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This document outlines the results of a survey conducted by the Centers for Medicare & Medicaid Services regarding deficiencies at the Cleveland Pines Nursing Center, along with a plan of correction.
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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
Start with the facility name and date at the top of the form.
02
List the specific deficiencies found during the survey process in the designated section.
03
For each deficiency, provide a detailed description of the issue, including the regulation that it violates.
04
Develop a plan of correction for each deficiency, detailing the steps that will be taken to address the issue.
05
Assign responsibilities to specific staff members for implementing the plan of correction.
06
Include a timeline for completing each step of the plan.
07
Review the completed statement for accuracy, clarity, and comprehensiveness.
08
Have the statement signed and dated by the appropriate authority within the facility.

Who needs STATEMENT OF DEFICIENCIES AND PLAN OF CORRECTION?

01
Healthcare facilities that have received deficiencies during inspections or surveys.
02
Organizations seeking to improve compliance with regulations.
03
Facility management and staff responsible for quality assurance and regulatory compliance.
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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 identify areas of non-compliance with regulatory standards and to outline the specific actions they will take to rectify these deficiencies.
Healthcare facilities such as hospitals, nursing homes, and other long-term care organizations that receive regulatory inspections or surveys 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 review the cited deficiencies, develop a corrective action plan for each deficiency, assign responsible parties, set timelines for completion, and ensure that the plan addresses how the deficiencies will be corrected.
The purpose of the Statement of Deficiencies and Plan of Correction is to assure regulatory bodies that the facility is aware of its deficiencies and is taking actionable steps to correct them, thereby improving the quality of care provided to patients.
The Statement of Deficiencies and Plan of Correction must report specific information including the nature of each deficiency, the regulatory standard violated, the plan to correct each deficiency, responsible persons, timelines for completion, and any follow-up actions required to ensure compliance.
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