Key result
Continuous dexmedetomidine cuts postoperative pulmonary complications ~44% vs. placebo in oral and maxillofacial surgery.
Why the study?
Postoperative pulmonary complications are common and significant in oral and maxillofacial surgery patients, and the effect of dexmedetomidine on reducing PPCs remains inconclusive.
Does dexmedetomidine reduce the incidence of postoperative pulmonary complications in patients undergoing oral and maxillofacial surgery with fibular free flap reconstruction?
RCT (n=160)
Double-blind
1:1 ratio using SAS 9.2
No
Does dexmedetomidine reduce the incidence of postoperative pulmonary complications in patients undergoing oral and maxillofacial surgery with fibular free flap reconstruction?
Relative Risk: 0.563 (95% CI 0.346–0.916)
Absolute Event Rate: 22.5% vs 40%
p-value: p=0.017
Continuous infusion of dexmedetomidine significantly reduced the incidence of postoperative pulmonary complications within 7 days after oral and maxillofacial surgery with fibular free flap reconstruction.
Supports dexmedetomidine infusion to reduce pulmonary complications after oral maxillofacial surgery; extends RCT evidence to fibular free flap reconstruction.
Background: Postoperative pulmonary complications (PPCs) are common and significant problems for oral and maxillofacial surgery patients. Dexmedetomidine (DEX), an α2-adrenoreceptor agonist, has been proven having lung protection effects. However, since now, there has not been final conclusion about whether DEX can reduce the incidence of PPCs. We hypothesize that, in oral and maxillofacial surgery with fibular free flap reconstruction patients, DEX may decrease the incidence of PPCs.Methods: This was a prospective, double-blind, randomized, placebo-controlled, single-centered trial with two parallel arms. A total of 160 patients at intermediate-to-high risk of PPCs undergoing oral and maxillofacial surgery with fibular free flap reconstruction and tracheotomy were enrolled and randomized to receive continuous infusion of either DEX or placebo (normal saline). 0.4 ug/kg of DEX was given over 10mins as an initial dose followed by a maintaining dose of 0.4 ug/kg/h till the second day morning after surgery. At the same time, the normal saline was administered a similar quantity. The primary outcome was the incidence of PPCs according to Clavien-Dindo score within 7 days after surgery. Results: The two groups had similar characteristics at baseline. 18(22.5%) of 80 patients administered DEX, and 32(40.0%) of 80 patient administered placebo experienced PPCs within the first 7 days after surgery (relative risk [RR] 0.563,95% confidence interval [CI] 0.346-0.916; P=0.017). In the first 7 days after surgery, the DEX group had a lower incidence of PPCs and a better postoperative survival probability (Log-rank test, P=0.019), and was less prone to occur PPCs (Cox regression, P=0.025, HR=0.516). When the total dose of DEX was more than 328μg, the patients were unlikely to have PPCs (ROC curve, AUC=0.614, P=0.009).Conclusions: For patients undergoing oral and maxillofacial surgery with fibular free flap reconstruction and tracheotomy who were at intermediate or high risk of developing PPCs, continuous infusion of DEX could decrease the occurrence of PPCs during the first 7 days after surgery and shorten the length of hospital stay after surgery, but did not increase the prevalence of bradycardia or hypotension. Trial registration: Chinese Clinical Trial Registry, www.chictr.org.cn, number: ChiCTR1800016153; Registered on May 15, 2018.
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Liu et al. (2020) conducted an RCT in Postoperative pulmonary complications (PPCs) (n=160). Dexmedetomidine vs. Placebo (normal saline) was evaluated on Incidence of postoperative pulmonary complications (PPCs) within 7 days after surgery (RR 0.563, 95% CI 0.346-0.916, p=0.017). Continuous infusion of dexmedetomidine significantly reduced the incidence of postoperative pulmonary complications within 7 days after surgery compared to placebo (22.5% vs 40.0%; RR 0.563) in patients undergoing oral and maxillofacial surgery.
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