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1.
Phlebology ; 37(3): 196-199, 2022 Apr.
Article in English | MEDLINE | ID: mdl-34846270

ABSTRACT

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.


Subject(s)
Ankle , Obesity , Ankle Joint , Body Mass Index , Humans , Lower Extremity , Obesity/complications
2.
Catheter Cardiovasc Interv ; 96(4): E484-E492, 2020 10 01.
Article in English | MEDLINE | ID: mdl-32558228

ABSTRACT

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.


Subject(s)
Calcium Chloride , Carotid Artery Diseases/chemically induced , Carotid Artery, Common/pathology , Vascular Calcification/chemically induced , Animals , Biomechanical Phenomena , Carotid Artery Diseases/diagnostic imaging , Carotid Artery Diseases/pathology , Carotid Artery, Common/diagnostic imaging , Disease Models, Animal , Elasticity , Male , Neointima , Sus scrofa , Time Factors , Tomography, Optical Coherence , Ultrasonography, Interventional , Vascular Calcification/diagnostic imaging , Vascular Calcification/pathology
3.
Dermatol Surg ; 46(11): e108-e111, 2020 11.
Article in English | MEDLINE | ID: mdl-32049707

ABSTRACT

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.


Subject(s)
Cryotherapy , Pain, Procedural/therapy , Sclerosing Solutions/administration & dosage , Sclerotherapy/adverse effects , Telangiectasis/therapy , Adult , Aged , Female , Humans , Leg , Middle Aged , Pain Management/methods , Pain Measurement , Pain Threshold/physiology , Pain, Procedural/diagnosis , Pain, Procedural/physiopathology , Sclerosing Solutions/adverse effects , Sclerotherapy/methods , Thigh , Treatment Outcome , Young Adult
4.
Clinics (Sao Paulo) ; 70(6): 435-40, 2015 Jun.
Article in English | MEDLINE | ID: mdl-26106963

ABSTRACT

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.


Subject(s)
Aortic Aneurysm, Abdominal/surgery , Blood Vessel Prosthesis , Endovascular Procedures/methods , Prosthesis Design , Animals , Aorta/anatomy & histology , Aortic Aneurysm, Abdominal/diagnosis , Blood Vessel Prosthesis Implantation/methods , Cattle , Humans , Models, Animal , Neck/anatomy & histology , Pilot Projects , Renal Artery/anatomy & histology , Stents , Swine
5.
Clinics ; 70(6): 435-440, 06/2015. tab, graf
Article in English | LILACS | ID: lil-749795

ABSTRACT

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. .


Subject(s)
Animals , Cattle , Humans , Aortic Aneurysm, Abdominal/surgery , Blood Vessel Prosthesis , Endovascular Procedures/methods , Prosthesis Design , Aorta/anatomy & histology , Aortic Aneurysm, Abdominal/diagnosis , Blood Vessel Prosthesis Implantation/methods , Models, Animal , Neck/anatomy & histology , Pilot Projects , Renal Artery/anatomy & histology , Stents , Swine
6.
Phlebology ; 29(7): 454-60, 2014 Aug.
Article in English | MEDLINE | ID: mdl-23761871

ABSTRACT

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.


Subject(s)
Cardiovascular Agents/therapeutic use , Venous Insufficiency/drug therapy , Biomechanical Phenomena , Brazil , Cardiovascular Agents/adverse effects , Chronic Disease , Coumarins/therapeutic use , Diosmin/therapeutic use , Double-Blind Method , Drug Therapy, Combination , Edema/diagnosis , Edema/physiopathology , Female , Foot Joints/drug effects , Foot Joints/physiopathology , Hesperidin/therapeutic use , Humans , Hydroxyethylrutoside/analogs & derivatives , Hydroxyethylrutoside/therapeutic use , Male , Plethysmography , Quality of Life , Range of Motion, Articular , Recovery of Function , Surveys and Questionnaires , Time Factors , Treatment Outcome , Venous Insufficiency/diagnosis , Venous Insufficiency/physiopathology , para-Aminobenzoates/therapeutic use
7.
HPB Surg ; 2009: 240780, 2009.
Article in English | MEDLINE | ID: mdl-19404409

ABSTRACT

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.


Subject(s)
Hemoperitoneum/etiology , Hemostasis, Surgical/methods , Hypertension, Portal/diagnosis , Liver Cirrhosis/complications , Varicose Veins/surgery , Abdominal Pain/diagnosis , Abdominal Pain/etiology , Blood Transfusion , Brazil , Disease Progression , Emergency Service, Hospital , Emergency Treatment/methods , Fatal Outcome , Female , Hemoperitoneum/diagnosis , Hemoperitoneum/surgery , Humans , Hypertension, Portal/complications , Laparotomy/methods , Ligation/methods , Liver Cirrhosis/diagnosis , Middle Aged , Multiple Organ Failure/diagnosis , Postoperative Complications/physiopathology , Retroperitoneal Space/blood supply , Rupture, Spontaneous/etiology , Rupture, Spontaneous/surgery , Severity of Illness Index , Varicose Veins/complications , Varicose Veins/diagnosis
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