Publications by authors named "Simon J C Lee"

Background: Recent modifications to low-dose CT (LDCT)-based lung cancer screening guidelines increase the number of eligible individuals, particularly among racial and ethnic minorities. Because these populations disproportionately live in metropolitan areas, we analyzed the association between travel time and initial LDCT completion within an integrated, urban safety-net health care system.

Methods: Using Esri's StreetMap Premium, OpenStreetMap, and the r5r package in R, we determined projected private vehicle and public transportation travel times between patient residence and the screening facility for LDCT ordered in March 2017 through December 2022 at Parkland Memorial Hospital in Dallas, Texas.

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Low-dose computed tomography-based lung cancer screening represents a complex clinical undertaking that could require multiple referrals, appointments, and time-intensive procedures. These steps may pose difficulties and raise concerns among patients, particularly minority, under-, and uninsured populations. The authors implemented patient navigation to identify and address these challenges.

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Unlabelled: Using Donabedian's quality of care model, this study assessed process (hospital multimodal treatment) and structure (hospital surgical case volume) measures to evaluate localized pancreatic cancer outcomes.

Background: Treatment at high surgical volume hospitals has been shown to improve short-term outcomes. However, multimodal treatment-surgery and chemotherapy-is the standard of care yet only received by 35% of US patients and has not been examined at the hospital level.

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As clinical trials have become more complex, with increasing numbers of required procedures and clinic visits, gaining access to promising new treatments has become even more challenging for many individuals. To address these barriers, we implemented a financial reimbursement and outreach program designed to increase the number and diversity of participants in cancer clinical trials at centers in Dallas, Houston, and Philadelphia. As endorsed by U.

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Background: Monitoring disease incidence rates over time with population surveillance data is fundamental to public health research and practice. Bayesian disease monitoring methods provide advantages over conventional methods including greater flexibility in model specification and the ability to conduct formal inference on model-derived quantities of interest. However, software platforms for Bayesian inference are often inaccessible to nonspecialists.

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  • - The study investigates false-positive results in uninsured minority women undergoing 3-D mammography, analyzing data from 21,022 women in the Breast Screening and Patient Navigation (BSPAN) program in North Texas.
  • - False-positive rates were found to be 11.8% in women aged 40-49 and 9.6% in women aged 50-64, with increased odds related to certain demographic factors like hormone replacement therapy and prior mammograms.
  • - The findings highlight the need for further research to reduce false-positive rates and optimize resource use in community outreach programs aimed at this vulnerable population.
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  • Lung cancer screening trials often involve healthier populations, prompting researchers to study the impact of comorbidities in a real-world group of patients receiving low-dose CT scans for screening.
  • The study analyzed 1,358 patients, finding that most had a moderate level of comorbidities, with chronic pulmonary disease being the most prevalent. Overall, 70% completed the LDCT, with no significant link found between comorbidity levels and completion or results.
  • The research concluded that while comorbidities were present, they did not affect the likelihood of completing the screening or the outcomes, although the rate of completion improved over time as experience with the process grew.
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  • The commentary explores ways to enhance cancer care over the next decade by leveraging evidence and advances in multi-level behavioral interventions.
  • It highlights strategic areas for future research, including cancer prevention, early detection, and comprehensive care to address clinician shortages and improve patient outcomes.
  • The authors emphasize adapting to challenges posed by COVID-19 and other crises within healthcare, while identifying new opportunities for innovation based on lessons learned from past implementation efforts in behavioral health.
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Background: The Breast Screening and Patient Navigation (BSPAN) Program provides access to no-cost breast cancer screening services to uninsured women in North Texas. Using data from the longitudinal BSPAN program (2012-2019), we assessed prevalence and correlates of (i) baseline adherence and (ii) longitudinal adherence to screening mammograms.

Methods: Outcomes were baseline adherence (adherent if women received second mammogram 9-30 months after the index mammogram) and longitudinal adherence (assessed among baseline adherent women and defined as being adherent 39 months from the index mammogram).

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Purpose: The COVID-19 pandemic has led to profound changes in clinical research, including remote consent, telehealth, off-site procedures, shipment of therapy, and remote study monitoring. We assessed longitudinal perceptions of these adjustments among clinical research professionals.

Methods: We distributed an anonymous survey assessing experiences, perceptions, and recommendations regarding COVID-19-related clinical research adjustments to cancer clinical research office personnel in May 2020 and again in November 2020.

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Background: Professional society guidelines are emerging for cardiovascular care in cancer patients. However, it is not yet clear how effectively the cancer survivor population is screened and treated for cardiomyopathy in contemporary clinical practice. As electronic health records (EHRs) are now widely used in clinical practice, we tested the hypothesis that an EHR-based cardio-oncology registry can address these questions.

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Background: Accrual to cancer clinical trials is suboptimal. Few data exist regarding whether financial reimbursement might increase accruals.

Objective: The objective of this study was to assess perceptions about reimbursement to overcome barriers to trial accrual.

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Background: Less than 5% of eligible individuals in the United States undergo lung cancer screening. Variation in clinicians' participation in lung cancer screening has not been determined.

Patients And Methods: We studied medical providers who ordered ≥ 1 low-dose computed tomography (LDCT) for lung cancer screening from February 2017 through February 2019 in an integrated safety-net healthcare system.

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  • * In a study of 3,247 cancer patients, 58.5% of ED visits were self-referred, while clinicians referred patients to the ED 61.3% of the time for management.
  • * Self-referred visits were not associated with more severe conditions compared to clinician-referred visits, indicating a need to explore barriers to accessing alternatives to the ED for acute care.
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  • Cancer-related financial hardship negatively impacts patient care and quality of life; understanding current financial screening practices is essential for creating effective interventions.
  • A 2017 survey revealed that 72% of cancer practice groups conduct financial screenings, and 50% have specialized financial navigators; those serving higher Medicaid populations and fewer racial/ethnic minorities were more likely to engage in these practices.
  • The findings suggest a gap in financial care for practices with more diverse patient populations, indicating a need for targeted interventions to address financial hardships and inequities in cancer care.
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Objectives: Previous studies have implicated therapeutic drug monitoring (TDM), by measuring serum or urine drug levels, as a highly reliable technique for detecting medication non-adherence but the attitudes of patients and physicians toward TDM have not been evaluated previously. Accordingly, we solicited input from patients with uncontrolled hypertension and their physicians about their views on TDM.

Design: Prospective analysis of responses to a set of questions during semistructured interviews.

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Background: During the COVID-19 public health emergency, the FDA and NIH altered clinical trial requirements to protect participants and manage study conduct. Given their detailed knowledge of research protocols and regular contact with patients, clinicians, and sponsors, clinical research professionals offer important perspectives on these changes.

Methods: We developed and distributed an anonymous survey assessing COVID-19-related clinical trial adjustment experiences, perceptions, and recommendations to Clinical Research Office personnel at the Harold C.

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Article Synopsis
  • The study investigated lung cancer screening patterns in individuals who were eligible but not enrolled in a screening trial.
  • Among the 900 individuals approached, 447 enrolled, revealing no significant demographic differences between the enrolled and nonenrolled groups.
  • LDCT completion rates were notably higher for enrolled participants (81%) compared to those who declined (73%) and those who could not be reached (49%), indicating that contact and participation in trials may enhance screening adherence.
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• Health systems, especially those caring for medically underserved populations, should consider a multi-level approach to patient and stakeholder engagement to advance adoption of population screening as guideline-based care. • Iterative engagement should inform design and activation of an electronic order set to (1) capture socio-demographic data to establish screening eligibility, and (2) provide CMS-mandated documentation of patient counseling, while minimizing order burden for referring clinicians. • Patients who most stand to benefit from guideline-based lung cancer screening may also be those least likely to complete the multi-step processes of screening.

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Objective: The introduction of oral cancer therapies presents new challenges to delivery of quality cancer care. Little is known about how patients and providers address and overcome these challenges. We conducted a qualitative study exploring the range of patient and provider perspectives on oral cancer therapies.

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Purpose: Did the creation of an urgent care clinic specifically for patients with cancer affect emergency department visits among adults newly diagnosed with cancer?

Patients And Methods: We applied an interrupted time series analysis to adjusted monthly emergency department visits made by adults age 18 years or older who were diagnosed with cancer between 2009 and 2016 at a comprehensive cancer center. Cancer registry patients were linked to a longitudinal regional database of emergency department and hospital visits. Because the urgent care clinic was closed on weekends, we took advantage of the natural experiment by comparing weekend visits as a control group.

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Purpose: Mobile devices provide individuals with rapid and frequent access to electronic patient portals. We investigated how oncology patients use this technology to review test results and communicate with providers.

Patients And Methods: We performed a retrospective study of patients enrolled in the MyChart electronic health portal associated with the Epic electronic medical record at the Harold C.

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Background: The growing numbers of cancer survivors challenge delivery of high-quality survivorship care by healthcare systems. Innovative ways to improve care coordination for patients with cancer and multiple chronic conditions ("complex cancer survivors") are needed to achieve better care outcomes, improve patient experience of care, and lower cost. Our study, Project CONNECT, will adapt and implement three evidence-based care coordination strategies, shown to be effective for primary care conditions, among complex cancer survivors.

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Background: The population of cancer survivors is rapidly growing in the United States. Long-term and late effects of cancer, combined with the ongoing management of other chronic conditions, make survivors particularly vulnerable to polypharmacy and its adverse effects. In the current study, the authors examined patterns of prescription medication use and polypharmacy in a population-based sample of cancer survivors.

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