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Pesquisa : C05.182.895.249 [Categoria DeCS]
Referências encontradas : 61 [refinar]
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[PMID]:29332910
[Au] Autor:Kato K; Kato T; Hayano S; Fukasawa Y; Numaguchi A; Hattori T; Saito A; Sato Y; Hayakawa M
[Ad] Endereço:Department of Pediatrics, Nagoya University Graduate School of Medicine.
[Ti] Título:Successful Infant Pneumonectomy with Unilateral Pulmonary Artery Occlusion Test.
[So] Source:Int Heart J;59(1):237-239, 2018 Jan 27.
[Is] ISSN:1349-3299
[Cp] País de publicação:Japan
[La] Idioma:eng
[Ab] Resumo:The use of unilateral pulmonary artery occlusion (UPAO) test for the preoperative evaluation of pneumonectomy was reported in adult patients. On the contrary, in infants, no strategies have yet been recommended to predict hemodynamics after pneumonectomy, nor has use of the UPAO test been reported. We describe the first case of infant with abnormal pulmonary circulation in whom successful pneumonectomy was performed after preoperative evaluation using UPAO test. Right pneumonectomy was planned for an 8-month-old girl, because of decreased right pulmonary function, high risk of pneumothorax, and impaired left lung expansion due to overexpansion caused by severe left bronchial stenosis and bronchomalacia. However, she had also prolonged pulmonary hypertension and there was difficulty in accurate echocardiographic evaluation of its severity due to concomitant left pulmonary artery stenosis. Furthermore, contrast-enhanced computer tomography suggested a certain degree of right pulmonary venous flow, discordant with the result showing scarce right pulmonary flow in perfusion scintigraphy. Predicting postoperative hemodynamic changes was therefore considered difficult. To evaluate these concerns, we performed cardiac catheterization and UPAO test to simulate postoperative hemodynamics. Pulmonary arteriography showed decreased but significant right pulmonary arterial and venous flows. Measurements including pulmonary artery pressure and cardiac index showed no marked changes after occlusion. Based on UPAO test results, the operation was successfully performed and hemodynamics remained stable postoperatively. The UPAO test may be useful for infants with cardiopulmonary impairment to evaluate the tolerability of pneumonectomy.
[Mh] Termos MeSH primário: Anormalidades Múltiplas
Broncomalácia/cirurgia
Testes de Função Cardíaca/métodos
Pneumonectomia/métodos
Artéria Pulmonar/fisiopatologia
Circulação Pulmonar/fisiologia
Estenose de Artéria Pulmonar/cirurgia
[Mh] Termos MeSH secundário: Angiografia
Broncomalácia/congênito
Broncomalácia/diagnóstico
Feminino
Seres Humanos
Lactente
Artéria Pulmonar/diagnóstico por imagem
Cintilografia
Estenose de Artéria Pulmonar/congênito
Estenose de Artéria Pulmonar/diagnóstico
Resistência Vascular
Função Ventricular Direita/fisiologia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1802
[Cu] Atualização por classe:180206
[Lr] Data última revisão:
180206
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:180116
[St] Status:MEDLINE
[do] DOI:10.1536/ihj.16-606


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[PMID]:28209649
[Au] Autor:Mani RK; Mishra V; Sharma M; Kumar RA
[Ad] Endereço:Department of Pulmonology Critical Care, Nayati Multi Super Speciality Hospital, Mathura, Uttar Pradesh, India.
[Ti] Título:Isolated pulmonary mucormycosis.
[So] Source:BMJ Case Rep;2017, 2017 Feb 16.
[Is] ISSN:1757-790X
[Cp] País de publicação:England
[La] Idioma:eng
[Mh] Termos MeSH primário: Broncomalácia/microbiologia
Pneumopatias Fúngicas/microbiologia
Mucormicose/complicações
[Mh] Termos MeSH secundário: Idoso
Broncomalácia/diagnóstico por imagem
Evolução Fatal
Feminino
Seres Humanos
Pneumopatias Fúngicas/diagnóstico por imagem
Mucormicose/diagnóstico por imagem
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170310
[Lr] Data última revisão:
170310
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170218
[St] Status:MEDLINE


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[PMID]:28196820
[Au] Autor:Pons-Odena M; Verges A; Arza N; Cambra FJ
[Ad] Endereço:Pediatric Intensive Care Unit, Hospital Sant Joan de Deu, Esplugues De Llobregat, Spain.
[Ti] Título:Combined use of Neurally Adjusted Ventilatory Assist (NAVA) and Vertical Expandable Prostethic Titanium Rib (VEPTR) in a patient with Spondylocostal dysostosis and associated bronchomalacia.
[So] Source:BMJ Case Rep;2017, 2017 Feb 14.
[Is] ISSN:1757-790X
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Jarcho-Levin syndrome is a rare disorder characterised by defects in vertebral and costal segmentation of varying severity. Respiratory complications are the main cause of death or severe comorbidity due to a restrictive rib cage. A 3 months old infant with Spondylocostal dysostosis and associated bronchomalacia experiencing severe asynchrony during the weaning process is reported. The Neurally Adjusted Ventilatory Assist (NAVA) mode was used to improve adaptation to mechanical ventilation after Vertical Expandable Prosthetic Titanium Ribs (VEPTRs) were implanted. The synchrony achieved with the NAVA mode allowed a decrease of the sedoanalgesia he received. A follow-up CT scan showed a reduction in the volume of the posterobasal atelectasis. The evolution of this patient suggests that the combined use of VEPTR for thoracic expansion and ventilation using NAVA can favour the global improvement. This mode could be an option to consider in selected patients with difficult weaning from mechanical ventilation in paediatric intensive care units.
[Mh] Termos MeSH primário: Anormalidades Múltiplas/cirurgia
Broncomalácia/cirurgia
Hérnia Diafragmática/cirurgia
Suporte Ventilatório Interativo
Próteses e Implantes
[Mh] Termos MeSH secundário: Broncomalácia/complicações
Hérnia Diafragmática/complicações
Seres Humanos
Lactente
Masculino
Costelas
Titânio
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
D1JT611TNE (Titanium)
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170306
[Lr] Data última revisão:
170306
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170216
[St] Status:MEDLINE


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[PMID]:27722899
[Au] Autor:Kusak B; Cichocka-Jarosz E; Jedynak-Wasowicz U; Lis G
[Ad] Endereço:Department of Pediatrics, Chair of Pediatrics Jagiellonian University Medical College, Krakow, Poland. beatakusak@gmail.com.
[Ti] Título:Types of laryngomalacia in children: interrelationship between clinical course and comorbid conditions.
[So] Source:Eur Arch Otorhinolaryngol;274(3):1577-1583, 2017 Mar.
[Is] ISSN:1434-4726
[Cp] País de publicação:Germany
[La] Idioma:eng
[Ab] Resumo:The aim of this study was to: (1) find out whether laryngomalacia (LM) types are related to clinical course; (2) which patients with LM are at higher risk of other airway malacia [tracheomalacia (TM) and/or bronchomalacia (BM)]; and (3) evaluate the prevalence of LM in our region. Patients with established LM diagnosis and complete clinical and endoscopy records were enrolled. They were classified into different LM types according to classification based on the side of supraglottic obstruction. One hundred ten children were included. The most common LM appearance was type I-58 children, followed by combine types (I + II and I + III)-38. The other airway malacia were found in 47 patients: TM in 31, BM in 10, and TM with BM in 6. Other comorbidities (cardiac, neurological, and genetic disorders) were identified in 30 children. Patients with combine types of LM differ from those with single type of LM in terms of prematurity (13 vs 31 %, p = 0.04) and higher weight on the examination day (p = 0.006). Patients with other airway malacia differ from children with isolated LM in terms of prematurity (40 vs 13 %, p = 0.008), comorbidities (38 vs 19 %, p = 0.024), and lower weight on the examination day (p = 0.014). The prevalence of clinically relevant LM was one in 2600-3100 newborns. Clinical course of LM cannot be anticipated on the basis of solely endoscopic evaluation of the larynx. Comorbidities and prematurity increase the risk of other airway malacia. The prevalence of LM is relatively high in the middle-south part of Poland.
[Mh] Termos MeSH primário: Obstrução das Vias Respiratórias
Broncomalácia/epidemiologia
Laringomalácia
Traqueomalácia/epidemiologia
[Mh] Termos MeSH secundário: Obstrução das Vias Respiratórias/patologia
Obstrução das Vias Respiratórias/fisiopatologia
Broncoscopia/métodos
Comorbidade
Feminino
Seres Humanos
Lactente
Recém-Nascido
Laringomalácia/classificação
Laringomalácia/epidemiologia
Laringomalácia/fisiopatologia
Masculino
Polônia/epidemiologia
Prevalência
Estudos Retrospectivos
Medição de Risco
Fatores de Risco
Supraglotite/patologia
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1705
[Cu] Atualização por classe:170515
[Lr] Data última revisão:
170515
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161011
[St] Status:MEDLINE
[do] DOI:10.1007/s00405-016-4334-5


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[PMID]:28298961
[Au] Autor:Sinha N
[Ad] Endereço:Houston Methodist Hospital, Houston, Texas.
[Ti] Título:Transplant Pulmonary Interventions: Translating Lung Transplant Interventions to Nontransplant Patients.
[So] Source:Methodist Debakey Cardiovasc J;12(4 Suppl):18-20, 2016 Oct-Dec.
[Is] ISSN:1947-6108
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:Roughly 10% of lung transplant recipients experience airway complications. Although the incidence has decreased dramatically since the first lung transplants were performed in the 1960s, airway complications have continued to adversely affect outcomes. Bronchoscopic interventions such as balloon dilation, airway stenting, and endobronchial electrocautery play an important role in ameliorating the morbidity and mortality associated with these complications. This review describes the array of bronchoscopic interventions used to treat airway complications after lung transplant and how these techniques can be used in nontransplant settings as well.
[Mh] Termos MeSH primário: Obstrução das Vias Respiratórias/terapia
Fístula Brônquica/terapia
Broncomalácia/terapia
Broncoscopia
Granuloma do Sistema Respiratório/terapia
Transplante de Pulmão/efeitos adversos
Pulmão/cirurgia
[Mh] Termos MeSH secundário: Obstrução das Vias Respiratórias/etiologia
Obstrução das Vias Respiratórias/mortalidade
Obstrução das Vias Respiratórias/fisiopatologia
Coagulação com Plasma de Argônio
Fístula Brônquica/etiologia
Fístula Brônquica/mortalidade
Fístula Brônquica/fisiopatologia
Broncomalácia/etiologia
Broncomalácia/mortalidade
Broncomalácia/fisiopatologia
Broncoscopia/efeitos adversos
Broncoscopia/instrumentação
Broncoscopia/métodos
Broncoscopia/mortalidade
Dilatação
Granuloma do Sistema Respiratório/etiologia
Granuloma do Sistema Respiratório/mortalidade
Granuloma do Sistema Respiratório/fisiopatologia
Seres Humanos
Pulmão/fisiopatologia
Transplante de Pulmão/métodos
Transplante de Pulmão/mortalidade
Fatores de Risco
Stents
Deiscência da Ferida Operatória
Resultado do Tratamento
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1707
[Cu] Atualização por classe:170724
[Lr] Data última revisão:
170724
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170317
[St] Status:MEDLINE
[do] DOI:10.14797/mdcj-12-4s1-18


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[PMID]:27863648
[Au] Autor:Sztanó B; Kiss G; Márai K; Rácz G; Szegesdi I; Rácz K; Katona G; Rovó L
[Ad] Endereço:Department of Otorhinolaryngology, Head and Neck Surgery, University of Szeged, Hungary. Electronic address: sztano.balazs@med.u-szeged.hu.
[Ti] Título:Biodegradable airway stents in infants - Potential life-threatening pitfalls.
[So] Source:Int J Pediatr Otorhinolaryngol;91:86-89, 2016 Dec.
[Is] ISSN:1872-8464
[Cp] País de publicação:Ireland
[La] Idioma:eng
[Ab] Resumo:OBJECTIVE: The solution of severe tracheobronchial obstructions in early childhood means a great challenge. Biodegradable stents were intended to be a minimally invasive temporary solution which may decrease the number of interventions and limit the possible complications of stenting procedures. However, our first experiences have brought out a new, - especially in childhood - potentially life-threatening complication of this concept. METHODS: Five SX-ELLA biodegradable polydioxanone stents was applied in three patients because of severe tracheobronchial obstruction: congenital tracheomalacia (7 day-old), acquired tracheomalacia (10 month-old), and congenital trachea-bronchomalacia (10 month-old). RESULTS: The breathing of all children improved right after the procedure. We observed degradation of the stent from the 5th postoperative week which resulted in large intraluminar fragments causing significant airway obstruction: one patient died of severe pneumonia, the other baby required urgent bronchoscopy to remove the obstructing 'foreign body' from the trachea. In the third case repeated stent placements successfully maintained the tracheal lumen. CONCLUSIONS: Polydioxanone stents may offer an alternative to metallic or silastic stents for collapse or external compression of the trachea in children; however, large decaying fragments mean a potential risk especially in the small size pediatric airway. The fragmentation of the stent, which generally starts in the 4-6 postoperative weeks, may create large sharp pieces. These may be anchored to the mucosa and covered by crust leading to obstruction. As repeated interventions are required, we do not consider the application of biodegradable stents unambiguously advantageous.
[Mh] Termos MeSH primário: Implantes Absorvíveis/efeitos adversos
Obstrução das Vias Respiratórias/etiologia
Corpos Estranhos/etiologia
Stents/efeitos adversos
Traqueia
[Mh] Termos MeSH secundário: Obstrução das Vias Respiratórias/cirurgia
Broncomalácia/terapia
Broncoscopia
Feminino
Corpos Estranhos/cirurgia
Seres Humanos
Lactente
Recém-Nascido
Masculino
Polidioxanona/efeitos adversos
Traqueomalácia/terapia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Nm] Nome de substância:
31621-87-1 (Polydioxanone)
[Em] Mês de entrada:1703
[Cu] Atualização por classe:171116
[Lr] Data última revisão:
171116
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161120
[St] Status:MEDLINE


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[PMID]:27729160
[Au] Autor:Hiebert JC; Zhao YD; Willis EB
[Ad] Endereço:Department of Otorhinolaryngology, The University of Oklahoma Health Sciences Center, 920 Stanton L. Young Blvd WP 1290, Oklahoma City, OK, 73104, USA. Electronic address: Jared-hiebert@ouhsc.edu.
[Ti] Título:Bronchoscopy findings in recurrent croup: A systematic review and meta-analysis.
[So] Source:Int J Pediatr Otorhinolaryngol;90:86-90, 2016 Nov.
[Is] ISSN:1872-8464
[Cp] País de publicação:Ireland
[La] Idioma:eng
[Ab] Resumo:IMPORTANCE: The etiology of recurrent croup is often anatomic. Currently there is no set criteria for determining who should undergo diagnostic bronchoscopy and which patients are at most risk for having a clinically significant finding. Few studies have addressed these questions. OBJECTIVE: To identify risk factors for clinically significant findings on bronchoscopy in children with recurrent croup and the frequency of bronchoscopy findings in general. DATA SOURCES: PUBMED, Ovid MEDLINE, EMBASE. STUDY SELECTION: Articles addressing bronchoscopy in children with recurrent croup, up to July 2016, were reviewed. Related keywords and medical subject headings were used during the search. The abstracts were reviewed to determine suitability for inclusion based on a set of criteria. Manual crosscheck of references was performed. DATA EXTRACTION: We analyzed the bronchoscopy findings of individual patients in each study and their associated risk factors when available. RESULTS: We reviewed 11 articles, published between 1992 and 2016, including 885 patients (654 males, 237 females). Only 5 studies, including 455 patients, had sufficient data for meta-analysis. Our study revealed that the three most common bronchoscopy findings were subglottic stenosis, reflux changes, and broncho/tracheomalacia. Only 8.7% of patients were noted to have clinically significant findings on bronchoscopy. Meta analysis showed an association between significant bronchoscopy findings and History of Intubation [OR = 5.17, 95% CI 2.65-10.09], Inpatient Consultation [OR = 4.01, 95% CI 1.44-11.20], Age < 3 [OR = 3.22, 95% 1.66-6.27], Age < 1 [OR = 2.86, 95% CI 1.28-6.40], and Prematurity [OR = 2.90, 95% CI 1.39-6.06]. Our study found a high incidence of a History of GERD (20%) and Asthma/Allergies (35%) among patients with recurrent croup, but these variables did not reach statistical significance in patients with significant bronchoscopy findings ([OR = 1.62, 95% CI 0.79-3.30], [OR = 0.57, 95% CI 0.30-1.08] respectively). CONCLUSION: The risk factors most associated with clinically significant bronchoscopy findings in recurrent croup are Intubation, Inpatient Consultation, Age < 3, Age <1, and Prematurity. A History of GERD and Asthma/Allergy, though highly prevalent in recurrent croup patients, were not statistically associated with significant bronchoscopy findings. RELEVANCE: The results should guide physicians in selecting which recurrent croup patients are most at risk for significant findings and thus may warrant bronchoscopy.
[Mh] Termos MeSH primário: Broncomalácia/diagnóstico por imagem
Broncoscopia
Crupe/etiologia
Refluxo Gastroesofágico/diagnóstico por imagem
Laringoestenose/diagnóstico por imagem
Traqueomalácia/diagnóstico por imagem
[Mh] Termos MeSH secundário: Fatores Etários
Broncomalácia/complicações
Pré-Escolar
Crupe/epidemiologia
Refluxo Gastroesofágico/complicações
Seres Humanos
Lactente
Intubação Intratraqueal
Laringoestenose/complicações
Nascimento Prematuro/epidemiologia
Recidiva
Encaminhamento e Consulta
Fatores de Risco
Traqueomalácia/complicações
[Pt] Tipo de publicação:JOURNAL ARTICLE; META-ANALYSIS; REVIEW
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:161013
[St] Status:MEDLINE


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[PMID]:27343517
[Au] Autor:Baird CW; Prabhu S; Buchmiller TL; Smithers C; Jennings R
[Ad] Endereço:Department of Cardiac Surgery, Boston Children's Hospital & Harvard Medical School, Boston, Massachusetts. Electronic address: christopher.baird@cardio.chboston.org.
[Ti] Título:Direct Tracheobronchopexy and Posterior Descending Aortopexy for Severe Left Mainstem Bronchomalacia Associated With Congenital Pulmonary Airway Malformation and Left Circumflex Aortic Arch.
[So] Source:Ann Thorac Surg;102(1):e1-4, 2016 Jul.
[Is] ISSN:1552-6259
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:Complex tracheobronchial obstruction and malacia can be associated with conotruncal and aortic arch anomalies. A circumflex aortic arch composed of a left aortic arch and right descending aorta is an extremely rare anomaly that can severely affect the distal trachea and mainstem bronchi, resulting in severe respiratory symptoms. We report the case of a patient with circumflex aortic arch and severe left mainstem bronchial obstruction and malacia in which the external aortic compression and residual bronchomalacia were addressed with direct bronchial and tracheal intervention.
[Mh] Termos MeSH primário: Aorta Torácica/anormalidades
Aorta Torácica/cirurgia
Brônquios/cirurgia
Broncomalácia/cirurgia
Traqueia/cirurgia
[Mh] Termos MeSH secundário: Brônquios/anormalidades
Broncopatias/cirurgia
Broncoscopia
Constrição Patológica/cirurgia
Feminino
Seres Humanos
Lactente
Radiografia Torácica
Tomografia Computadorizada por Raios X
Traqueia/anormalidades
Estenose Traqueal/cirurgia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1703
[Cu] Atualização por classe:170817
[Lr] Data última revisão:
170817
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:160626
[St] Status:MEDLINE


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[PMID]:25800226
[Au] Autor:Sadreameli SC; McGrath-Morrow SA
[Ad] Endereço:Johns Hopkins University. Electronic address: ssadrea1@jhmi.edu.
[Ti] Título:Respiratory Care of Infants and Children with Congenital Tracheo-Oesophageal Fistula and Oesophageal Atresia.
[So] Source:Paediatr Respir Rev;17:16-23, 2016 Jan.
[Is] ISSN:1526-0550
[Cp] País de publicação:England
[La] Idioma:eng
[Ab] Resumo:Despite acute respiratory and chronic respiratory and gastro-intestinal complications, most infants and children with a history of oesophageal atresia / trachea-oesophageal fistula [OA/TOF] can expect to live a fairly normal life. Close multidisciplinary medical and surgical follow-up can identify important co-morbidities whose treatment can improve symptoms and optimize pulmonary and nutritional outcomes. This article will discuss the aetiology, classification, diagnosis and treatment of congenital TOF, with an emphasis on post-surgical respiratory management, recognition of early and late onset complications, and long-term clinical outcomes.
[Mh] Termos MeSH primário: Hiper-Reatividade Brônquica/terapia
Broncomalácia/terapia
Atresia Esofágica/cirurgia
Aspiração Respiratória/terapia
Fístula Traqueoesofágica/cirurgia
Traqueomalácia/terapia
[Mh] Termos MeSH secundário: Assistência ao Convalescente
Hiper-Reatividade Brônquica/epidemiologia
Broncomalácia/epidemiologia
Criança
Pré-Escolar
Comorbidade
Transtornos de Deglutição/epidemiologia
Transtornos de Deglutição/terapia
Atresia Esofágica/diagnóstico por imagem
Atresia Esofágica/epidemiologia
Transtornos da Motilidade Esofágica/epidemiologia
Transtornos da Motilidade Esofágica/terapia
Estenose Esofágica/epidemiologia
Estenose Esofágica/terapia
Refluxo Gastroesofágico/epidemiologia
Refluxo Gastroesofágico/terapia
Seres Humanos
Lactente
Recém-Nascido
Aspiração Respiratória/epidemiologia
Fístula Traqueoesofágica/diagnóstico por imagem
Fístula Traqueoesofágica/epidemiologia
Traqueomalácia/epidemiologia
Disfunção da Prega Vocal/epidemiologia
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1701
[Cu] Atualização por classe:170210
[Lr] Data última revisão:
170210
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:150325
[St] Status:MEDLINE


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[PMID]:26593083
[Au] Autor:Amin RS; Rutter MJ
[Ad] Endereço:Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, 3333 Burnet Avenue, Cincinnati, OH 45229, USA; Department of Pediatrics, University of Cincinnati College of Medicine, 231 Albert Sabin Way, Cincinnati, OH 45267, USA. Electronic address: Raouf.Amin@cchmc.org.
[Ti] Título:Airway Disease and Management in Bronchopulmonary Dysplasia.
[So] Source:Clin Perinatol;42(4):857-70, 2015 Dec.
[Is] ISSN:1557-9840
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:This article presents an overview of the diagnosis and management of airway problems encountered in infants with severe bronchopulmonary dysplasia (BPD). Respiratory failure in premature infants develops as a result of parenchymal and airway diseases. The survival of increasingly premature infants and the ventilatory support required by premature lungs may result in airway disease. The management of respiratory failure depends on whether it is primarily caused by parenchymal versus airway diseases. Continuous airway pressure early in the neonatal period has favorably changed the incidence of BPD. This article discusses the indications, timing, and guidelines for care of tracheotomy.
[Mh] Termos MeSH primário: Broncomalácia/terapia
Displasia Broncopulmonar/terapia
Pressão Positiva Contínua nas Vias Aéreas/métodos
Laringoestenose/terapia
Síndrome do Desconforto Respiratório do Recém-Nascido/terapia
Traqueomalácia/terapia
[Mh] Termos MeSH secundário: Broncomalácia/complicações
Displasia Broncopulmonar/complicações
Seres Humanos
Recém-Nascido
Recém-Nascido Prematuro
Laringoestenose/complicações
Respiração Artificial/métodos
Traqueobroncomalácia/complicações
Traqueobroncomalácia/terapia
Traqueomalácia/complicações
Traqueotomia/métodos
Desmame do Respirador
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1609
[Cu] Atualização por classe:151123
[Lr] Data última revisão:
151123
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:151124
[St] Status:MEDLINE



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