Documented Care Template for Clinical Compliance Data Capture

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Healthcare providers face challenges in capturing and reporting comprehensive clinical data to meet complex regulatory requirements, often relying on inadequate internal systems that result in incomplete or delayed data, leading to time-consuming and error-prone manual processes.

Innovation Solution

A system and method for capturing compliance-qualified data at the point of clinical care using a documented care template that encodes necessary information, with a conditioning engine accessing compliance criteria to generate templates for contemporaneous data capture and automatic transmission to regulatory bodies.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Reliability

If retrospective review of patient accounting records is used for compliance data capture, then existing systems can be utilized, but data completeness and accuracy deteriorate due to lack of clinical detail and time delays

Engineering Contradiction:
Improvecompliance data accuracyVSAvoidtime delay in data capture
Core Design Contradiction:
ReliabilityVSLoss of time

Solution Approach 1:

The system performs preliminary action by capturing compliance-qualified data at the point of clinical care delivery, before retrospective review is needed. The documented care template is populated contemporaneously during patient care, ensuring data is ready for compliance reporting without requiring later manual review or backtracking through accounting records.

Inventive Principle:
Principle #10Preliminary action

Solution Approach 2:

The system introduces an intermediary layer - the documented care template and conditioning engine - that bridges clinical care delivery and compliance reporting. This intermediary captures and qualifies clinical data at the point of care, transforming it into compliance-qualified data without requiring direct reliance on incomplete accounting records.

Inventive Principle:
Principle #24Intermediary (Mediator)

2Reliability

If manual examination of patient charts and records is performed for compliance, then comprehensive data can be reviewed, but productivity decreases and human error increases

Engineering Contradiction:
Improvecompliance reporting accuracyVSAvoidcompliance data collection efficiency
Core Design Contradiction:
ReliabilityVSProductivity

Solution Approach 1:

The system enables self-service by automatically capturing and qualifying compliance data through the documented care template during routine clinical documentation. The conditioning engine automatically processes and qualifies data without requiring manual intervention from compliance personnel, transforming a manual review process into an automated system that serves itself.

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

The system replaces the mechanical manual review process with an automated electronic system. Instead of compliance personnel manually examining patient charts and records, the documented care template and conditioning engine automatically capture, process, and qualify data, substituting human labor with an automated information processing system.

Inventive Principle:
Principle #28Mechanics substitution (Replace mechanical system)

3Ease of manufacture

If internal patient accounting system is used for compliance data storage, then existing infrastructure is utilized, but data completeness deteriorates due to billing-focused design rather than clinical tracking

Engineering Contradiction:
Improvesystem implementation simplicityVSAvoidclinical data completeness
Core Design Contradiction:
Ease of manufactureVSLoss of information

Solution Approach 1:

The system achieves universality by making the documented care template serve multiple functions: it captures clinical data for patient care documentation, qualifies data for compliance reporting, and stores information in a structured format suitable for both clinical and regulatory purposes. This multi-functional approach eliminates the need for separate billing and compliance systems.

Inventive Principle:
Principle #6Universality (Multi-functionality)

Solution Approach 2:

The system applies parameter changes by transforming raw clinical data into compliance-qualified data through the conditioning engine. The template structure and data qualification processes modify the parameters of clinical information to meet regulatory requirements while maintaining the original clinical meaning and completeness.

Inventive Principle:
Principle #35Parameter changes

Data Source

PatentUS8751249B2System and method for capture of qualified compliance data at point of clinical care
Publication Date: 2014.06.10 CERNER INNOVATION INC
  • US8751249B2 patent drawing
  • US8751249B2 patent drawing
  • US8751249B2 patent drawing

AI summary

A system and related techniques generate and maintain a set of compliance-qualified data schemas or templates for deployment in a hospital or other clinical setting. According to conventional implementations, the clinical data required by regulatory reporting bodies such as CMS (Centers for Medicare and Medicaid Services), JCAHO (Joint Commission on Accreditation of Healthcare Organizations) or other government or private bodies may not be systematically captured or track, so that compliance officers and other managers are left to reconstruct compliance data after the face, for instance from patient accounting systems or other platforms not designed to filter or store regulatory data. Platforms and methods according to the invention, in contrast, may access regulatory or compliance criteria and generate a data capture or documented care template, according to which various clinical measures and other information which are required by compliance bodies are automatically captured, at the point of care. Thus patient labs, tests, outcomes and other clinically related data may be conditioned to include that information demanded by regulatory standards, including lab ratios and others, and that data may be automatically recorded, stored, and in embodiments, transmitted to regulatory bodies or agencies, electronically. The regulatory data store that results may likewise in embodiments be accessed by analytic tools to model various compliance and clinical scenarios.