90 results on '"Fitzgerald, Mark P."'
Search Results
2. Calcium supplementation during trauma resuscitation: a propensity score-matched analysis from the TraumaRegister DGU®
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Helsloot, Dries, Fitzgerald, Mark, Lefering, Rolf, Groombridge, Christopher, Becaus, Nathalie, Verelst, Sandra, and Missant, Carlo
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- 2024
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3. A miniaturized mode-of-action profiling platform enables high throughput characterization of the molecular and cellular dynamics of EZH2 inhibition
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Falkenstern, Lilia, Georgi, Victoria, Bunse, Stefanie, Badock, Volker, Husemann, Manfred, Roehn, Ulrike, Stellfeld, Timo, Fitzgerald, Mark, Ferrara, Steven, Stöckigt, Detlef, Stresemann, Carlo, Hartung, Ingo V., and Fernández-Montalván, Amaury
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- 2024
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4. Simvastatin in Critically Ill Patients with Covid-19.
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Hills, Thomas, Lorenzi, Elizabeth, Berry, Lindsay, Shyamsundar, Murali, Al-Beidh, Farah, Annane, Djillali, Arabi, Yaseen, Aryal, Diptesh, Au, Carly, Beane, Abigail, Bhimani, Zahra, Bonten, Marc, Bradbury, Charlotte, Brunkhorst, Frank, Burrell, Aidan, Buxton, Meredith, Calfee, Carolyn, Cecconi, Maurizio, Cheng, Allen, Cove, Matthew, Detry, Michelle, Estcourt, Lise, Fitzgerald, Mark, Goligher, Ewan, Goossens, Herman, Green, Cameron, Haniffa, Rashan, Harrison, David, Hashmi, Madiha, Higgins, Alisa, Huang, David, Ichihara, Nao, Jayakumar, Deva, Kruger, Peter, Lamontagne, François, Lampro, Lamprini, Lawler, Patrick, Marshall, John, Mason, Alexina, McGlothlin, Anna, McGuinness, Shay, McQuilten, Zoe, McVerry, Bryan, Mouncey, Paul, Murthy, Srinivas, Neal, Matthew, Nichol, Alistair, OKane, Cecilia, Parke, Rachael, Parker, Jane, Rabindrarajan, Ebenezer, Reyes, Luis, Rowan, Kathryn, Saito, Hiroki, Santos, Marlene, Saunders, Christina, Seymour, Christopher, Shankar-Hari, Manu, Sinha, Pratik, Thompson, B, Turgeon, Alexis, Turner, Anne, van de Veerdonk, Frank, Weis, Sebastian, Young, Ian, Zarychanski, Ryan, McArthur, Colin, Angus, Derek, Berry, Scott, Derde, Lennie, Webb, Steve, Gordon, Anthony, McAuley, Daniel, and Lewis, Roger
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Humans ,Bayes Theorem ,COVID-19 ,COVID-19 Drug Treatment ,Critical Illness ,Hospital Mortality ,Hydroxymethylglutaryl-CoA Reductase Inhibitors ,Simvastatin ,Treatment Outcome - Abstract
BACKGROUND: The efficacy of simvastatin in critically ill patients with coronavirus disease 2019 (Covid-19) is unclear. METHODS: In an ongoing international, multifactorial, adaptive platform, randomized, controlled trial, we evaluated simvastatin (80 mg daily) as compared with no statin (control) in critically ill patients with Covid-19 who were not receiving statins at baseline. The primary outcome was respiratory and cardiovascular organ support-free days, assessed on an ordinal scale combining in-hospital death (assigned a value of -1) and days free of organ support through day 21 in survivors; the analyis used a Bayesian hierarchical ordinal model. The adaptive design included prespecified statistical stopping criteria for superiority (>99% posterior probability that the odds ratio was >1) and futility (>95% posterior probability that the odds ratio was
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- 2023
5. Directional eddy current probe configuration for in-line detection of out-of-plane wrinkles
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Mussatayev, Meirbek, Yi, Qiuji, Fitzgerald, Mark, Maes, Vincent K., Wilcox, Paul, and Hughes, Robert
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Physics - Instrumentation and Detectors - Abstract
Real-time monitoring of carbon fibre composites during Automated Fibre Placement (AFP) manufacturing remains a challenge for non-destructive evaluation (NDE) techniques. An directional eddy-current (EC) probe with asymmetric transmit and differential receive (Tx-dRx) coils is designed, constructed and characterized to evaluate the detectability of out-of-plane wrinkles. Initial studies were conducted to determine suitable excitation frequencies and to analyse the impact of relative orientations of driver and pickup coils on wrinkle detectability. The probe configurations are evaluated experimentally and employ a new finite element modelling approach to better understand the relationship between eddy-current density and defect detection. The findings indicate that a probe configuration with an asymmetric driver coil normal to the material surface and aligned with the fibre directions, and with differential pickup coils 90 degrees to the scanning direction, shows the best capability for out-of-plane wrinkle detection, with SNR >20 for wrinkles over 1.3 mm in amplitude., Comment: [2024] Elsevier. This manuscript version is made available under the CC BY-NC-ND 4.0 license. [https://doi.org/10.1016/j.compositesb.2023.111048]
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- 2023
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6. De novo variants in DENND5B cause a neurodevelopmental disorder
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Acosta, Maria T., Adams, David R., Alvarez, Raquel L., Alvey, Justin, Allworth, Aimee, Andrews, Ashley, Ashley, Euan A., Afzali, Ben, Bacino, Carlos A., Bademci, Guney, Balasubramanyam, Ashok, Baldridge, Dustin, Bale, Jim, Bamshad, Michael, Barbouth, Deborah, Bayrak-Toydemir, Pinar, Beck, Anita, Beggs, Alan H., Behrens, Edward, Bejerano, Gill, Bellen, Hugo J., Bennett, Jimmy, Bernstein, Jonathan A., Berry, Gerard T., Bican, Anna, Bivona, Stephanie, Blue, Elizabeth, Bohnsack, John, Bonner, Devon, Botto, Lorenzo, Briere, Lauren C., Brown, Gabrielle, Burke, Elizabeth A., Burrage, Lindsay C., Butte, Manish J., Byers, Peter, Byrd, William E., Carey, John, Carrasquillo, Olveen, Cassini, Thomas, Chang, Ta Chen Peter, Chanprasert, Sirisak, Chao, HsiaoTuan, Chinn, Ivan, Clark, Gary D., Coakley, Terra R., Cobban, Laurel A., Cogan, Joy D., Coggins, Matthew, Cole, F. Sessions, Colley, Heather A., Cope, Heidi, Corona, Rosario, Craigen, William J., Crouse, Andrew B., Cunningham, Michael, D’Souza, Precilla, Dai, Hongzheng, Dasari, Surendra, Davis, Joie, Dayal, Jyoti G., Delgado, Margaret, Dell'Angelica, Esteban C., Dipple, Katrina, Doherty, Daniel, Dorrani, Naghmeh, Doss, Argenia L., Douine, Emilie D., Earl, Dawn, Eckstein, David J., Emrick, Lisa T., Eng, Christine M., Falk, Marni, Fieg, Elizabeth L., Fisher, Paul G., Fogel, Brent L., Forghani, Irman, Fu, Jiayu, Gahl, William A., Glass, Ian, Goddard, Page C., Godfrey, Rena A., Grajewski, Alana, Gropman, Andrea, Halley, Meghan C., Hamid, Rizwan, Hanchard, Neal, Hassey, Kelly, Hayes, Nichole, High, Frances, Hing, Anne, Hisama, Fuki M., Holm, Ingrid A., Hom, Jason, Horike-Pyne, Martha, Huang, Alden, Huang, Yan, Hutchison, Sarah, Introne, Wendy, Isasi, Rosario, Izumi, Kosuke, Jarvik, Gail P., Jarvik, Jeffrey, Jayadev, Suman, Jean-Marie, Orpa, Jobanputra, Vaidehi, Kaitryn, Emerald, Ketkar, Shamika, Kiley, Dana, Kilich, Gonench, Kobren, Shilpa N., Kohane, Isaac S., Kohler, Jennefer N., Korrick, Susan, Krakow, Deborah, Krasnewich, Donna M., Kravets, Elijah, Lalani, Seema R., Lam, Byron, Lam, Christina, Lanpher, Brendan C., Lanza, Ian R., LeBlanc, Kimberly, Lee, Brendan H., Levitt, Roy, Lewis, Richard A., Liu, Pengfei, Liu, Xue Zhong, Longo, Nicola, Loo, Sandra K., Loscalzo, Joseph, Maas, Richard L., Macnamara, Ellen F., MacRae, Calum A., Maduro, Valerie V., Maghiro, AudreyStephannie, Mahoney, Rachel, Malicdan, May Christine V., Mamounas, Laura A., Manolio, Teri A., Mao, Rong, Marom, Ronit, Marth, Gabor, Martin, Beth A., Martin, Martin G., Martínez-Agosto, Julian A., Marwaha, Shruti, McCauley, Jacob, McConkie-Rosell, Allyn, McCray, Alexa T., McGee, Elisabeth, Might, Matthew, Miller, Danny, Mirzaa, Ghayda, Morava, Eva, Moretti, Paolo, Morimoto, Marie, Mulvihill, John J., Nakano-Okuno, Mariko, Nelson, Stanley F., Nieves-Rodriguez, Shirley, Novacic, Donna, Oglesbee, Devin, Orengo, James P., Pace, Laura, Pak, Stephen, Pallais, J. Carl, Papp, Jeanette C., Parker, Neil H., Petcharet, Leoyklang, Phillips, John A., III, Posey, Jennifer E., Potocki, Lorraine, Swerdzewski, Barbara N. Pusey, Quinlan, Aaron, Rao, Deepak A., Raper, Anna, Raskind, Wendy, Renteria, Genecee, Reuter, Chloe M., Rives, Lynette, Robertson, Amy K., Rodan, Lance H., Rosenfeld, Jill A., Rosenthal, Elizabeth, Rossignol, Francis, Ruzhnikov, Maura, Sabaii, Marla, Sacco, Ralph, Sampson, Jacinda B., Saporta, Mario, Schaechter, Judy, Schedl, Timothy, Schoch, Kelly, Scott, Daryl A., Seto, Elaine, Sharma, Prashant, Shashi, Vandana, Shelkowitz, Emily, Sheppeard, Sam, Shin, Jimann, Silverman, Edwin K., Sinsheimer, Janet S., Sisco, Kathy, Smith, Edward C., Smith, Kevin S., Solnica-Krezel, Lilianna, Solomon, Ben, Spillmann, Rebecca C., Stergachis, Andrew, Stoler, Joan M., Sullivan, Kathleen, Sullivan, Jennifer A., Sutton, Shirley, Sweetser, David A., Sybert, Virginia, Tabor, Holly K., Tan, Queenie K.-G., Tan, Amelia L.M., Tarakad, Arjun, Taylor, Herman, Tekin, Mustafa, Telischi, Fred, Thorson, Willa, Tifft, Cynthia J., Toro, Camilo, Tran, Alyssa A., Ungar, Rachel A., Urv, Tiina K., Vanderver, Adeline, Velinder, Matt, Viskochil, Dave, Vogel, Tiphanie P., Wahl, Colleen E., Walker, Melissa, Walley, Nicole M., Wambach, Jennifer, Wan, Jijun, Wang, Lee-kai, Wangler, Michael F., Ward, Patricia A., Wegner, Daniel, Weisz Hubshman, Monika, Wener, Mark, Wenger, Tara, Westerfield, Monte, Wheeler, Matthew T., Whitlock, Jordan, Wolfe, Lynne A., Worley, Kim, Yamamoto, Shinya, Zhang, Zhe, Zuchner, Stephan, Scala, Marcello, Tomati, Valeria, Ferla, Matteo, Lena, Mariateresa, Cohen, Julie S., Fatemi, Ali, Brokamp, Elly, Koziura, Mary E., Nicouleau, Michael, Rio, Marlene, Siquier, Karine, Boddaert, Nathalie, Musante, Ilaria, Tamburro, Serena, Baldassari, Simona, Iacomino, Michele, Scudieri, Paolo, Bellus, Gary, Reed, Sara, Al Saif, Hind, Russo, Rossana Sanchez, Walsh, Matthew B., Cantagrel, Vincent, Crunk, Amy, Gustincich, Stefano, Ruggiero, Sarah M., Fitzgerald, Mark P., Helbig, Ingo, Striano, Pasquale, Severino, Mariasavina, Salpietro, Vincenzo, Pedemonte, Nicoletta, and Zara, Federico
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- 2024
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7. The Australian Trauma Registry (ATR): a leading clinical quality registry
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Fischer, Angela, Fitzgerald, Mark, Curtis, Kate, and Balogh, Zsolt J.
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- 2023
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8. A systematic review assessing incorporation of prophylactic splenic artery embolisation (pSAE) into trauma guidelines for the management of high-grade splenic injury
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Clements, Warren, Fitzgerald, Mark, Chennapragada, S. Murthy, Mathew, Joseph, Groombridge, Christopher, Ban, Ee Jun, and Lukies, Matthew W.
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- 2023
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9. Trauma-induced disturbances in ionized calcium levels correlate parabolically with coagulopathy, transfusion, and mortality: a multicentre cohort analysis from the TraumaRegister DGU®
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Helsloot, Dries, Fitzgerald, Mark, Lefering, Rolf, Verelst, Sandra, and Missant, Carlo
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- 2023
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10. A parametric model to jointly characterize rate, duration, and severity of exacerbations in episodic diseases
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Safari, Abdollah, Petkau, John, FitzGerald, Mark J., and Sadatsafavi, Mohsen
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- 2023
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11. Flail chest injury—changing management and outcomes
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Marasco, Silvana F., Nguyen Khuong, Jacqueline, Fitzgerald, Mark, Summerhayes, Robyn, Sekandarzad, Mir Wais, Varley, Vincent, Campbell, Ryan J., and Bailey, Michael
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- 2023
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12. Pamrevlumab plus nab-paclitaxel/gemcitabine (Pam + GA) as first- and second-line therapy in metastatic pancreatic cancer (mPDAC): Results from Precision Promise (PrP) Bayesian platform trial.
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Picozzi, Vincent J., Varghese, Anna M., Oberstein, Paul Eliezer, Hidalgo, Manuel, Wolpin, Brian M., Lim, Kian-Huat, McGlothlin, Anna, Graves, Todd, Detry, Michelle A., Fitzgerald, Mark, Bosse, Anna, Moravek, Cassadie, Pedersen, Samantha, Berkenblit, Anna, Chen, Jian, Carrier, Ewa, Adib, Deyaa R, Berry, Donald A., Simeone, Diane M., and Ko, Andrew H.
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- 2025
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13. Late-Onset Findings During Extended EEG Monitoring Are Rare in Critically Ill Children.
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Fung, France W., Parikh, Darshana S., Walsh, Kathleen, Fitzgerald, Mark P., Massey, Shavonne L., Topjian, Alexis A., and Abend, Nicholas S.
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- 2025
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14. Correction: Prophylaxis in healthcare workers during a pandemic: a model for a multi-centre international randomised controlled trial using Bayesian analyses
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Bruce, Pepa, Ainscough, Kate, Hatter, Lee, Braithwaite, Irene, Berry, Lindsay R., Fitzgerald, Mark, Hills, Thomas, Brickell, Kathy, Cosgrave, David, Semprini, Alex, Morpeth, Susan, Berry, Scott, Doran, Peter, Young, Paul, Beasley, Richard, and Nichol, Alistair
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- 2022
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15. Prophylaxis in healthcare workers during a pandemic: a model for a multi-centre international randomised controlled trial using Bayesian analyses
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Bruce Metadata, Pepa, Ainscough, Kate, Hatter, Lee, Braithwaite, Irene, Berry, Lindsay R., Fitzgerald, Mark, Hills, Thomas, Brickell, Kathy, Cosgrave, David, Semprini, Alex, Morpeth, Susan, Berry, Scott, Doran, Peter, Young, Paul, Beasley, Richard, and Nichol, Alistair
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- 2022
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16. Acute colonic pseudo-obstruction in polytrauma patients.
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Johnny, Cecil S., Schlegel, Richard N., Balachandran, Mayurathan, Casey, Laura, Mathew, Joseph, Carne, Peter, Varma, Dinesh, Ee-Jun Ban, and Fitzgerald, Mark C.
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- 2024
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17. Global modified Delphi consensus on diagnosis, phenotypes, and treatment of SCN8A‐related epilepsy and/or neurodevelopmental disorders
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Conecker, Gabrielle, primary, Xia, Maya Y., additional, Hecker, JayEtta, additional, Achkar, Christelle, additional, Cukiert, Cristine, additional, Devries, Seth, additional, Donner, Elizabeth, additional, Fitzgerald, Mark P., additional, Gardella, Elena, additional, Hammer, Michael, additional, Hegde, Anaita, additional, Hu, Chunhui, additional, Kato, Mitsuhiro, additional, Luo, Tian, additional, Schreiber, John M., additional, Wang, Yi, additional, Kooistra, Tammy, additional, Oudin, Madeleine, additional, Waldrop, Kayla, additional, Youngquist, J. Tyler, additional, Zhang, Dennis, additional, Wirrell, Elaine, additional, and Perry, M. Scott, additional
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- 2024
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18. Late-Onset Findings During Extended EEG Monitoring Are Rare in Critically Ill Children
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Fung, France W., primary, Parikh, Darshana S., additional, Walsh, Kathleen, additional, Fitzgerald, Mark P., additional, Massey, Shavonne L., additional, Topjian, Alexis A., additional, and Abend, Nicholas S., additional
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- 2024
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19. De novo variants in DENND5B cause a neurodevelopmental disorder
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Scala, Marcello, primary, Tomati, Valeria, additional, Ferla, Matteo, additional, Lena, Mariateresa, additional, Cohen, Julie S., additional, Fatemi, Ali, additional, Brokamp, Elly, additional, Bican, Anna, additional, Phillips, John A., additional, Koziura, Mary E., additional, Nicouleau, Michael, additional, Rio, Marlene, additional, Siquier, Karine, additional, Boddaert, Nathalie, additional, Musante, Ilaria, additional, Tamburro, Serena, additional, Baldassari, Simona, additional, Iacomino, Michele, additional, Scudieri, Paolo, additional, Rosenfeld, Jill A., additional, Bellus, Gary, additional, Reed, Sara, additional, Al Saif, Hind, additional, Russo, Rossana Sanchez, additional, Walsh, Matthew B., additional, Cantagrel, Vincent, additional, Crunk, Amy, additional, Gustincich, Stefano, additional, Ruggiero, Sarah M., additional, Fitzgerald, Mark P., additional, Helbig, Ingo, additional, Striano, Pasquale, additional, Severino, Mariasavina, additional, Salpietro, Vincenzo, additional, Pedemonte, Nicoletta, additional, Zara, Federico, additional, Acosta, Maria T., additional, Adams, David R., additional, Alvarez, Raquel L., additional, Alvey, Justin, additional, Allworth, Aimee, additional, Andrews, Ashley, additional, Ashley, Euan A., additional, Afzali, Ben, additional, Bacino, Carlos A., additional, Bademci, Guney, additional, Balasubramanyam, Ashok, additional, Baldridge, Dustin, additional, Bale, Jim, additional, Bamshad, Michael, additional, Barbouth, Deborah, additional, Bayrak-Toydemir, Pinar, additional, Beck, Anita, additional, Beggs, Alan H., additional, Behrens, Edward, additional, Bejerano, Gill, additional, Bellen, Hugo J., additional, Bennett, Jimmy, additional, Bernstein, Jonathan A., additional, Berry, Gerard T., additional, Bivona, Stephanie, additional, Blue, Elizabeth, additional, Bohnsack, John, additional, Bonner, Devon, additional, Botto, Lorenzo, additional, Briere, Lauren C., additional, Brown, Gabrielle, additional, Burke, Elizabeth A., additional, Burrage, Lindsay C., additional, Butte, Manish J., additional, Byers, Peter, additional, Byrd, William E., additional, Carey, John, additional, Carrasquillo, Olveen, additional, Cassini, Thomas, additional, Chang, Ta Chen Peter, additional, Chanprasert, Sirisak, additional, Chao, HsiaoTuan, additional, Chinn, Ivan, additional, Clark, Gary D., additional, Coakley, Terra R., additional, Cobban, Laurel A., additional, Cogan, Joy D., additional, Coggins, Matthew, additional, Cole, F. Sessions, additional, Colley, Heather A., additional, Cope, Heidi, additional, Corona, Rosario, additional, Craigen, William J., additional, Crouse, Andrew B., additional, Cunningham, Michael, additional, D’Souza, Precilla, additional, Dai, Hongzheng, additional, Dasari, Surendra, additional, Davis, Joie, additional, Dayal, Jyoti G., additional, Delgado, Margaret, additional, Dell'Angelica, Esteban C., additional, Dipple, Katrina, additional, Doherty, Daniel, additional, Dorrani, Naghmeh, additional, Doss, Argenia L., additional, Douine, Emilie D., additional, Earl, Dawn, additional, Eckstein, David J., additional, Emrick, Lisa T., additional, Eng, Christine M., additional, Falk, Marni, additional, Fieg, Elizabeth L., additional, Fisher, Paul G., additional, Fogel, Brent L., additional, Forghani, Irman, additional, Fu, Jiayu, additional, Gahl, William A., additional, Glass, Ian, additional, Goddard, Page C., additional, Godfrey, Rena A., additional, Grajewski, Alana, additional, Gropman, Andrea, additional, Halley, Meghan C., additional, Hamid, Rizwan, additional, Hanchard, Neal, additional, Hassey, Kelly, additional, Hayes, Nichole, additional, High, Frances, additional, Hing, Anne, additional, Hisama, Fuki M., additional, Holm, Ingrid A., additional, Hom, Jason, additional, Horike-Pyne, Martha, additional, Huang, Alden, additional, Huang, Yan, additional, Hutchison, Sarah, additional, Introne, Wendy, additional, Isasi, Rosario, additional, Izumi, Kosuke, additional, Jarvik, Gail P., additional, Jarvik, Jeffrey, additional, Jayadev, Suman, additional, Jean-Marie, Orpa, additional, Jobanputra, Vaidehi, additional, Kaitryn, Emerald, additional, Ketkar, Shamika, additional, Kiley, Dana, additional, Kilich, Gonench, additional, Kobren, Shilpa N., additional, Kohane, Isaac S., additional, Kohler, Jennefer N., additional, Korrick, Susan, additional, Krakow, Deborah, additional, Krasnewich, Donna M., additional, Kravets, Elijah, additional, Lalani, Seema R., additional, Lam, Byron, additional, Lam, Christina, additional, Lanpher, Brendan C., additional, Lanza, Ian R., additional, LeBlanc, Kimberly, additional, Lee, Brendan H., additional, Levitt, Roy, additional, Lewis, Richard A., additional, Liu, Pengfei, additional, Liu, Xue Zhong, additional, Longo, Nicola, additional, Loo, Sandra K., additional, Loscalzo, Joseph, additional, Maas, Richard L., additional, Macnamara, Ellen F., additional, MacRae, Calum A., additional, Maduro, Valerie V., additional, Maghiro, AudreyStephannie, additional, Mahoney, Rachel, additional, Malicdan, May Christine V., additional, Mamounas, Laura A., additional, Manolio, Teri A., additional, Mao, Rong, additional, Marom, Ronit, additional, Marth, Gabor, additional, Martin, Beth A., additional, Martin, Martin G., additional, Martínez-Agosto, Julian A., additional, Marwaha, Shruti, additional, McCauley, Jacob, additional, McConkie-Rosell, Allyn, additional, McCray, Alexa T., additional, McGee, Elisabeth, additional, Might, Matthew, additional, Miller, Danny, additional, Mirzaa, Ghayda, additional, Morava, Eva, additional, Moretti, Paolo, additional, Morimoto, Marie, additional, Mulvihill, John J., additional, Nakano-Okuno, Mariko, additional, Nelson, Stanley F., additional, Nieves-Rodriguez, Shirley, additional, Novacic, Donna, additional, Oglesbee, Devin, additional, Orengo, James P., additional, Pace, Laura, additional, Pak, Stephen, additional, Pallais, J. Carl, additional, Papp, Jeanette C., additional, Parker, Neil H., additional, Petcharet, Leoyklang, additional, Posey, Jennifer E., additional, Potocki, Lorraine, additional, Swerdzewski, Barbara N. Pusey, additional, Quinlan, Aaron, additional, Rao, Deepak A., additional, Raper, Anna, additional, Raskind, Wendy, additional, Renteria, Genecee, additional, Reuter, Chloe M., additional, Rives, Lynette, additional, Robertson, Amy K., additional, Rodan, Lance H., additional, Rosenthal, Elizabeth, additional, Rossignol, Francis, additional, Ruzhnikov, Maura, additional, Sabaii, Marla, additional, Sacco, Ralph, additional, Sampson, Jacinda B., additional, Saporta, Mario, additional, Schaechter, Judy, additional, Schedl, Timothy, additional, Schoch, Kelly, additional, Scott, Daryl A., additional, Seto, Elaine, additional, Sharma, Prashant, additional, Shashi, Vandana, additional, Shelkowitz, Emily, additional, Sheppeard, Sam, additional, Shin, Jimann, additional, Silverman, Edwin K., additional, Sinsheimer, Janet S., additional, Sisco, Kathy, additional, Smith, Edward C., additional, Smith, Kevin S., additional, Solnica-Krezel, Lilianna, additional, Solomon, Ben, additional, Spillmann, Rebecca C., additional, Stergachis, Andrew, additional, Stoler, Joan M., additional, Sullivan, Kathleen, additional, Sullivan, Jennifer A., additional, Sutton, Shirley, additional, Sweetser, David A., additional, Sybert, Virginia, additional, Tabor, Holly K., additional, Tan, Queenie K.-G., additional, Tan, Amelia L.M., additional, Tarakad, Arjun, additional, Taylor, Herman, additional, Tekin, Mustafa, additional, Telischi, Fred, additional, Thorson, Willa, additional, Tifft, Cynthia J., additional, Toro, Camilo, additional, Tran, Alyssa A., additional, Ungar, Rachel A., additional, Urv, Tiina K., additional, Vanderver, Adeline, additional, Velinder, Matt, additional, Viskochil, Dave, additional, Vogel, Tiphanie P., additional, Wahl, Colleen E., additional, Walker, Melissa, additional, Walley, Nicole M., additional, Wambach, Jennifer, additional, Wan, Jijun, additional, Wang, Lee-kai, additional, Wangler, Michael F., additional, Ward, Patricia A., additional, Wegner, Daniel, additional, Weisz Hubshman, Monika, additional, Wener, Mark, additional, Wenger, Tara, additional, Westerfield, Monte, additional, Wheeler, Matthew T., additional, Whitlock, Jordan, additional, Wolfe, Lynne A., additional, Worley, Kim, additional, Yamamoto, Shinya, additional, Zhang, Zhe, additional, and Zuchner, Stephan, additional
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- 2024
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20. Damage Control Interventional Radiology (DCIR): Evolving Value of Interventional Radiology in Trauma
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Mathew, Joseph K. and Fitzgerald, Mark C.
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- 2022
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21. Indigenous Data Sovereignty and Governance: The Australian Traumatic Brain Injury National Data Project
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Ryder, Courtney, Wilson, Roland, D’Angelo, Shane, O’Reilly, Gerard M., Mitra, Biswadev, Hunter, Kate, Kim, Yen, Rushworth, Nick, Tee, Jin, Hendrie, Delia, Fitzgerald, Mark C., and Curtis, Kate
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- 2022
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22. Periodic Discharges in Critically Ill Children: Predictors and Outcome
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Fung, France W., primary, Parikh, Darshana S., additional, Massey, Shavonne L., additional, Fitzgerald, Mark P., additional, Vala, Lisa, additional, Donnelly, Maureen, additional, Jacobwitz, Marin, additional, Kessler, Sudha K., additional, Xiao, Rui, additional, Topjian, Alexis A., additional, and Abend, Nicholas S., additional
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- 2023
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23. GETTING OUT OF THE LABYRINTH: GERALD BARRY'S WIENER BLUTAND THE PATH TO PETRA VON KANT
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Fitzgerald, Mark
- Abstract
AbstractGerald Barry's approach to composition has undergone a number of changes. Frequently these developments coincide with the composition of a large-scale opera. One of these points of transition in his output occurs in the period before he commenced work on The Bitter Tears of Petra von Kant. Between 1999 and 2000 Barry composed three works – 1998, The Eternal Recurrenceand Wiener Blut– in which he attempted to find a new compositional direction after a period in which canonic proliferation dominated his musical material. This article examines some of the main traits of these works, and Wiener Blutin particular, since it contains a greater variety of approaches than the other two compositions. The article also considers how Barry's shift in approach may have been linked to his decision to set Rainer Werner Fassbinder's play. Its quite plain, realistic prose was a contrast to the sort of text Barry had previously chosen to set, requiring a different musical response, and the article draws out some possible connections between Barry's three ‘pointillistic’ compositions and the opera.
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- 2024
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24. Dupilumab Reduces Exacerbations Independent of Changes in Biomarkers in Moderate-to-Severe Asthma
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Pavord, Ian D., Casale, Thomas B., Corren, Jonathan, FitzGerald, Mark J., Deniz, Yamo, Altincatal, Arman, Gall, Rebecca, Pandit-Abid, Nami, Radwan, Amr, Jacob-Nara, Juby A., Rowe, Paul J., and Busse, William W.
- Abstract
Changes from baseline in fractional exhaled nitric oxide (FeNO) and blood eosinophil count (Eos) may be related to efficacy outcomes in dupilumab-treated patients with moderate-to-severe asthma.
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- 2024
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25. Periodic Discharges in Critically Ill Children: Predictors and Outcome.
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Fung, France W., Parikh, Darshana S., Massey, Shavonne L., Fitzgerald, Mark P., Vala, Lisa, Donnelly, Maureen, Jacobwitz, Marin, Kessler, Sudha K., Rui Xiao, Topjian, Alexis A., and Abend, Nicholas S.
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- 2024
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26. A quality improvement initiative to improve folic acid supplementation counseling for adolescent females with epilepsy
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Molisani, Sara E., primary, Parikh, Darshana, additional, DiGiovine, Marissa, additional, Dlugos, Dennis, additional, Fitzgerald, Mark P., additional, Fried, Lawrence, additional, Helbig, Ingo, additional, Kessler, Sudha Kilaru, additional, McDonnell, Pamela Pojomovsky, additional, Melamed, Susan, additional, Prelack, Marisa S., additional, Sharif, Uzma, additional, Tefft, Sarah, additional, Tencer, Jaclyn, additional, Witzman, Stephanie, additional, Shaw, Kathy, additional, and Abend, Nicholas S., additional
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- 2023
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27. Precision Promise (PrP) Bayesian platform trial for metastatic pancreatic cancer (mPDAC): Results of the first experimental arm, SM-88 as second line therapy.
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Oberstein, Paul Eliezer, wang-gillam, Andrea, Varghese, Anna M., Ko, Andrew H., Hendifar, Andrew Eugene, Ocean, Allyson J., McGlothlin, Anna, Graves, Todd, Berry, Scott M., Detry, Michelle A., Fitzgerald, Mark, Bosse, Anna, Moravek, Cassadie, Feehan, Kelly, Howland, Carrie Meghann, Berry, Donald A., Simeone, Diane M., and Picozzi, Vincent J.
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- 2024
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28. Data from Suppression of Breast Cancer Stem Cells and Tumor Growth by the RUNX1 Transcription Factor
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Hong, Deli, primary, Fritz, Andrew J., primary, Finstad, Kristiaan H., primary, Fitzgerald, Mark P., primary, Weinheimer, Adam, primary, Viens, Adam L., primary, Ramsey, Jon, primary, Stein, Janet L., primary, Lian, Jane B., primary, and Stein, Gary S., primary
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- 2023
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29. Supplementary Figures 1-10 from Suppression of Breast Cancer Stem Cells and Tumor Growth by the RUNX1 Transcription Factor
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Hong, Deli, primary, Fritz, Andrew J., primary, Finstad, Kristiaan H., primary, Fitzgerald, Mark P., primary, Weinheimer, Adam, primary, Viens, Adam L., primary, Ramsey, Jon, primary, Stein, Janet L., primary, Lian, Jane B., primary, and Stein, Gary S., primary
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- 2023
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30. Leveraging electronic medical record-embedded standardised electroencephalogram reporting to develop neonatal seizure prediction models: a retrospective cohort study
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McKee, Jillian L, primary, Kaufman, Michael C, additional, Gonzalez, Alexander K, additional, Fitzgerald, Mark P, additional, Massey, Shavonne L, additional, Fung, France, additional, Kessler, Sudha K, additional, Witzman, Stephanie, additional, Abend, Nicholas S, additional, and Helbig, Ingo, additional
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- 2023
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31. Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders
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Burglen, Lydie, primary, Van Hoeymissen, Evelien, primary, Qebibo, Leila, additional, Barth, Magalie, additional, Belnap, Newell, additional, Boschann, Felix, additional, Depienne, Christel, additional, De Clercq, Katrien, additional, Douglas, Andrew GL, additional, Fitzgerald, Mark P, additional, Foulds, Nicola, additional, Garel, Catherine, additional, Helbig, Ingo, additional, Held, Katharina, additional, Horn, Denise, additional, Janssen, Annelies, additional, Kaindl, Angela M, additional, Narayanan, Vinodh, additional, Prager, Christina, additional, Rupin-Mas, Mailys, additional, Afenjar, Alexandra, additional, Zhao, Siyuan, additional, Ramaekers, Vincent Th, additional, Ruggiero, Sarah M, additional, Thomas, Simon, additional, Valence, Stéphanie, additional, Van Maldergem, Lionel, additional, Rohacs, Tibor, additional, Rodriguez, Diana, additional, Dyment, David, additional, Voets, Thomas, additional, and Vriens, Joris, additional
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- 2023
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32. A 12-year experience in the management of traumatic bladder rupture at an Australian level 1 trauma centre.
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Yao, Henry H., Fletcher, Jan, Grummet, Jeremy, Royce, Peter L., Fitzgerald, Mark, and Hanegbi, Uri
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Objective: To review the contemporary bladder trauma epidemiology, diagnosis and management over a 12-year period at a level 1 trauma centre in Australia. Patients and Methods: From July 2001 through June 2013, 97 multi-trauma patients at a level 1 trauma centre in Australia were identified to have sustained bladder rupture. Data on demographics, clinical presentation, diagnosis, management and complications were extracted from the TraumaNET database, medical records and health-coding database. Results: Of the 97 patients, 98% of bladder ruptures resulted from blunt trauma mostly from road accidents. There was a male preponderance of 64%. Intra-peritoneal bladder rupture (51%) was the most common type of injury followed by extra-peritoneal bladder ruptures (42%) and combined intra- and extra-peritoneal bladder ruptures (7%). Concomitant pelvic fractures occurred in 78% of patients and concurrent intra-abdominal injuries in 68%. Initial imaging missed 28% of bladder ruptures, with computed tomography with intravenous contrast missing 65% of bladder ruptures. The majority of intra-peritoneal bladder ruptures and 56% of extra-peritoneal bladder ruptures were repaired surgically, with 83% of repairs performed in conjunction with another surgical procedure. The in-hospital mortality rate was 9%, and all deaths were due to concomitant injuries. Conclusion: Traumatic bladder rupture is associated with a 9% mortality rate due to the frequently associated significant concurrent injuries. Computed tomography cystogram or plain cystogram is the imaging modality of choice in diagnosing bladder rupture. Intra-peritoneal bladder ruptures should be repaired surgically, while extra-peritoneal bladder ruptures can be treated conservatively in selected patients. The timing of surgical repair should be coordinated with other specialties. Level of evidence: 4 [ABSTRACT FROM AUTHOR]
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- 2023
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33. Hospitalisations and in‐hospital deaths following moderate to severe traumatic brain injury in Australia, 2015–20: a registry data analysis for the Australian Traumatic Brain Injury National Data (ATBIND) project.
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O'Reilly, Gerard M, Curtis, Kate, Mitra, Biswadev, Kim, Yesul, Afroz, Afsana, Hunter, Kate, Ryder, Courtney, Hendrie, Delia V, Rushworth, Nick, Tee, Jin, D'Angelo, Shane, Solly, Emma, Bhattacharya, Oashe, and Fitzgerald, Mark C
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Objective: To describe the frequency of hospitalisation and in‐hospital death following moderate to severe traumatic brain injury (TBI) in Australia, both overall and by patient demographic characteristics and the nature and severity of the injury. Design, setting: Cross‐sectional study; analysis of Australia New Zealand Trauma Registry data. Participants: People with moderate to severe TBI (Abbreviated Injury Score [head] greater than 2) who were admitted to or died in one of the twenty‐three major Australian trauma services that contributed data to the ATR throughout the study period, 1 July 2015 – 30 June 2020. Major outcome measures: Primary outcome: number of hospitalisations with moderate to severe TBI; secondary outcome: number of deaths in hospital following moderate to severe TBI. Results: During 2015–20, 16 350 people were hospitalised with moderate to severe TBI (mean, 3270 per year), of whom 2437 died in hospital (14.9%; mean, 487 per year). The mean age at admission was 50.5 years (standard deviation [SD], 26.1 years), and 11 644 patients were male (71.2%); the mean age of people who died in hospital was 60.4 years (SD, 25.2 years), and 1686 deaths were of male patients (69.2%). The overall number of hospitalisations did not change during 2015–20 (per year: incidence rate ratio [IRR], 1.00; 95% confidence interval [CI], 0.99–1.02) and death (IRR, 1.00; 95% CI, 0.97–1.03). Conclusion: Injury prevention and trauma care interventions for people with moderate to severe TBI in Australia reduced neither the incidence of the condition nor the associated in‐hospital mortality during 2015–20. More effective care strategies are required to reduce the burden of TBI, particularly among younger men. [ABSTRACT FROM AUTHOR]
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- 2023
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34. Pharmacists in Trauma: a randomised controlled trial of emergency medicine pharmacists in trauma response teams
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Roman, Cristina, Dooley, Michael, Fitzgerald, Mark, Smit, De Villiers, Cameron, Peter, and Mitra, Biswadev
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BackgroundAnalgesia is an important component for patient well-being, but commonly delayed during trauma resuscitation. The Pharmacists in Trauma trial assessed the effects of integrating pharmacists into trauma response teams to improve analgesia delivery and medication management.MethodsThis unblinded randomised trial compared emergency medicine (EM) pharmacist involvement in trauma callouts versus standard care at an Australian level 1 trauma centre. Randomisation was performed via an online single sequence randomisation service. Eligible patients included those managed with a trauma callout during working hours of an EM pharmacist. Pharmacists were able to prescribe medications using a Partnered Pharmacist Medication Charting model. The primary outcome was the proportion of patients who had first dose analgesia within 30 min compared using the χ2test.ResultsFrom 15 July 2021 until 31 January 2022, there were 119 patients randomised with 37 patients excluded as no analgesia was required. There were 82 patients included for analysis, 39 in the control arm and 43 in the intervention arm. The primary outcome was achieved in 25 (64.1%) patients in the control arm and 36 (83.7%) patients in the pharmacist arm (relative risk 1.31; 95% CI 1.0 to 1.71; p=0.042). Time to analgesia in the control arm was 28 (22–35) mins and 20 (15–26 mins) with pharmacist involvement; p=0.025. In the pharmacist arm, the initial dose of analgesia was prescribed by the pharmacist for 38 (88.4%) patients. There were 27 other medications prescribed by the pharmacist for the management of these patients. There were no differences in emergency and trauma centre or hospital length of stay.ConclusionAddition of the EM pharmacist in trauma response teams improved time to analgesia. Involvement of an EM pharmacist in trauma reception and resuscitation may assist by optimising medication management, with members of the team more available to focus on other life-saving interventions.Trial registration numberACTRN12621000338864.
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- 2024
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35. Author response: Gain-of-function variants in the ion channel gene TRPM3 underlie a spectrum of neurodevelopmental disorders
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Burglen, Lydie, primary, Van Hoeymissen, Evelien, primary, Qebibo, Leila, additional, Barth, Magalie, additional, Belnap, Newell, additional, Boschann, Felix, additional, Depienne, Christel, additional, De Clercq, Katrien, additional, Douglas, Andrew GL, additional, Fitzgerald, Mark P, additional, Foulds, Nicola, additional, Garel, Catherine, additional, Helbig, Ingo, additional, Held, Katharina, additional, Horn, Denise, additional, Janssen, Annelies, additional, Kaindl, Angela M, additional, Narayanan, Vinodh, additional, Prager, Christina, additional, Rupin-Mas, Mailys, additional, Afenjar, Alexandra, additional, Zhao, Siyuan, additional, Ramaekers, Vincent Th, additional, Ruggiero, Sarah M, additional, Thomas, Simon, additional, Valence, Stéphanie, additional, Van Maldergem, Lionel, additional, Rohacs, Tibor, additional, Rodriguez, Diana, additional, Dyment, David, additional, Voets, Thomas, additional, and Vriens, Joris, additional
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- 2022
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36. WE-180. Neonatal seizure prediction algorithms based on EMR-embedded standardized EEG reporting
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McKee, Jillian L., primary, Kaufman, Michael C., additional, Gonzalez, Alexander K., additional, Massey, Shavonne L., additional, Fung, France W., additional, Fitzgerald, Mark P., additional, Kessler, Sudha K., additional, Witzman, Stephanie, additional, Abend, Nicholas S., additional, and Helbig, Ingo, additional
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- 2022
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37. Seizure prediction in 1117 neonates leveraging EMR-embedded standardized EEG reporting
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McKee, Jillian L, primary, Kaufman, Michael, additional, Gonzalez, Alexander, additional, Fitzgerald, Mark P, additional, Massey, Shavonne L, additional, Fung, France, additional, Kessler, Sudha K, additional, Witzman, Stephanie, additional, Abend, Nicholas, additional, and Helbig, Ingo, additional
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- 2022
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38. Oral health literacy education and practice in US dental hygiene programs: A national survey.
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Lawler, Heather M., Farrell, Chris, Fitzgerald, Mark, Jones, Darlene, and Cullen, Jennifer
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Purpose/Objectives: Studies have shown a significant relationship between low oral health literacy (OHL) and poor oral health outcomes. National calls for action include better training of dental providers to meet the needs of the low OHL public. The purpose of this research was to determine the extent OHL education is being included in US dental hygiene (DH) education programs. Methods: In fall of 2020, a 23-itemdigital survey was sent to 321 Commission on Dental Accreditation-accredited DH schools in the US. Results: Survey generated 90 eligible responses (28%). Respondents reported that OHL education is being included in DH curricula to some degree. Communication strategies (82.4%) were the most likely OHL concept to be taught. Subject areas included community health (89%), cultural competency (78%), and special populations (78%). Respondents ranked lack of assessment instruments, lack of concrete activities, lack of clear understanding of OHL, and difficulty in implementing OHL concepts as the top barriers to incorporating OHL education in the DH curriculum. Conclusion(s): OHL is an established determinant of oral health. As prevention and patient education experts, dental hygienists play an important role in improving patient OHL. More fully integrating OHL into DH curricula would provide future DHs with the training needed to improve oral health outcomes and would better align DH education programs with national OHL initiatives. [ABSTRACT FROM AUTHOR]
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- 2023
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39. Child neurology telemedicine: Analyzing 14 820 patient encounters during the first year of the COVID‐19 pandemic.
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Kaufman, Michael C., Xian, Julie, Galer, Peter D., Parthasarathy, Shridhar, Gonzalez, Alexander K., McKee, Jillian L., Prelack, Marisa S., Fitzgerald, Mark P., Helbig, Ingo, Ruggiero, Sarah Mckeown, Craig, Sansanee, Rametta, Salvatore C., Molisani, Sara E., Sharif, Uzma, Melamed, Susan E., Digiovine, Marissa, Fried, Lawrence, Malcolm, Marissa P., Kessler, Sudha Kilaru, and Chadehumbe, Madeline
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COVID-19 pandemic ,PATIENT portals ,TELEMEDICINE ,NEUROMUSCULAR diseases ,NOSOLOGY - Abstract
Aim: To determine the long‐term impact of telemedicine in child neurology care during the COVID‐19 pandemic and with the reopening of outpatient clinics. Method: We performed an observational cohort study of 34 837 in‐person visits and 14 820 telemedicine outpatient visits across 26 399 individuals. We assessed differences in care across visit types, time‐period observed, time between follow‐ups, patient portal activation rates, and demographic factors. Results: We observed a higher proportion of telemedicine for epilepsy (International Classification of Diseases, 10th Revision G40: odds ratio [OR] 1.4, 95% confidence interval [CI] 1.3–1.5) and a lower proportion for movement disorders (G25: OR 0.7, 95% CI 0.6–0.8; R25: OR 0.7, 95% CI 0.6–0.9) relative to in‐person visits. Infants were more likely to be seen in‐person after reopening clinics than by telemedicine (OR 1.6, 95% CI 1.5–1.8) as were individuals with neuromuscular disorders (OR 1.6, 95% CI 1.5–1.7). Self‐reported racial and ethnic minority populations and those with highest social vulnerability had lower telemedicine participation rates (OR 0.8, 95% CI 0.8–0.8; OR 0.7, 95% CI 0.7–0.8). Interpretation: Telemedicine continued to be utilized even once in‐person clinics were available. Pediatric epilepsy care can often be performed using telemedicine while young patients with neuromuscular disorders often require in‐person assessment. Prominent barriers for socially vulnerable families and racial and ethnic minorities persist. [ABSTRACT FROM AUTHOR]
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- 2023
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40. Salmonella bovismorbificans abscess masking a primary testicular tumour in the retroperitoneum – A case report.
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Fitzgerald, Mark and Kamath, Sheshang
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Testicular tumours can present outside the testis in about 5 % of cases, including as a primary lesion within the retroperitoneal space. These arise insidiously and can be hard to detect. Salmonella is an uncommon cause of abscess formation and the subtype of bovismorbificans, arising from geckos, only scarcely reported to cause an abscess. We describe a case in line with SCARE Criteria where a retroperitoneal non-seminomatous germ cell tumour presented with a salmonella bovismorbificans abscess and subsequent bacteraemia. A 37 year old male presented unwell with fevers and right flank pain suggestive of pyelonephritis. He had a salmonella bacteraemia on initial blood cultures, subsequently isolated to be salmonella bovismorbificans, and a CT scan demonstrate a large 7.7 cm retroperitoneal mass with surrounding lymphadenopathy. An initial attempt at tissue sampling failed as the lesion was filled with purulent material requiring a pig tail drain to remain in place. He progressed slowly with resolution of fevers and bacteraemia however the lesion did not reduce in size despite adequate antibiotic treatment for two weeks. A repeat core biopsy and aspiration after 19 days revealed ongoing salmonella infection with a yolk sac tumour and seminoma. His AFP markers at this time were elevated at 3330kIU/L. A underlying malignancy should be consider when a retroperitoneal abscess fails to resolve with adequate treatment especially when a organism unknown to cause abscess is isolated. • Testicular tumour presenting primarily as an abscess outside of the testis is rare. • Commonly found within North Australian geckos, Salmonella Bovismorbificans can cause abscesses. • A retroperitoneal testicular cancer complicated by a salmonella Bovismorbificans abscess. [ABSTRACT FROM AUTHOR]
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- 2024
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41. Comparison of fibre-optic-guided endotracheal intubation through a supraglottic airway device versus hyperangulated video laryngoscopy by emergency physicians: A randomised controlled study in cadavers
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Groombridge, Christopher J, Maini, Amit, Mathew, Joseph, Fritz, Peter, Kim, Yesul, Fitzgerald, Mark, Smit, De Villiers, and O’Reilly, Gerard
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Background: After failed endotracheal intubation, using direct laryngoscopy, rescued using a supraglottic airway device, the choice of subsequent method to secure a definitive airway is not clearly determined.Objective: The aim of this study was to compare the time to intubation using a fibre-optic airway scope, to guide an endotracheal tube through the supraglottic airway device, with a more conventional approach using a hyperangulated video laryngoscope.Methods: A single-centre randomised controlled trial was undertaken. The population studied were emergency physicians working in an adult major trauma centre. The intervention was intubation through a supraglottic airway device guided by a fibre-optic airway scope. The comparison was intubation using a hyperangulated video laryngoscope. The primary outcome was time to intubation. The trial was registered with ANZCTR.org.au (ACTRN12621000018819).Results: Four emergency physicians completed intubations using both of the two airway devices on four cadavers for a total of 32 experiments. The mean time to intubation was 14.0 s (95% confidence interval = 11.1–16.8) in the hyperangulated video laryngoscope group compared with 29.2 s (95% confidence interval = 20.7–37.7) in the fibre-optic airway scope group; a difference of 15.2 s (95% confidence interval = 8.7–21.7, p< 0.001). All intubations were completed within 2 min, and there were no equipment failures or evidence of airway trauma.Conclusion: Successful intubation of the trachea without airway trauma by emergency physicians in cadavers is achievable by either fibre-optic airway scope via a supraglottic airway device or hyperangulated video laryngoscope. Hyperangulated video laryngoscope was statisticallybut arguably not clinicallysignificantly faster than fibre-optic airway scope via supraglottic airway device.
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- 2023
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42. Risk Stratification of Elderly Patients Undergoing Spinal Surgery Using the Modified Frailty Index
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Kweh, Barry Ting Sheen, Lee, Hui Qing, Tan, Terence, Tew, Kim Siong, Leong, Ronald, Fitzgerald, Mark, Matthew, Joseph, Kambourakis, Anthony, Liew, Susan, Hunn, Martin, and Tee, Jin Wee
- Abstract
Study Design: Retrospective cohort.Objectives: To validate the 11-item modified Frailty Index (mFI) as a perioperative risk stratification tool in elderly patients undergoing spine surgery.Methods: All consecutive cases of spine surgery in patients aged 65 years or older between July 2016 and June 2018 at a state-wide trauma center were retrospectively reviewed. The primary outcome was post-operative major complication rate (Clavien-Dindo Classification ≥ III). Secondary outcome measures included the rate of all complications, 6-month mortality and surgical site infection.Results: A total of 348 cases were identified. The major complication rate was significantly lower in patients with an mFI of 0 compared to ≥ 0.45 (18.3% versus 42.5%, P= .049). As the mFI increased from 0 to ≥ 0.45 there was a stepwise increase in risk of major complications (P< .001). Additionally, 6-month mortality rate was considerably lower when the mFI was 0 rather than ≥ 0.27 (4.2% versus 20.4%, P= .007). Multivariate analysis demonstrated an mFI ≥ 0.27 was significantly associated with an increased incidence of major complication (OR 2.80, 95% CI 1.46-5.35, P= .002), all complication (OR 2.93, 95% CI 1.70-15.11, P< .001), 6-month mortality (OR 7.39, 95% CI 2.55-21.43, P< .001) and surgical site infection (OR 4.43, 95% CI 1.71-11.51, P= .002). The American Society of Anesthesiologists’ (ASA) index did not share a stepwise relationship with any outcome.Conclusion: The mFI is significantly associated in a gradated fashion with increased morbidity and mortality. Patients with an mFI ≥ 0.27 are at greater risk of major complications, all-complications, 6-monthy mortality, and surgical site infection.
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- 2023
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43. The Australian Traumatic Brain Injury National Data (ATBIND) project: a mixed methods study protocol.
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O'Reilly, Gerard M, Curtis, Kate, Kim, Yesul, Mitra, Biswadev, Hunter, Kate, Ryder, Courtney, Hendrie, Delia V, Rushworth, Nick, Afroz, Afsana, D'Angelo, Shane, Tee, Jin, and Fitzgerald, Mark C
- Abstract
Background: Traumatic brain injury (TBI) is the largest contributor to death and disability in people who have experienced physical trauma. There are no national data on outcomes for people with moderate to severe TBI in Australia.Objectives: To determine the incidence and key determinants of outcomes for patients with moderate to severe TBI, both for Australia and for selected population subgroups, including Aboriginal and Torres Strait Islander Australians.Methods and Analysis: The Australian Traumatic Brain Injury National Data (ATBIND) project will analyse Australia New Zealand Trauma Registry (ATR) data and National Coronial Information Service (NCIS) deaths data. The ATR documents the demographic characteristics, injury event description and severity, processes of care, and outcomes for people with major injury, including TBI, assessed and managed at the 27 major trauma services in Australia. We will include data for people with moderate to severe TBI (Abbreviated Injury Scale [AIS] (head) score higher than 2) who had Injury Severity Scores [ISS] higher than 12 or who died in hospital. People will also be included if they died before reaching a major trauma service and the coronial report details were consistent with moderate to severe TBI. The primary research outcome will be survival to discharge. Secondary outcomes will be hospital discharge destination, hospital length of stay, ventilator-free days, and health service cost.Ethics Approval: The Alfred Ethics Committee approved ATR data extraction (project reference number 670/21). Further ethics approval has been sought from the NCIS and multiple Aboriginal health research ethics committees. The ATBIND project will conform with Indigenous data sovereignty principles.Dissemination Of Results: Our findings will be disseminated by project partners with the aim of informing improvements in equitable system-level care for all people in Australia with moderate to severe TBI.Study Registration: Not applicable. [ABSTRACT FROM AUTHOR]- Published
- 2022
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44. Bladder inflation to reduce hemorrhage secondary to a pelvic fracture
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Fitzgerald, Mark, Phan, Tuan, Fitzgerald, Sarah, Xiao, Yuewei, Green, Madeline, Johnny, Cecil, Mathew, Joseph, Gocentas, Robert, and Clements, Warren
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Bladder inflation may be a temporizing measure to tamponade pelvic bleeding in select trauma cases to bridge the patient to definitive interventions. Ultrasonographic confirmation of an intact bladder with an adjacent pelvic haematoma in a shocked adult with pelvic fracture is used for subject selection. An illustrative example of physiologic and interventional radiological control of pelvic bleeding following bladder inflation with sterile saline is presented.
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- 2024
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45. Molnupiravir plus usual care versus usual care alone as early treatment for adults with COVID-19 at increased risk of adverse outcomes (PANORAMIC): an open-label, platform-adaptive randomised controlled trial
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Butler, Christopher C, Hobbs, F D Richard, Gbinigie, Oghenekome A, Rahman, Najib M, Hayward, Gail, Richards, Duncan B, Dorward, Jienchi, Lowe, David M, Standing, Joseph F, Breuer, Judith, Khoo, Saye, Petrou, Stavros, Hood, Kerenza, Nguyen-Van-Tam, Jonathan S, Patel, Mahendra G, Saville, Benjamin R, Marion, Joe, Ogburn, Emma, Allen, Julie, Rutter, Heather, Francis, Nick, Thomas, Nicholas P B, Evans, Philip, Dobson, Melissa, Madden, Tracie-Ann, Holmes, Jane, Harris, Victoria, Png, May Ee, Lown, Mark, van Hecke, Oliver, Detry, Michelle A, Saunders, Christina T, Fitzgerald, Mark, Berry, Nicholas S, Mwandigha, Lazaro, Galal, Ushma, Mort, Sam, Jani, Bhautesh D, Hart, Nigel D, Ahmed, Haroon, Butler, Daniel, McKenna, Micheal, Chalk, Jem, Lavallee, Layla, Hadley, Elizabeth, Cureton, Lucy, Benysek, Magdalena, Andersson, Monique, Coates, Maria, Barrett, Sarah, Bateman, Clare, Davies, Jennifer C, Raymundo-Wood, Ivy, Ustianowski, Andrew, Carson-Stevens, Andrew, Yu, Ly-Mee, Little, Paul, Agyeman, Akosua A, Ahmed, Tanveer, Allcock, Damien, Beltran-Martinez, Adrian, Benedict, Oluseye E, Bird, Nigel, Brennan, Laura, Brown, Julianne, Burns, Gerard, Butler, Mike, Cheng, Zelda, Danson, Ruth, de Kare-Silver, Nigel, Dhasmana, Devesh, Dickson, Jon, Engamba, Serge, Fisher, Stacey, Fox, Robin, Frost, Eve, Gaunt, Richard, Ghosh, Sarit, Gilkar, Ishtiaq, Goodman, Anna, Granier, Steve, Howell, Aleksandra, Hussain, Iqbal, Hutchinson, Simon, Imlach, Marie, Irving, Greg, Jacobsen, Nicholas, Kennard, James, Khan, Umar, Knox, Kyle, Krasucki, Christopher, Law, Tom, Lee, Rem, Lester, Nicola, Lewis, David, Lunn, James, Mackintosh, Claire I., Mathukia, Mehul, Moore, Patrick, Morton, Seb, Murphy, Daniel, Nally, Rhiannon, Ndukauba, Chinonso, Ogundapo, Olufunto, Okeke, Henry, Patel, Amit, Patel, Kavil, Penfold, Ruth, Poonian, Satveer, Popoola, Olajide, Pora, Alexander, Prasad, Vibhore, Prasad, Rishabh, Razzaq, Omair, Richardson, Scot, Royal, Simon, Safa, Afsana, Sehdev, Satash, Sevenoaks, Tamsin, Shah, Divya, Sheikh, Aadil, Short, Vanessa, Sidhu, Baljinder S, Singh, Ivor, Soni, Yusuf, Thalasselis, Chris, Wilson, Pete, Wingfield, David, Wong, Michael, Woodall, Maximillian N J, Wooding, Nick, Woods, Sharon, Yong, Joanna, Yongblah, Francis, and Zafar, Azhar
- Abstract
The safety, effectiveness, and cost-effectiveness of molnupiravir, an oral antiviral medication for SARS-CoV-2, has not been established in vaccinated patients in the community at increased risk of morbidity and mortality from COVID-19. We aimed to establish whether the addition of molnupiravir to usual care reduced hospital admissions and deaths associated with COVID-19 in this population.
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- 2023
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46. Favipiravir for COVID-19 in adults in the community in PRINCIPLE, an open-label, randomised, controlled, adaptive platform trial of short- and longer-term outcomes.
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Hobbs, FD Richard, Gbinigie-Thompson, Oghenekome A., Shanyinde, Milensu, Yu, Ly-Mee, Harris, Victoria, Dorward, Jienchi, Hayward, Gail, Saville, Benjamin R., Berry, Nicholas S., Evans, Philip H., Thomas, Nicholas PB, Patel, Mahendra G., Richards, Duncan, Hecke, Oliver Van, Detry, Michelle A., Saunders, Christina T., Fitzgerald, Mark, Robinson, Jared, Latimer-Bell, Charlotte, and Allen, Julie
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Evidence for the effect of favipiravir treatment of acute COVID-19 on recovery, hospital admissions and longer-term outcomes in community settings is limited. In this multicentre. open-label, multi-arm, adaptive platform randomised controlled trial participants aged ≥18 years in the community with a positive test for SARS-CoV-2 and symptoms lasting ≤14 days were randomised to: usual care; usual care plus favipiravir tablets (loading dose of 3600 mg in divided doses on day one, then 800 mg twice a day for four days); or, usual care plus other interventions. Co-primary endpoints were time to first self-reported recovery and hospitalisation/death related to COVID-19, within 28 days, analysed using Bayesian models. Recovery at six months was the primary longer-term outcome. Trial registration: ISRCTN86534580. The primary analysis model included 8811 SARS-CoV-2 positive mostly COVID vaccinated participants, randomised to favipiravir (n = 1829), usual care (n = 3256), and other treatments (n = 3726). Time to self-reported recovery was shorter in the favipiravir group than usual care (estimated hazard ratio 1·23 [95% credible interval 1·14 to 1·33]), a reduction of 2·98 days [1·99 to 3·94] from 16 days in median time to self-reported recovery for favipiravir versus usual care alone. COVID-19 related hospitalisations/deaths were similar (estimated odds ratio 0·99 [0·61 to 1·61]; estimated difference 0% [−0·9% to 0·6%]). 14 serious adverse events occurred in the favipiravir group and 4 in usual care. By six months, the proportion feeling fully recovered was 74·9% for favipiravir versus 71·3% for usual care (RR = 1·05, [1·02 to 1·08]). In this open-label trial in a largely vaccinated population with COVID-19 in the community, favipiravir did not reduce hospital admissions, but shortened time to recovery and had a marginal positive impact on long term outcomes. [ABSTRACT FROM AUTHOR]
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- 2024
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47. Rib fixation in non-ventilator-dependent chest wall injuries: A prospective randomized trial.
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Marasco, Silvana Francesca, Balogh, Zsolt J., Wullschleger, Martin E., Hsu, Jeremy, Patel, Bhavik, Fitzgerald, Mark, Martin, Kate, Summerhayes, Robyn, and Bailey, Michael
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- 2022
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48. Initial Efforts to Manage IPE during the COVID-19 Pandemic: Reports from the Big Ten IPE Academic Alliance.
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Smith, Laura J., Romito, Laura, Congdon, Heather B., Ascione, Frank J., Fitzgerald, Mark, Karpa, Kelly, Pfiefle, Andrea, Sick, Brian, and Khalili, Hossein
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- 2022
49. Phenotype Spectrum of TRPM3‐Associated Disorders.
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Jolitz, Laura, Helbig, Ingo, Fitzgerald, Mark P., McKeown Ruggiero, Sarah, Cohen, Stacey, Angelini, Chloe, Vallespin, Elena, Michaud, Vincent, Gerasimenko, Anna, Cogne, Benjamin, Isidor, Bertrand, Keren, Boris, Dyment, David, Heron, Delphine, Karstensen, Helena Gásdal, Cuppen, Inge, Christodoulou, John, Wilson, Meredith, Lake, Nicole J., and Biskup, Saskia
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SYMPTOMS , *DEVELOPMENTAL delay , *INTELLECTUAL disabilities , *MOTOR ability , *EPILEPSY - Abstract
Objective Methods Results Interpretation Monoallelic variants in the transient receptor potential melastatin‐related type 3 gene (TRPM3) have been associated with neurodevelopmental manifestations, but knowledge on the clinical manifestations and treatment options is limited. We characterized the clinical spectrum, highlighting particularly the epilepsy phenotype, and the effect of treatments.We analyzed retrospectively the phenotypes and genotypes of 43 individuals with TRPM3 variants, acquired from GeneMatcher and collaborations (n = 21), and through a systematic literature search (n = 22). We included all patients with a pathogenic TRPM3 variant.The median age at the time of the study was 10 years, with a preponderance of girls (60%) versus boys (40%). Frequent findings were developmental delay and/or intellectual disability (93%), global or axial hypotonia (77%), ocular involvement (70%), musculoskeletal anomalies (65%), and dysmorphic features (58%). Epilepsy was diagnosed in 31 patients (72%), classified in all as developmental and epileptic encephalopathy with or without spike wave activation in sleep (DEE/DEE‐SWAS). Patients with the variant p.Val1002Met (n = 24) significantly more often had developmental delay and epilepsy. The most effective anti‐seizure medication was primidone. All treated patients showed an improvement in seizure frequency, motor and speech development, and/or learning capability with this drug.Developmental delay/intellectual disability and epilepsy are dominant phenotypic features in patients with TRPM3 variants. Given that epilepsy can negatively impact development, screening for awake and sleep electroencephalogram abnormalities and other manifestations are essential to offer early intervention. The TRPM3 channel blocker primidone has shown promising effects and should be considered in every child with a TRPM3 gain‐of‐function variant. ANN NEUROL 2025 [ABSTRACT FROM AUTHOR]
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- 2025
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50. Development of a model to predict electroencephalographic seizures in neonates with hypoxic ischemic encephalopathy treated with therapeutic hypothermia.
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Massey, Shavonne L., Sandoval Karamian, Amanda G., Fitzgerald, Mark P., Fung, France W., Abramson, Abigail, Salmon, Mandy K., Parikh, Darshana, and Abend, Nicholas S.
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CEREBRAL anoxia-ischemia , *RECEIVER operating characteristic curves , *EPILEPTIFORM discharges , *THERAPEUTIC hypothermia , *STATUS epilepticus - Abstract
Objective Methods Results Significance Electroencephalographic seizures (ES) are common in neonates with hypoxic–ischemic encephalopathy (HIE), but identification with continuous electroencephalographic (EEG) monitoring (CEEG) is resource‐intensive. We aimed to develop an ES prediction model.Using a prospective observational study of 260 neonates with HIE undergoing CEEG, we identified clinical and EEG risk factors for ES, evaluated model performance with area under the receiver operating characteristic curve (AUROC), and calculated test characteristics emphasizing high sensitivity. We assessed ES incidence and timing in neonates subdivided by ES risk group (low, moderate, high) as determined by EEG risk factors.ES occurred in 32% (83/260) of neonates. Performing CEEG for only 24 h would fail to identify the 7% (17/260) of neonates with later onset ES (20% of all neonates experiencing ES). Identifying 90% or 95% of neonates with ES would require CEEG for 63 or 74 h, respectively. The optimal model included continuity and epileptiform discharges, both assessed in the initial 1 h of CEEG. It yielded an AUROC of .80, and at a cutoff that emphasized sensitivity, had sensitivity of 94%, specificity of 45%, positive predictive value of 44%, and negative predictive value of 95%. The model would avoid CEEG beyond 1 h in 32% (84/260) of neonates, but 6% (5/83) of neonates with ES would not have ES identified. ES incidence was significantly different (p < .01) across ES risk groups (6% low, 40% moderate, and 83% high). Only ~6 h of CEEG would identify all neonates with ES in the low‐risk group, whereas 75 and 63 h of CEEG would be required to identify 95% of neonates with ES in the moderate‐risk and high‐risk groups, respectively.Among neonates with HIE, a model employing two EEG variables from a 1‐h screening EEG and stratifying neonates into low‐, moderate‐, and high‐risk groups could enable evidence‐based strategies for targeted CEEG use. [ABSTRACT FROM AUTHOR]
- Published
- 2024
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