Suhas Bajgur
University of Texas at Austin
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Featured researches published by Suhas Bajgur.
JAMA Neurology | 2016
Amrou Sarraj; Navdeep Sangha; Muhammad S Hussain; Dolora Wisco; Nirav A. Vora; Lucas Elijovich; Nitin Goyal; Michael G. Abraham; Manoj K. Mittal; Lei Feng; Abel Wu; Vallabh Janardhan; Suman Nalluri; Albert J. Yoo; Megan George; Randall C. Edgell; Rutvij J Shah; Clark W. Sitton; Emilio P. Supsupin; Suhas Bajgur; M. Carter Denny; Peng R. Chen; Mark Dannenbaum; Sheryl Martin-Schild; Sean I. Savitz; Rishi Gupta
Importance Randomized clinical trials have shown the superiority of endovascular therapy (EVT) compared with best medical management for acute ischemic strokes with large vessel occlusion (LVO) in the anterior circulation. However, of 1287 patients enrolled in 5 trials, 94 with isolated second (M2) segment occlusions were randomized and 51 of these received EVT, thereby limiting evidence for treating isolated M2 segment occlusions as reflected in American Heart Association guidelines. Objective To evaluate EVT safety and effectiveness in M2 occlusions in a cohort of patients with acute ischemic stroke. Design, Setting, and Participants This multicenter retrospective cohort study pooled patients with acute ischemic strokes and LVO isolated to M2 segments from 10 US centers. Patients with acute ischemic strokes and LVO in M2 segments presenting within 8 hours from their last known normal clinical status (LKN) from January 1, 2012, to April 30, 2015, were divided based on their treatment into EVT and medical management groups. Logistic regression was used to compare the 2 groups. Univariate and multivariate analyses evaluated associations with good outcome in the EVT group. Main Outcomes and Measures The primary outcome was the 90-day modified Rankin Scale score (range, 0-6; scores of 0-2 indicate a good outcome); the secondary outcome was symptomatic intracerebral hemorrhage. Results A total of 522 patients (256 men [49%]; 266 women [51%]; mean [SD] age, 68 [14.3] years) were identified, of whom 288 received EVT and 234 received best medical management. Patients in the medical management group were older (median [interquartile range] age, 73 [60-81] vs 68 [56-78] years) and had higher rates of intravenous tissue plasminogen activator treatment (174 [74.4%] vs 172 [59.7%]); otherwise the 2 groups were balanced. The rate of good outcomes was higher for EVT (181 [62.8%]) than for medical management (83 [35.4%]). The EVT group had 3 times the odds of a good outcome as the medical management group (odds ratio [OR], 3.1; 95% CI, 2.1-4.4; P < .001) even after adjustment for age, National Institute of Health Stroke Scale (NIHSS) score, Alberta Stroke Program Early Computed Tomographic Score (ASPECTS), intravenous tissue plasminogen activator treatment, and time from LKN to arrival in the emergency department (OR, 3.2; 95% CI, 2-5.2; P < .001). No statistical difference in symptomatic intracerebral hemorrhage was found (5.6% vs 2.1% for the EVT group vs the medical management group; P = .10). The treatment effect did not change after adjusting for center (OR, 3.3; 95% CI, 1.9-5.8; P < .001). Age, NIHSS score, ASPECTS, time from LKN to reperfusion, and successful reperfusion score of at least 2b (range, 0 [no perfusion] to 3 [full perfusion with filling of all distal branches]) were independently associated with good outcome of EVT. A linear association was found between good outcome and time from LKN to reperfusion. Conclusions and Relevance Although a randomized clinical trial is needed to confirm these findings, available data suggest that EVT is reasonable, safe, and effective for LVO of the M2 segment relative to best medical management.
PLOS ONE | 2015
Rahul Karamchandani; Farhaan Vahidy; Suhas Bajgur; Kim Yen Thi Vu; H. Alex Choi; Robert Kirk Hamilton; Mohammad H. Rahbar; Sean I. Savitz
Background and Purpose Post-stroke depression (PSD) is common but is not routinely assessed for in hospitalized patients. As a Comprehensive Stroke Center, we screen all stroke inpatients for depression, though the feasibility of early screening has not been established. We assessed the hypothesis that early depression screening in stroke patients is feasible. We also explored patient level factors associated with being screened for PSD and the presence of early PSD. Methods The medical records of all patients admitted with ischemic stroke (IS) or intracerebral hemorrhage (ICH) between 01/02/13 and 15/04/13 were reviewed. A depression screen, modified from the Patient Health Questionnaire-9, was administered (maximum score 27, higher scores indicating worse depression). Patients were eligible if they did not have a medical condition precluding screening. Feasibility was defined as screening 75% of all eligible patients. Results Of 303 IS and ICH inpatients, 70% (211) were eligible for screening, and 75% (158) of all eligible patients were screened. More than one-third of all patients screened positive for depression (score > 4). Women (OR 2.06, 95% CI 1.06–4.01) and younger patients (OR 0.97, 95% CI 0.96–0.99) were more likely to screen positive. Screening positive was not associated with poor discharge/day 7 outcome (mRS > 3; OR 1.45, 95% CI 0.74–2.83). Conclusions Screening stroke inpatients for depression is feasible and early depression after stroke is common. Women and younger patients are more likely to experience early PSD. Our results provide preliminary evidence supporting continued screening for depression in hospitalized stroke patients.
PLOS ONE | 2017
Kwang Wook Jo; Suhas Bajgur; Hoon Kyo Kim; Huimahn Alex Choi; Pil Woo Huh; Kiwon Lee
Malignant brain edema (MBE) due to hemispheric infarction can result in brain herniation, poor outcomes, and death; outcome may be improved if certain interventions, such as decompressive craniectomy, are performed early. We sought to generate a prediction score to easily identify those patients at high risk for MBE. 121 patients with large hemispheric infarction (LHI) (2011 to 2014) were included. Patients were divided into two groups: those who developed MBE and those who did not. Independent predictors of MBE were identified by logistic regression and a score was developed. Four factors were independently associated with MBE: baseline National Institutes of Health Stroke Scale (NIHSS) score (p = 0.048), Alberta Stroke Program Early Computed Tomography Score (ASPECTS) (p = 0.007), collateral score (CS) (p<0.001) and revascularization failure (p = 0.013). Points were assigned for each factor as follows: NIHSS ≤ 8 (= 0), 9–17 (= 1), ≥ 18 (= 2); ASPECTS≤ 7 (= 1), >8 (= 0); CS<2 (= 1), ≥2 (= 0); revascularization failure (= 1),success (= 0). The MBE Score (MBES) represents the sum of these individual points. Of 26 patients with a MBES of 0 to 1, none developed MBE. All patients with a MBES of 6 developed MBE. Both MBE development and functional outcomes were strongly associated with the MBES (p = 0.007 and 0.002, respectively). The MBE score is a simple reliable tool for the prediction of MBE.
Neurology | 2017
Jude P Savarraj; Kaushik Parsha; Georgene W. Hergenroeder; Liang Zhu; Suhas Bajgur; Sungho Ahn; Kiwon Lee; Tiffany R. Chang; Dong H. Kim; Yin Liu; H. Alex Choi
Objective: To investigate inflammatory processes after aneurysmal subarachnoid hemorrhage (aSAH) with network models. Methods: This is a retrospective observational study of serum samples from 45 participants with aSAH analyzed at multiple predetermined time points: <24 hours, 24 to 48 hours, 3 to 5 days, and 6 to 8 days after aSAH. Concentrations of cytokines were measured with a 41-plex human immunoassay kit, and the Pearson correlation coefficients between all possible cytokine pairs were computed. Systematic network models were constructed on the basis of correlations between cytokine pairs for all participants and across injury severity. Trends of individual cytokines and correlations between them were examined simultaneously. Results: Network models revealed that systematic inflammatory activity peaks at 24 to 48 hours after the bleed. Individual cytokine levels changed significantly over time, exhibiting increasing, decreasing, and peaking trends. Platelet-derived growth factor (PDGF)-AA, PDGF-AB/BB, soluble CD40 ligand, and tumor necrosis factor-α (TNF-α) increased over time. Colony-stimulating factor (CSF) 3, interleukin (IL)-13, and FMS-like tyrosine kinase 3 ligand decreased over time. IL-6, IL-5, and IL-15 peaked and decreased. Some cytokines with insignificant trends show high correlations with other cytokines and vice versa. Many correlated cytokine clusters, including a platelet-derived factor cluster and an endothelial growth factor cluster, were observed at all times. Participants with higher clinical severity at admission had elevated levels of several proinflammatory and anti-inflammatory cytokines, including IL-6, CCL2, CCL11, CSF3, IL-8, IL-10, CX3CL1, and TNF-α, compared to those with lower clinical severity. Conclusions: Combining reductionist and systematic techniques may lead to a better understanding of the underlying complexities of the inflammatory reaction after aSAH.
Pharmacotherapy | 2017
Sophie Samuel; Leigh Gomez; Jude P. Savarraj; Suhas Bajgur; Huimahn Alex Choi
To assess whether a positive linear association exists between body mass index (BMI) and incidence of venous thromboembolism (VTE) in overweight and obese hospitalized patients.
Cytokine | 2018
Jude P Savarraj; Mary F. McGuire; Kaushik Parsha; Georgene W. Hergenroeder; Suhas Bajgur; Sungho Ahn; Liang Zhu; Elena Espino; Tiffany R. Chang; Spiros Blackburn; Dong H. Kim; Pramod K. Dash; Huimahn Alex Choi
Background Unregulated inflammatory and thrombotic responses have been proposed to be important causes of early brain injury and worse clinical outcomes after subarachnoid hemorrhage (SAH). Objective We hypothesize that SAH is characterized by an increased inflammatory and thrombotic state and disruption of associations between these states. Methods This is a retrospective cohort study of 60 patients with SAH. 23 patients with unruptured aneurysms (UA) and 77 patients with traumatic brain injury (TBI) were chosen as controls. Plasma cytokine levels were measured using a 41‐plex human immunoassay kit, and cytokine patterns associated with SAH, UA and TBI were identified using statistical and informatics methods. Results SAH was characterized by an increase in several cytokines and chemokines, platelet‐derived factors, and growth factors. Cluster analysis identified several cytokine clusters common in SAH, UA and TBI groups – generally grouped as platelet‐derived, vascular and pro‐inflammatory clusters. In the UA group, the platelet‐derived cluster had an inverse relationship with the inflammatory cluster which was absent in SAH. Additionally, a cluster comprising of growth and colony stimulating factors was unique to SAH. Conclusions A cluster of cytokines involved in growth and colony stimulation was unique to SAH. Negative associations between the thrombotic and inflammatory molecules were observed in UA but not in SAH. Further studies to examine the pathophysiology behind the cluster unique to SAH and the associations between the thrombotic and inflammatory cytokines are required. HighlightsCytokines involved in inflammatory and thrombotic processes are elevated after SAH.Positive correlations between the processes were observed in SAH and UA.Negative correlations between the processes were present in UA but absent in SAH.A growth colony stimulating factor cluster was unique in SAH.
Critical Care Medicine | 2016
Chritina Luther; Jenna Snow; Angela Lauritano; Jacqueline Denzler; Suhas Bajgur; Elena Espino; Wamda Ahmed; Huimahn Alex Choi
Crit Care Med 2016 • Volume 44 • Number 12 (Suppl.) Higher SAH severity represented by lower GCS on initial presentation is associated with higher odds for developing SIRS within the first 96 hrs. Younger age is also associated with higher odds for early SIRS in SAH, criteria, possibly due to a more robust inflammatory response. SIRS within 96 hrs is an independent risk factor in-hospital SAH mortality. Further studies are necessary no determine the pathophysiology of SIRS in SAH and its role in SAH mortality.
Neurocritical Care | 2016
H. Alex Choi; Suhas Bajgur; Wesley Jones; Jude P Savarraj; Sang Bae Ko; Nancy J. Edwards; Tiffany R. Chang; Georgene W. Hergenroeder; Mark Dannenbaum; P. Roc Chen; Arthur L. Day; Dong H. Kim; Kiwon Lee; James C. Grotta
Journal of Thrombosis and Thrombolysis | 2017
Sophie Samuel; Suhas Bajgur; Jude P. Savarraj; Huimahn Alex Choi
Stroke | 2016
Maria I DeGuzman; Hari Indupuru; Suhas Bajgur; Sandi Shaw; Stephanie Cooper; Christine Glendening; Melvin R Sline; Hope Moser; Nicole Harrison; Amrou Sarraj; Sean I. Savitz; Farhaan Vahidy