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1.
Gynecol Obstet Invest ; 88(1): 37-46, 2023.
Artículo en Inglés | MEDLINE | ID: mdl-36577396

RESUMEN

OBJECTIVE: The aim of this study was to highlight the safety of OnabotulinumtoxinA (BTA) injections, with or without concurrent pudendal nerve block, in treating women with myofascial pelvic pain (MFPP). DESIGN: This was a retrospective cohort study. SETTING: The review was conducted in a tertiary care academic center. Participants/Materials: We conducted a chart review of patients who were diagnosed with MFPP and treated with BTA with or without pudendal nerve block between January 2010 and February 2022. METHODS: BTA was injected transvaginally into the pelvic floor muscle group. The primary outcomes were adverse events after BTA injections, and the secondary outcome was the effect of concomitant pudendal nerve block at the time of BTA injections. RESULTS: The cohort included 182 patients; 103 (56.6%) received BTA injections with pudendal nerve block, and 79 (43.4%) received BTA alone. There were no significant demographic differences between the two groups. Post-treatment complications of BTA administration included worsening of pelvic pain (11.5%), constipation (6.6%), urinary tract infection (2.7%), urinary retention (3.8%), and fecal incontinence (2.7%). No statistical difference was noted in the number of phone calls, patient-initiated electronic messages, emergency room visits, or clinic visits for both groups within 30 days post-treatment. The mean number of total injections was 1.6 in the BTA-only group and 1.7 in the BTA with pudendal block group (p = 0.421). Median time to re-intervention with a second BTA injection was 6.0 months; 5.6 months in the BTA with pudendal block group; and 6.8 months in the BTA-only group, p = 0.46. There were 63 re-intervention events after BTA injections. LIMITATIONS: Limitations of our study include the retrospective design making it vulnerable to missing or incomplete data available for review. CONCLUSION: OnabotulinumtoxinA is beneficial in treating women with MFPP; with a duration of therapeutic effect of approximately 6 months. The use of a concurrent pudendal nerve block did not impact clinical outcomes.


Asunto(s)
Toxinas Botulínicas Tipo A , Síndromes del Dolor Miofascial , Nervio Pudendo , Femenino , Humanos , Toxinas Botulínicas Tipo A/administración & dosificación , Toxinas Botulínicas Tipo A/efectos adversos , Toxinas Botulínicas Tipo A/uso terapéutico , Dolor Pélvico/tratamiento farmacológico , Dolor Pélvico/etiología , Estudios Retrospectivos , Atención Terciaria de Salud , Síndromes del Dolor Miofascial/tratamiento farmacológico , Bloqueo Nervioso , Inyecciones Intramusculares , Resultado del Tratamiento
2.
JAAPA ; 33(8): 50-52, 2020 Aug.
Artículo en Inglés | MEDLINE | ID: mdl-32740116

RESUMEN

Fecal incontinence often is underreported and can be associated with both social embarrassment and isolation. As patients often do not proactively discuss their symptoms, healthcare providers should screen for this distressing condition. The cause of fecal incontinence often is multifactorial, so no single therapy can guarantee perfect, risk-free outcomes. This article reviews the limited therapies for managing fecal incontinence, including a minimally invasive vaginal control device that may offer hope for managing fecal incontinence in women.


Asunto(s)
Terapia por Estimulación Eléctrica/instrumentación , Incontinencia Fecal/etiología , Incontinencia Fecal/terapia , Plexo Lumbosacro , Modalidades de Fisioterapia/instrumentación , Adulto , Anciano , Terapia Cognitivo-Conductual , Incontinencia Fecal/diagnóstico , Incontinencia Fecal/psicología , Femenino , Humanos , Persona de Mediana Edad , Calidad de Vida , Índice de Severidad de la Enfermedad , Adulto Joven
3.
JAAPA ; 32(12): 11-12, 2019 Dec.
Artículo en Inglés | MEDLINE | ID: mdl-31770299

RESUMEN

In small clinical trials, dehydroepiandrosterone (DHEA) has been found to relieve symptoms associated with postmenopausal conditions and infertility in women. DHEA may provide a cost-effective alternative to typical hormone therapies. Because of a lack of long-term and large-scale studies, only intravaginal DHEA supplementation is approved and recommended for treatment. Further investigation of DHEA supplementation is needed and encouraged to determine its safety and effectiveness.


Asunto(s)
Deshidroepiandrosterona/uso terapéutico , Dispareunia/tratamiento farmacológico , Técnicas Reproductivas Asistidas , Enfermedades Vaginales/tratamiento farmacológico , Enfermedades de la Vulva/tratamiento farmacológico , Administración Intravaginal , Administración Oral , Atrofia , Femenino , Ginecología , Humanos , Menopausia
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