Apnea Testing for the Determination of Brain Death: A Systematic Scoping Review.

Apnea is one of the three cardinal findings in brain death (BD). Apnea testing (AT) is physiologically and practically complex. We sought to review described modifications of AT, safety and complication rates, monitoring techniques, performance of AT on extracorporeal membrane oxygenation (ECMO), and other relevant considerations regarding AT. We conducted a systematic scoping review to answer these questions by searching the literature on AT in English language available in PubMed or EMBASE since 1980. Pediatric or animal studies were excluded. A total of 87 articles matched our inclusion criteria and were qualitatively synthesized in this review. A large body of the literature on AT since its inception addresses a variety of modifications, monitoring techniques, complication rates, ways to perform AT on ECMO, and other considerations such as variability in protocols, lack of uniform awareness, and legal considerations. Only some modifications are widely used, especially methods to maintain oxygenation, and most are not standardized or endorsed by brain death guidelines. Future updates to AT protocols and strive for unification of such protocols are desirable.

Introduction

The physiology of respiration is complex and beyond the scope of this review. The respiratory center with respiratory generators is located in the ventrolateral medulla oblongata [1]. If the function of these structures is irreversibly lost, a patient will not take any spontaneous breaths despite adequate stimulation. Therefore, AT assesses functionality of the lower brainstem by allowing the arterial carbon dioxide partial pressure (PaCO2) to increase and the CSF-pH to decrease to a level that maximally stimulates the respiratory centers in the medulla oblongata [2]. The exact carbon dioxide level at which the medullary chemoreceptors are maximally stimulated is unknown, but a PaCO2 value of 60 mm Hg (or 20 mm Hg above baseline) is generally considered an appropriate target for assessment of brain death [3].

Procedural flow for a standard AT in adults with oxygen insufflation according to the American Academy of Neurology (AAN) guidelines [4] is shown in Fig. 1. Blood pressure can (and should) be supported with pressors, possibly preemptively, but the test should be aborted if the SBP drops < 90 mm Hg [4] despite adequate vasopressor support. The target duration of the apnea test (8–10 min) is derived from the traditional assumption that PaCO2 increases at a rate of 3 mmHg/min. However, in practice, the rate of PaCO2 increase is highly variable, from 0.5 to 10.5 mm Hg per minute, and neither linear nor predictable [5]. During normothermia and in the absence of pulmonary disease, even 5 min of apneic oxygenation may be enough to raise the PaCO2 from 40 to above 60 mm Hg [6]. If the PaCO2 has not reached the designated threshold, and the patient is stable, the test is continued and repeat gases are checked until the patient meets the goal [7]. After conclusion of the AT, the patient is reconnected to the ventilator. Alternatively, the test can be repeated for a longer period of time (10–15 min) after repeat pre-oxygenation on the ventilator [4]. If the AT has to be aborted, an ABG should be sent off immediately prior to reconnecting the patient to the ventilator; if the PaCO2 has risen adequately, the test can be considered positive, but if not, the is test is considered inconclusive [4]. If pulmonary status cannot be optimized to repeat the test, an ancillary test is required [4, 8].

Fig. 1

Standard Apnea Test with Oxygen Insufflation according to the guidelines of the American Academy of Neurology [4]

Since inception of AT for the purpose of determination of brain death, a number of modifications, observations about safety and termination rates, practical considerations for AT conduction, new critical care technologies that affect AT and observations about AT in the context of worldwide application and society have been published.

Objectives

In this scoping review, we set out to address the following questions:

Which modifications to conventional apnea testing have been described?

What complications and termination rates have been documented for apnea testing?

What monitoring techniques are available for apnea testing?

How can apnea testing be performed on ECMO?

Are there other important considerations pertaining to apnea testing?

Methods

We conducted a database search (PubMed, EMBASE) and review of relevant medical literature from 1980 to 2019 on the topic of apnea testing for brain death determination. A search on registered work in progress studies similar to this topic on the International Prospective Register of Systematic Reviews (PROSPERO) revealed an ongoing review termed “Criteria for brain death: a worldwide comparison.” Hence, we decided to not focus on the details of worldwide differences in apnea testing; however, we included this topic as example for objective #5. Our review followed the Preferred Reporting Items for Scoping Reviews (PRISMA-ScR) guidelines [9]. Selected studies included English language articles concerning apnea testing using the search terms “brain death” with “apnea,” “apnea test,” “apnoea,” “apneoa test,” or “apnea/apnoea testing” (see Supplementary Material). Controlled trials, cohort studies, case series, case reports, and reviews on apnea testing for brain death determination in the adult population were included. Pediatric or animal studies were excluded. The search was most recently updated on Feb 12, 2020. Two reviewers independently screened the titles and abstracts and the selected full publications against the prespecified criteria. Disagreements regarding study selection were resolved by consensus. Selected studies were reviewed by both authors, and data were extracted for qualitative synthesis and grouped based on the prespecified objectives.

Results

A total of 391 articles were initially retrieved and reviewed for relevance. Figure 2 shows the flowchart of retrieved and included literature. Ultimately, 87 articles met our inclusion criteria and were included in qualitative data synthesis.

Fig. 2

Flow diagram of record identification, screening, eligibility and inclusion

Modifications to AT to Enable Successful AT Completion

A summary of described modifications to AT is displayed in Table 1.

Table 1

Modifications of Apnea testing

Method	Results	Reference(s)
Adjustment of oxygen insufflation	Avoidance of CO2 elimination by high flow rate of O2	Kramer et al. [12]
Maintenance of positive end-expiratory pressure
Comparison of AT with oxygen catheter, T-piece and CPAP	Significantly less decrease in PaO2 with CPAP versus oxygen catheter or T-piece	Levesque et al. [16]
Ambu Bag with PEEP valve	stable PaO2/FiO2 ratio	Park et al. [17] Park et al. [18]
Comparison of oxygen insufflation with CPAP-AT	gradual decrease of PaO2/FiO2 ratio with conventional AT vs no decrease in CPAP-AT	Solek-Pastuszka et al. [15]
Comparison of MAT to conventional AT	Similar mean duration of AT Similar change in PaCO2, PaO2 or pH Subgroups overweight patients and hanging injury: prevention of dramatic PaO2 reductions with MAT	Park et al. [19]
Comparison of oxygen insufflation versus Ambu bag with CPAP valve	no significant difference in the degree of PO2 reduction, rate of PCO2 rise or pH decline	Kramer et al. [12]
Carbon dioxide augmentation
Introduction of CO2 at 1L/min	Significant reduction of observation time	Lang [21]
	Less serious adverse events	Melano et al. [22]
Elevation of baseline CO2 level	Shorter duration of AT	Benzel et al. [23]
CO2 augmentation via ventilator	Avoidance of CO2 target over- or undershooting	Sharpe et al. [25] Pepe et al. [26]
Oxygen augmentation
Recruitment maneuvers compared to standard AT	Recruitment significantly increased PaO2/FiO2 ratio; occurrence of hypotension in recruitment group	Paries et al. [27]
Bulk diffusion method	Maintenance of PaO2	Al Jumah et al. [28]
Oxygen transporting solutions	Increase of pre-apnea and apnea-PaO2	Kolsanov et al. [29]

AT apnea test, CO carbon dioxide, CPAP continuous positive airway pressure, FiO fraction of inspired oxygen, MAT modified apnea test, O oxygen, PaO partial pressure of oxygen, PEEP positive end-expiratory pressure

Adjustment of the O2 Insufflation

While O2 insufflation—the AAN guidelines recommend 6 L/min3, however, recommended rates vary considerably largely between 4 and > 6 L/min [10]—is aimed at preventing hypoxia, high flow O2 insufflation might result in a small degree of CO2 elimination, decreasing the rate of CO2 accumulation, and prolonging the test [11]. This can be addressed by lowering the O2 flow from the initial insufflation rate, commonly 4–6 L/min, by 1–2 L/min without inducing desaturation to increase the CO2 [12].

Modified AT with Maintenance of Positive End-Expiratory Pressure

The modified apnea test (MAT) comprises delivery of 100% oxygen through the ETT and maintenance of positive end-expiratory pressure (PEEP) after disconnection from the ventilator, but does not interfere with the build-up of hypercapnia. This type of modification has been adopted widely and is included in the 2010 AAN guidelines as well as others (see below). Continuous positive airway pressure (CPAP) during AT can be generated in three ways: directly by the ventilator; through the use of a T-piece tube with a CPAP valve at the outflow end; and through the use of a traditional T-piece system with connection to a reservoir bag connected at one end with the distal outflow tubing immersed in water at a depth that can be adjusted depending on the target PEEP [13]. The first approach requires the use of a ventilator that allows disabling of rescue breaths for apnea. The 2010 AAN guidelines and the Austrian guidelines support AT with a T-piece and CPAP (second approach) if conventional AT resulted in poor oxygenation [4, 14]. Contrastingly, the Polish criteria recommend routine use of CPAP on a ventilator (CPAP-AT) [15]. These techniques can prevent the decruitment of lungs, reduce the risk of hypoxemia, and increase hemodynamic stability by prevention of blood pressure fluctuation compared to the traditional O2 insufflation method. This is especially true for patients on high PEEP and high doses of vasoconstrictor or inotropic medications [16, 30]. Various studies have shown success with using CPAP/PEEP during AT. In a Canadian study of 19 BD patients, the use of a 10-cm H2O PEEP valve attached to a T-piece with 12 L/min oxygen directly attached to the ETT was compared to the use of a simple T-piece (without CPAP valve, but with same 12 L/min oxygen flow) and to traditional oxygen insufflation with oxygen at 6 L/min. All patients had PaCO2 elevation > 60 mm Hg at the end of a 10 min trial, but the decrease in arterial oxygen partial pressure (PaO2) during AT was significantly less with the CPAP valve compared to the oxygen catheter or the plain T-piece [16]. In series of 4 and 26 BD patients by the same group, an Ambu bag with a PEEP valve was connected to the ETT with 10 L/min of 100% oxygen flow upon ventilator disconnection, resulting in stable PaO2/FiO2 (P/F) ratio when compared to prior to AT [17, 18]. In a recent comparison of the classic oxygen insufflation method with the CPAP-AT in 60 patients, a gradual decrease of P/F ratio was found throughout conventional AT, but not in the CPAP group [15]. In a Korean study comparing MAT to conventional AT, mean duration of AT was similar, without significant differences in change of PaCO2, PaO2 or pH. In overweight patients, however, MAT prevented dramatic PaO2 reductions, and in patients with hypoxic brain injury due to hanging, differences in PaO2 and SaO2 in the MAT group were significantly smaller than in the conventional AT group [19]. Less clear benefit was found in a multicenter Canadian study involving 14 ICUs with 77 patients comparing a group with O2 catheters placed inside the ETT to a group with an Ambu bag with a CPAP valve attached to the ETT, without significant difference in the degree of PO2 reduction, rate of PCO2 rise or pH decline [12]. Newer ventilators with the ability to switch the ventilator into complete apnea mode and keep the patient connected to the ventilator during the apnea test while using PEEP have shown success from a practical standpoint [20].

Carbon Dioxide Augmentation and Elevation of CO2 Level Prior to Apnea Testing

Carbon dioxide augmentation and elevation of the CO2 level prior to apnea testing are modifications that have been published as attempts to reach the same goal—proof that there is the absence of spontaneous respirations, but are neither widely adopted, standardized, nor supported by major guidelines. Carbon dioxide augmentation is limited by the need for steel CO2 containers, which are not readily available in most ICUs. Introduction of CO2 at a rate of 1 L/min into the circuit markedly reduced the observation time compared with conventional apneic oxygenation in a case series of 34 BD patients, allowing PaCO2 levels ≥ 60 mm Hg to be reached within 2 min [21]. A larger study from Argentina compared the same rate of CO2 administration for only 1 min duration followed by disconnection from the ventilator with the typical O2 insufflation method. Patients who received CO2 augmentation had less frequent serious adverse events (hypotension, cardiac arrest, arrhythmias, and hypoxemia). Pretest hypokalemia compared to normokalemia was a significant risk factor for complications in the group that received artificial CO2 augmentation. The authors recommended this CO2 augmentation method in patients who have low pretest PaO2/FiO2 ratio and higher risk of developing hypoxemia, but only after assuring normokalemia [22].

Intentional elevation of the baseline pre-apnea CO2 was reported in another study of 11 BD patients. Six patients who commenced AT at a CO2 of 40–45 mm Hg were compared to five patients who had a starting PCO2 level between 46 and 51 mm Hg. The group with higher baseline PCO2 reached a PaCO2 of 60 mm Hg in a shorter period. Both groups showed a PaCO2 rise of more than 20 mm Hg from baseline [23]. A similar modified apnea test, which allowed decrease in the minute ventilation to facilitate PaCO2 rise ≥ 20 mmHg from baseline, was also described in a case report of a patient who failed the regular apnea test and whose baseline PaCO2 level was 53 mm Hg. After 30 min of hypoventilation, the PaCO2 was 99 mmHg, no breaths were observed for 60 s and he was pronounced brain dead. The authors argue that the prior literature suggests that only 30–60 s are needed to confirm apnea. Furthermore, they discuss that a slower increase in PaCO2 compared to conventional AT does not result in CSF pH equilibrium based on animal data, indicating that if the hypoventilation process lasts less than 60 min, the CSF pH will not have enough time to equilibrate [24].

A combination of these two methods has also been described in 60 patients undergoing AT with CO2 augmentation, without disconnecting from the ventilator and with monitoring the end-tidal PCO2. The oxygen bayonet providing O2 to the ventilator from the wall O2 outlet was disconnected and reconnected to a Carbogen (97% O2/3% CO2) cylinder. The ventilator rate was set at 4 breaths/min and was gradually decreased by 1 breath/min until the predetermined end-tidal CO2 (PetCO2) was achieved, and then, adequate increase in PaCO2 was confirmed. The mean pre-apnea and post-apnea PaCO2 achieved by this method were 40 and 67 mmHg, respectively [25]. A similar process using Carbogen and capnometry, decreasing the ventilator set rate to 2–4 breaths/min and aiming for a calculated target PetCO2, has been reported in 24 BD patients. The mean post-apnea PetCO2 and PaCO2 were 63.2 and 71.5 mmHg, respectively, without major complications [26].

When considering these modifications that arguably infer a significant change when compared to conventional AT, it is important to view these modifications as a means to enable conduction of an AT—albeit significantly modified—as opposed to, in most instances, foregoing the AT altogether due to anticipated or manifest hemodynamic-respiratory instability.

Augmentation of Oxygenation

Among the following methods of augmentation of oxygenation, recruitment maneuvers may be the most practical ones to attempt if needed. A study describing the use of recruitment maneuvers compared 27 patients treated with recruitment maneuvers after completing AT to 27 matched controls. In the recruitment group, immediately after reconnection to the ventilator, PEEP was increased from 5 to 35 cm H2O and the respiratory rate was decreased to 0.5 breaths per minute for 40 s before reapplying the initial ventilation settings. P/F ratio increased significantly in the recruitment group, although hypotension was noted in 55% during the recruitment maneuver [27]. A method described, but not widely used, with intention to avoid hypoxemia is the bulk diffusion method. This involves delivery of a large flow (40–60 L/min) of 100% FiO2 at the orifice of the ETT via the ventilator circuitry (with CPAP set at zero or by turning off the ventilator and disconnecting the expiratory humidity trap), with the goal of minimizing hypoxia during the assessment [28]. This method was described in a study of 24 BD patients, of which 23 completed the test. (In one patient, the test was aborted due to hypotension.) Only five (20.8%) patients had a post-apnea PaO2 of < 100 torr. Another method that has not gained wide use and is majorly limited by regulations and availability describes the use of artificial oxygen transporting solutions, such as perfluorocarbon-based oxygen carriers. In a study from Russia, the use of intravenous Perftoran (a solution of perfluordecaline and perfluormethylcyclohexylpiperidine 2:1 in emulsion) increased the pre-apnea and apnea-PaO2 compared to controls without affecting the PaCO2 levels [29].

Other, single case modifications aimed at improved oxygenation and/or ability to conduct and complete AT described a pre-AT recruitment maneuver with incremental titration of PEEP and maintenance of PEEP via a CPAP valve [30], prolonged AT for 110 min due to suspected cardiac ventilations resulting in a very slow increase in carbon dioxide levels [31] and successful use of prone positioning with CPAP and T-piece in a severely hypoxic patient [32].

Safety, Complications and Termination Rates of AT

While AT is generally considered safe, intentional induction of hypercarbia and respiratory acidosis can lead to cardiac arrhythmias, hypotension, or hypoxemia [3]. The patient should always be monitored for desaturation with an oxygen saturation [SpO2] monitor and for hypotension, which may develop due to dilatation of the peripheral arterioles and depression of the myocardial contractility in the setting of CO2 elevation [33]). Moreover, AT may de-recruit lungs and lead to decreased oxygenation and lung quality for potential transplantation. In patients on high PEEP or hemodynamic support, hemodynamic instability may be observed upon ventilator disconnection due to a sharp decrease in the intrathoracic pressure with immediate increase in the venous return to the heart [13]. Reported complications of AT are summarized in Table 2.

Table 2

Complications of Apnea testing and risk factors for completion failure

Complication	Incidence	Reference(s)
Hypotension	7–39%	Wijdicks et al. [35] Datar et al. [36] Daneshmand et al. [37] Goudreau et al. [43] Jeret and Benjamin [42]
Hypoxemia	4–6.3%	Wijdicks et al. [35] Datar et al. [36] Daneshmand et al. [37]
Cardiac arrhythmias	<1%–1%	Goudreau et al. [43]
Cardiac arrest	0–0.7%	Scott et al. [54]
Pneumothorax, Pneumomediastinum, Pneumoperitoneum	Very rare–Rare	Thery et al. [44]
		Junsay and Bencheqroun [45]
		Hasan and Landsberg [46] Brandstetter et al. [47] Gorton et al. [51] Burns and Russell [52] Goranovic et al. [53]
Termination of Apnea test abortion	0–20%	Wijdicks et al. [35] Datar et al. [36] Daneshmand et al. [37] Kim and Kim [38] Yee et al. [39] Kim and Kim [40] Jeret and Benjamin [42] Giani et al. [41]
Risk factors for apnea test failure	Low SBP High A-a gradient hypoxemia Pretest acidemia age	Kim and Kim [38] Yee et al. [39] Kim and Kim [40]

Hypotension and Hypoxemia

In addition to hypoxemia, hypotension is a major risk during AT and may demand termination of AT. Occurrence of hypotension may be due to acidemia, but may also be due to changes in intrathoracic pressures (auto-PEEP may occur), leading to decreased preload and hypotension [34]. In a series of 228 BD patients, AT could not be performed in 7% of patients because of hemodynamic instability or poor oxygenation at baseline and was aborted in 3% because of hypoxemia or hypotension without major complications (cardiac arrest or pneumothorax) [35]. Polytrauma resulting in brain death was significantly more common in patients with aborted or not attempted apnea tests than in patients with completed AT in this study [35]. However, in a subsequent study by the same group, percentage of aborted apnea tests decreased from 3 to 1.6% with strict compliance with suggested prerequisites [36]. In this study of 63 patients, hypoxemia (6.3%) and hypotension (17.4%) were the most frequent complications. Of note, in this series, which showed markedly lower termination rate, AT was performed by experienced neurointensivists in 94% of cases. In another follow-up series using conventional oxygen insufflation in 116 patients, < 2% of cases were terminated [37]. In a study of 267 brain death examinations, 13 cases failed the apnea test with preexistent low systolic blood pressure and high A-a gradient being independent risk factors for failure [38].

Occurrence of cardiac arrhythmia, arrest, or pneumothorax was not observed in either of these series. Other series found termination rates in similar range. In a study of 207 BD patients, termination rate was 4.8% due to hypoxemia and/or hypotension and was associated with age, pretest pH, and higher A–a gradient after logistic regression analysis [39], with similar results in a study of 512 apnea tests in which 28 were aborted, with prediction of test failure if systolic blood pressure pretest was less than 105 mmHg, pretesting pH was less than 7.326, and starting A-a gradient exceeded 556.4 mmHg [40]. Another study of 167 BD patients including 25 on veno-arterial ECMO did not result in any AT termination despite 24% of the non-ECMO patients having baseline hypoxemia [41].

In a study of 70 apnea tests, 39% of patients either developed marked hypotension (≥ 15% drop in mean arterial pressure, 85%) or required vasopressor dose manipulation (15%). Out of 27 examinations in which hypotension developed, the test was aborted in 14 patients (52%, 20% of total AT), continued despite marked hypotension in two cases, tolerated with prophylactic administration of epinephrine or dopamine in four cases, and successfully completed after increase in the rate of ongoing dopamine infusion during the test in seven cases [42]. In another study, hypotension was the most common complication in 24% of 145 patients undergoing AT, but cardiac arrhythmias were observed in < 1%. The only significant variable predicting complications was inadequate pre-oxygenation [43].

Pneumothorax, Pneumomediastinum, and Pneumoperitoneum

Pneumothorax, pneumomediastinum, and pneumoperitoneum are rare complications of AT [44]. The most common risk is barotrauma if the cannula has a diameter close to that of the endotracheal tube (ETT), and O2 outflow is obstructed, like in a case of insertion of a 7.0 oxygen tube at 6 L/min inside a 7.5 endotracheal tube [45]. If this is the case, bilateral tension pneumothoraces can occur [46] or pneumomediastinum with subcutaneous emphysema and Hamman’s sign can result, as was the case in a patient where the internal cannula-to-ETT diameter ratio was 0.83 [47]. In a manikin study with oxygen flow of 6 L/min, internal cannula-to-ETT ratio ≥ 0.7 increased the airway pressures and volumes [48]. Based on these findings, the internal cannula diameter-to-ETT ratio should not be larger than 0.6–0.7. The cannula tip position inside the endotracheal tube (placed in distal 1/3 compared to proximal 1/3 increases the airway pressure) and the O2 flow rate (should be < 10 L/min) are also important factors determining the tracheal airway pressure during O2 insufflation [49]. Another option is to change the tubing inside a standard 7.0 ETT from standard O2 tubing (6 mm outside diameter) to pressure tubing (3 mm outside diameter) [50] in order to avoid tension pneumothoraxes and barotrauma.

A study reporting three cases of pneumothorax and summarizing the published literature found another nine cases. Information regarding oxygen cannula diameter was available for nine patients (range 2.3–5.3 mm), and flow rate was available for ten (mean 11 L/min). Eight of ten (80%) patients had an O2 flow rate ≥ 8 L/min. Pneumothorax was treated to resolution in the majority of patients, although only six completed AT and only three patients became organ donors [51]. Complications can also occur as a result of direct airway [52] or tracheal [53] perforation by the supplemental oxygen cannula.

In a review paper from 2013 summarizing all these complications, out of 608 patients undergoing AT in the literature, 111 (18%) had hypotension, 36 (6%) hypoxemia, 7 (1%) arrhythmia, but only 2 (0.3%) bradycardia and 4 (0.7%) cardiac arrest [54].

Monitoring Techniques During AT

Application of End-Tidal Capnometry

While it is standard to measure PaCO2 via ABG to assess for adequate development of hypercapnia during AT, EtCO2, while less accurate, may provide a helpful estimate and prevent overshooting the target PaCO2, thus avoiding complications associated with a profound respiratory acidosis [54]. Notably, an increase in PaCO2–PetCO2 gradient pre- versus post-apnea has been described in several studies, with varying differences in rise of the gradient from 7 to 9 mm Hg [25] in one study, and 0.7 ± 3.6 mmHg (pre-apnea testing) to 8.7 ± 7.1 mmHg (after 20 min of apnea) in another study [55]. Despite the increasing gradient, using a PetCO2 value of 60 mmHg as guidance, the mean duration of AT, hypercapnia, acidosis, and decrease in PaO2 at the end of the test were all significantly reduced after using EtCO2 as compared with not utilizing it [55]. Similar safety and test duration results with capnometry were reported in a Korean study of 61 BD patients comparing two groups, with and without EtCO2. The total duration of AT was shorter in the capnometry group, and the systolic blood pressure during apnea increased in the capnometry group and decreased in the controls [56].

Other Monitoring

Performance of ABGs at intervals determined by the attending physician versus regular 3–5 min intervals resulted in shorter test duration, smaller PCO2 rise and less pH reduction [12]. Other monitoring suggestions have targeted higher sensitivity than visual observation to monitor for spontaneous respirations. Using ultrasound and assessing for lung-sliding during AT have been reported [57], as well as monitoring of electrical activity of the diaphragm [58]. It is unclear, however, if these high-tech approaches offer relevant advantages compared to the visual inspection of the chest.

Apnea Testing on Extracorporeal Membrane Oxygenation (ECMO)

Physicians performing BD evaluations should be familiar with ECMO technology for two main reasons. The first is that the use of ECMO is increasing: In a study comparing ECMO use in 2006 to 2011, it increased from 11.4 to 60.9 cases per million adult discharges [59]. Another study showed that the use of ECMO-CPR increased dramatically between 1992 and 2017 [60]. The second reason why clinicians performing BD evaluations should be familiar with ECMO is that BD is not rare in patients on ECMO: In a study published in 2009, 21% of adult patients treated with ECMO-CPR ultimately were BD [61]. However, there are both practical and ethical challenges to performing AT on ECMO, and there is no clear guidance on how it should be done [62]. Of the published methods to complete AT on ECMO, none has been endorsed by society guidelines so far, and hemodynamic instability as well as failure rates may limit their generalizability.

In a retrospective study of 26 patients between 1995 and 2014 who were declared brain dead on ECMO and became organ donors, AT was not performed in 11 (42%) [63]. Traditional AT does not consider ECMO physiology or derecruitment of the lungs in this subset of critically ill patients. Patients may require high ventilatory support for underlying respiratory failure, and the contribution of the native, diseased lungs to the overall oxygenation in these patients is often small. Systolic blood pressure parameters in current guidelines also do not consider altered flow physiology. For patients who may already be supported by high-dose vasopressors and inotropes, the hypercapnic acidemic state induced by AT may lead to cardiovascular collapse. For successful conduct of AT in patients on ECMO, aspects to specifically consider include preventing hemodynamic instability, maximizing oxygenation, and reducing excessive carbon dioxide elimination. Table 3 summarizes the steps described in literature for completion of AT on ECMO.

Table 3

Apnea testing on extracorporeal membrane oxygenation (ECMO)

Goal	Methods/Results	Reference(s)
Preoxygenation	Optimization of ECMO flow and fractional inspired concentration Tracheal oxygen insufflation Use of CPAP Ambu bag with PEEP valve	Madden et al. [73] Saucha et al. [74] Shah and Lazaridis [71] Lie and Hwang [75] Giani et al. [41]
Reach Target PaCO2	Reduction of Sweep Gas Flow	Madden et al. [73] Saucha et al. [74] Shah and Lazaridis [71] Lie and Hwang [75] Solek-Pastuszka et al. [15] Giani et al. [41]
	Carbogen or CO2 supplementation	Andrews et al. [70] Madden et al. [76] Beam et al. [77]
Blood Gas Monitoring	Draw ABGs from two sites: radial and post-oxygenator site	Ihle et al. [80]

ABG arterial blood gas, CO carbon dioxide, CPAP continuous positive airway pressure, PEEP positive end-expiratory pressure

Preoxygenation and Reduction of Sweep Gas Flow

Most of the initial published experiences for AT on ECMO stem from small case series for both veno-arterial [64-70] and veno-venous ECMO [71-73]. The most common process includes pre-oxygenation with 100% FiO2 on the ventilator and 100% O2 on the ECMO flow, reduction in the sweep gas flow to 0–1 L/min and either retention of the patient on the ventilator or disconnection and placement on T-piece or on a cannula inside the ETT with oxygen insufflation at 6–9 L/min [71, 73, 74]. Tracheal oxygen insufflation with 4–9 L/min through a suction catheter or T-piece, and the use of CPAP to prevent alveolar derecruitment, has also been described [75].

In the largest reported series, a study of 169 BD patients (including 25 patients on ECMO), all with successful AT completion, AT was conducted (after pre-oxygenation with 100% FiO2 for 5 min) via an AMBU bag with adjustable PEEP valve (at the PEEP level as the ventilator) connected to an 8 L/min oxygen flow. For ECMO patients, the extracorporeal blood flow was not modified, but the sweep gas flow was reduced to 1 L/min, and FiO2 was increased to 100%. While no significant hemodynamic alterations occurred, severe hypoxia occurred in 8% of ECMO patients compared to only 2.4% of non-ECMO patients (p = 0.063) [41].

Carbogen or CO2 Supplementation

Another reported method of AT on ECMO is Carbogen supplementation via the ventilator circuit. This method was used in a case report of one patient on veno-arterial ECMO; the patient achieved the target CO2 goal within 8 min without hemodynamic instability [70]. In a retrospective review of AT using the carbogen method on five subjects, the targeted CO2 goal was reached in all patients, and there were no adverse events [76]. Another case report describes the addition of 8% CO2 volume to the ECMO circuit resulting in reliable elevation of PaCO2 above 60 mmHg, independent of patient size, ECMO circuit volume, or oxygenator surface. Not reliant on ventilator setting changes, this technique results in rapid and predictable rise of CO2 without trying to estimate the change in sweep gas flow and/or multiple gas draws. This method differs from previous descriptions of AT on ECMO which advocated for decreasing the sweep gas flow to decrease CO2 removal by the ECMO oxygenator [77].

Blood Gas Monitoring While on ECMO

In non-ECMO patients, PvCO2 is higher than PaCO2 before AT, but after AT, PaCO2 is higher than PvCO2 [78]. This is likely due to CO2 production by the lungs without elimination [79]. Although this difference is not important in non-ECMO patients undergoing AT, this may be significant in ECMO patients, so blood sampling should be done from two different sites. For patients on VA-ECMO, different gas tensions (i.e., PaCO2) may exist at different arterial sampling sites. This is due to the moving relative position of the aortic “water shed” or “mixing point” compared to the cerebral vessel take-off orifices. Given that these differences in gas tensions may not be recognized simply by peripheral arterial gas sampling, a protocol measuring both radial and post-oxygenator carbon dioxide (PaCO2) and oxygen (PaO2) gas tensions during AT may be necessary to ensure homogenous gas tensions reach the brain without compartmentalization [80].

Other Important Considerations About Apnea Testing

Variability of AT Protocols

As with brain death protocols in general, there is significant variability in the specifications for AT both within the USA and worldwide [81]. For the target laboratory value to signify a positive apnea test, most US protocols require a PaCO2 target of 60mmg Hg, but some require a different PaCO2 target < 60mmHg[10]; this variability also exists worldwide; for example, Korea requires the absence of spontaneous respiration when the PaCO2 is 50 mmHg or greater [19]. As opposed to the USA, where the common target apnea laboratory value is the PCO2 level, some countries require a target arterial pH < 7.30 [7] and some require pH ≤ 7.28 [82] in addition to the PaCO2elevation > 60 mm Hg. In the UK [83], there is no absolute PaCO2 target; instead, after starting with a PaCO2 level of 45 mm Hg and disconnecting the patient from the ventilator, they are observed for 5 min for signs of respiratory effort, and then, an ABG is obtained to confirm a 3.75 mm Hg rise has occurred.

With regard to the number and timing of AT, only one apnea test is required in the USA [4], although some individual institutions require more [4, 84]. Brazil, similarly, requires only one apnea test [85]. In the UK and Australia–New Zealand, two apnea tests are needed [7, 83]. In Canada, one apnea test is sufficient if two clinical brain death exams are done concurrently, but if done at different times, they should each be followed by an apnea test [82]. In Korea, two apnea tests separated by six hours are needed [19]. Regarding timing of AT, it is recommended that AT is performed at the end of the BD assessment to minimize risk of harm [4, 7, 15, 86].

Awareness About AT

It has repeatedly been demonstrated that knowledge about conduction of AT is suboptimal. In a recent survey from the USA, 30% of responders reported completing BD exams in their practice, and 76.1% reported to have had training on how to complete the exam. However, 28.3% of them ordered a confirmatory test in patients who, during the AT, take breaths[87]. Similarly, recent large studies across the world have demonstrated this. A survey on brain death practices in intensive care units in Turkey revealed that only 22% of clinicians found AT necessary for brain death determination; 78% of respondents stated that it could be used as an optional confirmatory test, while 66% were not familiar with modifications of AT [88]. A study on BD testing in China revealed that among 550 BD cases, AT was only completed in 50.7%, and in 42.0% AT had to be stopped because of instability [89].

Legal Considerations of AT

Pursuant to recent lawsuits about the need for consent prior to AT, there has been some discussion of this topic in the literature. [90, 91]. One argument for obtaining consent is that there are potential complications of AT, and the procedure has no benefit to a given patient, although a counterargument to this is that allowing for a dignifying death might present a strong benefit. In addition to the aforementioned established risks of AT, those who advocate for the need for consent prior to AT argue that theoretically, secondary injury can occur from elevation of intracranial pressure (ICP) during AT. In a study of 16 brain death evaluations performed in the presence of ICP monitoring, the mean ICP was 86.6, 95, and 83.8 mmHg before AT, during AT, and after AT, while the cerebral perfusion pressure (CPP) was 8.4, 13.5, and 1 mm Hg during the same periods. This data prompted some to conclude these patients did not have complete cerebral circulatory arrest prior to AT [92] and that changes in cerebral hemodynamics may cause secondary injury and lead to BD as a result of AT in patients who were not already BD [86, 90, 92]. However, in a more recent study analyzing ICP, CPP, and mean arterial pressure (MAP) in a total of 34 patients who fulfilled clinical brain death criteria prior to AT, during AT, and after AT, AT had no significant effect on ICP, CPP, MAP, or oxygenation [93]. Furthermore, similar to the aforementioned study, ICP was in the 80 s mmHg—values not compatible with viable brain. For these reasons, though apnea test should be performed last after the rest of the evaluation is completed, so hypercarbia does not confound the other cranial nerve exams [7], or, if two BD exams are planned, the apnea test should be performed with the second exam [86]. The currently practiced standard is that decision-making about performance of apnea testing should not be adjudicated in a courtroom and should not be left up to families, but should be the responsibility of clinicians [94-96]. Moreover, a survey of adult neurologists demonstrated that consent is not routinely obtained prior to AT [97, 98].

Conclusion

AT is physiologically and practically complex. A variety of modifications have been described to facilitate successful conduction of AT, yet complications can occur, and their knowledge is important. Furthermore, many of the suggested modifications would likely need further standardization prior to becoming widely adaptable. This is especially the case for AT while on ECMO, where there is not yet a standardized procedural guideline. Additionally, awareness of variations in AT protocols, monitoring, and awareness of legal aspects is also pivotal. Hence, AT is best performed by experienced providers. Future efforts to ensure that AT is performed safely and consistently should include consensus on timing of AT, number of tests, prerequisites, AT targets, AT technique, and an update to acceptable alternatives and modifications including guidelines for AT for patients on ECMO.

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