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Randomized Controlled Trial
. 2015 Apr 8:15:46.
doi: 10.1186/s12871-015-0026-8.

Stepwise tapering of remifentanil at the end of surgery decreased postoperative pain and the need of rescue analgesics after thyroidectomy

Affiliations
Randomized Controlled Trial

Stepwise tapering of remifentanil at the end of surgery decreased postoperative pain and the need of rescue analgesics after thyroidectomy

Sun Sook Han et al. BMC Anesthesiol. .

Abstract

Background: This study was designed to investigate whether stepwise tapering of remifentanil at the end of surgery could decrease postoperative pain scores and requirements of rescue analgesics after remifentanil-desflurane anesthesia in patients with thyroidectomy.

Methods: Sixty two patients undergoing thyroidectomy under general anesthesia were randomly allocated into two groups. All patients were anesthetised with desflurane and high-dose remifentanil. Remifentnail was infused at the rate of 0.3 μg/kg/min until the end of surgery in patients of the control group (group A) whereas remifentanil was tapered gradually from 0.3 to 0.1 μg/kg/min until the end of surgery for at least 30 minutes in patients with group B. Pain scores (0-100 numerical rating scale, NRS), rescue analgesic requirements and adverse events were assessed at 30 min, 2 h, 6 h, 12 h, and 24 h after operation.

Results: There was a significant decrease in pain scores at 30 min (20 [0-80] vs. 50 [0-100], P = 0.002) and 2 h (30 [10-60] vs. 40 [20-80], P = 0.018) after surgery in group B compared with group A. In addition, rescue analgesics are less required in group B than in group A postoperatively (2 [1-3] vs. 3 [2,3], P = 0.039). There were no significant differences in adverse events between the two groups.

Conclusions: Tapering of remifentanil at the end of surgery decreased postoperative pain scores immediately after thyroidectomy with desflurane and high-dose remifentanil anesthesia.

Trial registration: Clinical Research information Service (CRiS, registration number KCT0000589).

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Figures

Figure 1
Figure 1
Consort flow diagram. Seventy three patients were assessed for eligibility and 11 patients were excluded because of exclusion criteria (9 patients) and patient refusals (2 patients). Sixty two patients were randomized for the study and 57 patients were included in the final analysis. Five patients (4 patients from group A and 1 patient from group B) were excluded during the study period for protocol violations, intraoperative hypotension, re-operation and the use of NSAID on the day of operation.
Figure 2
Figure 2
End-tidal concentration of desflurane during the operation. Values are given as mean (SD). A group: no tapering group, B group: tapering group.

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