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20/04/2013

Hémorragie jonctionnelle: Un nouveau dispositif de compression

La prise en charge des hémorragies jonctionnelles est un des enjeux actuels de la chirurgie de guerre. Réaliser une compression artérielle fémorale peut être obtenu manuellement ou bien à l'aide de dispositifs mécaniques. L'utilisation du Combat Ready Clamp (CRoC) fait partie de la doctrine actuelle du TCCC américain. Un produit similaire est proposé: Le Junctionnal Emergency Treatment Tool (JETT). L'intérêt de ce type de dispositifs ne parait pas devoir être limité au préhospitalier. Ils sont en effet utilisés de manière courante à l'hôpital notamment pour comprimer les régions fémorales lors du retrait des dispositifs artériels fémoraux (femostop). Un troisième dispositif compressif vient compléter l'offre: Le SAM junctionnal tourniquet dont l'usage semble plus simple et qui offre surtout l'avantage de réaliser une stabilisation pelvienne. (voir ici sa validation sur cadavre)

Sam Tourniquet.JPG 

hémorragie,jonctionnel,garrot

hémorragie,jonctionnel,garrot

 

 

Cependant malgré tout leur intérêt potentiel aucun de ces produits n'a été vraiment validé 

23/03/2013

Tourniquet: Quel efficacité et avec quoi ?

Performance improvement in emergency tourniquet use during the Baghdad surge

Kragh JF et all. Am J Emerg Med 2013 Mar 4. pii: S0735-6757(12)00611-0.

 Cette lettre à l"éditeur rapporte l'étude comparée sur 3 périodes des conditions d'emploi et l'efficacité des garrrots pendant les combats s'étant déroulés pour le contrôle de la ville de Baghdad. 1252 garrots ont été posés chez 727 blessés sur 952 membres. L'emploi avant la structure chirurgicale est bien plus fréquente dans la dernière période avec un taux qui passe de 84% à 97% et un taux de survie de 86.6% à 90.8%.


 La réponse initiale à la pose de ce garrot est dans 87% une réduction du saignement. Dans 5% des cas le saignement n'est pas modifié. Il est augmenté dans 0.3%. La réponse au garrot n'est pas documentée dans 8% des cas.  Ce document confirme les précautions à prendre lors du déserrement de garrot rapportant une baisse de la pression artérielle d'au moins 30  mmHg chez 2% des blessés

Tourniquet efficacité 2.jpg

 Par ailleurs l'emploi isolé d'un  garrot ne s'observe que dans 18% des cas. Le plus souvent il est utilisé avec un pansement simple et dans 13% des cas avec un pansementcompressif et 1% un bandage compressif du membre.

Tourniquet efficacité.jpg

En résumé le garrot doit être posé plus tôt et plus souvent permettant d'obtenir une meilleure survie.

Approfondir   1   2   3

Fiche mémento

| Tags : tourniquet

04/02/2013

Le CROC: Une validation expérimentale

Assessment of users to  control simulated junctional hemorrhage with the combat ready clamp (CRoC™).

Mann-Salinas EA et all.  Int J Burn Trauma 2013;3(1):49-54

CROC.jpeg

The Combat Ready Clamp (CRoC™) was designed to control hemorrhage from the groin region, on the battlefield. The purpose of this experiment was to determine whether CRoC™ user performance varied by the surface the casualty laid on (flat-hard, flat-soft, and curved-soft) and how quickly the device could be applied. The commercial manikin selected to assess user performance was designed to train soldiers in CRoC™ use. The manikin simulated severe hemorrhage from an inguinal wound, controllable by correct use of the CRoC™. Each individual (n = 6) performed 3 iterations on each of the 3 surfaces (54 iterations total). The CRoC™ achieved hemorrhage control 100% of the time (54/54). Patient surface affected time to stop bleeding. The flat-soft surface (padded, 55 ± 9.7 seconds) was significantly different from the curved-soft surface (litter, 65 ± 16.5 seconds) and had the lowest overall total time (p = 0.007); time for the hard-flat surface was 58 ± 9.5 seconds. Users were trained to use the Combat Ready Clamp effectively, and the surface the casualty was lying on made some difference to user performance. All six persons trained had success in all nine of their iterations of CRoC™ use– a 100% rate. These findings indicate that training was effective and that training of other users is plausible, feasible, and practical within the scope of the present evidence.

 

19/01/2013

Hémorragies jonctionnelles: De quoi dispose-t-on en préhospitalier ?

La prise en charge d'hémorragies jonctionnelles est une véritable gageure en préhospitalier. Si ces hémorragies ne sont pas garrotables encore peut-on espérer d'en réduire le débit par la compression directe en ayant recours à l'association de packing de plaies, pansement hémostatiques et pansements compressifs. Depuis peu certains dispositifs mécaniques sont proposés bien que n'ayant pas fait l'objet de validation réelle. Une simple image vaut plus que de long commentaires, alors imprégnez vous de celles-ci.

1. Réaliser un pansement compressif:

PST Périné.jpg

Souvenez vous que vous devez disposer de pansement et que vous devez être en capacités de réaliser un pansement de ce type sur une racine de membres. Il doit être associer rembourage de toute cavité avec ce que vous avez sous la main, idéalement pansement hémostatique au contact de ce qui saigne et COMPRESSION forte.

2. Comprimer l'aorte abdominale:

Le garrot abdominal  (The Abdominal Aortic Tourniquet)

The-Abdominal-Aortic-Tourniquet.jpg

Ce dispositif existe depuis plusieurs années. Il a une assisse expérimentale mais n'est pas diffusé. On pourrait l'assimiler grossièrement au compartiment abdominal du pantalon antichoc

3. Comprimer l'artère fémorale au pli inguinal

Le CROC: (Combat Ready Clamp)

CROC.jpg

Ce dispsositif a été validé par l'armée US qui vient de l'intégrer au TCCC.

Le JETT (Junctional Emergency Treatment Tool)

JETT.JPG

Ce dispositif vient d'être présenté et semble être efficace

Lire aussi ce document

4. Réaliser l'équivalent d'un packing de plaie

Le Tournicath

Le principe est d'insérer un ballon que l'on gonfle dans la cavité. Ceci est faisable avec une sonde de foley, mais dans ce cas le ballon est de bien plus grand volume.

1264005969_extras_ladillos_1_0.jpg

wound_x600_8rkTV_54.jpg

5. Comprimer directement la zone hémorragique par un clamp

L'IT Clamp

clamp1-350x265.jpg

 

01/12/2012

Apport du fibrinogène: A la folie ou pas du tout ??

Une econférence qui fait parfaitement le point sur l'intérêt et les questions en suspens concernant l'intérêt du fibrinogène dans la réanimation hémostatique du traumasié qui saigne.

Fibrinogène.JPG

En condition de combat avant l'arivée en structure hopsitalière de campagne, l'apport de fibrinogène peut être réalisé par l'apport de plasma lyophylisé (PLYO) produit par le SSA (obtenu en moins de 6 min après reconstitution à température ambiante par adjonction d'eau PPI, chaque unité contient au moins 0,5g de fibrinogène). C'est une des composantes de la transfusion de plasma thérapeutique. qui doit désormais être envisagé au niveau du role 1 (poste de secours ou vecteur d'évacuation tactique).

Le recours au fibrinogène (Clottafact), qui apparaît être d'un intérêt majeur compte tenu d'un apport insuffisant par la transfusion de plasma. (Abstract Rourke et all.)

coagulopathie

Il ne peut (pour des raisons de logistique de production et de disponibilté) être apporté qu'à partir de la prise en charge hospitalière.

Pour approfondir avec en perspective le blessé de guerre hémorragique:

(1) Un revue générale sur la coagulopathie de l'hémorragie massive: "Hemodilution caused by trauma and major surgery induces complex hemostatic changes involving procoagulant factors as well as anticoagulant, fibrinolytic, and antifibrinolytic factors. The endothelial responses to shear stress, active proteases, and various inflammatory cells and cytokines add further complexity to the pathophysiology of massive hemodilution. In addition to the conventional transfusion products, which are often difficult to administer in a timely manner, purified factor concentrates of plasma origin and from recombinant synthesis are highly concentrated (i.e., small volume) for a rapid restoration of targeted factor(s). The use of point-of-care testing is desirable to optimize the dose and timing of such intervention. Additional clinical trials of different factor concentrate therapies are required to validate their efficacy and safety in patients after trauma or major surgery.152 Further understanding of the time course of pathophysiological changes in massive hemodilution is necessary to optimally balance hemostatic and anticoagulant therapies."

(2) Un focus sur le blessé de guerre: "In patients with combatrelated trauma requiring massive transfusion, the transfusion of an increased fibrinogen: RBC ratio was independently associated with improved survival to hospital discharge, primarily by decreasing death from hemorrhage. Prospective studies are needed to evaluate the best source of fibrinogen and the optimal empiric ratio of fibrinogen to RBCs in patients requiring massive transfusion."

(3) La stratégie transfusionnelle du blessé de guerre SFAR 2012: " En traumatologie, l’administration de fibrinogène est recommandée : dose initiale de 3 à 4 g suivie d’une administration régulière en cas d’hypofibrinogènémie biologique (<1,5 à 2 g/l) ou de signes thromboelastométriques de déficit fonctionnel en fibrinogène [8]. Une analyse nord-américaine rétrospective de 252 dossiers de BdG ayant nécessité une TM a permis de mettre en évidence qu’un apport faible de fibrinogène (< 0,2 g/CGR) au cours de la transfusion était associé à une majoration significative de la mortalité de ces blessés [39]. Le SSA américain utilise l’apport de cryoprécipités contenant surtout du fibrinogène et d’autres facteurs de coagulation pour compenser ces déficits [37]. Les recommandations du SSA français sont l’administration de fibrinogène de façon répétée afin de maintenir un fibrinogène plasmatique supérieur à 1,5 g/l ou en l’absence de laboratoire (situation des structures chirurgicales « légères »), d’administrer au moins 0,2 g de fibrinogène par CGR transfusé."

| Tags : coagulopathie

23/09/2012

Facteur VIIa: Intérêt pas prouvé !

Use of recombinant factor VIIA for control of combat-related haemorrhage.

Woodruff SI et all. Emerg Med J 2010;27:2 121-124

Ce travail  met en exergue que le recours au FVIIa n'a pas d'intérêt prouvé en cas de prise en charge de traumatismes pénétrants. Ceci est d'autant plus vrai qu'il est fait alors qu'une coagulopathie sévère est installée (The utility of recombinant factor VIIa as a last resort in trauma. Mamtani R. et all. World Journal of Emergency Surgery 2012, 7(Suppl 1):S7)

----------------------------------------------

Background 

Recombinant activated human coagulation factor VII (rFVIIa), an intravascular strategy to promote clotting, is being used as an adjunct to surgical control of bleeding in combat trauma patients.

Objective 

To describe the initial experiences with rFVIIa administered to combat casualties at US Navy-Marine Corps medical treatment facilities in Iraq, and to comparesurvival outcomes of those treated with rFVIIa to controls not receiving rFVIIa.

Methods

Medical encounter data from the US Navy-Marine Corps Combat Trauma Registry were retrospectively reviewed to identify all battle-injured patients documented as having received rFVIIa during the period May 2004 to January 2006 of Operation Iraqi Freedom. Available clinical and injury related data are presented to characterise the patients. To assess effects of rFVIIa on survival outcomes, rFVIIa cases were matched to controls on injury severity and age.

Results 

22 battle-injured patients from the Combat Trauma Registry received rFVIIa. Primarily young US Marines, these patients typically had penetrating injuries from improvised explosive devices and gunshot wounds. Injuries were often abdominal. The average dose used was similar to that reported in another study of civilian trauma patients, although dosing varies widely in the existing experimental and anecdotal literature. Over two-thirds (68%) of the rFVIIa patients surviveddan identical outcome seen for a matched control group of 22 patients.

Conclusions 

Survival of seriously injured combat casualties was good, although identical to that of a control group. Methodological limitations of this retrospective study preclude making firm conclusions about the effectiveness of rFVIIa. Future controlled studies are needed for safety and efficacy testing of rFVIIa in combat trauma patients.

----------------------------------------------

 

22/04/2012

Use of tourniquets and their effects on limb function in the modern combat environment

Use of tourniquets and their effects on limb function in the modern combat environment 

Kragh JF  Foot Ankle Clin N Am 15 (2010) 23–40


Un article à lire avec attention car il exprime bien à la fois l'histoire des garrots et les enjeux actuels

| Tags : tourniquet

10/03/2012

Garrot abdominal ?

L'arrêt des hémorragies lors de la prise en charge préhospitalière d'un traumatisme jonctionnel est particulièrement difficile. Nos amis anglais proposent une stratégie de prise en charge. Pendant la guerre du viet-nam les américains avaient recours au pantalon anti-choc dont il existe de nombreuses variantes (1) et dont l'utilité est très discutée en traumatologie civile (2). La mortalité des blessés notamment abdominaux antérieur serait accrue par le recours au PAC (3). Une autre critique est la complexité de sa mise en oeuvre. 

Récemment un dispositif appelé CROC a été présenté. Il permet de réaliser un point de compression en région ilio-inguinale. Bien qu'aucune étude n'ait été publiée, le Comité du TCCC a validé son emploi au combat.

Un autre dispositif de compression abdominale cette fois est présenté. Le tourniquet abdominal aortique (The Abdominal Aortic Tourniquet - AAT™) a pour objectif de réduire le saignement par une compression des structures vasculaires intra-abdominales.

AAT.JPG 

Il existe une documentation expérimentale pour son emploi dont le principe se rapproche du pantalon anti-choc mais dont la simplicité d'emploi semble être sans commune mesure autorisant son emploi en environnement exigu notamment en hélicoptère (?). A suivre

 

23/02/2012

Tourniquet: Le point vu du côté US

The Military Emergency Tourniquet Program's Lessons Learned With Devices and Designs

Kragh et all. MILITARY MEDICINE, 176, 10:1144, 2011

Un travail très intéressant qui porte sur l'analyse de 159 garrots après leur emploi. Les trois plus fréquemment rencontrés sont le CAT, le Delfi EMT et le SOFT-T. 119 était encore utilisables. 28 étaient inefficaces, 52 efficaces et pour le reste étaient non analysable.Le plus efficace est le Delfi EMT suivi par le CAT et le SOFT-T. Il n'a pas été identifié de pose de tourniquet à une main. L'efficacité globale du garrot est en partie rapporté à sa largeur. Une explication retneue d'inefficacité est une tension insuffisante du tourniquet avant la torsion. Des bris de barre de torsion du CAT sont observées. D'autres garrots que l'EMT, le CAT et le SOFT-T sont rencontrés: Le Tourniquet RATCHET LBT et les garrots improvisés dont un exemple est présenté ci-après.

Garrot improvisé.JPG

| Tags : tourniquet, garrot

13/12/2011

25 recommandations UK pour les traumas jonctionnels

http://www.medicalsca.com/files/emf_parker_junctional_tra...

Une affaire d'équipe pour une prise en charge "aggressive" qu'il faut avoir réfléchi AVANT

12/11/2011

Cause de décès en afghanistan: Actualités canadiennes

Causes of Death in Canadian Forces Members Deployed to Afghanistan and Implications on Tactical Combat Casualty Care Provision

Pannell D et all. J Trauma. 2011;71: S401–S407

DeathCan.JPG

Ce document identifie par ailleurs l'importance de la formation des personels à la gestion des voies aériennes, des mesures de stabilisation du rachis en cas d'IED, du recours aux sondes de foley pour le tamponenment des hémorragies jonctionnelles en cas de non application possible de pansement hémostatique.

-------Morceaux choisis:

We recommend that combat medical technicians should continue to practice surgical airways in live-tissue laboratories. In addition, didactic teaching should continue to review the indications for cricothyrotomy on the battlefield. .........

...... Based on this review, we also feel that future Canadian TCCC courses may be improved by giving battlefield providers a treatment option for dealing with exsanguination from small wounds at junctional areas (groin, axillary, and neck). Currently, TCCC providers only have hemostatic dressings to deal with this difficult problem. However, unfavorable wound geometry can make utilization of these products unfeasible. In addition, TCCC providers have no option for treating carotid artery hemorrhage in the neck. We suggest that combat medical technicians also carry urinary catheters; these can be inserted into wound tracts of small wounds. Insufflation of the balloon may provide temporary hemostasis of junctional bleeding and buy enough time for evacuation to a definitive surgical facility. Another option would be to pack such wounds with ribbon gauze. These options may also be used for posterior packing of lifethreatening epistaxis associated with facial fractures.
On our review, we also noted that three casualties.....

....we recommend that spinal immobilization be considered for all casualties suffering from blunt trauma or IED-related incidents during “Tactical Field Care,” if the tactical situation permits, and if the medical technician deems the situation to be safe enough to proceed with this procedure.

 

02/09/2011

La sonde de foley: Pour l'hémostase

Une sonde de foley est utile non pour réaliser un sondage urinaire sur le terrain mais comme moyen d'hémostase.

 L'emploi de sonde à ballonet pour rélaiser un tamponnement de lésions hémorragiques est une réalité.

 

Ces techniques peuvent trouver un champ d'application au combat notamment pour la prise en charge des traummatisés jonctionnels.

 

Premier exemple: Un saignement d'origine thoracique.

 

Ffoley Thorax.JPG

Balloon Foley catheter compression as a treatment for intercostal vessel bleeding. Chao BF et all Injury, Int. J. Care Injured 42 (2011) 958–959

Autres exemples:

Les plaies sous-clavières

Foley Sous Clav.JPG

 

 

Les plaies cervicales,

neckfoley.jpg

les plaies inguinales,

les épistaxis

| Tags : foley

30/08/2011

Exacyl: Bon aussi pour le blessé de guerre !

Une étude à paraître conduite par une équipe US a mis en évidence l'intérêt de l'acide tranexaminique.

----------------

Tranexamic acid decreases mortality following wartime injury: the Military Application of Tranexamic acid in Trauma Emergency Resuscitation Study (MATTERS) MAJ Jonathan J. Morrison, MB ChB, MRCS, RAMC(V), LT COL (sel) Joseph J. Dubose, MD, USAF MC, COL Todd E. Rasmussen, MD, USAF MC, SURG CAPT Mark Midwinter, BMedSci, MD FRCS RN

http://archsurg.ama-assn.org/cgi/content/short/archsurg.2...

A recent registry-based study of combat injured troops receiving blood in Afghanistan (January 2009 - December 2010) at the Bastion Role 3 facility has demonstrated findings supportive of TXA use in this population. In a review of 896 combat casualties treated at Bastion over this time frame, 32.7% (N=293) received TXA (mean ± SD dose: 2.3 ± 1.3g) while 67.2% (N=603) did not receive TXA. In the overall cohort, the TXA group was more severely injured (ISS: 25.2±16.6 vs. 22.5±18.5; p<0.001), required more blood (11.8±12.1 vs. 9.8±13.1 pRBC units; p<0.001), and had a lower Glasgow Coma Score (7.3±5.5 vs. 10.5±5.5; p<0.001) and initial systolic blood pressure (112±29.1 vs. 122.5±30.3 mmHg), but also had a lower unadjusted mortality than the no-TXA group (17.4% vs. 23.9%; p=0.028). In the massive transfusion cohort (N=321; 24 hour transfusion: 21.9±14.7 pRBC; 19.1±13.3 FFP and 3.5±3.2 apheresis platelet units), mortality was also lower in the TXA (mean ± SD dose: 2.4 ± 1.4g) compared to the no-TXA group (14.4% vs. 28.1%; p=0.004). In a multivariate regression model, TXA use in the massive transfusion cohort was independently associated with survival (odds ratio: 7.28; 95% confidence interval: 3.02-17.32. For all patients requiring at least one unit of blood after combat injury, patients receiving TXA had higher rates of DVT (2.4% vs. 0.2%, p = 0.001) and PE (2.7% vs. 0.3%, p =0.001), but were also more likely to have injury patterns associated with higher risk of thromboembolic events ; including higher mean ISS (25 vs 23, p < 0.001), more severe extremity injuries (extremity AIS >=3 66.6% in TXA group, 47.3% non-TXA, p < 0.001), and more commonly GCS < or = 8 (63.3% vs. 35.6%, p < 0.001). These survival benefit findings associated with TXA use support the hypothesis that the use of this adjunct, in conjunction with component-based resuscitation following combat injury, is associated with improved survival. This association is most prominent in those requiring massive transfusion.

 

e.jpg

L'article complet

 

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Exacyl 1g IV  au mieux dans l'heure et pas après 3 heures après la blessure

 

 

Les hémorragies jonctionnelles: Un nouvel outil, le CROC !

L'hémorragie jonctionnelle n'est pas garrotable, n'est pas forcément aisément comprimable directement. Parmi les solutions outre l'exacyl dans l'heure on peut avancer la compression des jonctions.

CROC.jpeg

 

Une recommandation d'emploi du CRoC ( combat ready clamp ) est hautement probable dans la prochaien version du TCCC. Lire ce document:  Hémorragies jonctionnelles.pdf . Regarder une vidéo d'entraînement.

 

l'alternative le femostop ?

26/07/2011

Un garrot: Oui mais surtout un garrot pneumatique

Un travail d'une portée majeure qui met en évidence l'importance de disposer de garrot pneumatique delfi dès que possible.

Les garrots du type du SOFTT ou du CAT doivent être posé à l'avant mais surtout doivent être doublé, associé à un pansement compressif et surtout  remplacé le plus tôt possible par un garrot pneumatique du type du garrot DELFI EMT.

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An Evaluation of Two Tourniquet Systems for the Control of Prehospital Lower Limb Hemorrhage.

Taylor DM et all. (J Trauma. 2011;XX: 000–000) DOI: 10.1097/TA.0b013e31820e0e41

Garrot.JPG

 

Background:

Hemorrhage remains the main cause of preventable death on the modern battlefield. As Improvised Explosive Devices in Afghanistan become increasingly powerful, more proximal limb injuries occur. Significant concerns now exist about the ability of the windlass tourniquet to control distal hemorrhage after mid-thigh application. To evaluate the efficacy of the Combat Application Tourniquet (CAT) windlass tourniquet in comparison to the newer Emergency and Military Tourniquet (EMT) pneumatic tourniquet.

Methods:

Serving soldiers were recruited from a military orthopedic outpatient clinic. Participants’ demographics, blood pressure, and body mass index were recorded. Doppler ultrasound was used to identify the popliteal pulses bilaterally. The CAT was randomly self-applied by the participant at midthigh level, and the presence or absence of the popliteal pulse on Doppler was recorded. The process was repeated on the contralateral leg with the CAT now applied by a trained researcher. Finally, the EMT tourniquet was applied to the first leg and popliteal pulse change Doppler recorded again.


Results:

A total of 25 patients were recruited with 1 participant excluded. The self-applied CAT occluded popliteal flow in only four subjects (16.6%). The CAT applied by a researcher occluded popliteal flow in two subjects (8.3%). The EMT prevented all popliteal flow in 18 subjects (75%). This was a statistically significant difference at p  0.001 for CAT versus EMT.


Conclusion:

This study demonstrates that the CAT tourniquet is ineffective in controlling arterial blood flow when applied at mid-thigh level. The EMT was successful in a significantly larger number of participants.

 

29/03/2011

Exacyl: OUI mais dans l'heure qui suit le trauma

L'exacyl est recommandé pour la prise en charge du traumatisé. L'étude Crash 2 l'a montré. Un complément d'analyse de cette étude précise cependant qu'il faut l'administer dans l'heure suivant le traumatisme.

---------------------------------------------------------------

The importance of early treatment with tranexamic acid in bleeding trauma patients: an exploratory analysis of the CRASH-2 randomised controlled trial

Findings

10 096 patients were allocated to tranexamic acid and 10 115 to placebo, of whom 10 060 and 10 067, respectively, were analysed. 1063 deaths (35%) were due to bleeding. We recorded strong evidence that the effect of tranexamic acid on death due to bleeding varied according to the time from injury to treatment (test for interaction p<0·0001). Early treatment (≤1 h from injury) significantly reduced the risk of death due to bleeding (198/3747 [5·3%] events in tranexamic acid group vs 286/3704 [7·7%] in placebo group; relative risk [RR] 0·68, 95% CI 0·57—0·82; p<0·0001). Treatment given between 1 and 3 h also reduced the risk of death due to bleeding (147/3037 [4·8%] vs 184/2996 [6·1%]; RR 0·79, 0·64—0·97; p=0·03). Treatment given after 3 h seemed to increase the risk of death due to bleeding (144/3272 [4·4%] vs103/3362 [3·1%]; RR 1·44, 1·12—1·84; p=0·004). We recorded no evidence that the effect of tranexamic acid on death due to bleeding varied by systolic blood pressure, Glasgow coma score, or type of injury.

Interpretation

Tranexamic acid should be given as early as possible to bleeding trauma patients. For trauma patients admitted late after injury, tranexamic acid is less effective and could be harmful.

Lire l'article

11/12/2010

Réduire l'hémorragie: IL FAUT ADMINISTRER DE L'EXACYL

Le consensus européen sur la prise en charge des hémorragies de cause traumatique évoque le recours à l'acide tranexaminique. L'exacyl a largement démontré son efficacité comme moyen pharmacologique d’épargne sanguine péri-opératoire. Son intérêt en traumatologie n'était pas jusqu'à présent bien documenté. L'étude Crash 2 publiée dans le lancet apporte un éclairage nouveau. 

Effects of tranexamic acid on death, vascular occlusive events, and blood transfusion in trauma patients with signifi cant haemorrhage (CRASH-2): a randomised, placebo-controlled trial

June 15, 2010 DOI:10.1016/S0140-6736(10)60835-5

10 096 patients were allocated to tranexamic acid and 10 115 to placebo, of whom 10 060 and 10 067, respectively, were analysed. All-cause mortality was significantly reduced with tranexamic acid (1463 [14·5%] tranexamic acid group vs 1613 [16·0%] placebo group; relative risk 0·91, 95% CI 0·85–0·97; p=0·0035). The risk of death due to bleeding was  significantly reduced (489 [4·9%] vs 574 [5·7%]; relative risk 0·85, 95% CI 0·76–0·96; p=0·0077). 

Il n'existe pas de protocole d'emploi bien formalisé. Dans l'étude crash 2, une dose de charge de 1 g est administrée en 10 minutes, suivie d'un entretien de 1 g perfusé en 08 h. De faibles posologies seraient efficaces. Certains proposent le régime suivant: bolus IV de 10 mg.kg-1 suivi d’une perfusion continue de 1 mg.kg-1 .h-1. Ce médicament est disponible en dotation. 

Pour en savoir plus  1  et  2  et  3 

22/11/2010

Quikclot Combat Gauze: Application

 

Cette version du quikclot est maintenant en dotation. Le manuel d'emploi est ici

| Tags : pansement

Tourniquet improvisé: Pas avec n'importe quoi !

Tourniquets improvisés: Avec les bons moyens

TQ_Post Accident_2

 
Points essentiels:

    1. Il vaut mieux avoir recours à des garrots prévus pour arrêter les hémorragies artérielles
    2. Les garrots doivent être portés sur soi et pas dans le sac
    3. Apprener les principes, et vous pourrez alors avoir recours à un garrot improvisé

Dans ce cas, il s'agit d'un accident sur un pas de tir

    Dans ce cas, il s'agit d'un accident sur un pas de tir

    1. La ceinture n'est pas une bonne idée
    2. Le garrot posé à la RACINE DU MEMBRE est ce qu'il faut faire, dans la mesure où il est correcement serré. L'hémorrgaie est arrêtée ET les pouls distaux ne sont plus perçus. Sinon il faut poser un second garrot.
    3. Vous pouvez utiliser comme garrot de fortune un bandage triangulaire, votre pansement israélien, toute bande compressive dont vous seriez porteur.
    4. Il est habituel de devoir associer rembourrage de plaie, pansement hémostatique, pansement compressif et garrot.

Vous devez avoir tout cela dans votre équipement

 

21/11/2010

Pansements hémostatiques: Une vision US

Prehospital topical hemostatic agents – A review of the current literature

PHTLS Executive Council

Lance E. Stuke, M.D. MPH

Background: The 6th edition of the PHTLS textbook discusses three topical hemostatic agents which were approved by the U.S. Food and Drug Administration and available for prehospital use at the time: HemCon dressing, QuikClot, and TraumaDex. Data on these products was based primarily on anecdotal military reports and very little data was available on their use in the civilian prehospital setting. Several new products have arrived on the market after the release of the 6th edition of PHTLS and several important new studies have been published which will be reviewed here. The vast majority of these products have been researched and developed for use in the military setting in Iraq and Afghanistan although some limited civilian data is also available.

The perfect hemostatic dressing does not exist. Ideally, the dressing should be lightweight, easy to store, and able to be rapidly applied to a hemorrhaging wound. It should be conformable to the wound, allowing the hemostatic agent to reach areas of injury which are difficult to access with direct pressure (i.e. deep groin wounds). The dressing should cause minimal local tissue destruction, be easily removable from the wound, and not contain particles which can spread systemically. Finally, the dressing must not be washed away by rapid bleeding from high-flow blood vessels.

Manufacturers have tried various methods to deliver hemostatic agents into bleeding wounds. Some products are packaged into a granular form which can be poured directly into the wound. Others are incorporated into a dressing or mesh which allows the provider to apply direct pressure to the site of injury. This dressing can be formed either as a rigid bandage, a small bag, or a gauze which must be unrolled prior to application. Each method of preparation has distinct advantages and disadvantages depending on the location and type of injury being treated.

Literature and Product Review:

HemCon: HemCon dressing (Hemorrhage Control Technologies, Portland, OR), is composed of chitosan, a substance derived from arthropod skeletons. Chitosan dressings are thought to function by mechanically sealing the wound and adhering to surrounding tissue. HemCon is a dual-sided 4 x 4 inch rectangular bandage: a chitosan-containing active side which must be placed directly on the wound and a nonstick side which the provider uses to apply pressure. The efficacy of HemCon depends entirely on the bandage adhering well to the wound, which is difficult in wounds which aren’t flat and easily accessible. The bandage isn’t flexible and can break when forced into a wound. It is best applied to flat, superficial wounds which are easily accessible. HemCon has been studied in both the military and civilian settings. The military demonstrated a 97% success rate in controlling bleeding with HemCon.1,2 The civilian experience has been less optimistic, controlling bleeding in 27 of 34 cases studied (79%). Of the seven failures, six were felt to be due to user error, possibly due to less training by civilian EMS providers in the proper use of the product.3 An additional study using a complex groin injury model in swine noted an increase in the rate of rebleeding and mortality between those treated with HemCon versus QuikClot. The authors noted that application of HemCon was more difficult than other agents and all failures of HemCon were due to the bandage not adhering to the injured tissue to which it was applied.4

As previously noted, a disadvantage of the HemCon dressing is that it is relatively non-conformable and difficult to pack into deeper wounds. ChitoFlex is the latest development from HemCon Medical Technologies. It utilizes the same chitosan-based hemostatic agent but packages it into a gauze form. This allows the dressing to be packed into deep bleeding wounds for improved access to the site of hemorrhage. ChitoFlex is available in several sizes, including 1”x3”, 3”x9”, and as a 3”x28” roll. In one study, ChitoFlex was found to be equivalent, but not superior to QuikClot and Celox (a chitosan granule).5

WoundStat: WoundStat was an FDA-approved mineral-based agent consisting of granular smectite, a nonmetallic clay. When the granules were exposed to blood they absorbed water, swelled, and formed a clay paste with strong adhesiveness to the surrounding tissue. Initial studies were promising6,7,8 and it was used by the U.S. Army for a short time. However, later data demonstrated that the granules could cause injury to the blood vessels and make repair difficult. The granules were also shown to enter the circulatory system and cause thrombosis in distal organs.9 Because of these potentially serious side effects, the U.S. Army announced in April 2009 that WoundStat would no longer be used by their medical personnel.

QuikClot: QuikClot (Z-Medica, Wallingford, CT) is a granular product consisting of kaolin, which is a combination of inert minerals such as silicon, aluminum, magnesium, and sodium found in volcanic rock. When placed in a bleeding wound, it absorbs water thereby increasing the local concentration of clotting factors, platelets, and red blood cells to stimulate clot formation. A byproduct of its mechanism is a severe exothermic reaction, with heat generation of up to 70̊ C (158o F). This heat generation causes local tissue destruction and even burns. QuikClot has been studied in both the military and civilian sector, with up to 92% effectiveness in stopping hemorrhage.10 QuikClot was issued to U.S. soldiers in the Iraq and Afghanistan conflicts. Civilian use has been by a wide range of providers, including EMT/firefighters, paramedics, and police. Examples of civilian use include treatment of severe lacerations, gunshot wounds to the neck and even hemodialysis catheter dislodgement. Trauma surgeons have also used QuikClot for successful treatment of bleeding during surgery in the chest, abdomen, and pelvis. QuikClot was noted to have two significant weaknesses. Since it is a granular powder poured into a wound, it had limited usefulness in high-pressure bleeding (i.e. femoral artery bleed)as the granules were washed away by the bleeding before they were able to form a clot. Furthermore, the heat generated from its use was associated with several burns.

QuikClot production was stopped after development of several newer generation products. These newer generation products have minimal heat production and are packaged both as gauzes and in a bagged form. Currently Z-Medica sells QuikClot packaged in 2”x2” and 4”x4” gauze pads for use on superficial lacerations which don’t have severe bleeding. QuikClot has also developed a small kaolin-impregnated pad (QuikClot ACS+) and as a laparotomy pad (QuikClot Trauma Pad) for use by trauma surgeons in the operating room for cases of severe bleeding during surgery. This later product remains in the research phase and is not yet approved for widespread use.

QuikClot Combat GauzeTM is a 3”x4 yard long roll of nonwoven gauze impregnated with kaolin. Combat Gauze has all the advantages of normal gauze (easy application, flexible, large coverage area, and easily removable) with the additional advantage of hemostatic function from the kaolin. It is designed for packing into deep wounds which are actively bleeding (i.e. arterial injury in the groin). Prehospital personnel can also use combat gauze as they would any standard Kerlix gauze. Combat Gauze was recently compared to several newer generation products, including the HemCon RTS, and found to be superior and had no apparent side effects.11 Currently, QuikClot Combat Gauze is the only product endorsed by the Tactical Combat Casualty Care Committee and they recommend it as first line treatment for life-threatening hemorrhage on external wounds not amendable to direct pressure and tourniquet placement.

Summary:

- Numerous topical hemostatic products have been developed and released onto the market.

- Some of these products have since been discontinued, while others are widely used.

-Economic and medical considerations continue to make this a rapidly evolving and growing area of prehospital care. It is important for the EMS provider to remain cognizant of these products and their advantages, disadvantages, and complications as they continue to evolve.

PHTLS Recommendation: Topical hemostatic agents may be used to control hemorrhage occurring in sites not amenable to tourniquet placement and which cannot be controlled by direct pressure alone.

 

 

Bibliography

  1. Achneck HE, Sileshi B, Jamiolkowski RM, et al. A comprehensive review of topical hemostatic agents: Efficacy and recommendations for use. Annals of Surgery 2010; 251: 217-228.

  2. Mabry R and McManus JG. Prehospital advances in the management of severe penetrating trauma. Crit Care Med. 2008:36(7);S258-266.

  3. Brown MA, Daya MR, Worley JA. Experience with chitosan dressings in a civilian EMS system. J Emerg Med. 2009;62:239-243.

  4. Kozen BG, Kircher SJ, Henao J, et al. An alternative hemostatic dressing: comparison of CELOX, HemCon, and QuikClot.Acad Emerg Med. 2008; 15:74-81.

  5. Devlin JJ, Kircher S, Kozen BG, et al. Comparison of ChitoFlex, CELOX, and QuikClot in control of hemorrhage. J Emerg Med. 2009 Apr 1 (Epub ahead of print).

  6. Ward KR, Tiba MH, Holbert WH, et al. Comparison of a new hemostatic agent to current combat hemostatic agents in a swine model of lethal arterial hemorrhage. J Trauma. 2007;63:276-284.

  7. Kheirabadi BS, Edens JW, Terrazas IB, et al. Comparison of new hemostatic granules/powders with currently deployed hemostatic products in a lethal model of extremioty arterial hemorrhage in swine. J Trauma. 2009;66:316-328.

  8. Arnaud F, Parreno-Sadalan D, Tomori T, et al. Comparison of 10 hemostatic dressings in a groin transaction model in swine. J Trauma. 2009;67:848-855.

  9. Bheirabadi BS, Mace JE, Terrazas IB, et al. Safety evaluation of new hemostatic agents, smectite granules, and kaolin-coated gauze in a vascular injury wound model in swine. J Trauma. 2010;68:269-278.

  10. Rhee P, Brown C, Martin M, et al. QuikClot use in trauma for hemorrhage control: case series of 103 documented uses. J Trauma. 2008;64:1093-1099.

  11. Kheirabadi BS, Scherer MR, Estep JS, et al. Determination of efficacy of new hemostatic dressings in a model of extremity arterial hemorrhage in swine. J Trauma. 2009;67:450-460.

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