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Health Sciences · Medicine

Patient Dignity and Privacy
Research Guide

What is Patient Dignity and Privacy?

Patient Dignity and Privacy refers to the preservation of a patient's autonomy, sense of worth, and confidentiality in healthcare settings, particularly through interventions like Dignity Therapy for end-of-life care in palliative settings.

This field encompasses 23,632 works focused on Dignity Therapy as a psychotherapeutic intervention for terminally ill patients in palliative care. Research examines preserving patient dignity, addressing psychological distress, and upholding privacy and human rights, especially in elderly care. Growth data over the past five years is not available.

Topic Hierarchy

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graph TD D["Health Sciences"] F["Medicine"] S["Public Health, Environmental and Occupational Health"] T["Patient Dignity and Privacy"] D --> F F --> S S --> T style T fill:#DC5238,stroke:#c4452e,stroke-width:2px
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23.6K
Papers
N/A
5yr Growth
114.1K
Total Citations

Research Sub-Topics

Why It Matters

Patient Dignity and Privacy directly influences end-of-life care quality by enhancing patient and family satisfaction while reducing stress, anxiety, and depression in relatives. Detering et al. (2010) in 'The impact of advance care planning on end of life care in elderly patients: randomised controlled trial' demonstrated that advance care planning, a key dignity-preserving practice, improved outcomes in a randomized controlled trial (ACTRN12608000539336). Ferrell et al. (2017) in 'Integration of Palliative Care Into Standard Oncology Care: American Society of Clinical Oncology Clinical Practice Guideline Update' provided evidence-based recommendations for integrating palliative care, which supports dignity through better symptom management and communication in oncology, cited 2004 times. These approaches apply in palliative oncology and elderly care, ensuring patients maintain autonomy as shown in competence assessments by Appelbaum (2007) in 'Assessment of Patients' Competence to Consent to Treatment'.

Reading Guide

Where to Start

'SPIKES—A Six-Step Protocol for Delivering Bad News: Application to the Patient with Cancer' by Baile et al. (2000), as it offers a practical, straightforward six-step protocol for communication that directly supports dignity and privacy in disclosing illness information.

Key Papers Explained

Baile et al. (2000) in 'SPIKES—A Six-Step Protocol for Delivering Bad News: Application to the Patient with Cancer' establishes communication basics (2920 citations), which Steinhauser (2000) in 'Factors Considered Important at the End of Life by Patients, Family, Physicians, and Other Care Providers' builds on by identifying role-specific dignity factors (2482 citations). Detering et al. (2010) in 'The impact of advance care planning on end of life care in elderly patients: randomised controlled trial' tests these empirically, showing satisfaction gains (2279 citations), while Ferrell et al. (2017) in 'Integration of Palliative Care Into Standard Oncology Care: American Society of Clinical Oncology Clinical Practice Guideline Update' integrates them into oncology guidelines (2004 citations). Appelbaum (2007) in 'Assessment of Patients' Competence to Consent to Treatment' complements by addressing autonomy assessment (1342 citations).

Paper Timeline

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graph LR P0["A history and theory of informed...
1986 · 2.3K cites"] P1["Information Privacy: Measuring I...
1996 · 2.2K cites"] P2["SPIKES—A Six-Step Protocol for D...
2000 · 2.9K cites"] P3["Factors Considered Important at ...
2000 · 2.5K cites"] P4["The impact of advance care plann...
2010 · 2.3K cites"] P5["A practical guide to using Inter...
2014 · 1.5K cites"] P6["Integration of Palliative Care I...
2017 · 2.0K cites"] P0 --> P1 P1 --> P2 P2 --> P3 P3 --> P4 P4 --> P5 P5 --> P6 style P2 fill:#DC5238,stroke:#c4452e,stroke-width:2px
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Most-cited paper highlighted in red. Papers ordered chronologically.

Advanced Directions

Current research emphasizes informed consent theory from Kapp (1986) reviewing Faden and Beauchamp, alongside privacy measurement by Smith et al. (1996), applied to modern palliative models like Quill and Abernethy (2013) on generalist-specialist integration. No recent preprints or news coverage available.

Papers at a Glance

Frequently Asked Questions

What is Dignity Therapy?

Dignity Therapy is a psychotherapeutic intervention designed for patients near the end of life in palliative care. It focuses on preserving patient dignity, reducing psychological distress, and improving quality of life. The cluster of 23,632 papers centers on its application in end-of-life settings.

How does advance care planning support patient dignity?

Advance care planning enhances end-of-life care by aligning treatments with patient wishes, thereby upholding autonomy and privacy. Detering et al. (2010) found it improves patient and family satisfaction while reducing stress, anxiety, and depression in a randomized controlled trial. This practice is particularly relevant in elderly care.

What protocol is used for delivering bad news to preserve dignity?

The SPIKES protocol provides a six-step method for disclosing unfavorable information to cancer patients. Baile et al. (2000) in 'SPIKES—A Six-Step Protocol for Delivering Bad News: Application to the Patient with Cancer' outlined steps including setting up the interview and checking patient perception. It meets research requirements for effective communication.

Why is patient competence assessment important for privacy?

Assessing competence ensures patients can consent to treatment while respecting their autonomy and privacy. Appelbaum (2007) in 'Assessment of Patients' Competence to Consent to Treatment' describes evaluating understanding in cases like a 75-year-old refusing amputation. This protects dignity in end-of-life decisions.

What factors do patients consider important at end of life?

Patients prioritize pain management, physician communication, death preparation, and a sense of completion. Steinhauser (2000) in 'Factors Considered Important at the End of Life by Patients, Family, Physicians, and Other Care Providers' identified these differ by role. They form the basis for quality end-of-life care.

How is privacy concern measured in healthcare?

Privacy concerns are measured by scales assessing organizational practices and individual worries. Smith et al. (1996) in 'Information Privacy: Measuring Individuals’ Concerns About Organizational Practices' developed an instrument based on public polls showing rising American concerns. It applies to healthcare confidentiality.

Open Research Questions

  • ? How can Dignity Therapy be adapted for non-palliative care settings to preserve dignity in chronic illness?
  • ? What metrics best quantify the long-term impact of SPIKES protocol on patient privacy perceptions post-bad news delivery?
  • ? In what ways do cultural differences affect factors deemed important for end-of-life dignity, beyond those identified by Steinhauser?
  • ? How does integration of generalist and specialist palliative care, as in Quill and Abernethy, optimize privacy in diverse healthcare teams?
  • ? What assessment tools beyond Appelbaum's can reliably measure competence while minimizing dignity violations in elderly patients?

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