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Dive into the research topics where Caroline Dorsen is active.

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Featured researches published by Caroline Dorsen.


American Journal of Public Health | 2015

Putting the Mouth Back in the Head: HEENT to HEENOT

Judith Haber; Erin Hartnett; Kenneth Allen; Donna Hallas; Caroline Dorsen; Julia Lange-Kessler; Madeleine Lloyd; Edwidge Thomas; Dorothy Wholihan

Improving oral health is a leading population health goal; however, curricula preparing health professionals have a dearth of oral health content and clinical experiences. We detail an educational and clinical innovation transitioning the traditional head, ears, eyes, nose, and throat (HEENT) examination to the addition of the teeth, gums, mucosa, tongue, and palate examination (HEENOT) for assessment, diagnosis, and treatment of oral-systemic health. Many New York University nursing, dental, and medical faculty and students have been exposed to interprofessional oral health HEENOT classroom, simulation, and clinical experiences. This was associated with increased dental-primary care referrals. This innovation has potential to build interprofessional oral health workforce capacity that addresses a significant public health issue, increases oral health care access, and improves oral-systemic health across the lifespan.


Gender & Development | 2009

The oral-systemic connection in primary care.

Judith Haber; Sheryl Strasser; Madeleine Lloyd; Caroline Dorsen; Rose Knapp; Carolyn Auerhahn; Robert H. Kennedy; Michael C. Alfano; Terry Fulmer

The Nurse Practitioner • March 2009 43 mproving access to healthcare and enhancing health promotion and disease prevention are major priorities for the well-being of the public and a central focus of current federal health initiatives. Furthermore, as recognized by the U.S. Surgeon General in 2000, evidence surrounding the critical importance of the oral-systemic connection is mounting. The unique partnership of the New York University (NYU) Colleges of Dentistry and Nursing provides an opportunity to put into operation a vision of how to increase access to primary healthcare and proactively address oral-systemic issues through an innovative NP-Managed Faculty Practice Model. The following article describes the evolution of the model, which has been guided by evidence-based research and federal legislation urging new paradigms of healthcare delivery.


Journal of Cardiovascular Nursing | 2015

Improving heart failure self-care through a community-based skill-building intervention: A study protocol

Victoria Vaughan Dickson; Gail D’Eramo Melkus; Caroline Dorsen; Stuart D. Katz; Barbara Riegel

Background:Self-care is the cornerstone of heart failure (HF) management. Numerous approaches to improving HF self-care, which involves adherence to the treatment plan, routine symptom monitoring, and the response to symptoms when they occur, have been developed with little impact on HF outcomes. On the basis of HF practice recommendations that patients receive education and counseling that emphasizes self-care and targets skill building of critical target behaviors, we are conducting a clinical trial designed to improve self-care among community-dwelling older adults using an innovative group-based, skill-building approach led by a trained health educator. Objective:This article describes the study design and research methods used to implement and evaluate the intervention. Methods:The study uses a staggered randomized controlled design to assess feasibility of providing an HF self-care intervention in a community group setting to improve HF self-care, knowledge, and health-related quality of life at 1 and 3 months. A community engagement approach is used to partner with the community throughout all phases of the project. Seventy-five older adults with HF are randomly assigned to the intervention consisting of six to eight 60-minute sessions held in community senior centers or to the wait-list control group. Focus groups are used to elicit feedback on the participants’ experience in the program. Results:Preliminary study participation data (n = 60; women, 48%; black, 27%; Hispanic, 32%; mean [SD] age, 70 [10] years) and focus group feedback suggest that the delivery approach is feasible and acceptable, and the participants are very satisfied with the program. Conclusions:Implementation of a community-based HF self-care intervention delivered in partnership with established community-based centers is an innovative approach to intervention. If efficacy is demonstrated, this intervention has far-reaching implications for helping the growing population of HF patients in ethnically diverse communities.


Journal of Interprofessional Care | 2012

Oral health care and smoking cessation practices of interprofessional home care providers for their patients with HIV

Nancy VanDevanter; Caroline Dorsen; Peter Messeri; Donna Shelley; Andresa Person

The need for oral health services among patients with HIV, especially those in advanced stages of disease and those who smoke, has been well documented. Patients receiving HIV-related home care services provide an opportunity for assessment of oral health and smoking cessation needs; however, the majority of home care providers lack formal training to provide these services, thus interprofessional collaborations may be of value. This study assessed the oral health and smoking cessation practices of a random sample of 81 HIV home care providers. Results showed very favorable attitudes toward providing these services with some differences across disciplines. More than 70% of nurses would like to receive additional training in comprehensive oral health assessment by dental professionals. The study provides evidence for the potential of expanding these services for patients with HIV through interprofessional collaboration, in particular with nurses and dentists.


Journal of the Association of Nurses in AIDS Care | 2011

Barriers to volunteer enrollment in HIV preventive vaccine clinical research trials: a review of the literature.

Arlene Hurley-Rosenblatt; Caroline Dorsen

Attempting to enroll volunteers into a clinical research study often presents a challenge to the investigative team. Potential subjects often look on the experience with suspicion; they might fear being treated like ‘‘guinea pigs.’’ Many preconceived biases about participating in research stem from one particular clinical study, the infamous Tuskegee syphilis experiment. In this study, which started in 1932 and lasted 40 years, 600 Black men (300 with syphilis and 201 without syphilis) from a rural area of Alabama were told by researchers that they were being treated for ‘‘bad blood,’’ a local term used to describe several ailments, including syphilis, anemia, and fatigue. In truth, they did not receive the proper treatment to cure syphilis. When the study was reviewed, an investigative panel found (a) no evidence that researchers had informed the participants about the study or its real purpose, (b) that the men had been misled and had not been given all the facts required to provide informed consent, and (c) nothing to show that subjects were ever given the choice of quitting the study, even when penicillin became the drug of choice for syphilis in 1947 (Centers for Disease Control and Prevention, 2009). Although codes have since been implemented to prevent such unethical behavior from recurring and thousands of studies have been conducted without incident, the fear of being harmed still haunts potential volunteers. When testing a preventive vaccine against HIV, the challenges to recruit, enroll, and retain volunteers for clinical trials become even more difficult because many communities have not been adequately informed or rather have been misinformed about HIV vaccine research, resulting in a basic mistrust of this research. Knowing the factors that influence enrollment of volunteers into HIV vaccine research can greatly affect recruitment and retention of volunteers. As McCluskey, Alexander, Larkin, Murguia, and Wakefield (2005) wrote, ‘‘A promising vaccine candidate without the volunteers needed to test it, or a vaccine that is not trusted by the people it is meant to benefit, will impair long-term success’’ (p. 650). The purpose of this article is to explore factors that deter recruitment of volunteers into HIV preventive vaccine trials.


Addiction Research & Theory | 2018

Ceremonial ‘Plant Medicine’ use and its relationship to recreational drug use: an exploratory study

Caroline Dorsen; Joseph J. Palamar; Michele G. Shedlin

Abstract Background: The ceremonial use of psychoactive/hallucinogenic plant based drugs, such as ayahuasca, psilocybin and others, is a growing trend in the United States (US) and globally. To date, there has been little research documenting how many people are using psychoactive substances in this context, who the users are, what benefits/risks exist in the use of these drugs and the relationship between ceremonial drug use and recreational drug use. In this paper we describe a cohort of plant medicine facilitators in the US and explore how they differentiate plant medicine use from recreational drug use. Methods: Using modified ethnography, individual interviews were conducted in 2016 with 15 participants who are currently facilitating plant medicine ceremonies in the US. Descriptive content analysis was performed to discover themes and to inform a larger mixed-method study. Results: Ceremonial drug use was seen by participants as a natural healing and treatment modality used in the context of community and ritual. Three main themes were identified relating to participants’ differentiation between ceremonial plant medicine use and recreational drug use: (1) participants see a clear delineation between plant medicine use and recreational drug use; (2) plant medicine is seen as a potential treatment for addiction, but concerns exist regarding potential interference with recovery; and (3) plant medicine use may influence recreational use. Conclusions: More research is needed on who is using plant medicine, motivators for use, perceived and real risks and benefits of plant medicine use and harm reduction techniques regarding safe ingestion.


Womens Health Issues | 2018

Cardiovascular Disease Risk in Sexual Minority Women (18-59 Years Old): Findings from the National Health and Nutrition Examination Survey (2001-2012)

Billy A. Caceres; Abraham A. Brody; Perry N. Halkitis; Caroline Dorsen; Gary Yu; Deborah Chyun

OBJECTIVE Sexual minority women (lesbian and bisexual) experience significant stigma, which may increase their cardiovascular disease (CVD) risk. The purpose of this study was to examine the prevalence of modifiable risk factors for CVD (including mental distress, health behaviors, blood pressure, glycosylated hemoglobin, and total cholesterol) and CVD in sexual minority women compared with their heterosexual peers. MATERIALS AND METHODS A secondary analysis of the National Health and Nutrition Examination Survey (2001-2012) was conducted. Multiple imputation with chained equations was performed. Logistic regression models adjusted for relevant covariates were run. Self-report (medical history and medication use) and biomarkers for hypertension, diabetes, and high total cholesterol were examined. RESULTS The final analytic sample consisted of 7,503 that included 346 sexual minority women (4.6%). Sexual minority women were more likely to be younger, single, have a lower income, and lack health insurance. After covariate adjustment, sexual minority women exhibited excess CVD risk related to higher rates of frequent mental distress (adjusted odds ratio [AOR], 2.05; 95% confidence interval [CI], 1.45-2.88), current tobacco use (AOR, 2.11; 95% CI, 1.53-2.91), and binge drinking (AOR, 1.66; 95% CI, 1.17-2.34). Sexual minority women were more likely to be obese (AOR, 1.61; 95% CI, 1.23-2.33) and have glycosylated hemoglobin consistent with prediabetes (AOR, 1.56; 95% CI, 1.04-2.34). No differences were observed for other outcomes. CONCLUSIONS Sexual minority women demonstrated increased modifiable risk factors for CVD, but no difference in CVD diagnoses. Several emerging areas of research are highlighted, in particular, the need for CVD prevention efforts that target modifiable CVD risk in sexual minority women.


The Diabetes Educator | 2018

Prevalence of Obesity, Prediabetes, and Diabetes in Sexual Minority Women of Diverse Races/Ethnicities: Findings From the 2014-2015 BRFSS Surveys

Kelley Newlin Lew; Caroline Dorsen; Gail D’Eramo Melkus; Monika Maclean

Purpose The purpose of this study is to assess the weighted prevalence and odds ratios of obesity, prediabetes, and diabetes by (1) female sexual orientation (lesbian, bisexual, and straight) with racial/ethnic (Hispanic, non-Hispanic black, and non-Hispanic white) groups combined and (2) across and within racial/ethnic groups by sexual orientation. Methods A secondary analysis of pooled 2014-2015 Behavioral Risk Factor Surveillance System data from 28 states (N = 136 878) was conducted. Rao-Scott chi-square test statistics were computed and logistic regression models were developed to assess weighted prevalence and odds ratios of obesity, prediabetes, and diabetes with adjustments for demographics (age, income, and education), depression, and health care access factors. Results With racial/ethnic groups combined, lesbian and bisexual women, relative to straight women, had a significantly increased likelihood for obesity when controlling for demographics. Bisexual women were found to have significantly reduced odds for diabetes, compared with straight women, with adjustments for demographics, depression, and health care access factors. Compared with their non-Hispanic white counterparts, Hispanic lesbian women had significantly increased odds for obesity and diabetes, while non-Hispanic black bisexual women had a significantly greater likelihood for obesity, holding demographics, depression, and health care access factors constant. Non-Hispanic white lesbian women had an increased likelihood for obesity relative to their straight, ethnic/racial counterparts. Prediabetes subsample analysis revealed the prevalence was low across all female sexual orientation groups. Conclusion Sexual minority women, particularly those of color, may be at increased risk for obesity and diabetes. Research is needed to confirm the findings.


The Diabetes Educator | 2018

Prevalence of Obesity, Prediabetes, and Diabetes in Sexual Minority Men: Results From the 2014 Behavioral Risk Factor Surveillance System

Kelley Newlin Lew; Caroline Dorsen; Thomas Lawrence Long

Purpose The purpose of this study is to assess the prevalence and related odds ratios for obesity, prediabetes, and diabetes in sexual minority men (SMM) in relation to straight men. Methods A secondary analysis of 2014 Behavioral Risk Factor Surveillance System data from 19 states (n = 53 542) was conducted. Weighted means and standard errors were computed to estimate prevalence rates of obesity, prediabetes, and diabetes across male sexual orientation groups, respectively. Unadjusted and adjusted (demographics, depression, and health care access factors) weighted logistic regression models were developed. Results Obesity prevalence was lower in gay men relative to straight men with logistic regression modeling indicating gay men were significantly less likely to be obese, relative to their straight counterparts, in the unadjusted and adjusted models. In terms of prediabetes, rates were low across all sexual orientation groups with no significant differences observed. Yet bisexual men, relative to straight men, had higher rates of diabetes with significantly increased odds for the disease in both the unadjusted and adjusted models. Conclusion Findings indicate gay men have reduced risk for obesity while bisexual men may have increased diabetes burden. Across all male sexual orientation groups, prediabetes prevalence was low, suggesting the need for more aggressive prediabetes screening. Additional research is necessary to confirm the findings.


Gender & Development | 2017

Pelvic pain in transgender men taking testosterone: Assessing the risk of ovarian cancer

Miles Harris; Lauren Kondel; Caroline Dorsen

Some guidelines on care for transgender men taking testosterone recommend oophorectomy to prevent ovarian cancer, while others recommend following guidelines for females. A review of the literature finds no strong evidence that transgender men are at increased risk for ovarian cancer. In transgender men taking testosterone without other risk factors, oophorectomy to prevent cancer is unnecessary.

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