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1.
Eur J Obstet Gynecol Reprod Biol ; 208: 81-85, 2017 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-27894033

RESUMEN

OBJECTIVE: As endometrioma frequently recurs after conservative surgery, long-term postoperative medical treatment for the prevention of recurrence is necessary. However, it has not been elucidated whether long-term postoperative medical treatment is crucial to all patients until menopause. Thereupon, this study was conducted to evaluate the age-related recurrence patterns after conservative surgery for endometrioma. STUDY DESIGN: A retrospective cohort study was performed on a total of 420 reproductive-aged women who underwent conservative surgery for endometrioma between January 2000 and December 2010. Ultrasonography was used during the follow-up period to detect endometrioma recurrence. Patients were classified into two groups according to the use of postoperative medications. The first group was observation only, while the second received gonadotropin releasing hormone agonists followed by cyclic oral contraceptives. The cumulative recurrence rate of endometrioma was compared according to the age at surgery (20-29 years, 30-39 years, 40-45 years) within each group. Subgroup analysis was performed according to the age between the two groups. RESULTS: The median follow-up duration after surgery was 29.0 months (range 6-159 months) for all patients. After adjusting for parity, size and bilaterality of cyst, and stage with American Society for Reproductive Medicine classification of endometriosis which was statistically different, within the group of no treatment, the cumulative recurrence rate in 40-45 years (10.2%) was significantly lower compared with those in 20-29 years (43.3%; hazard ratio (HR)=0.04; 95% confidence interval (CI)=0.01-0.52) and 30-39 years (22.5%; HR=0.19; 95% CI=0.04-0.92). However, there were no differences within the group of postoperative medical treatment. When we compared between the two groups, the cumulative recurrence rate was significantly different in 20-29 years (8.1 vs 43.3%; p<0.001) and 30-39 years (5.4 vs 22.5%; p=0.007), but there was no difference in 40-45 years (4.5 vs 10.2%; p=0.901). CONCLUSIONS: Our preliminary results demonstrate that the risk of endometrioma recurrence decreases with age. After the age of forty, the recurrence rate does not differ according to the use of postoperative medication. Based on our results, postoperative medical treatment may be individualized according to the patient's age at the time of surgery. Further studies are needed to identify patients who may benefit from postoperative medication.


Asunto(s)
Envejecimiento , Endometriosis/cirugía , Laparoscopía , Tratamientos Conservadores del Órgano , Enfermedades del Ovario/cirugía , Ovario/cirugía , Adulto , Terapia Combinada , Anticonceptivos Secuenciales Orales , Endometriosis/diagnóstico por imagen , Endometriosis/tratamiento farmacológico , Endometriosis/epidemiología , Femenino , Fármacos para la Fertilidad Femenina/antagonistas & inhibidores , Fármacos para la Fertilidad Femenina/uso terapéutico , Estudios de Seguimiento , Hormona Liberadora de Gonadotropina/agonistas , Humanos , Leuprolida/antagonistas & inhibidores , Leuprolida/uso terapéutico , Persona de Mediana Edad , Enfermedades del Ovario/diagnóstico por imagen , Enfermedades del Ovario/tratamiento farmacológico , Enfermedades del Ovario/epidemiología , Ovario/diagnóstico por imagen , República de Corea/epidemiología , Estudios Retrospectivos , Riesgo , Prevención Secundaria , Ultrasonografía , Adulto Joven
2.
Oncotarget ; 8(6): 9144-9154, 2017 Feb 07.
Artículo en Inglés | MEDLINE | ID: mdl-27880720

RESUMEN

Reproductive history and exogenous hormonal exposures are acknowledged risk factors for breast cancer in the general population. In women at increased breast cancer risk for genetic predisposition or positive family history, data regarding these risk factors are limited or conflicting, and recommendations for these categories are unclear. We evaluated the characteristics of reproductive life in 2522 women at increased genetic or familial breast cancer risk attending our Family Cancer Center. Breast cancers in BRCA mutation carriers were more likely to be hormone receptor negative, diagnosed at 35 years or before and multiple during the lifetime than tumors in women at increased familial risk, while the distribution of invasive cancers and HER2 positive tumors was similar in the different risk groups. At least one full-term pregnancy (HR 0.27; 95% CI 0.12-0.58; p = 0.001), breastfeeding either less (HR 0.24; 95% CI 0.09-0.66; p = 0.005) or more (HR 0.25; 95% IC 0.08-0.82; p = 0.022) than one year and late age at menopause (HR 0.10; 95% CI 0.01-0.82; p = 0.033) showed to be protective factors in BRCA mutation carriers, while in women at increased familial risk early age at first full-term pregnancy (HR 0.62; 95% IC 0.38-0.99; p = 0.048) and late menarche (HR 0.61; 95% CI 0.42-0.85; p = 0.004) showed to be the main protective factors. Finally, for the entire population, combined hormonal contraceptives demonstrated to do not increase breast cancer risk. The results of our study suggest that women at high familial risk and mutation carries develop tumors with different clinical-pathological characteristics and, consequently, are influenced by different protective and risk factors.


Asunto(s)
Proteína BRCA1/genética , Proteína BRCA2/genética , Biomarcadores de Tumor/genética , Neoplasias de la Mama/genética , Fertilidad , Mutación , Salud Reproductiva , Adulto , Anciano , Lactancia Materna , Neoplasias de la Mama/terapia , Distribución de Chi-Cuadrado , Anticonceptivos Secuenciales Orales/efectos adversos , Femenino , Predisposición Genética a la Enfermedad , Herencia , Humanos , Italia , Menarquia , Menopausia , Persona de Mediana Edad , Paridad , Linaje , Fenotipo , Embarazo , Modelos de Riesgos Proporcionales , Factores de Riesgo , Factores de Tiempo
3.
Clin Exp Obstet Gynecol ; 43(3): 334-40, 2016.
Artículo en Inglés | MEDLINE | ID: mdl-27328486

RESUMEN

PURPOSE OF INVESTIGATION: To compare the effects of desogestrel (DSG) 150 mcg/ethinyl estradiol (EE) 20 mcg for 21 days followed by either seven days of EE ten mcg (21/7-active) or no treatment (DSG/EE+no Tx) on hemostatic markers. MATERIALS AND METHODS: This was a randomized, multicenter, open-label study that enrolled healthy premenopausal women. Non-inferiority of 21/7-active to DSG/EE+no Tx was determined if the upper limit of the two-sided 95% CI of the mean treatment difference in prothrombin fragment 1+2 (F1+2) over 24 weeks between groups was < 130 pmol/L. RESULTS: 246 subjects (n = 125, 21/7-active; n = 121, DSG/EE+no Tx) comprised the primary analysis. Mean F1+2 levels increased in both 21/7-active and DSG/EE+no Tx regimens (least square [LS] mean changes +45 pmol/L and +56.8 pmol/L, respectively). LS mean treatment difference was -11.8 pmol/L (95% CI: -54.8, 31.2). CONCLUSION: The effect of adding EE ten mcg to the seven-day hormone-free interval of DSG/EE on F1+2 levels was non-inferior to traditional DSG/EE.


Asunto(s)
Coagulación Sanguínea/efectos de los fármacos , Anticonceptivos Orales Combinados/farmacología , Anticonceptivos Secuenciales Orales/farmacología , Desogestrel/farmacología , Etinilestradiol/farmacología , Productos de Degradación de Fibrina-Fibrinógeno/efectos de los fármacos , Fragmentos de Péptidos/efectos de los fármacos , Proteína C/efectos de los fármacos , Proteína S/efectos de los fármacos , Protrombina/efectos de los fármacos , Adulto , Antitrombinas/sangre , Anticonceptivos Orales Combinados/administración & dosificación , Anticonceptivos Secuenciales Orales/administración & dosificación , Desogestrel/administración & dosificación , Etinilestradiol/administración & dosificación , Femenino , Productos de Degradación de Fibrina-Fibrinógeno/metabolismo , Humanos , Tiempo de Tromboplastina Parcial , Fragmentos de Péptidos/sangre , Proteína C/metabolismo , Proteína S/metabolismo , Adulto Joven
4.
Eur J Obstet Gynecol Reprod Biol ; 195: 40-51, 2015 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-26476798

RESUMEN

BACKGROUND: Hydrosalpinx is a rare cause of abdominal pain in paediatric patients, though cases are documented in the literature. Its aetiology differs considerably from traditional hydrosalpinx due to ascending sexually transmitted infection. Hydrosalpinx can present mimicking an acute abdomen or can be asymptomatic. Management of paediatric hydrosalpinx varies, but often involves surgical removal of the affected tube. METHODS: In June 2015, a literature search using relevant keywords was completed on MEDLINE and EMBASE databases to determine best management of paediatric hydrosalpinx. RESULTS: We found 66 cases from 38 articles. Surgical intervention took place in 74% of cases (n=49). The most common surgical intervention was salpingectomy. In 3% of cases (n=2), nonsurgical medical management with hormonal therapy was utilized, with post-operative improvement in symptomology. In 23% of cases (n=15), conservative management was utilized: 2 of these cases torted, 4 cases persisted and 9 cases resolved. CONCLUSION: Overall, the results of this review demonstrate that there are comparable outcomes between surgical, medical and conservative management. However, medical and conservative management was not often offered, and more research is needed on the subject.


Asunto(s)
Anticonceptivos Femeninos/uso terapéutico , Anticonceptivos Secuenciales Orales/uso terapéutico , Enfermedades de las Trompas Uterinas/terapia , Acetato de Medroxiprogesterona/uso terapéutico , Salpingectomía , Anomalía Torsional/terapia , Adolescente , Niño , Manejo de la Enfermedad , Enfermedades de las Trompas Uterinas/complicaciones , Femenino , Humanos , Guías de Práctica Clínica como Asunto , Salpingostomía , Anomalía Torsional/etiología
5.
Gynecol Endocrinol ; 31(4): 332-6, 2015 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-25558892

RESUMEN

OBJECTIVES: To evaluate different oral contraceptive pill (OCP) pretreatment associated differential in-vitro fertilization (IVF)/intracytoplasmic sperm injection (ICSI) outcomes of polycystic ovary syndrome (PCOS) patients and explore enhanced hormonal balance induced by the pretreatment. METHODS: This retrospective study included 500 PCOS women and 565 normal ovulating counterparts undergoing IVF/ICSI. The PCOS patients were divided into three groups based on the OCP pretreatment regimens: non-OCP (without OCP pretreatment), unsuccessive OCP (the period of successive pretreatment ≤2 months) and successive OCP (the period of successive pretreatment ≥3 months) groups. Comprehensive hormonal and ultra-sonographic assessments were performed before/after IVF pretreatment. Confounding factors affecting pregnancy outcomes were analyzed with logistic regression. RESULTS: PCOS patients with significant endocrine disorders had reduced implantation and pregnancy rates and increased miscarriage rate. Successive, not unsuccessive OCP pretreatment, significantly improved the implantation and pregnancy rates, and reduced the incidence of monotocous small-for-gestational age infants, which was accompanied by remarkably decreased hyperandrogenism and antral follicles. CONCLUSION: PCOS is an independent risk factor for poor IVF outcome. Successive, not unsuccessive, OCP cyclical pretreatment could improve pregnancy outcome of PCOS patients, associated with reduction of hyperandrogenism and antral follicle excess.


Asunto(s)
Anticonceptivos Secuenciales Orales/uso terapéutico , Fertilización In Vitro , Hiperandrogenismo/prevención & control , Infertilidad Femenina/terapia , Síndrome de Hiperestimulación Ovárica/prevención & control , Inducción de la Ovulación/efectos adversos , Síndrome del Ovario Poliquístico/tratamiento farmacológico , Adulto , China/epidemiología , Femenino , Retardo del Crecimiento Fetal/etiología , Retardo del Crecimiento Fetal/prevención & control , Hospitales Universitarios , Humanos , Hiperandrogenismo/etiología , Infertilidad Femenina/etiología , Servicio Ambulatorio en Hospital , Síndrome de Hiperestimulación Ovárica/etiología , Síndrome del Ovario Poliquístico/fisiopatología , Embarazo , Índice de Embarazo , Estudios Retrospectivos , Inyecciones de Esperma Intracitoplasmáticas , Estadística como Asunto , Adulto Joven
6.
Fertil Steril ; 100(5): 1337-42, 2013 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-23953327

RESUMEN

OBJECTIVE: To evaluate the efficacy of continuous oral contraceptive (OC) use versus the usual cyclic fashion in the recurrence of endometriosis-related symptoms after surgery. DESIGN: Prospective cohort trial involving patients in two tertiary care units. SETTING: Academic institution in collaboration with a private hospital. PATIENT(S): 356 patients underwent surgical treatment by laparoscopy for symptomatic endometriosis. INTERVENTION(S): After surgical treatment for endometriosis, patients offered 6-month course of cyclic OC (including a 7-day pill-free period) or continuous OC. MAIN OUTCOME MEASURE(S): Recurrence rate of endometriosis-related symptoms and endometriomas after fertility-sparing surgery. RESULT(S): Out of 356 patients, 167 were placed on the usual cyclic OC course and 85 on continuous OC for a minimum of 6 months. The continuous OC group experienced a statistically significant reduction in recurrence rates for endometrioma, dysmenorrhea, and non-menstrual pelvic pain as compared with the cyclic OC group. There was no reduction in the recurrence of dyspareunia between the two groups. CONCLUSION(S): After surgical treatment of endometriosis, the use of both cyclic and continuous OC improves pain symptoms when compared with preoperative scores. Continuous OC appears to be associated with a reduced recurrence rate for dysmenorrhea, non-menstrual pelvic pain, and endometrioma but not for dyspareunia as compared with cyclic OC.


Asunto(s)
Anticonceptivos Hormonales Orales/administración & dosificación , Anticonceptivos Secuenciales Orales/administración & dosificación , Endometriosis/cirugía , Preservación de la Fertilidad , Laparoscopía , Adulto , Distribución de Chi-Cuadrado , Esquema de Medicación , Dismenorrea/etiología , Dismenorrea/prevención & control , Endometriosis/complicaciones , Endometriosis/diagnóstico , Femenino , Preservación de la Fertilidad/efectos adversos , Grecia , Humanos , Estimación de Kaplan-Meier , Laparoscopía/efectos adversos , Dolor Postoperatorio/etiología , Dolor Postoperatorio/prevención & control , Dolor Pélvico/etiología , Dolor Pélvico/prevención & control , Cuidados Posoperatorios , Estudios Prospectivos , Recurrencia , Centros de Atención Terciaria , Factores de Tiempo , Resultado del Tratamiento
8.
Arch Gynecol Obstet ; 287(3): 447-53, 2013 Mar.
Artículo en Inglés | MEDLINE | ID: mdl-23053314

RESUMEN

PURPOSE: To evaluate the changes in the volume of rectovaginal endometriotic nodules infiltrating the rectum during 12-month treatment with hormonal therapies. MATERIALS AND METHODS: This prospective, non-randomized, self-controlled clinical trial included patients with rectovaginal endometriotic nodules infiltrating at least the muscularis propria of the rectum, who received one of the following therapies: norethisterone acetate, triptorelin and tibolone, norethisterone acetate and letrozole, desogestrel, sequential oral contraceptive pill. The volume of the nodules was determined by virtual organ computer-aided analysis (VOCAL, GE Healthcare, USA) at baseline and after 6 and 12 months of treatment. RESULTS: Eighty-three women (90.2 %) completed the 12-month treatment. When compared with baseline values, the volume of the nodules decreased at 6-month (p < 0.001) and 12-month treatment (p < 0.001). After 12-month treatment, the volume of the nodules decreased in all study groups. The volume of the nodules decreased during therapy in 68 women (73.9 %) and increased in 11 women (12.0 %). CONCLUSION: 12-month administration of hormonal therapies reduces the volume of rectovaginal endometriotic nodules infiltrating the rectum in the majority of cases.


Asunto(s)
Endometriosis/tratamiento farmacológico , Enfermedades del Recto/tratamiento farmacológico , Enfermedades Vaginales/tratamiento farmacológico , Adulto , Inhibidores de la Aromatasa/uso terapéutico , Calcio/uso terapéutico , Colecalciferol/uso terapéutico , Anticonceptivos Secuenciales Orales/uso terapéutico , Anticonceptivos Sintéticos Orales/uso terapéutico , Desogestrel/uso terapéutico , Endometriosis/diagnóstico por imagen , Moduladores de los Receptores de Estrógeno/uso terapéutico , Femenino , Humanos , Procesamiento de Imagen Asistido por Computador , Letrozol , Nitrilos/uso terapéutico , Noretindrona/análogos & derivados , Noretindrona/uso terapéutico , Acetato de Noretindrona , Norpregnenos/uso terapéutico , Estudios Prospectivos , Enfermedades del Recto/diagnóstico por imagen , Resultado del Tratamiento , Triazoles/uso terapéutico , Pamoato de Triptorelina/uso terapéutico , Ultrasonografía , Enfermedades Vaginales/diagnóstico por imagen , Vitaminas/uso terapéutico
9.
Contraception ; 86(6): 659-65, 2012 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-22770787

RESUMEN

BACKGROUND: We sought to estimate the prevalence of types of combined oral contraceptives (COCs) used among US women. STUDY DESIGN: We analyzed interview-collected data from 12,279 women aged 15-44 years participating in the National Survey of Family Growth, 2006-2010. Analyses focused on COC use overall, by pill type, across sociodemographics and health factors. RESULTS: The prevalence of current COC use (88 different brands) was 17%. The majority of COC users used earlier-formulation COCs: ≥30 mcg (67%) versus <30 mcg estrogen (33%), monophasic (67%) versus multiphasic (33%) dosages and traditional 21/7 (88%) versus extended/other cycle regimens (12%) regimens. Norgestimate (32%) and norethindrone (20%) were the most commonly used progestins. Sociodemographic, gynecological and health risk factors were associated with type of COC use. CONCLUSION: Further investigation of specific COC use and of the factors associated with types of pills used among US women at the population level is needed.


Asunto(s)
Conducta Anticonceptiva , Anticonceptivos Orales Combinados/administración & dosificación , Anticonceptivos Hormonales Orales/administración & dosificación , Congéneres del Estradiol/administración & dosificación , Congéneres de la Progesterona/administración & dosificación , Adolescente , Adulto , Anticonceptivos Secuenciales Orales/administración & dosificación , Anticonceptivos Sintéticos Orales/administración & dosificación , Estudios Transversales , Composición Familiar , Femenino , Encuestas Epidemiológicas , Humanos , Noretindrona/administración & dosificación , Norgestrel/administración & dosificación , Norgestrel/análogos & derivados , Estados Unidos , Adulto Joven
10.
Drug Ther Bull ; 48(9): 102-5, 2010 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-20810709

RESUMEN

Around 25% of women in the UK aged 16-49 years use oral contraception.1 Annually, around 5 million combined oral contraceptive (COC) items are prescribed in primary care in England alone, at a cost of over pound40 million. The effectiveness of such contraception depends on correct and consistent use of the pills and is influenced by unwanted effects that can lead to discontinuation (e.g. bleeding irregularities), and by adherence to specified procedures for when a pill is missed. Qlaira (Bayer plc) is the first licensed COC in the UK to include the oestrogen estradiol valerate (E2V, which is metabolised to oestradiol, a natural human hormone) and the progestogen dienogest (DNG). It has been marketed as "the first and only COC to deliver...the same oestrogen as produced by a woman's body". In theory, it might be less likely than other COCs to cause unwanted effects. However, it has a complex dosage regimen, and has its own missed-pill guidance which differs substantially from that for other pills.3 Here we review the effectiveness and place of Qlaira.


Asunto(s)
Anticonceptivos Secuenciales Orales/farmacología , Estradiol/análogos & derivados , Nandrolona/análogos & derivados , Adolescente , Adulto , Anticonceptivos Secuenciales Orales/efectos adversos , Costos de los Medicamentos , Interacciones Farmacológicas , Estradiol/efectos adversos , Estradiol/farmacología , Femenino , Humanos , Persona de Mediana Edad , Nandrolona/efectos adversos , Nandrolona/farmacología , Guías de Práctica Clínica como Asunto , Ensayos Clínicos Controlados Aleatorios como Asunto , Adulto Joven
11.
Prescrire Int ; 19(106): 65-7, 2010 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-20568487

RESUMEN

A monophasic combination of ethinylestradiol plus levonorgestrel or norethisterone is the oral contraceptive with which we have most experience. A quadriphasic combination of estradiol and dienogest was recently authorised in various European Union member states. The results of two non-comparative trials and one comparative trial versus ethinylestradiol + levonorgestrel suggest that the contraceptive efficacy of the estradiol + dienogest combination is no better than that of other oral contraceptives. In addition, there is no tangible difference in regulation of the menstrual cycle compared to the ethinylestradiol + levonorgestrel combination, as assessed by bleeding during and after dosing. The estradiol + dienogest combination has the same frequent and mild adverse effects as other combined contraceptives, such as nausea, breast tenderness and headache. In contrast, little is known of the potential cardiovascular adverse effects of the new combination, including the risk of thrombosis. Use of this quadriphasic combination is inconvenient. The monthly blister pack contains 5 different tablets, with different compositions, that must be taken in exactly the right order. In addition, a woman must follow complicated directions for catching up if she misses a pill, and they differ throughout the cycle. In practice, it is better to continue to use a well-documented combined contraceptive such as the monophasic ethinylestradiol + levonorgestrel combination.


Asunto(s)
Anticonceptivos Secuenciales Orales/farmacología , Estradiol/administración & dosificación , Nandrolona/análogos & derivados , Interacciones Farmacológicas , Estradiol/efectos adversos , Femenino , Humanos , Nandrolona/administración & dosificación , Nandrolona/efectos adversos
12.
Med Sci Sports Exerc ; 42(7): 1314-23, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20019632

RESUMEN

PURPOSE: To compare the effects of a high-CHO diet (80% CHO) and glucose ingestion (2 g x kg(-1)) during exercise (120 min, 57% VO2max) on fuel selection in women taking (W+OC) or not (W-OC) oral contraceptives and in men (six in each group). METHODS: Substrate oxidation was measured using indirect respiratory calorimetry in combination with a tracer technique to compute the oxidation of exogenous (13C-glucose) and endogenous CHO. RESULTS: In the control situation (mixed diet with water ingestion during exercise), the percent contribution to the energy yield (%En) of CHO oxidation was higher in men than in women (62 vs 53 %En). The high-CHO diet and glucose ingestion during exercise separately increased the %En from CHO oxidation in both men (+12%) and women (+24%), and the sex difference observed in the control situation disappeared. However, the increase in the %En from total CHO oxidation observed when glucose was ingested during exercise and when combined with a high-CHO diet was larger in women than in men (+47 vs +17 %En). This was not attributable to a higher %En from exogenous glucose oxidation in women, for which no sex difference was observed (25 and 27 %En in men and women), but was attributable to a smaller decrease in endogenous glucose oxidation. No significant difference in fuel selection was observed between W+OC and W-OC. CONCLUSIONS: The increase in total CHO oxidation after the high-CHO diet was not different between sexes. Glucose ingestion during exercise, separately and combined to the high-CHO diet, had a greater effect in women than in men; this was mostly attributable to the smaller reduction in endogenous CHO oxidation.


Asunto(s)
Metabolismo de los Hidratos de Carbono/fisiología , Ejercicio Físico/fisiología , Glucosa/metabolismo , Adulto , Calorimetría Indirecta , Anticonceptivos Secuenciales Orales , Femenino , Preferencias Alimentarias , Humanos , Masculino , Consumo de Oxígeno , Factores Sexuales , Adulto Joven
13.
Fertil Steril ; 93(1): 52-6, 2010 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18973896

RESUMEN

OBJECTIVE: To evaluate long-term cyclic and continuous administration of oral contraceptive pills (OCP) in preventing ovarian endometrioma recurrence after laparoscopic cystectomy. DESIGN: Prospective, randomized, controlled trial. SETTING: Tertiary care University Hospital. PATIENT(S): Two hundred thirty-nine women who underwent laparoscopic excision of ovarian endometriomas. INTERVENTION(S): Patients were divided randomly into three groups: nonusers receiving no therapy and cyclic and continuous users receiving low-dose, monophasic OCP for 24 months in cyclic or continuous administration, respectively. MAIN OUTCOME MEASURE(S): Endometrioma recurrence, size of recurrent endometrioma, and growth rate during at least 2 years follow-up evaluated by transvaginal ultrasonography. RESULT(S): The crude recurrence rate within 24 months was significantly lower in cyclic (14.7%) and continuous users (8.2%) compared with nonusers (29%). The recurrence-free survival was significantly lower in nonusers compared with cyclic and continuous users. The mean recurrent endometrioma diameter at first observation was significantly lower in cyclic (2.17 +/- 0.45 cm) and continuous users (1.71 +/- 0.19 cm) compared with nonusers (2.73 +/- 0.56 cm). The mean diameter increase every 6 months of follow-up was significantly reduced in cyclic users (0.31 +/- 0.18 cm) and continuous users (0.25 +/- 0.09 cm) versus nonusers (0.48 +/- 0.3 cm). No significant differences between cyclic users and continuous users in terms of endometrioma recurrence were demonstrated. CONCLUSION(S): Long-term cyclic and continuous postoperative use of OCP can effectively reduce and delay endometrioma recurrence.


Asunto(s)
Anticonceptivos Orales Combinados/administración & dosificación , Anticonceptivos Hormonales Orales/administración & dosificación , Anticonceptivos Secuenciales Orales/administración & dosificación , Endometriosis/tratamiento farmacológico , Etinilestradiol/administración & dosificación , Laparoscopía , Norpregnenos/administración & dosificación , Enfermedades del Ovario/tratamiento farmacológico , Adulto , Terapia Combinada , Supervivencia sin Enfermedad , Esquema de Medicación , Endometriosis/diagnóstico por imagen , Endometriosis/cirugía , Femenino , Humanos , Estimación de Kaplan-Meier , Enfermedades del Ovario/diagnóstico por imagen , Enfermedades del Ovario/cirugía , Estudios Prospectivos , Prevención Secundaria , Índice de Severidad de la Enfermedad , Factores de Tiempo , Resultado del Tratamiento , Ultrasonografía
14.
Acta Pharm Hung ; 79(2): 88-91, 2009.
Artículo en Húngaro | MEDLINE | ID: mdl-19634640

RESUMEN

Application of counterfeit medicines is extremely dangerous, because neither their quality, nor their efficacy and the circumstances of their preparation are known. The most effective and well-known fight against counterfeit medicines is the assurance of closed medicine supply chain. In the present study beside the review of the anti-counterfeiting technologies, combined oral contraceptives purchased out of pharmacy were examined from the point of counterfeiting. Based on the results of the study it could be concluded that the medicines contained the correct ingredients, but the examined products were not marketing authorized in Hungary.


Asunto(s)
Anticonceptivos Secuenciales Orales/normas , Fraude , Preparaciones Farmacéuticas/normas , Farmacias/normas , Anticonceptivos Secuenciales Orales/química , Hungría , Legislación de Medicamentos , Espectroscopía Infrarroja por Transformada de Fourier
15.
Contraception ; 78(2): 113-9, 2008 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-18672111

RESUMEN

BACKGROUND: The study was conducted to evaluate the efficacy and safety for the prevention of pregnancy of a 28-day oral contraceptive (OC) containing 150 mcg desogestrel (DSG)/20 mcg ethinyl estradiol (EE) for 21 days followed by 7 days of 10 mcg EE (Cette-28). STUDY DESIGN: A 6-month, prospective, multicenter, single-arm study was conducted in 1302 women aged 18-45 years. RESULTS: Over six cycles of treatment, the cumulative risk of pregnancy among all treated subjects (n=1262) was 0.9%. The Pearl Index for women 18-35 years of age (n=1042) was 2.20, including 9 pregnancies with estimated conception dates during active drug ingestion or up to 7 days after the last combination tablet. The rate of unscheduled bleeding was low and the duration of scheduled bleeding was approximately 2 days during each of the six treatment cycles. The safety profile was similar to what has been reported for other OCs. CONCLUSION: This low-dose, 28-day OC incorporating 7 days of 10 mcg EE during the hormone free interval is effective and safe for the prevention of pregnancy and is well-tolerated by women.


Asunto(s)
Anticonceptivos Secuenciales Orales/administración & dosificación , Desogestrel/administración & dosificación , Etinilestradiol/administración & dosificación , Adulto , Anticonceptivos Secuenciales Orales/efectos adversos , Desogestrel/efectos adversos , Esquema de Medicación , Etinilestradiol/efectos adversos , Femenino , Humanos , Metrorragia/etiología , Embarazo , Resultado del Tratamiento
16.
Contraception ; 77(1): 34-9, 2008 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-18082664

RESUMEN

BACKGROUND: The study was conducted to evaluate the effects of low-dose estrogen compared to placebo on ovarian activity during the traditional 7-day hormone-free interval (HFI) of an oral contraceptive (OC). STUDY DESIGN: Women were randomized to placebo or low-dose estrogen for 7 days during the HFI. Serum levels of estradiol, follicle-stimulating hormone (FSH), luteinizing hormone and inhibin B were obtained before, during and after treatment. RESULTS: Mean hormone levels remained constant or only increased slightly for the low-dose estrogen group compared to greater more sustained increases observed for the placebo group. Estradiol, FSH and inhibin B levels were substantially higher for those on placebo. Differences were most noticeable by the end of the HFI and persisted into the subsequent cycle. CONCLUSION: Subjects receiving low-dose estrogen for 7 days during the HFI demonstrated more pronounced ovarian suppression compared to placebo as evidenced by attenuation of increases in serum inhibin B, FSH and estradiol levels.


Asunto(s)
Anticonceptivos Hormonales Orales/administración & dosificación , Anticonceptivos Secuenciales Orales/farmacología , Ovario/efectos de los fármacos , Adolescente , Adulto , Estradiol/sangre , Femenino , Hormona Folículo Estimulante/sangre , Humanos , Inhibinas/sangre , Inhibinas/efectos de los fármacos , Placebos/administración & dosificación , Estudios Prospectivos
17.
Med Arh ; 62(5-6): 289-93, 2008.
Artículo en Bosnio | MEDLINE | ID: mdl-19469273

RESUMEN

This study follows 94 patients, age 45 to 60, by controlled, random and prospective studies in time period of six months. Out of total number of patients, 53 were divided into research group and treated with hormonal therapy (2 mg of estradiol and 0,5 mg of norgestrel), 41 patients were divided into control group and treated with refemin (Cimicifuga recemosa). Results were statistically processed using Student test and ANOVA, giving us following results: use of HNL resulted with statistically significant changes--increase of heart frequency (*p<0,01), QTc-intervals (**p=0,01), increase of systolic pressure (**p=0,01), increase of diastolic pressure (**p=0,01), increase of body mass index (**p=0,01), endometrial thickness decrease (**p=0,01); use of Cimicifuge recemose resulted with statistically significant changes--increase of diastolic pressure(*p=0,01), increase of body mass index (BMI) (*p=0,01) and endometrial thickness decrease (*p=0,05). By testing research and controlled group with ANOVA test, we have determined that there is statistical difference in operating between recovered hormone therapy and Cimicifuge recemose within parameters of hearth frequency and diastolic pressure.


Asunto(s)
Anticonceptivos Hormonales Orales/administración & dosificación , Anticonceptivos Secuenciales Orales/administración & dosificación , Terapia de Reemplazo de Estrógeno , Combinación Etinil Estradiol-Norgestrel/administración & dosificación , Hemodinámica , Lípidos/sangre , Menopausia/fisiología , Adulto , Cimicifuga , Femenino , Humanos , Persona de Mediana Edad , Fitoterapia , Preparaciones de Plantas/uso terapéutico
18.
Ginecol Obstet Mex ; 75(1): 35-42, 2007 Jan.
Artículo en Español | MEDLINE | ID: mdl-17542267

RESUMEN

This review provides an update regarding newer options in hormonal contraception that include the progestin-releasing intrauterine system, the contraceptive patch and ring, the single rod progestin-releasing implant, extended and emergency oral contraception and recent advances in hormonal male contraception. These methods represent a major advancement in this field, allowing for the development of more acceptable, safety and effective birth control regimens.


Asunto(s)
Anticoncepción/tendencias , Administración Cutánea , Anticoncepción/métodos , Anticoncepción Postcoital/métodos , Dispositivos Anticonceptivos Femeninos , Anticonceptivos Hormonales Orales/administración & dosificación , Anticonceptivos Secuenciales Orales/administración & dosificación , Depresión Química , Implantes de Medicamentos , Estrógenos/administración & dosificación , Femenino , Antagonistas de Hormonas/administración & dosificación , Humanos , Dispositivos Intrauterinos Medicados , Masculino , Progestinas/administración & dosificación , Espermatogénesis/efectos de los fármacos
19.
Arch. med ; (14): 42-50, jun. 2007. ilus, tab
Artículo en Español | LILACS | ID: lil-467947

RESUMEN

El uso de anticonceptivos orales sin importar la generación no se ha correlacionado claramente como único factor para la producción de enfermedades del sistema circulatorio; cuando hay efectos adversos se encuentra relacionado con mayor edad, antecedente cardiovascular, diabetes mellitus, y cigarrillo.Al realizar la investigación no se encontró relación, con el uso prolongado de anticonceptivos orales y enfermedad coronaria, aunque se recomienda efectuarotros estudios


Asunto(s)
Anticonceptivos Orales , Anticonceptivos Orales Combinados , Anticonceptivos Hormonales Orales , Anticonceptivos Secuenciales Orales , Enfermedad Coronaria
20.
Contraception ; 72(2): 105-10, 2005 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-16022848

RESUMEN

OBJECTIVE: The objective of this study was to describe the characteristics of and outcomes and side effects in patients using triphasic oral contraceptives (OCs) in a continuous use regimen. METHODS: A retrospective review of patient charts from four community-based physician practices was conducted. All patients had been using triphasic OCs in a continuous regimen (i.e., to prevent withdrawal bleeding) for a planned duration of at least three 28-day cycles. Data collected through retrospective chart abstraction included demographic and clinical indicators, duration of and reason for continuous triphasic OC use, prior OC history and side effect incidence and treatment. RESULTS: Forty-three patients meeting the inclusion criteria had data of sufficient quality to be included in all analyses. These patients represented 603 total cycles. Nearly half of the patients (49%) indicated that their primary reason for continuous OC use was personal preference rather than medical reasons. More than half of the patients (56%) had previously used triphasic OCs in a noncontinuous regimen; 24% had no prior OC experience. The median duration of continuous use was 237 days (including right-censored patients; range, 55-994). Of the 39% of patients who terminated continuous use, the most common reason given was the desire to become pregnant (35%). Sixty-one percent of the patients reported no side effects from continuous use. The most common side effect occurring beyond Day 21 of continuous use was breakthrough bleeding (reported in four patients). Survival analysis indicated that time on continuous triphasic use was positively related to parity >0 (p<.05) and the absence of side effects (p<.1). CONCLUSION: The data suggest that successful continuous use is feasible with triphasic OCs, with few adverse side effects.


Asunto(s)
Anticoncepción , Anticonceptivos Orales Combinados/administración & dosificación , Anticonceptivos Secuenciales Orales/administración & dosificación , Anticonceptivos Sintéticos Orales/administración & dosificación , Ciclo Menstrual/efectos de los fármacos , Adolescente , Adulto , Índice de Masa Corporal , Anticonceptivos Orales Combinados/efectos adversos , Anticonceptivos Secuenciales Orales/efectos adversos , Anticonceptivos Sintéticos Orales/efectos adversos , Esquema de Medicación , Femenino , Humanos , Persona de Mediana Edad , Aceptación de la Atención de Salud , Estudios Retrospectivos , Fumar , Síndrome de Abstinencia a Sustancias
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