A lecture on patients' rights delivered to the staff of King Fahad Medical City in Riyadh on Monday 18/9/2017. It given an overview on patients' rights then focus on three of them: shared decision-making, privacy, and confidentiality
SCHS Topic 5: Privacy, Confidentiality and Medical RecordsDr Ghaiath Hussein
Series of lectures I gave for the PEER (Professionalism and Ethics Education for Residents) Project sponsored and organized by the Saudi Commission for Health Specialties (SCHS).
OUTLINE:
Definitions and differences
How to maintain the privacy of our patients?
How to maintain the confidentiality of our patients’ information?
When to disclose medical information
The document discusses patients' rights in Saudi Arabia. It outlines the ethical basis for patients' rights and defines key rights such as the right to treatment, access to care, choice of care, participation in decision making, privacy and confidentiality, seeking second opinions, and end-of-life care. It discusses these rights in the context of Islamic guidance and Saudi law. Specific patient rights addressed include consent to treatment, privacy, safety, participation in research studies, complaints procedures, and additional considerations for special groups like children, the elderly, and those with psychiatric or special needs. The document emphasizes informing both patients and healthcare providers about patients' rights.
The document discusses the principles of informed consent and the role of nurses in the informed consent process. It addresses why informed consent is needed, who is responsible for obtaining consent, and when it is required. It outlines the delivery methods for obtaining consent and ethical considerations. The document emphasizes that nurses have an important role in ensuring patient comprehension, addressing anxiety, identifying appropriate surrogates, and facilitating documentation. Nurses can help ensure the process complies with legal and regulatory standards to protect patient autonomy and participation in healthcare decisions.
This document outlines patient rights and ethics in healthcare. It defines a patient bill of rights as guaranteeing ethical care and decision making for clients. The purposes are to ensure ethical treatment for all people receiving care. A patient bill of rights typically articulates positive rights like access to records, informed consent, and privacy. It also discusses protecting patient privacy and concerns around trusting healthcare organizations with personal health information.
Lecture 13 privacy, confidentiality and medical recordsDr Ghaiath Hussein
A lecture on privacy, confidentiality and medical records delivered to Alfarabi Medical College undergraduate medical students in the week starting 27.11.2016
Teaching medical ethics for undergraduate medical studentsDr Ghaiath Hussein
The document discusses teaching medical ethics to undergraduate medical students by non-specialized staff. It outlines the workshop which will introduce key concepts in ethics, discuss the need to teach ethics and what topics to cover, and provide practical guidance on teaching ethics. The workshop will not provide a ready-made prescription, but rather introduce participants to fundamental concepts and considerations for developing ethics curriculum. It will also address challenges in teaching and evaluating ethics.
Medical ethics deals with moral principles that guide clinical practice and relationships. It considers the choices and actions of both medical practitioners and patients in light of duties and obligations. There are several core principles of medical ethics including respect for patient autonomy, beneficence, non-maleficence, justice, confidentiality, and veracity. These principles guide informed consent processes and the patient-practitioner relationship. Upholding ethics is important for maintaining trust between the medical field and society.
This document outlines patients' rights related to medical treatment. It discusses the definition and ethical basis of patients' rights, and then focuses on specific rights in more detail. These include the right to access care, choice of care, participate in decision making, privacy and confidentiality, seek second opinions or referrals, and receive compassionate end-of-life care. The document also discusses the ethics behind providing healthcare, including principles of autonomy, beneficence, non-maleficence, and justice. Key treatment-related rights like consent, continued care, and submitting complaints are also defined.
SCHS Topic 5: Privacy, Confidentiality and Medical RecordsDr Ghaiath Hussein
Series of lectures I gave for the PEER (Professionalism and Ethics Education for Residents) Project sponsored and organized by the Saudi Commission for Health Specialties (SCHS).
OUTLINE:
Definitions and differences
How to maintain the privacy of our patients?
How to maintain the confidentiality of our patients’ information?
When to disclose medical information
The document discusses patients' rights in Saudi Arabia. It outlines the ethical basis for patients' rights and defines key rights such as the right to treatment, access to care, choice of care, participation in decision making, privacy and confidentiality, seeking second opinions, and end-of-life care. It discusses these rights in the context of Islamic guidance and Saudi law. Specific patient rights addressed include consent to treatment, privacy, safety, participation in research studies, complaints procedures, and additional considerations for special groups like children, the elderly, and those with psychiatric or special needs. The document emphasizes informing both patients and healthcare providers about patients' rights.
The document discusses the principles of informed consent and the role of nurses in the informed consent process. It addresses why informed consent is needed, who is responsible for obtaining consent, and when it is required. It outlines the delivery methods for obtaining consent and ethical considerations. The document emphasizes that nurses have an important role in ensuring patient comprehension, addressing anxiety, identifying appropriate surrogates, and facilitating documentation. Nurses can help ensure the process complies with legal and regulatory standards to protect patient autonomy and participation in healthcare decisions.
This document outlines patient rights and ethics in healthcare. It defines a patient bill of rights as guaranteeing ethical care and decision making for clients. The purposes are to ensure ethical treatment for all people receiving care. A patient bill of rights typically articulates positive rights like access to records, informed consent, and privacy. It also discusses protecting patient privacy and concerns around trusting healthcare organizations with personal health information.
Lecture 13 privacy, confidentiality and medical recordsDr Ghaiath Hussein
A lecture on privacy, confidentiality and medical records delivered to Alfarabi Medical College undergraduate medical students in the week starting 27.11.2016
Teaching medical ethics for undergraduate medical studentsDr Ghaiath Hussein
The document discusses teaching medical ethics to undergraduate medical students by non-specialized staff. It outlines the workshop which will introduce key concepts in ethics, discuss the need to teach ethics and what topics to cover, and provide practical guidance on teaching ethics. The workshop will not provide a ready-made prescription, but rather introduce participants to fundamental concepts and considerations for developing ethics curriculum. It will also address challenges in teaching and evaluating ethics.
Medical ethics deals with moral principles that guide clinical practice and relationships. It considers the choices and actions of both medical practitioners and patients in light of duties and obligations. There are several core principles of medical ethics including respect for patient autonomy, beneficence, non-maleficence, justice, confidentiality, and veracity. These principles guide informed consent processes and the patient-practitioner relationship. Upholding ethics is important for maintaining trust between the medical field and society.
This document outlines patients' rights related to medical treatment. It discusses the definition and ethical basis of patients' rights, and then focuses on specific rights in more detail. These include the right to access care, choice of care, participate in decision making, privacy and confidentiality, seek second opinions or referrals, and receive compassionate end-of-life care. The document also discusses the ethics behind providing healthcare, including principles of autonomy, beneficence, non-maleficence, and justice. Key treatment-related rights like consent, continued care, and submitting complaints are also defined.
The document discusses training employees on patient confidentiality and the HIPAA Privacy Rule. It defines covered entities as health providers, health plans, and clearinghouses that are required to protect personal health information. Protected health information cannot be disclosed without patient authorization, and breaches of confidentiality are only allowed to facilitate treatment or operations with consent. The HIPAA Privacy Rule enforces penalties for violations, and sensitive patient information requires security controls like only accessing authorized information and not discussing cases in public areas.
AETCOM [ATTITUDE,ETHICS & COMMUNICATION IN MEDICAL EDUCATION] EDUCATIONanitasreekanth
This document outlines an Attitude, Ethics and Communication (AETCOM) module for medical students. The module aims to teach professionalism through 27 structured learning sessions over 4 years focusing on communication skills, medical ethics, and developing the right attitudes. Key elements include using case-based learning, maintaining competency logbooks, and assessments of students' professional development throughout their clinical training. The goal is to produce medical graduates who are compassionate, caring, and committed to serving patients and communities to a high standard of medical practice.
This document provides an overview of HIPAA privacy and confidentiality requirements for protected health information (PHI). It explains that HIPAA establishes national standards to give patients more control over their medical records and information while setting boundaries around how this sensitive data can be used and shared. Violations of HIPAA privacy rules carry civil and criminal penalties, and all healthcare staff, volunteers and students must be trained on and abide by these policies to protect patient privacy and build trust.
Some slides are taken from different textbooks of medicine like Davidson, Kumar and Clark and Oxford, and some from other presentations made by respected tutors. I'm barely responsible for compilation of various resources per my interest. These resources are free for use, and I do not claim any copyright. Hoping knowledge remains free for all, forever.
This document outlines patient safety in healthcare facilities. It defines key terms like patient safety, psychological safety, and safety culture. It discusses the roles of the patient safety committee and the components of a patient safety plan. Specific patient safety issues in the intensive care unit are examined, like collaboration among ICU staff and common errors. International patient safety goals are provided, such as accurately identifying patients and reducing healthcare-associated infections. Root cause analysis is introduced as a way to investigate incidents and prevent future errors.
This document discusses the history and principles of bioethics. It begins by explaining how advances in medicine raised new moral issues that ethicists worked to address. Notable cases of unethical human subject research helped establish principles like informed consent and respect for persons. Guidelines like the Nuremberg Code aimed to prevent future abuses. The document then examines key bioethical principles like autonomy, beneficence, nonmaleficence, and justice. It explores how these principles guide issues like informed consent, respecting patient values, avoiding harm, and fair allocation of resources. The challenges of applying principles to complex real-world cases are also discussed.
Managing Patient & Family Rights and Responsibilities Ahmad Thanin
This document outlines a hospital's policy to maintain patients' rights to receive information and participate in their care. The policy states that patients or their families have the right to be informed about diagnoses, treatment plans, costs, and participate in care decisions. Doctors are responsible for ensuring patients understand their conditions and options. All clinical staff must respect patients' preferences, privacy, and allow participation. The goal is to fulfill the ethical commitment to involve patients in their care through open communication and informed decision making.
This document discusses patient safety and medical errors. It notes that medical errors impact about 1 in 10 patients worldwide according to the WHO. The rates of death from medical errors in healthcare exceed those of other high-risk industries like commercial airlines or nuclear power. The document outlines some of the common causes of medical errors, including systemic flaws, communication issues, and patient ignorance. It emphasizes that a culture of safety and teamwork is needed to effectively address patient safety issues and prevent future errors.
Patient confidentiality refers to an individual's right to have their personal and identifiable medical information kept private. This information should only be accessible to physicians and necessary healthcare staff. Examples of confidentiality breaches include a doctor revealing patient information to the media or healthcare staff accessing medical records they have no need to see. To ensure confidentiality, healthcare workers must speak privately with patients, secure records, restrict access to electronic databases, and monitor offices for potential issues. Effective training at hire and periodically can help healthcare staff properly protect patient confidentiality.
This document discusses several important medico-legal issues that triage nurses need to be aware of, including: obtaining informed consent, duty of care, negligence, documentation, confidentiality, and preserving forensic evidence. The triage nurse must be knowledgeable, skilled, educated, professional and accountable. They use tools like the Australasian Triage Scale, physiological discriminators, and local policies/protocols. Triage involves assessing patients in a chaotic environment with many factors that can increase risk. Proper documentation, obtaining consent, maintaining confidentiality and adhering to the standard of care are important to avoid legal issues like charges of negligence or battery.
This document discusses patient confidentiality and preserving privacy of patient health records. It aims to increase awareness of legal requirements and best practices for maintaining confidentiality. The goals are to promote awareness of confidentiality laws, advocate for compliance with procedures to protect medical records, and exercise caution when handling documented and electronic patient information. Healthcare professionals must attend annual training on patient privacy laws like HIPAA and ensure sensitive patient data is only accessed by authorized individuals. Any breaches of confidentiality must be reported immediately and can result in penalties.
An introductory overview of the basic concepts of Healthcare Quality, a starter for beginners.
Prepared in 2014 for the new staff of the Quality Management Department in King Saud University Medical City in Riyadh as a part of their capacity building plan.
Acknowledgments:
*Dr. Magdy Gamal Yousef, MBBCh, MS, CPHQ - for his contribution in the scientific content
**Ms. Maram Baksh, MS, CPHQ - for the design of the full HCQ capacity building plan in KSUMC
A talk delivered by Prof Faisal Ghani for 3rd year medical students at Alfarabi Medical College about the patients' confidentiality, the measures to protect them, and when it is ethical to breach it.
This document outlines patients' rights and responsibilities regarding privacy and confidentiality at Najran Armed Forces Hospital. It discusses the right to privacy, confidentiality of personal health information, and staff responsibilities to maintain privacy and protect confidential patient data. Staff are expected to complete training on privacy and confidentiality policies and sign confidentiality agreements to protect patient information. The policy applies to all patients at the hospital, including minors, and protects their private health details.
Healthcare Information Privacy & Confidentiality: How To Work Very Well With ...Nawanan Theera-Ampornpunt
The presentation discussed key aspects of Thailand's draft Personal Data Protection Act, including requirements for informed consent, sensitive data protections, data security standards, and rights of data owners. It emphasized balancing privacy protections with enabling quality care, research, and operations through prioritizing compliance, assessing practices, and considering perspectives of lawyers, clinicians, technologists, and management. The presenter encouraged embracing privacy as a value, using laws as guidance, and addressing new technologies and non-digital data to maintain trust while enabling information sharing.
Definition: Patient-Centered Care
Definition Patient-centered care (patient centred care): “Is a model in which providers partner with families to identify and satisfy the full range of patient needs and preferences.”
To expand this definition, patient-centered care is dependent on the involvement of the staff and care team as well.
“To succeed, a patient-centered approach must also address the staff experience as staff’s ability and inclination to effectively care for patients is unquestionably compromised if they do not feel care for themselves" (Picker Institute).
Researchers from Harvard Medical School, on behalf of Picker Institute and The Commonwealth Fund, defined seven primary dimensions of patient-centered care model.
These factors are identified as:
Respect for patients’ values, preferences and expressed needs
Coordination and integration of care
Information, communication and education
Physical comfort
Emotional support and alleviation of fear and anxiety
Involvement of family and friends
Transition and continuity
Confidentiality in healthcare involves keeping patient information private without their consent for disclosure. Maintaining confidentiality is important to build trust in the physician-patient relationship and encourage patients to seek care. Personal information like names, addresses, diagnoses and social security numbers should be kept private. HIPAA provides federal laws protecting the confidentiality and security of patient healthcare information. Healthcare workers should only discuss patients in private settings and properly dispose of documents with identifying patient information to uphold patient confidentiality.
Delirium is a transient, usually reversible mental dysfunction characterized by a wide range of neuropsychiatric abnormalities. The pathophysiology is unclear but involves global functional derangement of the brain. Delirium is very common in hospitalized patients, especially post-operatively and in those with advanced cancer or dementia. It is caused by multiple factors including patient vulnerability, medical insults, organ dysfunction, and iatrogenic events. Symptoms include inattention, disorientation, cognitive and sleep impairments. It is evaluated using tools like the Confusion Assessment Method and treated by addressing risk factors and underlying causes.
This document discusses effective communication strategies for breaking bad news to cancer patients. It begins by defining communication and its importance in healthcare. It then discusses why communicating with cancer patients is complex, involving emotional reactions, expectations, family involvement, and balancing hope. It outlines common psychological reactions patients experience after receiving a cancer diagnosis. The document then recommends a six-step strategy called SPIKES for breaking bad news sensitively and provides behaviors to avoid, such as blocking, lecturing, and premature reassurance. The goal is to gather information from patients, provide understandable information, support patients emotionally, and develop a treatment plan together.
The document discusses training employees on patient confidentiality and the HIPAA Privacy Rule. It defines covered entities as health providers, health plans, and clearinghouses that are required to protect personal health information. Protected health information cannot be disclosed without patient authorization, and breaches of confidentiality are only allowed to facilitate treatment or operations with consent. The HIPAA Privacy Rule enforces penalties for violations, and sensitive patient information requires security controls like only accessing authorized information and not discussing cases in public areas.
AETCOM [ATTITUDE,ETHICS & COMMUNICATION IN MEDICAL EDUCATION] EDUCATIONanitasreekanth
This document outlines an Attitude, Ethics and Communication (AETCOM) module for medical students. The module aims to teach professionalism through 27 structured learning sessions over 4 years focusing on communication skills, medical ethics, and developing the right attitudes. Key elements include using case-based learning, maintaining competency logbooks, and assessments of students' professional development throughout their clinical training. The goal is to produce medical graduates who are compassionate, caring, and committed to serving patients and communities to a high standard of medical practice.
This document provides an overview of HIPAA privacy and confidentiality requirements for protected health information (PHI). It explains that HIPAA establishes national standards to give patients more control over their medical records and information while setting boundaries around how this sensitive data can be used and shared. Violations of HIPAA privacy rules carry civil and criminal penalties, and all healthcare staff, volunteers and students must be trained on and abide by these policies to protect patient privacy and build trust.
Some slides are taken from different textbooks of medicine like Davidson, Kumar and Clark and Oxford, and some from other presentations made by respected tutors. I'm barely responsible for compilation of various resources per my interest. These resources are free for use, and I do not claim any copyright. Hoping knowledge remains free for all, forever.
This document outlines patient safety in healthcare facilities. It defines key terms like patient safety, psychological safety, and safety culture. It discusses the roles of the patient safety committee and the components of a patient safety plan. Specific patient safety issues in the intensive care unit are examined, like collaboration among ICU staff and common errors. International patient safety goals are provided, such as accurately identifying patients and reducing healthcare-associated infections. Root cause analysis is introduced as a way to investigate incidents and prevent future errors.
This document discusses the history and principles of bioethics. It begins by explaining how advances in medicine raised new moral issues that ethicists worked to address. Notable cases of unethical human subject research helped establish principles like informed consent and respect for persons. Guidelines like the Nuremberg Code aimed to prevent future abuses. The document then examines key bioethical principles like autonomy, beneficence, nonmaleficence, and justice. It explores how these principles guide issues like informed consent, respecting patient values, avoiding harm, and fair allocation of resources. The challenges of applying principles to complex real-world cases are also discussed.
Managing Patient & Family Rights and Responsibilities Ahmad Thanin
This document outlines a hospital's policy to maintain patients' rights to receive information and participate in their care. The policy states that patients or their families have the right to be informed about diagnoses, treatment plans, costs, and participate in care decisions. Doctors are responsible for ensuring patients understand their conditions and options. All clinical staff must respect patients' preferences, privacy, and allow participation. The goal is to fulfill the ethical commitment to involve patients in their care through open communication and informed decision making.
This document discusses patient safety and medical errors. It notes that medical errors impact about 1 in 10 patients worldwide according to the WHO. The rates of death from medical errors in healthcare exceed those of other high-risk industries like commercial airlines or nuclear power. The document outlines some of the common causes of medical errors, including systemic flaws, communication issues, and patient ignorance. It emphasizes that a culture of safety and teamwork is needed to effectively address patient safety issues and prevent future errors.
Patient confidentiality refers to an individual's right to have their personal and identifiable medical information kept private. This information should only be accessible to physicians and necessary healthcare staff. Examples of confidentiality breaches include a doctor revealing patient information to the media or healthcare staff accessing medical records they have no need to see. To ensure confidentiality, healthcare workers must speak privately with patients, secure records, restrict access to electronic databases, and monitor offices for potential issues. Effective training at hire and periodically can help healthcare staff properly protect patient confidentiality.
This document discusses several important medico-legal issues that triage nurses need to be aware of, including: obtaining informed consent, duty of care, negligence, documentation, confidentiality, and preserving forensic evidence. The triage nurse must be knowledgeable, skilled, educated, professional and accountable. They use tools like the Australasian Triage Scale, physiological discriminators, and local policies/protocols. Triage involves assessing patients in a chaotic environment with many factors that can increase risk. Proper documentation, obtaining consent, maintaining confidentiality and adhering to the standard of care are important to avoid legal issues like charges of negligence or battery.
This document discusses patient confidentiality and preserving privacy of patient health records. It aims to increase awareness of legal requirements and best practices for maintaining confidentiality. The goals are to promote awareness of confidentiality laws, advocate for compliance with procedures to protect medical records, and exercise caution when handling documented and electronic patient information. Healthcare professionals must attend annual training on patient privacy laws like HIPAA and ensure sensitive patient data is only accessed by authorized individuals. Any breaches of confidentiality must be reported immediately and can result in penalties.
An introductory overview of the basic concepts of Healthcare Quality, a starter for beginners.
Prepared in 2014 for the new staff of the Quality Management Department in King Saud University Medical City in Riyadh as a part of their capacity building plan.
Acknowledgments:
*Dr. Magdy Gamal Yousef, MBBCh, MS, CPHQ - for his contribution in the scientific content
**Ms. Maram Baksh, MS, CPHQ - for the design of the full HCQ capacity building plan in KSUMC
A talk delivered by Prof Faisal Ghani for 3rd year medical students at Alfarabi Medical College about the patients' confidentiality, the measures to protect them, and when it is ethical to breach it.
This document outlines patients' rights and responsibilities regarding privacy and confidentiality at Najran Armed Forces Hospital. It discusses the right to privacy, confidentiality of personal health information, and staff responsibilities to maintain privacy and protect confidential patient data. Staff are expected to complete training on privacy and confidentiality policies and sign confidentiality agreements to protect patient information. The policy applies to all patients at the hospital, including minors, and protects their private health details.
Healthcare Information Privacy & Confidentiality: How To Work Very Well With ...Nawanan Theera-Ampornpunt
The presentation discussed key aspects of Thailand's draft Personal Data Protection Act, including requirements for informed consent, sensitive data protections, data security standards, and rights of data owners. It emphasized balancing privacy protections with enabling quality care, research, and operations through prioritizing compliance, assessing practices, and considering perspectives of lawyers, clinicians, technologists, and management. The presenter encouraged embracing privacy as a value, using laws as guidance, and addressing new technologies and non-digital data to maintain trust while enabling information sharing.
Definition: Patient-Centered Care
Definition Patient-centered care (patient centred care): “Is a model in which providers partner with families to identify and satisfy the full range of patient needs and preferences.”
To expand this definition, patient-centered care is dependent on the involvement of the staff and care team as well.
“To succeed, a patient-centered approach must also address the staff experience as staff’s ability and inclination to effectively care for patients is unquestionably compromised if they do not feel care for themselves" (Picker Institute).
Researchers from Harvard Medical School, on behalf of Picker Institute and The Commonwealth Fund, defined seven primary dimensions of patient-centered care model.
These factors are identified as:
Respect for patients’ values, preferences and expressed needs
Coordination and integration of care
Information, communication and education
Physical comfort
Emotional support and alleviation of fear and anxiety
Involvement of family and friends
Transition and continuity
Confidentiality in healthcare involves keeping patient information private without their consent for disclosure. Maintaining confidentiality is important to build trust in the physician-patient relationship and encourage patients to seek care. Personal information like names, addresses, diagnoses and social security numbers should be kept private. HIPAA provides federal laws protecting the confidentiality and security of patient healthcare information. Healthcare workers should only discuss patients in private settings and properly dispose of documents with identifying patient information to uphold patient confidentiality.
Delirium is a transient, usually reversible mental dysfunction characterized by a wide range of neuropsychiatric abnormalities. The pathophysiology is unclear but involves global functional derangement of the brain. Delirium is very common in hospitalized patients, especially post-operatively and in those with advanced cancer or dementia. It is caused by multiple factors including patient vulnerability, medical insults, organ dysfunction, and iatrogenic events. Symptoms include inattention, disorientation, cognitive and sleep impairments. It is evaluated using tools like the Confusion Assessment Method and treated by addressing risk factors and underlying causes.
This document discusses effective communication strategies for breaking bad news to cancer patients. It begins by defining communication and its importance in healthcare. It then discusses why communicating with cancer patients is complex, involving emotional reactions, expectations, family involvement, and balancing hope. It outlines common psychological reactions patients experience after receiving a cancer diagnosis. The document then recommends a six-step strategy called SPIKES for breaking bad news sensitively and provides behaviors to avoid, such as blocking, lecturing, and premature reassurance. The goal is to gather information from patients, provide understandable information, support patients emotionally, and develop a treatment plan together.
There is an evident deficiency on how best to break bad news in medicine. This is an essential communication skill that our patients expect of us. It is an essential requisite of Good Medical Practice. This presentation is part of a course held at Al Hammadi Hospital, Suwaidi, Riyadh, KSA on Breaking Bad News. 2017
The document outlines a patient's bill of rights, which includes the right to considerate and respectful care, the right to information about diagnosis, treatment, and prognosis, and the right to make decisions about their plan of care and refuse treatment. It also covers the rights to privacy, confidentiality, review of medical records, continuity of care, and informed consent regarding research studies. The document states that hospitals must respect patient dignity and values in all activities.
Though very few in number, there are elder care organizations in different parts of the country willing to provide the support we need for the care of the elderly in our homes. This is an endeavor to list the geriatric care facilities available in India.
The document outlines a patient's bill of rights, which lists protections and responsibilities for patients during hospitalization. It states patients have the right to receive medical information, make healthcare decisions, privacy, and confidentiality of medical records. While not legally binding, the bill of rights provides guidance for healthcare facilities and staff on treating patients and their families with courtesy, respect and responsiveness.
This document discusses in-home care for senior citizens. It notes that 82% of people prefer to stay in their homes as long as possible. In-home care offers more flexibility compared to hospitals or nursing homes. It can also be more cost-effective by avoiding costs for room and board. While technology has advanced to provide more hospital-level care at home, research shows it can be difficult to find high-quality in-home care services. When choosing a provider, it is important to find one with experienced registered nurses who are compassionate and committed to patient care standards.
The Expanded Senior Citizen Act of 2010 grants additional benefits and privileges to senior citizens aged 60 and above in the Philippines. It provides for a 20% discount on essential goods and services such as medicines, medical services, transportation, and lodging. It also exempts senior citizens from income tax if they are minimum wage earners, and provides for discounts on utilities, free vocational training, and continued government benefits. The law establishes local Offices of the Senior Citizens Affairs to issue IDs, monitor compliance, and address issues. It also forms a National Coordinating and Monitoring Board composed of various government agencies to oversee implementation.
This document discusses different types of discrimination including gender, caste, and language discrimination. It explains that gender discrimination involves restricting one sex to inferior roles based on gender identity. Caste discrimination involves treating those from lower castes as untouchables or inferior. Language discrimination involves treating groups differently based on their preferred language. The document also discusses marginalization, which excludes groups from fully participating in society due to poverty. Marginalization can happen to individuals and communities. It particularly impacts women, minorities, Dalits, Adivasis, and children. Overcoming marginalization of minorities can help national development and inclusive growth by reducing poverty and inequality.
Primer on the senior citizen's act of 2010Harve Abella
This document summarizes key points from MARIVIC ACOSTA-GALBAN's presentation on tax policies for senior citizens in the Philippines. It defines who qualifies as a senior citizen and resident citizen. It outlines various tax exemptions for senior citizens based on their income levels as well as discounts of 20% that senior citizens are entitled to for medicines, medical fees, transportation, hotels, restaurants and other services.
The document discusses patients' rights regarding informed consent for medical treatment. It outlines the rights to informed consent, informed decision, and informed choice. It defines key concepts like competence, disclosure, comprehension, and voluntariness that are important for ensuring informed consent. The document also discusses limitations to consent in emergency situations and the rights to privacy, confidentiality, and refusal of treatment. Overall, it establishes that patients have a fundamental right to make voluntary and informed decisions about their own healthcare.
Patient Rights outline basic rules between patients and medical caregivers as well as institutions to improve patient outcomes. They are based on the concept of human dignity and equality from the Universal Declaration of Human Rights. Patient Rights vary between countries and regions depending on cultural and social norms but generally include rights like access to treatment, privacy, non-discrimination, and taking part in treatment decisions. Both the U.S. and European perspectives on Patient Rights establish lists of rights and responsibilities in an effort to protect patients and support high quality healthcare.
The document outlines 19 rights that patients have as a hospital patient in New York State. These rights include the right to receive treatment without discrimination, considerate and respectful care in a safe environment, privacy and confidentiality regarding medical information and records, and to participate in decisions about treatment and discharge. Patients also have the right to understand their diagnosis and treatment plan, provide or refuse consent for procedures, refuse treatment or participation in research, and file complaints about their care without reprisal.
“I solemnly pledge myself to consecrate my life to service of humanity.” This is the first sentence a doctor utters while taking an oath when s/he enters into the medical profession. They are considered as God by people despite knowing the fact that they are human, as the profession gives ‘hope’ to live to a patient and his family. But due to the increasing number of medico legal issues in the country, there is a serious concern about the doctor-patient relationship. To raise awareness among the patients about their rights and responsibilities as patients and to build up a strong, safe and healthy doctor patient relationship, the Dr. Anamika Ray Memorial Trust observes June 25 as Patients’ Rights Day under the “STOP MEDICAL TERRORISM” movement for better and transparent healthcare services in India.
The Trust, in consultation with a panel of medical professionals of national and international repute, drafted the Patients’ Rights in 10 points and the responsibilities in another 10 points. The Rights and Responsibilities of the patients available at http://smt.armt.in in many Indian languages. It's a two page document. The Trust requests everyone to support the cause by downloading the document in their preferred language, printing it out and distributing it among patients in any hospital in India. The Trust believes that this initiative may save hundreds of lives and will be a great contribution for better and more transparent healthcare services in India.
The rights mentioned in the draft include the right to get the best possible medical care without discrimination; right to prompt, life-saving treatment; right to take part in all decisions relating to one’s health care; right to privacy; right to know the identity and role of people involved in treatment; right to dignity and to have caregivers’ respect; right to appropriate assessment and management of pain; right to receive visitors; right to refuse treatment and to leave the medical centre; and right to get necessary information related to the line of treatment as well as all health records.
The responsibilities mentioned in the draft include the responsibility to refrain from misbehaving and misconduct towards any medical service providers; responsibility to refrain from physical assault of any healthcare personnel or damage to property; responsibility to be truthful; responsibility to provide complete and accurate medical history; responsibility to cooperate with the agreed line of treatment; responsibility to meet the financial obligations; responsibility to refrain from initiating, participating or supporting fraudulent and illegal health care practices; responsibility to report illegal or unethical behaviour; responsibility to get a post-mortem done and responsibility to discuss end of life decisions.
The document provides an overview of informed consent and patient rights in healthcare. It discusses the historical lessons that led to greater emphasis on informed consent, including past unethical medical experiments. It defines informed consent as both a process of ongoing discussion and a signed document. The key principles of respect for patient autonomy, beneficence, and justice are outlined. Requirements for valid consent from patients and their representatives are covered. The document also discusses other important patient rights like privacy, no deposit laws, no detention laws, and rights of senior citizens.
Ppt senior citizens legal rights seminarcaishaan90
The Rotaract Club of Athena's Knights held a seminar on the legal rights of senior citizens. Several speakers addressed topics like legal remedies for abused or abandoned senior citizens, succession planning, reverse mortgages, and police safety mechanisms for seniors. Over 200 senior citizens attended the event, which included sessions from lawyers, retired bankers, and police representatives. The seminar aimed to educate seniors on their rights and how to protect themselves legally.
This document summarizes Republic Act No. 9994, which outlines benefits and protections for senior citizens in the Philippines. It defines senior citizens as those aged 60 and older, and entitles them to discounts, free services, exemptions, incentives, and government financial assistance. Specific benefits include a 20% discount on goods and services, social pension for indigent seniors, and mandatory PhilHealth coverage. It also describes penalties for violating the law and proposed bills to further assist senior citizens.
This document outlines patients' rights and responsibilities in healthcare facilities in Saudi Arabia. It begins by defining patients' rights as policies that must be protected by health facilities for patients and their families. It then lists 12 specific rights that include the right to privacy, safety, treatment options, complaint processes, and participation in care decisions. It also outlines additional rights for specific groups like children, elderly patients, and those with special needs or psychiatric conditions. The document concludes by listing responsibilities of patients and families, such as respecting staff, facilities, and other patients' privacy and values, as well as following treatment plans and facility rules.
This document discusses privacy, confidentiality, and medical records. It defines privacy as protecting a patient's body from being seen or interfered with by others, while confidentiality refers to protecting a patient's medical information. The document outlines measures to ensure privacy during examinations and confidentiality of medical records. It describes what types of patient information must be kept confidential and exceptions when information can be disclosed, such as for legal or public health reasons. Ethical and legal guidelines for maintaining privacy, confidentiality, and proper documentation in medical records are also reviewed.
Patients at Hospital Changkat Melintang have rights that respect their personal dignity, values, and preferences. They have the right to receive considerate care without discrimination. They also have the right to effective communication, involvement in treatment decisions, privacy and confidentiality, pain management, and understanding of medical charges. If patients have concerns about their care, the hospital provides processes to lodge and address complaints.
VVC Nursing : F10 General Hospital OrientationJustin Gatewood
The document provides an overview of patient rights and responsibilities at hospitals. It discusses 8 key rights that patients have, including the right to receive information, choose providers, access emergency services, participate in treatment decisions, refuse treatment, and expect confidentiality and respect. It also outlines responsibilities of patients such as providing accurate medical information and following treatment advice. The document reviews policies around advance directives, customer service, and violations of patient rights.
This document outlines the duties of healthcare practitioners towards patients, including: providing good treatment by listening to patients and showing respect; achieving the patient's interests and guarding their rights by limiting unnecessary procedures and informing them of treatment options; obtaining valid consent by ensuring the patient understands risks and can consent voluntarily; reassuring patients by addressing psychological needs and breaking bad news sensitively; maintaining patient confidentiality with exceptions to protect others or report crimes; and obtaining proper consent before photographing or recording patients.
Series of lectures I gave for the PEER (Professionalism and Ethics Education for Residents) Project sponsored and organized by the Saudi Commission for Health Specialties (SCHS).
OUTLINE:
What is an informed consent to treatment?
What is the elf basis to consent?
What makes the consent an ethically valid one?
Types of Consent
When it is needed? When could it be waived?
How to take an informed consent?
What if the patient is not able to give consent?
Documentation of Consent
Special Issues about Consent
This document discusses patients' rights in healthcare. It begins by defining a patient's bill of rights as a list of guarantees for those receiving medical care, including the right to information, fair treatment, and autonomy over decisions. The document then outlines specific rights in more detail, such as the right to receive respectful and safe care, provide informed consent, privacy and confidentiality, refuse treatment, and make complaints. It discusses patients' rights during medication and treatment. Overall, the document aims to clearly define the rights and protections that should be afforded to all patients.
PRESENTATION ON Patients right and responsibilitiesBhavaniBangaram1
The document provides an overview of patient rights, including definitions, purposes, and key areas. It defines a patient as a person receiving medical treatment and outlines some basic patient rights such as privacy, informed consent, and quality care. It discusses the nurse's role in safeguarding patient rights and protecting patients from unethical practices. The presentation aims to help patients feel more confident in the healthcare system and stress the important relationship between patients and providers.
This document discusses patients' rights and advocacy in nursing. It outlines various patients' bills of rights which guarantee patients access to information, treatment, and medical decision making. Specific rights mentioned include the right to privacy, informed consent, and making complaints. The role of nurses as advocates who help patients understand and exercise their rights is described. Nurses act as advocates by developing relationships with patients and making decisions with them. They may also be whistleblowers by calling attention to unethical or illegal actions. The document is authored by Prof. Dr. Ram Sharan Mehta on the topics of patient rights and advocacy in nursing.
This document outlines various patient rights and ethics related to healthcare. It discusses the purpose of delineating patient rights to ensure ethical treatment. Some key rights mentioned include the right to informed consent, privacy, access medical records, file complaints, and continuity of care. It also discusses ethics principles like autonomy, beneficence, nonmaleficence, justice and various codes of ethics for healthcare professionals. Additionally, it provides an overview of the US Senate passed Patient's Bill of Rights that would ensure patients have rights like access to specialists and emergency care.
Admission+Discharge+Rights OF b.SC NURSING PSYCHIATRIC NURSING.pptelizakoirala3
This document discusses the legal aspects of psychiatric care, including admission and discharge procedures for mentally ill patients, the rights of mentally ill persons, and relevant mental health acts and policies. It provides details on voluntary versus involuntary admission, the admission process, types of discharge including conditional discharge, and the rights of mentally ill persons to privacy, confidentiality, consent in treatment, and least restrictive care.
Informed consent is required for any medical procedure and involves educating the patient on the nature, risks, and benefits of the procedure. Key aspects of informed consent include voluntary agreement from the patient, disclosure of relevant medical information, and the patient's competence to consent. Exceptions may apply in emergencies or for therapeutic reasons. Standards for obtaining informed consent aim to respect patient autonomy while balancing ethical obligations of beneficence.
This document discusses several core ethics principles: autonomy, beneficence, nonmaleficence, justice, informed consent, confidentiality, and others. It provides definitions and examples for each principle. Several case studies involving ethical dilemmas in healthcare are also presented, including conflicts between patient/family wishes and physician recommendations for treatment. The document advocates using an ethical decision-making process and calling an ethics consultation to help resolve complex cases.
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November 17, 2021 @ 4:00 pm - 5:00 pm EST
Speaker:
Ghaiath Hussein, Assistant Professor, Medical Ethics and Law, Trinity College Dublin, Ireland
About this Seminar:
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This slide is very helpful for physiotherapy students and also for other medical and healthcare students.
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2. Outline
O Why do we need to know about and
respects patients’ rights?
O Ethical and Legal aspects inpatients’ rights
O Overview on consent to treatment
O Overview on privacy and confidentiality
O Summary points
5. Professional/Legal
requirement
O Patient’s Bill of Rights and Responsibilities (KSA)
http://www.moh.gov.sa/en/HealthAwareness/Educati
onalContent/HealthTips/Pages/Tips-2011-1-29-
001.aspx
O Law of Practicing Healthcare Professions:
O “Article 5:
O Healthcare professionals shall serve the best interest of
individuals and society within the framework of
respecting human right to life, safety and dignity and
shall observe customs and traditions prevailing in the
Kingdom, and eschew exploitation.”
6. Rights of Patients & Their Families
1. Knowing Patient and
Family Rights and
Responsibilities
2. Getting Health Care
3. Privacy and
Confidentiality
4. Safety and Protection
5. Respect and
Appreciation
6. Participation in the
Healthcare Plan
7. Refuse Treatment
8. Participation in
Research Studies
9. Organ and Tissues
Donation Policies and
Procedures
10. Health Insurance and
Financial Policy
11. Clear and
Comprehensive
Declaration Forms
12. Complaints and
Suggestions Policies
and Procedures
O Child Patient Rights
O Elderly Patient Rights
O Psychiatric Patient Rights
O Special Needs Patient
Rights
7. Participation in decision-making
Receive Relevant
Information
Diagnosis
Treatment
Prognosis
Post-Discharge Care
Hospital policies
Consent to
Treatment
Relevant facts
explained
Patients are free from
undue influence
Patients assign
Substitute decision
maker (SDM)
Right to Refuse
Treatment
Relevant alternatives
explained
Risks explained, and
consent taken
8. CAPACITY
VOLUNTARINES
S
DISCLOSURE
•The patients has
the ability to:
• Understand
medical
information
• Appreciate the
risks
• Memorize the
information
•Communicate
the decision
•Freedom from
undue influence:
• Financial
• Social pressure
•Physical
restraint
•Information:
•Diagnosis
• Possible
prognosis
• Benefits and
risk of treatment
• Expected
outcome
• In a language
understood by
the patient
9. Right to Privacy & Confidentiality
Confidentiality :
- Is the right of an
individual to have
personal, identifiable
medical information
kept out of reach of
others.
Privacy:
- A right or expectation to
not be interfered with
- Be free from
surveillance
- A moral right to be left
alone.
RESPECTS PATIENT’S
BODY
RESPECTS PATIENT’S
INFORMATION
10. Measures to Protect Privacy (KSA guidelines)
1. Make sure examination takes place in isolation from
other patients, unauthorized family members, and/or
staff
2. Provide gender-sensitive waiting and examination
rooms
3. Provide proper clothing for the admitted patients
4. Make sure patients are well covered when transferred
from one place to another in the hospital
5. Make sure your patient’s body is exposed ONLY as
much as needed by the examination or investigation
6. Patients should have separate lifts and be given
priority
11. Measures to Protect Privacy
7. Make sure there is another person (chaperone, nurse)
of the same sex as the patient present all the time of
the examination
8. Always take permission from the patient before
examination
9. Insure privacy when taking information from patients
10. Avoid keeping patients for periods more than required
by the procedure.
11. It’s prohibited to examine the patient in the corridors or
in the waiting area.
12. During examination, no foreign person unrelated to the
patient allowed
13. Give patients enough time to expose the part with pain
14. Only relevant personnel are allowed to enter the
examination room
13. What is Confidential?
O All identifiable patient information, whether written,
computerised, visually or audio recorded or simply
held in the memory of health professionals, is subject
to the duty of confidentiality.
It covers:
O Past, present or future physical or mental condition,
O Individual diagnosis or treatment;
O A picture, photograph, video, audiotape or other images of
the patient;
O Who the patient’s doctor is and what clinics patients attend;
O Anything else that may be used to identify patients directly or
indirectly
O The past, present, or future payment
14. Confidentiality Measures
1. Limit the accessibility to the medical records
2. Do not discuss the patient’s medical information
with unauthorized family members
3. Do not disclose patient’s information without his/her
consent, or in established exceptions (below)
4. Do NOT collect information not related to the
provision of care
5. Set policies that regulate access to medical
information and how any breach to confidentiality is
managed
6. Limit sharing of information with other staff, unless
in cases of consultations and second opinion
15. Conditions to breach confidentiality
1. Approval from the patients or their substitute decision
maker,
2. If the information is required by judiciary
3. Consultation or second opinion
4. Notification of events of public health interest/threats
(birth, death, notifiable diseases, etc.)
5. Prevent individual/personal threats (e.g. prevent
crimes)
6. If needed by the doctor to defend him/herself before
judges, or discipline committee
7. If the patient consciously and truly admits committing
a crime on which another person was
accused/punished
Remember: Disclosure should be only to the
concerned party & not beyond the needed limits
الضابطفيكشف أو سترمنع هو المريض سر عن الطبيبالمفسدة ظهور
16. 4- Continued care, Seeking 2nd opinion & Referral
The patients have the right to:
Receive uninterrupted care from his/her doctor.
To be referred to other health care providers when
necessary.
Receive a second opinion when the patient or his/her
doctor requests one.
The second opinion must be provided by a qualified
health care professional within the same organization.
Saudi Commission for Health Specialties
17. Compassionate EOL Care
The patient have the right to:
Have her physical pain assessed and managed
Have Advance Directive Plan (Living Will)
Assign a family member to be the SDM
Have her/his emotional and spiritual needs
addressed
Saudi Commission for Health Specialties
18. Appeal and Complaint Submission
The patient have the right to:
Be told on how to process her problems or complaints
Voice his/her concerns about the care she/he receives
Ask questions and express concerns about hospital
health care and services, without fear of reprisal
Have his/her complaint responded to in a timely and
satisfactory manner
Saudi Commission for Health Specialties
19. Additional Rights for special groups
Children Elderly
• Examined by
specialized team.
• Appropriate
environment
• Assign a companion
• Report any violence
against children to the
concerned authority.
• Avoid isolating the
patient unless it's
medically necessary.
• Meet their special
needs in the health
facility.
• Provide needed
health and treatment
services to the
patient.
• Facilitate making
appointments and
having their medical
reports
Saudi Commission for Health Specialties
20. Psychiatric Special Needs Patient
• Protect psychiatric
patients from harm.
• Ensure the patient’s
freedom of movement
and shouldn’t isolate
him/her unless it’s
medically necessary.
• Allocating mental health
clinics
• Provide suitable
education and
rehabilitation methods
• Respect the patient’s
dignity, independency
in addition to his/her
personal decisions.
• Provide specialized
equipments and tools
for special needs
patients.
• Assist the patient in
moving
• Provide suitable aisles
and bathrooms.
• Allocate parking spaces
for special needs
Saudi Commission for Health Specialties
Additional Rights for special groups
21. Key messages
Make sure you and your patients know
your and their rights
Train your colleagues on patient’s rights
Knowing and providing these rights
protects you professionally and legally
Patient rights guide you to achieve your
ethical and professional goals of availing
the best service to your patients
Rights are rights! They are required by
LAW, needed for accreditation, and not
gifts that you may or may not give.
Saudi Commission for Health Specialties
22. References
O Saudi Council for Health Specialties
Manual of Ethics of the Medical
Profession
O Patient’s Bill of Rights and
Responsibilities MOH, KSA
O Law of Practicing Healthcare
Professions
O Professionalism and Ethics Handbook
for Residents (Saudi Commission for
Health Specialties, Riyadh – 2015)