Search

Your search keyword '"CreveCoeur, Travis S."' showing total 22 results
Start Over Author "CreveCoeur, Travis S."
22 results on '"CreveCoeur, Travis S."'

1. Timing of intraoperative neurophysiological monitoring (IONM) recovery and clinical recovery after termination of pediatric spinal deformity surgery due to loss of IONM signals

Author

CreveCoeur, Travis S., Iyer, Rajiv R., Goldstein, Hannah E., Delgardo, Mychael W., Hankinson, Todd C., Erickson, Mark A., Garg, Sumeet, Skaggs, David L., Andras, Lindsay, Kennedy, Benjamin C., Cahill, Patrick J., Lenke, Lawrence G., Angevine, Peter D., Roye, Benjamin D., Vitale, Michael G., Mendiratta, Anil, and Anderson, Richard C.E.

Published
2024
Full Text
View/download PDF

7. Building consensus for the medical management of children with moderate and severe acute spinal cord injury: a modified Delphi study

Author

CreveCoeur, Travis S., primary, Alexiades, Nikita G., additional, Bonfield, Christopher M., additional, Brockmeyer, Douglas L., additional, Browd, Samuel R., additional, Chu, Jason, additional, Figaji, Anthony A., additional, Groves, Mari L., additional, Hankinson, Todd C., additional, Harter, David H., additional, Hwang, Steven W., additional, Jea, Andrew, additional, Kernie, Steven G., additional, Leonard, Jeffrey R., additional, Martin, Jonathan E., additional, Oetgen, Matthew E., additional, Powers, Alexander K., additional, Rozzelle, Curtis J., additional, Skaggs, David L., additional, Strahle, Jennifer M., additional, Wellons, John C., additional, Vitale, Michael G., additional, and Anderson, Richard C. E., additional

Published
2023
Full Text
View/download PDF

11. Socioeconomic and demographic factors in the diagnosis and treatment of Chiari malformation type I and syringomyelia

Author

Akbari, Syed Hassan A., primary, Rizvi, Asad A., additional, CreveCoeur, Travis S., additional, Han, Rowland H., additional, Greenberg, Jacob K., additional, Torner, James, additional, Brockmeyer, Douglas L., additional, Wellons, John C., additional, Leonard, Jeffrey R., additional, Mangano, Francesco T., additional, Johnston, James M., additional, Shah, Manish N., additional, Iskandar, Bermans J., additional, Ahmed, Raheel, additional, Tuite, Gerald F., additional, Kaufman, Bruce A., additional, Daniels, David J., additional, Jackson, Eric M., additional, Grant, Gerald A., additional, Powers, Alexander K., additional, Couture, Daniel E., additional, Adelson, P. David, additional, Alden, Tord D., additional, Aldana, Philipp R., additional, Anderson, Richard C. E., additional, Selden, Nathan R., additional, Bierbrauer, Karin, additional, Boydston, William, additional, Chern, Joshua J., additional, Whitehead, William E., additional, Dauser, Robert C., additional, Ellenbogen, Richard G., additional, Ojemann, Jeffrey G., additional, Fuchs, Herbert E., additional, Guillaume, Daniel J., additional, Hankinson, Todd C., additional, O’Neill, Brent R., additional, Iantosca, Mark, additional, Oakes, W. Jerry, additional, Keating, Robert F., additional, Klimo, Paul, additional, Muhlbauer, Michael S., additional, McComb, J. Gordon, additional, Menezes, Arnold H., additional, Khan, Nickalus R., additional, Niazi, Toba N., additional, Ragheb, John, additional, Shannon, Chevis N., additional, Smith, Jodi L., additional, Ackerman, Laurie L., additional, Jea, Andrew H., additional, Maher, Cormac O., additional, Narayan, Prithvi, additional, Albert, Gregory W., additional, Stone, Scellig S. D., additional, Baird, Lissa C., additional, Gross, Naina L., additional, Durham, Susan R., additional, Greene, Stephanie, additional, McKinstry, Robert C., additional, Shimony, Joshua S., additional, Strahle, Jennifer M., additional, Smyth, Matthew D., additional, Dacey, Ralph G., additional, Park, Tae Sung, additional, and Limbrick, David D., additional

Published
2022
Full Text
View/download PDF

12. Occipital-Cervical Fusion and Ventral Decompression in the Surgical Management of Chiari-1 Malformation and Syringomyelia: Analysis of Data From the Park-Reeves Syringomyelia Research Consortium

Author

CreveCoeur, Travis S, primary, Yahanda, Alexander T, additional, Maher, Cormac O, additional, Johnson, Gabrielle W, additional, Ackerman, Laurie L, additional, Adelson, P David, additional, Ahmed, Raheel, additional, Albert, Gregory W, additional, Aldana, Phillipp R, additional, Alden, Tord D, additional, Anderson, Richard C E, additional, Baird, Lissa, additional, Bauer, David F, additional, Bierbrauer, Karin S, additional, Brockmeyer, Douglas L, additional, Chern, Joshua J, additional, Couture, Daniel E, additional, Daniels, David J, additional, Dauser, Robert C, additional, Durham, Susan R, additional, Ellenbogen, Richard G, additional, Eskandari, Ramin, additional, Fuchs, Herbert E, additional, George, Timothy M, additional, Grant, Gerald A, additional, Graupman, Patrick C, additional, Greene, Stephanie, additional, Greenfield, Jeffrey P, additional, Gross, Naina L, additional, Guillaume, Daniel J, additional, Haller, Gabe, additional, Hankinson, Todd C, additional, Heuer, Gregory G, additional, Iantosca, Mark, additional, Iskandar, Bermans J, additional, Jackson, Eric M, additional, Jea, Andrew H, additional, Johnston, James M, additional, Keating, Robert F, additional, Kelly, Michael P, additional, Khan, Nickalus, additional, Krieger, Mark D, additional, Leonard, Jeffrey R, additional, Mangano, Francesco T, additional, Mapstone, Timothy B, additional, McComb, J Gordon, additional, Menezes, Arnold H, additional, Muhlbauer, Michael, additional, Oakes, W Jerry, additional, Olavarria, Greg, additional, O’Neill, Brent R, additional, Park, Tae Sung, additional, Ragheb, John, additional, Selden, Nathan R, additional, Shah, Manish N, additional, Shannon, Chevis, additional, Shimony, Joshua S, additional, Smith, Jodi, additional, Smyth, Matthew D, additional, Stone, Scellig S D, additional, Strahle, Jennifer M, additional, Tamber, Mandeep S, additional, Torner, James C, additional, Tuite, Gerald F, additional, Wait, Scott D, additional, Wellons, John C, additional, Whitehead, William E, additional, and Limbrick, David D, additional

Published
2021
Full Text
View/download PDF

13. Association between supratentorial pediatric high-grade gliomas involved with the subventricular zone and decreased survival: a multi-institutional retrospective study

Author

Mistry, Akshitkumar M., primary, Mummareddy, Nishit, additional, CreveCoeur, Travis S., additional, Lillard, Jock C., additional, Vaughn, Brandy N., additional, Gallant, Jean-Nicolas, additional, Hale, Andrew T., additional, Griffin, Natalie, additional, Wellons, John C., additional, Limbrick, David D., additional, Klimo, Paul, additional, and Naftel, Robert P., additional

Published
2020
Full Text
View/download PDF

20. Role of resting state MRI temporal latency in refractory pediatric extratemporal epilepsy lateralization.

Author

Shah, Manish N., Nguyen, Ryan D., Pao, Ludovic P., Zhu, Liang, CreveCoeur, Travis S., Mitra, Anish, and Smyth, Matthew D.

Abstract

Background: Pediatric epilepsy affects 0.5-1% of children, with 10-30% of these children refractory to medical anticonvulsant therapy and potentially requiring surgical intervention. Analysis of resting state functional MRI (rsMRI) signal temporal differences (latency) has been proposed to study the pathological cognitive processes.Purpose/hypothesis: To quantitatively and qualitatively analyze the correlation of rsMRI signal latency to pediatric refractory extratemporal epilepsy seizure foci lateralization.Study Type: Retrospective review.Population: With Institutional Review Board approval, rsMRI and anatomical MRI scans were obtained from 38 registered pediatric epilepsy surgery patients from Washington University and 259 healthy control patients from the ADHD-200 dataset.Field Strength/sequence: 3 T echo planar imaging (EPI) blood oxygenation level-dependent (BOLD) sequence.Assessment: The images were transformed to pediatric atlases in Talairach space. Preoperative voxelwise latency maps were generated with parabolic interpolation of the rsMRI signal lateness or earliness when compared with the global mean signal (GMS) using cross-covariance analysis.Statistical Tests: Latency z-score maps were created for each epilepsy patient by voxelwise calculation using healthy control mean and standard deviation maps. Voxelwise hypothesis testing was performed via multiple comparisons corrected (false discovery and familywise error rate) and uncorrected methods to determine significantly late and early voxels. Significantly late and/or early voxels were counted for the right and left hemisphere separately. The hemisphere with the greater proportion of significantly late and/or early voxels was hypothesized to contain the seizure focus. Preoperative rsMRI latency analysis hypotheses were compared with postoperative seizure foci lateralization determined by resection images.Results: Preoperative rsMRI latency analysis correctly identified seizure foci lateralization of 64-85% of postoperative epilepsy resections with the proposed methods. RsMRI latency lateralization analysis was 77-100% sensitive and 58-79% specific. In some patients, qualitative analysis yielded preoperative rsMRI latency patterns specific to procedure performed.Data Conclusion: Preoperative rsMRI signal latency of pediatric epilepsy patients was correlated with seizure foci lateralization. J. Magn. Reson. Imaging 2019;49:1347-1355. [ABSTRACT FROM AUTHOR]

Published
2019
Full Text
View/download PDF

22. Socioeconomic and demographic factors in the diagnosis and treatment of Chiari malformation type I and syringomyelia.

Author

Akbari SHA, Rizvi AA, CreveCoeur TS, Han RH, Greenberg JK, Torner J, Brockmeyer DL, Wellons JC, Leonard JR, Mangano FT, Johnston JM, Shah MN, Iskandar BJ, Ahmed R, Tuite GF, Kaufman BA, Daniels DJ, Jackson EM, Grant GA, Powers AK, Couture DE, Adelson PD, Alden TD, Aldana PR, Anderson RCE, Selden NR, Bierbrauer K, Boydston W, Chern JJ, Whitehead WE, Dauser RC, Ellenbogen RG, Ojemann JG, Fuchs HE, Guillaume DJ, Hankinson TC, O'Neill BR, Iantosca M, Oakes WJ, Keating RF, Klimo P, Muhlbauer MS, McComb JG, Menezes AH, Khan NR, Niazi TN, Ragheb J, Shannon CN, Smith JL, Ackerman LL, Jea AH, Maher CO, Narayan P, Albert GW, Stone SSD, Baird LC, Gross NL, Durham SR, Greene S, McKinstry RC, Shimony JS, Strahle JM, Smyth MD, Dacey RG, Park TS, and Limbrick DD

Abstract

Objective: The goal of this study was to assess the social determinants that influence access and outcomes for pediatric neurosurgical care for patients with Chiari malformation type I (CM-I) and syringomyelia (SM)., Methods: The authors used retro- and prospective components of the Park-Reeves Syringomyelia Research Consortium database to identify pediatric patients with CM-I and SM who received surgical treatment and had at least 1 year of follow-up data. Race, ethnicity, and insurance status were used as comparators for preoperative, treatment, and postoperative characteristics and outcomes., Results: A total of 637 patients met inclusion criteria, and race or ethnicity data were available for 603 (94.7%) patients. A total of 463 (76.8%) were non-Hispanic White (NHW) and 140 (23.2%) were non-White. The non-White patients were older at diagnosis (p = 0.002) and were more likely to have an individualized education plan (p < 0.01). More non-White than NHW patients presented with cerebellar and cranial nerve deficits (i.e., gait ataxia [p = 0.028], nystagmus [p = 0.002], dysconjugate gaze [p = 0.03], hearing loss [p = 0.003], gait instability [p = 0.003], tremor [p = 0.021], or dysmetria [p < 0.001]). Non-White patients had higher rates of skull malformation (p = 0.004), platybasia (p = 0.002), and basilar invagination (p = 0.036). Non-White patients were more likely to be treated at low-volume centers than at high-volume centers (38.7% vs 15.2%; p < 0.01). Non-White patients were older at the time of surgery (p = 0.001) and had longer operative times (p < 0.001), higher estimated blood loss (p < 0.001), and a longer hospital stay (p = 0.04). There were no major group differences in terms of treatments performed or complications. The majority of subjects used private insurance (440, 71.5%), whereas 175 (28.5%) were using Medicaid or self-pay. Private insurance was used in 42.2% of non-White patients compared to 79.8% of NHW patients (p < 0.01). There were no major differences in presentation, treatment, or outcome between insurance groups. In multivariate modeling, non-White patients were more likely to present at an older age after controlling for sex and insurance status (p < 0.01). Non-White and male patients had a longer duration of symptoms before reaching diagnosis (p = 0.033 and 0.004, respectively)., Conclusions: Socioeconomic and demographic factors appear to influence the presentation and management of patients with CM-I and SM. Race is associated with age and timing of diagnosis as well as operating room time, estimated blood loss, and length of hospital stay. This exploration of socioeconomic and demographic barriers to care will be useful in understanding how to improve access to pediatric neurosurgical care for patients with CM-I and SM.

Published
2021
Full Text
View/download PDF

Catalog

Books, media, physical & digital resources
See catalog results