South Carolina 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.

The South Carolina Medication Data Form (SC MDF) is a standardized tool used by healthcare professionals to track medication errors and near misses within the state's healthcare system. The form is designed to gather critical information regarding these incidents, allowing for analysis and improvement of medication safety practices. Key features of the South Carolina Medication Data Form include: 1. Medication Error Classification: The SC MDF categorizes medication errors into various types to help identify patterns and trends. These classifications include prescribing errors, dispensing errors, administration errors, monitoring errors, and documentation errors. 2. Near Miss Classification: The form also captures near misses, which are situations where errors almost occur but are intercepted before reaching the patient. Near misses provide valuable insights into potential vulnerabilities in the medication use process, allowing for proactive interventions to prevent future errors. 3. Data Collection: The SC MDF collects a range of data elements related to medication errors and near misses. These include patient demographics, medication details, contributing factors, severity of the incident, outcomes, and any preventive measures taken. This comprehensive data collection helps in understanding the causes and consequences of medication errors for appropriate analysis and improvement initiatives. 4. Analytical Capabilities: The SC MDF serves as a valuable data source for organizations and policymakers in South Carolina by facilitating analysis of medication errors and near misses. The data collected can be used to identify system-wide issues, develop targeted interventions, and measure the effectiveness of quality improvement initiatives. Different types of South Carolina Medication Data Form — Medication Error and Near Miss Classification can include: 1. Individual Healthcare Facility Forms: Various healthcare facilities within South Carolina may have their own customized versions of the SC MDF, tailored to their specific needs and reporting requirements. 2. Statewide Standardized Form: In addition to facility-specific forms, there may be an official statewide standardized version of the SC MDF, endorsed by regulatory bodies or professional organizations. This ensures consistency and uniformity in reporting across the state. 3. Specialized Forms: Depending on the organization or program, specialized versions of the SC MDF may exist to focus on specific areas of medication errors or near misses. These may include forms dedicated to pediatric incidents, long-term care facilities, or specific healthcare settings. In conclusion, the South Carolina Medication Data Form — Medication Error and Near Miss Classification is a comprehensive tool used to document and analyze medication errors and near misses in healthcare settings across the state. By collecting standardized data, this form enables healthcare professionals to identify patterns, implement targeted interventions, and ultimately enhance patient safety.

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

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.

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

SECTION 40-43-30. Definitions. For purposes of this chapter: (1) "Administer" means the direct application of a drug or device pursuant to a lawful order of a practitioner to the body of a patient by injection, inhalation, ingestion, topical application, or any other means.

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.

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.

Wrong dose, missing doses, and wrong medication are the most commonly reported administration errors. Contributing factors to patient and caregiver error include low health literacy, poor provider?patient communication, absence of health literacy, and universal precautions in the outpatient clinic.

Types of Medication Errors Prescribing. Omission. Wrong time. Unauthorized drug. Improper dose. Wrong dose prescription/wrong dose preparation. Administration errors include the incorrect route of administration, giving the drug to the wrong patient, extra dose, or wrong rate.

A near miss is defined as "any event that could have had adverse consequences but did not and was indistinguishable from fully fledged adverse events in all but outcome." (Some studies use the related terms "potential adverse event" and "close call.") In a near miss, an error was committed, but the patient did not ...

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.

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Jan 1, 2018 — DDSN Service Providers will be required to complete Medication Error Reporting documentation in Therap. This will assist each provider agency ... (54) "Manufacturer" means a person engaged in the manufacture of prescription drugs or devices. (55) "Material safety data sheet" or "MSDS" means a resource ...by S Crane — Barriers and motivators for making error reports from family medicine offices: a ... How to complete a near miss reporting form (video) · External Link Disclaimer ... Paramedic shall submit a complete application with the Department, on a form prescribed, prepared, ... The South Carolina Medical Control Committee and the South ... by S Zhou · 2018 · Cited by 18 — Using multiclass classification to automate the identification of patient safety incident reports by type and severity. BMC Medical ... by DA South · 2015 · Cited by 10 — Because the error is corrected before the medication is administered, this transcription error can be classified as a near-miss transcription ... by ZSY Wong · 2020 · Cited by 8 — Presently many incident reporting systems in the world capture incidents of medication errors using free text without indicating the medication- ... 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. Nov 8, 2017 — A system for reporting and reviewing errors is an es- sential component of a medication safety system; the goal is to enhance patient safety and ... This survey collected information about the number of medication errors and near-misses reported in the year prior to joining the project, the extent to ...

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South Carolina Medication Data Form - Medication Error and Near Miss Classification