THANK YOU FOR TAKING THE TIME!
Curious as to why you would extract three teeth with “no periodontal issues or bone defects� But assuming there was a valid rationale, let’s pose the following questions:ANSWERED BELOW
1. Following extraction, was there bleeding from the osteotomies? GOOD BLEEDING DURING. PRIMARY CLOSURE, NO BLEEDING UPON RELEASING PT. PT DID NOT NEED THE GUAZE.
2. If the bleeding index was poor, did you decorticate the walls of the osteotomy prior to placing the graft? I DID, BUT PERHAPS NOT VIGOROUSLY ENOUGH? I REMEMBER THINKING I SHOULDVE BEEN MORE AGGRESSIVE BUT I HAD SUFFICIENT BLOOD, IN FACT I USED IT TO MIX THE GRAFT INSTEAD OF SALINE.
3. What type of graft did you use and was it of high or low crystallinity? What is the recommended resorption time? DYNACORE ALLOGRAFT 70:30 Cort/Can and DYNAMATRIX MEMBRANE... CRYSTALLINITY?
4. Was there any tissue movement or microtrauma to the flap during healing? NO
5. Why did you use a corticosteriod immediately post-operatively, what was the dosage and for how long was the patient using it? If you want to interfere with the early inflammatory phase and resorption of the graft, then you chose the right drug. (2) 4 MG TABS. 1 THE DAY OF, 1 THE NEXT DAY
6. Why did use mix clindamycin with the graft rather than metronidazole and what was the dosage? CLINDAMYCIN 300MG X30 WERE GIVEN FOR PT TO TAKE ORALLY. I DIDNT MIX WITH THE GRAFT.
I know I have been critical of these types of cases on this site in the past, and have received my share of “hate†mail after my posts, but this is just basic biology guys. Without a respect for basic pathways of healing, you can expect to see these results routinely. But these “empirical†cocktails have no longer have a place in implantology. Take a good bone augmentation course and get caught up with current protocols. NO HATE MAIL HEAR, I ASSURE YOU. JUST APPRECIATION