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Radecki Breitkopf, Carmen

Mayo Clinic

Deborah J. Rhodes, Carmen Radecki Breitkopf, Sarah M. Jenkins, and Celine M. Vachon, Mayo Clinic, Rochester; and Jeanette Y. Ziegenfuss, HealthPartners Institute for Education and Research, Minneapolis, MN.

Citations 8

Internet Use by Gynecologic Oncology Patients and Its Relationship with Anxiety
Corrales, Dalia M, Wells, Ali , Breitkopf, Carmen Radecki , Peña, Gabriela de la, Kaplan, Alan L., King, Lorrie S, Robazetti, Sonia C., Dinh, Tri A., Wells, Ali E, Radecki Breitkopf, Carmen, Corrales, Dalia M

Journal of Health Communication | February 23, 2018 | Volume: 23 | Issue: 3 | Pages: 299-305

10.1080/10810730.2018.1442529 Get It

Management of Adolescent–Parent Dyads’ Discordance for Willingness to Participate in a Reproductive Health Clinical Trial
Francis, Jenny , Fraiz, Lauren Dapena, Roche, Ariel M. de, Catallozzi, Marina , Breitkopf, Carmen Radecki , Rosenthal, Susan L. , Francis, Jenny K R , Radecki Breitkopf, Carmen, Roche, Ariel M. de

Journal of Empirical Research on Human Research Ethics | December 11, 2017 | Volume: 13 | Issue: 1 | Pages: 42-49

10.1177/1556264617745409 Get It

The objective of this study is to understand the resolution of discordance between adolescent–parent dyads about participation in research. Adolescent (14-17 years) and parent dyads were recruited from NYC pediatric clinics to assess attitudes toward research participation. A subset of dyads participated in videotaped discussions about participation in a hypothetical study. Videos from dyads that held strongly discordant opinions about participation ( n = 30) were content-coded and analyzed using a thematic framework approach. Strategies used to resolve discordance included asserting authority, granting autonomy, or recognizing inaccurate assumptions using a variety of communication behaviors. Missed opportunities to enroll initially discordant dyads may be avoided by allowing time for adolescents and parents to elicit information, clarify a situation, or convince the other.
A Population-Based Study of Sociodemographic and Geographic Variation in HPV Vaccination
Wilson, Patrick M. , Jacobson, Debra J., Agunwamba, Amenah A. , Breitkopf, Carmen Radecki , Sauver, Jennifer L. St. , Finney Rutten, Lila J, Radecki Breitkopf, Carmen, Jacobson, Robert M. , St Sauver, Jennifer L, Rutten, Lila J. Finney , St Sauver, Jennifer L

Cancer Epidemiology, Biomarkers & Prevention | February 14, 2017 | Volume: 26 | Issue: 4 | Pages: 533-540

10.1158/1055-9965.epi-16-0877 Get It

Abstract Background: Human papillomavirus (HPV) vaccination rates in the United States remain low and lag behind other recommended adolescent vaccines. Studies evaluating the association of geographic and area-level characteristics with HPV vaccination rates provide a valuable resource for public health planning. Method: We used the Rochester Epidemiology Project data linkage system to ascertain HPV vaccination rates between 2010 and 2015 in a 7-county region of southern Minnesota. Geocoded individual patient data were spatially linked to socioeconomic data from the American Community Survey at the census block group level. Bayesian hierarchical logistic regression was used to model incident vaccination rates, adjusting for individual- and area-level sociodemographic characteristics, and geolocation. Geolocation was modeled as an approximated Gaussian field using a Stochastic Partial Differential Equations approach. All models were estimated using Integrated Nested Laplace Approximations. Results: In adjusted models, increasing age and female sex were associated with increased HPV vaccination. Lower socioeconomic status was associated with decreased rates of initiation [adjusted odds ratio (AOR); 95% confidence interval = 0.90 (0.86–0.95)], completion of the second dose [AOR = 0.88 (0.83–0.93)], and completion of the third dose [AOR = 0.85 (0.80–0.92)]. Geographic spatial analysis demonstrated increased odds of vaccination for the eastern region and in the greater Rochester metropolitan area, showing significant spatial variation not explained by individual level characteristics and ACS block group-level data. Conclusions: HPV vaccination rates varied geographically and by individual and geographically indexed sociodemographic characteristics. Impact: Identifying geographic regions with low HPV vaccination rates can help target clinical and community efforts to improve vaccination rates. Cancer Epidemiol Biomarkers Prev; 26(4); 533–40. ©2017 AACR. See all the articles in this CEBP Focus section, “Geospatial Approaches to Cancer Control and Population Sciences.”
Awareness and knowledge of Human Papillomavirus (HPV), HPV‐related cancers, and HPV vaccines in an uninsured adult clinic population
Breitkopf, Carmen Radecki , Findley, Victoria, Jacobson, Debra J., Wilson, Patrick M. , Albertie, Monica, Colón‐Otero, Gerardo , Radecki Breitkopf, Carmen, Finney Rutten, Lila J, Jacobson, Robert M. , Rutten, Lila J. Finney

Cancer Medicine | October 17, 2016 | Volume: 5 | Issue: 11 | Pages: 3346-3352

10.1002/cam4.933 Get It

AbstractHuman papillomavirus (HPV) vaccines offer primary prevention of cervical cancer and protection against other HPV‐associated cancers. HPV vaccine coverage in the United States (U.S.) remains low, particularly among older adolescents/young adults, and the uninsured. We assessed awareness and knowledge of HPV disease, HPV‐related cancers, and HPV vaccines among working, uninsured adults. Data from the 2014 Health Information National Trends Survey (HINTS 4, Cycle 4) were used as a benchmark. Patients were surveyed in late 2014 at the Volunteers in Medicine free clinic in Duval County, Florida. Surveys contained validated measures of HPV disease and vaccine knowledge; HPV‐related cancer knowledge was also assessed. Two‐hundred and ninety‐six surveys were analyzable with an 84% participation rate. Half (50.3%) of participants had heard of HPV, and 32.1% had heard of the HPV vaccine; in HINTS, these estimates were 63.6% and 62.7%, respectively (both P < 0.0001). In adjusted models, high HPV disease knowledge was associated with white race and increased education; high vaccine knowledge was associated with white race, increased education, and female sex. Recognition of HPV as a causative agent was 43.9% for cervical, 9.1% for anal, and 11.1% for throat cancers. For all HPV‐associated cancers, participants had lower knowledge/recognition relative to HINTS. The uninsured, socioeconomically disadvantaged adults we surveyed were unaware of a ubiquitous virus that can cause cancer and the existence of a vaccine to protect against it. These findings point to settings and populations in which initiatives to promote HPV vaccination as a cancer prevention tool remain critical.
Ovarian cancer patients’ and their family members’ perspectives on novel vaccine and virotherapy trials
Breitkopf, Carmen Radecki , Ridgeway, Jennifer L. , Asiedu, Gladys B. , Carroll, Katherine , Tenney, Meaghan , Jatoi, Aminah , Radecki Breitkopf, Carmen, Ridgeway, Jennifer L

Clinical Trials | June 28, 2016 | Volume: 13 | Issue: 6 | Pages: 660-664

10.1177/1740774516654445 Get It

Background/aims: Some of the most promising avenues of cancer clinical investigation center on immunotherapeutic approaches. These approaches have provided notable gains in cancer therapeutics with recent Food and Drug Administration approvals of agents of this class in several types of cancers, although gains for ovarian cancer lag behind. This study examined perceptions of therapeutic trials including immunotherapy and virotherapy among ovarian cancer patients and their family members. Methods: A total of 72 semi-structured qualitative interviews were conducted with 33 patients and 39 family members at two National Cancer Institute–designated comprehensive cancer centers. Eligible patients were diagnosed with epithelial ovarian, primary peritoneal, or fallopian tube carcinoma and had experience with clinical trial conversations; family members were nominated by patients and interviewed separately. Applied thematic analysis was used to understand and interpret the data. Results: More participants were aware of vaccine trials than virus trials, although more than half had heard of at least one of them. Initial reactions to vaccine trials were generally favorable. For many, childhood experience with vaccines lent a familiar frame of reference. Virus trials elicited more negative initial reactions, including the use of adjectives such as “scary” and “dreadful.” Viruses seemed contagious or difficult to control. Increased receptivity to these trials occurred in the context of limited therapeutic options and cancer recurrence. Most participants, including those not immediately drawn to these types of trials, indicated openness to learning more. Conclusion: Although vaccine and viral trials are both immunologically based therapeutic approaches, patients who are offered these trials may perceive their potential benefit and safety quite differently. There is a need to consider terminology, solicit and address “gut reactions,” and provide information that enables patients and their family members to better understand the science behind these trials.
The Effect of Message Framing on African American Women’s Intention to Participate in Health-Related Research
Balls‐Berry, Joyce E. , Parker, Monica W. , Halyard, Michele Y. , Albertie, Monica, Pinn, Vivian W. , Breitkopf, Carmen Radecki , Hayes, Sharonne, Halyard, Michele, Enders, Felicity , Radecki Breitkopf, Carmen, Hayes, Sharonne N. , Balls-Berry, Joyce Joy E

Journal of Health Communication | April 14, 2016 | Volume: 21 | Issue: 5 | Pages: 527-533

10.1080/10810730.2015.1103333 Get It

The impact of a spiritual legacy intervention in patients with brain cancers and other neurologic illnesses and their support persons
Piderman, Katherine M. , Breitkopf, Carmen Radecki , Jenkins, Sarah M. , Kwete, Gracia M., Sytsma, Terin T. , Lovejoy, Laura A., Yoder, Timothy J., Jatoi, Aminah , Radecki Breitkopf, Carmen, Lapid, Maria I.

Psycho-Oncology | December 9, 2015 | Volume: 26 | Issue: 3 | Pages: 346-353

10.1002/pon.4031 Get It

AbstractObjectiveThe objectives were to assess the feasibility of using a novel, comprehensive chaplain‐led spiritual life review interview to develop a personal Spiritual Legacy Document (SLD) for persons with brain tumors and other neurodegenerative diseases and to describe spiritual well‐being (SWB), spiritual coping, and quality of life (QOL) of patients and their support persons (SP) before and after receipt of the SLD.MethodsPatient‐SP pairs were enrolled over a 2‐year period. Assessments included the Functional Assessment of Chronic Illness Therapy‐Spiritual Expanded Version, Brief Religious Coping Scale, Brief COPE Inventory, and QOL Linear Analog Scale. Baseline assessments were completed prior to an audio‐recorded spiritual life review interview with a chaplain.ResultsThirty‐two patient/SP pairs were enrolled; 27 completed baseline assessments and the interview. Twenty‐four reviewed their SLD and were eligible for follow‐up. A total of 15 patients and 12 SPs completed the 1‐month follow‐up; 10 patients and seven SPs completed the 3‐month follow‐up. Patients endorsed high levels of SWB and spiritual coping at baseline. Both patients and SPs evidenced improvement on several aspects of SWB, spiritual coping, and QOL at 1 month, but patients' decreased financial well‐being was also observed. Patients and SPs demonstrated favorable changes in peacefulness and positive religious coping at both time points.ConclusionsA chaplain‐led spiritual life review is a feasible intervention for patients with neurodegenerative disease and results in beneficial effects on patients and SPs. Copyright © 2015 John Wiley & Sons, Ltd.
Awareness of Breast Density and Its Impact on Breast Cancer Detection and Risk
Rhodes, Deborah J. , Breitkopf, Carmen Radecki , Jenkins, Sarah M. , Vachon, Celine M. , Radecki Breitkopf, Carmen, Ziegenfuss, Jeanette Y. , Vachon, Celine M.

Journal of Clinical Oncology | March 3, 2015 | Volume: 33 | Issue: 10 | Pages: 1143-1150

10.1200/jco.2014.57.0325 Get It

Purpose Legislation mandating disclosure of breast density (BD) information has passed in 21 states; however, actual awareness of BD and knowledge of its impact on breast cancer detection and risk are unknown. Methods We conducted a national cross-sectional survey administered in English and Spanish using a probability-based sample of screening-age women, with oversampling of Connecticut, the only state with BD legislation in effect for > 1 year before the survey. Results Of 2,311 women surveyed, 65% responded. Overall, 58% of women had heard of BD, 49% knew that BD affects breast cancer detection, and 53% knew that BD affects cancer risk. After multivariable adjustment, increased BD awareness was associated with white non-Hispanic race/ethnicity (Hispanic v white non-Hispanic: odds ratio [OR], 0.23; P < .001), household income (OR, 1.07 per category increase; P < .001), education (OR, 1.19 per category increase; P < .001), diagnostic evaluation after a mammogram (OR, 2.64; P < .001), and postmenopausal hormone therapy (OR, 1.69; P = .002). Knowledge of the masking effect of BD was associated with higher household income (OR, 1.10; P < .001), education (OR, 1.22; P = .01), prior breast biopsy (OR, 2.16; P < .001), and residing in Connecticut (Connecticut v other states: OR, 3.82; P = .003). Connecticut residents were also more likely to have discussed their BD with a health care provider (67% v 43% for residents of other US states; P = .001). Conclusion Disparities in BD awareness and knowledge exist by race/ethnicity, education, and income. BD legislation seems to be effective in increasing knowledge of BD impact on breast cancer detection. These findings support continued and targeted efforts to improve BD awareness and knowledge among women eligible for screening mammography.