MR-compatible methods and systems for cardiac monitoring and gating

• US 7,054,676 B2
• Filed: 04/24/2001
• Issued: 05/30/2006
• Est. Priority Date: 04/24/2001
• Status: Expired due to Fees

• Current Assignee: Duke University
• Original Assignee: Duke University
• Inventors: Brau, Anja C. S., Johnson, G. Allan, Hedlund, Laurence W., Wheeler, Charles T.
• Primary Examiner(s): ROBINSON, DANIEL LEON
• Application Number:
  US09/840,029
• Publication Number:
  US 20020156371A1
• Time in Patent Office: 1,862 Days
• Field of Search: 600/413, 600/410, 600/407, 600/428, 600/425, 600/421, 324/307, 324/308, 324/309
• US Class Current: 600/413
• CPC Class Codes: G01R 33/5604 Microscopy; Zooming
• CPC Class Codes: G01R 33/5673 Gating or triggering based on a physiological signal other than an MR signal, e.g. ECG gating or motion monitoring using optical systems for monitoring the motion of a fiducial marker

Abstract

Noninvasive, MR-compatible methods and systems optically detect mechanical cardiac activity by anatomic (e.g., esophageal) movements. Most preferably, esophageal motion is detected optically and is indicative rhythmic cardiac activities. This esophageal motion may then be detected and used to provide a signal indicative of periods of cardiac activity and inactivity. The signal may be further processed so as to generate a trigger signal that may be input to a MR scanner. In such a manner, MR microscopy may be accomplished to acquire information at a specific phase of the cardiac cycle, for example, in synchrony with periods of cardiac inactivity. Moreover, since mechanical cardiac activity is detected and employed, instead of electrical activity as is employed in conventional techniques, the present invention is immune to electromagnetic interference during MR microscopy. As a result, robust cardiac signals may be monitored and gated during 2-dimensional and 3-dimensional in vivo microscopy. The present invention is therefore especially well suited for MR microscopy of small animals, such as laboratory mice and rats.

Claims

1. A method for detecting a phase in a cardiac cycle comprising the steps of:

(a) optically detecting movements of an anatomic structure affected by cardiac activity;

(b) deriving a cardiac signal in response to said optically detected movements which is indicative of a phase in a cardiac cycle; and

(c) generating a trigger signal in response to said derived cardiac signal which is indicative of said phase of the cardiac cycle.

2. The method of claim 1, wherein step (a) is practiced by inserting an optical fiber esophageal probe into an esophagus.

3. The method of claim 2, which comprises directing laser light onto a site within the esophagus through at least one optical fiber in the probe, and receiving reflected light from said esophagus site through at least one other optical fiber in the probe.

4. The method of claim 3, which comprises directing said reflected light to a photodetector which derives said cardiac signal therefrom.

5. The method of claim 4, which comprises receiving the derived cardiac signal from said photodetector and generating said trigger signal therefrom.

6. A method of conducting magnetic resonance (MR) microscopy comprising the steps of:

(a) optically detecting internal anatomic physical movement in response to rhythmic periods of cardiac activity and inactivity during a cardiac cycle;

(b) conducting MR microscopy during said periods of cardiac inactivity; and

(c) using the derived cardiac signal to produce cardiac images at specific phases of the cardiac cycle.

7. The method of claim 6, wherein step (a) includes deriving a cardiac signal indicative of said rhythmic periods of cardiac activity and inactivity.

8. The method of claim 7, wherein step (a) further includes generating a trigger signal in response to said derived cardiac signal of said periods of cardiac inactivity.

9. The method of claim 6, wherein step (a) includes generating a trigger signal in response to said optically detected periods of cardiac inactivity.

10. The method of claim 6, wherein step (a) is practiced by inserting an optical fiber esophageal probe into the esophagus.

11. The method of claim 10, wherein step (a) is practiced by optically detecting esophageal movements indicative of said periods of cardiac activity and inactivity.

12. The method of claim 11, comprising directing laser light onto a site within the esophagus through at least one optical fiber in the probe, and receiving reflected light from said esophagus site through at least one other optical fiber in the probe.

13. The method of claim 12, which comprises directing said reflected light to a photodetector which derives said cardiac signal therefrom.

14. The method of claim 13, which comprises processing the derived cardiac signal by receiving the derived cardiac signal from said photodetector and generating said trigger signal therefrom.

15. A magnetic resonance (MR) microscopy method comprising the steps of:

(a) inserting an optical fiber probe into a vertebrate esophagus;

(b) illuminating a site of the esophagus with light emitted by said probe;

(c) detecting reflected light from the esophagus site by a photodetector coupled optically to said probe;

(d) determining movements of the esophagus at said site indicative of rhythmic periods of cardiac activity and inactivity based on said detected reflected light and generating an output signal therefrom; and

(e) providing said output signal to a MR scanner and synchronizing MR microscopy in response to said detected periods of cardiac inactivity.

16. The method of claim 15, wherein the vertebrate esophagus is the esophagus of a laboratory animal.

17. The method of claim 16, wherein the laboratory animal is a rodent.

18. A method of conducting magnetic resonance (MR) microscopy using a MR microscopy unit, said method comprising the steps of:

(a) deriving a cardiac signal indicative of rhythmic periods of cardiac activity and inactivity by optically detecting internal anatomic physical movement in response to rhythmic periods of said cardiac activity and inactivity during a cardiac cycle;

(b) generating a trigger signal in response to said derived cardiac signal being indicative of said periods of cardiac inactivity; and

(c) operating the MR microscopy unit in response to receiving said trigger signal so that MR microscopy is conducted only during said periods of cardiac inactivity.

19. The method of claim 18, wherein step (a) is practiced by inserting an optical fiber esophageal probe into the esophagus and operating the esophageal probe to derive said cardiac signal.

20. The method of claim 19, wherein step (a) is practiced by optically detecting esophageal movements indicative of said periods of cardiac activity and inactivity.

21. The method of claim 20, comprising directing laser light onto a site within the esophagus through at least one optical fiber in the probe, and receiving reflected light from said esophagus site through at least one other optical fiber in the probe.

22. The method of claim 21, which comprises directing said reflected light to a photodetector which derives said cardiac signal therefrom.

23. The method of claim 22, which comprises processing the derived cardiac signal by receiving the derived cardiac signal from said photodetector and generating said trigger signal therefrom.