Portable automated blood pressure monitoring apparatus and method

• US 4,889,132 A
• Filed: 09/26/1986
• Issued: 12/26/1989
• Est. Priority Date: 09/26/1986
• Status: Expired due to Term

• Current Assignee: University of North Carolina At Chapel Hill (University of North Carolina System)
• Original Assignee: University of North Carolina At Chapel Hill (University of North Carolina System)
• Inventors: Flaugher, David J., Watts, Charles E., Obrist, Paul A., Hutcheson, J. Stanford, Lutz, Richard W.
• Primary Examiner(s): JAWORSKI, FRANCIS J
• Application Number:
  US06/913,677
• Time in Patent Office: 1,187 Days
• Field of Search: 128/680-683, 128/630, 128/663, 128/666-668
• US Class Current: 600/493
• CPC Class Codes: A61B 5/02208 using the Korotkoff method

Abstract

A portable auscultatory blood pressure and heart rate measurement system is wearable by an ambulatory patient and measures systolic and diastolic pressure upon request or at random time intervals within a user-programmed range. Cuff inflation pressure and deflation rate are also user programmable. During cuff deflation, pressure and korotkoff sound signal amplitudes are obtained and stored in timed relation to the user'"'"'s ECG, a threshold level is derived from pressure signal amplitudes and system noise level, and systolic and diastolic pressure determined and validated by trend analysis in relation to this threshold level. Analysis results are stored along with a sample number and time of measurement under on-board digital signal processor control, in both a solid state memory and an analog serial data storage medium such as magnetic tape. Data may be retrieved by local display, for example, in a biofeedback setting, or display on an external video display or printer, or can be downloaded in digital form to a local or remote digital computer.

Claims

1. A method for automatically measuring at least one cardiovascular parameter of a subject, comprising the steps of:

(1) producing a random value;

(2) converting the random value produced in said producing step to a time duration;

(3) timing said time duration;

(4) when said time duration timed by said timing step (3) has elapsed, measuring and storing at least one cardiovascular parameter of the subject; and

(5) repeating said producing step (1), converting step (2), timing step (3), and measuring and storing step (4) to obtain a series of measurements of said at least one parameter.

2. A method as in claim 1 wherein:

said method further includes the steps, performed after said producing step (1) and before said converting step (2), of;

determining whether the random value produced by said producing step (1) falls within a predetermined range, and

repeating said producing step (1) and said determining step if the random value is not within said predetermined range; and

said converting step (2) converts into time durations only random values determined by said determining step to fall within said predetermined

3. A method as in claim 2 further including the preliminary step of programming said predetermined range.

4. A method as in claim 1 wherein said measuring and storing step (4) includes the steps of:

inflating an occluding cuff worn by said subject to a pressure in excess of the systolic blood pressure of said subject;

continuously sensing the pressure of said cuff;

controllably deflating said cuff;

sensing Korotkoff sounds produced by said subject during said deflating step;

storing indicia of said sensed sounds and pressure in analog form on an analog serial storage device;

producing digital signals representing said cardiovascular at least one parameter of said subject in response to said pressure sensed by said cuff pressure sensing step and said sounds sensed by said Korotkoff sounds sensing step; and

storing said digital signals representing said cardiovascular at least one parameter in digital form in a solid state memory device.

5. A method of automatically measuring the blood pressure of a subject comprising the steps of:

(1) inflating an occluding cuff disposed on said subject to a first predetermined pressure;

(2) deflating said cuff at a controlled rate until the pressure within said cuff falls to a second predetermined pressure less than said first pressure;

(3) during said deflating step (2), sensing the pressure within said cuff;

(4) during said deflating step (2), sensing the amplitude level of sounds generated by said subject as a result of said cuff deflation;

(5) during said deflating step (2), periodically storing levels representing said sensed pressures and sensed sound amplitude levels; and

(6) after said deflating step (2), selecting, in response to said stored sensed sound amplitude levels, the stored pressure levels indicating the systolic and diastolic blood pressures of said subject, said selecting step including the steps of;

(a) determining the time of occurrence of a predetermined number of stored sound amplitude levels measured consecutively in time which have the highest mean level, said time of occurrence being the time of the center of maximum Korotkoff sound activity;

(b) determining the stored sound amplitude level measured latest in time before said time of the center of maximum Korotkoff sound activity which is less than a predetermined threshold level;

(c) selecting as the systolic blood pressure of said subject the stored pressure level measured simultaneously with said stored sound amplitude level determined by said determining step (b);

(d) determining the stored sound amplitude level measured earliest in time after said time of the center of maximum Korotkoff sound activity which is less than said predetermined threshold level; and

(e) selecting as the diastolic blood pressure of the subject the stored pressure level measured simultaneously with said stored sound amplitude level determined by said determining step (d).

6. A method as in claim 5 wherein:

said sensing step (4) includes the steps of;

(a) sensing R-waves produced by the brain of said subject,

(b) continuously measuring the amplitude level of sound produced by said subject, and

(c) determining the sensed peak sound amplitude level occurring between each pair of adjacent R-waves sensed by said sensing step (a); and

said storing step (5) includes the step of storing each of said sensed peak amplitude levels determined by determining step (c) together with the pressure sensed by sensing step (3) occurring simultaneously with said each sensed peak amplitude levels.

7. A method as in claim 5 wherein:

said sensing step (4) includes the steps of;

detecting sounds generated by said subject as a result of deflation of said cuff, and

amplifying the sound detected by said detecting step by a predetermined gain to produce a signal indicating the amplitude level of said sounds; and

said method further includes the step of dynamically adjusting said gain in response to said highest mean level determined by said determining step (a).

8. A method as in claim 5 further including the steps of:

(a1) calculating the mean value of all of said sound amplitude levels stored by said storing step (5);

(a2) calculating the mean value of all of said stored amplitude levels stored by said storing step (5) which are less than the mean value calculated by said calculating step (a1); and

(a3) setting said predetermined threshold level to a value between said mean value calculated by said calculating step (a1) and the mean value calculated by said calculating step (a2).

9. A method as in claim 8 wherein said setting step (a3) comprises the step of setting said predetermined threshold level to be half of the sum of said mean value calculated by said calculating step (a1) and the mean value calculated by said calculating step (a2) to which the mean value calculated by said calculating step (a2) has been added.

10. A method as in claim 5 wherein:

said determining step (b) also determines whether at least one stored sound amplitude level measured immediately before said sound amplitude level measured latest in time before said time of the center of maximum Korotkoff sound activity which is less than said predetermined threshold level is also less than said threshold level; and

said determining step (d) also determines whether at least one stored sound amplitude level measured immediately after said stored sound amplitude level measured earliest in time after said time of the center of maximum Korotkoff sound activity which is less than said predetermined threshold level is also less than said threshold level.

11. A method as in claim 10 further including the steps of verifying that the cuff pressures associated with the respective stored sound amplitude levels determined in determining steps (b) and (d) are substantially at expected pressure values derived from said controlled rate of cuff deflation.

12. A method of automatically measuring the systolic and diastolic blood pressures of a subject, comprising the steps of:

(1) disposing an occluding cuff, a sound transducer and ECG electrodes on a subject;

(2) inflating the cuff to a pressure greater than the systolic blood pressure of said subject;

(3) linearly deflating said cuff at a controlled rate until the pressure within said cuff falls to less than the diastolic blood pressure of said subject;

(4) during said deflating step (3), continuously producing a first signal indicating the amplitude of sound detected by said sound transducer;

(5) during said deflating step (3), continuously producing a second signal indicating the pressure within said cuff;

(6) detecting the onset of each cardiac cycle of said subject in response to signals generated by said ECG electrodes;

(7) for each cardiac cycle detected by said detecting step (6) during deflation of said cuff, detecting the peak level PKS of said first signal;

(8) for each cardiac cycle detected by said detecting step (6) during deflation of said cuff, detecting the level PRE of said second signal at the time said peak level PKS is detected by said detecting step (7);

(9) for each cardiac cycle detected by said detecting step (6) during deflation of said cuff, storing said peak level PKS detected by said detecting step (7) and said level PRE detected by said detecting step (8);

(10) determining, in response to said stored peak levels PKS, a predetermined number of consecutive cardiac cycles generating the highest average peak level of said first signal;

(11) calculating the mean value AKSN of all of said peak levels PKS stored by said storing step (9);

(12) calculating the mean value ANOISE of all of said peak levels PKS stored by said storing step (9) which are less than said mean value AKSN calculated by said calculating step (11);

(13) calculating a threshold level ##EQU3## (14) determining the stored peak level PKS measured for last cardiac cycle occurring before the center one of said predetermined number of consecutive cardiac cycles determined by said determining step (10) which is less than K-THRESHOLD;

(15) selecting said level PRE stored by said storing step (9) for said last cardiac cycle determined by said determining step (14) as the systolic blood pressure of said subject;

(16) determining the stored peak level PKS measured for the first cardiac cycle occurring after the center one of said predetermined number of consecutive cardiac cycles determined by said determining step (10) which is less than K-THRESHOLD; and

(17) selecting said level PRE stored by said storing step (9) for said first cardiac cycle determined by said determining step (16) as the diastolic blood pressure of said subject.

13. A system for automatically measuring at least one cardiovascular parameter of a subject comprising:

means for producing a random value and for converting said random value to a time duration;

means for timing said at least one time duration;

means for measuring at least one cardiovascular parameter of a subject hen said duration timed by said timing means has elapsed;

means for storing said parameter measured by said measuring means; and

automatic sequencing means operatively connected to said random value producing and converting means, timing means, measuring means and storing means, for repeatedly causing, in sequence, (1) said random value producing and converting means to produce a random value and convert said random value to a time duration, (2) said timing means to time said time duration, (3) said measuring means to measure said cardiovascular at least one parameter after said time duration timed by said timing means has elapsed, and (4) said storing means to store said parameter produced by said producing means, to obtain a series of measurements of said at least one parameter.

14. A system as in claim 13 wherein:

said sequencing means also determines whether random values produced by said random value producing and converting means fall within a predetermined range, and controls said random value producing and converting means to produce an additional random value when a produced random value is not within said predetermined range.

15. A system as in claim 14 further including means for programming said predetermined range.

16. A system as in claim 13 wherein:

said measuring means includes;

an occluding cuff disposed on said subject,

means for selectively inflating said occluding cuff to a pressure in excess of the systolic blood pressure of said subject,

means for continuously sensing the pressure of said cuff;

means for controllably deflating said cuff; and

means for sensing Korotkoff sounds produced by said subject; and

said system further includes;

serial storing means for storing analog indicia of said sensed sounds and pressure,

means for producing digital signals representing the cardiovascular at least one parameter of said subject in response to the cuff pressure sensed by said pressure means and the Korotkoff sounds sensed by said sound sensing means, and

solid state memory means for storing said digital signals representing said cardiovascular at least one parameter.

17. A system for automatically measuring the blood pressure of a subject comprising:

means for inflating an occluding cuff disposed on said subject to a first predetermined pressure;

means for deflating said cuff at a controlled rate until the pressure within said cuff falls to a second predetermined pressure less than said first pressure;

means for sensing the pressure within said cuff;

means for sensing the amplitude level of sounds generated by said subject as a result of said cuff deflation;

means for periodically storing levels representing pressures sensed by said pressure sensing means and sound amplitude levels sensed by said sound amplitude level sensing means during deflation of said cuff; and

means for selecting, in response to said sensed sound amplitude levels stored in said storing means, the stored pressure levels indicating the systolic and diastolic blood pressures of said subject, said selecting means comprising a digital signal processing means for;

(a) determining the time of occurrence of a predetermined number of stored sound amplitude levels measured consecutively in time which have the highest mean level, said time of occurrence being the time of the center of maximum Korotkoff sound activity;

(b) determining the stored sound amplitude level measured latest in time before said determined time of the center of maximum Korotkoff sound activity which is less than a predetermined threshold level;

(c) selecting as the systolic blood pressure of said subjecting the stored pressure level measured simultaneously with said determined sound amplitude level measured latest in time;

(d) determining the stored sound amplitude level measured earliest in time after said determined time of the center of maximum Korotkoff sound activity which is less than said predetermined threshold level; and

(e) selecting as the diastolic blood pressure of the subject the stored pressure level measured simultaneously with said determined earliest in time sound amplitude level.

18. A system as in claim 17 wherein:

said system further includes;

means for sensing R-waves produced by the brain of said subject, and

means for determining the peak sound amplitude level sensed by said sound amplitude level sensing means occurring between each pair of adjacent R-waves sensed by said R-wave sensing means; and

said storing means stores each of said sensed peak amplitude levels determined by said determining means together with the pressure sensed by said pressure sensing means occurring simultaneously with said each sensed peak amplitude levels.

19. A system as in claim 17 wherein:

said sound amplitude sensing means includes;

means for detecting sound generated by said subject as a result of deflation of said cuff, and

means for amplifying the sounds detected by said sound detecting means by a predetermined gain to produce a signal indicating the amplitude level of said sounds; and

said processing means also dynamically adjusts said gain in response to said determined highest mean level.

20. A system as in claim 17 wherein said processing means also:

(a1) calculates the mean value of all of said sound amplitude levels stored by said storing means;

(a2) calculates a further mean value of all of said stored amplitude levels stored by said storing means which are less than said calculated mean value of all of said stored sound amplitude levels; and

(a3) sets said predetermined threshold level to a value between said mean value and said further mean value.

21. A system as in claim 20 wherein said processing means sets said predetermined threshold level to be half of the sum of said mean value and said further mean value to which the further mean value is added.

22. A system as in claim 17 wherein said processing means also:

determines whether at least one stored sound amplitude level measured immediately before said sound, amplitude level measured latest in time before said determined time of the center of maximum Korotkoff sound activity which is less than said predetermined threshold level is also less than said threshold level; and

determines whether at least one stored sound amplitude level measured immediately after said stored sound amplitude level measured earliest in time after said determined time of the center of maximum Korotkoff sound activity which is less than said predetermined threshold level is also less than said threshold level.

23. A system as in claim 17 further including means for verifying that the cuff pressures associated with the respective stored sound amplitude levels determined by said digital signal processing means are substantially at expected pressure values derived from said controlled rate of cuff deflation.

24. A system for automatically measuring the systolic and diastolic blood pressures of a subject, said system of the type including an occluding cuff, a Korotkoff sound transducer and ECG electrodes, said system comprising:

means for inflating said cuff to a pressure greater than the systolic blood pressure of said subject;

means for linearly deflating said cuff at a controlled rate until the pressure within said cuff falls to less than the diastolic blood pressure of said subject;

means for continuously producing a first signal indicating the amplitude of sound detected by said Korotkoff sound transducer;

means for continuously producing a second signal indicating the pressure within said cuff;

means for detecting the onset of each cardiac cycle of said subject in response to signals generated by said ECG electrodes;

storing means for storing digital signals; and

digital signal processing means for;

(a) determining the peak level PKS of said first signal for each cardiac cycle detected by said cardiac cycle detecting means,

(b) determining the level PRE of said second signal at the time said peak level PKS is determined for each cardiac cycle detected by said cardiac cycle detecting means,

(c) storing, in said storing means, said peak level PKS and said determined level PRE for each cardiac cycle detected by said cardiac cycle detecting means,

(d) determining, in response to said peak levels PKS stored by said storing means, a predetermined number of consecutive cardiac cycles having the highest average peak level,

(e) calculating the mean value AKSN of all of said peak levels PKS stored by said storing means,

(f) calculating the mean value ANOISE of all of said peak levels PKS stored by said storing means which are less than said mean value AKSN,

(g) calculating a threshold level ##EQU4## (h) determining the stored peak level PKS measured for the last cardiac cycle occurring before the center cardiac cycle of said predetermined number of consecutive cardiac cycles determined to have the highest average peak level which is less than K-THRESHOLD,

(i) selecting said level PRE stored by said storing means for said last cardiac cycle as the systolic blood pressure of said subject,

(j) determining the stored peak level PKS measured for the first cardiac cycle occurring after the center cardiac cycle of said predetermined number of consecutive cardiac cycles determined to have the highest average peak level which is less than K-THRESHOLD, and

(k) selecting said level PRE stored by said storing means for said first cardiac cycle as the diastolic blood pressure of said subject.