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This document outlines the deficiencies cited during a health survey of Surgicare Surgical Associates of Englewood Cliffs by the New Jersey Department of Health & Senior Services, including regulations
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How to fill out Statement of Deficiencies

01
Review the template provided for the Statement of Deficiencies.
02
Gather all necessary documentation and evidence related to the deficiencies.
03
Clearly identify each deficiency with a specific reference according to the relevant standards.
04
Provide detailed descriptions of each deficiency, including the impact and context.
05
Include corrective actions taken or planned to rectify each identified deficiency.
06
Ensure that all information is clear, concise, and free of jargon.
07
Double-check for accuracy and completeness before submission.

Who needs Statement of Deficiencies?

01
Organizations or facilities undergoing regulatory inspections.
02
Healthcare providers requiring compliance documentation.
03
Administrators needing to address areas of concern in their operations.
04
Quality assurance teams looking to improve service delivery.
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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.
The CMS-2567 form is used for reporting deficiencies identified during health care facility surveys. It provides a detailed account of compliance issues and corrective action plans. This form is essential for facilities seeking to maintain accreditation and compliance with federal and state regulations.
A deficiency citation consists of (a) a regulatory reference, (b) a statement of deficient practice, and (c) relevant findings.
Deficiency citation or "cited deficiency" means written docu- mentation by the department that describes a nursing home's deficien- cy(ies); the requirement that the deficiency(ies) violates; and the reasons for the determination of noncompliance.
The deficient practice statement indicates the part of the requirement that is not met. It summarizes the issues that demonstrate the agency's actions or failures to act that resulted in noncompliance with the requirement. It also indicates the extent of the deficient practice.
Deficiency Citation: an entry made on the Form CMS-2567 that includes: 1) the alpha prefix and data tag number (D-Tag), 2) the Code of Federal Regulations (CFR), 3) the language from the reference which pinpoints the aspect(s) of the requirement with which the laboratory failed to comply, 4) an explicit statement that
Elements to include: Author of paper. Year of publication (in round brackets) Title of paper (in single quotation marks) Title of conference proceedings: subtitle (in italics) Location and date of conference. Place of publication: Publisher. Page references for the paper.
The statement of deficient entity practice includes: (1) the specific action(s), error(s), lack of action (deficient practice); (2) when possible, resultant outcome(s) relative to the deficient practice; (3) a description of the extent of the deficient practice or the number of deficient cases relative to the total

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A Statement of Deficiencies is a formal document that outlines non-compliance or deficiencies identified during inspections or audits, often related to healthcare facilities or programs.
Organizations and facilities that participate in federal healthcare programs, such as nursing homes or hospitals, are required to file a Statement of Deficiencies when non-compliance is found.
To fill out a Statement of Deficiencies, one must provide detailed descriptions of the deficiencies, reference the regulatory standards violated, and include any corrective actions taken or planned.
The purpose of a Statement of Deficiencies is to document compliance issues, inform the involved parties, ensure corrective actions are taken, and protect the safety and well-being of individuals receiving care.
The information that must be reported includes the date of the inspection, specific regulatory citations, detailed descriptions of the deficiencies, the time frame for compliance, and any corrective action plans.
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