Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 5 de 5
Filtrar
Adicionar filtros








Intervalo de ano
1.
Int. braz. j. urol ; 44(5): 987-995, Sept.-Oct. 2018. tab, graf
Artigo em Inglês | LILACS | ID: biblio-975639

RESUMO

ABSTRACT Objective: To compare standard urotherapy with a combination of urotherapy and biofeedback sessions and to determine the changes that these therapies promote in children with dysfunctional voiding. Patients and Methods: The data of 45 patients who participated in the study from January 2010 to March 2013 were evaluated. All patients underwent urinary system ultrasonography to determine post-void residual urine volumes and urinary system anomalies. All patients were diagnosed using uroflowmetry - electromyography (EMG). The flow pattern, maximum flow rate, and urethral sphincter activity were evaluated in all patients using uroflowmetry - EMG. Each patient underwent standard urotherapy, and the results were recorded. Subsequently, biofeedback sessions were added for all patients, and the changes in the results were recorded and statistically compared. Results: A total of forty - five patients were included, of which 34 were female and 11 were male and the average age of the patients was 8.4 ± 2.44 years (range: 5 - 15 years). After the standard urotherapy plus biofeedback sessions, the post-void residual urine volumes, incontinence rates and infection rates of patients were significantly lower than those with the standard urotherapy (p < 0.05). A statistically significant improvement in voiding symptoms was observed after the addition of biofeedback sessions to the standard urotherapy compared with the standard urotherapy alone (p < 0.05). Conclusions: Our study showed that a combination of urotherapy and biofeedback was more effective in decreasing urinary incontinence rates, infection rates and post - void residual urine volumes in children with dysfunctional voiding than standard urotherapy alone, and it also showed that this combination therapy corrected voiding patterns significantly and objectively.


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Adolescente , Transtornos Urinários/terapia , Biorretroalimentação Psicológica , Urodinâmica , Resultado do Tratamento , Eletromiografia
2.
Int. braz. j. urol ; 40(5): 650-655, 12/2014. tab
Artigo em Inglês | LILACS | ID: lil-731126

RESUMO

Purpose We aimed to compare the outcomes of pneumatic (PL), ultrasonic (UL) and combined (PL/UL) lithotripsy performed in percutaneous lithotripsy (PNL) according to success rates and stone clearence. Materials and Methods The medical records of 512 patients treated with PNL between April 2010 and April 2013 were evaluated. Postoperative stone analysis revealed as calcium oxalate in 408 of these patients. The operation notes of 355 patients recorded in detail with complete parameters were reviewed. According to stone disintegration method, patients were divided into three groups: PL only in Group I, UL only in Group II, and UL/PL combination in Group III. Number of patients was 155, 110 and 90, respectively. Results Fluoroscopy screening time was significantly shorter in group II, and III compared to group I (p<0.001). The failure rates were 13.5% (21 patients) for group I, 3.6% (4 patients) for group II, and 3.3% (3 patients) for group III. There was a significant statistical difference in favor of group II and III by means of success (p=0.023). Group II and III had larger FSA, and this was statistically significant (p=0.032). Stone disintegration time (SDT) was 64.0±41.92 minutes for group I, 49.5±34.63 for group II, and 37.7±16.89 for group III. Group III has a statistically significant shorter SDT (p=0.011). Conclusions We concluded that, in cases with high stone burden, where faster and efficient lithotripsy is needed, combined ultrasonic / pneumatic lithotripter may be the ideal choice and in suitable cases ultrasonic lithotripter usage provides important advantages to the surgeon. .


Assuntos
Adulto , Feminino , Humanos , Masculino , Pessoa de Meia-Idade , Terapia Combinada/instrumentação , Cálculos Renais/terapia , Litotripsia/instrumentação , Nefrostomia Percutânea/instrumentação , Análise de Variância , Terapia Combinada/métodos , Desenho de Equipamento , Fluoroscopia , Tempo de Internação , Litotripsia/métodos , Nefrostomia Percutânea/métodos , Duração da Cirurgia , Estatísticas não Paramétricas , Fatores de Tempo , Resultado do Tratamento
3.
Int. braz. j. urol ; 40(5): 683-689, 12/2014. graf
Artigo em Inglês | LILACS | ID: lil-731135

RESUMO

We aimed, in this study, to determine the distribution of α-1 AR subtypes in rat and human pelvis and calyces, and to evaluate, by comparing these two species, the possibility of rats to be used as models for humans. Twenty patients with renal carcinoma were included into the study. The patients underwent radical nephrectomy for renal cell carcinoma (RCC). After nephrectomy, specimens were evaluated and excisional biopsies from healthy pelvis and calyces tissues were performed. When pathology confirmed the non-invasion of RCC, specimen was included into the study. A total of 7 adult Wistar Albino (250-300 g) female rats were used in this study. Specimens included renal pelvis and calyces. All specimens were evaluated under light microscope histopathologically. The concentrations of the receptor densities did not differ between the two groups. With the demonstration of the α receptors in rat kidneys and calyces, many receptor-based studies concerning both humans and rats can take place. Novel medication targeting these subtypes -in this matter α1A and α1D for renal pelvis and calyces- may be helpful for expulsive therapy and/or pain relief. With the demonstration of similar receptor densities between human and rat tissues, rat model may be useful for α-receptor trials for renal pelvis and calyces.


Assuntos
Animais , Feminino , Humanos , Cálices Renais/química , Pelve Renal/química , Modelos Animais , Receptores Adrenérgicos alfa/análise , Biópsia , Carcinoma de Células Renais/química , Imuno-Histoquímica , Neoplasias Renais/química , Nefrectomia , Ratos Wistar , Reprodutibilidade dos Testes
4.
Int. braz. j. urol ; 39(4): 513-518, Jul-Aug/2013. tab
Artigo em Inglês | LILACS | ID: lil-687309

RESUMO

Purpose To evaluate the long term efficacy and safety of the use of propiverine and terazosine combination in patients with LUTS and DO by a placebo controlled study. Materials and Methods One hundred patients were enrolled in the study. They were randomized into two groups (each group consisted of 50 patients). Terazosine and placebo were administered to the patients in Group 1 and terazosine plus propiverine HCL was administered to Group 2. The patients were evaluated by international prostate symptom score (IPSS), the first four questions of IPSS (IPSS4), the 8th question of IPSS (quality of life-QoL), overactive bladder symptom score questionnaire (OAB-q V8), PSA test, urodynamic studies, post voiding residue (PVR). All patients were followed for one year and were reassessed for comparison. Results IPSS, IPSS4, OAB symptoms, QoL score, PVR, and Qmax scores of the groups did not differ. After one year treatment, there was significant improvement in IPSS, IPSS4, OAB symptoms, QoL and Qmax values in Group 2. No significant improvement was noted for the same parameters in Group 1. Conclusion This is the first study to show long term safety and efficacy of anticholinergic therapy for patients with LUTS. In patients with OAB or DO, long term anticholinergic treatment may be regarded as a treatment option. .


Assuntos
Adulto , Humanos , Masculino , Pessoa de Meia-Idade , Benzilatos/uso terapêutico , Sintomas do Trato Urinário Inferior/tratamento farmacológico , Antagonistas Muscarínicos/uso terapêutico , Prazosina/análogos & derivados , Bexiga Urinária Hiperativa/tratamento farmacológico , Método Duplo-Cego , Quimioterapia Combinada/métodos , Prazosina/uso terapêutico , Qualidade de Vida , Inquéritos e Questionários , Fatores de Tempo , Resultado do Tratamento
5.
Int. braz. j. urol ; 38(6): 795-801, Nov-Dec/2012. tab
Artigo em Inglês | LILACS | ID: lil-666015

RESUMO

Purpose

To compare totally tubeless and standard percutaneous nephrolitotomy procedures on many parameters. Materials and Methods

Percutaneous nephrolitotomy was performed on 195 patients between June 2009 and May 2012. The data of those patients were evaluated retrospectively. Totally tubeless cases were enrolled to Group 1, and Group 2 consisted of non-tubeless cases (re-entry or Foley catheter). Results

Group 1 included 85 cases and group 2 a total of 110 patients. Paper tracing values for the kidney stones were 321.25 ± 102.4 mm2 and 324.10 ± 169.5 mm2 respectively. Mean fluoroscopy time was 4.9 ± 1.9 min and 5.08 ± 2.7 min, mean operation time was 78.8 ± 27.9 min and 81.9 ± 28.77 min and mean decrease in hematocrit was 2.6 ± 1.6 and 3.74 ± 1.9 respectively. All these comparisons were statistically significant. Length of hospitalization was 1.6 ± 1.1 and 3.5 ± 1.5 days for Groups 1 and 2 respectively. Mean superficial pain score was 5.8 ± 1.6 and 6.7 ± 1.2 respectively for both groups after 1 hour. At 6 hours, the scores changed to 3.87 ± 1.22 and 4.84 ± 1.3 respectively. The analgesic dose was 1.00 ± 0.7 and 1.53 ± 0.6 for the groups respectively at 6 hours. All the statistical differences were significant for these three parameters. Conclusions

We believe that, because of their post operative patient comfort and decreased length of hospital stay, totally tubeless procedures should be considered as an alternative to standard percutaneous nephrolitotomy. .


Assuntos
Humanos , Cálculos Renais/cirurgia , Nefrostomia Percutânea/métodos , Tempo de Internação , Nefrostomia Percutânea/instrumentação , Duração da Cirurgia , Medição da Dor , Dor Pós-Operatória , Estudos Retrospectivos , Fatores de Tempo , Resultado do Tratamento , Cateterismo Urinário
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA