Effects of immersion on the breathing parameters of patients with Duchenne muscular dystrophy
DOI:
https://doi.org/10.5935/0104-7795.20120005Keywords:
Muscular Dystrophy, Duchenne, Hydrotherapy, Immersion, Pulmonary VentilationAbstract
In many rehabilitation centers, Aquatic Physiotherapy is commonly used as an optional treatment for Duchenne Muscular dystrophy (DMD) patients. However, there is so little scientific evidence about the immersion effects on the breathing parameters of these patients. Objective: Our goal was to evaluate the immersion effects to the depth of the seventh cervical vertebra (C7), related to the breathing parameters in DMD patients. Method: Fifteen boys with DMD participated of the study, averaging 12 years in age. Clinical history and general information were investigated, and the following parameters were evaluated on the ground and inside the pool: Partial Oxygen Saturation (SpO2), heart rate (HR), maximal inspiratory (PI Max.) and expiratory (PE Max.) pressures, minute volume (MV), respiratory rate (RR), tidal volume (TV), Forced Vital Capacity (FVC) and peak expiratory flow (PEF). The SpO2 diminished after the aquatic evaluation when compared to values beforehand (p = 0.01). RR was higher inside the pool than outside (p = 0.02). PI Max. and PE Max. did not change inside the pool. Results: Analyzing the results for volumes, FVC and EPF were reduced inside the pool when compared to evaluation on solid ground (p = 0.004). MV and TV did not change. A positive correlation between ground and pool values of FVC and PEF was seen (FVC: r = 0.692, p = 0.006; EPF: r = 0.913, p = 0.0001). C7 immersion was able to reduce SpO2, FVC, and PEF, while increasing the RR of DMD patients. Conclusion: With the correlation between ground and pool values of FVC and PEF encountered in this study, there is a possibility of predicting pool values for these parameters using only the ground data. These findings could lead to a scientific base for a better Aquatic Physiotherapy prescription for DMD patients, at different pathology stages.
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References
Silva JDM, Costa KS, Cruz MC. Distrofia muscular de Duchenne: um enfoque cinesioterapêutico. Lato & Sensu. 2003;4(1):3-5.
Finder JD, Birnkrant D, Carl J, Farber HJ, Gozal D, Iannaccone ST, et al. Respiratory care of the patient with Duchenne muscular dystrophy: ATS consensus statement. Am J Respir Crit Care Med. 2004;170(4):456-65.
Slutzky, LC. Fisioterapia respiratória nas doenças neuromusculares. Rio de Janeiro: Revinter; 1997.
Inkley SR, Oldenburg FC, Vignos PJ Jr. Pulmonary function in Duchenne muscular dystrophy related to stage of disease. Am J Med. 1974;56(3):297-306.
McDonald CM, Abresch RT, Carter GT, Fowler WM Jr, Johnson ER, Kilmer DD,et al. Profiles of neuromuscular diseases. Duchenne muscular dystrophy. Am J Phys Med Rehabil. 1995;74(5 Suppl):S70-92.
Hapke EJ, Meek JC, Jacobs J. Pulmonary function in progressive muscular dystrophy. Chest. 1972;61(1):41-7.
Rideau Y, Jankowski LW, Grellet J. Respiratory function in the muscular dystrophies. Muscle Nerve. 1981;4(2):155-64.
Eäckman E, Nylander E. The heart in Duchenne muscular dystrophy: a non-invasive longitudinal study. Eur Heart J. 1992;13(9):1239-44.
Adams MA, Chandler LS. Effects of physical therapy program on vital capacity of patients with muscular dystrophy. Phys Ther. 1974;54(5):494-6.
Barbé F, Quera-Salva MA, McCann C, Gajdos P, Raphael JC, Lattre J, et al. Sleep-related respiratory disturbances in patients with Duchenne muscular dystrophy. Eur Respir J. 1994;7(8):1403-8.
Griggs RC, Donohoe KM, Utell MJ, Goldblatt D, Moxley RT 3rd. Evaluation of pulmonary function in neuromuscular disease. Arch Neurol. 1981;38(1):9-12.
Hahn A, Bach JR, Delaubier A, Renardel-Irani A, Guillou C, Rideau Y. Clinical implications of maximal respiratory pressure determinations for individuals with Duchenne muscular dystrophy. Arch Phys Med Rehabil. 1997;78(1):1-6.
Cole AJ, Becker BE. Comprehensive aquatic therapy. Philadelphia: Elsevier; 2004.
Taylor NA, Morrison JB. Lung volume changes in response to altered breathing gas pressure during upright immersion. Eur J Appl Physiol Occup Physiol. 1991;62(2):122-9.
Taylor NA, Morrison JB. Static and dynamic pulmonary compliance during upright immersion. Acta Physiol Scand. 1993;149(4):413-7.
Taylor NA, Morrison JB. Static respiratory muscle work during immersion with positive and negative respiratory loading. J Appl Physiol. 1999;87(4):1397-403.
Choukroun ML, Kays C, Varène P. Effects of water temperature on pulmonary volumes in immersed human subjects. Respir Physiol. 1989;75(3):255-65.
Arborelius M Jr, Ballidin UI, Lilja B, Lundgren CE. Hemodynamic changes in man during immersion with the head above water. Aerosp Med. 1972;43(6):592-8.
Hall J, Bisson D, O'Hare P. The physiology of immersion. Physiology. 1990;76:517-21.
Bach JR, Gonçalves MR. Noninvasive ventilation or paradigm paralysis? Eur Respir J. 2004;23(4):651.
Agostoni E, Gurtner G, Torri G, Rahn H. Respiratory mechanics during submersion and negativepressure breathing. J Appl Physiol. 1966;21(1):251-8.
Hong SK, Cerretelli P, Cruz JC, Rahn H. Mechanics of respiration during submersion in water. J Appl Physiol. 1969;27(4):535-8.
Hong SK, Ting EY, Rahn H. Lung volumes at different depths of submersion. J Appl Physiol. 1960;15:550-3.
Craig AB Jr, Ware DE. Effect of immersion in water on vital capacity and residual volume of the lungs. J Appl Physiol. 1967;23(4):423-5.
Carey CR, Schaefer KE, Alvis HJ. Effect of skin diving on lung volumes. J Appl Physiol. 1956;8(5):519-23.
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