buscando diferencias significativas entre los segmentos de las arterias intervenidas, estratificados en proximal, medio distal y superior, lateral, inferior u ostial. Con seguimiento a los pacientes a tres, seis y doce meses en cuanto a presión arterial de consultorio. Resultados: Se evaluaron 150 puntos de denervación renal exitosos, correspondientes a 23 arterias renales de 11 procedimientos. La mediana de edad fue 56 años. Al realizar un modelo de regresión lineal no se encontró ninguna diferencia estadísticamente significativa entre las impedancias de ninguno de los segmentos de las arterias ni sitios anatómicos. Se documentó disminución de presión arterial sistólica a tres meses, seis meses y doce meses de 14 mmHg (RIQ 10-33mmHg), 21 mmHg (RIQ 12-42mmHg) y 19 mmHg (RIQ 11-42 mmHg) respectivamente

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Introducción. La hipertensión arterial es una de las patologías más representativas en términos de morbi-mortalidad y afectación de la calidad de vida de los usuarios de una EPS privada en Bogotá. Se cuenta en la literatura con múltiples prácticas para favorecer la adherencia al tratamiento de la hipertensión, pero se evidencia que en muchos pacientes no se logran las metas terapéuticas establecidas, generando a largo plazo complicaciones que impactan en la calidad de vida de los pacientes y en el costo en salud. Es por esto que en la EPS se establece desde el 2012 el programa: Ruta para la gestión del autocuidado, como una estrategia de intervención complementaria sobre los pacientes con enfermedades crónicas, con el fin de apoyar a los usuarios del programa de promoción y prevención Atención Específica integral (AEI) en el cumplimiento de las recomendaciones terapéuticas farmacológicas y no farmacológicas generadas por el equipo de salud. La ruta está dirigida especialmente al grupo de pacientes hipertensos con dificultades en la adherencia al programa de promoción y prevención, o en el logro de metas terapéuticas, y busca implementar estrategias de intervención educativa orientadas a fomentar la capacidad de las personas para adaptarse y auto gestionar los desafíos que representa convivir con el diagnóstico de una patología crónica. Por lo anterior la presente investigación busca evaluar el efecto del programa Ruta para la gestión del autocuidado en el control de cifras tensionales en pacientes hipertensos en en una EPS privada de Bogotá en el año 2015. Objetivo. Establecer si la participación en el programa Ruta para la gestión del autocuidado influye en los valores de cifras tensionales de pacientes hipertensos, graduados del programa en una EPS privada de Bogotá en el año 2015. Metodología. Estudio con enfoque cuantitativo, observacional longitudinal retrospectivo de una intervención antes y después, para evaluar el efecto del programa Ruta de gestión de autocuidado, en el control de cifras tensionales, índice de masa corporal y perímetro abdominal de pacientes con diagnóstico de hipertensión arterial afiliados a la EPS privada en Bogotá, graduados del programa entre el 1 de Enero de 2015 a Diciembre de 2015. Población del estudio 409 pacientes, con muestreo por conveniencia. La recolección de datos fue a partir de fuentes secundarias de historia clínica sistematizada de la EPS. Resultados. La población de estudio fueron 409 pacientes, de los cuales el 69,2% son mujeres (n=283). El promedio de la edad de los pacientes fue de 60,16+/-0.9 años, los mayores de 60 años son el grupo más representativo con un 54% (n=220), el estrato socioeconómico 1 es el 77% (n=315), , el tiempo de duración de la ruta de autocuidado de la población analizada más frecuente fue de 4 a 6 meses con un 60,4% (n=247) y el tratamiento más utilizado es el combinado con 53,1% (n=217). Antes del inicio de la Ruta de gestión de autocuidado, 138 pacientes tuvieron valores de tensión arterial sistólica en rangos de hipertensión, al finalizar la misma disminuyeron los valores a rangos de normalidad 96 pacientes (69,6%). De los pacientes que iniciaron con tensión arterial sistólica en rangos de normalidad (n=271), el 12,5% al finalizar la ruta tuvieron valores en rangos de hipertensión (n=34). El cambio en los rangos de tensión arterial sistólica evidenció que es estadísticamente significativo (p=0.000) con un OR de 2,8:1, lo cual indica que la variación de pacientes con valores de tensión arterial sistólica en rangos de hipertensión a valores en rango de normotensión, ocurre 2,8 veces más en quienes realizan la ruta de gestión de autocuidado que los que no. Antes del inicio de la Ruta de gestión de autocuidado, 70 pacientes tuvieron valores de tensión arterial diastólica en rangos de hipertensión, al finalizar la misma disminuyeron los valores a rangos de normalidad 56 pacientes (80%). De los pacientes que iniciaron con tensión arterial diastólica en rangos de normalidad (n=339), el 8,3% al finalizar la ruta tuvieron valores en rangos de hipertensión (n=28). El cambio en los rangos de tensión arterial diastólica, evidenció que es estadísticamente significativo (p=0.001) con un OR de 2,0:1, lo cual indica que la variación de pacientes con valores de tensión arterial diastólica en rangos de hipertensión a valores en rango de normotensión, ocurre 2 veces más en quienes realizan la ruta de gestión de autocuidado que los que no. Conclusión. La implementación de modelos educativos en la atención primaria en salud en las unidades de atención de servicios ambulatorios en la EPS, generan un impacto positivo en el control de las cifras tensionales. El tener pacientes controlados incide en la disminución de morbimortalidad, costos de hospitalización médica y mejora en la calidad de vida.

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The shortage of donor hearts for patients with end stage heart failure has accelerated the development of ventricular assist devices (VAD) that act as a replacement heart. Mechanical devices involving pulsatile, axial and centrifugal devices have been proposed. Recent clinical developments indicate that centrifugal devices are not only beneficial for bridge to transplantation applications, but may also aid myocardial recovery. The results of a recent study have shown that patients who received a VAD have extended lives and improved quality of life compared to recipients of drug therapy. Unfortunately 25% of these patients develop right heart failure syndrome, sepsis and multi-organ failure. It was reported that 17% of patients initially receiving an LVAD later required a right ventricular assist device (RVAD). Hence, current research focus is in the development of a bi-ventricular assist device (BVAD). Current BVAD technology is either too bulky or necessitates having to implant two pumps working independently. The latter requires two different controllers for each pump leading to the potential complication of uneven flow dynamics and the requirements for a large amount of body space. This paper illustrates the combination of the LVAD and RVAD as one complete device to augment the function of both the left and right cardiac chambers with double impellers. The proposed device has two impellers rotating in counter directions, hence eliminating the necessity of the body muscles and tubing/heart connection to restrain the pump. The device will also have two separate chambers with independent rotating impeller for the left and right chambers. A problem with centrifugal impellers is the fluid stagnation underneath the impeller. This leads to thrombosis and blood clots.This paper presents the design, construction and location of washout hole to prevent thrombus for a Bi-VAD centrifugal pump. Results using CFD will be used to illustrate the superiority of our design concept in terms of preventing thrombus formation and hemolysis.

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Aim: In the current climate of medical education, there is an ever-increasing demand for and emphasis on simulation as both a teaching and training tool. The objective of our study was to compare the realism and practicality of a number of artificial blood products that could be used for high-fidelity simulation. Method: A literature and internet search was performed and 15 artificial blood products were identified from a variety of sources. One product was excluded due to its potential toxicity risks. Five observers, blinded to the products, performed two assessments on each product using an evaluation tool with 14 predefined criteria including color, consistency, clotting, and staining potential to manikin skin and clothing. Each criterion was rated using a five-point Likert scale. The products were left for 24 hours, both refrigerated and at room temperature, and then reassessed. Statistical analysis was performed to identify the most suitable products, and both inter- and intra-rater variability were examined. Results: Three products scored consistently well with all five assessors, with one product in particular scoring well in almost every criterion. This highest-rated product had a mean rating of 3.6 of 5.0 (95% posterior Interval 3.4-3.7). Inter-rater variability was minor with average ratings varying from 3.0 to 3.4 between the highest and lowest scorer. Intrarater variability was negligible with good agreement between first and second rating as per weighted kappa scores (K = 0.67). Conclusion: The most realistic and practical form of artificial blood identified was a commercial product called KD151 Flowing Blood Syrup. It was found to be not only realistic in appearance but practical in terms of storage and stain removal.

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For the last two decades heart disease has been the highest single cause of death for the human population. With an alarming number of patients requiring heart transplant, and donations not able to satisfy the demand, treatment looks to mechanical alternatives. Rotary Ventricular Assist Devices, VADs, are miniature pumps which can be implanted alongside the heart to assist its pumping function. These constant flow devices are smaller, more efficient and promise a longer operational life than more traditional pulsatile VADs. The development of rotary VADs has focused on single pumps assisting the left ventricle only to supply blood for the body. In many patients however, failure of both ventricles demands that an additional pulsatile device be used to support the failing right ventricle. This condition renders them hospital bound while they wait for an unlikely heart donation. Reported attempts to use two rotary pumps to support both ventricles concurrently have warned of inherent haemodynamic instability. Poor balancing of the pumps’ flow rates quickly leads to vascular congestion increasing the risk of oedema and ventricular ‘suckdown’ occluding the inlet to the pump. This thesis introduces a novel Bi-Ventricular Assist Device (BiVAD) configuration where the pump outputs are passively balanced by vascular pressure. The BiVAD consists of two rotary pumps straddling the mechanical passive controller. Fluctuations in vascular pressure induce small deflections within both pumps adjusting their outputs allowing them to maintain arterial pressure. To optimise the passive controller’s interaction with the circulation, the controller’s dynamic response is optimised with a spring, mass, damper arrangement. This two part study presents a comprehensive assessment of the prototype’s ‘viability’ as a support device. Its ‘viability’ was considered based on its sensitivity to pathogenic haemodynamics and the ability of the passive response to maintain healthy circulation. The first part of the study is an experimental investigation where a prototype device was designed and built, and then tested in a pulsatile mock circulation loop. The BiVAD was subjected to a range of haemodynamic imbalances as well as a dynamic analysis to assess the functionality of the mechanical damper. The second part introduces the development of a numerical program to simulate human circulation supported by the passively controlled BiVAD. Both investigations showed that the prototype was able to mimic the native baroreceptor response. Simulating hypertension, poor flow balancing and subsequent ventricular failure during BiVAD support allowed the passive controller’s response to be assessed. Triggered by the resulting pressure imbalance, the controller responded by passively adjusting the VAD outputs in order to maintain healthy arterial pressures. This baroreceptor-like response demonstrated the inherent stability of the auto regulating BiVAD prototype. Simulating pulmonary hypertension in the more observable numerical model, however, revealed a serious issue with the passive response. The subsequent decrease in venous return into the left heart went unnoticed by the passive controller. Meanwhile the coupled nature of the passive response not only decreased RVAD output to reduce pulmonary arterial pressure, but it also increased LVAD output. Consequently, the LVAD increased fluid evacuation from the left ventricle, LV, and so actually accelerated the onset of LV collapse. It was concluded that despite the inherently stable baroreceptor-like response of the passive controller, its lack of sensitivity to venous return made it unviable in its present configuration. The study revealed a number of other important findings. Perhaps the most significant was that the reduced pulse experienced during constant flow support unbalanced the ratio of effective resistances of both vascular circuits. Even during steady rotary support therefore, the resulting ventricle volume imbalance increased the likelihood of suckdown. Additionally, mechanical damping of the passive controller’s response successfully filtered out pressure fluctuations from residual ventricular function. Finally, the importance of recognising inertial contributions to blood flow in the atria and ventricles in a numerical simulation were highlighted. This thesis documents the first attempt to create a fully auto regulated rotary cardiac assist device. Initial results encourage development of an inlet configuration sensitive to low flow such as collapsible inlet cannulae. Combining this with the existing baroreceptor-like response of the passive controller will render a highly stable passively controlled BiVAD configuration. The prototype controller’s passive interaction with the vasculature is a significant step towards a highly stable new generation of artificial heart.