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008 200222s2019 ua dho f m 000 0 eng d
040 _aEG-GiCUC
_beng
_cEG-GiCUC
041 0 _aeng
049 _aDeposite
097 _aM.Sc
099 _aCai01.09.09.M.Sc.2019.Ib.E
100 0 _aIbrahim Hasan Bashier Garoushi
245 1 0 _aEvaluation of the neurosensory disturbances after inferior alveolar nerve lateralization with and without isolation of the simultaneously placed implants using collagen membrane :
_bRandomized clinical trial /
_cIbrahim Hasan Bashier Garoushi ; Supervised Rami Elbialy , Mohamed Atef
246 1 5 _aتقييم {uئإ٨ؤ}ستجابة {uئإ٨ؤ}لإحساس {uئإ٨ؤ}لعصبى بعد تحر{uئإئ٣}ك {uئإ٨ؤ}لعصب {uئإ٨ؤ}لسنخى {uئإ٨ؤ}لسفلى مع عزل {uئإ٨ؤ}و بدون عزل {uئإ٨ؤ}لغرسا{uئإ٩٥} {uئإ٨ؤ}لموضوعة فى نفس {uئإ٨ؤ}لوقت بغشاء {uئإ٨ؤ}لكولاجين :
_bتجربة سر{uئإئ٣}ر{uئإئ٣}ة عشوائيه
260 _aCairo :
_bIbrahim Hasan Bashier Garoushi ,
_c2019
300 _a83 P. :
_bcharts , facsimiles , photographs ;
_c25cm
502 _aThesis (M.Sc.) - Cairo University - Faculty of Oral and Dental Medicine - Department of Prosthodontics
520 _aInferior alveolar nerve lateralization with simultaneous implant placement has been presented with different modifications in the literature to overcome or decrease the postoperative complications. The present study is a randomized clinical trial to evaluate the neurosensory disturbances, primary stability and marginal bone loss after IAN lateralization with and without isolation of the IAN by collagen membrane.A total of 30 sites with severely atrophied posterior mandibular ridge wereselected for IAN lateralization procedure; 15 sites received a collagen membrane as an isolation between the nerve and implant, while the other 15 sites had no isolationbetween the nerve and implant surface with a follow up period of up to 6 months.Neurosensory evaluation using the modified MRC scale was carried outpostoperatively after 2 weeks, 1month, 3 months and 6 months. Implant stability values were taken using Osstell device immediately after surgery and 6 months postoperative. Immediate CBCT sections to measure the level of the crestal bonerelative to implant platform, and 6 months postoperative measurements were recorded and calculated for marginal bone loss assessment. For group A, a grade of S3 and/or S3+ was achieved at 26.7%, 60% and 73.3% of the sites at time intervals of 2 weeks, 1 month and 3 months, respectively. While in group B, a grade of S3 and/or S3+ was achieved at 33.3%, 86.7% and 53.3% of the sites at time intervals of 2 weeks, 1 month and 3 months, respectively. For both groups, all patients reached a grade of S4 (which is considered to be a 2normal sensation3) after a period of 6 months. The marginal bone loss recorded was in between the mean range of 0.02 to 0.55 mm after 6 months of implant placement with no significant statistical difference between group A and group B. The primary stability of both groups immediately after the procedure ranged between ISQ values of 60-69, whereas 6 months postoperative assessment results ranged between ISQ values of 72-80
530 _aIssued also as CD
653 4 _aIAN
653 4 _aImplant
653 4 _aLateralization
700 0 _aMohamed Atef ,
_eSupervisor
700 0 _aRami Elbialy ,
_eSupervisor
856 _uhttp://172.23.153.220/th.pdf
905 _aAsmaa
_eCataloger
905 _aNazla
_eRevisor
942 _2ddc
_cTH
999 _c76727
_d76727