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1.
Gynecol Obstet Invest ; 88(1): 37-46, 2023.
Artigo em Inglês | MEDLINE | ID: mdl-36577396

RESUMO

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.


Assuntos
Toxinas Botulínicas Tipo A , Síndromes da Dor Miofascial , Nervo Pudendo , Feminino , Humanos , Toxinas Botulínicas Tipo A/administração & dosagem , Toxinas Botulínicas Tipo A/efeitos adversos , Toxinas Botulínicas Tipo A/uso terapêutico , Dor Pélvica/tratamento farmacológico , Dor Pélvica/etiologia , Estudos Retrospectivos , Atenção Terciária à Saúde , Síndromes da Dor Miofascial/tratamento farmacológico , Bloqueio Nervoso , Injeções Intramusculares , Resultado do Tratamento
2.
JAAPA ; 33(8): 50-52, 2020 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-32740116

RESUMO

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.


Assuntos
Terapia por Estimulação Elétrica/instrumentação , Incontinência Fecal/etiologia , Incontinência Fecal/terapia , Plexo Lombossacral , Modalidades de Fisioterapia/instrumentação , Adulto , Idoso , Terapia Cognitivo-Comportamental , Incontinência Fecal/diagnóstico , Incontinência Fecal/psicologia , Feminino , Humanos , Pessoa de Meia-Idade , Qualidade de Vida , Índice de Gravidade de Doença , Adulto Jovem
3.
JAAPA ; 32(12): 11-12, 2019 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-31770299

RESUMO

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.


Assuntos
Desidroepiandrosterona/uso terapêutico , Dispareunia/tratamento farmacológico , Técnicas de Reprodução Assistida , Doenças Vaginais/tratamento farmacológico , Doenças da Vulva/tratamento farmacológico , Administração Intravaginal , Administração Oral , Atrofia , Feminino , Ginecologia , Humanos , Menopausa
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