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[PMID]:29224761
[Au] Autor:Propst EJ; Zawawi F; Kirsch RE; Honjo O
[Ad] Endereço:Department of Otolaryngology-Head and Neck Surgery, Hospital for Sick Children, University of Toronto, Toronto, Ontario, Canada. Electronic address: Evan.propst@utoronto.ca.
[Ti] Título:Direct tracheobronchopexy via left lateral thoracotomy for severe tracheobronchomalacia.
[So] Source:Int J Pediatr Otorhinolaryngol;103:32-35, 2017 Dec.
[Is] ISSN:1872-8464
[Cp] País de publicação:Ireland
[La] Idioma:eng
[Ab] Resumo:An infant with pulmonary atresia/ventricular septal defect/major aortopulmonary collateral arteries underwent unifocalization, ventriculoseptal defect closure and placement of a right ventricle to pulmonary artery conduit via median sternotomy. Aortopexy and pulmonary arteriopexy via redo sternotomy were insufficient to allow weaning of continuous positive airway pressure and he required direct tracheobronchopexy via left lateral thoracotomy to alleviate posterior trachealis intrusion along the length of the trachea and left main bronchus. He also underwent laryngotracheoplasty with placement of a posterior costal cartilage graft for bilateral vocal cord paralysis. The patient was weaned from positive pressure and discharged in stable condition.
[Mh] Termos MeSH primário: Brônquios/cirurgia
Toracotomia/métodos
Traqueia/cirurgia
Traqueobroncomalácia/cirurgia
[Mh] Termos MeSH secundário: Broncoscopia
Circulação Colateral
Comunicação Interventricular/cirurgia
Seres Humanos
Lactente
Masculino
Artéria Pulmonar/cirurgia
Atresia Pulmonar/cirurgia
Tomografia Computadorizada por Raios X
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1712
[Cu] Atualização por classe:171226
[Lr] Data última revisão:
171226
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:171212
[St] Status:MEDLINE


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[PMID]:28901225
[Au] Autor:Rabinowitz EJ; Epstein S; Kohn N; Meyer DB
[Ad] Endereço:1 Division of Pediatric Cardiology, Cohen Children's Heart Center, Cohen Children's Medical Center of New York-Hofstra Northwell School of Medicine, New Hyde Park, NY, USA.
[Ti] Título:Promoting Pulmonary Arterial Growth via Right Ventricle-to-Pulmonary Artery Connection in Children With Pulmonary Atresia, Ventricular Septal Defect, and Hypoplastic Pulmonary Arteries.
[So] Source:World J Pediatr Congenit Heart Surg;8(5):564-569, 2017 Sep.
[Is] ISSN:2150-136X
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Complete repair of pulmonary atresia (PA) ventricular septal defect (VSD) with hypoplastic or absent native pulmonary arteries, often with major aortopulmonary collateral arteries (MAPCAs), involves construction of an adequate sized pulmonary arterial tree. We report our results with a previously described staged strategy using initial right ventricle (RV)-to-reconstructed pulmonary arterial tree (RV-PA) connection to promote pulmonary arterial growth and facilitate later ventricular septation. METHODS: We retrospectively reviewed data for all patients (N = 10) with initial echocardiographic diagnosis of PA-VSD and hypoplastic pulmonary arteries operated in our center from October 2008 to August 2016. Pulmonary arterial vessel size measured on preoperative and postoperative angiography was used to calculate Nakata index. RESULTS: Seven patients had PA-VSD, three had virtual PA-VSD, and seven had MAPCAs. All underwent creation of RV-PA connection at a median age of 7.5 days and weight 3.6 kg. Eight patients had RV-PA conduits, two had a transannular patches, and seven had major pulmonary artery reconstruction simultaneously. There were no deaths or serious morbidity; one conduit required revision prior to complete repair. Complete repair with ventricular septation and RV pressure less than half systemic was achieved in all patients at a median age of 239 days. Nakata index in neonatal period was 54 mm /m (range 15-144 mm /m ) and at time of septation 184 mm /m (range 56-510 mm /m ; P = .004). Growth rates of right and left branch pulmonary arteries were similar. The 10 patients underwent 28 catheterizations with 13 interventions in 8 patients prior to full repair. CONCLUSION: Early palliative RV-PA connection promotes pulmonary arterial growth and facilitates eventual full repair with VSD closure with low RV pressure and operative risk.
[Mh] Termos MeSH primário: Anormalidades Múltiplas
Comunicação Interventricular/cirurgia
Ventrículos do Coração/cirurgia
Artéria Pulmonar/cirurgia
Atresia Pulmonar/cirurgia
[Mh] Termos MeSH secundário: Criança
Pré-Escolar
Ecocardiografia
Feminino
Comunicação Interventricular/diagnóstico
Ventrículos do Coração/anormalidades
Ventrículos do Coração/diagnóstico por imagem
Seres Humanos
Lactente
Masculino
Período Pós-Operatório
Artéria Pulmonar/diagnóstico por imagem
Atresia Pulmonar/diagnóstico
Estudos Retrospectivos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171012
[Lr] Data última revisão:
171012
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170914
[St] Status:MEDLINE
[do] DOI:10.1177/2150135117717266


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[PMID]:28870391
[Au] Autor:Hobbes B; d'Udekem Y; Zannino D; Konstantinov IE; Brizard C; Brink J
[Ad] Endereço:Department of Cardiac Surgery, Royal Children's Hospital, Melbourne, Australia; Heart Research Group, Murdoch Children's Research Institute, Melbourne, Australia.
[Ti] Título:Determinants of Adverse Outcomes After Systemic-To-Pulmonary Shunts in Biventricular Circulation.
[So] Source:Ann Thorac Surg;104(4):1365-1370, 2017 Oct.
[Is] ISSN:1552-6259
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Systemic-to-pulmonary shunts are useful palliative procedures, although many teams have been deterred by high mortality and morbidity. We aimed to identify predictors of adverse outcomes after shunts in biventricular lesions. METHODS: From 2004 to 2014, 173 children had shunt procedures. Morphologies included: tetralogy of Fallot, pulmonary atresia with ventricular septal defect (VSD) with and without major aortopulmonary collaterals (MAPCAs), transposition of great arteries with pulmonary stenosis, and double outlet right ventricle. Median age was 22 days (range, 3 to 3,438 days) and median weight 3.2 kg (range, 1.7 to 20 kg). Shunt sizes ranged from 3 to 5 mm with median shunt size/weight ratio 1.03 mm/kg (range, 0.3 to 2.5 mm/kg). RESULTS: In-hospital mortality was 5.2% for the initial shunt procedure. Inter-stage mortality was 3.6%. Overall, 86% of patients progressed to corrective surgery. Acute events were observed in 41 patients, leading to 6 deaths. Events included 30 emergency chest openings, 16 shunt thrombosis, and 17 pulmonary overcirculation. Independent predictors of acute events or in-hospital mortality were genetic or extracardiac anomalies (hazard ratio [HR] = 1.9, p = 0.04), and preoperative shock/acidosis (HR = 2.73, p = 0.003). Diagnosis of pulmonary atresia with VSD and MAPCAs was protective (HR = 0.23, p = 0.042). Weight, shunt size, and size/weight ratios were not significant risk factors. Shunt thrombosis occurred at a median 3 hours (range, 0 to 46 hours) postoperatively, leading to 33% of in-hospital deaths. Low postoperative oxygen saturation and higher platelet counts in intensive care were independent predictors of thrombosis (p = 0.022, p = 0.005 respectively). CONCLUSIONS: Early adverse events contribute to mortality and morbidity for the shunt procedure. Patients with lower oxygen saturation and higher platelet counts in the postoperative period are at higher risk of shunt thrombosis.
[Mh] Termos MeSH primário: Procedimento de Blalock-Taussig/efeitos adversos
Cardiopatias Congênitas/cirurgia
Mortalidade Hospitalar
Atresia Pulmonar/cirurgia
Trombose/etiologia
[Mh] Termos MeSH secundário: Procedimento de Blalock-Taussig/mortalidade
Criança
Pré-Escolar
Feminino
Cardiopatias Congênitas/mortalidade
Seres Humanos
Lactente
Recém-Nascido
Masculino
Oxigênio/sangue
Contagem de Plaquetas
Atresia Pulmonar/mortalidade
Estudos Retrospectivos
Fatores de Risco
Trombose/mortalidade
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Nm] Nome de substância:
S88TT14065 (Oxygen)
[Em] Mês de entrada:1710
[Cu] Atualização por classe:171010
[Lr] Data última revisão:
171010
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170906
[St] Status:MEDLINE


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[PMID]:28823330
[Au] Autor:Luxford JC; Arora N; Ayer JG; Verrall CE; Cole AD; Orr Y; d'Udekem Y; Sholler GF; Winlaw DS
[Ad] Endereço:Sydney Medical School, University of Sydney, Sydney, New South Wales, Australia.
[Ti] Título:Neonatal Ebstein Anomaly: A 30-year Institutional Review.
[So] Source:Semin Thorac Cardiovasc Surg;29(2):206-212, 2017 Summer.
[Is] ISSN:1532-9488
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:This study aimed to review our 30-year, single-center experience of neonates admitted with Ebstein anomaly. Between January 1985 and August 2015, 80 neonates with Ebstein anomaly were managed. The primary outcome measures were early and late survival, freedom from reoperation, and functional status. Pulmonary atresia or critical stenosis occurred in 18 neonates. Twenty-seven (34%) patients required intervention: 13 systemic-to-pulmonary shunts, 5 balloon pulmonary valvotomy, 3 relief of right ventricular outflow tract obstruction, 3 Starnes procedures, and 3 other procedures. Sixty-nine (86%) of the neonates survived to hospital discharge. Overall 15-year survival estimate was 67% (SE = 6.5), with a superior prognosis for those able to be managed medically (15-year survival of 79%, SE = 7.0) compared with those in whom surgical or catheter intervention was undertaken (15-year survival of 45%, SE = 11.2, P = 0.005). For early survivors of neonatal surgery, freedom from reoperation at 10 years was 16% (SE = 8.5). For long-term survivors, 96% were classified as New York Heart Association Class I or II. Neonates with Ebstein anomaly who can be managed without intervention have a good prognosis. Substantial mortality risk remains in those who require intervention, especially those complicated by pulmonary atresia.
[Mh] Termos MeSH primário: Valvuloplastia com Balão
Procedimentos Cirúrgicos Cardíacos
Anomalia de Ebstein/cirurgia
Procedimentos Cirúrgicos Vasculares
[Mh] Termos MeSH secundário: Fatores Etários
Valvuloplastia com Balão/efeitos adversos
Valvuloplastia com Balão/mortalidade
Procedimentos Cirúrgicos Cardíacos/efeitos adversos
Procedimentos Cirúrgicos Cardíacos/mortalidade
Intervalo Livre de Doença
Anomalia de Ebstein/complicações
Anomalia de Ebstein/mortalidade
Anomalia de Ebstein/fisiopatologia
Feminino
Seres Humanos
Recém-Nascido
Estimativa de Kaplan-Meier
Masculino
New South Wales
Complicações Pós-Operatórias/etiologia
Complicações Pós-Operatórias/terapia
Modelos de Riscos Proporcionais
Atresia Pulmonar/complicações
Atresia Pulmonar/fisiopatologia
Retratamento
Estudos Retrospectivos
Fatores de Risco
Fatores de Tempo
Resultado do Tratamento
Procedimentos Cirúrgicos Vasculares/efeitos adversos
Procedimentos Cirúrgicos Vasculares/mortalidade
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:171005
[Lr] Data última revisão:
171005
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170822
[St] Status:MEDLINE


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[PMID]:28591888
[Au] Autor:Hahn F; Russe MF; Langer M
[Ti] Título:Unkorrigierte Pulmonalatresie mit Ventrikelseptumdefekt bei einer 31-jährigen Patientin: MRT-Untersuchung des Herzens zur Bestimmung der Anatomie und der Flüsse der aberranten Gefäße..
[So] Source:Rofo;189(6):547-548, 2017 Jun.
[Is] ISSN:1438-9010
[Cp] País de publicação:Germany
[La] Idioma:ger
[Mh] Termos MeSH primário: Técnicas de Imagem Cardíaca/métodos
Cardiopatias Congênitas/diagnóstico por imagem
Imagem por Ressonância Magnética/métodos
Atresia Pulmonar/diagnóstico por imagem
[Mh] Termos MeSH secundário: Adulto
Diagnóstico Diferencial
Feminino
Seres Humanos
Doenças Raras
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170830
[Lr] Data última revisão:
170830
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170608
[St] Status:MEDLINE
[do] DOI:10.1055/s-0043-101524


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[PMID]:28527961
[Au] Autor:Patrick WL; Mainwaring RD; Reinhartz O; Punn R; Tacy T; Hanley FL
[Ad] Endereço:Division of Pediatric Cardiac Surgery, Lucile Packard Children's Hospital/Stanford University, Stanford, California.
[Ti] Título:Major Aortopulmonary Collateral Arteries With Anatomy Other Than Pulmonary Atresia/Ventricular Septal Defect.
[So] Source:Ann Thorac Surg;104(3):907-916, 2017 Sep.
[Is] ISSN:1552-6259
[Cp] País de publicação:Netherlands
[La] Idioma:eng
[Ab] Resumo:BACKGROUND: Major aortopulmonary collateral arteries (MAPCAs) are frequently found in association with pulmonary atresia with ventricular septal defect (PA/VSD). However, some patients with MAPCAs do not have PA/VSD but have a variety of other "atypical" anatomic diagnoses. METHODS: This was a retrospective review of patients with MAPCAs and atypical anatomy. The 50 patients with MAPCAs could be divided into two subgroups: (1) single ventricle anatomy (n = 33) and (2) two ventricle anatomy (n = 17). RESULTS: The 33 patients with MAPCAs and single ventricle included 15 with unbalanced complete atrioventricular canal (CAVC), 6 with pulmonary atresia-intact ventricular septum, and 12 with other forms of single ventricle. The initial cardiac operation included unifocalization/shunt in 24 patients and creation of aortopulmonary window or central shunt in 9 patients. There were seven operative and eight late deaths. Sixteen patients have had a bidirectional Glenn procedure and 6 had a Fontan procedure. The 17 patients with MAPCAs and two ventricles included 5 with CAVC, 4 with corrected transposition, 3 with double outlet right ventricle, 3 with scimitar syndrome, and 2 with complex D-transposition. The initial cardiac operation included single-stage complete repair in 5 patients, unifocalization/shunt in 10 patients, and aortopulmonary window in 2 patients. There were two operative and two late deaths. Thirteen patients have achieved complete repair status. CONCLUSIONS: The data demonstrate the wide diversity of anatomy seen in patients with MAPCAs when evaluating diagnoses other than PA/VSD. Two-thirds of the patients had single ventricle and was associated with a relatively high mortality.
[Mh] Termos MeSH primário: Aorta Torácica/anormalidades
Circulação Colateral
Defeitos dos Septos Cardíacos/diagnóstico
Artéria Pulmonar/anormalidades
Atresia Pulmonar/diagnóstico
[Mh] Termos MeSH secundário: Angiografia
Aorta Torácica/diagnóstico por imagem
California/epidemiologia
Procedimentos Cirúrgicos Cardíacos/métodos
Procedimentos Cirúrgicos Cardíacos/mortalidade
Pré-Escolar
Ecocardiografia
Feminino
Seguimentos
Defeitos dos Septos Cardíacos/fisiopatologia
Defeitos dos Septos Cardíacos/cirurgia
Seres Humanos
Lactente
Masculino
Artéria Pulmonar/diagnóstico por imagem
Atresia Pulmonar/fisiopatologia
Atresia Pulmonar/cirurgia
Circulação Pulmonar
Estudos Retrospectivos
Taxa de Sobrevida/tendências
Fatores de Tempo
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170914
[Lr] Data última revisão:
170914
[Sb] Subgrupo de revista:AIM; IM
[Da] Data de entrada para processamento:170522
[St] Status:MEDLINE


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[PMID]:28520535
[Au] Autor:Awori MN; Mehta NP; Mitema FO; Kebba N
[Ad] Endereço:1 Department of Surgery, School of Medicine, College of Health Sciences, University of Nairobi, Nairobi, Kenya.
[Ti] Título:Optimal Z-Score Use in Surgical Decision-Making in Pulmonary Atresia With Intact Ventricular Septum.
[So] Source:World J Pediatr Congenit Heart Surg;8(3):385-388, 2017 May.
[Is] ISSN:2150-136X
[Cp] País de publicação:United States
[La] Idioma:eng
[Ab] Resumo:OBJECTIVES: In the surgical treatment of pulmonary atresia with intact ventricular septum, the size of the tricuspid valve annulus (as measured by z-scores) has emerged as a significant factor in deciding which repair to perform. Various tricuspid valve annulus z-scores are reported as "cutoffs" for successful biventricular repair. We aimed to determine whether the use of different z-score data sets contributed to the gross variation in "cutoffs" for successful biventricular repair reported in the literature. METHODS: A single search was made of PubMed using the "advanced" setting with the following search terms: pulmonary, atresia, intact, septum, z, and score. The filters "title" and "title/abstract" were used for the first four and last two terms, respectively; the instruction "AND" combined all terms. Articles that identified which z-score data set was used in patients with biventricular repairs were included. RESULTS: From 13 articles, 1,392 patients were studied, 410 (29.5%) of which achieved biventricular repair. Three z-score data sets were quoted; mean tricuspid valve annulus z-scores in biventricular repair patients ranged between -0.53 and -5.1. After correcting for discrepancies between z-score data sets, no study reported a mean tricuspid valve annulus z-score <-2.8 in biventricular repair patients and 83.3% reported mean tricuspid valve annuli z-scores >-1.7. CONCLUSION: The use of varied tricuspid valve annuli z-score data sets may have contributed to gross variations in reported "cutoffs" for successful biventricular repair. This could lead to inappropriate surgical pathway allocation.
[Mh] Termos MeSH primário: Procedimentos Cirúrgicos Cardíacos/métodos
Tomada de Decisões
Cardiopatias Congênitas/cirurgia
Atresia Pulmonar/cirurgia
[Mh] Termos MeSH secundário: Seres Humanos
Recém-Nascido
[Pt] Tipo de publicação:JOURNAL ARTICLE; REVIEW
[Em] Mês de entrada:1709
[Cu] Atualização por classe:170929
[Lr] Data última revisão:
170929
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170519
[St] Status:MEDLINE
[do] DOI:10.1177/2150135117701407


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[PMID]:28496023
[Au] Autor:Nagatomo Y; Muneuchi J; Watanabe M; Joo K; Ochiai Y
[Ad] Endereço:Department of Pediatrics, JCHO Kyushu Hospital.
[Ti] Título:Bilateral Coronary-Pulmonary Artery Fistulas in Pulmonary Atresia With Ventricular Septal Defect.
[So] Source:Int Heart J;58(3):463-465, 2017 May 31.
[Is] ISSN:1349-3299
[Cp] País de publicação:Japan
[La] Idioma:eng
[Ab] Resumo:We present a very rare case of bilateral coronary to pulmonary artery fistulas associated with pulmonary atresia with ventricular septal defect. The courses of coronary to pulmonary artery fistulas have to be clearly delineated by detailed angiography prior to corrective surgery.
[Mh] Termos MeSH primário: Anormalidades Múltiplas
Fístula Artério-Arterial/diagnóstico
Vasos Coronários
Defeitos dos Septos Cardíacos/diagnóstico
Artéria Pulmonar
Atresia Pulmonar/diagnóstico
[Mh] Termos MeSH secundário: Fístula Artério-Arterial/cirurgia
Procedimentos Cirúrgicos Cardíacos/métodos
Angiografia Coronária
Defeitos dos Septos Cardíacos/cirurgia
Seres Humanos
Recém-Nascido
Masculino
Atresia Pulmonar/cirurgia
[Pt] Tipo de publicação:CASE REPORTS; JOURNAL ARTICLE
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170809
[Lr] Data última revisão:
170809
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170513
[St] Status:MEDLINE
[do] DOI:10.1536/ihj.16-324


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[PMID]:28441832
[Au] Autor:Hong NC; Sun K
[Ti] Título:[Fetal cardiac interventions for pulmonary atresia].
[So] Source:Zhonghua Er Ke Za Zhi;55(4):311-314, 2017 Apr 02.
[Is] ISSN:0578-1310
[Cp] País de publicação:China
[La] Idioma:chi
[Mh] Termos MeSH primário: Doenças Fetais/terapia
Atresia Pulmonar/terapia
[Mh] Termos MeSH secundário: Coração Fetal
Seres Humanos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170807
[Lr] Data última revisão:
170807
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170427
[St] Status:MEDLINE
[do] DOI:10.3760/cma.j.issn.0578-1310.2017.04.017


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[PMID]:28441821
[Au] Autor:Zhao QM; Liu F; Wu L; Ye M; Jia B; Ma XJ; Huang GY
[Ad] Endereço:Pediatric Heart Center, Children's Hospital of Fudan University, Shanghai 201102, China.
[Ti] Título:[Assessment of undiagnosed critical congenital heart disease before discharge from the maternity hospital].
[So] Source:Zhonghua Er Ke Za Zhi;55(4):260-266, 2017 Apr 02.
[Is] ISSN:0578-1310
[Cp] País de publicação:China
[La] Idioma:chi
[Ab] Resumo:Undiagnosed critical congenital heart disease (CCHD) was assessed before discharge from maternity hospital.Basic information was provided for screening CCHD in the early neonatal stage.Chi-squared test was used for comparison of categorical variables(detection rate of different types of CCHD). A retrospective cohort study was conducted in neonates with CCHD who were admitted to Children's Hospital of Fudan University between 1 January 2012 and 31 December 2015. For comparing with the previously reported undiagnosed rate of CCHD at discharge, CCHD was defined as all duct dependent congenital heart disease (DDCHD) and any cyanotic CHD that required early surgery. A total of 1 036 infants with CCHD were included. The prenatal detection rate of CCHD was 14.04%(122/869). As a whole, 52.51% (544/1 036) of CCHD cases were undiagnosed at discharge, and 14.09%(146/1 036)were still missed after 6-week examination. The diagnoses most likely to be unrecognized at discharge included critical coarctation of the aorta (COA) (75.00%), total anomalous pulmonary venous connection (61.54%), pulmonary atresia (PA) with ventricle septal defect (VSD) (61.45%), single ventricle (SV) (60.10%) and critical aortic stenosis (52.94%). Among newborns diagnosed prior to discharge, 54.88% (270/492) due to symptom or prenatal ultrasonographic diagnosis, 45.12% (222/492) due to abnormal findings in routine examination. Among asymptomatic CCHD cases without prenatal diagnosis, 71.02% (544/766) were undiagnosed and the most common delayed diagnosis was SV (82.78%), interrupted aortic arch (81.82%), transposition of the great arteries with intact ventricular septum (79.63%), PA/VSD (79.07%), and critical COA (78.57%). Newborns with DDC were more likely to develop symptoms within the first few days after birth, in comparison with non-DDC cases. However, their detection rates were close to each other. The rate of misdiagnosis of CCHD before discharge from maternity hospitals is high in China, indicates the importance of implementation of CCHD screening in Chinese maternity hospitals, so as to give timely diagnosis and proper treatment.
[Mh] Termos MeSH primário: Cardiopatias Congênitas/diagnóstico
Triagem Neonatal
[Mh] Termos MeSH secundário: Coartação Aórtica
China
Diagnóstico Tardio
Erros de Diagnóstico
Feminino
Comunicação Interventricular
Hospitalização
Maternidades
Seres Humanos
Lactente
Recém-Nascido
Oximetria
Alta do Paciente
Diagnóstico Pré-Natal
Atresia Pulmonar
Estudos Retrospectivos
Transposição dos Grandes Vasos
[Pt] Tipo de publicação:JOURNAL ARTICLE
[Em] Mês de entrada:1708
[Cu] Atualização por classe:170807
[Lr] Data última revisão:
170807
[Sb] Subgrupo de revista:IM
[Da] Data de entrada para processamento:170427
[St] Status:MEDLINE
[do] DOI:10.3760/cma.j.issn.0578-1310.2017.04.006



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