Surgical technique for alveolar ridge augmentation with maxillary sinus elevation (lateral approach) using a pre-portioned and ready pre-packaged bone graft composition in gelatin bag and method of producing it
12419752 ยท 2025-09-23
Inventors
Cpc classification
C08L3/02
CHEMISTRY; METALLURGY
A61F2/4601
HUMAN NECESSITIES
A61F2002/30064
HUMAN NECESSITIES
A61F2002/2835
HUMAN NECESSITIES
C08L3/02
CHEMISTRY; METALLURGY
C08L5/00
CHEMISTRY; METALLURGY
A61F2/2846
HUMAN NECESSITIES
A61L27/3608
HUMAN NECESSITIES
C08L1/00
CHEMISTRY; METALLURGY
A61L27/3691
HUMAN NECESSITIES
C08L89/06
CHEMISTRY; METALLURGY
C08L1/00
CHEMISTRY; METALLURGY
C08L5/08
CHEMISTRY; METALLURGY
C08L89/06
CHEMISTRY; METALLURGY
C08L5/00
CHEMISTRY; METALLURGY
C08L5/08
CHEMISTRY; METALLURGY
A61L27/50
HUMAN NECESSITIES
International classification
A61L27/50
HUMAN NECESSITIES
A61C8/00
HUMAN NECESSITIES
A61L27/36
HUMAN NECESSITIES
Abstract
The present embodiment relates generally to methods of performing surgical technique maxillary sinus floor augmentation with a lateral approach using a pre-portioned and ready pre-packaged bone graft composition in gelatin bags and method of producing gelatin bags. In addition the present inventions can be widely used in other medical fields such as dentistry, orthopedic surgery, spine surgery, plastic and reconstruction surgery, sport medicine, trauma surgery, phinoplasty surgery and veterinary.
Claims
1. A method of treating edentulous patients comprising: mixing different types of bone graft materials, the bone graft material types consisting of two or more bone graft material types from a list of autologous bone grafting, autogenous bone grafting, allogeneic grafts, xenografts, synthetic substitutes; placing the bone graft materials on a film, wherein the film has a thickness of up to 50 m, the film comprising gelatin and a polysaccharide derivative; sealing the bone graft materials in the film formed into a bag; making an incision in soft tissue of a patient's mouth cavity; placing the bag into a space behind the incision; and suturing the incision.
2. The method of claim 1 further comprising modeling the bone graft materials by press agglomeration.
3. The method of claim 1 wherein the bone graft materials comprises coherent mass bone graft chips harvested from cortical human bone.
4. The method of claim 1 wherein the bone graft materials comprises coherent mass bone graft chips harvested from cancellous human bone.
5. The method of claim 1 wherein the bone graft materials comprises artificial bone graft particles.
6. The method of claim 1 wherein the bone graft materials comprises synthetic bone graft particles.
7. The method of claim 1 further comprising pulling back a soft tissue flap created by the incision, exposing a lateral wall of a sinus in a maxilla jaw.
8. The method of claim 7 further comprising creating a window in a sinus boney wall.
9. The method of claim 8 wherein the bag is placed in the window.
10. The method of claim 1 wherein the polysaccharide derivative is starch.
11. The method of claim 1 wherein the polysaccharide derivative is glycogen.
12. The method of claim 1 wherein the polysaccharide derivative is cellulose.
Description
BRIEF DESCRIPTION OF THE DRAWINGS
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DETAILED DESCRIPTION OF THE PREFERRED EMBODIMENT
(16) Referring to the representation of the images now, the present invention describes a dental surgical technique for maxillary sinus lift and dental implant placement that includes using gelatin bag with a pre-portioned bone graft composition.
(17) In practice, prior to then start of the sinus lift augmentation procedure described above, a current treatment plan must be established based on diagnostic evaluation such as an oral exam, radiographic evaluation from verity radiographs: cone beam computer tomography (CBCT) must be taken to measure the sinus's width and height, panoramic X-ray and full mouth series x-ray is taken to calibrate the patient's upper jaw and maxillary sinuses.
(18) As demonstrated in
(19) A pre-operative Cone Beam Computed Tomography was performed and used to estimate the efficiency of bone lamina for sinus lifting surgery and bone formation with biomaterials (
(20) An additional analysis was performed on periapical radiograph (
(21) The procedure is performed from inside the oral cavity of patient's mouth (
EXAMPLE
(22) The surgical procedure discussed in this case was performed at Privet Dental Office in Los Angeles, California, USA.
(23) A 49-year-old Caucasian female, with a good health status (ASA score: 0), was attended to at the dental office; written informed consent was obtained from the patient to have the case details. Patient was informed regarding the use of a new approach in sinus lift augmentation surgery. She was indicated for a prosthetic implant rehabilitation procedure in the upper right quadrant after a maxillary sinus lift procedure for atrophy of the maxillary bone at the first molar level to install one dental implant.
(24) A pre-operative evaluation of the patient's maxillary sinus for implant planning was performed using CBCT images before surgery,
(25) The surgery was performed under antibiotic prophylaxis: Amoxicillin 2 gr 1 hour before the surgery. For the local anesthesia (4% Septocaine with 1/100,000 epinephrine 1.7 ml 2 cartridges) were administrated in buccal and palatal areas around the tooth. The patient was placed on systemic antibiotics for seven day: Amoxicillin 500 mg (1 capsule every 8 hours).
(26) A full-thickness flap (
(27) Through delicate instrumentation, the sinus membrane was carefully reflected and peeled from the inner surface of the sinus cavity wall (
(28) A particular mass of bone graft chips can be harvested from different parts of patient jaw or harvested from an individual other than the receiving patient or bone substitutes had its origin from a species other than human or synthetic bone particles.
(29) At the same time the process to prepare pre-portioned and ready pre-packaged biocompatible osteogenic bone graft composition is started, creating the single dose in the bags of blood-soluble gelatin film (
(30) The mass of bone graft consist of a different variety of sizes of bone chips.
(31) The coherent mass of bone graft chips can harvest from cortical, cancellous or mix of both types of bone.
(32) The bone graft was positioned in the newly formed subantral cavity to preserve the sinus membrane, and the space was then filled with the single doses in the bags of blood-soluble and saliva-soluble gelatin film (
(33) The maxillary sinus entry was packed with gelatin bags (
(34) A regular size of root form implant (having a 4.2 mm in diameter size and length of 10 mm) was placed (
(35) The soft tissue around the dental implant healed good with minimal discomfort for patient.
(36) The importance of continuing a high standard of oral hygiene was addressed to the patient.
(37) Tooth brushing and flossing techniques were reinforced.
(38) During the postoperative period, the patient received antibiotic therapy (Amoxillin 500 mg (1 tablet every 8 hours for 7 days) and performed oral rinses with 0.2% Chlorhexidine (Peridex, 0.12%) was prescribed for three times/day for 10 days. (Azizi B, Budimir A, Mehmeti B, Jakovljevid S, Bago I, Gjorgievska E, Gabrio D., Antimicrobial Efficacy of Photodynamic Therapy and Light-Activated Disinfection Against Bacterial Species on Titanium Dental Implants. Int J Oral Maxillofac Implants. 2018 July/August; 33(4):831-837-incorporated herein by reference).
(39) The prognosis of current surgical procedure was highly favorable. The patient received full explanation regarding long-term prognosis and oral hygiene maintenance. During the time of follow-up no hard and soft tissue changes was detected.
(40) Delayed dental implant placement and delayed loading was planned to allow continue chewing function of the patient.
(41) The surgical technique described in this article developed new approach of alveolar ridge augmentation with maxillary sinus elevation (lateral approach) using a pre-portioned and ready pre-packaged bone graft composition in gelatin bags.
(42) This method eliminates the several commonly found complications such as sinus or Schneiderian membrane perforation, bone graft exposure, postoperative incidences of dislodgement of the bone graft, loss of bone graft and difficulties during manipulation with bone grafting.
(43) Method that can be used to enhance the stability of bone graft for instance, to tightly pack of the graft particles.
(44) Thereby, the above-mentioned discussion discloses and describes simply exemplary embodiments of the present inventions. As doctors will understand, the present inventions can be implemented in other specific forms without changing the main idea of current innovations. Respectively, the disclosure of the present embodiment is planned to be illustrated, but not limiting of the capability of the inventions, as well as other claims.