U.S. Pat. No. 8,702,609, which is assigned to the assignee of the present application, discloses an image guided-therapy catheter that uses ultrasound to form an image of the interior of a blood vessel directly in front of the catheter, to determine the locations of plaque, and then permits the use of this information in driving a set of RF ablation electrodes to selectively ablate plaque, while avoiding damaging the interior surfaces of the blood vessel. A number of challenging issues are presented in the design of this type of device. Among these is the acoustic characteristics of the medical device and how to avoid harmful interference to the returning signal from signal that has reflected from the portion of the device proximal (that is, further back from the tip) to the ultrasound array.
Another troublesome issue in the design of the system is the multiplexing of the driving/receiving coax lines for the ultrasound elements. With a large array, it would be impossible to have a separate coax line for each element. Multiplexors, however, require an increasing number of control inputs for an increasing number of multiplexed lines. With catheter space at an extreme premium, fitting a high number of control lines into a catheter is also very problematic.
The following embodiments and aspects thereof are described and illustrated in conjunction with systems, tools and methods which are meant to be exemplary and illustrative, not limiting in scope. In various embodiments, one or more of the above-described problems have been reduced or eliminated, while other embodiments are directed to other improvements.
The present invention may take the form of an intravenous ultrasound catheter having a distal tip and having a forward-facing array of ultrasound elements near to the distal tip of the device. Also, an integrated circuit (IC) die, abuts and is proximal to the ultrasound elements, having a thickness of less than 80 μm, and further having a first face, facing the forward-facing array, and having an array of ultrasound element driving and receiving contacts, in mating arrangement to the array of ultrasound elements, so that the array of ultrasound element driving and receiving contacts collectively physically abut and electrically connect to each of the ultrasound elements; a second face, opposed to the first face, and having a set of input-output signal contacts, the set being fewer in number than the array of ultrasound element driving and receiving contacts and each being switchable into contact with any one of a set of the ultrasound element driving and receiving contacts, the second face also having a set of control contacts, wherein inputs received by the control contacts positively collectively command some aspect of operation of the IC die; and a set of amplifiers, interposed between the first face and the second face, including an amplifier for each one of the driving and receiving electrical contacts. A flex circuit assembly is proximal to the integrated circuit and includes coax cables and a contact portion, has a set of contact pads abutting and electrically connects the input-output signal contacts of the IC die to the coax cables. Finally, backing material, abutting and directly proximal to the contact portion, thereby forming an interface and wherein the backing material and the contact portion material have equal acoustic impedance, thereby preventing reflection at the interface.
In addition to the exemplary aspects and embodiments described above, further aspects and embodiments will become apparent by reference to the drawings and by study of the following detailed descriptions.
Exemplary embodiments are illustrated in referenced drawings. It is intended that the embodiments and figures disclosed herein are to be considered illustrative rather than restrictive.
Referring to
The basic function of the chip 18 is to allow 32 micro-coax acoustic channels to selectively connect to any group of thirty-two ultrasound array elements and to amplify the return signals from the ultrasound elements, as they are transmitted to the coax signal lines 16. On power-up, the ultrasound system resets the chip 18 and asserts the Tx/Rx line placing the MUX in transmit mode for elements 1-32. The ultrasound system 10 then transmits an electrical analog pulse through each of the micro-coax cables 16 to contacts 17. The electrical pulses are then transferred to elements 1-32 of the piezoelectric array. After the ultrasonic pulses have left elements 1-32, the Tx/Rx line is de-asserted placing the MUX in receive mode. In the receive mode, mechanical energy reflected from the tissue or blood is converted to electrical energy by the piezoelectric elements 1-32 and the power transferred back through the chip 18 where the signal is amplified (using power received on contact pad 23), matched to the cable and sent back through each micro-coax to the ultrasound system for conversion to digital data at the front end of the imaging system. The receive mode lasts for approximately 8 μS. Tx/Rx is then re-asserted and the cycle repeats for elements 33-64 and so forth. A chip ground 25 is electrically connected to a further ground at the proximal end of a linear conductor.
During the transmit cycle, the input electrical impedance of the IC chip 18 on the flex side of the chip 18 is matched to that of the coaxial cable 16 (typically 50 to 100 Ohm characteristic impedance), whereas the output impedance of the IC chip 18 is matched, or optimized, to the electrical impedance of the individual piezoelectric elements of the array 30 (typically 10,000 Ohms). The electrical impedance matching scheme works also in the receive cycle to enable optimal transmission of power.
In summary, the IC chip 18 performs multiple functions in the operation of the imaging system 10: It enables the electrical connection of multiple micro-coaxial cables 16 to the individual elements of the array 30, it matches the electrical impedance of the coaxial cables 16 to that of the piezoelectric elements, it acts as multiplexer so the entire array 30 of elements can be addressed and as an amplifier of the weak receive signals (of the order of a few microvolts) in receive mode.
In one scheme of driving the ultrasound array 30, the following transmit receive sequence is performed, where B1 is the first block of elements, B2 is the second block of elements and so on until B32 is the 32nd block of elements and TBn indicates transmission through the nth block of elements, and RBn means receiving on the nth block of elements:
TB1,RB1,TB1,RB2, . . . ,TB1,RBn,TB2,RB1,TB2,RB2, . . . TB2,RBn, . . . ,TBnRB1, . . . TBnRBn (S1)
In a catheter designed to be introduced into cardiac arteries, space is at a great premium, and any design aspects that reduce the number of lines that must extend through the catheter yield a great benefit. Although a traditional multiplex device would permit any block 32 to be chosen at any time, this would require five control lines (yielding 32 combinations), not counting a transmit/receive choice line. Lowering the number of blocks to 16 would require blocks of 36—requiring four more coax signal lines 16, also difficult to fit into the catheter. To accommodate the above pattern of transmit and receive sequences, in one preferred embodiment control line 20b is a transmit line increment. In one preferred embodiment, chip 18 includes an incrementing register for transmit periods, incremented by a transmit increment line 20b and a separate incrementing register for receive periods, incremented by a receive increment line 20c. A transmit/receive selector line 20a thereby permits each to be incremented through its repeated cycles, as shown in sequence S1, listed above. In another embodiment, transmit/receive selector line 20a is used to increment the transmit and receive block registers, with for example, each rising edge counting as a transmit block increment and each falling edge counting as received block increments. A counter is placed in series with the transmit register so that only every 18th transition to transmit increments the transmit register and with every transition to receive incrementing the receive register, as indicated in sequence S1. This permits the transmit and receive increment lines to be eliminated. In yet another preferred embodiment, a single block increment line steps through the 18×18 (324) transmit/receive pairs sequence S1, which must be stored in a memory 36 of chip 18.
Chip 18 is connected to array 30, by way of different techniques such as a flip chip bonding technique, pressure bonding through a thin layer of low viscosity adhesive (1-2 microns) or indium bonding. These are known techniques in the semiconductor/microchip industry. In the case of flip chip bonding, for example, a solder ball 40 (
The waveforms created by waveform generator 14 are typically two-cycle 35 MHz pulses, having pulse width of 5.7 nsec and pulse repetition frequency for 6 mm maximum penetration of 125 kHz or pulse repetition period of 8 usec. It should be noted that other frequencies in the range of 25 to 50 MHz may be utilized depending on resolution or penetration desired.
Referring, now, to
Referring to
Catheter 80 is configured for placement through opening O and into body B of a human patient or subject, as schematically represented in
Referring to
Referring now to
If the supporting tip surface is constructed of a suitable synthetic material capable of withstanding the high temperatures generated by the electrodes, the electrode material may be deposited or applied directly onto the tip. Suitable synthetic materials include high temperature plastics (e.g. Torlon, available from Solvay Advanced Polymers LLC, Alpharetta, Ga.) or silicone rubber materials (e.g. RTV325, Eager Plastics, Inc. Chicago, Ill. or RTV 560 GE Plastics). Another suitable material, TPX (4-polymethylpentene) is available from Mitsui Chemicals Inc., Tokyo, Japan. TPX is a solid plastic with acoustic properties similar to human tissue and therefore transports acoustic energy to tissue efficiently with little loss. The acoustic impedance of human tissue is about 1.55 MRayls while that of TPX is 1.78 MRayls (implying 93% transmission). TPX also has a relatively high softening temperature (about 350 F) and melting temperature of about 460 F, which makes it suitable for the ablation application, in which elevated temperatures may occur.
While a number of exemplary aspects and embodiments have been discussed above, those possessed of skill in the art will recognize certain modifications, permutations, additions and sub-combinations thereof. It is therefore intended that the following appended claims and claims hereafter introduced are interpreted to include all such modifications, permutations, additions and sub-combinations as are within their true spirit and scope.
This application is a continuation-in-part of U.S. patent application Ser. No. 15/633,716, filed Jun. 26, 2017, which is incorporated by reference as if fully set forth herein.
Number | Name | Date | Kind |
---|---|---|---|
3827115 | Bom | Aug 1974 | A |
3938502 | Bom | Feb 1976 | A |
4446395 | Hadjicostis | May 1984 | A |
4532924 | Auth et al. | Aug 1985 | A |
4643186 | Rosen et al. | Feb 1987 | A |
4682596 | Bales et al. | Jul 1987 | A |
4794931 | Yock | Jan 1989 | A |
4939826 | Schoup | Jul 1990 | A |
5010886 | Passafaro et al. | Apr 1991 | A |
5098431 | Rydell | Mar 1992 | A |
5159931 | Pini | Nov 1992 | A |
5176141 | Bom et al. | Jan 1993 | A |
5240003 | Lancee et al. | Aug 1993 | A |
5291893 | Slayton | Mar 1994 | A |
5327905 | Avitall | Jul 1994 | A |
5359760 | Busse et al. | Nov 1994 | A |
5425364 | Imran | Jun 1995 | A |
5454809 | Janssen | Oct 1995 | A |
5592730 | Greenstein et al. | Jan 1997 | A |
5622177 | Breimesser et al. | Apr 1997 | A |
5626576 | Janssen | May 1997 | A |
5749914 | Janssen | May 1998 | A |
5771895 | Slager | Jun 1998 | A |
5788636 | Curley | Aug 1998 | A |
5840030 | Ferek-Petric et al. | Nov 1998 | A |
5840031 | Crowley | Nov 1998 | A |
5857974 | Eberle et al. | Jan 1999 | A |
5893832 | Song | Apr 1999 | A |
5924993 | Hadjicostis et al. | Jul 1999 | A |
5935108 | Kathoh et al. | Aug 1999 | A |
6047216 | Carl et al. | Apr 2000 | A |
6066096 | Smith et al. | May 2000 | A |
6099524 | Lipson et al. | Aug 2000 | A |
6356790 | Maguire et al. | Mar 2002 | B1 |
6394956 | Chandrasekaran et al. | May 2002 | B1 |
6560472 | Hill et al. | May 2003 | B2 |
6572551 | Smith et al. | Jun 2003 | B1 |
6582369 | Huang et al. | Jun 2003 | B1 |
6582423 | Thapliyal | Jun 2003 | B1 |
6679845 | Ritter et al. | Jan 2004 | B2 |
6709396 | Flesch et al. | Mar 2004 | B2 |
6783497 | Grenon et al. | Aug 2004 | B2 |
6852109 | Winston et al. | Feb 2005 | B2 |
6858006 | MacCarter et al. | Feb 2005 | B2 |
6892438 | Hill et al. | May 2005 | B1 |
6899682 | Eberle et al. | May 2005 | B2 |
6925693 | Takeuchi et al. | Aug 2005 | B2 |
6962567 | Eberle et al. | Nov 2005 | B2 |
6972018 | Ryan et al. | Dec 2005 | B2 |
6994674 | Sheljaskow et al. | Feb 2006 | B2 |
7004940 | Ryan et al. | Feb 2006 | B2 |
7022088 | Keast et al. | Apr 2006 | B2 |
7045108 | Jiang et al. | May 2006 | B2 |
7053530 | Baumgartner et al. | May 2006 | B2 |
7060033 | White et al. | Jun 2006 | B2 |
7066895 | Podany | Jun 2006 | B2 |
7074218 | Washington et al. | Jul 2006 | B2 |
7112196 | Brosch et al. | Sep 2006 | B2 |
7115092 | Park et al. | Oct 2006 | B2 |
7156812 | Seward et al. | Jan 2007 | B2 |
7156938 | Baumgartner et al. | Jan 2007 | B2 |
7195179 | Miller et al. | Mar 2007 | B2 |
7226417 | Eberle et al. | Jun 2007 | B1 |
7519410 | Taimisto et al. | Apr 2009 | B2 |
7596415 | Brabec et al. | Sep 2009 | B2 |
7844347 | Brabec et al. | Nov 2010 | B2 |
8414492 | Hadjicostis | Apr 2013 | B2 |
8425421 | Hadjicostis | Apr 2013 | B2 |
8702609 | Hadjicostis | Apr 2014 | B2 |
8974446 | Nguyen et al. | Mar 2015 | B2 |
9138290 | Hadjicostis | Sep 2015 | B2 |
10188368 | Hadjicostis | Jan 2019 | B2 |
20030055308 | Friemel et al. | Mar 2003 | A1 |
20040068191 | Seward et al. | Apr 2004 | A1 |
20040092806 | Sagon et al. | May 2004 | A1 |
20040147920 | Keidar | Jul 2004 | A1 |
20040254471 | Hadjicostis et al. | Dec 2004 | A1 |
20040254570 | Hadjicostis et al. | Dec 2004 | A1 |
20050033182 | Cerofolini | Feb 2005 | A1 |
20050107783 | Tom et al. | May 2005 | A1 |
20050159739 | Paul et al. | Jul 2005 | A1 |
20050228290 | Borovsky | Oct 2005 | A1 |
20050251127 | Brosch et al. | Nov 2005 | A1 |
20060030844 | Knight et al. | Feb 2006 | A1 |
20070167804 | Park et al. | Jul 2007 | A1 |
20070189761 | Sudol | Aug 2007 | A1 |
20070246821 | Lu et al. | Oct 2007 | A1 |
20080200815 | Van Der Steen | Aug 2008 | A1 |
20130267853 | Dausch et al. | Oct 2013 | A1 |
20140180101 | Hadjicostis | Jun 2014 | A1 |
20150099976 | Ghaffari et al. | Apr 2015 | A1 |
20160008067 | Hadjicostis | Jan 2016 | A1 |
20160113633 | Hadjicostis | Apr 2016 | A1 |
20160374710 | Sinelnikov et al. | Dec 2016 | A1 |
20180368805 | Hadjicostis | Dec 2018 | A1 |
Number | Date | Country |
---|---|---|
106037803 | Oct 2016 | CN |
1717601 | Feb 2008 | EP |
2136603 | Dec 2009 | EP |
H02134149 | May 1990 | JP |
H02140156 | May 1990 | JP |
20060112244 | Oct 2006 | KR |
9519143 | Jul 1995 | WO |
9745157 | Dec 1997 | WO |
9912489 | Mar 1999 | WO |
Number | Date | Country | |
---|---|---|---|
20190150893 A1 | May 2019 | US |
Number | Date | Country | |
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Parent | 15633716 | Jun 2017 | US |
Child | 16259740 | US |