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1.
J Laryngol Otol ; 137(6): 685-690, 2023 Jun.
Article in English | MEDLINE | ID: mdl-35871793

ABSTRACT

OBJECTIVE: To evaluate the long-term functional outcomes in patients who received primary radiotherapy for tumour-node stage T2N0 glottic carcinoma, stratified for tumour extension. METHODS: A cross-sectional study was performed on patients who were treated with radiotherapy for T2N0 glottic carcinoma. Four questionnaires were used to measure different aspects of functional outcome. In addition, objective evaluation and perceptual analysis were performed. RESULTS: Fourteen patients were included in this study. The median time between the start of radiotherapy and assessment was 42 months (range, 26-143 months). Patients reported high-level functioning, with low symptom scores and good swallowing function, and showed a median dysphonia grade of 1.5. The median Voice Handicap Index-30 score was 17.5. CONCLUSION: Patients with T2N0 glottic carcinoma treated with radiotherapy had good long-term quality of life, with low symptom scores, good swallowing functioning and slightly elevated voice outcome parameters.


Subject(s)
Carcinoma , Dysphonia , Laryngeal Neoplasms , Humans , Quality of Life , Cross-Sectional Studies , Treatment Outcome , Dysphonia/etiology , Laryngeal Neoplasms/radiotherapy , Laryngeal Neoplasms/pathology , Carcinoma/pathology , Glottis/pathology , Radiotherapy/adverse effects
2.
Int J Pediatr Otorhinolaryngol ; 150: 110891, 2021 Nov.
Article in English | MEDLINE | ID: mdl-34425354

ABSTRACT

OBJECTIVE: To evaluate the long-term ipsi- and contralateral hearing of patients with a unilateral enlarged vestibular aqueduct (EVA). STUDY DESIGN: Multicenter retrospective cohort study. SETTING: Three tertiary otology and audiology referral centers. PATIENTS AND DIAGNOSTIC INTERVENTIONS: A total of 34 children with a unilateral enlarged vestibular aqueduct as identified on CT and/or MR imaging were evaluated with pure tone and speech perception audiometry. MEAN OUTCOME MEASURES: Radiologic measurements of the vestibular aqueduct, ipsi- and contralateral hearing loss, ipsi- and contralateral hearing loss progression over time and DNA test results. RESULTS: All patients in this cohort with unilateral EVA presented with hearing loss. Hearing loss was progressive in 38% of the ipsilateral ears. In 29% of the children, hearing loss was also found in the contralateral ear without EVA. In 90%, the contralateral hearing was stable, with a mean follow up of 4.2 years. We found a significant correlation between the severity of the hearing loss and the size of the EVA. A genetic diagnosis associated with EVA and/or SNHL was found in only 7%. CONCLUSION: About a third of the children with unilateral EVA are at risk of developing hearing loss in the contralateral ear. This indicates that at least in some patients with a unilateral EVA, a bilateral pathogenic process underlies the hearing loss, in contrary to what the imaging results suggest. These findings are important for counseling of EVA patients and their parents and have implications for follow up.


Subject(s)
Hearing Loss, Sensorineural , Hearing Loss , Vestibular Aqueduct , Child , Hearing Loss, Sensorineural/diagnostic imaging , Humans , Retrospective Studies , Vestibular Aqueduct/abnormalities , Vestibular Aqueduct/diagnostic imaging
3.
AJNR Am J Neuroradiol ; 41(3): 529-534, 2020 03.
Article in English | MEDLINE | ID: mdl-32029469

ABSTRACT

BACKGROUND AND PURPOSE: Ménière disease is characterized by endolymphatic hydrops, whereas perilymphatic enhancement on MR imaging has been suggested to be of additional value in diagnosing Ménière disease. This study evaluates the presence of endolymphatic hydrops and perilymphatic enhancement in patients with Ménière disease and with other vertigo-associated inner ear pathology. MATERIALS AND METHODS: A 3D-FLAIR sequence 4 hours after intravenous gadolinium injection was performed to visualize the endolymph and perilymph in 220 patients suspected of having Ménière disease. Patients' ears were retrospectively categorized as having Ménière disease (probable or definite) or other vertigo-associated inner ear pathology not attributable to Ménière disease. Endolymphatic hydrops was evaluated using a visual classification system, and perilymphatic enhancement was scored both visually and quantitatively. RESULTS: Endolymphatic hydrops was present in 137 (91.9%) of the definite Ménière disease ears and in 9 (7.0%) of the ears with other vertigo-associated inner ear pathology (P < .001). The combination of endolymphatic hydrops and visually increased perilymphatic enhancement was present in 122 (81.9%) definite Ménière disease ears compared with 4 (3.1%) ears with other vertigo-associated inner ear pathology (P < .001). This combination increases the positive predictive value from 0.94 for endolymphatic hydrops and 0.91 for perilymphatic enhancement to 0.97. The addition of measured perilymphatic enhancement leads to a moderate decrease in sensitivity from 0.92 for endolymphatic hydrops to 0.86. CONCLUSIONS: The combination of perilymphatic enhancement and endolymphatic hydrops in patients suspected of having Ménière disease increases the positive predictive value in the diagnosis of definite Ménière disease.


Subject(s)
Magnetic Resonance Imaging/methods , Meniere Disease/diagnostic imaging , Perilymph/diagnostic imaging , Adult , Aged , Aged, 80 and over , Endolymphatic Hydrops/diagnostic imaging , Female , Gadolinium DTPA , Humans , Male , Middle Aged , Predictive Value of Tests , Retrospective Studies
4.
Eur Arch Otorhinolaryngol ; 273(12): 4225-4240, 2016 Dec.
Article in English | MEDLINE | ID: mdl-27324890

ABSTRACT

To provide an overview of anomalies of the temporal bone in CHARGE syndrome relevant to cochlear implantation (CI), anatomical structures of the temporal bone and the respective genotypes were analysed. In this retrospective study, 42 CTs of the temporal bone of 42 patients with CHARGE syndrome were reviewed in consensus by two head-and-neck radiologists and two otological surgeons. Anatomical structures of the temporal bone were evaluated and correlated with genetic data. Abnormalities that might affect CI surgery were seen, such as a vascular structure, a petrosquamosal sinus (13 %), an underdeveloped mastoid (8 %) and an aberrant course of the facial nerve crossing the round window (9 %) and/or the promontory (18 %). The appearance of the inner ear varied widely: in 77 % of patients all semicircular canals were absent and the cochlea varied from normal to hypoplastic. A stenotic cochlear aperture was observed in 37 %. The middle ear was often affected with a stenotic round (14 %) or oval window (71 %). More anomalies were observed in patients with truncating mutations than with non-truncating mutations. Temporal bone findings in CHARGE syndrome vary widely. Vascular variants, aberrant route of the facial nerve, an underdeveloped mastoid, aplasia of the semicircular canals, and stenotic round window may complicate cochlear implantation.


Subject(s)
CHARGE Syndrome/diagnostic imaging , Cochlear Implantation , DNA Helicases/genetics , DNA-Binding Proteins/genetics , Temporal Bone/abnormalities , Adolescent , Adult , CHARGE Syndrome/complications , Child , Child, Preschool , Cochlea/abnormalities , Cochlea/diagnostic imaging , Cochlear Implantation/methods , Cochlear Implants , Ear, Middle/abnormalities , Ear, Middle/diagnostic imaging , Facial Nerve/abnormalities , Female , Humans , Infant , Infant, Newborn , Male , Mastoid/abnormalities , Mastoid/diagnostic imaging , Middle Aged , Otolaryngology , Radiology , Retrospective Studies , Round Window, Ear/abnormalities , Round Window, Ear/diagnostic imaging , Semicircular Canals/abnormalities , Temporal Bone/diagnostic imaging , Temporal Bone/pathology , Tomography, X-Ray Computed
5.
Clin Otolaryngol ; 41(5): 571-8, 2016 Oct.
Article in English | MEDLINE | ID: mdl-26452334

ABSTRACT

OBJECTIVES: The aim of this study was to assess the reproducibility of different measurement methods and define the most workable technique for measuring head and neck paragangliomas, to determine the best method for evaluating tumour growth. The evaluation of tumour growth is vital for a 'wait-and-scan' policy, a management strategy that became increasingly important. STUDY DESIGN: Method comparison study. SETTING AND PARTICIPANTS: Thirty tumours, including carotid body, vagal body, jugulotympanic tumours and conglomerates of multiple tumours, were measured in duplicate, using linear dimensions, manual area tracing and an automated segmentation method. MAIN OUTCOME MEASURES: Reproducibility was assessed using the Bland-Altman method. RESULTS: The smallest detectable difference using the linear dimension method was 11% for carotid body and 27% for vagal body tumours, compared with 17% and 20% for the manual area tracing method. Due to the irregular shape of paragangliomas in the temporal bone and conglomerates, the manual area tracing method showed better results in these tumours (26% and 8% versus 54% and 47%). The linear dimension method was significantly faster (median 4.27 versus 18.46 minutes, P < 0.001). The automatic segmentation method yielded smallest detectable differences between 39% and 75%, and although fast (2.19 ± 1.49 minutes), it failed technically. CONCLUSIONS: Due to a relatively good reproducibility, fast and easy application, we found the linear dimension method to be the most pragmatic approach for evaluation of growth of carotid and vagal body paragangliomas. For jugulotympanic tumours, the preferred method is manual area tracing. However, volumetric changes of these tumours may be of less clinical importance than changes in relation to surrounding anatomical structures.


Subject(s)
Head and Neck Neoplasms/pathology , Paraganglioma/pathology , Female , Head and Neck Neoplasms/diagnostic imaging , Humans , Image Interpretation, Computer-Assisted , Magnetic Resonance Angiography , Male , Paraganglioma/diagnostic imaging , Reproducibility of Results , Tumor Burden
6.
Eur J Cancer ; 52: 77-84, 2016 Jan.
Article in English | MEDLINE | ID: mdl-26655558

ABSTRACT

PURPOSE: To study the feasibility of induction chemotherapy added to concomitant cisplatin-based chemoradiotherapy (CRT) in patients with locally advanced head and neck cancer (LAHNC). PATIENTS AND METHODS: LAHNC patients were treated with 4 courses of docetaxel/cisplatin/5-fluorouracil (TPF) followed by randomization to either cisplatin 100 mg/m(2) with conventional radiotherapy (cis100 + RT) or cisplatin 40 mg/m(2) weekly with accelerated radiotherapy (cis40 + ART). Primary endpoint was feasibility, defined as receiving ≥ 90% of the scheduled total radiation dose. Based on power analysis 70 patients were needed. RESULTS: 65 patients were enrolled. The data safety monitoring board advised to prematurely terminate the study, because only 22% and 41% (32% in total) of the patients treated with cis100 + RT (n = 27) and cis40 + ART (n = 29) could receive the planned dose cisplatin during CRT, respectively, even though the primary endpoint was reached. Most common grade 3-4 toxicity was febrile neutropenia (18%) during TPF and dehydration (26% vs 14%), dysphagia (26% vs 24%) and mucositis (22% vs 57%) during cis100 + RT and cis40 + ART, respectively. For the patients treated with cis100 + RT and cis40 + ART, two years progression free survival and overall survival were 70% and 78% versus 72% and 79%, respectively. CONCLUSION: After TPF induction chemotherapy, cisplatin-containing CRT is not feasible in LAHNC patients, because the total planned cisplatin dose could only be administered in 32% of the patients due to toxicity. However, all but 2 patients received more than 90% of the planned radiotherapy. Clinical Trials Information: NCT00774319.


Subject(s)
Antineoplastic Combined Chemotherapy Protocols/therapeutic use , Chemoradiotherapy/methods , Cisplatin/therapeutic use , Fluorouracil/therapeutic use , Head and Neck Neoplasms/therapy , Taxoids/therapeutic use , Adult , Aged , Antineoplastic Combined Chemotherapy Protocols/adverse effects , Chemoradiotherapy/adverse effects , Chemoradiotherapy/mortality , Cisplatin/adverse effects , Disease Progression , Disease-Free Survival , Docetaxel , Early Termination of Clinical Trials , Feasibility Studies , Female , Fluorouracil/adverse effects , Head and Neck Neoplasms/mortality , Head and Neck Neoplasms/pathology , Humans , Induction Chemotherapy , Kaplan-Meier Estimate , Male , Middle Aged , Neoplasm Metastasis , Neoplasm Recurrence, Local , Netherlands , Radiotherapy Dosage , Risk Factors , Taxoids/adverse effects , Time Factors , Treatment Outcome
7.
AJNR Am J Neuroradiol ; 36(2): 378-83, 2015 Feb.
Article in English | MEDLINE | ID: mdl-25147195

ABSTRACT

BACKGROUND AND PURPOSE: In many centers, MR imaging of the inner ear and auditory pathway performed on 1.5T or 3T systems is part of the preoperative work-up of cochlear implants. We investigated the applicability of clinical inner ear MR imaging at 7T and compared the visibility of inner ear structures and nerves within the internal auditory canal with images acquired at 3T. MATERIALS AND METHODS: Thirteen patients with sensorineural hearing loss eligible for cochlear implantation underwent examinations on 3T and 7T scanners. Two experienced head and neck radiologists evaluated the 52 inner ear datasets. Twenty-four anatomic structures of the inner ear and 1 overall score for image quality were assessed by using a 4-point grading scale for the degree of visibility. RESULTS: The visibility of 11 of the 24 anatomic structures was rated higher on the 7T images. There was no significant difference in the visibility of 13 anatomic structures and the overall quality rating. A higher incidence of artifacts was observed in the 7T images. CONCLUSIONS: The gain in SNR at 7T yielded a more detailed visualization of many anatomic structures, especially delicate ones, despite the challenges accompanying MR imaging at a high magnetic field.


Subject(s)
Ear, Inner/anatomy & histology , Hearing Loss, Sensorineural/pathology , Adult , Aged , Artifacts , Cochlear Implants , Ear, Inner/innervation , Female , Humans , Image Processing, Computer-Assisted , Magnetic Resonance Imaging/methods , Male , Middle Aged , Prospective Studies
8.
AJNR Am J Neuroradiol ; 35(12): E11, 2014 Dec.
Article in English | MEDLINE | ID: mdl-25324498
9.
Int J Pediatr Otorhinolaryngol ; 77(7): 1152-7, 2013 Jul.
Article in English | MEDLINE | ID: mdl-23726953

ABSTRACT

OBJECTIVES: To report the hearing impairment in a new autosomal recessive metabolic disorder due to a mutation in the ANKH gene and to report the outcomes of exploratory tympanotomy. STUDY DESIGN: Retrospective chart study. SETTING: Tertiary referral center. PATIENTS: One large consanguineous family was examined. Three patients underwent exploratory tympanotomy. INTERVENTION: Exploratory tympanotomies in three patients. MAIN OUTCOME MEASURES: Medical and otological histories; postoperative hearing outcomes. RESULTS: In the patients who received tympanotomies, a postoperative hearing gain of between 5 and 20 dB was noted, with a residual air-bone gap of between 6 and 35 dB (follow-up between 4 and 67 months). The sensorineural component of the hearing impairment varies greatly, between 4 and 23 dB, and this factor might also affect the final hearing outcome. CONCLUSIONS: Exploratory tympanotomy might improve the hearing outcome in patients with this syndrome and therefore surgery has a limited audiometric benefit in general. Based on anatomical findings, a congenital origin for the ossicular chain anomaly seems likely. It remains unclear whether the sensorineural component of the hearing impairment is progressive and this should be investigated further.


Subject(s)
Consanguinity , Hearing Loss/genetics , Hearing Loss/surgery , Middle Ear Ventilation/methods , Mutation , Phosphate Transport Proteins/genetics , Adolescent , Adult , Bone Diseases, Developmental/diagnostic imaging , Bone Diseases, Developmental/genetics , Child , Craniofacial Abnormalities/diagnostic imaging , Craniofacial Abnormalities/genetics , Female , Humans , Hyperostosis/diagnostic imaging , Hyperostosis/genetics , Hypertelorism/diagnostic imaging , Hypertelorism/genetics , Male , Middle Aged , Pedigree , Radiography , Retrospective Studies , Tertiary Care Centers , Treatment Outcome , Turkey , Young Adult
10.
JBR-BTR ; 95(4): 226-8, 2012.
Article in English | MEDLINE | ID: mdl-23019987

ABSTRACT

A rare case of aseptic thrombosis of the left vein of Labbé in a young woman is reported. Cerebral venous thrombosis was suggested by computed tomography and confirmed after intravenous administration of contrast by computed tomography venography. The combination of the clinical setting with the findings on the non-enhanced CT may favour the diagnosis of vein of Labbé thrombosis. The diagnosis can be confirmed on computed tomography venography.


Subject(s)
Contrast Media , Intracranial Thrombosis/diagnostic imaging , Radiographic Image Enhancement/methods , Adult , Anticoagulants/therapeutic use , Cerebral Angiography/methods , Cerebral Veins/diagnostic imaging , Cranial Sinuses/diagnostic imaging , Diagnosis, Differential , Female , Follow-Up Studies , Humans , Imaging, Three-Dimensional , Intracranial Thrombosis/drug therapy , Sinus Thrombosis, Intracranial/diagnostic imaging , Sinus Thrombosis, Intracranial/drug therapy , Tomography, X-Ray Computed
11.
Neuromuscul Disord ; 20(4): 251-4, 2010 Apr.
Article in English | MEDLINE | ID: mdl-20153965

ABSTRACT

Theoretically, 13% of patients with Duchenne muscular dystrophy may benefit from antisense-mediated skipping of exon 51 to restore the reading frame, which results in the production of a shortened dystrophin protein. We give a detailed description with longitudinal follow up of three patients with Becker muscular dystrophy with in-frame deletions in the DMD gene encompassing exon 51. Their internally deleted, but essentially functional, dystrophins are identical to those that are expected as end products in DMD patients treated with the exon 51 skipping therapy. The mild phenotype encourages further development of exon 51 skipping therapy.


Subject(s)
Dystrophin/genetics , Exons/genetics , Genetic Predisposition to Disease/genetics , Genetic Therapy/methods , Muscular Dystrophy, Duchenne/genetics , Mutation/genetics , Adolescent , Aged , Child , Child, Preschool , DNA Mutational Analysis , Dystrophin/chemistry , Dystrophin/metabolism , Genetic Testing , Humans , Male , Middle Aged , Molecular Weight , Muscular Dystrophy, Duchenne/metabolism , Muscular Dystrophy, Duchenne/physiopathology , Oligoribonucleotides, Antisense/pharmacology , Oligoribonucleotides, Antisense/therapeutic use , Open Reading Frames/genetics , Phenotype , Severity of Illness Index
12.
J Neurol ; 256(12): 2009-13, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19603245

ABSTRACT

Dysphagia is an important yet inconsistently recognized symptom of inclusion body myositis (IBM). It can be disabling and potentially life-threatening. We studied the prevalence and symptom-sign correlation of dysphagia. Fifty-seven IBM patients were interviewed using a standard questionnaire for dysphagia and 43 of these underwent swallowing videofluoroscopy (VFS). Symptoms of dysphagia were present in 37 of 57 patients (65%). Nevertheless, only 17 of these patients (46%) had previously and spontaneously complained about swallowing to their physicians. Both symptoms of impaired propulsion (IP) (59%) and aspiration-related symptoms (52%) were frequently mentioned. Swallowing abnormalities on VFS were present in 34 of 43 patients (79%) with IP of the bolus in 77% of this group. The reported feeling of IP was confirmed by VFS in 92% of these patients. Dysphagia in IBM is common but underreported by the vast majority of patients if not specifically asked for. In practice, two questions reliably predict the presence of IP on VFS: 'Does food get stuck in your throat' and 'Do you have to swallow repeatedly in order to get rid of food'. These questions are an appropriate means in selecting IBM patients for further investigation through VFS and eventual treatment.


Subject(s)
Deglutition Disorders/diagnosis , Disability Evaluation , Myositis, Inclusion Body/diagnosis , Aged , Cohort Studies , Deglutition Disorders/etiology , Deglutition Disorders/physiopathology , Diagnosis, Differential , Female , Humans , Male , Middle Aged , Myositis, Inclusion Body/complications , Myositis, Inclusion Body/physiopathology , Surveys and Questionnaires
13.
AJNR Am J Neuroradiol ; 29(7): 1382-8, 2008 Aug.
Article in English | MEDLINE | ID: mdl-18483188

ABSTRACT

BACKGROUND AND PURPOSE: Postoperative imaging of cochlear implants (CIs) needs to provide detailed information on localization of the electrode array. We evaluated visualization of a HiFocus1J array and accuracy of measurements of electrode positions for acquisitions with 64-section CT scanners of 4 major CT systems (Toshiba Aquilion-64, Philips Brilliance-64, GE LightSpeed-64, and Siemens Sensation-64). MATERIALS AND METHODS: An implanted human cadaver temporal bone, a polymethylmethacrylate (PMMA) phantom containing a CI, and a point spread function (PSF) phantom were scanned. In the human cadaver temporal bone, the visibility of cochlear structures and electrode array were assessed by using a visual analog scale (VAS). Statistical analysis was performed with a paired 2-tailed Student t test with significant level set to .008 after Bonferroni correction. Distinction of individual electrode contacts was quantitatively evaluated. Quantitative assessment of electrode contact positions was achieved with the PMMA phantom by measurement of the displacement. In addition, PSF was measured to evaluate spatial resolution performance of the CT scanners. RESULTS: VAS scores were significantly lower for Brilliance-64 and LightSpeed-64 compared with Aquilion-64 and Sensation-64. Displacement of electrode contacts ranged from 0.05 to 0.14 mm on Aquilion-64, 0.07 to 0.16 mm on Brilliance-64, 0.07 to 0.61 mm on LightSpeed-64, and 0.03 to 0.13 mm on Sensation-64. PSF measurements show an in-plane and longitudinal resolution varying from 0.48 to 0.68 mm and 0.70 to 0.98 mm, respectively, over the 4 scanners. CONCLUSION: According to PSF results, electrode contacts of the studied CI can be visualized separately on all of the studied scanners unless curvature causes intercontact spacing narrowing. Assessment of visibility of CI and electrode contact positions, however, varies between scanners.


Subject(s)
Cochlear Implants , Image Processing, Computer-Assisted , Phantoms, Imaging , Postoperative Complications/diagnostic imaging , Tomography, Spiral Computed , Cadaver , Cochlea/diagnostic imaging , Electrodes, Implanted , Equipment Failure Analysis , Humans , Pain Measurement , Prosthesis Fitting , Sensitivity and Specificity , Temporal Bone/diagnostic imaging
14.
Ear Hear ; 26(6): 577-92, 2005 Dec.
Article in English | MEDLINE | ID: mdl-16377994

ABSTRACT

OBJECTIVE: To study the clinical outcomes concerning speech perception of the Clarion CII HiFocus 1 with and without a positioner and link those outcomes with the functional implications of perimodiolar electrode designs, focusing on intrascalar position, insertion depth, stimulation levels, and intracochlear conductivity pathways. DESIGN: The speech perception scores of 25 consecutive patients with the Clarion CII HiFocus 1 implanted with a positioner and 20 patients without a positioner were prospectively determined. Improved multislice CT imaging was used to study the position of the individual electrode contacts relative to the modiolus and their insertion depth. Furthermore, stimulation thresholds, maximum comfort levels, and dynamic ranges were obtained. Finally, these data were associated with intracochlear conductivity paths as calculated from the potential distribution acquired with electrical field imaging. RESULTS: Implantation with a Clarion Hifocus 1 with positioner showed significantly higher speech perception levels at 3 mos, 6 mos, and 1 yr (p < 0.05) after implantation. Basally, the positioner brought the electrode contacts significantly closer to the modiolus, whereas apically no difference in distance toward the modiolus was present. Moreover, the patients with the electrode array in a perimodiolar position showed deeper insertions. The T-levels and dynamic range were not significantly different between the positioner and nonpositioner patients. Furthermore, the intracochlear conductivity paths showed no significant differences. However, a basal current drain is present for the shallowly inserted nonpositioner patients. CONCLUSIONS: A basally perimodiolar electrode design benefits speech perception. The combination of decreased distance to the modiolus, improved insertion depth, and insulating properties of the electrode array have functional implications for the clinical outcomes of the perimodiolar electrode design. Further research is needed to elucidate their individual contributions to those outcomes.


Subject(s)
Cochlea/diagnostic imaging , Cochlear Implantation/methods , Cochlear Implants , Hearing Loss/rehabilitation , Hearing Loss/surgery , Speech Perception/physiology , Adolescent , Adult , Aged , Audiometry, Pure-Tone , Auditory Threshold , Cochlea/surgery , Cochlear Implantation/standards , Cochlear Implants/standards , Electric Impedance , Female , Humans , Male , Middle Aged , Prospective Studies , Prosthesis Design , Regression Analysis , Tomography, X-Ray Computed
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