METHODS, SYSTEMS AND COMPUTER-READABLE PRODUCTS FOR OPTIMIZING AEROSOL PARTICLE ADMINISTRATION TO THE LUNGS

• US 20090178672A1
• Filed: 12/04/2008
• Published: 07/16/2009
• Est. Priority Date: 12/05/2007
• Status: Abandoned Application

• Current Assignee: Activaero GmbH
• Original Assignee: Activaero GmbH
• Inventors: Kroneberg, Philipp, Wencker, Marion, Mullinger, Bernhard
• Application Number:
  US12/327,940
• Publication Number:
  US 20090178672A1
• Time in Patent Office: Days
• US Class Current: 128/200.140
• CPC Class Codes: A61M 11/005 using ultrasonics spraying or atomising liquids using ultrasonic vibrations in general B05B17/06
• CPC Class Codes: A61M 15/00 Inhalators drug delivery in endotracheal tubes A61M16/04
• CPC Class Codes: A61M 16/107 in the inspiratory path
• CPC Class Codes: A61M 2016/0027 pressure meter
• CPC Class Codes: A61M 2205/52 with memories providing a history of measured variating parameters of apparatus or patient
• CPC Class Codes: A61M 2209/084 Supporting bases, stands for equipment

Abstract

The present invention is directed to methods, systems and computer-readable products for optimizing aerosol particle administration to the lungs. More specifically, the present invention relates to methods of tailoring inhaling maneuvers for aerosol particle administration using the subject'"'"'s lung function data and to systems and computer-readable products carrying out such methods.

Claims

1. A method for determining aerosol particle administration to the lungs, the method comprising:

deriving aerosol parameters for an inhalation system based on at least one measured pulmonary function parameter to thereby adapt the aerosol particle administration to a subject'"'"'s lung function.

2. The method of claim 1, further comprising measuring at least one pulmonary function parameter of the subject.

3. The method of claim 1, wherein, when the pulmonary function parameter is a measure of an inspiratory function, the deriving aerosol parameters step comprises:

comparing the value of the pulmonary function parameter with predetermined ranges for prespecified aerosol parameter groups, each aerosol parameter group having predefined aerosol parameters; and

selecting a prespecified aerosol parameter group based on the comparison of the value of the pulmonary function parameters with the predetermined ranges.

4. The method of claim 1, wherein, when the pulmonary function parameter is a measure of an expiratory function, said deriving aerosol parameters step comprises:

selecting a corrective coefficient using the measured expiratory function from among a plurality of corrective coefficients derived from a standard;

multiplying the measured expiratory function by the corrective coefficient to obtain a corrected pulmonary function parameter value;

comparing the corrected pulmonary function parameter value with predetermined ranges for prespecified aerosol parameter groups, each aerosol parameter group having predefined aerosol parameters; and

selecting a prespecified aerosol parameter group based on the comparison of the corrected pulmonary function parameter value with the predetermined ranges.

5. The method of claim 4, wherein the corrective coefficient is based on a severity grade of the subject'"'"'s lung disease.

6. The method of claim 1, wherein the pulmonary function parameter is maximum expiratory flow, forced expiratory flow, forced expiratory vital capacity or forced expiratory volume, or forced expiratory volume per second.

7. The method of claim 2, wherein the pulmonary function parameter is maximum expiratory flow, forced expiratory flow, forced expiratory vital capacity, or forced expiratory volume, or forced expiratory volume per second.

8. The method of claim 4, wherein the pulmonary function parameter is maximum expiratory flow, forced expiratory flow, forced expiratory vital capacity, or forced expiratory volume, or forced expiratory volume per second.

9. The method of claim 5, wherein the pulmonary function parameter is maximum expiratory flow, forced expiratory flow, forced expiratory vital capacity, forced expiratory volume, or forced expiratory volume per second.

10. A computer readable medium comprising encoding means for implementing the method of claim 1.

12. The system of claim 11, wherein the controller uses encoding means causing the system to implement the method of claim 1.

13. The system of claim 11, wherein the system comprises a reader for reading the computer readable medium of claim 10 or for reading a memory means having a subject'"'"'s individual data and aerosol parameters stored thereon, wherein the controller has a memory for storing the subject'"'"'s individual data and aerosol parameters.

17. The method of claim 3, wherein the inspiratory function is inspiratory capacity.

11. An inhalation system for administering aerosol particles to the lungs comprising:

a controller for adapting aerosol parameters for the inhalation system based on at least one measured pulmonary function parameter.

14. The system of claim 11, further comprising a monitor for measuring at least one pulmonary function parameter of a subject.

15. The system of claim 11, wherein the aerosol parameters comprise inspiratory volume of aerosol particles, inspiratory volume of aerosol-free particles, inspiratory flow rate, inspiratory timing of inspiratory flow of aerosol particles, or inspiratory timing of inspiratory flow of aerosol-free particles.

16. The system of claim 11, wherein the system is a portable, hand-held inhalation device.