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1.
Zhonghua Fu Chan Ke Za Zhi ; 43(4): 247-50, 2008 Apr.
Artigo em Chinês | MEDLINE | ID: mdl-18843961

RESUMO

OBJECTIVE: To compare the efficacy and safety of tranexamic acid (TA) and norethisterone (NET) for the treatment of patients with ovulatory menorrhagia in China. METHODS: One hundred and thirty one patients with proven ovulatory menorrhagia from gynecologic clinics of 5 teaching hospitals located in 4 different cities in China were enrolled during Jul 2004 to Dec 2006. Among them 128 completed the study. Patients were randomly divided into two therapeutic regimen groups: TA 1 g thrice daily during menstrual cycle days (D) 1-5, 69 cases; or NET 5 mg twice daily on D19-26, 59 cases. The drugs were administered for 2 consecutive cycles, then withdrawn and patients were followed-up for 1 more cycle. Data on menstrual blood loss [estimated by pictorial blood assessment chart (PBAC)], length of menstrual periods, quality of life (QOL) evaluated by a 6 item health-related questionnaire were collected before, during each cycle and were compared. RESULTS: Both treatments led to significant decreases of mean PBAC scores and shorter duration of menstrual periods, and improved the QOL ranking during the two treatment cycles. The mean percentages of PBAC decrements in the TA first and second cycles were significantly greater than those in the NET corresponding cycles(35% vs 17% , P = 0.004; 44% vs 34%, P = 0.04 respectively). The success rate of TA second cycle was higher than that of the NET second cycle (41% vs 24%, P = 0.04). Improvement of QOL ranking in the TA first cycle was also significantly better than those in the NET first cycle (P = 0.03). The percentage of patients with at least 1 adverse event in TA group (19%) was significantly lower than that in NET group (35%, P = 0.04). Patients' willingness to continue the treatment in the TA second and follow-up cycles (94%, 79% respectively) were significantly higher than those in the corresponding cycles of NET groups (79%, 59% respectively; P = 0.01, P = 0.02). CONCLUSION: The regimen of TA 3 g daily during menstrual days 1-5 is a more effective and tolerable treatment than luteal phase norethisterone for patients with ovulatory menorrhagia.


Assuntos
Antifibrinolíticos/uso terapêutico , Menorragia/tratamento farmacológico , Menstruação/efeitos dos fármacos , Noretindrona/uso terapêutico , Ácido Tranexâmico/uso terapêutico , Administração Oral , Adulto , Antifibrinolíticos/farmacologia , Feminino , Humanos , Pessoa de Meia-Idade , Noretindrona/efeitos adversos , Noretindrona/farmacologia , Estudos Prospectivos , Qualidade de Vida , Ácido Tranexâmico/efeitos adversos , Ácido Tranexâmico/farmacologia , Resultado do Tratamento
2.
Artigo em Chinês | MEDLINE | ID: mdl-16866153

RESUMO

Total DNA was extracted from T. vaginalis with Chelex-100 method and used as templates for PCR. The ferredoxin gene was directionally cloned into plasmid pMD-18T vector and subcloned into eukaryotic expression vector pcDNA3. 1 (+). The transformants were screened and identified by PCR and restriction analysis. The size of amplified ferredoxin gene was 306bp and the DNA sequence of cloned gene was same with that published.


Assuntos
Células Eucarióticas/metabolismo , Ferredoxinas/genética , Proteínas de Protozoários/genética , Trichomonas vaginalis/genética , Animais , Sequência de Bases , Clonagem Molecular , Expressão Gênica , Vetores Genéticos/genética , Plasmídeos/genética , Reação em Cadeia da Polimerase
3.
Artigo em Chinês | MEDLINE | ID: mdl-16042202

RESUMO

OBJECTIVE: To construct a recombinant plasmid containing ferredoxin gene of Trichomonas vaginalis. METHODS: Total DNA was extracted from Trichomonas vaginalis with Chelex-100 method and used as templates for PCR. Primers were designed based on the published sequence of the ferredoxin gene and used to amplify the Trichomonas vaginalis gene using PCR method. The ferredoxin gene obtained by PCR technique was directionally cloned into plasmid pMD-18T simple vector. The constructed recombinant plasmid was transferred into E. coli JM109. The transformants were screened and identified by PCR and restriction analysis. The DNA sequence of the gene was determined by Sanger's method. RESULTS: The size of amplified ferredoxin gene was 306bp. The correct recombinant plasmid was isolated and confirmed by PCR and restriction analysis. The DNA sequence of cloned gene was the same as the published sequence. CONCLUSION: The ferredoxin gene was successfully amplified and cloned into plasmid pMD-18T simple vector. The cloned ferredoxin gene could be used to produce recombinant protein and for study of its function.


Assuntos
Ferredoxinas/genética , Trichomonas vaginalis/genética , Sequência de Aminoácidos , Animais , Sequência de Bases , Clonagem Molecular , Escherichia coli/genética , Ferredoxinas/química , Dados de Sequência Molecular , Plasmídeos/genética , Reação em Cadeia da Polimerase
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