Delivery of a sympatholytic cardiovascular agent to the central nervous system
First Claim
1. A system for delivering a drug dosage from a drug dispenser to receptors of the central nervous system of a patient'"'"'s body to therapeutically treat symptoms of cardiac insult or impaired cardiac performance;
- wherein the central nervous system site comprises one of;
the sub-arachnoid space;
the sub-arachnoid space of the spinal cord;
the sub-arachnoid space of the thoracic spinal cord;
the sub-arachnoid space between the first and fifth thoracic vertebrae;
the sympathetic preganglionic cell bodies located in the intermediolateral cell column of the spinal cord;
the preganglionic sympathetic neurons that provide innervation to the heart; and
the preganglionic sympathetic neurons that provide innervation to the kidneys;
wherein the system comprises;
a drug infusion catheter adapted to be implanted in the patient'"'"'s body so that a distal drug delivery portion is disposed at a predetermined central nervous system site;
a drug delivery pump coupled to a proximal end of the drug infusion catheter having a drug reservoir holding a volume of a sympatholytic cardiovascular agent;
means for operating the drug delivery pump to discharge a predetermined dosage of the sympatholytic cardiovascular agent to a central nervous system site effective to alleviate such symptoms of cardiac insult or impaired cardiac performance;
a physiologic sensor adapted to be surgically implanted in the patient'"'"'s body;
means for operating the physiologic sensor to derive a physiologic parameter associated with cardiac insult or impaired cardiac performance, including at least one of the group;
a myocardial ischemia condition, a cardiac arrthymia condition, an episode of angina, a hypertension condition, a chronically elevated stress level, a chronically elevated anxiety level, and a relatively elevated sympathetic drive condition; and
means for adjusting the dosage as a function of the monitored physiologic parameter associated with cardiac insult or impaired cardiac performance;
wherein the sympatholytic agent comprises clonidine delivered from into the central nervous system by continuous intrathecal infusion at a dosage of 0.01 to 1.0 mg/day; and
wherein the physiologic sensor comprises an EGM sensor, and the operating means further comprises determining one or more of heart rate, heart rate variability, and aberrations in the PQRST segment include changes in morphology, ST segment elevation, electrical alternans, and interval changes associated with cardiac insult or impaired cardiac performance.
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Accused Products
Abstract
A sympatholytic cardiovascular agent delivered by a drug delivery pump to a central nervous system site to alleviate symptoms of acute or chronic cardiac insult or impaired cardiac performance. The drug delivery pump can be external or implantable infusion pump (IIP) coupled with a drug infusion catheter extending to the site. A patient activator can command delivery of a dosage and/or an implantable heart monitor (IHM) coupled with a sensor can detect physiologic parameters associated with cardiac insult or impaired cardiac performance and trigger dosage delivery. The IIP and IHM can be combined into a single implantable medical device (IMD) or can constitute separate IMDs that communicate by any of known communication mechanisms. The sympatholytic cardiovascular agent is one of the group consisting of an alpha-adrenergic agonist and an alpha2-adrenergic agonist (e.g., clonidine, p-aminoclonidine, guanabenz, lidamidine, tizanidine, moxonidine, methyldopa, xylazine, guanfacine, detomidine, medetomidine, and dexmedetomidine).
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Citations
7 Claims
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1. A system for delivering a drug dosage from a drug dispenser to receptors of the central nervous system of a patient'"'"'s body to therapeutically treat symptoms of cardiac insult or impaired cardiac performance;
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wherein the central nervous system site comprises one of; the sub-arachnoid space;
the sub-arachnoid space of the spinal cord;
the sub-arachnoid space of the thoracic spinal cord;
the sub-arachnoid space between the first and fifth thoracic vertebrae;
the sympathetic preganglionic cell bodies located in the intermediolateral cell column of the spinal cord;
the preganglionic sympathetic neurons that provide innervation to the heart; and
the preganglionic sympathetic neurons that provide innervation to the kidneys;wherein the system comprises; a drug infusion catheter adapted to be implanted in the patient'"'"'s body so that a distal drug delivery portion is disposed at a predetermined central nervous system site;
a drug delivery pump coupled to a proximal end of the drug infusion catheter having a drug reservoir holding a volume of a sympatholytic cardiovascular agent;means for operating the drug delivery pump to discharge a predetermined dosage of the sympatholytic cardiovascular agent to a central nervous system site effective to alleviate such symptoms of cardiac insult or impaired cardiac performance; a physiologic sensor adapted to be surgically implanted in the patient'"'"'s body; means for operating the physiologic sensor to derive a physiologic parameter associated with cardiac insult or impaired cardiac performance, including at least one of the group;
a myocardial ischemia condition, a cardiac arrthymia condition, an episode of angina, a hypertension condition, a chronically elevated stress level, a chronically elevated anxiety level, and a relatively elevated sympathetic drive condition; andmeans for adjusting the dosage as a function of the monitored physiologic parameter associated with cardiac insult or impaired cardiac performance; wherein the sympatholytic agent comprises clonidine delivered from into the central nervous system by continuous intrathecal infusion at a dosage of 0.01 to 1.0 mg/day; and wherein the physiologic sensor comprises an EGM sensor, and the operating means further comprises determining one or more of heart rate, heart rate variability, and aberrations in the PQRST segment include changes in morphology, ST segment elevation, electrical alternans, and interval changes associated with cardiac insult or impaired cardiac performance. - View Dependent Claims (2, 3, 4, 5, 6, 7)
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Specification