Abstract

BackgroundMissed injury is commonly used as a quality indicator in trauma care. The trauma tertiary survey (TTS) has been proposed to reduce missed injuries. However a systematic review assessing the effect of the TTS on missed injury rates in trauma patients found only observational studies, only suggesting a possible increase in early detection and reduction in missed injuries, with significant potential biases. Therefore, more robust methods are necessary to test whether implementation of a formal TTS will increase early in-hospital injury detection, decrease delayed diagnosis and decrease missed injuries after hospital discharge.Methods/DesignWe propose a cluster-randomised, controlled trial to evaluate trauma care enhanced with a formalised TTS procedure. Currently, 20 to 25% of trauma patients routinely have a TTS performed. We expect this to increase to at least 75%. The design is for 6,380 multi-trauma patients in approximately 16 hospitals recruited over 24 months. In the first 12 months, patients will be randomised (by hospital) and allocated 1:1 to receive either the intervention (Group 1) or usual care (Group 2). The recruitment for the second 12 months will entail Group 1 hospitals continuing the TTS, and the Group 2 hospitals beginning it to enable estimates of the persistence of the intervention. The intervention is complex: implementation of formal TTS form, small group education, and executive directive to mandate both. Outcome data will be prospectively collected from (electronic) medical records and patient (telephone follow-up) questionnaires. Missed injuries will be adjudicated by a blinded expert panel. The primary outcome is missed injuries after hospital discharge; secondary outcomes are maintenance of the intervention effect, in-hospital missed injuries, tertiary survey performance rate, hospital and ICU bed days, interventions required for missed injuries, advanced diagnostic imaging requirements, readmissions to hospital, days of work and quality of life (EQ-5D-5 L) and mortality.DiscussionThe findings of this study may alter the delivery of international trauma care. If formal TTS is (cost-) effective this intervention should be implemented widely. If not, where already partly implemented, it should be abandoned. Study findings will be disseminated widely to relevant clinicians and health funders.Trial registrationANZCTR: ACTRN12613001218785, prospectively registered, 5 November 2013Electronic supplementary materialThe online version of this article (doi:10.1186/s13063-015-0733-y) contains supplementary material, which is available to authorized users.

Highlights

  • Missed injury is commonly used as a quality indicator in trauma care

  • The findings of this study may alter the delivery of international trauma care

  • Description Before trauma tertiary survey (TTS), or as result of TTS - in-hospital: Injury missed at initial assessment, but detected within 24 hours, before or through formal TTS. After TTS, in-hospital: Injury missed by TTS, detected in hospital after 24 hours. After TTS, after hospital discharge: Injury missed during hospital stay including TTS, the same injury twice due to systematic error or persistent cognitive error

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Summary

Discussion

Outcomes and significance Missed injury in trauma is a common condition in young adults, with potential to lead to prolonged morbidity. The findings of this study may alter the delivery of international trauma care. If formal TTS is (cost-) effective this intervention should be implemented widely, inform guidelines and change practice. If not, where already partly implemented, it should be abandoned. Study findings will be disseminated widely to relevant clinicians and health funders. Trial status Recruitment has not yet begun because we are awaiting funding. Competing interests The authors declare that they have no competing interests. Authors’ contributions GK, CdM and LG conceived and designed the study. CdM and LG contributed to further iterations. JB provided health economic advice and EB provided statistical advice. All authors read and approved the final manuscript

Background
Patients are not required to participate in any way whilst in hospital
Findings
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