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1.
Cleft Palate Craniofac J ; 60(5): 526-535, 2023 05.
Artículo en Inglés | MEDLINE | ID: mdl-34982012

RESUMEN

A consortium of global cleft professionals, predominantly from low- and middle-income countries, identified adaptations to cleft care protocols during and after COVID-19 as a priority learning area of need.A multidisciplinary international working group met on a videoconferencing platform in a multi-staged process to make consensus recommendations for adaptations to cleft protocols within resource-constrained settings. Feedback was sought from a roundtable discussion forum and global organizations involved in comprehensive cleft care.Foundational principles were agreed to enable recommendations to be globally relevant and two areas of focus within the specified topic were identified. First the safety aspects of cleft surgery protocols were scrutinized and COVID-19 adaptations, specifically in the pre- and perioperative periods, were highlighted. Second, surgical procedures and cleft care services were prioritized according to their relationship to functional outcomes and time-sensitivity. The surgical procedures assigned the highest priority were emergent interventions for breathing and nutritional requirements and primary palatoplasty. The cleft care services assigned the highest priority were new-born assessments, pediatric support for children with syndromes, management of acute dental or auditory infections and speech pathology intervention.A collaborative, interdisciplinary and international working group delivered consensus recommendations to assist with the provision of cleft care in low- and middle-income countries. At a time of global cleft care delays due to COVID-19, a united approach amongst global cleft care providers will be advantageous to advocate for children born with cleft lip and palate in resource-constrained settings.


Asunto(s)
COVID-19 , Labio Leporino , Fisura del Paladar , Niño , Humanos , Fisura del Paladar/cirugía , Labio Leporino/cirugía , Países en Desarrollo
2.
Cleft Palate Craniofac J ; 57(6): 687-693, 2020 06.
Artículo en Inglés | MEDLINE | ID: mdl-32394745

RESUMEN

OBJECTIVE: To test the feasibility of implementing a high-fidelity cleft palate simulator during a workshop in Santiago, Chile, using a novel video endoscope to assess technical performance. DESIGN: Sixteen cleft surgeons from South America participated in a 2-day cleft training workshop. All 16 participants performed a simulated repair, and 13 of them performed a second simulated repair. The repairs were recorded using a low-cost video camera and a newly designed camera mouth retractor attachment. Twenty-nine videos were assessed by 3 cleft surgeons using a previously developed cleft palate objective structured assessment of technical skill (CLOSATS with embedded overall score assessment) and global rating scale. The reliability of the ratings and technical performance in relation to minimum acceptable scores and previous experience was assessed. RESULTS: The video setup provided acceptable recording quality for the purpose of assessment. Average intraclass correlation coefficient for the CLOSATS, global, and overall performance score was 0.69, 0.75, and 0.82, respectively. None of the novice surgeons passed the CLOSATS and global score for both sessions. One participant in the intermediate group, and 2 participants in the advanced group passed the CLOSATS and global score for both sessions. There were highly experienced participants who failed to pass the CLOSATS and global score for both sessions. CONCLUSIONS: The cleft palate simulator can be practically implemented with video-recording capability to assess performance in cleft palate repair. This technology may be of assistance in assessing surgical competence in cleft palate repair.


Asunto(s)
Fisura del Paladar , Chile , Fisura del Paladar/cirugía , Competencia Clínica , Humanos , Reproducibilidad de los Resultados , Grabación en Video
3.
Plast Reconstr Surg ; 149(4): 919-929, 2022 Apr 01.
Artículo en Inglés | MEDLINE | ID: mdl-35171871

RESUMEN

BACKGROUND: Craniofacial microsomia is associated with maxillomandibular hypoplasia, microtia, soft-tissue deficiency, and variable severity of cranial nerve dysfunction, most often of the facial nerve. This study evaluated the incidence of facial paralysis in patients with craniofacial microsomia and outcomes after free functioning muscle transfer for dynamic smile reconstruction. METHODS: A single-center, retrospective, cross-sectional study was performed from 1985 to 2018 to identify pediatric patients with craniofacial microsomia and severe facial nerve dysfunction who underwent dynamic smile reconstruction with free functioning muscle transfer. Preoperative and postoperative facial symmetry and oral commissure excursion during maximal smile were measured using photogrammetric facial analysis software. RESULTS: This study included 186 patients with craniofacial microsomia; 41 patients (21 male patients, 20 female patients) had documented facial nerve dysfunction (22 percent) affecting all branches (51 percent) or the mandibular branch only (24 percent). Patients with severe facial paralysis (n = 8) underwent smile reconstruction with a free functioning muscle transfer neurotized either with a cross-face nerve graft (n = 7) or with the ipsilateral motor nerve to masseter (n =1). All patients achieved volitional muscle contraction with improvement in lip symmetry and oral commissure excursion (median, 8 mm; interquartile range, 3 to 10 mm). The timing of orthognathic surgery and facial paralysis reconstruction was an important consideration in optimizing patient outcomes. CONCLUSIONS: The authors' institution's incidence of facial nerve dysfunction in children with craniofacial microsomia is 22 percent. Free functioning muscle transfer is a reliable option for smile reconstruction in children with craniofacial microsomia. To optimize outcomes, a novel treatment algorithm is proposed for craniofacial microsomia patients likely to require both orthognathic surgery and facial paralysis reconstruction. CLINICAL QUESTION/LEVEL OF EVIDENCE: Therapeutic, IV.


Asunto(s)
Parálisis Facial , Síndrome de Goldenhar , Transferencia de Nervios , Procedimientos de Cirugía Plástica , Niño , Estudios Transversales , Nervio Facial/cirugía , Parálisis Facial/complicaciones , Parálisis Facial/cirugía , Femenino , Síndrome de Goldenhar/complicaciones , Síndrome de Goldenhar/cirugía , Humanos , Masculino , Estudios Retrospectivos , Sonrisa/fisiología , Resultado del Tratamiento
4.
Plast Reconstr Surg ; 131(2): 253-257, 2013 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-23357986

RESUMEN

BACKGROUND: The anatomy of the facial nerve and its branches has been well documented. The course of the extratemporal facial nerve, its anatomical planes, and the surface landmarks of the temporal division and marginal mandibular division are well known. However, the surface landmark of the middle division of the facial nerve has not been studied to date. METHODS: Eighteen hemifacial dissections in 10 fresh human cadavers were performed through a preauricular face-lift incision. An 18-gauge needle with brilliant green dye was used to mark the nerve through the skin before dissection. The exact location of the middle division branches of the facial nerve was documented in relation to the transcutaneous marking. RESULTS: The middle division branches of the facial nerve were found to lie at a mean of 2.3 mm from the tattooed point, with a range of 0 to 6 mm. A nerve branch was found directly tattooed by the needle seven of 18 times, inferior to the tattoo five of 18 times, and superior to the tattoo six of 18 times. CONCLUSIONS: The zygomatic/buccal motor branch that innervates the zygomaticus major muscle can be reliably found at the midway point on a line drawn from the root of the helix and the lateral commissure of the mouth. This study will help guide surgeons to the middle division of the facial nerve as it applies to facial surgery.


Asunto(s)
Nervio Facial/anatomía & histología , Cadáver , Humanos
5.
Pediatr Surg Int ; 23(9): 923-6, 2007 Sep.
Artículo en Inglés | MEDLINE | ID: mdl-17437118

RESUMEN

Abdominal wall reconstruction in omphalopagus twins poses a difficult reconstructive challenge, as separation often results in a large abdominal wall defect. A number of options are available for closure, including tissue flaps, expanders and patches made of foreign material. Surgisis is a new biodegradable small intestine scaffolding substrate that permits tissue in-growth and results in a permanent durable scar. We describe its use in abdominal wall reconstruction after separation of a set of conjoined twins. A set of omphalopagus conjoined twins shared liver and abdominal wall. After separation at 6 months of age, Twin A's abdomen could be closed primarily, but Twin B could not. A 4-ply Surgisis mesh was used in the upper abdominal closure, and a skin flap was created, to completely cover the patch. Both twins survived the operation. A small portion of the skin flap over the Surgisis broke down, healing by secondary intention. In follow up of over 18 months post procedure, there have been no wound infections and the abdominal wall is intact with no evidence of a hernia. Surgisis can be successfully used for the reconstruction of complex abdominal wall defects in the pediatric patient, including reconstruction after separation of conjoined twins.


Asunto(s)
Pared Abdominal/cirugía , Materiales Biocompatibles , Procedimientos de Cirugía Plástica/métodos , Mallas Quirúrgicas , Gemelos Siameses/cirugía , Pared Abdominal/anomalías , Estudios de Seguimiento , Humanos , Lactante , Intestino Delgado/cirugía , Hígado/anomalías , Hígado/cirugía , Masculino
6.
J Craniofac Surg ; 16(1): 161-4, 2005 Jan.
Artículo en Inglés | MEDLINE | ID: mdl-15699667

RESUMEN

Congenital epulis is a rare benign hamartoma of the alveolar ridge found in the newborn. The clinical characteristics of this lesion show some variability, and opinion of its pathogenesis lacks consensus. Congenital epulis can cause feeding or respiratory compromise. A case report and review of the literature is presented. The diagnosis, pathology, and treatment are reviewed.


Asunto(s)
Neoplasias Gingivales/congénito , Tumor de Células Granulares/congénito , Diagnóstico Diferencial , Femenino , Enfermedades de las Encías/congénito , Hamartoma/congénito , Humanos , Recién Nacido , Maxilar
7.
Can J Anaesth ; 52(8): 837-44, 2005 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-16189336

RESUMEN

BACKGROUND: Moebius sequence is a rare congenital absence of the sixth and seventh cranial nerves, although there may be additional congenital cranial neuropathies. Developmental delay, cardiac and musculoskeletal abnormalities may also co-exist. Oro-facial manifestations include bilateral facial nerve palsy resulting in a mask like facies, drooling, incomplete eye closure, and strabismus secondary to the extra-ocular muscle imbalance. This condition has multiple implications for anesthetic care. METHODS: We reviewed 111 anesthesia records of 46 patients with Moebius sequence for anesthesia technique and related complications. RESULTS: Facial nerve palsy was universally present and bilateral in 44 (93.6%) patients. Thirty-two (68%) had concomitant sixth nerve palsy. Oro-facial and limb abnormalities were present in 16 (35%) and 18 (39%) of patients respectively. Endotracheal intubation, when attempted, was easy in 76 of 106 cases. Tracheal intubation was consistently difficult in seven patients and intubation failure occurred in a single patient only. Statistically significant factors associated with difficult tracheal intubation included structural abnormalities of the mandible and palate and abnormalities of four cranial nerves (IX, X, XI, XII). CONCLUSION: We confirm that tracheal intubation may be difficult in patients with Moebius sequence. We identify disease features that might predict a difficult tracheal intubation and thus allow the anesthesiologist an opportunity to plan accordingly.


Asunto(s)
Nervio Abducens/anomalías , Anomalías Múltiples/cirugía , Anestesia , Nervio Facial/anomalías , Nervio Abducens/cirugía , Adolescente , Niño , Preescolar , Nervio Facial/cirugía , Parálisis Facial/etiología , Femenino , Humanos , Lactante , Intubación Intratraqueal , Masculino , Respiración Artificial , Estudios Retrospectivos , Síndrome
8.
J Craniofac Surg ; 14(6): 876-9, 2003 Nov.
Artículo en Inglés | MEDLINE | ID: mdl-14600630

RESUMEN

Congenital nevi are characterized by the appearance of pigmented areas that range in size, shape, surface texture, and hairiness. In most cases, the nevus remains stable and benign, but because of possible malignant transformation, nevi are often excised. In this case, a young boy was born with a hairy nevus below his lip extending inferiorly down the left side of his chin and upper neck. After two surgical excisions, the wound healing process was interrupted when his incision wound was split while jumping on his bed. With the professional assistance of occupational therapists, the scar should heal in an esthetically pleasing manner.


Asunto(s)
Neoplasias Faciales/congénito , Nevo Pigmentado/congénito , Preescolar , Mentón , Estética , Neoplasias Faciales/cirugía , Humanos , Masculino , Nevo Pigmentado/cirugía , Dehiscencia de la Herida Operatoria/etiología , Dehiscencia de la Herida Operatoria/cirugía
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