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This document outlines deficiencies identified during a state licensure survey for a residential group home, along with required corrective actions.
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How to fill out statement of deficiencies and

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How to fill out STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION

01
Begin with the facility information, including name, address, and identification number.
02
List the date of the survey or inspection that identified the deficiencies.
03
Clearly outline each deficiency found, referencing the specific regulations or standards that were violated.
04
Provide a detailed description of each deficiency, including the impact on residents or patients.
05
Develop a corrective action plan for each deficiency, including specific steps to be taken, responsible parties, and timelines for completion.
06
Include a system for monitoring the effectiveness of the corrective actions implemented.
07
Gather signatures from relevant personnel to endorse the plan.

Who needs STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION?

01
Healthcare facilities that receive regulatory inspections or surveys.
02
Facilities seeking to address and rectify compliance issues.
03
Providers looking to improve quality of care and meet regulatory standards.
04
Organizations involved in quality assurance and compliance training.
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There are three scope levels assigned to a deficiency: isolated, pattern, or widespread. The survey agency determines the scope and severity levels for each deficiency cited on a survey.
Element 1: How the corrective action will be accomplished for identified affected individuals. Element 2: How will other individuals with the potential to be affected or in similar situations be identified and protected. Element 3: What systemic changes will ensure that the deficient practice will not recur.
There are three scope levels assigned to a deficiency: isolated, pattern, or widespread. The survey agency determines the scope and severity levels for each deficiency cited on a survey.
An acceptable Plan of Correction will include both immediate corrective actions to correct the violation and long-term quality improvement actions, with each element including who is responsible, when it will be done, and what action has been or will be taken.
A facility is not required to submit a plan of correction when it has deficiencies that are isolated and have a potential for minimal harm, but no actual harm has occurred.
In all cases of immediate jeopardy, the provider agreement must be terminated by CMS or State Medicaid Agency no later than 23 calendar days from the last day of the survey if the immediate jeopardy is not removed.
To write a Statement of Deficiencies, three elements must be completed: • Gather enough strong evidence. Differentiate finding and deficient practice or noncompliance. Based on a regulation/requirement, recognize what the entity failed to do. Don't wait until near the end of the survey.

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The Statement of Deficiencies and Plan of Correction (SOD/PAC) is a formal document used by healthcare facilities to report areas of non-compliance identified during inspections or audits. It outlines specific deficiencies in meeting regulatory standards and presents a plan to address and rectify these issues.
Healthcare facilities that are subject to regulatory inspections, such as nursing homes, hospitals, and other long-term care facilities, are required to file a Statement of Deficiencies and Plan of Correction when deficiencies are identified by regulatory bodies.
To fill out a Statement of Deficiencies and Plan of Correction, facilities must first review the inspection report to identify specific deficiencies. Then, they should complete the form by detailing each deficiency, outlining the steps they will take to correct the deficiencies, assigning responsibility for the corrective actions, and setting a timeline for implementation.
The purpose of the Statement of Deficiencies and Plan of Correction is to ensure that healthcare facilities acknowledge their deficiencies, provide a clear plan to address those issues, and improve their compliance with regulatory standards, ultimately enhancing patient safety and quality of care.
The information that must be reported includes the specific deficiencies identified, references to relevant regulations, the proposed corrective actions for each deficiency, the responsible party for implementation, and the timeline for the completion of the plan.
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