Relationship between supramaximal flow during cough and mortality in motor neurone disease

被引:61
作者
Chaudri, MB
Liu, C
Hubbard, R
Jefferson, D
Kinnear, WJ
机构
[1] Univ Nottingham Hosp, Dept Resp Med, Nottingham NG7 2UH, England
[2] Univ Nottingham Hosp, Dept Neurol, Nottingham NG7 2UH, England
[3] City Hosp Nottingham, Dept Resp Med, Nottingham, England
关键词
Bulbar function; cough spikes; expiratory muscle weakness; motor neurone disease; survival;
D O I
10.1183/09031936.02.00082702
中图分类号
R56 [呼吸系及胸部疾病];
学科分类号
摘要
The main function of cough is clearance of intrathoracic airways. A normal cough is characterized by a transient increase in expiratory flow above the maximal How-volume loop envelope, known as cough "spikes". They may be absent in patients with motor neurone disease. The relationship between cough pattern, pulmonary function and survival was studied. Fifty-three patients were recruited (25 bulbar). Vital capacity, maximal inspiratory and expiratory mouth pressures and cough flow/volume curves were performed on ail patients, and the presence or absence of spikes were recorded. The primary endpoints were mortality or initiation of ventilatory support over a period of 18 months. Thirty-five patients died over the 18-month period of the study (including the six who were started on noninvasive ventilation). Twelve of the 24 patients with spikes died compared to 23 out of 29 patients without spikes (p<0.05). Patients without spikes were more likely to be bulbar on clinical grounds (p<0.0001) and had poorer lung function. The results showed an association between the absence of cough spikes and increased mortality. However the main determinants of survival in motor neurone disease are age, vital capacity and inspiratory mouth pressure, and it remains to be shown whether regular monitoring of cough conveys any additional advantage.
引用
收藏
页码:434 / 438
页数:5
相关论文
共 24 条
[1]   COUGH DYNAMICS DURING PROGRESSIVE EXPIRATORY MUSCLE WEAKNESS IN HEALTHY CURARIZED SUBJECTS [J].
ARORA, NS ;
GAL, TJ .
JOURNAL OF APPLIED PHYSIOLOGY, 1981, 51 (02) :494-498
[2]   AMYOTROPHIC-LATERAL-SCLEROSIS - PREDICTORS FOR PROLONGATION OF LIFE BY NONINVASIVE RESPIRATORY AIDS [J].
BACH, JR .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 1995, 76 (09) :828-832
[3]  
BEARDSMORE CS, 1987, B EUR PHYSIOPATH RES, V23, P465
[4]   Radiological evidence of subclinical dysphagia in motor neuron disease [J].
Briani, C ;
Marcon, M ;
Ermani, M ;
Costantini, M ;
Bottin, R ;
Iurilli, V ;
Zaninotto, G ;
Primon, D ;
Feltrin, G ;
Angelini, C .
JOURNAL OF NEUROLOGY, 1998, 245 (04) :211-216
[6]   REFERENCE VALUES OF MAXIMAL RESPIRATORY MOUTH PRESSURES - A POPULATION-BASED STUDY [J].
BRUSCHI, C ;
CERVERI, I ;
ZOIA, MC ;
FANFULLA, F ;
FIORENTINI, M ;
CASALI, L ;
GRASSI, M ;
GRASSI, C .
AMERICAN REVIEW OF RESPIRATORY DISEASE, 1992, 146 (03) :790-793
[7]   SPIROMETRY IN AMYOTROPHIC LATERAL SCLEROSIS [J].
FALLAT, RJ ;
JEWITT, B ;
BASS, M ;
KAMM, B ;
NORRIS, FH .
ARCHIVES OF NEUROLOGY, 1979, 36 (02) :74-80
[8]   Cough in motor neuron disease: a review of mechanisms [J].
Hadjikoutis, S ;
Wiles, CM ;
Eccles, R .
QJM-MONTHLY JOURNAL OF THE ASSOCIATION OF PHYSICIANS, 1999, 92 (09) :487-494
[9]   Amyotrophic lateral sclerosis - Successful treatment of mucous plugging by mechanical insufflation-exsufflation [J].
Hanayama, K ;
Ishikawa, Y ;
Bach, JR .
AMERICAN JOURNAL OF PHYSICAL MEDICINE & REHABILITATION, 1997, 76 (04) :338-339
[10]   NATURAL-HISTORY OF AMYOTROPHIC-LATERAL-SCLEROSIS IN A DATABASE POPULATION - VALIDATION OF A SCORING SYSTEM AND A MODEL FOR SURVIVAL PREDICTION [J].
HAVERKAMP, LJ ;
APPEL, V ;
APPEL, SH .
BRAIN, 1995, 118 :707-719