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1.
Aust N Z J Obstet Gynaecol ; 50(6): 562-7, 2010 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-21133868

RESUMEN

BACKGROUND: Miscarriage is common and may result in significant psychological morbidity for women. Recent research has revealed that health care professionals often tend to neglect this factor. This negligence may lead to delayed diagnosis and appropriate care. AIMS: To assess health care professionals' and patients' attitudes towards the psychological impact of miscarriage. METHODS: A prospective, cross-sectional survey of nearly 3000 subjects was conducted. Of these, 1269 were health care professionals and 1519 were pregnant women or their spouses. Their perceptions of the psychological impact of miscarriage, in comparison with postnatal depression were studied. RESULTS Health care professionals were less aware of the psychological impact of miscarriage compared with postnatal depression (91.9 vs 98.4%, P = 0.02). Furthermore, they believed that the psychological impact of miscarriage was less than that of postnatal depression (79.9 vs 88.9%, P < 0.001). However, more patients believed that psychological impact after miscarriage can seriously affect women (59.0 vs for health care professionals 38.3%, P < 0.001). A higher proportion of patients compared with health care professionals (85.2 vs 74.3%, P < 0.001) believed that routine psychological support should be provided after miscarriage, but few agreed that primary health professionals were the most suitable people to provide this care although most health care professionals thought this to be appropriate (9.1 vs 59.7%, P < 0.001). CONCLUSION: Health care professionals should be more aware of the psychological morbidity associated with miscarriage and also be sensitive to a currently unmet need for psychological care.


Asunto(s)
Aborto Espontáneo/psicología , Personal de Salud/psicología , Pacientes/psicología , Relaciones Médico-Paciente , Aborto Espontáneo/epidemiología , Estudios Transversales , Femenino , Humanos , Percepción , Embarazo , Estudios Prospectivos , Índice de Severidad de la Enfermedad , Esposos/psicología
2.
Menopause ; 11(4): 416-22, 2004.
Artículo en Inglés | MEDLINE | ID: mdl-15243279

RESUMEN

OBJECTIVE: To investigate the effects of 6-month treatment of tibolone on menopause symptoms, psychological well-being, and the dyadic relationship of postmenopausal Chinese women and their spouses. DESIGN: A randomized, double-blind, crossover study was conducted in 100 postmenopausal Hong Kong Chinese women who received tibolone (2.5mg/day) and placebo. At baseline, 6-month and 13-month visits, the women filled in the Greene Climacteric Scale (GCS), 12-item General Health Questionnaire (GHQ) and Dyadic Adjustment Scale (DAS), and their spouses completed GHQ and DAS. RESULTS: Both tibolone and placebo treatment were associated with a significant reduction in the GCS total scores after the first 6-month interventional period (95% CI: -8.0 to -2.5 for tibolone, and -5.7 to -0.7 for placebo). After the correction for placebo response, tibolone treatment was associated with a significant reduction in the GCS somatic subscore (-1.1 +/- 0.4 for tibolone group versus 0.6 +/- 0.5 for placebo group, P < 0.05). There were no significant changes in the GHQ and DAS total scores of the women and their spouses after tibolone treatment, both with and without the correction for placebo response. CONCLUSIONS: Tibolone treatment had a significant beneficial effect on the somatic menopause symptoms but had no effect on the psychological well-being or marital relationship of the postmenopausal Chinese women and their spouses.


Asunto(s)
Moduladores de los Receptores de Estrógeno/uso terapéutico , Relaciones Interpersonales , Norpregnenos/uso terapéutico , Posmenopausia/efectos de los fármacos , China , Estudios Cruzados , Método Doble Ciego , Emociones/efectos de los fármacos , Femenino , Indicadores de Salud , Humanos , Masculino , Persona de Mediana Edad , Posmenopausia/fisiología , Conducta Sexual/efectos de los fármacos , Esposos , Negativa del Paciente al Tratamiento
3.
Hum Reprod ; 22(12): 3116-23, 2007 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-17947376

RESUMEN

BACKGROUND: The aim of this study was to quantify the three-dimensional (3D) ultrasound characteristics of ovaries in Caucasian women with polycystic ovarian syndrome (PCOS) and to examine if these values differed between different phenotypic forms. METHODS: 3D pelvic ultrasound was performed in 40 women with PCOS and in 40 controls. Total ovarian volume, stromal volume and echogenicity and antral follicle count (AFC) were measured and ovarian blood flow was quantified using both 3D power Doppler and two-dimensional pulsed-wave Doppler. RESULTS: Women with PCOS had a higher AFC (median 16.3 versus 5.5 per ovary, P < 0.001) and ovarian volume (12.56 versus 5.66 ml, P < 0.001). Stromal volume (10.79 versus 4.69 ml, P < 0.001) and stromal vascularization (VI: 3.85 versus 2.79%, P < 0.001; VFI: 1.27 versus 0.85, P < 0.001) were also increased in women with PCOS. There were no significant differences in stromal echogenicity or pulsed-wave Doppler indices between women with PCOS and the controls. Among the women with PCOS, ovarian vascularity was significantly higher in 30 women who were hirsute compared with normoandrogenic women (FI: 33.94 versus 29.30, P < 0.05) and in 14 women with PCOS who were of normal weight compared with obese women (VI: 4.51 versus 3.25%, P < 0.05; VFI: 1.56 versus 1.22, P < 0.05). CONCLUSIONS: Based on 3D ultrasound, women with PCOS have an increased stromal volume and vascularity. Stromal vascularity is significantly higher in women with PCOS who are hirsute and of normal weight.


Asunto(s)
Infertilidad Femenina/diagnóstico por imagen , Ovario/diagnóstico por imagen , Síndrome del Ovario Poliquístico/diagnóstico por imagen , Ultrasonografía Doppler/métodos , Adulto , Peso Corporal , Femenino , Humanos , Imagenología Tridimensional , Variaciones Dependientes del Observador , Ovario/irrigación sanguínea , Fenotipo , Estudios Prospectivos , Ultrasonografía Doppler/estadística & datos numéricos
4.
Gynecol Endocrinol ; 21(5): 248-56, 2005 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-16373243

RESUMEN

Recently, two large randomized placebo-controlled studies on long-term postmenopausal hormone replacement therapy, the Heart and Estrogen/progestin Replacement Study (HERS) and the Women's Health Initiative (WHI), have raise a lot of controversies, especially on the cardiovascular aspects. We briefly review these two trials and discuss what we know and do not know about postmenopausal hormone therapy, including the evidence on novel choices such as raloxifene and tibolone.


Asunto(s)
Terapia de Reemplazo de Estrógeno/efectos adversos , Terapia de Reemplazo de Estrógeno/tendencias , Posmenopausia , Anciano , Neoplasias de la Mama/epidemiología , Neoplasias del Colon/epidemiología , Enfermedad Coronaria/epidemiología , Enfermedad Coronaria/etiología , Enfermedad Coronaria/prevención & control , Demencia/prevención & control , Neoplasias Endometriales/epidemiología , Femenino , Fracturas de Cadera/epidemiología , Fracturas de Cadera/prevención & control , Humanos , Persona de Mediana Edad , Neoplasias/epidemiología , Placebos , Progestinas/administración & dosificación , Ensayos Clínicos Controlados Aleatorios como Asunto , Factores de Riesgo , Accidente Cerebrovascular/epidemiología , Trombosis de la Vena/epidemiología , Salud de la Mujer
5.
Acta Obstet Gynecol Scand ; 82(7): 589-96, 2003 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-12790838

RESUMEN

The benefits of a single course of antenatal corticosteroids on neonatal outcomes are well established. There is, however, much controversy about how long this treatment should continue, and whether repeated courses should be administered if the women remain at risk for preterm delivery 7 days after the initial therapy. This review aims to discuss current evidence on the effectiveness and safety of repeated courses of antenatal corticosteroids.


Asunto(s)
Glucocorticoides/administración & dosificación , Trabajo de Parto Prematuro , Atención Prenatal , Betametasona/administración & dosificación , Betametasona/efectos adversos , Dexametasona/administración & dosificación , Dexametasona/efectos adversos , Esquema de Medicación , Femenino , Glucocorticoides/efectos adversos , Humanos , Recién Nacido , Recien Nacido Prematuro , Enfermedades del Prematuro/prevención & control , Pulmón/efectos de los fármacos , Pulmón/embriología , Embarazo , Estudios Prospectivos , Ensayos Clínicos Controlados Aleatorios como Asunto , Estudios Retrospectivos
6.
Urology ; 59(1): 73-8, 2002 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-11796285

RESUMEN

OBJECTIVES: To determine the value of the before and after treatment level of prostate-specific antigen (PSA) to predict the time to androgen-independent progression (AIP) in patients with advanced prostate cancer who received androgen-deprivation therapy (ADT) at the time of recurrence or progression. METHODS: The records of 153 patients with advanced or metastatic prostate cancer who were treated with ADT were retrospectively reviewed. Fifty-six percent of the patients were initially treated with ADT. In the remainder, ADT was started at progression and/or failure. AIP was defined as two consecutive elevations of serum PSA above the nadir value by any threshold. Kaplan-Meier and multiple logistic regression analyses were used to determine the potential predictors of AIP. RESULTS: The median duration of the PSA response was 24 months. The most important predictors of the time to AIP were the initial Gleason grade and the nadir PSA level after the initiation of ADT. The odds ratio of having a response greater than 24 months was 15-times higher in patients achieving an undetectable serum PSA level versus those who did not. For each point increase in the Gleason sum, patients had a five times higher chance of progressing to AIP in 24 months or less. CONCLUSIONS: The ability to achieve an undetectable nadir PSA level and the initial Gleason grade are significant predictors of the time to AIP in men treated with ADT for metastatic and advanced prostate cancer.


Asunto(s)
Antígeno Prostático Específico/sangre , Neoplasias de la Próstata/sangre , Anciano , Antagonistas de Andrógenos/uso terapéutico , Progresión de la Enfermedad , Hormona Liberadora de Gonadotropina/análogos & derivados , Humanos , Masculino , Oportunidad Relativa , Orquiectomía , Neoplasias de la Próstata/patología , Neoplasias de la Próstata/terapia , Estudios Retrospectivos , Factores de Tiempo
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