The efficacy and safety of intrathecal dexmedetomidine for parturients undergoing cesarean section: a double-blind randomized controlled trial

被引:11
|
作者
Li, Xiao-xiao [1 ]
Li, Yu-mei [2 ]
Lv, Xue-li [1 ]
Wang, Xing-he [1 ]
Liu, Su [1 ,3 ]
机构
[1] Xuzhou Med Univ, Jiangsu Prov Key Lab Anesthesiol, Xuzhou, Jiangsu, Peoples R China
[2] Feng Xian Peoples Hosp Jiangsu Prov, Xuzhou, Jiangsu, Peoples R China
[3] Xuzhou Med Univ, Dept Anesthesiol, Affiliated Hosp, 99 Huaihai West Rd, Xuzhou 221000, Jiangsu, Peoples R China
关键词
Intrathecal dexmedetomidine; Spinal anesthesia; Cesarean section; SPINAL-ANESTHESIA; POSTOPERATIVE QUALITY; RECOVERY SCORE; BUPIVACAINE; BLOCK; CLONIDINE; AGONISTS;
D O I
10.1186/s12871-020-01109-4
中图分类号
R614 [麻醉学];
学科分类号
100217 ;
摘要
Background: The efficacy and safety of spinal anesthesia by intrathecal dexmedetomidine (DEX) for parturients undergoing cesarean section are still lack of evidence. This aim of our study was to evaluate the efficacy and safety of intrathecal DEX for parturients undergoing cesarean section to provide more data evidence for intrathecal applications. Methods: Three hundred parturients undergoing cesarean section under spinal anesthesia were randomly assigned into three groups: group B: 9.0 mg (1.2 ml) of 0.75% bupivacaine with saline (1 ml); group FB: 9.0 mg (1.2 ml) of 0.75% bupivacaine with 20 mu g of fentanyl (1 ml); group DB: 9.0 mg (1.2 ml) of 0.75% bupivacaine with 5 mu g of DEX (1 ml). Intraoperative block characteristics, parturients' postoperative quality of recovery, maternal and neonatal outcomes and the plasma concentration of DEX were measured. All parturients were followed up for 30 days to determine whether nerve injury occurred. Results: Compared with group B, the duration of sensory block in group FB and group DB were significantly prolonged (108.4 min [95% Confidence Interval (CI) = 104.6-112.3] in group B, and 122.0 min [95% CI = 116.8-127.3] in group FB, 148.2 min [95% CI = 145.3-151.1] in group DB). The overall score of quality recovery in group DB (71.6 [95% CI = 71.0-72.2]) was significantly higher than that in group FB (61.5 [95% CI = 60.8-62.2]) and group B (61.7 [95% CI = 61.0-62.4]). There was no statistically significant difference among the three groups for PH, PaO2, and PaCO(2)of newborn. The plasma concentration of DEX in umbilical artery and umbilical vein was low and cannot be detected. The 30-days follow-up of parturients did not show any new onset of back, buttock or leg pain or paresthesia. Conclusions: DEX is a potential local anesthetic adjuvant that the intrathecal combination of 5 mu g DEX can safely exhibit a facilitatory block effect and improve parturients' recovery quality.
引用
收藏
页数:9
相关论文
共 50 条
  • [41] Anterior quadratus lumborum catheters for elective cesarean section: A double-blind, randomized, placebo-controlled trial
    Hansen, Christian K.
    Steingrimsdottir, Gudny E.
    Dam, Mette
    Nielsen, Martin V.
    Tanggaard, Katrine
    Poulsen, Troels D.
    Lebech, Morten
    Borglum, Jens
    [J]. ACTA ANAESTHESIOLOGICA SCANDINAVICA, 2024, 68 (02) : 254 - 262
  • [42] Efficacy and safety of oral tolvaptan in patients undergoing hemodialysis: a Phase 2, double-blind, randomized, placebo-controlled trial
    Ogata, Hiroaki
    Shimofurutani, Naoko
    Okada, Tadashi
    Nagamoto, Hisashi
    Akizawa, Tadao
    [J]. NEPHROLOGY DIALYSIS TRANSPLANTATION, 2021, 36 (06) : 1088 - 1097
  • [43] Efficacy and Safety of Tauroursodeoxycholic Acid in the Treatment of Liver Cirrhosis: A Double-blind Randomized Controlled Trial
    潘晓莉
    赵莉
    李靓
    李爱华
    叶进
    杨玲
    徐可树
    侯晓华
    [J]. Current Medical Science, 2013, (02) : 189 - 194
  • [44] Efficacy and safety of tauroursodeoxycholic acid in the treatment of liver cirrhosis: A double-blind randomized controlled trial
    Xiao-li Pan
    Li Zhao
    Liang Li
    Ai-hua Li
    Jin Ye
    Ling Yang
    Ke-shu Xu
    Xiao-hua Hou
    [J]. Journal of Huazhong University of Science and Technology [Medical Sciences], 2013, 33 : 189 - 194
  • [45] Comparison of dexmedetomidine and fentanyl as adjuvants to intrathecal levobupivacaine in lower segment cesarean section: A prospective, randomized double blind study
    Rastogi, Kapil
    Bharti, Alok Kumar
    Singh, Yashpal
    Ranjan, Pushkar
    [J]. ANAESTHESIA PAIN & INTENSIVE CARE, 2020, 24 (04) : 383 - 388
  • [46] Safety and Efficacy of Levamisole in Loiasis: A Randomized, Placebo-controlled, Double-blind Clinical Trial
    Campillo, Jeremy T.
    Bikita, Paul
    Hemilembolo, Marlhand
    Louya, Frederic
    Missamou, Francois
    Pion, Sebastien D. S.
    Boussinesq, Michel
    Chesnais, CedricB
    [J]. CLINICAL INFECTIOUS DISEASES, 2022, 75 (01) : 19 - 27
  • [47] Safety and efficacy of tibolone and menopausal transition: a randomized, double-blind placebo-controlled trial
    Maria, Morais-Socorro
    Alvaro, Cavalcanti Maciel
    Rand, Martins
    Paulo, Neto Francisco
    Adriana, Rezende
    George, Azevedo
    Maria, Almeida
    [J]. GYNECOLOGICAL ENDOCRINOLOGY, 2012, 28 (06) : 483 - 487
  • [48] Efficacy and Safety of Pregabalin for Muscle Cramps in Liver Cirrhosis: A Double-Blind Randomized Controlled Trial
    Ahn, Sohyun
    Hong, Yoon-Ho
    Lee, Dong Hyeon
    Joo, Sae Kyung
    Jung, Yong Jin
    Sohn, Sung-Yeon
    Choi, Kyomin
    Kim, Won
    [J]. JOURNAL OF KOREAN MEDICAL SCIENCE, 2022, 37 (07)
  • [49] Efficacy and safety of tauroursodeoxycholic acid in the treatment of liver cirrhosis: A double-blind randomized controlled trial
    Pan, Xiao-li
    Zhao, Li
    Li, Liang
    Li, Ai-hua
    Ye, Jin
    Yang, Ling
    Xu, Ke-shu
    Hou, Xiao-hua
    [J]. JOURNAL OF HUAZHONG UNIVERSITY OF SCIENCE AND TECHNOLOGY-MEDICAL SCIENCES, 2013, 33 (02) : 189 - 194
  • [50] Efficacy and Safety of Baclofen for Alcohol Dependence: A Randomized, Double-Blind, Placebo-Controlled Trial
    Garbutt, James C.
    Kampov-Polevoy, Alexei B.
    Gallop, Robert
    Kalka-Juhl, Linda
    Flannery, Barbara A.
    [J]. ALCOHOLISM-CLINICAL AND EXPERIMENTAL RESEARCH, 2010, 34 (11) : 1849 - 1857