文献速递复苏与心脏骤停镇静镇痛与谵妄重症综合管理

罗库溴铵与琥珀胆碱用于快速序贯诱导插管:知晓、肌松与插管后镇静

Rocuronium vs Succinylcholine for RSI: Awareness, Paralysis, and Post-Intubation Sedation
RSS 订阅 · REBEL EM · 2026-06-22
一句话结论使用罗库溴铵的急诊RSI患者插管后首次镇静与镇痛时间分别比琥珀胆碱延迟2分钟和3分钟,但罗库溴铵可能导致患者在诱导剂消退后仍处于肌松状态而产生知晓。

这是一项包含2000余例急诊插管患者的回顾性队列研究,比较罗库溴铵与琥珀胆碱在RSI中的插管后镇静镇痛时机。研究纳入使用依托咪酯诱导的成人急诊插管患者。结果显示罗库溴铵组首次镇静中位时间为12分钟vs琥珀胆碱组10分钟,首次镇痛中位时间为24分钟vs 21分钟。琥珀胆碱组更早获得镇静(aHR 1.3,95%CI 1.2-1.5)和镇痛(aHR 1.4,95%CI 1.1-1.6)。仅44.8%患者在急诊期间同时接受了镇静和镇痛。罗库溴铵组院内死亡率更高(20.1% vs 11.0%),提示基线存在重要差异。

要点

  • 使用罗库溴铵进行RSI时,插管后首次镇静中位时间为12分钟,比琥珀胆碱(10分钟)延迟2分钟;首次镇痛中位时间为24分钟vs 21分钟,延迟3分钟
  • 罗库溴铵肌松作用持续20-75分钟,而琥珀胆碱仅5-10分钟,当依托咪酯等短效诱导剂消退后,罗库溴铵可能导致患者清醒但仍处于肌松状态
  • 琥珀胆碱组更早获得插管后镇静(aHR 1.3,95%CI 1.2-1.5)和镇痛(aHR 1.4,95%CI 1.1-1.6)
  • 仅44.8%急诊插管患者在急诊期间同时接受了镇静和镇痛;插管后低血压降低接受镇静的可能性(aHR 0.7,95%CI 0.5-0.8)
  • 急诊药师床旁参与与改善镇静时机相关(aHR 1.1,95%CI 1.0-1.3)

适用人群与场景

  • 成人(≥18岁)急诊插管患者,使用依托咪酯作为诱导剂,并使用罗库溴铵或琥珀胆碱作为肌松剂
  • 研究来自3家城市三级学术急诊科(包括2家一级创伤中心),时间跨度2012年6月至2022年6月
  • 排除未使用肌松剂或诱导剂插管的患者,以及使用依托咪酯以外诱导剂的患者

诊断标准与关键阈值

  • 原文未提及

处置流程与药物剂量

  • 琥珀胆碱组插管后首次镇静中位时间为10分钟,首次镇痛中位时间为21分钟
  • 罗库溴铵组插管后首次镇静中位时间为12分钟,首次镇痛中位时间为24分钟
  • 插管后镇静与镇痛应在RSI前规划,特别是使用长效肌松剂时

红旗征与不能漏的情况

  • 罗库溴铵作用持续20-75分钟可能超过诱导剂,导致患者清醒但无法移动或表达不适(知晓伴肌松)
  • 插管后低血压与较低的接受镇静可能性相关(aHR 0.7,95%CI 0.5-0.8),但这些患者同样需要镇静镇痛评估
  • 仅44.8%患者在急诊期间同时接受镇静和镇痛,提示插管后镇静镇痛管理存在重大缺口

研究设计与关键结果

  • 回顾性队列研究,纳入2000余例急诊插管患者,来自单一医疗系统内3家城市三级学术急诊科
  • 主要终点:罗库溴铵组插管后首次镇静中位时间12分钟vs琥珀胆碱组10分钟,首次镇痛中位时间24分钟vs 21分钟
  • 校正后分析:琥珀胆碱与更早获得镇静相关(aHR 1.3,95%CI 1.2-1.5)及更早获得镇痛相关(aHR 1.4,95%CI 1.1-1.6)
  • 罗库溴铵组平均镇静时间延迟7.9分钟,平均镇痛时间延迟12.8分钟
  • 罗库溴铵组院内死亡率20.1% vs琥珀胆碱组11.0%,提示两组基线存在重要未测量差异
  • 急诊药师床旁参与与改善镇静时机相关(aHR 1.1,95%CI 1.0-1.3)

证据类型、等级与局限

  • 证据类型:回顾性队列研究,通过Epic电子病历系统回顾
  • 局限性:仅纳入依托咪酯诱导患者,结果可能不适用于氯胺酮或丙泊酚;肌松剂选择非随机化,存在选择偏倚和适应证混杂风险
  • 局限性:未直接评估患者知晓情况,无患者访谈确认肌松期间的清醒、疼痛或回忆
  • 局限性:罗库溴铵组院内死亡率高9.1%,提示疾病严重程度、创伤状态、气道复杂性等重要基线差异未被充分校正
  • 局限性:中位时间差异小(镇静2分钟、镇痛3分钟),临床意义不确定;且时间终点为疾病导向而非患者导向指标

对床旁实践的改变

  • 使用罗库溴铵进行RSI时,应在插管前就准备好插管后镇静镇痛方案,避免诱导剂消退后患者仍处于肌松状态而产生知晓
  • 琥珀胆碱作用时间短(5-10分钟),当肌松消退时患者可通过体动表达不适,提供追加镇静镇痛的视觉线索;罗库溴铵无此优势
  • 插管后低血压患者虽然镇静镇痛延迟风险更高,但仍需评估镇静镇痛需求,不应因血流动力学问题而忽视
  • 急诊药师床旁参与可改善插管后镇静时机,提示多学科协作的价值
  • 本研究仅适用于依托咪酯诱导的患者,使用氯胺酮或丙泊酚诱导时结论可能不同

指南或共识出处

  • 原文未提及

以上提炼依据论文摘要(全文未开放获取,或许可不允许翻译转载);全文请点「阅读原文」。

原文图文 · 图 24 张

REBEL Rundown

Key Points

Rocuronium was associated with delayed post-intubation sedation and analgesia compared with succinylcholine in adult ED patients induced with etomidate.

The absolute median differences were small: 2 minutes to sedation and 3 minutes to analgesia, making the clinical significance uncertain.

The real concern is awareness during paralysis: rocuronium may outlast the induction agent, leaving patients awake but unable to move or communicate.

This was a retrospective observational study, and the 9.1% higher in-hospital mortality in the rocuronium group suggests important unmeasured baseline differences.

Post-intubation sedation and analgesia should be planned before RSI, especially when using long-acting paralytics.

Introduction

Rapid sequence intubation in the emergency department involves the use of an induction agent and neuromuscular blocker. Two commonly used neuromuscular blockers with differing durations are succinylcholine (5-10 minutes) and rocuronium (20-75 minutes). The most common induction agents (etomidate, ketamine, propofol) have relatively short half-lives. When a short-lived paralytic wears off, we can assess discomfort providing us with a visual cue for additional sedation and analgesia. If sedation ends prior to paralysis, patients may be conscious but paralyzed or in discomfort without the ability to express it – a situation that may occur with longer acting paralytics like rocuronium.

Paper

Hwang C, et al. Impact of paralytic choice on postintubation sedation and analgesia in the emergency department. Am J Health Syst Pharm. 2025;82(Supplement_3):S2929-S2936. PMID: 40037283

Previously Covered On REBEL

The CURASMUR Trial: Roc Rocks & Sux Sucks?

Succinylcholine or Rocuronium for 1st Pass Success Rate

Succinylcholine vs Rocuronium for RSI in Traumatic Brain Injury

The ED-AWARENESS Study: Awareness with Paralysis

Optimal Order of Drug Administration in Rapid Sequence Intubation

What They Did

CLINICAL QUESTION

Do patients receiving rocuronium during RSI have a delay in postintubation sedation and analgesia compared to those receiving succinylcholine?

STUDY DESIGN

Retrospective cohort study

Review of Epic electronic health records

3 urban tertiary care academic EDs – single health system in 1 stateTwo Level 1 trauma centers

Selection of medications (induction, paralysis, sedation, analgesia) based on physician preference not protocol driven.

EM clinical pharmacists present at each site

Time period – ED #1: November 2017 to June 2022

ED #2: April 2014 to June 2022

ED #3: June 2012 to June 2022.

POPULATION

Inclusion Criteria:

All ED patients who underwent endotracheal intubation, adults 18 years of age or older, received etomidate and either succinylcholine or rocuronium.

Exclusion Criteria:

Intubated without paralytic or induction medications, use of induction agents other than etomidate.

INTERVENTION & COMPARATOR

Intervention Group:

Rocuronium used as the neuromuscular blocker during RSI in adult ED patients who received etomidate as the induction agent.

Comparator Group:

Succinylcholine used as the neuromuscular blocker during RSI in adult ED patients who received etomidate as the induction agent.

OUTCOMES

Primary Outcome:

Time from paralytic administration to the first dose of post-intubation sedation or analgesia

Additional Outcomes:

Time to first sedative, time to first analgesic, medication selection and dosing, hypotension, pharmacist presence, ED/hospital mortality, survival to discharge, and ED length of stay.

Results:

Critical Results

Sedation timing: Median time to first sedative was 12 minutes with rocuronium vs 10 minutes with succinylcholine.

Analgesia timing: Median time to first analgesic was 24 minutes with rocuronium vs 21 minutes with succinylcholine.

Adjusted sedation outcome: Succinylcholine was associated with improved time to sedation: aHR 1.3; 95% CI 1.2–1.5.

Adjusted analgesia outcome: Succinylcholine was associated with improved time to analgesia: aHR 1.4; 95% CI 1.1–1.6.

Absolute mean difference: Rocuronium was associated with longer mean time to sedation by 7.9 minutes and longer mean time to analgesia by 12.8 minutes.

Sedation/analgesia gap: Only 44.8% of patients received both sedation and analgesia during their ED stay.

Hypotension effect: Post-RSI hypotension was associated with lower likelihood of receiving sedation: aHR 0.7; 95% CI 0.5–0.8.

Pharmacist presence: ED pharmacist bedside presence was associated with improved sedation timing: aHR 1.1; 95% CI 1.0–1.3.

Mortality imbalance: In-hospital mortality was higher in the rocuronium group: 20.1% vs 11.0%, suggesting important baseline differences between groups.

Strengths

Clinically important question: This study addresses a real ED problem: care does not end when the tube passes through the cords. Post-intubation sedation and analgesia are part of airway management.

Large sample size: More than 2,000 ED intubations were included, giving this study a larger cohort than many prior studies on post-intubation analgosedation.

Multicenter ED cohort: The study included three urban tertiary care academic EDs, including two Level 1 trauma centers, capturing variation in ED airway practice.

Relevant bedside comparison: Rocuronium and succinylcholine are the two most common paralytics used for RSI, making the comparison directly applicable to ED practice.

Granular medication timing: The authors evaluated the timing of medication administration rather than simply reporting whether sedation or analgesia was eventually given.

Appropriate time-to-event analysis: The authors used an adjusted Cox proportional hazards model, which fits the clinical question because the outcome is not just whether sedation or analgesia occurred, but when it occurred.

Attempted adjustment for confounding: The analysis adjusted for paralytic choice, post-RSI hypotension, ED pharmacist presence, and practice site. This does not eliminate confounding, but it strengthens the analysis compared with a simple unadjusted comparison.

Site-level stratification: The model was stratified by participating site, which is important because sedation practices, trauma volume, patient populations, and local RSI culture may differ across EDs.

Practice-pattern detail: The authors reported which sedatives and analgesics were used, along with initial dosing. This helps clinicians compare the study sites’ practice patterns with their own.

Pharmacist presence examined: The study evaluated ED pharmacist bedside presence, highlighting a potentially modifiable system factor associated with improved sedation timing.

Biologic plausibility: The findings fit the pharmacology: etomidate wears off quickly, succinylcholine wears off relatively quickly, and rocuronium lasts much longer, creating a plausible pathway to awareness with paralysis.

Consistent with prior literature: The findings align with prior studies associating rocuronium use with delayed or reduced post-intubation analgesia and sedation.

Limitations

Etomidate-only cohort: Only patients induced with etomidate were included, so findings may not apply to RSI with ketamine or propofol.

Small absolute time difference: Although statistically significant, the median difference was only 2 minutes for sedation and 3 minutes for analgesia, making clinical significance unclear.

Disease-centered outcome: Time to first sedative or analgesic is not patient-centered and does not tell us whether patients experienced awareness, pain, distress, or recall.

No direct awareness assessment: Patients were not interviewed for recollection of awareness while paralyzed.

Baseline imbalance: The rocuronium group had a 9.1% higher in-hospital mortality rate, suggesting important unmeasured baseline differences.

Retrospective observational design: Paralytic choice was not randomized, creating risk of selection bias and confounding by indication.

Residual confounding: Illness severity, trauma status, airway complexity, and contraindications to succinylcholine may have influenced paralytic choice.

Mortality signal is not causal: Higher mortality in the rocuronium group should not be interpreted as rocuronium causing harm.

No sedation-depth data: The study does not report RASS scores or whether adequate sedation was achieved.

First dose only: Timing of the first dose does not address dose adequacy, repeat dosing, infusion titration, or ongoing comfort.

EHR timing limitations: Medication administration times may reflect documentation timing rather than true bedside administration.

Pharmacist presence misclassification: Bedside pharmacist presence was inferred from schedules, not directly confirmed.

Limited generalizability: The study was performed in three EDs within one health system in one state.

Different study periods by site: Practice patterns may have changed over time across the included EDs.

COVID-era effects: Pandemic workflows, isolation precautions, and staffing strain may have affected post-intubation care.

Missing data: Blood pressure and pre-RSI GCS data were incomplete, limiting adjustment for severity of illness.

No protocolized sedation approach: Local clinician preference and workflow likely influenced medication timing.

Discussion

Awareness During Paralysis Is the Core Concern

“Paralyzed, conscious, and intubated” is a frightening situation for any patient. Choice of paralytic may affect our ability to recognize this situation based on duration of effect. When paralysis wears off, patients may begin to move, cough, breathe asynchronously, grimace, or show other signs of discomfort. Those signs often become a visual cue for additional sedation or analgesia. If the induction agent wears off before paralysis resolves, the patient may be awake, uncomfortable, and unable to communicate.

Anticipate the need for post-intubation sedation and analgesia before RSI, rather than waiting for movement, ventilator dyssynchrony, or visible distress to trigger treatment. This matters most when using rocuronium because the patient may not be able to demonstrate distress after the induction agent has worn off.

Interpreting the Signal

The results were statistically significant, but the absolute median differences were small: 2 minutes for sedation and 3 minutes for analgesia. Although no patient wants to be paralyzed and conscious for any length of time, it is unclear whether these small median differences reflect clinically meaningful delays.

The authors report both median times and mean differences. The mean differences were larger than the median differences, suggesting skewed data and likely influential outliers. This may be where the clinical signal lives. The issue may not be that every rocuronium patient receives sedation a few minutes later. The issue may be that some rocuronium patients may experience much longer delays.

Rocuronium was also associated with higher in-hospital mortality, 20.1% vs 11.0%, a 9.1% absolute difference. Which suggests the presence of unmeasured baseline differences between groups. Clinicians may have selected rocuronium for older, sicker, more complex patients.

The Practical Takeaway Is Workflow, Not Paralytic Tribalism

One can read this study as support for succinylcholine over rocuronium. A better interpretation is that when using rocuronium, clinicians must be more deliberate about timely sedation and analgesia. This is not an argument to abandon rocuronium. Rocuronium remains an important RSI medication. The problem is using a long-acting paralytic without an equally deliberate plan for post-intubation comfort. The bottom line is simple: do not wait for the patient to move. Have sedation and analgesia ready, reassess early, support blood pressure when needed, and titrate to patient comfort and safety.

Author's Conclusion

“Use of rocuronium for RSI was associated with reduced likelihood of timely post-RSI sedation and analgesia. Coupled with low initial sedation dosing, our findings suggest that patients intubated with rocuronium are at increased risk of being awake during paralysis.”

Our Conclusion

In adult ED patients undergoing RSI, the use of rocuronium for neuromuscular blockade was associated with delayed time to sedation and analgesia compared to succinylcholine, a statistically significant difference of a few minutes, but the concern is clinically important because rocuronium may mask awareness long after the induction agent has worn off.

This study should not push clinicians to reflexively choose succinylcholine over rocuronium. It should push us to build better RSI workflows: post-intubation sedation and analgesia should be anticipated, ordered, prepared, and administered promptly, especially when using long-acting paralysis.

Clinical Bottom Line

Regardless of which paralytic is used, have sedation and analgesia ready before intubation.

References

Hwang C, Michaels B, Park K, et al. Impact of paralytic choice on postintubation sedation and analgesia in the emergency department. Am J Health Syst Pharm. 2025;82(Supplement_3):S2929-S2936. PMID: 40037283

Post Peer Reviewed By: Anand Swaminathan, MD, MPH (IG: @emswami), and Marco Propersi, DO (X: @Marco_Propersi)

Meet the Authors

Amil Badoolah

DO

Assistant Progressor

Emergency Medicine,

NYU Grossman, Long Island School of Medicine, NY

Meet The Team

Your Deep-Dive Starts Here

REBEL Core Cast 112.0 – Awareness During Paralysis

Take Home Points: Dose your RSI meds correctly. Reach for post-intubation sedation at ...

Resuscitation

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The ED-AWARENESS Study: Awareness with Paralysis

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Procedures and Skills

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参考来源

  1. REBEL EM:Rocuronium vs Succinylcholine for RSI: Awareness, Paralysis, and Post-Intubation Sedation

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