DEVICES AND METHODS FOR TREATING CANCER AND CARDIAC WASTING
Disclosed herein are methods that can comprise detecting a cardiopulmonary measurement in a subject. Disclosed herein are methods that can comprise monitoring a disease in a patient by detecting a cardiopulmonary measurement. Disclosed herein are methods that can comprise treating a patient after detecting a cardiopulmonary measurement in a subject.
1 . (canceled)
2 . A method comprising actuating a cardioverter defibrillator that is directly or indirectly contacted with a subject in need thereof, wherein actuating the cardioverter defibrillator comprises delivering a low-energy pacing, a cardioversion therapy, a defibrillation therapy, or a combination thereof, based on a detection of a cardiopulmonary measurement, wherein the cardiopulmonary measurement comprises measuring at least two members selected from the group consisting of:
(i) from about 10 to about 5,000,000 premature ventricular contractions in a time period of from about 30 seconds to about 3 weeks,
(ii) an average heart rate during a time period of from about 60 to about 100 bpm and a standard deviation of a 5-minute average NN interval (SDANN) during a time period of from about 1 minute to about 60 minutes that comprises less than about 100 msec,
(iii) a percentage of successive normal sinus R-R intervals >50 msec (pNN50) that comprises less than 10% and an SDANN during a time period of from about 1 minute to about 60 minutes of at least 100 msec, and
(iv) a left ventricular (LV) mass of from about 1% to about 70% below that of an LV mass of an average human or below the previously determined LV mass of the subject, as determined by a computer tomography (CT) scan.
3 . The method of claim 2 , wherein the subject has or is suspected of having cardiac wasting, is at risk of developing cardiac wasting, or a combination thereof.
4 . The method of claim 3 , wherein the actuating treats, prevents, delays, or ameliorates the cardiac wasting in the subject.
5 . The method of claim 2 , wherein the cardiopulmonary measurement comprises a left ventricular (LV) mass of from about 2% to about 20% below that of an LV mass of an average human or below the previously determined LV mass of the subject, as determined by a computer tomography (CT) scan; and further comprising diagnosing the subject with a cardiac wasting.
6 . The method of claim 5 , wherein the diagnosing comprises performing echocardiography, or a magnetic resonance imaging (MRI) assessment, or a positron emission tomography-computed tomography (PET-CT) assessment or a scintigraphy assessment on the subject.
7 . The method of claim 6 , wherein the subject has a terminal illness and is considered to be in need of a palliative care, a hospice care, an end of life care, an improved quality of life, or any combination thereof.
8 . The method of claim 7 , wherein the palliative care or the hospice care is at home or in an institutional care structure.
9 . The method of claim 7 , wherein a life expectancy of the subject is less than about 12 months.
10 . The method of claim 7 , wherein a life expectancy of the subject is less than about 6 months.
11 . The method of claim 3 , wherein the subject has elevated plasma levels of a natriuretic peptide, as compared to a healthy subject.
12 . The method of claim 11 , wherein the natriuretic peptide comprises an atrial natriuretic peptide (ANP), a brain natriuretic peptide (BNP), a c-type natriuretic peptide (CNP), a dendroaspis natriuretic peptide (DNP), a urodilatin, or any combination thereof.
13 . The method of claim 2 , wherein the subject has congestion.
14 . The method of claim 3 , wherein the subject has elevated plasma levels of a troponin, as compared to a healthy subject.
15 . The method of claim 14 , wherein the troponin comprises troponin I or troponin T.
16 . The method of claim 3 , wherein the subject has elevated plasma levels of aldosterone, as compared to a healthy subject.
17 . The method of claim 2 , wherein the cardioverter defibrillator comprises an implantable cardioverter defibrillator.
18 . The method of claim 2 , wherein the cardioverter defibrillator is leadless.
19 . The method of claim 2 , wherein the cardioverter defibrillator comprises a wearable cardioverter defibrillator.
20 .- 24 . (canceled)
25 . A method of preventing or treating cardiac wasting in a subject having cardiac wasting or suspected of being at risk of cardiac wasting, comprising detecting a cardiopulmonary measurement, wherein the cardiopulmonary measurement comprises at least two measurements selected from the group consisting of:
(i) from about 10 to about 5,000,000 premature ventricular contractions in a time period of from about 30 seconds to about 3 weeks,
(ii) an average heart rate during a time period of from about 60 to about 100 bpm and a standard deviation of a 5-minute average NN interval (SDANN) during a time period of from about 1 minute to about 60 minutes that comprises less than about 100 msec,
(iii) a percentage of successive normal sinus R-R intervals >50 msec (pNN50) that comprises less than 10% and an SDANN during a time period of from about 1 minute to about 60 minutes of at least 100 msec, and
(iv) a left ventricular (LV) mass of from about 1% to about 70% below that of an LV mass of an average human or below the previously determined LV mass of the subject, as determined by a computer tomography (CT) scan; and
administering a medicament to the subject based at least in part on the cardiopulmonary measurement, thereby treating or preventing the cardiac wasting in the subject.
26 .- 50 . (canceled)
51 . A method of using an interoperable electronic device configured to measure a cardiopulmonary measurement, interpret a risk of a presence of a wasting of a left ventricular muscle mass based on the cardiopulmonary measurement using an algorithm stored on a computer readable memory operatively coupled to the interoperable electronic device, and transmit a detection of the risk of the presence of the wasting of the left ventricular muscle mass to a second device.
52 .- 121 . (canceled)
122 . The method of claim 51 , wherein the cardiopulmonary measurement comprises:
(i) from about 10 to about 5,000,000 premature ventricular contractions in a time period of from about 30 seconds to about 3 weeks,
(ii) an average heart rate during a time period of from about 60 to about 100 bpm and a standard deviation of a 5-minute average NN interval (SDANN) during a time period of from about 1 minute to about 60 minutes that comprises less than about 100 msec,
(iii) a percentage of successive normal sinus R-R intervals >50 msec (pNN50) that comprises less than 10% and an SDANN during a time period of from about 1 minute to about 60 minutes of at least 100 msec,
(iv) a left ventricular (LV) mass of from about 1% to about 70% below that of an LV mass of an average human or below the previously determined LV mass of the subject, as determined by a computer tomography (CT) scan, or
(v) any combination of (i)-(iv).
123 . The method of claim 122 , wherein the interoperable electronic device comprises a loop recorder, a cardioverter defibrillator, or a combination thereof.
124 . The method of claim 122 , wherein the interoperable electronic device comprises a wearable device.