CA2029668A1 - Sterile surgical needle-suture combination - Google Patents
Sterile surgical needle-suture combinationInfo
- Publication number
- CA2029668A1 CA2029668A1 CA002029668A CA2029668A CA2029668A1 CA 2029668 A1 CA2029668 A1 CA 2029668A1 CA 002029668 A CA002029668 A CA 002029668A CA 2029668 A CA2029668 A CA 2029668A CA 2029668 A1 CA2029668 A1 CA 2029668A1
- Authority
- CA
- Canada
- Prior art keywords
- suture
- needle
- diameter
- monofilament
- reduced diameter
- Prior art date
- Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
- Abandoned
Links
Classifications
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
- A61B17/06166—Sutures
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
- A61B17/06004—Means for attaching suture to needle
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61L—METHODS OR APPARATUS FOR STERILISING MATERIALS OR OBJECTS IN GENERAL; DISINFECTION, STERILISATION OR DEODORISATION OF AIR; CHEMICAL ASPECTS OF BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES; MATERIALS FOR BANDAGES, DRESSINGS, ABSORBENT PADS OR SURGICAL ARTICLES
- A61L17/00—Materials for surgical sutures or for ligaturing blood vessels ; Materials for prostheses or catheters
- A61L17/14—Post-treatment to improve physical properties
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
- A61B17/06195—Apparatus or means for preparing the cut end of the suture thread to be attached to the needle, e.g. tipping to prevent brooming
-
- A—HUMAN NECESSITIES
- A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
- A61B—DIAGNOSIS; SURGERY; IDENTIFICATION
- A61B17/00—Surgical instruments, devices or methods, e.g. tourniquets
- A61B17/04—Surgical instruments, devices or methods, e.g. tourniquets for suturing wounds; Holders or packages for needles or suture materials
- A61B17/06—Needles ; Sutures; Needle-suture combinations; Holders or packages for needles or suture materials
- A61B17/06004—Means for attaching suture to needle
- A61B2017/06028—Means for attaching suture to needle by means of a cylindrical longitudinal blind bore machined at the suture-receiving end of the needle, e.g. opposite to needle tip
Abstract
ABSTRACT
A needle-suture combination with reduced diameter portion of the suture being attached to the blunt end of the needle. The maximum diameter of the suture being almost the same but no larger than the diameter of the blunt end of the needle and the reduced diameter portion of the suture having a tensile strength greater than the remainder of the suture.
0270n
A needle-suture combination with reduced diameter portion of the suture being attached to the blunt end of the needle. The maximum diameter of the suture being almost the same but no larger than the diameter of the blunt end of the needle and the reduced diameter portion of the suture having a tensile strength greater than the remainder of the suture.
0270n
Description
-`` 2~2~
STEB~LE SURG I CAI, NEEDLE- sI~rruRE COMB I NATION
Background of ~he Invention In many surgical procedures, it is desirable that when joining tissue using surgical nesdles and sutures, that the ma~imum diameter of the needle; that is, the diameter at the b~unt end of the needle, and the ma~imum diameter of the suture be as close to the sa~e size as possible. This design is necessary so that the hole in the tissue produced by passing the needle through the tissue is substsntially filled by the suture. This is especially important when joining vascular tissue to prevent oozing or seepage of blood through the hole produced by the needle.
Originally, surgical needles had an eye at the blunt end through which the suture was atta~hed. As can be appreciated, this meant that the blunt en~ of the needle had sufficient size to allow for an eye to be placed in and that at least double the maximum diameter of the suture would be placed through that eye so that the hole produced when the needle was passed through tissue was substantially greater than the diameter of the suture. Over the years, to improve surgical procedures, Yarious techniques have been developed to eliminate the eye in the blunt end of the needle and find other techniques by which the suture can be attached to the blunt end of the needle.
Some of the techniques that have been developed are to place a channel in the blunt end and crimp the suture in ~hat ch3nnel or swage the suture into a hole drilled in the blunt end of the needle. As can be appreciated, it is s~ill required that the diameter of th~ blunt end of the needle be substantially larger ' -' .
" ' - ` . . :
. - , . , ` .
STEB~LE SURG I CAI, NEEDLE- sI~rruRE COMB I NATION
Background of ~he Invention In many surgical procedures, it is desirable that when joining tissue using surgical nesdles and sutures, that the ma~imum diameter of the needle; that is, the diameter at the b~unt end of the needle, and the ma~imum diameter of the suture be as close to the sa~e size as possible. This design is necessary so that the hole in the tissue produced by passing the needle through the tissue is substsntially filled by the suture. This is especially important when joining vascular tissue to prevent oozing or seepage of blood through the hole produced by the needle.
Originally, surgical needles had an eye at the blunt end through which the suture was atta~hed. As can be appreciated, this meant that the blunt en~ of the needle had sufficient size to allow for an eye to be placed in and that at least double the maximum diameter of the suture would be placed through that eye so that the hole produced when the needle was passed through tissue was substantially greater than the diameter of the suture. Over the years, to improve surgical procedures, Yarious techniques have been developed to eliminate the eye in the blunt end of the needle and find other techniques by which the suture can be attached to the blunt end of the needle.
Some of the techniques that have been developed are to place a channel in the blunt end and crimp the suture in ~hat ch3nnel or swage the suture into a hole drilled in the blunt end of the needle. As can be appreciated, it is s~ill required that the diameter of th~ blunt end of the needle be substantially larger ' -' .
" ' - ` . . :
. - , . , ` .
2~2~8 ~ 2 --than the diameter of the body of the suture and he~ce when such a needle-s~ture combination is used to join tissue, the suture still does not completely fill the hole formed by the needle.
In recent years, various techniques have been developed to reduce the diameter o the suture at the end tha~ i8 to be attached to the blunt end of the needle and in many instances this has b~en accomplished so that the diameter of the body of the suture is substantially the same as the diameter of the blunt end of the needle. Some of these techniques are more fully described in U.S. Patents, 3,890,975 and 3,926,194.
Though these techniques produce a needle-suture combination wherein the maximum diameter of the suture is close to the diameter of the blunt end of the needle, in order to accomplish this they all greatly reduce the strength of the suture in that area of the suture that is attached to the needle or immediately adjacent that area. This, of course, produces a weakened needle-suture combination. This problem restricts the various sizes o ~utures that can be produced by these techniques especially the extremely ine size sutures. It also limits the types of materials that can be used to produce the sutures in that you must greatly i w rease ~he overall strengt~
of the suture to have sufficient strength at the reduced diameter portion.
~ummary_Qf the Present Inven~ion It is an object of the present invention to produce a needle-suture c~mbination, which when used to join tissue, the hole produced by the needle is substantially filled by the suture joining the tissue. It is a further object of the present invention to produce a needle-suture combination ;n which the area of the suture joi~ed to the needle and the area ~djacent that area has a tensile strength substantially greater than the remainder of the suture. It is a ~ur~her object of 2~2~g ~ 3 --the present invention to produce preferred n~edle-suture combination~ wherein the diameter of the body of the suture is almost the same as the diameter of the blunt end of the needle. It is yet a further object of the present invention to be able to attain these desirable characteristics with all suture sizes especially the smaller size sutures.
The surgical needle-~uture combination of the present invention comprises a surgical needle having a blunt end and a sharp point. A surgical suture has one end of the suture attached to the blunt end of the surgical needle. The diameter of the blunt end of the needle is somewhat larger or substantially the same as the maximum diameter of the suture or the diameter of the body of the suture. The portion of the lS suture attached to the blunt end of the needle and usually ~he portion immediately adjacent such attached portion has a reduced diameter as compared to the diameter of the body of the suture. In the preferred embodiments of the surgical needle-suture combinatiuns of the present invention, the reduced diameter portion has a tensile strength at least 50%
greater than the tensile ~trength of the body o the suture.
The present invention also includes the method for producing a surgical suture having a reduced diameter po~tion from monofilaments of various polymeric material The monofilament is helically wound to form a cylinder comprising a multiplicity of convolutions of the monofilament. Adjacent portions of each convolution are heated to an elevated temperature and the heated portions are then drawn to increase the length o the heated portions while reducing the diameter of the heated portions. This heating and drawing also increases the density and crystallini~y of the heated and drawn portion. Each convolution is sev~red to ~orm a suture having a reduced diameter end por~ion. Preferably, each convolution ;s . .
.
. .
, . . ' .
,:
2 ~
severed appro~imately in the center of ths reduced diarneter portion to form a suture having both ends of a reduced diameter.
Brief Des~ription of the Prawing~
Figure 1 is a perspecti~e view of a sterile surgical needle-suture combination of the present invention.
Figure 2 is a cross-sectional view of the needle-suture combination of Fig. 1.
Figure 3 is a perspective view o~ another e~bodiment o~
the sterile surgical needle-suture combina~ion o the present invention.
Figure g is a diagramatic ~iew of various steps in the process for producing needle-suture combinations.
Figure 5 is a perspecti~e view of the stretching drum used in the present invention.
Figure 6 is an end view of the stretching drum in its closed or initial original position.
25Fiqure 7 is an end view o~ the stretching drum of Fig. 6 in its open position.
Figure 8 is an end view of the stretching mechanism of Figs. 6 or 7 which also shows mechanism~ for moving the drum from the position shown in Fig. 6 to the position shown in Fig.
7.
Figure 9 is a top view of the mechanism shown in Figure ~.
- ~2~fi~
Detailçd Descript;on of the_Invention Referring to the drawings, in Fig . 1 there i~ shown one embodiment of this sterile surgical needle-suture combination 20 of tha present invention. The needle 21 has a sharp end 22 or point and a blunt end 23. Attached to the blunt end is a surgical suture 24. As more clearly shown ;n the cross-sectional view in Fig. 2, the blunt end 2~ has a hole 25 drilled into the center of the blunt end. The ~uture has a reduced d;ameter portion 26 which is inserted into that hole and attached to the blunt end of the needle. As may be seen in Fig. 2, the ma~imum diameter of the suture or the diameter of the body of the suture, is substantially the same as the maximum diameter of the needle or the blunt end of the needle.
In Fiq. 3, ther~ is shown another embodiment of the sterile surgical-needle suture combination 30 of the present invention In this embodiment, the blunt end 31 of the needle 32 has a channel 33. The reduced diameter portion 34 of the suture 35 is placed in that channel and the channel crimped about the reduced portion of the suture to attach the suture to the needle.
The sutures used to produce the needle-suture combinations of t~e present invention may be any of the monofilament sutures such as polyethylene, polypropylene, polyester, nylon, poly~lycolides, polyfluoro carbons, etc. The needles used in producing the needle-suture combinations of the present invention may be made from various metals such as stainless steel. The suture may be attached to the needle by any of the various techniques which allow for attachment of the suture to the blunt end of the needle, such as dr;lling a hole in the blunt end of the needle ~nd adhering or attaching the suture into that hole either using adhesive or by crimping or . .
2 ~
by placing the suture in a channel ~nd adhering it in the channel by crimping and/or adhesion or by various ot~.er techniques well known in the art.
Referring to Fig. 4, there is shown diagramatically one method for producinq surgical sutures which may be used in producing the surgical needle-suture combinations of the present invention. ~xtruded monofilaments 40 are supplied from a supply roll 41 and passed around a pair of rolls 42 and 43 called a ~Godet~ and the e~truded monofilament then passed through a hot oven 44. The monofilament is then taken up on a second pair of rolls 45 and 46 or second ~Godet~ and then wound up on a wind up roll 47. The second pair of drawing rolls 45 and 45 are operated at a speed 16% slower than the first pair lS of drawing rolls 42 and 43, so ~hat as the e~truded mono-filament passes through the oven the monofilament is relaxed.
Depending upon the composi~ion of the monofilament, the oven will be heated to a suitable temperature to allow the monofilament to relas. If a polypropylene monofilament suture is being produced, the oven would be maintained at about 285F. The wound up rela~ed monofilament on the wind-up roll 47 is moved to another feed station 48 and wound on a split drum 49~ The diameter of the drum is ~uch as to allow for the production of the desired length of sutures. A portion of the surface of the drum has been flattened and there are a pair of bars 50 and 51 or xollers at the edges of this flattened surface so that when the monofilament is helically wound around the circumference of the drum, the portion of the monofilament e~tending between these two bars is displaced from the surface of the drum. The filaments are held in positlon by clamps 58 and S9 placed on the outside of the 1attened section adjacent the rollers. A heater bar 52 is placed adjacent the portion of the monofilament which passes between these two bars and the monofilament warmed or heated. If the monofilament is made from polypropylene, it is heated ~y this heating bar to about 2~2~
300~F for from about 3 to 5 minutes. One section 53 or half of the drum is then di~placed from the stationery half 54 of the drum to increase the circumference of the drum and draw or stretch the portion of the monofilament e~tending between the roller bars. The distance the filament i~ drawn or~Jtretc~ed stretched will depend on the si~e of the suture being produced but may vary from two inches to ~hree inches or more. Upon drawing, the d~ameter of the filament is reduced in the area that ~s drawn, that is, the area between the bars. After drawing, a cutting board 55 may ~e placed underneath the drawn portion and the drawn portion of the wound monofilament cut with a razor knife 56 substantially in the center of the drawn or stretched area. The cut sutures having reduced diameter portions at each end are dropped onto a tray 57. The tray is taken to another station where needles are attached to each end by swaging or other known tec~niques. The double-armed sutures are then wound and packaged as is well known. The needle-su~ure combination may then be sterilized by any of the technigues known in the art such as ethylene oside, radiation, etc.
It is important that the drawing or ~tretching drum be circular or substantially circular in configuration to minimize any set or kink developing in the monofilament as a result of the processing.
The stretching drum will be mora fully described in conjunction with Figs. 5 through 9. The drum 60 comprises two halves 61 and 62. Preferably, the drawn is split sli~htly off-center so that th~ stationery half 61 is slightly larger than the moveable half 62. This configuration will allow the shaft 74 to be placed at the center of tha closed drum. When the hal~es are adjacent, the drum has a substantially c;rcular cross-section. The split drum i~ flattened for abou~ 4 inches at the area 63 where one of the halves meets the other half of , '~2~8 the drum. Disposed in this flat area about 4 inches apart are a pair of roller bars 64 and 65. One half of the drum is stationery and is attached to a stationery stand 66. The opposite half of the drum is moveable and is attached through a moveable yoke mechanism 67. The e~truded monofilament is ~ound about the circumference of the drum. The length of the drum will determina the number of s~rands that can be made around the drum, and the diameter of the drum will determine the length of the sutures to be produced.
Opposite the flat section of the drum, the drums are attached by a hinge 68.
Once the sutures are wound about the drum, i~mediately adjacent each side of the flattened portion there are clamps 69 and 70 which are used to clamp the estruded monofilament winds to the surface of the drum. A moveable heater bar 71 is placed adjacent the monofilament winds at the 1att~ned area of the drum to heat these portions of the winds to the desired temperature.
Once this portion has been heated sufficiently, the moveable yoke is moved away so as to displace the moveable half of the drum from the stationery half o the drum with the gap at its widest portion being from about two to four inches.
This stretches each monofilament wind in the portion of the wind between the roller bars. A cu~ting sur~ace 72 is placed under the stretched portion of the winds of the monofilament and a suitable razor knife 73 is passed along this cutting board to cut the monofilaments in the stretched areas and produce a plurality of sutures having a reduced diameter portion at each end of the suture. The sutures are collected, needles attached and packa~ed as is well ~nown in the artO
2 ~
The stretching ~f the monofilament material at the desired temperature produces a reduced diameter portion which portion has a tensile strength substantially greater than the remainder of the ~uture. The tensile strength may be as much as 50% to 60% greater than the tensile strength of the body of the suture.
The followinq is specific example for producing needle-suture co~binations accordinq to the present invention.
Example An extruded monofilament of polypropylene is produce and wound on a wind-up roll. The propylene monofilament is fed to a first ~odet~. The first ~Godet~ is operated at a speed of appro~imately 70 feet per min~te and the monofilament is wrapped about this "Godet~ approsimately ~i~ times. The filament is pas~ed ~hrough a hot air oven with the oven maintained at a temperature of about 285F. ~he filament is wound on a ~econd ~Godet~ with the second ~odet~ being operated at a speed of appro~imately 60 feet per minute, so that as the monofilament passes through the oven it is relaxed about 16%. The rela~ed monofilament is taken from ~he second ~Godet~ and wound up on a suitable wind-up roll.
The rela~ed polypropylene monofilament is then wound on a split drum as described in conjunctions with Fi~s. 5-9. The drum i~ about twelve inches in diameter and about 300 winds of the r~la~ed polypropylene monofilament cover the surface of the drum. An electric heater bar is placed against the portion of the monofilaments that pass ~etween the two bars forming a portion of the surface o~ the drum. The polypropylene is heated to a appro~imately 300F for about 5 minutes. The moveable ~ection of ~he drum is then di~placed from the stationery section of the drum to draw the heated portion of . ~
; ` ~ '.
, , 2~9~
the monofilaments about 3 inches, to reduce the diameter of the monofilament in the portion that passes between the two bar~.
A cutting surface is pla~ed beneath the ~tretched portions of the monofilament~ and a razor knife passea down the center of the stretched portions to cut the winds on the drum and form separate sutures which have a reduced diameter portion at each end. The cut sutures are collected and a needls having a channel in the blunt end is attached to each reduced diameter end of the suture to produce a double-armed suture. The sutures are suitably wound and packaged and sterilized using cobalt radiation. Size 3~0, 4/0 and 5/0 polypropylene sutures are produced as described above. The diameter, density (which is an indication of crystallinity) and the tensile strength of both the body portion and the reduced diameter portion of each o~ the sutures is measured. The 3/0 suture has a diameter in the body portion of 9.85 mils, a density of 0.9085 gm/cc3 and a tensile strength of 67,000 lbs. per s~uare inch while the reduced diameter portion of the size 3~0 suture has a diameter of 7.1 mils, a density of 0.9113 gm/cc3 ana a tensile strength of 109,000 lbs. per sguare inch. The diameter of the ~ody portion of the 9/0 suture is 7.6 mil~, a density of 0.9085 gm~cc3 and the tensile strength 73,000 lbs. per sguare inch while the reduced diameter portion has a diameter of 5.2 mils, a density of 0.9112 gk/cc3 and a tensile strength of 138,000 lbs. per square inch. The S/0 suture has a diameter in the body portion of 5.7 m~ls, a density of 019103 gm/cc3 and a tensile strength in this portion of 75,000 lbs. per square inch while the reduced diameter portion of the 5/0 suture has a diameter of 4.0 mils, a density of 0.9112 ~m~cc3 and a tensile stren~th of 129,000 lbs. per square inch.
The ratio of the diameter of the blunt en~ of the needle to the body diameter of the 3/0 suture i~ 1.46 to 1 as compared to a ratio of 2.08 to 1 for conventional 3/0 needle-~uture combinations. The ratio of the diameter of the blunt end of , ' ' ~2~8 the needle to the body diameter of the 4/0 suture is 1.51 to 1 as compared to a ratio o~ 2.24 to 1 for a conventional 4/0 needle-suture. The ratio of th0 diameter of the blunt end of the needle to the body diameter of a 5~0 suture is 1.62 to 1 as compared to 3 ratio of2.16 to 1 for a 5/0 needle-suture.
Test methods used for determining the physical properties of monofilament suturQ materials w~re as follows:
Tensile strength is determined by A.S.T.M. method D-2256-66T a~ a constant rate of e~tension using an INSTRON table Model 4200 universal testing instrument manufactured by the Instxon Corporation of Canton, Massachusetts, With the instrument sample clamps set 5 inches apart, 5-inch lengths of su~ure were elonqated at a rate of 12 inches per minute until fracture.
The INSTRON instrument was set or th~ correct suture diameter, ~nd Young's Modulus was calculated in psi from the initial stress-strain data generated during the straight tensile strength test. Young'~ ~odulus is the ratio of applied stress to strain ~n the elastic region of the suture and measures the elastic component of a suture's resistance to stress. This value is rclated to the fleYibility of a suture.
As many apparently widely different embodiments of this invention may be made without departing ~rom the ~pirit and scope thereo~, it is to be understood tha~ the invent~on ~ not limited to the specific embodiment~ ~hereof e~cept as defined in the following claims.
.
.
In recent years, various techniques have been developed to reduce the diameter o the suture at the end tha~ i8 to be attached to the blunt end of the needle and in many instances this has b~en accomplished so that the diameter of the body of the suture is substantially the same as the diameter of the blunt end of the needle. Some of these techniques are more fully described in U.S. Patents, 3,890,975 and 3,926,194.
Though these techniques produce a needle-suture combination wherein the maximum diameter of the suture is close to the diameter of the blunt end of the needle, in order to accomplish this they all greatly reduce the strength of the suture in that area of the suture that is attached to the needle or immediately adjacent that area. This, of course, produces a weakened needle-suture combination. This problem restricts the various sizes o ~utures that can be produced by these techniques especially the extremely ine size sutures. It also limits the types of materials that can be used to produce the sutures in that you must greatly i w rease ~he overall strengt~
of the suture to have sufficient strength at the reduced diameter portion.
~ummary_Qf the Present Inven~ion It is an object of the present invention to produce a needle-suture c~mbination, which when used to join tissue, the hole produced by the needle is substantially filled by the suture joining the tissue. It is a further object of the present invention to produce a needle-suture combination ;n which the area of the suture joi~ed to the needle and the area ~djacent that area has a tensile strength substantially greater than the remainder of the suture. It is a ~ur~her object of 2~2~g ~ 3 --the present invention to produce preferred n~edle-suture combination~ wherein the diameter of the body of the suture is almost the same as the diameter of the blunt end of the needle. It is yet a further object of the present invention to be able to attain these desirable characteristics with all suture sizes especially the smaller size sutures.
The surgical needle-~uture combination of the present invention comprises a surgical needle having a blunt end and a sharp point. A surgical suture has one end of the suture attached to the blunt end of the surgical needle. The diameter of the blunt end of the needle is somewhat larger or substantially the same as the maximum diameter of the suture or the diameter of the body of the suture. The portion of the lS suture attached to the blunt end of the needle and usually ~he portion immediately adjacent such attached portion has a reduced diameter as compared to the diameter of the body of the suture. In the preferred embodiments of the surgical needle-suture combinatiuns of the present invention, the reduced diameter portion has a tensile strength at least 50%
greater than the tensile ~trength of the body o the suture.
The present invention also includes the method for producing a surgical suture having a reduced diameter po~tion from monofilaments of various polymeric material The monofilament is helically wound to form a cylinder comprising a multiplicity of convolutions of the monofilament. Adjacent portions of each convolution are heated to an elevated temperature and the heated portions are then drawn to increase the length o the heated portions while reducing the diameter of the heated portions. This heating and drawing also increases the density and crystallini~y of the heated and drawn portion. Each convolution is sev~red to ~orm a suture having a reduced diameter end por~ion. Preferably, each convolution ;s . .
.
. .
, . . ' .
,:
2 ~
severed appro~imately in the center of ths reduced diarneter portion to form a suture having both ends of a reduced diameter.
Brief Des~ription of the Prawing~
Figure 1 is a perspecti~e view of a sterile surgical needle-suture combination of the present invention.
Figure 2 is a cross-sectional view of the needle-suture combination of Fig. 1.
Figure 3 is a perspective view o~ another e~bodiment o~
the sterile surgical needle-suture combina~ion o the present invention.
Figure g is a diagramatic ~iew of various steps in the process for producing needle-suture combinations.
Figure 5 is a perspecti~e view of the stretching drum used in the present invention.
Figure 6 is an end view of the stretching drum in its closed or initial original position.
25Fiqure 7 is an end view o~ the stretching drum of Fig. 6 in its open position.
Figure 8 is an end view of the stretching mechanism of Figs. 6 or 7 which also shows mechanism~ for moving the drum from the position shown in Fig. 6 to the position shown in Fig.
7.
Figure 9 is a top view of the mechanism shown in Figure ~.
- ~2~fi~
Detailçd Descript;on of the_Invention Referring to the drawings, in Fig . 1 there i~ shown one embodiment of this sterile surgical needle-suture combination 20 of tha present invention. The needle 21 has a sharp end 22 or point and a blunt end 23. Attached to the blunt end is a surgical suture 24. As more clearly shown ;n the cross-sectional view in Fig. 2, the blunt end 2~ has a hole 25 drilled into the center of the blunt end. The ~uture has a reduced d;ameter portion 26 which is inserted into that hole and attached to the blunt end of the needle. As may be seen in Fig. 2, the ma~imum diameter of the suture or the diameter of the body of the suture, is substantially the same as the maximum diameter of the needle or the blunt end of the needle.
In Fiq. 3, ther~ is shown another embodiment of the sterile surgical-needle suture combination 30 of the present invention In this embodiment, the blunt end 31 of the needle 32 has a channel 33. The reduced diameter portion 34 of the suture 35 is placed in that channel and the channel crimped about the reduced portion of the suture to attach the suture to the needle.
The sutures used to produce the needle-suture combinations of t~e present invention may be any of the monofilament sutures such as polyethylene, polypropylene, polyester, nylon, poly~lycolides, polyfluoro carbons, etc. The needles used in producing the needle-suture combinations of the present invention may be made from various metals such as stainless steel. The suture may be attached to the needle by any of the various techniques which allow for attachment of the suture to the blunt end of the needle, such as dr;lling a hole in the blunt end of the needle ~nd adhering or attaching the suture into that hole either using adhesive or by crimping or . .
2 ~
by placing the suture in a channel ~nd adhering it in the channel by crimping and/or adhesion or by various ot~.er techniques well known in the art.
Referring to Fig. 4, there is shown diagramatically one method for producinq surgical sutures which may be used in producing the surgical needle-suture combinations of the present invention. ~xtruded monofilaments 40 are supplied from a supply roll 41 and passed around a pair of rolls 42 and 43 called a ~Godet~ and the e~truded monofilament then passed through a hot oven 44. The monofilament is then taken up on a second pair of rolls 45 and 46 or second ~Godet~ and then wound up on a wind up roll 47. The second pair of drawing rolls 45 and 45 are operated at a speed 16% slower than the first pair lS of drawing rolls 42 and 43, so ~hat as the e~truded mono-filament passes through the oven the monofilament is relaxed.
Depending upon the composi~ion of the monofilament, the oven will be heated to a suitable temperature to allow the monofilament to relas. If a polypropylene monofilament suture is being produced, the oven would be maintained at about 285F. The wound up rela~ed monofilament on the wind-up roll 47 is moved to another feed station 48 and wound on a split drum 49~ The diameter of the drum is ~uch as to allow for the production of the desired length of sutures. A portion of the surface of the drum has been flattened and there are a pair of bars 50 and 51 or xollers at the edges of this flattened surface so that when the monofilament is helically wound around the circumference of the drum, the portion of the monofilament e~tending between these two bars is displaced from the surface of the drum. The filaments are held in positlon by clamps 58 and S9 placed on the outside of the 1attened section adjacent the rollers. A heater bar 52 is placed adjacent the portion of the monofilament which passes between these two bars and the monofilament warmed or heated. If the monofilament is made from polypropylene, it is heated ~y this heating bar to about 2~2~
300~F for from about 3 to 5 minutes. One section 53 or half of the drum is then di~placed from the stationery half 54 of the drum to increase the circumference of the drum and draw or stretch the portion of the monofilament e~tending between the roller bars. The distance the filament i~ drawn or~Jtretc~ed stretched will depend on the si~e of the suture being produced but may vary from two inches to ~hree inches or more. Upon drawing, the d~ameter of the filament is reduced in the area that ~s drawn, that is, the area between the bars. After drawing, a cutting board 55 may ~e placed underneath the drawn portion and the drawn portion of the wound monofilament cut with a razor knife 56 substantially in the center of the drawn or stretched area. The cut sutures having reduced diameter portions at each end are dropped onto a tray 57. The tray is taken to another station where needles are attached to each end by swaging or other known tec~niques. The double-armed sutures are then wound and packaged as is well known. The needle-su~ure combination may then be sterilized by any of the technigues known in the art such as ethylene oside, radiation, etc.
It is important that the drawing or ~tretching drum be circular or substantially circular in configuration to minimize any set or kink developing in the monofilament as a result of the processing.
The stretching drum will be mora fully described in conjunction with Figs. 5 through 9. The drum 60 comprises two halves 61 and 62. Preferably, the drawn is split sli~htly off-center so that th~ stationery half 61 is slightly larger than the moveable half 62. This configuration will allow the shaft 74 to be placed at the center of tha closed drum. When the hal~es are adjacent, the drum has a substantially c;rcular cross-section. The split drum i~ flattened for abou~ 4 inches at the area 63 where one of the halves meets the other half of , '~2~8 the drum. Disposed in this flat area about 4 inches apart are a pair of roller bars 64 and 65. One half of the drum is stationery and is attached to a stationery stand 66. The opposite half of the drum is moveable and is attached through a moveable yoke mechanism 67. The e~truded monofilament is ~ound about the circumference of the drum. The length of the drum will determina the number of s~rands that can be made around the drum, and the diameter of the drum will determine the length of the sutures to be produced.
Opposite the flat section of the drum, the drums are attached by a hinge 68.
Once the sutures are wound about the drum, i~mediately adjacent each side of the flattened portion there are clamps 69 and 70 which are used to clamp the estruded monofilament winds to the surface of the drum. A moveable heater bar 71 is placed adjacent the monofilament winds at the 1att~ned area of the drum to heat these portions of the winds to the desired temperature.
Once this portion has been heated sufficiently, the moveable yoke is moved away so as to displace the moveable half of the drum from the stationery half o the drum with the gap at its widest portion being from about two to four inches.
This stretches each monofilament wind in the portion of the wind between the roller bars. A cu~ting sur~ace 72 is placed under the stretched portion of the winds of the monofilament and a suitable razor knife 73 is passed along this cutting board to cut the monofilaments in the stretched areas and produce a plurality of sutures having a reduced diameter portion at each end of the suture. The sutures are collected, needles attached and packa~ed as is well ~nown in the artO
2 ~
The stretching ~f the monofilament material at the desired temperature produces a reduced diameter portion which portion has a tensile strength substantially greater than the remainder of the ~uture. The tensile strength may be as much as 50% to 60% greater than the tensile strength of the body of the suture.
The followinq is specific example for producing needle-suture co~binations accordinq to the present invention.
Example An extruded monofilament of polypropylene is produce and wound on a wind-up roll. The propylene monofilament is fed to a first ~odet~. The first ~Godet~ is operated at a speed of appro~imately 70 feet per min~te and the monofilament is wrapped about this "Godet~ approsimately ~i~ times. The filament is pas~ed ~hrough a hot air oven with the oven maintained at a temperature of about 285F. ~he filament is wound on a ~econd ~Godet~ with the second ~odet~ being operated at a speed of appro~imately 60 feet per minute, so that as the monofilament passes through the oven it is relaxed about 16%. The rela~ed monofilament is taken from ~he second ~Godet~ and wound up on a suitable wind-up roll.
The rela~ed polypropylene monofilament is then wound on a split drum as described in conjunctions with Fi~s. 5-9. The drum i~ about twelve inches in diameter and about 300 winds of the r~la~ed polypropylene monofilament cover the surface of the drum. An electric heater bar is placed against the portion of the monofilaments that pass ~etween the two bars forming a portion of the surface o~ the drum. The polypropylene is heated to a appro~imately 300F for about 5 minutes. The moveable ~ection of ~he drum is then di~placed from the stationery section of the drum to draw the heated portion of . ~
; ` ~ '.
, , 2~9~
the monofilaments about 3 inches, to reduce the diameter of the monofilament in the portion that passes between the two bar~.
A cutting surface is pla~ed beneath the ~tretched portions of the monofilament~ and a razor knife passea down the center of the stretched portions to cut the winds on the drum and form separate sutures which have a reduced diameter portion at each end. The cut sutures are collected and a needls having a channel in the blunt end is attached to each reduced diameter end of the suture to produce a double-armed suture. The sutures are suitably wound and packaged and sterilized using cobalt radiation. Size 3~0, 4/0 and 5/0 polypropylene sutures are produced as described above. The diameter, density (which is an indication of crystallinity) and the tensile strength of both the body portion and the reduced diameter portion of each o~ the sutures is measured. The 3/0 suture has a diameter in the body portion of 9.85 mils, a density of 0.9085 gm/cc3 and a tensile strength of 67,000 lbs. per s~uare inch while the reduced diameter portion of the size 3~0 suture has a diameter of 7.1 mils, a density of 0.9113 gm/cc3 ana a tensile strength of 109,000 lbs. per sguare inch. The diameter of the ~ody portion of the 9/0 suture is 7.6 mil~, a density of 0.9085 gm~cc3 and the tensile strength 73,000 lbs. per sguare inch while the reduced diameter portion has a diameter of 5.2 mils, a density of 0.9112 gk/cc3 and a tensile strength of 138,000 lbs. per square inch. The S/0 suture has a diameter in the body portion of 5.7 m~ls, a density of 019103 gm/cc3 and a tensile strength in this portion of 75,000 lbs. per square inch while the reduced diameter portion of the 5/0 suture has a diameter of 4.0 mils, a density of 0.9112 ~m~cc3 and a tensile stren~th of 129,000 lbs. per square inch.
The ratio of the diameter of the blunt en~ of the needle to the body diameter of the 3/0 suture i~ 1.46 to 1 as compared to a ratio of 2.08 to 1 for conventional 3/0 needle-~uture combinations. The ratio of the diameter of the blunt end of , ' ' ~2~8 the needle to the body diameter of the 4/0 suture is 1.51 to 1 as compared to a ratio o~ 2.24 to 1 for a conventional 4/0 needle-suture. The ratio of th0 diameter of the blunt end of the needle to the body diameter of a 5~0 suture is 1.62 to 1 as compared to 3 ratio of2.16 to 1 for a 5/0 needle-suture.
Test methods used for determining the physical properties of monofilament suturQ materials w~re as follows:
Tensile strength is determined by A.S.T.M. method D-2256-66T a~ a constant rate of e~tension using an INSTRON table Model 4200 universal testing instrument manufactured by the Instxon Corporation of Canton, Massachusetts, With the instrument sample clamps set 5 inches apart, 5-inch lengths of su~ure were elonqated at a rate of 12 inches per minute until fracture.
The INSTRON instrument was set or th~ correct suture diameter, ~nd Young's Modulus was calculated in psi from the initial stress-strain data generated during the straight tensile strength test. Young'~ ~odulus is the ratio of applied stress to strain ~n the elastic region of the suture and measures the elastic component of a suture's resistance to stress. This value is rclated to the fleYibility of a suture.
As many apparently widely different embodiments of this invention may be made without departing ~rom the ~pirit and scope thereo~, it is to be understood tha~ the invent~on ~ not limited to the specific embodiment~ ~hereof e~cept as defined in the following claims.
.
.
Claims (8)
1. A sterile surgical needle suture combination comprising a surgical needle having a blunt end and a sharp point and a suture, one end of which is attached to the blunt end of the surgical needle, the diameter of the blunt end of the needle being slightly larger or substantially the same as the maximum diameter of the suture, the portion of the suture attached to the blunt and of the needle having a reduced diameter as compared to the maximum diameter of said suture and said reduced diameter portion of said suture having a tensile strength greater than the remainder of the suture.
2. A sterile surgical needle-suture combination according to Claim 1 wherein the tensile strength of the reduced diameter portion of the suture is at least 50% greater than the tensile strength of the remainder of the suture.
3. A sterile surgical needle-suture combination according to Claim 1 wherein the suture is polypropylene.
4. A sterile surgical-needle suture combination according to Claim 1 wherein the blunt end of the needle includes a channel and the reduced diameter portion of the suture is attached to the channel.
5. A needle-suture combination of Claim 1 wherein the blunt end of the needle includes a drilled hole and the reduced diameter portion of the suture is attached in the hole at the blunt end.
6. A method for producing a surgical suture having a reduced diameter end portion comprising:
a) winding a monofilament in a helical configuration;
b) heating a portion of said monofilament to an elevated temperature;
c) drawing said heated portion while in said helical configuration to reduce the diameter of said heated and drawn portion; and d) severing said monofilament to produce a suture having a reduced diameter end portion.
a) winding a monofilament in a helical configuration;
b) heating a portion of said monofilament to an elevated temperature;
c) drawing said heated portion while in said helical configuration to reduce the diameter of said heated and drawn portion; and d) severing said monofilament to produce a suture having a reduced diameter end portion.
7. A method according to Claim 6 wherein the monofilament is wound in a helical configuration having multiple convolutions and adjacent portions of the convolutions are helical and drawn to reduce their diameter.
8. A method according to Claim 6 or 7 wherein the monofilament is severed in the reduced diameter portion to produce a suture having a reduced diameter portion at each of its ends.
Applications Claiming Priority (2)
| Application Number | Priority Date | Filing Date | Title |
|---|---|---|---|
| US434,399 | 1989-11-13 | ||
| US07/434,399 US5007922A (en) | 1989-11-13 | 1989-11-13 | Method of making a surgical suture |
Publications (1)
| Publication Number | Publication Date |
|---|---|
| CA2029668A1 true CA2029668A1 (en) | 1991-05-14 |
Family
ID=23724081
Family Applications (1)
| Application Number | Title | Priority Date | Filing Date |
|---|---|---|---|
| CA002029668A Abandoned CA2029668A1 (en) | 1989-11-13 | 1990-11-09 | Sterile surgical needle-suture combination |
Country Status (12)
| Country | Link |
|---|---|
| US (1) | US5007922A (en) |
| EP (1) | EP0428110B1 (en) |
| JP (1) | JP2965667B2 (en) |
| AU (2) | AU635980B2 (en) |
| BR (1) | BR9005726A (en) |
| CA (1) | CA2029668A1 (en) |
| DE (1) | DE69010840T2 (en) |
| DK (1) | DK0428110T3 (en) |
| ES (1) | ES2056338T3 (en) |
| GR (1) | GR1000961B (en) |
| IE (1) | IE65358B1 (en) |
| PT (1) | PT95873B (en) |
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| CA2704219C (en) * | 1990-12-13 | 2011-01-04 | United States Surgical Corporation | Method and apparatus for tipping sutures |
| CA2071083A1 (en) * | 1991-06-14 | 1992-12-15 | Matthew E. Hain | Dynamic treatment of suture strand |
| CA2088458A1 (en) * | 1992-01-30 | 1993-07-31 | Cheng-Kung Liu | Polyamide monofilament suture manufactured from higher order polyamide |
| US5279783A (en) * | 1992-01-30 | 1994-01-18 | United States Surgical Corporation | Process for manufacture of polyamide monofilament suture |
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| Publication number | Priority date | Publication date | Assignee | Title |
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| US3422181A (en) * | 1966-05-23 | 1969-01-14 | American Cyanamid Co | Method for heat setting of stretch oriented polyglycolic acid filament |
| US3630205A (en) * | 1969-07-31 | 1971-12-28 | Ethicon Inc | Polypropylene monofilament sutures |
| US3799169A (en) * | 1972-05-11 | 1974-03-26 | Ethicon Inc | Lateral release suture |
| TR17343A (en) * | 1972-05-31 | 1975-03-24 | Ethicon Inc | SUETUER THAT CAN BE RELEASED BY CONTROL |
| US3980177A (en) * | 1973-10-26 | 1976-09-14 | Johnson & Johnson | Controlled release suture |
| US3926194A (en) * | 1974-11-20 | 1975-12-16 | Ethicon Inc | Sutures with reduced diameter at suture tip |
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| US4034763A (en) * | 1976-06-10 | 1977-07-12 | Frazier Calvin H | Ligament forming suture |
| ZA773904B (en) * | 1976-08-10 | 1978-09-27 | American Cyanamid Co | Isotactic polypropylene surgical sutures |
| US4224946A (en) * | 1978-08-14 | 1980-09-30 | American Cyanamid Company | Surgical sutures derived from segmented polyether-ester block copolymers |
| US4911165A (en) * | 1983-01-12 | 1990-03-27 | Ethicon, Inc. | Pliabilized polypropylene surgical filaments |
| US4621638A (en) * | 1984-07-30 | 1986-11-11 | Pfizer Hospital Products Group, Inc. | Hard elastic sutures |
| US4832025A (en) * | 1987-07-30 | 1989-05-23 | American Cyanamid Company | Thermoplastic surgical suture with a melt fused length |
-
1989
- 1989-11-13 US US07/434,399 patent/US5007922A/en not_active Expired - Lifetime
-
1990
- 1990-11-07 AU AU65878/90A patent/AU635980B2/en not_active Ceased
- 1990-11-09 CA CA002029668A patent/CA2029668A1/en not_active Abandoned
- 1990-11-12 ES ES90121637T patent/ES2056338T3/en not_active Expired - Lifetime
- 1990-11-12 IE IE407390A patent/IE65358B1/en not_active IP Right Cessation
- 1990-11-12 DK DK90121637.4T patent/DK0428110T3/en active
- 1990-11-12 DE DE69010840T patent/DE69010840T2/en not_active Expired - Lifetime
- 1990-11-12 EP EP90121637A patent/EP0428110B1/en not_active Expired - Lifetime
- 1990-11-12 BR BR909005726A patent/BR9005726A/en not_active IP Right Cessation
- 1990-11-13 JP JP2304231A patent/JP2965667B2/en not_active Expired - Lifetime
- 1990-11-13 PT PT95873A patent/PT95873B/en not_active IP Right Cessation
- 1990-11-13 GR GR900100805A patent/GR1000961B/en not_active IP Right Cessation
-
1993
- 1993-02-03 AU AU32800/93A patent/AU646362B2/en not_active Expired
Also Published As
| Publication number | Publication date |
|---|---|
| JP2965667B2 (en) | 1999-10-18 |
| AU646362B2 (en) | 1994-02-17 |
| BR9005726A (en) | 1991-09-17 |
| US5007922A (en) | 1991-04-16 |
| IE904073A1 (en) | 1991-05-22 |
| DK0428110T3 (en) | 1994-08-29 |
| AU635980B2 (en) | 1993-04-08 |
| PT95873A (en) | 1991-09-13 |
| PT95873B (en) | 1997-12-31 |
| EP0428110B1 (en) | 1994-07-20 |
| AU3280093A (en) | 1993-03-25 |
| ES2056338T3 (en) | 1994-10-01 |
| GR1000961B (en) | 1993-03-16 |
| DE69010840T2 (en) | 1995-03-23 |
| AU6587890A (en) | 1991-05-16 |
| IE65358B1 (en) | 1995-10-18 |
| EP0428110A1 (en) | 1991-05-22 |
| JPH03210251A (en) | 1991-09-13 |
| DE69010840D1 (en) | 1994-08-25 |
| GR900100805A (en) | 1992-04-17 |
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