Instrument access device
10321934 ยท 2019-06-18
Assignee
Inventors
- Frank BONADIO (County Wicklow, IE)
- Trevor VAUGH (County Offaly, IE)
- Ronan B. McManus (County Wicklow, IE)
- Shane J. MacNALLY (County Wicklow, IE)
- Michael Mulhall (County Galway, IE)
Cpc classification
A61B17/3468
HUMAN NECESSITIES
A61B17/3462
HUMAN NECESSITIES
A61B2017/3484
HUMAN NECESSITIES
A61B17/3423
HUMAN NECESSITIES
A61B2017/3466
HUMAN NECESSITIES
A61B2017/3445
HUMAN NECESSITIES
A61B17/0293
HUMAN NECESSITIES
A61B2017/3449
HUMAN NECESSITIES
A61B17/3498
HUMAN NECESSITIES
International classification
Abstract
An instrument access device 1 comprises a proximal member 25 for location externally of an opening into a body cavity. A first connector 20 extends between the proximal member 25 and a first instrument receiver 2. A second connector 21 extends between the proximal member and a second instrument receiver 3. Instrument seals can be housed in relatively rigid housings for added strength.
Claims
1. A medical device, comprising: a wound protector, including: a proximal ring assembly including a proximal ring member having a central longitudinal axis, a distal ring, a wound-engaging sleeve extending between the proximal ring member and the distal ring, and the proximal ring assembly further including a sealing member having a plurality of access portions that provide access through the sealing member into the wound-engaging sleeve, wherein the plurality of access portions include: a central access portion having a central longitudinal axis coaxial with the central longitudinal axis of the proximal ring member, and a peripheral access portion having a central longitudinal axis offset from the central longitudinal axis of the central access portion, wherein a width of the peripheral access portion is less than a width of the central access portion, wherein the central access portion includes a first tube extending proximal to a proximalmost end of the proximal ring member, the width of the central access portion being a width of the first tube at a first location proximal to the proximalmost end of the proximal ring member, and the peripheral access portion includes a second tube extending proximal to the proximalmost end of proximal ring member, the width of the peripheral access portion being a width of the second tube at a second location proximal to the proximalmost end of the proximal ring member.
2. The medical device of claim 1, wherein the sealing member further includes at least one seal for sealing at least one of the plurality of access portions.
3. The medical device of claim 1, wherein the peripheral access portion is one of a plurality of peripheral access portions having central longitudinal axes offset from the central longitudinal axis of the central access portion.
4. The medical device of claim 1, wherein the sealing member further comprises a reinforcing ring enveloped by a flexible material, where the reinforcing ring is more rigid than the flexible material.
5. The medical device of claim 1, wherein the sealing member further comprises a reinforcing ring enveloped by a flexible material, where the reinforcing ring is more rigid than the flexible material.
6. A medical device, comprising: a wound protector, including: a proximal ring assembly including a proximal ring member, a distal ring, a wound-engaging sleeve extending between the proximal ring member and the distal ring, and the proximal ring assembly further including a sealing member having a central longitudinal axis and a plurality of access portions that provide access through the sealing member into the wound-engaging sleeve, wherein the plurality of access portions include: a central access portion having a central longitudinal axis coaxial with the central longitudinal axis of the sealing member, and a peripheral access portion having a central longitudinal axis offset from the central longitudinal axis of the central access portion, wherein a width of the peripheral access portion is less than a width of the central access portion, wherein the width of the central access portion is at a position where the central access portion has a circular cross-section, and the width of the peripheral access portion is at a position where the peripheral access portion has a circular cross-section.
7. The medical device of claim 6, wherein the peripheral access portion is one of a plurality of peripheral access portions having central longitudinal axes offset from the central longitudinal axis of the central access portion.
8. The medical device of claim 6, wherein the central longitudinal axis of the sealing member is coaxial with a central longitudinal axis of the proximal ring member.
9. The medical device of claim 6, wherein the sealing member further includes at least one seal for sealing at least one of the plurality of access portions.
10. The medical device of claim 6, wherein at least one of the central and peripheral access portions includes a tubular member extending proximal to the proximal ring member, and the width of the at least one of the central and peripheral access portions is a width of the tubular member proximal to a proximalmost edge of the proximal ring member.
11. The medical device of claim 6, wherein the sealing member engages a proximalmost end of the proximal ring member.
12. A medical device, comprising: a wound protector, including: a proximal ring assembly including a proximal ring member having a central longitudinal axis, a distal ring, a wound-engaging sleeve extending between the proximal ring member and the distal ring, the wound-engaging sleeve, and the proximal ring assembly further including a cover having a plurality of passageways that provide access through the cover into the wound-engaging sleeve, wherein the plurality of passageways include: a first passageway having a central longitudinal axis coaxial with the central longitudinal axis of the proximal ring member, and a second passageway having a central longitudinal axis offset from the central longitudinal axis of the central access portion, wherein a width of the second passageway is less than a width of the first passageway, and wherein the widths of the first and second passageways are measured at a position proximal to a proximalmost end of the wound protector, wherein the width of the first passageway is a diameter of a circular portion of the first passageway, and the width of the second passageway is a diameter of a circular portion of the second passageway.
13. The medical device of claim 12, wherein one of the first passageway and the second passageway includes a tubular member extending proximal to the proximal ring member.
14. The medical device of claim 13, wherein the tubular member has a proximal end, and the cover further includes a valve at the proximal end for sealing the tubular member.
15. The medical device of claim 12, wherein the cover further includes at least one valve for sealing at least one of the plurality of passageways.
16. The medical device of claim 12, wherein the cover comprises a flexible material, and a reinforcing ring for stiffening the flexible material.
17. The medical device of claim 12, wherein the cover extends proximal to the proximal ring member.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
(1) The invention will be more clearly understood from the following description of some embodiments thereof, given by way of example only, with reference to the accompanying drawings, in which:
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DETAILED DESCRIPTION
(40) Referring to the drawings and initially to
(41) The insertion device 2 comprises a lipseal 10 through which an instrument 11 is insertable and a second seal member 12 having a passageway extending therethrough, through which the instrument 11 is insertable. The first insertion device 2 also has a reducer cap 15 which has a further lipseal 16 which is smaller than the lipseal 10. To insert large diameter instruments, the cap 15 is removed. To insert smaller diameter instruments the cap 15 is in place.
(42) Referring to
(43) The lipseal valve 10 is located proximally of the duckbill valve 12 so that a double seal is provided to substantially prevent leakage of insufflation gas.
(44) The lipseal 10 may be of any suitable material. For example it may be of an elastomeric material, a foamtype material or a gelatinous material. The duckbill valve 12 may be of any suitable material. For example, it may be of a flexible polymeric material.
(45) The second and third instrument insertion devices 3, 4 may be of the same or different construction as that of the first instrument insertion device 2.
(46) The instrument access device of the invention is suitable for use during laparoscopic surgery to facilitate instrument access to an insufflated abdominal cavity while maintaining pneumoperitoneum.
(47) The instrument access device of the invention comprises a first connector 20 for connecting the first instrument insertion device 2 to a connector base 25, a second connector 21 for connecting the second instrument insertion device 3 to the base 25, and a third connector 22 for connecting the third instrument insertion device 4 to the base 25.
(48) The base 25 is mounted to a proximal ring assembly 26 of a retractor which includes a sleeve 27 which may extend in two layers between a distal anchoring ring (not shown) and the proximal ring assembly 26. One such retractor is described in our US 2005-0090717A, the entire contents of which are incorporated herein by reference. The base 25 has a tab 29 to aid dismounting of the base member 25 from the retractor. A pull ring 30 may be used to aid release of the retractor.
(49) The instrument insertion devices 2, 3, 4 are arranged in sealing relationship to a body of a patient, in use. The instrument seals 2, 3, 4 are spaced proximally of the proximal ring assembly 26.
(50) The connectors 20, 21, 22 connect the proximal ring assembly 26 to the instrument seals 2, 3, 4. The connectors 20, 21, 22 may be integral with the connector base 25 and the seals 2, 3, 4 subsequently attached, for ease of manufacture. In addition, instrument seals 2, 3, 4 can be housed in relatively rigid housings for added strength whilst maintaining connector flexibility.
(51) In use, a wound opening is created in a tissue wall, and the distal anchoring ring is inserted through the wound opening into the wound interior. The proximal ring assembly 26 is located externally of the wound opening, with the retractor member extending proximally from the distal anchoring member through the wound opening. The second end of the retractor member is pulled proximally relative to the proximal ring assembly 26 to retract laterally the sides of the wound opening. Instruments may then be inserted through the instrument seals 2, 3, 4, extended through the connectors 20, 21, 22, and extended through the retracted wound opening and into the wound interior.
(52) Referring especially to
(53) In the embodiment of
(54) In the case of the devices of
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(62) The device 200 of
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(64) The device 250 of
(65) In the case of the access devices of
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(67) The device 300 of
(68) A base part of the access device of
(69) The instrument insertion devices may be coded such as by indicia or colour coding to indicate a particular instrument size that may be used with a particular device size. For example, the colour blue may be used to indicate use with an instrument of up to 5 mm in size, white for up to 10 mm instruments, grey for up to 12 mm instruments, and orange for up to 15 mm instruments.
(70) It will be appreciated that features described with reference to one embodiment of the invention may be utilised with any of the other embodiments.
(71) The invention is not limited to the embodiments hereinbefore described which may be varied in detail.