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This document details deficiencies identified during a state licensure survey of a residential facility, along with corrective action plans that must be implemented.
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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 by clearly identifying the facility or organization involved.
02
List the specific deficiencies found during the inspection in detail.
03
Include relevant dates of the inspection and the timeline of when the deficiencies were identified.
04
For each deficiency, write a corresponding plan of correction outlining the steps that will be taken to address the issue.
05
Assign responsibility for implementing the corrective actions to specific individuals or teams.
06
Establish deadlines for when each corrective action will be completed.
07
Review the completed form for accuracy and completeness before submitting.
08
Ensure the signatures of responsible parties are included to indicate agreement with the plan.

Who needs STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION?

01
Facilities that are subject to regulatory inspections, such as nursing homes, hospitals, and other healthcare providers.
02
Organizations that receive federal or state funding and must comply with certain standards.
03
Management teams responsible for quality assurance and compliance within health care settings.
04
Inspectors and regulatory bodies who evaluate compliance with health and safety regulations.
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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 is a formal document used by healthcare facilities to outline deficiencies in compliance with standards set by regulatory agencies, along with a detailed plan on how to correct those deficiencies.
Healthcare facilities and organizations that are subject to regulatory inspections and have been found to have deficiencies are required to file a Statement of Deficiencies and Plan of Correction.
To fill out the Statement of Deficiencies and Plan of Correction, facilities must accurately identify each deficiency based on inspection results, describe the actions they will take to correct each deficiency, assign responsibility, and set a timeline for completion.
The purpose of the Statement of Deficiencies and Plan of Correction is to ensure that healthcare facilities address and rectify compliance issues to provide safe and high-quality care to patients and to meet regulatory standards.
The information that must be reported includes the specific deficiencies identified, the corrective actions planned, the timeline for implementation, the persons responsible for the corrections, and any supporting documentation as required by the regulatory agency.
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