Whole-Course Application of Dexmedetomidine Combined with Ketorolac in Nonnarcotic Postoperative Analgesia for Patients with Lung Cancer Undergoing Thoracoscopic Surgery: A Randomized Control Trial.


Journal

Pain physician
ISSN: 2150-1149
Titre abrégé: Pain Physician
Pays: United States
ID NLM: 100954394

Informations de publication

Date de publication:
03 2020
Historique:
entrez: 28 3 2020
pubmed: 28 3 2020
medline: 8 9 2020
Statut: ppublish

Résumé

Opioid-based postoperative analgesia provides adequate analgesia with much adverse effects and immunosuppression. Dexmedetomidine and ketorolac have properties of opioid-sparing, antiinflammation, and immune protection. To investigate the efficacy and safety of whole-course application of dexmedetomidine combined with ketorolac in nonnarcotic postoperative analgesia and its effect on inflammatory response and immune function in thoracoscopic surgery of lung cancer. Double-blind, randomized control trial. The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China. Sixty patients scheduled for thoracoscopic surgery were enrolled and randomly divided into 2 groups to receive a combination of intraoperative usage of dexmedetomidine and postoperative patient-controlled intravenous analgesia of dexmedetomidine 0.1 µg/kg/h and ketorolac 3 mg/kg (DEX group) or only postoperative patient-controlled intravenous analgesia of sufentanil 1.5 µg/kg and ketorolac 3 mg/kg (SUF group) for 48 hours. Vital signs, postoperative Visual Analog Scale (VAS) score, Ramsay sedation score, patient-controlled analgesia pressing times, consumption of sufentanil and rescue drug, and complications were compared between the 2 groups. The levels of inflammatory factors and immune function were also compared. A significant reduction in median blood pressures and heart rates within 48 hours after surgery and perioperative consumption of sufentanil were observed in the DEX group compared with the SUF group (P < 0.05). No statistically significant difference was found in VAS scores, patient-controlled analgesia pressing times, and rescue drug consumption between the 2 groups (P > 0.05). The incidence of nausea was significantly lower in the DEX group compared with the SUF group (P < 0.05). A significant decrease of interleukin (IL)-1 beta, IL-6, tumor necrosis factor (TNF)-alpha, and increased CD4+ and CD4+/CD8+ were observed in the DEX group compared with the SUF group at 24 and 48 hours after surgery (P < 0.05). There was no difference in the levels of CD8+ and natural killer cells between the 2 groups (P > 0.05). This study was limited by its sample size. Whole-course application of dexmedetomidine combined with ketorolac in nonnarcotic postoperative analgesia provided adequate and safe postoperative analgesia, reduced sufentanil consumption, analgesia-related complications, alleviated inflammatory response, and immunosuppression compared with sufentanil-based analgesia in thoracoscopic surgery. Dexmedetomidine, ketorolac, sufentanil, thoracoscopic surgery, postoperative analgesic, patient-controlled analgesia, inflammatory response, immune function.

Sections du résumé

BACKGROUND
Opioid-based postoperative analgesia provides adequate analgesia with much adverse effects and immunosuppression. Dexmedetomidine and ketorolac have properties of opioid-sparing, antiinflammation, and immune protection.
OBJECTIVES
To investigate the efficacy and safety of whole-course application of dexmedetomidine combined with ketorolac in nonnarcotic postoperative analgesia and its effect on inflammatory response and immune function in thoracoscopic surgery of lung cancer.
STUDY DESIGN
Double-blind, randomized control trial.
SETTING
The First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning, China.
METHODS
Sixty patients scheduled for thoracoscopic surgery were enrolled and randomly divided into 2 groups to receive a combination of intraoperative usage of dexmedetomidine and postoperative patient-controlled intravenous analgesia of dexmedetomidine 0.1 µg/kg/h and ketorolac 3 mg/kg (DEX group) or only postoperative patient-controlled intravenous analgesia of sufentanil 1.5 µg/kg and ketorolac 3 mg/kg (SUF group) for 48 hours. Vital signs, postoperative Visual Analog Scale (VAS) score, Ramsay sedation score, patient-controlled analgesia pressing times, consumption of sufentanil and rescue drug, and complications were compared between the 2 groups. The levels of inflammatory factors and immune function were also compared.
RESULTS
A significant reduction in median blood pressures and heart rates within 48 hours after surgery and perioperative consumption of sufentanil were observed in the DEX group compared with the SUF group (P < 0.05). No statistically significant difference was found in VAS scores, patient-controlled analgesia pressing times, and rescue drug consumption between the 2 groups (P > 0.05). The incidence of nausea was significantly lower in the DEX group compared with the SUF group (P < 0.05). A significant decrease of interleukin (IL)-1 beta, IL-6, tumor necrosis factor (TNF)-alpha, and increased CD4+ and CD4+/CD8+ were observed in the DEX group compared with the SUF group at 24 and 48 hours after surgery (P < 0.05). There was no difference in the levels of CD8+ and natural killer cells between the 2 groups (P > 0.05).
LIMITATIONS
This study was limited by its sample size.
CONCLUSIONS
Whole-course application of dexmedetomidine combined with ketorolac in nonnarcotic postoperative analgesia provided adequate and safe postoperative analgesia, reduced sufentanil consumption, analgesia-related complications, alleviated inflammatory response, and immunosuppression compared with sufentanil-based analgesia in thoracoscopic surgery.
KEY WORDS
Dexmedetomidine, ketorolac, sufentanil, thoracoscopic surgery, postoperative analgesic, patient-controlled analgesia, inflammatory response, immune function.

Identifiants

pubmed: 32214297

Substances chimiques

Analgesics, Non-Narcotic 0
Dexmedetomidine 67VB76HONO
Ketorolac YZI5105V0L

Types de publication

Journal Article Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

E185-E193

Commentaires et corrections

Type : ErratumIn

Auteurs

Zhuang Miao (Z)

Department of Anesthesiology, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Ping Wu (P)

Department of Anesthesiology, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Jing Wang (J)

Anesthesiology Department, Dalian Medical of University, Dalian, China; 3Department of Thoracic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Fa-Chen Zhou (FC)

Anesthesiology Department, Dalian Medical of University, Dalian, China; 3Department of Thoracic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Yun Lin (Y)

Anesthesiology Department, Dalian Medical of University, Dalian, China; 3Department of Thoracic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Xin-Yu Lu (XY)

Department of Anesthesiology, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Run Lv (R)

Anesthesiology Department, Dalian Medical of University, Dalian, China; 3Department of Thoracic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Qian-Hao Hou (QH)

Anesthesiology Department, Dalian Medical of University, Dalian, China; 3Department of Thoracic Surgery, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

Qing-Ping Wen (QP)

Department of Anesthesiology, The First Affiliated Hospital of Dalian Medical University, Dalian, China.

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Classifications MeSH