M. Schurmann et al., Peripheral sympathetic function as a predictor of complex regional pain syndrome type I (CRPS I) in patients with radial fracture, AUTON NEURO, 86(1-2), 2000, pp. 127-134
Complex regional pain syndrome type I (CRPS I) is a frequent complication a
fter injuries of the upper limbs. The pathophysiology of this disease remai
ns unclear, although disturbances of the sympathetic nervous system have be
en detected in several clinical studies, and sympathetic blocks resolve the
symptoms in many of the cases. To investigate the meaning of sympathetic d
ysfunction at the beginning of the disease. 27 patients with distal radial
fracture were examined prospectively during the course of the disease with
regard to their clinical symptoms and their peripheral sympathetic nervous
function. Sympathetic nervous function was examined by testing the vasocons
trictor response to sympathetic stimuli - recorded with laser Doppler fluxm
etry - of the fingertips of both hands. Four patients developed CRPS I duri
ng the 12-week observation time and two patients presented an incomplete cl
inical CRPS I picture ('borderline patients'). The complaints of all patien
ts (normal fracture patients, CRPS I patients, borderline patients) were si
milar during the first week after trauma with focus on pain, motoric distur
bances and autonomic symptoms. After 1 or 2 weeks, a larger clinical differ
ence developed between normal fracture patients and CRPS I or 'borderline p
atients'. In CRPS I patients and 'borderline patients', the sympathetic vas
oconstrictor response was diminished or absent from the first posttraumatic
day throughout the observation time, whereas the normal Fracture patients
revealed slightly impaired sympathetic nervous function on the first posttr
aumatic day and normal results during the rest of the observation time. Wit
h regard to the unaffected contralateral hand, CRPS I patients also showed
impaired sympathetic nervous function. The results of the present study sug
gest that the disturbances in the sympathetic nervous system in CRPS I pati
ents are systemic and not limited to the affected limb. Their occurrence be
fore the clinical breakout of the disease may serve as a marker that might
be useful for early therapy and lead to further understanding of the pathop
hysiology of CRPS I. (C) 2000 Elsevier Science B.V. All rights reserved.