Your browser doesn't support javascript.
loading
Show: 20 | 50 | 100
Results 1 - 9 de 9
Filter
1.
Int. braz. j. urol ; 42(6): 1190-1194, Nov.-Dec. 2016. graf
Article in English | LILACS | ID: biblio-828942

ABSTRACT

ABSTRACT Objective: Previous series have demonstrated that Clomiphene Citrate (CC) is an effective treatment to increase Total Testosterone (TT) in Late Onset Hypogonadism (LOH) patients. However, what happens to TT levels after ending CC treatment is still debatable. The objective of this study is to evaluate TT levels 3 months after the discontinuation of CC in patients with LOH who were previously successfully treated with the same drug. Materials and Methods: Twenty-seven patients with LOH that were successfully treated (achieved TT levels >11nmol/l) with CC 50mgs daily for 50 days were prospectively recruited in our Andrological outpatient clinic. CC was then stopped for 3 months and TT levels were measured at the end of this period. Results: Mean TT level before discontinuation of CC was 22.7±8.1nmol/L (mean±SD). Three months after discontinuation, mean TT level significantly decreased in all patients, 10.2±3.9nmol/l (p<0.01). Twenty-one patients (78%) decreased TT levels under 11nmol/L. Six patients (22%) had TT levels that remained within the normal recommended range (≥11nmol/l). No statistical significant differences were observed between both groups. Conclusion: In the short term LOH does not seem to be a reversible condition in most patients after CC treatment. More studies with longer follow-up are needed to evaluate the kinetics of TT in LOH.


Subject(s)
Humans , Adult , Aged , Testosterone/blood , Clomiphene/therapeutic use , Estrogen Antagonists/therapeutic use , Hypogonadism/therapy , Luteinizing Hormone/blood , Prospective Studies , Follow-Up Studies , Treatment Outcome , Clomiphene/administration & dosage , Estrogen Antagonists/administration & dosage , Follicle Stimulating Hormone/blood , Hypogonadism/surgery , Middle Aged
2.
Int. braz. j. urol ; 38(4): 512-518, July-Aug. 2012. ilus, tab
Article in English | LILACS | ID: lil-649445

ABSTRACT

INTRODUCTION: Male testosterone deficiency is associated with bad sexual function and quality of life (QoL). The aim of this study was to determine whether a daily dose of 25 mg clomiphene citrate (CC) is effective in stimulating the endogenous testosterone production pathway and to address the applicability of this medication as a therapeutic option for symptomatic hypogonadism. MATERIALS AND METHODS: This was a prospective study. Men with low sexual desire and testosterone levels (T) below 400 ng/dL were selected to receive CC. Blood samples were obtained to determine baseline measurements of serum T, estradiol, LH, lipid profile and fasting plasma glucose. Each patient was treated with a daily dose of 25 mg CC for at least 3 months. Patients were asked if they experienced any side effects related to the use of CC and if they experienced any improvement in their sexual profile. Paired samples T-test was utilized to analyze responses to therapy. RESULTS: Our cohort consisted of 125 men with hypogonadism and low libido. Mean age was 62 years (± 11.1 years). Serum T levels ranged from 309 ng/dL (baseline, mean value) to 642 ng/dL (3 months after CC initiation, mean value) (p < 0.001). Serum cholesterol levels ranged from 197 to 186 mg/dL (p = 0.003). There were no statistically significant differences when comparing pre and post-treatment HDL-Cholesterol, triglycerides, fasting plasma glucose and prolactin. All men reported improvements in the post-treatment QoL scores. No serious adverse events were recorded. CONCLUSIONS: The CC was effective in stimulating the endogenous production of testosterone. A lower level of total cholesterol was verified after three months of treatment. This medication should be considered as a therapeutic option for some patients with symptomatic male testosterone deficiency.


Subject(s)
Adult , Aged , Humans , Male , Middle Aged , Clomiphene/administration & dosage , Estrogen Antagonists/administration & dosage , Hypogonadism/drug therapy , Testosterone/deficiency , Age Factors , Epidemiologic Methods , Luminescence , Quality of Life , Time Factors , Treatment Outcome , Testosterone/blood , Testosterone/metabolism
4.
Journal of Korean Medical Science ; : 445-451, 2008.
Article in English | WPRIM | ID: wpr-69845

ABSTRACT

We initiated this study to investigate whether combining Helicobacter pylori eradication with immunosuppressive therapy provides an additional benefit to patients with idiopathic thrombocytopenic purpura (ITP) that has relapsed or has not responded to steroid and/or danazol therapy in patients who have H. pylori infection. Thirty- four patients with chronic ITP that had relapsed or failed to steroid and/or danazol therapy were assessed for H. pylori infection. Of the 21 confirmed cases, 12 patients were given H. pylori eradication therapy alone (EA), while 9 patients received eradication therapy combined with immunosuppressive therapy (EI). The response rate was not significantly different between patients in the EA and those in the EI group (41.7% in the EA group vs. 66.7% in the EI group, p=0.345). The median platelet count at 6 months after therapy was higher in the EI group patients (75X10(9)/L in the EI group patients vs. 18x109/L in the EA group patients, p=0.028). The median response duration was also longer in the EI group patients (9 months in the EI group patients vs. 3 months in the EA group patients, p=0.049). These results show that a significant benefit is gained by the use of H. pylori eradication combined with immunosuppressive therapy over the use of eradication therapy alone for patients with chronic ITP.


Subject(s)
Adult , Aged , Female , Humans , Male , Middle Aged , Anti-Bacterial Agents/administration & dosage , Chronic Disease , Danazol/administration & dosage , Drug Therapy, Combination , Estrogen Antagonists/administration & dosage , Helicobacter Infections/complications , Helicobacter pylori , Immunosuppressive Agents/administration & dosage , Purpura, Thrombocytopenic, Idiopathic/complications , Steroids/administration & dosage , Treatment Outcome
5.
Article in English | IMSEAR | ID: sea-44458

ABSTRACT

OBJECTIVE: To determine the day of ovulation by the salivary ferning test in clomiphene citrate-treated women. DESIGN: A descriptive study. SETTING: Department of Obstetrics and Gynecology, Faculty of Medicine, Chulalongkorn University, Bangkok, Thailand. SUBJECT: Seventy-five infertile women with regular menstrual cycles. MATERIAL AND METHOD: Infertile women were given 100 mg of clomiphene citrate for five days and collected their saliva samples daily until seven days after ovulation. Transvaginal ultrasound was performed daily to detect ovulation. The salivary ferning formation was examined by a normal light microscope and graded from 1-3, according to its extent and intensity. MAIN OUTCOME MEASURE: The salivary ferning score, the peak salivary ferning day, and the day of ovulation detected by ultrasound. RESULTS: The patients' age and cycle length (mean +/- SD) were 32.9 +/- 3.7 years and 28.4 +/- 1.3 days. The peak salivary ferning day corresponded with the ultrasound ovulation day in only 7.1%. There were two peaks of median salivary ferning scores; one was two days prior ovulation and the other was five days post ovulation. There was no correlation between the peak salivary ferning day and day of ovulation detected by ultrasound (r = 0.102, p > 0.05). CONCLUSION: In clomiphene citrate-stimulated cycles, the saliva ferning test does not seem to associate with ovulation.


Subject(s)
Adult , Clomiphene/administration & dosage , Endometrium/drug effects , Estrogen Antagonists/administration & dosage , Female , Fertility Agents, Female/administration & dosage , Follicle Stimulating Hormone , Humans , Infertility, Female/diagnostic imaging , Luteinizing Hormone , Menstrual Cycle/drug effects , Ovulation/drug effects , Ovulation Detection/methods , Ovulation Induction , Saliva , Thailand , Time
6.
Arq. bras. oftalmol ; 67(4): 631-635, jul.-ago. 2004. tab, graf
Article in Portuguese | LILACS | ID: lil-386034

ABSTRACT

OBJETIVO: O tamoxifeno é um antiestrógeno utilizado como agente terapêutico eficaz no câncer de mama. A droga pode causar efeitos tóxicos oculares em dosagens altas. O objetivo deste estudo foi determinar possíveis efeitos retino-tóxicos centrais usando o eletrorretinograma multifocal (mfERG) em grupo de pacientes tratadas com baixa dosagem de tamoxifeno (20 mg/dia) após cirurgia do câncer de mama. MÉTODOS: O eletrorretinograma multifocal (mfERG) de 30 graus centrais da retina foi obtido em 3 diferentes grupos: Grupo experimental - 15 mulheres (41-59 anos, média 48,6 ± 4,5) com fundo de olho normal, tratadas com tamoxifeno em baixa dosagem por 1 a 55 meses. Grupo controle - 6 mulheres (30 -76 anos, média 49,9±18,8) com diagnóstico prévio de câncer de mama que não receberam tratamento com tamoxifeno até o teste do eletrorretinograma multifocal. Grupo controle normal - 15 voluntárias normais (30-71 anos, média 47,7 ± 12,9). A amplitude e a latência de eletrorretinograma multifocal para N1-P1 foram analisados estatisticamente (análise de variância de uma via). RESULTADOS: As amplitudes médias N1-P1 (nV/grau²) foram comparáveis para respostas de diferentes excentricidades (0 a 25 graus) nos três grupos. Não houve diferença estatisticamente significativa para a latência de N1 e P1 (ms) do eletrorretinograma multifocal entre os 3 grupos. CONCLUSÕES: O tratamento com baixa dosagem de tamoxifeno não mostrou efeitos retino-tóxicos em pequeno grupo de mulheres após cirurgia do câncer de mama. Investigação seriada proporcionará melhor compreensão desses efeitos.


Subject(s)
Humans , Female , Adult , Middle Aged , Estrogen Antagonists/adverse effects , Estrogen Antagonists/toxicity , Breast Neoplasms , Electroretinography , Retina , Tamoxifen , Estrogen Antagonists/administration & dosage , Tamoxifen
7.
P. R. health sci. j ; 23(1): 13-18, Mar. 2004.
Article in English | LILACS | ID: lil-359654

ABSTRACT

Hereditary (HAE) and acquired (AAE) angioedema are vascular reactions involving the sub mucosal tissues, representing localized edema caused by dilatation and increased permeability of the capillaries. HAE and AAE are clinical disorders characterized by angioedema that require prompt differentiation from other causes of angioedema in order to receive the most pertinent and effective therapeutic interventions. The aim of this report is to describe the clinical characteristics of patients with both HAE and AAE identified and followed at the Immunology Clinic of the University Hospital at the Puerto Rico Medical Center, their response and side effects to danazol therapy and their comparison with other series of similar patients reported in the literature. Overall, the patients in this sample presented a similar clinical profile compared to other reported series in the literature.


Subject(s)
Humans , Male , Female , Child , Adolescent , Adult , Middle Aged , Angioedema , Estrogen Antagonists/administration & dosage , Estrogen Antagonists/adverse effects , Estrogen Antagonists/therapeutic use , Complement C1 , Complement C1q , Complement C4 , Data Interpretation, Statistical , Diagnosis, Differential , Danazol/administration & dosage , Danazol/adverse effects , Danazol/therapeutic use , Enzyme-Linked Immunosorbent Assay , Immunodiffusion , Complement Inactivating Agents/analysis , Time Factors
8.
J Indian Med Assoc ; 2001 Aug; 99(8): 436, 438-40
Article in English | IMSEAR | ID: sea-96475

ABSTRACT

Endometriosis is defined as the presence of tissue, histologically similar to endometrium, in any other site but that of uterine cavity. Transplantation of endometrial tissue that comes as a retrograde menstrual flow is the most accepted possible theory. Endometriosis is associated with marked subfertility, but the mechanism of causation of infertility is poorly understood unless it has caused very definite anatomical distortion of internal genitalia. Management of infertility in endometriosis is discussed in detail.


Subject(s)
Adult , Aged , Danazol/administration & dosage , Endometriosis/complications , Estrogen Antagonists/administration & dosage , Female , Gonadotropin-Releasing Hormone/administration & dosage , Humans , Incidence , India/epidemiology , Infertility, Female/epidemiology , Middle Aged , Progesterone/administration & dosage , Prognosis , Risk Factors , Severity of Illness Index
9.
J. bras. ginecol ; 100(8): 249-50, ago. 1997. tab
Article in Portuguese | LILACS | ID: lil-197969

ABSTRACT

Quarenta e seis pacientes com carcinoma avançado de mama foram tratadas com antiestrogênio (Tamoxifen) no Setor de Patologia Mamária do HCPA. Após quatro anos. 35 pacientes apresentavam seguimento adequado para tabulaçäo dos resultados quanto à eficácia do tratamento, duraçäo da resposta e efeitos colaterais. Os autores concluem que o tratamento com Tamoxifeno é a primeira escolha em hormonioterapia na pós-menopausa, para tratamento do câncer de mama


Subject(s)
Humans , Female , Estrogen Antagonists/administration & dosage , Estrogen Antagonists/therapeutic use , Breast Neoplasms/drug therapy , Breast Neoplasms/therapy , Postmenopause , Tamoxifen/administration & dosage , Tamoxifen/therapeutic use
SELECTION OF CITATIONS
SEARCH DETAIL