Methods and apparatus for monitoring the cardiovascular condition of patients with sleep disordered breathing
An apparatus for assessing patient breathing and cardiovascular condition of a patient includes a storage medium for storing data regarding the breathing and cardiovascular condition of the patient, a processor in communication with the storage medium, the processor being configured to prompt the patient with a series of queries relating to patient breathing and cardiovascular condition, a display for presenting the patient with the series of queries and a date entry device for receiving responses to the series of queries. The processor is configured to tally positive responses to the series of queries to generate a sleep disordered breathing index.
1. A system for monitoring sleep disordered breathing (SDB) related information, the system comprising:
a sensor for measuring SDB related information of a patient;
a sense tube for conveying the sleep disordered breathing related information from the patient to the sensor;
a display device for presenting the patient with an SDB questionnaire comprising a plurality of different questions;
an input device for receiving responses to the plurality of questions; and
one or more processors in communication with the sensor, the display device, and the input device, the one or more processors configured to:
identify a number of received responses indicative of SDB;
calculate an SDB index based on the number of received responses identified as being indicative of SDB;
generate a first warning message for display on the display device if the SDB index is greater than a first predetermined threshold; and
generate a second warning message for display on the display device if the SDB index is both less than the first predetermined threshold and greater than a second predetermined threshold.
2. The system of claim 1 , wherein the first warning message comprises a recommendation for a full SDB assessment.
3. The system of claim 2 , wherein the second warning message comprises an indication that a full SDB assessment is unnecessary.
4. The system of claim 1 , wherein the display device is further configured to display the calculated SDB index.
5. The system of claim 1 , wherein the sensor is configured to measure at least one of oxygen concentration, pressure, or flow in the sense tube.
6. The system of claim 1 , wherein the first and second warning messages comprise statistical data derived from the measured SDB related information.
7. The system of claim 6 , wherein the statistical data comprises an apnea hypopnea index (AHI) derived from the measured SDB related information.
8. The system of claim 7 , wherein the one or more processors are further configured to:
detect an apnea event if a moving average ventilation derived from the measured SDB related information drops below a predetermined average ventilation value for a predetermined time period; and
calculate the AHI based on a plurality of detected apnea events.
9. The system of claim 7 , wherein the one or more processors are further configured to:
detect a hypopnea event if a moving average ventilation derived from the measured SDB related information (a) drops below a first predetermined average ventilation value and (b) remains above a second predetermined average ventilation value for a predetermined time period; and
calculate the AHI based on a plurality of detected hypopnea events.
10. The system of claim 1 , wherein the one or more processors are further configured to:
detect at least one of central apneas, obstructive apneas, hypopneas, partial obstructions, or snoring from the measured SDB related information; and
generate a statistical summary for display on the display device based on the detected central apneas, obstructive apneas, hypopneas, partial obstructions, or snoring.
11. The system of claim 1 , wherein at least one question of the SDB questionnaire determines a gender, an age, a height, or a weight of the patient.
12. The system of claim 1 , wherein at least one question of the SDB questionnaire determines a presence of snoring.
13. The system of claim 1 , wherein at least one question of the SDB questionnaire determines a presence of excessive sleepiness.
14. The system of claim 1 , wherein at least one question of the SDB questionnaire determines a presence of breathlessness at nighttime.
15. The system of claim 1 , wherein at least one question of the SDB questionnaire determines a presence of cessation of breathing during sleep.
16. The system of claim 1 , wherein at least one question of the SDB questionnaire determines a subjective quality of sleep.
17. The system of claim 1 further comprising:
a blower for providing a respiratory therapy to the patient according to one or more treatment protocols.
18. The system of claim 1 , wherein the one or more processors are further configured to:
monitor changes in the measured SDB related information; and
adjust the treatment protocol of the blower based on the monitored changes in the measured SDB related information.
19. The system of claim 1 , wherein a single unit comprises the display device, the input device, and the one or more processors.
20. The system of claim 1 , wherein a remote device comprises the display device and the input device.