Sumbal Janjua
Harvard University
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Featured researches published by Sumbal Janjua.
Journal of Trauma-injury Infection and Critical Care | 2011
de Moya M; Bramos T; Suresh Agarwal; Karim Fikry; Sumbal Janjua; David R. King; H.B. Alam; George C. Velmahos; Peter A. Burke; William D. Tobler
BACKGROUND In trauma patients, open reduction and internal fixation of rib fractures remain controversial. We hypothesized that patients who have open reduction and internal fixation of rib fractures would experience less pain compared with controls and thus require fewer opiates. Further, we hypothesized that improved pain control would result in fewer pulmonary complications and decreased length of stay. METHODS This is a retrospective bi-institutional matched case-control study. Cases were matched 1:2 by age, injury severity Score, chest abbreviated injury severity score, head abbreviated injury severity score, pulmonary contusion score, and number of fractured ribs. The daily total doses of analgesic drugs were converted to equianalgesic intravenous morphine doses, and the primary outcome was inpatient narcotic administration. RESULTS Sixteen patients between July 2005 and June 2009 underwent rib fixation in 5 ± 3 days after injury using an average of 3 (1-5) metallic plates. Morphine requirements decreased from 110 mg ± 98 mg preoperatively to 63 ± 57 mg postoperatively (p = 0.01). There were no significant differences between cases and controls in the mean morphine dose (79 ± 63 vs. 76 ± 55 mg, p = 0.65), hospital stay (18 ± 12 vs. 16 ± 11 days, p = 0.67), intensive care unit stay (9 ± 8 vs. 7 ± 10 days, p = 0.75), ventilation days (7 ± 8 vs. 6 ± 10, p = 0.44), and pneumonia rates (31% vs. 38%, p = 0.76). CONCLUSION The need for analgesia was significantly reduced after rib fixation in patients with multiple rib fractures. However, no difference in outcomes was observed when these patients were compared with matched controls in this pilot study. Further study is required to investigate these preliminary findings.
Archives of Surgery | 2011
Karim Fikry; George C. Velmahos; Athanasios Bramos; Sumbal Janjua; Marc de Moya; David R. King; Hasan B. Alam
OBJECTIVE To determine whether selective nonoperative management of abdominal gunshot wounds (AGSW) is safe in trauma centers with a low volume of penetrating trauma. DESIGN Retrospective study. SETTING Academic level 1 trauma center with approximately 10% penetrating trauma. PATIENTS All patients with anterior and posterior AGSW (January 1, 1999, through December 31, 2009), excluding tangential injuries, transfers, and deaths in the emergency department. Patients with hemodynamic instability or peritonitis received an urgent laparotomy. The remaining patients had selective nonoperative management. A delayed laparotomy was offered for worsening symptoms or worrisome computed tomography findings. MAIN OUTCOME MEASURES Hospital stay, complications, and mortality. RESULTS Of 125 AGSW patients, 38 (30%) were initially managed by selective nonoperative management (25 of 99 anterior and 13 of 26 posterior AGSW patients). Seven selective nonoperative management patients received delayed laparotomy as late as 11 hours after admission. At the end, 30 of the 125 patients (24%) were successfully managed without an operation (20 of 99 anterior and 10 of 26 posterior AGSW patients). There were no predictors of delayed laparotomy and no complications or mortality attributed to it. Ten patients (8%) had a nontherapeutic laparotomy, and 3 of them developed complications. CONCLUSIONS Selective nonoperative management of AGSW is feasible and safe in trauma centers with low penetrating trauma volumes. Nearly 1 in 4 AGSW patients does not need a laparotomy, and nontherapeutic laparotomies are associated with complications. The volume of AGSW per se should not be an excuse for routine laparotomies. These data become particularly important because penetrating trauma volumes are decreasing around the country.
Journal of the American College of Cardiology | 2017
Sumbal Janjua; Virginia A. Triant; Daniel Addison; Bálint Szilveszter; Susan Regan; Pedro V. Staziaki; Steven A. Grinspoon; Udo Hoffmann; Markella V. Zanni; Tomas G. Neilan
There is a 2.5-fold increased risk of incident heart failure (HF) among women living with human immunodeficiency virus (HIV) (WLWHIV) [(1)][1]. Whether HF outcomes differ by HIV status among women has not been established. Leveraging data from a large, current and established U.S. health care system
Jacc-cardiovascular Imaging | 2017
Hamed Emami; Richard A. P. Takx; Thomas Mayrhofer; Sumbal Janjua; Jakob Park; Amit Pursnani; Ahmed Tawakol; Michael T. Lu; Maros Ferencik; Udo Hoffmann
OBJECTIVES This study sought to determine prognostic value of nonobstructive coronary artery disease (CAD) for atherosclerotic cardiovascular disease (ASCVD) events and to determine whether incorporation of this information into the pooled cohort equation reclassifies recommendations for statin therapy as defined by the 2013 guidelines for cholesterol management of the American College of Cardiology and American Heart Association (ACC/AHA). BACKGROUND Detection of nonobstructive CAD by coronary computed tomography angiography may improve risk stratification and permit individualized and more appropriate allocation of statin therapy. METHODS This study determined the pooled hazard ratio of nonobstructive CAD for ASCVD events from published studies and incorporated this information into the ACC/AHA pooled cohort equation. The study calculated revised sex- and ethnicity-based 10-year ASCVD risk and determined boundaries corresponding to the original 7.5% risk for ASCVD events. It also assessed reclassification for statin eligibility by incorporating the results from meta-analysis to individual patients from a separate cohort. RESULTS This study included 2 studies (2,295 subjects; 66% male; prevalence of nonobstructive CAD, 47%; median follow-up, 49 months; 67 ASCVD events). The hazard ratio of nonobstructive CAD for ASCVD events was 3.2 (95% confidence interval: 1.5 to 6.7). Incorporation of this information into the pooled cohort equation resulted in reclassification toward statin eligibility in individuals with nonobstructive CAD, with an original ASCVD score of 3.0% and 5.9% or higher in African-American women and men and a score of 4.4% and 4.6% or higher in Caucasian women and men, respectively. The absence of nonobstructive CAD resulted in reclassification toward statin ineligibility if the original ASCVD score was as 10.0% and 17.9% or lower in African-American women and men and 13.7% and 14.3% or lower in Caucasian women and men, respectively. Reclassification is observed in 14% of patients. CONCLUSIONS Detection of nonobstructive CAD by coronary computed tomography angiography improves risk stratification and permits individualized and more appropriate allocation of statin therapy across sex and ethnicity groups.
Circulation-cardiovascular Imaging | 2017
Daniel O. Bittner; Thomas Mayrhofer; Fabian Bamberg; Travis R. Hallett; Sumbal Janjua; Daniel Addison; John T. Nagurney; James E. Udelson; Michael T. Lu; Quynh A. Truong; Pamela K. Woodard; Judd E. Hollander; Chadwick D. Miller; Anna Marie Chang; Harjit Singh; Harold I. Litt; Udo Hoffmann; Maros Ferencik
Background— Coronary artery calcification (CAC) may impair diagnostic assessment of coronary computed tomography angiography (CTA). We determined whether CAC affects efficiency of coronary CTA in patients with suspected acute coronary syndrome (ACS). Methods and Results— This is a pooled analysis of ACRIN-PA (American College of Radiology Imaging Network–Pennsylvania) 4005 and the ROMICAT-II trial (Rule Out Myocardial Infarction/Ischemia Using Computer Assisted Tomography) comparing an initial coronary CTA strategy to standard of care in acute chest pain patients. In the CTA arms, we investigated appropriateness of downstream testing, cost, and diagnostic yield to identify patients with obstructive coronary artery disease on subsequent invasive coronary angiography across CAC score strata (Agatston score: 0, >0–10, >10–100, >100–400, >400). Out of 1234 patients (mean age 51±8.8 years), 80 (6.5%) had obstructive coronary artery disease (≥70% stenosis) and 68 (5.5%) had ACS. Prevalence of obstructive coronary artery disease (1%–64%), ACS (1%–44%), downstream testing (4%–72%), and total (2337–8484 US
Journal of stroke | 2018
Daniel Addison; Patrick R. Lawler; Hamed Emami; Sumbal Janjua; Pedro V. Staziaki; Travis R. Hallett; Orla Hennessy; Hang Lee; Bálint Szilveszter; Michael T. Lu; Negar Mousavi; Matthew Nayor; Francesca N. Delling; Javier Romero; Lori J. Wirth; Annie W. Chan; Udo Hoffmann; Tomas G. Neilan
) and diagnostic cost (2310–6678 US
Journal of the American Heart Association | 2017
Daniel Addison; Sara B. Seidelmann; Sumbal Janjua; Hamed Emami; Pedro V. Staziaki; Travis R. Hallett; Bálint Szilveszter; Michael T. Lu; Richard P. Cambria; Udo Hoffmann; Annie W. Chan; Lori J. Wirth; Tomas G. Neilan
) increased across CAC strata (P<0.001). As the increase in testing and cost were lower than the increase of ACS rate in patients with CAC>400, cost to diagnose one ACS was lowest in this group (19 283 US
International Journal of Cardiology | 2017
Daniel O. Bittner; Richard A. P. Takx; Pedro V. Staziaki; Sumbal Janjua; Tomas G. Neilan; Nandini M. Meyersohn; Michael T. Lu; Anand M. Prabhakar; John T. Nagurney; Udo Hoffmann; Brian B. Ghoshhajra
versus 464 399 US
Circulation-cardiovascular Imaging | 2017
Sumbal Janjua; Pedro V. Staziaki; Bálint Szilveszter; Richard A. P. Takx; Thomas Mayrhofer; Orla Hennessy; Hamed Emami; Jakob Park; Alexander R. Ivanov; Travis R. Hallett; Michael T. Lu; Javier Romero; Steven Grinspoon; Udo Hoffmann; Markella V. Zanni; Tomas G. Neilan
) as compared with patients without CAC. The diagnostic yield of invasive coronary angiography was highest in patients with CAC>400 (87% versus 38%). Conclusions— Downstream testing, total, and diagnostic cost increased with increasing CAC, but were found to be appropriate because obstructive coronary artery disease and ACS were more prevalent in patients with high CAC. In patients with acute chest pain undergoing coronary CTA, cost-efficient testing and excellent diagnostic yield can be achieved even with high CAC burden. Clinical Trial Registration— URL: http://www.clinicaltrials.gov. Unique identifiers: NCT01084239 and NCT00933400.
PLOS ONE | 2018
Puja Kohli; Pedro V. Staziaki; Sumbal Janjua; Daniel Addison; Travis R. Hallett; Orla Hennessy; Richard A. P. Takx; Michael T. Lu; Florian J. Fintelmann; Marc J. Semigran; R. S. Harris; Bartolome R. Celli; Udo Hoffmann; Tomas G. Neilan
Background and Purpose Interventions to reduce the risk for cerebrovascular events (CVE; stroke and transient ischemic attack [TIA]) after radiotherapy (RT) for head and neck cancer (HNCA) are needed. Among broad populations, statins reduce CVEs; however, whether statins reduce CVEs after RT for HNCA is unclear. Therefore, we aimed to test whether incidental statin use at the time of RT is associated with a lower rate of CVEs after RT for HNCA. Methods From an institutional database we identified all consecutive subjects treated with neck RT from 2002 to 2012 for HNCA. Data collection and event adjudication was performed by blinded teams. The primary outcome was a composite of ischemic stroke and TIA. The secondary outcome was ischemic stroke. The association between statin use and events was determined using Cox proportional hazard models after adjustment for traditional and RT-specific risk factors. Results The final cohort consisted of 1,011 patients (59±13 years, 30% female, 44% hypertension) with 288 (28%) on statins. Over a median follow-up of 3.4 years (interquartile range, 0.1 to 14) there were 102 CVEs (89 ischemic strokes and 13 TIAs) with 17 in statin users versus 85 in nonstatins users. In a multivariable model containing known predictors of CVE, statins were associated with a reduction in the combination of stroke and TIA (hazard ratio [HR], 0.4; 95% confidence interval [CI], 0.2 to 0.8; P=0.01) and ischemic stroke alone (HR, 0.4; 95% CI, 0.2 to 0.8; P=0.01). Conclusions Incidental statin use at the time of RT for HNCA is associated with a lower risk of stroke or TIA.