Non-invasive tension time index in relation to severity of disease in children with cystic fibrosis

Pediatric Pulmonology

Volumn 43, Issue 10, 2008, Pages 973-981

  Hahn, Andreas ^a,d   Ankermann, Tobias ^b   Claass, Andreas ^b   Mann, Marion ^c   Lindemann, Hermann ^d   Neubauer, Bernd A ^a  

^a JUSTUS LIEBIG UNIVERSITY   (Germany)

^b UNIVERSITY HOSPITAL SCHLESWIG HOLSTEIN   (Germany)

^c Institute of Medical Statistics   (Germany)

^d Department of Pediatric Pulmonology ^*  (Germany)

Author keywords

Childhood; Respiratory muscle fatigue; Respiratory muscle strength; Respiratory muscles

Indexed keywords

ADOLESCENT; ADULT; AIRWAY OBSTRUCTION; ARTICLE; BREATHING MUSCLE; CLINICAL ARTICLE; COMPARATIVE STUDY; CONTROLLED STUDY; CYSTIC FIBROSIS; DISEASE SEVERITY; FEMALE; HUMAN; LUNG DISEASE; LUNG FUNCTION TEST; MALE; METHODOLOGY; NON INVASIVE TENSION TIME INDEX; OXYGEN SATURATION; PRIORITY JOURNAL; RESPIRATORY TRACT DISEASE; SCHOOL CHILD;

ADOLESCENT; ADULT; CHILD; CYSTIC FIBROSIS; FEMALE; FORCED EXPIRATORY VOLUME; HUMANS; LUNG VOLUME MEASUREMENTS; MALE; MUSCLE TONUS; SEVERITY OF ILLNESS INDEX; TIME FACTORS;

EID: 55049106687     PISSN: 87556863     EISSN: 10990496     Source Type: Journal    
DOI: 10.1002/ppul.20887     Document Type: Article

References (30)

1. Liou TG, Adler FR, Cox DR, Cahill BC. Lung transplantation and survival in children with cystic fibrosis. N Engl J Med 2007;357:2143-2152.
2. Szeinberg A, England S, Mindorff C, Fraser JM, Levison H. Maximal inspiratory and expiratory pressures are reduced in hyperinflated malnourished, young adult males with cystic fibrosis. Am Rev Respir Dis 1986;132:766-769.
3. Marks J, Pasterkamp H, Tal A, Leahy F. Relationship between respiratory muscle strength, nutritional status, and lung volume in cystic fibrosis and asthma. Am Respir Rev Dis 1986;133:414-447.
4. Mier A, Redington A, Brophy C, Hodson M, Green M. Respiratory muscle function in cystic fibrosis. Thorax 1990;45:750-752.
5. Lands LC, Heigenhauser GJF, Jones NL. Respiratory and peripheral muscle function in cystic fibrosis. Am Rev Respir Dis 1993;147:865-869.
6. Pradal U, Polese G, Braggion C, Poggi R, Zanolla L, Mastella G, Rossi A. Determinants of transdiaphragmatic pressure in adults with cystic fibrosis. Am J Respir Crit Care Med 1994;150:167-173.
7. Cropp GJ, Pullano TP, Cerny FJ, Nathanson IT. Exercise tolerance and cardiorespiratory adjustments at peak work capacity in cystic fibrosis. Am Rev Respir Dis 1982;126:211-216.
8. Hayot M, Guillaumont S, Ramonatxo M, Voisin M, Préfaut C. Determinants of the tension-time index of inspiratory muscles in children with cystic fibrosis. Pediatr Pulmonol 1997;23:336-343.
9. Keochkerian D, Chlif M, Delanaud S, Gauthier R, Maingourd Y, Ahmaidi S. Timing and driving components of the breathing strategy in children with cystic fibrosis during exercise. Pediatr Pulmonol 2005;40:449-456.
10. Bellemare F, Grassino A. Effect of pressure and timing of contraction on human diaphragmatic fatigue. J Appl Physiol 1982;53:1190-1195.
11. Bellemare F, Grassino A. Evaluation of human diaphragmatic fatigue. J Appl Physiol 1982;53:1196-1206.
12. Hayot M, Ramonatxo M, Matecki S, Milic-Emili J, Préfaut C. Noninvasive assessment of inspiratory muscle function during exercise. Am J Respir Crit Care Med 2000;162:2201-2207.
13. Ramonatxo M, Boulard P, Préfaut C. Validation of a non-invasive tension-time index of inspiratory muscles. J Appl Physiol 1995;78:646-653.
14. Mulreany LT, Weiner DJ, McDonough JM, Panitch HB, Allen JL. Noninvasive measurement of the tension-time index in children with neuromuscular disease. J Appl Physiol 2003;95:931-937.
15. Ramsey BW, Farrell PM, Pencharz P, The Consensus Committee. Nutritional assessment and management in cystic fibrosis: a consensus report. Am J Clin Nutr 1992;55:108-116.
16. Gibson LE, Cook RE. A test for concentration of electrolytes in sweat in cystic fibrosis of the pancreas using pilocarpine iontophoresis. Pediatrics 1959;23:545-549.
17. Cabrera ME, Lough MD, Doershuk CF, Salvator AE. An expanded scoring system including an index of nutritional status for patients with cystic fibrosis. Pediatr Pulmonol 1994;18:199-205.
18. Quanjer PH, Tammeling JE, Cotes JE. Lung volumes and forced ventilatory flows. Report working party standardization of lung function tests. European community for steel and coal Luxemburg. Official statement of the European Respiratory Society. Eur Respir J 1993;6:5-40.
19. Zapletal A, Motoyama EK, van de Woestijne KP, Hunt VR, Bouhuys A. Maximum expiratory flow-volume curves and airway conductance in children and adolescents. J Appl Physiol 1969;26:308-316.
20. Wilson SH, Cooke NT, Edwards RHT, Spiro SG. Predicted normal values for maximal respiratory pressures in Caucasian adults and children. Thorax 1984;39:535-538.
21. Ringqvist T. The ventilatory capacity in healthy subjects. An analysis of causal factors with special reference to the respiratory force. Scand J Clin Lab Invest 1966;88:5-176.
22. Gaultier C, Boule M, Girard F. Inspiratory force reserve of the respiratory muscles in children with chronic obstructive pulmonary disease. Am Rev Respir Dis 1985;131:811-815.
23. Bureau MA, Lupien L, Begin R. Neural drive and ventilatory strategy in normal children and patients with cystic fibrosis and asthma. Pediatrics 1981;68:187-194.
24. Gaultier C. Tension-time index of inspiratory muscles in children. Pediatr Pulmonol 1997;23:327-329.
25. O'Neill S, Leahy F, Pasterkamp H, Tal A. The effects of chronic hyperinflation, nutritional status, and posture on respiratory muscle strength in cystic fibrosis. Am Rev Respir Dis 1983;128:1051-1054.
26. Lands L, Desmond KJ, Demizio D, Pavilanis A, Coates AL. The effect of nutritional status and hyperinflation on respiratory muscle strength in children and young adults. Am Rev Respir Dis 1990;141:506-509.
27. Caronia CG, Silver P, Nimkoff L, Gorvoj J, Quinn C, Sagy M. Use of bilevel positive airway pressure (BIPAP) in end-stage patients with cystic fibrosis awaiting lung transplantation. Clin Pediatr 1998;37:555-559.
28. Granton JT, Shapiro C, Kesten S. Noninvasive nocturnal ventilatory support in advanced lung disease from cystic fibrosis. Respir Care 2002;47:675-681.
29. Efrati O, Modan-Moses D, Barak A, Boujanover Y, Augarten A, Szeiberg AM, Levy I, Yahav Y. Long-term non-invasive positive pressure ventilation among cystic fibrosis patients awaiting lung transplantation. Isr Med Assoc J 2004;6:527-530.
30. Piper AJ, Parker S, Torzillo PJ, Sullivan CE, Bye BTP. Nocturnal nasal IPPV stabilizes patients with cystic fibrosis and hypercapnic respiratory failure. Chest 1992;102:846-850.