ABSTRACT
OBJECTIVE: To describe effects of non-ablative erbium-doped:yttrium-aluminium-garnet (Er:YAG) laser on vaginal atrophy induced by iatrogenic menopause in the ewe. DESIGN: Animal experimental, randomised, sham and estrogen-treatment controlled study with blinding for primary outcome. SETTING: KU Leuven, Belgium. SAMPLE: Twenty-four ewes. METHODS: Menopause was surgically induced, after which the ewes were randomised to three groups receiving vaginal Er:YAG laser application three times, with a 1-month interval; three sham manipulations with a 1-month interval; or estrogen replacement and sham manipulations. At given intervals, ewes were clinically examined and vaginal wall biopsies were taken. Vaginal compliance was determined by passive biomechanical testing from explants taken at autopsy. MAIN OUTCOME MEASURES: Vaginal epithelial thickness (primary), composition of the lamina propria (collagen, elastin, glycogen and vessel content), vaginal compliance, clinical signs. RESULTS: Animals exposed to Er:YAG laser application and sham manipulation, but not to estrogens, displayed a significant and comparable increase in vaginal epithelial thickness between baseline and 7 days after the third application (69% and 67%, respectively, both P < 0.0008). In laser-treated ewes, temporary vaginal discharge and limited thermal injury were observed. Estrogen-substituted ewes displayed a more prominent increase in epithelial thickness (202%; P < 0.0001) and higher vaginal compliance (P < 0.05). None of the interventions induced changes in the lamina propria. CONCLUSIONS: Vaginal Er:YAG laser has comparable effect to sham manipulation in menopausal ewes. TWEETABLE ABSTRACT: Vaginal Er:YAG laser has comparable effect to sham manipulation in menopausal ewes #LASER #GSM #RCT.
Subject(s)
Atrophy , Estrogen Replacement Therapy/methods , Estrogens/pharmacology , Lasers, Solid-State/therapeutic use , Low-Level Light Therapy , Menopause , Vagina/pathology , Vaginal Diseases , Animals , Atrophy/diagnosis , Atrophy/drug therapy , Atrophy/etiology , Atrophy/radiotherapy , Biopsy/methods , Disease Models, Animal , Female , Low-Level Light Therapy/adverse effects , Low-Level Light Therapy/methods , Sheep , Treatment Outcome , Vaginal Diseases/drug therapy , Vaginal Diseases/pathology , Vaginal Diseases/radiotherapyABSTRACT
OBJECTIVE: The objective of the study is to analyze the predictors of unplanned cesarean section in nulliparae. DESIGN: Prospective cohort study. SETTING: Institute for the Care of Mother and Child in Prague. METHODS: This study consisted of nulliparae giving birth between the 37th and 42nd weeks of singleton low-risk pregnancy, with the fetus in vertex position and without primary indication for CS. Selected prenatal and intranatal factors were analyzed in relation to acute CS due to a failure to progress in labor and/or fetal distress. Using logistic regression analysis (LR1-3) and the classification tree method (chi-square automatic interaction detector 1-2), five prediction models were tested. RESULTS: Of 3,728 nulliparae, 908 (24.4%) had an acute CS. All logistic regression models were comparable (receiver operating characteristic (ROC) 0.837-0.0881) and identified the occiput posterior position (OPP) of the fetus, maternal age, and epidural analgesia as the most influential risk factors. Spontaneous onset of labor, oxytocin administration, and maternal body height decreased are likely indicated for acute CS. The ability to predict a vaginal delivery was 95.7-96.3% and CS was 58.5-61.8%. The classification tree method (ROC 0.860-0.861) identified similar risk factors such as the OPP, peridural analgesia, and spontaneous onset of labor. The prediction abilities were similar at 94.5-96.4% for vaginal delivery and 64.6-59.0% for CS. CONCLUSION: OPP of the fetus was the strongest risk factor for the unsuccessful trial of vaginal labor.
Subject(s)
Analgesia, Epidural , Labor, Obstetric , Cesarean Section , Child , Delivery, Obstetric , Female , Humans , Pregnancy , Prospective StudiesABSTRACT
OBJECTIVE: The aim of the study is to analyse the musculo-fascial component of the pelvic floor in symptomatic group of woman with pelvic organ prolapse before planned vaginal reconstruction using synthetic vaginal mesh. DESIGN: Observational cohort study. SETTING: Department of Obstetrics and Gynaecology, Hospital in Frýdek-Místek; GONA Ltd, Prague; Institute for Care of Mother and Child, Prague; 3rd Faculty of Medicine CHU Prague. METHODOLOGY: The study involved 285 female volunteers (6 nulliparous, all other patients gave birth vaginally at least once) that in the period 2008-2015 before the planned reconstructive vaginal operations have undergone a comprehensive urogynaecology examination supplemented by magnetic resonance imaging (MRI) of the pelvic floor. Assessed was musculofascial component of the pelvic floor containing -musculus levator ani (MLA), endopelvic fascia (EF) and sacrouterine ligaments (SUL). MLA and EF were evaluated at two levels. The first level corresponds to the puborectalis muscle (evaluation of MRI trauma stage and avulsion), the second level correspondes to the iliococcygeus muscule (evaluation only avulsion injury to the muscle). RESULTS: Normal appereance of musculus puborectalis (level 1) was captured only in 25 (8.8) women. In 117 (41.1%) of women were present MRI minor trauma, 143 (50,2%) women were present with MRI major trauma. Avulsion of the muscle was captured in 85 cases (29.8%) at level 1 and in 165 cases (57.9%) in level 2. Preserved architecture of the EF was caught only 99 (34.7%) of the cases in level 1 and in 47 cases (16.5%) in level 2. Sacrouterine ligaments showed normal morphology in 100 cases (35.1%).Conslusion: Defects of musculofascial component of the pelvic floor is found frequently in women with symptomatic pelvic organ prolapse. Often a combination of defects MLA, EF and SUL are found. These comprehensive pelvic floor defects require careful urogynecological examination and planing operating methods with a view to minimizing the likelihood of recurrence of the descent. In indicated cases the use of the synthetic vaginal mesh is as a method of first choice.
Subject(s)
Magnetic Resonance Imaging , Pelvic Floor/diagnostic imaging , Pelvic Organ Prolapse/diagnostic imaging , Pelvic Organ Prolapse/surgery , Vagina/surgery , Adult , Cohort Studies , Female , Humans , Middle Aged , Pelvic Floor/surgery , PregnancyABSTRACT
OBJECTIVE: The aim of the study is to compare the results of five years follow-up prospective study of vaginal prolapse repaired by prolift total mesh surgery or sacrospinous fixation. STUDY DESIGN: A single-center prospective, cohort study, in patients with defect grade II and more by POP-Q. SETTING: The Institute for the Care of Mather and Child; 3rd Medical Faculty Charles university, Prague. METHODS: Comparison of the preoperative state and the five years after the operation according POP Q, ICIQ-SF, PISQ 12, VAS. Comparison of intraoperative and postoperative complications. RESULTS: The study was attended by 142 patients; 75 patients underwent surgery Prolift Total and 67 patients sacrospinous fixation by Amreich Richter. On clinical examination at 5-year follow-up, we observed 15 (20.0%) case of anatomical failure in the Prolift group and 30 (44.8%) in the SSF group. Anatomic failure was defined clinically as Ba, C or Bp at the hymen or below. In assessing the overall condition before and five years after surgery using a VAS occurred in patients in the cohort Prolift Total decrease to 2.9 (± 1.9) from the original 7.8 (± 1.8). VAS in SSF group decreased after 5 years to 4.2 (± 2.7) of the original 7.8 (± 1.4). Values ICIQ-SF, analyzing the state of voiding PT group showed a decline from the original 6.7 (± 6.9) to 5.5 (± 5.3). A similar trend was evident even after the SSF. Parameters questionnaire PISQ-12 showed a positive increase from the original 28.6 (± 9.5) to 31.8 (± 7.9) points. PISQ-12 was improved from 28.7 (± 9.8) to 32.2 (± 7.5). CONCLUSION: Recurrences were observed more frequently in patients after sacrospinous fixation, while the quality of life questionnaires yielded comparable postoperative results. Quantity of intraoperative complications is low and both groups do not differ.
Subject(s)
Gynecologic Surgical Procedures/methods , Pelvic Organ Prolapse/surgery , Surgical Mesh , Uterine Prolapse/surgery , Child , Cohort Studies , Female , Follow-Up Studies , Humans , Pelvic Organ Prolapse/psychology , Prospective Studies , Quality of Life , Treatment Outcome , Uterine Prolapse/psychologyABSTRACT
OBJECTIVE: To analyse the results of the long-term prospective follow-up study of vaginal prolapse reconstructed using a Prolift Posterior. STUDY DESIGN: Prospective, cohort study. SETTING: Institute for the Care of Mother and Child, Prague. METHODS: Over a 5-year period (I/2006 - XII/2011) we prospectively followed a cohort of patients with posterior vaginal wall defect who underwent surgical reconstruction using a monofilament polypropylene implant Prolift Posterior (Gynecare, Ethicon, Inc., Piscataway, NJ, USA). Patients were invited for review at six weeks, three months, six months, 12 months and then yearly up to five years. Postoperative follow-up included the clinical examination and subjective evaluation using VAS, PISQ 12 and ICIQ SF. RESULTS: One hundred twenty-four women were included in the study, of which 14 (11.3%) had no prolapse surgery in their health history. There were no concomitant vaginal procedures such as hysterectomy or another implant surgery. The average operation time and blood loss were 64.25 min (min. 10, max. 205 min) and 115 ml (min. 10 ml, max. 1000 ml), respectively. Only one patient had a blood loss 1000 ml. There were no injuries of the urinary bladder or intestines during the needle insertion of the mesh. In the five-year period, the recurrence of posterior vaginal wall defect was observed in 4 cases (3.3%). The average time to the posterior vaginal wall recurrence prolapse was 19.5 months (min. 6, max. 36). De novo prolapse in the anterior compartment was observed in 25 patients (20.5%). CONCLUSION: In this prospective single centre study, we observed anatomical improvement in the implanted compartment with low recurrence rate. During five years follow-up period there was de novo anterior vaginal wall defect observed in 20.5% cases. The question of implant employment in urogynecology remain to be answered, however, our results show that implants have their position in reconstructive surgery.
Subject(s)
Gynecologic Surgical Procedures/methods , Pelvic Organ Prolapse/surgery , Surgical Mesh , Uterine Prolapse/surgery , Child , Cohort Studies , Female , Follow-Up Studies , Humans , Prospective Studies , Treatment OutcomeABSTRACT
OBJECTIVE: A short literature review of ewe as an experimental model in research of effects of pregnancy, delivery and urogynecological surgical procedures on the pelvic floor. DESIGN: Literature overview. SETTING: Institute for the Care of Mother and Child, Third Faculty of Medicine, Prague. METHODS: This is an overview of recent literature on experiments using ewes as a model for biomechanical and morphological changes of the vagina induced by pregnancy, delivery and transvaginal graft implantation. RESULTS AND CONCLUSION: The ovine pelvic floor and vagina have comparable morphology to human. Its biomechanical and biochemical properties get changed during the pregnancy and postpartum similarly to clinical findings. Sheep could be used for testing of urogynaecological implants vaginally and simultaneously implanted in the abdominal wall to provide better understanding of anatomical environment differences. The size of the ovine vagina gives the opportunity to perform comprehensive biomechanical, histological and biochemical testing. Experiments and observation may improve our understanding of pathology and physiology of vaginal wall changes induced by hormones, prolapse or surgery.
Subject(s)
Delivery, Obstetric , Models, Animal , Pelvic Floor/surgery , Pregnancy , Sheep , Vagina/surgery , Animals , Female , Gynecologic Surgical Procedures , Postpartum Period , Urologic Surgical ProceduresABSTRACT
OBJECTIVE: The aim of this article is to review current options of prenatal diagnosis and management of fetuses with congenital diaphragmatic hernia at the Institute for the Care of Mother and Child. SETTING: Institute for the Care of Mother and Child, 3. LF UK, Prague. METHODS: Review of the literature. RESULTS: Prenatal diagnosis of congenital diaphragmatic hernia based on 2D ultrasound. Measurement of the lung-to-head ratio (LHR), observed to expected lung to head ratio (O/E LHR), side of the diaphragmatic defect, assessment of the liver position and presence of associated anomalies (negative prognostic factors) are used for prediction of outcome. Prenatal diagnosis can be suplemented by 3D ultrasonography and magnetic resonace imaging. An important part of succesful management of CDH is the referal of cases to a specialised center.
Subject(s)
Hernias, Diaphragmatic, Congenital , Prenatal Care , Ultrasonography, Prenatal , Echocardiography, Three-Dimensional , Female , Hernia, Diaphragmatic/diagnostic imaging , Hernia, Diaphragmatic/therapy , Humans , Infant, Newborn , Magnetic Resonance Imaging , PregnancyABSTRACT
With ongoing evolution of advanced ultrasound diagnostic in prenatal care the trend is to detect potential fetal anomalies in the first trimester if possible. Complex knowledge of normal fetal anatomy, embryology and ultrasound anatomy is important to be able to identify subtle abnormalities. In this review we demonstrate the possibilities of ultrasound imaging of fetal brain at late first trimester and describe normal central nervous system development week by week. Original images are presented.
Subject(s)
Central Nervous System/embryology , Gestational Age , Ultrasonography, Prenatal , Central Nervous System/abnormalities , Central Nervous System/diagnostic imaging , Female , Humans , PregnancyABSTRACT
OBJECTIVE: The aim of this article is to review the current options of prenatal diagnosis in congential diaphragmatic hernia (CDH). SUBJECT: Systematic review. SETTING: Institute for the Care of Mother and Child, 3rd Medical Faculty, Prague. SUBJECT AND METHOD: Review of recent published data. CONCLUSION: The basic method for prenatal diagnosis of congenital diaphragmatic hernia is 2D ultrasonography: measurement of lung-to-head ratio (LHR), observed to expected lung to head ratio (observed to expected LHR - O/E LHR), localization of diaphragmatic defect, assessment of liver position and presence of associated anomalies (negative prognostic factors). Prenatal diagnosis can be supplied with 3D ultrasonography and magnetic resonace (imaging methods for valid measurement of fetal lung volume and/or presence of associated congenital defects confirmation). The reactivity of intrapulmonary arteries are evaluated by hyperoxygenation test and measurement of arterial Doppler parameters. Isolated diaphragmatic hernia is not an indication for invasive prenatal diagnostic methods. Important part of succesful prenatal diagnosis and therapy of CDH is concentration of cases in specialized centre.
