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This document outlines deficiencies identified during the state licensure survey of Hinson Retirement and Care Center and provides a plan of correction for compliance with health care regulations.
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How to fill out STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION

01
Start by obtaining the STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION form from the appropriate regulatory agency.
02
Review the instructions provided with the form carefully to understand each section.
03
Identify and list the deficiencies cited during the inspection in the designated section.
04
For each deficiency, provide a detailed explanation of how it occurred and its impact on the facility.
05
Develop a specific plan of correction for each deficiency, outlining the steps that will be taken to address the issue.
06
Assign responsibilities to staff members for implementing each part of the correction plan.
07
Establish a timeline for completing the corrections and document expected completion dates.
08
Include any supporting documents or evidence that may strengthen your case, like training records or policy changes.
09
Review the completed form for accuracy and completeness before submitting it.
10
Submit the form to the regulatory agency by the deadline specified.

Who needs STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION?

01
Healthcare facilities that have undergone inspection and received citations for deficiencies.
02
Organizations seeking to demonstrate compliance with state or federal regulations.
03
Providers who need to outline corrective actions to ensure quality care and avoid penalties.
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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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A Statement of Deficiencies and Plan of Correction is a formal document that outlines the deficiencies identified during a regulatory inspection and describes the plan to rectify these issues to comply with applicable regulations.
Typically, healthcare facilities, such as nursing homes or hospitals, that have undergone a regulatory inspection and have identified deficiencies must file a Statement of Deficiencies and Plan of Correction.
To fill out a Statement of Deficiencies and Plan of Correction, a facility should first identify the specific deficiencies noted by the inspectors, then outline clear corrective actions for each deficiency, including timelines for implementation and responsible parties.
The purpose of the Statement of Deficiencies and Plan of Correction is to ensure that identified issues are addressed in a timely manner to protect the health and safety of patients and to maintain compliance with regulatory standards.
The information that must be reported includes the specific deficiencies cited, the corrective actions planned for each deficiency, timelines for corrections, and individuals responsible for implementing these actions.
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