Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 20 de 35
Filtrar
1.
Infant Ment Health J ; 39(2): 242-253, 2018 03.
Artigo em Inglês | MEDLINE | ID: mdl-29489020

RESUMO

This study examines the attachment quality and how this changed over time among infants who had cleft lip and palate (CLP), by conducting a prospective longitudinal study addressing the effects of this type of perinatal event on the parent-infant relationship and the emotional development of the infants. At 12 months of age, the Strange Situation Paradigm (SSP; M. Ainsworth, M.C. Blehar, E. Waters, & T. Wall, 1978) was administered to a sample of 38 CLP infants (born between 2003 and 2010) and 17 healthy controls. At 4 years of age, the Attachment Story Completion Task (ASCT; I. Bretherton, D. Ridgeway, & J. Cassidy, 1990) was administered to 32 individuals from the CLP sample and 14 from the control group. As reported in the literature, CLP infants display secure attachment behaviors as frequently as do control infants (55%). However, a more detailed analysis of the attachment scales revealed that CLP infants show more avoidance and less proximity seeking. In addition, a closer examination of the subcategories of attachment styles revealed that most CLP infants (71%) displayed distal attachment strategies such as the B1/B2 or A1/A2 subcategories. At 4 years old, CLP infants clearly displayed more deactivation and less security than did the control sample. Moreover, when detailing the evolution of attachment individually, almost 60% of the CLP children showing distal strategies at 12 months became deactivated or disorganized when they reached 4 years. Indeed, subtle differences in attachment behaviors at 12 months old-which can be considered marginally secure at that age-may reveal attachment vulnerabilities, which seem to be more apparent over the course of development.


Assuntos
Fenda Labial/psicologia , Fissura Palatina/psicologia , Relações Mãe-Filho/psicologia , Apego ao Objeto , Adulto , Estudos de Casos e Controles , Pré-Escolar , Fenda Labial/complicações , Fissura Palatina/complicações , Feminino , Humanos , Lactente , Estudos Longitudinais , Masculino , Pais/psicologia , Estudos Prospectivos , Psicologia da Criança , Fatores de Risco , Estresse Psicológico/psicologia , Suíça
2.
Cleft Palate Craniofac J ; 55(1): 88-97, 2018 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-34162054

RESUMO

OBJECTIVE: To investigate the evolution of maternal representations (ie, the way parents perceive their child in term of temperament, character, behaviors, etc) of children with a cleft at 3 major milestones: before/after reconstructive surgeries and at school age. Parenting style was also analyzed and compared with parents of children born without a cleft. DESIGN AND PARTICIPANTS: The sample was composed of 30 mothers of children with an orofacial cleft and 14 mothers of children without a cleft. Maternal representations were assessed when the child was 2 months (before surgery), 12 months (after surgery), and 5 years of age (when starting school) using semistructured interviews that were transcribed and coded according to the subscales of the Working Model of the Child Interview and the Parental Development Interview. At the 5-year appointment, mothers also completed a questionnaire about parenting style. RESULTS: Results showed no difference across groups (cleft/noncleft) in maternal representations at the 2-month, 12-month, and 5-year assessments. In the cleft group, significant differences were shown between 2 and 12 months in caregiving sensitivity, perceived infant difficulty, fear for the infant's safety, and parental pride, all factors being higher at 12 months. Those differences in parental representations over time were not found in the noncleft group. Additionally, mothers of the cleft group were significantly more authoritarian than mothers of children without a cleft. CONCLUSION: The absence of differences across cleft and noncleft groups suggests that having a child with a cleft does not affect maternal representations and emotions between 2 months and 5 years of the child's age. However, parenting style seems to be influenced by the presence of a cleft in the present sample.

3.
Int J Pediatr Otorhinolaryngol ; 79(12): 2243-7, 2015 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-26545794

RESUMO

OBJECTIVE: Grommets may be considered as the treatment of choice for otitis media with effusion (OME) in children born with a cleft. But the timing and precise indications to use them are not well established. The aim of the study is to compare the results of hearing and speech controls at three and six year-old in children born with total cleft or cleft palate in the presence or not of grommets. METHODS: This retrospective study concerns non syndromic children born between 1994 and 2006 and operated for a unilateral cleft lip palate (UCLP) or a cleft palate (CP) alone, by one surgeon with the same schedule of operations (Malek procedure). We compared the results of clinical observation, tympanometry, audiometry and nasometry at three and six year-old. The Borel-Maisonny classification was used to evaluate the velar insufficiency. None of the children had preventive grommets. The Fisher Exact Test was used for statistical analysis with p<0.05 considered as significant. RESULTS: Seventy-seven patients were analyzed in both groups. Abnormal hearing status was statistically more frequent in children with UCLP compared to children with CP, at three and six years (respectively, 80-64%, p<0.03 and 78-60%, p<0.02), with the use of grommets at six years in 43% of cases in both groups. Improvement of hearing status between three and six year-old was present in 5% of children with UCLP and 9% with CP, without the use of grommets. CONCLUSION: The use of grommets between three and six year-old was not associated to any improvement of hearing status or speech results children with UCLP or with CP, with a low risk of tympanosclerosis. These results favor the use of grommets before the age of three, taking into account the risk of long term tympanosclerosis.


Assuntos
Fenda Labial/complicações , Fissura Palatina/complicações , Audição , Ventilação da Orelha Média , Otite Média com Derrame/cirurgia , Fala , Audiometria , Criança , Pré-Escolar , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Feminino , Transtornos da Audição/etiologia , Testes Auditivos , Humanos , Masculino , Ventilação da Orelha Média/instrumentação , Otite Média com Derrame/complicações , Estudos Retrospectivos , Distúrbios da Fala/etiologia , Insuficiência Velofaríngea/etiologia
4.
Rev Med Suisse ; 11(460): 357-61, 2015 Feb 04.
Artigo em Francês | MEDLINE | ID: mdl-25854046

RESUMO

Vascular anomalies are rare conditions that could be observed at all ages. They are classified, according to their histology, in vascular tumors or vascular malformations. The general practitioner plays a significant role in diagnosis and patient management, diagnosis being suspected on clinical history. In case of vascular anomaly, ultrasound-Doppler assessment is helpful to characterize morphologic and hemodynamic changes of the lesion and permits to monitor the evolution and to detect complications. Further investigations are often necessary prior to multidisciplinary management. In this article, a brief overview of vascular anomalies, their multidisciplinary management and the exemple of Klippel-Trenaunay syndrome are presented.


Assuntos
Comunicação Interdisciplinar , Síndrome de Klippel-Trenaunay-Weber/terapia , Malformações Vasculares/terapia , Clínicos Gerais/organização & administração , Humanos , Síndrome de Klippel-Trenaunay-Weber/diagnóstico , Síndrome de Klippel-Trenaunay-Weber/fisiopatologia , Papel do Médico , Ultrassonografia Doppler , Malformações Vasculares/diagnóstico , Malformações Vasculares/fisiopatologia
5.
Eur Arch Otorhinolaryngol ; 272(5): 1277-85, 2015 May.
Artigo em Inglês | MEDLINE | ID: mdl-25411074

RESUMO

Patients with cleft palate are prone to velopharyngeal insufficiency. In minor cases or when hypernasal speech does not resolve after velopharyngoplasty, an augmentation pharyngoplasty with autologous fat can be proposed. The aim of the present study is to evaluate the short-term (within 2 months) and long-term efficiency (during the 24 months following the procedure) of our procedure in the setting of velopharyngeal insufficiency related to a cleft palate. Twenty-two patients with cleft palate related velopharyngeal insufficiency were included in this retrospective study. All patients were operated following the same technique, in the same institution. The pre- and postoperative evaluations included a nasometry, a subjective evaluation using the Borel-Maisonny score, and a nasofibroscopy to assess the degree of velopharyngeal closure. Scores of Borel-Maisonny and nasometry were compared before, shortly after the procedure (within 2 months) and long term after the procedure (within 24 months). Forty-one procedures in 22 patients with a cleft palate performed in our institution between October 2004 and January 2012 were included in the study. Nine patients had a previous velopharyngoplasty with persistent rhinolalia despite intensive speech therapy. In 14 patients the procedure was repeated because of recurrent hypernasal speech after the first injection. The average number of procedures per patient was 1.8. Postoperative nasometry and Borel-Maisonny scores were statistically significantly improved and remained stable until the end of the follow-up (median 42 months postoperative) in most patients. Complications were rare and minor. Autologous fat injection is a simple procedure for treatment of minor velopharyngeal insufficiencies in patients with cleft palate, with good long-term results and few complications.


Assuntos
Fissura Palatina , Faringe/cirurgia , Procedimentos de Cirurgia Plástica , Complicações Pós-Operatórias , Gordura Subcutânea Abdominal/transplante , Insuficiência Velofaríngea , Adolescente , Adulto , Criança , Fissura Palatina/complicações , Fissura Palatina/cirurgia , Feminino , Humanos , Injeções/métodos , Masculino , Cirurgia Endoscópica por Orifício Natural/métodos , Complicações Pós-Operatórias/diagnóstico , Complicações Pós-Operatórias/terapia , Procedimentos de Cirurgia Plástica/efeitos adversos , Procedimentos de Cirurgia Plástica/métodos , Estudos Retrospectivos , Distúrbios da Fala/etiologia , Distúrbios da Fala/terapia , Fonoterapia/métodos , Resultado do Tratamento , Insuficiência Velofaríngea/diagnóstico , Insuficiência Velofaríngea/etiologia , Insuficiência Velofaríngea/cirurgia
6.
Swiss Med Wkly ; 144: w13943, 2014 Mar 07.
Artigo em Inglês | MEDLINE | ID: mdl-24610228

RESUMO

BACKGROUND: Infantile haemangiomas (IHs) are very common vascular tumours. Propranolol is at present the first-line treatment for problematic and complicated haemangioma. In accordance with a Swiss protocol, children are monitored for 2 days at the start of the treatment to detect possible side effects of this drug. Our study advocates a simplification of the pretreatment monitoring process. METHODS: All children with a problematic and complicated haemangioma treated with propranolol between September 2009 and September 2012 were included in the study. All patients were hospitalised under constant nurse supervision for 48 hours at the start of the treatment and subjected to cardiac and blood measurements. The dosage of propranolol was 1 mg/kg/day on the first day and 2 mg/kg/day from the second day. Demographic data, clinical features, treatment outcome and complications were analysed. RESULTS: Twenty-nine infants were included in our study. Of these, 86.2% responded immediately to the treatment. There were no severe adverse reactions. Six patients presented transient side effects such as bradycardia, hypotension after the first dose and hypoglycaemia later. No side effects occurred after the second dose. Treatment was never interrupted. CONCLUSION: Propranolol (a ß-blocker) is a safe treatment for problematic IH. Side effects may occur after the first dose. A strict 48 hour monitoring in hospital is expensive and may be unnecessary as long as the contraindications for the drug are respected.


Assuntos
Monitoramento de Medicamentos/métodos , Neoplasias Faciais/tratamento farmacológico , Neoplasias dos Genitais Femininos/tratamento farmacológico , Hemangioma Capilar/tratamento farmacológico , Síndromes Neoplásicas Hereditárias/tratamento farmacológico , Propranolol/uso terapêutico , Neoplasias Cutâneas/tratamento farmacológico , Vasodilatadores/uso terapêutico , Glicemia/metabolismo , Pressão Sanguínea , Ecocardiografia , Eletrocardiografia , Feminino , Hospitalização , Humanos , Lactente , Testes de Função Renal , Masculino , Propranolol/efeitos adversos , Estudos Retrospectivos , Vasodilatadores/efeitos adversos
7.
Cleft Palate Craniofac J ; 51(2): 189-99, 2014 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-24555489

RESUMO

OBJECTIVE: The main objective of the study is to identify practical and cultural factors influencing the mental health of mothers of children with an orofacial cleft in Benin and to compare it with a sample of Swiss mothers in the same conditions. METHOD: Thirty-six mothers of children with an orofacial cleft in Benin and 40 mothers of children with an orofacial cleft in Switzerland were interviewed about practical and emotional aspects concerning their child and their own lives. Then, they completed the Perinatal Postraumatic Stress Questionnaire and the Beck Depression Inventory. RESULTS: Mothers in Benin had significantly higher posttraumatic stress and depression symptoms compared with mothers in Switzerland. Depression symptoms were higher in Beninese mothers coming from urban areas, in Beninese mothers with few or no other children, and in Beninese mothers whose child was operated on at a more advanced age. DISCUSSION: This study stressed the importance of cultural differences in perceptions of orofacial clefts in order to provide appropriate care to patients and their families. In particular, wide campaigns of information should help parents to understand the cleft origin and the medical staff in small dispensaries to provide adequate support and care. This may diminish anxiety concerning the child's short- and long-term prognosis. Creation of a Beninese parental support group for children with clefts and their families could be another way to provide information and support where multidisciplinary care is not available.


Assuntos
Fenda Labial/psicologia , Fissura Palatina/psicologia , Saúde Mental , Mães/psicologia , Benin , Características Culturais , Feminino , Humanos , Recém-Nascido , Entrevistas como Assunto , Masculino , Escalas de Graduação Psiquiátrica , Suíça
8.
Cleft Palate Craniofac J ; 50(6): 704-12, 2013 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-24218985

RESUMO

Objective : The main objective of this study was to assess mother-child patterns of interaction in relation to later quality of attachment in a group of children with an orofacial cleft compared with children without cleft. Design : Families were contacted when the child was 2 months old for a direct assessment of mother-child interaction and then at 12 months for a direct assessment of the child's attachment. Data concerning socioeconomical information and posttraumatic stress symptoms in mothers were collected at the first appointment. Participants : Forty families of children with a cleft and 45 families of children without cleft were included in the study. Families were recruited at birth in the University Hospital of Lausanne. Results : Results showed that children with a cleft were more difficult and less cooperative during interaction at 2 months of age with their mother compared with children without a cleft. No significant differences were found in mothers or in dyadic interactive styles. Concerning the child's attachment at 12 months old, no differences were found in attachment security. However, secure children with a cleft were significantly more avoidant with their mother during the reunion episodes than secure children without cleft. Conclusion : Despite the facial disfigurement and the stress engendered by treatment during the first months of the infant's life, children with cleft and their mothers are doing as well as families without cleft with regard to the mothers' mental health, mother-child relationships, and later quality of attachment. A potential contribution for this absence of difference may be the pluridisciplinary support that families of children with cleft benefit from in Lausanne.


Assuntos
Relações Mãe-Filho , Apego ao Objeto , Criança , Humanos , Lactente , Mães/psicologia
9.
Artigo em Inglês | MEDLINE | ID: mdl-23611443

RESUMO

Objective : The main objective of this study was to assess mother-child patterns of interaction in relation to later quality of attachment in a group of children with an orofacial cleft compared with children without cleft. Design : Families were contacted when the child was 2 months old for a direct assessment of mother-child interaction and then at 12 months for a direct assessment of the child's attachment. Data concerning socioeconomical information and posttraumatic stress symptoms in mothers were collected at the first appointment. Participants : Forty families of children with a cleft and 45 families of children without cleft were included in the study. Families were recruited at birth in the University Hospital of Lausanne. Results : Results showed that children with a cleft were more difficult and less cooperative during interaction at 2 months of age with their mother compared with children without a cleft. No significant differences were found in mothers or in dyadic interactive styles. Concerning the child's attachment at 12 months old, no differences were found in attachment security. However, secure children with a cleft were significantly more avoidant with their mother during the reunion episodes than secure children without cleft. Conclusion : Despite the facial disfigurement and the stress engendered by treatment during the first months of the infant's life, children with cleft and their mothers are doing as well as families without cleft with regard to the mothers' mental health, mother-child relationships, and later quality of attachment. A potential contribution for this absence of difference may be the pluridisciplinary support that families of children with cleft benefit from in Lausanne.

11.
World J Surg ; 36(8): 1963-9, 2012 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-22538390

RESUMO

BACKGROUND: This study reviews the 15 year program of our Department of Pediatric Surgery for the treatment and follow-up of children born with a cleft in Benin and Togo. METHODS: We analyzed files of children born in Africa with a cleft. They were referred to us through a nongovernmental organization (NGO) between 1993 and 2008 and assessed in Africa by local pediatricians before and after surgery. Operations were performed by our team. RESULTS: Two hundred files were reviewed: 60 cases of unilateral cleft lip, seven of bilateral cleft lip, 44 of unilateral cleft lip palate (UCLP), 29 of bilateral cleft lip palate (BCLP), 53 of cleft palate (CP), three of bilateral oro-ocular cleft, one of unilateral and two of median clefts (Binder), and one of commissural cleft. Sixty-nine (35 %) of these cases were not operated in Africa: 25 (12.5 %) had not shown up, 28 (15 %) were considered unfit for surgery (Down's syndrome, HIV-positive, malnutrition, cardiac malformation), and 16 (7.5 %) were transferred to Switzerland. Palatal fistula occurred in 20 % of UCLP, 30 % of BCLP, and 16 % of CP. Evaluation of speech after palate surgery gave less than 50 % of socially acceptable speech. CONCLUSIONS: Our partnership with a NGO and a local team makes it possible to treat and subsequently follow children born with a cleft in West Africa. Surgery is performed under good conditions. If aesthetic results are a success, functional results after palate surgery need further improvement to promote integration in school and social life.


Assuntos
Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Benin/epidemiologia , Fenda Labial/epidemiologia , Fissura Palatina/epidemiologia , Feminino , Seguimentos , Humanos , Masculino , Missões Médicas , Procedimentos de Cirurgia Plástica/métodos , Togo/epidemiologia , Falha de Tratamento , Resultado do Tratamento
12.
Cleft Palate Craniofac J ; 48(4): 419-24, 2011 Jul.
Artigo em Inglês | MEDLINE | ID: mdl-20500071

RESUMO

OBJECTIVE: The announcement, prenatally or at birth, of a cleft lip and/or palate represents a challenge for the parents. The purpose of this study is to identify parental working internal models of the child (parental representations of the child and relationship in the context of attachment theory) and posttraumatic stress disorder symptoms in mothers of infants born with a cleft. METHOD: The study compares mothers with a child born with a cleft (n  =  22) and mothers with a healthy infant (n  =  36). RESULTS: The study shows that mothers of infants with a cleft more often experience insecure parental working internal models of the child and more posttraumatic stress symptoms than mothers of the control group. It is interesting that the severity or complexity of the cleft is not related to parental representations and posttraumatic stress disorder symptoms. The maternal emotional involvement, as expressed in maternal attachment representations, is higher in mothers of children with a cleft who had especially high posttraumatic stress disorder symptoms, as compared with mothers of children with a cleft having fewer posttraumatic stress disorder symptoms. DISCUSSION: Mothers of children with a cleft may benefit from supportive therapy regarding parent-child attachment, even when they express low posttraumatic stress disorder symptoms.


Assuntos
Fenda Labial/psicologia , Fissura Palatina/psicologia , Comportamento Materno/psicologia , Relações Mãe-Filho , Apego ao Objeto , Transtornos de Estresse Pós-Traumáticos/psicologia , Adaptação Psicológica , Adulto , Desenvolvimento Infantil , Feminino , Humanos , Lactente , Masculino , Mães/psicologia , Poder Familiar/psicologia , Personalidade , Estresse Psicológico/psicologia
13.
J Craniofac Surg ; 21(5): 1615-8, 2010 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-20856058

RESUMO

The aim of the study was to determine the influence of the dissection of the palate during primary surgery and the type of orthognathic surgery needed in cases of unilateral total cleft. The review concerns 58 children born with a complete unilateral cleft lip and palate and treated between 1994 and 2008 at the appropriate age for orthognathic surgery. This is a retrospective mixed-longitudinal study. Patients with syndromes or associated anomalies were excluded. All children were treated by the same orthodontist and by the same surgical team. Children are divided into 2 groups: the first group includes children who had conventional primary cleft palate repair during their first year of life, with extensive mucoperiosteal undermining. The second group includes children operated on according to the Malek surgical protocol. The soft palate is closed at the age of 3 months, and the hard palate at 6 months with minimal mucoperiosteal undermining. Lateral cephalograms at ages 9 and 16 years and surgical records were compared. The need for orthognathic surgery was more frequent in the first than in the second group (60% vs 47.8%). Concerning the type of orthognathic surgery performed, 2- or 3-piece Le Fort I or bimaxillary osteotomies were also less required in the first group. Palate surgery following the Malek procedure results in an improved and simplified craniofacial outcome. With a minimal undermining of palatal mucosa, we managed to reduce the amount of patients who required an orthognathic procedure. When this procedure was indicated, the surgical intervention was also greatly simplified.


Assuntos
Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Cirurgia Ortognática , Adolescente , Cefalometria , Criança , Feminino , Necessidades e Demandas de Serviços de Saúde , Humanos , Lactente , Estudos Longitudinais , Masculino , Osteogênese por Distração , Osteotomia de Le Fort , Estudos Retrospectivos , Resultado do Tratamento
14.
Arch Dis Child Fetal Neonatal Ed ; 95(6): F447-51, 2010 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-20584802

RESUMO

OBJECTIVE: To evaluate the incidence and severity of nasal trauma secondary to nasal continuous positive airway pressure (nCPAP) in neonates. DESIGN: Prospective observational study. SETTING: Neonatal intensive care unit (NICU) of the University Hospital of Lausanne, Switzerland. PATIENTS: All neonates admitted between January 2002 and December 2007 treated by nCPAP were eligible. METHODS: Patients' noses were monitored during nCPAP. Nasal trauma was reported into three stages: (I) persistent erythema; (II) superficial ulceration; and (III) necrosis. RESULTS: 989 neonates were enrolled. Mean gestational age was 34 weeks (SD 4), mean birth weight 2142 g (SD 840). Nasal trauma was reported in 420 (42.5%) patients and it was of stage I, II and III in 371 (88.3%), 46 (11%) and 3 (0.7%) patients, respectively. Incidence and severity of trauma were inversely correlated with gestational age and birth weight. The risk of nasal trauma was greater in neonates <32 weeks of gestational age (OR 2.48, 95% CI 1.59 to 3.86), weighing <1500 g at birth (OR 2.28, 95% CI 1.43 to 3.64), treated >5 days by nCPAP (OR 5.36, 95% CI 3.82 to 7.52), or staying >14 days in the NICU (OR 1.67, 95% CI 1.22 to 2.28). Most cases of nasal trauma (90%) appeared during the first 6 days of nCPAP. Persistent visible scars were present in two cases. CONCLUSIONS: Nasal trauma is a frequent complication of nCPAP, especially in preterm neonates, but long-term cosmetic sequelae are very rare. This study provides a description of nasal trauma and proposes a simple staging system. This could serve as a basis to develop strategies of prevention and treatment of this iatrogenic event.


Assuntos
Pressão Positiva Contínua nas Vias Aéreas/efeitos adversos , Nariz/lesões , Peso ao Nascer , Pressão Positiva Contínua nas Vias Aéreas/métodos , Eritema/etiologia , Feminino , Idade Gestacional , Humanos , Recém-Nascido , Recém-Nascido Prematuro , Terapia Intensiva Neonatal/métodos , Masculino , Necrose , Doenças Nasais/etiologia , Estudos Prospectivos , Índices de Gravidade do Trauma , Úlcera/etiologia
15.
Eur Arch Otorhinolaryngol ; 267(6): 977-83, 2010 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-20033195

RESUMO

Velopharyngeal insufficiency (VPI) is a structural or functional trouble, which causes hypernasal speech. Velopharyngeal flaps, speech therapy and augmentation pharyngoplasty, using different implants, have all been used to address this trouble. We hereby present our results following rhinopharyngeal autologous fat injection in 18 patients with mild velopharyngeal insufficiency (12 soft palate clefts, 4 functional VPI, 2 myopathy). 28 injections were carried out between 2004 and 2007. The degree of hypernasal speech was evaluated pre- and postoperatively by a speech therapist and an ENT specialist and quantified by an acoustic nasometry (Kay Elemetrics). All patients were exhaustively treated with preoperative speech therapy (average, 8 years). The mean value of the nasalance score was 37% preoperatively and 23% postoperatively (p = 0.015). The hypernasality was reduced postoperatively in all patients (1-3 degrees of the Borel-Maisonny score). There were no major complications, two minor complications (one hematoma, one cervical pain). The autologous fat injection is a simple, safe, minimally invasive procedure. It proves to be efficient in cases of mild velopharyngeal insufficiency or after a suboptimal velopharyngoplasty.


Assuntos
Tecido Adiposo/transplante , Insuficiência Velofaríngea/cirurgia , Adolescente , Adulto , Criança , Fissura Palatina/cirurgia , Síndrome de DiGeorge/cirurgia , Feminino , Seguimentos , Humanos , Masculino , Pessoa de Meia-Idade , Fonação/fisiologia , Complicações Pós-Operatórias/etiologia , Espectrografia do Som , Inteligibilidade da Fala , Insuficiência Velofaríngea/etiologia , Distúrbios da Voz/etiologia , Distúrbios da Voz/cirurgia , Qualidade da Voz/fisiologia , Adulto Jovem
16.
Swiss Med Wkly ; 139(37-38): 535-9, 2009 Sep 19.
Artigo em Inglês | MEDLINE | ID: mdl-19838870

RESUMO

QUESTION UNDER STUDY: Domestic accidents are an important problem in paediatric medicine. This study was designed to gain a better understanding of burn mechanisms and target prevention. METHODS: Children treated for burn lesions in the Department of Paediatric Surgery between August 2004 and August 2005 were included in this prospective study. The burn mechanisms, the children's ages and the circumstances in which children were burned as well as their home environment variables were analyzed. RESULTS: The current study included eighty-nine patients, aged between 2 months and 15 years. Seventy-eight percent were less than 5 years old. More than half were boys. Hot liquid scalding was the most frequent mechanism. There does not seem to be an increased risk in the immigrant population or in low economic status families. In most cases, an adult person was present at time of injury. CONCLUSIONS: If we were to describe the highest "at risk" candidate for a burn in our region, it would be a boy aged 15 months to 5 years who is burned by a cup of hot liquid on his hand, at home, around mealtime, in the presence of one or both parents. Reduced attention in the safe domestic setting is probably responsible.


Assuntos
Queimaduras/epidemiologia , Acidentes Domésticos/prevenção & controle , Acidentes Domésticos/estatística & dados numéricos , Adolescente , Fatores Etários , Queimaduras/diagnóstico , Queimaduras/prevenção & controle , Causalidade , Criança , Pré-Escolar , Emigrantes e Imigrantes , Feminino , Humanos , Lactente , Masculino , Estudos Prospectivos , Fatores de Risco , Índice de Gravidade de Doença , Fatores Sexuais , Classe Social , Suíça/epidemiologia
17.
J Pediatr Surg ; 43(10): e15-8, 2008 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-18926197

RESUMO

The oro-ocular cleft no. 4 according to the Tessier classification is one of the rarest facial cleft, and to this day, few cases have been reported in the literature. We describe the case of a 9-month-old girl with a complete bilateral facial cleft. On the right cornea protruded a hard lesion, a corneal staphyloma. We describe the 3 primary surgical steps used to restore the possibility of satisfactory feeding, to promote language acquisition, and to protect vision in the nonaffected eye. The psychological and social aspects of severe facial deformities in developing countries are also tackled.


Assuntos
Anormalidades Múltiplas , Fenda Labial/complicações , Fissura Palatina/complicações , Doenças da Córnea/congênito , Olho Artificial , Face/anormalidades , Anormalidades Múltiplas/cirurgia , Fenda Labial/cirurgia , Fissura Palatina/cirurgia , Coloboma/complicações , Coloboma/cirurgia , Doenças da Córnea/complicações , Doenças da Córnea/cirurgia , Países em Desenvolvimento , Anormalidades do Olho/cirurgia , Pálpebras/anormalidades , Pálpebras/cirurgia , Face/cirurgia , Feminino , Humanos , Lactente , Maxila/anormalidades , Nervo Óptico/anormalidades , Órbita/anormalidades , Vasos Retinianos/anormalidades
18.
J Pediatr Gastroenterol Nutr ; 46(3): 299-307, 2008 Mar.
Artigo em Inglês | MEDLINE | ID: mdl-18376248

RESUMO

OBJECTIVES: To determine the epidemiology of biliary atresia (BA) in Switzerland, the outcome of the children from diagnosis, and the prognostic factors. PATIENTS AND METHODS: The records of all patients with BA born in Switzerland between January 1994 and December 2004 were analyzed. Survival rates were calculated with the Kaplan-Meier method, and prognostic factors evaluated with the log rank test. Median follow up was 58 months (range, 5-124). RESULTS: BA was diagnosed in 48 children. Incidence was 1 in 17,800 live births (95% confidence interval 1/13,900-1/24,800), without significant regional, annual, or seasonal variation. Forty-three children underwent a Kasai portoenterostomy (PE) in 5 different Swiss pediatric surgery units. Median age at Kasai PE was 68 days (range, 30-126). Four-year survival with native liver after Kasai PE was 37.4%. Liver transplantation (LT) was needed in 31 in 48 children with BA, including 5 patients without previous Kasai PE. Four patients (8%, all born before 2001) died while waiting for LT, and 29 LT were performed in 27 patients (28 in Geneva and 1 in Paris). All of the transplanted patients are alive. Four-year overall BA patient survival was 91.7%. Four-year survival with native liver was 75% in patients who underwent Kasai PE before 46 days, 33% in patients operated on between 46 and 75 days, and 11% in patients operated on after 75 days (P = 0.02). CONCLUSIONS: Overall survival of patients with BA in Switzerland compares favorably with current international standards, whereas results of the Kasai operation could be improved to reduce the need for LTs in infancy and early childhood.


Assuntos
Atresia Biliar/epidemiologia , Atresia Biliar/mortalidade , Transplante de Fígado/mortalidade , Portoenterostomia Hepática/mortalidade , Fatores Etários , Atresia Biliar/cirurgia , Feminino , Humanos , Incidência , Lactente , Recém-Nascido , Estimativa de Kaplan-Meier , Masculino , Prognóstico , Estudos Retrospectivos , Suíça/epidemiologia , Resultado do Tratamento
19.
J Pediatr Surg ; 43(4): 668-74, 2008 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-18405714

RESUMO

BACKGROUND: The aim of this retrospective study was to evaluate speech outcome and need of a pharyngeal flap in children born with nonsyndromic Pierre Robin Sequence (nsPRS) vs syndromic Pierre Robin Sequence (sPRS). METHODS: Pierre Robin Sequence was diagnosed when the triad microretrognathia, glossoptosis, and cleft palate were present. Children were classified at birth in 3 categories depending on respiratory and feeding problems. The Borel-Maisonny classification was used to score the velopharyngeal insufficiency. RESULTS: The study was based on 38 children followed from 1985 to 2006. For the 25 nsPRS, 9 (36%) pharyngeal flaps were performed with improvements of the phonatory score in the 3 categories. For the 13 sPRS, 3 (23%) pharyngeal flaps were performed with an improvement of the phonatory scores in the 3 children. There was no statistical difference between the nsPRS and sPRS groups (P = .3) even if we compared the children in the 3 categories (P = .2). CONCLUSIONS: Children born with nsPRS did not have a better prognosis of speech outcome than children born with sPRS. Respiratory and feeding problems at birth did not seem to be correlated with speech outcome. This is important when informing parents on the prognosis of long-term therapy.


Assuntos
Transtornos da Articulação/prevenção & controle , Síndrome de Pierre Robin/reabilitação , Síndrome de Pierre Robin/cirurgia , Retalhos Cirúrgicos , Transtornos da Articulação/etiologia , Pré-Escolar , Feminino , Seguimentos , Humanos , Lactente , Masculino , Fonética , Síndrome de Pierre Robin/classificação , Síndrome de Pierre Robin/complicações , Prognóstico , Estudos Retrospectivos , Fonoterapia , Resultado do Tratamento
20.
Pediatr Surg Int ; 24(1): 37-47, 2008 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-17962961

RESUMO

Myoblast transfer therapy has been extensively studied for a wide range of clinical applications, such as tissue engineering for muscular loss, cardiac surgery or Duchenne Muscular Dystrophy treatment. However, this approach has been hindered by numerous limitations, including early myoblast death after injection and specific immune response after transplantation with allogenic cells. Different cell sources have been analyzed to overcome some of these limitations. The object of our study was to investigate the growth potential, characterization and integration in vivo of human primary fetal skeletal muscle cells. These data together show the potential for the creation of a cell bank to be used as a cell source for muscle cell therapy and tissue engineering. For this purpose, we developed primary muscular cell cultures from biopsies of human male thigh muscle from a 16-week-old fetus and from donors of 13 and 30 years old. We show that fetal myogenic cells can be successfully isolated and expanded in vitro from human fetal muscle biopsies, and that fetal cells have higher growth capacities when compared to young and adult cells. We confirm lineage specificity by comparing fetal muscle cells to fetal skin and bone cells in vitro by immunohistochemistry with desmin and 5.1 H11 antibodies. For the feasibility of the cell bank, we ensured that fetal muscle cells retained intrinsic characteristics after 5 years cryopreservation. Finally, human fetal muscle cells marked with PKH26 were injected in normal C57BL/6 mice and were found to be present up to 4 days. In conclusion we estimate that a human fetal skeletal muscle cell bank can be created for potential muscle cell therapy and tissue engineering.


Assuntos
Músculo Esquelético/embriologia , Distrofias Musculares/cirurgia , Mioblastos Esqueléticos/transplante , Transplante de Células-Tronco/métodos , Adolescente , Adulto , Animais , Biópsia , Sobrevivência Celular , Células Cultivadas , DNA/genética , Desmina/biossíntese , Desmina/genética , Feminino , Regulação da Expressão Gênica no Desenvolvimento , Humanos , Imuno-Histoquímica , Masculino , Camundongos , Camundongos Endogâmicos C57BL , Microscopia de Fluorescência , Músculo Esquelético/metabolismo , Músculo Esquelético/transplante , Mioblastos Esqueléticos/citologia , Mioblastos Esqueléticos/metabolismo , Gravidez , Reação em Cadeia da Polimerase Via Transcriptase Reversa , Engenharia Tecidual/métodos
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...