دورية أكاديمية
Functional capacity and quality of life in children and adolescents with sickle cell anemia.
| العنوان: | Functional capacity and quality of life in children and adolescents with sickle cell anemia. |
|---|---|
| المؤلفون: | Silva JLD; University Nove de Julho, UNINOVE, Sao Paulo, Sao Paulo, Brazil., Soares BA; Department of Physical Therapy, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil., Silva JC; University Nove de Julho, UNINOVE, Sao Paulo, Sao Paulo, Brazil., Blum PB; Darcy Vargas Children's Hospital, Sao Paulo, Sao Paulo, Brazil., Reimberg MM; University Nove de Julho, UNINOVE, Sao Paulo, Sao Paulo, Brazil., Corso SD; University Nove de Julho, UNINOVE, Sao Paulo, Sao Paulo, Brazil., Lanza FC; University Nove de Julho, UNINOVE, Sao Paulo, Sao Paulo, Brazil.; Department of Physical Therapy, Universidade Federal de Minas Gerais (UFMG), Belo Horizonte, Minas Gerais, Brazil. |
| المصدر: | Pediatric pulmonology [Pediatr Pulmonol] 2023 Apr; Vol. 58 (4), pp. 1100-1105. Date of Electronic Publication: 2023 Feb 02. |
| نوع المنشور: | Journal Article |
| اللغة: | English |
| بيانات الدورية: | Publisher: Wiley-Liss Country of Publication: United States NLM ID: 8510590 Publication Model: Print-Electronic Cited Medium: Internet ISSN: 1099-0496 (Electronic) Linking ISSN: 10990496 NLM ISO Abbreviation: Pediatr Pulmonol Subsets: MEDLINE |
| أسماء مطبوعة: | Publication: <2005-> : Hoboken, NJ : Wiley-Liss Original Publication: [Philadelphia, PA] : W.B. Saunders, [c1985- |
| مواضيع طبية MeSH: | Quality of Life* , Anemia, Sickle Cell*, Humans ; Child ; Adolescent ; Cross-Sectional Studies ; Reproducibility of Results ; Walking/physiology |
| مستخلص: | Objective: To evaluate the functional and exercise capacity, lung function, quality of life of children and adolescents with sickle cell anemia (SCA HbSS) and to test the reproducibility of functional capacity tests in this population. Method: Cross-sectional study with volunteers with SCA Hb-SS (SCAG), aged 6-18 years matched in age and gender to the control group (CG) with healthy individuals. Spirometry, 5-repetition sit-to-stand test (5STS-test), modified shuttle test (MST), and Pediatric Quality of Life Questionnaire (PedsQL) were performed. The reproducibility of 5STS-test and MST was evaluated: RESULTS: Forty eight volunteers of SCAG and 48 of CG were evaluated. Lung function of SCAG (FVC: 92 ± 15% pred.; FEV Conclusion: Children and adolescents with sickle cell anemia presented worse capacity to walk or run, and to perform sit-to-stand test when compared with their control peers. Additionally, they have poorer quality of life. The MST and 5STS-test showed good reproducibility to be applied in pediatric individuals with SCA. (© 2023 Wiley Periodicals LLC.) |
| References: | Vieira AK, Alvim CG, Carneiro MCM, et al. Pulmonary function in children and adolescents with sickle cell disease: have we paid proper attention to this problem? J Brasileiro Pneumol. 2016;42(6):409-415. Haupt HM, Moore GW, Bauer TW, Hutchins GM. The lung in sickle cell disease. Chest. 1982;81(3):332-337. Hostyn SV, de Carvalho WB, Johnston C, Braga JAP. Evaluation of functional capacity for exercise in children and adolescents with sickle-cell disease through the six-minute walk test. J Pediatr. 2013;89(6):588-594. Barbeau P, Woods KF, Ramsey LT, et al. Exercise in sickle cell anemia: effect on inflammatory and vasoactive mediators. Endothelium. 2001;8(2):147-155. Souza LCNA, Viegas CAA. Qualidade de sono e função pulmonar em adolescentes portadores de anemia falciforme clinicamente estáveis. J Brasileiro Pneumolog. 2007;33(3):275-281. Silva LBP, Mercês de Jesus G, Bessa Junior J, et al. Exercise capacity and biomarkers among children and adolescents with sickle cell disease. Pediatr Exerc Sci. 2022:1-8. Agha H, El Tagui M, El Ghamrawy M, Hady MA. The 6-min walk test: an independent correlate of elevated tricuspid regurgitant jet velocity in children and young adult sickle cell patients. Ann Hematol. 2014;93(7):1131-1138. Gomes ÉLFD, Sampaio LMM, Costa IP, et al. Analysis of autonomic modulation during maximal and submaximal work rate and functional capacity in asthmatic children. J Asthma. 2013;50:613-618. Tsopanoglou SP, Davidson J, Goulart AL, de Moraes Barros MC, dos Santos AMN. Functional capacity during exercise in very low birth weight premature children. Pediatr Pulmonol. 2014;49:91-98. Selvadurai HC, Cooper PJ, Meyers N, et al. Validation of shuttle tests in children with cystic fibrosis. Pediatr Pulmonol. 2003;35:133-138. Lanza FC, Reimberg MM, Ritti-Dias R, et al. Validation of the modified shuttle test to predict peak oxygen uptake in youth asthma patients under regular treatment. Front Physiol. 2018;9:9199. Combret Y, Boujibar F, Gennari C, et al. Measurement properties of the one-minute sit-to-stand test in children and adolescents with cystic fibrosis: A multicenter randomized cross-over trial. PLoS One. 2021;16(2):e0246781. Zeren M, Gurses HN, Denizoglu Kulli H, Ucgun H, Cakir E. Sit-to-stand test in children with bronchiectasis: does it measure functional exercise capacity? Heart & Lung. 2020;49(6):796-802. Thorpe N, Harniess P, Main E, et al. Feasibility, safety and acceptability of select outcome measures in a physiotherapy study protocol for boys with haemophilia. Pilot Feasibility Stud. 2021;7(1):105. doi:10.1186/s40814-021-00831-1. Nielsen MKF, Christensen JF, Frandsen TL, et al. Testing physical function in children undergoing intense cancer treatment-a RESPECT feasibility study. Pediatr Blood Cancer. 2018;65(8):e27100. Miller MR, JHankinson J, Brusasco V, et al. Standardisation of spirometry. Eur Respir J 2005;26:319-338. Pereira CA. Espirometria. diretrizes para testes de função pulmonar. J Bras Pneumol. 2002;28:S1-S82. Laveneziana P, Albuquerque A, Aliverti A, et al. ERS statement on respiratory muscle testing at rest and during exercise. Eur Respir J. 2019;53:1801214. Lanza FC, Santos MLM, Selman JPR, et al. Reference equation for respiratory pressures in pediatric population: a multicenter study. PLoS One. 2015;10(8):e0135662. Klatchoian DA, Len CA, Terreri MTRA, et al. Qualidade de vida de crianças e adolescentes de são paulo: confiabilidade e validade da versão brasileira do questionário genérico pediatric quality of life Inventory™ versão 4.0. J Pediatr. 2008;84(4):308-315. Varni JW, Seid M, Rode CA. The PedsQL: measurement model for the pediatric quality of life inventory. Med Care. 1999;37:126-139. Bradley J, Howard J, Wallace E, Elborn S. Reliability, repeatability, and sensitivity of the modified shuttle test in adult cystic fibrosis. Chest. 2000;117(6):1666-1671. Lanza FC, Zagatto EP, Silva JC, et al. Reference equation for the incremental shuttle walk test in children and adolescents. J Pediatr. 2015;167(5):1057-1061. Sim J, Wright CC. The kappa statistic in reliability studies: use, interpretation, and sample size requirements. Phys Ther. 2005;85(3):257-268. Connes P, Machado R, Hue O, Reid H. Exercise limitation, exercise testing and exercise recommendations in sickle cell anemia. Clin Hemorheol Microcirc. 2011;49(1-4):151-163. Petto J, Jesus JB, Vasques LMR, et al. Resting blood lactate in individuals with sickle cell disease. Rev Bras Hematol Hemoter. 2011;33(1):26-30. Ohara DG, Ruas G, Castro SS, Martins PRJ, Walsh IAP. Musculoskeletal pain, profile and quality of life of individuals with sickle cell disease. Braz J Phys Ther. 2012;16(5):431-438. Campbell A, Minniti CP, Nouraie M, et al. Prospective evaluation of haemoglobin oxygen saturation at rest and after exercise in paediatric sickle cell disease patients. Br J Haematol. 2009;147(3):352-359. Barden EM, et al. Total resting energy expenditure in children with sickle cell disease. J Pediatr. 2000;36(1):73-79. Al-Saqladi AWM, Cipolotti R, Fijnvandraat K, Brabin B. Growth and nutritional status of children with homozygous sickle cell disease. Ann Trop Paediatr. 2008;28(3):165-189. Novelli EM, Gladwin MT. Crises in sickle cell disease. Chest. 2016;149(4):1082-1093. Chaudry RA, Cikes M, Karu T, et al. Paediatric sickle cell disease: pulmonary hypertension but normal vascular resistance. Arch Dis Child. 2011;96(2):131-136. Tanaka H, Monahan KD, Seals DR. Age - predicted maximal heart rate revisited. JACC. 2001;37(1):153-156. Waltz X, Romana M, Lalanne Mistrih ML, et al. Hematologic and hemorheological determinants of resting and exercise-induced hemoglobin oxygen desaturation in children with sickle cell disease. Haematologica. 2013;98:1039-1044. Panepinto JA, O'Mahar KM, DeBaun MR, Loberiza FR, Scott JP. Health-related quality of life in children with sickle cell disease: child and parent perception. Br J Haematol. 2005;130:437-444. Buchowski MS, Townsend KM, Williams R, Chen KY. Patterns and energy expenditure of free-living physical activity in adolescents with sickle cell anemia. J Pediatr. 2002;140(1):86-92. Bohannon, Richard, RW. Test-retest reliability of the Five-Repetition Sit-to-Stand test: a systematic review of the literature involving adults. J Strength Cond Res. 2011;25(11):3205-3207. |
| فهرسة مساهمة: | Keywords: adolescents; children; exercise; functional capacity; sickle cell anemia |
| تواريخ الأحداث: | Date Created: 20230103 Date Completed: 20230320 Latest Revision: 20230425 |
| رمز التحديث: | 20231215 |
| DOI: | 10.1002/ppul.26300 |
| PMID: | 36593732 |
| قاعدة البيانات: | MEDLINE |
Full Text Finder كن أول من يترك تعليقا!