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4. Exploring options for POP treatment: Patient selection, surgical approaches, and ways to manage risks: Four expert gynecologic surgeons offer tips on diagnosis, surgical and nonsurgical treatment approaches, and patient factors to consider

Author

Gebhart, John B., Karram, Mickey M., Ridgeway, Beri M., and Walters, Mark D.

Subjects
United States. Food and Drug Administration -- Management, Surgery -- Methods, Physicians -- Methods, Hospital patients -- Care and treatment -- Methods, Conferences and conventions, Prolapse, Company business management, Health
Abstract

A number of presentations at the 2019 Pelvic Anatomy and Gynecologic Surgery (PAGS) Symposium (Las Vegas, Nevada, December 12-14, 2019) focused on pelvic organ prolapse (POP) repair, including anatomic considerations, [...]

Published
2020

5. Homozygous Truncating Intragenic Duplication in TUSC3 Responsible for Rare Autosomal Recessive Nonsyndromic Intellectual Disability with No Clinical or Biochemical Metabolic Markers

Author

El Chehadeh, S., Bonnet, C., Callier, P., Béri, M., Dupré, T., Payet, M., Ragon, C., Mosca-Boidron, A. L., Marle, N., Mugneret, F., Masurel-Paulet, A., Thevenon, J., Seta, N., Duplomb, L., Jonveaux, P., Faivre, L., Thauvin-Robinet, C., Zschocke, Johannes, Editor-in-chief, Baumgartner, Matthias, editor, Morava, Eva, editor, Patterson, Marc, editor, Rahman, Shamima, editor, and Peters, Verena, editor

Published
2015
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8. Contributors

Author

Alahwal, Hazem, Sakr Esa, Wael Ali, Ayoub, Mohamad, Bhalla, Tarun, Brown, David L., Cata, Juan P., Chepanoske, Michael, Cubillos, Javier, Cummings, Kenneth C., III, Das, John, Drake, Richard L., Chehade, Nour El Hage, Elsharkawy, Hesham, Farag, Ehab, Farag, Rebecca, Forero, Mauricio, Gadsden, Jeff, Hall, Emily Barney, Hawke, Aaron, Hochaimi, Nour, Karroum, Rami, Kolli, Sree, Kwater, Andrzej P., Faysal Malik, Mohammed, Muse, Iyabo, Nair, Harsha, Narouze, Samer, Oweidat, Adeeb, Rahimi, Michael, Ridgeway, Beri M., Roqués-Escolar, Vicente, Samuel, Samuel W., Schneider, Keith Matthew, Seif, Christian, Seif, John, Skinner, Chelsea, Mounir-Soliman, Loran, Souza, Dmitri, Stamper, Samantha, Sánchez-Amador, Ana Isabel, Taleb, Husien, Toda, Chihiro, Trela, Stefan R., Wong, Cynthia A., Xu, Jeff L., and Yared, Maria

Published
2025
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10. Vulvodynia

Author

Ridgeway, Beri M., Jelovsek, J. Eric, Walters, Mark D., Klein, Eric A., editor, and Potts, Jeannette M., editor

Published
2008
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11. Risk Factors Associated With Postoperative Mortality Among COVID-19 Positive Patients: Results of 3027 Operations and Procedures

Author

Sumeyye Yilmaz, Ipek Sapci, Xue Jia, Maged Argalious, Mark A. Taylor, Beri M. Ridgeway, Georges-Pascal Haber, and Scott R. Steele

Subjects
Male, Postoperative Complications, Risk Factors, Elective Surgical Procedures, Humans, COVID-19, Surgery, Female, Middle Aged, Pandemics, Retrospective Studies
Abstract

To investigate the predictors of postoperative mortality in coronavirus disease 2019 (COVID-19)-positive patients.COVID-19-positive patients have more postoperative complications. Studies investigating the risk factors for postoperative mortality in COVID-19-positive patients are limited.COVID-19-positive patients who underwent surgeries/procedures in Cleveland Clinic between January 2020 and March 2021 were identified retrospectively. The primary outcome was postoperative/procedural 30-day mortality. Secondary outcomes were length of stay, intensive care unit admission, and 30-day readmission.A total of 2543 patients who underwent 3027 surgeries/procedures were included. Total 48.5% of the patients were male. The mean age was 57.8 (18.3) years. A total of 71.2% had at least 1 comorbidity. Total 78.7% of the cases were elective. The median operative time was 94 (47.0-162) minutes and mean length of stay was 6.43 (13.4) days. Postoperative/procedural mortality rate was 4.01%. Increased age [odds ratio (OR): 1.66, 95% CI, 1.4-1.98; P0.001], being a current smoker [2.76, (1.3-5.82); P =0.008], presence of comorbidity [3.22, (1.03-10.03); P =0.043], emergency [6.35, (3.39-11.89); P0.001] and urgent versus [1.78, (1.12-2.84); P =0.015] elective surgery, admission through the emergency department [15.97, (2.00-127.31); P =0.009], or inpatient service [32.28, (7.75-134.46); P0.001] versus outpatients were associated with mortality in the multivariable analysis. Among all specialties, thoracic surgery [3.76, (1.66-8.53); P =0.002] had the highest association with mortality. Total 17.5% of the patients required intensive care unit admission with increased body mass index being a predictor [1.03, (1.01-1.05); P =0.005].COVID-19-positive patients have higher risk of postintervention mortality. Risk factors should be carefully evaluated before intervention. Further studies are needed to understand the impact of pandemic on long-term surgical/procedural outcomes.

Published
2022

19. Reply

Author

Chang, Olivia H., primary, Shepherd, Jonathan P., additional, Ridgeway, Beri M., additional, and Cadish, Lauren A., additional

Published
2021
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21. Contributors

Author

Barber, Matthew D., primary, Bradley, Linda D., additional, Diwadkar, Gouri B., additional, Escobar, Pedro F., additional, Falcone, Tommaso, additional, Jelovsek, J. Eric, additional, Paraiso, Marie Fidela R., additional, Park, Amy J., additional, Ridgeway, Beri M., additional, Tizzano, Anthony P., additional, Uranga, Rebecca S., additional, Walters, Mark D., additional, Whiteside, James L., additional, Wieder, Devorah R., additional, Chen, Chi Chiung Grace, additional, Frick, Anna C., additional, Gebhart, John B., additional, Karram, Mickey, additional, Kho, Rosanne M., additional, Magrina, Javier F., additional, and Muir, Tristi W., additional

Published
2010
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24. Delineation of 15q13.3 microdeletions

Author

Masurel-Paulet, A, Andrieux, J, Callier, P, Cuisset, J M, Le Caignec, C, Holder, M, Thauvin-Robinet, C, Doray, B, Flori, E, Alex-Cordier, M P, Beri, M, Boute, O, Delobel, B, Dieux, A, Vallee, L, Jaillard, S, Odent, S, Isidor, B, Beneteau, C, Vigneron, J, Bilan, F, Gilbert-Dussardier, B, Dubourg, C, Labalme, A, Bidon, C, Gautier, A, Pernes, P, Pinoit, J M, Huet, F, Mugneret, F, Aral, B, Jonveaux, P, Sanlaville, D, and Faivre, L

Published
2010
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26. Defining the Effect of the 16p11.2 Duplication on Cognition, Behavior, and Medical Comorbidities

Author

D'Angelo, D., Lebon, S., Chen, Q., Martin-Brevet, S., Snyder, L. G., Hippolyte, L., Hanson, E., Maillard, A. M., Faucett, W. A., Mace, A., Pain, A., Bernier, R., Chawner, S. J. R. A., David, A., Andrieux, J., Aylward, E., Baujat, G., Caldeira, I., Conus, P., Ferrari, C., Forzano, F., Gerard, M., Goin-Kochel, R. P., Grant, E., Hunter, J. V., Isidor, B., Jacquette, A., Jonch, A. E., Keren, B., Lacombe, D., Le Caignec, C., Martin, C. L., Mannik, K., Metspalu, A., Mignot, C., Mukherjee, P., Owen, M. J., Passeggeri, M., Rooryck-Thambo, C., Rosenfeld, J. A., Spence, S. J., Steinman, K. J., Tjernagel, J., Van Haelst, M., Shen, Y., Draganski, B., Sherr, E. H., Ledbetter, D. H., van den Bree, M. B. M., Beckmann, J. S., Spiro, J. E., Reymond, A., Jacquemont, S., Chung, W. K., Knoers, N. V. A. M., Martinet, D., Belfiore, M., Cuvellier, J. -C., Devries, B., Delrue, M. -A., Doco-Fenzy, M., Lebel, R., Leheup, B., Lewis, S., Mencarelli, M. A., Minet, J. -C., Vincent-Delorme, C., Moerman, A., Mucciolo, M., Ounap, K., Rajcan-Separovic, E., Renieri, A., Sanlaville, D., Faas, B. H., Koolen, D. A., Vulto-Van Silfhout, A., de Leeuw, N., Rosanfeld, J. A., Filges, I., Achatz, E., Roetzer, K. M., Bonneau, D., Guichet, A., Lazaro, L., Plessis, G., Kroisel, P. M., Reis, A., Jonveaux, P., Chantot-Bastaraud, S., Rauch, A., Demeer, B., Nordgren, A., Labalme, A., Ferrarini, A., Ramelli, G. P., Guilmatre, A., Joly-Helas, G., Haize, S., Layet, V., Le Gallic, S., de Freminville, B., Touraine, R., Van Binsbergen, E., Mathieu-Dramard, M., Barth, M., Blaumeiser, B., Masurel, A., Cailler, P., Olivier-Faivre, L., Malacarne, M., Coutton, C., Dieterich, K., Satre, V., Wallgren-Pettersson, C., Tensgrom, C., Kaksonen, S., Duban-Bedu, B., Holder, M., Rossi, M., Gaillard, D., Bock, D., Bednarek, N., Guillin, O., Bizzarri, V., Flori, E., Silengo, M., Kooy, R. F., Aboura, A., Beri, M., Delobel, B., Drunat, S., Jaros, Z., Kolk, A., Reigo, A., Zufferey, F., Beckmann, N., Faravelli, F., Alupay, H., Aaronson, B., Ackerman, S., Ankenman, K., Anwar, A., Atwell, C., Bowe, A., Beaudet, A. L., Benedetti, M., Berg, J., Berman, J., Berry, L. N., Bibb, A. L., Blaskey, L., Brennan, J., Brewton, C. M., Buckner, R., Bukshpun, P., Burko, J., Cali, P., Cerban, B., Chang, Y., Cheong, M., Chow, V., Chu, Z., Chudnovskaya, D., Cornew, L., Dale, C., Dell, J., Dempsey, A. G., Deschamps, T., Earl, R., Edgar, J., Elgin, J., Endre, J., Evans, Y. L., Findlay, A., Fischbach, G. D., Fisk, C., Fregeau, B., Gaetz, B., Gaetz, L., Garza, S., Gerdts, J., Glenn, O., Gobuty, S. E., Golembski, R., Greenup, M., Heiken, K., Hines, K., Hinkley, L., Jackson, F. I., Jenkins, J., Jeremy, R. J., Johnson, K., Kanne, S. M., Kessler, S., Khan, S. Y., Ku, M., Kuschner, E., Laakman, A. L., Lam, P., Lasala, M. W., Lee, H., La, K., Levy, S., Lian, A., Llorens, A. V., Loftus, K., Luks, T. L., Marco, E. J., Martin, S., Martin, A. J., Marzano, G., Masson, C., Mcgovern, K. E., Keehn, R. M., Miller, D. T., Miller, F. K., Moss, T. J., Murray, R., Nagarajan, S. S., Nowell, K. P., Owen, J., Paal, A. M., Packer, A., Page, P. Z., Paul, B. M., Peters, A., Peterson, D., Poduri, A., Pojman, N. J., Porche, K., Proud, M. B., Qasmieh, S., Ramocki, M. B., Reilly, B., Roberts, T. P. L., Shaw, D., Sinha, T., Smith, B., Snow, A., Swarnakar, V., Thieu, T., Triantafallou, C., Vaughan, R., Wakahiro, M., Wallace, A., Ward, T., Wenegrat, J., Wolken, A., Blaumeiser, Bettina, Kooy, Frank, Other departments, Cardiff University Experiences of Children With Copy Number Variants (ECHO) Study, 16p11.2 European Consortium, Simons Variation in Individuals Project (VIP) Consortium, Knoers, VA., Martinet, D., Belfiore, M., Cuvellier, JC., de Vries, B., Delrue, MA., Doco-Fenzy, M., Lebel, R., Leheup, B., Lewis, S., Mencarelli, MA., Minet, JC., Vincent-Delorme, C., Moerman, A., Mucciolo, M., Ounap, K., Rajcan-Separovic, E., Renieri, A., Sanlaville, D., Faas, BH., Koolen, DA., Vulto-van Silfhout, A., de Leeuw, N., Rosenfeld, JA., Filges, I., Achatz, E., Roetzer, KM., Bonneau, D., Guichet, A., Lazaro, L., Plessis, G., Kroisel, PM., Reis, A., Jonveaux, P., Chantot-Bastaraud, S., Rauch, A., Demeer, B., Nordgren, A., Labalme, A., Ferrarini, A., Ramelli, GP., Guilmatre, A., Joly-Helas, G., Haize, S., Layet, V., Le Gallic, S., de Fréminville, B., Touraine, R., Van Binsbergen, E., Mathieu-Dramard, M., Barth, M., Blaumeiser, B., Masurel, A., Cailler, P., Olivier-Faivre, L., Malacarne, M., Coutton, C., Dieterich, K., Satre, V., Wallgren-Pettersson, C., Tensgrom, C., Kaksonen, S., Duban-Bedu, B., Holder, M., Rossi, M., Gaillard, D., Bock, D., Bednarek, N., Guillin, O., Bizzarri, V., Flori, E., Silengo, M., Kooy, RF., Aboura, A., Beri, M., Delobel, B., Drunat, S., Jaros, Z., Kolk, A., Reigo, A., Zufferey, F., Beckmann, N., Faravelli, F., Alupay, H., Aaronson, B., Ackerman, S., Ankenman, K., Anwar, A., Atwell, C., Bowe, A., Beaudet, AL., Benedetti, M., Berg, J., Berman, J., Berry, LN., Bibb, AL., Blaskey, L., Brennan, J., Brewton, CM., Buckner, R., Bukshpun, P., Burko, J., Cali, P., Cerban, B., Chang, Y., Cheong, M., Chow, V., Chu, Z., Chudnovskaya, D., Cornew, L., Dale, C., Dell, J., Dempsey, AG., Deschamps, T., Earl, R., Edgar, J., Elgin, J., Olson, JE., Evans, YL., Findlay, A., Fischbach, GD., Fisk, C., Fregeau, B., Gaetz, B., Gaetz, L., Garza, S., Gerdts, J., Glenn, O., Gobuty, SE., Golembski, R., Greenup, M., Heiken, K., Hines, K., Hinkley, L., Jackson, FI., Jenkins J.<Suffix>3rd</Suffix>, Jeremy, RJ., Johnson, K., Kanne, SM., Kessler, S., Khan, SY., Ku, M., Kuschner, E., Laakman, AL., Lam, P., Lasala, MW., Lee, H., LaGuerre, K., Levy, S., Lian Cavanagh, A., Llorens, AV., Loftus Campe, K., Luks, TL., Marco, EJ., Martin, S., Martin, AJ., Marzano, G., Masson, C., McGovern, KE., McNally Keehn, R., Miller, DT., Miller, FK., Moss, TJ., Murray, R., Nagarajan, SS., Nowell, KP., Owen, J., Paal, AM., Packer, A., Page, PZ., Paul, BM., Peters, A., Peterson, D., Poduri, A., Pojman, NJ., Porche, K., Proud, MB., Qasmieh, S., Ramocki, MB., Reilly, B., Roberts, TP., Shaw, D., Sinha, T., Smith-Packard, B., Snow Gallagher, A., Swarnakar, V., Thieu, T., Triantafallou, C., Vaughan, R., Wakahiro, M., Wallace, A., Ward, T., Wenegrat, J., Wolken, A., Human genetics, Amsterdam Neuroscience - Complex Trait Genetics, and Amsterdam Reproduction & Development (AR&D)

Subjects
Male, 0301 basic medicine, Proband, Pediatrics, Autism Spectrum Disorder, Developmental Disabilities, Chromosome Disorders, Comorbidity, Nonverbal learning disorder, Cohort Studies, Cognition, 0302 clinical medicine, Cerebellum, Chromosome Duplication, Gene duplication, Copy-number variation, Non-U.S. Gov't, Child, 2. Zero hunger, Intelligence quotient, Research Support, Non-U.S. Gov't, Middle Aged, Psychiatry and Mental health, Microcephaly, Female, Schizophrenic Psychology, Chromosome Deletion, Psychology, Rare cancers Radboud Institute for Health Sciences [Radboudumc 9], Human, Adult, medicine.medical_specialty, Adolescent, DNA Copy Number Variations, Research Support, Nervous System Malformations, Article, Chromosomes, Young Adult, 03 medical and health sciences, Intellectual Disability, Journal Article, medicine, Humans, Autistic Disorder, Preschool, Psychiatry, Neurodevelopmental disorders Donders Center for Medical Neuroscience [Radboudumc 7], Epilepsy, Pair 16, Other Research Radboud Institute for Health Sciences [Radboudumc 0], Case-control study, Autism Spectrum Disorder/epidemiology, Autism Spectrum Disorder/genetics, Autistic Disorder/epidemiology, Autistic Disorder/genetics, Case-Control Studies, Cerebellum/abnormalities, Child, Preschool, Chromosome Disorders/epidemiology, Chromosome Disorders/genetics, Chromosomes, Human, Pair 16/genetics, Developmental Disabilities/epidemiology, Developmental Disabilities/genetics, Epilepsy/epidemiology, Epilepsy/genetics, Intellectual Disability/epidemiology, Intellectual Disability/genetics, Microcephaly/epidemiology, Microcephaly/genetics, Nervous System Malformations/epidemiology, Nervous System Malformations/genetics, Schizophrenia/epidemiology, Schizophrenia/genetics, medicine.disease, 030104 developmental biology, Chromosomes, Human, Pair 16, Schizophrenia, Autism, Human medicine, 030217 neurology & neurosurgery
Abstract

Contains fulltext : 167711.pdf (Publisher’s version ) (Closed access) IMPORTANCE: The 16p11.2 BP4-BP5 duplication is the copy number variant most frequently associated with autism spectrum disorder (ASD), schizophrenia, and comorbidities such as decreased body mass index (BMI). OBJECTIVES: To characterize the effects of the 16p11.2 duplication on cognitive, behavioral, medical, and anthropometric traits and to understand the specificity of these effects by systematically comparing results in duplication carriers and reciprocal deletion carriers, who are also at risk for ASD. DESIGN, SETTING, AND PARTICIPANTS: This international cohort study of 1006 study participants compared 270 duplication carriers with their 102 intrafamilial control individuals, 390 reciprocal deletion carriers, and 244 deletion controls from European and North American cohorts. Data were collected from August 1, 2010, to May 31, 2015 and analyzed from January 1 to August 14, 2015. Linear mixed models were used to estimate the effect of the duplication and deletion on clinical traits by comparison with noncarrier relatives. MAIN OUTCOMES AND MEASURES: Findings on the Full-Scale IQ (FSIQ), Nonverbal IQ, and Verbal IQ; the presence of ASD or other DSM-IV diagnoses; BMI; head circumference; and medical data. RESULTS: Among the 1006 study participants, the duplication was associated with a mean FSIQ score that was lower by 26.3 points between proband carriers and noncarrier relatives and a lower mean FSIQ score (16.2-11.4 points) in nonproband carriers. The mean overall effect of the deletion was similar (-22.1 points; P < .001). However, broad variation in FSIQ was found, with a 19.4- and 2.0-fold increase in the proportion of FSIQ scores that were very low (100) compared with the deletion group (P < .001). Parental FSIQ predicted part of this variation (approximately 36.0% in hereditary probands). Although the frequency of ASD was similar in deletion and duplication proband carriers (16.0% and 20.0%, respectively), the FSIQ was significantly lower (by 26.3 points) in the duplication probands with ASD. There also were lower head circumference and BMI measurements among duplication carriers, which is consistent with the findings of previous studies. CONCLUSIONS AND RELEVANCE: The mean effect of the duplication on cognition is similar to that of the reciprocal deletion, but the variance in the duplication is significantly higher, with severe and mild subgroups not observed with the deletion. These results suggest that additional genetic and familial factors contribute to this variability. Additional studies will be necessary to characterize the predictors of cognitive deficits.

Published
2016
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27. Antenatal magnesium sulfate and the need for mechanical ventilation in the first three days of life

Author

Ololade Okito, Adeolu Aromolaran, Beri Massa-Buck, Dinan Abdelatif, Hany Aly, and Mohamed A. Mohamed

Subjects
antenatal magnesium, neonatal resuscitation, RDS, VLBW, Pediatrics, RJ1-570
Abstract

Background: Antenatal administration of magnesium sulfate (MgSO4) to women in preterm labor has gained widespread use. This study examined the relationship between MgSO4 exposure with neonatal respiratory outcomes. Methods: Very low birth weight (VLBW) infants exposed to antenatal MgSO4 were included. Infants who were intubated anytime during the first three days of life were compared to those who were not intubated regarding their demographic and clinical characteristics, MgSO4 therapy, immediate respiratory outcomes, and occurrence of intraventricular hemorrhage (IVH) using student t-test, chi square testing and logistic regression analysis to control for confounding variables. Correlation coefficient of MgSO4 cumulative dose given and duration of infusion with delivery room resuscitation and need for mechanical ventilation in the first 3 days of life were also calculated. Multilinear regression analysis was used to control for confounding factors. Results: Intubated group included 96 infants while non-intubated group included 171 infants. Although, intubated group has younger gestational age (26 vs. 29 weeks, p

Published
2023
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28. American Urogynecologic Society Best-Practice Statement on Evaluation of Obstructed Defecation

Author

Milena M. Weinstein, Elena Tunitsky-Bitton, and Beri M Ridgeway

Subjects
Reconstructive surgery, medicine.medical_specialty, Constipation, Manometry, Urology, Pelvic Organ Prolapse, Pelvic Floor Disorders, 03 medical and health sciences, 0302 clinical medicine, medicine, Humans, Medical History Taking, Physical Examination, Ultrasonography, Pelvic organ, 030219 obstetrics & reproductive medicine, business.industry, General surgery, Obstetrics and Gynecology, Magnetic Resonance Imaging, body regions, Rectal Diseases, Fluoroscopy, 030211 gastroenterology & hepatology, Surgery, Female, Obstructed defecation, medicine.symptom, business, Gastrointestinal Motility, Intestinal Obstruction
Abstract

The symptoms of constipation and obstructed defecation are common in women with pelvic floor disorders. Female pelvic medicine and reconstructive surgery specialists evaluate and treat women with these symptoms, with the initial consultation often occurring when a woman has the symptom or sign of posterior compartment pelvic organ prolapse (including rectocele or enterocele) or if a rectocele or enterocele is identified in pelvic imaging. This best-practice statement will review techniques used to evaluate constipation and obstructed defecation, with a special focus on the relationship between obstructed defecation, constipation, and pelvic organ prolapse.

Published
2018

29. Reply

Author

Cadish, Lauren A., primary, Ridgeway, Beri M., additional, and Shepherd, Jonathan P., additional

Published
2019
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31. Contributors

Author

Amundsen, Cindy L., Dayan, Yehudith Assouline, Attaran, Marjan, Barber, Matthew D., Bordeianou, Liliana, Bradley, Catherine S., Bradley, Megan S., Cundiff, Geoffrey W., Dmochowski, Roger R., Dwarica, Denicia S., Egnot, Brittany R., Ferrando, Cecile A., Fields, Ian C., Gebhart, John B., Gregory, W. Thomas, Grisales, Tamara, Handa, Victoria L., Hartigan, Siobhan M., Hickman, Lisa C., Hoover, Mallorie L., Jelovsek, John Eric, Karram, Mickey M., Kelley, Erika L., Kenne, Kimberly A., Kingsberg, Sheryl A., Knight, Katrina M., Kowalski, Joseph T., Kraus, Stephen R., Lin, Frank C., Mahdy, Ayman, Maheshwari, Deepali, Matthews, Catherine A., Mendhiratta, Neil, Meriwether, Kate V., Moalli, Pamela A., Mueller, Elizabeth R., Muir, Tristi W., Newman, Diane K., Nitti, Victor W., Paquette, Ian M., Patterson, Danielle, Pedersen, Karina, Pham, Thythy T., Quiroz, Lieschen H., Rezaee, Roya L., Richter, Holly E., Ridgeway, Beri M., Rosenman, Amy, Rourke, Elizabeth, Routzong, Megan R., Shaffer, Rebecca, Siddiqui, Nazema Y., Slobodov, Gennady, Solomon, Ellen R., Sung, Vivian W., Takacs, Elizabeth B., Tarnay, Christopher, Vasavada, Sandip P., Visco, Anthony G., Walters, Mark D., and Yuen, Hoi Tik Hyde

Published
2022
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32. Methods for the defining mechanisms of anterior vaginal wall descent (DEMAND) study.

Author

Moalli, Pamela A., Bowen, Shaniel T., Abramowitch, Steven D., Lockhart, Mark E., Ham, Michael, Hahn, Michael, Weidner, Alison C., Richter, Holly E., Rardin, Charles R., Komesu, Yuko M., Harvie, Heidi S., Ridgeway, Beri M., Mazloomdoost, Donna, Shaffer, Amanda, and Gantz, Marie G.

Subjects
VAGINAL surgery, COLPORRHAPHY, MAGNETIC resonance imaging, VAGINAL hysterectomy, GENEALOGY
Abstract

Introduction and hypothesis: The protocol and analysis methods for the Defining Mechanisms of Anterior Vaginal Wall Descent (DEMAND) study are presented. DEMAND was designed to identify mechanisms and contributors of prolapse recurrence after two transvaginal apical suspension procedures for uterovaginal prolapse. Methods: DEMAND is a supplementary cohort study of a clinical trial in which women with uterovaginal prolapse randomized to (1) vaginal hysterectomy with uterosacral ligament suspension or (2) vaginal mesh hysteropexy underwent pelvic magnetic resonance imaging (MRI) at 30–42 months post-surgery. Standardized protocols have been developed to systematize MRI examinations across multiple sites and to improve reliability of MRI measurements. Anatomical failure, based on MRI, is defined as prolapse beyond the hymen. Anatomic measures from co-registered rest, maximal strain, and post-strain rest (recovery) sequences are obtained from the "true mid-sagittal" plane defined by a 3D pelvic coordinate system. The primary outcome is the mechanism of failure (apical descent versus anterior vaginal wall elongation). Secondary outcomes include displacement of the vaginal apex and perineal body and elongation of the anterior wall, posterior wall, perimeter, and introitus of the vagina between (1) rest and strain and (2) rest and recovery. Results: Recruitment and MRI trials of 94 participants were completed by May 2018. Conclusions: Methods papers which detail studies designed to evaluate anatomic outcomes of prolapse surgeries are few. We describe a systematic, standardized approach to define and quantitatively assess mechanisms of anatomic failure following prolapse repair. This study will provide a better understanding of how apical prolapse repairs fail anatomically. [ABSTRACT FROM AUTHOR]

Published
2021
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33. Contributors

Author

Delaney, Conor P., Benninger, Michael S., Capizzani, Tony R., Falcone, Tommaso, Grobmyer, Stephen R., Kaouk, Jihad, Kroh, Matthew, Lyden, Sean P., Rodriguez, John H., Rosen, Michael J., Siegel, Christopher T., Siperstein, Allan, Steele, Scott R., Walsh, R. Matthew, Abouassaly, Robert, Abu-Elmagd, Kareem, Ahmad, Usman, Alarhayem, Abdul Q., Antiporda, Michael, Asfaw, Sofya H., Aucejo, Federico, Augustin, Toms, Beach, Jocelyn M., Benay, Cassandre, Berber, Eren, Bertolo, Riccardo, Bolshinsky, Vladimir, Bryson, Paul C., Caputo, Francis J., Cha, Walter S., Champagne, Bradley J., Chang, Julietta, Church, James M., D’Amico, Giuseppe, Davalos, Gerardo, DeBernardo, Robert, Diago-Uso, Teresa, Djohan, Risal, Droz, Nathan, Eghtesad, Bijan, El-Hayek, Kevin, Fafaj, Aldo, Farivar, Behzad S., Farma, Jeffrey M., Fathalizadeh, Alisan, Flannagan, Molly, Fujiki, Masato, Garisto, Juan, Glover, Keith, Goldfarb, David A., Gorgun, Emre, Gruner, Morgan, Guerron, Alfredo D., Haber, Georges-Pascal, Hardy, David M., Hashimoto, Koji, Hocevar, Barbara J., Holler, Kristen, Holubar, Stefan D., Husain, Farah A., Kagedan, Daniel J., Kalady, Matthew F., Kessler, Hermann, Khaitan, Leena, Khithani, Amit, Kirksey, Lee, Klein, Eric A., Krishnamurthi, Venkatesh, Krpata, David M., Ku, Jamie A., David Kwon, Choon Hyuck, Laczynski, David J., Landis-Erdman, Judith, Larson, Kelsey E., Lavertu, Pierre, Leavitt, Tripp, Lim, Sungho, Lipman, Jeremy M., Lyo, Victoria, Mann, Gary N., Marong, Jeannine L., Mascarenhas, Christopher, McBeath, Evan R., Michener, Chad M., Miller, Charles, Miller, Eric T., Moore, Edwina C., Nair, Amit, Naples, Robert, Nassar, Ahmed, O’Halloran, Eileen A., Okubo, Keita, Parodi, F. Ezequiel, Perry, Will, Petro, Clayton C., Ponsky, Lee, Prabhu, Ajita, Pratt, Debra, Quintini, Cristiano, Raja, Siva, Reavis, Kevin M., Reghunathan, Saranya, Ridgeway, Beri M., Rosen, David R., Rosenblatt, Steven, Sasaki, Kazunari, Schwarz, Graham, Shawki, Sherief, Simon, Robert, Smolock, Christopher J., Steenberge, Sean P., Sullivan, Rachael C., Tang, Andrew, Tassone, Patrick, Tastaldi, Luciano, Thomas, Lewis J., IV, Valente, Michael A., Valente, Stephanie A., Vilchez, Valery, Weber, Cynthia E., Wee, Alvin C., Wu, James S., Zender, Chad A., and Zutshi, Massarat

Published
2021
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44. Contributors

Author

Matthew D. Barber, Linda D. Bradley, Gouri B. Diwadkar, Pedro F. Escobar, Tommaso Falcone, J. Eric Jelovsek, Marie Fidela R. Paraiso, Amy J. Park, Beri M. Ridgeway, Anthony P. Tizzano, Rebecca S. Uranga, Mark D. Walters, James L. Whiteside, Devorah R. Wieder, Chi Chiung Grace Chen, Anna C. Frick, John B. Gebhart, Mickey Karram, Rosanne M. Kho, Javier F. Magrina, and Tristi W. Muir

Published
2010
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46. Vulvodynia

Author

Ridgeway, Beri M., primary, Jelovsek, J. Eric, additional, and Walters, Mark D., additional

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47. Molecular characterization of 1q44 microdeletion in 11 patients reveals three candidate genes for intellectual disability and seizures.

Author

Thierry, G., Beneteau, C., Pichon, O., Flori, E., Isidor, B., Popelard, F., Delrue, M.A., Duboscq-Bidot, L., Thuresson, A.C., Bon, B.W.M. van, Cailley, D., Rooryck, C., Paubel, A., Metay, C., Dusser, A., Pasquier, L., Beri, M., Bonnet, C., Jaillard, S., Dubourg, C., Tou, B., Quere, M.P., Soussi-Zander, C., Toutain, A., Lacombe, D., Arveiler, B., Vries, L.B.A. de, Jonveaux, P., David, A., Caignec, C. Le, Thierry, G., Beneteau, C., Pichon, O., Flori, E., Isidor, B., Popelard, F., Delrue, M.A., Duboscq-Bidot, L., Thuresson, A.C., Bon, B.W.M. van, Cailley, D., Rooryck, C., Paubel, A., Metay, C., Dusser, A., Pasquier, L., Beri, M., Bonnet, C., Jaillard, S., Dubourg, C., Tou, B., Quere, M.P., Soussi-Zander, C., Toutain, A., Lacombe, D., Arveiler, B., Vries, L.B.A. de, Jonveaux, P., David, A., and Caignec, C. Le

Abstract

1 juli 2012, Item does not contain fulltext, Patients with a submicroscopic deletion at 1q43q44 present with intellectual disability (ID), microcephaly, craniofacial anomalies, seizures, limb anomalies, and corpus callosum abnormalities. However, the precise relationship between most of deleted genes and the clinical features in these patients still remains unclear. We studied 11 unrelated patients with 1q44 microdeletion. We showed that the deletions occurred de novo in all patients for whom both parents' DNA was available (10/11). All patients presented with moderate to severe ID, seizures and non-specific craniofacial anomalies. By oligoarray-based comparative genomic hybridization (aCGH) covering the 1q44 region at a high resolution, we obtained a critical deleted region containing two coding genes-HNRNPU and FAM36A-and one non-coding gene-NCRNA00201. All three genes were expressed in different normal human tissues, including in human brain, with highest expression levels in the cerebellum. Mutational screening of the HNRNPU and FAM36A genes in 191 patients with unexplained isolated ID did not reveal any deleterious mutations while the NCRNA00201 non-coding gene was not analyzed. Nine of the 11 patients did not present with microcephaly or corpus callosum abnormalities and carried a small deletion containing HNRNPU, FAM36A, and NCRNA00201 but not AKT3 and ZNF238, two centromeric genes. These results suggest that HNRNPU, FAM36A, and NCRNA00201 are not major genes for microcephaly and corpus callosum abnormalities but are good candidates for ID and seizures.

Published
2012

48. Mirror extreme BMI phenotypes associated with gene dosage at the chromosome 16p11.2 locus

Author

Jacquemont, S., Reymond, A., Zufferey, F., Harewood, L., Walters, R.G., Kutalik, Z., Martinet, D., Shen, Y., Valsesia, A., Beckmann, N.D., Thorleifsson, G., Belfiore, M., Bouquillon, S., Campion, D., Leeuw, N. de, Vries, L.B.A. de, Esko, T., Fernandez, B.A., Fernandez-Aranda, F., Fernandez-Real, J.M., Gratacos, M., Guilmatre, A., Hoyer, J., Jarvelin, M.R., Kooy, R.F., Kurg, A., Caignec, C. Le, Mannik, K., Platt, O.S., Sanlaville, D., Haelst, M.M. van, Villatoro Gomez, S., Walha, F., Wu, B.L., Yu, Y., Aboura, A., Addor, M.C., Alembik, Y., Antonarakis, S.E., Arveiler, B., Barth, M., Bednarek, N., Bena, F., Bergmann, S., Beri, M., Bernardini, L., Blaumeiser, B., Bonneau, D., Bottani, A., Boute, O., Brunner, H.G., Cailley, D., Callier, P., Chiesa, J., Chrast, J., Coin, L., Coutton, C., Cuisset, J.M., Cuvellier, J.C., David, A., Freminville, B. de, Delobel, B., Delrue, M.A., Demeer, B., Descamps, D., Didelot, G., Dieterich, K., Disciglio, V., Doco-Fenzy, M., Drunat, S., Duban-Bedu, B., Dubourg, C., El-Sayed Moustafa, J.S., Elliott, P., Faas, B.H.W., Faivre, L., Faudet, A., Fellmann, F., Ferrarini, A., Fisher, R., Flori, E., Forer, L., Gaillard, D., Gerard, M., Gieger, C., Gimelli, S., Gimelli, G., Grabe, H.J., Guichet, A., Guillin, O., Hartikainen, A.L., Heron, D., Hippolyte, L., Holder, M., Homuth, G., Isidor, B., Jaillard, S., Jaros, Z., Jimenez-Murcia, S., Helas, G.J., et al., Jacquemont, S., Reymond, A., Zufferey, F., Harewood, L., Walters, R.G., Kutalik, Z., Martinet, D., Shen, Y., Valsesia, A., Beckmann, N.D., Thorleifsson, G., Belfiore, M., Bouquillon, S., Campion, D., Leeuw, N. de, Vries, L.B.A. de, Esko, T., Fernandez, B.A., Fernandez-Aranda, F., Fernandez-Real, J.M., Gratacos, M., Guilmatre, A., Hoyer, J., Jarvelin, M.R., Kooy, R.F., Kurg, A., Caignec, C. Le, Mannik, K., Platt, O.S., Sanlaville, D., Haelst, M.M. van, Villatoro Gomez, S., Walha, F., Wu, B.L., Yu, Y., Aboura, A., Addor, M.C., Alembik, Y., Antonarakis, S.E., Arveiler, B., Barth, M., Bednarek, N., Bena, F., Bergmann, S., Beri, M., Bernardini, L., Blaumeiser, B., Bonneau, D., Bottani, A., Boute, O., Brunner, H.G., Cailley, D., Callier, P., Chiesa, J., Chrast, J., Coin, L., Coutton, C., Cuisset, J.M., Cuvellier, J.C., David, A., Freminville, B. de, Delobel, B., Delrue, M.A., Demeer, B., Descamps, D., Didelot, G., Dieterich, K., Disciglio, V., Doco-Fenzy, M., Drunat, S., Duban-Bedu, B., Dubourg, C., El-Sayed Moustafa, J.S., Elliott, P., Faas, B.H.W., Faivre, L., Faudet, A., Fellmann, F., Ferrarini, A., Fisher, R., Flori, E., Forer, L., Gaillard, D., Gerard, M., Gieger, C., Gimelli, S., Gimelli, G., Grabe, H.J., Guichet, A., Guillin, O., Hartikainen, A.L., Heron, D., Hippolyte, L., Holder, M., Homuth, G., Isidor, B., Jaillard, S., Jaros, Z., Jimenez-Murcia, S., Helas, G.J., and et al.

Abstract

Contains fulltext : 96105.pdf (publisher's version ) (Closed access), Both obesity and being underweight have been associated with increased mortality. Underweight, defined as a body mass index (BMI)

Published
2011

49. Colaboradores

Author

APONTE, MARGARITA M., ASHBURN, JEAN H., ATTARAN, MARJAN, BARBER, MATTHEW D., BENT, ALFRED E., BOLOGNA, RAYMOND A., BURGIO, KATHRYN L., CHEN, CHI CHIUNG GRACE, CLEMONS, JEFFREY L., CUNDIFF, GEOFFREY W., EVANS, JANELLE, FLEMING, EVELYN L., FRICK, ANNA C., GEBHART, JOHN B., GREGORY, W. THOMAS, HALE, DOUGLASS S., HAMPTON, B. STAR, HUANG, WEN-CHEN, HULL, TRACY L., JELOVSEK, J. ERIC, KARRAM, MICKEY M., KINGSBERG, SHERYL A., MAHDY, AYMAN, MATTHEWS, CATHERINE A., MOALLI, PAMELA A., MOORE, COURTENAY K., MUFFLY, TYLER M., MUIR, TRISTI W., NITTI, VICTOR W., PARAISO, MARIE FIDELA R., RACKLEY, RAYMOND R., REZAEE, ROYA L., RICHTER, HOLLY E., RIDGEWAY, BERI M., SHAFFER, REBECCA, SIBAI, BAHA M., SILVA, WILLIAM ANDRE, SOLOMON, ELLEN R., SOUTH, MARY M., STEPP, KEVIN J., SULTANA, CARMEN J., SUNG, VIVIAN W., TARR, MEGAN E., TIZZANO, ANTHONY P., TUNITSKY-BITTON, ELENA, UNGER, CECILE A., VACCARO, CHRISTINE M., VASAVADA, SANDIP P., WALTERS, MARK D., WHITESIDE, JAMES L., WHITMORE, KRISTENE E., and ZUTSHI, MASSARAT

Published
2016

50. Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis

Author

Démurger, F., primary, Pasquier, L., additional, Dubourg, C., additional, Dupé, V., additional, Gicquel, I., additional, Evain, C., additional, Ratié, L., additional, Jaillard, S., additional, Beri, M., additional, Leheup, B., additional, Lespinasse, J., additional, Martin-Coignard, D., additional, Mercier, S., additional, Quelin, C., additional, Loget, P., additional, Marcorelles, P., additional, Laquerrière, A., additional, Bendavid, C., additional, Odent, S., additional, and David, V., additional

Published
2013
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