Endoscopic Suturing Device with Suction Chamber for Permanent Tissue Joining

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Solution Overview

Problem

Current endoscopic suturing methods for reducing gastric volume, such as endoscopic plications, often result in non-permanent sutures and risk internal lesions, leading to high morbidity and treatment costs.

Innovation Solution

An endoscopic suturing device with a pressure joining mechanism that uses a tensioning element and suturing elements with a mechanical interference fit to ensure permanent tissue approximation, reducing the risk of lesions and simplifying the surgical procedure.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If conventional endoscopic plication sutures are used to reduce gastric volume, then the procedure is less invasive, but the sutures become undone in a short while and do not present permanent treatment

Engineering Contradiction:
Improveless invasive procedureVSAvoidpermanent suture result
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The closing wall is configured with an inclined surface that forms an angle between 20° and 80° with the longitudinal axis of the chamber. This curved/angled configuration allows the suction force to be applied at an optimal angle to the tissue, enhancing the approximation and pressing effect on the sutured tissues, thereby ensuring permanent merging while maintaining the less invasive endoscopic approach

Inventive Principle:
Principle #14Spheroidality (Curvature)

Solution Approach 2:

The device utilizes suction (negative pressure) applied through the closing wall to create a pressing effect on the sutured tissues. The suction force, combined with the inclined closing wall geometry, ensures continuous and effective approximation of the tissue edges, preventing suture failure and achieving permanent treatment results

Inventive Principle:
Principle #29Pneumatics and hydraulics

2Ease of operation

If conventional endoscopic plication sutures are used, then the procedure can be performed endoscopically, but internal lesions may occur leading to patient death

Engineering Contradiction:
Improveendoscopic procedureVSAvoidinternal lesions
Core Design Contradiction:
Ease of operationVSObject-affected harmful factors

Solution Approach 1:

The device incorporates a visual inspection mechanism through the endoscope that allows real-time monitoring of the suturing process and tissue approximation. The operator can observe the tissue handling and adjust the suction force or suture placement to prevent excessive tension or damage, thereby reducing the risk of internal lesions while maintaining the endoscopic approach

Inventive Principle:
Principle #23Feedback

Solution Approach 2:

The device allows controlled adjustment of suction parameters (pressure level) and suture tension to optimize tissue approximation without causing damage. By dynamically adjusting these parameters, the procedure achieves effective suturing while minimizing the risk of internal lesions and complications

Inventive Principle:
Principle #35Parameter changes

3Volume of moving object

If conventional endoscopic plication sutures are used, then the procedure can reduce intragastric volume, but the sutures do not present sufficient approximation under pressure

Engineering Contradiction:
Improveintragastric volume reductionVSAvoidapproximation under pressure
Core Design Contradiction:
Volume of moving objectVSStrength

Solution Approach 1:

The inclined closing wall configured at 20°-80° creates an optimized force transmission path from the suction source to the tissue. This angular geometry ensures that the suction force is effectively converted into radial pressing action on the sutured tissues, achieving sufficient approximation and strong holding effect to maintain intragastric volume reduction

Inventive Principle:
Principle #14Spheroidality (Curvature)

Solution Approach 2:

The device employs controlled suction (negative pressure) that is transmitted through the closing wall to the sutured tissues. This pneumatic force, combined with the mechanical suture structure, provides sufficient approximation strength to maintain effective intragastric volume reduction without requiring excessive mechanical force that could cause tissue damage

Inventive Principle:
Principle #29Pneumatics and hydraulics

Applied Scientific Principles

This section explains which scientific principles are used to turn an abstract innovation direction into a practical engineering solution.

Function Achieved in This Case

The device achieves permanent tissue merging under pressure, reducing morbidity and treatment costs by ensuring stable and long-lasting sutures, while minimizing the risk of internal lesions during endoscopic procedures.

Implementation Method 1

a suction system connected to said chamber so as to be able to create negative pressure inside said chamber

Methodology Applied
Scientific EffectNegative pressure (suction): Vacuum

Implementation Method 2

an elongated tubular element which extends as from a tensioning element associated to an elongated tensionable suturing element

Methodology Applied
Scientific EffectMechanical force (tension): Mechanical Force

Data Source

PatentUS20240090896A1Endoscopic suturing device and endoscopic suction and suturing chamber
Publication Date: 2024.03.21 SOC BENEFICENTE DE SENHORAS HOSPITAL SIRIO LIBANES
  • US20240090896A1 patent drawing
  • US20240090896A1 patent drawing
  • US20240090896A1 patent drawing

AI summary

The present invention refers to an endoscopic suturing device and to an endoscopic suction and suturing chamber for joining tissues which offers effective and permanent result in therapeutic processes, in addition to the reduction in morbidity and in the costs involved in the surgical procedures. The endoscopic suturing device (10) comprises an elongated tubular element (20) which extends from a tensioning element (30) associable with an elongated tensionable suturing element (40) comprising proximal end (41) and distal end (42), the proximal end (41) comprising suturing elements (50, 51) so that the distal end (42) enters the receptacle (21) for fastening to the tension point (31), and the suturing elements (50, 51) are delimited by the limiting region (22) and rigidly joined to each other when the tensioning element (30) is activated.