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Artificial cervical disc replacement versus anterior cervical discectomy and fusion in the management of single level cervical disc prolapse : Randomized control single blinded study / Hesham Mohammed Edwal ; Supervised Mohammed Ahmed Sawan , Mohammed Alaaeldein Thabet , Mohamme Adel Elmallwany

By: Contributor(s): Material type: TextTextLanguage: English Publication details: Cairo : Hesham Mohammed Edwal , 2017Description: 103 P. : charts , facsimiles ; 25cmOther title:
  • دراسة مقارنـه بين التثبيت الاستاتيكي باقفاص كربونيه والتثبيت الديناميكي باستخدام غضروف صناعي في العلاج الجراحي لأمراض أنزلاق الغضروف العنقي أحادي المستوى [Added title page title]
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Dissertation note: Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Neurosurgery Summary: Objective: This study details analysis of the indications, safety, efficacy and complications of artificial cervical disc for replacement of cervical disc in cases cervical disc diseases compared to PEEK cage insertion. Methods: A prospective study conducted on 30 patients with single level cervical disc diseases like herniated or degenerative lesions treated with fixed and dynamic prosthesis, confirmed by clinical and radiological data,. Results: Average age of presentation was 37.7 years for both groups, female ratio for the fixed group was 1.5:1, and 1:1.08 for the dynamic group, with age ranged between 18 and 50 years for both studies. The average duration of symptoms was 51.4 weeks.The average follow up period in our study was 6 months, 21 cases had left sided radiculopathy, 10 cases had right sided affection. The most common presenting symptom after brachialgia (100%) was neck pain, most common sign was sensory changes. Most common operated level was C5-6 for both groups. The average follow up period in our study was 12 months with no recurrence, instability or progressive kyphosis Conclusion:artificial cervical disc is the alternative to cage fusion and total disc prosthesis with a wider range of indications. offers stable, artificial cervical disc controlled (adequate) motion to already significantly degenerated motion segments. In addition the implant is axial compliant offering capabilities to avoid overloading and accelerated degeneration of the adjacent segments above and below the treated segment
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Thesis Thesis قاعة الرسائل الجامعية - الدور الاول المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.20.M.Sc.2017.He.A (Browse shelf(Opens below)) Not for loan 01010110074560000
CD - Rom CD - Rom مخـــزن الرســائل الجـــامعية - البدروم المكتبة المركزبة الجديدة - جامعة القاهرة Cai01.11.20.M.Sc.2017.He.A (Browse shelf(Opens below)) 74560.CD Not for loan 01020110074560000

Thesis (M.Sc.) - Cairo University - Faculty of Medicine - Department of Neurosurgery

Objective: This study details analysis of the indications, safety, efficacy and complications of artificial cervical disc for replacement of cervical disc in cases cervical disc diseases compared to PEEK cage insertion. Methods: A prospective study conducted on 30 patients with single level cervical disc diseases like herniated or degenerative lesions treated with fixed and dynamic prosthesis, confirmed by clinical and radiological data,. Results: Average age of presentation was 37.7 years for both groups, female ratio for the fixed group was 1.5:1, and 1:1.08 for the dynamic group, with age ranged between 18 and 50 years for both studies. The average duration of symptoms was 51.4 weeks.The average follow up period in our study was 6 months, 21 cases had left sided radiculopathy, 10 cases had right sided affection. The most common presenting symptom after brachialgia (100%) was neck pain, most common sign was sensory changes. Most common operated level was C5-6 for both groups. The average follow up period in our study was 12 months with no recurrence, instability or progressive kyphosis Conclusion:artificial cervical disc is the alternative to cage fusion and total disc prosthesis with a wider range of indications. offers stable, artificial cervical disc controlled (adequate) motion to already significantly degenerated motion segments. In addition the implant is axial compliant offering capabilities to avoid overloading and accelerated degeneration of the adjacent segments above and below the treated segment

Issued also as CD

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