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1.
Zhonghua Nan Ke Xue ; 15(11): 1049-52, 2009 Nov.
Artigo em Chinês | MEDLINE | ID: mdl-20218321

RESUMO

OBJECTIVE: To evaluate the safety and efficacy of Qianliean Suppository in the treatment of chronic prostatitis of damp-heat and blood-stasis syndrome. METHODS: We conducted a randomized, single-blind, parallel-controlled, multi-centered clinical trial among 467 subjects, who were assigned to a trial group (n = 349) and a control group (n = 118), the former treated with Qianliean Suppository anally one pill per night for 28 days and the latter given Yejuhua Suppository in the same way. The efficacy was evaluated by the TCM syndrome, NIH-CPSI, main clinical symptoms and WBC count in EPS. RESULTS: After the treatment, the total rates of recovery, excellence and effectiveness for the TCM syndrome were 4.4%, 58.0% and 90.7% respectively in the trial group, significantly higher than 0.9%, 33.1% and 70.4% in the control group (P < 0.025). Remarkable decreases were observed in the NIH-CPSI total score and the scores on pain and discomfort, voiding symptoms and quality of life in the former group compared with the latter (P < 0.025). The trial group also showed a marked alleviation of such main chronic prostatitis symptoms as urgent micturition and perineal pain and discomfort (P < 0.05), as well as an obvious improvement (55.2%) of the WBC count in EPS as compared with 32.4% in the control group (P < 0.05). No serious adverse events occurred in either of the two groups (0.56% [2/349 ] vs 0.83% [1/118]). CONCLUSIONS: Qianliean Suppository is safe and effective for the treatment of chronic prostatitis of damp-heat and blood-stasis syndrome.


Assuntos
Medicamentos de Ervas Chinesas/uso terapêutico , Fitoterapia , Prostatite/tratamento farmacológico , Adolescente , Adulto , Doença Crônica , Medicamentos de Ervas Chinesas/efeitos adversos , Humanos , Masculino , Pessoa de Meia-Idade , Método Simples-Cego , Resultado do Tratamento , Adulto Jovem
2.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-326486

RESUMO

<p><b>OBJECTIVE</b>To investigate the pathologic monitoring of intestinal graft rejection in auxiliary en-bloc liver-small bowel transplantation in pigs.</p><p><b>METHODS</b>Fifty outbred long-white pigs were randomized into three groups, and the auxiliary composite liver-small bowel allotransplantations were undertaken in 10 pigs in group A and group B while segment small bowel allotransplantations were undertaken in 10 pigs in group C. Group A and C were not treated with immunosuppressive drugs while group B was treated with cyclosporine A and methylprednisolone. The postoperative intestinal graft rejections were monitored by biopsy through the jejunostomy or ileuostomy on 1, 3, 5, 7, 14, 21 and 30 days after operation. Through routine management, the specimens were directly examined via optical and electronic microscope respectively.</p><p><b>RESULTS</b>As shown from pathological data, the median initial time of postoperative rejection in group A was 8 days (ranged from 7 to 12), later than that in group C (5 days:ranged from 3 to 5), P<0.05). On the 7th day postoperatively, the rejection scores in group A was 1.11+/-0.20, lower than that in group C(2.56+/-0.18, P<0.05), but higher than that in group B(0.20+/-0.13, P<0.05). Ultrastructure also showed more severe intestinal graft rejection in intestinal transplantation than that in combined transplantation. The median survival time was 9 days(ranged from 7 to 25) in group A and 12 days(ranged from 7 to 20) in group C, while all the pigs in group B lived longer than 30 days.</p><p><b>CONCLUSION</b>The pathological assessment through the jejunostomy or ileuostomy biopsy is a convenient method to monitor the postoperative graft rejections in intestinal related transplantation.</p>


Assuntos
Animais , Feminino , Masculino , Rejeição de Enxerto , Sobrevivência de Enxerto , Intestino Delgado , Patologia , Transplante , Transplante de Fígado , Alergia e Imunologia , Suínos , Transplante Homólogo
3.
Chinese Journal of Surgery ; (12): 810-813, 2009.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-299733

RESUMO

<p><b>OBJECTIVE</b>To report preliminary experience of the protocol of combining Campath 1H induction with low-dose monotherapy of tacrolimus and no steroid in two cases of small bowel transplantation.</p><p><b>METHODS</b>Campath 1H 30 mg was infused during the small bowel transplantation, and the patients were given 1 gram of methylprednisolone followed by the Campath 1H and another gram of methylprednisolone before reperfusion. Tacrolimus was infused just after the reperfusion. The tacrolimus was administered from vein first and then from gut tract, the blood tacrolimus level was controlled at 10 to 15 microg/L within the first 3 months after the operation, and reduced to 5 microg/L thereafter.</p><p><b>RESULTS</b>The two recipients have survived more than 1 year, one received surgical closure of intestinal graft terminal stoma 13 months after the transplantation. One episode of indeterminate to mild acute rejection was verified by pathology through routine ileoscopical biopsy in each cases, and one episode of mild to moderate acute rejection occurred 8 months after the transplantation, and the patients recovered after low dose or bolus steroid therapy. The peripheral lymphocyte counts and monocyte counts decreased greatly after Campath 1H was given, and recovered very slowly thereafter. No sign of infection and graft versus host disease (GVHD) was found, and the grafted intestine achieved excellent function. The total parenteral nutrition was ceased on the day 21 and 14 after the operation, respectively, and the patients lived on oral intake to maintain nutrition status.</p><p><b>CONCLUSIONS</b>It's showed that the protocol combining Campath 1H induction with low-dose monotherapy of tacrolimus without steroid in small bowel transplantation can control graft rejection effectively without increasing the opportunity of infection, no sign of GVHD is found, and the grafted intestine could achieve excellent function.</p>


Assuntos
Feminino , Humanos , Masculino , Adulto Jovem , Alemtuzumab , Anticorpos Monoclonais , Usos Terapêuticos , Anticorpos Monoclonais Humanizados , Anticorpos Antineoplásicos , Usos Terapêuticos , Quimioterapia Combinada , Rejeição de Enxerto , Imunossupressores , Usos Terapêuticos , Intestino Delgado , Transplante , Tacrolimo , Usos Terapêuticos
4.
Chinese Journal of Surgery ; (12): 45-47, 2004.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-311155

RESUMO

<p><b>OBJECTIVE</b>To report the first case of non-composite combined liver and intestinal allotransplantation in China. The technical aspects of the case and pros and cons of such an approach versus composite technique were discussed.</p><p><b>METHODS</b>The patient suffered from short bowel syndrome and TPN-related liver damage. A non-composite technique was used in this case. During operation, the whole 380 cm intestine was transplanted with systemic drainage and aortic inflow, while the liver graft was placed in a piggyback fashion. Warm ischemic time of donor graft was 2 min and 30 seconds, and cold ischemic duration for intestinal and liver graft was 6 hours and 40 and 8 hours and 7 utes respectively. Postoperative immunosuppression management includes tacrolimus, methylprednisolone, MMF and Zenapax.</p><p><b>RESULTS</b>The recipient recovered smoothly with no evidence of rejection on days' follow up. Now he is maintained well on enteral nutrition.</p><p><b>CONCLUSION</b>Non-composite technique should be considered in adult recipients, especially those with a history of abdominal infections or multiple laparotomies.</p>


Assuntos
Adulto , Humanos , Masculino , Intestinos , Transplante , Transplante de Fígado , Síndrome do Intestino Curto , Terapêutica , Transplante Homólogo , Métodos , Resultado do Tratamento
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