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Remifentanil versus dexmedetomidine for treatment of cardiac surgery patients with moderate to severe noninvasive ventilation intolerance (REDNIVIN): a prospective, cohort study.
Hao, Guang-Wei; Luo, Jing-Chao; Xue, Yan; Ma, Guo-Guang; Su, Ying; Hou, Jun-Yi; Yu, Shen-Ji; Liu, Kai; Zheng, Ji-Li; Tu, Guo-Wei; Luo, Zhe.
Afiliação
  • Hao GW; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Luo JC; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Xue Y; Department of Nursing, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Ma GG; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Su Y; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Hou JY; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Yu SJ; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Liu K; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Zheng JL; Department of Nursing, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Tu GW; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
  • Luo Z; Department of Critical Care Medicine, Zhongshan Hospital, Fudan University, Shanghai, China.
J Thorac Dis ; 12(10): 5857-5868, 2020 Oct.
Article em En | MEDLINE | ID: mdl-33209418
ABSTRACT

BACKGROUND:

The use of sedation to noninvasive ventilation (NIV) patients remains controversial, however, for intolerant patients who are uncooperative, administration of analgesics and sedatives may be beneficial before resorting to intubation. The aim of this study was to evaluate the efficacy of remifentanil (REM) versus dexmedetomidine (DEX) for treatment of cardiac surgery (CS) patients with moderate to severe NIV intolerance.

METHODS:

This prospective cohort study of CS patients with moderate to severe NIV intolerance was conducted between January 2018 and March 2019. Patients were treated with either REM or DEX, decided by the bedside intensivist. Depending on the treatment regimen, the patients were allocated to one of two groups the REM group or DEX group.

RESULTS:

A total of 90 patients were enrolled in this study (52 in the REM group and 38 in the DEX group). The mitigation rate, defined as the percentage of patients who were relieved from the initial moderate to severe intolerant status, was greater in the REM group than DEX group at 15 min and 3 h (15 min 83% vs. 61%, P=0.029; 3 h 92% vs. 74%, P=0.016), although the mean mitigation rate (81% vs. 85%, P=0.800) was comparable between the two groups. NIV failure, defined as reintubation or death over the course of study, was comparable between the two groups (19.2% vs. 21.1%, respectively, P=0.831). There were no significant differences between the two groups in other clinical outcomes, including tracheostomy (15.4% vs. 15.8%, P=0.958), in-hospital mortality (11.5% vs. 10.5%, P=0.880), ICU length of stay (LOS) (7 vs. 7 days, P=0.802), and in-hospital LOS (17 vs. 19 days, P=0.589).

CONCLUSIONS:

REM was as effective as DEX in CS patients with moderate to severe NIV intolerance. Although the effect of REM was better than that of DEX over the first 3 h, the cumulative effect was similar between the two treatments.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies Idioma: En Revista: J Thorac Dis Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Etiology_studies / Observational_studies Idioma: En Revista: J Thorac Dis Ano de publicação: 2020 Tipo de documento: Article País de afiliação: China