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1.
Catheter Cardiovasc Interv ; 96(4): E484-E492, 2020 10 01.
Artículo en Inglés | MEDLINE | ID: mdl-32558228

RESUMEN

OBJECTIVE: The present study evaluated the effect of endovascular administration of calcium chloride to the carotid artery of swines, to create a model of arterial calcification. METHODS: Fifteen Large White pigs were used for the study. Via endovascular treatment, carotid arteries were exposed during 9 min to either calcium chloride (experimental artery) or saline (control artery) with the use of the TAPAS catheter. Intravascular ultrasound (IVUS) imaging was obtained at baseline, postprocedure and at 30 days. Optical coherence tomography (OCT) imaging was obtained in vitro after carotids were harvested. Longitudinally cut parallel arterial segments were placed in a system of delicate clamps and underwent uniaxial strain test. All arteries underwent histopathological examination. RESULTS: Calcium chloride treated segments showed extensive circumferential parietal calcification evident on both IVUS and OCT. Reduction in minimal lumen area on IVUS was evident in experimental arteries both at 24 hr and 30 days postprocedure. Histopathologic assessment (Von Kossa stain) confirmed medial calcification with mild intimal thickening. Biomechanical testing showed treated segments to have smaller breaking strength and less elastic deformation than controls. CONCLUSION: We developed a nonexpensive, reproducible model of early carotid medial calcification in pigs. Our model has the potential to help the development of research to unravel mechanisms underlying arterial calcification, the use of current or new devices to treat calcified lesions as well as to serve as an option for training interventionalists on the use of such devices.


Asunto(s)
Cloruro de Calcio , Enfermedades de las Arterias Carótidas/inducido químicamente , Arteria Carótida Común/patología , Calcificación Vascular/inducido químicamente , Animales , Fenómenos Biomecánicos , Enfermedades de las Arterias Carótidas/diagnóstico por imagen , Enfermedades de las Arterias Carótidas/patología , Arteria Carótida Común/diagnóstico por imagen , Modelos Animales de Enfermedad , Elasticidad , Masculino , Neointima , Sus scrofa , Factores de Tiempo , Tomografía de Coherencia Óptica , Ultrasonografía Intervencional , Calcificación Vascular/diagnóstico por imagen , Calcificación Vascular/patología
2.
Dermatol Surg ; 46(11): e108-e111, 2020 11.
Artículo en Inglés | MEDLINE | ID: mdl-32049707

RESUMEN

BACKGROUND: Liquid sclerotherapy is the treatment of choice for telangiectasias. However, pain caused by the procedure is a barrier to treatment adherence by patients. OBJECTIVE: To evaluate the use of skin cooling for the management of pain in patients undergoing liquid sclerotherapy. METHODS AND MATERIALS: A total of 230 lower limbs from 115 patients with telangiectasias classified as C1 according to the Clinical-Etiological-Anatomical-Pathophysiological classification were included. Patients underwent liquid sclerotherapy with and without skin cooling during the procedure. Pain was assessed using a visual analog scale, applied immediately after the procedure, according to each lower limb area treated. RESULTS: Visual analog scale pain scores were significantly lower for sclerotherapy with the use of cooling for pain management during the procedure than for sclerotherapy without cooling both in the thigh and leg (p < .0001). CONCLUSION: The use of a cooling system is effective in reducing pain in patients undergoing liquid sclerotherapy of telangiectasias, providing more comfort to patients.


Asunto(s)
Crioterapia , Dolor Asociado a Procedimientos Médicos/terapia , Soluciones Esclerosantes/administración & dosificación , Escleroterapia/efectos adversos , Telangiectasia/terapia , Adulto , Anciano , Femenino , Humanos , Pierna , Persona de Mediana Edad , Manejo del Dolor/métodos , Dimensión del Dolor , Umbral del Dolor/fisiología , Dolor Asociado a Procedimientos Médicos/diagnóstico , Dolor Asociado a Procedimientos Médicos/fisiopatología , Soluciones Esclerosantes/efectos adversos , Escleroterapia/métodos , Muslo , Resultado del Tratamiento , Adulto Joven
3.
Phlebology ; 37(3): 196-199, 2022 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-34846270

RESUMEN

AIM: The aim of the present study was to show that an increase in weight leads to the aggravation of limited joint mobility. METHOD: One hundred sixteen patients with varicose veins of the lower limbs and body mass index (BMI) higher than 30 kg/m2 were evaluated at the Belczak Clinic in Maringá, Brazil. All patients were evaluated by the same physician, and the goniometric readings were performed on all patients by a physiotherapist. The participants were then divided into three groups based on BMI: Group I-BMI between 30 and 40. Group II-BMI between 40 and 50, and Group III-BMI > 50. RESULTS: There is a significant difference between the groups detected. CONCLUSION: The present findings show that an increased BMI in obese individuals with chronic venous disease is associated with a progressive limitation of ankle mobility.


Asunto(s)
Tobillo , Obesidad , Articulación del Tobillo , Índice de Masa Corporal , Humanos , Extremidad Inferior , Obesidad/complicaciones
4.
Clinics (Sao Paulo) ; 70(6): 435-40, 2015 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-26106963

RESUMEN

OBJECTIVES: To analyze angiotomographic parameters of juxtarenal aneurysms to assess the applicability of an endograft model to patients and to create in vitro and in vivo models to assess the new endograft. METHODS: A total of 49 patients with juxtarenal aneurysms were submitted to angiotomographic evaluation, and parameters such as the aortic diameter, the length of the neck, and the angulations of the celiac trunk, superior mesenteric artery and renal arteries; the distances between them; and anatomic variations were analyzed. Based on these parameters, an endograft model was developed and tested in a newly created in vitro model of juxtarenal aneurysm. An experimental model of juxtarenal aneurysm was then established in six pigs weighing 50-60 kg to assess the new endograft model. RESULTS: The angiotomographic parameters of juxtarenal aneurysm measured in this study were similar to those reported in the literature and allowed the development of an endograft based on the hourglass concept, which was applicable to 85.8% of the patients. The in vitro model of juxtarenal aneurysm evidenced good radiopacity and functionality and permitted adjustments in the new device and technical improvements in the procedures for treating these aneurysms. In addition, the porcine model of juxtarenal aneurysm was successfully created in all six animals using a bovine pericardial patch, and use of the new endograft in three pilot procedures evidenced its feasibility. CONCLUSIONS: The Hourglass endograft was rendered applicable to treatment of the majority of patients with juxtarenal aneurysms simply by changing its diameter. Moreover, the new in vitro and in vivo models were shown to be effective for assessing both the presented endograft and experiments assessing the endovascular treatment of juxtarenal aneurysms.


Asunto(s)
Aneurisma de la Aorta Abdominal/cirugía , Prótesis Vascular , Procedimientos Endovasculares/métodos , Diseño de Prótesis , Animales , Aorta/anatomía & histología , Aneurisma de la Aorta Abdominal/diagnóstico , Implantación de Prótesis Vascular/métodos , Bovinos , Humanos , Modelos Animales , Cuello/anatomía & histología , Proyectos Piloto , Arteria Renal/anatomía & histología , Stents , Porcinos
5.
Phlebology ; 29(7): 454-60, 2014 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-23761871

RESUMEN

INTRODUCTION: Our current understanding of the pathophysiology of chronic venous disease (CVD) suggests that veno-active drugs (VAD) can provide effective symptom relief. Few studies have conducted head-to-head comparisons of VAD and placebo while also assessing objective measures (such as water plethysmography findings and tibiotarsal joint range of motion) and patient-reported quality of life outcomes. OBJECTIVES: To compare the effects of different VAD on limb volume reduction, tibiotarsal range of motion, and quality of life. METHODS: 136 patients with CVD (CEAP grades 2-5) were randomly allocated into four groups to receive micronized diosmin + hesperidin, aminaphthone, coumarin + troxerutin, or placebo (starch). Patients were administered a questionnaire consisting of a quality of life (QoL) measure designed specifically for persons with CVD, and underwent tibiotarsal joint angle measurement and water plethysmography of the lower extremity before and 30 days after pharmacological intervention. Assessors were blind to the treatment groups. RESULTS: Nine patients dropped out of the trial. Data collected from the 127 remaining patients was considered for statistical analysis. There were no differences in tibiotarsal joint range of motion. Volume reductions ≥100 mL were more frequent in the diosmin + hesperidin group than in any other group. QoL scores were best in the aminaphthone group, and between-group differences were found on individual analysis of questionnaire items. CONCLUSIONS: Use of VAD was associated with significant improvements in QoL as compared with placebo. VAD may be effective for providing symptom relief in patients with CVD.


Asunto(s)
Fármacos Cardiovasculares/uso terapéutico , Insuficiencia Venosa/tratamiento farmacológico , Fenómenos Biomecánicos , Brasil , Fármacos Cardiovasculares/efectos adversos , Enfermedad Crónica , Cumarinas/uso terapéutico , Diosmina/uso terapéutico , Método Doble Ciego , Quimioterapia Combinada , Edema/diagnóstico , Edema/fisiopatología , Femenino , Articulaciones del Pie/efectos de los fármacos , Articulaciones del Pie/fisiopatología , Hesperidina/uso terapéutico , Humanos , Hidroxietilrutósido/análogos & derivados , Hidroxietilrutósido/uso terapéutico , Masculino , Pletismografía , Calidad de Vida , Rango del Movimiento Articular , Recuperación de la Función , Encuestas y Cuestionarios , Factores de Tiempo , Resultado del Tratamiento , Insuficiencia Venosa/diagnóstico , Insuficiencia Venosa/fisiopatología , para-Aminobenzoatos/uso terapéutico
6.
Clinics ; 70(6): 435-440, 06/2015. tab, graf
Artículo en Inglés | LILACS | ID: lil-749795

RESUMEN

OBJECTIVES: To analyze angiotomographic parameters of juxtarenal aneurysms to assess the applicability of an endograft model to patients and to create in vitro and in vivo models to assess the new endograft. METHODS: A total of 49 patients with juxtarenal aneurysms were submitted to angiotomographic evaluation, and parameters such as the aortic diameter, the length of the neck, and the angulations of the celiac trunk, superior mesenteric artery and renal arteries; the distances between them; and anatomic variations were analyzed. Based on these parameters, an endograft model was developed and tested in a newly created in vitro model of juxtarenal aneurysm. An experimental model of juxtarenal aneurysm was then established in six pigs weighing 50-60 kg to assess the new endograft model. RESULTS: The angiotomographic parameters of juxtarenal aneurysm measured in this study were similar to those reported in the literature and allowed the development of an endograft based on the hourglass concept, which was applicable to 85.8% of the patients. The in vitro model of juxtarenal aneurysm evidenced good radiopacity and functionality and permitted adjustments in the new device and technical improvements in the procedures for treating these aneurysms. In addition, the porcine model of juxtarenal aneurysm was successfully created in all six animals using a bovine pericardial patch, and use of the new endograft in three pilot procedures evidenced its feasibility. CONCLUSIONS: The Hourglass endograft was rendered applicable to treatment of the majority of patients with juxtarenal aneurysms simply by changing its diameter. Moreover, the new in vitro and in vivo models were shown to be effective for assessing both the presented endograft and experiments assessing the endovascular treatment of juxtarenal aneurysms. .


Asunto(s)
Animales , Bovinos , Humanos , Aneurisma de la Aorta Abdominal/cirugía , Prótesis Vascular , Procedimientos Endovasculares/métodos , Diseño de Prótesis , Aorta/anatomía & histología , Aneurisma de la Aorta Abdominal/diagnóstico , Implantación de Prótesis Vascular/métodos , Modelos Animales , Cuello/anatomía & histología , Proyectos Piloto , Arteria Renal/anatomía & histología , Stents , Porcinos
7.
HPB Surg ; 2009: 240780, 2009.
Artículo en Inglés | MEDLINE | ID: mdl-19404409

RESUMEN

The rupture of retroperitoneal varices is a rare and catastrophic complication of portal hypertension. We describe a case of this nature, the first in Brazilian medical literature, and also reviewing all previous 34 cases. We systematically analyzed all therapeutic approach and propose a management algorithm for diagnosis and treatment of this lethal condition. The majority of the patients presented with abdominal pain, distention and hypotension, and developed hemorrhagic shock. Rupture of retroperitoneal varices can be properly managed if an early diagnosis is made and surgery is performed promptly, which is the only effective treatment. Arteriography should be used when the suspicion is of rupture of hepatocellular carcinoma.


Asunto(s)
Hemoperitoneo/etiología , Hemostasis Quirúrgica/métodos , Hipertensión Portal/diagnóstico , Cirrosis Hepática/complicaciones , Várices/cirugía , Dolor Abdominal/diagnóstico , Dolor Abdominal/etiología , Transfusión Sanguínea , Brasil , Progresión de la Enfermedad , Servicio de Urgencia en Hospital , Tratamiento de Urgencia/métodos , Resultado Fatal , Femenino , Hemoperitoneo/diagnóstico , Hemoperitoneo/cirugía , Humanos , Hipertensión Portal/complicaciones , Laparotomía/métodos , Ligadura/métodos , Cirrosis Hepática/diagnóstico , Persona de Mediana Edad , Insuficiencia Multiorgánica/diagnóstico , Complicaciones Posoperatorias/fisiopatología , Espacio Retroperitoneal/irrigación sanguínea , Rotura Espontánea/etiología , Rotura Espontánea/cirugía , Índice de Severidad de la Enfermedad , Várices/complicaciones , Várices/diagnóstico
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