Although transplantation remains an effective intervention for many end-stage organ diseases, a significant limitation is the scarcity of available donations. Death can be determined using two types of criteria: death determination by circulatory criteria (DCC) and death determination by neurologic criteria (DNC). When circulatory criteria are used to determine death, the donation process is known as donation after circulatory determination of death (DCD) and has also been referred to as donation after circulatory death, donation after cardiac death, or non-heart-beating organ donation. Donation after circulatory determination of death can further be classified as either uncontrolled or controlled.
1 Uncontrolled DCD refers to the process whereby organs are recovered from those who die following an unexpected cardiac arrest with unsuccessful resuscitation. Controlled DCD refers to cases where organ donors die following planned withdrawal of life-sustaining measures (WLSM) or medical assistance in dying (MAID). Regardless, for a donation to ensue, there must be adherence to the “dead donor” rule; the donor must be dead before retrieval of their organs.
2 For DCD, death determination is based on the permanent cessation of circulation. Since increased time can cause loss of a donation opportunity or impact organ viability for transplant, death determination for DCD must be done in a timely fashion.
The criteria for determining death in DCD have been established in guidelines.
3‐5 In both adult and pediatric Canadian guidelines, the preferred method to confirm the absence of blood pressure is invasive arterial blood pressure (IAP) monitoring.
4,5 In the development of the updated Canadian Clinical Practive Guideline for death determination featured in this month’s Special Issue of the
Journal,
6 it was recognized that in many situations IAP is uncommon, such as DCD in children and patients donating after MAID. Clinical studies outside of the context of DCD have examined other monitoring methods to confirm the absence of circulation using palpable pulse, electrocardiograms (ECGs), ultrasound images of arterial flow or cardiac motion, and regional tissue oximetry as less invasive alternatives to IAP monitoring. Our specific research question was, “In patients who are potential organ donors undergoing DCC, can alternate noninvasive means of measuring circulation versus IAP be used to diagnose cessation of circulation?” The purpose of this systematic review is to summarize the literature, as it relates to DCD, of patients monitored around a period of cessation of circulation, on the diagnostic accuracy of noninvasive methods for measuring circulation compared with the current gold standard (IAP monitoring).
Methods
The protocol for this systematic review was registered on PROSPERO (CRD42021258936); first submitted 16 June 2021. This review was part of a larger project to establish an updated clinical practice guideline for death determination in collaboration with the Canadian Critical Care Society, Canadian Medical Association, and the Canadian Blood Services. This manuscript adhers to the Preferred Reporting Items for Systematic Reviews and Meta-Analyses (PRISMA) for Diagnostic Test Accuracy checklist and guidelines.
7
Eligibility criteria
We included studies on patients who were monitored around a period of cessation of circulation by comparing methods to measure circulation. Our target population was potential DCD donors (both controlled and uncontrolled), but we did not restrict our search to this population. We included all ages of participants and types of settings. We included studies on extracorporeal support if they compared methods that assess for the presence or absence of a pulse.
The intervention of interest was any noninvasive method for the measurement of circulation and could include any combination of palpable pulse, electrocardiogram, ultrasonography, or other techniques.
Our reference standard of interest was IAP monitoring, but we included any reference test that measured circulation. We were intentionally broad with our inclusion criteria given the anticipated paucity of research in this area, coupled with our desire to include data using other reference tests to provide evolving evidence that may inform future research.
We excluded animal studies. We accepted all study designs, except for commentaries, editorials, and ethical analyses. Studies had to compare methodologies for determining circulation, so studies predicting future return of spontaneous circulation (ROSC) were excluded.
Although Sarti
et al.
8 focused on a period of hypotension and not cessation of circulation, we included this study to provide valuable specificity data in pediatrics that also used the target reference standard, IAP monitoring.
We searched MEDLINE, Embase, Web of Science, and the Cochrane Central Register of Controlled Trials from inception to 27 April 2021. The latest search was completed on 27 April 2021.
Search strategy
We developed the search strategy with an information specialist (R. F.) in consultation with content experts, and this strategy was then peer-reviewed by a second information specialist (D. C.) not involved in the study using the 2020 Cochrane protocol peer review assessment form (available at community.cochrane.org). Keywords and related terms such as “heart arrest,” “measurement,” and “blood pressure” were used. The full search strategy can be found in the Electronic Supplementary Material [ESM], eAppendices 1–4. We restricted our inclusion to articles in English or French.
Selection process
Retrieved citations were imported into EndNote™ X9 (Clarivate™, London, UK) for reference management and duplicates were removed automatically. Titles and abstracts were screened independently and in duplicate using a standardized study eligibility form through InsightScope (
https://insightscope.ca/), a crowdsourcing platform for reviews, using predetermined selection criteria. Prospective reviewers from the platform must have obtained a total sensitivity of 0.8 after screening a set of 100 test citations. Disagreements between reviewers were resolved through discussion and a third reviewer if necessary. The same procedure was followed for full-text screening. See ESM eAppendices 5 and 6.
Data collection and items
Reviewers (J. A. K., A.-V. N., L. H.) abstracted relevant study details onto a form (Microsoft Excel, Microsoft Corporation, Redmond, WA, USA) independently and in duplicate. We abstracted data including study design, inclusion and exclusion criteria, recruitment period, outcomes, details on the index, and reference test (e.g., definitions of circulation, thresholds). Any statistical comparisons between measurement methods were recorded for each study (e.g., sensitivity, specificity). We calculated sensitivity and/or specificity if not reported by the authors and there were sufficient data to do so. The data abstraction items can be found in ESM eAppendices 7–28. Our target condition was absence of circulation. Throughout this review, sensitivity was defined as the proportion of patients with absence of circulation that were correctly identified as not having circulation; taken in the death determination context, determining someone dead who is dead. Specificity was defined as the proportion of patients with present circulation that were correctly identified as having circulation; taken in the death determination context, determining someone alive who is alive.
Risk of bias assessment
The risk of bias was assessed independently in duplicate for our study question specifically using the Quality Assessment of Diagnostic Accuracy Studies (QUADAS-2) tool.
9 We reviewed four domains: 1) patient selection; 2) index tests; 3) reference standard; and 4) flow and timing. Conflicts were resolved through discussion and, if needed, a third assessor. QUADAS-2 was a post hoc choice to be specific to diagnostic accuracy studies.
Synthesis methods
Meta-analysis was not possible because of heterogeneity in study design, index and reference tests, statistical analysis, and outcomes. We summarized with descriptive synthesis. Data on our population of interest (potential DCD donors, including patients undergoing withdrawal of life-sustaining measures [WLST]) were considered direct evidence while data on other populations (e.g., cardiopulmonary bypass) were considered indirect evidence.
Certainty assessment and reporting bias assessment
We assessed quality in the same aggregate body of evidence using the Grading of Recommendations Assessment, Development and Evaluation (GRADE) framework, which classifies quality as very low, low, moderate, or high based on evaluation of risk of bias, inconsistency, indirectness, imprecision, and publication bias.
10 Publication bias was assessed in accordance with the GRADE recommendations.
Our study team deemed false positives (determining someone dead who is alive) a critical outcome because this would violate the dead donor rule. A test with perfect specificity (for pulselessness) will never classify an alive person as dead; therefore, a very highly specific test is critical to protect the dead donor rule.
Our study team deemed false negatives (determining someone alive who is dead) an important outcome. A highly sensitive test (for pulselessness) will almost never classify a dead person as alive; therefore, a highly sensitive test minimizes diagnostic delays that can compromise a donation opportunity or reduce organ viability for transplant.
Discussion
In this systematic review on diagnostic test accuracy for cessation of circulation during death determination, we identified 21 studies evaluating six different noninvasive index tests (palpable pulse, POCUS pulse check, ECG, POCUS cardiac motion assessment, cerebral NIRS, and CNAP) with very low to moderate quality of evidence. Ten studies addressed the target question with IAP monitoring as reference (10/21, 47%). Our findings show insufficient evidence to support the use of any other diagnostic method as equivalent or superior to IAP monitoring for the determination of death in potential DCD donors. Isoelectric ECG had zero false positive events (determining someone dead who is not), but likely delays the time to death determination. For the purpose of DCD, ECG may be appropriate to use in specific contexts such as pediatric DCD and DCD following MAID. Point-of-care ultrasound assessment of pulse and cardiac motion are emerging therapies, but the body of evidence is currently limited by indirectness and imprecision. Although the evidence is limited, there are data suggesting that palpable pulse and NIRS should not be used for DCC (low and very low quality) in potential DCD donors. We found limited or no evidence for specific subgroups (children, MAID, uncontrolled DCD).
The last Canadian adult DCD guideline published in 2006 states that IAP monitoring is the “preferred method to confirm the absence of blood pressure.”
4 Subsequently, Canadian pediatric guidelines in 2017 also recommended the use of IAP monitoring for DCC.
5 European recommendations for uncontrolled DCD have suggested determining death using ECG or alternatively, echocardiography or IAP “in case of electro-mechanical dissociation.”
31 In some countries’ guidelines, the method is not defined, or they state that any of the three previously mentioned techniques can be used.
1 This review is driven by consideration of the potential negative impacts of the use of IAP monitoring in the context of DCD; it is invasive, may be technically challenging to obtain, especially in pediatrics, and requires trained personnel as well as a hospital setting to insert and monitor. There are certain situations, such as MAID, where the patient may choose environments without invasive monitoring to die or may be able to make an informed decision preferring alternative methods.
Pulse palpation requires no additional equipment, but had unacceptably low specificity in all studies (four studies; range, 0.41–0.79; low quality evidence).
8,11‐13 Diagnostic tests with low specificity would have higher false positives (determining someone dead who is alive), which we deemed a critical outcome as this could violate the dead donor rule. In contrast to pulse palpation, evidence for the use of isoelectric ECG included more robust, multicentre prospective studies and zero false positives (0%, 0/510 patients, two studies).
19,20 There was a strong and consistent association that, although the specificity was excellent, the use of isoelectric ECG delays the time to death determination. The median time for this delay in the largest (
n = 480) included study was 3 min 37 sec (range, 0 sec–83 min 28 sec).
20 A longer warm ischemia time may come at the cost of graft function if isoelectric ECG is used.
32 Nevertheless, the priority to avoid false positives (determining someone dead who is alive) outweighs the impact on warm ischemia times. The two ECG studies were in the setting of WLSM. The duration between loss of pulsatile pressure and an isoelectric ECG in MAID may be shorter than seen in WLSM associated with medication administration for MAID (such as bupivacaine or potassium chloride). Indeed, warm ischemia times for MAID are reported to be shorter compared with conventional DCD donors.
33‐35 Medical assistance in dying patients may be a population in which the use of ECG is a suitable alternative given patient preference for noninvasive monitoring if the method of MAID includes medication causing rapid electrocardiographic arrest.
Besides MAID, situations may occur with neonates and pediatric patients where IAP may not be present. Invasive arterial blood pressure monitoring in children may be more technically challenging given smaller patient sizes and high rates of arterial line malfunction.
36 As pediatric guidelines evolve, there is a balance in allowing some flexibility in monitoring while still ensuring safeguards. Family members have described the lost opportunity of DCD as “a waste of precious life-giving organs and hospital resources.”
37 In pediatrics, use of ECG may be an appropriate alternative where IAP monitoring is not technically feasible.
Point-of-care ultrasound has become a common part of many clinical assessments. Nevertheless, the results of our study suggest that its use cannot be recommended given that data are limited because IAP monitoring was not included as a reference, event numbers were small, studies were on a cardiac bypass or cardiac arrest population, and/or videos were only reviewed and not also acquired in real-time. There was imprecision due to a low number of events. Point-of-care ultrasound techniques also have real-world challenges such as the requirement for training, maintenance of competence, need for standards for interpretation, and time demands on these trained individuals. There is a larger body of evidence assessing POCUS techniques for the prediction of ROSC and survival.
38,39 Tsou
et al. meta-analyzed 15 studies and reported that spontaneous cardiac movement had a pooled sensitivity of 0.95 (95% CI, 0.72 to 0.99) and specificity of 0.80 (95% CI, 0.63 to 0.91) in predicting ROSC during cardiac arrest, with a positive likelihood ratio of 4.8 (95% CI, 2.5 to 9.4) and a negative likelihood ratio of 0.06 (95% CI, 0.01 to 0.39).
39 These studies on ROSC predict a future event and have limited application to the question on real-time cessation of circulation.
Death determination by circulatory criteria and DNC are aligned towards a single brain-based definition of death, recognizing a common biomedical pathway of death.
40‐42 In our review, we assessed evidence on cerebral NIRS as a potential noninvasive modality for DCC. Although a correlation was identified between NIRS and blood pressure, there was a concerning overlap between baseline saturation and saturation either during cessation of circulation or in patients already determined dead by cardiac criteria.
23‐25,27‐29 Given this, NIRS likely has poor discrimination for DCC (three studies,
n = 30 patients, very low-quality evidence).
Our study is strengthened by the comprehensive search strategy and an a priori protocol. We assessed the studies’ risk of bias using a standardized tool and performed the quality of evidence assessment using GRADE methodology. Nevertheless, there are several important limitations. First, none of the studies included were specifically designed to compare noninvasive methods with IAP monitoring in the context of DCD. Second, the landscape of research we found generally consisted of small, observational studies, often further limited by a case-control or unblinded design. Third, only half of the included studies used IAP monitoring as the reference standard (10/21, 47%), and few defined what their threshold for pulse pressure was. Fourth, only 14% (3/21) of the studies included potential DCD candidates or WLST; no studies included potential MAID or uncontrolled DCD candidates. Finally, our search had language restrictions. Future research should continue to assess POCUS methods, compare IAP monitoring and ECG in subgroups of uncontrolled DCD and MAID, increase representation of pediatric patients, assess the success and complication rates of IAP monitoring, assess the effect of arterial cathether location (e.g., central vs peripheral), and explore other creative noninvasive options such as CNAP.
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