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This document outlines deficiencies found during a state licensure survey of a residential care facility and provides a plan of correction that the facility must submit to address the identified issues.
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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 identification of the facility's name, address, and contact information at the top of the form.
02
Enter the date of the survey or inspection that led to the deficiencies being reported.
03
Clearly list each deficiency found during the survey, using specific language to describe the issue.
04
For each deficiency, provide the regulatory citation or standard that has been violated.
05
Describe the plan of correction for each noted deficiency, including steps to be taken, responsible party, and timeline for completion.
06
Obtain signatures from the facility administrator and relevant staff members to confirm acknowledgment of the deficiencies and the proposed corrective actions.
07
Submit the completed Statement of Deficiencies and Plan of Correction to the appropriate regulatory agency.

Who needs STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION?

01
Healthcare facilities undergoing inspections or surveys by regulatory agencies.
02
Facilities that have received findings of non-compliance in order to address deficiencies.
03
Administrators and staff responsible for quality assurance and compliance within healthcare settings.
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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 that outlines the deficiencies identified during inspections or audits of healthcare facilities and the corrective actions that will be taken to address those deficiencies.
Healthcare facilities that are found to have deficiencies during regulatory inspections are required to file a Statement of Deficiencies and Plan of Correction with the relevant regulatory authority.
To fill out the Statement of Deficiencies and Plan of Correction, facilities should review the deficiencies identified, develop specific and actionable plans to address each deficiency, document timelines for completion, and assign responsibility for the corrective actions.
The purpose of the Statement of Deficiencies and Plan of Correction is to ensure that healthcare facilities acknowledge deficiencies, demonstrate accountability, and take appropriate steps to improve compliance with regulations and enhance patient care.
The information that must be reported includes a description of each deficiency, the specific regulatory requirements that were not met, the corrective actions planned or implemented, timelines for compliance, and the individual responsible for overseeing the correction.
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