Syringe Pump Pressure Sensor Assembly for Adaptive Infusion

Resolve Bottlenecks,
Find Innovative Solutions
Generate Solutions

Solution Overview

Problem

Syringe pumps used in medical applications face challenges in accurately delivering fluids over extended periods and adapting to different syringe sizes, with existing systems lacking efficient pressure monitoring and interchangeable pump assembly capabilities.

Innovation Solution

A syringe pump design featuring a housing with a motor, gearbox, pressure sensor, and interchangeable pump assemblies that can convert between syringe and peristaltic pumps, including a sliding block assembly with a cam mechanism for engaging and disengaging with a lead screw, and a clamping mechanism for various plunger flange sizes, along with redundant sensors for fail-safe operation.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Adaptability or versatility

If a syringe pump uses a fixed pump assembly design, then the structure is simple, but it cannot adapt to different syringe sizes or convert to peristaltic pump mode

Engineering Contradiction:
Improveadaptability to different syringe sizesVSAvoidpump assembly structure
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The pump assembly is designed with movable and adjustable components, including a sliding block assembly with cam mechanism that can be repositioned along the lead screw, and a clamping mechanism that can adjust to different plunger flange sizes. This dynamic design allows the same pump assembly to accommodate various syringe dimensions while maintaining structural integrity.

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The pump assembly is designed to perform multiple functions: it can operate with different syringe sizes using the adjustable clamping mechanism, and can be converted between syringe pump mode and peristaltic pump mode by repositioning the sliding block and cam mechanism. This multi-functional design eliminates the need for separate pump assemblies for different applications.

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

2Adaptability or versatility

If the syringe pump includes interchangeable pump assembly capabilities, then versatility is improved, but device complexity increases

Engineering Contradiction:
Improveinterchangeable pump assembly capabilitiesVSAvoidassembly interchangeability
Core Design Contradiction:
Adaptability or versatilityVSDevice complexity

Solution Approach 1:

The pump system is divided into modular components: a base pump unit and interchangeable pump assemblies. The pump assembly can be removed and replaced by detaching it from the base, allowing users to switch between different pump configurations (syringe pump, peristaltic pump) without redesigning the entire system. This segmentation reduces overall complexity by standardizing the interface between modules.

Inventive Principle:
Principle #1Segmentation

Solution Approach 2:

The pump assembly incorporates dynamic elements such as the sliding block assembly that can move along the lead screw and the cam mechanism that can be repositioned. These dynamic features enable the assembly to adapt to different operating modes and syringe sizes, making the interchangeability practical and versatile without requiring completely different rigid structures for each mode.

Inventive Principle:
Principle #15Dynamics

3Measurement precision

If the syringe pump lacks pressure monitoring, then the device is simpler, but fluid delivery accuracy over extended periods deteriorates

Engineering Contradiction:
Improvepressure monitoringVSAvoidsensor assembly
Core Design Contradiction:
Measurement precisionVSDevice complexity

Solution Approach 1:

The pressure sensor provides real-time feedback on the pressure within the syringe barrel during fluid delivery. The controller monitors this pressure data and can adjust the motor speed and plunger actuation to maintain accurate flow rates, compensate for occlusions, and ensure precise delivery over extended periods. This feedback loop significantly improves measurement precision and delivery accuracy.

Inventive Principle:
Principle #23Feedback

Solution Approach 2:

The patent replaces complex mechanical pressure indication systems with an electronic pressure sensor and digital control system. Instead of using mechanical gauges or pressure-sensitive mechanical components, the system uses an electronic sensor that integrates with the controller to provide precise, real-time pressure monitoring and automated adjustments, reducing mechanical complexity while improving precision.

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

4Reliability

If the syringe pump uses redundant sensors, then reliability is improved, but device complexity increases

Engineering Contradiction:
Improvefail-safe operationVSAvoidsensor redundancy
Core Design Contradiction:
ReliabilityVSDevice complexity

Solution Approach 1:

The system incorporates redundant sensors (such as multiple position sensors or pressure sensors) that serve as backup measurements before failure occurs. If one sensor provides erroneous data or fails, the controller can detect the discrepancy through cross-validation and switch to using data from the redundant sensor, ensuring continuous reliable operation without interruption to fluid delivery.

Inventive Principle:
Principle #11Beforehand cushioning (Prior cushioning)

Data Source

PatentUS10391241B2Syringe pump having a pressure sensor assembly
Publication Date: 2019.08.27 DEKA PRODUCTS LP
  • US10391241B2 patent drawing
  • US10391241B2 patent drawing
  • US10391241B2 patent drawing

AI summary

A syringe pump is disclosed that includes a body, a syringe seat, a syringe actuator, a memory, and one or more processors. The syringe seat is coupled to the body. The syringe actuator is configured to actuate a syringe secured within the syringe seat. The memory is configured to store a plurality of instructions. The one or more processors, in accordance with the plurality of instructions, is/are configured to: prime the syringe pump in a prime phase; determine if an occlusion exists during the prime phase using a first test; stop the prime phase; initiate fluid delivery into a patient; enter into a start-up phase; determine if an occlusion exists using a second test during the start-up phase; transition from the start-up phase into a steady-state phase; and determine if an occlusion exists during the steady-state phase using a third test.