IV Fluid Container Identification System for Medication Tracking

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Solution Overview

Problem

Current systems face challenges in accurately tracking and documenting IV fluid medications, particularly in clinical settings, due to difficulties in managing residual medications and ensuring proper disposal of controlled substances, which can lead to errors and diversion issues.

Innovation Solution

An IV fluid container identification system with unique identification elements, such as labels or RFID tags, that can be applied at various stages of the medication delivery process, allowing for real-time tracking and data collection through sensors and devices, ensuring accurate documentation and disposal processes.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Measurement precision

If manual verification of residual IV fluid is performed, then accuracy of medication tracking is improved, but time consumption and workload increase

Engineering Contradiction:
Improveaccuracy of medication trackingVSAvoidtime consumption
Core Design Contradiction:
Measurement precisionVSLoss of time

Solution Approach 1:

The IV fluid container automatically reports its own residual volume through an integrated sensor system that measures the remaining fluid level and communicates this data to the medication administration record system without requiring manual verification by the caregiver

Inventive Principle:
Principle #25Self-service

Solution Approach 2:

Manual visual inspection and measurement of residual IV fluid is replaced by an automated sensor-based measurement system that electronically determines and reports the remaining fluid volume, eliminating the need for manual verification steps

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

2Reliability

If rigorous disposal procedures for controlled substances are implemented, then security against diversion is improved, but complexity of disposal process increases

Engineering Contradiction:
Improvesecurity against diversionVSAvoidcomplexity of disposal process
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The disposal process is merged with the existing medication administration documentation system, where the same sensor system that tracks medication administration also automatically documents residual fluid disposal, eliminating the need for separate complex disposal procedures

Inventive Principle:
Principle #5Merging (Combining)

Solution Approach 2:

The system provides automatic feedback and verification of disposal actions through electronic communication with the medication administration record, where the sensor-measured residual volume is automatically recorded and verified, ensuring accountability without requiring complex manual verification procedures

Inventive Principle:
Principle #23Feedback

3Productivity

If tracking of IV fluid containers is automated, then productivity of documentation is improved, but device complexity increases

Engineering Contradiction:
Improveproductivity of documentationVSAvoiddevice complexity
Core Design Contradiction:
ProductivityVSDevice complexity

Solution Approach 1:

The sensor system and electronic communication capabilities integrated into the IV fluid container serve multiple functions: tracking medication administration, monitoring residual fluid levels, verifying disposal, and maintaining medication administration records, thereby improving productivity without requiring multiple separate devices

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

Data Source

PatentUS20210042695A1Characterizing Medication Container Preparation, Use, and Disposal Within a Clinical Workflow
Publication Date: 2021.02.11 CRISI MEDICAL SYSTEMS INC
  • US20210042695A1 patent drawing
  • US20210042695A1 patent drawing
  • US20210042695A1 patent drawing

AI summary

Data characterizing a medication container (e.g., an identifier, etc.) is received from a manually administrable medication device within a clinical workflow. Thereafter, one or more data records are generated, modified, or appended to include a portion of the received data. Subsequent requests that include the medication source from remote sources are answered by transmitting data stored in the one or more data records. Related apparatus, systems, methods, and articles are also described.