Truth Disclosure

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  Subject Areas on Research

  • "Notify your partners--it's the law": HIV providers and mandatory disclosure. 
  • A comprehensive process for identifying and managing conflicts of interest reduced perceived bias at a specialty society annual meeting. 
  • A qualitative analysis of partner selection, HIV serostatus disclosure, and sexual behaviors among HIV-positive urban men. 
  • A tale worth telling: the impact of the diagnosis experience on disclosure of genetic disorders. 
  • ACCF/AHA consensus conference report on professionalism and ethics. 
  • Acceptance of HIV testing during prenatal care. Perinatal Guidelines Evaluation Project. 
  • Afterword: Giving good advice: it is not what doctors say, but how they say it. 
  • Are patients willing to participate in medical education? 
  • Associations between understanding of current treatment intent, communication with healthcare providers, preferences for invasive life-sustaining interventions and decisional conflict: results from a survey of patients with advanced heart failure in Singapore. 
  • Avoidant Coping Mediates the Relationship Between Self-Efficacy for HIV Disclosure and Depression Symptoms Among Men Who Have Sex with Men Newly Diagnosed with HIV. 
  • Battling the Chimaera: How Much Disclosure of Rare Risks Is Necessary? 
  • Communicating breast cancer risks to women using different formats. 
  • Communicating prognosis with parents of critically ill infants: direct observation of clinician behaviors. 
  • Conflicts of interest for medical publishers and editors: protecting the integrity of scientific scholarship. 
  • Consistency of financial interest disclosures in the biomedical literature: the case of coronary stents. 
  • Developmental trajectories of externalizing and internalizing behaviors: factors underlying resilience in physically abused children. 
  • Disclosing diagnosis, continued. 
  • Disclosure between patients with gastrointestinal cancer and their spouses. 
  • Do clinicians tell patients they have prehypertension? 
  • Do patients participating in clinical trials want to know study results? 
  • Don't ask, don't tell? Revealing placebo responses to research participants and patients. 
  • Erosion in medical students' attitudes about telling patients they are students. 
  • Ethical aspects of banking placental blood for transplantation. 
  • Ethical standards for cardiothoracic surgeons' participation in social media. 
  • Evaluation of breastfeeding Web sites for patient education. 
  • Formulary tiers, medication cost sharing, and transparency in bronze and silver qualified health plans in 2014 vs 2018. 
  • GIS modeling of air toxics releases from TRI-reporting and non-TRI-reporting facilities: impacts for environmental justice. 
  • HIV serostatus disclosure in the treatment cascade: evidence from Northern Tanzania. 
  • HIV status disclosure during acute HIV infection in Malawi. 
  • HIV-related stigma, isolation, discrimination, and serostatus disclosure: a global survey of 2035 HIV-infected adults. 
  • Health Care Professionals' Responses to Religious or Spiritual Statements by Surrogate Decision Makers During Goals-of-Care Discussions. 
  • Heart Failure Fake News: How Do We Distinguish the Truth? 
  • Helping patients decide: ten steps to better risk communication. 
  • How does PLoS medicine manage competing interests? 
  • Improving the measurement of self-reported medication nonadherence. 
  • Informing women about their breast cancer risks: truth and consequences. 
  • Instrumentation and practice standards for electrocardiographic monitoring in special care units. A report for health professionals by a Task Force of the Council on Clinical Cardiology, American Heart Association. 
  • Intraoperative apnea: medication error with disclosure (simulation case scenario). 
  • Managed care organizations should not disclose their physicians' financial incentives. 
  • Modality of Primary HIV Disclosure and Association with Mental Health, Stigma, and Antiretroviral Therapy Adherence in Tanzanian Youth Living with HIV. 
  • Needlestick injuries among surgeons in training. 
  • New policy on disclosure of interest for American College of Rheumatology Journals. 
  • Obesity prevention and the primary care pediatrician's office. 
  • Open letter on the asbestos industry in India. 
  • Pain communication in the context of osteoarthritis: patient and partner self-efficacy for pain communication and holding back from discussion of pain and arthritis-related concerns. 
  • Parent perceptions of early prognostic encounters following children's severe traumatic brain injury: 'locked up in this cage of absolute horror'. 
  • Patterns of HIV disclosure and condom use among HIV-infected young racial/ethnic minority men who have sex with men. 
  • Perceptions of patients and physicians regarding phase I cancer clinical trials: implications for physician-patient communication. 
  • Prenatal diagnosis of Down syndrome: how best to deliver the news. 
  • Prognostic Communication Between Oncologists and Parents of Children With Advanced Cancer. 
  • Protecting whistleblowers. Employers should respond to the message, not shoot the messenger. 
  • Race as a predictor of patient preferences for biopsy result communication. 
  • Right Brain: Breaking bad news: Communication education for neurology trainees. 
  • Self-disclosure of HIV status, disclosure counseling, and retention in HIV care in Cameroon. 
  • Serostatus disclosure to sexual partners among people living with HIV: examining the roles of partner characteristics and stigma. 
  • Sexual behavior of HIV discordant couples after HIV counseling and testing. 
  • Should doctors ever lie on behalf of patients? 
  • Specialist Physicians' Attitudes and Practice Patterns Regarding Disclosure of Pre-referral Medical Errors. 
  • The Disclosure Dilemma: Willingness to Disclose a Positive HIV Status Among Individuals Preparing for HIV Testing During Antenatal Care in Tanzania. 
  • The Emotional and Behavioral Impact of Delivering Bad News to Virtual versus Real Standardized Patients: A Pilot Study. 
  • The concept of voluntary consent. 
  • The correlation between patient characteristics and expectations of benefit from Phase I clinical trials. 
  • The dilemmas of parents of adolescents and young adults with congenital heart disease. 
  • The hazards of correcting myths about health care reform. 
  • The prevalence and process of pediatric HIV disclosure: A population-based prospective cohort study in Zimbabwe. 
  • The process of HIV status disclosure to HIV-positive youth in Kinshasa, Democratic Republic of the Congo. 
  • The use of standardized patients for mock oral board exams in neurology: a pilot study. 
  • To tell the truth: potential liability for concealing physician impairment. 
  • Trial summaries on results databases and journal publication. 
  • Truth in the most optimistic way. 
  • Understanding of an aggregate probability statement by patients who are offered participation in Phase I clinical trials. 
  • Voices of Women Facing HIV-Related Stigma in the Deep South. 
  • Why journals should not publish articles funded by the tobacco industry. 
  • Youth self-report of physical and sexual abuse: a latent class analysis. 
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  Keywords of People

  • Dodge, Kenneth A., William McDougall Distinguished Professor of Public Policy Studies, Duke Science & Society
  • Yancy Jr., William Samuel, Professor of Medicine, Medicine, General Internal Medicine