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Maryland Medication Data Form - Medication Error and Near Miss Classification

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Multi-State
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US-02260BG
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This form is a generic example that may be referred to when preparing such a form for your particular state. It is for illustrative purposes only. Local laws should be consulted to determine any specific requirements for such a form in a particular jurisdiction.


The Maryland Medication Data Form is a document designed to capture and classify medication errors and near misses that occur in healthcare settings within the state of Maryland. It serves as a standardized reporting tool to track and analyze incidents related to medication errors, ensuring patient safety and quality improvement. Keywords: Maryland Medication Data Form, medication errors, near miss classification, healthcare, standardized reporting tool, incidents, patient safety, quality improvement. 1. Purpose of the Maryland Medication Data Form: The primary purpose of the Maryland Medication Data Form is to collect comprehensive data on medication errors and near misses, enabling healthcare organizations to identify trends, implement proactive measures, and improve medication management processes and patient outcomes. 2. Features and Components of the Form: The Maryland Medication Data Form typically gathers information on various aspects of medication incidents, such as the type of error, contributing factors, stage of medication process (prescribing, dispensing, administration), healthcare personnel involved, severity of the incident, and potential harm or adverse effects caused to the patient. 3. Key Benefits of the Form: By utilizing the Maryland Medication Data Form, healthcare institutions can monitor medication errors and near misses more effectively. It aids in identifying areas of improvement, developing targeted interventions, educating staff, and implementing strategies to reduce the likelihood of future errors, ultimately enhancing patient safety. 4. Types of Medication Errors Covered: The Maryland Medication Data Form broadly encompasses various types of medication errors, encompassing but not limited to prescribing errors, dispensing errors, administration errors, wrong dose, wrong medication, wrong route, drug interactions, or use of expired medications. 5. Near Miss Classification: The Maryland Medication Data Form also includes a classification system to capture near misses, which refer to incidents where error or harm was narrowly avoided. Near misses are considered valuable opportunities for learning, as they highlight potential vulnerabilities and enable the identification of system weaknesses before harm occurs. 6. Reporting and Analysis: Once completed, the Maryland Medication Data Form data should be reported to designated entities within the healthcare system. Analysis of this aggregated data allows for the identification of patterns, trends, or common contributing factors, enabling targeted interventions and system-level improvements. 7. Integration with Reporting Systems: To streamline the reporting process, the Maryland Medication Data Form can be integrated into existing incident reporting systems or electronic health records (Ears). This interoperability enhances data collection efficiency and reduces duplicate data entry, facilitating real-time incident tracking and analysis. Having a standardized reporting tool like the Maryland Medication Data Form in place promotes a culture of open communication, encourages healthcare providers to disclose errors, and facilitates shared learning across organizations, ultimately driving improvements in medication safety statewide.

The Maryland Medication Data Form is a document designed to capture and classify medication errors and near misses that occur in healthcare settings within the state of Maryland. It serves as a standardized reporting tool to track and analyze incidents related to medication errors, ensuring patient safety and quality improvement. Keywords: Maryland Medication Data Form, medication errors, near miss classification, healthcare, standardized reporting tool, incidents, patient safety, quality improvement. 1. Purpose of the Maryland Medication Data Form: The primary purpose of the Maryland Medication Data Form is to collect comprehensive data on medication errors and near misses, enabling healthcare organizations to identify trends, implement proactive measures, and improve medication management processes and patient outcomes. 2. Features and Components of the Form: The Maryland Medication Data Form typically gathers information on various aspects of medication incidents, such as the type of error, contributing factors, stage of medication process (prescribing, dispensing, administration), healthcare personnel involved, severity of the incident, and potential harm or adverse effects caused to the patient. 3. Key Benefits of the Form: By utilizing the Maryland Medication Data Form, healthcare institutions can monitor medication errors and near misses more effectively. It aids in identifying areas of improvement, developing targeted interventions, educating staff, and implementing strategies to reduce the likelihood of future errors, ultimately enhancing patient safety. 4. Types of Medication Errors Covered: The Maryland Medication Data Form broadly encompasses various types of medication errors, encompassing but not limited to prescribing errors, dispensing errors, administration errors, wrong dose, wrong medication, wrong route, drug interactions, or use of expired medications. 5. Near Miss Classification: The Maryland Medication Data Form also includes a classification system to capture near misses, which refer to incidents where error or harm was narrowly avoided. Near misses are considered valuable opportunities for learning, as they highlight potential vulnerabilities and enable the identification of system weaknesses before harm occurs. 6. Reporting and Analysis: Once completed, the Maryland Medication Data Form data should be reported to designated entities within the healthcare system. Analysis of this aggregated data allows for the identification of patterns, trends, or common contributing factors, enabling targeted interventions and system-level improvements. 7. Integration with Reporting Systems: To streamline the reporting process, the Maryland Medication Data Form can be integrated into existing incident reporting systems or electronic health records (Ears). This interoperability enhances data collection efficiency and reduces duplicate data entry, facilitating real-time incident tracking and analysis. Having a standardized reporting tool like the Maryland Medication Data Form in place promotes a culture of open communication, encourages healthcare providers to disclose errors, and facilitates shared learning across organizations, ultimately driving improvements in medication safety statewide.

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The ASHP classifies errors as prescribing error, dispensing error, omission error, wrong time error, unauthorized drug error, improper dose error, wrong dosage-form error, wrong drug-preparation error, wrong administration-technique error, deteriorated drug error, monitoring error, compliance error, and other ...

Medication error procedures: Immediately notify the supervisor and physician. Follow agency policy to notify appropriate professionals. Know and follow your facility's policy for medication errors. Complete a medication error report in ance with regulations and agency policies.

Write a note in the medical record documenting what happened, the impact on the patient, treatment provided, and results. You can include who was told about it, what they were told, and when.

The Institute for Safe Medication Practices further defines a near miss as ?any event or situation that didn't produce patient injury, but only because of chance.?2 For reporting purposes, a near miss is considered an error, as is a medication error that doesn't result in patient harm.

A medication error is defined as "any preventable event that may cause or lead to inappropriate medication use or patient harm while the medication is in the control of the healthcare professional, patient, or consumer,? ing to the National Coordinating Council for Medication Error Reporting and Prevention.

Health care professionals and consumers have the opportunity to report the occurrence of medication errors to a variety of organizations. Examples include the Institute of Safe Medication Practices (ISMP) and the Food and Drug Administration (FDA). These organizations collectively review error submissions.

Draw a single line through the erroneous entry and write the time, date, and your name. Identify the reason for the correction. Include the rationale in your notation; for example, ?mistaken entry, wrong medication name written.? Follow facility policy when adding late information.

Adopt a reporting system. The only way to reduce medication errors is to develop a reporting system and then make changes to prevent similar errors from reoccurring. Even a near miss should be reported. The staff should be encouraged to report without any repercussions.

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Jul 11, 2015 — DATAFORM 3 Medication Error and Near Miss Classification Form. Category, Description, Example. A, No error, capacity to cause error, NA. B, Error that did not reach the patient, NA. C, Error that reached patient but ...by RA Nosek Jr · 2005 · Cited by 34 — The user then can select a single error from the spreadsheet and view all the pertinent details from the incident in report form. Go to: Centralized reporting. by S Crane — Introduction. Near-miss events are errors that occur in the process of providing medical care that are detected and corrected before a patient is harmed. by ZR Wolf · 2008 · Cited by 231 — This chapter focuses on the assertion that reporting errors that result in patient harm as well as seemingly trivial errors and near misses has the potential to ... Jul 23, 2015 — The purpose of this taxonomy is to provide a standard language and structure of medication error-related data for use in developing databases. by A Mulac · 2021 · Cited by 59 — Incident reports with insufficient information to classify the degree of harm were coded as missing. Understanding the context of the data. The data on ... by M Hoppes · 2014 · Cited by 1 — Classify the level of harm—5 levels /1 near miss. 2. Take action guided by serious safety event classification (see Table 2/page13). Things to consider ... 1 The report estimated that as many as 98,000 people die annually from medical errors in hospitals. The report challenged the health care industry to reduce the ... The purpose of this study is to assess the rates of perioperative medication errors (MEs) and adverse drug events (ADEs) as percentages of medication ...

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Maryland Medication Data Form - Medication Error and Near Miss Classification