Discussion
To address challenges with ED crowding in our level 1 trauma center that result in delays or denials of transfers, we designed and implemented a protocol to increase timely access to care. In a prospective cohort study, we found that DA was effective more than 80% of the time in enabling access to high-level trauma care at our institution. Previous to implementation of the DA protocol, these patients would have been denied access. In addition, DA appears to be safe. There were no morbidity or mortality events attributed to the DA process after quality review by a group of evaluators composed of trauma surgeons and nurses. In addition, adverse events such as up-triage to an ICU, rapid response and cardiopulmonary arrest within 24 hours of transfer using DA were no different from transfers via the ED during the same period. Overall hospital mortality was also not different between the two cohorts.
Our findings offer evidence in support of DA as a viable strategy for level 1 or 2 trauma centers with highly congested EDs that threaten the timely transfer of trauma patients. Though we found a trend toward transfers in the DA cohort taking longer to arrive at our hospital by approximately 45 min, this difference was not statistically significant. We found that all transfers in the DA cohort who were successfully transferred had a time from initial call to decision communicated to the referring ED within the a priori defined target of 10 minutes. It is unclear whether there may be other aspects of the DA process that may cause a delay.
Though we cannot conclude that without the DA process patients would have received inadequate trauma care, we expect that the DA process is likely efficacious in ensuring more timely care for the patient, given that the selection of which level 1 trauma center to transfer a patient is typically (though not always) based on geographical proximity to the referring hospital. Thus, the DA process increases the likelihood that the patient gets access to the geographically more proximate hospital without needing to call additional hospitals for transfer that are less likely to be geographically as close by.
To our knowledge, our study is the first to report on the design and feasibility of DA for trauma patients. Previous literature regarding the development of strategies to ensure timely transfer to high-level care has focused on the geographical distribution of facilities and their proximity to patients.12–14 Several studies have demonstrated that delays in transfer to a higher-level trauma center result in worse outcomes.1–3 The American College of Surgeons recently published a study concluding that ‘access delayed is accessed denied’.15 In their study, Hashmi et al demonstrated that among more than 1.9 million trauma patients, states with better access to trauma care had lower age-adjusted mortality. DA represents one strategy to help ensure the optimization of patient safety in trauma system care and potentially to improve outcomes. Future studies should explore this relationship.
Several aspects of the DA protocol were essential to ensure appropriate care for these patients, and hospitals designing DA protocols should be attentive to these. First, the presence of the trauma team on arrival of the patient in the general care ward or ICU was critical. In many trauma bays at high-level centers, trauma team members maintain a continuous presence within the ED and are therefore present to ensure rapid assessment of the patient on arrival. In DA, patients are transferred directly to the inpatient location, which may not have trauma team members located there continuously. Within our DA protocol, when the trauma surgeon accepted the patient for transfer, trauma team members were informed about the expected arrival time of the patient, and a member of the trauma team, the bedside nurse and the nurse manager were designated to be present on the arrival of the patient. Primary surveys were performed for all patients at the time of arrival by the trauma team at the bedside, which included an attending and resident physician, as well as two or more nurses (bedside nurse and resource nurse).
In addition, the trauma team at the bedside that received the patient analyzed whether any further imaging was needed. For any imaging studies that were emergently indicated, the trauma team followed a protocol using an order system that indicated urgency and a hotline to connect with the radiologist. Radiologists at our hospital were educated about DA and were prepared to prioritize the patient for rapid imaging when indicated by the operation team. Ensuring ready access to imaging may be a challenge for hospitals. Hospitals implementing DA protocols should consider tracking metrics such as time to CT scan. In our study, this metric was similar for DA and ED-to-ED cohorts.
Given the impact of ED crowding on patient safety, an important future direction of DA would be to analyze whether such a pathway could be implemented to prevent ED overcrowding rather than purely in reaction to it, as our pathway was designed. By routinely performing DA in trauma patients, the ED may be less crowded with acutely injured patients and may be better able to care for those entering the ED from the street.
This study has several limitations. First, it was designed and implemented in a single center. The feasibility and effectiveness of the DA protocol at our institution may not be generalizable to other centers. In addition, we compared the cohort of patients exposed to the DA protocol with a contemporaneous control cohort that was not exposed to the DA protocol. Although we found no differences in the primary and secondary outcomes, the relatively lower number of patients in the DA cohort raises the possibility of type II error. Importantly, though the mortality rate was slightly higher in the DA cohort, the cause of mortality in each case was not attributable to any aspect of the DA process. In addition, though there were patients in the DA cohort who underwent operating room procedures, we did not observe any direct-to-operating room transfers. Thus, this aspect of the DA pathway needs to be further assessed for feasibility and safety. Finally, the major difference between the DA and non-DA populations was that the patients in the DA protocol were transferred to our institution during Code Help, a period of severe ED congestion, whereas those in the ED-to-ED pathway were transferred during a less congested period. Though the DA protocol specifically bypasses the ED, it is possible that significant ED congestion affects care on the general care wards, ICUs and operating rooms where these patients received care. As such, this may have impacted our results in a manner that we could not predict.