TREATING CRT NON-RESPONDERS USING CARDIAC CONTRACTILITY MODULATION THERAPY
A method of selecting a patient for cardiac contractility modulation therapy, comprising: selecting a patient meeting a criteria for cardiac resynchronization therapy (CRT); detecting a potential difficulty in effective delivery of CRT to the patient; and determining that the patient can benefit from cardiac contractility modulation therapy in spite of said potential difficulty.
1 . A method of selecting a patient for cardiac contractility modulation therapy, comprising:
selecting a patient meeting a criteria for cardiac resynchronization therapy (CRT);
detecting a potential difficulty in effective delivery of said CRT to said patient; and
determining that said patient can benefit from cardiac contractility modulation therapy in spite of said potential difficulty.
2 . (canceled)
3 . A method according to claim 1 , wherein said detecting comprises receiving an indication that said patient suffers from one or more comorbidities selected from a list comprising renal insufficiency, diabetes mellitus, chronic obstructive pulmonary disease, sleeping disorders like apnea, and anemia.
4 . A method according to claim 1 , wherein said detecting comprises receiving an indication that said patient suffers from cardiac arrhythmia.
5 . A method according to claim 4 , wherein said cardiac arrhythmia comprises a non-left bundle branch block (non-LBBB).
6 . A method according to claim 1 , wherein said determining comprises receiving an indication that said patient suffers from heart failure in NYHA classes II-IV.
7 . A method according claim 1 , wherein said determining comprises receiving an indication that said patient suffers from a left ventricular ejection fraction in a range between 25% - 55%.
8 . A method according to claim 7 , wherein said determining comprises receiving an indication that the patient exhibits a normal QRS duration, which is larger than 130 ms.
9 . A method according to claim 1 , wherein said determining comprises setting a pulse generator of a cardiac device with parameters of a testing electric field for cardiac contractility modulation to be delivered through at least one electrode lead to the heart, and determining that an effect of said testing electric field on said patient indicates that said patient can benefit from cardiac contractility modulation therapy through said at least one electrode lead.
10 - 11 . (canceled)
12 . A method according to claim 1 , comprising:
selecting a cardiac tissue location suitable for delivery of cardiac contractility modulation and CRT therapy through said at least one electrode lead.
13 - 15 . (canceled)
16 . A method according to claim 1 , comprising:
identifying that an effect of CRT is not a planned effect.
17 . (canceled)
18 . A method according to claim 16 , wherein said identifying comprises identifying that said CRT effect comprises at least one undesired side effect.
19 . A method according to claim 18 , wherein said at least one undesired side effect comprises pain sensation and/or arrhythmia.
20 - 21 . (canceled)
22 . A method according to claim 1 , comprising selecting a treatment plan in which a dual purpose device is configured to generate electric fields for both CRT and cardiac contractility modulation therapy.
23 . A method according to claim 22 , wherein said dual purpose device is configured to time said CCM electric field during a refractory period of the heart as a train of biphasic bipolar pulses.
24 - 25 . (canceled)
26 . A method according to claim 1 , wherein said treating comprises treating said patient with cardiac contractility modulation therapy in combination with CRT.
27 . (canceled)
28 . A method according to claim 26 , wherein said treating comprises delivering an electric field for CRT and cardiac contractility modulation therapy through a same electrode lead.
29 . (canceled)
30 . A method according to claim 26 , wherein said treating comprises delivering an extended pacing signal for both CRT and cardiac contractility modulation therapy effects during a non-refractory period of the right ventricle.
31 . A method according to claim 26 , comprising:
determining if treating said patient with said cardiac contractility modulation and said CRT has a desired effect on cardiac output and/or heart contraction;
modifying said CRT therapy based on the results of said determining.
32 . A method of selecting a patient for cardiac contractility modulation therapy comprising:
identifying that an effect of CRT delivered is not a beneficial effect on said patient; and
modifying a setting of a cardiac device controller to generate a cardiac contractility modulation electric field based on the results of said identifying.
33 - 35 . (canceled)
36 . A method according to claim 1 , wherein said detecting comprises identifying that said CRT delivery to said patient does not result in a beneficial effect on at least one of ejection fraction, intracardiac pressure, intra cardiac pressure gradient over a selected time period, NYHA class score, Peak VO2 and 6 minute walk score.
37 - 46 . (canceled)
47 . A method for testing at least one electrode lead for delivery of cardiac contractility modulation therapy, comprising:
determining to deliver CRT to a patient;
implanting in said patient two or more electrode leads in the heart at locations suitable for delivery of said CRT; and
testing if at least one electrode lead out of the two or more electrode leads is suitable for delivery of cardiac contractility modulation therapy.
48 - 63 . (canceled)