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1.
Endocr Pract ; 19(2): 252-8, 2013.
Article in English | MEDLINE | ID: mdl-23543030

ABSTRACT

OBJECTIVES: Successful surgery does not always resolve all the clinical consequences of hypercortisolism in patients with Cushing's disease (CD). Our purpose was to integrally evaluate a group of CD patients cured by pituitary surgery and look for the persistence of CD symptoms, signs, and comorbidities. METHODS: We performed clinical and biochemical evaluations of 29 CD patients (2 males) cured by pituitary surgery. All patients underwent early (median 12 months) and late (median 58 months) postoperative evaluations. We sought information regarding hypercortisolism-related symptoms and signs, as well as metabolic, cardiovascular, reproductive, and psychologic comorbidities. RESULTS: The prevalence of obesity dropped from 72.4% at diagnosis to 31% at early evaluation but increased again to 44.8% at the late evaluation. Diabetes was present in 14 patients (48.3%) at diagnosis and persisted in 9 at the late evaluation. Hypertriglyceridemia was present in 58.6% and 55.1% of patients at diagnosis and at the late follow-up, respectively. The prevalence of hypercholesterolemia was 79.3% at diagnosis, decreased to 55.1% at the early evaluation, and increased to 65.5% at the late evaluation. Menstrual abnormalities were originally present in 15 of 20 women, and 8 of the 15 had recovered normal periods when seen at the last evaluation. Among the 24 patients with depression at diagnosis, 11 and 6 still exhibited mood abnormalities at the early and late evaluations, respectively. CONCLUSIONS: In a variable proportion of patients, the cardiovascular, metabolic, and emotional comorbidities of CD persist after long-term remission, irrespective of the initial degree of hypercortisolism.


Subject(s)
Cushing Syndrome/surgery , Depression/epidemiology , Fatigue/epidemiology , Hirsutism/prevention & control , Hypertension/prevention & control , Pituitary Gland/surgery , Acne Vulgaris/epidemiology , Acne Vulgaris/prevention & control , Adolescent , Adult , Cohort Studies , Comorbidity , Cushing Syndrome/epidemiology , Cushing Syndrome/metabolism , Cushing Syndrome/physiopathology , Depression/prevention & control , Fatigue/prevention & control , Female , Follow-Up Studies , Hirsutism/epidemiology , Hirsutism/etiology , Humans , Hydrocortisone/blood , Hydrocortisone/metabolism , Hydrocortisone/urine , Hypertension/epidemiology , Hypertension/etiology , Hypokalemia/epidemiology , Hypokalemia/prevention & control , Male , Menstruation Disturbances/epidemiology , Menstruation Disturbances/etiology , Menstruation Disturbances/prevention & control , Mexico/epidemiology , Middle Aged , Pituitary Gland/metabolism , Prevalence , Young Adult
2.
Contraception ; 86(6): 698-703, 2012 Dec.
Article in English | MEDLINE | ID: mdl-22770794

ABSTRACT

BACKGROUND: Although acceptability of combined oral contraceptives (COCs) is widespread, patients are often unaware of the noncontraceptive benefits. STUDY DESIGN: An opinion survey through telephone interview was conducted to evaluate the knowledge of 500 Brazilian women 15-45 years of age who were current users or had recently used COCs. Data were obtained on their knowledge of adverse events, the effects of COCs on health- and menstrual-related symptoms, noncontraceptive benefits and aspects related to sexual response. RESULTS: Most of the women interviewed learned about the pill from doctors or the Internet. Other than the pill, the best-known contraceptive methods were the condom and intrauterine device. The majority of women believe that COCs do not change the risk of gynecological cancers. Most believed that they had no significant effect on sexual response. CONCLUSIONS: COCs users in Brazil lack precise information on aspects related to general health, particularly menstrual-related symptoms and noncontraceptive health benefits.


Subject(s)
Contraceptives, Oral, Combined , Patient Medication Knowledge , Urban Health , Adolescent , Adolescent Behavior , Adult , Brazil , Condoms/adverse effects , Contraception Behavior , Contraceptives, Oral, Combined/adverse effects , Contraceptives, Oral, Combined/therapeutic use , Female , Humans , Internet , Intrauterine Devices/adverse effects , Menstruation Disturbances/prevention & control , Middle Aged , Patient Education as Topic , Physician's Role , Young Adult
3.
Rev. chil. obstet. ginecol ; 76(5): 344-353, 2011. ilus
Article in Spanish | LILACS | ID: lil-608805

ABSTRACT

Objetivo: Demostrar la influencia sobre las molestias emocionales y físicas (beneficios no anticonceptivos) experimentadas durante el primer año de uso de un anticonceptivo oral combinado (AOC) que contiene 0,02 mg de etinilestradiol (EE) y 2 mg de acetato de clormadinona (ACM) administrado en un régimen de 24 + 4 días de placebo. Diseño del estudio: Análisis adicional de las sensaciones subjetivas registradas en los diarios de 1665 participantes de un estudio de Fase III multicéntrico, no controlado, de administración múltiple, después de 13 ciclos de EE/ACM en un régimen de administración de 24 + 4 días, publicado previamente. Resultados: Se informó de menor frecuencia de molestias emocionales y físicas en el ciclo de medicación 13 en comparación con los datos en la admisión y en el ciclo 1. La incidencia de ánimo depresivo se redujo en 84,5 por ciento y 72,2 por ciento respectivamente, y la irritabilidad en 87,3 por ciento y 66,0 por ciento. Las cefaleas se redujeron en 75,5 por ciento y 74,7 por ciento, las molestias mamarias en 77,1 por ciento y 66,1 por ciento, y la dismenorrea preexistente en 77,9 por ciento y 67,6 por ciento respectivamente. El abandono prematuro del estudio a causa de las molestias fue marginal, y el perfil del sangrado fue aceptable. Conclusiones: Un AOC de baja dosis que contiene 0,02 mg de EE + 2 mg de ACM, administrado en un régimen de 24 + 4 días, reduce significativamente la mayor parte de las molestias emocionales y físicas que se presentan durante los ciclos espontáneos de las mujeres, y se combina con un adecuado perfil de sangrado.


Objective: To demonstrate the influence on physical and psychological complaints during the first year of intake of the combined oral contraceptive (COC) 0.02 mg ethinylestradiol (EE)/2 mg chlormadinone acetate (CMA), administered in a regimen of 24 days of CMA/EE intake followed by 4 days of placebo intake. Study design: The subjective feelings of non-contraceptive benefits registered in women's diaries of 1,665 subjects participating in a multicentre, uncontrolled, multiadministration, Phase III trial, published elsewhere, were analyzed post-hoc after 13 cycles intake of EE/CMA in a 24 +4 days intake regimen. Results: Emotional complaints were reported less frequently at medication cycle 13 compared with admission and cycle 1. Depressive mood was reduced by 84.5 percent and 72.2 percent, irritability by 87.3 percent and 66.0 percent; physical complaints were also reduced: headaches by 75.5 percent and 74.7 percent, breast discomfort by 77.1 percent and 66.1 percent; pre-existing dysmenorrhea by 77.9 percent and 67.6 percent. Premature termination due to complaints was only marginal, the bleeding profile was accepted. Conclusions: The low-dose COC, 0.02 mg EE/2 mg CMA, administered in a 24 +4 day regimen, reduces significantly most of the emotional and physical complaints occurring during spontaneous cycles of women, combined with an adequate bleeding profile.


Subject(s)
Humans , Adolescent , Adult , Female , Chlormadinone Acetate/administration & dosage , Contraceptives, Oral, Combined/administration & dosage , Menstrual Cycle , Ethinyl Estradiol/administration & dosage , Headache/prevention & control , Dose-Response Relationship, Drug , Depression/prevention & control , Dysmenorrhea/prevention & control , Fatigue/prevention & control , Irritable Mood , Uterine Hemorrhage/prevention & control , Multicenter Studies as Topic , Placebos , Menstruation Disturbances/prevention & control
4.
Nutrition ; 25(6): 634-9, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19230616

ABSTRACT

OBJECTIVE: Female athlete triad (FAT) is a syndrome characterized by the simultaneous presence of disordered eating, amenorrhea, and osteopenia or osteoporosis. The aim of this study was to assess the prevalence of FAT in adolescent elite women swimmers. METHODS: The sample was composed of 78 athletes in the age range of 11-19 y from Rio de Janeiro (Brazil). The presence of disordered eating was assessed through three questionnaires (Eating Attitudes Test, Bulimic Investigatory Test Edinburgh, and Body Shape Questionnaire); the presence of menstrual dysfunctions, through a validated questionnaire; and bone dysfunctions, through assessment of bone mineral density by applying the method of dual-energy X-ray absorptiometry. The t test was used to compare means. The chi-square test was used to evaluate the association among categorical variables (P < 0.05). Pearson's coefficients of simple linear correlation between the variables of lean body mass and body mineral density at the spine (L1-L4) and overall in the body were calculated. Kaplan-Meier survival curves to estimate mean menarche age were obtained. All analyses were conducted in SPSS 13.0. RESULTS: The athletes' mean age at menarche was 12.38 +/- 0.2 y. It was verified that 44.9%, 19.2%, and 15.4% of the athletes met the criteria for disordered eating, menstrual irregularity, and low bone mass, respectively. Among participants, 47.4% (37 of 78) met one criterion of FAT, 15.4% (12 of 78) met two criteria, and 1.3% (1 of 78) met all three criteria, corresponding with the development of the syndrome. Only 35.9% (28 of 78) of the athletes did not present positive results for any of the criteria assessed. CONCLUSION: The prevalence of FAT was low. However, a significant number of athletes presented a partial status of FAT, especially of disordered eating. The present study suggests the need to monitor the causes of these disorders to create preventive actions that will reverse or avoid the development of the syndrome, thus preserving the athletes' health.


Subject(s)
Bone Diseases, Metabolic/epidemiology , Feeding and Eating Disorders/epidemiology , Female Athlete Triad Syndrome/epidemiology , Menstruation Disturbances/epidemiology , Swimming , Absorptiometry, Photon , Adolescent , Bone Density/physiology , Bone Diseases, Metabolic/diagnosis , Bone Diseases, Metabolic/prevention & control , Brazil/epidemiology , Chi-Square Distribution , Child , Cross-Sectional Studies , Feeding and Eating Disorders/diagnosis , Feeding and Eating Disorders/prevention & control , Female , Female Athlete Triad Syndrome/diagnosis , Female Athlete Triad Syndrome/prevention & control , Humans , Kaplan-Meier Estimate , Menarche/physiology , Menstruation Disturbances/diagnosis , Menstruation Disturbances/prevention & control , Prevalence , Surveys and Questionnaires , Young Adult
5.
Contraception ; 69(2): 115-9, 2004 Feb.
Article in English | MEDLINE | ID: mdl-14759615

ABSTRACT

The objectives of this study were to compare effects of medroxyprogesterone acetate 25 mg + estradiol cypionate 5 mg (Cyclofem) and norethisterone enanthate (NET-EN) upon the menstrual pattern and determine changes in lipoprotein parameters after 12 months of use. One-hundred females were included and 87 (45 with Cyclofem and 42 with NET-EN) women completing 12 months were evaluated. Menstrual changes were the leading complaint among users. At the end of 12 months, 20/45 (44.4%) and 18/41 (43.9%) Cyclofem and NET-EN users, respectively, had normal menstrual pattern. Irregular and infrequent bleeding were the two most important changes that occurred. The discontinuation rate at 12 months due to menstrual disturbances did not show any significant differences between the two preparations, but showed lower incidence compared to other studies. Total cholesterol, high-density, low-density and very low-density lipoprotein cholesterol and triglyceride levels decreased at 12 months in both groups and these changes were statistically significant.


Subject(s)
Contraceptive Agents, Female/adverse effects , Contraceptives, Oral, Combined/adverse effects , Estradiol/analogs & derivatives , Estradiol/adverse effects , Lipids/blood , Medroxyprogesterone Acetate/adverse effects , Menstruation Disturbances/chemically induced , Norethindrone/analogs & derivatives , Norethindrone/adverse effects , Adolescent , Adult , Cholesterol/metabolism , Contraceptive Agents, Female/administration & dosage , Contraceptives, Oral, Combined/administration & dosage , Drug Combinations , Estradiol/administration & dosage , Female , Humans , Injections, Intramuscular , Medroxyprogesterone Acetate/administration & dosage , Menstruation Disturbances/prevention & control , Middle Aged , Norethindrone/administration & dosage
6.
Reprod. clim ; 13(3): 151-5, set. 1998.
Article in Portuguese | LILACS | ID: lil-226139

ABSTRACT

A perimenopausa tem sido reconhecida cada vez mais como uma entidade separada no processo da menopausa precoce ou tardio. A menopausa näo deve ser vista necessariamente como um declínio, mas sim pode ser uma experiência pessoal positiva e o começo de uma vida de transiçäo satisfatória. Esperar pela parada das menstruaçöes antes de iniciar tratamento näo tem uma base fisiológica.


Subject(s)
Humans , Female , Adult , Middle Aged , Estrogens/deficiency , Menstruation/physiology , Menstrual Cycle/physiology , Premenopause/physiology , Estrogen Replacement Therapy , Menstruation Disturbances/prevention & control , Menstruation Disturbances/therapy , Uterine Hemorrhage/etiology , Women's Health , Contraceptives, Oral/therapeutic use , Depressive Disorder/etiology , Depressive Disorder/prevention & control , Depressive Disorder/therapy , Cardiovascular Diseases/prevention & control , Estrogens/therapeutic use , Osteoporosis/prevention & control , Progesterone/therapeutic use , Risk Factors
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