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A Randomized Controlled Study to Evaluate the Efficacy of Noninvasive Limb Cover for Chronic Phantom Limb Pain Among Veteran Amputees
被引:21
作者:
Hsiao, An-Fu
[1
,2
]
York, Robyn
[1
]
Hsiao, Ian
[1
]
Hansen, Ed
[1
]
Hays, Ron D.
[3
,6
]
Ives, John
[5
]
Coulter, Ian D.
[4
,6
]
机构:
[1] VA Long Beach Healthcare Syst, Long Beach, CA USA
[2] Univ Calif Irvine, Dept Med, Irvine, CA 92717 USA
[3] Univ Calif Los Angeles, Dept Med, Los Angeles, CA 90024 USA
[4] Univ Calif Los Angeles, Sch Dent, Los Angeles, CA 90024 USA
[5] Samueli Inst, Alexandria, VA USA
[6] RAND Corp, Santa Monica, CA USA
来源:
ARCHIVES OF PHYSICAL MEDICINE AND REHABILITATION
|
2012年
/
93卷
/
04期
关键词:
Phantom limb pain;
Rehabilitation;
SPINAL-CORD-INJURY;
SOMATOSENSORY CORTEX;
REORGANIZATION;
FARABLOC;
NERVE;
D O I:
10.1016/j.apmr.2011.11.021
中图分类号:
R49 [康复医学];
学科分类号:
100215 ;
摘要:
Hsiao A-F, York R, Hsiao I, Hansen E, Hays RD, Ives J, Coulter ID. A randomized controlled study to evaluate the efficacy of noninvasive limb cover for chronic phantom limb pain among veteran amputees. Arch Phys Med Rehabil 2012;93:617-22. Objective: To assess the efficacy of a noninvasive limb cover for treating chronic phantom limb pain (PLP). Design: Randomized, double-blind, placebo-controlled trial. Setting: Outpatient clinic. Participants: We randomly assigned 57 subjects to 2 groups: true noninvasive limb cover (n=30) and sham noninvasive limb cover (n=27). Inclusion criteria included age of 18 years or greater, upper or lower extremity amputation with healed residual limb, and 3 or more episodes of PLP during the previous 6 weeks. Interventions: Subjects received 2 true or sham noninvasive limb covers to be worn over the prosthesis and residual limbs 24 hours a day for 12 weeks. Main Outcome Measures: Primary outcome measure was the numerical pain rating scale of PLP level (0-10). Secondary outcomes included overall pain level (0-10), PLP frequency per week, and the Veterans RAND 12-Item Health Survey (VR-12). We collected data at baseline and at 6- and 12-week follow-up visits. Results: Demographic and clinical characteristics were not significantly different between groups. The true noninvasive limb cover group reported nonsignificant reductions in PLP from 5.9 +/- 1.9 at baseline to 3.9 +/- 1.7 at the 12-week follow-up. The sham noninvasive limb cover group also had nonsignificant reducations in PLP from 6.5 +/- 1.8 to 4.2 +/- 2.3. PLP did not differ significantly between the 2 groups at 6 weeks (mean difference, 0.8; 95% confidence interval [CI], -1.4 to 3) or at 12 weeks (mean difference, 0.2; 95% CI, -1.9 to 2.3). Similarly, overall pain level, PLP episodes per week, and VR-12 physical and mental health component scores did not differ between the 2 groups at 6 and 12 weeks. Conclusions: A true noninvasive limb cover did not significantly decrease PLP levels or the frequency of PLP episodes per week, overall bodily pain levels, or VR-12 physical and mental health component scores compared with a sham noninvasive limb cover in our veteran amputee sample.
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页码:617 / 622
页数:6
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