Physical complaints in ageing persons with spinal muscular atrophy

被引:37
作者
de Groot, IJM
de Witte, LP
机构
[1] Inst Rehabil Res, iRv, NL-6430 AD Hoensbroek, Netherlands
[2] Maastricht Univ, Dept Rehabil, Maastricht, Netherlands
关键词
spinal muscular atrophy; ageing; physical problems; physical complaints;
D O I
10.1080/16501970510030156
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective: While life expectancy is improving for persons with spinal muscular atrophy, new physical complaints may arise. To investigate this, we studied persons with a long duration and severe course (high functional limitations) of the disease. Design: Cross-sectional descriptive study. Subjects/Patients: Persons with spinal muscular atrophy. Methods: Questionnaires and structured interviews on prevalence of physical complaints and their duration. Of 190 questionnaires 99 were returned; of 23 persons (with the longest disease duration and high functional limitation level) selected for structured medical interviews 9 participated. Results: Patterns common within and different between the different types of spinal muscular atrophy were identified. Of the 10 most common complaints, types 1-2 had a significantly higher prevalence of kyphoscoliosis, difficulty in coughing, joint contractures and voice/speech problems, while type 3 had a significantly higher prevalence of fatigue. No statistically significant correlation was found between the appearance of physical complaints and disease duration. However, sleeping and swallowing problems were in the 5 most common complaints with the shortest mean time of appearance. The structured interview revealed hypermobility in the hand, suffusion of the eyes, and itching as new complaints with high prevalence. Conclusion: There are indications that the frequency of less well-known physical complaints increases with ageing.
引用
收藏
页码:258 / 262
页数:5
相关论文
共 21 条
[1]  
Benditt J O, 1998, Phys Med Rehabil Clin N Am, V9, P167
[2]   Treatment of type I spinal muscular atrophy with noninvasive ventilation and gastrostomy feeding [J].
Birnkrant, DJ ;
Pope, JF ;
Martin, JE ;
Repucci, AH ;
Eiben, RM .
PEDIATRIC NEUROLOGY, 1998, 18 (05) :407-410
[3]  
BRUIN AF, 1994, J CLIN EPIDEMIOL, V47, P407
[4]  
CARTER CT, 1995, AM J PHYS MED REHAB, V74, pS150, DOI 10.1097/00002060-199509001-00009
[5]  
Cerveri I, 1993, Monaldi Arch Chest Dis, V48, P318
[6]  
Elkohen M, 1996, ARCH MAL COEUR VAISS, V89, P611
[7]  
EMERY AEH, 1997, DIAGNOSTIC CRITERIA, pCH8
[8]   Cardiac involvement in Werdnig-Hoffmann's spinal muscular atrophy [J].
Finsterer, J ;
Stöllberger, C .
CARDIOLOGY, 1999, 92 (03) :178-182
[9]   LONG-TERM VENTILATORY SUPPORT IN SPINAL MUSCULAR-ATROPHY [J].
GILGOFF, IS ;
KAHLSTROM, E ;
MACLAUGHLIN, E ;
KEENS, TG .
JOURNAL OF PEDIATRICS, 1989, 115 (06) :904-909
[10]   Sleep-disordered breathing in neuromuscular disease [J].
Christian Guilleminault ;
Ravinder P. Shergill .
Current Treatment Options in Neurology, 2002, 4 (2) :107-112