Balloon dilation catheter for use in sinus drainage pathways
The present disclosure provides a balloon dilation catheter that includes a handle ( 102 ), a substantially rigid inner guide member ( 108 ) coupled to the handle, a shaft ( 118 ) arranged over the inner guide member, a balloon ( 120 ) coupled to the inner guide member, and a polymer ball tip ( 122 ) positioned at a distal end of the balloon. To treat a sinus drainage pathway of a subject using the balloon dilation catheter, the substantially rigid inner guide member is positioned into the drainage pathway of the sinus of the subject via a nasal passageway. The balloon is then inflated to expand or otherwise remodel the drainage pathway.
1. A balloon dilation catheter for dilating sinus drainage pathways comprising:
a handle having a proximal end and a distal end, the handle configured to be gripped by an operator;
a substantially rigid inner guide member having a distal end and a proximal end, wherein the substantially rigid inner guide member includes a lumen extending between the distal end and the proximal end of the substantially rigid inner guide member, wherein the substantially rigid inner guide member extends longitudinally from the distal end of the handle, and wherein the distal end of the substantially rigid inner guide member includes a curved portion with a radius of curvature greater than zero;
a shaft arranged over the substantially rigid inner guide member;
a balloon coupled to the shaft such that the balloon is fixed relative to the shaft, wherein the balloon is positioned over the curved portion of the substantially rigid inner guide member; and
a polymer ball tip positioned at a distal end of the balloon, wherein the polymer ball tip is formed from excess balloon material such that the polymer ball tip is directly coupled to the distal end of the balloon, and wherein the polymer ball tip is distal of the distal end of the substantially rigid inner guide member.
2. The balloon dilation catheter of claim 1 , wherein the balloon is fixed relative to the shaft and further fixed relative to the substantially rigid inner guide member.
3. The balloon dilation catheter of claim 1 , wherein the distal end of the substantially rigid inner guide member is intractable such that the radius of curvature of the curved portion of the substantially rigid inner guide member is constant and cannot be shaped by the operator.
4. The balloon dilation catheter of claim 1 , wherein the substantially rigid inner guide member comprises a precipitation-hardened material.
5. The balloon dilation catheter of claim 1 , further comprising:
a first port positioned at the proximal end of the handle, wherein the proximal end of the substantially rigid inner guide member forms a sealing arrangement with the first port; and
a second port positioned at the proximal end of the handle, wherein the second port is in fluid communication with the balloon via an inflation lumen.
6. The balloon dilation catheter of claim 5 , wherein the first port comprises an adjustable connector configured to receive a guidewire, wherein the adjustable connector enables the operator to adjust a position of a distal end of the guidewire in relation to the distal end of the substantially rigid inner guide member.
7. The balloon dilation catheter of claim 1 , wherein a guidewire is arranged within the lumen of the substantially rigid inner guide member,
wherein the guidewire is a light emitting guidewire, and
wherein the light emitting guidewire comprises:
a light emitting diode; and
an optical fiber having a proximal end and a distal end, wherein a diameter of the distal end of the optical fiber is less than a diameter of the proximal end of the optical fiber such that the optical fiber is flared at the proximal end.
8. The balloon dilation catheter of claim 1 , wherein the polymer ball tip and the lumen of the substantially rigid inner guide member comprise respective apertures that are configured for aspiration of blood or secretions.
9. A method of treating a sinus drainage pathway of a patient, comprising:
providing a balloon dilation catheter of claim 1 , wherein the balloon dilation catheter comprises:
a handle having a proximal end and a distal end, the handle configured to be gripped by an operator,
a substantially rigid inner guide member having a distal end and a proximal end, wherein the substantially rigid inner guide member includes a lumen extending between the distal end and the proximal end of the substantially rigid inner guide member, wherein the substantially rigid inner guide member extends longitudinally from the distal end of the handle, and wherein the distal end of the substantially rigid inner guide member includes a curved portion with a radius of curvature greater than zero,
a shaft arranged over the substantially rigid inner guide member,
a balloon coupled to the shaft such that the balloon is fixed relative to the shaft, wherein the balloon is positioned over the curved portion of the substantially rigid inner guide member, and
a polymer ball tip positioned at a distal end of the balloon, wherein the polymer ball tip is formed from excess balloon material such that the polymer ball tip is directly coupled to the distal end of the balloon, and wherein the polymer ball tip is distal of the distal end of the substantially rigid inner guide member;
directing the distal end of the substantially rigid inner guide member into a head of a patient through a nostril;
directing the distal end of the substantially rigid inner guide member to a position within the sinus drainage pathway; and
inflating the balloon to dilate tissue defining the position of the sinus drainage pathway.
10. The method of claim 9 , further comprising:
positioning a guidewire within the lumen of the substantially rigid inner guide member, wherein the balloon dilation catheter further comprises a first port positioned at the proximal end of the handle, wherein the proximal end of the substantially rigid inner guide member forms a sealing arrangement with the first port, and wherein the first port comprises an adjustable connector configured to receive the guidewire, the method further comprising:
adjusting a position of a distal end of the guidewire in relation to the distal end of the substantially rigid inner guide member via the adjustable connector.
11. The method of claim 9 , further comprising aspirating blood or secretions through the lumen of the substantially rigid inner guide member, wherein the polymer ball tip and the lumen of the substantially rigid inner guide member comprise respective apertures that are configured for aspiration of the blood or secretions.