Neutral wrist splinting in carpal tunnel syndrome: A comparison of night-only versus full-time wear instructions

被引:90
作者
Walker, WC
Metzler, M
Cifu, DX
Swartz, Z
机构
[1] Virginia Commonwealth Univ, Med Coll Virginia, Dept Phys Med & Rehabil, Richmond, VA 23298 USA
[2] Hunter Holmes McGuire Vet Adm Med Ctr, Richmond, VA USA
来源
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION | 2000年 / 81卷 / 04期
关键词
median neuropathy; carpal tunnel syndrome; orthosis; wrist splint; nerve condition;
D O I
10.1053/mr.2000.3856
中图分类号
R49 [康复医学];
学科分类号
100215 ;
摘要
Objective: To compare the effects of night-only to full-time splint wear instructions on symptoms, function, and impairment in carpal tunnel syndrome (CTS). Design: Randomized clinical trial with 6-week follow-up. Setting: Veterans Administration Medical Center, outpatient clinic. Subjects: Outpatients with untreated CTS were consecutively recruited from our electrodiagnostics lab. Twenty-one patients (30 hands) were enrolled, and 17 patients (24 hands) completed the study. Interventions: Thermoplastic, custom-molded, neutral wrist splints with subjects receiving either full-time or night-only wear instructions. Outcome Measures: Symptoms and functional deficits were measured by Levine's self-administered questionnaire, and physiologic impairment was measured by median nerve sensory and motor distal latency. Compliance and Crossover: Almost all (92%) of the combined sample reported frequent splint use, but their adherence to specific wearing instructions was limited. A majority (73%) of the full-time group reported splint wear less than one half of waking hours, and some (23%) of the night-only group reported occasional daytime wear. Despite this tendency for treatment crossover, the two treatment groups differed in daytime wear as intended (chi(2) analysis, p = .004). Results: The combined sample improved in three of four outcome measures: sensory distal latency (mean = .28msec, standard deviation [SD] = .37, p = .004), symptom severity (mean = .64, SD = .46, p = .0001), and functional deficits (mean = .49, SD = .51, p = .0001). Severity of CTS was a factor only in sensory distal latency improvement (more improvement in severe CTS). Subjects receiving full-time wear instructions showed superior distal latency improvement, both motor (.35 vs -.07msec, p = .04) and sensory (.46 vs .13msec, p = .05) when compared with subjects receiving night-only wear instructions. Conclusions: This study provides added scientific evidence to support the efficacy of neutral wrist splints in CTS and suggests that physiologic improvement is best with full-time splint wear instructions.
引用
收藏
页码:424 / 429
页数:6
相关论文
共 48 条
[1]  
*AM ASS EL MED AM, 1993, MUSCLE NERVE, V16, P1389
[2]  
BAUMAN TD, 1981, CLIN ORTHOP RELAT R, V156, P151
[3]   A CRITICAL-REVIEW OF COMPLIANCE STUDIES IN RHEUMATOID-ARTHRITIS [J].
BELCON, MC ;
HAYNES, RB ;
TUGWELL, P .
ARTHRITIS AND RHEUMATISM, 1984, 27 (11) :1227-1233
[4]  
BRAIN WR, 1947, LANCET, V252, P278
[5]  
BUCHATHAL F, 1974, J NEUROL NEUROSUR PS, V34, P243
[6]   SPLINTING FOR CARPAL-TUNNEL SYNDROME - IN SEARCH OF THE OPTIMAL ANGLE [J].
BURKE, DT ;
BURKE, MM ;
STEWART, GW ;
CAMBRE, A .
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION, 1994, 75 (11) :1241-1244
[7]   Soft versus hard resting hand splints in rheumatoid arthritis: Pain relief, preference, and compliance [J].
Callinan, NJ ;
Mathiowetz, V .
AMERICAN JOURNAL OF OCCUPATIONAL THERAPY, 1996, 50 (05) :347-353
[8]   COMPARISON OF MEDIAN AND RADIAL NERVE SENSORY LATENCIES IN THE ELECTROPHYSIOLOGICAL DIAGNOSIS OF CARPAL-TUNNEL SYNDROME [J].
CARROLL, GJ .
ELECTROENCEPHALOGRAPHY AND CLINICAL NEUROPHYSIOLOGY, 1987, 68 (02) :101-106
[9]   Oral drug of choice in carpal tunnel syndrome [J].
Chang, MH ;
Chiang, HT ;
Lee, SSJ ;
Ger, LP ;
Lo, YK .
NEUROLOGY, 1998, 51 (02) :390-393
[10]   INTER-EXAMINER AND INTRA-EXAMINER RELIABILITY OF NERVE-CONDUCTION MEASUREMENTS IN NORMAL SUBJECTS [J].
CHAUDHRY, V ;
CORNBLATH, DR ;
MELLITS, ED ;
AVILA, O ;
FREIMER, ML ;
GLASS, JD ;
REIM, J ;
RONNETT, GV ;
QUASKEY, SA ;
KUNCL, RW .
ANNALS OF NEUROLOGY, 1991, 30 (06) :841-843