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1.
J Trauma Acute Care Surg ; 88(1): 180-185, 2020 01.
Article in English | MEDLINE | ID: mdl-31688832

ABSTRACT

BACKGROUND: Intravenous ketamine is commonly used for pain management in the civilian prehospital setting. Several studies have evaluated its effectiveness in the military setting. To date, there has been no report reviewing the published data on the use of ketamine in this context. The objective of this systematic review was to analyze the content and quality of published data on the use of ketamine for prehospital pain management in military trauma. METHODS: The MEDLINE database was searched for studies on ketamine use in combat prehospital settings, at point of injury or during evacuation, published between 2000 and 2019. The systematic review was conducted following PRISMA guidelines, and the protocol was registered on PROSPERO (CRD42019115728). Civilian reports and case series lacking systematic data collection were excluded. RESULTS: Eight studies were included with 2029 casualties receiving ketamine. All but one were American reports from Afghanistan and Iraq conflicts. Studies implied retrospective cohorts or prospective observational analysis. Ketamine use rose from 3.9% during the period preceding its addition to the Tactical Combat Casualty Care guidelines in 2012 to 19.8% thereafter. It was the most common analgesic administered (up to 52% of casualties) in one of the studies. Ketamine was more likely given during tactical medical evacuation when no analgesic was provided at the point of injury. The median total intravenous dose was 50 mg. Pain intensity decreased from moderate or severe to mild or none, sometimes after only one dose. In one study, ketamine administration during tactical evacuation was associated with increased systolic blood pressure as opposed to morphine. Incoherent speech, extremity movements, and hallucinations were the main adverse events reported. CONCLUSION: Published data on ketamine use in military trauma are rare and heterogeneous. Though, all studies tend to strengthen the belief in the efficacy and safety of ketamine when given at 50-mg to 100-mg intravenous for prehospital analgesia in combat casualties. LEVEL OF EVIDENCE: Systematic Review, Level IV.


Subject(s)
Analgesics/administration & dosage , Drug Utilization/statistics & numerical data , Ketamine/administration & dosage , Military Medicine/statistics & numerical data , Pain/drug therapy , War-Related Injuries/complications , Administration, Intravenous , Afghan Campaign 2001- , Analgesics/adverse effects , Blood Pressure/drug effects , Dose-Response Relationship, Drug , Drug Administration Schedule , Drug Utilization/standards , First Aid/methods , First Aid/standards , First Aid/statistics & numerical data , Humans , Iraq War, 2003-2011 , Ketamine/adverse effects , Military Medicine/methods , Military Medicine/standards , Pain/diagnosis , Pain/etiology , Pain Management/methods , Pain Management/standards , Pain Management/statistics & numerical data , Pain Measurement , Practice Guidelines as Topic , War-Related Injuries/drug therapy
2.
J Trauma ; 71(6): 1761-4; discussion 1764-5, 2011 Dec.
Article in English | MEDLINE | ID: mdl-22182886

ABSTRACT

BACKGROUND: Modern warfare causes severe injuries, and despite rapid transportation to theater regional trauma centers, casualties frequently arrive coagulopathic and in shock. Massive hemorrhage management includes transfusion of red blood cells and plasma in a 1:1 ratio. Fresh frozen plasma requires thawing and badly fits the emergency criteria. Since 1994, the French Military Blood Bank has been producing freeze-dried plasma (FDP) and providing it for overseas operation. The aim of our study was to evaluate the use of FDP in war settings and to assess its clinical efficiency and safety. PATIENTS: We performed a prospective study of the FDP delivered at the International Security Assistance Force Role 3 Military Medical Treatment Facility in the Kabul Afghanistan International Airport between February 2010 and February 2011. We included every patient who received at least one unit of FDP. Basic clinical data were recorded at admission. Transfusion requirements were monitored. Biological testing were performed before and after administration of FDP including hemoglobin concentration, platelets count, fibrinogen level, prothrombin time (PT), and thromboelastography. RESULTS: Eighty-seven casualties received FDP during 93 episodes of transfusion. On average, 3.5 FDP units were transfused per episodes of transfusion. Of the 87 patients studied, 7 died because of nonsurvivable injuries and outcomes were unavailable for 11. The other 59 patients survived. PT significantly declined by an average of 3.3 seconds after FDP transfusion. This moderate decrease in PT reflects continued bleeding and resuscitation. It nevertheless suggests improvement in hemostasis before surgical control of bleeding. All FDP users reported ease of use, clinically observed efficacy equivalent to fresh frozen plasma and the absence of adverse effects associated with FDP. CONCLUSION: Our results provide evidence of the effectiveness of FDP for the prevention or correction of coagulopathy and hemorrhage in combat casualties.


Subject(s)
Blood Component Transfusion/methods , Hemostatic Techniques , Intensive Care Units , Shock, Hemorrhagic/therapy , Adult , Afghanistan , Cohort Studies , Critical Care/methods , Female , France , Freeze Drying , Hospitals, Military , Humans , Male , Middle Aged , Prospective Studies , Risk Assessment , Shock, Hemorrhagic/diagnosis , Shock, Hemorrhagic/mortality , Survival Rate , Treatment Outcome , Warfare , Young Adult
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