已发表论文

术中右美托咪定可减轻经皮肾镜取石术患者术后的全身炎症反应综合征:一个回顾性队列研究

 

Authors Tan F, Gan X, Deng Y, Li X, Guo N, Hei Z, Zhu Q, Chen ZG, Zhou S

Received 17 November 2017

Accepted for publication 22 December 2017

Published 14 February 2018 Volume 2018:14 Pages 287—293

DOI https://doi.org/10.2147/TCRM.S157320

Checked for plagiarism Yes

Review by Single-blind

Peer reviewers approved by Dr Hoa Le

Peer reviewer comments 2

Editor who approved publication: Professor Deyun Wang

Purpose: Dexmedetomidine (DEX) has been reported to attenuate inflammation in rats. The present retrospective cohort study aimed to investigate whether intraoperative administration with DEX could reduce the incidence of postoperative systemic inflammatory response syndrome (SIRS) in patients following percutaneous nephrolithotomy (PCNL).
Patients and methods:
 A total of 251 patients were included in the analysis. Among these patients, 175 received intravenous DEX infusion during the intraoperative period and 76 did not. The primary outcome measures were the incidences of postoperative SIRS and fever. Secondary outcomes included patient-controlled analgesia (tramadol) requirements, length of postoperative hospitalization stay, serum creatinine (Scr) and serum blood urea nitrogen (BUN) concentration, and adverse events (bradycardia, hypotension, renal artery thrombosis).
Results:
 Administration of DEX not only significantly attenuated the incidence of SIRS and fever (=0.029, =0.042, respectively), but also reduced analgesia requirements (=0.028). The length of postoperative hospitalization stay, Scr and BUN concentration, and adverse events did not differ significantly between the two groups. Further univariate and multivariate logistic regression analysis indicated that intraoperative DEX administration was a protective factor against SIRS after PCNL (OR 0.476 [95% CI: 0.257–0.835]; =0.019).
Conclusion: 
Intraoperative administration of DEX might be associated with reductions in the incidences of SIRS and fever after PCNL.
Keywords: PCNL, SIRS, risk factor, dexmedetomidine