1. A supervisory controlling method for supervising and controlling an optical repeater based on supervisory control information to be transmitted together with a wavelength-division multiplexed signal light propagated through an optical transmission path in an optical amplifying-and-repeating transmission system for amplifying and repeatingly transmitting said wavelength-division multiplexed signal light by said optical repeater, comprising:
supplying a plurality of excitation lights of different wavelengths from the optical repeater to a Raman amplifying medium on said optical transmission path,
Raman amplifying and repeatingly transmitting the wavelength-division multiplexed signal light propagated through said optical transmission path, among the plurality of excitation lights to be supplied to said Raman amplifying medium, and
applying a modulation onto the excitation light enabling Raman amplification of the signal lights at a longer wavelength side included in said wavelength-division multiplexed signal light, to thereby return a response signal to a supervisory controlling command.
2. A supervisory controlling method for supervising and controlling an optical repeater according to claim 1,
wherein, among said plurality of excitation lights to be supplied to said Raman amplification medium, the excitation light enabling Raman amplification of the optical signal at a shorter wavelength side included in said wavelength-division multiplexed signal light, is applied with the modulation of a phase opposite to that of the excitation light enabling Raman amplification of said optical signal at the longer wavelength side.
3. A supervisory controlling system for supervising and controlling an optical repeater based on supervisory control information to be transmitted together with a wavelength-division multiplexed signal light propagated through an optical transmission path in an optical amplifying-and-repeating transmission system for amplifying and repeatingly transmitting said wavelength-division multiplexed signal light by said optical repeater, comprising:
an excitation light supplying section that supplies a plurality of excitation lights of different wavelengths to a Raman amplifying medium on said optical transmission path, to Raman amplify and repeatingly transmit the wavelength-division multiplexed signal light propagated through said optical transmission path, and
an excitation light modulating section that applies, among the plurality of excitation lights to be supplied to said Raman amplifying medium, a modulation onto the excitation light enabling Raman amplification of the signal lights at a longer wavelength side included in said wavelength-division multiplexed signal light, to thereby return a response signal to a supervisory controlling command by the modulation components included in the signal lights at the longer wavelength side that have been Raman amplified by the excitation light modulated by said excitation light modulating section.
4. A supervisory controlling system for supervising and controlling an optical repeater according to claim 3,
wherein said excitation light modulating section applies, among said plurality of excitation lights to be supplied by said excitation light supplying section to said Raman amplification medium, the modulation onto the excitation light to enable Raman amplification of the optical signal at a shorter wavelength side included in said wavelength-division multiplexed signal light, wherein said modulation has a phase opposite to the modulation onto the excitation light to enable Raman amplification of said optical signal at the longer wavelength side.
5. A method for controlling an optical repeater based on supervisory control information to be transmitted together with a wavelength-division multiplexed signal light propagated through an optical transmission path, comprising:
supplying a plurality of excitation lights of different wavelengths from the optical repeater to a Raman amplifying medium on the optical transmission path;
Raman amplifying and repeatingly transmitting the wavelength-division multiplexed signal light propagated through the optical transmission path; and
applying a modulation onto the excitation light enabling Raman amplification of the signal lights to return a response signal to a supervisory controlling command.
The claims below are in addition to those above.
All refrences to claim(s) which appear below refer to the numbering after this setence.
1. An implantable subcutaneous device, comprising:
a housing configured for subcutaneous non-intrathoracic placement;
detection circuitry provided in the housing and configured to produce a cardiac electrophysiologic signal;
energy delivery circuitry provided in the housing;
at least one electrode configured for subcutaneous non-intrathoracic placement and coupled to the detection and energy delivery circuitry;
an implantable blood sensor configured to produce a blood sensor signal; and
a processor provided in the housing and coupled to the blood sensor, the detection circuitry, and the energy delivery circuitry, the processor using the blood sensor signal to verify that the cardiac electrophysiologic signal comprises a cardiac signal having a QRS complex, the processor configured to discriminate between a tachyarrhythmia condition that requires cardioversion or defibrillation therapy and a condition that does not require cardioversion or defibrillation therapy using the cardiac electrophysiologic signal verified to have a QRS complex and the blood sensor signal, the processor configured to withhold delivery of cardioversion or defibrillation therapy in response to determining, using the blood sensor signal, that the condition does not require cardioversion or defibrillation therapy.
2. The device of claim 1, wherein the processor is configured to detect the tachyarrhythmia condition using the cardiac electrophysiologic signal and confirm presence of the tachyarrhythmia condition using the blood sensor signal.
3. The device of claim 1, wherein the processor is configured to identify a cardiac rhythm as the tachyarrhythmia condition using the cardiac electrophysiologic signal and a relative change in the blood sensor signal.
4. The device of claim 1, wherein the processor is configured to activate the blood sensor and evaluate the tachyarrhythmia condition using the cardiac electrophysiologic signal and the blood sensor signal in response to detecting the tachyarrhythmia condition using the cardiac electrophysiologic signal.
5. The device of claim 1, wherein the processor is configured to deliver the therapy to treat the tachyarrhythmia condition in response to confirming presence of the tachyarrhythmia condition, the processor configured to deactivate the blood sensor before or after delivery of the therapy.
6. The device of claim 1, wherein the processor is configured to discriminate between the tachyarrhythmia condition that requires the therapy and noise.
7. The device of claim 1, wherein the device comprises a plurality of electrodes, and the processor is configured to detect the tachyarrhythmia condition by analyzing an activation pattern of the cardiac electrophysiologic signal using the plurality of electrodes.
8. The device of claim 1, wherein the blood sensor comprises optical signal sensing circuitry, a blood oxygen saturation sensor, a pulse oximeter or photoplethysmography circuitry.
9. The device of claim 1, wherein the processor is configured, in response to detecting an unidentifiable cardiac rhythm using the cardiac electrophysiologic signal, to activate the blood sensor to facilitate identification of the unidentifiable cardiac rhythm using the blood sensor signal.
10. The device of claim 1, wherein the processor is configured to determine a hemodynamic state using the cardiac electrophysiologic signal and the blood sensor signal.
11. The device of claim 1, wherein the processor is configured to use the blood sensor signal for assessing oxygen saturation.
12. The device of claim 1, wherein the processor is configured to deliver the therapy to treat the tachyarrhythmia condition in response to confirming presence of the tachyarrhythmia condition.
13. The device of claim 1, wherein the processor is configured to discriminate between the tachyarrhythmia condition that requires the cardioversion or defibrillation therapy and the condition that does not require the cardioversion or defibrillation therapy by performing a correlation between the electrocardiogram signal and the blood sense signal.
14. The device of claim 1, wherein the processor is configured to selectively power-up the blood sensor for producing the blood sensor signal based on an indication of arrhythmia identified from the cardiac electrophysiologic signal.
15. The device of claim 1, wherein the processor is configured to, in response to detecting an unidentifiable cardiac rhythm using the cardiac electrophysiologic signal, power-up the blood sensor facilitating identification of the unidentifiable cardiac rhythm using the blood sensor signal and discrimination between the tachyarrhythmia condition that requires cardioversion or defibrillation therapy and the condition that does not require cardioversion or defibrillation therapy.
16. The device of claim 1, wherein the processor is configured to use the blood sensor signal for assessing afterload by analyzing the morphology of the blood sensor signal.
17. The device of claim 1, wherein the processor is configured to identify the tachyarrhythmia condition based on the cardiac electrophysiologic signal and a relative change in the blood sensor signal.
18. The device of claim 1, wherein the processor, in response to detecting a tachyarrhythmia using the cardiac electrophysiologic signal, is configured to activate the blood sensor and evaluate the tachyarrhythmia using the cardiac electrophysiologic signal and the blood sensor signal to discriminate between the tachyarrhythmia condition that requires cardioversion or defibrillation therapy and the condition that does not require cardioversion or defibrillation therapy.
19. An implantable subcutaneous device, comprising:
a housing configured for subcutaneous non-intrathoracic placement;
detection circuitry provided in the housing and configured to produce a cardiac electrophysiologic signal;
energy delivery circuitry provided in the housing;
at least one electrode configured for subcutaneous non-intrathoracic placement and coupled to the detection and energy delivery circuitry;
an implantable photoplethysmography sensor configured for deployment between a layer of skin and a layer of extrathoracic muscle tissue and having a photodetector arrangement oriented towards the muscle tissue, and to produce a blood sensor signal; and
a processor provided in the housing and coupled to the blood sensor, the detection circuitry, and the energy delivery circuitry, the processor configured to identify an indication of a tachyarrhythmia condition based on the cardiac electrophysiologic signal, activate the blood sensor to produce the blood sensor signal based on the identification of the indication of the tachyarrhythmia condition, verify that the cardiac electrophysiologic signal comprises a QRS complex using the blood sensor signal, confirm presence of the tachyarrhythmia condition based on the cardiac electrophysiologic signal verified to have a QRS complex and the blood sensor signal, and initiate delivery of an electrical cardiac therapy to treat the tachyarrhythmia condition using the energy delivery circuitry based on the confirmed presence of the tachyarrhythmia condition, wherein the electrical cardiac therapy is withheld by the processor if the tachyarrhythmia condition is not confirmed from the blood sensor signal.
20. The device of claim 19, wherein the implantable photoplethysmography sensor is configured to be oriented toward the muscle tissue in a manner that reduces interference from ambient light sources.
21. The device of claim 19, comprising an opaque barrier arranged to direct light into the photodetector arrangement of the implantable photoplethysmography sensor.
22. The device of claim 19, wherein the processor is configured to cooperate with the photoplethysmography sensor to verify that the cardiac electrophysiologic signal comprises a cardiac signal having a QRS complex.
23. The device of claim 22, wherein the processor is configured to discriminate between a tachyarrhythmia condition that requires a cardioversion or defibrillation therapy and a condition that does not require cardioversion or defibrillation therapy using the cardiac electrophysiologic signal verified to have a QRS complex and the blood sensor signal.