We questioned whether the side effects outweighed the advantages of pr
iming doses of nondepolarizing neuromuscular relaxants in awake patien
ts. We have assessed lung function and clinical evidence of muscle wea
kness in 10 elderly patients, eight women and two men, aged 67-78 yr,
ASA grade I or II, before and 3 min after a priming dose (0.01 mg/kg)
of vecuronium. Forced vital capacity (FVC), forced expiratory volume i
n 1 s (FEV1), maximum midexpiratory flow rate (MMEF), peak expiratory
flow rate (PEFR), inspiratory capacity (IC), functional residual capac
ity (FRC), expiratory reserve volume (ERV), residual volume (RV), slow
vital capacity (SVC), and total lung capacity (TLC) were measured by
using a Morgan transfer test machine and oxygen saturation (SpO2) was
measured by pulse oximetery. All the patients developed ptosis, six ha
d diplopia and were unable to perform the Valsalva maneuver for 10 s,
and four were unable to swallow or lift their head for >4 s, demonstra
ting significant muscle weakness. Significant reductions occurred in F
VC, FEV1, FRC, ERV, SVC, and TLC. SpO2 decreased in 8 of 10 patients,
and in 4 the decrease exceeded 4%. We conclude that priming with vecur
onium 0.01 mg/kg in elderly patients causes significant impairment of
lung function and a significant decrease in oxygen saturation.