Hypoxia and hypotension in patients intubated by physician staffed helicopter emergency medical services - a prospective observational multi-centre study
The effective treatment of airway compromise in trauma and non-trauma patients is important. Hypoxia and hypotension are predictors of negative patient outcomes and increased mortality, and may be important quality indicators of care provided by emergency medical services. Excluding cardiac arrests, critical trauma and non-trauma patients remain the two major groups to which helicopter emergency medical services (HEMS) are dispatched. Several studies describe the impact of pre-hospital hypoxia or hypotension on trauma patients, but few studies compare this in trauma and non-trauma patients. The primary aim was to describe the incidence of pre-hospital hypoxia and hypotension in the two groups receiving pre-hospital tracheal intubation (TI) by physician-staffed HEMS.
Methods
Data were collected prospectively over a 12-month period, using a uniform Utstein-style airway template. Twenty-one physician-staffed HEMS in Europe and Australia participated. We compared peripheral oxygen saturation and systolic blood pressure before and after definitive airway management. Data were analysed using Cochran–Mantel–Haenszel methods and mixed-effects models.
Results
Eight hundred forty three trauma patients and 422 non-trauma patients receiving pre-hospital TI were included. Non-trauma patients had significantly lower predicted mean pre-intervention SpO2 compared to trauma patients. Post-intervention and admission SpO2 for the two groups were comparable. However, 3% in both groups were still hypoxic at admission. For hypotension, the differences between the groups were less prominent. However, 9% of trauma and 10% of non-trauma patients were still hypotensive at admission. There was no difference in short-term survival between trauma (97%) and non-trauma patients (95%). Decreased level of consciousness was the most frequent indication for TI, and was associated with increased survival to hospital (cOR 2.8; 95% CI: 1.4–5.4).
Conclusions
Our results showed that non-trauma patients had a higher incidence of hypoxia before TI than trauma patients, but few were hypoxic at admission. The difference for hypotension was less prominent, but one in ten patients were still hypotensive at admission. Further investigations are needed to identify reversible causes that may be corrected to improve haemodynamics in the pre-hospital setting. We found high survival rates to hospital in both groups, suggesting that physician-staffed HEMS provide high-quality emergency airway management in trauma and non-trauma patients.
Trial registration
Clinicaltrials.gov Identifier: NCT01502111. Registered 22 Desember 2011.
Keywords
Physician staffed HEMSAirway managementIntubationAir ambulanceHelicopter emergency medical servicesAdvanced trauma life supportCritical care
Background
Pre-hospital advanced airway management including tracheal intubation (TI) has high priority in the management of critically ill patients [1–3]. Drug-assisted rapid sequence intubation (RSI) is the definitive method of securing the airways of patients who are unable to maintain patent airways or adequate ventilation [2]. However, TI in the pre-hospital setting may be challenging, with sub-optimal working conditions for critical care providers [4]. Several studies report a high incidence of unanticipated difficult airways, first TI attempt failures and complications during pre-hospital advanced airway management, comparable to emergency airway management outside the operating room [5–8]. Critically ill patients may be susceptible to hypoxia and hypotension in conjunction with emergency anaesthesia and airway management [9–11]. The full range of optimal emergency airway management requires an experienced and trained provider to manage it, and hospital-level care to patients in the field is often provided by physician-staffed helicopter emergency medical services (HEMS) [12–14].
Pre-hospital hypoxia and hypotension are predictors of negative patient outcomes and increased in-hospital mortality in non-cardiac arrest patients, and avoidance or mitigation of hypoxia and hypotension may be considered important measures of quality of care provided by the emergency medical services (EMS) [15–17]. Sadly, core data on physiological responses and how they relate to pre-hospital TI are inconsistently reported. Standardised data from pre-hospital airway management could improve our knowledge about the challenges of hypoxia and hypotension in TI [18–20].
The target group of this multi-centre study were non-cardiac arrest patients requiring pre-hospital TI by physician-staffed HEMS. By excluding out-of-hospital cardiac arrests, critical trauma and non-trauma patients are the major groups to which HEMS are dispatched [21]. Several studies describe the impact of pre-hospital hypoxia or hypotension on trauma patients but few studies compare this to the impact hypoxia and hypotension has on non-trauma patients needing pre-hospital TI. This knowledge could be important for how the two groups are handled in pre-hospital care [15, 22]. The primary aim of our study was to describe the incidence of pre-hospital hypoxia and hypotension in the two groups. Secondarily, we wanted to assess whether survival to hospital differed between trauma and non-trauma patients.
Methods
Study design and setting
This prospective multi-centre study collected uniform data on advanced pre-hospital airway management from 21 HEMS in Australia, England, Finland, Hungary, Norway and Switzerland, to analyse differences between trauma and non-trauma patients requiring TI in the field. To include the full range of resuscitative interventions on-scene, only physician-staffed HEMS participated. Necessary ethical and institutional approvals were acquired prior to patient enrolment.
Participants
Trauma and non-trauma patients requiring pre-hospital TI on primary missions were included. Primary out-of-hospital cardiac arrests were excluded. Airway management and RSI protocols were part of local standard operating procedures. Service-specific anaesthetic agents, sedatives, analgesics and neuromuscular blocking agents were used to facilitate TI.
Data collection
Data collections lasted for 1 year for the majority of centres, commencing on the 1st of January 2012 for the majority of centres and concluded on the 15th of March 2013 for the last centre. Two centres, Kent Surrey Sussex HEMS (England) and REGA-Basel (Switzerland), participated for 9 and 6 months, respectively. Prospective airway data were collected according to dataset definitions described in the Utstein style template [23]. Survival data was available only for the pre-hospital phase, as in-hospital follow-up was beyond the scope of this study. Data regarding airway management success rates and complications have previously been published [24].
Variables
Patient demographics were described by category (trauma or non-trauma), age, sex, and indications for TI. Burns and strangulation were classified as trauma in the template, while drownings and asphyxia were classified as non-trauma. We compared lowest oxygen saturation (SpO2) and systolic blood pressure (SBP) before and after completion of TI as described in the airway template. An intubation attempt was defined as attempted laryngoscopy with the intent to intubate. Hypoxia was defined as SpO2 < 90% and hypotension as SBP < 90 mmHg. SPO2 and SBP were measured as first value recorded on scene and first value recorded after finalised airway management. Glasgow Coma Score (GCS) and pre-intervention comorbidity (American Society of Anesthesiologists Physical Status (ASA-PS)) were recorded. The variables are defined in the airway template paper [23].
Statistical analysis
Categorical demographical variables are presented as counts and percentages. The multi-centre nature of the study introduces an internal clustering in the data, and the statistical methods that take this into account have thus been applied [25]. We were mainly interested in the intra-site association between the recorded variables. For binary outcomes we applied Cochran–Mantel–Haenszel methods to estimate conditional odds ratios (cOR) and corresponding 95% confidence intervals (CIs), while for continuous outcomes we used mixed-effects models with random intercepts for sites for single-value outcomes and for sites and patients for longitudinal data. Results from these models are presented as predicted means. The predicted mean is an estimate of the mean for a patient from a ‘typical’ site, i.e. with the random effect(s) set to zero, and can roughly be interpreted as a ‘mean of means’ estimate. Marginal estimates are also presented. The amount of missing data for the main outcomes was generally low, and we have therefore performed complete-case analyses throughout.
We used IBM SPSS Statistics version 21.0 (IBM Corp., Armonk, New York) for storing and preparing the data for statistical analysis and R version 3.2.1 and 3.2.3 (R Foundation for Statistical Computing, Vienna, Austria) for performing the analyses [26]. For fitting the mixed-effects models, we used the R packages ‘nlme’ version 3.1–123 and ‘lme4’ version 1.1–10.
Results
Demographics
Overall, 2327 (16%) of patients attended required advanced airway interventions during the study period. We included 1265 patients receiving pre-hospital TI in the analysis. Of these, 843 were trauma patients and 422 non-trauma patients. Patients handled with bag-valve-mask ventilation (BVM), supraglottic airway devices (SAD) or continous positive airway pressure (CPAP) instead of TI and patients with missing data relative to airway management, short-term survival status or trauma categories were excluded from the analysis (Fig. 1). Patient characteristics, indication for TI and number of attempts are summarised in Table 1. Decreased level of consciousness was the most frequent indication recorded in both trauma (61%) and non-trauma patients (69%). Emergency surgical airway was done in two trauma patients (0.2%), one after failed primary TI and one was a primary surgical airway. The proportion of males did not differ significantly between trauma and non-trauma patients (cOR: 1.27; 95% CI: 0.94–1.73). There was a large difference in predicted mean age between trauma and non-trauma patients (43 and 54 years; CI of difference: 8–14 years). Non-trauma patients had a predicted mean initial GCS of 2.1 points lower (95% CI: 1.6–2.6) than trauma patients (predicted means 5.6 and 7.6, respectively).
Fig. 1
Study population flow chart. Flow chart of study population. One thousand two hundred sixty five non-cardiac arrest patients that received pre-hospital tracheal intubation were included
Table 1
Marginal/crude patient characteristics
Patient category
Trauma
Non-trauma
All patients
P-value
n
%
n
%
n
%
Patients
843
100%
422
100%
1265
100%
Age
< 0.001
0–5 years
19
2%
22
5%
41
3%
6–14 years
36
4%
9
2%
45
4%
15–29 years
227
27%
38
9%
265
21%
30–49 years
276
33%
83
20%
359
29%
50–69 years
185
22%
151
37%
336
27%
> 70 years
83
10%
109
26%
192
16%
Missing data
17
2%
10
2%
27
2%
Sex
< 0.001
Male
622
74%
266
64%
888
70%
Missing data
1
0%
3
1%
4
0%
Comorbidity (ASA-PS)
< 0.001
ASA class 1
500
67%
100
26%
600
53%
ASA class 2
188
25%
146
38%
334
29%
ASA class 3
58
8%
120
31%
178
16%
ASA class 4
4
1%
19
5%
23
2%
ASA class 5
0
0%
4
1%
4
0%
Missing data
90
11%
29
7%
119
9%
Indication for pre-hospital TI
< 0.001
Decreased consciousness
510
61%
277
69%
787
64%
Ineffective ventilation
69
8%
58
14%
127
10%
Combative or uncooperative
93
11%
9
2%
102
8%
Impending airway obstruction
68
8%
12
3%
80
6%
Hypoxia
26
3%
25
6%
51
4%
Relief of pain or distress
44
5%
4
1%
48
4%
Existing airway obstruction
13
2%
12
3%
25
2%
Other
8
1%
6
1%
14
1%
Missing data
12
1%
19
5%
31
2%
Attempts at pre-hospital TI
< 0.001
One attempt
772
92%
360
86%
1132
90%
Multiple attempts
68
8%
60
14%
128
10%
Missing data
3
0%
2
0%
5
0%
Characteristics of patients requiring pre-hospital TI by physician-staffed HEMS, TI Tracheal intubation, HEMS Helicopter emergency medical services, ASA-PS American Society of Anesthesiologists Physical Status. All percentages except for the ‘Missing data’ rows are calculated based on the non-missing data
Oxygen saturation
Non-trauma patients had significantly lower pre-intervention SpO2 (p < 0.001) and post-intervention SpO2 (p = 0.001) than trauma patients, predicted means 89 vs. 94%, and 96 vs. 97%, respectively (Fig. 2). Admissions mean SpO2 was 98% for both groups. In both groups, 3% of patients were still hypoxic at admission (Table 2). Rates of hypoxia and hypotension in patients with decreased level of consciousness are presented in Table 3.
Fig. 2
Patient vitals across airway intervention. Predicted means for patients SBP and SPO2 across airway intervention for trauma and non-trauma patients, based on linear mixed-effects models with time, trauma category and their interaction as fixed effects and random intercepts for patients and HEMS. Vertical lines show 95% pointwise confidence intervals. Non-trauma patients had a significantly lower mean SPO2, and higher mean SBP, before TI compared to trauma patients. Post-intervention and admission values for the two groups showed little difference. SBP: systolic blood pressure. SPO2: oxygen saturation. HEMS: helicopter emergency medical services
Table 2
Hypotension and hypoxia rates before and after airway intervention
Patients
Trauma
Non-trauma
P-valuea
All patients
Missing data
843
100%
442
100%
–
1265
100%
–
–
Hypoxiab
Pre-intervention
126
18%
114
33%
0.01
240
23%
212
17%
Post-intervention
40
5%
31
8%
0.17
71
6%
106
8%
Admission to hospital
23
3%
12
3%
0.30
35
3%
164
13%
Hypotensionc
Pre-intervention
87
12%
56
15%
0.83
143
13%
157
12%
Post-intervention
100
13%
63
16%
0.97
163
14%
77
6%
Admission to hospital
68
9%
37
10%
0.12
105
9%
148
12%
The reported rates are marginal rates
aBased on Cochran–Mantel–Haenszel chi-squared tests
bHypoxia was defined as oxygen saturation (SpO2) < 90%
cHypotension was defined as systolic blood pressure (SBP) < 90 mmHg
Table 3
Hypotension and hypoxia in patients with decreased level of consciousness
Patients
Trauma
Non-trauma
P-valuea
All patients
Missing data
510
100%
277
100%
–
787
100%
–
–
Hypoxiab
Pre-intervention
63
15%
55
23%
0.23
118
18%
118
15%
Post-intervention
17
4%
13
5%
0.37
30
4%
56
7%
Admission to hospital
7
2%
3
1%
0.19
10
1%
83
11%
Hypotensionc
Pre-intervention
48
11%
27
11%
0.63
75
11%
88
11%
Post-intervention
55
11%
28
11%
0.44
83
11%
38
5%
Admission to hospital
34
7%
17
7%
0.20
51
7%
77
10%
The reported rates are marginal rates
aBased on Cochran–Mantel–Haenszel chi-squared tests
bHypoxia was defined as oxygen saturation (SpO2) < 90%
cHypotension was defined as systolic blood pressure (SBP) < 90 mmHg
Systolic blood pressure
There was a significant difference in predicted mean pre-intervention SBP between non-trauma and trauma patients (p = 0.002), but not for SBP at post-intervention or at admission (Fig. 2). For non-trauma patients, there was a significant decrease (p < 0.001) in SBP during the airway intervention from a pre-intervention (predicted mean) SBP of 135 mmHg to post-intervention SBP 120 mmHg, and a subsequent significant increase to hospital admission SBP of 124 mmHg. For trauma patients, there was a significant (p < 0.001) decrease in SBP during the airway interventions from 127 mmHg to 121 mmHg, but post-intervention SBP was equal to the admission SBP of 121 mmHg. Nine percent of trauma patients and 10% of non-trauma patients were still hypotensive at admission (Table 2).
Short-term survival
Overall, 97% of patients survived to hospital admission. There was no difference in short-term survival between trauma patients (97%) and non-trauma patients (95%) (cOR = 0.78; 95% CI: 0.34–1.68; p = 0.56). The large group intubated for decreased level of consciousness showed a more positive association with survival to hospital (cOR = 2.8; 95% CI: 1.4–5.4; p < 0.001) than other indications for TI combined (Table 1). This effect was strong for non-trauma patients (cOR = 10.7; 95% CI: 2.7–42.1; p = 0.001) but not present for trauma patients (cOR = 1.2; 95% CI: 0.49–2.9; p = 0.69).
Discussion
Main findings
Non-trauma patients had a significantly higher incidence of hypoxia before TI than trauma patients. Post-intervention and admission SpO2 for the two groups were comparable, and 3 % in both groups were still hypoxic at admission. For hypotension, the differences between the groups were less prominent, but one in ten trauma and non-trauma patients were still hypotensive at admission. There was no difference in survival to hospital between the groups studied, but patients intubated due to decreased level of consciousness showed a positive association with short-term survival than patients with other indications for TI.
Vital signs and emergency anaesthesia
Vital signs are commonly used for initial assessment and triage of patients, both in the pre-hospital setting and emergency department [27]. Hypoxia and hypotension in the field are predictors of increased in-hospital mortality, but patients’ vital signs across airway interventions are infrequently reported [16, 18, 28]. Physiological variables like SBP and SpO2 may represent indications for TI, but they are also markers of success or complications following airway intervention and the level of critical care provided in the field [23, 29]. As the pathophysiology behind pre-hospital hypoxia and hypotension are diverse, it is important that these vital signs are interpreted along with other clinical variables and the mechanism of injury or illness [27, 30]. Resuscitative interventions are often initiated before the cause of hypotension or hypoxia is clearly identified [31]. The objectives of emergency anaesthesia and TI is to secure oxygenation and ventilation, but also to avoid secondary insults caused by hypoxia and hypotension to vital organs [1]. After initial resuscitation and stabilisation of the patient on-scene, pre-hospital critical care also includes a transition from anaesthesia to mobile critical care during the evacuation and transport of the patient to hospital. Although proper regular monitoring of vital signs is a priority in patients receiving emergency anaesthesia in the field, careful preparation and adequate monitoring to avoid complications can be more difficult in a pre-hospital setting than in a hospital [1, 32].
Hypoxia
One in three non-trauma patients in our study presented with pre-intervention hypoxia, and this was significantly more frequent than for trauma patients. However, in both groups 3 % remained hypoxic at hospital admission after pre-hospital TI. Similar results have been reported from other physician-manned EMS [33, 34]. As desaturation may develop more rapidly in critically ill patients receiving emergency anaesthesia, strategies to improve preoxygenation during RSI in the field, like apnoeic oxygenation, may be important to reduce hypoxia in these patients [9, 22, 35]. We have previously published data showing a non-linear association between the patient’s age and the TI failure risk, with the highest risk for middle-aged patients and significantly lower risk for both younger and older patients [24]. Another study demonstrated significantly higher age among all patients experiencing desaturation during pre-hospital RSI, and also showed that the duration of hypoxia was significantly longer in non-trauma patients compared to trauma patients [22]. Physician-staffed EMS provide TI success rates of close to 100% with very high first pass success rates and robust RSI procedures that are effective in preventing or correcting hypoxia. Highest quality airway management can be provided before arrival in hospital [18, 36, 37].
Hypotension
Hypotension in trauma patients is often due to hypovolemia from blood loss, while non-traumatic hypotension may be due to a variety of causes, including hypovolemic, cardiogenic, septic or neurological factors, and it may be difficult to determine the exact cause of non-traumatic hypotension in the pre-hospital setting [16, 31]. In-hospital mortality rates in non-trauma patients after pre-hospital hypotension have also shown to be high across all age groups [16, 17]. Furthermore, sustained hypotension or shock in trauma and non-trauma patients correlates with higher in-hospital mortality [17, 38]. Although clinical thresholds for hypotension related to patient outcomes, e.g. 90 mmHg for severe traumatic brain injury (TBI), has been suggested, recent studies indicate a possible linear association between pre-hospital SBP and the probability of death, suggesting that using thresholds might not be so meaningful [15, 30, 39]. Nonetheless, a limit of 90 mmHg to indicate hypotension was used in our study, in agreement with clinical guidelines and other systems handling critical ill patients [16, 31, 40]. The reductions in SBP across TI within the groups studied were statistically significant, but these changes may not be clinically significant. They may be the result of the effect of sedatives or anaesthetics perturbing physiology in critical illness or the illness itself, such as hypovolemia. Since it was not possible to standardise the medication or intravenous fluid protocols in the participating international centres, variation in use of these with hypotensive side effects can be possible confounders. The recorded SBP after TI in our study suggests that the HEMS teams have provided good pre-hospital critical care from scene to hospital admission for these patients. Despite this, one in ten patients in both groups were hypotensive at arrival in hospital. This is a relatively high number and should warrant further investigation to identify if there are reversible causes that can be corrected to improve haemodynamics before arrival in hospital.
Decreased level of consciousness
Patients with severe TBI and patients with decreased level of consciousness are at high risk of airway obstruction and hypoxia on-scene due to loss of protective airway reflexes and aspiration of blood and gastric contents [14]. Decreased level of consciousness was the main indication for TI in nearly two thirds of the trauma and non-trauma patients in our study, showing that these patients are an important advanced airway indication group in pre-hospital critical care. Competent airway management is vital in preventing secondary insults and improving outcome in trauma and non-trauma patients with decreased level of consciousness [14, 41]. In our study, the rates of hypoxia and hypotension decreased after TI, and there was little difference between the groups studied from TI to hospital admission.
In trauma patients a GCS score below nine is generally considered as an absolute indication for TI, especially in isolated brain injury [42]. In non-trauma patients however, a GCS score cannot be applied in the same way to support the decision to intubate or not [43]. Decreased level of consciousness must therefore be used in a broader context to support decision-making, e.g. when accompanied by persistent hypoxia despite supplemental oxygen administration [42, 43]. However, some trauma and non-trauma patients with higher GCS scores may benefit from pre-hospital TI to maintain adequate oxygenation and ventilation [44]. A reduction in mortality in patients with GCS below nine receiving pre-hospital physician-led care (instead of paramedic-provided pre-hospital TI) has been shown earlier [45, 46]. A recent review addressing the effect of pre-hospital TI on mortality in patients with severe TBI found a clear trend towards survival when highly trained providers performed TI compared to providers with limited experience [14]. We found that survival to hospital for patients intubated due to decreased level of consciousness was more favourable than for other indications for TI in physician-staffed HEMS. This effect was strong for non-trauma patients, although they presented with lower mean GCS, higher mean age, and had a higher degree of comobidity than trauma patients.
Survival
In trauma, there is still a high number of potentially preventable deaths on-scene [47]. Massive haemorrhage and non-compressible haemorrhage are important causes of preventable pre-hospital trauma deaths [48, 49]. In both trauma and non-trauma patients, there may be patient-related factors (e.g. cardiopulmonary instability or preexisting comorbidities) that may contribute to lower survival [1]. We have previously shown that pre-hospital TI is safe, with few complications, in the hands of HEMS physicians [24]. In the current study, short-term survival to hospital was not significantly different between trauma and non-trauma patients, and the majority of patients requiring pre-hospital emergency anaesthesia and TI by physician-staffed HEMS presented at the hospital alive.
Limitations
Although a randomised controlled trial including a control group would have been the preferable standard, this was not feasable in our pre-hospital study setting. The study was therefore designed from a methodological and practical view as a prospective multicenter observational study. Study inclusion was limited to patients who received TI. Those patients for whom TI was attempted but failed and SAD provided were excluded. The data was re-analyzed with these patients included and the results were the same. The strength of this study is the prospective design and the use of a uniform template for data reporting across international HEMS systems. Standardised variables can enhance the quality of data reported, allowing high-quality research data to be compared across patient populations [50]. We believe our results may be generalised to other physician-staffed HEMS. The main limitation was the lack of in-hospital outcome and survival data, which was beyond the scope of this study. Also, the treating physicians recorded the data themselves, with the risk of registration or recall bias. Using anonymous case report forms in this study may have reduced this effect. Automated data capture was not available in the pre-hospital study setting, and physiological data collected at key intervals according to template definitions may not capture all changes in patient physiology.
Conclusions
Our results showed that non-trauma patients had a higher incidence of hypoxia before TI than trauma patients, but few were hypoxic at admission. The difference for hypotension was less prominent, but one in ten patients were still hypotensive at admission. Further investigations are needed to identify reversible causes that may be corrected to improve haemodynamics in the pre-hospital setting. We found high survival rates to hospital in both groups, suggesting that physician-staffed HEMS provide high-quality emergency airway management in trauma and non-trauma patients.
Abbreviations
ASA-PS:
American Society of Anesthesiologists Physical Status
BVM:
Bag-valve-mask ventilation
CI:
Confidence interval
cOR:
Conditional Odds Ratio
CPAP:
Continous positive airway pressure
EMS:
Emergency medical services
GCS:
Glasgow Coma Score
HEMS:
Helicopter Emergency Medical Services
RSI:
Rapid sequence intubation
SAD:
Supraglottic airway devices
SBP:
Systolic blood pressure
SpO2
:
Oxygen saturation
TBI:
Traumatic brain injury
TI:
Tracheal intubation
Declarations
Acknowledgements
Assistance with the article: We are grateful to our fellow HEMS physicians for their efforts in submitting patient data in this study. Also, we are indebted to research staff Elizabeth Foster (LAA) and Sandra Ware (GSA-HEMS) for making their service data available. A special thanks to Stig Atle Gjøen for developing and maintaining the database at Haukeland University Hospital. Lastly, our sincere thanks to HEMS colleagues who were instrumental in making this study possible in their home services: Falko Harm, Mathias Zuercher, Péter Temesvári, Andreas Jørgensen, Tom Silfvast, Antti Kämäräinen, Bjørn Ole Reid, Ann-Elin Tomlinson and Lars Jacobsen.
Availability of data and material
The datasets generated during and/or analysed during the current study are available from the corresponding author on reasonable request.
Funding
Financial support and sponsorship: A PhD-grant (50%) for GAS was funded by Norwegian Air Ambulance Foundation, Drøbak, Norway. The participating centres, HEMS physicians and study coordinators received no financial support for their participation in this study.
Authors’ contributions
GAS conceived the study, designed the study protocol, was responsible for ethical applications in Norway, developed and supervised the web-based data collection system, contributed to patient recruitment and data collection, and wrote the first draft and the subsequent manuscript. JKH designed the study protocol, contributed to patient recruitment and data collection, wrote the first draft, and helped draft the manuscript. DL was responsible for ethical applications in UK, contributed to patient recruitment, data collection and helped draft the manuscript. BB was responsible for ethical applications in Australia, contributed to patient recruitment, data collection and helped draft the manuscript. MS contributed to patient recruitment, data collection and helped draft the manuscript. KOH performed the statistical analyses, prepared the figures and tables, and helped draft the manuscript. JR helped draft the manuscript, and contributed in the interpretation of the statistical analysis. KF contributed to patient recruitment, data collection and helped draft the manuscript. AS was responsible for ethical applications in Hungary, contributed to patient recruitment, data collection and helped draft the manuscript. RL was responsible for ethical applications in UK, contributed to patient recruitment, data collection and helped draft the manuscript. HJ was responsible for ethical applications in Finland, contributed to patient recruitment, data collection and helped draft the manuscript. SJMS conceived the study, designed the study protocol, and helped draft the manuscript. All authors have read and approved the final version of the manuscript.
Ethics approval and consent to participate
Norway: The Regional Committee for Medical and Health Research Ethics in Western Norway considered the study as a service evaluation study and exempted it from ethical review (Reference number: 2011/1123/REK VEST). Australia: The Royal Prince Alfred Hospital Human Research Ethics Committee approved the study. Hungary: Egészségügyi Tudományos Tanács, Tudományos és Kutatásetikai Bizottság – Scientific and Research Ethics Committee of the Medical Research Council approved the study (Reference number: 98/2012/EKU (3/PI/12.)). Switzerland: Ethikkommission beider Basel approved the study (Reference number: EK: 233/12). England: The Barts Health R&D department (for London’s Air Ambulance), and the UK National Institute for Health Research and local Ethics and Research Committee (for Kent Surrey Sussex HEMS), approved the study as a service evaluation project and exempted it from ethical review. Finland: The Ethics Committee of Kuopio University Hospital, Kuopio, approved the study (Reference number Kupio / Vantaa / Tampere132/2011, and Tampere ETL code R12020). Requirement for written informed consents was waived.
Consent for publication
See above. Consent for publication is not applicable.
Competing interests
The authors declare they have no conflict of interest.
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Authors’ Affiliations
(1)
Norwegian Air Ambulance Foundation
(2)
Department of Anaesthesia and Intensive Care, Haukeland University Hospital
(3)
Department of Health Sciences, University of Stavanger
(4)
Air Ambulance Department, Oslo University Hospital
(5)
Faculty of Medicine, University of Oslo
(6)
University of Surrey
(7)
Kent, Surrey & Sussex Air Ambulance Trust
(8)
UiT - The Arctic University of Norway
(9)
The University Hospital of North Norway
(10)
Sydney HEMS, NSW Ambulance
(11)
Sydney Medical School, University of Sydney
(12)
Centre for Clinical Research, Haukeland University Hospital
(13)
Hungarian Air Ambulance Nonprofit Ltd
(14)
Centre for Pre-hospital Emergency Care, Kuopio University Hospital
(15)
London’s Air Ambulance, Bartshealth NHS Trust
(16)
Department of Medical Sciences, University of Bergen
(17)
Norwegian Air Ambulance Foundation
References
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