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2.
J Am Coll Dent ; 82(3): 21-4, 2015.
Article in English | MEDLINE | ID: mdl-26697651

ABSTRACT

The central point in the U.S. Supreme Court upholding the Federal Trade Commission's action against the North Carolina State Board of Dental Examiners was that they acted without proper supervision from the State of North Carolina in curbing commercial activity: issuing cease and desist orders to teeth-whitening businesses, for example. It appears unlikely that the law of the land will allow professions to enforce and may substantially limit a profession's voice in defining nearby commercial activity. The line between professional services and commercial ones is not clear. Vending whitening agents, as drug stores do, is commercial but may not be professional. Providing such services in the dental office certainly should be professional, but is also certainly commercial. As dentistry becomes more overtly commercial in nature, it is likely that the profession will have less say over defining and enforcing oral healthcare practices.


Subject(s)
Dentists/ethics , Ethics, Dental , Licensure, Dental/ethics , Social Responsibility , Advertising , Allied Health Personnel/legislation & jurisprudence , Dentists/legislation & jurisprudence , Dissent and Disputes/legislation & jurisprudence , Economic Competition/legislation & jurisprudence , Humans , Licensure, Dental/legislation & jurisprudence , Marketing of Health Services , North Carolina , Professional Autonomy , Self Care , Tooth Bleaching , United States
7.
N C Med J ; 69(5): 408-10, 2008.
Article in English | MEDLINE | ID: mdl-19006938
8.
J Adolesc Health ; 40(4): 334-41, 2007 Apr.
Article in English | MEDLINE | ID: mdl-17367726

ABSTRACT

PURPOSE: Doctors must understand patients' priorities to create an effective treatment partnership. Little is known about whether subspecialist pediatricians understand chronically ill adolescents' preferences. METHODS: A survey was conducted of 155 adolescents with chronic illnesses and 52 subspecialty physicians recruited from the same clinics of a children's hospital. Adolescents and physicians rated the importance that adolescents place on items relating to quality of care and physician-patient communication styles using a previously validated measure. RESULTS: For quality of care items, rank order correlation between physicians and patient responses was high (r = .63, p < .001) and both rated pain management items as most important. Physicians underestimated the importance adolescents placed on communicating with the physician as a friend and medical-technical aspects of care. For communication items, physicians' responses were significantly different than adolescents for 13 of 17 items. Except for three items pertaining to autonomy, physician and patient responses were in the same direction, but adolescent responses were less extreme. CONCLUSIONS: Physicians understood the importance of pain management to adolescents with chronic illnesses, but overestimated their desired level of autonomy. Asking adolescents for their preferences may be the first step in improving adolescents' experience of care.


Subject(s)
Adolescent Health Services/statistics & numerical data , Pain Management , Physician-Patient Relations , Quality of Health Care/statistics & numerical data , Adolescent , Adolescent Behavior/psychology , Adolescent Health Services/organization & administration , Adult , Anemia, Sickle Cell/complications , Arthritis, Juvenile/complications , Child , Chronic Disease , Cystic Fibrosis/complications , Female , Health Services Needs and Demand/statistics & numerical data , Humans , Inflammatory Bowel Diseases/complications , Male , Pain/etiology , Pain/psychology , Patient Satisfaction , Population Surveillance , Surveys and Questionnaires
9.
N C Med J ; 66(1): 78, 2005.
Article in English | MEDLINE | ID: mdl-15786687
11.
Pediatrics ; 114(5): 1272-80, 2004 Nov.
Article in English | MEDLINE | ID: mdl-15520107

ABSTRACT

BACKGROUND: Efforts to make health care for adolescents with chronic illnesses more patient-centered must be grounded in an understanding and clear measures of adolescents' preferences and priorities. OBJECTIVE: To develop a measure of health care preferences of adolescents with chronic illnesses and to determine demographic, developmental, and health factors associated with adolescents' preferences. DESIGN: Mixed-method questionnaire development and survey. SETTING: Subspecialty clinics of a tertiary care children's hospital. PARTICIPANTS: All adolescents (age: 11-19 years) with juvenile rheumatoid arthritis, sickle cell disease, inflammatory bowel disease, or cystic fibrosis of at least 2-year duration who were being treated at the participating center were eligible to participate, and 155 of 251 did so (62%). The participants had a mean age of 15.5 +/- 2.4 years, 45% were male, and 75% were white. INTERVENTION: None. MAIN OUTCOME MEASURES: Ratings of 65 items related to quality of care and 17 items related to physician-patient communication styles. RESULTS: An 82-item questionnaire, devised from qualitative analysis of focus group results, contained 65 Likert scale items that adolescents considered important for health care quality and 17 forced-choice items related to adolescents' preferences for communication. Among the first 65 items, the group of questions related to physician trust and respect had the highest rating of 5.24 +/- 0.62 of 6, followed by patient power and control (mean rating: 4.72 +/- 0.77) and then caring and closeness in the patient-doctor relationship (mean rating: 4.19 +/- 0.91). For the communication items, the adolescents, on average, preferred communication directly to them rather than to their parents and were nearly neutral regarding physicians' inquiries about personal issues. CONCLUSIONS: Participants rated aspects of interpersonal care (especially honesty, attention to pain, and items related to respect) as most important in their judgments of quality. As in most previous studies of adults, technical aspects of care were also rated highly, suggesting that adolescents understand and value both scientific and interpersonal aspects of care.


Subject(s)
Attitude to Health , Chronic Disease/therapy , Delivery of Health Care , Adolescent , Adolescent Health Services , Adult , Anemia, Sickle Cell/therapy , Arthritis, Juvenile/therapy , Child , Cystic Fibrosis/therapy , Data Collection , Female , Health Services Research , Humans , Inflammatory Bowel Diseases/therapy , Male , Multivariate Analysis , Physician-Patient Relations , Quality of Health Care , Risk-Taking , Surveys and Questionnaires
13.
N C Med J ; 65(2): 68-77, 2004.
Article in English | MEDLINE | ID: mdl-15239503

ABSTRACT

North Carolina is indeed fortunate to have avoided many of the extreme shortages of nurses reported in other states. Yet, there are important developments on the horizon that have the potential to cause such shortages. Taking action today to expand the production of new nurses, enhance their education, augment school-to-work transitions, and improve the nursing workplace environment can help reduce the likelihood of a future nursing workforce crisis. Some steps will require new financial commitments either from public or private sources. Others will require a renewed commitment on the part of employers, educators, regulators and the nursing community. However, these steps are necessary if we are to recruit and retain well-prepared and motivated nurses who are needed to meet our healthcare needs now and in the future. Nursing, especially nursing at the bedside in hospitals and in long-term care, requires increasingly sophisticated technical skills and continues to demand intellectual, physical and emotional energy beyond what would be required in many other professions and occupations. It is hoped that the recommendations offered here will help focus the efforts of legislators, educators, employers, the nursing community, trade associations, foundations and the public at large to ensure an adequate supply of well-trained nursing personnel for the future.


Subject(s)
Advisory Committees , Nurses/supply & distribution , Adult , Education, Nursing, Graduate/organization & administration , Humans , Male , Middle Aged , North Carolina , Personnel Selection , Policy Making , Workplace
16.
Annu Rev Public Health ; 24: 227-46, 2003.
Article in English | MEDLINE | ID: mdl-12668757

ABSTRACT

Recent efforts to attain near-complete coverage of child populations by recommended vaccines have included initiatives by federal and state agencies, as well as private foundations, to develop and implement statewide or community-based childhood immunization registries. Plans for a single, national registry have been set aside in favor of a national network of local and state registries linked through the use of common definitions and unique child identifiers. However, both operational/technical and financing difficulties have slowed their development. The experience to date in selected areas has provided useful lessons for further development of a registry system and has underscored the potential of such systems to assure the success of childhood immunization initiatives.


Subject(s)
Immunization Programs , Public Health Informatics , Registries , Child Welfare , Child, Preschool , Confidentiality/legislation & jurisprudence , Health Insurance Portability and Accountability Act , Humans , Public Health Informatics/legislation & jurisprudence , United States
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