João Bruno Piantino Dias Moura Silveira, Aida Luiza Ribeiro Turquetto, Luciana Patrick Amato, Daniela Regina Agostinho, Luiz Fernando Caneo, Maria Angelica Binotto, Maria Isabel da Costa Soares Lopes, Joaquim Carlos Rodrigues, Marcus Vinicius Barbosa Santos, Patricia Alves Oliveira, Ana Cristina Sayuri TanaKa, Marcelo Biscegli Jatene
{"title":"方坦手术后儿童与健康儿童呼吸和功能结果的比较分析。","authors":"João Bruno Piantino Dias Moura Silveira, Aida Luiza Ribeiro Turquetto, Luciana Patrick Amato, Daniela Regina Agostinho, Luiz Fernando Caneo, Maria Angelica Binotto, Maria Isabel da Costa Soares Lopes, Joaquim Carlos Rodrigues, Marcus Vinicius Barbosa Santos, Patricia Alves Oliveira, Ana Cristina Sayuri TanaKa, Marcelo Biscegli Jatene","doi":"10.1007/s00246-024-03666-8","DOIUrl":null,"url":null,"abstract":"<p><p>Studies have shown that respiratory muscle training enhances functional capacity and pulmonary function in Fontan patients. However, diaphragm muscle characteristics in Fontan children have not been fully elucidated. The aim of this study was to compare respiratory function, maximal and submaximal functional capacities, and quality of life, as well as to assess diaphragm mobility and thickness, between Fontan patients aged 8 to 12 years and healthy individuals. This cross-sectional study included 45 children-27 Fontan patients, Fontan Group (FG) and 18 healthy control Group (CG) subjects. Different examinations were performed: spirometry was used to analyze pulmonary volume and capacity; manovacuometry was used to determine respiratory muscle strength; chest ultrasound was used to determine diaphragm muscle characteristics; cardiopulmonary exercise and the six-minute walk test (6MWT) were used to determine functional capacity; the AUQEI questionnaire was used to determine quality of life. Descriptive analysis and intergroup comparisons were performed for all the data. Compared with the CG, the FG exhibited impaired pulmonary function and reduced functional capacity. Significant differences in median values were noted for forced expiratory volume in one second (FEV<sub>1</sub>): 2.39 L/min, p = 0.002; forced vital capacity (FVC): 1.73 vs. 3.06 L/min, p = 0.002; maximal inspiratory pressure: - 73 vs. - 117 cmH<sub>2</sub>O, p = 0.007; absolute peak VO<sub>2</sub>: 1.09 vs. 1.51 L/min, p < 0.001; relative peak VO<sub>2</sub>: 31.9 vs. 42.5 mL/kg/min, p = 0.003; and 6MWT distance: 420 vs. 586 m, p < 0.001. Diaphragmatic thickness, mobility and quality of life were similar between the groups. Despite the reduced functional capacity, impaired pulmonary volume and capacity, and respiratory muscle weakness of the FG compared to those of the CG, the diaphragm characteristics and quality of life were similar between the groups.</p>","PeriodicalId":19814,"journal":{"name":"Pediatric Cardiology","volume":" ","pages":""},"PeriodicalIF":1.5000,"publicationDate":"2024-10-21","publicationTypes":"Journal Article","fieldsOfStudy":null,"isOpenAccess":false,"openAccessPdf":"","citationCount":"0","resultStr":"{\"title\":\"Comparative Analysis of Respiratory and Functional Outcomes in Children Post-Fontan Procedure Versus Healthy Peers.\",\"authors\":\"João Bruno Piantino Dias Moura Silveira, Aida Luiza Ribeiro Turquetto, Luciana Patrick Amato, Daniela Regina Agostinho, Luiz Fernando Caneo, Maria Angelica Binotto, Maria Isabel da Costa Soares Lopes, Joaquim Carlos Rodrigues, Marcus Vinicius Barbosa Santos, Patricia Alves Oliveira, Ana Cristina Sayuri TanaKa, Marcelo Biscegli Jatene\",\"doi\":\"10.1007/s00246-024-03666-8\",\"DOIUrl\":null,\"url\":null,\"abstract\":\"<p><p>Studies have shown that respiratory muscle training enhances functional capacity and pulmonary function in Fontan patients. However, diaphragm muscle characteristics in Fontan children have not been fully elucidated. The aim of this study was to compare respiratory function, maximal and submaximal functional capacities, and quality of life, as well as to assess diaphragm mobility and thickness, between Fontan patients aged 8 to 12 years and healthy individuals. This cross-sectional study included 45 children-27 Fontan patients, Fontan Group (FG) and 18 healthy control Group (CG) subjects. Different examinations were performed: spirometry was used to analyze pulmonary volume and capacity; manovacuometry was used to determine respiratory muscle strength; chest ultrasound was used to determine diaphragm muscle characteristics; cardiopulmonary exercise and the six-minute walk test (6MWT) were used to determine functional capacity; the AUQEI questionnaire was used to determine quality of life. Descriptive analysis and intergroup comparisons were performed for all the data. Compared with the CG, the FG exhibited impaired pulmonary function and reduced functional capacity. Significant differences in median values were noted for forced expiratory volume in one second (FEV<sub>1</sub>): 2.39 L/min, p = 0.002; forced vital capacity (FVC): 1.73 vs. 3.06 L/min, p = 0.002; maximal inspiratory pressure: - 73 vs. - 117 cmH<sub>2</sub>O, p = 0.007; absolute peak VO<sub>2</sub>: 1.09 vs. 1.51 L/min, p < 0.001; relative peak VO<sub>2</sub>: 31.9 vs. 42.5 mL/kg/min, p = 0.003; and 6MWT distance: 420 vs. 586 m, p < 0.001. Diaphragmatic thickness, mobility and quality of life were similar between the groups. 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引用次数: 0
摘要
研究表明,呼吸肌训练可提高丰坦患者的功能能力和肺功能。然而,丰坦儿童的膈肌特征尚未完全阐明。本研究旨在比较 8 至 12 岁丰坦患者和健康人的呼吸功能、最大和次最大功能能力、生活质量,并评估膈肌的活动度和厚度。这项横断面研究包括45名儿童--27名Fontan患者、Fontan组(FG)和18名健康对照组(CG)。研究人员进行了不同的检查:肺活量测定用于分析肺容量和肺活量;压力测定用于确定呼吸肌力量;胸部超声波用于确定膈肌特征;心肺运动和六分钟步行测试(6MWT)用于确定功能能力;AUQEI问卷用于确定生活质量。对所有数据进行了描述性分析和组间比较。与 CG 相比,FG 的肺功能受损,功能能力下降。一秒钟用力呼气容积(FEV1)的中位值存在显著差异:2.39 L/min,p = 0.002;用力肺活量(FVC):1.73 vs. 3.06 L/min,p = 0.003:1.73 vs. 3.06 L/min,p = 0.002;最大吸气压力:- 73 vs. - 117 cmH2O,p = 0.007;绝对峰值 VO2:1.09 vs. 1.51 L/min,p 2:31.9 vs. 42.5 mL/kg/min,p = 0.003;6MWT 距离:420 vs. 586 m,p = 0.003:420 米对 586 米,p
Comparative Analysis of Respiratory and Functional Outcomes in Children Post-Fontan Procedure Versus Healthy Peers.
Studies have shown that respiratory muscle training enhances functional capacity and pulmonary function in Fontan patients. However, diaphragm muscle characteristics in Fontan children have not been fully elucidated. The aim of this study was to compare respiratory function, maximal and submaximal functional capacities, and quality of life, as well as to assess diaphragm mobility and thickness, between Fontan patients aged 8 to 12 years and healthy individuals. This cross-sectional study included 45 children-27 Fontan patients, Fontan Group (FG) and 18 healthy control Group (CG) subjects. Different examinations were performed: spirometry was used to analyze pulmonary volume and capacity; manovacuometry was used to determine respiratory muscle strength; chest ultrasound was used to determine diaphragm muscle characteristics; cardiopulmonary exercise and the six-minute walk test (6MWT) were used to determine functional capacity; the AUQEI questionnaire was used to determine quality of life. Descriptive analysis and intergroup comparisons were performed for all the data. Compared with the CG, the FG exhibited impaired pulmonary function and reduced functional capacity. Significant differences in median values were noted for forced expiratory volume in one second (FEV1): 2.39 L/min, p = 0.002; forced vital capacity (FVC): 1.73 vs. 3.06 L/min, p = 0.002; maximal inspiratory pressure: - 73 vs. - 117 cmH2O, p = 0.007; absolute peak VO2: 1.09 vs. 1.51 L/min, p < 0.001; relative peak VO2: 31.9 vs. 42.5 mL/kg/min, p = 0.003; and 6MWT distance: 420 vs. 586 m, p < 0.001. Diaphragmatic thickness, mobility and quality of life were similar between the groups. Despite the reduced functional capacity, impaired pulmonary volume and capacity, and respiratory muscle weakness of the FG compared to those of the CG, the diaphragm characteristics and quality of life were similar between the groups.
期刊介绍:
The editor of Pediatric Cardiology welcomes original manuscripts concerning all aspects of heart disease in infants, children, and adolescents, including embryology and anatomy, physiology and pharmacology, biochemistry, pathology, genetics, radiology, clinical aspects, investigative cardiology, electrophysiology and echocardiography, and cardiac surgery. Articles which may include original articles, review articles, letters to the editor etc., must be written in English and must be submitted solely to Pediatric Cardiology.