Abstract

ContextSurvival rates after severe injury are improving, but complication rates and outcomes are variable.ObjectiveThis cohort study addressed the lack of longitudinal data on the steroid response to major trauma and during recovery.DesignWe undertook a prospective, observational cohort study from time of injury to 6 months postinjury at a major UK trauma centre and a military rehabilitation unit, studying patients within 24 hours of major trauma (estimated New Injury Severity Score (NISS) > 15).Main outcome measuresWe measured adrenal and gonadal steroids in serum and 24-hour urine by mass spectrometry, assessed muscle loss by ultrasound and nitrogen excretion, and recorded clinical outcomes (ventilator days, length of hospital stay, opioid use, incidence of organ dysfunction, and sepsis); results were analyzed by generalized mixed-effect linear models.FindingsWe screened 996 multiple injured adults, approached 106, and recruited 95 eligible patients; 87 survived. We analyzed all male survivors <50 years not treated with steroids (N = 60; median age 27 [interquartile range 24–31] years; median NISS 34 [29–44]). Urinary nitrogen excretion and muscle loss peaked after 1 and 6 weeks, respectively. Serum testosterone, dehydroepiandrosterone, and dehydroepiandrosterone sulfate decreased immediately after trauma and took 2, 4, and more than 6 months, respectively, to recover; opioid treatment delayed dehydroepiandrosterone recovery in a dose-dependent fashion. Androgens and precursors correlated with SOFA score and probability of sepsis.ConclusionThe catabolic response to severe injury was accompanied by acute and sustained androgen suppression. Whether androgen supplementation improves health outcomes after major trauma requires further investigation.

Highlights

  • MethodsStudy design and protocol This prospective cohort study was conducted in the Royal. Military and civilian trauma patients with an estimated New Injury Severity Score (NISS) >15 were recruited [12]

  • O ver 5 million people worldwide die each year from serious injury [1], with almost 25% caused by road traffic collisions (RTC) [2]

  • Improvement in survival is often offset during the weeks following acute major trauma by the systemic inflammatory response syndrome (SIRS), which is associated with increased risks of infection, multiorgan dysfunction or failure (MOD/MOF), and death [7, 8]

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Summary

Methods

Study design and protocol This prospective cohort study was conducted in the Royal. Military and civilian trauma patients with an estimated New Injury Severity Score (NISS) >15 were recruited [12]. Study design and protocol This prospective cohort study was conducted in the Royal The protocol was approved by the NRES Committee South West – Frenchay 11/ SW/0177 and MOD REC 116/Gen/10

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