Pedersen, Peter Heide; Xavier, Fred; Vergari, Claudio; Skalli, Wafa; Eiskjær, Søren Peter; Vialle, Raphael
In: Spine Deform, vol. 5, no. 6, pp. 444, 2017, ISSN: 2212-1358.
@article{pmid31997201,
title = {Paper #9: Nano-Dose Protocol for 3D Reconstruction of the Spine in Early Onset Scoliosis: Preliminary Results of a Phantom Based and Clinically Validated Study using Stereo-Radiography},
author = {Peter Heide Pedersen and Fred Xavier and Claudio Vergari and Wafa Skalli and Søren Peter Eiskjær and Raphael Vialle},
doi = {10.1016/j.jspd.2017.09.012},
issn = {2212-1358},
year = {2017},
date = {2017-11-01},
journal = {Spine Deform},
volume = {5},
number = {6},
pages = {444},
abstract = {This is a prospective study validating the reproducibility of 3D reconstruction of the spine using a new reduced micro-dose protocol. A pilot group of children with scoliosis underwent micro-dose- and additional reduced micro-dose (nano-dose) full-spine imaging. 3D reconstructions of both protocols were evaluated.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Lamerain, Mayalen; Bachy, Manon; Dubory, Arnaud; Kabbaj, Reda; Scemama, Caroline; Vialle, Raphaël
In: Clin Spine Surg, vol. 30, no. 7, pp. E857–E863, 2017, ISSN: 2380-0194.
@article{pmid27404854,
title = {All-Pedicle Screw Fixation With 6-mm-Diameter Cobalt-Chromium Rods Provides Optimized Sagittal Correction of Adolescent Idiopathic Scoliosis},
author = {Mayalen Lamerain and Manon Bachy and Arnaud Dubory and Reda Kabbaj and Caroline Scemama and Raphaël Vialle},
doi = {10.1097/BSD.0000000000000413},
issn = {2380-0194},
year = {2017},
date = {2017-08-01},
journal = {Clin Spine Surg},
volume = {30},
number = {7},
pages = {E857--E863},
abstract = {PURPOSE: Recently introduced cobalt-chromium (CoCr) rods that rely solely on pedicle screws produce very good results in correcting scoliotic curves. All-pedicle screws constructs are also suspected of decreasing thoracic kyphosis. The current study was designed to evaluate sagittal correction in adolescent idiopathic scoliosis patients, using 6-mm CoCr rods and all-screw constructs.nnMATERIALS AND METHODS: A total of 61 patients treated by posterior spinal fusion and instrumentation, using all-pedicle screw constructs were included. The mean age at surgery was 15.4 years (range, 12-18 y). Forty-five patients (group A) were diagnosed with decreased thoracic kyphosis, and 16 patients (group B) had normal (35-50 degrees) thoracic kyphosis.nnRESULTS: The preoperative main Cobb angle was 62.93±19.38 degrees in group A and 73.45±22.13 degrees in group B. In group A, the postoperative main Cobb angle was 23.33±12.71 degrees. In group B, the postoperative main Cobb angle was 27.20±10.04 degrees. The T4-T12 thoracic kyphosis improved postoperatively from 18.15±10.29 to 28.18±8.35 degrees in group A. In group B, the postoperative T4-T12 thoracic kyphosis was 40.34±3.13 degrees. Statistical analysis showed a significant improvement between preoperative and postoperative values of T4-T12 thoracic kyphosis in group A. In group B, the differences in T4-T12 thoracic kyphosis values were not statistically significant.nnCONCLUSIONS: Our result demonstrates a significant improvement of T4-T12 thoracic kyphosis in the hypokyphotic group of patients and confirms that CoCr rods can produce sagittal corrections in hypokyphotic adolescent idiopathic scoliosis patients. Our results confirm the benefit of combining all-pedicle screw constructs with a posterolateral translational in situ bending procedure to correct hypokyphosis directly.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Fetoscopic patch coverage of experimental myelomenigocele using a two-port access in fetal sheep
Guilbaud, Lucie; Roux, Nathalie; Friszer, Stéphanie; Garabedian, Charles; Dhombres, Ferdinand; Bessières, Bettina; Fallet-Bianco, Catherine; Rocco, Federico Di; Zerah, Michel; Jouannic, Jean-Marie
In: Childs Nerv Syst, vol. 33, no. 7, pp. 1177–1184, 2017, ISSN: 1433-0350.
@article{pmid28550526,
title = {Fetoscopic patch coverage of experimental myelomenigocele using a two-port access in fetal sheep},
author = {Lucie Guilbaud and Nathalie Roux and Stéphanie Friszer and Charles Garabedian and Ferdinand Dhombres and Bettina Bessières and Catherine Fallet-Bianco and Federico Di Rocco and Michel Zerah and Jean-Marie Jouannic},
doi = {10.1007/s00381-017-3461-7},
issn = {1433-0350},
year = {2017},
date = {2017-07-01},
journal = {Childs Nerv Syst},
volume = {33},
number = {7},
pages = {1177--1184},
abstract = {PURPOSE: This study aims to assess the feasibility and the effectiveness of a fetoscopic myelomeningocele (MMC) coverage using a sealed inert patch through a two-port access, in the sheep model.nnMETHODS: Forty-four fetuses underwent surgical creation of a MMC defect at day 75 and were divided into four groups according to the MMC repair technique, performed at day 90. Group 1 remained untreated. Group 2 had an open surgery using suture of the defect. Groups 3 and 4 underwent defect coverage using a Gore®-polytetrafluoroethylene patch secured with surgical adhesive (Bioglue®), with an open approach (group 3) and a fetoscopic one (group 4). Lambs were killed at term, and histological examinations were performed.nnRESULTS: Fetoscopic patch coverage was achieved in all the lambs of group 4. All the fetuses of group 2 had a complete closure of the defect whereas only 38% in group 3 and 14% in group 4. Fetal loss rate seems to be lower in group 4 than in groups 2 and 3.nnCONCLUSION: Fetoscopic coverage of MMC defect can be performed using a sealed patch through a two-port access, but the patch and glue correction may not be the ideal technique to repair fetal MMC.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Maurice, P; Dhombres, F; Blondiaux, E; Friszer, S; Guilbaud, L; Lelong, N; Khoshnood, B; Charlet, J; Perrot, N; Jauniaux, E; Jurkovic, D; Jouannic, J-M
In: J Gynecol Obstet Hum Reprod, vol. 46, no. 5, pp. 423–429, 2017, ISSN: 2468-7847.
@article{pmid28934086,
title = {Towards ontology-based decision support systems for complex ultrasound diagnosis in obstetrics and gynecology},
author = {P Maurice and F Dhombres and E Blondiaux and S Friszer and L Guilbaud and N Lelong and B Khoshnood and J Charlet and N Perrot and E Jauniaux and D Jurkovic and J-M Jouannic},
doi = {10.1016/j.jogoh.2017.03.004},
issn = {2468-7847},
year = {2017},
date = {2017-05-01},
journal = {J Gynecol Obstet Hum Reprod},
volume = {46},
number = {5},
pages = {423--429},
abstract = {INTRODUCTION: We have developed a new knowledge base intelligent system for obstetrics and gynecology ultrasound imaging, based on an ontology and a reference image collection. This study evaluates the new system to support accurate annotations of ultrasound images. We have used the early ultrasound diagnosis of ectopic pregnancies as a model clinical issue.nnMATERIAL AND METHODS: The ectopic pregnancy ontology was derived from medical texts (4260 ultrasound reports of ectopic pregnancy from a specialist center in the UK and 2795 Pubmed abstracts indexed with the MeSH term "Pregnancy, Ectopic") and the reference image collection was built on a selection from 106 publications. We conducted a retrospective analysis of the signs in 35 scans of ectopic pregnancy by six observers using the new system.nnRESULTS: The resulting ectopic pregnancy ontology consisted of 1395 terms, and 80 images were collected for the reference collection. The observers used the knowledge base intelligent system to provide a total of 1486 sign annotations. The precision, recall and F-measure for the annotations were 0.83, 0.62 and 0.71, respectively. The global proportion of agreement was 40.35% 95% CI [38.64-42.05].nnDISCUSSION: The ontology-based intelligent system provides accurate annotations of ultrasound images and suggests that it may benefit non-expert operators. The precision rate is appropriate for accurate input of a computer-based clinical decision support and could be used to support medical imaging diagnosis of complex conditions in obstetrics and gynecology.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Rouissi, Jihane; Arvieu, Robin; Dubory, Arnaud; Vergari, Claudio; Bachy, Manon; Vialle, Raphaël
In: Childs Nerv Syst, vol. 33, no. 2, pp. 337–341, 2017, ISSN: 1433-0350.
@article{pmid28028597,
title = {Intra and inter-observer reliability of determining degree of pelvic obliquity in neuromuscular scoliosis using the EOS-CHAIR® protocol},
author = {Jihane Rouissi and Robin Arvieu and Arnaud Dubory and Claudio Vergari and Manon Bachy and Raphaël Vialle},
doi = {10.1007/s00381-016-3326-5},
issn = {1433-0350},
year = {2017},
date = {2017-02-01},
journal = {Childs Nerv Syst},
volume = {33},
number = {2},
pages = {337--341},
abstract = {PURPOSE: Scoliosis with pelvic obliquity (PO) could be investigated with the EOS-CHAIR protocol as the most common deformity especially in patients with trunk hypotonia and quadriplegia. However, the intra-observer and inter-observer reliability of various angles assessing PO was not investigated with this new imaging protocol.nnMETHODS: A retrospective cohort of 36 EOS frontal full-spine acquisitions made in sitting position was used. The sacroiliac pelvic obliquity angle, iliac crest pelvic obliquity angle, and ischiatic pelvic obliquity angle were assessed in an intra-observer and inter-observer study.nnRESULTS: The use of the EOS-CHAIR protocol was implemented satisfactory with a high acceptance rate by all caregivers and patients and their families. Intra-observer and inter-observer reliability was excellent for the three tested angular measurements.nnDISCUSSION: As for idiopathic scoliosis, we postulate the EOS system as being superior to standard radiographs to assess 3D spinal deformities in neuromuscular conditions. The EOS-CHAIR protocol improves preoperative comprehension of the lumbosacral junction anatomy in patients with poor standing or sitting postures. Our results show a very high reliability of three different angular measurements of the frontal pelvic obliquity in sitting position. Then it is possible to use one of these three angles as well as the others to assess frontal pelvic obliquity in neuromuscular patients. This frontal pelvic obliquity protocol in sitting position with the EOS-CHAIR is a validated measurement technique that needs to be used now to measure PO as a critical parameter of the global trunk balance in neuromuscular patients.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Limited Dorsal Myeloschisis: A Diagnostic Pitfall in the Prenatal Ultrasound of Fetal Dysraphism
Friszer, Stéphanie; Dhombres, Ferdinand; Morel, Baptiste; Zerah, Michel; Jouannic, Jean-Marie; Garel, Catherine
In: Fetal Diagn Ther, vol. 41, no. 2, pp. 136–144, 2017, ISSN: 1421-9964.
@article{pmid27160821,
title = {Limited Dorsal Myeloschisis: A Diagnostic Pitfall in the Prenatal Ultrasound of Fetal Dysraphism},
author = {Stéphanie Friszer and Ferdinand Dhombres and Baptiste Morel and Michel Zerah and Jean-Marie Jouannic and Catherine Garel},
doi = {10.1159/000445995},
issn = {1421-9964},
year = {2017},
date = {2017-01-01},
journal = {Fetal Diagn Ther},
volume = {41},
number = {2},
pages = {136--144},
abstract = {OBJECTIVE: To determine the ultrasonographic characteristics of limited dorsal myeloschisis (LDM) at prenatal ultrasound (US) and to highlight the main features that may help differentiate LDM and myelomeningocele (MMC).nnMETHODS: In a tertiary reference center in fetal medicine, we prospectively collected the medical data and ultrasonographic characteristics of all patients referred for in utero prenatal repair of MMC between November 1, 2013 and April 30, 2015.nnRESULTS: Among the 29 patients assessed, the diagnosis of MMC was revised in 7 cases. In 6 cases, the diagnosis of LDM was established. On US scan, LDM was characterized by a spinal saccular lesion with a thick peripheral lining in continuity with the adjacent skin. Within the saccular lesion, a thick hyperechoic well-delineated structure was present in continuity with the spinal cord. Cerebral structures were normal except for 2 cases showing a cisterna magna slightly decreased in size. In the remaining 22 cases MMC was confirmed, with cerebral anomalies present in 21/22 cases (95.5%).nnCONCLUSION: LDM is a form of closed dysraphism accessible to prenatal diagnosis by US that may mimic MMC. Considering the major difference in prognosis between these two entities, physicians should be aware of the existence and ultrasonographic characteristics of LDM.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
Prenatal Sacral Anomalies Leading to the Detection of Associated Spinal Cord Malformations
Morel, Baptiste; Friszer, Stéphanie; Jouannic, Jean-Marie; Pointe, Hubert Ducou Le; Blondiaux, Eléonore; Garel, Catherine
In: Fetal Diagn Ther, vol. 42, no. 4, pp. 294–301, 2017, ISSN: 1421-9964.
@article{pmid28463829,
title = {Prenatal Sacral Anomalies Leading to the Detection of Associated Spinal Cord Malformations},
author = {Baptiste Morel and Stéphanie Friszer and Jean-Marie Jouannic and Hubert Ducou Le Pointe and Eléonore Blondiaux and Catherine Garel},
doi = {10.1159/000457795},
issn = {1421-9964},
year = {2017},
date = {2017-01-01},
journal = {Fetal Diagn Ther},
volume = {42},
number = {4},
pages = {294--301},
abstract = {INTRODUCTION: Systematic analysis of the spine is recommended as part of the basic sonographic examination. The aim of our study is to assess the proportion of spinal cord anomalies diagnosed following detection of a sacral anomaly.nnMATERIAL AND METHODS: We analyzed retrospectively collected data in a prenatal tertiary center during a 9-year period. Patients were referred for second-line ultrasound in the context of diabetes mellitus or following detection of pelvic or lower spine anomalies. We included all cases of sacral anomalies with available postnatal or postmortem outcomes (imaging and/or pathologic data) and excluded all cases of open dysraphism (myelomeningocele).nnRESULTS: Nineteen patients were included. The mean gestational age was 28 weeks (21-39). Sacral anomalies included 2 cases of complete agenesis, 12 cases of partial agenesis, 4 segmentation anomalies, and 1 case of abnormal angulation of the sacral spine. Fourteen associated spinal cord malformations included 8 tethered spinal cords, 5 truncated spinal cords, and 1 lipoma of the filum terminale. All anomalies were confirmed by postnatal or postmortem examinations.nnCONCLUSIONS: Sacral anomalies detected during basic sonographic examination represent an important warning sign for associated spinal cord anomalies, with possible poor neonatal outcome.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
[Ultrasound screening for birth defects: A medico-economic review]
Ferrier, C; Dhombres, F; Guilbaud, L; Durand-Zaleski, I; Jouannic, J-M
In: Gynecol Obstet Fertil Senol, vol. 45, no. 7-8, pp. 408–415, 2017, ISSN: 2468-7189.
@article{pmid28720225,
title = {[Ultrasound screening for birth defects: A medico-economic review]},
author = {C Ferrier and F Dhombres and L Guilbaud and I Durand-Zaleski and J-M Jouannic},
doi = {10.1016/j.gofs.2017.06.007},
issn = {2468-7189},
year = {2017},
date = {2017-01-01},
journal = {Gynecol Obstet Fertil Senol},
volume = {45},
number = {7-8},
pages = {408--415},
abstract = {OBJECTIVES: The systematic use of ultrasound during pregnancy aims at birth defect detection. Our objective was to assess the economic efficiency of prenatal ultrasound screening for fetal malformations.nnMETHODS: We carried out a literature review on Medline via PubMed between 1985 and 2015, from the economic perspective of the prenatal ultrasound screening for fetal malformations.nnRESULTS: The literature on this subject was sparse and we selected only twelve articles presenting relevant economic data, of which only eight were proper medico-economic studies. We found arguments for the economic effectiveness of ultrasound screening for fetal malformation detection, which is largely linked to the terminations of pregnancies and to the cost of the handicaps "avoided". However, none of the reviewed articles could reach medico-economic conclusions. Additionally, we highlighted various elements making economic analyses more complex in this field: the choice of the method, the uncertainty around two essential parameters (the efficiency of ultrasound and the costs of procedures) and the difficulties to compare or to generalize results. We also noticed important methodological heterogeneity among the studies and the absence of French study.nnCONCLUSIONS: Previously published data are insufficient to assess the economic efficiency of prenatal ultrasound screening for fetal malformations.},
keywords = {},
pubstate = {published},
tppubtype = {article}
}
[No title]
0000.
@proceedings{pmid38024482,
title = {[No title]},
keywords = {},
pubstate = {published},
tppubtype = {proceedings}
}
