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Vermont Medication Data Form - Medication Error and Near Miss Classification

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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.

Vermont Medication Data Form (MDF) is a standardized tool implemented to collect and analyze data related to medication errors and near misses in healthcare settings in Vermont. This form serves as a crucial means of identifying and understanding medication-related incidents, allowing healthcare professionals to implement improvement strategies effectively. Keywords: Vermont Medication Data Form, Medication Error, Near Miss Classification, healthcare settings, standardized tool, data collection, analysis, medication-related incidents, improvement strategies. There are different types of Vermont Medication Data Forms available, each serving a specific purpose: 1. MDF Medication Error Classification: This form categorizes medication errors based on their nature, severity, and various contributing factors. It helps to identify specific areas for improvement, track trends, and implement preventive measures. 2. MDF Near Miss Classification: This form focuses on documenting near misses or close calls that could have resulted in medication errors but were intercepted before causing harm to patients. Analyzing near misses provides valuable insights into potential vulnerabilities within medication management processes and offers opportunities for system enhancements. 3. MDF Data Collection and Analysis: This component of the MDF focuses on accurately capturing and organizing medication-related data. It includes fields for crucial information such as date, time, location, involved staff, medications involved, patient information, contributing factors, consequences, and outcome of the incident. Collecting this detailed data enables in-depth analysis and facilitates targeted interventions. 4. MDF Reporting and Feedback: The MDF allows for the reporting of medication errors and near misses to the appropriate stakeholders, including healthcare professionals, administrators, and regulatory bodies. Feedback loops are established to ensure that incidents are thoroughly investigated, lessons learned are disseminated, and effective corrective actions are implemented. 5. MDF Continuous Quality Improvement: The Vermont Medication Data Form serves as a foundation for continuous quality improvement efforts. By identifying patterns, trends, and potential causes, healthcare facilities can implement proactive measures, develop standardized protocols, and promote interdisciplinary collaboration to enhance medication safety. To summarize, the Vermont Medication Data Form — Medication Error and Near Miss Classification is a comprehensive tool enabling healthcare establishments to collect, classify, and analyze medication errors and near misses. By utilizing this standardized form, healthcare organizations can prioritize patient safety, identify system weaknesses, and implement targeted interventions to reduce the occurrence of medication-related incidents.

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Table of Contents CategoryDescriptionANo error, capacity to cause errorBError that did not reach the patientCError that reached patient but unlikely to cause harm (omissions considered to reach patient)DError that reached the patient and could have necessitated monitoring and/or intervention to preclude harm5 more rows

Class C error or prohibited practice Type of action/inaction committed by staff that generally involves: ? The death of a person ? Injury requiring hospitalization or medical treatment at an emergency department, clinic or health care provider's office ? Falsification of records and/or certification paperwork ? ...

Common causes of medication error include incorrect diagnosis, prescribing errors, dose miscalculations, poor drug distribution practices, drug and drug device related problems, incorrect drug administration, failed communication and lack of patient education.

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.

Medication errors occur when weak medication systems and/or human factors such as fatigue, poor environmental conditions or staff shortages affect prescribing, transcribing, dispensing, administration and monitoring practices, which can then result in severe harm, disability and even death.

34.1 Category I An error occurred that may have contributed to or resulted in the patient's death. [ Classify each medication involved in a medication error. Include the intended product for use, as well as the actual product used, if these are different.

Medication errors can be classified, invoking psychological theory, as knowledge-based mistakes, rule-based mistakes, action-based slips, and memory-based lapses.

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Jan 27, 2020 — If a patient is refusing a medication you MUST notify MD and document on back of MAR and/or nursing note as to why. We must fill out an AIMS ... Please complete all sections of this form by printing or typing the ... ☐ Patient death or serious injury associated with a medication error (e.g., errors ...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. 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 A Samsiah · 2016 · Cited by 53 — They said that theoretically both actual errors and near misses should be reported as this will portray a complete picture of all sources of ... by N Hall · 2022 · Cited by 2 — These examples demonstrate how the definition of a as 'near miss' can depend on: whether a medicine had been dispensed or reached the patient, ... Oct 23, 2015 — ... the term 'near miss' is used as synonym for describing what is classified 'intercepted error' for pharmacovigilance purposes. A near miss from a. by LT Kohn · Cited by 26143 — medication class (12.1 percent); using the wrong drug name, dosage form, or ... pation in error reporting systems that focus on “near misses” or errors. medication's labeling (e.g., Core Data Sheet, SPC, Investigators Brochure, local label, ... • Medication errors or near misses (including dispensing errors, ... The VAERS program follows up on reports classified as serious by attempting to obtain medical records to better understand the event. These requests for medical ...

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Vermont Medication Data Form - Medication Error and Near Miss Classification