Background: Because pregnancy increases the sensitivity of nervous tissue t
o local anaesthetics, pregnant patients may be at higher risk of developing
neurologic deficits after spinal block than non-pregnant patients. Therefo
re, we evaluated prospectively the incidence and type of neurologic symptom
s after spinal anaesthesia with hyperbaric bupivacaine for caesarean sectio
n.
Methods: In this prospective follow-up study we recorded neurologic complic
ations during anaesthesia and postoperatively until discharge from the hosp
ital of 219 patients, who underwent caesarean section under spinal anaesthe
sia with hyperbaric bupivacaine (5 mg/ml, mean 13 mg). The patients filled
in a questionnaire on the first and fifth postoperative days. In the case o
f complaints typical of neurologic symptoms they were checked first by the
anaesthesiologist and, in the case of persistent symptoms, afterwards addit
ionally by a neurologist.
Results: Twenty-six of 219 patients were not included in the further evalua
tion because of incomplete return of their questionnaires. Seventeen mother
s (8.8%) complained of transient neurologic symptoms (TNSs), lasting mostly
1-2 days, in the buttocks and/or legs during the first three postoperative
days. Eleven patients (5.7%) complained of postdural puncture head-ache. T
wo patients (emergency caesarean section because of protracted labour in on
e and elective caesarean section because of previous caesarean section in t
he other) complained of persisting pain or sensory abnormalities, Neither o
f them felt paraesthesia during lumbar puncture.
Conclusion: Women after caesarean section under a spinal block seem to suff
er more often from TNSs than non-pregnant women. The conclusions are, howev
er, uncertain since we had no control group operated on under other than sp
inal anaesthesia. The persisting neurologic symptoms in two patients might
also be due to the obstetric procedure itself. To find out about the validi
ty and possible underlying causes of our results, we need randomised studie
s with control groups receiving epidural or general anaesthesia.