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1.
Quintessence Int ; 38(10): E572-6, 2007.
Article in English | MEDLINE | ID: mdl-18197315

ABSTRACT

OBJECTIVES: To clinically evaluate the jet injection Injex (Rösch AG Medizintechnik) using 2 different anesthetic solutions, and to compare the jet injection and the standard needle injection techniques. METHOD AND MATERIALS: Of the 32 patients in the study, 10 received mepivacaine 3% anesthetic solution by means of the jet injection technique, while the remaining 22 patients received lidocaine 2% with epinephrine 1:80,000 by the same method. The 14 patients in whom pulp anesthesia was achieved were selected for an additional evaluation of the pulp reaction using standard needle injection anesthesia. The differences between the 2 compounds with Injex were statistically evaluated by means of independent-samples t test analysis. The differences between subgroups receiving both jet injection and needle injection anesthesia were evaluated by means of paired t test analysis. RESULTS: The administration of mepivacaine 3% using Injex did not achieve pulp anesthesia in any of the 10 patients, although the soft tissue anesthesia was successful. The administration of lidocaine with epinephrine using Injex resulted in pulp anesthesia in only 14 patients; soft tissue anesthesia was observed in all patients of this group. There was no statistically significant difference between Injex and the needle injection technique in onset of anesthesia. However, the duration of anesthesia was significantly longer for the needle infiltration group than for the Injex injection group. CONCLUSION: The anesthetic solution should be combined with a vasoconstriction agent when the Injex technique is implemented.


Subject(s)
Anesthesia, Dental/methods , Anesthesia, Local/methods , Anesthetics, Local/administration & dosage , Dental Pulp/drug effects , Anesthesia Recovery Period , Anesthesia, Dental/instrumentation , Anesthesia, Local/instrumentation , Double-Blind Method , Epinephrine/administration & dosage , Humans , Injections, Jet , Lidocaine/administration & dosage , Mepivacaine/administration & dosage , Mouth Mucosa/drug effects , Needles , Vasoconstrictor Agents/administration & dosage
2.
Implant Dent ; 15(4): 386-94, 2006 Dec.
Article in English | MEDLINE | ID: mdl-17172957

ABSTRACT

PURPOSE: It has been reported that previous Biogran (3i Implant Innovations, Inc., Palm Beach Gardens, FL) can be converted in vitro into hydroxyapatite (Biogran II) to accelerate new bone formation. The purpose of this study was to evaluate the bone regeneration around implants placed in critical-sized defects in rabbit tibia using granular and spherical forms of Biogran II in regards to implant contact, bone-to-graft contact, bone graft area, and total bone volume. MATERIALS AND METHODS: Twelve adult New Zealand rabbits were used, offering 24 surgical sites (1 in each tibia), where 6-mm round defects were created allowing the homocentric insertion of a screw type experimental implant with Osseotite (3i Implant Innovations, Inc.) surface. Half of the defects (group A) were filled up with spherical and half (group B) with granular forms of Biogran II. Ossix (3i Implant Innovations, Inc.) membranes covered the surgical sites. RESULTS: The histological evaluation after 8 weeks showed new bone formation in both groups, without any statistically significant differences in regards to bone-to-implant contact, bone-to-graft contact, bone graft area, and bone volume. Both dissolution of the outer shell and inner silica gel of the particles were observed mostly in spherical particles. In addition, new bone formation within the protected pouch interconnected with the surrounding new bone was observed exclusively in spherical particles of Biogran II. CONCLUSION: Faster dissolution of both outer and inner portions of spherical particles of Biogran II led to better integration with the surrounding new bone during an 8-week period of healing.


Subject(s)
Biocompatible Materials/therapeutic use , Bone Regeneration/physiology , Bone Substitutes/therapeutic use , Dental Implants , Glass , Animals , Bone Diseases/pathology , Bone Diseases/surgery , Membranes, Artificial , Osseointegration/physiology , Rabbits , Solubility , Surface Properties , Tibia/pathology , Tibia/surgery , Wound Healing/physiology
3.
Int J Neurosci ; 116(1): 67-75, 2006 Jan.
Article in English | MEDLINE | ID: mdl-16319000

ABSTRACT

The purpose of this study was the examination of the role of temperature in the action of lidocaine via electrophysiological recordings on the sciatic nerve of the rat in vitro and in vivo. 20 Male Wistar rats were used in each type of experiment. In vitro, lidocaine shows no statistically significant difference regarding the onset of anesthesia but at the temperature of 25 degrees C it is significantly more potent on the establishment of anesthesia compared to the temperature of 36.5 degrees C. In vivo, lidocaine at the temperature of 4 degrees C is statistically significantly more effective in the establishment and the duration of anesthesia related to the temperature of 20 degrees C.


Subject(s)
Anesthetics, Local/pharmacology , Lidocaine/pharmacology , Sciatic Nerve/drug effects , Temperature , Action Potentials/drug effects , Animals , Body Temperature , Electrophysiology , In Vitro Techniques , Male , Rats , Rats, Wistar
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