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Dive into the research topics where Jane D. Scott is active.

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Featured researches published by Jane D. Scott.


Journal of Trauma-injury Infection and Critical Care | 2000

External fixation as a bridge to intramedullary nailing for patients with multiple injuries and with femur fractures: damage control orthopedics.

Thomas M. Scalea; Sharon Boswell; Jane D. Scott; Kimberly A. Mitchell; Mary E. Kramer; Andrew N. Pollak

BACKGROUND The advantages of early fracture fixation in patients with multiple injuries have been challenged recently, particularly in patients with head injury. External fixation (EF) has been used to stabilize pelvic fractures after multiple injury. It potentially offers similar benefits to intramedullary nail (IMN) in long-bone fractures and may obviate some of the risks. We report on the use of EF as a temporary fracture fixation in a group of patients with multiple injuries and with femoral shaft fractures. METHODS Retrospective review of charts and registry data of patients admitted to our Level 1 trauma center July of 1995 to June of 1998. Forty-three patients initially treated with EF of the femur were compared to 284 patients treated with primary IMN of the femur. RESULTS Patients treated with EF had more severe injuries with significantly higher Injury Severity Scores (26.8 vs. 16.8) and required significantly more fluid (11.9 vs. 6.2 liters) and blood (1.5 vs. 1.0 liters) in the initial 24 hours. Glasgow Coma Scale score was lower (p < 0.01) in those treated with EF (11 vs. 14.2). Twelve patients (28%) had head injuries severe enough to require intracranial pressure monitoring. All 12 required therapy for intracranial pressure control with mannitol (100%), barbiturates (75%), and/or hyperventilation (75%). Most patients had more than one contraindication to IMN, including head injury in 46% of cases, hemodynamic instability in 65%, thoracoabdominal injuries in 51%, and/or other serious injuries in 46%, most often multiple orthopedic injuries. Median operating room time for EF was 35 minutes with estimated blood loss of 90 mL. IMN was performed in 35 of 43 patients at a mean of 4.8 days after EF. Median operating room time for IMN was 135 minutes with an estimated blood loss of 400 mL. One patient died before IMN. One other patient with a mangled extremity was treated with amputation after EF. There was one complication of EF, i.e., bleeding around a pin site, which was self-limited. Four patients in the EF group died, three from head injuries and one from acute organ failure. No death was secondary to the fracture treatment selected. One patient who had EF followed by IMN had bone infection and another had acute hardware failure. CONCLUSION EF is a viable alternative to attain temporary rigid stabilization in patients with multiple injuries. It is rapid, causes negligible blood loss, and can be followed by IMN when the patient is stabilized. There were minimal orthopedic complications.


Annals of Emergency Medicine | 1997

An Evaluation of Technologies for Identifying Acute Cardiac Ischemia in the Emergency Department: A Report from a National Heart Attack Alert Program Working Group

Harry P. Selker; Robert J Zalenski; Elliott M. Antman; Tom P. Aufderheide; Sheilah Ann Bernard; Robert O. Bonow; W. Brian Gibler; Michael D Hagen; Paula A. Johnson; Joseph Lau; Robert A McNutt; Joseph P. Ornato; J.Sanford Schwartz; Jane D. Scott; Paul A Tunick; W. Douglas Weaver

Abstract [Selker HP, Zalenski RJ, Antman EM, Aufderheide TP, Bernard SA, Bonow RO, Gibler WB, Hagen MD, Johnson P, Lau J, McNutt RA, Ornato J, Schwartz JS, Scott JD, Tunick PA, Weaver WD: An evaluation of technologies for identifying acute cardiac ischemia in the emergency department: A report from a National Heart Attack Alert Program Working Group. Ann Emerg Med January 1997;29:13-87.]


Annals of Emergency Medicine | 1997

An Evaluation of Technologies for Identifying Acute Cardiac Ischemia in the Emergency Department: Executive Summary of a National Heart Attack Alert Program Working Group Report ☆ ☆☆ ★

Harry P. Selker; Robert J Zalenski; Elliott M. Antman; Tom P. Aufderheide; Sheilah Ann Bernard; Robert O. Bonow; W. Brian Gibler; Michael D Hagen; Paula A. Johnson; Joseph Lau; Robert A McNutt; Joseph P. Ornato; J.Sanford Schwartz; Jane D. Scott; Paul A Tunick; W. Douglas Weaver

Abstract [Selker HP, Zalenski RJ, Antman EM, Aufderheide TP, Bernard SA, Bonow RO, Gibler WB, Hagen MD, Johnson P, Lau J, McNutt RA, Ornato J, Schwartz JS, Scott JD, Tunick PA, Weaver WD: An evaluation of technologies for identifying acute cardiac ischemia in the emergency department: Executive Summary of a National Heart Attack Alert Program Working Group report. Ann Emerg Med January 1997;29:1-12.]


Injury-international Journal of The Care of The Injured | 2002

Trauma deaths in an Italian urban area: an audit of pre-hospital and in-hospital trauma care

Osvaldo Chiara; Jane D. Scott; Stefania Cimbanassi; Aldo Marini; Riccardo Zoia; Aurelio Rodriguez; Thomas M. Scalea

In Italy, a comprehensive regional study of trauma deaths has never been performed. We examined the organization and delivery of trauma care in the city area of Milan, using panel review of trauma deaths. Two panels evaluated the appropriateness of care of all trauma victims occurred during 1 year, applying predefined criteria and judging deaths as not preventable (NP), possible preventable (PP), and definitely preventable (DP). Two hundred and fifty-five deaths were reviewed. Blunt trauma were 78.04% and motor vehicle crashes accounted for over 50%. Most victims (73.72%) died during pre-hospital settings and 91.1% died within the first 6h, principally because of central nervous system injuries in blunt and hemorrhage in penetrating trauma. Panels judged 57% of deaths NP, 32% PP, 11% DP (inter-panel K-test 0.88). Preventable deaths were higher after in-hospital admission. Main failures of treatment were lack in airway control or intravenous infusions in pre-hospital and mismanagement with missed injuries in emergency department. The high rate of avoidable deaths in Milan supports the need of trained pre-hospital personnel and of well equipped referring hospitals for trauma.


Journal of Trauma-injury Infection and Critical Care | 1999

Early fracture fixation may be 'just fine' after head injury: No difference in central nervous system outcomes

Thomas M. Scalea; Jane D. Scott; Robert J. Brumback; Andrew R. Burgess; Kimberly A. Mitchell; Clifford H. Turen; Howard R. Champion

BACKGROUND Recent reports suggest that early fracture fixation worsens central nervous system (CNS) outcomes. We compared discharge Glasgow Coma Scale (GCS) scores, CNS complications, and mortality of severely injured adults with head injuries and pelvic/lower extremity fractures treated with early versus delayed fixation. METHODS Using trauma registry data, records meeting preselected inclusion criteria from the years 1991 to 1995 were examined. We identified 171 patients aged 14 to 65 years (mean age, 32.7 years) with head injuries and fractures who underwent early fixation (< or = 24 hours after admission) (n = 147) versus delayed fixation (> 24 hours after admission) (n = 24). RESULTS Patients were severely injured, with a mean admission GCS score of 9.1, Revised Trauma Score of 6.2, Injury Severity Score of 38, median intensive care unit length of stay of 16.5 days, and hospital length of stay of 23 days. No differences between groups were found by age, admission GCS score, Injury Severity Score, Revised Trauma Score, intensive care unit length of stay, hospital length of stay, shock, vasopressors, major nonorthopedic operative procedures, total intravenous fluids or blood products, or mortality rates. In survivors, no differences in discharge GCS scores or CNS complications were found. CONCLUSION We found no evidence to suggest that early fracture fixation negatively influences CNS outcomes or mortality.


Annals of Emergency Medicine | 2010

NIH Roundtable on Emergency Trauma Research

Charles B. Cairns; Ronald V. Maier; Opeolu Adeoye; Darryl C. Baptiste; William G. Barsan; Lorne H. Blackbourne; Randall S. Burd; Christopher R. Carpenter; David Chang; William G. Cioffi; Edward E. Cornwell; J. Michael Dean; Carmel Bitondo Dyer; David Jaffe; Geoff Manley; William J. Meurer; Robert W. Neumar; Robert Silbergleit; Molly W. Stevens; Michael Wang; Debra L. Weiner; David W. Wright; Robin Conwit; Billy Dunn; Basel Eldadah; Debra Egan; Rosemarie Filart; Giovanna Guerrero; Dallas Hack; Michael Handigan

STUDY OBJECTIVE The National Institutes of Health (NIH) formed an NIH Task Force on Research in Emergency Medicine to enhance NIH support for emergency care research. The NIH Trauma Research Roundtable was convened on June 22 to 23, 2009. The objectives of the roundtable are to identify key research questions essential to advancing the scientific underpinnings of emergency trauma care and to discuss the barriers and best means to advance research by exploring the role of trauma research networks and collaboration between NIH and the emergency trauma care community. METHODS Before the roundtable, the emergency care domains to be discussed were selected and experts in each of the fields were invited to participate in the roundtable. Domain experts were asked to identify research priorities and challenges and separate them into mechanistic, translational, and clinical categories. During and after the conference, the lists were circulated among the participants and revised to reach a consensus. RESULTS Emergency trauma care research is characterized by focus on the timing, sequence, and time sensitivity of disease processes and treatment effects. Rapidly identifying the phenotype of patients on the time spectrum of acuity and severity after injury and the mechanistic reasons for heterogeneity in outcome are important challenges in emergency trauma research. Other research priorities include the need to elucidate the timing, sequence, and duration of causal molecular and cellular events involved in time-critical injuries, and the development of treatments capable of halting or reversing them; the need for novel experimental models of acute injury; the need to assess the effect of development and aging on the postinjury response; and the need to understand why there are regional differences in outcomes after injury. Important barriers to emergency care research include a limited number of trained investigators and experienced mentors, limited research infrastructure and support, and regulatory hurdles. CONCLUSION The science of emergency trauma care may be advanced by facilitating the following: (1) development of an acute injury template for clinical research; (2) developing emergency trauma clinical research networks; (3) integrating emergency trauma research into Clinical and Translational Science Awards; (4) developing emergency care-specific initiatives within the existing structure of NIH institutes and centers; (5) involving acute trauma and emergency specialists in grant review and research advisory processes; (6) supporting learn-phase or small, clinical trials; (7) performing research to address ethical and regulatory issues; and (8) training emergency care investigators with research training programs.


Annals of Emergency Medicine | 2010

Summary of NIH Medical-Surgical Emergency Research Roundtable Held on April 30 to May 1, 2009

Amy H. Kaji; Roger J. Lewis; Tony Beavers-May; Robert A. Berg; Eileen M. Bulger; Charles B. Cairns; Clifton W. Callaway; Carlos A. Camargo; Joseph A. Carcillo; Roberta L. DeBiasi; Tania Diaz; Francine Ducharme; Seth W. Glickman; Katherine L. Heilpern; Robert W. Hickey; Terry L. Vanden Hoek; Judd E. Hollander; Susan L. Janson; Gregory J. Jurkovich; Arthur L. Kellermann; Stephen F. Kingsmore; Jeffrey A. Kline; Nathan Kuppermann; Robert A. Lowe; David McLario; Larry A. Nathanson; Graham Nichol; Andrew B. Peitzman; Lynne D. Richardson; Arthur B. Sanders

STUDY OBJECTIVE In 2003, the Institute of Medicine Committee on the Future of Emergency Care in the United States Health System convened and identified a crisis in emergency care in the United States, including a need to enhance the research base for emergency care. As a result, the National Institutes of Health (NIH) formed an NIH Task Force on Research in Emergency Medicine to enhance NIH support for emergency care research. Members of the NIH Task Force and academic leaders in emergency care participated in 3 roundtable discussions to prioritize current opportunities for enhancing and conducting emergency care research. The objectives of these discussions were to identify key research questions essential to advancing the scientific underpinnings of emergency care and to discuss the barriers and best means to advance research by exploring the role of research networks and collaboration between the NIH and the emergency care community. METHODS The Medical-Surgical Research Roundtable was convened on April 30 to May 1, 2009. Before the roundtable, the emergency care domains to be discussed were selected and experts in each of the fields were invited to participate in the roundtable. Domain experts were asked to identify research priorities and challenges and separate them into mechanistic, translational, and clinical categories. After the conference, the lists were circulated among the participants and revised to reach a consensus. RESULTS Emergency care research is characterized by focus on the timing, sequence, and time sensitivity of disease processes and treatment effects. Rapidly identifying the phenotype and genotype of patients manifesting a specific disease process and the mechanistic reasons for heterogeneity in outcome are important challenges in emergency care research. Other research priorities include the need to elucidate the timing, sequence, and duration of causal molecular and cellular events involved in time-critical illnesses and injuries, and the development of treatments capable of halting or reversing them; the need for novel animal models; and the need to understand why there are regional differences in outcome for the same disease processes. Important barriers to emergency care research include a limited number of trained investigators and experienced mentors, limited research infrastructure and support, and regulatory hurdles. The science of emergency care may be advanced by facilitating the following: (1) training emergency care investigators with research training programs; (2) developing emergency care clinical research networks; (3) integrating emergency care research into Clinical and Translational Science Awards; (4) developing emergency care-specific initiatives within the existing structure of NIH institutes and centers; (5) involving emergency specialists in grant review and research advisory processes; (6) supporting learn-phase or small, clinical trials; and (7) performing research to address ethical and regulatory issues. CONCLUSION Enhancing the research base supporting the care of medical and surgical emergencies will require progress in specific mechanistic, translational, and clinical domains; effective collaboration of academic investigators across traditional clinical and scientific boundaries; federal support of research in high-priority areas; and overcoming limitations in available infrastructure, research training, and access to patient populations.


Academic Emergency Medicine | 2014

Gender-specific research for emergency diagnosis and management of ischemic heart disease: proceedings from the 2014 Academic Emergency Medicine Consensus Conference Cardiovascular Research Workgroup.

Basmah Safdar; John T. Nagurney; Ayodola Anise; Holli A. DeVon; Gail D'Onofrio; Erik P. Hess; Judd E. Hollander; Mariane J. Legato; Alyson J. McGregor; Jane D. Scott; Semhar Z. Tewelde; Deborah B. Diercks

Coronary artery disease (CAD) is the most common cause of death for both men and women. However, over the years, emergency physicians, cardiologists, and other health care practitioners have observed varying outcomes in men and women with symptomatic CAD. Women in general are 10 to 15 years older than men when they develop CAD, but suffer worse postinfarction outcomes compared to age-matched men. This article was developed by the cardiovascular workgroup at the 2014 Academic Emergency Medicine (AEM) consensus conference to identify sex- and gender-specific gaps in the key themes and research questions related to emergency cardiac ischemia care. The workgroup had diverse stakeholder representation from emergency medicine, cardiology, critical care, nursing, emergency medical services, patients, and major policy-makers in government, academia, and patient care. We implemented the nominal group technique to identify and prioritize themes and research questions using electronic mail, monthly conference calls, in-person meetings, and Web-based surveys between June 2013 and May 2014. Through three rounds of nomination and refinement, followed by an in-person meeting on May 13, 2014, we achieved consensus on five priority themes and 30 research questions. The overarching themes were as follows: 1) the full spectrum of sex-specific risk as well as presentation of cardiac ischemia may not be captured by our standard definition of CAD and needs to incorporate other forms of ischemic heart disease (IHD); 2) diagnosis is further challenged by sex/gender differences in presentation and variable sensitivity of cardiac biomarkers, imaging, and risk scores; 3) sex-specific pathophysiology of cardiac ischemia extends beyond conventional obstructive CAD to include other causes such as microvascular dysfunction, takotsubo, and coronary artery dissection, better recognized as IHD; 4) treatment and prognosis are influenced by sex-specific variations in biology, as well as patient-provider communication; and 5) the changing definitions of pathophysiology call for looking beyond conventionally defined cardiovascular outcomes to patient-centered outcomes. These emergency care priorities should guide future clinical and basic science research and extramural funding in an area that greatly influences patient outcomes.


Circulation Research | 2012

K08 and K99 Cardiovascular Training: Comparisons and Trends among Current Awardees

Jane D. Scott; Drew E. Carlson

Training the next generation of independent cardiovascular investigators has been a longstanding interest to the Circulation Research community, as evidenced by an editorial in the first volume of this journal.1 Since then, National Institutes of Health (NIH) training mechanisms have expanded from a single offering of postdoctoral fellowships to the current offerings composed of institutional predoctoral and postdoctoral traineeships, individual predoctoral and postdoctoral fellowships, and individual early career development awards. The transition from postdoctoral trainee to independent status has always challenged aspiring young investigators and is especially difficult during fiscally constrained times. As resources dwindle, we wanted to compare the 2 training programs (K99/R00, K08) that most often launch cardiovascular bench science careers and describe the characteristics of individuals trained under each program. The NIH initiated the K99/R00 Pathway to Independence award to support this transition to independence for promising candidates. Participation by the National Heart, Lung, and Blood Institute (NHLBI) in the K99/R00 funding opportunity complements its long-standing participation in the K08 Mentored Clinical Scientist Award program. We compare the first 4 years of trainees in the cardiovascular K99/R00 portfolio with the concurrent experience with the K08 cardiovascular portfolio. The results highlight differences and similarities in the populations and institutions served and the training structures and skills developed. Continued analysis of this comparison will inform future approaches to maintain a vibrant, innovative, productive, and engaged biomedical research community. The K08 and K99/R00 programs have fundamental differences. The K08 provides up to 5 years of mentored research during the assistant professor years, whereas the last 3 years of the K99/R00 (the R00) is an independent award and starts with the first faculty appointment. We analyzed 4 years of data to compare and contrast the K08 with K99/R00 programs to determine the attributes of trainees and comment on the program …


Annals of Emergency Medicine | 2016

Confronting Ethical and Regulatory Challenges of Emergency Care Research With Conscious Patients

Neal W. Dickert; Jeremy Brown; Charles B. Cairns; Aaliyah Eaves-Leanos; Sara F. Goldkind; Scott Y. H. Kim; Graham Nichol; Katie J. O’Conor; Jane D. Scott; Richard Sinert; David Wendler; David W. Wright; Robert Silbergleit

Barriers to informed consent are ubiquitous in the conduct of emergency care research across a wide range of conditions and clinical contexts. They are largely unavoidable; can be related to time constraints, physical symptoms, emotional stress, and cognitive impairment; and affect patients and surrogates. US regulations permit an exception from informed consent for certain clinical trials in emergency settings, but these regulations have generally been used to facilitate trials in which patients are unconscious and no surrogate is available. Most emergency care research, however, involves conscious patients, and surrogates are often available. Unfortunately, there is neither clear regulatory guidance nor established ethical standards in regard to consent in these settings. In this report-the result of a workshop convened by the National Institutes of Health Office of Emergency Care Research and Department of Bioethics to address ethical challenges in emergency care research-we clarify potential gaps in ethical understanding and federal regulations about research in emergency care in which limited involvement of patients or surrogates in enrollment decisions is possible. We propose a spectrum of approaches directed toward realistic ethical goals and a research and policy agenda for addressing these issues to facilitate clinical research necessary to improve emergency care.

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Joseph P. Ornato

Virginia Commonwealth University

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Elliott M. Antman

Brigham and Women's Hospital

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J.Sanford Schwartz

National Institutes of Health

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Michael D Hagen

National Institutes of Health

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Paul A Tunick

National Institutes of Health

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Paula A. Johnson

Brigham and Women's Hospital

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Robert A McNutt

National Institutes of Health

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Robert J Zalenski

National Institutes of Health

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