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Preoxygenation before intubation in adult patients with acute hypoxemic respiratory failure: a network meta-analysis of randomized trials

Critical Care volume 23, Article number: 319 (2019) Cite this article

Abstract

Background

Patients with acute hypoxemic respiratory failure are at risk for life-threatening complications during endotracheal intubation. Preoxygenation might help reduce the risk of hypoxemia and intubation-related complications. This network meta-analysis summarizes the efficacy and safety of preoxygenation methods in adult patients with acute hypoxemic respiratory failure.

Methods

We searched PubMed, EMBASE, and the Cochrane Library Central Register of Controlled Trials through April 2019 for randomized controlled trials (RCT) that studied the use of conventional oxygen therapy (COT), high-flow nasal cannula (HFNC), noninvasive ventilation (NIV), and HFNC and NIV as preoxygenation before intubation in patients with acute hypoxemic respiratory failure. Citations’ screening, study selection, data extraction, and risk of bias assessment were independently performed by two authors. The primary outcome was the lowest SpO2 during the intubation procedure.

Results

We included 7 RCTs (959 patients). Patients preoxygenated with NIV had significantly less desaturation than patients treated with COT (mean difference, MD 5.53, 95% CI 2.71, 8.34) and HFNC (MD 3.58, 95% CI 0.59, 6.57). Both NIV (odds ratio, OR 0.43, 95% CI 0.21, 0.87) and HFNC (OR 0.49, 95% CI 0.28, 0.88) resulted in a lower risk of intubation-related complications than COT. There were no significant mortality differences among the use of NIV, HFNC, COT, and HFNC and NIV during preoxygenation.

Conclusions

In adult patients with acute hypoxemic respiratory failure, NIV is a safe and probably the most effective preoxygenation method.

Background

Patients with acute hypoxemic respiratory failure are at increased risk for life-threatening complications during endotracheal intubation. Profound desaturation (SpO2 < 80%) during intubation was reported in 25% of patients [1]. Cardiac arrest occurred in 1 out of 40 intubations, and it was associated with hypoxemia and absence of preoxygenation [2]. Preoxygenation might help reduce the risk of hypoxemia and intubation-related complications.

Apart from conventional oxygen therapy (COT) delivered through bag-valve mask or face mask, noninvasive ventilation (NIV) and high-flow nasal cannula (HFNC) have been increasingly used in the intensive care units (ICU) as preoxygenation devices. Both HFNC [3,4,5] and NIV [6, 7] have been shown to offer better preoxygenation than COT. The recently published FLORALI-2 study comparing HFNC and NIV has added new insight to this battlefield [8].

Network meta-analysis (NMA) has been increasingly advocated in medical research [9]. Through a combination of direct and indirect estimates of effects, NMA allows comparison of multiple interventions and improved precision. The aim of this NMA is to evaluate the impact of preoxygenation, which includes desaturation during intubation, intubated-related complications, and mortality, by various devices including COT, HFNC, and NIV, in adults with acute hypoxemic respiratory failure.

Methods

We adhered to the Preferred Reporting Items for Systematic Reviews and Meta-analyses extension statement for reporting network meta-analyses (PRISMA-NMA) (Additional file 1) [10]. The protocol for this review was registered in the International Prospective Register of Systematic Reviews (CRD42018085866).

Data sources and searches

We searched PubMed, EMBASE, and the Cochrane Library Central Register of Controlled Trials through April 2019 for potentially relevant studies published in English. Our PubMed search strategy is presented in Additional file 2: Table S1. Reference lists of relevant articles were also reviewed. We included randomized controlled trials (RCT) of adult patients with acute hypoxemic respiratory failure investigating any form of preoxygenation devices during endotracheal intubation. Acute hypoxemic respiratory failure was defined by the individual authors in the included studies. Preoxygenation devices included COT via bag-valve mask or face mask, HFNC, or NIV. We defined preoxygenation as oxygen delivery during the period before induction of anesthesia, till initiation of laryngoscopy. Apneic oxygenation was defined as oxygen delivery to the nasopharynx during the time between initiation of laryngoscopy to the intubation of the trachea (Additional file 2: Figure S1). We excluded studies focusing only on apneic oxygenation. The following were excluded: studies evaluating only the duration of preoxygenation, decision on ventilation or preoxygenation during anesthesia or interventional procedures, or enrolling healthy volunteers or animals.

Study selection and data extraction

Two authors (KF and SA) independently screened citations and abstracts in duplicate and independently. All references judged potentially relevant were evaluated for full-text eligibility. Discrepancies were solved by consensus with the third author (GN). When relevant data or information was missing, we attempted to contact authors of the studies.

Outcome measures

The primary outcome was the lowest SpO2 during the intubation procedure (from beginning of laryngoscopy to confirmation of endotracheal intubation by capnography). The secondary outcomes were proportion of patients with severe desaturation (SpO2 < 80%), intubation-related complications (aspiration or new infiltrate on post-intubation chest radiograph, hemodynamic instability, and cardiac arrest), and mortality.

Risk of bias assessment

Two authors (SA and GN) independently assessed the risk of bias of included studies. We assessed the risk of bias of RCTs using the revised Cochrane risk-of-bias tool for randomized trials [11]. In case of disagreement for the attribution of risk of bias, it was solved by discussion and consensus with the third author (KF).

Statistical analysis and quality of evidence

We performed a random effect network meta-analysis using a frequentist framework, calculating mean differences (MD) for continuous outcomes and odds ratios (OR) for dichotomous outcomes. Where data were not available, we converted the median and interquartile range to mean and standard deviations using a published equation [12].

We used the package “netmeta” (version 1.0-1) in R (version 3.4.2, The R Foundation for Statistical Computing) to perform network meta-analysis [13]. The “netmeta” package is based on an approach that follows the graph-theoretical methodology. We ranked the treatment using the P-score which are based on the frequentist point estimates and their standard errors [14]. It represented the extent of certainty that a treatment is better than the other treatments—the P-score would be close to 1 when a treatment is certain to be the best and close to 0 when a treatment was certain to be the worst. Precision of the ranking is also taken into account by looking at confidence intervals. Homogeneity and consistency assumptions were checked using a generalized Cochrane’s Q statistics for multivariate meta-analysis [15]. Inconsistency in the random effect model was assessed by between-study Q statistic that was calculated based on design-by-treatment interaction model [16]. Sensitivity analysis was conducted by sequentially omitting one study each time.

We applied the modified Grading of Recommendations Assessment, Development and Evaluation (GRADE) approach for network meta-analysis [17, 18]. The contribution of all direct estimates to the network estimates was evaluated from the contribution matrix [19]. We would rate down the quality of evidence when intransitivity was present, or when there was incoherence between direct and indirect estimates. When both direct and indirect evidence were available, we chose the higher of the two quality ratings for the NMA estimate [17].

Results

Literature search

The initial search yielded 909 citations; 13 proved potentially eligible after reviewing the full-text articles. Seven studies met our inclusion criteria, representing 959 patients (Fig. 1).

Fig. 1
figure 1

PRISMA flow diagram of the search results

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Study characteristics

Of the 7 eligible trials, 3 compared HFNC with COT; 2, NIV with COT; 1, NIV with HFNC; and 1, HFNC and NIV with NIV (Table 1). Trial sample size ranged from 40 to 313 patients. Results of the individual studies could be found in Additional file 2: Tables S2–S3.

Table 1 Characteristics of the included studies
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Risk of bias

The risk of bias was high in 1 trial, low in 3 trials, and with some concerns in 3 trials (Fig. 2).

Fig. 2
figure 2

Risk of bias of included studies

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Quality of evidence

Direct comparisons often suffered from imprecision and limitations of risk of bias. There were no significant concerns regarding intransitivity. There was no significant incoherence detected by statistical testing nor visual inspection of direct and indirect estimates (Table 2).

Table 2 Direct, indirect, and network meta-analysis estimates of the effects of different preoxygenation methods
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Clinical outcomes

Lowest SpO2 during intubation

Seven trials (959 patients) reported the lowest SpO2 during intubation (Additional file 2: Table S2). The network geometry was shown in Additional file 2: Figure S2. The network estimate provided high-to-moderate quality evidence (Table 2). Patients preoxygenated with NIV had significantly less desaturation than patients treated with COT (network estimate, MD 5.53, 95% CI 2.71, 8.34) and HFNC (network estimate, MD 3.58, 95% CI 0.59, 6.57) (Fig. 3). Although HFNC and NIV was ranked to be the best treatment (Table 3), there was no evidence that HFNC and NIV was superior than NIV (direct estimate, MD − 3.10, 95% CI − 11.18, 4.98), and thus, the result should be interpreted with caution. NIV ranked the 2nd among the four methods. The heterogeneity and consistency were low (I2 = 23.6%; Q statistics total: p = 0.264, within design: p = 0.162, between designs: p = 0.750).

Fig. 3
figure 3

Forest plot of lowest SpO2 during intubation. I2 = 23.6%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.264, within designs: p = 0.162, between designs: p = 0.750. COT, conventional oxygen therapy (bag-valve mask or facial mask); HFNC, high-flow nasal cannula; NIV, noninvasive ventilation; MD, mean difference; NMA, network meta-analysis

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Table 3 The P-score statistics
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SpO2 < 80% during intubation

Seven trials (959 patients) reported the incidence of SpO2 < 80% during intubation (Additional file 2: Table S2). The network estimate provided moderate-quality evidence (Table 2). Significant desaturation with SpO2 < 80% was less common in patients preoxygenated with NIV than that with COT (network estimate OR 0.43, 95%CI 0.19, 0.97) (Fig. 4). The combined use of HFNC and NIV was ranked to be the best preoxygenation method. However, the confidence interval of its treatment effect estimates was very wide because of the small sample size (direct estimate OR 0.16, 95% CI 0.01, 1.80). NIV ranked the 2nd among the four preoxygenation methods (Table 3).

Fig. 4
figure 4

Forest plot of SpO2 < 80% during intubation. I2 = 48%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.104, within designs: p = 0.072, between designs: p = 0.409. COT, conventional oxygen therapy (bag-valve mask or facial mask); HFNC, high-flow nasal cannula; NIV, noninvasive ventilation; OR, odds ratio; NMA, network meta-analysis

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Intubation-related complications

Seven trials (959 patients) reported the intubation-related complications) (Additional file 2: Table S3). The network estimate ranged from high- to low-quality evidence (Table 2). Both NIV (network estimate OR 0.43, 95% CI 0.21, 0.87) and HFNC (network estimate OR 0.49, 95% CI 0.28, 0.88) resulted in a lower risk of intubation-related complications than COT (Fig. 5). NIV ranked the 1st and HFNC 2nd among the four preoxygenation methods (Table 3).

Fig. 5
figure 5

Forest plot of intubation-related complications. I2 = 0%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.978, within designs: p = 0.914, between designs: p = 0.892. Intubation-related complications were defined as aspiration or new infiltrate on post-intubation chest radiograph, hemodynamic instability, and cardiac arrest. COT, conventional oxygen therapy (bag-valve mask or facial mask); HFNC, high-flow nasal cannula; NIV, noninvasive ventilation; OR, odds ratio; NMA, network meta-analysis

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Mortality

Six trials (919 patients) reported the mortality (Additional file 2: Table S2). The network estimate ranged from high- to low-quality evidence (Table 2): There was no evidence showing the superiority of one particular preoxygenation method as determined by the confidence interval (Fig. 6). Thus, the ranking by P-scores should be interpreted with caution (Table 3).

Fig. 6
figure 6

Forest plot of mortality. I2 = 0%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.533, within designs: p = 0.545, between designs: p = 0.322. COT, conventional oxygen therapy (bag-valve mask or facial mask); HFNC, high-flow nasal cannula; NIV, noninvasive ventilation; OR, odds ratio; NMA, network meta-analysis

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Sensitivity analysis

We performed sensitivity analysis by excluding the study by Guitton et al. [5] as subjects with mild hypoxemia were included, compared with the other included studies which recruited subjects with moderate to severe respiratory failure. Results of direct, indirect, and network estimates were similar (Additional file 2: Figures S3–S6). There was no change in ranking based on P-scores (Additional file 2: Table S5).

Discussion

In this network meta-analysis, we included 7 RCTs enrolling 959 patients comparing three preoxygenation methods—COT, HFNC, and NIV. Hypoxemic patients treated with NIV during intubation desaturated less (as reflected by absolute difference of lowest SpO2 and incidence of SpO2 < 80%) than those patients treated with HFNC or COT (moderate quality of evidence). The risk of intubation-related complications (aspiration or new infiltrate on postintubation chest radiograph, hemodynamic instability, and cardiac arrest) was lower with NIV than with any other preoxygenation methods (moderate quality of evidence). Among the methods of preoxygenation examined, it seems that combined use of HFNC and NIV is the most effective in minimizing the drop in SpO2 and the incidence of SpO2 < 80% during intubation. However, this determination is limited to data from only one single-center study in which no head-to-head comparisons were performed against all other methods.

HFNC has several physiological advantages, including its ability to deliver high-flow oxygen, generation of low level of PEEP, and allowing apneic oxygenation [21]. Despite the clear benefit of HFNC in patients with acute hypoxemic respiratory failure and after planned extubation [22, 23], the evidence for HFNC in preoxygenation remains conflicting. The single-center before-after study by Miguel-Montanes et al. [24] has excluded patients with severe hypoxemia. Its positive results have not been reproducible in the subsequent trials by Vourc’h et al. [3] and Simon et al. [4] which recruited patients with severe hypoxemia and patients with mild-moderate hypoxemia respectively. While Guitton et al. [5] have shown a reduction in intubation-related adverse events with the use of HFNC in non-severely hypoxemic patient, it was not accompanied by an improvement in the lowest SpO2. The effectiveness of HFNC is undermined by the loss of PEEP effect due to mouth opening in patients in respiratory distress [25]. These patients can have a dramatic increase in inspiratory nasal and oral flow rate of up to 110 L/min and 280 L/min respectively, and that could not be matched by the HFNC [26]. Another possible explanation is that apneic oxygenation requires a continuous oxygen extraction from the functional residual capacity (FRC) during the apnea period, thus generating a pressure gradient to allow oxygen flow from the nose into the alveoli. These mechanisms are hindered by the reduction of FRC and shunt physiology in diseased lungs [27]. Airflow may also be limited by the use of cricoid pressure possibly obstructing the space between the oropharynx and trachea [28].

NIV allows the delivery of high level of FiO2 and positive intrathoracic pressure, encouraging alveolar recruitment which could possibly improve the efficiency of gaseous exchange. It has also been shown to counteract inward air leaks and improve face-mask seal [29]. The theoretical risk of gastric distention and aspiration remains unproven based on our analysis. Although the mask must be removed during laryngoscopy, patients preoxygenated with NIV still desaturated less during intubation than patients preoxygenated with other modalities. The authors thus recommend the use of NIV for preoxygenation in patients with acute hypoxemic respiratory failure.

The next question would be whether the addition of HFNC to NIV could produce extra benefit during preoxygenation. The pilot study by Jaber et al. [20] published in 2016 showed promising results. However, one must be cautious in the interpretation of the findings in the use of HFNC and NIV, in view of the small sample size that tends to overestimate the treatment effect and the possibility of publication bias. Additionally, the optimal way to minimize air leak with concomitant use of HFNC and NIV has not been well-delineated. It would be interesting to consider whether nasal continuous positive airway pressure mask could play a special role in preoxygenation. Visualization of glottic view by laryngoscopy may be feasible with the nasal mask in situ, maintaining oxygenation during intubation.

Another practical but unaddressed consideration would be the oxygen device used prior to the decision of intubation. Based on the mortality difference shown in FLORALI-1 trial, it would not be surprising to see a surge in the use of HFNC in patients with acute hypoxemic respiratory failure. A more recent systematic review also confirmed a reduced risk of requiring intubation with the use of HFNC compared with COT [22]. All existing studies placed no restriction in the patient enrollment based on the oxygen devices they used prior to inclusion and the number of patients on advanced oxygen device varied across studies (Additional file 2: Table S4). As shown in the study by Baillard et al. [7], there was an increased risk of adverse events including severe desaturation with SpO2 < 80% in patients initially put on NIV, who were then randomized to receive COT during preoxygenation. It would be uncertain whether the lowered complication risks during preoxygenation with NIV was in fact a reflection of a higher risk of complication in patients “de-escalated” from a more advanced oxygen support (NIV) to a simpler device (COT). Additionally, whether the advantage of oxygenation in NIV would be less evident in patients who were already put on NIV or HFNC remained unclear.

The study is the first systematic review using network meta-analysis to evaluate preoxygenation methods in patients with acute hypoxemic respiratory failure. NMA allows the comparison of multiple preoxygenation methods and increases the precision by combining direct and indirect estimates. Other strengths of this study included the comprehensive search, duplicate and independent citation screening and data abstraction, use of the latest modified Cochrane risk of bias assessment tool, and the adherence to the PRISMA-NMA guideline.

This study had some limitations. Despite an extensive literature search, the number of trials for each comparison of preoxygenation methods remained small. Funnel plot was not constructed because of the limited number of studies, so it is not possible to estimate possible publication bias. While pulse oximetry was frequently used as the outcome measure in clinical trials studying preoxygenation, it is, however, not the best surrogate to reflect systematic oxygenation [30]. Arterial oxygen saturation or end-tidal oxygen is more relevant to assess the adequacy of preoxygenation, but they may not be readily available in case of clinical emergency settings.

Conclusions

In adult patients with acute hypoxemic respiratory failure, NIV is a safe and probably the most effective preoxygenation method. Further research should be performed to evaluate the benefits of the combination strategy of NIV plus HFNC.

Availability of data and materials

All data generated or analyzed during the present study are included in this published article and its supplementary information files.

Abbreviations

COT:

Conventional oxygen therapy

NIV:

Noninvasive ventilation

HFNC:

High-flow nasal cannula

ICU:

Intensive care unit

PEEP:

Positive end-expiratory pressure

NMA:

Network meta-analysis

RCT:

Randomized controlled trials

MD:

Mean difference

OR:

Odds ratio

CI:

Confidence interval

NR:

Not reported

RR:

Respiratory rate

bpm:

Breath per minute

GCS:

Glasgow coma scale

RSI:

Rapid sequence induction

BVM:

Bag-valve mask

SBP:

Systolic blood pressure

SOFA:

Sequential Organ Failure Assessment

SD:

Standard deviation

IQR:

Interquartile range

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Authors and Affiliations

  1. Department of Intensive Care, Queen Elizabeth Hospital, 30 Gascoigne Road, Kowloon, Hong Kong SAR

    Ka Man Fong, Shek Yin Au & George Wing Yiu Ng

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  1. Ka Man Fong
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  2. Shek Yin Au
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Contributions

KF conceived the study, performed the literature search, analyzed the data, and drafted the manuscript. SA and GN did the acquisition of data and the revision of the manuscript. All authors read and approved the final manuscript.

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Correspondence to Ka Man Fong.

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Additional file 1:

PRISMA checklist. (DOCX 23.5 kb)

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Figure S1. Timing of preoxygenation methods. Figure S2. Network of preoxygenation methods for evaluating lowest SpO2. The size of the nodes was proportional to the number of patients randomized to each preoxygenation methods and thickness of the lines to the number of direct comparisons. Figure S3.Sensitivity analysis of forest plot of lowest SpO2 during intubation. I2 = 42.6%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.156, within designs: p = 0.083, between designs: p = 0.616. Figure S4. Sensitivity analysis of forest plot of SpO2 < 80% during intubation. I2 = 0%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.574, within designs: p = 0.354, between designs: p = 0.615. Figure S5. Sensitivity analysis of forest plot of intubation-related complications. I2 = 0%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.933, within designs: p = 0.749, between designs: p = 0.848. Figure S6. Sensitivity analysis of forest plot of mortality. I2 = 0%. Q-statistics for heterogeneity (within designs) and inconsistency (between designs). Total: p = 0.574, within designs: p = 0.354, between designs: p = 0.615. Table S1. PubMED search strategy. Table S2. Lowest SpO2, incidence of SpO2 < 80% during intubation, and mortality. NR, not reported; SD, standard deviation. aICU mortality. b28-day mortality. cOnly median and interquartile range were provided in the study: NIV 92 (84–98), COT 88 (79–95). Data were transformed into mean and standard deviation using a published equation [12]. Table S3. Intubation-related complications. NR, not reported; COT, conventional oxygen therapy (bag-valve mask or facial mask); HFNC, high-flow nasal cannula; NIV, noninvasive ventilation; aAdverse events including cardiac arrest, hemodynamic instability and aspiration of gastric contents were included as outcome measure and it was reported that there were no adverse events related to intubation in the study. Table S4. Advanced oxygen devices used before study inclusion. NR, not reported; COT, conventional oxygen therapy (bag-valve mask or facial mask); HFNC, high-flow nasal cannula; NIV, noninvasive ventilation. Table S5. P-scores statistics of sensitivity analysis. (DOCX 840 kb)

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Fong, K.M., Au, S.Y. & Ng, G.W.Y. Preoxygenation before intubation in adult patients with acute hypoxemic respiratory failure: a network meta-analysis of randomized trials. Crit Care 23, 319 (2019). https://doi.org/10.1186/s13054-019-2596-1

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Keywords

Critical Care

ISSN: 1364-8535