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Dive into the research topics where Muhammad Alvi is active.

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Featured researches published by Muhammad Alvi.


Stroke | 2013

Systemic Inflammatory Response Syndrome in Tissue-Type Plasminogen Activator–Treated Patients is Associated With Worse Short-term Functional Outcome

Amelia K Boehme; Niren Kapoor; Karen C. Albright; Michael Lyerly; Pawan V. Rawal; Reza Bavarsad Shahripour; Muhammad Alvi; J. Thomas Houston; April Sisson; T. Mark Beasley; Anne W. Alexandrov; Andrei V. Alexandrov; David W. Miller

Background and Purpose— Systemic inflammatory response syndrome (SIRS) is a generalized inflammatory state. The primary goal of the study was to determine whether differences exist in outcomes in SIRS and non-SIRS intravenous tissue-type plasminogen activator–treated patients. Methods— Consecutive patients were retrospectively reviewed for the evidence of SIRS during their admission. SIRS was defined as the presence of ≥2 of the following: body temperature <36°C or >38°C, heart rate >90, respiratory rate >20, and white blood cells <4000/mm or >12 000 mm, or >10% bands. Patients diagnosed with infection (via positive culture) were excluded. Results— Of the 241 patients, 44 had evidence of SIRS (18%). Adjusting for pre–tissue-type plasminogen activator National Institutes of Health Stroke Scale, age, and race, SIRS remained a predictor of poor functional outcome at discharge (odds ratio [OR], 2.58; 95% confidence interval [CI], 1.16–5.73; P=0.0197). Conclusions— In our sample of tissue-type plasminogen activator–treated (tPA) patients, ~1 in 5 patients developed SIRS. Furthermore, we found the presence of SIRS to be associated with poor short-term functional outcomes and prolonged length of stay.


Journal of Stroke & Cerebrovascular Diseases | 2014

Predictors of Systemic Inflammatory Response Syndrome in Ischemic Stroke Undergoing Systemic Thrombolysis with Intravenous Tissue Plasminogen Activator

Amelia K Boehme; Niren Kapoor; Karen C. Albright; Michael Lyerly; Pawan V. Rawal; Reza Bavarsad Shahripour; Muhammad Alvi; J. Thomas Houston; April Sisson; T. Mark Beasley; Anne W. Alexandrov; Andrei V. Alexandrov; David W. Miller

BACKGROUND Systemic inflammatory response syndrome (SIRS) is an inflammatory process associated with poor outcomes in acute ischemic stroke (AIS) patients. However, no study to date has investigated predictors of SIRS in AIS patients treated with intravenous (IV) tissue plasminogen activator (tPA). METHODS Consecutive patients were retrospectively reviewed for evidence of SIRS during their acute hospitalization. SIRS was defined as the presence of 2 or more of the following: (1) body temperature less than 36°C or greater than 38°C, (2) heart rate greater than 90, (3) respiratory rate greater than 20, or (4) white blood cell count less than 4000/mm or greater than 12,000/mm or more than 10% bands for more than 24 hours. Those diagnosed with an infection were excluded. A scoring system was created to predict SIRS based on patient characteristics available at the time of admission. Logistic regression was used to evaluate potential predictors of SIRS using a sensitivity cutoff of ≥65% or area under the curve of .6 or more. RESULTS Of 212 patients, 44 had evidence of SIRS (21%). Patients with SIRS were more likely to be black (61% versus 54%; P = .011), have lower median total cholesterol at baseline (143 versus 167 mg/dL; P = .0207), and have history of previous stroke (51% versus 35%; P = .0810). Ranging from 0 to 6, the SIRS prediction score consists of African American (2 points), history of hypertension (1 point), history of previous stroke (1 point), and admission total cholesterol less than 200 (2 points). Patients with an SIRS score of 4 or more were 3 times as likely to develop SIRS when compared with patients with a score of ≤3 (odds ratio = 2.815, 95% confidence interval 1.43-5.56, P = .0029). CONCLUSIONS In our sample of IV tPA-treated AIS patients, clinical and laboratory characteristics available on presentation were able to identify patients likely to develop SIRS during their acute hospitalization. Validation is required in other populations. If validated, this score could assist providers in predicting who will develop SIRS after treatment with IV tPA.


International Scholarly Research Notices | 2013

Hemorrhagic Transformation (HT) and Symptomatic Intracerebral Hemorrhage (sICH) Risk Prediction Models for Postthrombolytic Hemorrhage in the Stroke Belt

James E. Siegler; Muhammad Alvi; Amelia K Boehme; Michael Lyerly; Karen C. Albright; Reza Bavarsad Shahripour; Pawan V. Rawal; Niren Kapoor; April Sisson; J. Thomas Houston; Anne W. Alexandrov; Sheryl Martin-Schild; Andrei V. Alexandrov

Background Symptomatic intracerebral hemorrhage (sICH) remains the most feared complication of intravenous tissue plasminogen activator (IV tPA) treatment. We aimed to investigate how previously validated scoring methodologies would perform in treated patients in two US Stroke Belt states. Methods and Results We retrospectively reviewed consecutive patients from two centers in two Stroke Belt states who received IV tPA (2008–2011). We assessed the ability of three models to predict sICH. sICH was defined as a type 2 parenchymal hemorrhage with deterioration in National Institutes of Health Stroke Scale (NIHSS) score of ≥4 points or death. Among 457 IV tPA-treated patients, 19 (4.2%) had sICH (mean age 68, 26.3% Black, 63.2% female). The Cucchiara model was most predictive of sICH in the entire cohort (AUC: 0.6528) and most predictive of sICH among Blacks (OR = 6.03, 95% CI 1.07–34.1, P = 0.0422) when patients were dichotomized by score. Conclusions In our small sample from the racially heterogeneous US Stroke Belt, the Cucchiara model outperformed the other models at predicting sICH. While predictive models should not be used to justify nontreatment with thrombolytics, those interested in understanding contributors to sICH may choose to use the Cucchiara model until a Stroke Belt model is developed for this region.


Journal of Stroke & Cerebrovascular Diseases | 2014

Investigating the Utility of Previously Developed Prediction Scores in Acute Ischemic Stroke Patients in the Stroke Belt

Amelia K Boehme; Pawan V. Rawal; Michael Lyerly; Karen C. Albright; Reza Bavarsad Shahripour; Paola Palazzo; Niren Kapoor; Muhammad Alvi; J. Thomas Houston; Mark R. Harrigan; Luis Cava; April Sisson; Anne W. Alexandrov; Andrei V. Alexandrov

BACKGROUND To assess the utility of previously developed scoring systems, we compared SEDAN, named after the components of the score (baseline blood Sugar, Early infarct signs and (hyper) Dense cerebral artery sign on admission computed tomography scan, Age, and National Institutes of Health Stroke Scale on admission), Totaled Health Risks in Vascular Events (THRIVE), Houston Intra-arterial Therapy (HIAT), and HIAT-2 scoring systems among patients receiving systemic (intravenous [IV] tissue plasminogen activator [tPA]) and endovascular (intra-arterial [IA]) treatments. METHODS We retrospectively reviewed all IV tPA and IA patients presenting to our center from 2008-2011. The scores were assessed in patients who were treated with IV tPA only, IA only, and a combination of IV tPA and IA (IV-IA). We tested the ability of THRIVE to predict discharge modified Rankin scale (mRS) 3-6, HIAT and HIAT-2 discharge mRS 4-6, and SEDAN symptomatic intracerebral hemorrhage (sICH). RESULTS Of the 366 patients who were included in this study, 243 had IV tPA only, 89 had IA only, and 34 had IV-IA. THRIVE was predictive of mRS 3-6 in the IV-IA (odds ratio [OR], 1.95; 95% confidence interval [CI], 1.30-2.91) and the IV group (OR, 1.71; 95% CI, 1.43-2.04), but not in the IA group. HIAT was predictive of mRS 4-6 in the IA (OR, 3.55; 95% CI, 1.65-7.25), IV (OR, 3.47; 95% CI, 2.26-5.33), and IV-IA group (OR, 6.48; 95% CI, 1.41-29.71). HIAT-2 was predictive of mRS 4-6 in the IA (OR, 1.39; 95% CI, 1.03-1.87) and IV group (OR, 1.36; 95% CI, 1.18-1.57), but not in the IV-IA group. SEDAN was not predictive of sICH in the IA or the IV-IA group, but was predictive in the IV group (OR, 1.54; 95% CI, 1.01-2.36). CONCLUSIONS Our study demonstrated that although highly predictive of outcome in the original study design treatment groups, prediction scores may not generalize to all patient samples, highlighting the importance of validating prediction scores in diverse samples.


Southern Medical Journal | 2015

Patient Selection for Drip and Ship Thrombolysis in Acute Ischemic Stroke.

Michael Lyerly; Karen C. Albright; Amelia K Boehme; Reza Bavarsad Shahripour; John Donnelly; James T Houston; Pawan V. Rawal; Niren Kapoor; Muhammad Alvi; April Sisson; Anne W. Alexandrov; Andrei V. Alexandrov

Objectives The drip and ship model is a method used to deliver thrombolysis to acute stroke patients in facilities lacking onsite neurology coverage. We sought to determine whether our drip and ship population differs from patients treated directly at our stroke center (direct presenters). Methods We retrospectively reviewed consecutive patients who received thrombolysis at an outside facility with subsequent transfer to our center between 2009 and 2011. Patients received thrombolysis after telephone consultation with a stroke specialist. We examined demographics, vascular risk factors, laboratory values, and stroke severity in drip and ship patients compared with direct presenters. Results Ninety-six patients were identified who received thrombolysis by drip and ship compared with 212 direct presenters. The two groups did not differ with respect to sex, ethnicity, vascular risk factors, or admission glucose. The odds ratio (OR) of arriving at our hospital as a drip and ship for someone 80 years or older was 0.31 (95% confidence interval [CI] 0.15–0.61, P < 0.001). Only 21% of drip and ship patients were black versus 38% of direct presenters (OR 0.434, 95% CI 0.25–0.76, P = 0.004). Even after stratifying by age (<80 vs ≥80), a smaller proportion of drip and ship patients were black (OR 0.44, 95% CI 0.24–0.81, P = 0.008). Furthermore, we found that fewer black patients with severe strokes arrived by drip and ship (OR 0.33, 95% CI 0.11–0.98, P = 0.0028). Conclusions Our study showed that a smaller proportion of blacks and older adults arrived at our center by the drip and ship model. This may reflect differences in how patients are selected for thrombolysis and transfer to a higher level of care.


Journal of Stroke & Cerebrovascular Diseases | 2014

Safety of Protocol Violations in Acute Stroke tPA Administration

Michael Lyerly; Karen C. Albright; Amelia K Boehme; Reza Bavarsad Shahripour; James T Houston; Pawan V. Rawal; Niren Kapoor; Muhammad Alvi; April Sisson; Anne W. Alexandrov; Andrei V. Alexandrov


Journal of neurological disorders | 2013

The Potential Impact of Maintaining a 3-Hour IV Thrombolysis Window: How Many More Patients can we Safely Treat?

Michael Lyerly; Karen C. Albright; Amelia K Boehme; Reza Bavarsad Shahripour; James T Houston; Pawan V. Rawal; Niren Kapoor; Muhammad Alvi; April Sisson; Anne W. Alexandrov; Andrei V. Alexandrov


Stroke | 2013

Abstract 5: Management Of Intravenous tPA In Non-ICU Environments: Safety, Clinical Outcome, And Cost Savings

Kisha C Coleman; Paola Palazzo; Reza Bavarsad Shahripour; Amy Brooks; Mary A Cronin; Kara Sands; Michael Lyerly; April Sisson; Thomas K. Houston; Pawan V. Rawal; Muhammad Alvi; Niren Kapoor; Karen C. Albright; Amelia K Boehme; Andrei V. Alexandrov; Anne W. Alexandrov


Stroke | 2015

Abstract W P333: Seizure as the Presenting Symptom of ICH Patient Characteristics and EEG Utilization

Kanika Arora; Alyssa Gadpaille; Karen C. Albright; Muhammad Alvi; Ayaz Khawaja; Harn Shiue; Kara Sands; Mark R. Harrigan


Stroke | 2015

Abstract W P309: Serum Albumin Predicts Outcome In Primary Intracerebral Hemorrhage

Harn Shiue; Karen C. Albright; Kara Sands; Angela Hays; Alissa Gadpaille; Ayaz Khawaja; April Sisson; Muhammad Alvi; Reza Bavarsad Shahripour; Mark R. Harrigan

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Karen C. Albright

University of Alabama at Birmingham

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Reza Bavarsad Shahripour

University of Alabama at Birmingham

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Andrei V. Alexandrov

University of Alabama at Birmingham

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April Sisson

University of Alabama at Birmingham

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Michael Lyerly

University of Alabama at Birmingham

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Niren Kapoor

University of Alabama at Birmingham

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Pawan V. Rawal

University of Alabama at Birmingham

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Anne W. Alexandrov

University of Tennessee Health Science Center

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James T Houston

University of Alabama at Birmingham

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