WHO Patient Safety Rights Charter: A Comprehensive Medical Analysis of the 10 Fundamental Rights for Safer Healthcare

The World Health Organization (WHO) has launched the Patient Safety Rights Charter – a landmark document that establishes 10 fundamental patient rights essential for mitigating risks and preventing harm in healthcare settings. This comprehensive medical article provides a detailed analysis of each patient safety right, exploring its clinical implications, ethical foundations, and practical applications for healthcare professionals, policymakers, patients, and families.

Drawing on international human rights instruments, the charter links patient safety with the right to health, dignity, information, privacy, non-discrimination, and fair resolution. Unsafe healthcare is a leading cause of morbidity and mortality worldwide, and this charter represents a critical framework for transforming health systems into safer, more equitable, and patient-centred environments.


1. Introduction: The Global Imperative for Patient Safety

Patient safety is a fundamental principle of healthcare. Yet, every year, unsafe care causes millions of preventable deaths and disabilities worldwide. According to the Organisation for Economic Co-operation and Development (OECD), the economic burden of patient harm is substantial, with billions of dollars lost due to extended hospital stays, litigation, and lost productivity. A landmark systematic review and meta-analysis published in the BMJ (Panagioti et al., 2019) found that preventable patient harm is prevalent across medical care settings, affecting millions of patients annually.

The WHO Patient Safety Rights Charter was developed through a consultative process with members of the World Patient Safety Day 2023 planning group, engaging a diverse range of stakeholders including patient advocates, patient safety experts, hospital safety experts, human rights experts, health workers, policymakers, and healthcare leaders. The charter is based on a comprehensive review of existing patient rights charters and legal instruments from across the world. A draft underwent critical review by participants of the WHO Global Conference “Engaging Patients for Patient Safety”, held on 12–13 September 2023 at WHO headquarters in Geneva.

The charter is universally applicable across all healthcare settings and relevant at every level of healthcare provision. It covers the complete spectrum of health services, including:

DomainExamples
PromotiveHealth education, lifestyle counselling
ProtectiveVaccination, screening programmes
PreventiveRisk assessment, early intervention
CurativeDiagnosis, treatment, surgery
RehabilitativePhysical therapy, recovery support
PalliativeEnd-of-life care, symptom management

The charter recognises the importance of engaging and empowering families and caregivers in healthcare processes and health systems at national, subnational, and community levels.


2. Human Rights Foundations of Patient Safety

The charter explores the linkages between patient safety, the right to health, and human rights more broadly. Human rights are enshrined in various international instruments, including:

InstrumentYearKey Provisions
Universal Declaration of Human Rights1948Dignity, liberty, security, equality
International Covenant on Economic, Social and Cultural Rights1966Right to health, work, education
Convention on the Elimination of All Forms of Discrimination against Women (CEDAW)1979Gender equality in healthcare
Convention on the Rights of the Child (CRC)1989Children’s right to healthcare
Convention on the Rights of Persons with Disabilities (CRPD)2008Accessibility, reasonable accommodation

2.1 The Right to Health

The right to health is the right of everyone to the enjoyment of the highest attainable standard of physical and mental health. All WHO Member States have ratified at least one international human rights treaty that incorporates this right. Countries have a legal obligation to develop and implement legislation and policies that ensure universal access to safe and quality health services.

Given that unsafe healthcare is a leading cause of morbidity and mortality worldwide, patient safety grounded in the ethical principle “First, do no harm” is an indispensable element of ensuring the safe engagement of patients with the health system and fulfilling the right to health.

2.2 The Right to Life, Liberty and Personal Security

The right to life extends beyond the avoidance of intentional harm; it includes the right to healthcare that is free from unintentional harm, especially when preventable based on available evidence. The right to liberty prohibits arbitrary deprivation of liberty based on disability or impairment, including mental health conditions. Personal security in healthcare involves ensuring that patients are treated in a safe environment, shielded from any form of abuse, neglect, violence, or exploitation.

2.3 The Right to Dignity

The right to dignity involves healthcare that is culturally appropriate and respects each patient’s humanity, autonomy, will, and preferences in relation to the acceptability of health services provided.

2.4 The Right to Information

Every patient has the right to be provided with information about their health condition, treatment options, potential risks, benefits, and prognosis in an accessible and understandable format. This empowers patients to actively participate in their health journey and make informed decisions.

2.5 The Right to Privacy

The right to privacy is essential in healthcare settings and directly impacts patient safety. Patients are entitled to expect the safeguarding of their physical privacy, personal matters, and medical information.

2.6 The Right to Non-Discrimination

Safe healthcare must be accessible for every patient, everywhere, at all times, regardless of age, gender, ethnicity, language, religion, disability, socioeconomic status, or any other status as established by human rights standards.

2.7 The Right to Freedom from Cruel, Inhuman or Degrading Treatment

This right safeguards individuals from actions that put their physical, mental, emotional, and psychological well-being in jeopardy. It calls for a healthcare environment where patients are treated with compassion and respect.

Patient safety represents a tangible manifestation of realising health-related human rights and is a litmus test of the global commitment towards respecting, protecting, and fulfilling those rights.


3. The 10 Patient Safety Rights: Detailed Clinical Analysis

The following sections provide a detailed medical and clinical analysis of each of the 10 patient safety rights established by the WHO Charter.


Right 1: Right to Timely, Effective and Appropriate Care

Definition: Patients have the right to receive timely and effective care tailored to their health needs, particularly in situations where delays could lead to disease progression, clinical deterioration, failure to rescue, and poor outcomes such as preventable patient harm.

3.1 Clinical Implications

AspectClinical Significance
TimelinessDelays in diagnosis or treatment can convert a treatable condition (e.g., sepsis, stroke, myocardial infarction) into a fatal or disabling one. “Time is tissue” applies across many conditions.
24/7 AvailabilityCare must be available around the clock, including out-of-hours periods, weekends, and public holidays.
Notification of critical resultsPatients have the right to be promptly notified of any critical test results, especially after discharge.
Post-discharge careTimely and effective post-discharge care ensures monitoring of recovery and early identification of complications.

3.2 Evidence Base

  • In sepsis, each hour of delay in antibiotic administration increases mortality by 7–8%.
  • In acute ischaemic stroke, earlier thrombolysis (within 60 minutes of arrival) significantly improves functional outcomes.
  • In myocardial infarction, door-to-balloon times >90 minutes are associated with higher mortality.

3.3 Practical Implementation

ActionResponsible Parties
Implement triage systems (e.g., Manchester Triage System)Emergency departments
Establish rapid response teams for deteriorating patientsHospitals
Develop electronic alert systems for critical laboratory resultsLaboratory and IT departments
Schedule follow-up appointments before dischargeDischarge planning teams

Right 2: Right to Safe Health Care Processes and Practices

Definition: Patients have the right to expect that health workers follow safe processes and practices and implement measures to identify, prevent, and manage risks and reduce preventable harm.

3.4 Key Safe Practices

Practice AreaRequired Actions
Patient identificationUse at least two identifiers before any intervention (e.g., name, medical record number, date of birth)
DocumentationAccurate, legible, timely, and complete medical records
Clinical and diagnostic pathwaysEvidence-based protocols for common conditions
Handovers and referralsStructured communication tools (e.g., SBAR – Situation, Background, Assessment, Recommendation)
Medication safetyReconciliation, independent double-checks for high-alert medications, avoidance of look-alike/sound-alike errors
Surgical safetyWHO Surgical Safety Checklist (Sign-In, Time-Out, Sign-Out)
Blood transfusion safetyPre-transfusion checks, patient identification, monitoring for reactions
Infection prevention and controlHand hygiene (WHO 5 Moments), aseptic technique, standard precautions
Diagnostic accuracyAvoid overdiagnosis and underdiagnosis; appropriate test utilisation

3.5 Clinical Example: The WHO Surgical Safety Checklist

Implementation of the WHO Surgical Safety Checklist has been associated with:

  • Reduction in surgical mortality by 25–50%
  • Reduction in surgical complications by one-third
  • Improved teamwork and communication in operating theatres

Right 3: Right to Qualified and Competent Health Workers

Definition: Patients have the right to receive care from health workers who possess the necessary qualifications, skills, and competencies aligned with national and international standards.

3.6 Who Are Health Workers?

The charter defines health workers broadly:

  • Clinical professionals: Doctors, nurses, pharmacists, midwives
  • Public health professionals
  • Laboratory, health, and medical technicians
  • Community health workers and traditional medicine practitioners
  • Health management and support workers: Hospital administrators, district health managers, social workers, cleaners, drivers
  • Care workers: Those providing direct personal care services in acute care, long-term care, public health, community-based care, social care, and home care

3.7 Implications

RequirementAction
Credentialing and privilegingVerify qualifications, licences, and ongoing competency before granting clinical privileges
Continuing professional developmentMandatory ongoing education and skills maintenance
Disclosure to patientsPatients are entitled to be informed about the names of their healthcare team and details about facilities (licensing, certification, safety ratings)
Compassionate careCare should be delivered with professional integrity, compassion, empathy, and respect

3.8 Patient Safety Impact

Studies consistently show that higher nurse staffing levels and better-educated nurses are associated with lower mortality rates, fewer medication errors, and improved patient outcomes.


Right 4: Right to Safe Medical Products and Their Safe and Rational Use

Definition: Patients have the right of access to medical products they need, including medicines, vaccines, medical devices, diagnostics, blood and blood products, traditional and complementary medicines, and assistive and medical technologies that meet recognised safety, quality, and efficacy standards.

3.9 Scope of Medical Products

CategoryExamples
Medicines and vaccinesPrescription drugs, OTC products, biologicals
Medical devicesImplants, infusion pumps, diagnostic equipment
DiagnosticsLaboratory tests, imaging, point-of-care tests
Blood and blood productsWhole blood, packed red cells, platelets, plasma
Traditional and complementary medicinesHerbal products, acupuncture, traditional remedies
Assistive technologiesWheelchairs, hearing aids, prosthetics

3.10 Safe and Rational Use Encompasses

StageActivities
Prescribing/orderingAppropriate indication; correct drug, dose, route, duration
StorageCorrect temperature, security, labelling
DispensingAccuracy, patient counselling
PreparationAseptic technique (e.g., for IV medications)
AdministrationFive rights (right patient, drug, dose, route, time)
MonitoringTherapeutic drug monitoring, adverse reaction surveillance

3.11 Pharmacovigilance Obligations

Health workers and patients alike must be empowered on:

  • Identification and reporting of suspected adverse drug reactions (ADRs)
  • Transfusion reactions
  • Adverse events following immunisation (AEFIs)
  • Medication errors
  • Substandard and falsified medicines and other medical products

Reporting should be made to relevant authorities (e.g., national pharmacovigilance centres, FDA, EMA, MHRA, national medicine regulatory authorities).


Right 5: Right to Safe and Secure Health Care Facilities

Definition: Patients have the right to receive care in health care facilities that are safe, resilient, and easily accessible to everyone.

3.12 Key Components

ComponentRequirements
AccessibilityUniversal design for persons with disabilities; reasonable accommodation when universal design is not feasible
Structural integrityBuilding safety, seismic resilience, climate resilience
Critical systemsPower, illumination, water, sanitation, waste management, ventilation, infusion systems – especially in operating theatres and isolation units
Fire safetyFire detection, suppression systems, evacuation protocols
Electrical safetyGrounding, backup power, regular inspections
Radiation safetyLead shielding, dosimetry, staff training
Infection preventionClean water, proper sanitation, hand hygiene facilities, safe waste management
Environmental safetySmoke-free surroundings, safe food (tailored to dietary and cultural needs, with allergy considerations)
Emergency preparednessEvacuation pathways, disaster response plans

3.13 Special Considerations

  • Persons with disabilities: Universal design is of utmost importance. Where not feasible, reasonable accommodation must be provided.
  • Emergencies and disasters: Facilities must maintain robust infrastructure to ensure continuity of essential services.
  • Nutrition: Patients are entitled to safe and appropriate food tailored to their dietary and cultural needs, with consideration of known allergies.

Right 6: Right to Dignity, Respect, Non-Discrimination, Privacy and Confidentiality

Definition: All patients have the right to be treated with dignity and respect throughout their health care journey, irrespective of their background, beliefs, values, cultures or preferences.

3.14 Key Elements

ElementClinical Application
DignityCulturally appropriate care; respecting autonomy and choices; honouring end-of-life preferences
Freedom from abuse/neglectProtection from physical, emotional, sexual, or financial abuse; zero tolerance for violence
Non-discriminationCare that is impartial and inclusive; active protection for vulnerable populations (children, women, older persons, persons with disabilities, Indigenous Peoples, refugees, migrants, sexual/gender/ethnic minorities, people in humanitarian emergencies)
PrivacyPrivate consultation spaces; discreet medical procedures away from public view; confidential conversations
ConfidentialitySafeguarding all personal and medical information; disclosure only with explicit patient consent or as required by law

3.15 Vulnerable Populations

The charter explicitly calls for active protection of:

  • Children
  • Women
  • Older persons
  • Persons with disabilities
  • Indigenous Peoples
  • Refugees and migrants
  • People in humanitarian emergencies
  • Sexual, gender and ethnic minorities

Principle: “It is essential that care is equitable, and that at-risk patients and communities are partners in shaping the care they receive.”

3.16 Privacy and Confidentiality in the Digital Age

With the increasing use of electronic health records (EHRs), telemedicine, and artificial intelligence (AI), the charter reinforces the fundamental right to privacy and confidentiality. Patients are entitled to:

  • Safeguarding of physical privacy
  • Protection of personal matters
  • Confidential handling of medical information
  • Assurance that identifiable information is only disclosed with explicit consent or as required by law

“Upholding privacy and confidentiality are essential for establishing and maintaining trust between patients and the health care team.”


Right 7: Right to Information, Education and Supported Decision-Making

Definition: Patients have the right to receive timely, accurate and complete information about their health, and to actively participate in discussions about their care and the decision-making process.

3.17 Information That Must Be Provided

Type of InformationDetails
Medical conditionDiagnosis, prognosis, natural history
Management planTreatment goals, steps, timeline
Medications/medical productsNames, purpose, benefits, possible adverse effects, interactions, contraindications, alternatives
Self-care instructionsHow to manage their condition at home
Risks and benefitsOf proposed treatments and of not treating
AI in healthcareStrengths, limitations, and risks of AI used in patient education and decision-making

3.18 Supported Decision-Making

Patients have the right to:

  • Active participation in discussions and decisions about their care
  • Access to adequate support before consenting to treatment (one-to-one consultations, decision aids, educational materials, videos)
  • Exercise legal capacity by involving a legally authorised representative of their choice
  • Receive effective communication that is culturally appropriate and tailored to their age, literacy, and individual needs (including interpretation services and alternative/accessible formats for language or sensory barriers)

3.19 Emergency Situations

In emergencies where obtaining formal consent is not feasible and a designated family member, caregiver, or legal representative is unavailable:

“Health workers will expend their greatest effort to arrive at the best interpretation of the patient’s will and preferences to guide their actions.”

3.20 The Right to Refuse Care

Patients have the right to refuse care without coercion, pressure, or undue influence from anyone. This right is fundamental to autonomy and informed consent.


Right 8: Right to Access to Medical Records

Definition: Patients have the right to access or obtain a copy of their records in a usable and understandable format.

3.21 Key Provisions

ProvisionDescription
AccessRight to view and obtain copies of physical and electronic records
FormatRecords must be usable and understandable
AccuracyRecords must be accurate and up to date
CorrectionRight to request corrections to factual inaccuracies
ControlRight to control the use of their information
TransferRight to easily transfer medical records when seeking second opinions or changing facilities
RepresentativeRight to designate a representative to access or obtain records

3.22 Clinical Importance

  • Second opinions: Access to records facilitates informed second opinions, reducing diagnostic errors.
  • Care continuity: Transfer of records between facilities reduces duplication of tests and medication errors.
  • Patient empowerment: Access to records enables patients to understand their condition and participate in management.

Right 9: Right to Be Heard and Fair Resolution

Definition: Patients have the right to share their experiences, file complaints, and report safety incidents occurring during their care, without fear of retribution or negative repercussions.

3.23 Scope of Reporting

Patients may report:

  • Adverse events leading to patient harm
  • Near misses (incidents that could have caused harm but did not)
  • Any other safety risks they perceive or safety concerns they have

3.24 Elements of Fair Resolution

ElementDescription
Supportive environmentCulture of safety; fear-free reporting
Clear explanationPatients entitled to understand what happened, why it happened, and actions taken for redressal
Prevention of recurrenceCommitment to implementing learnings from incident analysis
Independent investigationClear pathway for independent investigation and accountability
ReconciliationFair and just process for addressing harm
CompensationIn line with harm experienced, national legislation, and best practices
Psychological supportOngoing psychological and other forms of support as needed
ReassuranceCommitment that the facility will implement learnings to prevent future occurrences

3.25 Just Culture vs. Blame Culture

The charter emphasises a culture of safety whereby patients’ voices are heard and concerns expressed without fear of retribution. This aligns with the “Just Culture” principle, which distinguishes between human error, at-risk behaviour, and reckless behaviour.


Right 10: Right to Patient and Family Engagement

Definition: Patients have the right to be active partners in their care, with a particular focus on ensuring their safety at every step of care provision.

3.26 Elements of Partnership

ElementDescription
Self-determinationFreedom to make choices about their care
Informed participationUnderstanding and managing potential risks
Planning and monitoringContributing to treatment plans and ongoing assessment
Choice of provider/facilityFreedom to choose preferred option of care, health workers, or healthcare facility
Right to refuse careWithout coercion, pressure, or undue influence
Advance directivesRight to outline healthcare preferences for future scenarios where unable to make decisions
Second opinionsRight to seek opinion of another physician at any stage
Family/caregiver supportRight to seek support from designated family members throughout the healthcare journey

3.27 Role of Families and Caregivers

Family members, as designated by the patient, have the right to:

  • Be actively involved in discussions and decisions regarding the patient’s care
  • Play a vital role in identifying and flagging potential safety risks, particularly when patients are unable to communicate or make decisions themselves

3.28 System-Level Engagement

Patients, families, patient organisations, and the public have the right to be involved in shaping their health system to promote patient safety. This may take the form of:

Form of EngagementExamples
Public actionHealth awareness campaigns, educational campaigns
Policy developmentParticipation in policy development
Service deliveryInput into service design and delivery
Monitoring and evaluationParticipation in assessment and monitoring
ResearchPatient and public involvement in research
GovernanceParticipation in patient and family advisory committees, healthcare facility boards and committees

4. Target Audiences and Applicability

The charter is intended for a diverse range of stakeholders:

Stakeholder GroupRole
Patients, families, caregivers and the general publicRights-holders; active participants in their care
Civil society organisations, patient organisations, patient groups and patient advocatesAdvocates for patient rights; support for implementation
Health workersDuty-bearers; frontline implementers of safe care
Policy-makers, health care leaders and health care facility managersEnablers of safe systems; accountable for safety culture
Professional associations, patient safety experts, international organisations and intergovernmental organisationsGuidance, standard-setting, and technical support
National and subnational regulatory authoritiesRegulatory oversight; enforcement of standards
Human rights experts, advocates, activists and organisationsHuman rights perspective and accountability
Academia and research institutionsResearch, education, and evidence generation

5. Call for Adoption by Countries and Stakeholders

WHO invites Member States and all stakeholders to adopt, disseminate, and implement the Patient Safety Rights Charter through the following multifaceted actions:

5.1 Stakeholder Engagement

Conduct stakeholder analysis to identify relevant stakeholders, including patient organisations, the private sector, and the non-health sector, to raise awareness, secure commitment, and ensure active participation.

5.2 Legislative Framework and Regulatory Mechanisms

  • Conduct comprehensive analysis of existing national and subnational legal instruments and regulatory mechanisms in relation to human rights
  • Adopt or adapt the charter at national and institutional levels
  • Incorporate the rights articulated in the charter into existing national instruments and regulatory frameworks

5.3 Incorporation into Policies and Professional Guidelines

Collaborate with stakeholders to incorporate the principles of the charter into:

  • Existing national and subnational policies (patient safety and quality improvement frameworks)
  • Professional guidelines and operational procedures

5.4 Accountability, Remedial and Incentive Mechanisms

  • Create or use existing mechanisms for holding healthcare institutions and health workers accountable for informing patients of the charter and upholding these rights
  • Designate clear channels for reporting violations of patients’ rights
  • Establish remedial actions to address non-compliance
  • Consider introducing support measures to enhance adherence, such as designating “Charter champions” in healthcare facilities, especially those in underserved areas

5.5 Communication and Advocacy

  • Launch comprehensive awareness campaigns promoting the charter, its purpose, and its long-term impact
  • Adapt communication messages per target audience
  • Leverage various communication channels
  • Evaluate the effectiveness of communication and advocacy interventions
  • Boost public health literacy
  • Collaborate with media outlets to disseminate information about safe medical practices, self-care interventions, and other relevant healthcare topics

5.6 Capacity-Building of Health Workers and Patient Advocates

Strengthen the capacity of health workers and patient advocates with the competencies necessary for advocating and implementing patient safety practices, including those outlined in the charter. This can be achieved by incorporating patient safety into the education and training of health workers and patient advocates.

5.7 Monitoring, Evaluation and Improvement

  • Establish mechanisms for ongoing monitoring, evaluation, and improvement of the charter and its implementation strategies
  • Regularly assess the effectiveness of various approaches and make adjustments as needed
  • Set up independent mechanisms (or use existing mechanisms) to assess compliance with patient safety rights, investigate complaints, and ensure transparency

5.8 Research

Allocate resources to support research related to:

  • Patient rights and safety
  • Adoption of the charter by various stakeholders
  • Implementation strategies
  • The charter’s impact on patient safety culture, burden of patient harm, patient experience and satisfaction, and health outcomes

5.9 International Collaboration and Sharing of Best Practices

Engage in international collaboration and sharing of best practices, challenges, and successes in implementing the charter. This could include establishing a platform for information exchange or regular international forums focused on patient safety rights.


6. Clinical and Practical Implications for Healthcare Professionals

6.1 Key Takeaways for Clinicians

RightClinical Action
Right 1: Timely careRecognise and act on deteriorating patients; expedite critical results notification
Right 2: Safe processesUse checklists, SBAR for handovers, medication reconciliation
Right 3: Competent workersMaintain competence through CPD; introduce yourself to patients
Right 4: Safe productsFollow five rights of medication administration; report ADRs
Right 5: Safe facilitiesEnsure infection control; participate in safety drills
Right 6: Dignity and privacyUse private consultation spaces; obtain consent before examinations
Right 7: Information and decision-makingUse teach-back; provide decision aids; respect refusal of care
Right 8: Medical recordsEnsure accurate documentation; facilitate patient access to records
Right 9: Being heardEncourage patient reporting; participate in incident analysis
Right 10: EngagementInvolve patients and families in rounds, safety huddles, and committees

6.2 The Role of Pharmacovigilance

The charter explicitly links patient safety with pharmacovigilance through Right 4 (safe medical products and their safe and rational use). Healthcare professionals must:

  • Report suspected adverse drug reactions to national pharmacovigilance centres (e.g., FDA FAERS, EMA EudraVigilance, MHRA Yellow Card, Egyptian Pharmacovigilance Centre)
  • Report medication errors and near misses
  • Be vigilant for substandard and falsified medicines
  • Empower patients to recognise and report adverse reactions
  • Document medication histories accurately
  • Perform medication reconciliation at transitions of care

6.3 Implications for Hospital Administrators

ActionExpected Outcome
Establish patient and family advisory councilsImproved patient-centred care and safety culture
Implement safety reporting systems with non-punitive responsesIncreased reporting of incidents and near misses
Train staff on patient rightsReduced violations and complaints
Ensure accessible complaint and resolution pathwaysTimely and fair resolution of patient concerns
Designate “Charter champions”Enhanced adherence and accountability

7. Measuring Impact and Success

7.1 Key Performance Indicators

IndicatorData Source
Patient awareness of rightsPatient surveys
Healthcare worker training completion ratesTraining records
Incident reporting ratesSafety reporting systems
Patient complaints resolved within defined timeframeComplaint tracking systems
Patient satisfaction with safetyPatient experience surveys
Rates of preventable patient harmClinical audits, HAI surveillance
Medication error ratesPharmacy and nursing reports

7.2 Global Reporting

WHO encourages countries to share best practices, challenges, and successes in implementing the charter. This may include establishing a platform for information exchange or regular international forums focused on patient safety rights.


8. Conclusion: A New Era for Patient Safety

The WHO Patient Safety Rights Charter represents a paradigm shift in how patient safety is conceptualised and operationalised globally. By linking safety directly to fundamental human rights, the charter elevates patient safety from a technical healthcare quality issue to a legal and ethical imperative.

The 10 rights provide a comprehensive framework that addresses:

  • Clinical processes and practices
  • Health worker competence
  • Safe medical products
  • Physical infrastructure
  • Dignity, respect, and non-discrimination
  • Information and decision-making
  • Access to records
  • Fair resolution
  • Patient and family engagement

For healthcare professionals, the charter is both a guide and a call to action. Every interaction with a patient is an opportunity to uphold these rights. Every adverse event reported, every safety checklist completed, every moment of respectful communication, and every family member invited into the care team brings us closer to the goal of healthcare that is truly safe for all.

The ultimate message: Patient safety is not a privilege – it is a right. Unsafe care is not an unfortunate inevitability – it is a preventable violation of human dignity. The WHO Patient Safety Rights Charter provides the roadmap. Now, implementation must follow.


References

  1. World Health Organization. Patient Safety Rights Charter. Geneva: World Health Organization; 2024.
  2. Slawomirski L, Klazinga N. The economics of patient safety: from analysis to action. Paris: Organisation for Economic Co-operation and Development; 2020.
  3. Panagioti M, Khan K, Keers RN, et al. Prevalence, severity, and nature of preventable patient harm across medical care settings: systematic review and meta-analysis. BMJ. 2019;366:l4185.
  4. United Nations. Universal Declaration of Human Rights. 1948.
  5. United Nations. International Covenant on Economic, Social and Cultural Rights. 1966.
  6. United Nations. Convention on the Elimination of All Forms of Discrimination against Women (CEDAW). 1979.
  7. United Nations. Convention on the Rights of the Child (CRC). 1989.
  8. United Nations. Convention on the Rights of Persons with Disabilities (CRPD). 2008.
  9. World Health Organization. WHO Surgical Safety Checklist. Geneva: WHO; 2009.
  10. World Health Organization. WHO guidelines on hand hygiene in health care. Geneva: WHO; 2009.

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