Dose Titration Control for Obstructive Sleep Apnea Pharmacotherapy

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Solution Overview

Problem

Existing pharmacotherapy for obstructive sleep apnea faces challenges in determining optimal medicament doses over time due to changes in patient physiology and tolerance, with existing methods failing to account for individual subject responses and varying side effects.

Innovation Solution

A computer-implemented method for dose titration that adjusts medicament doses based on individual subject responses, using various monitoring signals to optimize therapeutic efficacy while minimizing side effects, incorporating oxybutynin and atomoxetine to enhance airway patency during REM and NREM sleep.

Engineering Contradictions & Design Principles

VSEngineering Contradiction Analysis

1Ease of operation

If pharmacotherapy is used to treat OSA, then treatment comfort is improved compared to CPAP, but determining optimal dose levels over time becomes difficult due to changing patient physiology and tolerance

Engineering Contradiction:
Improvetreatment comfortVSAvoiddose determination complexity
Core Design Contradiction:
Ease of operationVSDevice complexity

Solution Approach 1:

The system implements automated feedback loops where patient response data (efficacy measures and side effect measures) are continuously collected and fed back to adjust medicament dose levels. This automated feedback mechanism resolves the contradiction by eliminating the need for complex manual dose determination while maintaining treatment comfort through pharmacotherapy.

Inventive Principle:
Principle #23Feedback

Solution Approach 2:

The system enables self-service dose optimization by automatically monitoring patient responses and adjusting doses without requiring complex external intervention. The automated determination of dose titration based on collected data allows the system to self-regulate optimal dosing, reducing the burden on healthcare providers while maintaining comfort.

Inventive Principle:
Principle #25Self-service

2Ease of operation

If fixed dose levels are used, then treatment simplicity is maintained, but efficacy decreases as patients change over time in weight, sleeping position, age

Engineering Contradiction:
Improvetreatment simplicityVSAvoidtreatment efficacy
Core Design Contradiction:
Ease of operationVSReliability

Solution Approach 1:

The system transitions from static fixed dosing to dynamic dose adjustment by continuously adapting medicament levels based on changing patient physiology. The automated dose titration mechanism allows treatment to evolve with patient changes in weight, age, and sleeping position, maintaining both simplicity and reliability simultaneously.

Inventive Principle:
Principle #15Dynamics

Solution Approach 2:

The system automatically adjusts dosing parameters (medicament levels) in response to detected changes in patient parameters (weight, age, sleeping position). This dynamic parameter adjustment maintains treatment efficacy while preserving simplicity through automated adaptation rather than manual intervention.

Inventive Principle:
Principle #35Parameter changes

3Reliability

If higher medicament levels are used, then therapeutic efficacy is improved, but side effects increase requiring close monitoring

Engineering Contradiction:
Improvetherapeutic efficacyVSAvoidside effects
Core Design Contradiction:
ReliabilityVSObject-generated harmful factors

Solution Approach 1:

The system uses real-time feedback from side effect monitoring to automatically adjust medicament levels, preventing excessive dosing that would cause harmful side effects. This feedback mechanism allows the system to push therapeutic efficacy close to the optimal limit while automatically retreating when side effects appear, achieving high efficacy with minimal harm.

Inventive Principle:
Principle #23Feedback

Solution Approach 2:

The system employs a trial-and-error approach where medicament levels are temporarily increased to test efficacy thresholds, then adjusted downward when side effects manifest. This partial excessive action allows the system to explore optimal dosing boundaries while the automated monitoring ensures side effects are quickly detected and corrected.

Inventive Principle:
Principle #16Partial or excessive action

4Device complexity

If manual dose adjustment is used, then system complexity is reduced, but time consumption increases for determining optimal doses

Engineering Contradiction:
Improvesystem complexityVSAvoidtime for dose determination
Core Design Contradiction:
Device complexityVSLoss of time

Solution Approach 1:

The system replaces manual mechanical dose adjustment processes with automated electronic monitoring and calculation systems. Although this increases device complexity, it dramatically reduces time consumption by eliminating manual assessment and calculation, allowing rapid adaptation to patient changes without prolonged determination periods.

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

Solution Approach 2:

The system performs self-service dose optimization by automatically collecting data, analyzing responses, and determining optimal doses without external intervention. This automation reduces time consumption for dose determination while the standardized algorithms keep system complexity manageable.

Inventive Principle:
Principle #25Self-service

Data Source

PatentEP4222753B1Methods and systems for performing dose titration
Publication Date: 2026.04.15 KONINKLIJKE PHILIPS NV
  • EP4222753B1 patent drawingFigure 1
  • EP4222753B1 patent drawingFigure 2
  • EP4222753B1 patent drawingFigure 3A~3B

AI summary

The invention provides a computer-implemented method for controlling a dose titration of a medicament to be provided to a subject for treating obstructive sleep apnea. The method includes obtaining a dose level of a previous dose of the medicament, the previous dose having been provided to the subject and obtaining a medicament efficacy measure based on a response of the subject to the previous dose. A dose titration for a future dose of the medicament is determined based on the medicament efficacy measure and the dose level of the previous dose.