US20140257133A1

US20140257133A1 - Bone Marrow Aspiration Needle

Info

Publication number: US20140257133A1
Application number: US14/281,168
Authority: US
Inventors: Matthew D. Landrigan; James M. McKale
Original assignee: Biomet Biologics LLC
Current assignee: Zb Manufacturing LLC; Biomet Manufacturing LLC
Priority date: 2010-08-03
Filing date: 2014-05-19
Publication date: 2014-09-11
Also published as: US8728008B2; US20120035501A1

Abstract

A bone marrow aspiration assembly including a cannulated introducer needle and an aspiration needle. The cannulated introducer needle is curved to approximate a natural curvature of an iliac crest. The aspiration needle includes apertures for aspirating bone marrow. The aspiration needle is configured to be received in, and extend from, the cannulated introducer needle to reach a bone marrow aspiration site in the iliac crest.

Description

CROSS-REFERENCE TO RELATED APPLICATIONS

This application is a divisional application of U.S. patent application Ser. No. 12/849,412 filed on Aug. 3, 2010, the entire disclosure of which is incorporated by reference herein.

FIELD

The present disclosure relates to bone marrow aspiration needles.

BACKGROUND

This section provides background information related to the present disclosure which is not necessarily prior art.
Autologous stem cell therapies often utilize a patient's bone marrow or concentrated bone marrow aspirate to deliver autologous adult mononuclear stem cells to the patient for the treatment of a wide variety of disorders. Concentrated autologous cell therapies utilize in vitro cell culture to expand a desired cell line, or a point-of-care device to concentrate the mononuclear cell-rich fraction (CRF), for delivery to a desired treatment site. An exemplary point-of-care device is the MarrowStim™ device by Biomet Biologics, LLC of Warsaw, Ind.
Concentration of the mononuclear CRF is limited by the number of recovered mononuclear cells in the aspirate. Often, aspiration of four 1 ml aspirates recovers almost twice the number of osteoblast progenitor cells as compared to a single 4 ml aspirate. This discrepancy is often attributed to aspirate dilution from peripheral blood. Harvesting smaller volumes of aspirate from a variety of different locations, such as along the curved iliac crest of the pelvis, can improve the baseline and concentrated mononuclear CRF, which will lead to more effective stem cell therapies.

SUMMARY

This section provides a general summary of the disclosure, and is not a comprehensive disclosure of its full scope or all of its features.
The present teachings provide for a bone marrow aspiration assembly including a cannulated introducer needle and an aspiration needle. The cannulated introducer needle is curved to approximate a natural curvature of an iliac crest. The aspiration needle includes apertures for aspirating bone marrow. The aspiration needle is configured to be received in, and extend from, the cannulated introducer needle to reach a bone marrow aspiration site in the iliac crest.
The present teachings further provide for a bone marrow aspiration assembly including a cannulated bone piercing needle, a rigid, cannulated introducer needle, and a flexible aspiration needle. The rigid, cannulated introducer needle is curved to approximate a natural curvature of an iliac crest. The rigid, cannulated introducer needle has a length longer than the cannulated bone piercing needle and is configured to be received within and pass through the cannulated bone piercing needle. The flexible aspiration needle has apertures for aspirating bone marrow, and is configured to be received in, and extend from, the rigid, cannulated introducer needle to reach a bone marrow aspiration site in the iliac crest.
The present teachings also provide for a method for aspirating bone marrow. The method includes piercing bone with a cannulated bone piercing needle; inserting into the cannulated bone piercing needle a rigid, cannulated introducer needle that is curved to approximate a natural curvature of an iliac crest and has a length longer than the cannulated bone piercing needle such that at least a tip of the rigid, cannulated introducer needle extends out from within the cannulated bone piercing needle; and inserting into the rigid, cannulated introducer needle a flexible aspiration needle having apertures for aspirating bone marrow such that the flexible aspiration needle extends from the rigid, cannulated introducer needle to reach a bone marrow aspiration site in the iliac crest.
Further areas of applicability will become apparent from the description provided herein. The description and specific examples in this summary are intended for purposes of illustration only and are not intended to limit the scope of the present disclosure.

DRAWINGS

The drawings described herein are for illustrative purposes only of selected embodiments and not all possible implementations, and are not intended to limit the scope of the present disclosure.

FIG. 1 is a perspective view of a bone marrow aspiration assembly according to the present teachings;

FIG. 2 illustrates an inner needle assembly separated from an outer needle assembly of the bone marrow aspiration assembly of FIG. 1;

FIG. 3 is a cross-sectional view of the bone marrow aspiration assembly;

FIG. 3A is an enlarged cross-sectional view of the bone marrow aspiration assembly showing cooperation between the inner needle assembly and the outer needle assembly;

FIG. 4 is a perspective view of an insert of the outer needle assembly;

FIG. 4A is a cross-sectional view of the insert of FIG. 4;

FIG. 5 is a top view of the insert;

FIG. 6 is a perspective view of a handle of the outer needle assembly;

FIG. 7A illustrates a distal end of each of an outer cannula (right side of Figure) and an inner cannula (left side of Figure) of the bone marrow aspiration assembly;

FIG. 7B illustrates the inner cannula seated within the outer cannula;

FIG. 8 illustrates a distal end of each of another outer cannula (right side of Figure) and another inner cannula (left side of Figure) according to the present teachings;

FIG. 9 is a perspective view of a distal side of a handle of the inner needle assembly;

FIG. 9A is a perspective view of a connection region of the handle of the inner needle assembly;

FIG. 9B is a planar view of a distal end of the connection region;

FIG. 10 is a perspective view of a trocar (left side of Figure) configured to be received by the outer needle assembly (right side of Figure);

FIG. 11 is an assembled view of the trocar in cooperation with the outer needle assembly;

FIG. 12 is a posterior view of a pelvis with the inner cannula and the outer cannula engaging the iliac crest;

FIG. 13 is a cross-sectional view of the pelvis and illustrates the bone marrow aspiration assembly engaging the pelvis, the assembly including a trocar mounted to the outer needle assembly;

FIG. 14 is a cross-sectional view of the pelvis and illustrates the bone marrow aspiration assembly engaging the pelvis, the assembly including the outer needle assembly and the inner needle assembly;

FIG. 15A is a top, cross-sectional view of interaction between the inner needle assembly and the outer needle assembly in a first position;

FIG. 15B is a top, cross-sectional view of interaction between the inner needle assembly and the outer needle assembly in a second position;

FIG. 15C is a top, cross-sectional view of interaction between the inner needle assembly and the outer needle assembly in a third position;

FIG. 16 is a cross-sectional view of the pelvis and the bone marrow aspiration assembly of FIG. 1 in the first position engaging the pelvis, and a syringe for aspirating bone marrow from the pelvis;

FIG. 17 is a cross-sectional view of the bone marrow aspiration assembly engaging the pelvis with the inner needle assembly and the outer needle assembly each in a first position such that openings of outer and inner distal opening groups are aligned;

FIG. 18 is a cross-sectional view of the bone marrow aspiration assembly engaging the pelvis with the inner needle assembly and the outer needle assembly each in a second position such that openings of outer and inner intermediate opening groups are aligned;

FIG. 19 is a cross-sectional view of the bone marrow aspiration assembly engaging the pelvis with the inner needle assembly and the outer needle assembly each in a third position such that openings of outer and inner proximal opening groups are aligned;

FIG. 20 illustrates an outer needle assembly (right side of Figure) and an inner needle assembly (left side of Figure) of another bone marrow aspiration assembly of the present teachings;

FIG. 20A is another distal tip that may be provided with the outer needle assembly of FIG. 20;

FIG. 21 is a perspective view of a bone piercing needle of the present teachings;

FIG. 22 is a posterior view of a pelvis with the bone piercing needle of FIG. 21 and the bone marrow aspiration assembly of FIG. 20 seated therein;

FIG. 23A illustrates a curved introducer needle according to the present teachings;

FIG. 23B illustrates a flexible needle assembly according to the present teachings;

FIG. 24 is a cross-sectional view of the pelvis with the bone piercing needle of FIG. 21, the introducer needle of FIG. 23A, and the flexible needle of FIG. 23B seated therein; and

FIG. 24A is similar to FIG. 24, but with the flexible needle including a plurality of circular openings.

Corresponding reference numerals indicate corresponding parts throughout the several views of the drawings.

DETAILED DESCRIPTION

Example embodiments will now be described more fully with reference to the accompanying drawings.
With initial reference to FIG. 1 and FIG. 2, a bone marrow aspiration assembly according to the present teachings is generally illustrated at reference numeral 10. The assembly 10 generally includes an outer needle assembly 12 and an inner needle assembly 14.
The outer needle assembly 12 includes an outer handle 16 and an outer cannula 18 extending therefrom. With additional reference to FIG. 3 and FIG. 3A, the outer handle 16 includes a proximal surface 20 and a distal surface 22 opposite to the proximal surface 20. The distal surface 22 has a raised neck 24 at a center thereof. The raised neck 24 includes a distal portion 26.
With reference to FIGS. 3 and 3A, the outer handle 16 defines a through bore 28 extending between the proximal surface 20 and a center of the distal portion 26 of the raised neck 24. A longitudinal axis A extending through an axial center of the through bore 28 is perpendicular to each of a plane extending across the proximal surface 20, a plane extending across the distal surface 22, and a plane extending across the distal portion 26 of the raised neck 24.
With reference to FIG. 3A, at approximately a mid-point of the through bore 28, the outer handle 16 defines a stepped, annular retention surface 30. Between the retention surface 30 and the proximal surface 20 is an annular flange 31 protruding into the through bore 28 toward the longitudinal axis A. The outer handle 16 defines a plurality of diameter areas of the through bore 28 having diameters of various sizes.
A first area 29 is between the proximal surface 20 and the flange 31. From the proximal surface 20, the first area 29 tapers inward toward the longitudinal axis A, and retains a generally uniform diameter about the longitudinal axis A as it extends in the distal direction (toward the distal surface 22) until it reaches the flange 31. A second area 33 is at the flange 31. The second area 33 has a diameter that is smaller than the diameter of the first area 29. A third area 35 is adjacent to the flange 31 on a distal side thereof (closest to the distal surface 22). The third area 35 has a diameter that is similar in size to the diameter of the first area 29. A fourth area 37 is between the annular retention surface 30 and the third area 35. A fifth area 39 is between the annular retention surface 30 and the distal portion 26 of the neck 24. The fifth area 39 has the smallest diameter, which is generally uniform throughout its length. The fourth area 37 has a diameter that is greater than the diameter of the fifth area 39, but smaller than the diameter of the second area 33.
With additional reference to FIGS. 4 and 4A, an insert 32 is seated within the through bore 28. The insert 32 defines a center channel 34 having a longitudinal axis that is common with the longitudinal axis A. Near a proximal end 36 of the insert 32, but spaced apart therefrom, is an annular recess 38 extending around an outer surface 40 of the insert 32. Proximate to a distal end 42 of the insert 32, but spaced apart therefrom, is an annular collar 44 extending from the insert 32 in a direction perpendicular to the longitudinal axis A. Between the annular recess 38 and the annular collar 44, but closer to the annular recess 38, is a pair of flexible retention fins 46.
The diameter of the center channel 34 is greatest at a portion 48 that is at the proximal end 36. The diameter of the center channel 34 tapers inward from the proximal end 36 to a point along the length of the center channel 34 that is approximately even with the fins 46. The remainder of the center channel 34, which extends along the longitudinal axis A to the distal end 42 has a generally uniform diameter.
With additional reference to FIG. 5, protruding from a portion of the insert 32 defining the large diameter portion 48 of the center channel 34 are a series of raised surfaces or bumps 50. A first pair 52 a, a second pair 52 b, and a third pair 52 c of the bumps 50 are arranged at 120° intervals around the large diameter portion 48. The two bumps 50 of each pair 52 a, 52 b, and 52 c are spaced apart to securely receive a portion of the inner handle 90 therebetween, as described herein. FIGS. 4 and 5 also illustrate six planar surfaces 54 of the outer surface 40, which are in a hexagonal arrangement and are between the collar 4 and the fins 46. The planar surfaces 54 restrict rotational movement of the insert 32 about the longitudinal axis A when seated in the through bore 28.
As illustrated in FIGS. 3A and 6 for example, the insert 32 is positioned within the through bore 28 of the handle 16 such that the proximal end 36 is at, or closely proximate to, the plane extending across the proximal surface 20 of the outer handle 16 and such that the distal end 42 extends beyond the distal portion 26 of the raised neck 24. The collar 44 abuts the distal portion 26 of the raised neck 24 and the fins 46 are seated on the retention surface 30. The handle 16 can be manufactured such that the insert 32 is a separately formed component that is inserted into the through bore 28 at the distal portion 26 until the annular, flexible fins 46 pass across the annular retention surface 30, at which point they expand from a contracted or first position to an expanded or second position to contact the annular retention surface 30. The collar 44 and the flexible fins 46 retain the insert 32 within the through bore 28.
Alternatively, the handle 16 can be manufactured such that the insert 32 is molded together with the remainder of the handle 16 or the insert 32 can be formed integral with the remainder of the handle 16 during manufacturing. The handle 16 and the insert 32 may also be manufactured in any other suitable manner. Both the handle 16 and the insert 32 can be made of any suitable material, such as a suitable polymer.
With reference to FIGS. 2 and 3 for example, the outer cannula 18 includes a proximal end 58 and a distal end 60 and defines an outer cannula passageway 62 that extends an entire length of the outer cannula 18, from the proximal end 58 to the distal end 60. A longitudinal axis A extending through an axial center of the outer cannula passageway 62 is aligned with the longitudinal axis A of the through bore 28 (see FIG. 3); thus the longitudinal axis of the outer cannula passageway 62 is also designated with reference letter A.
With additional reference to FIG. 7A, the distal end 60 is open and includes a plurality of sharpened edges or teeth 64. The outer cannula 18 defines a plurality of openings 66 between the distal end 60 and the proximal end 58. The openings 66 provide communication between the passageway 62 and an exterior of the outer cannula 18.
As illustrated in FIG. 2, an outer distal set 68 and an outer proximal set 70 of the openings 66 are provided. Each of the outer distal set 68 and the outer proximal set 70 include multiple openings 66 spaced apart along the longitudinal axis A of the outer cannula 18. The outer distal set 68 is substantially similar to the outer proximal set 70. The description of the outer distal set 68 below is therefore also sufficient to describe the outer proximal set 70. Only one of the outer distal set 68 and the outer proximal set 70 may be provided in some applications. Additional sets of the openings 66 may also be included.
With specific reference to FIG. 7A, the outer distal set 68 will now be described. The outer distal set 68 includes an outer distal opening group 72 a, an outer intermediate opening group 72 b, and an outer proximal opening group 72 c. The different outer opening groups 72 a, 72 b, and 72 c are not radially aligned, but rather radially offset 120° from each other about axis A.
The outer distal opening group 72 a includes a first distal array 74 a of openings 66 and a second distal array 74 b of openings 66. The first and the second distal arrays 74 a and 74 b are spaced 180° apart about the radius of the outer cannula 18. Each of the first and the second distal arrays 74 a and 74 b include a plurality of the openings 66 aligned parallel to the longitudinal axis A in the distal-to-proximal direction. The first distal array 74 a includes four of the openings 66 and the second distal array 74 b includes three of the openings 66. None of the openings 66 of the first distal array 74 a are aligned in the distal to proximal direction with any of the openings 66 of the second distal array 74 b, but rather the openings 66 are spaced apart.
The intermediate opening group 72 b includes a first intermediate array 76 a of openings 66 and a second intermediate array 76 b of openings 66, which are each substantially similar to the first and the second distal arrays 74 a and 74 b respectively. The only substantial difference between the intermediate opening group 72 b and the distal opening group 72 a is that the first and the second intermediate arrays 76 a and 76 b are each radially rotated or shifted approximately 120° about the longitudinal axis A as compared to the first and the second distal arrays 74 a and 74 b.
The proximal opening group 72 c includes a first proximal array 78 a of openings 66 and a second proximal array 78 b of openings 66. The first proximal array 78 a is substantially similar to both the first intermediate array 76 a and the first distal array 74 a. The second proximal array 78 b is substantially similar to both the second intermediate array 76 b and the second distal array 74 b. The only substantial difference between the proximal opening group 72 c and both the intermediate opening group 72 b and the distal opening group 72 a is that the first and the second proximal arrays 78 a and 78 b are each radially rotated or shifted approximately 120° about the longitudinal axis A such that the first and the second proximal arrays 78 a and 78 b are not radially aligned with either the first and the second intermediate arrays 76 a and 76 b or the first and the second distal arrays 74 a and 74 b.
With additional reference to FIG. 8, the outer cannula 18 can alternatively include elongated slots 80, instead of the openings 66, which each extend parallel to the longitudinal axis A. Each of the arrays 74 a, 74 b (obscured behind array 74 a in FIGS. 8), 76 a, 76 b, 78 a, and 78 b include two slots 80 that are radially aligned with each other. The slots 80 of each of the first arrays 74 a, 76 a, and 78 a are aligned with the slots 80 of each of the corresponding second arrays 74 b, 76 b, and 78 b such that they overlap along the longitudinal axis A. The distal opening group 72 a, the intermediate opening group 72 b, and the proximal opening group 72 c are each orientated such that the slots 80 of the different opening groups 72 a, 72 b, and 72 c are not radially aligned, but rather offset by 120° degrees each as illustrated. This offset can also be 180°.
With reference to FIGS. 3 and 3A, the proximal end 58 of the outer cannula 18 includes a pair of opposing flared surfaces 82 that extend outward and away from the longitudinal axis A. At least a portion of the proximal end 58, including the flared surfaces 82, is seated within the insert 32 to mount the outer cannula 18 to the outer handle 16 by way of the insert 32. The flared surfaces 82 extend within the portion of the insert 32 defining the center channel 34 to secure the outer cannula 18 to the insert. The outer cannula 18 may also be secured to the insert 32 with a suitable adhesive or the insert 32 can be molded to the outer cannula 18 during manufacturing. The outer cannula passageway 62 is aligned with the center channel 34 of the insert 32 to provide a continuous passage from the proximal surface 20 of the handle 16 to the distal end 60 of the outer cannula 18.
The outer cannula 18 can be made of any suitable polymer or metal and can be rigid or flexible, as further discussed herein. For example, rigid stainless steel can be used, as well as flexible material, such as Nitinol.
With reference to FIG. 2, the inner needle assembly 14 generally includes an inner handle 90 and an inner cannula 92 that extends from the inner handle 90 along longitudinal axis B. The inner handle 90 includes a distal surface 94 and a proximal surface 96 that is opposite to the distal surface 94. With continued reference to FIG. 2 and additional reference to FIGS. 9, 9A, and 9B, the distal surface 94 includes a connection region 98 at a center thereof. The connection region 98 includes a connection cone 100 between two connection tabs 102.
The connection cone 100 has a tapered outer surface 104 that is tapered in the proximal to distal direction such that a diameter of the outer surface 104 is greatest at the distal surface 94. Extending from the tapered outer surface 104 is a first ridge 106 a, a second ridge 106 b, and a third ridge 106 c that are each positioned at 120° intervals about the outer surface 104 of the cone 100. The ridges 106 are elongated and extend along a portion of a length of the outer surface 104. An inner surface 108 of the connection cone 100 defines an inner connection channel 110 that extends through the connection cone 100. The inner surface 108 is cylindrical and has a generally uniform diameter throughout, which provides the inner connection channel 110 with a uniform diameter.
The connection tabs 102 each terminate at a tooth 112. The teeth 112 extend from their respective connection tabs 102 towards each other and oppose each other. The teeth 112 are sized to be received within the annular recess 38 of the insert 32.
The inner connection channel 110 is aligned along the longitudinal axis B with, and in communication with, a syringe receptacle 114 defined by the inner handle 90, as illustrated in FIG. 3A for example. The receptacle 114 extends from the proximal surface 96 and into a portion of the inner handle 90. The receptacle 114 has an inner diameter that is greatest at the proximal surface 96 of the inner cannula handle 90. From the proximal surface 96, the inner diameter of the syringe receptacle 114 tapers inward toward the longitudinal axis B, which is at an axial center of the syringe receptacle 114 and is co-linear with the longitudinal axis A when the inner needle assembly 14 is in cooperation with the outer needle assembly 12, as illustrated in FIGS. 3 and 3A.
The inner cannula 92 includes a proximal end 120 extending to the receptacle 114 and a distal end 122 that terminates at a closed tip 124. The inner cannula 92 defines an inner cannula passageway 126, as illustrated in FIGS. 3 and 3A, for example. The longitudinal axis B extends through an axial center of the inner cannula passageway 126. Between the proximal end 120 and the distal end 122 of the inner cannula 92 are a plurality of openings or ports 128, which provide communication between the inner cannula passageway 126 and an exterior of the inner cannula 92. As illustrated in FIG. 2, the openings 128 are arranged in an inner distal set 130 and an inner proximal set 132. The inner distal set 130 is substantially similar to the inner proximal set 132 and thus the below description of the inner distal set 130 also describes the inner proximal set 132. As with the outer distal and proximal sets 68 and 70, only one of the inner sets 130 and 132 need be provided, or additional inner sets of the openings 128 can be provided depending on the application. The number of sets of openings 128 provided will generally correspond to the number and sets of openings 66 provided.
With reference to FIG. 7A, the inner distal set 130 includes an inner distal opening group 134 a, an inner intermediate opening group 134 b, and an inner proximal opening group 134 c. Unlike the outer opening groups 72 a, 72 b, and 72 c of the outer distal set 68, the inner opening groups 134 a, 134 b, and 134 c are all radially aligned along the longitudinal axis B.
The inner distal opening group 134 a includes a first inner distal array 136 a of openings 128 and a second inner distal array 136 b of openings 128. The first inner distal array 136 a is radially spaced apart 180° from the second inner distal array 136 b. The first inner distal array 136 a is substantially similar to the first outer distal array 74 a of openings 66. The second inner distal array 136 b is substantially similar to the second outer distal array 74 b. Thus, the first inner distal array 136 a includes four openings 128 radially aligned and spaced apart along a line parallel to the longitudinal axis B and the second inner distal array 136 b includes three openings 128 that are radially aligned and spaced apart along a line parallel to the longitudinal axis B. The openings 128 of the first inner distal array 136 a and the openings 128 of the second inner distal array 136 b are not aligned in the distal to proximal direction, but rather staggered such that the openings 128 of the second inner distal array 136 b are between the openings 128 of the first inner distal array 136 a in the distal to proximal direction of the inner cannula 92.
The inner intermediate opening group 134 b and the inner proximal opening group 134 c are radially aligned with, and are substantially similar to, the inner distal opening group 134 a, but spaced apart from the inner distal opening group 134 a along the longitudinal axis B. Therefore, the description of the inner distal opening group 134 a is also sufficient to describe both the inner intermediate opening group 134 b and the inner proximal opening group 134 c.
As illustrated in FIG. 3A, the proximal end 120 of the inner cannula 92 includes a syringe connector 140 having external threads 142. The syringe connector 140 may have any configuration suitable to couple a syringe to the inner cannula 92 in order to aspirate material there through, such as bone marrow, as further described herein.
The inner cannula 92 can be made of a suitable polymer or metal and can be rigid or flexible. For example, rigid stainless steel can be used, as well as flexible material, such as Nitinol.
As illustrated in FIG. 8, in place of the circular openings 128 the inner cannula 92 can include openings 129 shaped as elongated slots extending parallel to the longitudinal axis B. Each inner opening group 134 a, 134 b, and 134 c can include a pair of the slotted openings 129 orientated at 180° relative to each other. The pairs of openings 129 of the inner distal opening groups 134 a, 134 b, and 134 c are each radially aligned.
With additional reference to FIGS. 10 and 11, a trocar is illustrated at reference numeral 200. The trocar 200 generally includes a trocar handle 202 and a trocar needle 204 extending therefrom. The trocar handle 202 includes a distal surface 206 and a proximal surface 208 that is opposite to the distal surface 206. The trocar needle 204 includes a proximal end 210 and a distal end 212. The proximal end 210 is attached to a connector 214 at a center of the distal surface 206 of the trocar handle 202 with a press-fit, for example. The distal end 212 includes a pointed tip 216. The trocar needle 204 is rigid and made from any suitable rigid material, such as a suitable metal. At opposite sides of the connector 214 are locking tabs 218 configured to cooperate with the annular recess 38 of the insert 32 of the outer handle 16 to secure the trocar 200 to the outer handle 16, as further described herein.
With continued reference to FIGS. 1-11 and additional reference to FIGS. 12-19, use of the outer needle assembly 12, the inner needle assembly 14, and the trocar 200 to aspirate bone marrow will now be described. While aspiration of bone marrow from a posterior iliac crest 302 of a pelvis 300 is described, the outer needle assembly 12, the inner needle assembly 14, and the trocar 200 can be used to retrieve/isolate a variety of biological materials from a variety of different sources.
With initial reference to FIGS. 12 and 13, cortical bone 304 and cancellous bone 306 of the iliac crest 302 is initially pierced with a suitable piercing device, such as the trocar 200. As illustrated in FIG. 13, the trocar 200 can be coupled with the outer needle assembly 12 such that the trocar needle 204 extends through the outer cannula passageway 62 and the distal end 212 of the trocar needle 204, including the pointed tip 216, extends beyond the teeth 64 of the distal end 60 of the outer cannula 18. The teeth 64 facilitate piercing and cutting of the cortical bone 304 and the cancellous bone 306 of the iliac crest 302.
The trocar 200 can be secured to the outer needle assembly 12 through cooperation between the locking tabs 218 of the handle 202 and the annular recess 38 of the insert 32 of the outer handle 16. Once the outer cannula 18 is in a desired position and at a desired bone depth within the cancellous bone 306, the trocar 200 can be removed from cooperation with the outer needle assembly 12, which is left in position in the iliac crest 302.
With reference to FIG. 14, the inner needle assembly 14 is coupled to the outer needle assembly 12 seated in the iliac crest 302 by inserting the inner cannula 92 within the outer cannula 18 such that the distal end 122 of the inner cannula 92, including the closed tip 124, extends beyond the distal end 60 of the outer cannula 18. The connection tabs 102 are coupled to the annular recess 38 of the insert 32 of the outer handle 16 to lock the inner needle assembly 14 to the outer needle assembly 12. The connection cone 100 of the inner cannula handle 90 is seated within the insert 32 such that each of the ridges 106 of the cone 100 are between bumps 50 of each pair of bumps 52, as illustrated in FIG. 15A.
The longitudinal axis A of the outer needle assembly 12 is aligned with the longitudinal axis B when the inner needle assembly 14 is coupled to the outer needle assembly 12, as illustrated in FIGS. 3 and 3A for example. The outer cannula 18 and the inner cannula 92 are arranged such that the outer distal set 68 and the outer proximal set 70 of openings 66 are each aligned along the longitudinal axes A and B with the inner distal set 130 and the inner proximal set 132 of openings 128 respectively.
Because the recess 38 is annular, the inner needle assembly 14 can be rotated with respect to the outer needle assembly 12 about the longitudinal axis A of the outer needle assembly 12, while maintaining alignment of the longitudinal axis A and the longitudinal axis B. The inner needle assembly 14 is generally rotated between a first position (FIG. 15A), a second position (FIG. 15B), and a third position (FIG. 15C).
As illustrated in FIG. 15A, in the first position the first ridge 106 a of the connection core 100 is between the bumps 50 of the first pair of bumps 52 a, the second ridge 106 b is seated between the bumps 50 of the second pair of bumps 52 b, and the third ridge 106 c is seated between the bumps 50 of the third pair of bumps 52 c. Each opening 66 of the outer distal opening group 72 a is aligned with an opening 128 of the inner distal opening group 134 a. In particular and with reference to FIGS. 16 and 17, the openings 66 of the first and the second outer distal arrays 74 a/74 b are aligned with the openings 128 of the first and the second inner distal arrays 136 a and 136 b respectively, thus permitting aspiration of material, such as bone marrow, there through. In contrast, the openings 66 of the outer intermediate and outer proximal arrays 76 a, 76 b, 78 a, and 78 b are not aligned with the openings 128 of the inner intermediate and inner proximal arrays 138 a, 138 b, 140 a, and 140 b, thus restricting aspiration of bone marrow there through.
With reference to FIG. 16, aspiration is performed using any suitable device, such as a syringe 400. The syringe 400 generally includes a luer lock 402 with threads 404 and a chamber 406 including a plunger 408 (chamber 406 and plunger 408 are conventional features that are partially illustrated). The syringe 400 is connected to the inner handle 90 through cooperation between the threads 404 of the luer lock 402 and the threads 142 at the proximal end 120 of the inner cannula 92. As the plunger 408 is pulled away from the luer lock 402, a negative pressure is established in the chamber 406 and in the passageway 126 of the inner cannula 92, thereby drawing bone marrow through the aligned openings 66 and 128 through the passageway 126 of the inner cannula 92 and into the chamber 406 of the syringe 400. Thus, when the inner needle assembly 14 is in the first position relative to the outer needle assembly 12, bone marrow can be aspirated from an area of the iliac crest 302 that is in close proximity to the outer distal opening group 72 a and the inner distal opening group 134 a.
With reference to FIGS. 15B and 18, to aspirate bone marrow from an area of the iliac crest 302 that is proximate to the outer intermediate opening group 72 b and the inner intermediate opening group 134 b, the inner needle assembly 14 is rotated 120° about the longitudinal axes A and B from the first position to the second position. In the second position, the first ridge 106 a is locked between the bumps 50 of the second pair of bumps 52 b, the second ridge 106 b is locked between the bumps 50 of the third pair of bumps 52 c and the third ridge 106 c is locked between the bumps 50 of the first pair of bumps 52 a. In this second position, as illustrated in FIG. 18, the openings 66 of the first and the second outer intermediate arrays 76 a/76 b are aligned with the openings 128 of the first and the second inner intermediate arrays 138 a/138 b respectively, thus permitting aspiration of material, such as bone marrow, there through. In contrast, the openings 66 of the outer distal and proximal arrays 74 a, 74 b, 78 a, and 78 b are not aligned with the openings 128 of the inner distal and proximal arrays 136 a, 136 b, 140 a, 140 b, thus restricting aspiration of bone marrow there through.
With reference to FIGS. 15 c and 19, to aspirate bone marrow from an area of the iliac crest 302 that is proximate to the outer proximal opening group 72 c and the inner proximal opening group 134 c, the inner needle assembly 14 is rotated 120 degrees about the longitudinal axes A and B from the second position to the third position. In the third position, the first ridge 106 a is locked between the bumps 50 of the third pair of bumps 52 c, the second ridge 106 b is locked between the bumps 50 of the first pair of bumps 52 a, and the third ridge 106 c is locked between the bumps 50 of the second pair of bumps 52 b. In this third position, as illustrated in FIG. 19, the openings 66 of the first and the second outer proximal arrays 78 a/78 b are aligned with the openings 128 of the first and the second inner proximal arrays 140 a/140 b respectively, thus permitting aspiration of material, such as bone marrow, there through. In contrast, the openings 66 of the outer distal and intermediate arrays 74 a, 74 b, 76 a, and 76 b are not aligned with the openings 128 of the inner distal and intermediate arrays 136 a, 136 b, 138 a, 138 b, thus restricting aspiration of bone marrow there through.
The outer proximal set 70 of openings 66 is substantially similar to the outer distal set 68 of openings 66. The inner proximal set 132 of openings 128 is substantially similar to the inner distal set 130 of openings 128. Thus, alignment of the openings 66 and the openings 128 of the outer proximal and inner proximal sets 70 and 132 respectively in each of the first position, the second position, and the third position is the same as the alignment of the openings 66 and 128 of the outer and the inner distal sets 68 and 130 in each of the first, the second, and the third positions.
Thus, cooperation between the outer needle assembly 12 and the inner needle assembly 14 permits aspiration of bone marrow from three different areas of the iliac crest 250. The three different areas are relatively offset both radially and longitudinally without having to move the outer needle assembly 12. Such movement may cause patient discomfort and increase the complexity of the procedure.
With additional reference to FIG. 20, another bone marrow aspiration assembly according to the present teachings is illustrated at reference numeral 10′. The aspiration assembly 10′ is similar to the assembly 10 described above and thus like features are designated with the same reference numerals, but include the prime symbol (′). The assembly 10 generally includes an outer needle assembly 12′ including an outer cannula 18′ and an inner needle assembly 14′ including an inner cannula 92′.
The outer cannula 18′ and the inner cannula 92′ are both flexible and can be made of any suitable flexible material, such as a suitable polymer or Nitinol. The outer cannula 18′ is illustrated as including slots 80′ and the inner cannula 92′ is illustrated as including slots 129′ arranged in the same manner as illustrated in FIG. 8 on the assembly 10 (i.e. proximal, intermediate, and distal groups of slots 80/129 each positioned 120° apart radially). However, the slots 80′ and 129′ can be provided in any suitable arrangement and/or shape to permit aspiration through selective slots 80′ and 129′ (or openings 66/128) by rotating the inner cannula 92′ with respect to the outer cannula 18′. For example, the slots 80′ and 129′ can be arranged in two groups of slots 80′/129′ positioned 120° apart radially or can have the arrangement of circular openings 66/128 illustrated in, for example, FIGS. 7A and 7B.
With reference to FIG. 21, a bone piercing needle is illustrated at reference numeral 450. The bone piercing needle 450 includes a head 452, a cannula 454 terminating at an open tip 456, and a collar 458 between the head 452 and the cannula 454. The bone piercing needle 450 is substantially shorter in length than the bone marrow aspiration assembly 10′ and is rigid throughout. The cannula 454 is about 3-4 inches in length. The bone piercing needle 450 can be made of any suitable rigid material, such as a metal.
With additional reference to FIG. 22, use of the bone piercing needle 450 and the aspiration assembly 10′ to aspirate bone marrow from the pelvis 300 will now be described. The bone piercing needle 450 is driven into the pelvis 300 such that the collar 458 is at an outer surface of the iliac crest 302 and the cannula 454 extends through the cortical bone 304 to the cancellous bone 306. With the inner needle assembly 14′ mated with the outer needle assembly 12′, the inner and outer cannulas 18′ and 92′ are inserted into the iliac crest 302 either through the cannula 454 when the bone piercing needle 450 is left in the pelvis 300 or through the opening created in the pelvis 300 when the bone piercing needle 450 is removed. Because the inner and outer cannulas 18′ and 92′ are flexible, they are able to track along a curved perimeter 308 of the iliac crest 302, which is typically a rich source of bone marrow. To aspirate bone marrow from the iliac crest 302, a syringe is attached to the assembly 10′, which is operated in the same manner as the assembly 10 described above.
The assembly 10′ may also include the trocar 200 of FIG. 10, or any other suitable trocar or rigid device, which can be inserted within the outer cannula 18′ to facilitate insertion of the outer cannula 18′ into the iliac crest 302. The outer cannula 18′ may have an open tip 60′ as illustrated in FIG. 20, or it may have a closed tip (FIG. 20A). When the tip 60′ is open, the trocar 200 may extend beyond the tip 60′.
With additional reference to FIG. 23A, an introducer needle is illustrated at reference numeral 500. The introducer needle 500 generally includes a handle 502 and a cannula 504. The handle 502 includes a center connector 506 with an annular recess 508 extending about an exterior surface thereof. The connector 506 includes an opening 510 extending through a center thereof. The opening 510 extends through the handle 502 and is in communication with the cannula 504.
The cannula 504 includes a proximal end 512 secured to the handle 502 and a distal end 514 that is opposite to the proximal end 512. The distal end 514 includes an open tip 516 that may include sharpened edges 518 to facilitate positioning of the of the introducer needle 500 at an implantation site. The cannula 504 defines a channel 520 that extends between the proximal end 512 and the distal end 514. The channel 520 is in cooperation with the opening 510 to provide a continuous passageway through the introducer needle 500.
The cannula 504 is rigid and curved between the proximal end 512 and the distal end 514. The cannula 504 can have any suitable shape and any suitable degree of curvature to match or closely approximate either the overall natural curve of the iliac crest or specific portions thereof to facilitate positioning the cannula 504 proximate to areas with the greatest amount of bone marrow. The cannula 504 can be curved along its entire length or only portions thereof. The cannula 504 can be made of any suitable material, such as a suitable metal. The cannula 504 can optionally include holes along its length in communication with the channel 520, such as the openings 66 or the slots 80 of the outer cannula 18, which can be provided in any suitable size, shape, and arrangement, such as the arrangement herein with respect to the outer cannula 18.
A flexible needle assembly 550 is illustrated in FIG. 23B. The flexible needle assembly 550 is substantially similar to the inner needle assembly 14′ and therefore similar features are designated with the same reference numerals, but with the prime (′) symbol added. Unlike the inner needle assembly 14′, the assembly 550 as illustrated includes only a single pair of slots 129′ at the distal end 122′, but can include any suitable number of slots 129′ or openings (such as openings 128 as arranged in FIGS. 2 and 7A) in any suitable shape, number, or arrangement, such as is provided with the inner needle assembly 14 or 14′.
With additional reference to FIG. 24, use of the curved introducer needle 500 to aspirate bone marrow from the iliac crest 302 of the pelvis 300 will now be described. The cortical bone 304 of the iliac crest 302 is initially pierced with the bone piercing needle 450, which is driven within the iliac crest 302 such that the open tip 456 extends to within the cancellous bone 306. The cannula 504 of the introducer needle 500 is then inserted through the cannula 454 of the bone piercing needle 450 and into the iliac crest 302. The bone piercing needle 450 can be curved, as illustrated, to accommodate the introducer needle. The curvature of the cannula 504 is similar to the curvature of the perimeter 308 of the iliac crest 302 and thus the cannula 504 can be positioned proximate to the perimeter 308, an area rich in bone marrow, along at least a majority of its length. Alternatively, the bone piercing needle 450 can be removed prior to insertion of the cannula 504, which can be inserted through the opening in the iliac crest 302 formed by insertion of the cannula 454.
Once the cannula 504 of the introducer needle 500 is at an area of the iliac crest 302 from which bone marrow is to be aspirated, the flexible needle assembly 550 can be mated with the introducer needle 500 such that the tabs 102′ are coupled to the annular recess 508 and the inner cannula 92′ extends through the channel 520 such that the distal end 122′, including a portion with the slots 129′ (illustrated as a plurality of circular openings in FIG. 24A), extends beyond the distal end 514. To aspirate bone marrow, a syringe 400 can be coupled to threads of the cannula handle 90′ (in a manner substantially similar to that illustrated in FIG. 16) to aspirate bone marrow through the slots 129′ of the inner cannula. Alternatively, a syringe can be attached directly to the connector 506 of the introducer needle 500 to aspirate bone marrow directly through the open tip 516. The flexible needle assembly 550 can be rotated to aspirate bone marrow from different areas of the iliac crest 302.
When the cannula 504 includes the slots 80 or the openings 66 of the outer cannula 18 and the cannula 92′ includes the slots 129 or the openings 128 of the inner cannula 92, as arranged in FIGS. 7A and 8 for example, bone marrow may be aspirated through select slots 80/129 or openings 66/128 by rotating the flexible needle assembly 550 relative to the cannula 504 to provide selective alignment, and selective aspiration, through the different slots 80/129 or openings 66/128 in the same manner as described in FIGS. 15 and 17-19 with respect to use of the outer needle assembly 12 and the inner needle assembly 14.
The foregoing description of the embodiments has been provided for purposes of illustration and description. It is not intended to be exhaustive or to limit the invention. Individual elements or features of a particular embodiment are generally not limited to that particular embodiment, but, where applicable, are interchangeable and can be used in a selected embodiment, even if not specifically shown or described. The same may also be varied in many ways. Such variations are not to be regarded as a departure from the invention, and all such modifications are intended to be included within the scope of the invention.

Claims

What is claimed is:

1. A bone marrow aspiration assembly comprising:

a cannulated introducer needle curved to approximate a natural curvature of an iliac crest; and

an aspiration needle including apertures for aspirating bone marrow, the aspiration needle is configured to be received in, and extend from, the cannulated introducer needle to reach a bone marrow aspiration site in the iliac crest.

2. The bone marrow aspiration assembly of claim 1, wherein the cannulated introducer needle includes an open tip and is without aspiration openings about a radius thereof.

3. The bone marrow aspiration assembly of claim 1, wherein the cannulated introducer needle includes a connector configured to mate with an aspiration syringe for aspirating bone marrow directly through the cannulated introducer needle.

4. The bone marrow aspiration assembly of claim 1, wherein the aspiration needle includes a single group of apertures.

5. The bone marrow aspiration assembly of claim 1, wherein the aspiration needle includes a distal group, an intermediate group, and a proximal group of apertures each having a first array of apertures and a second array of apertures, each of the groups are arranged 120° apart and each of the first arrays are arranged 180° apart from each of the second arrays.

6. The bone marrow aspiration assembly of claim 1, wherein the cannulated introducer needle is rigid and the aspiration needle is flexible.

7. A bone marrow aspiration assembly comprising:

a cannulated bone piercing needle;

a rigid, cannulated introducer needle that is curved to approximate a natural curvature of an iliac crest, the rigid, cannulated introducer needle has a length longer than the cannulated bone piercing needle and is configured to be received within and pass through the cannulated bone piercing needle; and

a flexible aspiration needle having apertures for aspirating bone marrow, the flexible aspiration needle is configured to be received in, and extend from, the rigid, cannulated introducer needle to reach a bone marrow aspiration site in the iliac crest.

8. The bone marrow aspiration assembly of claim 7, wherein the rigid, cannulated introducer needle has an open tip and is without aspiration openings about a radius thereof.

9. The bone marrow aspiration assembly of claim 7, wherein the rigid, cannulated introducer needle includes a connector configured to mate with an aspiration syringe for aspirating bone marrow directly through the rigid, cannulated introducer needle.

10. The bone marrow aspiration assembly of claim 7, wherein the flexible aspiration needle includes a single group of apertures.

11. The bone marrow aspiration assembly of claim 7, wherein the flexible aspiration needle includes a distal group, an intermediate group, and a proximal group of apertures each having a first array of apertures and a second array of apertures, each of the groups are arranged 120° apart and each of the first arrays are arranged 180° apart from each of the second arrays.

12. A method for aspirating bone marrow comprising:

piercing bone with a cannulated bone piercing needle;

inserting into the cannulated bone piercing needle a rigid, cannulated introducer needle that is curved to approximate a natural curvature of an iliac crest and has a length longer than the cannulated bone piercing needle such that at least a tip of the rigid, cannulated introducer needle extends out from within the cannulated bone piercing needle; and

inserting into the rigid, cannulated introducer needle a flexible aspiration needle having apertures for aspirating bone marrow such that the flexible aspiration needle extends from the rigid, cannulated introducer needle to reach a bone marrow aspiration site in the iliac crest.

13. The method of claim 12, further comprising mating an aspiration syringe with a connector of the cannulated introducer needle for aspirating bone marrow directly through the cannulated introducer needle.

14. The method of claim 12, further comprising aspirating bone marrow through a single group of apertures of the flexible aspiration needle.

15. The method of claim 12, further comprising aspirating bone marrow through a distal group, an intermediate group, and a proximal group of apertures of the flexible aspiration needle each having a first array of apertures and a second array of apertures, each of the groups are arranged 120° apart and each of the first arrays are arranged 180° apart from each of the second arrays.

16. The method of claim 12, wherein the cannulated introducer needle includes an open tip and is without aspiration openings about its radius.