期刊论文详细信息
BMC Pulmonary Medicine
Increased respiratory drive relates to severity of dyspnea in systemic sclerosis
Jan Stolk2  Annemie JM Schuerwegh1  Willem BGJ Hamersma2  Maarten K Ninaber2 
[1] Rheumatology, Leiden University Medical Center, Leiden, the Netherlands;Department of Pulmonology (C3), Leiden University Medical Center, PO Box 9600, Leiden 2300RC, the Netherlands
关键词: Dyspnea evaluation;    Systemic sclerosis;    Respiratory drive;   
Others  :  863091
DOI  :  10.1186/1471-2466-14-57
 received in 2013-07-20, accepted in 2014-03-28,  发布年份 2014
PDF
【 摘 要 】

Background

Dyspnea may be a presenting symptom in progressive systemic sclerosis (SSc). Respiratory drive (mouth occlusion pressure, MOP, at rest and during CO2 rebreathing, 7% CO2, 93% O2) is a major determinant of dyspnea and may relate to the magnitude of dyspnea.

Methods

In a prospective design, MOP at 0.1 sec (P0.1) was measured in 73 SSc patients while breathing room air and during CO2 rebreathing. An abnormal V’E/P0.1 is defined as < 8 L/min/cm H2O. Dyspnea scores were assessed by a shortness of breath questionnaire (UCSD dyspnea scale).

Results

Mean P0.1 in patients with normal V’E/P0.1 (n = 45) was 1.1 ± 0.04 and 1.6 ± 0.08 cm H2O in patients with abnormal V’E/P0.1 (n = 28), p <0.001. ∆P0.1/∆PetCO2 differed significantly between these groups (0.45 versus 0.75 cm H2O/mmHg, P < 0.001), but no significant difference was present in ∆V’E/∆PetCO2. V’E/P0.1 showed the highest significant correlation with the UCSD dyspnea score (r = -0.76, p <0.001). UCSD cut-off value for abnormal V’E/P0.1 was 8.5 (sensitivity 93%, specificity 96%, area under the curve 0.98).

Conclusions

In SSc patients an abnormal V’E/P0.1 better relates to the severity of dyspnea than traditional lung function parameters and can easily be assessed at first outpatient consultation.

【 授权许可】

   
2014 Ninaber et al.; licensee BioMed Central Ltd.

【 预 览 】
附件列表
Files Size Format View
20140725024922206.pdf 256KB PDF download
48KB Image download
【 图 表 】

【 参考文献 】
  • [1]Black CM, Stephen C: Systemic Sclerosis (Scleroderma) And Related Disorders. In Oxford Textbook of Rheumatology. Edited by MadisonPJ IDA, WooP GDN. Oxford: Oxford University Press; 1993:771.
  • [2]LeRoy EC, Black C, Fleischmajer R, Jablonska S, Krieg T, Medsger TA Jr, Rowell N, Wollheim F: Scleroderma (systemic sclerosis): classification, subsets and pathogenenis. J Rheumatol 1988, 15:202-205.
  • [3]Whitelaw WA, Derenne JP, Milic-Emili J: Occlusion pressure as a measure of respiratory center output in conscious man. Resp Physiol 1975, 23:181-199.
  • [4]Nageh TT, Du Bois RM: Non-invasive ventilation in hypercapnic respiratory failure secondary to sclerodermic chest wall restriction. Respir Med 1998, 92:1170-1172.
  • [5]Pugazhenthi M, Cooper D, Ratnakant BS, Postlethwaite A, Carbone L: Hypercapnic respiratory failure in systemic sclerosis. J Clin Rheumatol 2003, 9:43-46.
  • [6]Cherniack RM, Snidal DP: The effect of obstruction to breathing on the ventilatory response to CO2. J Clin Invest 1956, 35:1286-1290.
  • [7]Gorini M, Spinelli A, Ginanni R, Duranti R, Gigliotti F, Arcangeli P, Scano G: Neural respiratory drive and neuromuscular coupling with CO2 rebreathing in patients with chronic interstitial lung disease. Chest 1989, 96:824-830.
  • [8]Patrick J: The influence of age, sex, body size and lung size on the control and pattern of breathing during CO2 inhalation in Caucasians. Respir Physiol 1972, 16:337-350.
  • [9]Milic-Emili J, Whitelaw WA, Derenne JP: Occlusion pressure, a simple measure of the respiratory center output. N Engl J Med 1975, 293:1029-1031.
  • [10]Scott GC, Burki NK: The relationship between resting ventilation to mouth occlusion pressure. An index of resting respiratory function. Chest 1990, 98:900-906.
  • [11]Calverley PMA: Ventilatory Control And Dyspnea. In Chronic Obstructive Pulmonary Disease. Edited by Calverley PMA, Pride NB. London: Chapman and Hall; 1995:205-242.
  • [12]ATS Board of Directors: ATS/ERS Statement on respiratory muscle testing. Am J Respir Crit Care Med 2002, 166:518-624.
  • [13]Jordan C: Automatic method for measuring mouth occlusion pressure response to carbon dioxide inhalation. Med Biol Eng Comput 1981, 19:279-286.
  • [14]MacIntyre N: Standardisation of the single-breath determination of carbon monoxide uptake in the lung. Eur Respir J 2005, 26:720-735.
  • [15]Miller MR: Standardisation of spirometry. Eur Respir J 2005, 26:319-338.
  • [16]Montes de Oca M, Celli BR: Mouth occlusion pressure, CO2 response and hypercapnia in severe obstructive pulmonary disease. Eur Respir J 1998, 12:666-671.
  • [17]Read DJC: A clinical method for assessing ventilatory response to carbon dioxide. Aust Ann Med 1967, 16:20-32.
  • [18]Rietjens GJWM, Kuipers H, Kester ADM, Keizer HA: Validation of a computerized metabolic measurement system (Oxycon-Pro) during low and high intensity exercise. Int J Sports Med 2001, 22:291-294.
  • [19]Eakin EG, Resnikoff PM, Prewitt LM, Ries AL, Kaplan RM: Validation of a new dyspnea measure. The UCSD shortness of breath questionnaire. Chest 1998, 113:619-624.
  • [20]Nishino T: Dyspnoea: underlying mechanisms and treatment. Br J Anaesth 2011, 106:463-474.
  • [21]Walterspacher S, Schlager D, Walker DJ, Muller-Quernheim J, Windisch W, Kabitz HJ: Respiratory muscle function in interstitial lung disease. Eur Respir J 2013, 42:211-219.
  • [22]DiMarco AF, Kelsen SG, Cherniack NS, Gothe B: Occlusion pressure and breathing pattern in patients with interstitial lung disease. Am Rev Respir Dis 1983, 127:425-430.
  文献评价指标  
  下载次数:3次 浏览次数:1次