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1.
BMC Microbiol ; 24(1): 112, 2024 Apr 04.
Artículo en Inglés | MEDLINE | ID: mdl-38575862

RESUMEN

BACKGROUND: Postpartum women often experience stress urinary incontinence (SUI) and vaginal microbial dysbiosis, which seriously affect women's physical and mental health. Understanding the relationship between SUI and vaginal microbiota composition may help to prevent vaginal diseases, but research on the potential association between these conditions is limited. RESULTS: This study employed 16S rRNA gene sequencing to explore the association between SUI and vaginal dysbiosis. In terms of the vaginal microbiota, both species richness and evenness were significantly higher in the SUI group. Additionally, the results of NMDS and species composition indicated that there were differences in the composition of the vaginal microbiota between the two groups. Specifically, compared to postpartum women without SUI (Non-SUI), the relative abundance of bacteria associated with bacterial dysbiosis, such as Streptococcus, Prevotella, Dialister, and Veillonella, showed an increase, while the relative abundance of Lactobacillus decreased in SUI patients. Furthermore, the vaginal microbial co-occurrence network of SUI patients displayed higher connectivity, complexity, and clustering. CONCLUSION: The study highlights the role of Lactobacillus in maintaining vaginal microbial homeostasis. It found a correlation between SUI and vaginal microbiota, indicating an increased risk of vaginal dysbiosis. The findings could enhance our understanding of the relationship between SUI and vaginal dysbiosis in postpartum women, providing valuable insights for preventing bacterial vaginal diseases and improving women's health.


Asunto(s)
Microbiota , Incontinencia Urinaria de Esfuerzo , Enfermedades Vaginales , Femenino , Humanos , Incontinencia Urinaria de Esfuerzo/etiología , Disbiosis/microbiología , ARN Ribosómico 16S/genética , Vagina/microbiología , Microbiota/genética , Lactobacillus/genética , Bacterias/genética , Enfermedades Vaginales/complicaciones
2.
BMC Infect Dis ; 23(1): 836, 2023 Nov 27.
Artículo en Inglés | MEDLINE | ID: mdl-38012631

RESUMEN

BACKGROUND: The purpose of this study was to evaluate the vaginal microecology and the distribution of human papillomavirus (HPV) subtypes in patients with uterine adhesions and explore the correlation between HPV infection and vaginal microecology imbalance and the occurrence of intrauterine adhesion (IUA). METHODS: A total of 479 women were enrolled in the study, including 259 in the normal group and 220 in the IUA group. Vaginal microecological and HPV analyses were performed on all participants. Significant differences between the two groups were analyzed, and Spearman correlation analysis was performed. RESULTS: The incidence of IUA in patients between 31 and 40 years of age was high. The I-II degree of vaginal cleanliness in the IUA group was significantly lower than that in the normal group, and the number of III-IV degree was significantly higher than that in the normal group. Moreover, the incidences of VVC (vulvovaginal candidiasis) and vaginal disorders and infections with HPV 16 and HPV 52 subtypes were significantly higher in the IUA group than in the normal group. The incidence of high-risk HPV infection combined with vaginal disorders in the IUA group was higher than that in the normal group. Correlation analysis showed that the occurrence of IUAs was positively correlated with HPV infection and negatively correlated with PH and vaginal microecological imbalance. CONCLUSION: The HPV infection rate and vaginal microecology disorders affect the occurrence of IUAs. For patients with IUAs, control of the HPV infection rate and the prevention of vaginal microecological disorders should be improved.


Asunto(s)
Infecciones por Papillomavirus , Adherencias Tisulares , Enfermedades Uterinas , Enfermedades Vaginales , Femenino , Humanos , Estudios Transversales , Pueblos del Este de Asia , Infecciones por Papillomavirus/complicaciones , Infecciones por Papillomavirus/epidemiología , Infecciones por Papillomavirus/virología , Enfermedades Uterinas/epidemiología , Enfermedades Uterinas/etiología , Vagina/microbiología , Enfermedades Vaginales/complicaciones , Enfermedades Vaginales/epidemiología , Enfermedades Vaginales/microbiología , Adherencias Tisulares/epidemiología , Adherencias Tisulares/etiología , Adherencias Tisulares/microbiología , Adherencias Tisulares/virología , China
3.
Obstet Gynecol ; 141(6): 1219-1223, 2023 06 01.
Artículo en Inglés | MEDLINE | ID: mdl-37141593

RESUMEN

BACKGROUND: Batteries are known to cause damage to mucosal surfaces. Unfortunately, the timing of serious sequelae and recommendations for removal of a vaginally inserted battery in a premenopausal patient are not well characterized. This case report aims to detail the timeline of events and complications after vaginal insertion of a 9-volt alkaline battery and to further clarify the recommendation for urgent removal. CASE: A 24-year-old nulliparous woman with significant psychiatric and trauma history was admitted for ingestion and insertion of multiple foreign objects, including a 9-volt battery that she inserted into her vagina during her hospital admission. Examination under anesthesia was required for removal of the battery, with cervical and vaginal necrosis and partial-thickness burns noted. Removal occurred approximately 5.5 hours after insertion. Management included vaginal irrigation and topical estrogen. CONCLUSION: Given our findings of rapid and severe damage to the vaginal mucosa, urgent removal of a vaginally inserted battery is indicated.


Asunto(s)
Cuerpos Extraños , Enfermedades Vaginales , Humanos , Femenino , Adulto Joven , Adulto , Corrosión , Vagina/cirugía , Vagina/lesiones , Enfermedades Vaginales/complicaciones , Cuerpos Extraños/complicaciones , Cuerpos Extraños/cirugía , Suministros de Energía Eléctrica
4.
Menopause ; 30(2): 174-178, 2023 02 01.
Artículo en Inglés | MEDLINE | ID: mdl-36696641

RESUMEN

OBJECTIVE: This prospective pilot study aimed to evaluate the effects of a modified vaginal erbium laser (VEL) protocol, using the hyperstack mode on the vaginal vestibulum and introitus to treat superficial dyspareunia in postmenopausal breast cancer survivors suffering from the genitourinary syndrome of menopause. METHODS: In this pilot, prospective, randomized study, two groups of postmenopausal women suffering from superficial dyspareunia were included: 34 women (VEL group) were treated with erbium laser crystal yttrium-aluminum-garnet (XS Fotona SMOOTH; Fotona, Ljubljana, Slovenia) with a wavelength of 2,940 nm; for the other 34 (hyperstack group), a modified second step of the VEL protocol for the treatment of vestibulum and introitus was used, with hyperstacked (repeating a number of) subablative, long pulses with very low fluences. For each group, three laser applications at 30-day intervals were performed. Symptoms were assessed before, after each application, and after 1 and 3 months from the last laser application, using the visual analog scale score for superficial dyspareunia. RESULTS: Superficial dyspareunia improved in both groups over time (P < 0.001), regardless of age and years since menopause status. The reduction in visual analog scale score after the third laser application was 58% in VEL versus 73.5% in hyperstack. The hyperstack group, since the first laser application, showed a greater (P < 0.001) and persistent improvement of superficial dyspareunia. CONCLUSIONS: The hyperstack treatment of the introitus and vestibulum in breast cancer survivors leads to a more significant improvement in superficial dyspareunia than the VEL alone.


Asunto(s)
Neoplasias de la Mama , Supervivientes de Cáncer , Dispareunia , Láseres de Estado Sólido , Enfermedades Vaginales , Femenino , Humanos , Dispareunia/etiología , Dispareunia/terapia , Enfermedades Vaginales/complicaciones , Enfermedades Vaginales/cirugía , Erbio , Proyectos Piloto , Neoplasias de la Mama/complicaciones , Estudios Prospectivos , Resultado del Tratamiento , Láseres de Estado Sólido/uso terapéutico
5.
Int Urogynecol J ; 33(7): 1833-1838, 2022 07.
Artículo en Inglés | MEDLINE | ID: mdl-33991221

RESUMEN

INTRODUCTION AND HYPOTHESIS: Evidence and recommendations for the use of intravaginal estrogen for prevention of bacterial vaginosis and pessary-related complications are limited and controversial. We hypothesized that adding intravaginal estrogen to pessary use would decrease the incidence of bacterial vaginosis and other pessary-related complications. METHODS: A single-center, open-label, randomized, parallel study was conducted between April 2018 and August 2020. Participants were randomized to either receive intravaginal estriol 0.03 mg plus Lactobacillus acidophilus 100 million viable cell vaginal tablets or have no treatment. The Amsel criteria, normal flora index, visual analog scale, Thai version of the ICIQ-VS (International Consultation on Incontinence Questionnaire-Vaginal symptoms) questionnaire, vaginal abrasions and vaginal bleeding were evaluated at entry and at 2- and 14-week follow-up. RESULTS: Seventy-eight women were included and randomized to two groups (39 women per group). At 2-week follow-up, one participant in the intervention group and two participants in the control group were diagnosed with bacterial vaginosis (2.7% vs. 5.7%, p = 0.609). At 14-week follow-up, two participants in the intervention group and two participants in the control group were diagnosed with bacterial vaginosis (5.7% vs. 6.2%, p = 0.926). Normal flora index was significantly different at 2-week follow-up [8 (6.3) vs. 5 (6.0), p = 0.032]. There was no significant difference in the visual analog scale, Thai version of the ICIQ-VS, vaginal abrasions and vaginal bleeding between the 2- and 14-week follow-ups. CONCLUSIONS: This study shows no benefit of intravaginal estrogen in reducing bacterial vaginosis, vaginal abrasions, vaginal bleeding and pain in postmenopausal women using a vaginal pessary for pelvic organ prolapse treatment.


Asunto(s)
Prolapso de Órgano Pélvico , Enfermedades Vaginales , Vaginosis Bacteriana , Estrógenos , Femenino , Humanos , Prolapso de Órgano Pélvico/complicaciones , Prolapso de Órgano Pélvico/terapia , Pesarios/efectos adversos , Posmenopausia , Hemorragia Uterina/etiología , Enfermedades Vaginales/complicaciones , Vaginosis Bacteriana/complicaciones , Vaginosis Bacteriana/prevención & control
7.
J Gynecol Obstet Hum Reprod ; 50(4): 102095, 2021 Apr.
Artículo en Inglés | MEDLINE | ID: mdl-33592348

RESUMEN

AIM: To investigate the effects of isolated posterior vaginal compartment prolapse to lower urinary tract symptoms (LUTS). MATERIALS-METHODS: Patients who were admitted with any kind of LUTS and diagnosed with posterior compartment defects were retrospectively analyzed at urogynecology units of 2 different tertiary referral centers. Patients were included in the analysis if they had isolated posterior vaginal compartment defects with no clinically significant anterior and apical compartment defects. The control group consisted of patients with no pelvic organ prolapse (POP). All pelvic examinations were performed by the same 2 specialists. The responses to a detailed LUTS questionnaire in the unit were assessed. RESULTS: Of the 340 women with posterior POP, 280 were excluded from the analysis due to combined anterior and/or apical POP with posterior POP and stage 4 POP. When we compared the symptoms between the control group and the remaining 60 patients with isolated posterior POP, there was a statistically significant difference in urge, frequency, nocturia, abnormal emptying, vaginal winding, difficult stool passage (p = 0.031, p < 0.001, p < 0.001, p = 0.022, p = 0.041, and p = 0.039, respectively). CONCLUSION: Women with posterior POP should be carefully examined not only for anorectal or bulging symptoms but also for LUTS.


Asunto(s)
Síntomas del Sistema Urinario Inferior/etiología , Prolapso Uterino/complicaciones , Enfermedades Vaginales/complicaciones , Estudios de Casos y Controles , Femenino , Humanos , Síntomas del Sistema Urinario Inferior/diagnóstico , Persona de Mediana Edad , Estudios Retrospectivos
8.
Rev. esp. investig. quir ; 24(4): 141-142, 2021. ilus
Artículo en Español | IBECS | ID: ibc-219953

RESUMEN

La dehiscencia de la cúpula vagina tras una histerectomía es una complicación poco frecuente con una mayor incidencia en casos de cirugía laparoscópica. Su diagnóstico es clínico y, en caso de acompañarse de evisceración de contenido intraabdominal, supone una auténtica emergencia quirúrgica debido al riesgo de lesión intestinal y peritonitis. Respecto a la vía de abordaje para su tratamiento continua existiendo controversia, recomendándose la laparoscopia si la situación de la paciente lo permite. Presentamos el caso de una paciente con antecedente de histerectomía total y doble anexectomía 3 meses antes con exploración compatible con abdomen agudo y TC indicativa de perforación de víscera hueca. En la cirugía por vía laparoscópica se evidenció una dehiscencia a nivel de la cúpula vaginal. (AU)


Vaginal cuff dehiscence after hysterectomy is a rare complication. It is more frequent in laparoscopic surgery and its diagnosis isclinical. In case of bowel evisceration it is a surgical emergency due to the risk of bowel injury and peritonitis. Controversy existsregarding the surgical approach. If the patient´s situation allows it, laparoscopy is recommended. We present the case of a patientwith total hysterectomy with bilateral salpingo-oophorectomy 3 months before. She presented an acute abdomen and the CT scanwas indicative of hollow viscus perforation. Laparoscopic surgery showed a vaginal cuff dehiscence. (AU)


Asunto(s)
Humanos , Femenino , Adulto , Dehiscencia de la Herida Operatoria/terapia , Enfermedades Vaginales/complicaciones , Abdomen Agudo/cirugía , Exenteración Pélvica , Laparoscopía , Medicina de Emergencia
9.
Breast ; 54: 216-221, 2020 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-33160147

RESUMEN

BACKGROUND: Studies in the adjuvant setting have shown that endocrine therapy related side effects predict breast cancer recurrence risk. Here, we assess the relationship between early reported side effects and incidence of breast cancer in women randomised to tamoxifen for cancer prevention in the International Breast Intervention Study (IBIS)-I trial. METHODS: Women randomised to tamoxifen in the IBIS-I trial and for whom side effect status was known at the 6-month follow-up visit were included in this analysis. Side effects included in this analysis were hot flushes, vaginal discharge, and vaginal dryness. The primary endpoint was all breast cancer and secondary endpoint was oestrogen receptor (ER) positive breast cancer. Cox proportional hazard models were used to investigate breast cancer incidence in the tamoxifen group with and without side effects reported within 6 months of randomisation. RESULTS: Women randomised to tamoxifen and reporting hot flushes at the 6-month follow-up visit had a non-statistically significant increase in breast cancer compared to those without hot flushes (HR = 1.26 (0.98-1.62), P = 0.08). A significant higher breast cancer risk was observed for postmenopausal women who reported hot flushes at the 6-month follow-up visit compared to those without hot flushes (HR = 1.59 (1.12-2.26), P = 0.01). A higher risk was observed for ER-positive breast cancer in postmenopausal women (HR = 1.81 (1.19-2.74), P = 0.01). No significant associations between gynaecological side effects and breast cancer occurrence was observed. CONCLUSIONS: Overall, no association between side effects reported at 6 months and subsequent breast cancer occurrence was observed. Some side effects might be useful markers for breast cancer occurrence in postmenopausal women.


Asunto(s)
Antineoplásicos Hormonales/efectos adversos , Neoplasias de la Mama/inducido químicamente , Neoplasias de la Mama/epidemiología , Efectos Colaterales y Reacciones Adversas Relacionados con Medicamentos/complicaciones , Tamoxifeno/efectos adversos , Neoplasias de la Mama/prevención & control , Femenino , Estudios de Seguimiento , Sofocos/inducido químicamente , Sofocos/complicaciones , Humanos , Incidencia , Persona de Mediana Edad , Posmenopausia , Modelos de Riesgos Proporcionales , Ensayos Clínicos Controlados Aleatorios como Asunto , Receptores de Estrógenos/metabolismo , Estudios Retrospectivos , Resultado del Tratamiento , Excreción Vaginal/inducido químicamente , Excreción Vaginal/complicaciones , Enfermedades Vaginales/inducido químicamente , Enfermedades Vaginales/complicaciones
10.
Obstet Gynecol ; 136(5): 933-941, 2020 11.
Artículo en Inglés | MEDLINE | ID: mdl-33030871

RESUMEN

OBJECTIVE: To assess independent risk factors for surgical failure and worsening pelvic floor symptoms within 5 years after vaginal prolapse surgery. METHODS: This secondary analysis includes OPTIMAL (Operations and Pelvic Muscle Training in the Management of Apical Support Loss) (n=374) and E-OPTIMAL (Extended) (n=285) trial participants. Surgical failure was defined as apical descent greater than one third of the total vaginal length, anterior or posterior vaginal wall past the hymen, subsequent surgery or bothersome vaginal bulge. Worsening pelvic floor symptoms were defined as increases from baseline as large as the minimally important difference for subscale scores of the Pelvic Floor Distress Inventory: 11 for the Urinary Distress Inventory and Colorectal-Anal Distress Inventory and 34.3 for the Pelvic Organ Prolapse Distress Inventory. Outcomes were measured at 6 months then 1, 2, 3, 4, and 5 years. Chi-square and t test results from bivariate models and clinical relevance were used to inform final models. RESULTS: Baseline risk factors for surgical failure were Hispanic ethnicity (adjusted odds ratio [aOR] 1.92, 95% CI 1.17-3.15), perineal body (aOR 1.34, 95% CI 1.09-1.63), and pretreatment Pelvic Organ Prolapse Distress Inventory score (aOR 1.16, 95% CI 1.05-1.28). Risk factors for worsening of pelvic floor symptoms were pretreatment Pelvic Organ Prolapse Distress Inventory score (aOR 0.75, 95% CI 0.60-0.94) for worsening Pelvic Organ Prolapse Distress Inventory score, vaginal deliveries (aOR 1.26, 95% CI 1.10-1.44) and pretreatment Urinary Distress Inventory score (aOR 0.86, 95% CI 0.80-0.93) for worsening Urinary Distress Inventory score, and age (aOR 1.03, 95% CI 1.01-1.05) and pretreatment Colorectal-Anal Distress Inventory score (aOR 0.95, 95% CI 0.92-0.98) for worsening Colorectal-Anal Distress Inventory score. CONCLUSIONS: Hispanic ethnicity, larger preoperative perineal body, and higher pretreatment Pelvic Organ Prolapse Distress Inventory scores were risk factors for surgical failure up to 5 years after vaginal prolapse repair. Participants with higher baseline Pelvic Floor Distress Inventory scores were less likely to worsen. Risk factors for worsening Urinary Distress Inventory and Colorectal-Anal Distress Inventory scores included more vaginal deliveries and increased age, respectively. CLINICAL TRIAL REGISTRATION: NCT00597935, NCT01166373.


Asunto(s)
Procedimientos Quirúrgicos Ginecológicos/efectos adversos , Prolapso de Órgano Pélvico/cirugía , Complicaciones Posoperatorias/etiología , Vagina/cirugía , Enfermedades Vaginales/cirugía , Adulto , Anciano , Progresión de la Enfermedad , Incontinencia Fecal/etiología , Incontinencia Fecal/cirugía , Femenino , Humanos , Persona de Mediana Edad , Oportunidad Relativa , Prolapso de Órgano Pélvico/complicaciones , Periodo Posoperatorio , Calidad de Vida , Ensayos Clínicos Controlados Aleatorios como Asunto , Factores de Riesgo , Índice de Severidad de la Enfermedad , Factores de Tiempo , Insuficiencia del Tratamiento , Incontinencia Urinaria de Esfuerzo/etiología , Incontinencia Urinaria de Esfuerzo/cirugía , Enfermedades Vaginales/complicaciones
11.
BMJ Case Rep ; 13(8)2020 Aug 24.
Artículo en Inglés | MEDLINE | ID: mdl-32843410

RESUMEN

Transverse vaginal septum is one of the variants of Mullerian duct anomaly, caused as a result of defective fusion or recanalisation of vaginal and Mullerian organs. At an early age, it commonly presents as primary amenorrhea along with cyclical abdominal pain while later on usually it presents as dyspareunia and infertility. Our 22-year-old patient presented with secondary amenorrhea. It is very unusual for a transverse vaginal septum to cause secondary amenorrhea. MRI and clinical examination raised the suspicion of transverse vaginal septum causing secondary amenorrhea. She attained regular menstrual cycle after septum excision. The proposed theory behind it is obliteration of microperforated transverse vaginal septum because of menstrual blood and cell debris. Thus, a rare possibility of transverse vaginal septum should also be considered as a differential diagnosis of secondary amenorrhea.


Asunto(s)
Vagina , Enfermedades Vaginales , Adulto , Amenorrea/etiología , Femenino , Procedimientos Quirúrgicos Ginecológicos , Humanos , Vagina/anomalías , Vagina/cirugía , Enfermedades Vaginales/complicaciones , Enfermedades Vaginales/diagnóstico , Enfermedades Vaginales/patología , Enfermedades Vaginales/cirugía , Adulto Joven
13.
J Low Genit Tract Dis ; 24(4): 411-416, 2020 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-32569019

RESUMEN

OBJECTIVE: Breastfeeding-related hypoestrogenic state has been reported as a possible risk factor for postpartum dyspareunia. This study aimed to evaluate the prevalence and characteristics of postpartum vulvovaginal atrophy according to 3 different diagnostic methods and to estimate its association with postpartum dyspareunia and daily vulvovaginal symptoms. METHODS: This is a prospective cohort study of puerperal women attending a routine postpartum checkup. Participants completed a questionnaire and underwent a gynecological examination. Atrophy was diagnosed separately according to gynecologist impression, vaginal pH measurement (≥5.1), and cytologic vaginal maturation index. Patients were followed up with a telephone survey 2-3 months later, inquiring about symptoms possibly associated with atrophy. RESULTS: Of 117 participants, vaginal atrophy was diagnosed in 48% by gynecological examination, 62% by a pH level of 5.1 or greater, and 40.2% had cytological atrophy. Of the 35.9% of women who had resumed sexual intercourse (42/117), 69% reported dyspareunia. No significant association was found between dyspareunia and atrophy parameters. There was no difference in the rates of dyspareunia among women who were exclusively breastfeeding (21/27 = 78%), partially breastfeeding (4/7 = 57%), or not breastfeeding (4/8, 50%). Atrophy was more common in breastfeeding women according to the 3 criteria (gynecological examination: 57.6% vs 16.7%, p = .006; pH: 70% vs 22%, p < .001; vaginal maturation index: 51.1% vs 0%, p < .001). Of the 117 participants, 47% reported daily vulvovaginal symptoms. Those with daily symptoms reported more dyspareunia as compared with those without daily symptoms (85% vs 52%, p = .025). CONCLUSIONS: A high prevalence of atrophy was observed in puerperal women in association with breastfeeding. There was no significant association between atrophy and dyspareunia or daily vulvovaginal symptoms.


Asunto(s)
Lactancia Materna/efectos adversos , Dispareunia/epidemiología , Enfermedades Vaginales/epidemiología , Enfermedades de la Vulva/epidemiología , Adulto , Atrofia/patología , Dispareunia/complicaciones , Femenino , Humanos , Israel/epidemiología , Periodo Posparto , Prevalencia , Estudios Prospectivos , Factores de Riesgo , Vagina/patología , Enfermedades Vaginales/complicaciones , Enfermedades Vaginales/patología , Vulva/patología , Enfermedades de la Vulva/complicaciones , Enfermedades de la Vulva/patología , Adulto Joven
14.
Pediatr Obes ; 15(8): e12632, 2020 08.
Artículo en Inglés | MEDLINE | ID: mdl-32174046

RESUMEN

BACKGROUND/OBJECTIVES: Several exposures during pregnancy are associated with offspring body mass index (BMI). The objective of this study was to evaluate whether third trimester antibiotic use and vaginal infections are associated with BMI in preschool children. SUBJECTS/METHODS: The study population included singletons from the NINFEA birth cohort with available anthropometric measurements at the age of 4 (3151 born with vaginal and 1111 born with caesarean delivery). Self-reported use of antibiotics and the presence of vaginal infection in the third trimester were analysed in association with the child's BMI, classified into three categories: thinness, normal and overweight/obesity, using both the International Obesity Task Force (IOTF) and the World Health Organization (WHO) recommended cut-offs. RESULTS: Maternal vaginal infections in the third trimester of pregnancy were associated with higher relative risk ratios (RRR) for overweight/obesity at age of four in children delivered vaginally: 1.92 (95% confidence interval [CI]: 1.37 to 2.70). This association appeared stronger for children born to women with pre-pregnancy BMI >25 kg/m2 (RRR: 4.78; 95% CI 2.45 to 9.35), and was robust when different obesity cut-offs were used. The results regarding third trimester antibiotic use in vaginal deliveries were less conclusive (RRRs for overweight/obesity: 1.43 (0.92 to 2.21) and 1.11 (0.57 to 2.20), for the IOTF and WHO cut-offs, respectively). Third trimester vaginal infections were not associated with BMI in children delivered by caesarean section. CONCLUSIONS: Maternal third trimester vaginal infections are associated with an increased overweight/obesity risk in children born by vaginal delivery, and especially in children of mothers with pre-pregnancy overweight/obesity.


Asunto(s)
Antibacterianos/efectos adversos , Sobrepeso/etiología , Obesidad Infantil/etiología , Complicaciones Infecciosas del Embarazo/tratamiento farmacológico , Enfermedades Vaginales/complicaciones , Adulto , Índice de Masa Corporal , Preescolar , Femenino , Humanos , Embarazo , Tercer Trimestre del Embarazo , Enfermedades Vaginales/tratamiento farmacológico
15.
Menopause ; 27(4): 423-429, 2020 04.
Artículo en Inglés | MEDLINE | ID: mdl-32068686

RESUMEN

OBJECTIVE: To estimate the impact of vulvovaginal atrophy (VVA) on sexual function in a clinical population of postmenopausal women. METHODS: Women 45 to 75 years old and more than 12 months after the last menstruation, who attended menopausal/gynecological centers in Italy and Spain, were included. Women with at least one VVA symptom completed the following questionnaires: Day-to-Day Impact of Vaginal Aging (DIVA), Female Sexual Function Index (FSFI), and Female Sexual Distress Scale revised (FSDS-R). A physical gynecological examination was performed to confirm the VVA diagnosis. Data were analyzed by chi-square and Student's t tests. RESULTS: In all, 2,160 evaluable women were included in the study. VVA was confirmed in 90% of the included participants. The negative impact on sexual function was significantly higher in women with than in women without confirmed VVA, as evaluated with the sexual function component (DIVA-C) of the DIVA questionnaire (P = 0.013). Statistically significant differences (P < 0.0005) were also detected in the scores of overall FSDS-R, the overall FSFI, and of all the FSFI subdomains (desire, arousal, lubrication, orgasm, satisfaction, and pain). CONCLUSION: For postmenopausal women with at least one VVA symptom, the presence of physician-confirmed VVA is associated with significant impaired sexual function, as shown by unadjusted analyses. Given the impact on quality of life and the prevalence of VVA, further research to improve and reduce VVA is warranted.


Asunto(s)
Atrofia/diagnóstico , Dispareunia/etiología , Disfunciones Sexuales Fisiológicas/etiología , Enfermedades Vaginales/diagnóstico , Enfermedades de la Vulva/diagnóstico , Anciano , Atrofia/complicaciones , Estudios de Casos y Controles , Estudios Transversales , Femenino , Humanos , Persona de Mediana Edad , Posmenopausia , Encuestas y Cuestionarios , Enfermedades Vaginales/complicaciones , Enfermedades de la Vulva/complicaciones
16.
J Obstet Gynaecol ; 40(4): 512-519, 2020 May.
Artículo en Inglés | MEDLINE | ID: mdl-31496326

RESUMEN

Vulvovaginal atrophy (VVA) has an impact on the quality of life (QoL) of women. This post hoc analysis of the EVES study provides an overview of the QoL in postmenopausal Italian women in relation with VVA severity. We included 1066 women attending menopause/gynaecologic centres. A face-to-face survey (including QoL and sexual life questionnaires), joining an objective gynaecological examination to confirm VVA, were performed. The 65.5% of the participants presented severe vaginal, vulvar and/or urinary symptoms; an 86.9% had an objective confirmed VVA. Women with severe symptoms presented with significantly worse QoL scores than the women without. We found there were moderately significant correlations between vaginal and vulvar symptoms' severity and lower overall DIVA QoL scores (p<.0005, in both cases). Women with a confirmed VVA presented worse QoL scores than women without confirmation. Our data suggest a clear relationship between VVA severity and a decrease in QoL in postmenopausal Italian women.IMPACT STATEMENTWhat is already known on this subject? Vulvovaginal atrophy (VVA) appears as a common chronic disorder in postmenopausal women that, as soon as the oestrogen levels decrease, becomes a severe condition affecting their quality of life (QoL).What do the results of this study add? We provide new insight about QoL related to VVA severity in Italian postmenopausal women. Our local data demonstrates that QoL in Italian women suffering from menopause is directly related to the severity of vaginal and vulvar symptoms. The same correlation exists for urinary symptoms. QoL is also reduced in patients with an objectively confirmed VVA diagnosis.What are the implications of these findings for clinical practice and/or further research? The implications of our findings involve the need for a better management, not only of the physical aspects of VVA, but also of the non-physical dimensions. Clinicians should ask for the impact of VVA on QoL aspects, making postmenopausal women aware about the possible affected spheres. Medical personnel should conduct future campaigns in the Italian general population, not only in those asking for medical help, to make all women conscious about this silent disorder affecting physical and non-physical dimensions and in order to treat it at early stages.


Asunto(s)
Dispareunia , Posmenopausia , Calidad de Vida , Enfermedades Vaginales , Enfermedades de la Vulva , Atrofia/complicaciones , Atrofia/patología , Atrofia/fisiopatología , Estudios de Cohortes , Dispareunia/etiología , Dispareunia/patología , Dispareunia/prevención & control , Dispareunia/psicología , Intervención Médica Temprana/métodos , Femenino , Examen Ginecologíco/métodos , Humanos , Italia/epidemiología , Persona de Mediana Edad , Posmenopausia/fisiología , Posmenopausia/psicología , Índice de Severidad de la Enfermedad , Vagina/patología , Enfermedades Vaginales/complicaciones , Enfermedades Vaginales/patología , Enfermedades Vaginales/fisiopatología , Vulva/patología , Enfermedades de la Vulva/complicaciones , Enfermedades de la Vulva/patología , Enfermedades de la Vulva/fisiopatología
17.
J Minim Invasive Gynecol ; 27(3): 577-578, 2020.
Artículo en Inglés | MEDLINE | ID: mdl-31352071

RESUMEN

STUDY OBJECTIVE: To demonstrate the application of the so-called reverse technique to approach deep infiltrating endometriosis nodules affecting the retrocervical area, the posterior vaginal fornix, and the anterior rectal wall. In Video 1, the authors describe the complete procedure in 10 steps in order to standardize it and facilitate the comprehension and the reproduction of such a procedure in a simple and safe way. DESIGN: A case report. SETTING: A private hospital in Curitiba, Paraná, Brazil. PATIENT: A 32-year-old woman was referred to our service complaining about cyclic dysmenorrhea, dyspareunia, chronic pelvic pain, and cyclic dyschezia. Transvaginal ultrasound with bowel preparation showed a 2.4-cm endometriotic nodule at the retrocervical area, uterosacral ligaments, posterior vaginal fornix, and anterior rectal wall, infiltrating up to the muscularis 10 cm far from the anal verge. INTERVENTIONS: Not applicable. MEASUREMENTS AND MAIN RESULTS: Under general anesthesia, the patient was placed in the dorsal decubitus position with her arms alongside her body and her lower limbs in abduction. Pneumoperitoneum was achieved using a Veress needle placed at the umbilicus. Four trocars were placed according to the French technique as follows: a 10-mm trocar at the umbilicus for the 0 degree laparoscope; a 5-mm trocar at the right anterosuperior iliac spine; a 5-mm trocar in the midline between the umbilicus and the pubic symphysis, approximately 8 to 10 cm inferior to the umbilical trocar; and a 5-mm trocar at the left anterosuperior iliac spine. The entire pelvis was inspected for endometriotic lesions (step 1). The implants located at the ovarian fossae were completely removed (step 2). The ureters were identified bilaterally, and both pararectal fossae were dissected, preserving the hypogastric nerves (step 3). The lesion was separated from the retrocervical area, and the posterior vaginal fornix was resected (reverse technique), leaving the disease attached to the anterior surface of the rectum (step 4). The lesion was shaved off the anterior rectal wall using a harmonic scalpel (step 5). The anterior rectal wall was closed using X-shaped stitches of 3-0 polydioxanone suture in 2 layers (step 6). The specimen was extracted through the vagina (step 7). The posterior vaginal fornix was reattached to the retrocervical area using X-shaped sutures of 0 poliglecaprone 25 (step 8). A pneumatic test was performed to check the integrity of the suture (step 9). At the end of the procedure, hemostasis was controlled, and the abdominal cavity was irrigated using Lactate ringer solution (step10). CONCLUSION: The laparoscopic reverse technique is an alternative approach to face retrocervical or rectovaginal nodules infiltrating the anterior rectal wall. In this technique, the separation of the nodule from the rectal wall is performed at the end of the surgery and not at the beginning as performed within the traditional technique. This enables the surgeon to perform a more precise dissection of the endometriotic nodule from the rectal wall because of the increased mobility of the bowel. The wider range of movements serves as an ergonomic advantage for the subsequent dissection of the lesion from the rectum, allowing the surgeon to decide the best technique to apply for the treatment of the bowel disease (rectal shaving or discoid or segmental resection).


Asunto(s)
Endometriosis/cirugía , Laparoscopía/métodos , Enfermedades del Recto/cirugía , Enfermedades Vaginales/cirugía , Adulto , Brasil , Dolor Crónico/etiología , Dolor Crónico/cirugía , Dismenorrea/etiología , Dismenorrea/cirugía , Dispareunia/etiología , Dispareunia/cirugía , Endometriosis/complicaciones , Femenino , Humanos , Dolor Pélvico/etiología , Dolor Pélvico/cirugía , Enfermedades del Recto/complicaciones , Enfermedades Vaginales/complicaciones
18.
Menopause ; 26(11): 1259-1264, 2019 11.
Artículo en Inglés | MEDLINE | ID: mdl-31688572

RESUMEN

OBJECTIVE: The softgel 17ß-estradiol (E2) vaginal inserts (4 and 10 µg; Imvexxy; TherapeuticsMD, Boca Raton, FL) are FDA approved for treating moderate to severe dyspareunia associated with postmenopausal vulvar and vaginal atrophy (VVA). The objective here was to determine responder rates at week 2 and whether week-2 findings predicted week-12 responders in the REJOICE trial. METHODS: Postmenopausal women received E2 vaginal inserts 4, 10, or 25 µg, or placebo for 12 weeks. Proportion of responders (having ≥2 of the following: vaginal superficial cells >5%, vaginal pH <5.0, or dyspareunia improvement of ≥1 category) were calculated. Odds ratios (ORs) for positive response at week 12 given a positive response at week 2 were determined in the efficacy evaluable (EE) population. RESULTS: The responder rate (in EE population [n = 695]) was 74% to 82% with E2 inserts versus 24% with placebo at week 2, and 72% to 80% versus 33% at week 12. Positive treatment responses were 9- to 14-fold higher with vaginal E2 than with placebo at week 2, and 5- to 8-fold higher at week 12. Response at week 2 predicted response at week 12 in the total population (OR 13.1; 95% CI, 8.8-19.7) and with active treatment only (OR 7.9; 95% CI, 4.7-13.2). CONCLUSIONS: A high percentage of postmenopausal women with moderate to severe dyspareunia responded with the E2 softgel vaginal insert at week 2, and a positive response at week 2 predicted a positive response at week 12.


Asunto(s)
Dispareunia/tratamiento farmacológico , Estradiol/administración & dosificación , Estrógenos/administración & dosificación , Vagina/patología , Enfermedades Vaginales/tratamiento farmacológico , Vulva/patología , Enfermedades de la Vulva/tratamiento farmacológico , Administración Intravaginal , Adulto , Anciano , Atrofia/tratamiento farmacológico , Método Doble Ciego , Dispareunia/complicaciones , Dispareunia/patología , Femenino , Humanos , Persona de Mediana Edad , Posmenopausia , Resultado del Tratamiento , Enfermedades Vaginales/complicaciones , Enfermedades Vaginales/patología , Enfermedades de la Vulva/complicaciones , Enfermedades de la Vulva/patología
20.
Menopause ; 26(12): 1436-1442, 2019 12.
Artículo en Inglés | MEDLINE | ID: mdl-31644509

RESUMEN

OBJECTIVE: The aim of the study was to determine the most used methods for assessing genitourinary syndrome of menopause by the latest studies on the subject, and to critically assess their differences and comparability. METHODS: A narrative review of the literature was conducted, employing the terms genitourinary syndrome, vaginal atrophy, urogenital atrophy, and atrophic vaginitis, to analyze methods used to assess treatment efficacy. Only controlled randomized clinical trials assessing improvement of genitourinary syndrome of menopause, conducted in the last 5 years, and considering all types of treatment, were selected. RESULTS: Of the 37 studies included, 24 combined both objective and subjective methods thereby ensuring reproducibility and efficacy of symptom relief of the treatment analyzed. The vaginal maturation index was the most used objective method, followed by vaginal pH. One study used histological and immunohistochemistry tests. Regarding subjective methods, the "Most bothering Symptom" and other questionnaires as the Female Sexual Function Index for sex life, the Verbal Rating Scale, among others, were used. CONCLUSIONS: Despite the heterogeneity observed, particularly for subjective assessment of symptoms, there was a tendency to standardize methods and to use an objective method together with a subjective, which seems to be fundamental to guarantee reproducibility and comparability of results of each treatment analyzed. Histological and immunohistochemistry tests may be an option as an objective method in further studies, to better assess thickness, vascularization, among other parameters.


Asunto(s)
Atrofia/fisiopatología , Enfermedades Urogenitales Femeninas/fisiopatología , Menopausia , Disfunciones Sexuales Fisiológicas/etiología , Enfermedades Vaginales/fisiopatología , Atrofia/tratamiento farmacológico , Atrofia/etiología , Femenino , Enfermedades Urogenitales Femeninas/complicaciones , Enfermedades Urogenitales Femeninas/tratamiento farmacológico , Humanos , Ensayos Clínicos Controlados Aleatorios como Asunto , Proyectos de Investigación , Disfunciones Sexuales Fisiológicas/complicaciones , Síndrome , Enfermedades Vaginales/complicaciones , Enfermedades Vaginales/tratamiento farmacológico , Salud de la Mujer
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