The Experts below are selected from a list of 288 Experts worldwide ranked by ideXlab platform
Noriyuki Azuma - One of the best experts on this subject based on the ideXlab platform.
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Exudative retinal detachment following cataract surgery in Hallermann-Streiff Syndrome
Graefe's Archive for Clinical and Experimental Ophthalmology, 2008Co-Authors: Sachiko Nishina, Yumi Suzuki, Noriyuki AzumaAbstract:Purpose To report two cases of Hallermann-Streiff Syndrome with exudative retinal detachment after cataract surgery. Methods Case report. Results Four eyes of two patients with Hallermann-Streiff Syndrome developed exudative retinal detachments after lensectomy and anterior vitrectomy at 2 and 4 months of age. Both patients had extreme microphthalmia. The exudative retinal detachment regressed spontaneously in three of the four eyes; however, one eye required subscleral sclerectomy. In one patient, the best-corrected visual acuity was 20/200 at 3 years of age; the other patient had good fixation and following behavior in each eye at 1 year of age. Conclusions Early surgery to treat congenital cataracts in extremely microphthalmic eyes associated with the Hallermann-Streiff Syndrome may induce exudative retinal detachment. However, the retinal detachments tend to regress and may not cause severe visual impairment.
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exudative retinal detachment following cataract surgery in Hallermann Streiff Syndrome
Graefes Archive for Clinical and Experimental Ophthalmology, 2008Co-Authors: Sachiko Nishina, Yumi Suzuki, Noriyuki AzumaAbstract:Purpose To report two cases of Hallermann-Streiff Syndrome with exudative retinal detachment after cataract surgery.
Gagan Arora - One of the best experts on this subject based on the ideXlab platform.
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lighted stylet guided intubation via the intubating laryngeal airway in a patient with Hallermann Streiff Syndrome
Canadian Journal of Anaesthesia-journal Canadien D Anesthesie, 2009Co-Authors: David T Wong, Gagan AroraAbstract:Purpose Hallermann-Streiff Syndrome is a congenital Syndrome associated with oculomandibulofacial abnormalities and potentially difficult airways. This case report describes the novel use of a lighted stylet-guided tracheal tube insertion through a new supraglottic airway, the intubating laryngeal airway (ILA™), in a patient with Hallermann-Streiff Syndrome who had anticipated difficult airway.
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lighted stylet guided intubation via the intubating laryngeal airway in a patient with Hallermann Streiff Syndrome l intubation guidee avec un stylet lumineux via un masque larynged intubation chez un patient souffrant du Syndrome d Hallermann streif
2009Co-Authors: David T Wong, Gagan AroraAbstract:Purpose Hallermann-Streiff Syndrome is a congenital Syndrome associated with oculomandibulofacial abnormalities and potentially difficult airways. This case report describes the novel use of a lighted stylet-guided tracheal tube insertion through a new supraglottic airway, the intubating laryngeal airway (ILA TM ), in a patient with Hallermann-Streiff Syndrome who had anticipated difficult airway. Clinical features A 26-year-old male with HallermannStreiff Syndrome was scheduled for a vitrectomy. The patient had mandibulofacial dystocia with a bird-like appearance, a mouth opening of 4 cm, a receding chin, and a Mallampati class 3 examination. The surgeon requested muscle paralysis and no movement during surgery. After receiving midazolam, fentanyl and propofol, a size 3.5 ILA TM was inserted and lung ventilation was easy to perform. A 7.5-mm internal diameter tracheal tube was mounted on a lighted stylet with its inner rigid stylet removed. After succinylcholine administration, the lighted stylet-tracheal tube assembly was inserted via the ILA TM
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Lighted stylet-guided intubation via the intubating laryngeal airway in a patient with Hallermann-Streiff Syndrome
Canadian Journal of Anesthesia Journal canadien d'anesthésie, 2008Co-Authors: David T Wong, Gagan AroraAbstract:Purpose Hallermann-Streiff Syndrome is a congenital Syndrome associated with oculomandibulofacial abnormalities and potentially difficult airways. This case report describes the novel use of a lighted stylet-guided tracheal tube insertion through a new supraglottic airway, the intubating laryngeal airway (ILA™), in a patient with Hallermann-Streiff Syndrome who had anticipated difficult airway. Clinical features A 26-year-old male with Hallermann-Streiff Syndrome was scheduled for a vitrectomy. The patient had mandibulofacial dystocia with a bird-like appearance, a mouth opening of 4 cm, a receding chin, and a Mallampati class 3 examination. The surgeon requested muscle paralysis and no movement during surgery. After receiving midazolam, fentanyl and propofol, a size 3.5 ILA™ was inserted and lung ventilation was easy to perform. A 7.5-mm internal diameter tracheal tube was mounted on a lighted stylet with its inner rigid stylet removed. After succinylcholine administration, the lighted stylet-tracheal tube assembly was inserted via the ILA™ until the transillumination just vanished below the sternal notch. The lighted stylet was removed, the circuit was connected, and capnography confirmed tracheal placement of tube. The ILA™ was deflated and left in situ. Upon emergence from anesthesia, the tracheal tube, and subsequently the ILA™, were removed without complications. Conclusions This case presents a novel use of a lighted stylet-guided tracheal tube insertion through the ILA™ in a patient with Hallermann-Streiff Syndrome. This intubation technique can be considered in patients with difficult airways as a primary route of intubation, or as a secondary rescue strategy. Objectif Le Syndrome d’Hallermann-Streiff-François est un Syndrome congénital associée à des anomalies oculo-mandibulo-faciales et des voies aériennes potentiellement difficiles. Cette présentation de cas décrit l’utilisation novatrice d’une sonde trachéale guidée par stylet lumineux pour l’intubation via un nouveau dispositif supraglottique de gestion des voies aériennes, le masque laryngé d’intubation ILA™, chez un patient souffrant du Syndrome d’Hallermann-Streiff-François chez qui on prévoyait des voies aériennes difficiles. Éléments cliniques Un homme de 26 ans souffrant du Syndrome d’Hallermann-Streiff-François a été admis pour subir une vitrectomie. Le patient souffrait de dystocie mandibulo-faciale et présentait une apparence d’oiseau, une ouverture buccale de 4 cm, un menton effacé, et un score de Mallampati de classe 3. Le chirurgien a demandé que les muscles soient paralysés et qu’il n’y ait aucun mouvement pendant la chirurgie. Après l’administration de midazolam, de fentanyl et de propofol, un ILA™ de taille 3 a été inséré et la ventilation des poumons a été facile à réaliser. Une sonde trachéale de 7,5 mm de diamètre interne a été fixée à un stylet lumineux dont le stylet intérieur rigide avait été retiré. Après l’administration de succinylcholine, le montage sonde trachéale – stylet lumineux a été inséré via le ILA™ jusqu’à ce que la diaphanoscopie disparaisse juste sous l’échancrure sternale. Le stylet lumineux a été enlevé, le circuit connecté, et la capnographie a confirmé le positionnement trachéal de la sonde. L’ILA™ a été dégonflé et laissé in situ . Lors du réveil de l’anesthésie, la sonde trachéale, puis l’ILA™, ont été extraits sans complications. Conclusion Ce cas présente une utilisation innovante de l’insertion d’une sonde trachéale guidée par stylet lumineux via un ILA™ chez un patient souffrant du Syndrome d’Hallermann-Streiff-François. Cette technique d’intubation peut être envisagée pour les patients présentant des voies aériennes difficiles comme voie d’intubation principale, ou comme stratégie de sauvetage secondaire.
Massimiliano Serafino - One of the best experts on this subject based on the ideXlab platform.
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Hallermann Streiff Syndrome with severe bilateral enophthalmos and radiological evidence of silent brain Syndrome a new congenital silent brain Syndrome
Clinical Ophthalmology, 2011Co-Authors: Paolo Nucci, Carlo De Conciliis, Matteo Sacchi, Massimiliano SerafinoAbstract:Background We present the first case of a congenital form of silent brain Syndrome (SBS) in a young patient affected by Hallermann–Streiff Syndrome (HSS) and the surgical management of the associated eyelid anomalies.
Sachiko Nishina - One of the best experts on this subject based on the ideXlab platform.
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Exudative retinal detachment following cataract surgery in Hallermann-Streiff Syndrome
Graefe's Archive for Clinical and Experimental Ophthalmology, 2008Co-Authors: Sachiko Nishina, Yumi Suzuki, Noriyuki AzumaAbstract:Purpose To report two cases of Hallermann-Streiff Syndrome with exudative retinal detachment after cataract surgery. Methods Case report. Results Four eyes of two patients with Hallermann-Streiff Syndrome developed exudative retinal detachments after lensectomy and anterior vitrectomy at 2 and 4 months of age. Both patients had extreme microphthalmia. The exudative retinal detachment regressed spontaneously in three of the four eyes; however, one eye required subscleral sclerectomy. In one patient, the best-corrected visual acuity was 20/200 at 3 years of age; the other patient had good fixation and following behavior in each eye at 1 year of age. Conclusions Early surgery to treat congenital cataracts in extremely microphthalmic eyes associated with the Hallermann-Streiff Syndrome may induce exudative retinal detachment. However, the retinal detachments tend to regress and may not cause severe visual impairment.
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exudative retinal detachment following cataract surgery in Hallermann Streiff Syndrome
Graefes Archive for Clinical and Experimental Ophthalmology, 2008Co-Authors: Sachiko Nishina, Yumi Suzuki, Noriyuki AzumaAbstract:Purpose To report two cases of Hallermann-Streiff Syndrome with exudative retinal detachment after cataract surgery.
David T Wong - One of the best experts on this subject based on the ideXlab platform.
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lighted stylet guided intubation via the intubating laryngeal airway in a patient with Hallermann Streiff Syndrome
Canadian Journal of Anaesthesia-journal Canadien D Anesthesie, 2009Co-Authors: David T Wong, Gagan AroraAbstract:Purpose Hallermann-Streiff Syndrome is a congenital Syndrome associated with oculomandibulofacial abnormalities and potentially difficult airways. This case report describes the novel use of a lighted stylet-guided tracheal tube insertion through a new supraglottic airway, the intubating laryngeal airway (ILA™), in a patient with Hallermann-Streiff Syndrome who had anticipated difficult airway.
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lighted stylet guided intubation via the intubating laryngeal airway in a patient with Hallermann Streiff Syndrome l intubation guidee avec un stylet lumineux via un masque larynged intubation chez un patient souffrant du Syndrome d Hallermann streif
2009Co-Authors: David T Wong, Gagan AroraAbstract:Purpose Hallermann-Streiff Syndrome is a congenital Syndrome associated with oculomandibulofacial abnormalities and potentially difficult airways. This case report describes the novel use of a lighted stylet-guided tracheal tube insertion through a new supraglottic airway, the intubating laryngeal airway (ILA TM ), in a patient with Hallermann-Streiff Syndrome who had anticipated difficult airway. Clinical features A 26-year-old male with HallermannStreiff Syndrome was scheduled for a vitrectomy. The patient had mandibulofacial dystocia with a bird-like appearance, a mouth opening of 4 cm, a receding chin, and a Mallampati class 3 examination. The surgeon requested muscle paralysis and no movement during surgery. After receiving midazolam, fentanyl and propofol, a size 3.5 ILA TM was inserted and lung ventilation was easy to perform. A 7.5-mm internal diameter tracheal tube was mounted on a lighted stylet with its inner rigid stylet removed. After succinylcholine administration, the lighted stylet-tracheal tube assembly was inserted via the ILA TM
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Lighted stylet-guided intubation via the intubating laryngeal airway in a patient with Hallermann-Streiff Syndrome
Canadian Journal of Anesthesia Journal canadien d'anesthésie, 2008Co-Authors: David T Wong, Gagan AroraAbstract:Purpose Hallermann-Streiff Syndrome is a congenital Syndrome associated with oculomandibulofacial abnormalities and potentially difficult airways. This case report describes the novel use of a lighted stylet-guided tracheal tube insertion through a new supraglottic airway, the intubating laryngeal airway (ILA™), in a patient with Hallermann-Streiff Syndrome who had anticipated difficult airway. Clinical features A 26-year-old male with Hallermann-Streiff Syndrome was scheduled for a vitrectomy. The patient had mandibulofacial dystocia with a bird-like appearance, a mouth opening of 4 cm, a receding chin, and a Mallampati class 3 examination. The surgeon requested muscle paralysis and no movement during surgery. After receiving midazolam, fentanyl and propofol, a size 3.5 ILA™ was inserted and lung ventilation was easy to perform. A 7.5-mm internal diameter tracheal tube was mounted on a lighted stylet with its inner rigid stylet removed. After succinylcholine administration, the lighted stylet-tracheal tube assembly was inserted via the ILA™ until the transillumination just vanished below the sternal notch. The lighted stylet was removed, the circuit was connected, and capnography confirmed tracheal placement of tube. The ILA™ was deflated and left in situ. Upon emergence from anesthesia, the tracheal tube, and subsequently the ILA™, were removed without complications. Conclusions This case presents a novel use of a lighted stylet-guided tracheal tube insertion through the ILA™ in a patient with Hallermann-Streiff Syndrome. This intubation technique can be considered in patients with difficult airways as a primary route of intubation, or as a secondary rescue strategy. Objectif Le Syndrome d’Hallermann-Streiff-François est un Syndrome congénital associée à des anomalies oculo-mandibulo-faciales et des voies aériennes potentiellement difficiles. Cette présentation de cas décrit l’utilisation novatrice d’une sonde trachéale guidée par stylet lumineux pour l’intubation via un nouveau dispositif supraglottique de gestion des voies aériennes, le masque laryngé d’intubation ILA™, chez un patient souffrant du Syndrome d’Hallermann-Streiff-François chez qui on prévoyait des voies aériennes difficiles. Éléments cliniques Un homme de 26 ans souffrant du Syndrome d’Hallermann-Streiff-François a été admis pour subir une vitrectomie. Le patient souffrait de dystocie mandibulo-faciale et présentait une apparence d’oiseau, une ouverture buccale de 4 cm, un menton effacé, et un score de Mallampati de classe 3. Le chirurgien a demandé que les muscles soient paralysés et qu’il n’y ait aucun mouvement pendant la chirurgie. Après l’administration de midazolam, de fentanyl et de propofol, un ILA™ de taille 3 a été inséré et la ventilation des poumons a été facile à réaliser. Une sonde trachéale de 7,5 mm de diamètre interne a été fixée à un stylet lumineux dont le stylet intérieur rigide avait été retiré. Après l’administration de succinylcholine, le montage sonde trachéale – stylet lumineux a été inséré via le ILA™ jusqu’à ce que la diaphanoscopie disparaisse juste sous l’échancrure sternale. Le stylet lumineux a été enlevé, le circuit connecté, et la capnographie a confirmé le positionnement trachéal de la sonde. L’ILA™ a été dégonflé et laissé in situ . Lors du réveil de l’anesthésie, la sonde trachéale, puis l’ILA™, ont été extraits sans complications. Conclusion Ce cas présente une utilisation innovante de l’insertion d’une sonde trachéale guidée par stylet lumineux via un ILA™ chez un patient souffrant du Syndrome d’Hallermann-Streiff-François. Cette technique d’intubation peut être envisagée pour les patients présentant des voies aériennes difficiles comme voie d’intubation principale, ou comme stratégie de sauvetage secondaire.
