Dual Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy

• US 20100094417A1
• Filed: 10/13/2009
• Published: 04/15/2010
• Est. Priority Date: 10/15/2008
• Status: Abandoned Application

• Current Assignee: Christopher Robert Johnson, James Schumacher, Janet Ellen Morris
• Original Assignee: Christopher Robert Johnson, James Schumacher, Janet Ellen Morris
• Inventors: Schumacher, James, Morris, Janet Ellen, Johnson, Christopher Robert
• Application Number:
  US12/578,273
• Publication Number:
  US 20100094417A1
• Time in Patent Office: Days
• US Class Current: 623/9
• CPC Class Codes: A61D 1/00 Surgical instruments for veterinary use
• CPC Class Codes: A61D 7/04 Devices for anaesthetising animals by gases or vapours; Inhaling devices
• CPC Class Codes: A61F 2/20 Epiglottis; Larynxes; Tracheae combined with larynxes or for use therewith tracheae, bronchi per se A61F2/04 ; tracheostomy tubes A61M16/0465

Abstract

In a horse with left recurrent laryngeal neuropathy, abduction of the arytenoid cartilage on the affected side of the larynx cannot be achieved, causing progressive collapse of the arytenoid cartilage and vocal cord into the airway as negative inspiratory pressure increases. This produces airflow limitations that result in more rapid development of hypoxemia, hypercarbia, and metabolic acidosis, causing early fatigue and poor performance. Horses with left recurrent laryngeal neuropathy have a history of upper airway obstruction during exercise, including abnormal inspiratory respiratory noise and exercise intolerance. This noise is the result of air turbulence created as air passes over the affected vocal cord and ventricle, which acts as resonators. The DHLCP caudal and cranial device'"'"'s are placed between the cricoid and the arytenoid cartilages and will permanently abduct the affected arytenoid cartilage. Once abducted sufficiently, it will provide unobstructed respiration during exercise, but not so much that saliva, food, and water are aspirated during swallowing.

Claims

1. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy comprising:

a. a caudal device; and

b. a cranial device.

2. The Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 1, wherein each of the caudal and cranial devices further comprises:

i. a dual-hook anchor arrangement (2);

ii. a shank (4);

iii. a first swedge (7);

iv. a stranded cable (5);

v. a monofilament leader (6);

vi. a second swedge (8);

vii. a half-circle cutting needle (3).

3. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 2, wherein the dual-hook anchor arrangement for each of the caudal and cranial devices further comprises:

a. two hooks (9) that connect to the shank (4) at approximately a 65 degree angle to each other;

each hook (9) has a total length of 10 mm and a diameter of 0.5 mm;

when connected to the shank (4), the bend of each hook (9) begins at 5 mm and turns upward and parallel to the shank (4);

and from the bend upward, the hook (9) has a length of 5 mm;

the shank (4) has a length of 7 mm and a diameter of 1 mm;

the dual-hook anchor arrangement (2) is swedged to the stranded cable (5) with the first swedge (7).

4. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 2, wherein the first swedge (7) for each of the caudal and cranial devices has a length of 4 mm and a diameter of 1.25 mm.

5. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 2, wherein the stranded cable (5) for each of the caudal and cranial devices has a length of 355.6 mm and a diameter of 1 mm.

6. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 2, wherein the monofilament leader (6) for each of the caudal and cranial devices has a length of 152.4 mm and a diameter of 1 mm.

7. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 2, wherein the caudal device has a 36 mm half-circle cutting needle (3) swedged to an end of the monofilament leader (6) by a second swedge (8).

8. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 2, wherein the cranial device has a 26 mm half-circle cutting needle (3) swedged to an end of the monofilament leader (6) by a second swedge (8).

9. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 7, wherein the second swedge (8) for each of the caudal and cranial devices has a length of 4 mm and a diameter of 1.25 mm.

10. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 8, wherein the second swedge (8) for each of the caudat and cranial devices has a length of 4 mm and a diameter of 1.25 mm.

11. A Dual-Hook Laryngeal Cable Prosthesis (DHLCP) used to correct airflow in the larynx of horses affected with left recurrent laryngeal neuropathy according to claim 2, wherein the DHLCP is made of surgical stainless steel.

12. A method of instrumenting the dorsal aspect of the larynx of a horse using a dual-hook laryngeal cable prosthesis (DHLCP), said method comprising the steps of:

a. walking off a half-circle cutting needle (3) from the caudal aspect of the cricoid cartilage just lateral to the dorsal midline until the point slips beneath the cartilage using the left index finger as a guide;

b. advancing the half-circle cutting needle (3) of the caudal device in a cranial direction and avoiding penetration of the point of the half-circle cutting needle (3) through the laryngeal mucosa;

c. rotating the half-circle cutting needle (3) of the caudal device to penetrate the cricoid cartilage 1.5 cm to 2 cm cranial to its caudal border and lateral to the dorsal ridge;

d. drawing the half-circle cutting needle (3) of the caudal device through the cricoid cartilage and out of an incision using the left index finger to ascertain the site of penetration;

e. seating the dual-hook anchor arrangement (2) of the caudal device onto the caudal edge of the cricoid cartilage and applying tension to the stranded cable (5) of the caudal device using the left hand;

f. passing a large hemostat beneath the cranial aspect of the cricopharyngeus muscle, and bringing out the hemostats jaws at the site of penetration of the half-circle cutting needle (3) of the caudal device in the cricoid cartilage;

g. grasping and drawing the end of the stranded cable (5) of the caudal device beneath the cricopharyngeus muscle and bringing the stranded cable (5) out of the incision;

h. positioning the half-circle cutting needle (3) of the cranial device on the caudomedial aspect of the muscular process of the arytenoid cartilage and passing in a caudomedial to craniolateral direction through the arytenoid cartilage, after retracting the cricopharyngeus muscle caudally to expose the muscular process of the arytenoid cartilage;

i. pulling the monofilament leader (6) and stranded cable (5) of the cranial device through the arytenoid cartilage;

j. positioning the dual-hook anchor arrangement (2) of the cranial device tightly against the muscular process of the arytenoid cartilage by removing slack and tensioning the stranded cable (5) and bringing the stranded cable (5) out of the incision;

k. removing the half-circle cutting needles (3) from both of the caudal and cranial devices from the monofilament leaders (6);

l. passing the leading ends of each of the stranded cables (5) from the caudal and cranial devices through a crimp in opposite directions;

m. applying tension from a cinch tightener on the stranded cables (5) of each of the caudal and cranial devices until the desired abduction (observed endoscopically) of the arytenoid cartilage is reached;

n. applying a crimper to a crimp to secure the stranded cables (5) of the caudal and cranial devices together, and removing any excess length of the stranded cables (5) from the caudal and cranial devices with a cable cutter.