Stephen C. Cook
Current Organizations / Institutes
The organizations/institutes from the scholar's latest article
Previous Organizations / Institutes
The organizations / institutes from the scholar's other articles in the past ten years
Stephen C. Cook has a total of 13 co-authors. Here are the top co-authors by number of shared publications:
Bennett P. Samuel
Congenital Heart Center, Spectrum Health Helen DeVos Children's Hospital, Grand Rapids, MI 49503, USA
2 shared publications- Bennett P. Samuel
Congenital Heart Center, Spectrum Health Helen DeVos Children's Hospital, Grand Rapids, Michigan, USA
2 shared publications Darcy N. Marckini
Congenital Heart Center, Spectrum Health Helen DeVos Children's Hospital, Grand Rapids, Michigan, USA
2 shared publicationsJessica L. Parker
Office of Research and Education, Spectrum Health, Grand Rapids, Michigan, USA
2 shared publicationsSihong Huang
Congenital Heart Center, Spectrum Health Helen DeVos Children's Hospital, Grand Rapids, MI 49503, USA
2 shared publicationsAllison J. Sterk
Congenital Heart Center, Helen DeVos Children’s Hospital, Adult Congenital Heart Disease Program, Spectrum Health, Grand Rapids, USA
1 shared publication
Latest Publications
- Open Access
- 9 December 2020
- Published by Wolters Kluwer Health in Maternal-Fetal Medicine
- Vol. 3 (1) , 71-74
The Pregnancy Heart Team Approach for the Adult with Hypertrophic Cardiomyopathy and Severe Left Ventricular Outflow Tract Obstruction
Hypertrophic cardiomyopathy (HCM), the most common single-gene cardiovascular disease, is associated with increased risk for arrhythmias, heart failure, and sudden cardiac death. The hemodynamic changes known to occur during pregnancy can exacerbate heart failure and arrhythmias in women with HCM. We present a 30-year-old woman with HCM to illustrate the benefits of multidisciplinary team management of severe left ventricular outflow tract obstruction (peak gradient >100 mmHg) for optimal maternal and fetal outcomes.
- 9 December 2020
- Published by Wolters Kluwer Health in Maternal-Fetal Medicine
- Vol. 3 (1) , 71-74
Open AccessThe Pregnancy Heart Team Approach for the Adult with Hypertrophic Cardiomyopathy and Severe Left Ventricular Outflow Tract Obstruction
Hypertrophic cardiomyopathy (HCM), the most common single-gene cardiovascular disease, is associated with increased risk for arrhythmias, heart failure, and sudden cardiac death. The hemodynamic changes known to occur during pregnancy can exacerbate heart failure and arrhythmias in women with HCM. We present a 30-year-old woman with HCM to illustrate the benefits of multidisciplinary team management of severe left ventricular outflow tract obstruction (peak gradient >100 mmHg) for optimal maternal and fetal outcomes.
- Open Access
- 13 October 2020
- Published by Springer Nature in SN Comprehensive Clinical Medicine
- Vol. 2 (11) , 2479-2481
Unrepaired Transitional Atrioventricular Septal Defect in a Geriatric Woman with Down Syndrome. Case Report
- 13 October 2020
- Published by Springer Nature in SN Comprehensive Clinical Medicine
- Vol. 2 (11) , 2479-2481
Open AccessUnrepaired Transitional Atrioventricular Septal Defect in a Geriatric Woman with Down Syndrome. Case Report
- 1 July 2020
- Published by Elsevier in Canadian Journal of Cardiology
- Vol. 36 (7) , 1098-1103
Complex Determinants of Work Ability in Adults With Congenital Heart Disease and Implications for Clinical Practice
- 1 July 2020
- Published by Elsevier in Canadian Journal of Cardiology
- Vol. 36 (7) , 1098-1103
Complex Determinants of Work Ability in Adults With Congenital Heart Disease and Implications for Clinical Practice
- 3 January 2019
- Published by Tech Science Press in Congenital Heart Disease
- Vol. 14 (3) , 356-361
Electronic health record associated stress: A survey study of adult congenital heart disease specialists
Background Physician burnout has many undesirable consequences, including negative impact on patient care delivery and physician career satisfaction. Electronic health records (EHRs) may exacerbate burnout by increasing physician workload. Objective To determine burnout in adult congenital heart disease (ACHD) specialists by assessing stress associated with EHRs. Design Electronic survey study of ACHD providers. Setting Canada and United States. Participants Three hundred eighty‐three ACHD specialists listed on the Adult Congenital Heart Association directory between February and April 2017. Outcome Measures Burnout was measured using the Maslach Burnout Inventory (MBI) to understand factors contributing to work life and EHR satisfaction. Chi‐square and Wilcoxon Rank Sum tests were used for statistical analysis. Results Of the 383 invited participants, 110 (28.7%) completed surveys with the majority (n = 88, 80.7%) reporting from an academic medical center. Burnout was defined as high scores on the emotional exhaustion and/or depersonalization MBI subscales. When comparing the 40% (n = 44) that met criteria for burnout with those that did not, there was strong disagreement that a reasonable amount of time is spent on clerical tasks related to direct (P = .0043) or indirect (P = .0004) patient care. There was strong disagreement that EHRs increased efficiency (P = .006) or the patient portal improved patient care (P = .0215). Finally, physicians who met criteria for burnout had lower personal accomplishment scores (P = .0355). Conclusions Our results suggest time spent on EHRs creates clerical burden exacerbating ACHD physician burnout. The high levels of emotional exhaustion may decrease quality of ACHD care by directing focus away from physician‐patient interaction. Health care systems must develop best practice for EHR design and implementation to optimize patient advocacy and care, and decrease physician burnout.
- 3 January 2019
- Published by Tech Science Press in Congenital Heart Disease
- Vol. 14 (3) , 356-361
Electronic health record associated stress: A survey study of adult congenital heart disease specialists
Background Physician burnout has many undesirable consequences, including negative impact on patient care delivery and physician career satisfaction. Electronic health records (EHRs) may exacerbate burnout by increasing physician workload. Objective To determine burnout in adult congenital heart disease (ACHD) specialists by assessing stress associated with EHRs. Design Electronic survey study of ACHD providers. Setting Canada and United States. Participants Three hundred eighty‐three ACHD specialists listed on the Adult Congenital Heart Association directory between February and April 2017. Outcome Measures Burnout was measured using the Maslach Burnout Inventory (MBI) to understand factors contributing to work life and EHR satisfaction. Chi‐square and Wilcoxon Rank Sum tests were used for statistical analysis. Results Of the 383 invited participants, 110 (28.7%) completed surveys with the majority (n = 88, 80.7%) reporting from an academic medical center. Burnout was defined as high scores on the emotional exhaustion and/or depersonalization MBI subscales. When comparing the 40% (n = 44) that met criteria for burnout with those that did not, there was strong disagreement that a reasonable amount of time is spent on clerical tasks related to direct (P = .0043) or indirect (P = .0004) patient care. There was strong disagreement that EHRs increased efficiency (P = .006) or the patient portal improved patient care (P = .0215). Finally, physicians who met criteria for burnout had lower personal accomplishment scores (P = .0355). Conclusions Our results suggest time spent on EHRs creates clerical burden exacerbating ACHD physician burnout. The high levels of emotional exhaustion may decrease quality of ACHD care by directing focus away from physician‐patient interaction. Health care systems must develop best practice for EHR design and implementation to optimize patient advocacy and care, and decrease physician burnout.
- 22 August 2018
- Published by Springer Nature in Current Cardiology Reports
- Vol. 20 (10) , 1-8
It Is Not Taboo: Addressing Sexual Function in Adults with Congenital Heart Disease
Purpose of the Review To review the current state of literature on sexual dysfunction in adults with congenital heart disease (ACHD). Recent Findings The prevalence of sexual dysfunction in ACHD is approximately 28%. Compared to age-matched cohorts, the prevalence of sexual dysfunction among ACHD cohorts demonstrates significant variability. ACHD have a lower rate of ever having sexual intercourse and often at a later age. Regardless of complexity, ACHD with sexual dysfunction have higher level of distress, decreased quality of life, and worse New York Heart Association classification. Patients, including heart failure and ACHD, treated with dual angiotensin receptor neprilysin inhibitor have reported improved sexual relationships. Summary The prevalence of sexual dysfunction in ACHD patients is high and sexual dysfunction research in ACHD remains limited. Therefore, the relationship between sexual dysfunction and ACHD remains ill-defined. Cardiologists that participate in the care of these patients should proactively discuss sexual health and provide counseling and therapies to provide high-quality healthcare for ACHD.
- 22 August 2018
- Published by Springer Nature in Current Cardiology Reports
- Vol. 20 (10) , 1-8
It Is Not Taboo: Addressing Sexual Function in Adults with Congenital Heart Disease
Purpose of the Review To review the current state of literature on sexual dysfunction in adults with congenital heart disease (ACHD). Recent Findings The prevalence of sexual dysfunction in ACHD is approximately 28%. Compared to age-matched cohorts, the prevalence of sexual dysfunction among ACHD cohorts demonstrates significant variability. ACHD have a lower rate of ever having sexual intercourse and often at a later age. Regardless of complexity, ACHD with sexual dysfunction have higher level of distress, decreased quality of life, and worse New York Heart Association classification. Patients, including heart failure and ACHD, treated with dual angiotensin receptor neprilysin inhibitor have reported improved sexual relationships. Summary The prevalence of sexual dysfunction in ACHD patients is high and sexual dysfunction research in ACHD remains limited. Therefore, the relationship between sexual dysfunction and ACHD remains ill-defined. Cardiologists that participate in the care of these patients should proactively discuss sexual health and provide counseling and therapies to provide high-quality healthcare for ACHD.