US20070203398A1 - Surgical device for retracting and/or sealing an incision - Google Patents

Abstract

A wound protector retractor comprises an inner O-ring for insertion through a wound opening and a connecting sleeve extending between the O-ring and outer mounting means. The outer means are provided by rings between which the sleeve is led. The rings are rotated relative to each other and the inner ring to form a centralised lumen of reduced cross section and to shorten the axial extent of the sleeve. A wound is both retracted and protected.

Description

BACKGROUND OF THE INVENTION
• The present invention relates to a surgical device. More specifically, the invention relates to devices for retraction of an incision or natural bodily opening during surgery and for protecting the edges of incisions from infection or tumour seeding during surgery.
• Wound Retraction
• Adequate anatomical exposure is required in modern surgical procedures to allow procedures to be safely and effectively performed. Anatomical exposure is achieved by separating the walls of a natural orifice or spreading apart the margins of a surgical incision. A difficult surgical procedure can be simplified by adequate retraction whereas a relatively simple procedure can be made more difficult or even dangerous by the lack of adequate retraction. Exposure is maximised with correct incision placement and well directed retraction.
• Retraction can be achieved in several different ways. The most common method of surgical wound retraction is by the use of hand held retractors. These may be made of metal or thermoplastics and allow an operator to apply a retraction force to the wound edges. They are disposable or reusable and come in a variety of shapes and sizes to satisfy the requirements of different surgical procedures.
• Another type of retractor are Frame mounted retractor devices are also known. Such devices consist of a rigid circular or horseshoe-shaped frame on which multiple, detachable and movable paddle retractors are attached. The device may be mounted to an operating table to provide secure anchorage. Retraction may be applied in required directions. Typically such retractors are made of stainless steel to facilitate cleaning and sterilisation for reuse. Some of the more complex retractors need to be taken apart before sterilisation and reassembled before use. These devices always apply retraction at a few specific locations on the wound. This is a disadvantage of such devices as it can lead to regional ischaemia on parts the wound edge.
• A wound retractor and protector is disclosed in U.S. Pat. No. 5,524,644 (Crook). This device consists of an open-ended sleeve of polymeric material with a flexible ring at each end. One ring is inserted into the incision and the sleeve is manually rolled up around the other ring to apply tension to the polymeric material to achieve retraction. The device is often difficult to use because of the manual dexterity required, especially when the surgeons hands are wet. In addition, the device is incrementally adjustable. This restricts the efficiency of the device across all abdominal wall thicknesses.
• U.S. Pat. No. 5,545,179 (Williamson IV) describes a device having an elastomeric sealing element and a tubing conduit. The device protects the edges of the wound from contamination. However, the device is specifically for laparoscopic instruments and is not suitable for hand assisted surgery because the wound opening is not sufficiently retracted.
• WO-A-96/36283 (Mollenauer) describes a trocar device for retracting and sealing an incision and providing a sealed access port for surgical instruments. Whilst this incision and providing a sealed access port for surgical instruments. Whilst this device provides both retraction and protection to the wound edge is not suitable for use in hand assisted surgery due to size limitations. The device retracts and protects due to the inflation of one or one or more balloons and because these close the lumen when inflated it is not possible to visualise the contents of the abdomen through the device.
• WO-A-98/48724 discloses a device for use in hand assisted laparoscopic surgery. The device has a wound retractor/protector component and a component for sealing around the wrist of the surgeon. The wound protector component consists of an inner ring and two outer inflatable doughnut-shaped rings mounted vertically on top of another. The inner and outer rings are linked by an elastomeric sleeve. Inflation of the two outer rings causes retraction of the elastomeric sleeve. This device provides wound retraction and protection but it is not suitable for device has a large vertical profile due to the outer rings. This restructs reach into the incision and extends the fulcrum of any instruments used in such a way that their effective reach and breath of lateral movement would be severely restricted.
• Wound Protection
• The sides of an open wound are susceptible to infection and cross contamination if they are touched by contaminated material such as body parts or fluids as they pass through the opening of a wound. Serious problems can also result from cancerous material coming into contact with the wound edge. It is well known that cancerous cells may become seeded in wound areas, especially at trocar sites.
• To avoid such problems great care is taken to protect the edges of an incision using drapes that are impervious to liquids. An incision liner is disclosed in U.S. Pat. No. 3,397,692 (Creager). This linear comprises a sheet of polymeric material. The sheet has a hole cut out in the centre and the edges of the hole are reinforced using a semi-rigid ring. This ring can be inserted into the incision allowing a surgical procedure to proceed through the ring while the material attached to the ring protects the edges of the incision from contaminants in the wound site. These device marketed as “Steridrape” by 3M Corporation and comes in a variety of sizes for different wound sizes. However such devices do not adequately retract an incision.
• In general known devices are of either complex construction, do not effectively seal a wound and/or are difficult to operate.
• There is therefore a need for an improved surgical device that will overcome at least some of these problems.
STATEMENTS OF INVENTION
• According to the invention there is provided a surgical device comprising:
• • an inner mounting means for insertion through a wound opening;
  • a first outer mounting means for mounting external of a wound opening; and
  • connecting means extending between the inner and outer mounting means;
  • the connecting means being movable to shorten the axial extent of the connecting means.
• In a particularly preferred embodiment of the invention the outer mounting means is movable relative to the inner mounting means to twist the connecting means to form a lumen of reduced cross section and to shorten the axial extent of the connecting means.
• Most preferably the outer mounting means is rotatable relative to the inner mounting means to twist the connecting means.
• In a particularly preferred embodiment of the invention the connecting means is a sleeve of pliable material extending between the inner and outer mounting means.
• In one aspect the device includes a second outer mounting means, the connecting means extending between the first outer mounting means, the inner mounting means, and the second outer mounting means.
• In this case preferably the first and second outer mounting means are rotatable relative to one another to twist the connecting means and to draw the inner mounting means towards the outer mounting means. The outer rings also rotate relative to the inner mounting means.
• In a particularly preferred embodiment the inner mounting means is an O-ring. Preferably the connecting means is a sleeve which is led from the first outer mounting means to the O-ring and from the O-ring to the second outer mounting means.
• In a preferred embodiment of the invention the device includes locking means for locking the first outer mounting means relative to the second outer mounting means.
• In one arrangement one of the outer mounting means is located or locatable within the other outer mounting means.
• Preferably the inner diameter of the sleeve is greater than or equal to the axial length of the sleeve.
• In a preferred arrangement the inner diameter of the sleeve is greater than the axial length of the sleeve by an amount less than the thickness of an average abdominal wall, which is typically 2 to 6 cm. This assists in achieving a retraction force.
• Preferably a substantially gas tight seal is formed between the outer mounting means on shortening of the length of the sleeve. Ideally, the sleeve extending between the first and second outer mounting means defines an inflatable space.
• In one embodiment of the invention the device includes a port for connection to an inflation means.
• The invention also provides a surgical device comprising:—
• • an inner mounting means for insertion through a wound opening;
  • a first outer mounting means;
  • a second outer mounting means; and
  • a sleeve of pliable material extending from the second outer mounting means to the inner mounting means and from the inner mounting means to the first outer mounting means.
• Preferably one or both of the first and second outer mounting means are movable relative to one another to adjust the diameter of the lumen defined by a twist in the sleeve extending therebetween.
• Ideally, the first and second outer mounting means are rotatable relative to one another.
• In one embodiment of the invention the sleeve is releasably mounted to the second outer mounting means for adjustment of the length of the sleeve.
• Preferably the second mounting means comprises a receiver and the sleeve is mounted or mountable to a ring which is releasably mounted to the receiver.
• In another embodiment of the invention the inner mounting means is configured to reduce the size thereof for ease of insertion into a wound opening.
• Typically in this case the inner mounting means comprises a ring which includes a hinge means for reducing the size of the ring.
• A device as claimed in claim1 wherein the connecting means is translated to shorten the axial extent of the connecting means.
• A device as claimed in claim23 wherein the connecting means comprises a sleeve which is translated by a drawstring mechanism.
• A device as claimed in claim24 wherein the connecting means comprises a plurality of straps attached to the inner mounting means, the straps being pulled upwardly to shorten the axial extend of the connecting means.
• Typically the outer mounting means includes a holder for holding a surgical instrument.
• The surgical device may form a wound retractor, a wound protector or a wound protector retractor.
BRIEF DESCRIPTION OF DRAWINGS
• The invention will be more clearly understood from the following description thereof given by way of example only with reference to the accompanying drawings, in which:—
• FIG. 1 is a perspective view of a surgical device according to the invention;
• FIG. 2 is a cross sectional view of the device ofFIG. 1;
• FIG. 3 is a cross sectional view of the device in one position of use;
• FIG. 4 is a cross sectional view of the device in another position of use;
• FIG. 5 is a top plan view of the device in the position ofFIG. 4;
• FIGS. 6 and 7 are respectively perspective and cross sectional views illustrating a method of forming the device of FIGS.1 to5;
• FIG. 8 is a perspective view of another surgical device according to the invention;
• FIG. 9 is a cross sectional view of the device ofFIG. 8 in one position of use;
• FIG. 10 is a cross sectional view of the device ofFIG. 8 in another position of use;
• FIGS. 11 and 12 are cross sectional views of another surgical device according to the invention in different positions of use;
• FIG. 13 is a plan view of the device ofFIG. 11;
• FIG. 14 is a cross sectional view of a further surgical device according to the invention;
• FIGS. 15A and 15B are cross sectional views of the device ofFIG. 14, in use;
• FIG. 16 is plan view of the device ofFIG. 14;
• FIG. 17 is a cross section view of another surgical device of invention;
• FIG. 18 is a plan view of the device ofFIG. 17;
• FIG. 19 is a cross sectional view of another surgical device of the invention;
• FIG. 20 is a plan view of the device ofFIG. 19;
• FIG. 21 is a cross sectional view of a further surgical device of the invention;
• FIG. 22 is a cross sectional view of a still further surgical device of the invention;
• FIG. 23 is plan view of the device ofFIG. 22;
• FIG. 24 is a perspective view of another surgical device of the invention;
• FIG. 25 is a perspective view of the device ofFIG. 24 being adjusted;
• FIG. 26 is a side, partially cross sectional view of the device ofFIGS. 24 and 25;
• FIG. 27 is a view similar toFIG. 26 of the device partially disassembled;
• FIG. 28 is a view similar toFIG. 26 with the device ofFIG. 27 re-assembled;
• FIG. 29 is a diagrammatic perspective view of another surgical device of the invention;
• FIG. 30 is a perspective view of the device ofFIG. 29 in a wound inserting configuration;
• FIGS. 31 and 32 are respectively diagrammatic perspective and plan views of an inner ring part of the device ofFIGS. 29 and 30;
• FIG. 33 is a cross sectional view of two surgical devices ready for assembly;
• FIG. 34 is a cross sectional view of the devices ofFIG. 33, assembled;
• FIG. 35 is a plan view of another surgical device according to the invention;
• FIG. 36 is a cross sectional view on the line A-A inFIG. 35 with the device in position in an incision;
• FIG. 37 is a plan view of the device ofFIGS. 35 and 36 in another position of use; and
• FIG. 38 is a cross sectional view on the line B-B ofFIG. 37.
DETAILED DESCRIPTION
• Referring to the drawings and initially toFIG. 1 to7 thereof there is illustrated a surgical device, especially for use in laproscopic surgery. The device1 in this case is used in surgery involving anincision2 in a wall3 of a patients abdomen. The wound is, in this case, both protected and retracted by the device1 of the invention. Thus, the invention in this case provides a wound protector retractor.
• The device1 comprises an inner mounting means in the form of an O-ring10 of flexible material such as of elastomeric material for insertion through thewound opening2, an outer mounting means for mounting external of thewound opening2 and a connecting means, in this case in the form of asleeve11 extending between the inner10 and outer mounting means. The outer mounting means is movable, in this case rotatable, relative to the inner O-ring10 to twist thesleeve11 to form acentralised lumen12 of reduced cross section and to shorten the axial extent of thesleeve11. As thesleeve11 is twisted the inner O-ring10 is drawn upwardly from the inserted position illustrated inFIG. 3 to the in-use position illustrated inFIG. 4 in which the wound is sealed and a radial retraction force is applied to the wound. A surgeon inserts a sealed gloved hand/arm/instrument through the sealed and retracted wound to perform a surgical procedure within the abdomen.
• In this preferred case the outer mounting means comprises a first outer mounting means in the form of a firstannular ring20 and a second outer mounting means in the form of a secondannular ring21. Thesleeve11 is of biocompatible pliable gas impermeable plastics material and is attached at one end to thering20 and at an opposite end to thering21. Thesleeve11 is connected to thering20, led over the O-ring10 and back up for attachment to thering21 as best illustrated inFIG. 2.
• In use, a surgeon makes an incision in the abdominal cavity and the O-ring10 is flexed and inserted through the incision as illustrated inFIG. 3. The outer rings20,21 are then rotated relative to one another in the direction of the arrows A and B inFIG. 3. This relative rotation twists thesleeve11 and shortens the sleeve until the device is in the operative position ofFIG. 4. In this position the inner O-ring10 is engaged against the inside of the interior of the anterior abdominal wall and therings21 and22 are external of the wound opening with thesleeve11 shortened in axial extent. The twisting of thesleeve11 provides acentral lumen12 of reduced size, which depends on the degree of twist. A full 180° relative twist would result in closing down of the lumen. The reducedlumen12 provides access for instruments and/or a surgeons arm while maintaining a wound seal.
• Locking means of any suitable type may be provided to lock therings20,21 together. The locking means may, for example comprise a releasable latching system such as a ratchet and pawl arrangement or the like.
• Preferably a gas tight seal is formed between therings20,21 in use. The sleeve in this case provides aninflatable space30 between therings20,21 and the inner O-ring10. An inflation connection port may be provided in the device to facilitate inflation. On inflation, a wound engaging section11aof the sleeve is pushed radially outwardly to provide a highly efficient wound protector/seal and wound retractor. The inner sleeve section11bis inflated to further restrict thelumen12 and provide highly efficient sealing engagement with a surgeons forearm, a device or an instrument inserted through the lumen.
• For efficient sealing engagement it is preferred that the inner diameter (d) of thesleeve11 is greater than or equal to the axial length (l) of thesleeve11 as illustrated inFIG. 7. Preferably the inner diameter of the sleeve is greater than the axial length of the sleeve by an amount which is less than the thickness of an average abdominal wall. With this configuration on twisting of thesleeve11, sealing and retraction forces are applied to the wound opening.
• The surgical device1 may be formed from acylindrical sleeve50 of pliable plastic material attached to a pair ofrings20,21 as illustrated inFIGS. 6 and 7. A flexible O-ring10 is fitted over thesleeve50. Theflexible sleeve50 is then turned over on itself so that the O-ring10 is confined between inner and outer sleeve sections11a,11band therings20,21 are in the configuration illustrated inFIGS. 1 and 2.
• The device of the invention applies a force to the wound edges to achieve adequate exposure without causing ischaemic injury to the wound edges. The device protects wound edges from cross infection or seeding by cancerous or otherwise malignant cells. Another advantage is that the device is sufficiently inexpensive that it can be disposed of after a single use thereby obviating the need for cleaning and sterilisation between use. In addition, the device is simple to place into a desired position in a wound or natural bodily opening and easy to remove, especially without negating the benefits gained from use of the device as a wound protector.
• Referring to FIGS.8 to10 there is illustrated another surgical device60 according to the invention. The device60 is similar to the device1 and like parts are assigned the same reference numerals. In this case thesleeve61 is a single wall sleeve and there is only one outer mountingring62. On rotation of theouter ring62 relative to the inner ring10 a twist is formed in the sleeve which is shortened, drawing theinner ring10 upwardly against the interior of the anterior abdominal wall as illustrated inFIGS. 9 and 10.
• It will be appreciated that the inner O-ring may be fixed, for example, by adhesives to the sleeve of the surgical device. It will also be appreciated that one or more of the mounting means may be shaped to positively engage with tissue. For example, the mounting means may include tissue-engaging projections to lock the mounting means in position.
• It will be appreciated that while for efficient retraction and wound protection it is preferred that the connecting means between the outer and inner mounting means is in the form of a sleeve of pliable material, the connecting means may be discontinuous. For example the sleeve may be in the form of elongate strips or the like.
• Referring to FIGS.11 to13 there is illustrated anothersurgical device70 according to the invention. In this case the connecting means comprises a plurality ofstraps71 which are drawn upwardly to shorten the axial extent and to form a wound retractor. Thestraps71 are retained in the shortened configuration illustrated by any suitable locking means such as bywedge elements72. In this case an irisdiaphragm type device80 is provided in the wound opening which is inflatable from the rest configuration illustrated inFIG. 11 to the pressurised inflated configuration illustrated inFIG. 12.
• Referring to FIGS.14 to16 there is illustrated anotherdevice85 according to the invention in which the connecting means is defined by a plurality ofstraps86 which are movable between aninner mounting ring83 and anouter mounting ring84 bybuckle devices87 from the initial position illustrated inFIG. 15B to the wound retracting position ofFIG. 15 A. Theinner ring83 is first inserted though the incision. Theouter ring82 is then brought down to skin level by taking up the slack in thestraps86. To achieve the retraction effect thestraps86 are pulled taut causing the wound edge to be displaced out from the centrepoint of the wound. Thestraps86 may be adjusted until optimum retraction is achieved. Tension in thestraps86 is maintained by thebuckles86 which may hold thestrap86 taut either by friction or using a clasp mechanism.
• Referring toFIGS. 17 and 18 anothersurgical device90 similar to thedevice85 is illustrated. In this case the inner and outer mounting rings82,83 are of oval shape in transverse cross section to smooth the movement of thestraps86. This device operates in a similar manner to thedevice85.
• Referring toFIGS. 19 and 20 there is illustrated anothersurgical device93 which has single legged straps94. This device operates in a similar manner todevices85 anddevice90. In this case straps94 do not loop around theinner ring83 but are directly attached to it.
• Referring toFIG. 21 there is illustrated a furthersurgical device95 havingstraps96 which are locked in position by a locking mechanism. The locking mechanism comprises a wedge97 inserted into a hole through which thestrop96 passes to hold thestrap96 in position by friction. A ratchet mechanism may also be used or some other adjustable locking mechanism to hold the strap in position.
• Thedevice98 illustrated inFIGS. 22 and 23 is similar to the device ofFIG. 21 except that a different construction of wedge or ratchet99 is used to lock the straps in position.
• Referring to FIGS.24 to26 there is illustrated another surgical device according to the invention. In this case the surgical device is awound protector retractor200 of similar construction as that described above with reference to FIGS.1 to10. The device1 comprises an inner mounting means in the form of a first O-ring201, a first outer mounting means in the form of a second O-ring202 mounted in afirst receiver203, and a second mounting means in the form of a third O-ring205 mounted in asecond receiver206. Thereceivers203,206 are in this case interconnectable as illustrated and a fourth O-ring207 is provided between thereceivers203,206 on assembly.
• Asleeve210 of flexible pliable plastics material extends from the secondouter receiver206 to the inner O-ring201 and from the inner O-ring201 to the firstouter receiver203. Thereceivers203,206 are de-mountable as illustrated inFIG. 25 to facilitate relative rotation therebetween in the direction of the arrows to vary the degree of twist in thesleeve210.
• Referring toFIGS. 27 and 28 there is illustrated anothersurgical device220 which is similar to the device of FIGS.24 to26 and like parts are assigned the same reference numerals. In this case the O-ring205 is de-mountable from thereceiver206 to facilitate length adjustment of thesleeve210. On removal of the O-ring205 thesleeve210 is adjusted to a desired length d. In this way asingle device220 may be used for a variety of thickness of abdomens. The lumen diameter defined by the twist does not need to be changed to cater for a range of abdomen sizes. The excess sleeve may be cut off or wound around the O-ring seal205.
• Referring now to FIGS.29 to32 there is illustratedpart230 of another surgical device according to the invention which is similar to the devices of FIGS.24 to28 and like parts are assigned the same reference numerals. An inner mounting means231 is configured to reduce the size thereof for ease of insertion into a wound opening. In this case the inner mounting means231 is in the form of a split ring which is hinged at232 to facilitate a reduction in the diameter of thering231 as illustrated. It will of course be appreciated that the hinge may be integrally formed and indeed, there may be a number of such hinges.
• Referring toFIGS. 33 and 34 there is illustrated an assembly of twosurgical devices250,260. Thedevice250 is a forearm seal and thedevice260 is a wound protector retractor which is assembled to anouter sealing device250. Thesealing device250 provides an outer sealed access port through which a surgeon may insert his forearm or for insertion of an instrument or the like.
• Referring to FIGS.35 to38 there is illustrated anothersurgical device300 according to the invention. Thedevice300 is a wound protector retractor similar to those described above. In this case thewound protector retractor300 comprises aninner ring301 of semi-rigid elastomeric material and anouter ring302 which is of similar material. Asleeve303 of pliable material extends between therings301,302.Drawstrings305 are fitted to thesleeve303, the drawstrings being pulled outwardly in the direction of the arrows to pull thesleeve303 upwardly to tighten in the incision and provide a wound protector and retractor.
• Reference is also made to appropriate alternatives and modifications which are outlined in our parallel applications referenced ATRO1/C, ATRO12/C, ATRO14/C/, ATRO15/C, ATRO16/C/, ATRO17/C, the entire contents of which are incorporated herein by reference.
• The invention is not limited to the embodiments hereinbefore described which may be varied in construction and detail.

Claims (14)

1.-37. (canceled)

38. A surgical device for use in minimally invasive surgery of the type using an inflated body cavity accessible to a surgeon through an access port, defined by the device, surrounding an incision in a patient's body, the device having:

body cavity engagement means for insertion into the incision to locate the device in position;

fixing means for attaching the device to a patient's skin, the fixing means including a proximal ring;

a sleeve connected between the body cavity engagement means and the fixing means, wherein the sleeve is adjustable by the positioning of the proximal ring so that the positioning of the proximal ring retracts the sleeve to cause the sleeve to apply outward pressure against the patient's body to retract the incision to define an access port and create a seal between the incision and sleeve; and

sealing means, at least one of mounted on the sleeve and operating on the sleeve, to prevent substantial leakage of gas from the body cavity on inflation when in an inoperative position and formed to mould about a substantial portion of a surgeon's hand or surgical instrument on insertion in an operating position.

39. The surgical device ofclaim 38 in which the body cavity engagement means is provided by a distal ring formed for insertion into the incision.

40. The surgical device ofclaim 39, in which the sealing means includes a self-sealing valve mounted on the sleeve.

41. The surgical device ofclaim 39, in which the fixing means incorporates adjustment means for modifying the length of the sleeve, so as to ensure that the fixing means and the distal ring may be brought into close contact with the abdominal wall ensuring a good seal is maintained and that the device is firmly mounted in position.

42. The surgical device ofclaim 38, further including a connector ring mounted adjacent said proximal ring.

43. The surgical device ofclaim 38, in which the sleeve is made of an elastomer material, whereby insertion of the distal ring into an incision stretches the elastomer material causing tension between the distal ring and proximal ring.

44. The surgical device ofclaim 38, wherein said sealing means is an external proximal valve mounted adjacent to said proximal ring.

45. The surgical device ofclaim 38, wherein said sealing means is an internal distal valve.

46. The surgical device ofclaim 38, wherein said sealing means is a self-sealing spring valve including a tensioned member mounted on the sleeve.

47. A surgical device for use in minimally invasive surgery of the type using an inflated cavity accessible to a surgeon through an access port, defined by the device, surrounding an incision in a patient's body, the device comprising:

body cavity engagement means for insertion into the incision to locate the device in position, said body cavity engagement means including a distal ring;

fixing means for attaching the device to a patient's skin, said fixing means including a proximal ring;

a sleeve connected between the body cavity engagement means and the fixing means, said sleeve having an adjustable length that shortens to cause said sleeve to apply outward pressure against the patient's body sufficient to retract the incision to define the access port; and

one of an external proximal sealing valve mounted adjacent to said proximal ring and an internal distal sealing valve mounted adjacent to said distal ring, to prevent substantial leakage of gas from the body cavity on inflation when in an operative position and formed to mold about a substantial portion of a surgeon's hand or surgical instrument on insertion in an operating position.

48. The surgical device ofclaim 47, wherein said one of an external proximal sealing valve mounted adjacent to said proximal ring and an internal distal sealing valve mounted adjacent to said distal ring is a self-sealing spring valve including a tensioned member mounted on the sleeve.

49. A surgical device for use in minimally invasive surgery of the type using an inflated cavity accessible to a surgeon through an access port, defined by the device, surrounding an incision in a patient's body, the device comprising:

body cavity engagement means for insertion into the incision to locate the device in position, said body cavity engagement means including a distal ring;

fixing means for attaching the device to a patient's skin, said fixing means including a proximal ring;

a sleeve connected between the body cavity engagement means and the fixing means, said sleeve having a length;

wherein said proximal ring includes an adjustment means for adjusting the length of said sleeve to cause said sleeve to apply outward pressure against the patient's body sufficient to retract sides of the incision; and

one of an external proximal sealing valve mounted adjacent to said proximal ring and an internal distal sealing valve mounted adjacent to said distal ring, to prevent substantial leakage of gas from the body cavity on inflation when in an operative position and formed to mold about a substantial portion of a surgeon's hand or surgical instrument on insertion in an operating position.

50. The surgical device ofclaim 49, wherein said one of an external proximal sealing valve mounted adjacent to said proximal ring and an internal distal sealing valve mounted adjacent to said distal ring is a self-sealing spring valve including a tensioned member mounted on the sleeve.

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