Monitoring respiratory muscle strength assists in early diagnosis of respiratory dysfunction as opposed to the isolated use of pulmonary function evaluation in amyotrophic lateral sclerosis;Monitoramento da força muscular respiratória em detrimento do uso isolado da avaliação da função pulmonar para o diagnóstico precoce de disfunção respiratória em pacientes com esclerose lateral amiotrófica

Arquivos de Neuro-Psiquiatria

Volumn 71, Issue 3, 2013, Pages 146-152

  Fregonezi, Guilherme ^a   Araújo, Palomma Russelly Saldanha ^a   Macêdo, Tathiana Lindemberg Ferreira ^a   Dourado Junior, Mario Emilio ^a   Resqueti, Vanessa Regiane ^b   de Andrade, Armele de Fátima Dornelas ^b  

^a FEDERAL UNIVERSITY OF RIO GRANDE DO NORTE   (Brazil)

^b FEDERAL UNIVERSITY OF PERNAMBUCO   (Brazil)

Author keywords

Muscle weakness; Neuromuscular diseases; Pulmonary function test; Respiratory muscles

Indexed keywords

ADULT; AMYOTROPHIC LATERAL SCLEROSIS; ANTHROPOMETRIC PARAMETERS; ARTICLE; BODY MASS; BODY WEIGHT; BREATHING MUSCLE; CLINICAL ARTICLE; CONTROLLED STUDY; CROSS-SECTIONAL STUDY; EARLY DIAGNOSIS; FEMALE; FORCED EXPIRATORY VOLUME; FORCED VITAL CAPACITY; HUMAN; LUNG FUNCTION; MALE; MAXIMAL EXPIRATORY FLOW; MUSCLE STRENGTH; MUSCLE WEAKNESS; RESPIRATORY FAILURE; SENSITIVITY AND SPECIFICITY; SPIROMETRY;

EID: 84875746424     PISSN: 0004282X     EISSN: 16784227     Source Type: Journal    
DOI: 10.1590/S0004-282X2013000300004     Document Type: Article

References (29)

1. Lima NMFV, Nucci A. Clinical attention and assistance profile of patients with amyotrophic lateral sclerosis. Arq Neuropsiquiatr 2011;69:170-175.
2. Hirtz D, Thurman DJ, Gwinn-Hardy K, Mohamed M, Chaudhuri AR, Zalutsky R. How common are the common neurological disorders? Neurology 2007:68;326-337.
3. Spataro R, LoRe M, Piccoli T, Piccoli F, La Bella V. Causes and place of death in Italian patients with amyotrophic lateral sclerosis. Acta Neurol Scand 2010;122:217-223.
4. Kurian KM, Forbes RB, Colville S, Swingler RJ. Cause of death and clinical grading criteria in a cohort of amyotrophic lateral sclerosis cases undergoing autopsy from the Scottish Motor Neurone Disease Register. J Neurol Neurosurg Psychiatry 2009;80:84-87.
5. Corcia P, Pradat PF, Salachas F, et al. Causes of death in a post-mortem series of ALS patients. Amyotroph Lateral Scler 2008;9:59-62.
6. Resqueti VR, Araújo PRS, Dourado Junior ME, Fregonezi GAF. Esclerose lateral amiotrófica (ELA) e músculos respiratórios. Ter Man 2011;9:503-508.
7. Uldry C, Janssens JP, de Muralt B, Fitting JW. Sniff nasal inspiratory pressure in patients with chronic obstructive pulmonary disease. Eur Respir J 1997;10:1292-1296.
8. Nava S, Ambrosino N, Crotti P, Fracchia C, Rampulla C. Recruitment of some respiratory muscles during three maximal inspiratory maneuvers. Thorax 1993;48:702-707.
9. Katagiri M, Abe T, Yokoba M, Dobashi Y, Tomita T, Easton PA. Neck and abdominal muscle activity during a sniff. Respir Med 2003;97:1027-1035.
10. Hart N, Polkey MI, Sharshar T, et al. Limitations of sniff nasal pressure in patients with severe neuromuscular weakness Neurol Neurosurg Psychiatry 2003;74:1685-1687.
11. Azevedo IG, Severino FG, Araújo TL, Resqueti VR, Bruno S, Fregonezi GAF. Relação entre pressão inspiratória nasal e pressão inspiratória máxima em pacientes com distrofia miotônica. Ter Man 2010;8:224-230.
12. O'Neill CL, Williams TL, Peel ET, et al. Non-invasive ventilation in motor neuron disease: an update of current UK practice. J Neurol Neurosurg Psychiatry 2012;83:371-376.
13. Miller MR, Hankinson J, Brusasco V, et al. ATS/ERS Task Force. Standardisation of spirometry. Eur Respir 2005;26:319-338.
14. Pereira CAC, Sato T, Rodrigues SC. New reference values for forced spirometry in white adults in Brazil. J Bras Pneumol 2007;33:397-406.
15. Lechtzin N, Wiener CM, Shade DM, Clawson L, Diette GB. Spirometry in the supine position improves the detection of diaphragmatic weakness in* patients with amyotrophic lateral sclerosis. Chest 2002;121;436-442.
16. Black LF, Hyatt RE. Maximal respiratory pressures: normal values and relationship to age and sex. Am Rev Respir Dis 1969;99:696-702.
17. Neder JA, Andreoni S, Lerario MC, Nery LE. References values for lung function tests. Maximal respiratory pressures and voluntary ventilation. Braz J Med Biol Res 1999;32:719-727.
18. Severino FG, Resqueti VR, Bruno SS, Azevedo IG, Vieira RHG, Fregonezi GAF. Comparação entre o manovacuômetro nacional e o importado para medida da pressão inspiratória nasal. Rev Bras Fisioter 2010;14:426-431.
19. Lofaso F, Nicot F, Lejaille M, et al. Sniff nasal inspiratory pressure: what is the optimal number of sniffs? Eur Respir J 2006;27:980-982.
20. Steier J, Kaul S, Seymour J, et al. The value of multiple tests of respiratory muscle strength. Thorax 2007;62:975-980.
21. Araujo PRS, Resqueti VR, Nascimento Jr JF, et al. Maximal sniff nasal inspiratory pressure in Brazilian healthy subjects: a multicenter study. Maximal respiratory pressure in Brazilian health population: a multicenter study (in press).
22. Fregonezi GAF, Araujo PRS, Dornelas de Andrade AF, et al. Maximal sniff nasal inspiratory pressure in Brazilian healthy subjects: a multicenter study. In: XXI European Annual Congress, 2011, Amsterdam. Eur Resp J 2011;239.
23. Lechtzin N, Wiener CM, Shade DM, et al. Spirometry in the supine position improves the detection of diaphragmatic weakness in patients with amyotrophic lateral sclerosis. Chest 2002;121:436-442.
24. Tsara V, Serasli E, Steiropoulos P, Tsorova A, Antoniadou M, Zisi P. Respiratory function in amyotrophic lateral sclerosis patients. The role of sleep studies. Hippokrattia 2010;14:33-36.
25. Singh D, Verma R, Garg RK, et al. Assessment of respiratory functions by spirometry and phrenic nerve studies in patients of amyotrophic lateral sclerosis. J Neurol Sci 2011;306:76-81.
26. Silva LBC, Mourão LF, Silva AA, et al. Amyotrophic lateral sclerosis: combined nutritional, respiratory and functional assessment. Arq Neuropsiquiatr 2008;66:354-359.
27. Almeida SRM, Silva LBC, Guerreiro CAM, Nucci A. Amyotrophic lateral sclerosis: prospective study on respiratory parameters. Arq Neuropsiquiatr 2010;68:258-262
28. Qureshi MM, Hayden D, Urbinelli L, et al. Analysis of factors that modify susceptibility and rate of progression in amyotrophic lateral sclerosis (ALS). Amyotrophic Lateral Sclerosis 2006;7:173-182.
29. Fallat RJ, Jewitt B, Bass M, Kamm B, Norris FH Jr. Spirometry in amyotrophic lateral sclerosis. Arch Neurol 1979;36:74-80.