Tight control over the delivery of insulin in both type I (usually juvenile onset) and type II (usually late adult onset), has been shown to improve the quality of life as well as the general health of these patients. Insulin delivery has been dominated by subcutaneous injections of both long acting insulin to cover the basal needs of the patient and by short acting insulin to compensate for meals and snacks. Recently, the development of electronic, external insulin infusion pumps has allowed the continuous infusion of fast acting insulin for the maintenance of the basal needs as well as the compensatory doses for meals and snacks. These infusion systems have shown to improve control of blood glucose levels, however, they suffer the drawbacks of size, cost, and complexity, which prevents many patients from accepting this technology over the standard subcutaneous injections. These pumps are electronically controlled and must be programmed to supply the desired amounts of basal and bolus insulin.
In one embodiment, the invention provides a disposable infusion device comprising a base arranged to adhere to a patient's skin, a cannula arranged to extend from the base to beneath the patient's skin to deliver a liquid medicament to the patient, and a source arranged to provide the cannula with a liquid medicament. The source includes a pump that pumps the liquid medicament to the cannula and comprises a compressible tube.
The source may further include a reservoir that holds the liquid medicament and the compressible tube preferably communicates with the reservoir.
The source may further comprise a tube compressor that compresses a length of the compressible tube to pump the liquid medicament to the cannula. The tube compressor may comprise a strap fixed to an end of the compressible tube and extending along the compressible tube. The tube compressor may further include an actuator that pulls the strap against the compressible tube to compress the compressible tube. The tube compressor may further include a disk having a circumferential surface that supports the compressible tube and the actuator may be arranged to pull the strap and compress the compressible tube against the disk circumference. The device may further include a volume adjuster that adjusts the volume of liquid medicament pumped to the cannula with each actuation of the actuator. The tube compressor may further include a disk having a circumferential surface that supports the compressible tube, the actuator may be arranged to pull the strap and compress the compressible tube against the disk circumference, and the volume adjuster may comprise a groove within the circumferential surface of the disk. The groove may have a depth that increases along the disk circumference and arranged to receive the compressible tube. The disk is preferably rotatable to vary the length of the groove receiving the compressible tube to adjust the volume of liquid medicament pumped to the cannula with each actuation of the actuator. The disk may be further arranged so that as the length of the groove receiving the compressible tube decreases, the volume of liquid medicament pumped to the cannula increases.
The source may include a reservoir that holds the liquid medicament and the compressible tube preferably communicates with the reservoir. The tube compressor may then comprise a strap fixed to an end of the compressible tube and extending along the compressible tube. An actuator may be employed to pull the strap against the compressible tube to compress the compressible tube. The tube compressor may further include a disk having a circumferential surface that supports the compressible tube and the actuator may be arranged to pull the strap and compress the compressible tube against the disk circumference. The device may further include a volume adjuster that adjusts the volume of liquid medicament pumped to the cannula with each actuation of the actuator.
In another embodiment, a disposable infusion device comprises a base arranged to adhere to a patient's skin, a cannula arranged to extend from the base to beneath the patient's skin to deliver a liquid medicament to the patient, and a source arranged to provide the cannula with a liquid medicament. The source may include a reservoir that contains the liquid medicament and a pump that pumps the liquid medicament from the reservoir to the cannula. The pump may comprise a compressible tube and a tube compressor that compresses a length of the compressible tube to pump the liquid medicament to the cannula.
The tube compressor mat be adjustable for varying the length of the compressible tube that is compressed. The tube compressor may further include a disk having a circumferential surface that supports the compressible tube and the actuator may be arranged to pull the strap and compress the compressible tube against the disk circumference. The disk circumferential surface may include a groove arranged to receive the compressible tube and the length of the groove receiving the compressible tube may be adjustable for varying the length of the compressible tube that is compressed.
The features of the present invention which are believed to be novel are set forth with particularity in the appended claims. The invention, together with further features and advantages thereof, may best be understood by making reference to the following description taken in conjunction with the accompanying drawings, in the several figures of which like reference numerals identify identical elements, and wherein:
The port 10 further includes a cannula 15. The cannula 15 is carried by the funnel port 12. As known in the art, once the needle 14 and cannula 15 are positioned beneath the skin 18 as shown, the needle 14 is removed leaving the cannula 15 in a deployed position and ready to deliver insulin to the patient.
In the case when the system 30 includes multiple reservoirs, the system may have a mechanism for the selection of which insulin is infused at any given time. It also may provide control over how much of each particular insulin is determined to be delivered by having the patient depress the actuator 38 a desired number of times. For example, each activation might deliver 0.5 units of insulin. Therefore, if 3 units of insulin are desired, 6 depressions will deliver the desired amount.
The insulin in reservoir 52 is constantly delivered under the control of a mechanical timer pump 56. The timer pump is of the type known in the art to include a winder 58, a wind-up spring 60, and gears 62. The gears 62 drive a worm gear 63 and lead screw 65 to drive a piston 67. The piston 67 thus pressurizes the reservoir 52 to provide a constant flow of insulin to the cannula 66. When a bolus of fast acting insulin is required, such as at meals, the port 54 is used to inject the fast acting insulin into the reservoir 52. When the reservoir is full, further injected insulin will displace a like quantity of insulin from reservoir 52 thereby injecting the same into and out of the cannula 66.
Referring now to
More specifically, the device 120 includes a reservoir 122 for containing a fast acting insulin. The device further includes disk 124 having a groove 126 that increases in depth along the circumference of the disk 124. A flexible tube 130 extends from the reservoir 122 around the disk 124 and within the groove 126. A strap 132 extends from a fixed tie point 134 along the tube 130 to an actuator 136. As the disk is rotated in the clockwise direction, an increasing length of the tube 130 will reside in the groove 126. Conversely, counter-clockwise rotation of disk 124 will cause a decreased length of the tube 130 to reside in the groove 126. When the actuator 136 is moved in the direction of arrow 138, the strap 132 acts upon (compresses) the portion of the tube 130 not in the groove 126 to cause a measured bolus of insulin to be delivered to the infusion tube 140. Hence, as more tubing is acted upon by the strap 132, a larger volume bolus is delivered by peristaltic action. The disk 124 may be rotated by a dial, such as the dial 82 of the device 86 of
As may be noted, the pump includes a resilient membrane 174 sealed to a base 176 by a sealing ring 178. The base may be adhered to the patient's skin by adhesive tape (not shown). The pump 170 also includes an intake valve 180 which permits insulin to enter the inner cavity 184 formed by the membrane 174 and base 176 when the membrane returns to the configuration shown in
While particular embodiments of the present invention have been shown and described, modifications may be made, and it is therefore intended in the appended claims to cover all such changes and modifications which fall within the true spirit and scope of the invention as defined by those claims.
This application claims priority to U.S. Provisional Application Ser. No. 60/782,941, filed on Mar. 16, 2006, which is incorporated by reference.
Number | Name | Date | Kind |
---|---|---|---|
4263909 | Bush | Apr 1981 | A |
4340048 | Eckenhoff | Jul 1982 | A |
4360019 | Portner et al. | Nov 1982 | A |
4552561 | Eckenhoff | Nov 1985 | A |
4604994 | Sealfon | Aug 1986 | A |
4643723 | Smit | Feb 1987 | A |
4681560 | Schulte et al. | Jul 1987 | A |
4696671 | Epstein et al. | Sep 1987 | A |
4705464 | Arimond | Nov 1987 | A |
4734092 | Millerd | Mar 1988 | A |
4773900 | Cochran | Sep 1988 | A |
4781688 | Thoma et al. | Nov 1988 | A |
4816016 | Schulte et al. | Mar 1989 | A |
4850955 | Newkirk | Jul 1989 | A |
5061243 | Winchell et al. | Oct 1991 | A |
5230706 | Duquette | Jul 1993 | A |
5308334 | Sancoff | May 1994 | A |
5431634 | Brown | Jul 1995 | A |
5492534 | Athayde et al. | Feb 1996 | A |
5545143 | Fischell | Aug 1996 | A |
5752930 | Rise et al. | May 1998 | A |
5776103 | Kriesel | Jul 1998 | A |
5785688 | Joshi et al. | Jul 1998 | A |
6056716 | Dantonio et al. | May 2000 | A |
6126637 | Kriesel et al. | Oct 2000 | A |
6200055 | Fusaro, Jr. | Mar 2001 | B1 |
6270481 | Mason et al. | Aug 2001 | B1 |
6497680 | Holst et al. | Dec 2002 | B1 |
6500150 | Gross et al. | Dec 2002 | B1 |
6719728 | Mason et al. | Apr 2004 | B2 |
7201746 | Olsen | Apr 2007 | B2 |
7255690 | Gray et al. | Aug 2007 | B2 |
20010056259 | Skinkle et al. | Dec 2001 | A1 |
20030088238 | Poulsen et al. | May 2003 | A1 |
20030187394 | Wilkinson | Oct 2003 | A1 |
20030229310 | Flaherty et al. | Dec 2003 | A1 |
20040068222 | Brian | Apr 2004 | A1 |
20040092865 | Flaherty et al. | May 2004 | A1 |
20050273081 | Olsen | Dec 2005 | A1 |
20060069382 | Pedersen | Mar 2006 | A1 |
20060184121 | Brockman et al. | Aug 2006 | A1 |
20060264835 | Nielsen et al. | Nov 2006 | A1 |
20100198183 | Lanigan et al. | Aug 2010 | A1 |
20100232992 | Gray | Sep 2010 | A1 |
Number | Date | Country |
---|---|---|
0941741 | Sep 1999 | EP |
2005039673 | May 2005 | WO |
Entry |
---|
PCT/US07-06181, International Search Report Dec. 20, 2007. |
International Search Report for PCT/US07/06116 dated May 14, 2008, 2 pages. |
International Search Report for PCT/US07/06182 dated Sep. 24, 2008, 2 pages. |
International Search Report for PCT/US07/06115 dated Nov. 14, 2007, 2 pages. |
International Search Report for PCT/US07/06243 dated Nov. 7, 2007, 2 pages. |
International Search Report for PCT/US07/06190 dated Oct. 1, 2008, 2 pages. |
Number | Date | Country | |
---|---|---|---|
20070299408 A1 | Dec 2007 | US |
Number | Date | Country | |
---|---|---|---|
60782941 | Mar 2006 | US |