A single dose of propofol at the end of surgery for the prevention of emergence agitation in children undergoing strabismus surgery during sevoflurane anesthesia.

BACKGROUND: Emergence agitation in children after sevoflurane is common. Different drugs have been used to decrease its occurrence with variable efficacy. The authors compared the incidence and severity of emergence agitation in children who received a single dose of propofol at the end of strabismus surgery versus children who received saline. METHODS: In this prospective, randomized, double-blind study, the authors enrolled 80 healthy children aged 2-6 yr. The children were randomly allocated to the propofol group (n = 41), which received 1 mg/kg propofol at the end of surgery, or to the saline group (n = 39), which received saline. RESULTS: The mean scores on the Pediatric Anesthesia Emergence Delirium scale were significantly lower in the propofol group compared with the saline group (8.6 +/- 3.9 vs. 11.5 +/- 4.5; P = 0.004). Also, the incidence of agitation was significantly lower in the propofol group compared with the saline group (19.5% vs. 47.2%; P = 0.01). A threshold score greater than 10 on the Pediatric Anesthesia Emergence Delirium scale was the best discriminator between presence and absence of emergence agitation. Times to removal of the laryngeal mask airway (10.6 +/- 1.5 vs. 9.4 +/- 1.9 min; P = 0.004) and emergence times (23.4 +/- 5.7 vs. 19.7 +/- 5 min; P = 0.004) were significantly longer in the propofol group. However, discharge times were similar between the two groups (propofol: 34.1 +/- 8.4 min; saline: 34.9 +/- 8.6 min). More parents in the propofol group were satisfied. CONCLUSIONS: In children undergoing strabismus surgery, 1 mg/kg propofol at the end of surgery after discontinuation of sevoflurane decreases the incidence of agitation and improves parents' satisfaction without delaying discharge from the postanesthesia care unit.

Unilateral anterior uveitis complicating zoledronic acid therapy in breast cancer.

BACKGROUND: Zoledronic acid is very widely used in patients with metastatic bone disease and osteoporosis. Only one case of bilateral uveitis was recently reported related to its use. CASE PRESENTATION: We report the first case of severe unilateral anterior uveitis in a patient with breast cancer and an intraocular lens. Following zoledronic acid infusion, the patient developed severe and dramatic right eye pain with decreased visual acuity within 24 hours and was found to have a fibrinous anterior uveitis of moderate severity The patient was treated with topical prednisone and atropine eyedrops and recovered slowly over several months. CONCLUSION: Internists, oncologists, endocrinologists, and ophtalmologists should be aware of uveitis as a possible complication of zoledronic acid therapy. Patients should be instructed to report immediately to their physicians and treatment with topical prednisone and atropine eyedrops should be instituted immediately at the onset of symptoms. This report documents anterior uveitis as a complication of zoledronic acid therapy. This reaction could be an idiosyncratic one but further research may shed more light on the etiology.

Comparison of the immediate with the 24-hour postoperative prism and cover measurements in adjustable muscle surgery: is immediate postoperative adjustment reliable?

PURPOSE: Immediate postoperative adjustment after adjustable-suture strabismus surgery has been suggested as a viable alternative to the classic adjustment that is performed, usually within 6 to 24 hours after surgery. The purpose of this study was to compare the immediate postoperative eye measurements with those taken 24 hours postoperatively and to determine whether there was any significant difference between the 2 measurements. METHODS: This was a prospective study of strabismus patients who were candidates for muscle surgery using the adjustable-suture technique. All patients received a total intravenous general anesthesia, which allowed rapid recovery of consciousness. Measurements using the simultaneous prism cover test were obtained in the recovery room immediately after the patients regained consciousness and again 24 hours after surgery. Both measurements were taken before adjustment and were compared. RESULTS: A total of 25 patients were studied. The postoperative alignment changed significantly during the first 24 hours in 84% of our patients. The mean drift in alignment during the first 24 hours measured 7.2 +/- 4.3 prism diopters and was significantly different from 0 ( P < 0.001). CONCLUSION: The immediate postoperative ocular alignment after adjustable strabismus surgery is significantly different from the 24 hours postoperative alignment. This difference was noticed despite using an anesthesia protocol that allowed rapid recovery and full regaining of consciousness shortly after the conclusion of surgery. This early drift should be taken into consideration if adjustment is to be made in the immediate postoperative period.