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1.
Kaohsiung J Med Sci ; 33(3): 144-151, 2017 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-28254117

RESUMO

We aim to investigate the correlation of benign prostatic obstruction (BPO)-related complications with clinical outcomes in patients after transurethral resection of the prostate in China. We reviewed the medical history of all patients who underwent surgery from 1992 to 2013. We assessed the preoperative clinical profile, clinical management, and operative complications. Overall, 2271 patients were enrolled in the study. Of these patients, 1193 (52.5%) had no BPO-related complications and 1078 (46.3%) had BPO-related complications. Compared with patients without BPO-related complications, those with BPO-related complications were older (p = 0.001) and usually had other urologic comorbidities (p = 0.003). Additionally, they tended to have more tissue resected (p < 0.001), a higher American Society of Anesthesiologists grade (p = 0.002), and larger prostates (p < 0.001). Nonetheless, there was no obvious difference in surgical complications between both groups (p > 0.05). Among patients with BPO-related complications, compared with the bladder stone group, only the bladder stone+ group tended to have a greater urinary infection risk after transurethral resection of the prostate. Compared with patients with one or two BPO-related complications, those with three BPO-related complications tended to have a higher risk of pulmonary embolism and acute coronary syndrome (p < 0.05). Despite the widespread use of medication, patients with BPO-related complications were older and had larger prostates; however, transurethral resection of the prostate is still considered a safe and recommended surgical treatment. Nevertheless, those with three or more complications were at a higher risk of severe complication after surgery, and active surgical intervention is needed once BPO-related complications develop.


Assuntos
Próstata/cirurgia , Hiperplasia Prostática/cirurgia , Ressecção Transuretral da Próstata/métodos , Cálculos da Bexiga Urinária/cirurgia , Síndrome Coronariana Aguda/etiologia , Síndrome Coronariana Aguda/patologia , Idoso , Humanos , Masculino , Pessoa de Meia-Idade , Tamanho do Órgão , Complicações Pós-Operatórias/patologia , Próstata/patologia , Hiperplasia Prostática/complicações , Hiperplasia Prostática/patologia , Embolia Pulmonar/etiologia , Embolia Pulmonar/patologia , Estudos Retrospectivos , Índice de Gravidade de Doença , Trombose/etiologia , Trombose/patologia , Ressecção Transuretral da Próstata/instrumentação , Resultado do Tratamento , Cálculos da Bexiga Urinária/complicações , Cálculos da Bexiga Urinária/patologia , Urodinâmica
2.
Lab Anim ; 44(3): 226-30, 2010 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20385652

RESUMO

The zinc disc implantation-induced urinary bladder calculi model in the rat is commonly used for preclinical evaluation of the antiurolithiatic activity of test compounds. Certain published reports state that relatively long durations for which zinc discs must be implanted in the bladders of rats. Hence, there is a need to refine this model. These investigations aimed to determine whether long-term studies using the zinc disc implantation model provide any additional data that affect the final outcomes of the study. In this study, we evaluated the effects of a well-known antiurolithiatic polyherbal drug, Cystone, for different treatment durations of 10, 20 and 48 days postimplantation. Our results indicate that even the shortest duration of 10 days is sufficient to reveal antiurolithiatic effects of a test drug. Hence, in the zinc disc implantation-induced urinary bladder calculi model, the study duration is proposed to be minimized so as to reduce the distress caused to the rats due to long-term exposure to the implant. Further, it is suggested that the growth of the bladder calculi can be monitored by taking X-ray radiographs of the bladder deposits to decide the time to terminate the study. Use of preformed calcium oxalate crystal instead of zinc discs, as suggested in earlier reports by others, may also be considered to avoid the sacrifice of rats at the end of the study.


Assuntos
Bem-Estar do Animal , Modelos Animais de Doenças , Determinação de Ponto Final/ética , Corpos Estranhos/complicações , Cálculos da Bexiga Urinária/etiologia , Zinco/efeitos adversos , Alternativas ao Uso de Animais , Animais , Oxalato de Cálcio/efeitos adversos , Determinação de Ponto Final/métodos , Corpos Estranhos/tratamento farmacológico , Corpos Estranhos/patologia , Masculino , Ayurveda , Extratos Vegetais/farmacologia , Plantas Medicinais , Radiografia , Ratos , Ratos Wistar , Bexiga Urinária/diagnóstico por imagem , Cálculos da Bexiga Urinária/tratamento farmacológico , Cálculos da Bexiga Urinária/patologia
3.
Int J Toxicol ; 22(3): 227-32, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-12851155

RESUMO

The purpose of this study was to investigate the effect of oral administration of manganese acetate on the kidneys and urinary bladder of Sprague-Dawley (SD) rats. Male and female SD rats (150 to 175 g), 6 weeks old, were administered varying doses of manganese acetate for 63 days by oral gavage. At the end of 63 days, 50% of the animals were sacrificed and kidney tissue was isolated and fixed for histopathological studies (study A). The remaining 50% were cross-mated and dosing ceased. Animals were sacrificed after 2 weeks (study B). Male treated animals were noted to have viscous, gritty urine in the urinary bladder, and the high-dose groups had urinary bladder stones (uroliths). Histopathologically, the most striking lesions were observed in the kidneys and prostate glands of male animals. Mild-to-moderate tubulointerstitial nephritis with tubular proteineous and glomerulosclerosis was observed in animals of all treatment groups. Urolithiasis in the urinary bladder was confirmed in 33% to 66% of treated animals. Female animals did not show a significant difference above controls in renal tissues. Results of this study suggest that male rats are more sensitive to the effects of high levels of manganese given orally than female rats and that the genitourinary structures represent target organs of toxicity.


Assuntos
Rim/efeitos dos fármacos , Manganês/farmacologia , Nefrite Intersticial/induzido quimicamente , Bexiga Urinária/efeitos dos fármacos , Administração Oral , Animais , Relação Dose-Resposta a Droga , Feminino , Rim/patologia , Masculino , Manganês/administração & dosagem , Nefrite Intersticial/patologia , Próstata/efeitos dos fármacos , Próstata/patologia , Proteinúria/induzido quimicamente , Proteinúria/patologia , Ratos , Ratos Sprague-Dawley , Testes de Toxicidade , Bexiga Urinária/patologia , Cálculos da Bexiga Urinária/induzido quimicamente , Cálculos da Bexiga Urinária/patologia
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