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1.
Arch Gynecol Obstet ; 309(4): 1467-1473, 2024 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-38353721

RESUMEN

INTRODUCTION: Pelvic floor disorders (PFD) occur in about 40% of women after delivery. Less is known about the intervention and care needs of women with postpartum PFD. The aim of this analysis was to analyze care needs and self-initiated measures to strengthen the pelvic floor in postpartum women in relation to incontinence and sexual dysfunction. Furthermore, influencing factors for self-initiated measures were evaluated. PATIENTS AND METHODS: An anonymous online survey (via LimeSurvey) was conducted between September and October 2022 and distributed via social media (Instagram and Facebook). The survey explicitly addressed mothers with and without pelvic floor disorders up to 5 years postpartum (inclusion criteria). Validated instruments were employed to assess incontinence (ICIQ-SF) and sexual functioning (PISQ-IR: Condition Impact). The questions on the use of services and preventive measures, as well as on the interaction with a gynecologist, were based on self-developed items. RESULTS: In total, 49.4% of the participants of the survey showed symptoms of urinary incontinence (UI). Furthermore, only 40.3% (n = 241) of women were actively asked by their gynecologists for the occurrence of UI or PFD among those who suffered from PFD. Overall, 79.3% of the participants of the survey with UI underwent measures to deal with the complaints. The ICIQ-SF Score was significantly associated with all self-induced measures. High School diplomas and academic degrees were associated with the use of love balls (p < 0.05). CONCLUSION: The results of the study show the unmet needs of postpartum women. PFD should be addressed more frequently in the outpatient setting. Furthermore, more systematic information about the treatment of PFD could help to address unmet information needs and improve interventions.


Asunto(s)
Trastornos del Suelo Pélvico , Prolapso de Órgano Pélvico , Disfunciones Sexuales Fisiológicas , Medios de Comunicación Sociales , Incontinencia Urinaria , Femenino , Humanos , Trastornos del Suelo Pélvico/complicaciones , Incontinencia Urinaria/epidemiología , Periodo Posparto , Disfunciones Sexuales Fisiológicas/epidemiología , Encuestas y Cuestionarios
2.
Oncol Rep ; 39(1): 160-172, 2018 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-29192327

RESUMEN

Retinoblastoma (RB) is the most common malignant intraocular tumor in early childhood. Imminent chemotherapy resistance diminishes the clinical-therapeutic options and emphasizes the necessity for new therapeutic approaches. The present study aimed at characterizing and comparing etoposide and cisplatin-resistant human RB cell lines with regard to changes in proliferation and apoptosis levels, anchorage independent growth behavior in vitro as well as tumor formation capacity in vivo. The proliferation rates were significantly increased in the etoposide-resistant RB cell lines Y-79, WERI-Rb1 and RB-355 reflecting significantly higher growth kinetics compared to the parental controls. In line with these findings in in vivo chicken chorioallantoic (CAM) assays, etoposide-resistant cell lines generated significantly increased numbers of tumors with higher tumor weights compared to their parental counterparts. In contrast to etoposide, the cisplatin-resistant RB cell lines Y-79, WERI-Rb1 and RB-355 displayed significantly increased apoptosis rates and reduced proliferation rates resulting in significantly decreased growth kinetics. Tumor formation capacity of cisplatin-resistant cell lines did not significantly change, and in comparison with parental controls cisplatin-resistant Y-79 cells displayed significantly reduced tumor weight. Soft agarose assays indicated that anchorage-independent growth of all chemotherapy-resistant cell lines analyzed was significantly decreased. Summarizing, one can state that etoposide-resistant RB cells behave more aggressively than the tumor cells of origin and potentially represent a risk factor for local relapse, while cisplatin-resistant cells show a significantly decreased tumorigenic potential.


Asunto(s)
Cisplatino/farmacología , Resistencia a Antineoplásicos , Etopósido/farmacología , Neoplasias de la Retina/patología , Retinoblastoma/patología , Animales , Apoptosis , Línea Celular Tumoral , Proliferación Celular , Supervivencia Celular , Pollos , Membrana Corioalantoides/efectos de los fármacos , Membrana Corioalantoides/patología , Humanos , Trasplante de Neoplasias , Neoplasias de la Retina/tratamiento farmacológico , Retinoblastoma/tratamiento farmacológico
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