Method of evaluating gastroparesis using an ingestible capsule

• US 20080287833A1
• Filed: 09/06/2007
• Published: 11/20/2008
• Est. Priority Date: 05/16/2007
• Status: Abandoned Application

• Current Assignee: The Smartpill Corporation (Medtronic Plc)
• Original Assignee: The Smartpill Corporation (Medtronic Plc)
• Inventors: Semler, John R., Kuo, Braden
• Application Number:
  US11/899,540
• Publication Number:
  US 20080287833A1
• Time in Patent Office: Days
• US Class Current: 600/593
• CPC Class Codes: A61B 5/037 Measuring oesophageal pressure
• CPC Class Codes: A61B 5/073 Intestinal transmitters
• CPC Class Codes: A61B 5/14539 for measuring pH
• CPC Class Codes: A61B 5/42 Detecting, measuring or recording for evaluating the gastrointestinal, the endocrine or the exocrine systems A61B1/00, A61B5/4857, A61B5/486, A61B5/4866, A61B5/4869 take precedence

Abstract

A method of evaluating gastroparesis comprising the steps of providing an ingestible capsule having a pH sensor and a pressure sensor, having a subject ingest the capsule, recording pH measurements from the pH sensor as a function of time as the capsule moves through at least a portion of the gastrointestinal tract of the subject, recording pressure measurements from the pressure sensor as a function of time as the capsule moves through at least a portion of the gastrointestinal tract of the subject, determining the capsule'"'"'s location at a first position in the gastrointestinal tract, deriving a pressure pattern as a function of time and the pressure measurements, providing a reference pressure pattern, and analyzing the subject'"'"'s pressure pattern relative to the reference pressure pattern to evaluate the subject with respect to gastroparesis. The location may be the junction between the stomach and the small bowel of the subject. The pressure pattern may be the number of contractions relative to a baseline over a given time interval or area under the curve of pressure measurements over a given time interval.

Claims

1. A method of evaluating gastroparesis comprising the steps of:

providing an ingestible capsule having a pH sensor and a pressure sensor;

having a subject ingest said capsule;

recording pH measurements from said pH sensor as a function of time as said capsule moves through at least a portion of the gastrointestinal tract of said subject;

recording pressure measurements from said pressure sensor as a function of time as said capsule moves through at least a portion of said gastrointestinal tract of said subject;

determining said capsules location at a position in said gastrointestinal tract;

deriving a pressure pattern as a function of time and said pressure measurements;

providing a reference pressure pattern; and

analyzing said subject'"'"'s pressure pattern relative to said reference pressure pattern to evaluate said subject with respect to gastroparesis.

2. The method set forth in claim 1, wherein said position is the junction between the stomach and the small bowel of said subject.

3. The method set forth in claim 1, wherein said pressure pattern is the number of contractions relative to a baseline for a given time interval.

4. The method set forth in claim 1, wherein said pressure pattern is the area under the curve of said pressure measurements for a given time interval.

5. The method set forth in claim 1, wherein said pressure pattern is amplitude.

6. The method set forth in claim 1, wherein said step of evaluating said subject comprises diagnosing gastroparesis.

7. The method set forth in claim 3, wherein said step of analyzing said pressure pattern comprises the step of determining if said subject'"'"'s pressure pattern is significantly lower than said reference pressure pattern, wherein said reference pressure pattern is derived from a healthy control group.

8. The method set forth in claim 7, wherein said subject'"'"'s pressure pattern is at least ten percent less than said reference pressure pattern.

9. The method set forth in claim 1, wherein said time is the time said capsule resides in the stomach of said subject.

10. The method set forth in claim 1, wherein said time extends from about one hour before said capsules is determined to be at said position to about the time said capsule is determined to be at said position.

11. The method set forth in claim 1, wherein said step of analyzing said subject'"'"'s pressure pattern relative to said reference pressure pattern to evaluate said subject with respect to gastroparesis comprises the step of comparing said subject'"'"'s pressure pattern to said reference pressure pattern for three consecutive twenty minute intervals before and after said capsule is determined to be at said position.

12. The method set forth in claim 1, and further comprising the steps of determining the transit time between a first location and a second location, and evaluating said transit time relative to a reference transit time.

13. The method set forth in claim 12, wherein said first location is the point at which said capsule is ingestible by said subject and said second location is the junction between the stomach and the small bowel of said subject.

14. The method set forth in claim 13, wherein said step of evaluating said transit time relative to a reference transit time comprises the step of determining whether said transit time is greater than or less than said reference transit time.

15. The method set forth in claim 14, wherein said reference said transit time is about 5 hours.

16. The method set forth in claim 1, wherein said step of deriving a pressure pattern as a function of time and said pressure measurements comprises the step of conditioning said recorded pressure measurements.

17. The method set forth in claim 16, wherein said conditioning comprises the step of normalizing said data points by applying a baseline compensation.

18. The method set forth in claim 17, wherein said baseline is about 3 mmHg.

19. The method set forth in claim 16, wherein said conditioning comprises the steps of filtering out data points in said pressure measurements above an upper limit and filtering out data points in said pressure measurements below a lower limit.

20. The method set forth in claim 17, wherein said upper limit is about 200 mmHg and said lower limit is about 9 mmHg.

21. The method set forth in claim 1, and further comprising the steps of deriving a pH pattern as a function of time and said pH measurements and analyzing said pH pattern for said subject and said pressure pattern for said subject relative to a pH reference pattern and a pressure reference pattern to determine said capsule'"'"'s location at a second position.

22. The method set forth in claim 21, and further comprising the steps of determining transit time between said first position and said second position, and evaluating said transit time relative to a reference transit time.

23. The method set forth in claim 22, wherein said first position is a junction between the stomach and the small bowel of said gastrointestinal tract of said subject and said second position is a junction between the ileum and the caecum of said gastrointestinal tract of said subject.

24. The method set forth in claim 22, wherein said first position is the junction between the ileum and the caecum of said gastrointestinal tract of said subject and said second position is the point at which said capsule is discharged from said gastrointestinal tract of said subject.

25. The method set forth in claim 1, and further comprising the steps of:

deriving a second pressure pattern different from said first pressure pattern as a function of time and said pressure measurements;

providing a second reference pressure pattern; and

analyzing said second pressure pattern variations for said subject relative to said second reference in determining said capsule'"'"'s location at said position.

26. The method set forth in claim 25, wherein said first pressure pattern is frequency of contractions relative to a baseline over a given time interval and said second pressure pattern is motility index.

27. The method set forth in claim 21, and further comprising the steps of:

deriving a second pressure pattern different from said first pressure pattern as a function of time and said pressure measurements;

providing a second reference pressure pattern; and

analyzing said second pressure pattern variations for said subject relative to said second reference in determining said capsule'"'"'s location at said second position.

28. The method set forth in claim 27, wherein said first pressure pattern is frequency of contractions and said second pressure pattern is motility index.

29. The method set forth in claim 1, wherein said step of determining said capsules location at a position in said gastrointestinal tract comprises the steps of:

providing a reference pH;

analyzing said pH measurements for said subject relative to said reference pH to determine said capsule'"'"'s location at said position.

30. The method set forth in claim 1, wherein said step of analyzing said pressure pattern comprises the step of determining if said subject'"'"'s pressure pattern is substantially similar to said reference pressure pattern, wherein said reference pressure pattern is derived from a gastroparetic control group.

31. A method of evaluating gastroparesis comprising the steps of:

providing an ingestible capsule having a pH sensor;

having a subject ingest said capsule;

recording pH measurements from said pH sensor as a function of time as said capsule moves through at least a portion of the gastrointestinal tract of said subject;

determining said capsules position at a junction between the stomach and the small bowel of said subject as a function of said pH measurements;

determining a transit time of said capsule between the time said capsule is ingested by said subject and the time said capsule is determined to be at said position;

providing a reference transit time; and

evaluating said transit time relative to said reference transit time.

32. The method set forth in claim 31, and further comprising having said subject ingest a low fat meal with said ingestion of said capsule.

33. The method set forth in claim 31, wherein said step of evaluating said transit time relative to said reference transit time comprises the step of determining whether said transit time is greater than or less than said reference transit time.

34. The method set forth in claim 31, wherein said reference transit time is about 5 hours.