Management of pediatric patients with complex regional pain syndrome

被引:81
作者
Wilder, Robert T. [1 ]
机构
[1] Mayo Clin, Mayo Eugenio Litta Childrens Hosp, Rochester, MN 55902 USA
关键词
complex regional pain syndrome; pediatric;
D O I
10.1097/01.ajp.0000194283.59132.fb
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
This review Summarizes current information about diagnosis and treatment of complex regional pain syndrome (CRPS) in children. Although it has been widely held that CRPS in children is intrinsically different from adults, there appear to be relatively few differences. However, there is a marked preponderance of lower extremity cases in children. Historically, psychological factors have been invoked to explain the genesis and persistence of CRPS in children, but the evidence is not compelling. Treatment outcome studies are limited but indicate that children generally respond to a primary focus on physical therapy.,Multidisciplinary treatment reports are particularly encouraging. The general perception that children have a milder course may relate to the potentially greater willingness of children to actively participate in appropriately targeted treatment rather than to innate differences in the disease process itself. Recurrence rates appear higher than in adults, but response to reinitiation of treatment seems to proceed efficiently. Clinical judgment dictates the extent of medication or interventional therapy added to the treatment to facilitate rehabilitation. In many ways, the approach to the treatment of children mirrors that of adults, with perhaps greater restraint in the use of medications and invasive procedures. The rehabilitation of children with CRPS. like that of adults with CRPS, needs further rigorous investigation.
引用
收藏
页码:443 / 448
页数:6
相关论文
共 68 条
[1]   Epidemiology of complex regional pain syndrome: a retrospective chart review of 134 patients [J].
Allen, G ;
Galer, BS ;
Schwartz, L .
PAIN, 1999, 80 (03) :539-544
[2]   REFLEX SYMPATHETIC DYSTROPHY SYNDROME IN CHILDREN [J].
ASHWAL, S ;
TOMASI, L ;
NEUMANN, M ;
SCHNEIDER, S .
PEDIATRIC NEUROLOGY, 1988, 4 (01) :38-42
[3]   Surgical sympathectomy for reflex sympathetic dystrophy syndromes [J].
Bandyk, DF ;
Johnson, BL ;
Kirkpatrick, AF ;
Novotney, ML ;
Back, MR ;
Schmacht, DC .
JOURNAL OF VASCULAR SURGERY, 2002, 35 (02) :269-277
[4]   THERMAL BIOFEEDBACK IN THE TREATMENT OF SYMPTOMS ASSOCIATED WITH REFLEX SYMPATHETIC DYSTROPHY [J].
BAROWSKY, EI ;
ZWEIG, JB ;
MOSKOWITZ, J .
JOURNAL OF CHILD NEUROLOGY, 1987, 2 (03) :229-232
[5]   REFLEX NEUROVASCULAR DYSTROPHY IN CHILDHOOD [J].
BERNSTEIN, BH ;
SINGSEN, BH ;
KENT, JT ;
KORNREICH, H ;
KING, K ;
HICKS, R ;
HANSON, V .
JOURNAL OF PEDIATRICS, 1978, 93 (02) :211-215
[6]  
BETEND B, 1981, ARCH FR PEDIATR, V38, P121
[7]  
BOAS RA, 1996, REFLEX SYMPATHETIC D, P79
[8]   REVERSAL OF A SUDECKS ATROPHY BY THE ADJUNCTIVE USE OF TRANS-CUTANEOUS ELECTRICAL NERVE-STIMULATION - A CASE-REPORT [J].
BODENHEIM, R ;
BENNETT, JH .
PHYSICAL THERAPY, 1983, 63 (08) :1287-1288
[9]   Reflex sympathetic dystrophy arising in a patient with familial Mediterranean fever [J].
Bodur, H ;
Gündüz, OH ;
Yücel, M .
RHEUMATOLOGY INTERNATIONAL, 1999, 19 (1-2) :69-70
[10]  
BROMMEL B, 1993, Z PSYCHOSOM MED PSYC, V39, P346