Please use this identifier to cite or link to this item:
https://dora.health.qld.gov.au/qldresearchjspui/handle/1/3229
Title: | How Many Maneuvers Should We Do for Maximal Inspiratory and Expiratory Muscle Pressure Testing in Children: A Retrospective Review in Children with Cystic Fibrosis | Authors: | McElrea, M. S. Marchant, J. M. Chang, Anne Boonjindasup, W. Irons, J. Y. |
Issue Date: | 2021 | Source: | 199, (2), 2021, p. 213-222 | Pages: | 213-222 | Journal: | Lung | Abstract: | Objectives: Maximal inspiratory pressure (MIP) and maximal expiratory pressure (MEP) could be useful clinical parameters in monitoring many conditions including cystic fibrosis (CF). However, current protocols for undertaking the measurements lack standardization including the number of repeated attempts to achieve best values. We aimed to (a) determine the optimum number of attempts to achieve best MIP/MEP values, and (b) evaluate if the number of attempts is consistent across two different test days. Methods: We analyzed data of a previous randomized controlled trial involving the effect of singing on respiratory muscle strength in 35 children with CF. On two different days (T1, T2) children performed MIP/MEP with at least ten attempts each to achieve < 10% repeatability. Results: All children achieved repeatable MIP/MEP values within 10–11 attempts with 24 (68.6%) and 26 (74.3%) of these achieving best values of MIP and MEP, respectively, at attempts 6–11. Median values of the pressures by three, five, eight and all attempts significantly increased with more attempts (all p < 0.05). At T2, 56% required fewer attempts to achieve best values, but 32% required more attempts, indicating that the number of attempts required was inconsistent between test days. Conclusion: It is likely that at least ten attempts (best two within < 10% variability) is required to achieve best and reliable MIP/MEP in children with CF. A larger sample size in children with CF and various conditions is required to consolidate these findings.L20104969712021-03-01 | DOI: | 10.1007/s00408-021-00422-0 | Resources: | https://www.embase.com/search/results?subaction=viewrecord&id=L2010496971&from=exporthttp://dx.doi.org/10.1007/s00408-021-00422-0 | | Keywords: | clinical article;controlled study;cystic fibrosis;female;follow up;forced expiratory volume;forced vital capacity;human;lung function;lung function test;male;maximal expiratory pressure;article;maximal respiratory pressure;muscle strength;priority journal;randomized controlled trial;randomized controlled trial (topic);retrospective study;singing;spirometry;manometeradolescent;maximal inspiratory pressure;body mass;breathing muscle;child | Type: | Article |
Appears in Sites: | Children's Health Queensland Publications |
Show full item record
Items in DORA are protected by copyright, with all rights reserved, unless otherwise indicated.