STENT MONITORING ASSEMBLY AND METHOD OF USE THEREOF
Assemblies are provided comprising a stent and a sensor positioned on and/or in the stent. Within certain aspects the sensors are wireless sensors, and include for example one or more fluid pressure sensors, contact sensors, position sensors, accelerometers, pulse pressure sensors, blood volume sensors, blood flow sensors, blood chemistry sensors, blood metabolic sensors, mechanical stress sensors and/or temperature sensors. Within certain aspects these stents may be utilized to assist in stent placement, monitor stent function, identify complications of stent treatment, monitor physiologic parameters and/or medically image a body passageway, e.g., a vascular lumen.
1 - 89 . (canceled)
90 . An assembly comprising a first stent in combination with a second stent, wherein each of the first and second stents is a unitary stent; and a sensor positioned on or within each of said first and second stents, wherein the assembly further comprises an antenna for sending and receiving data.
91 . The assembly according to claim 90 wherein the sensor is positioned on an outer wall of the first stent or on an inner wall of the first stent.
92 . The assembly according to claim 90 wherein the sensor is positioned within the first stent material itself.
93 . The assembly according to claim 90 wherein the sensor of the first stent is a fluid pressure sensor.
94 . The assembly according to claim 90 wherein the sensor of the first stent is a blood volume sensor
95 . The assembly according to claim 90 wherein the sensor of the first stent is a blood flow sensor.
96 . The assembly according to claim 90 wherein the sensor of the first stent is a blood chemistry sensor.
97 . The assembly according to claim 90 wherein the sensor of the first stent is a blood metabolic sensor.
98 . The assembly according to claim 90 , wherein the sensor of the first stent measures the development of restenosis.
99 . The assembly according to claim 90 , wherein the sensor of the first stent measures the development of a thrombus, atherosclerosis, tumor, inflammation, abscess or other space occupying lesion.
100 . The assembly according to claim 90 wherein the first stent is a vascular, gastrointestinal, pulmonary, head and neck, or genitourinary stent.
101 . The assembly according to claim 98 wherein said vascular stent is a coronary stent, carotid stent, cerebral stent, vertebral stent, iliac stent, femoral stent, popliteal stent, or stent for the arteries of the lower extremities.
102 . The assembly according to claim 90 wherein the first said stent is a non-biodegradable stent.
103 . The assembly according to claim 90 wherein the sensor of the first stent is connected to a wireless microprocessor.
104 . The assembly according to claim 90 wherein a plurality of sensors are positioned on or within the first stent.
105 . The assembly according to claim 90 wherein the sensor of the first stent has a unique sensor identification number.
106 . The assembly according to claim 90 wherein the sensor of the first stent is uniquely defined within a specific position on or within said assembly.
107 . A method for monitoring the assembly of claim 1 when the assembly is located in situ in a patient, the method comprising
a. sending a wireless signal from an interrogation module positioned outside the skin of the patient to the assembly;
b. sending data from a sensor of the assembly of claim 1 by way of a wireless RF signal back to the interrogation module
c. collecting the data in a home of the patient.
108 . The method of claim 108 wherein the data accumulated at the home is collected and transmitted via the Internet to a physician's office for analysis.