Team of doctors using a laptop to review grievance policy documents

Creating an Effective Grievance Policy: A Guide for Hospital Leaders

An effective hospital grievance policy is key for protecting patient rights, resolving complaints, and improving satisfaction scores. Learn how to avoid common policy pitfalls, ensure regulatory alignment, and build trust through transparent, accountable patient grievance management.

Table of Contents

Among the many important responsibilities in hospital administration, establishing a clear and effective grievance policy stands out as a key driver of patient satisfaction, compliance, and operational consistency. Well-designed grievance policies not only streamline complaint resolution but also reinforce patient trust and institutional accountability.

This guide provides healthcare leaders with clear insights into creating, enhancing, and implementing effective grievance policies and procedures.

Grievance Policy

Why Hospitals Need Patient Grievance Policies and Procedures

Understanding what constitutes a hospital grievance policy is relatively straightforward. It defines how a patient or their representative can formally address concerns about care, treatment, or services, and how hospital staff must respond. These policies establish a structured process for resolving issues fairly and promptly.

However, creating and implementing a robust grievance policy is a more complex undertaking. For healthcare organization quality and risk management leaders, this means not only identifying what needs to be included in a grievance policy, but also determining how to implement these procedures effectively throughout the organization.

Establishing a comprehensive patient grievance policy and procedure helps mitigate risk, improve service quality, and contribute to long-term gains in patient complaint management and patient satisfaction.

What Needs to Be Included in a Hospital Grievance Policy?

According to an article published by the Healthcare Financial Management Association (HFMA), effective hospital policies should include:

  • A clear purpose statement explaining why the policy exists and its intended outcomes
  • Clear definitions of key terms, ideally linked to an online glossary for easy reference
  • Detailed action steps that staff must follow (i.e., the grievance procedures)
  • Supporting documentation, including forms, flow charts, and background materials

Including these elements not only ensures compliance but also improves usability and consistency across the organization.

Grievance Policy and Procedure Checklist

The following are key elements to include in a patient grievance policy and procedure template:

  • Definition of a grievance: The University of Texas Health Science Center defines a grievance as a formal verbal or written expression of dissatisfaction with some aspect of care or service that has not been resolved to the patient’s or family’s satisfaction at the point of service. This includes complaints related to abuse, neglect, patient harm or risk of harm, and violations of patient rights.
  • Eligibility to file: Policies should specify that grievances may be filed by patients or their authorized representatives.
  • Types of grievances: Typical grievance categories include care quality, communication, scheduling and access, pain management, neglect, and response delays.
  • How to file a grievance: Policies must offer clear directions on how to submit a grievance, including contact points and necessary documentation.
  • Grievance investigation and resolution process: The policy should describe how complaints are reviewed, investigated, and resolved by staff.
  • Patient grievance timelines: CMS requires that hospitals acknowledge grievances within seven days and resolve them within a reasonable timeframe. Including specific internal timelines helps set expectations and improve transparency.
  • Non-retaliation assurance: Patients must be protected from retaliation or adverse consequences for submitting grievances.
  • Recordkeeping procedures: Clearly describe how grievances and their resolutions will be documented and stored.
  • Explanation of patient rights: Policies should reinforce the patient’s right to voice concerns without fear of reprisal or discrimination.

Best Practices for Implementing a Grievance Policy

Including the right components in a policy is only half the battle. Equally important is how the patient grievance policy and procedure is written, distributed, and monitored. American Data Network’s Hospital Complaints and Grievances Software supports these efforts by centralizing documentation, tracking, and reporting, helping hospitals maintain compliance and improve response times.

Best practices include:

  • Putting everything in writing and avoiding reliance on verbal or informal processes
  • Writing clearly and concisely
  • Defining terms that may be unfamiliar to the reader
  • Using a standard format that aligns with other hospital policies
  • Ensuring policies are accessible to all staff members who need them

According to HFMA, hospital leaders should also:

  • Benchmark grievance processes against similar organizations
  • Circulate a first draft of the grievance policy to subject-matter experts and frontline staff for feedback
  • Use clear headings and subheadings to enhance readability
  • Establish monitoring processes to ensure compliance
  • Schedule regular reviews and updates to maintain relevance
  • Archive expired versions per legal and organizational requirements

Hospital leaders who adopt these practices demonstrate a commitment not only to compliance, but also to patient advocacy and continuous improvement.

Avoiding Common Grievance Policy Pitfalls

A report titled Taking a Systematic Approach to Hospital Policy Development identifies several pitfalls that undermine policy effectiveness:

  • Poorly written language (either overly complex or too simplistic)
  • Inconsistent styles and formatting across documents
  • Out-of-date or inaccurate information
  • Policies that are difficult to locate, access, or interpret
  • Lack of central management or oversight of policy documentation

By proactively addressing these issues, hospital leadership can ensure that their hospital grievance policy functions as a vital risk management and quality improvement tool. An effective complaints and grievances application can also track required response timelines, prompt staff to act before deadlines, and document every step — ensuring you stay compliant without relying on manual tracking.

Measuring the Impact of a Grievance Policy on Patient Satisfaction

Developing a patient grievance procedure is just one step toward improving care experiences. To evaluate effectiveness, hospitals must understand how to measure patient satisfaction in hospitals and correlate it with complaint and grievance trends.

Common methods include:

  • Patient satisfaction surveys (e.g., HCAHPS)
  • Complaint trend analysis to identify recurring concerns
  • Time-to-resolution metrics for grievances
  • Staff response rates and timeliness
  • Audit and compliance reviews

By linking these metrics to grievance management processes, hospitals can identify systemic weaknesses, allocate resources more effectively, and proactively respond to patient needs.

Turning a Grievance Policy into Patient-Centered Progress

A well-crafted grievance policy supports transparency, accountability, and trust in healthcare settings. For hospital leaders, taking ownership of the development, implementation, and refinement of patient grievance policies and procedures isn’t just a regulatory requirement—it’s a vital part of delivering high-quality, patient-centered care.

When combined with best practices, ongoing staff training, and outcome measurement, a strong hospital grievance policy becomes an essential foundation for patient satisfaction, risk reduction, and operational excellence.

Frequently Asked Questions (FAQ)

What is the purpose of a hospital grievance policy?

A hospital grievance policy provides a structured method for patients or their representatives to report concerns about care, services, or treatment. Its purpose is to ensure timely, fair, and documented resolution of complaints and to promote accountability and continuous improvement in patient care.

Who can file a patient grievance?

Patients and their representatives (e.g., family members, legal guardians, or appointed advocates) may file a grievance, depending on hospital policy and applicable laws.

What qualifies as a patient grievance?

Any formal verbal or written complaint that involves abuse, neglect, poor communication, care delays, or rights violations qualifies as a grievance. These must be addressed formally through the hospital’s grievance procedure.

How are patient grievances typically handled?

Hospitals typically follow CMS grievance procedures, which require acknowledgment of a grievance within seven days, investigation, formal review, and a written resolution with documentation.

Is there a difference between a complaint and a grievance?

Yes. According to The Joint Commission, a complaint is usually addressed informally and immediately at the point of care, while a grievance requires formal documentation and follow-up due to unresolved or serious issues.

How can hospitals measure the effectiveness of their grievance policy?

Hospitals can use HCAHPS survey data, track grievance resolution timelines, monitor recurring complaint trends, and evaluate internal audit results to determine how effectively the grievance policy supports patient satisfaction.

Where can I find examples of patient grievance policies and procedure documents?

You can refer to:

These templates are for informational use and represent publicly available grievance policies from various healthcare organizations. Hospital leaders should evaluate each policy’s applicability in the context of their institution’s needs, regulatory requirements, and legal counsel before use or adaptation.

Streamline Your Complaints and Grievances Process

Simplify and automate the management of patient complaints and grievances with our intuitive, compliant software solution. Improve your hospital’s efficiency, compliance, and patient satisfaction.

Explore Our Complaints & Grievances Software →

Doctors reviewing cms grievance response requirements paperwork

Navigating Complaints and CMS Grievance Response Requirements

Hospitals must comply with CMS grievance response requirements to maintain Medicare and Medicaid eligibility. This guide explains how to distinguish between complaints and grievances, outlines key CMS guidelines, and offers practical strategies for managing patient feedback effectively.

Table of Contents

Understanding and navigating the CMS grievance response requirements is essential for hospital leadership and staff. These guidelines, detailed in the Conditions of Participation (CoP), are not just regulatory instructions—they are prerequisites for hospitals seeking to remain eligible for federal funding through the Centers for Medicare and Medicaid Services (CMS). A clear grasp of what constitutes a general patient complaint versus a formal grievance, how to process grievances correctly, and how to meet CMS’s documentation and communication expectations is essential for compliance and patient satisfaction.

Hospitals must utilize robust Complaints and Grievances applications for prompt responses, thorough investigation, and transparent communication. This not only satisfies CMS mandates but also strengthens patient trust in the institution’s commitment to quality care.

Complaints and CMS Grievance Response Requirements

CMS Guidelines for Complaints and Grievances: Where to Find Them

CMS outlines its complaint and grievance requirements in the State Operations Manual (SOM), Appendix A, which contains the survey protocol, regulations, and interpretive guidelines for hospitals. As of April 2024, Appendix A was most recently updated, continuing to reference core requirements under Section 482.13(a)(2). The foundational Conditions of Participation were first introduced in 1986, and though specific interpretive guidance around grievances was last substantively revised in 2008, the expectations remain highly relevant.

The SOM details several requirements that hospitals must meet:

  • Procedures for submitting both written and verbal grievances
  • Defined timelines for reviewing and responding to grievances
  • Written communication to patients or representatives outlining investigation results
  • Designation of a contact person responsible for grievance resolution
  • Oversight by the hospital’s governing body or a formally delegated grievance committee

Distinguishing Complaints of Patients from Formal Patient Grievances

While both complaints and grievances may originate from patient dissatisfaction, the distinction between them is crucial. A complaint is an issue that can typically be resolved immediately by the staff present, such as a concern about room temperature or a missed meal. In contrast, a grievance involves concerns that cannot be promptly addressed and often require formal investigation, such as complaints about clinical care, potential neglect, or issues involving CMS Conditions of Participation.

For example, if a patient requests clean bedding and the staff provides it promptly, the issue remains a complaint. However, if a patient reports inadequate pain control and the staff must consult with a physician or adjust treatment, this typically requires further evaluation and cannot be resolved immediately. Per CMS and CIHQ standards, such situations qualify as a grievance.

Responding to Patient Grievances: Timeliness and CMS Grievance Response Requirements

CMS emphasizes the importance of prompt grievance resolution. While there is no hard deadline, hospitals are expected to respond within seven days on average. When delays are unavoidable—due to factors like case complexity or staff availability—CMS requires hospitals to document the cause and notify the patient or representative with an estimated timeline for follow-up, per the hospital’s grievance policy.

The right hospital complaints and grievances software can make this process faster, easier, and more compliant. By automating timeline tracking, flagging overdue cases, and centralizing communication records, hospitals can respond promptly, keep patients informed, and maintain a complete audit trail for CMS review—without adding administrative strain.

To remain compliant, hospitals should:

  • Track grievance timelines closely and document any delays
  • Notify patients if resolution exceeds the standard timeframe
  • Provide written responses that include findings, actions taken, contact information, and completion date
  • Respond electronically if the patient has requested communication via email

Governing Body Oversight in the Patient Grievance Process

The hospital’s governing body holds ultimate accountability for the grievance process. While operational responsibilities may be delegated to a designated grievance committee—typically made up of at least two individuals—the governing body must approve the policy and ensure regular reviews are conducted to confirm its effectiveness. A successful grievance process requires clearly defined roles, routine internal audits, and mechanisms to evaluate whether policies are being followed and improved.

Patient Rights and the Hospital Grievance Policy

Transparent communication is essential to compliance. Patients must be informed of their rights related to the grievance process at the time of admission. While hospitals are not obligated to refer grievances to external Quality Improvement Organizations (QIOs), they are required to inform patients that such an escalation is available should they remain dissatisfied with the hospital’s response. This ensures patients are empowered to advocate for their care without obstruction.

Common Pitfalls in Managing Patient Complaints and Grievances

Despite best intentions, hospitals can face several pitfalls in grievance management. Common issues include:

  • Failing to document grievances thoroughly
  • Confusing complaints with grievances
  • Missing deadlines for written responses to patients

Hospitals can mitigate these risks by training staff regularly, using automated reminders, and conducting internal audits to verify adherence to CMS timelines and definitions — see how complaints and grievances technology can streamline the process.

CMS Guidelines for Complaints and Grievances: Key Interpretations

SOM Appendix A provides additional clarity on several key areas. It defines what qualifies as a grievance and outlines the required process, from submission and investigation to follow-up. Hospitals must allow grievances to be submitted verbally and in writing, and respond formally in writing within a reasonable timeframe. The appendix encourages flexibility when needed, while still requiring communication with the patient during delays.

The following elements must be part of the grievance response process:

  • Instructions for patients on how to file a grievance
  • Clear internal processes for investigation
  • Documentation of all steps and communications
  • Final written notice including resolution and responsible contact

These expectations reflect CMS’s commitment to both regulatory standards and patient-centered care.

Improving the Patient Grievance Process Through Effective Management

Hospitals that approach complaints and CMS grievance requirements not just as a compliance exercise, but as an opportunity to improve communication and care, will be better positioned to meet both federal expectations and patient needs. Leadership should champion an organization-wide commitment to responsiveness, clarity, and follow-through in all grievance-related interactions.

When hospitals train their staff effectively, keep policies current, communicate clearly with patients, and adhere to response timelines, they are better equipped to navigate CMS’s complex—but essential—grievance response requirements.

Frequently Asked Questions

What are CMS grievance response requirements?

CMS grievance response requirements are federal mandates outlined in the Conditions of Participation. These rules define how hospitals must receive, process, and resolve formal patient grievances—including written responses, timelines for resolution, documentation standards, and oversight by a hospital’s governing body.

What is the difference between a complaint and a grievance in a hospital setting?

A complaint refers to an issue that can be resolved promptly by staff present at the time it is raised, such as a request for extra blankets or assistance with adjusting television settings. A grievance involves more serious or unresolved concerns—such as clinical care, neglect, abuse, or policy violations—and must follow a process that includes investigation and written follow-up.

What is included in a patient grievance process?

The patient grievance process must include:

  • Clear instructions for verbal or written grievance submission
  • Timely review and investigation of the grievance
  • Written communication of the resolution to the patient
  • Optional referral to external organizations like QIOs

All steps must comply with CMS guidelines for complaints and grievances and be incorporated into the hospital’s approved grievance policy.

Are verbal complaints subject to CMS grievance requirements?

Verbal complaints are not automatically considered grievances. If the issue is resolved immediately to the patient’s satisfaction, it is classified as a complaint. However, if resolution is delayed, requires investigation, or the problem cannot be handled by staff at the time, it qualifies as a patient grievance under CMS grievance response requirements.

How quickly must hospitals respond to patient complaints or grievances?

  • Complaints: Should be resolved immediately whenever possible.
  • Grievances: CMS recommends a seven-day average resolution period. If more time is needed, the hospital must notify the patient of delays and provide an updated timeline as defined in the hospital grievance policy.

How should hospitals document and manage patient complaints?

Even quickly resolved complaints of patients should be documented for internal tracking and quality improvement. For grievances, thorough documentation is essential—including the grievance content, investigation steps, communications with the patient, resolution details, and completion date.

Who is responsible for handling patient complaints and grievances?

  • Complaints: Typically handled by unit-level or frontline staff.
  • Grievances: Managed by a designated grievance committee or department, with ultimate oversight by the hospital’s governing body.

This structure ensures compliance with CMS grievance response requirements.

Can patients escalate unresolved complaints or grievances?

Yes. Patients have the right to escalate grievances involving care quality or discharge concerns to an external Quality Improvement Organization (QIO). Hospitals are required to inform patients of this right as part of the patient grievance process.

How can hospitals improve how they manage patient complaints and grievances?

To stay compliant and improve patient satisfaction, hospitals should:

  • Train staff to distinguish between complaints and grievances
  • Maintain a transparent and accessible patient grievance process
  • Review and audit the hospital grievance policy regularly
  • Use complaint and grievance data to guide performance improvement

Transform Your Complaints and Grievances Process

Simplify and automate the management of patient complaints and grievances with our intuitive, compliant software solution. Improve your hospital’s efficiency, compliance, and patient satisfaction.

Explore Our Complaints & Grievances Software →

Men and women thoroughly wash their hands

Leveraging Data and a Hand Hygiene Monitoring System to Improve Infection Control

 Hand hygiene monitoring systems can empower healthcare organizations to track compliance, reduce healthcare-associated infections, and create safer clinical environments. Learn how to choose the right tools, overcome monitoring challenges, and turn hygiene data into action.

Table of Contents

It’s widely acknowledged that hand hygiene can reduce healthcare-associated infections (HAIs), but some healthcare organizations are not following best practices. Reliable data and a well-implemented hand hygiene monitoring system can help improve adherence—and ultimately patient and healthcare worker safety.

Hand Hygiene Monitoring systems

Why a Hand Hygiene Monitoring System Matters for Reducing Healthcare-Associated Infections

Healthcare-associated infections are extremely frustrating, especially since patients get treatment to get better, not worse. But simple handwashing can help. According to the World Health Organization (WHO), infection prevention and control (IPC) interventions, including hand hygiene, can reduce HAIs by 35–70%. The WHO also estimates that for every $1 spent on hand hygiene, up to $16.50 in healthcare costs can be saved.

Following effective hand hygiene practices has long been recognized as the most important way to reduce the transmission of pathogens in healthcare settings. The WHO, the Centers for Disease Control and Prevention (CDC), and others have issued hand hygiene guidelines for healthcare workers. These guidelines specify a wide range of hand hygiene behaviors, including:

  • When hand hygiene is indicated
  • How to cleanse hands
  • What agents to use and how to choose them
  • How to dry hands, how long to dry them, and what instruments to use
  • When and how to use disposable gloves
  • The impact associated with wearing artificial nails and jewelry on hand hygiene
  • The infrastructure needed to support optimal hand hygiene

Despite this, hand hygiene compliance remains low. Global average adherence hovers around 40%, while in critical care units it reaches only about 60%, according to WHO data.

What Is a Hand Hygiene Monitoring System?

A hand hygiene monitoring system is a set of tools and technologies used to track, evaluate, and improve compliance with hand hygiene protocols in healthcare environments. These systems give organizations the data needed to influence behavior, drive improvement, and reduce infections.

Common Types of Hand Hygiene Monitoring Tools

  • Direct observation: Human auditors track handwashing behavior.
  • Product usage tracking: Quantifies soap/sanitizer use.
  • Electronic hand hygiene monitoring systems: Use sensors, badges, and real-time locating systems (RTLS) for automated tracking.

A well-designed hand hygiene monitoring tool captures compliance data continuously, helping organizations reinforce accountability and transparency.

How Hand Hygiene Data and Monitoring Systems Guide Better Practices

Better hand hygiene data leads to better decision-making. According to the CDC, leveraging data from hand hygiene compliance monitoring systems can:

  • Reduce infection rates
  • Identify performance gaps
  • Benchmark across organizations
  • Drive staff training and improvement
  • Support regulatory compliance

High-quality hand hygiene data can ultimately result in more efficient and cost-effective infection prevention and control programs, improved quality and safety of care, and better patient outcomes.

Improving Data Collection with a Hand Hygiene Monitoring System

For quality leaders seeking to enhance infection prevention without overburdening staff, collecting hand hygiene data efficiently is paramount. Manual observation methods can be time-consuming, inconsistent, and difficult to scale—making it essential to ask the right questions before implementing a more streamlined system:

  • What level of compliance is the organization aiming to achieve?
  • Who will be responsible for overseeing data collection and taking action, and how can their manual workload be minimized?
  • How will data be visualized and shared to maximize insights while reducing administrative burden?

By addressing these questions early, healthcare organizations can lay the groundwork for a data-driven approach that minimizes manual effort while driving measurable improvements. Using a combination of hand hygiene data collection methods typically produces more reliable results than relying on a single approach, according to the Joint Commission on Accreditation of Healthcare Organizations.

Core Data Collection Methods in Hand Hygiene Compliance Monitoring

MethodDescriptionProsCons
Direct ObservationManual tracking by auditorsContext-richObserver bias, time-intensive
Product UsageMeasures soap/sanitizer useEasy to scaleNo behavior details
SurveysStaff/patient feedbackCultural insightSubjective
Electronic MonitoringSensors & badgesReal-time, scalableCost, integration hurdles

Some healthcare organizations are enhancing hand hygiene data collection by adopting streamlined, low-cost tools. One organization, featured in the American Journal of Infection Control, developed a platform-independent system using Google Forms and Spreadsheets to simplify data entry and automate analytics. This approach not only provided rapid feedback to frontline staff but also reduced the data management burden on infection preventionists. As a result, leaders were able to focus more on targeted interventions and improving overall hand hygiene adherence.

Other healthcare organizations, according to a review article in the Journal of Medical Internet Research, have integrated electronic hand hygiene monitoring systems into the daily routines of healthcare workers to measure their hand hygiene compliance and quality. These tools include application-assisted direct observation, camera-assisted observation, sensor-assisted observation, and real-time locating systems.

Hand Hygiene Monitoring System Challenges

Implementing hand hygiene compliance monitoring systems isn’t without obstacles. Major challenges include:

  • Measurement inconsistencies: Lack of standard definitions for compliance
  • High volume of hand hygiene “moments” across departments
  • Observer bias is difficult to eliminate
  • Resource constraints for monitoring and analytics
  • Technical limitations of automated tools (e.g., misreadings, false positives)
  • Data integration issues with electronic health records and privacy protocols

As with any other performance measure rate, organizations should only compare hand hygiene performance to others that have defined, collected, and reported the same data in exactly the same way, according to the Joint Commission.

Using Hand Hygiene Data to Improve Outcomes

Data is only valuable if it informs action. In the pursuit of patient safety and infection control, hand hygiene compliance is a foundational metric—but traditional manual observation methods can fall short. Modern, advanced hand hygiene monitoring systems bridge this gap by delivering timely, actionable insights that drive behavioral change and organizational accountability. These systems may help healthcare facilities turn raw data into meaningful improvements through:

  • Real-time dashboards for staff feedback
  • Alerts for missed events
  • Analytics by shift, unit, or job role
  • Gamification and recognition programs
  • Automated reporting to leadership teams

By reducing the manual workload for infection preventionists, these tools free up time for root cause analysis and targeted interventions—ultimately improving hand hygiene compliance and reducing HAIs.

Choosing the Right Hand Hygiene Compliance Monitoring Tool

Some facilities adopt electronic hand hygiene monitoring systems with badge-based tracking, while others use simpler hybrid models that blend digital surveys with product use metrics. When evaluating solutions, organizations should consider:

  • Does it measure both frequency and technique?
  • Is it easy to use and understand?
  • Can it integrate with your hospital’s IT infrastructure?
  • Does it protect patient and staff privacy?
  • Is the ROI justifiable (e.g., fewer infections, less staff burden)?

Improving hand hygiene is more than a policy—it’s a systems challenge. With the right hand hygiene monitoring system, healthcare leaders can turn compliance into a measurable, trackable, and ultimately improvable process. By leveraging data, organizations not only reduce healthcare-associated infections but also support a culture of safety and accountability.

bed in the recovery room

Hospital Grievance Risk: Can Your Facility Afford Unresolved Complaints?

Unresolved hospital grievances don’t just risk compliance—they silently erode your bottom line. Use our free calculator to uncover how much revenue your organization could be losing and learn how to take control with a smarter grievance strategy.

Table of Contents

Effective hospital grievance management is not just a regulatory obligation—it’s a financial imperative. While complaints and grievances are often categorized as patient satisfaction or compliance issues, their true impact runs deeper. Every unresolved grievance represents a potential loss in patient revenue, trust, and future referrals. With the average hospital stay valued at over $18,000, even a small number of unresolved grievances can translate into millions in lost income. This article explores the hidden financial risk of hospital grievances—and shows you how to calculate it for your organization.

Hospital Grievance

Hospital Grievances: More Than a Compliance Issue

Unresolved complaints and grievances aren’t just customer service problems—they’re significant financial risks. Every unresolved hospital grievance can contribute to revenue loss, reputational harm, and increased regulatory scrutiny.

Hospitals thrive on trust, transparency, and accountability. Yet, when a patient grievance is overlooked or mismanaged, the consequences go far beyond the individual case. They ripple through your community, affect future patient decisions, and quietly drain your revenue.

The True Cost of an Unresolved Hospital Grievance

Based on 2023 Hospital Cost Report data, the average net patient revenue per adjusted discharge for U.S. acute care and critical access hospitals is approximately $18,426. That’s how much your hospital could lose each time a patient walks away dissatisfied.

Now imagine your hospital fields 100 patient grievances annually, and 30% remain unresolved. That’s 30 lost patients—equating to $552,780 in direct revenue losses. But the impact doesn’t stop there.

Dissatisfied patients talk—on average to 9–15 people. If just 10 others choose not to seek care from your facility, that’s another $5,527,800 in lost potential revenue.

Total potential loss: over $6 million. From just 30 unresolved grievances.

Use Our Calculator to Estimate Your Hospital Grievance Risk

To help you quantify this risk, we developed the Hospital Complaints and Grievances Financial Impact Calculator.

This free tool allows you to:

  • Input your hospital’s grievance volume
  • Adjust your resolution rate
  • Estimate how many people each dissatisfied patient influences

With just a few clicks, you’ll get a personalized snapshot of your financial exposure—and the potential value of improving your grievance management process.

Why a Structured Hospital Grievance Process Drives Financial Performance

Managing grievances isn’t just about checking a compliance box—it’s about protecting long-term revenue. Hospitals with clear, well-executed grievance processes respond faster, resolve issues more effectively, and retain more patients.

A structured grievance process helps you:

  • Address concerns quickly and reduce patient attrition
  • Improve transparency and rebuild trust through timely updates
  • Ensure accountability by routing issues to the right teams
  • Identify recurring service breakdowns that affect satisfaction and revenue

Grievance policies aligned with CMS and accreditor expectations (like The Joint Commission or DNV) don’t just prevent fines—they also reduce risk of lost revenue due to unmanaged dissatisfaction.

Manual Hospital Grievance Processes Increase Risk

Many hospitals still manage complaints and grievances using spreadsheets, email threads, or paper forms. These outdated systems make it easy for grievances to fall through the cracks—delaying resolutions, missing deadlines, and eroding patient trust.

A dedicated hospital grievance management system, like ADN’s specialized software, helps you:

  • Route grievances to the correct department automatically
  • Track deadlines to ensure timely follow-up
  • Document every step to maintain compliance
  • Report on trends to support continuous improvement

Explore our full solution here:
👉 Hospital Complaints and Grievances Software

Protect Revenue with Proactive Hospital Grievance Management

Hospitals that treat grievance management as a strategic priority—not just a regulatory requirement—see improvements in patient satisfaction, retention, and revenue.

Steps to take now:

  • Revisit your hospital grievance policy to ensure compliance and clarity
  • Train your staff on consistent grievance response workflows
  • Track and resolve grievances efficiently using digital tools
  • Use our calculator to understand your current financial exposure

Ready to See the Numbers?

Unresolved grievances cost more than you think. Quantify the risk and discover how proactive grievance management can protect your hospital’s bottom line.

→ Try the Hospital Grievance Financial Impact Calculator Now

a group of people sitting at a desk

Complaints and Grievances in Healthcare: Understanding the Key Differences and Requirements

Discover the essential differences between complaints and grievances in healthcare, why understanding them matters for regulatory compliance, and how effectively managing patient concerns can boost patient satisfaction and hospital quality.

Table of Contents

While hospitals aim for excellent patient experiences, complaints and grievances in healthcare settings inevitably arise. Healthcare quality, safety, and risk management professionals must understand the critical difference between grievances and complaints to effectively manage these concerns and remain compliant with regulations.

Complaints and Grievances in Healthcare

Complaints and Grievances in Healthcare: What’s the Difference?

Knowing the difference between grievance and complaint in healthcare is the foundation for effective management.

Complaints are issues that can usually be resolved promptly—within 24 hours—by immediate staff, such as nurses, administrative personnel, or patient advocates. Complaints typically don’t require written responses. Examples include:

  • Difficulty sleeping
  • Poor communication
  • Environmental concerns, like room temperature or noise
  • Lack of courtesy from staff

Grievances are more serious, typically formalized in writing or raised verbally but requiring further investigation. According to the Centers for Medicare and Medicaid Services (CMS), grievances often involve issues such as:

  • Persistent difficulties in obtaining appointments or access to care
  • Disrespectful or rude behavior by doctors, nurses, or hospital staff
  • Alleged patient abuse or neglect
  • Patient rights violations

Understanding and properly categorizing patient issues ensures appropriate responses and helps hospitals maintain compliance with regulatory requirements.

Note: A complaint may escalate into a grievance if the patient, family member, or representative feels the concern was not adequately resolved or expresses deeper dissatisfaction. In such cases, even issues initially treated as routine complaints must be documented and handled according to the hospital’s formal grievance process.

Regulatory Requirements for Complaints and Grievances in Healthcare

Hospitals must meet specific regulatory standards when managing complaints and grievances in healthcare. Non-compliance invites regulatory scrutiny, particularly from CMS. Essential CMS and Joint Commission requirements include:

  • Establishing processes for prompt resolution of patient complaints and grievances.
  • Ensuring hospital grievance policies are approved by the governing body.
  • Clearly communicating grievance filing procedures to patients.
  • Defining timeframes for grievance resolution—typically within 7-10 business days.
  • Providing patients with timely written notifications outlining actions taken.

Additionally, hospitals must comply with applicable federal regulations, such as OCR Section 1557 of the Affordable Care Act (ensuring nondiscrimination and accessibility), as well as the specific standards set forth by their accrediting body:

Consequences of Non-Compliance with Complaint and Grievance Regulations

Failure to properly address complaints and grievances in healthcare can lead to serious consequences, including:

  • Legal penalties and potential loss of licensing or accreditation.
  • Damage to hospital reputation and patient trust.
  • Increased regulatory oversight and scrutiny.
  • Potential patient harm from unresolved issues.

Non-compliance diverts resources away from patient care toward legal defense and remediation, negatively impacting hospital operations (Healthcare Compliance Journal).

Are Complaints and Grievances Costing Your Hospital?

Hospital Complaints and Grievances Financial Impact Calculator

Unaddressed or poorly managed complaints and grievances not only risk compliance violations but also impose significant financial burdens. Quantify the financial impact on your organization using our interactive Complaints and Grievances Financial Impact Calculator. Identify your potential savings and redirect resources back to patient care.

Calculate Your Hospital’s Potential Savings →

Strategies for Effective Complaint and Grievance Management in Healthcare

Healthcare organizations should strive to resolve complaints informally and immediately when possible. Effective complaint management includes:

  • Quick, professional responses to patient concerns.
  • Standard response times for addressing common complaints.
  • Sincere apologies and clear, empathetic solutions.
  • Documentation for ongoing quality improvement efforts.

Grievances, requiring more formal handling, should follow a structured process:

  • Clearly inform patients about their rights and grievance procedures.
  • Ensure confidentiality and compliance with HIPAA.
  • Train hospital staff thoroughly in grievance management.
  • Conduct timely, thorough investigations, providing written responses to patients.

A typical grievance workflow includes:

  1. Patient contacts a dedicated grievance line or patient advocate.
  2. Grievance intake form is completed and forwarded to medical leadership.
  3. Medical leadership conducts an investigation, documenting findings.
  4. A written response detailing the investigation outcomes and resolution actions is provided to the patient within established timeframes (usually 7-10 business days).

Avoiding Common Pitfalls When Addressing Complaints and Grievances

To manage patient complaints and grievances effectively, hospital leadership must avoid common pitfalls identified by the National Institute for Health and Care Research:

  • Offering insincere or defensive apologies.
  • Excusing inappropriate staff behavior due to stressful environments.
  • Engaging in overly defensive responses or debating irrelevant clinical details.

Using Complaints and Grievances as Opportunities to Improve Healthcare

Effectively addressing complaints and grievances in healthcare helps identify opportunities for improvement. As demonstrated in research from The Joint Commission Journal, systematically reviewing patient feedback can lead to meaningful enhancements in patient safety, quality, and satisfaction.

Streamline Your Complaints and Grievances Process

Simplify and automate the management of patient complaints and grievances with our intuitive, compliant software solution. Improve your hospital’s efficiency, compliance, and patient satisfaction.

Explore Our Complaints & Grievances Software →

Group of young contemporary pharmacologists discussing new medicament

Ultimate Guide to the National Patient Safety Goals 2025 (NPSGs)

An authoritative guide designed for healthcare leaders detailing evidence-based tactics for successfully implementing each of The Joint Commission’s 2025 National Patient Safety Goals.

Table of Contents

Hospital leaders – especially Directors or VPs of Quality and Patient Safety – can drive safer care by systematically implementing each National Patient Safety Goal. Below is an authoritative guide to the eight NPSGs for 2025, detailing each goal and element of performance, followed by actionable tactics supported by recent research, best-practice guidelines, and real-world implementation examples.

View the full list of 2025 National Patient Safety Goals and associated Elements of Performance.

National Patient Safety Goals 2025

National Patient Safety Goals 2025: #1 Identify Patients Correctly

 

2025 National Patient Safety Goal: NPSG 01.01.01:
Use at least two patient identifiers when providing care, treatment, and services.
Element(s) of performance for NPSG 01.01.01
EP 1Use at least two patient identifiers when administering medications, blood, or blood components; when collecting blood samples and other specimens for clinical testing; and when providing treatments or procedures. The patient’s room number or physical location is not used as an identifier. (See also MM.05.01.09, EPs 7, 10; PC.02.01.01, EP 10)
EP 2Label containers used for blood and other specimens in the presence of the patient. (See also PC.02.01.01, EP 10)
EP 3

Use distinct methods of identification for newborn patients.

Note: Examples of methods to prevent misidentification may include the following:

  • Distinct naming systems could include using the mother’s first and last names and the newborn’s gender (for example, “Smith, Judy Girl” or “Smith, Judy Girl A” and “Smith, Judy Girl B” for multiples).
  • Standardized practices for identification banding (for example, using two body sites and/or bar coding for identification).
  • Establish communication tools among staff (for example, visually alerting staff with signage noting newborns with similar names).

Accurately identifying patients is foundational to preventing wrong-patient errors. This goal emphasizes using multiple patient identifiers and standardized processes so every test, medication, or procedure is matched to the correct person. Hospitals must eliminate identification mistakes by hardwiring verification steps into care workflows.

Use at Least Two Identifiers for Every Patient Encounter

Ensure staff always verify at least two distinct identifiers (for example, name and date of birth) before providing any care, administering medications, drawing labs, or performing procedures​ (Source: ​jointcommission.org). This practice is required by NPSG standards and has been effective in avoiding misidentifications. Electronic health records (EHRs) and wristband systems should make it easy to check identifiers, and never allow room numbers or physical location to be used as an identifier (to avoid mix-ups if patients move rooms) ​(Source: psnet.ahrq.gov).

Implement Barcode Scanning and Other Technology Aids

Use bar-code medication administration (BCMA) and patient wristband scanning systems to verify patient identity at the point of care. Scanning the patient’s ID band provides an electronic double-check before medications, blood products, or tests are given. A meta-analysis found that wristband barcode scanning reduced medical errors by 57.5% ​​(Source: psnet.ahrq.gov). Many hospitals have reported sharp drops in wrong-patient errors after deploying barcode systems that prompt staff if the patient’s ID does not match the order.

Label Specimens and Diagnostics at the Bedside

Require that blood tubes, specimen containers, imaging requisitions, and other labeled materials be labeled in the presence of the patient immediately after collection. This ensures the label is attached to the correct patient’s sample. Incorporate two-identifier verification into the labeling process (e.g., patient states name/DOB while the phlebotomist labels the tube) to catch errors on the spot.

Related Reading: Specimen Study Helps 15 Hospitals Make Critical Process Changes to Prevent Errors

Address Look-Alike/Sound-Alike Names and Engage Patients in ID Checks

Flag patients with similar names in the EHR (e.g. alert banners for “J. Smith” vs “John Smith Jr.”) to prompt extra caution. For high-risk procedures (such as blood transfusions or surgeries), use an independent double-check – two clinicians should separately confirm the patient’s identity and agreement of identifiers. Encourage patients to participate by stating their name and DOB and speak up if an ID check does not occur. This patient engagement adds another layer of safety ​​​(Source: psnet.ahrq.gov). The Joint Commission’s Speak Up Patient Safety Program is another tactic that can help encourage patient engagement in their own care.

Audit and Train for Compliance

Continuously monitor compliance with patient ID protocols (e.g. random audits of whether two identifiers are used). Provide refresher training and share incident learnings. If near-misses occur (like a wrong patient near-miss caught by scanning), treat them as teaching opportunities. A culture of “zero tolerance” for skipping ID checks reinforces that every staff member is accountable for patient identification safety.

Leverage Patient Photos in EHRs to Prevent Misidentification

Integrating patient photographs into electronic health records provides an additional visual identifier to help staff quickly verify patient identity, especially in busy clinical settings. Recent studies have demonstrated that displaying patient photos in EHRs can significantly reduce wrong-patient order entry (WPOE) errors.

A notable study conducted at Brigham and Women’s Hospital found that the inclusion of patient photographs in EHRs led to a 35% reduction in wrong-patient order entry errors. Similarly, research published in JAMA Network Open reported that displaying patient photographs prominently in the EHR banner was associated with a significant decrease in the rate of wrong-patient orders.

Further, an evaluation from the Agency for Healthcare Research and Quality (AHRQ) highlighted patient photos as a noninterruptive decision-support tool, effectively improving patient identification without causing alert fatigue among healthcare providers (AHRQ Digital Healthcare Research).

Implementing patient photos can therefore serve as a practical, cost-effective approach to reinforcing patient identification accuracy, directly contributing to safer clinical care processes.

National Patient Safety Goals 2025: #2 Improve Staff Communication

2025 National Patient Safety Goal: NPSG 02.03.01:
Report critical results of tests and diagnostic procedures on a timely basis.
Element(s) of performance for NPSG 02.03.01
EP 1

Develop and implement written procedures for managing the critical results of tests and diagnostic procedures that address the following:

  • The definition of critical results of tests and diagnostic procedures
  • By whom and to whom critical results of tests and diagnostic procedures are reported
  • The acceptable length of time between the availability and reporting of critical results of tests and diagnostic procedures

Ⓓ Documentation is required.

EP 2Evaluate the timeliness of reporting the critical results of tests and diagnostic procedures.

Effective communication among caregivers is critical for timely, safe care. This goal focuses on standardized communication of critical information – whether during handoffs, when conveying critical test results, or in daily interactions. Hospitals should implement structured communication tools and “closed-loop” confirmation practices to ensure information is reliably exchanged and understood.

Use Structured Hand-off Protocols Like I-PASS

Implement standardized patient handoff protocols for shift-to-shift handoffs and inter-departmental transfers. Tools like the I-PASS handoff bundle ensure that critical patient information is not omitted. A 2025 systematic review published in BMJ Quality & Safety evaluated structured handoff protocols. This review found moderate-certainty evidence that the I-PASS tool reduces medical errors and adverse events ​​(Source: ​qualitysafety.bmj.com). Make these formats mandatory for both verbal handoffs and written handoff summaries in the EHR.

Report Critical Test Results in a Timely, “Closed-Loop” Manner

Establish a policy that critical lab values and diagnostic findings (e.g. dangerously high potassium or a radiology finding of a pneumothorax) are reported to the responsible provider within a set time frame. Use a reliable communication method that ensures receipt – for instance, a dedicated call center or an automated alert system that continuously tries providers until results are acknowledged ​​​(Source: cdc.gov). Many hospitals are adopting secure texting for critical results: one study demonstrated a reduction in average notification time from 11.3 minutes to 3.0 minutes by sending critical lab results directly to physicians’ smartphones, with 95% of providers preferring this over pager call-backs ​​​(Source: pmc.ncbi.nlm.nih.gov)​. Whatever the method, require that the receiving clinician confirms the result (closed-loop), and document the communication time.

Implement Read-Back Verification for Verbal Orders and Results

For any critical value relayed by phone or any telephone order, staff must perform a read-back – repeating the information received – to verify accuracy (Source: ​jointcommission.org). For example, if a lab calls a critical result, the nurse should write it down and read it back (“…confirming, potassium 2.8 for John Doe”). This practice, mandated by Joint Commission standards, has prevented innumerable errors caused by misheard information. Train all clinicians on read-back and enforce it as a standard operating procedure, especially in high-risk situations (critical lab values, verbal medication orders, etc.).

Leverage Team Training and Communication Coaching

Invest in programs like TeamSTEPPS, which is an evidence-based teamwork system aimed at improving communication and safety culture ​​(Source: ​ahrq.gov). Conduct simulation exercises for high-risk scenarios (e.g. emergency response, OR to ICU handoff) to practice clear communication and teamwork. A formal TeamSTEPPS training or similar communication workshops can improve staff assertiveness to speak up about concerns and foster habits like checking back and clarifying questions​. In a high-reliability organization, every team member should feel responsible for sharing critical information and confirming it was received – e.g., a nurse should feel empowered to call a physician if a critical report was not acknowledged within the policy timeframe.

Use Communication Tools for Special Situations

Implement condition-specific communication protocols, such as rapid response team alerts, critical lab result escalation trees, or patient deterioration watchlists. For example, an SBAR can be required when a nurse calls a physician about a patient’s urgent issue, to organize the information. Similarly, use pre-surgery briefings and post-op debriefings to make sure key information is transferred between teams. By institutionalizing these communication practices, staff know what to communicate, when, and how – reducing errors caused by miscommunication.

Enhance Critical Result Management with AI-Driven Alerts

Artificial intelligence (AI) tools are increasingly being utilized to prioritize and escalate critical test results automatically, ensuring timely provider acknowledgment. AI-driven communication systems can identify delays, trigger escalation protocols, and enhance the overall reliability of critical result reporting, thereby closing communication gaps.

Recent studies have demonstrated the effectiveness of AI in this domain. For instance, a study published in JAMA Internal Medicine found that implementing an AI-enabled early warning system was associated with a significant reduction in the risk of clinical deterioration and subsequent care escalation in hospitalized patients. The study concluded that such AI interventions could enhance patient safety by facilitating timely clinical responses. (Source: jamanetwork.com)

Another study at Mount Sinai Health System reported that hospitalized patients were 43% more likely to have their care escalated and significantly less likely to die if their care team received AI-generated alerts signaling adverse changes in their health. This underscores the potential of AI-driven alerts in improving patient outcomes. (Source: news-medical.net)

By integrating AI-driven alert systems into clinical workflows, healthcare providers can enhance the timeliness and effectiveness of their responses to critical patient data, ultimately improving patient outcomes and safety.

National Patient Safety Goals 2025: #3 Use Medicines Safely

2025 National Patient Safety Goal: NPSG 03.04.01:

Label all medications, medication containers, and other solutions on and off the sterile field in perioperative and other procedural settings.

Note: Medication containers include syringes, medicine cups, and basins.

Element(s) of performance for NPSG 03.04.01
EP 1

In perioperative and other procedural settings both on and off the sterile field, label medications and solutions that are not immediately administered. This applies even if there is only one medication being used.

Note: An immediately administered medication is one that an authorized staff member prepares or obtains, takes directly to a patient, and administers to that patient without any break in the process.

EP 2In perioperative and other procedural settings both on and off the sterile field, labeling occurs when any medication or solution is transferred from the original packaging to another container.
EP 3

In perioperative and other procedural settings both on and off the sterile field, medication or solution labels include the following:

  • Medication or solution name
  • Strength
  • Amount of medication or solution containing medication (if not apparent from the container)
  • Diluent name and volume (if not apparent from the container)
  • Expiration date and time

Note: The date and time are not necessary for short procedures, as defined by the hospital.

EP 4Verify all medication or solution labels both verbally and visually. Verification is done by two individuals qualified to participate in the procedure whenever the person preparing the medication or solution is not the person who will be administering it.
EP 5

Label each medication or solution as soon as it is prepared, unless it is immediately administered.

Note: An immediately administered medication is one that an authorized staff member prepares or obtains, takes directly to a patient, and administers to that patient without any break in the process.

2025 National Patient Safety Goal: NPSG 03.05.01:

Reduce the likelihood of patient harm associated with the use of anticoagulant therapy.

Note: This requirement does not apply to routine situations in which short-term prophylactic anticoagulation is used for preventing venous thromboembolism (for example, related to procedures or hospitalization).

Element(s) of performance for NPSG 03.05.01
EP 2The hospital uses approved protocols and evidence-based practice guidelines for reversal of anticoagulation and management of bleeding events related to each anticoagulant medication.
EP 3

The hospital uses approved protocols and evidence-based practice guidelines for perioperative management of all patients on oral anticoagulants.

Note: Perioperative management may address the use of bridging medications, timing for stopping an anticoagulant, and timing and dosing for restarting an anticoagulant.

EP 7

The hospital uses only oral unit-dose products, prefilled syringes, or premixed infusion bags when these types of products are available.

Note: For pediatric patients, prefilled syringe products should be used only if specifically designed for children.

2025 National Patient Safety Goal: NPSG 03.06.01:
Maintain and communicate accurate patient medication information.
Element(s) of performance for NPSG 03.06.01
EP 1

Obtain information on the medications the patient is currently taking when they are admitted to the hospital or seen in an outpatient setting. This information is documented in a list or other format that is useful to those who manage medications.

Note 1: Current medications include those taken at scheduled times and those taken on an as-needed basis. See the Glossary for a definition of medications.

Note 2: It is often difficult to obtain complete information on current medications from a patient. A good faith effort to obtain this information from the patient and/or other sources will be considered as meeting the intent of the EP.

Ⓓ Documentation is required.

EP 2

Define the types of medication information (for example, name, dose, route, frequency, purpose) to be collected in non-24-hour settings.

Note: Examples of non-24-hour settings include the emergency department, primary care, outpatient radiology, ambulatory surgery, and diagnostic settings.

EP 3

Compare the medication information the patient brought to the hospital with the medications ordered for the patient by the hospital in order to identify and resolve discrepancies.

Note: Discrepancies include omissions, duplications, contraindications, unclear information, and changes. A qualified individual, identified by the hospital, does the comparison.

EP 4

Provide the patient (or family, caregiver, or support person as needed) with written information on the medications the patient should be taking when they are discharged from the hospital or at the end of an outpatient encounter (for example, name, dose, route, frequency, purpose).

Ⓓ Documentation is required.

EP 3

Explain the importance of managing medication information to the patient when they are discharged from the hospital or at the end of an outpatient encounter.

Note: Examples include instructing the patient to give a list to their primary care provider; to update the information when medications are discontinued, doses are changed, or new medications (including over-the-counter products) are added; and to carry medication information at all times in the event of emergency situations. (For patient education on medications, refer to Standards MM.06.01.03, PC.02.03.01, and PC.04.01.05.)

Medication safety efforts aim to prevent errors at all stages – ordering, dispensing, administering, and monitoring. The 2025 NPSG priorities for medication safety include proper labeling of medications, safe management of high-risk drugs (like anticoagulants), and thorough medication reconciliation during care transitions. Hospitals should adopt best practices and technology to minimize medication errors that could harm patients.

Label All Medications and Solutions, Especially in Procedural Settings

Unlabeled syringes, cups, or basins can lead to dangerous mix-ups. Require that every medication or solution is labeled with name, concentration, and expiration immediately after it is prepared or placed into a container, unless it’s going to be used instantly (Source: ​jointcommission.org). This is particularly vital in the operating room or other procedural areas where multiple drugs (saline, anesthetics, etc.) might be on a table – for example, a syringe on the sterile field must have a label if it’s not administered right away. The Joint Commission highlights medication labeling as a simple but critical step to avoid inadvertent drug swaps. Conduct regular audits in areas like ORs, cath labs, and EDs to ensure labeling compliance.

Implement Safeguards for High-Risk Medications (Especially Anticoagulants)

Anticoagulant therapy (like heparin or warfarin) is a common source of serious adverse drug events, so specific protocols are needed. Use standardized, evidence-based protocols for initiating and managing anticoagulation (Source: ​jointcommission.org) – for instance, weight-based heparin dosing with checks, warfarin nomograms, and specified INR monitoring frequency. Also put in place protocols for reversal of anticoagulation and management of bleeding complications (e.g., ready availability of vitamin K, protamine, or reversal agents for DOACs, guided by current guidelines). Many hospitals have created multidisciplinary anticoagulation stewardship programs that review all hospital anticoagulation orders, ensure dosing is appropriate, and follow up on lab results. Such programs have been shown to reduce anticoagulation errors and bleeding events. Additionally, provide patient-specific education on anticoagulants – patients should be counseled on dose timing, dietary interactions (for warfarin), signs of bleeding, and the importance of follow-up lab tests.

Ensure Medication Reconciliation at Every Transition of Care

Create a robust process to maintain and communicate accurate medication information for each patient​ (Source: ​jointcommission.org). On admission, collect a “best possible” medication history (consider using pharmacy staff or medication history technicians to improve accuracy). Compare that list to admission orders and resolve discrepancies. Similarly, at discharge, reconcile the hospital medications with pre-admission meds and produce an updated, clear medication list for the patient (and their next providers). This prevents inadvertent omissions or duplications (for example, continuing a home blood pressure medication that was held in hospital, or inadvertently prescribing two drugs in the same class). A pharmacy-led medication reconciliation program at one hospital reduced drug discrepancies significantly. Analysis of the discharge reconciliation process revealed that medication errors were reduced from 90% to 47% on the surgical unit and from 57% to 33% on the medicine unit (Source: ​academic.oup.com). Best practices include using EHR tools to flag changes, involving patients in verifying their med lists, and educating them on any new medications added or stopped. Monitor reconciliation completion rates and intervene if compliance falters.

Leverage Technology for Medication Safety

Utilize available technology to minimize human error. For instance, Barcode Medication Administration (BCMA), which involves scanning the patient and medication barcode before giving doses, ensures the “five rights” – right patient, drug, dose, time, route. Hospitals using BCMA have reported significant reductions in wrong-medication and wrong-patient errors ​(Source: psnet.ahrq.gov). Smart infusion pumps with dose-error reduction software should be used for continuous IV infusions (such as heparin drips) – the Joint Commission now requires programmable pumps for heparin to prevent infusion rate errors ​(Source: jointcommission.org). In the pharmacy, use automated dispensing cabinets with safety features (like alerts for look-alike/sound-alike drugs) and limit access to high-alert meds. Technology is not foolproof, so also address any workarounds (e.g., if nurses bypass scanning due to equipment issues, fix those issues and retrain staff rather than allowing workarounds to persist​ (Source: pmc.ncbi.nlm.nih.gov).

Educate Patients and Staff on Medication Safety

Ensure that patients are counseled about their medications – especially high-risk ones – in plain language. For example, a heart failure patient on a new anticoagulant should know why it’s needed and the bleeding precautions to take. Engage patients to be a final check (e.g., encourage them to speak up if a pill looks different than before). For staff, provide periodic training on medication safety, such as safe anticoagulation practices, opioid monitoring, or insulin management. Use real case studies of errors (anonymized) to reinforce lessons. A culture of safety encourages staff to report “near-miss” medication errors without fear – each near-miss is a chance to identify system weaknesses (like confusing labeling or pharmacy dispensing errors) and address them before harm occurs.

National Patient Safety Goals 2025: #4 Use Alarms Safely

2025 National Patient Safety Goal: NPSG 06.01.01:
Improve the safety of clinical alarm systems.
Element(s) of performance for NPSG 06.01.01
EP 1Leaders establish alarm system safety as a hospital priority.
EP 2

Identify the most important alarm signals to manage based on the following:

  • Input from the medical staff and clinical departments
  • Risk to patients if the alarm signal is not attended to or if it malfunctions
  • Whether specific alarm signals are needed or unnecessarily contribute to alarm noise and alarm fatigue
  • Potential for patient harm based on internal incident history
  • Published best practices and guidelines

(For more information on managing medical equipment risks, refer to Standard EC.02.04.01)

EP 3

Establish policies and procedures for managing the alarms identified above that, at a minimum, address the following:

  • Clinically appropriate settings for alarm signals
  • When alarm signals can be disabled
  • When alarm parameters can be changed
  • Who in the organization has the authority to set alarm parameters
  • Who in the organization has the authority to change alarm parameters
  • Who in the organization has the authority to set alarm parameters to “off”
  • Monitoring and responding to alarm signals
  • Checking individual alarm signals for accurate settings, proper operation, and detectability

(For more information, refer to Standard EC.02.04.03)

Ⓓ Documentation is required.

Clinical alarm systems – cardiac monitors, pulse oximeters, IV pumps, ventilators, etc. – are crucial for patient monitoring, but alarm fatigue from excessive or non-actionable alarms is a well-documented safety hazard. This NPSG calls for hospitals to better manage alarm policies, ensuring that critical alarms are responded to while unnecessary alarms are reduced. The goal is a safer, quieter environment where clinicians do not become desensitized to important alarms.

Establish Alarm Safety as a Leadership Priority and Inventory Alarms

Hospital leadership should convene a multidisciplinary alarm management committee (including clinical engineers, nurses, physicians) to review all alarm-equipped devices in the hospital. Identify which alarm signals are most important for patient safety – for example, asystole or apnea alarms are life-critical, whereas an IV pump “infusion complete” alarm might be less urgent. By cataloguing alarm types and default settings, the team can prioritize which alarms require immediate response and which can be adjusted. The Joint Commission expects hospitals to designate the “most important alarms to manage” based on their own environment (Source: ​jointcommission.org)​. Focus on areas like intensive care, telemetry units, and OR/PACU where alarm overload is common.

Develop Policies to Reduce Non-Actionable Alarms and Prevent Alarm Fatigue

Create evidence-based policies for alarm parameters and default settings. This can include widening default alarm limits (within safe ranges) to reduce false alarms, tailoring alarm thresholds to the individual patient’s condition, and establishing delays or tiered escalation for certain alarms. For example, in some units pulse oximeter alarms for brief desaturations (a few seconds) can be delayed to alarm only if sustained, preventing constant chimes for self-correcting dips. Johns Hopkins Hospital and others have reported success by daily customization of cardiac monitor alarms (adjusting heart rate thresholds per patient) and eliminating duplicate alarms, resulting in a dramatic drop in alarm rate​ (Source: pmc.ncbi.nlm.nih.gov). All alarm settings changes should be done according to policy and tracked. The policy should also address who can modify alarm parameters (ensuring only competent staff do so, and critical alarms are not disabled). Regular maintenance of equipment to prevent nuisance alarms (e.g., ECG electrodes changed daily to reduce false leads-off alarms) is another tactic. A 2023 quality improvement study at Mayo Clinic implemented such interventions – stopping continuous monitoring on patients who didn’t need it and educating staff – and saw a ~17% reduction in total alarm load in just two months (Source: ​pmc.ncbi.nlm.nih.gov).

Train and Educate Staff about Proper Alarm Management

All clinical staff should be educated on the new alarm policies, the rationale behind them (reducing noise and improving safety), and their responsibility to respond promptly to alarms. Emphasize the dangers of alarm fatigue, where caregivers become desensitized – multiple studies link alarm overload to missed alarms and patient harm​ (Sources: sciencedirect.com​, psnet.ahrq.gov). Training should cover how to properly set alarm parameters for each patient, how to distinguish alarm priority levels (if the system has escalating tones or visual cues), and the protocol for responding (e.g., what to do if an alarm is sounding and it’s not your patient). Simulation drills can help – for instance, on a telemetry unit, a drill where an alarm is ignored can be used to discuss how to ensure someone always “owns” responding. Importantly, foster a culture where silencing or pausing alarms inappropriately is unacceptable; staff should never permanently silence an alarm without addressing the patient condition or fixing the cause.

Improve Alarm Notification and Response Workflows

Consider technologies that route critical alarms directly to the responsible nurse or a central monitor watcher to ensure alarms are not missed. Some hospitals use middleware to send alarm alerts to a nurse’s smartphone or pager, reducing reliance on hearing the alarm sound. Assign accountability – e.g., a unit might have a dedicated monitor technician who notifies nurses of lethal arrhythmias immediately. Audit response times to critical alarms and adjust staffing or roles if needed (for example, if nurses are tied up and can’t respond, a “backup responder” should be alerted). Ensure that for every alarm that triggers, there is a clear action – even if it’s assessing the patient – so that alarms are never ignored. The Joint Commission in 2021 set national targets to eliminate alarm-related fatalities by improving these alarm response systems, underscoring how crucial this issue is. (Source: pmc.ncbi.nlm.nih.gov).

Deploy Alarm Analytics Dashboards and Predictive AI Tools

Advanced hospitals are enhancing patient safety by integrating real-time alarm data into clinical analytics dashboards. These dashboards consolidate alerts from various monitoring devices, enabling clinicians to quickly identify critical alarms and respond promptly. For instance, GE Healthcare’s alarm management solutions incorporate centralized monitoring units that streamline alarm notifications, reducing response times and improving patient outcomes. (Source: gehealthcare.com)

In addition to dashboards, predictive AI algorithms are being utilized to anticipate patient deterioration events. Nationwide Children’s Hospital implemented a machine learning tool known as the Deterioration Risk Index (DRI), which analyzes electronic medical records to identify patients at risk of clinical deterioration. Over an 18-month period, the use of DRI led to a more than two-thirds reduction in deterioration events among inpatients. ​(Source: childrenshospitals.org)

Similarly, Stanford Health Care employed an AI model to predict clinical deterioration events, such as unplanned ICU transfers, within a 6- to 18-hour window. This proactive approach resulted in a 20% reduction in such events, demonstrating the efficacy of predictive analytics in improving patient care. (Source: healthcareitnews.com)

By leveraging alarm analytics dashboards and predictive AI tools, healthcare providers can not only reduce alarm fatigue but also intervene earlier in patient care, thereby enhancing overall safety and outcomes.

Continuous Evaluation of Alarm Data

Monitor alarm metrics regularly – how many alarms per bed per day? What percentage are true vs false? Use this data to fine-tune your approaches. Success can be seen in places like UCSF, which reduced audible monitor alarms in ICUs by more than 60% through interdisciplinary alarm management and saw no adverse events as a result (Source: jointcommissionjournal.com). If alarm-related incidents or near misses occur, perform a root cause analysis: Was the alarm volume too low? Did staff assume “false alarm” incorrectly? Use these learnings to further adjust policies or retrain staff. Alarm safety improvement is an ongoing process, but it pays off in better patient outcomes and a calmer healing environment.

Related Reading: Improving Clinical Alarm Management: Guidance and Strategies

National Patient Safety Goals 2025: #5 Prevent Infection

2025 National Patient Safety Goal: NPSG 07.01.01:
Comply with either the current Centers for Disease Control and Prevention (CDC) hand hygiene guidelines and/or the current World Health Organization (WHO) hand hygiene guidelines.
Element(s) of performance for NPSG 07.01.01
EP 1Implement a program that follows categories IA, IB, and IC of either the current Centers for Disease Control and Prevention (CDC) and/or the current World Health Organization (WHO) hand hygiene guidelines. (See also IC.06.01.01, EP 3)
EP 2Set goals for improving compliance with hand hygiene guidelines.
EP 3Improve compliance with hand hygiene guidelines based on established goals.

Healthcare-associated infections (HAIs) are a major patient safety risk, but they are often preventable through diligent infection prevention and control practices. This goal highlights adherence to proven guidelines (like hand hygiene compliance) and the use of evidence-based bundles to prevent device-related and surgical infections. Hospitals should treat infection prevention as a top priority, with the aim of zero preventable infections.

Enforce Rigorous Hand Hygiene Practices Hospital-Wide

  • Adhere to CDC and WHO Guidelines: Implement and enforce a hand hygiene program following CDC or WHO guidelines, emphasizing the “5 Moments for Hand Hygiene”—before touching a patient, before clean/aseptic procedures, after body fluid exposure, after touching a patient, and after touching patient surroundings (CDC, 2023; WHO, 2023).
  • Enhance Accessibility to Hand Hygiene Products: Ensure alcohol-based hand sanitizers and handwashing facilities are readily accessible at patient care points and high-traffic areas throughout the hospital to facilitate compliance.
  • Compliance Monitoring and Feedback: Employ electronic monitoring systems or regular observational audits to track compliance rates. Provide staff with immediate, specific feedback to encourage continuous improvement in hand hygiene adherence.

Leadership Engagement and Staff Training on Hand Hygiene

  • Leadership Accountability: Hospital leadership should visibly support and prioritize hand hygiene compliance, incorporating it into institutional safety culture.
  • Ongoing Education: Offer regular, evidence-based educational programs to reinforce correct hand hygiene practices among all healthcare staff. Training should address common compliance barriers and emphasize the critical role of hand hygiene in infection prevention.

Patient and Visitor Engagement in Hand Hygiene

  • Involve Patients in Hand Hygiene: Encourage patients to participate actively in infection prevention by asking healthcare providers if they’ve cleaned their hands before care. Provide visible reminders in patient rooms and waiting areas.
  • Visitor Hand Hygiene: Ensure visitors understand the importance of hand hygiene through clear signage and readily accessible hand hygiene stations at hospital entrances, patient rooms, and communal areas.

Set Clear, Measurable Hand Hygiene Goals

  • Establish and Track Compliance Targets: Define clear compliance goals (e.g., greater than 90% adherence hospital-wide) and publicly display unit-level performance. Regularly celebrate improvements to sustain momentum and demonstrate the importance of hand hygiene to staff.
  • Continuous Improvement Initiatives: Use hand hygiene compliance data to inform ongoing quality improvement efforts. Address gaps promptly by identifying and mitigating barriers to compliance, such as workload pressures or inadequate product availability.

By focusing specifically on these rigorous hand hygiene practices, hospitals can significantly reduce the incidence of healthcare-associated infections, protect patients, and enhance overall safety outcomes.

National Patient Safety Goals 2025: #6 Reduce the Risk for Suicide

2025 National Patient Safety Goal: NPSG 15.01.01:

Reduce the risk for suicide.

Note: EPs 2–7 apply to patients in psychiatric hospitals or patients being evaluated or treated for behavioral health conditions as their primary reason for care. In addition, EPs 3–7 apply to all patients who express suicidal ideation during the course of care.

Element(s) of performance for NPSG 15.01.01
EP 1

For psychiatric hospitals and psychiatric units in general hospitals: The hospital conducts an environmental risk assessment that identifies features in the physical environment that could be used to attempt suicide; the hospital takes necessary action to minimize the risk(s) (for example, removal of anchor points, door hinges, and hooks that can be used for hanging).

For nonpsychiatric units in general hospitals: The organization implements procedures to mitigate the risk of suicide for patients at high risk for suicide, such as one-to-one monitoring, removing objects that pose a risk for self-harm if they can be removed without adversely affecting the patient’s medical care, assessing objects brought into a room by visitors, and using safe transportation procedures when moving patients to other parts of the hospital.

Note: Nonpsychiatric units in general hospitals do not need to be ligature resistant. Nevertheless, these facilities should routinely assess clinical areas to identify objects that could be used for self-harm and remove those objects, when possible, from the area around a patient who has been identified as high risk for suicide. This information can be used for training staff who monitor high-risk patients (for example, developing checklists to help staff remember which equipment should be removed when possible).

Ⓓ Documentation is required.

EP 2

Screen all patients for suicidal ideation who are being evaluated or treated for behavioral health conditions as their primary reason for care using a validated screening tool.

Note: The Joint Commission requires screening for suicidal ideation using a validated tool starting at age 12 and above.

EP 3

Use an evidence-based process to conduct a suicide assessment of patients who have screened positive for suicidal ideation. The assessment directly asks about suicidal ideation, plan, intent, suicidal or self-harm behaviors, risk factors, and protective factors.

Note: EPs 2 and 3 can be satisfied through the use of a single process or instrument that simultaneously screens patients for suicidal ideation and assesses the severity of suicidal ideation.

EP 4Document patients’ overall level of risk for suicide and the plan to mitigate the risk for suicide.
EP 5

Follow written policies and procedures addressing the care of patients identified as at risk for suicide. At a minimum, these should include the following:

  • Training and competence assessment of staff who care for patients at risk for suicide
  • Guidelines for reassessment
  • Monitoring patients who are at high risk for suicide

Ⓓ Documentation is required.

EP 6Follow written policies and procedures for counseling and follow-up care at discharge for patients identified as at risk for suicide.
EP 7Monitor implementation and effectiveness of policies and procedures for screening, assessment, and management of patients at risk for suicide and take action as needed to improve compliance.

Hospitals must proactively identify patients at risk for harm – particularly those at risk of suicide or self-harm. This goal involves systematic screening for risk factors (like suicidal ideation) and taking action to mitigate those risks in the hospital environment and beyond. By recognizing at-risk individuals early, hospitals can prevent tragic events and ensure patients get the help they need.

Screen All Patients for Suicide Risk when Indicated Using Validated Tools

For hospitals that treat behavioral health conditions or emergency patients with psychiatric complaints, implement a suicide risk screening on admission (or initial evaluation) for those populations (Source: jointcommission.org). The Joint Commission requires that all patients being treated for emotional or behavioral disorders be screened for suicidal ideation. Many hospitals have expanded this to universal screening in emergency departments and inpatient units – using tools like the Columbia-Suicide Severity Rating Scale (C-SSRS) or the PHQ-9 depression questionnaire (which has suicide ideation questions). The screening should be done by trained staff in a sensitive manner, and positive screens should trigger an immediate, more thorough risk assessment by a qualified professional. In one landmark study (ED-SAFE), implementing suicide screening in the ER and follow-up care led to a 30% reduction in suicide attempts among those patients in the following year – demonstrating the life-saving potential of systematic screening and intervention (Source: jamanetwork.com).

Conduct a Thorough Risk Assessment and Level-of-Risk Stratification

If a patient screens positive or otherwise is suspected to be at risk (e.g., expresses suicidal thoughts, has recent suicide attempt, or shows self-harm behavior), perform a formal suicide risk assessment using a standardized approach. This includes evaluating the patient’s suicidal ideation frequency and intensity, intentions or plan, past attempts, mental health and substance use history, and access to means (like firearms or medications) (Source: jointcommission.org). Document the findings and an immediate safety plan/mitigation strategy. For example, a high-risk patient might be placed on one-to-one observation, in a ligature-resistant room, with removal of any personal belongings that could be used for self-harm. Moderate risk might warrant 15 minute checks and secured unit placement. The assessment should also consider other safety risks inherent in the population – for instance, in older adults, risk of falls; in those on opioids, risk of overdose. Addressing patient safety risks means looking at each individual’s context.

Create a Safe Environment for At-Risk Patients

For patients identified as high risk for suicide, take immediate actions to minimize environmental hazards. This includes using ligature-resistant rooms or safe rooms whenever possible (rooms with no anchor points for hanging, tamper-proof fixtures, etc.), removing unnecessary medical equipment, cords, or objects that could be used for self-harm, and ensuring supervision. Train staff to perform a safety sweep of the room and patient’s belongings. Many hospitals have a checklist for making a room “suicide safe.” In psychiatric units, maintaining a ligature-resistant environment is mandatory under Joint Commission standards. Additionally, adjust care processes: e.g., no unsupervised passes, monitored bathrooms, plastic utensils for meals, etc., as needed for safety. Assign sitters or 1:1 observers for patients who require continuous observation (per your risk protocol)​. All staff (nurses, techs, sitters) should be briefed on the patient’s risk and what to monitor (e.g., patient trying to obtain sharp objects).

Engage Mental Health Expertise and Initiate Treatment

Identifying the risk is only the first step; ensure that at-risk patients get expert evaluation and intervention promptly. This might mean psychiatry consults for patients on medical units who voice suicidal ideation, or evaluation by a licensed mental health professional in the ED. Start interventions such as safety planning (a brief intervention where the provider works with the patient on coping strategies and sources of support) and, when appropriate, begin or adjust medications for underlying conditions (e.g., antidepressants, anti-anxiety meds). Sometimes just the act of a compassionate suicide risk assessment and engagement in care can reduce a patient’s immediate sense of crisis. For patients with substance use contributing to self-harm risk, involve addiction medicine as well. Train staff on de-escalation and empathetic communication, so that at-risk patients feel heard and safe, not judged – this can diffuse potential violence or agitation, which is also a safety risk.

Provide Continuous Observation and Frequent Re-assessment

Suicide risk can fluctuate, so re-assess patients periodically (for instance, each shift or each day) and adjust the precautions accordingly (Source: jointcommission.org). If a patient’s mood improves or they contract for safety, you might be able to step down from 1:1 observation to frequent checks, but do so cautiously and with team consensus. Conversely, if a patient becomes more agitated or hopeless, intensify precautions. Always communicate risk status at handoffs (e.g., a banner in the chart “Suicide Risk – high” and verbal sign-out highlighting it). Maintain observation until the patient is formally cleared by mental health professionals.

Ensure Safe Discharge and Follow-up for Patients At Risk

A very vulnerable time is when a patient leaves the hospital. Before discharge, create a personalized safety plan: this includes recognizing warning signs, listing coping strategies, people or agencies to contact in a crisis, and removing access to lethal means (for example, involving family to temporarily lock up firearms or unused medications at home). Provide the patient and family with emergency contact information such as the 988 Suicide & Crisis Lifeline, local crisis center numbers, and arrange prompt follow-up appointments with outpatient behavioral health providers. If possible, make a connection while still inpatient – some hospitals do a warm handoff by having a case manager or peer support specialist schedule the first therapy session or ensure the patient has a follow-up within days of discharge. Research shows post-discharge follow-up (calls or visits) significantly reduces suicide rates ​(Source: psychiatryonline.org). Therefore, consider programs where staff reach out within 24-48 hours post-discharge to check on the patient’s well-being and remind them of their support. Document the discharge plan and educate the patient’s family on what to do if risk escalates again. By taking these steps, hospitals can extend the safety net beyond their walls, during the critical transition period.

National Patient Safety Goals 2025: #7 Improve Health Care Equity

2025 National Patient Safety Goal: NPSG 16.01.01:
Improving health care equity for the hospital’s patients is a quality and safety priority.
Element(s) of performance for NPSG 16.01.01
EP 1

The hospital designates an individual(s) to lead activities to improve health care equity for the hospital’s patients.

Note: Leading the hospital’s activities to improve health care equity may be an individual’s primary role or part of a broader set of responsibilities.

EP 2

The hospital assesses the patient’s health-related social needs (HRSNs) and provides information about community resources and support services.

Note 1: Hospitals determine which HRSNs to include in the patient assessment. Examples of a patient’s HRSNs may include the following:

  • Access to transportation
  • Difficulty paying for prescriptions or medical bills
  • Education and literacy
  • Food insecurity
  • Housing insecurity

Note 2: HRSNs may be identified for a representative sample of the hospital’s patients or for all the hospital’s patients.

Ⓓ Documentation is required.

EP 3

The hospital identifies health care disparities in its patient population by stratifying quality and safety data using the sociodemographic characteristics of the hospital’s patients.

Note 1: Hospitals may focus on areas with known health care disparities identified in the scientific literature (for example, organ transplantation, maternal care, diabetes management) or select measures that affect all patients (for example, experience of care and communication).

Note 2: Hospitals determine which sociodemographic characteristics to use for stratification analyses. Examples of sociodemographic characteristics may include the following:

  • Age
  • Gender
  • Preferred language
  • Race and ethnicity

Ⓓ Documentation is required.

EP 4

The hospital develops a written action plan that describes how it will improve health care equity by addressing at least one of the health care disparities identified in its patient population.

Ⓓ Documentation is required.

EP 5

The hospital acts when it does not achieve or sustain the goal(s) in its action plan to improve health care equity.

Ⓓ Documentation is required.

EP 6At least annually, the hospital informs key stakeholders, including leaders, licensed practitioners, and staff, about its progress to improve health care equity.

Achieving equity in healthcare is now recognized as a patient safety imperative – meaning that every patient should receive high-quality, safe care regardless of their race, ethnicity, language, or socioeconomic status. This new NPSG (effective 2023) requires hospitals to identify disparities in their outcomes and take action to improve equity. In practice, this involves analyzing data to find care gaps, engaging leadership in an equity strategy, addressing patients’ social needs, and implementing targeted improvements for underserved groups.

National data show, for example, Black patients received worse care than White patients on 36% of patient safety metrics, and low-income households fared worse than higher-income households on 33% of safety metrics​ (Source: psnet.ahrq.gov). These inequities highlight the need for focused equity interventions.

Use Data to Identify Care Disparities in Your Hospital

Start by stratifying key quality and safety data by patients’ sociodemographic characteristics to uncover any inequities. For example, analyze infection rates, readmissions, surgical complications, or patient experience scores by race, ethnicity, primary language, gender, insurance type, etc. This analysis may reveal gaps – perhaps surgical infection rates are higher in patients with limited English proficiency, or pain control is worse in minority patients. Your hospital’s own data will pinpoint where to focus. Use a robust data approach (your quality analytics team can use EHR data, safety event reports, patient surveys, etc.). Importantly, involve frontline staff and community representatives in discussing the data – they can provide context for why a disparity might exist and ideas for addressing it.

Designate an Equity Leader and Develop a Strategic Plan

Improving equity must be an organizational priority. Appoint a dedicated leader or team responsible for health equity initiatives (Source: ​ihs.gov). Many hospitals now have a Chief Equity Officer or an interdisciplinary health equity committee. This leader/coordinator will drive efforts such as staff education, data monitoring, and improvement projects. Next, develop a written action plan to address at least one identified disparity, as per Joint Commission requirements. The plan should clearly state: the specific disparity you’re targeting (e.g., higher 30-day readmission rates in Medicaid patients), the population of focus, a measurable goal, strategies or interventions to achieve improvement, and how progress will be monitored. For instance, if data show that non-English speaking patients have lower medication understanding and higher readmissions, your plan might involve providing multilingual pharmacist counseling and follow-up calls to those patients, aiming to cut readmissions by X%. Make sure leadership allocates resources for these efforts – improvement won’t happen without buy-in from the top. Some hospitals have incorporated equity metrics into their quality dashboards and executive performance goals, underscoring that equitable care is as important as any clinical target.

Address Patients’ Health-Related Social Needs as Part of Care

Recognize that social determinants of health (SDOH) – like lack of transportation, food insecurity, or unstable housing – can directly impact patient safety and outcomes. Integrate a process to assess patients’ social needs and connect them with resources (Source: ​ihs.gov). For example, upon admission or in the ED, patients could be screened with a brief SDOH questionnaire (many validated tools exist) to identify needs such as difficulty affording medications or unsafe living conditions. If needs are identified, have a system to provide information or referrals to community resources (food banks, housing assistance, free transportation services, etc.). Under NPSG 16, hospitals are required to at least assess some patient population for health-related social needs and provide resource information​. By systematically addressing social needs, you not only demonstrate respect and caring, but you may prevent safety issues (e.g., a patient won’t skip follow-up because they lacked a ride, or won’t split pills due to cost – factors that disproportionately affect vulnerable groups). Ensure staff (nurses, case managers, social workers) are trained and empowered to act on these screenings.

Implement Targeted Interventions to Reduce Identified Disparities

Based on the disparities you find, launch quality improvement projects just as you would for any clinical issue – but tailor them to the affected population. If data show fewer minorities receive core measures in cardiac care, initiate an equity-focused review of those cases to identify gaps (maybe implicit bias or communication barriers) and intervene (through training or process changes). Set specific goals (e.g., eliminate the gap in blood pressure control between Black and White patients within 1 year) and measure outcomes continuously (Source: ​ihs.gov). Use the Plan-Do-Study-Act (PDSA) cycle or other QI frameworks for these projects. Celebrate improvements and communicate them hospital-wide to show that equity efforts yield results.

Educate and Equip the Workforce to Provide Equitable Care

Improving equity also means tackling issues like implicit bias and cultural competency among staff. Conduct training sessions on recognizing implicit biases in healthcare – for example, how pain might be underestimated in certain racial groups due to stereotypes (Source: ​psnet.ahrq.gov). Training should provide clinicians with tools to ensure all patients are heard and respected (use of interpreter services for language needs, understanding cultural health beliefs, etc.). Encourage diverse hiring and include patient representatives from the community in advisory councils to bring forward issues minority patients face. Another strategy is standardizing care protocols to minimize biased decisions – if everyone gets the same fall assessment or the same discharge checklist, there’s less room for subjective differences in care. The Joint Commission’s new standards also require that leaders periodically inform key stakeholders (like the Board, community groups) about the progress in improving health equity. Transparency and accountability go a long way. Some hospitals publish an annual equity report with performance data stratified by race/ethnicity, along with actions taken – this level of openness can motivate continued improvement and trust with the community.

Sustain and Spread Successful Equity Initiatives

Once you’ve demonstrated improvement in one disparity, integrate those practices into standard operations and then tackle the next disparity. For instance, if you successfully improved diabetes control in one clinic for a vulnerable population by using patient navigators, consider spreading that model to other clinics or for other chronic diseases. Hardwire equity by adding equity considerations into all safety and quality committees (e.g., if a new sepsis protocol is developed, ensure it works for non-English speakers, etc.). The goal is to embed an equity lens so thoroughly that it becomes part of everyone’s daily work – analogous to infection control or medication safety. By systematically reducing disparities, hospitals will not only meet the NPSG requirements but will truly ensure all patients are safer.

National Patient Safety Goals 2025: #8 Prevent Mistakes in Surgery

2025 National Patient Safety Goal: UP 01.01.01:
Conduct a preprocedure verification process.
Element(s) of performance for UP 01.01.01
EP 1

Implement a preprocedure process to verify the correct procedure, for the correct patient, at the correct site.

Note: The patient is involved in the verification process when possible.

EP 2

Identify the items that must be available for the procedure and use a standardized list to verify their availability. At a minimum, these items include the following:

  • Relevant documentation (for example, history and physical, signed procedure consent form, nursing assessment, and preanesthesia assessment)
  • Labeled diagnostic and radiology test results (for example, radiology images and scans, or pathology and biopsy reports) that are properly displayed
  • Any required blood products, implants, devices, and/or special equipment for the procedure

Note: The expectation of this element of performance is that the standardized list is available and is used consistently during the preprocedure verification. It is not necessary to document that the standardized list was used for each patient.

Ⓓ Documentation is required.

2025 National Patient Safety Goal: UP 01.02.01:
Mark the procedure site.
Element(s) of performance for UP 01.02.01
EP 1

Identify those procedures that require marking of the incision or insertion site. At a minimum, sites are marked when there is more than one possible location for the procedure and when performing the procedure in a different location would negatively affect quality or safety.

Note: For spinal procedures, in addition to preoperative skin marking of the general spinal region, special intraoperative imaging techniques may be used for locating and marking the exact vertebral level.

EP 2Mark the procedure site before the procedure is performed and, if possible, with the patient involved.
EP 3

The procedure site is marked by a licensed practitioner who is ultimately accountable for the procedure and will be present when the procedure is performed. In limited circumstances, the licensed practitioner may delegate site marking to an individual who is permitted by the organization to participate in the procedure and has the following qualifications:

  • An individual in a medical postgraduate education program who is being supervised by the licensed practitioner performing the procedure; who is familiar with the patient; and who will be present when the procedure is performed
  • A licensed individual who performs duties requiring a collaborative agreement or supervisory agreement with the licensed practitioner performing the procedure (that is, an advanced practice registered nurse [APRN] or physician assistant [PA]); who is familiar with the patient; and who will be present when the procedure is performed.

Note: The hospital’s leaders define the limited circumstances (if any) in which site marking may be delegated to an individual meeting these qualifications.

EP 4

The method of marking the site and the type of mark is unambiguous and is used consistently throughout the hospital.

Note: The mark is made at or near the procedure site and is sufficiently permanent to be visible after skin preparation and draping. Adhesive markers are not the sole means of marking the site.

EP 5

A written, alternative process is in place for patients who refuse site marking or when it is technically or anatomically impossible or impractical to mark the site (for example, mucosal surfaces or perineum).

Note: Examples of other situations that involve alternative processes include:

  • Minimal access procedures treating a lateralized internal organ, whether percutaneous or through a natural orifice
  • Teeth
  • Premature infants, for whom the mark may cause a permanent tattoo

Ⓓ Documentation is required.

2025 National Patient Safety Goal: UP 01.03.01:
A time-out is performed before the procedure.
Element(s) of performance for UP 01.03.01
EP 1Conduct a time-out immediately before starting the invasive procedure or making the incision.
EP 2

The time-out has the following characteristics:

  • It is standardized, as defined by the hospital.
  • It is initiated by a designated member of the team.
  • It involves the immediate members of the procedure team, including the individual performing the procedure, the anesthesia providers, the circulating nurse, the operating room technician, and other active participants who will be participating in the procedure from the beginning.
EP 3When two or more procedures are being performed on the same patient, and the person performing the procedure changes, perform a time-out before each procedure is initiated.
EP 4

During the time-out, the team members agree, at a minimum, on the following:

  • Correct patient identity
  • The correct site
  • The procedure to be done
EP 5

Document the completion of the time-out.

Note: The hospital determines the amount and type of documentation.

Ⓓ Documentation is required.

Wrong-site, wrong-procedure, or wrong-patient surgeries are catastrophic events that are fully preventable with rigorous protocols. The Universal Protocol and the WHO Surgical Safety Checklist provide a framework to eliminate surgical mistakes. This goal entails a series of pre-operative and intra-operative checks – from verifying the patient and procedure, to marking the surgical site, to taking a final “time-out” pause – as well as fostering teamwork in the OR. When reliably implemented, these practices have proven to significantly reduce surgical errors and complications.

Conduct a Pre-Procedure Verification (“Surgical Checklist”) for Every Case

Well before the patient enters the operating room (for example, in the pre-op holding area), have a standardized verification process to confirm all the relevant documents and studies are available and correct (Source: jointcommission.org). This includes verifying the patient’s identity with two identifiers, the procedure planned, the site/side of the procedure, and that consent forms have been signed and match the intended surgery. Also verify that any required implants, special equipment, or imaging results are ready. Many hospitals use a checklist for this phase – often a nurse, with the patient involved, will review each item (e.g., “Mrs. Jones, we have you scheduled for a left knee arthroscopy, is that correct?”). Resolving discrepancies at this stage (such as discovering a consent form is missing or the x-ray isn’t in the room) prevents downstream errors. As part of the Universal Protocol, this pre-procedure verification is a mandatory step and should involve all relevant team members (pre-op nurse, anesthesiologist, surgeon) as appropriate.

Mark the Surgical Site Unambiguously

For procedures involving laterality (left vs right), multiple structures (e.g., fingers, limbs), or levels (spinal surgery), the correct site must be marked on the patient’s body before the surgery. The Joint Commission requires that the mark be made by a licensed provider who will be involved in the procedure (often the surgeon) and that it should be sufficiently permanent to be visible after skin prep (usually marking with a surgical marker “YES” or surgeon’s initials on the correct site). For example, if operating on the left eye, the surgeon should mark “left eye” or initials above that eye. Do not mark non-operative sites (to avoid confusion) except in cases like a possible level spine surgery (then initial the level that was verified by x-ray). Have a policy on acceptable site marking – some use an “X” not to operate on or a line pointing to the correct vertebral level after radiographic confirmation, etc. The patient (if awake and able) should be involved: “We are marking the left knee you’re having surgery on, correct?” Marking has prevented many a near-miss – if a clinician is about to prep the right side and sees no mark (because the left was the correct side and is marked), they know to stop. Special cases: for teeth, a dental diagram is used; for some minimal access procedures (endoscopy), site marking might not apply – have those exceptions defined. Overall, site marking is a simple but powerful visual communication that everyone in the OR can see, serving as a final check against wrong-site errors.

Perform a “Time-Out” in the OR Immediately Before Incision

The surgical time-out is a final pause performed in the OR with the entire surgical team immediately before the procedure begins (for example, after anesthesia induction and patient positioning, but before the incision). During the time-out, all activity should pause and the team verbally confirms critical information: correct patient identity, correct site and side (pointing to the mark), correct procedure to be done, and as applicable any special considerations (having the correct implants, antibiotics given, patient positioning, etc.)​(Source: jointcommission.org). The surgeon, anesthesiologist, circulating nurse, scrub tech – everyone participates and must be in agreement. This active communication time-out is required by the Universal Protocol and is extremely effective in catching any last-minute discrepancies. For instance, if the consent said left hip but the OR schedule said right hip, this is the moment someone might speak up. It is important that the time-out is done consistently for every case – even minor procedures – and that it is not pro forma. Encourage a culture where anyone in the OR can halt the start of surgery if something doesn’t sound right. Document the time-out in the record (many ORs have a checklist sheet or an EHR flow sheet to tick off that the time-out was completed and what was verified).

Adopt the WHO Surgical Safety Checklist for Comprehensive Safety

The WHO 19-item Surgical Safety Checklist (which includes steps for sign-in, time-out, and sign-out) covers not only patient/procedure verification but also other safety measures (like ensuring prophylactic antibiotics are given, counting instruments and sponges, and discussing post-op plans). Many hospitals worldwide have implemented it and seen significant drops in post-op complication rates and mortality – studies showed a 30%+ reduction in surgical complications and deaths after checklist adoption (Source: ​who.int). Incorporate the checklist into your workflow: for example, a “sign-in” phase in the anesthetic room (checking allergies, airway risk, etc.), the “time-out” in OR (patient, site, procedure, etc.), and a “sign-out” before the team leaves the OR (discussing specimen labeling, instrument counts correct, any equipment problems, and post-op management plans). This creates multiple layers of verification and promotes teamwork.

If your hospital already uses a checklist, periodically audit its completion and quality – ensure it’s done with meaning, not just ticking boxes. Engage surgeons by sharing data or stories of checklist catches (near-misses averted), so they champion its use rather than see it as bureaucratic.

Foster a Culture of Speaking Up in the OR

Even with protocols, human factors matter. Encourage surgeons and OR staff to adopt a team mentality – where any team member can question a discrepancy (like “Is this definitely the correct implant size?” or “Did we confirm the spinal level with x-ray?”) without hesitation. Research shows communication issues are a root cause of many surgical errors. Techniques from crew resource management (CRM) can be applied: having briefings and debriefings, flattening hierarchy so that even a junior nurse feels comfortable stopping the line if something is amiss. Some hospitals conduct after-action reviews for near-misses (like catching a wrong-level spine case before cutting) to learn how to improve processes and to positively reinforce the individuals who spoke up. Over time, as these practices become ingrained, wrong-site surgeries and other “never events” can truly become relics of the past. In fact, many organizations have gone years without a wrong-site surgery due to rigorous adherence to these protocols. Consistency is key – every patient, every time – no shortcuts, even when the schedule is running behind or for “quick cases.”

Your Roadmap to Safer Care: Implementing the National Patient Safety Goals 2025

By diligently implementing each of these 2025 National Patient Safety Goals with leadership support, staff training, patient engagement, and continuous improvement, hospitals can measurably enhance patient safety. Each goal’s tactics – from the basics of patient identification and hand hygiene to the newer focus on health equity – are backed by evidence and real-world success stories. As healthcare leaders, insisting on these best practices and providing the resources and accountability to carry them out will drive your organization toward zero harm. Remember, achieving excellence in patient safety is an ongoing journey of learning and improving – but with these targeted efforts in 2025, you will be closer to the ultimate goal of zero preventable patient harm.

You may also like:

Health care with stethoscope and pills glass tube

How to Improve Medication Errors in Hospitals

Medication errors remain a critical patient safety issue. Learn actionable strategies for quality improvement in medication errors, from reporting enhancements to tech solutions like CPOE and BCMA.

Table of Contents

Hospital administrators often express concerns about patient safety and seek effective strategies for how to improve medication errors. These types of errors cause harm to about 1.3 million people annually on a global scale and are responsible for one death daily in the United States, according to the World Health Organization. The worldwide impact of medication errors totals about $42 billion per year, the organization reports.

How to improve medication errors

Understanding the Scope for Improving Medication Errors

“The downstream effects include physical and emotional harm of patients and family members, losing trust in the healthcare system, and increased healthcare costs,” says Farzana Samad, a pharmacist who is the health scientist administrator at the Agency for Healthcare Research and Quality. (Statistics source: WHO).

In healthcare settings, improving medication errors requires addressing various causes such as wrong administration, incorrect orders, improper holds, wrong doses, improper storage, omissions, duplicates, and lack of monitoring, Samad explains. In hospitals, factors such as culture, technology, processes, and available resources influence medication error rates.

Why Underreporting Impacts a Quality Improvement Project for Medication Errors

Knowing how to improve medication errors begins with measuring their occurrence nationally. However, underreporting remains a significant barrier. In addition, reporting requirements vary between states, and a centralized database doesn’t exist, says Christina Michalek, a pharmacist and director of Membership and Patient Safety Organization (PSO) at the Institute for Safe Medication Practices (ISMP) and administrative coordinator for the Medication Safety Officers Society.

Reporting errors is vital for designing a quality improvement project for medication errors. Understanding systemic gaps allows hospitals to implement best practices that prevent harm, Samad notes. Lower reported rates might reflect not only ineffective strategies but also fear of reporting or cumbersome reporting systems.

Even errors that don’t reach patients offer lessons for a safety improvement plan for medication errors. “Severity bias might cause underreporting,” Samad explains, underscoring the need for a cultural shift toward learning and transparency.

Why Benchmarking Fails in Quality Improvement for Medication Errors

Although progress exists, quantifying medication error improvements remains challenging. Many healthcare systems mistakenly rely on benchmarking comparisons to gauge safety improvements.

Michalek cautions: “There is no acceptable incident rate for medication errors.” Instead of focusing on how many errors are reported, organizations should prioritize the quality improvement initiative for medication errors — analyzing error types and improving systemic weaknesses.

Significant variability exists across institutions in definitions, thresholds, and reporting habits. “The easiest way to improve your error rate is to stop reporting—and that’s certainly no way for organizations to learn and improve,” Michalek adds.

Best Practices for a Safety Improvement Plan for Medication Errors

Instead of benchmarking, ISMP recommends a proactive safety improvement plan for medication errors that focuses on actionable steps:

  • Boost reporting of close calls (good catches).
  • Educate leadership and the board about the importance of reporting.
  • Focus on system improvements based on real-world events.

Increasing the number of safety interventions demonstrates a quality improvement initiative for medication errors that fosters a true culture of learning and safety.

Technology’s Role in Decreased Medication Administration Errors and Quality Improvement

Hospitals can strengthen their quality improvement for medication errors by implementing critical technology tools. Katie Stewart of The Leapfrog Group emphasizes the importance of:

  • Computerized Provider Order Entry (CPOE): Used to catch common prescribing errors. Studies show CPOE reduces harm from prescriber errors by up to 55%.
  • Bar Code Medication Administration (BCMA): Scanning medications at the bedside ensures the right drug is administered at the correct time and dose.

Two measures in the Leapfrog Hospital Safety Grade reveal progress. In 2018, only 65.6% of hospitals met CPOE standards, but by 2024, that number rose to 88.1%. Similarly, BCMA adoption jumped from 47.3% in 2018 to 86.9% in 2024.

These systems are essential components of any quality improvement project for medication errors.

Staffing Solutions to Support Quality Improvement Medication Errors Initiatives

Beyond technology, staffing innovations help with decreased medication administration errors quality improvement. A study in the Journal of Nursing Management highlights the role of pharmaceutical technical assistants on nursing wards.

Their support freed up nurses for direct patient care, which nurses perceived as contributing to fewer errors. “Clear communication procedures and continuity were vital for success,” researchers concluded.

This staffing model provides a strong, people-centered strategy for hospitals aiming for sustained quality improvement medication errors outcomes.

How AI Technology Boosts a Quality Improvement Initiative for Medication Errors

Emerging tech, such as AI-enabled wearable cameras, offers another layer of protection. At the University of Washington, Dr. Kelly Michaelsen explored using wearable cameras to detect medication errors during administration.

Serving as a “second set of eyes,” the AI system could identify the contents of a syringe before injection, reducing errors caused by distraction or time pressure. Michaelsen stresses the importance of coupling technology with a culture of safety — minimizing interruptions and ensuring providers have sufficient time for checks. (Source: https://www.nature.com/articles/s41746-024-01295-2)

AI applications could become a powerful part of future safety improvement plans for medication errors.

You may also like: