Literature DB >> 31751349

Direct transport vs secondary transfer to level I trauma centers in a French exclusive trauma system: Impact on mortality and determinants of triage on road-traffic victims.

Sophie Rym Hamada1,2, Nathalie Delhaye3, Samuel Degoul4, Tobias Gauss5, Mathieu Raux6, Marie-Laure Devaud7, Johan Amani8, Fabrice Cook9, Camille Hego10, Jacques Duranteau11, Alexandra Rouquette12,13.   

Abstract

BACKGROUND: Transporting a severely injured patient directly to a trauma center (TC) is consensually considered optimal. Nevertheless, disagreement persists regarding the association between secondary transfer status and outcome. The aim of the study was to compare adjusted mortality between road traffic trauma patients directly or secondarily transported to a level 1 trauma center (TC) in an exclusive French trauma system with a physician staffed prehospital emergency medical system (EMS).
METHODS: A retrospective cohort study was performed using 2015-2017 data from a regional trauma registry (Traumabase®), an administrative database on road-traffic accidents and prehospital-EMS records. Multivariate logistic regression models were computed to determine the role of the modality of admission on mortality and to identify factors associated with secondary transfer. The primary outcome was day-30 mortality.
Results: During the study period, 121.955 victims of road-traffic accident were recorded among which 4412 trauma patients were admitted in the level 1 regional TCs, 4031 directly and 381 secondarily transferred from lower levels facilities. No significant association between all-cause 30-day mortality and the type of transport was observed (Odds ratio 0.80, 95% confidence interval (CI) [0.3-1.9]) when adjusted for potential confounders. Patients secondarily transferred were older, with low-energy mechanism and presented higher head and abdominal injury scores. Among all 947 death, 43 (4.5%) occurred in lower-level facilities. The population-based undertriage leading to death was 0.15%, 95%CI [0.12-0.19].
CONCLUSION: In an exclusive trauma system with physician staffed prehospital care, road-traffic victims secondarily transferred to a TC do not have an increased mortality when compared to directly transported patients.

Entities:  

Mesh:

Year:  2019        PMID: 31751349      PMCID: PMC6872206          DOI: 10.1371/journal.pone.0223809

Source DB:  PubMed          Journal:  PLoS One        ISSN: 1932-6203            Impact factor:   3.240


Background

Major trauma and road traffic accidents in particular remain an important cause of death and disability worldwide, especially among young and economically active adults [1]. Part of the answer is the organization of trauma care into structured regional trauma systems embedded into guidelines and along a national policy. Efforts and experiences from the United States [2,3], United Kingdom [4,5], Germany [6], Norway [7], or Netherlands revealed improved outcomes over the last 20 years. The provision of structured and coordinated trauma care from the scene to the rehabilitation unit has a far higher impact on outcome than any single medical intervention [2]. An exclusive trauma system is based on the provision of care by a limited number of highly specialized designated hospitals, so-called level 1 trauma centers (TC). Providing trauma care within a TC is now known to save lives and prevent long-term disability [2], so the direct transportation of severely injured patients to designated centers, while bypassing closer non-specialized facilities, is considered optimal. Nevertheless, few studies have analyzed the relationship between mortality and direct or secondary transport to TC and they generated conflicting results [8-12]. Those studies were exclusively conducted in paramedic staffed prehospital emergency medical systems without physician-staffed pre-hospital teams [13,14]. In France, as in some other European countries, the organization of prehospital care and trauma systems is systematically provided and coordinated by specialized physicians [15]. The main objective of this study was to compare adjusted intrahospital mortality between road traffic patients directly transported to a referral level 1 TC and patients secondarily transferred from a lower level facility. Secondary goals were 1/ to identify factors associated with secondary transfer (considered as undertriage), and 2/ to evaluate the proportion of patients deceased in lower level facilities before admission to a level 1 TC (considered as undertriage) and calculate a population-based undertriage.

Methods

Study design and setting

This is a retrospective cohort study conducted on prospectively collected data in the administrative area of Paris (Île de France region) which is organized as an exclusive trauma system with six level 1 TCs designated by the Regional Health Agency. The Île de France region gathers 12 million inhabitants, so about 20% of mainland France population and records an average of 42.000 road traffic accidents (RTA) each year. The emergency medical system (EMS) of the Île de France region is described in Fig 1, and also detailed in previous studies by Hamada et al. [16,17].
Fig 1

Map of the region Île-de-France with trauma center, SAMU dispatch center and ambulance stations location.

The Île de France region gathers 8 central emergency medical system dispatch centers (SAMU- Service d’Aide Médicale Urgente), 43 prehospital enhanced mobile care team stations (SMUR- Service Mobile d’Urgence et de Réanimation) and 6 level 1 Trauma Centers (TCs). The region is organized as an exclusive trauma system, conceiving severe trauma care only in the 6 designated TC among all existing tertiary care facilities (n = 87).

Map of the region Île-de-France with trauma center, SAMU dispatch center and ambulance stations location.

The Île de France region gathers 8 central emergency medical system dispatch centers (SAMU- Service d’Aide Médicale Urgente), 43 prehospital enhanced mobile care team stations (SMUR- Service Mobile d’Urgence et de Réanimation) and 6 level 1 Trauma Centers (TCs). The region is organized as an exclusive trauma system, conceiving severe trauma care only in the 6 designated TC among all existing tertiary care facilities (n = 87). In France, dispatching physicians located in centralized SAMUs are available 24/7 and decide which emergency vector (paramedic-staffed ambulance or physician-staffed mobile intensive care unit) is to be deployed based on information provided during the emergency call. After clinical assessment, patient’s triage is decided jointly by the physician on scene (when present) and the dispatching physician according to a national algorithm [18] and to the Mechanism, Glasgow coma scale and Arterial Pressure (MGAP) score [19]. All patients suspected of severe trauma are necessarily cared for by a physician-lead enhanced care team in a mobile intensive care unit and directly transported to a level 1 TC. The patient can also be transported to lower level of care facilities, with or without physician escort. Sometimes severe patients are first admitted to lower level of care facilities to allow initial stabilization, then transferred to a specialized center.

Population and databases

This study included all the patients involved in a RTA in the Île de France region between January 1, 2015 and December 31, 2017. All patients admitted to one of the six level 1 TCs of the region were prospectively registered in the regional trauma registry (Traumabase, http://traumabase.eu). The Traumabase obtained approval from the Advisory Committee for Information Processing in Health Research (CCTIRS, 11.305bis) and from the National Commission for data protection (CNIL, 911461), and meets the national institutional review board requirements (Comité de Protection des Personnes Paris VI, Paris France). The information is given to the patients (or next of kin, in case of comatose patients) about the existence of the trauma registry, but the institutional review board waived the need for informed consent. Data are anonymized from the time they are collected in the case report file. Sociodemographic, clinical, biological and therapeutic data (from the prehospital phase to the discharge of hospital) are systematically collected for all recorded patients. In parallel, for all RTA involving any vehicle in France, the Police collects descriptive variables on the road user, vehicle, location and conditions of the crash. These road accident analysis reports (RAAR) are sent to the Ministry of the Interior once the 30-day survival status is completed. The RAARs constitute a nation-wide database of more than 10 million accidents since 1953. Records from the RAAR and Traumabase were linked in order to evaluate the frequency of patients deceased in non-TC facilities (considered as inappropriate triage). The process of data management and linking is detailed in the supporting information (S1 File) and synthetized in the Flow chart (Fig 2). For individuals recorded as dead in the RAAR, but who could not be linked to any patient recorded in the Traumabase, archives from the 8 central dispatch centers of the Île de France region (SAMU) were examined to establish where the death occurred (either on scene or in an identified hospital).
Fig 2

Flow charts of the study.

Green filling: Traumabase data. Black boxes: RAAR and Traumabase linkage to identifiy the place of death of patients dead outside the trauma centre. Blue filling: Data extracted from SAMU archives. Pie: Population of hospital admissions extracted from RAAR, Traumabase and SAMU archives joint analysis

Flow charts of the study.

Green filling: Traumabase data. Black boxes: RAAR and Traumabase linkage to identifiy the place of death of patients dead outside the trauma centre. Blue filling: Data extracted from SAMU archives. Pie: Population of hospital admissions extracted from RAAR, Traumabase and SAMU archives joint analysis

Variable definitions and outcome

The primary outcome was the 30-day in-hospital all-causes mortality of RTA patients alive on admission to the TC. The causes of death were determined by the physicians in charge. The modality of admission was defined as direct transport if the patient was directly transported from the scene to a level 1 TC, and as secondary transfer if the patient was transferred to a level 1 TC within the first 48 hours after the RTA but after a previous admission in a lower level facility. Available prehospital variables included the mechanism of accident and distance to TC (categorized in inner or outer region as in Fig 1), demographic variables (age and gender) and worst vital signs during prehospital phase among: minimal Glasgow Coma Scale (GCS), maximal heart rate (HR), minimal systolic arterial blood pressure (SAP), minimal peripheral oxygen saturation (SpO2) [20], early on scene capillary hemoglobin concentration [21], MGAP score [19], tracheal intubation and vasopressor administration. The assessment of high speed was reported according to the Vittel criteria and the total number Vittel criteria was quantified [18]. The Abbreviated Injury Scale (AIS) of body regions version 2005 and the Injury Severity Score (ISS) were used as surrogate measures of injury severity. Comorbidities were classified according American Society of Anesthesiologists physical status classification (ASA) and antiplatelet or anticoagulation therapy intake. Available variable on admission were hemodynamic status, initial blood sample results, surgery within the first day and the Simplified Acute Physiologic Score II (SAPS2) and both intensive care unit and hospital length of stay at discharge. The expected probability of survival was calculated using the Trauma Related Injury Severity Score (TRISS) with most recent coefficients [22,23] using a respiratory rate of 20 min–1 in all patients [20]. Undertriage, defined as severe patients not ending in a TC, was computed according to three approaches: 1/ TC-based undertriage: (number of secondarily transferred patients) ÷ (number of admission in the TCs), 2/ Population-based undertriage leading to death according to the Cribari matrix method [24]: (number of death among patients first admitted in non TC) ÷ (number of admission in non TC) (Fig 2), 3/ Considering the boundaries of the 95% confidence interval of the observed mortality in patients directly admitted to the TC, we computed (with a Chi2 approach) the hypothetic systemic undertriage rate range outside which the crude mortality of inappropriately triaged patients (dead after initial transport in non-TC) would be significantly different than in TC-directly admitted patients. Overtriage, defined as transport to the trauma center of patients ending with ISS < 16, was computed according to the Cribari method.

Statistical analyses

The report follows the Strobe guidelines [25]. Continuous data were described as mean (standard deviation) or median [1st– 3rd quartile] according to their distribution, and categorical variables as count (percentages) [26]. Bivariate analyses were performed using Chi2 test and Student t tests (or Mann-Whitney test) depending on variable type, to identify covariates associated with 30-day mortality and/or with secondary transfer. Two multivariate logistic models were computed 1/ to identify the determinants of secondary transfer among prehospital available characteristics and 2 /to assess the association between secondary transfer and 30-day mortality adjusted on prehospital characteristics and characteristics available at admission. All confounders, i.e. the variables associated with the outcomes (p-value <0.05) in univariate analyses, were selected for multivariate analyses except in case of collinear variables (Spearman correlation coefficients >0.8), where the most clinically relevant variable was selected [27]. Initial physiologic variables (arterial pressure, heart rate and oxygen saturation) were withdrawn from the model because they were missing not at random in the secondary transfer group for more than 22% (vs <2% in the direct transport group). Multiple imputation via factor analysis for mixed data was used to handle missing data [28] as the average rate of missing data was 5.5% (maximum 15.7%) for variables candidate to multivariate analyses. Then, the variables were entered altogether into a multivariate logistic regression model and selection was performed using a backward stepwise procedure to optimize the Akaike criterion and the area under the receiver operating curve (AUC). The clinically relevant pairwise univariate interactions were tested. Model calibration was assessed using the Hosmer and Lemeshow statistic [29]. Model discrimination was assessed using the AUC and a bootstrap methodology (1000 samples) was used to quantify any optimism (averaged difference between the apparent AUC of the model developed on each bootstrap sample and its AUC on the original sample) in the final prediction model [30]. A sensitivity analysis was performed with a model on “complete cases” gathering all prehospital physiologic variables. Based on an hypothesized prevalence of secondary transfer of 10% and an hypothesized overall mortality of 6%, our sample size was sufficient to show a mortality difference of 4% between the two groups with a power of 80% and a type one error of 5%[31]. All tests were two-sided and a p ≤ 0.05 was considered significant. R 3.5.1 software (R Foundation for Statistical Computing, Vienna, Austria) was used for analyses.

Results

During the study period, 121 955 road traffic accidents were recorded by the Police (RAAR) and 4412 patients were admitted to the regional TCs following a road traffic accident in the Île de France region (Traumabase). Direct transportation to TC occurred for 4031 patients (91%), whereas 381 (9%) patients were secondarily transferred (Flow chart Fig 2). Overall, 278 (6%) in-hospital deaths were recorded over the 30 days following admission in the TC. The causes of death are detailed in the Table 1. There was no significant difference in the causes of death between the direct and secondary transfer groups (p = 0.07).
Table 1

Characteristics of patients deceased during the 30 days after admission depending on the cause of death.

CNSHSHypoxia/AnoxiaMOFSeptic shockTCAUnknown
DirectSTDirectDirectDirectDirectDirectSTDirectST
n172534439210183
Demography and outcome
Age (year)40 [26–60]82 [66–87]46 [33–64]64 [45–76]46 [29–65]72 [69, 74]43 [32–52]5665 [51–70]85 [85–88]
Male (%)123 (72)3 (60)24 (71)3 (75)31 (80)1 (50)8 (80)07 (88)2 (67)
ICU LOS3 [2–6]4 [3–113]1 [1–1]8 [1–17]2 [1–6]5 [4–6]1 [0–1]08 [6–9]11 [10–18]
Mechanism of injury (%)
MVA49 (28)1 (20)9 (27)2 (50)12 (31)04 (40)1 (100)1 (13)1 (33)
Motorbike45 (26)09 (27)2 (50)15 (39)1 (50)4 (40)01 (13)0
Bicycle12 (7)1 (20)2 (6)0001 (10)000
Pedestrian60 (35)3 (60)11 (32)011 (28)1 (50)1 (10)06 (74)2 (67)
Other6 (4)03 (9)01 (3)00000
Severity of head injury
Head AIS5 [4–5]5 [5–5]0 [0–4]5 [5–5]3 [0–4]3 [3–3]3 [3–5]01 [0–3]0 [1–0]

Data are expressed as median [quartile 1, 3], or n (%).

AIS: abbreviated injury scale, CNS: central nervous system, HS: Hemorrhagic shock/ exsanguination, ICU: intensive care unit, LOS: length of stay, MOF: multiple organ failure, MVA: motor vehicle accident, Direct: direct transportation, ST: secondary transfer, TCA: traumatic cardiac arrest.

278 in-hospital deaths recorded at 30-day (6%) in the trauma centers.

Data are expressed as median [quartile 1, 3], or n (%). AIS: abbreviated injury scale, CNS: central nervous system, HS: Hemorrhagic shock/ exsanguination, ICU: intensive care unit, LOS: length of stay, MOF: multiple organ failure, MVA: motor vehicle accident, Direct: direct transportation, ST: secondary transfer, TCA: traumatic cardiac arrest. 278 in-hospital deaths recorded at 30-day (6%) in the trauma centers. The characteristics of patients directly and secondarily transferred to the TCs are presented in Table 2 (prehospital available characteristics) and Table 3 (severity and hospital course).
Table 2

Prehospital demographic, physiologic and injury characteristics of patients according to the type of transport (# included in the multivariate analysis).

Direct transportation(n = 4031)Secondary transfer(n = 381)p
Demography and outcome
Age (year)37 (17)43 (20)< 0.001 #
Male (%)3118 (78%)293 (77%)0.89
BMI (kg/m2)25 (6)25 (5)0.82
ASA< 0.001 #
12888 (72%)248 (65%)
2869 (22%)106 (28%)
≥ 390 (2%)18 (5%)
Unknown184 (5%)9 (2%)
AC/AP therapy146 (4%)40 (11%)< 0.001 #
Professional situation< 0.001 #
Working1936 (63%)193 (59%)
Student420 (14%)44 (13%)
No activity595 (19%)74 (23%)
Other118 (4%)18 (6%)
Mechanism of injury (all blunt)< 0.001 #
MVA1343 (33%)98 (26%)
Motorbike1753 (44%)147 (37%)
Bicycle171 (4%)41 (11%)
Pedestrian668 (17%)83 (22%)
Other96 (2%)12 (3%)
Hospital on-call period2818 (70%)268 (70%)0.75
Ejection1319 (42%)96 (38%)0.23
Global assessment of speed2630 (76%)187 (58%)< 0.001 #
Death in the same vehicle105 (3%)2 (0.8%)0.04
Entrapment572 (14%)26 (7%)< 0.001 #
Unstable pelvic trauma195 (5%)21 (6%)0.47
Traumatic cardiac arrest99 (36%)27 (0.7%)< 0.001 #
Sum of Vittel criteria ≥ 13999 (92%)317 (83%)<0.01#
MGAP < 23817 (21%)33 (11%)<0.001
Prehospital variables
 SAP min (mmHg)115 (25)122 (23)< 0.001
 HR max (beats/min)94 (23)90 (19)0.01
 SpO2 min (%)98 [95–100]98 [96–100]0.85
 Glasgow Coma Scale15 [14–15]15 [15–15]< 0.001#
 Pre-admission intubation (%)896 (22%)22 (6%)<0.001

Qualitative variables expressed as n (%) and quantitative variables as mean (SD) or median [quartile1, 3] according to the distribution.

†: average missing data 22–26% (not missing at random)SAP (Systolic arterial blood pressure): 22.8% missing, HR (Heart rate): 22.6% missing, SpO (peripheral oxygen saturation): 25.7% missing.

BMI: body mass index, ASA: American society of anesthesiologists, AC/AP therapy: anticoagulant and/or antiplatelet therapy, MVA: motor vehicle accident, min: minimal, max: maximal.

Vittel Criteria: French triage algorithm gathering 26 criteria to transport in a TC [18].

MGAP: Mechanism, Glasgow coma scale, Age, and arterial blood Pressure (prehospital score predictive of mortality) [20].

Table 3

Severity, clinical characteristics and hospital course of trauma patients according to the type of transport.

Direct transportation(n = 4031)Secondary transfer(n = 381)p
Severity of injuries
SOFA (day 1)1 [0–4]0 [0–2]0.02
SAPS II (day 1)17 [10–31]15 [10–25]0.03
ISS11 [5–22]14 [9–22]< 0.001
Major trauma ISS ≥ 161557 (39%)147 (48%)0.001
Head and neck AIS ≥ 3900 (22%)103 (27%)0.04
Face AIS ≥ 2468 (12%)29 (8%)0.02
Thorax AIS ≥ 31148 (29%)120 (32%)0.23
Abdomen AIS ≥ 3408 (10%)76 (20%)< 0.001
Extremities pelvis AIS ≥ 31115 (29%)58 (15%)< 0.001
At admission
SAP (mmHg)129 (27)128 (24)0.63
Hemoglobin (g/dL)13.3 (2.1)13.0 (2.0)0.04
Lactate (mmol/L)2.5 (2.2)2.1 (1.5)0.01
Prothrombin rate (%)82 (18)83 (15)0.12
Surgery in the first 24h1941 (48%)152 (40%)0.01
Specific characteristics
Hemorrhagic shock266 (7%)14 (4%)0.03
Severe head trauma405 (10%)4 (1%)< 0.001
Spine trauma451 (11%)85 (22%)< 0.001
Medullary injury116 (3%)22 (6%)1
Evolution and outcome
Infection176 (23%)16 (14%)0.03
ICU LOS (days)2 [2–5]3 [2–7]< 0.001
Hospital LOS (days)7 [2–17]9 [5–16]< 0.001
Discharge from ICU< 0.001
Ward2938 (79%)326 (88%)
Home697 (19%)34 (9%)
Other ICU7 (0%)4 (1%)
Rehabilitation82 (2%)7 (2%)
Day 30 mortality269 (7%)9 (2%)0.001
Mortality over hospital stay289 (7%)9 (2%)0.001
Predicted mortality by TRISS (%)8.8%4.7%0.001

Qualitative variables expressed as n (%) and quantitative variables as mean (SD) or median [quartile1, 3] according to the distribution.

SOFA: sequential organ failure assessment, SAPS II: simplified acute physiologic score, ISS: injury severity score, AIS: abbreviated injury scale, SAP: systolic arterial blood pressure, ICU: intensive care unit, LOS: length of stay, TRISS: trauma related injury severity score.

Hemorrhagic shock: receiving ≥ 4 packed red blood cells concentrate within 6 hours.

Severe head trauma: Glasgow coma scale ≤ 8 and head AIS > 1.

Qualitative variables expressed as n (%) and quantitative variables as mean (SD) or median [quartile1, 3] according to the distribution. †: average missing data 22–26% (not missing at random)SAP (Systolic arterial blood pressure): 22.8% missing, HR (Heart rate): 22.6% missing, SpO (peripheral oxygen saturation): 25.7% missing. BMI: body mass index, ASA: American society of anesthesiologists, AC/AP therapy: anticoagulant and/or antiplatelet therapy, MVA: motor vehicle accident, min: minimal, max: maximal. Vittel Criteria: French triage algorithm gathering 26 criteria to transport in a TC [18]. MGAP: Mechanism, Glasgow coma scale, Age, and arterial blood Pressure (prehospital score predictive of mortality) [20]. Qualitative variables expressed as n (%) and quantitative variables as mean (SD) or median [quartile1, 3] according to the distribution. SOFA: sequential organ failure assessment, SAPS II: simplified acute physiologic score, ISS: injury severity score, AIS: abbreviated injury scale, SAP: systolic arterial blood pressure, ICU: intensive care unit, LOS: length of stay, TRISS: trauma related injury severity score. Hemorrhagic shock: receiving ≥ 4 packed red blood cells concentrate within 6 hours. Severe head trauma: Glasgow coma scale ≤ 8 and head AIS > 1. The multivariate analysis identified 10 prehospital variables independently associated with the type of transport (Table 4). Identified risk factors for secondary transfer were age (Odds ratio (OR) 1.4, 95% confidence interval (CI) [1.1–1.9] and 1.9, 95% CI [1.3–2.8] for ages 45 to 64 years and 65 to 100 years respectively), bicycle or pedestrian accidents (OR 2.2, 95% CI [1.4–3.4] and 1.5, 95% CI [1.0–2.1] respectively), high GCS score (OR 1.4, 95% CI [1.3–1.5]) and antiplatelet or anticoagulation therapy intake (OR 2.0, 95% CI [1.3–3.1]). In contrast, entrapment (OR 0.6, 95% CI [0.4–0.9]), high speed mechanisms (OR 0.6, 95% CI [0.5–0.8]) and pelvic injuries (OR 0.5, 95% CI [0.3–0.6]) were associated with a direct transfer. To notice, the only pairwise univariate interaction retained was between head and abdomen injury severity (AIS ≥ 3) which was negatively associated with secondary transfer (OR 0.1, 95% CI [0.02–0.3]). The Hosmer and Lemeshow test showed a good calibration of the model (p = 0.69). The discrimination as evaluated by the AUC was 0.76 (95% CI [0.73–0.78]) and the optimism adjusted AUC was evaluated at 0.75 (95% CI [0.72–0.77]). In the sensitivity analysis, the values of the OR of all the identified predictors were marginally modified by prehospital physiologic variables (S2 File).
Table 4

Results of the multivariate analysis to identify variables associated to the secondary transfer.

VariableOR, CI 95%pOveral test F
Intercept<0.001
Age0.01
[0,17]1.5 [0.9–2.3]0.07
]17,44]1-
]44,64]1.4 [1.1–1.9]0.01
]64, 100]1.9 [1.3–2.8]0.01
Mecanism0.01
MVA1-
Bicycle2.2 [1.4–3.4]<0.001
Pedestrian1.5 [1.0–2.1]0.03
Motorcycle1.1 [0.8–1.5]0.44
Other2.0 [1.0–4.0]0.04
Entrapment0.6 [0.4–0.9]0.03
Speed0.6 [0.5–0.8]<0.001
GCS initial*1.4 [1.3–1.5]<0.001
AC/AP therapy2.0 [1.3–3.1]0.01
AIS head ≥ 33.2 [2.4–4.3]<0.001
AIS face*0.7 [0.6–0.9]<0.001
AIS abdomen ≥ 33.6 [2.6–4.9]<0.001
AIS pelvis ≥ 30.5 [0.3–0.6]<0.001
AIS head ≥3 *AIS abdomen ≥ 30.1 [0.02–0.3]<0.001

OR, CI 95%: Odds ratio and its 95% confidence interval.

MVA: motor vehicle accident, GCS: Glasgow coma scale, AC/AP therapy: anticoagulant or antiplatelet therapy, AIS: Abbreviated Injury Scale.

Severe head trauma: head AIS ≥ 3.

Severe abdominal trauma:

* Continuous variables

Akaike criteria: 2290

Hosmer Lemeshow: p = 0.70

AUC Roc curve: 0.76 [0.73–0.78]

Optimism: 0.0095

OR, CI 95%: Odds ratio and its 95% confidence interval. MVA: motor vehicle accident, GCS: Glasgow coma scale, AC/AP therapy: anticoagulant or antiplatelet therapy, AIS: Abbreviated Injury Scale. Severe head trauma: head AIS ≥ 3. Severe abdominal trauma: * Continuous variables Akaike criteria: 2290 Hosmer Lemeshow: p = 0.70 AUC Roc curve: 0.76 [0.73–0.78] Optimism: 0.0095 The univariate comparison of the patients deceased at 30-day versus survivors is presented in the Supporting Information (S1 and S2 Tables). While crude mortality was significantly lower when patients were secondarily transferred (2% (n = 9) vs 7% (n = 269), p < 0.001), there was no significant association between 30-day mortality and the type of transport (OR 0.80, 95% CI [0.30–1.91]) when adjusted on predefined potential confounders in the multivariate analysis. In total, 3538 (80%) of the 4412 patients from the Traumabase could be matched to the RAAR files. Among the 278 patients who died during the first 30 days in the TC, 251 (90%) could be matched, leaving 696 patients to investigate (Fig 2). The research performed in the medical records of the 8 central dispatch centers of the Île de France region (SAMU) allowed to identify 43 (4.5% of all death) who died in peripheral non-specialized centers. The remaining patients died on-scene (n = 569, 60%) or in TC (n = 40, 4%, missing or unmatched with records from the Traumabase) and 44 (4.5%) could not be found in the SAMUs’ records (illustrated in the Flow Chart Fig 2). Those latter were considered as dead outside the TCs. So, the population based undertriage leading to death was 0.15%, 95% CI [0.12–0.18], and the overtriage was estimated at 60%, 95% CI [59-61]. The comparison of mortality between direct transport and secondary transfer groups could not be performed because no adjustment was possible given the available information in the RAAR and SAMU records. Nevertheless, considering the observed mortality in patients directly admitted to the TCs (7.6%, 95%CI [6.8–8.4]), the range of systemic undertriage calculated was 1.5–2.8%, 95%CI [1.4–2.9].

Discussion

The results of this study suggest that in the most densely populated French region, and within an exclusive trauma system, secondarily transferred patients were not at increased risk of mortality after adjusting for confounding factors. This is consistent with the results of two meta-analyses which recently tried to evaluate the effect of secondary transfer on outcome and found no additional risk on mortality (pooled OR = 1.06, 95% CI [0.90–1.25][13,14].

The trauma system performance

Our results can be partly explained by the structure of the trauma system in France which is entirely covered by a physician-staffed prehospital emergency care. This prehospital management was found associated with a significantly reduced 30-day mortality compared to paramedics in a study gathering 2700 patients with severe blunt trauma [15]. At the level of the TC, the observed rate of secondary transfer (9%) was lower than described in existing studies (ranging between 28% and 37% [32-35]). This can be explained both by a better initial orientation and by the available supply of TCs within the Île de France region. In the study by Garwe et al. (30% of secondary transfer), Oklahoma state was endowed of only one level 1 TC (and two level 2 TCs) for an average of 3.5 million inhabitants over 181.195 km2 [33]. In the Île de France region, one TC covered for an average of 2 million inhabitants over an average of 2.000 km2. This ratio of TC to area cover might have allowed to cope with a higher overtriage (60%) than previously observed, and to maintain a low rate of undertriage. The observed rate of secondary transfer remained higher than the recommended rate of “below 5%” [36]. Nevertheless, the patients that benefit most of early time-critical care, i.e. hemorrhagic shock or severe head trauma, were directly transported in 95% and 99% of cases respectively [37]. Most of the time, those patients are identified and triaged in the prehospital setting, according to the physiologic variables (for hemorrhagic shock) and to the GCS (for severe head trauma), except when their clinical status deteriorates secondarily.

Determinants of secondary transfer

The main challenge in interpreting the determinants of secondary transfer is the discrimination between three types of cases: 1/ cases where initial severity was under-appreciated (undertriage) [33], 2/ cases that benefitted from initial stabilization in non-TC hospitals before transfer [12], and 3/ occasions of system saturation that triggered the initial work up to be completed in a non-TC hospital before confirmation as major trauma case and secondary transfer to a TC. These three situations could not be elucidated with the available data in our study. Despite this fact, the variables found to be associated with secondary transfer and the direction of these associations were in agreement with previously published studies [11,38]. Paradoxically, road users considered as more vulnerable, either by lack of physical protection such as pedestrians or cyclists, or due to age-related frailty, were more likely to be secondarily transferred. The challenge is actually the clinical recognition of traumatic brain injury, especially in elderly patients and/or after low energy transfer mechanisms (pedestrian or bicycle) [32,39]. Indeed, high-force injuries such as high energy transfer motor vehicle accidents are usually the prerogative of younger patients and also result in clinically more obvious injuries easier to triage, as exemplified with facial trauma, clinically obvious pelvic fracture or combined severe injuries which where protective factors of secondary transfer. In our study, secondarily transferred patients presented with higher injury scores (48% ISS ≥ 16 vs 39%) but had a lower non-adjusted mortality. This shows that, while considered as “undertriaged”, these patients were properly cared for by the system, but obviously, their identification has to be improved in the region to streamline the triage process and to reduce the rate of secondary transfer.

Population based analyses

The linkage of administrative databases to medical registries has blossomed in epidemiological studies in the last decade [40]. Trauma registries have historically provided the main source of data [41], targeting the most severely injured patients transported to a TC and focusing on hospital-centered outcomes. Linking to non-research database (e.g. administrative) now allows creating population-based injury databases, spanning all phases of care, gathering data on severe and non-severe patients. This is the first study in France enabling the drawing of the regional triage profile and the estimation of the death rate on scene within the studied trauma system. First, the rate of undertriage leading to death was low (0.15%, 95%CI [0.12–0.19]). Then, if we admit that the systemic undertriage was over 1.5%, the crude mortality in patients admitted to non-TC (secondarily transferred or not) was not significantly different than in directly admitted patients. And if we logically admit that patients would not die more when directly transported, then, the upper limit of our regional undertriage would be 2.8%, 95%CI [2.7–2.9]. Finally, death occurred on-scene in 60% of patients. This observation is in agreement with data from the US [42]. Many of these patients were too critically injured to survive transport to any hospital, but some of these patients may be classified as preventable deaths. Indeed, the median time to death among patients with severe trauma is less than two hours [43]. The mean total pre-hospital time in our study was between 70 and 80 minutes, far longer than recently reported times in the PamPer (40 minutes) [44] or COMBAT trial (16 minutes) [45]. So, a more rapid transport to a TC might have prevented some deaths? To this concern, it is to note that in the physician staffed system in France, patients are carried in the mobile intensive care ambulance after immediate life-saving intervention, and resuscitation is continued on the way, even in futile cases. Thus, the observed 43 deaths in non-TC hospital might be a source of overestimation of the undertriage compared to other countries as the death is never pronounced during the transfer.

Limitations

Our study presents some limitations. First, its retrospective design precluded the measurement and adjustment on confounding factors such as provider experience, quality, timing, or appropriateness of care at the initial facility which were not available in the databases. Second, multiple imputation was used to handle with missing data for most of the variables except for prehospital physiological variables for which data were not missing at random. Nevertheless, as the rate of missing data was low (max: 5.5%) for these variables, the potential resulting bias was likely to be limited. Third, a potential for selection bias (survivor bias) may have been introduced by severely injured patients deceased in local hospitals before transfer to TC. However, efforts have been made to evaluate it using the linkage of Traumabase and RAAR, and return to the archives from the 8 central dispatch centers of the region but adjustment could not be performed on these data as confounding variables were not available. A large observational study in France is about to begin and will allow to have an integrated database across all facilities of the participating regions to answer these points. An Australian study even showed that, in a well-resourced and coordinated trauma network, mortality was lower in non-TC when adjusted for age and injury severity [46]. Fourth, a probabilistic linkage had to be performed between the Traumabase and RAAR as both datasets did not have a unique common identifier and the performances of the matching algorithm we designed could not be evaluated before implementation. However, this method has already been used to match EMS records to hospital outcomes in the US [47,48] and has been validated among injured patients [49]. Fifth, the external validity of this kind of regional study is a complex issue but the present data shed light onto the triage process in an exclusive physican-staffed trauma system. Finally, beyond the part of uncertainty inherent to this type of epidemiological research, we intended to address the known potential pitfalls of such a process [40] and all computations were made to assess the maximum risk (including unidentified patients as dead in non-TC).

Conclusion

Our study suggests that, in the context of exclusive trauma system with physician driven prehospital care, RTA trauma patients secondarily transferred to trauma center do not have an increased mortality when compared to directly transported patients. Patients identified as dead in non-specialized centers before transfer represented 4.5% of all fatalities.

Database linking process.

(DOCX) Click here for additional data file.

Sensitivity analysis: Results of the multivariate analysis to identify variables associated to the secondary transfer with only “complete cases” for prehospital physiologic variables.

Complete cases included 3868 patients in the direct group and 262 in the secondary transfer), SAP remained in the final model but not HR and SpO2. As it can be seen by comparing to Table 4, the values of the OR of all the identified predictors were marginally modified in this sensitivity analyses. Data missing not at random are known to introduce bias, so we chose to withdraw these prehospital variables and we showed that it had no meaningful impact on our results with these sensitivity analyses. (DOCX) Click here for additional data file.

Prehospital demographic, physiologic and injury characteristics of patients according to the 30-day mortality outcome.

BMI: body mass index, ASA: American society of anesthesiologists, AC/AP therapy: anticoagulant and/or antiplatelet therapy, MVA: motor vehicle accident, SAP: systolic arterial blood pressure, HR: Heart rate, SpO2: peripheral oxygen saturation, min: minimal, max: maximal. (DOCX) Click here for additional data file.

Severity, clinical characteristics and hospital course of trauma patients according to the 30-day mortality outcome.

SOFA: sequential organ failure assessment, SAPS II: simplified acute physiologic score, ISS: injury severity score, AIS: abbreviated injury scale, SAP: systolic arterial blood pressure, ICU: intensive care unit, LOS: length of stay. Hemorrhagic shock: receiving ≥ 4 packed red blood cells concentrate within 6 hours. Severe head trauma: Glasgow coma scale ≤ 8 and head AIS > 1. (DOCX) Click here for additional data file. 2 Aug 2019 PONE-D-19-19735 Direct transport vs secondary transfer to level I trauma centers in a French exclusive trauma system: impact on mortality and determinants of triage on road-traffic victims PLOS ONE Dear Dr Hamada, Thank you for submitting your manuscript to PLOS ONE. After careful consideration, we feel that it has merit but does not fully meet PLOS ONE’s publication criteria as it currently stands. Therefore, we invite you to submit a revised version of the manuscript that addresses the points raised during the review process. We would appreciate receiving your revised manuscript by Sep 16 2019 11:59PM. When you are ready to submit your revision, log on to https://www.editorialmanager.com/pone/ and select the 'Submissions Needing Revision' folder to locate your manuscript file. If you would like to make changes to your financial disclosure, please include your updated statement in your cover letter. To enhance the reproducibility of your results, we recommend that if applicable you deposit your laboratory protocols in protocols.io, where a protocol can be assigned its own identifier (DOI) such that it can be cited independently in the future. For instructions see: http://journals.plos.org/plosone/s/submission-guidelines#loc-laboratory-protocols Please include the following items when submitting your revised manuscript: A rebuttal letter that responds to each point raised by the academic editor and reviewer(s). This letter should be uploaded as separate file and labeled 'Response to Reviewers'. 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For information on unacceptable data access restrictions, please see http://journals.plos.org/plosone/s/data-availability#loc-unacceptable-data-access-restrictions. In your revised cover letter, please address the following prompts: a) If there are ethical or legal restrictions on sharing a de-identified data set, please explain them in detail (e.g., data contain potentially identifying or sensitive patient information) and who has imposed them (e.g., an ethics committee). Please also provide contact information for a data access committee, ethics committee, or other institutional body to which data requests may be sent. b) If there are no restrictions, please upload the minimal anonymized data set necessary to replicate your study findings as either Supporting Information files or to a stable, public repository and provide us with the relevant URLs, DOIs, or accession numbers. 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The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Partly Reviewer #2: Yes ********** 2. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: I Don't Know Reviewer #2: Yes ********** 3. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: No Reviewer #2: No ********** 4. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 5. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: needs a good statistician. Not convinced by numbers. otherwise a nice paper (maybe prehospital J might be more interested Reviewer #2: Interesting study from a well developed trauma system in Paris. My only major comment is that I don't get a sense of the total number of non trauma centres in that region, so the comment regarding "exclusive" trauma system is somewhat intriguing. Inclusive or exclusivity really depends on the proportion of major tertiary hospitals that are designated trauma centres (Level 1 or 2), so it may be argued that having 6 TCs in central Paris is really indicative of an inclusive system, depending on the number of similar sized tertiary hospitals within Paris. The only other major issue is survivor bias for patients undergoing secondary transfer and the need to report matched mortality for patients not transferred to the TC. The authors have identified this I think, but some discussion on the need for an integrated database across all facilities, non trauma and trauma centres, is warranted given the volume of trauma being reported. Lastly, I think a recent paper by Cornwall et al Injury 2019 on trauma transfers within a network in Australia outlining similar results would be worthwhile to place these results in context ********** 6. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. 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Submitted filename: PLOS review.docx Click here for additional data file. 28 Aug 2019 All answers are provided in the Response. to reviewers file (10 pages) Submitted filename: Response to Reviewers.docx Click here for additional data file. 30 Sep 2019 Direct transport vs secondary transfer to level I trauma centers in a French exclusive trauma system: impact on mortality and determinants of triage on road-traffic victims PONE-D-19-19735R1 Dear Dr. Hamada, We are pleased to inform you that your manuscript has been judged scientifically suitable for publication and will be formally accepted for publication once it complies with all outstanding technical requirements. Within one week, you will receive an e-mail containing information on the amendments required prior to publication. When all required modifications have been addressed, you will receive a formal acceptance letter and your manuscript will proceed to our production department and be scheduled for publication. Shortly after the formal acceptance letter is sent, an invoice for payment will follow. To ensure an efficient production and billing process, please log into Editorial Manager at https://www.editorialmanager.com/pone/, click the "Update My Information" link at the top of the page, and update your user information. If you have any billing related questions, please contact our Author Billing department directly at authorbilling@plos.org. If your institution or institutions have a press office, please notify them about your upcoming paper to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, you must inform our press team as soon as possible and no later than 48 hours after receiving the formal acceptance. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information, please contact onepress@plos.org. With kind regards, Zsolt J. Balogh, MD, PhD, FRACS Academic Editor PLOS ONE Additional Editor Comments (optional): Reviewers' comments: Reviewer's Responses to Questions Comments to the Author 1. If the authors have adequately addressed your comments raised in a previous round of review and you feel that this manuscript is now acceptable for publication, you may indicate that here to bypass the “Comments to the Author” section, enter your conflict of interest statement in the “Confidential to Editor” section, and submit your "Accept" recommendation. Reviewer #1: (No Response) Reviewer #2: All comments have been addressed ********** 2. Is the manuscript technically sound, and do the data support the conclusions? The manuscript must describe a technically sound piece of scientific research with data that supports the conclusions. Experiments must have been conducted rigorously, with appropriate controls, replication, and sample sizes. The conclusions must be drawn appropriately based on the data presented. Reviewer #1: Yes Reviewer #2: Yes ********** 3. Has the statistical analysis been performed appropriately and rigorously? Reviewer #1: Yes Reviewer #2: Yes ********** 4. Have the authors made all data underlying the findings in their manuscript fully available? The PLOS Data policy requires authors to make all data underlying the findings described in their manuscript fully available without restriction, with rare exception (please refer to the Data Availability Statement in the manuscript PDF file). The data should be provided as part of the manuscript or its supporting information, or deposited to a public repository. For example, in addition to summary statistics, the data points behind means, medians and variance measures should be available. If there are restrictions on publicly sharing data—e.g. participant privacy or use of data from a third party—those must be specified. Reviewer #1: Yes Reviewer #2: Yes ********** 5. Is the manuscript presented in an intelligible fashion and written in standard English? PLOS ONE does not copyedit accepted manuscripts, so the language in submitted articles must be clear, correct, and unambiguous. Any typographical or grammatical errors should be corrected at revision, so please note any specific errors here. Reviewer #1: Yes Reviewer #2: Yes ********** 6. Review Comments to the Author Please use the space provided to explain your answers to the questions above. You may also include additional comments for the author, including concerns about dual publication, research ethics, or publication ethics. (Please upload your review as an attachment if it exceeds 20,000 characters) Reviewer #1: All suggestions have been incorporated or discussed appropriately. The paper is ready for publication Reviewer #2: All my comments have been addressed and clarifying the structure of the trauma system in that region of Paris ********** 7. PLOS authors have the option to publish the peer review history of their article (what does this mean?). If published, this will include your full peer review and any attached files. If you choose “no”, your identity will remain anonymous but your review may still be made public. Do you want your identity to be public for this peer review? For information about this choice, including consent withdrawal, please see our Privacy Policy. Reviewer #1: No Reviewer #2: No 12 Nov 2019 PONE-D-19-19735R1 Direct transport vs secondary transfer to level I trauma centers in a French exclusive trauma system: impact on mortality and determinants of triage on road-traffic victims Dear Dr. Hamada: I am pleased to inform you that your manuscript has been deemed suitable for publication in PLOS ONE. Congratulations! Your manuscript is now with our production department. If your institution or institutions have a press office, please notify them about your upcoming paper at this point, to enable them to help maximize its impact. If they will be preparing press materials for this manuscript, please inform our press team within the next 48 hours. Your manuscript will remain under strict press embargo until 2 pm Eastern Time on the date of publication. For more information please contact onepress@plos.org. For any other questions or concerns, please email plosone@plos.org. Thank you for submitting your work to PLOS ONE. With kind regards, PLOS ONE Editorial Office Staff on behalf of Dr. Zsolt J. Balogh Academic Editor PLOS ONE
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