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1.
Medicine (Baltimore) ; 103(27): e38585, 2024 Jul 05.
Article de Anglais | MEDLINE | ID: mdl-38968535

RÉSUMÉ

Endometriosis is one of the most frequent gynecologic disorders. The pathognomonic symptom of endometriosis is pelvic pain. The recommended pain medications are oral hormonal contraceptives, progestin therapy, danazol, gonadotropin-releasing hormone analogs, nonsteroidal anti-inflammatory drugs, and aromatase inhibitors. In this study, we aimed to compare the efficiency of costing dienogest (DNG) and low-cost oral contraceptives regarding visual analog scores (VAS) score of pelvic pain and also cancer antigen-125 (CA-125), anti-Mullerian hormone (AMH) levels, and size of endometrioma in the patients with endometriosis which is a chronic disease that requires a lifelong management plan. In our study, 18 to 45-year-old patients presented to our institution's gynecology and obstetrician department for various complaints over 2 years, and endometriosis diagnoses were included. Patients were divided into 3 groups (20 patients in each medication group) according to the given medication: cyclic DNG (Visanne) or 0.03 mg ethinylestradiol combined with 2 mg DNG (Dienille) or estradiol valerate combined with 2 mg DNG (Qlarista). We recorded all patients' CA-125/AMH values and VAS scores of pelvic pain. All patients gave informed consent. There was no statistically significant difference between pre-medication and post-medication levels of CA-125, AMH, VAS score, and cyst size in all groups. However, statistically, significant decreases were seen in the cyst size and VAS score, indicating response to therapy in all groups. In conclusion, we think it is more reasonable to use cost-effective oral contraceptive medications, which also cause common side effects, instead of costing DNG since all drugs have the same efficiency and success.


Sujet(s)
Endométriose , Oestradiol , Éthinyloestradiol , Nandrolone , Mesure de la douleur , Douleur pelvienne , Humains , Femelle , Endométriose/traitement médicamenteux , Endométriose/complications , Nandrolone/analogues et dérivés , Nandrolone/usage thérapeutique , Nandrolone/administration et posologie , Adulte , Études prospectives , Douleur pelvienne/traitement médicamenteux , Douleur pelvienne/étiologie , Éthinyloestradiol/usage thérapeutique , Éthinyloestradiol/administration et posologie , Oestradiol/analogues et dérivés , Oestradiol/usage thérapeutique , Adulte d'âge moyen , Association médicamenteuse , Antigènes CA-125/sang , Jeune adulte , Hormone antimullérienne/sang , Adolescent
2.
Front Cell Infect Microbiol ; 14: 1417276, 2024.
Article de Anglais | MEDLINE | ID: mdl-38975329

RÉSUMÉ

Chronic prostatitis/chronic pelvic pain syndrome (CP/CPPS) is a common pelvic pain syndrome in males, seriously affecting patients' quality of life. For a long time, CP/CPPS has been considered a complex and variable disease, and its pathogenesis remains incompletely understood. Currently, CP/CPPS is believed to be a group of diseases characterized by pelvic pain or discomfort, urinary abnormalities, and other symptoms, each with its unique etiology, clinical characteristics, and outcomes, likely resulting from the action of pathogens or (and) certain non-infectious factors. Traditionally, CP/CPPS was thought to be unrelated to bacterial infections. However, in recent years, with the development of microbiology and the advancement of high-throughput sequencing technology, an increasing number of studies have suggested that microorganisms in the reproductive system may play an important role in the pathogenesis of CP/CPPS. The unique characteristics of CP/CPPS, such as its refractory nature and tendency to recur, may be closely related to the microbiota and their biological functions in the reproductive system. The relationship between CP/CPPS and reproductive system microorganisms is one of the current hot topics in microbiology and urology, receiving considerable attention from scholars in recent years and making a series of new advances. Through this review, we will comprehensively explore the relationship between CP/CPPS and reproductive system microorganisms, and look forward to future research directions, aiming to provide new ideas and methods for clinical diagnosis and treatment, thereby improving the treatment outcomes and quality of life of CP/CPPS patients.


Sujet(s)
Microbiote , Douleur pelvienne , Prostatite , Prostatite/microbiologie , Humains , Mâle , Douleur pelvienne/microbiologie , Douleur pelvienne/étiologie , Animaux , Qualité de vie , Douleur chronique/microbiologie , Douleur chronique/étiologie , Système génital/microbiologie , Maladie chronique
3.
Int J Mol Sci ; 25(12)2024 Jun 12.
Article de Anglais | MEDLINE | ID: mdl-38928175

RÉSUMÉ

Endometriosis (EM), a chronic condition in endometrial tissue outside the uterus, affects around 10% of reproductive-age women, significantly affecting fertility. Its prevalence remains elusive due to the surgical confirmation needed for diagnosis. Manifesting with a range of symptoms, including dysmenorrhea, dyschezia, dysuria, dyspareunia, fatigue, and gastrointestinal discomfort, EM significantly impairs quality of life due to severe chronic pelvic pain (CPP). Psychological manifestations, notably depression and anxiety, frequently accompany the physical symptoms, with CPP serving as a key mediator. Pain stems from endometrial lesions, involving oxidative stress, neuroinflammation, angiogenesis, and sensitization processes. Microbial dysbiosis appears to be crucial in the inflammatory mechanisms underlying EM and associated CPP, as well as psychological symptoms. In this scenario, dietary interventions and nutritional supplements could help manage EM symptoms by targeting inflammation, oxidative stress, and the microbiome. Our manuscript starts by delving into the complex relationship between EM pain and psychological comorbidities. It subsequently addresses the emerging roles of the microbiome, inflammation, and oxidative stress as common links among these abovementioned conditions. Furthermore, the review explores how dietary and nutritional interventions may influence the composition and function of the microbiome, reduce inflammation and oxidative stress, alleviate pain, and potentially affect EM-associated psychological disorders.


Sujet(s)
Endométriose , Inflammation , Stress oxydatif , Humains , Femelle , Endométriose/métabolisme , Endométriose/microbiologie , Endométriose/complications , Inflammation/métabolisme , Microbiote , Douleur pelvienne/métabolisme , Douleur pelvienne/microbiologie , Douleur pelvienne/étiologie , Troubles mentaux/métabolisme , Troubles mentaux/microbiologie , Troubles mentaux/étiologie
4.
BMC Womens Health ; 24(1): 370, 2024 Jun 26.
Article de Anglais | MEDLINE | ID: mdl-38918726

RÉSUMÉ

OBJECTIVE: Underdiagnosis of female genital tuberculosis (FGTB) often leads to infertility. In this study, we aimed to determine the site and histopathologic patterns of FGTB and its correlation with clinical presentation and acid-fast bacilli (AFB) status. METHODS: A retrospective cross-sectional study was conducted on 122 patients with a histopathological diagnosis of FGTB at the Department of Pathology, College of Health Sciences (CHS), Tikur Anbessa Specialized Hospital (TASH), Addis Ababa University (AAU), from January 1, 2013, to August 30, 2022. RESULTS: Female genital tuberculosis was found in 0.94% of the gynecology specimens examined. The most common presentations were menstrual disturbance, abdominopelvic pain, and infertility. Among patients with FGTB, 4.6% exhibited misleading clinical and radiologic findings, leading to suspicion of malignancy and subsequent aggressive surgical management. The endometrium was the most frequently affected organ, followed by the fallopian tube, ovary, cervix, and vulva. In the majority of tuberculous endometritis cases (53.3%), histopathology revealed early-stage granulomas. Acid-fast bacilli were found in a significant proportion (42.6%) of FGTB tissues with TB histopathology. The ovary had the highest rate of AFB detection, followed by the fallopian tube, endometrium, and cervix. CONCLUSION: Female genital tuberculosis should be considered in reproductive-age women presenting with menstrual irregularities, abdominopelvic pain, infertility, or an abdominopelvic mass. The endometrium is commonly affected, displaying early granulomas with low AFB positivity.


Sujet(s)
Tuberculose de l'appareil génital féminin , Humains , Femelle , Tuberculose de l'appareil génital féminin/anatomopathologie , Tuberculose de l'appareil génital féminin/diagnostic , Tuberculose de l'appareil génital féminin/complications , Études transversales , Études rétrospectives , Adulte , Éthiopie/épidémiologie , Jeune adulte , Adulte d'âge moyen , Troubles de la menstruation/anatomopathologie , Infertilité féminine/étiologie , Endomètre/anatomopathologie , Endomètre/microbiologie , Adolescent , Col de l'utérus/anatomopathologie , Col de l'utérus/microbiologie , Douleur pelvienne/étiologie , Trompes utérines/anatomopathologie , Trompes utérines/microbiologie , Ovaire/anatomopathologie , Douleur abdominale/étiologie , Vulve/anatomopathologie , Vulve/microbiologie , Endométrite/anatomopathologie , Endométrite/microbiologie , Endométrite/diagnostic
5.
Curr Opin Obstet Gynecol ; 36(4): 273-281, 2024 Aug 01.
Article de Anglais | MEDLINE | ID: mdl-38837702

RÉSUMÉ

PURPOSE OF REVIEW: In this review article, we discuss myofascial-related chronic pelvic pain, pathophysiology, symptomology, and management options. RECENT FINDINGS: Despite high prevalence of myofascial pelvic pain, screening is not routinely performed by providers. Treatment modalities include pelvic floor physical therapy, pelvic floor trigger point injections with anesthetics or botulinum toxin A and cryotherapy. Other adjunct modalities, such as muscle relaxants and intravaginal benzodiazepines, are used, but data regarding their effectiveness is sparse. SUMMARY: Myofascial pelvic pain is an important, though overlooked component of chronic pelvic pain. Multimodal, multidisciplinary approach including patient education, pelvic floor physical therapy, and trigger point injections is the mainstay of the management of myofascial pelvic pain.


Sujet(s)
Douleur chronique , Syndromes de la douleur myofasciale , Douleur pelvienne , Humains , Douleur pelvienne/thérapie , Douleur pelvienne/étiologie , Femelle , Douleur chronique/thérapie , Syndromes de la douleur myofasciale/thérapie , Plancher pelvien/physiopathologie , Techniques de physiothérapie , Toxines botuliniques de type A/usage thérapeutique , Points de déclenchement , Cryothérapie/méthodes
6.
Curr Opin Obstet Gynecol ; 36(4): 287-295, 2024 Aug 01.
Article de Anglais | MEDLINE | ID: mdl-38837727

RÉSUMÉ

PURPOSE OF REVIEW: Adenomyosis is a common cause of abnormal uterine bleeding (AUB), dysmenorrhea, and pelvic pain. Definitive diagnosis and treatment have historically been by uterine histopathology at time of hysterectomy; however, advances in imaging have supported earlier diagnosis and subsequent conservative treatment. This review aims to update the evidence supporting the uterine-sparing, procedural management options with a focus on clinical outcomes. RECENT FINDINGS: Uterine artery embolization (UAE), radiofrequency ablation (RFA), high-intensity focused ultrasound (HIFU), percutaneous microwave ablation (PMWA), and adenomyomectomy are minimally invasive interventions proven to be effective in reducing AUB and dysmenorrhea due to adenomyosis. Symptom improvement is associated with a decrease in uterine volume. Studies support the use of alternative treatment options given the overall low rates of symptom recurrence and reintervention. Combination therapy may be more effective than monotherapy. SUMMARY: This review provides the current evidence for use of alternative treatment options for adenomyosis. Access to ablative therapies in the USA is limited and primarily off label, given lack of FDA approval. High-quality prospective and randomized controlled trials are needed in order to further delineate treatment comparisons, efficacy, safety, and ideal patient selection for these treatments. More data are needed to assess safety and utility in those desiring future fertility.


Sujet(s)
Endométriose intra-utérine , Embolisation d'artère utérine , Humains , Femelle , Endométriose intra-utérine/thérapie , Résultat thérapeutique , Ablation par ultrasons focalisés de haute intensité , Dysménorrhée/thérapie , Dysménorrhée/étiologie , Ablation par radiofréquence/méthodes , Hémorragie utérine/thérapie , Hémorragie utérine/étiologie , Douleur pelvienne/thérapie , Douleur pelvienne/étiologie
7.
Radiology ; 311(3): e231863, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38916503

RÉSUMÉ

HISTORY: A 30-year-old female patient with a history of infertility and no pregnancy presented to the gynecologic endometriosis clinic for follow-up 1 month after oocyte retrieval, to be evaluated for pelvic optimization before potential embryo transfer, with worsening dysmenorrhea, dyspareunia, and overall pelvic pain. Eleven years prior, the patient had undergone left ovarian cystectomy for treatment of endometrioma, as well as excision of deep infiltrative endometriosis. The oocyte retrieval procedure, where more than 30 eggs were retrieved, was complicated by ovarian hyperstimulation syndrome and intraperitoneal bleeding, which necessitated admission to the intensive care unit (ICU) for 3 days. Following discharge from the ICU, the patient experienced occasional on-and-off pressure of the urinary bladder and persistent aching pelvic pain. At the 1-month follow-up appointment, the patient's vital signs were assessed (blood pressure, 142/94 mm Hg; pulse rate, 95 per minute; temperature, 96.8 °F [36 °C]). Routine blood investigations, including white blood cell count, were within normal limits. Physical examination showed the abdomen was soft but there was mild pelvic tenderness. The serum ß-human chorionic gonadotropin test result was negative for pregnancy, and urinalysis testing showed no leukocyte esterase or nitrites. MRI of the pelvis (Figs 1-3) was performed to evaluate the worsening pain.


Sujet(s)
Imagerie par résonance magnétique , Humains , Femelle , Adulte , Imagerie par résonance magnétique/méthodes , Endométriose/imagerie diagnostique , Endométriose/chirurgie , Endométriose/complications , Diagnostic différentiel , Douleur pelvienne/imagerie diagnostique , Douleur pelvienne/étiologie
8.
Tech Coloproctol ; 28(1): 69, 2024 Jun 21.
Article de Anglais | MEDLINE | ID: mdl-38907168

RÉSUMÉ

Chronic pelvic pain is a hidden issue which needs to involve many different usually uncoordinated specialists. For this reason there is a risk that treatments, in the absence of well-defined pathways, common goals, and terminology, may be poorly effective. The aim of the present paper is to summarize the evidence on anorectal pelvic pain, offering useful evidence-based practice parameters for colorectal surgeons' daily activity. Analysis of chronic anorectal and pelvic pain syndromes, the diagnostic and clinical optimal needs for evaluation, and the innumerable low evidence treatments and therapeutic options currently available suggests that a multimodal individualized management of pain may be the most promising approach. The limited availability of dedicated centers still negatively affects the applicability of these principles.


Sujet(s)
Douleur chronique , Chirurgie colorectale , Douleur pelvienne , Humains , Douleur pelvienne/thérapie , Douleur pelvienne/chirurgie , Douleur pelvienne/étiologie , Douleur chronique/thérapie , Chirurgie colorectale/normes , Syndrome , Maladies du rectum/chirurgie , Maladies du rectum/thérapie , Italie , Sociétés médicales , Canal anal/chirurgie , Gestion de la douleur/méthodes
9.
BMC Womens Health ; 24(1): 340, 2024 Jun 14.
Article de Anglais | MEDLINE | ID: mdl-38877485

RÉSUMÉ

BACKGROUND: Endometriosis affects 10-15% of women of reproductive age and is considered a critical gynecological problem. Endometriosis causes pain and infertility, both of which can impair the patient's quality of life. Sleep disorders account for the most bothersome presentation of impaired quality of life. This study investigated the frequency and severity of sleep disorders in women with endometriosis. METHODS: In this analytical cross-sectional study, 665 women referred to three hospitals in Tehran, Rasool-e-Akram, Pars, and Nikan, were included (463 patients with endometriosis and 202 women without endometriosis). All of them were informed about the study design and the aim of the research, and then they were asked to sign the consent form and complete the Pittsburgh Sleep Quality Index (PSQI). After data gathering and entering, they were analyzed by SPSS version 22 and were considered significant with P < 0.05. RESULTS: The study population's mean age was 35.4 ± 7.9 years. The mean global PSQI score in the case group (endometriosis patients) was higher than in the control group (non-endometriosis patients) (10.6 vs. 7.1; P < 0.001). Patients with dyspareunia, dysuria, pelvic pain, and dyschezia had a significantly higher PSQI score (P < 0.05). CONCLUSION: According to the findings of the present study, the sleep quality in endometriosis patients is low, and there is a need to pay greater attention to these patients. This may result in some changes in the therapeutic strategies for this disease.


Sujet(s)
Endométriose , Troubles de la veille et du sommeil , Humains , Femelle , Endométriose/complications , Endométriose/épidémiologie , Études transversales , Adulte , Troubles de la veille et du sommeil/épidémiologie , Troubles de la veille et du sommeil/complications , Iran/épidémiologie , Douleur pelvienne/épidémiologie , Douleur pelvienne/étiologie , Qualité de vie , Dyspareunie/épidémiologie , Dyspareunie/étiologie , Enquêtes et questionnaires , Adulte d'âge moyen , Indice de gravité de la maladie , Qualité du sommeil
10.
BMC Womens Health ; 24(1): 353, 2024 Jun 19.
Article de Anglais | MEDLINE | ID: mdl-38890641

RÉSUMÉ

BACKGROUND: The SCHUMANN study evaluated the efficacy and safety of the selective P2 × 3 antagonist eliapixant in patients with endometriosis-associated pelvic pain (EAPP). METHODS: SCHUMANN was a randomized, placebo- and active comparator-controlled, double-blind to placebo and open-label to comparator, parallel-group, multicenter, dose-finding phase 2b study. The participants were women with surgically diagnosed endometriosis who fulfilled defined EAPP criteria. Participants were randomized 1:1:1:1 to twice daily (BID) 25 mg, 75 mg, or 150 mg oral eliapixant or a placebo for 12 weeks. An exploratory once-daily elagolix 150 mg treatment group was also included. The primary endpoint was the absolute change in mean worst EAPP from baseline to the end of intervention (EOI). RESULTS: Overall, 215 participants were randomized for treatment (44 to eliapixant 25 mg, 44 to eliapixant 75 mg, 43 to eliapixant 150 mg, 43 to a placebo, and 41 to elagolix 150 mg). For safety reasons, the study was terminated early; both treatment and enrollment stopped immediately, producing less than 50% of the planned number of completers. The study found no significant differences in EAPP reduction from baseline between groups and no significant dose-response model. The elagolix 150 mg group showed better pain reduction than any of the other groups. No new safety signals were observed, relative to the previously known safety profile of eliapixant, which was generally well tolerated. However, one case of moderate and probably drug-induced liver injury in a participant receiving eliapixant 150 mg BID supported the association between eliapixant and a potential increase in liver function values, defined before the start of the phase 2 program. CONCLUSIONS: This study did not meet its primary objective as no statistically significant or clinically relevant differences in changes of mean worst EAPP from baseline were observed between treatment groups. The single observed case of moderate, probably drug-induced liver injury was the second case in the eliapixant phase 2 program conducted in the following indications: refractory or unexplained chronic cough, diabetic neuropathic pain, overactive bladder, and EAPP. Due to this, the benefit-risk ratio for the study was no longer considered to be positive. CLINICAL TRIAL REGISTRATION: ClinicalTrials.gov identifier NCT04614246; registered November 3, 2020.


Sujet(s)
Endométriose , Douleur pelvienne , Humains , Femelle , Endométriose/complications , Endométriose/traitement médicamenteux , Douleur pelvienne/traitement médicamenteux , Douleur pelvienne/étiologie , Adulte , Méthode en double aveugle , Résultat thérapeutique , Adulte d'âge moyen , Hydrocarbures fluorés/usage thérapeutique , Hydrocarbures fluorés/effets indésirables , Relation dose-effet des médicaments , Mesure de la douleur , Pyrimidines
11.
BMJ Open ; 14(6): e085879, 2024 Jun 03.
Article de Anglais | MEDLINE | ID: mdl-38830733

RÉSUMÉ

OBJECTIVES: Synthesis of the experience of women with pain from pelvic or vaginal mesh or its removal, to identify pain-related problems and to formulate psychological aspects of pain. DESIGN: Systematic review and thematic analysis of qualitative studies of pain from pelvic or vaginal mesh, or mesh removal, in women over 18 years, using individual interviews, focus groups, free text, or written or oral contributions to formal enquiries. DATA SOURCES: Medline, Embase and PsycINFO, from inception to 26 April 2023. ELIGIBILITY CRITERIA: Qualitative studies of pain and other symptoms from pelvic or vaginal mesh or its removal; adults; no language restriction. DATA EXTRACTION AND SYNTHESIS: Line-by-line coding of participant quotations and study author statements by one author to provide codes that were applied to half the studies by another author and differences resolved by discussion. Codes were grouped into subthemes and themes by both authors, then scrutinised and discussed by a focus group of mesh-injured women for omissions, emphasis and coherence. Studies were appraised using an amalgamation of the CASP and COREQ tools. RESULTS: 2292 search results produced 9 eligible studies, with 7-752 participants, a total of around 2000. Four recruited patients, four totally or partially from mesh advocacy groups, and two were national enquiries (UK and Australia). Four major themes were as follows: broken body, broken mind; distrust of doctors and the medical industry; broken life and keeping going-a changed future. Psychological content mainly concerned the loss of trust in medical care, leaving women unsupported in facing an uncertain future. Mesh-injured women strongly endorsed the findings. CONCLUSIONS: Pain and other problems associated with pelvic mesh are profound and far-reaching for women affected. Worse, they feel subject to continued gaslighting, including denial of their mesh-related problems and dismissal of their concerns about continued mesh insertion. PROSPERO REGISTRATION NUMBER: CRD42022330527.


Sujet(s)
Recherche qualitative , Filet chirurgical , Humains , Femelle , Filet chirurgical/effets indésirables , Prolapsus d'organe pelvien/chirurgie , Prolapsus d'organe pelvien/psychologie , Douleur pelvienne/psychologie , Douleur pelvienne/étiologie
12.
BMC Womens Health ; 24(1): 321, 2024 Jun 04.
Article de Anglais | MEDLINE | ID: mdl-38834977

RÉSUMÉ

Violence against women is a phenomenon that involves at least 35% of women worldwide. Violence can be sexual, physical, and/or psychological, perpetrated by the partner, another family member, or a stranger. Violence is a public health problem because its consequences include higher morbidity, higher mortality, and short and long-term physical and psychological health diseases. Most studies prove an association between any type of violence and some chronic pain diagnoses but no one has done a complete collection of this evidence. This systematic review and meta-analysis aimed to evaluate whether this association is statistically significant, including the largest number of studies. Through the inclusion of 37 articles, the association has been demonstrated. Compared with no history of violence, women who did experience violence showed 2 times greater odds of developing chronic pain. The impact of violence was significant also on fibromyalgia separately, but not on pelvic pain.PROSPERO registrationPROSPERO CRD42023425477.


Sujet(s)
Douleur chronique , Humains , Douleur chronique/psychologie , Douleur chronique/épidémiologie , Femelle , Douleur pelvienne/psychologie , Douleur pelvienne/épidémiologie , Douleur pelvienne/étiologie , Fibromyalgie/psychologie , Fibromyalgie/épidémiologie , Fibromyalgie/complications
13.
Can J Urol ; 31(3): 11898-11903, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38912944

RÉSUMÉ

INTRODUCTION: Interstitial cystitis/bladder pain syndrome (IC/BPS) is characterized by chronic pelvic pain and usually accompanies lower urinary tract symptoms. We have previously reported that amniotic bladder therapy (ABT) provides symptomatic improvement in refractory IC/BPS patients for up to 3 months. Herein, we evaluated the durability of ABT up to 6 months. MATERIALS AND METHODS: Consecutive IC/BPS patients received intra-detrusor injections of 100 mg micronized amniotic membrane. Clinical evaluation and patient-reported outcome measurements including Interstitial Cystitis Symptom Index (ICSI), Interstitial Cystitis Problem Index (ICPI), Bladder Pain/ Interstitial Cystitis Symptom Score (BPIC-SS) and Overactive Bladder Assessment Tool (OAB) were assessed. RESULTS: Twenty-five consecutive recalcitrant IC/BPS patients were included in the study with an average age of 47.4 ± 14.4 years (29-67 years). After ABT, the IC/BPS symptoms improved gradually up to 3 months in all patients with an average improvement in ICSI, ICPI, BPIC-SS and OAB score of 72.8%, 71.9%, and 66.6%, (p < 0.001) respectively, at 3 months. At 4 months after ABT, 7 patients experienced a rebound in symptoms and requested another injection which resulted in a significant improvement in IC/BPS symptoms after 2, 4, and 8 weeks (p < 0.01). For the 18 patients who received only one injection, the IC/BPS symptoms were still significantly lower at 5 and 6 months compared to baseline (p < 0.01), suggesting a possible durable effect based on the ICSI, ICPI, BPIC-SS, and OAB questionnaire scores. CONCLUSIONS: ABT provided an improvement in pain and lower urinary tract symptoms up to 6 months post-treatment in some refractory IC/BPS patients.


Sujet(s)
Cystite interstitielle , Humains , Cystite interstitielle/thérapie , Cystite interstitielle/complications , Adulte d'âge moyen , Adulte , Femelle , Sujet âgé , Études de suivi , Mâle , Facteurs temps , Amnios/transplantation , Résultat thérapeutique , Douleur pelvienne/thérapie , Douleur pelvienne/étiologie
17.
Curr Opin Obstet Gynecol ; 36(4): 282-286, 2024 Aug 01.
Article de Anglais | MEDLINE | ID: mdl-38934105

RÉSUMÉ

PURPOSE OF REVIEW: Hysterectomy is the most common gynecologic surgical procedure performed on women in the United States. While there are data supporting that hysterectomy for benign indication often does not reduce sexual function and may in fact improve sexual function as fibroids and endometriosis are resected, it remains unclear if there are factors within the perioperative period that affect sexual function in the years following surgery. To date, there is no consensus on what factors can optimize patients' sexual function after hysterectomy. RECENT FINDINGS: We present the current literature that assesses factors which may contribute to sexual function after hysterectomy. Preoperative demographic factors, including increasing age, pelvic pain, and preoperative sexual dysfunction, play a large role in postoperative sexual function. Perioperatively, there is a growing amount of data suggesting that premenopausal salpingo-oophorectomy at the time of hysterectomy may increase the risk of sexual dysfunction after hysterectomy, and no conclusive evidence that subtotal hysterectomy improves sexual function. The route of hysterectomy and technique of cuff closure can impact sexual function after hysterectomy due to the risk of shortening the vaginal length. SUMMARY: There is a lack of high-quality evidence that can provide a consensus on factors to optimize sexual function after hysterectomy. A growing area of research in the excision of endometriosis procedures is the consideration of nerve-sparing surgery. Considering the many variables that exist when counseling a patient on benign hysterectomy and its effects on sexual function, it is critical to understand the current research that exists with regards to these factors.


Sujet(s)
Hystérectomie , Troubles sexuels d'origine physiologique , Humains , Femelle , Hystérectomie/effets indésirables , Troubles sexuels d'origine physiologique/étiologie , Facteurs de risque , Endométriose/chirurgie , Complications postopératoires/étiologie , Douleur pelvienne/étiologie , Douleur pelvienne/chirurgie , Salpingo-ovariectomie
18.
Arch Ital Urol Androl ; 96(2): 12582, 2024 Jun 27.
Article de Anglais | MEDLINE | ID: mdl-38934521

RÉSUMÉ

OBJECTIVE: The management of chronic prostatitis/ chronic pelvic pain syndrome type III (CP/CPPS) has been always considered complex due to several biopsychological factors underlying the disease. In this clinical study, we aimed to evaluate the efficacy of the treatment with Palmitoylethanolamide, Epilobium and Calendula extract in patients with CP/CPPS III. MATERIALS AND METHODS: From June 2023 to July 2023, we enrolled 45 consecutive patients affected by CP/CPPS type III in three different institution. We included patients aged between 18 and 75 years with symptoms of pelvic pain for 3 months or more before the study, a total National Institutes of Health Chronic Prostatitis Symptom Index (NIH-CPSI) score ≥ 12 point and diagnosed with NIH category III, according to 4-glass test Meares-Stamey test. Patients were then allocated to receive rectal suppositories of PEA, Epilobium and Calendula, 1 suppository/ die for 1 month. All patients have been tested with standard urinalysis in order to assess urinary leukocytes (U-WBC). The primary endpoint of the study was the reduction of NIHCPSI. The secondary outcomes were the change of peak flow, post-void residual (PVR), IIEF-5, VAS score, PSA and decrease of U-WBC. RESULTS: A total of 45 patients concluded the study protocol. At baseline, the median age of all the patients included in the cohort was 49 years, the median PSA was 2.81 ng/ml, the median NIH-CPSI was 18.55, the median IIEF-5 was 18.27, the median U-WBC was 485.3/mmc, the median VAS score was 6.49, the median PVR was 26.5 ml and the median peak flow was 16.3 ml/s. After 1 month of therapy we observed a statistically significant improvement of NIH-CPSI, U-WBC, PSA, IIEF-5, peak flow, PVR and VAS. CONCLUSIONS: In this observational study, we showed the clinical efficacy of the treatment with PEA, Epilobium and Calendula, 1 suppository/die for 1 month, in patients with CP/CPPS III. The benefits of this treatment could be related to the reduction of inflammatory cells in the urine that could imply a reduction of inflammatory cytokines. These results should be confirmed in further studies with greater sample size.


Sujet(s)
Amides , Calendula , Épilobium , Éthanolamines , Acides palmitiques , Extraits de plantes , Prostatite , Humains , Mâle , Adulte d'âge moyen , Adulte , Prostatite/traitement médicamenteux , Suppositoires , Amides/administration et posologie , Amides/usage thérapeutique , Sujet âgé , Acides palmitiques/administration et posologie , Acides palmitiques/usage thérapeutique , Résultat thérapeutique , Jeune adulte , Éthanolamines/administration et posologie , Éthanolamines/usage thérapeutique , Extraits de plantes/administration et posologie , Extraits de plantes/usage thérapeutique , Adolescent , Maladie chronique , Douleur pelvienne/traitement médicamenteux , Douleur pelvienne/étiologie
19.
Minerva Obstet Gynecol ; 76(3): 250-256, 2024 Jun.
Article de Anglais | MEDLINE | ID: mdl-38939979

RÉSUMÉ

BACKGROUND: Pelvic congestion syndrome (PCS) is associated with chronic pelvic pain (CPP). The efficacy of flavonoids for treating PCS symptoms is still a matter of debate, and little has been published. The aim of this study was to assess the efficacy of a mixture of diosmin, troxerutin, and hesperidin in improving symptoms of patients with PCS, observing a direct effect on circulation by specific color Doppler ultrasonography (CDU) evaluations. METHODS: This was a pilot, prospective, independent, cross-over, daily-diary-based trial. Women were evaluated with CDU for 3 times (baseline, 60 days, 120 days). Data about N.=13 women who completed the study were analyzed. RESULTS: During the treatment, we recorded a significant reduction of intermenstrual and menstrual pain intensity (total points) (P<0.05). The satisfaction after treatment was significantly higher than after placebo (P<0.0001). A significant reduction in the diameter of the major ovarian vein (P=0.004 compared to placebo), associated with an increase in peak systolic velocity (P=0.01) and a corresponding significant increase in the Resistivity Index (P<0.0001) were recorded during treatment. CONCLUSIONS: The use of a mixture of diosmin, troxerutin and hesperidin in women with PCS can significantly help to manage typical symptoms of pelvic pain and it is associated with an evident Doppler effect on pelvic microcirculation.


Sujet(s)
Études croisées , Diosmine , Hespéridine , O-(bêta-Hydroxyéthyl)rutosides , Douleur pelvienne , Échographie-doppler couleur , Humains , Femelle , O-(bêta-Hydroxyéthyl)rutosides/analogues et dérivés , O-(bêta-Hydroxyéthyl)rutosides/usage thérapeutique , O-(bêta-Hydroxyéthyl)rutosides/pharmacologie , Diosmine/usage thérapeutique , Diosmine/pharmacologie , Diosmine/administration et posologie , Hespéridine/usage thérapeutique , Douleur pelvienne/traitement médicamenteux , Douleur pelvienne/imagerie diagnostique , Douleur pelvienne/étiologie , Adulte , Études prospectives , Projets pilotes , Syndrome , Jeune adulte , Résultat thérapeutique , Ovaire/effets des médicaments et des substances chimiques , Ovaire/imagerie diagnostique , Ovaire/vascularisation , Association médicamenteuse
20.
J Med Case Rep ; 18(1): 259, 2024 May 25.
Article de Anglais | MEDLINE | ID: mdl-38790071

RÉSUMÉ

BACKGROUND: Wandering spleen is a rare clinical entity in which the spleen is hypermobile and migrate from its normal left hypochondriac position to any other abdominal or pelvic position as a result of absent or abnormal laxity of the suspensory ligaments (Puranik in Gastroenterol Rep 5:241, 2015, Evangelos in Am J Case Rep. 21, 2020) which in turn is due to either congenital laxity or precipitated by trauma, pregnancy, or connective tissue disorder (Puranik in Gastroenterol Rep 5:241, 2015, Jawad in Cureus 15, 2023). It may be asymptomatic and accidentally discovered for imaging done for other reasons or cause symptoms as a result of torsion of its pedicle and infarction or compression on adjacent viscera on its new position. It needs to be surgically treated upon discovery either by splenopexy or splectomy based on whether the spleen is mobile or not. CASE PRESENTATION: We present a case of 39 years old female Ethiopian patient who presented to us complaining constant lower abdominal pain especially on the right side associated with swelling of one year which got worse over the preceding few months of her presentation to our facility. She is primiparous with delivery by C/section and a known case of HIV infection on HAART. Physical examination revealed a right lower quadrant well defined, fairly mobile and slightly tender swelling. Hematologic investigations are unremarkable. Imaging with abdominopelvic U/S and CT-scan showed a predominantly cystic, hypo attenuating right sided pelvic mass with narrow elongated attachment to pancreatic tail and absent spleen in its normal position. CT also showed multiple different sized purely cystic lesions all over both kidneys and the pancreas compatible with AD polycystic kidney and pancreatic disease. With a diagnosis of wandering possibly infarcted spleen, she underwent laparotomy, the finding being a fully infarcted spleen located on the right half of the upper pelvis with twisted pedicle and dense adhesions to the adjacent distal ileum and colon. Release of adhesions and splenectomy was done. Her post-operative course was uneventful. CONCLUSION: Wandering spleen is a rare clinical condition that needs to be included in the list of differential diagnosis in patients presenting with lower abdominal and pelvic masses. As we have learnt from our case, a high index of suspicion is required to detect it early and intervene by doing splenopexy and thereby avoiding splenectomy and its related complications.


Sujet(s)
Rate flottante , Adulte , Femelle , Humains , Douleur abdominale/étiologie , Douleur pelvienne/étiologie , Rate/imagerie diagnostique , Splénectomie , Tomodensitométrie , Rate flottante/complications , Rate flottante/chirurgie , Rate flottante/imagerie diagnostique
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