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Effects of droperidol dosage on postoperative emetic symptoms following pediatric strabismus surgery
Stanley W Stead1, Christopher D Beatie, Mary A Keyes
1Department of Anesthesiology, Jules Stein Eye Institute, University of California at Los Angeles, Los Angeles, CA 90095, USA.
Insights
Droperidol effectively reduces postoperative nausea and vomiting in pediatric strabismus surgery patients. The 80 microg.kg(-1) dose is most effective, without delaying discharge times.
Area of Science:
- Anesthesiology
- Pediatric Surgery
- Pharmacology
Background:
- Postoperative nausea and vomiting (PONV) are common complications in pediatric strabismus surgery.
- Effective antiemetic prophylaxis is crucial for optimizing patient recovery and discharge.
Purpose of the Study:
- To evaluate the efficacy of four different doses of droperidol in preventing postoperative emetic symptoms.
- To assess the safety and side effects associated with varying droperidol dosages in pediatric patients.
Main Methods:
- A randomized, blinded study was conducted with 82 pediatric patients (1-16 years) undergoing outpatient strabismus surgery.
- Patients received intravenous droperidol at doses of 10, 20, 40, or 80 microg.kg(-1) immediately after anesthesia induction.
- Emetic symptoms and side effects were monitored postoperatively, with a focus on predischarge and peak symptom occurrences.
Main Results:
- A dose-dependent reduction in emetic symptoms was observed with increasing droperidol dosage.
- The 80 microg.kg(-1) dose showed the lowest incidence of predischarge (5%) and peak (15%) emetic symptoms.
- No significant increase in recovery or hospitalization times was noted with higher droperidol doses; sedation and extrapyramidal symptoms were absent.
- Emetic symptoms, however, significantly delayed discharge time by approximately 76 minutes.
Conclusions:
- Prophylactic administration of droperidol at 80 microg.kg(-1) is the most effective dose for reducing postoperative emetic symptoms in pediatric strabismus surgery.
- This optimal dose does not prolong patient discharge time.
- Prompt management of emetic symptoms is essential to prevent significant delays in patient discharge.
Study Objective:
To compare the frequency of postoperative emetic symptoms and side effects in pediatric strabismus surgery using four doses of droperidol.
Design:
Randomized, blinded study.
Setting:
University eye institute.
Patients:
82 ASA physical status I and II pediatric patients, aged 1 to 16 years, undergoing outpatient strabismus surgery.
Interventions:
Patients were assigned to one of four doses of droperidol (10, 20, 40, or 80 microg.kg(-1)) (Groups 1, 2, 3, and 4, respectively). All patients received the same anesthetic management, with droperidol administered intravenously immediately after induction of anesthesia.
Measurements And Main Results:
Postoperatively, patients were evaluated for emetic symptoms (nausea, retching, and/or vomiting) and side effects (postoperative sedation or extrapyramidal symptoms). There was a dose-dependent reduction of emetic symptoms seen with increasing droperidol dose. Predischarge emetic symptoms were 50%, 15%, 15%, and 5% in Groups 1, 2, 3, and 4, respectively (p < 0.009). Peak emetic symptoms were observed after discharge: 75%, 40%, 35%, and 15% in Groups 1, 2, 3, and 4, respectively (p < 0.003). Convalescence times, including awakening, extubation, recovery, and hospitalization, were unaffected by increasing droperidol dose. Sedation was similar in all groups and no patient exhibited any side effects. However, when patients exhibited emetic symptoms, discharge time increased from 207 +/- 57 minutes to 283 +/- 128 minutes (p < 0.001).
Conclusions:
Prophylactic administration of droperidol 80 microg.kg(-1) is most effective in reducing postoperative emetic symptoms without increasing time to discharge. In those patients with emetic symptoms who also received prophylactic droperidol, time to discharge was significantly delayed.
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