1 / 61

Traumatic Hemorrhagic Shock and Massive Transfusion Protocols in Children

Traumatic Hemorrhagic Shock and Massive Transfusion Protocols in Children. Philip C. Spinella , MD. FCCM Associate Professor, Department of Pediatrics Critical Care Translational Research Program Director Washington University in St Louis. Epidemiology.

oren-ochoa
Télécharger la présentation

Traumatic Hemorrhagic Shock and Massive Transfusion Protocols in Children

An Image/Link below is provided (as is) to download presentation Download Policy: Content on the Website is provided to you AS IS for your information and personal use and may not be sold / licensed / shared on other websites without getting consent from its author. Content is provided to you AS IS for your information and personal use only. Download presentation by click this link. While downloading, if for some reason you are not able to download a presentation, the publisher may have deleted the file from their server. During download, if you can't get a presentation, the file might be deleted by the publisher.

E N D

Presentation Transcript

  1. Traumatic Hemorrhagic Shock and Massive Transfusion Protocols in Children Philip C. Spinella, MD. FCCM Associate Professor, Department of Pediatrics Critical Care Translational Research Program Director Washington University in St Louis

  2. Epidemiology • Trauma most common cause of death • Children > 1 year of age in US • Hemorrhage most common cause of preventable death • 66-80% of preventable deaths are from hemorrhage • Hemorrhagic death occurs fast – 6-12 hours • Prevention of early death from hemorrhage - important • Greatest Impact on Survival

  3. Objective: Incidence, association with mortality • Shock and coagulopathy • Retrospective: Combat Support Hospitals • 744 children in Iraq and Afghanistan from 2002-2009 • Coagulopathy and Shock • INR ≥1.5 • Base deficit (BD) ≥6.

  4. Coagulopathy 27% (202/744) of patients presented w/ coagulopathy

  5. Shock 38.3% (285/744) of patients presented with early shock

  6. Adjusted Analysis Table 3. Logistic regression results for in-hospital mortality Coagulopathy & shock, OR =3.8 (95% CI 2.0-7.4), (p<0.001)

  7. PEDIATRICS Vol. 127 No. 4 April 1, 2011 pp. e892 -e897

  8. Results • 707 patients from the derivation set and • 1101 patients in the validation set. Table 2. Multivariate Logistic Regression for Mortality INR, International Normalized Ratio

  9. Results • Pediatric “BIG” score • (Base Deficit + (2.5xINR) + (15-GCS) • AUC for derivation and validation datasets • 0.89 (95% CI 0.83-0.95) • 0.89 (95% CI 0.87-0.92)

  10. Grade V liver injury has a 76% mortality in academic Level 1 Trauma Centers

  11. DCR • INDICATION: LIFE THREATENING INJURY

  12. Massive Transfusion Protocol • MTP Principles • Rapid surgical control • Avoid overuse of crystalloids to minimize dilutional coagulopathy • Continuously monitor patient temperature • Avoid and treat hypothermia (use fluid warmer and Bair hugger if needed) • Avoid and treat acidosis as needed; (pH<7.2 treat with bicarbonate or THAM) • Treat low ionized calcium for hemostatic and hemodynamic effects Laboratory evaluation upon admission I stat: blood gas, lactate, Hb, ionized calcium and electrolytes, INR/PT. Laboratory: Type & Screen, CBC, Fibrinogen, TEG (if available) – STAT Laboratory Evaluation q hour until MTP stops I stat: blood gas, lactate, Hb, ionized calcium and electrolytes, INR/PT. Laboratory: CBC, Fibrinogen, TEG (if available) – STAT

  13. PEDS MTP

  14. Adjunctive Therapies • Fibrinogen concentrates • 30-50 mg/kg • Fibrinogen concentration or TEG based • Prothrombin complex concentrates • Factors II, IX, X • Factors II, VII, IX and X, Protein C and S – FDA IND • Anti-fibrinolytics • Tranexamic Acid (TXA) • rFVIIa

  15. CRASH-2 Trial • Clinical Randomization of an Antifibrinolytic in Significant Hemorrhage (Lancet, 2010) • Prospective of 20,211 patients • Multicenter (270 Hospitals) • Multinational (40 Nations) • Randomized, Blinded, Placebo-controlled • One gram tranexamic acid over ten minutesfollowed by one gram tranexamic acid given over eight hours • Normal saline placebo

  16. CRASH-2 Trial • Inclusion Criteria: • Adult Trauma victim • Systolic blood pressure less than 90 mmHg • Heart rate greater than 110 • Deemed to be at risk of significant hemorrhage

  17. CRASH-2 Trial • Endpoints: • Primary: In-hospital death within four weeks of injury • Secondary • Vascular occlusive events • Surgical interventions • Blood Transfusions • Total units of blood transfused

  18. CRASH-2 Trial- Results • Decreased mortality: • All-comers, 14.5% vs. 16.0% (p=0.0035) • Deaths from bleeding, 4.9% vs. 5.7% (p=0.0077)

  19. CRASH-2 Trial- Results • Treatment ≤1 h from injury reduced risk of death due to bleeding • 5.3% in TXA vs 7.7% in placebo • RR 0.68, (95% CI 0.57–0.82), (p<0.0001) • Treatment from 1- 3 h also reduced risk of death due to bleeding • 4.8% vs. 6.1% • RR 0.79, (0.64–0.97) (p=0.03). • Treatment > 3 h increased the risk of death due to bleeding • 4.4% vs. 3.1%, • RR 1.44, (1.12–1.84), (p=0.004)

  20. MATTERs Study • Military Application of Tranexamic Acid in Trauma Emergency Resuscitation (Arch Surg, 2012) • Retrospective, observational of: • 896 Combat-injured patients (both soldiers and nationals) presenting to Camp Bastion Surgical Hospital in Afghanistan • Requiring a minimum transfusion of one unit packed red blood cells

  21. MATTERs Study • Endpoints: • Primary: 24-hour, 48-hour, and in-hospital mortality • Secondary: • Transfusion requirement • Correction of PT and PTT between admission and ICU • Thromboembolic events

  22. MATTERs Study • Results (896 patients, 293 receiving TXA): • Greater injury severity in TXA-treated group • (ISS 25.2 vs. 22.5, p<0.001) • Greater transfusion requirement in TXA-treated group • (All products) • Decreased Mortality in TXA treated: • 48-hour (11.3 vs. 18.9%, p=0.004) • In-hospital (17.4 vs. 23.9%, p=0.030) • Reduction in hypocoagulability in TXA-treated group from ED to ICU

  23. MATTERs Study • Thromboembolic events increased with TXA: • PE • (8 vs. 2, p=0.001) • DVT • (7 vs. 1, p=0.001)

  24. Should TXA be used in Peds MTPs? • No evidence at all in children • Adult data appears supportive • Standard in Adult MTPs • Reasonable to add • Reasonable to wait for additional data

  25. Fibrinogen Concentrates • Provide high amount of fibrinogen rapidly • Not frozen, rapidly reconstituted and given • High cost • No comparative data with cryoprecipitate in trauma patients

  26. Goal Directed Hemostatic Resuscitation • Hemostatic Resuscitation = 1:1:1 • Goal directed hemostatic resuscitation • 1:1:1 that is tailored to patients needs

  27. Thromboelastography (TEG) • Whole blood test • Plasma-platelet interaction • Patient temperature • Functional measurement of • Clot initiation, amplification, propagation, lysis • TEG system • Laboratory based • Point of care • Remote - networked

  28. TEG Parameter Summary TEG Parameter Summary

  29. Back to the Future With Whole Blood ?

  30. Whole Blood Availability • Classic teaching is that Platelets stored at 4C are non functional • Current data indicates IMPROVED function • If whole blood can be stored for 10 days at 4C. • Improved hemostatic effects in vivo • Increase clinical utility significantly

  31. Average ± SEM ADP-, collagen-, ASPI-, and TRAP-6-stimulated aggregation in WB stored at 4º C versus 22º C (p<0.001 for all four agonists by repeated measures ANOVA). Pidcoke,H.F., Pidcoke, Heather, Transfusion. 2013 Jan;53 Suppl 1:137S-49S.

  32. Manno - Methods • Prospective double-blinded study • 161 children requiring cardiac surgery • Patients were randomized to • Warm FWB (< 6 hours at 20 degrees C) • Cold FWB (24 - 48 hours at 4-6 C) • Reconstituted whole blood (1:1:1) • (RBCs ≤ 5 days of storage, FFP, and platelets). Manno CS, et al. Blood 1991;77:930-6.

  33. Manno - Results • Patient groups similar • Sex and Age • Surgical severity score • By pass and circulatory arrest time • # requiring circulatory arrest

  34. Manno - Results ∞ cold vs recon § warm and cold vs recon Manno CS, et al. Blood 1991;77:930-6.

  35. Warm FWB Benefits & Risks • Benefits • Less dilutionaleffect than components • Less anti-coagulants and preservatives1 • More functional fresh product 2 • No storage lesion (adverse effects) of RBC • Risks • Infectious, GVHD, WBC mediated 1 Spinella PC, J Trauma. 2009;66:S69-76 2 Manno CS. Blood 1991;77:930-6.

  36. Cold Whole Blood Trials • Liver Transplant • Burn • Trauma

  37. Case Example Intraoperative Hemorrhagic Shock • A 9 year old 20 kilogram male, who previously underwent a right nephrectomy and pulmonary resection for Wilmstumor, presented one year later with a new lesion in the right lobe of his liver

  38. Case Example • The patient was taken to the operating room (OR) and a right hepatectomy was performed • Due to severe intra-operative bleeding the MT protocol was activated

  39. Case Example • During the 4 hours that the MT protocol was activated, a total of 10 units RBCs, 14 units FFP, and 15 units of platelets were transfused. (20 kg child) • With EBL of over 4 liters no laboratory evidence of a metabolic acidosis or shock indicated by normal base deficit values

  40. Case Example • Upon admission to the (ICU) • After receiving an intraoperative total of 13,100 milliliters (ml) of blood products • (8 blood volumes) • And 4,500 ml of normal saline • Patient had no physical evidence of pulmonary edema or anasarca.

  41. Case Example • Patient had no physical evidence of pulmonary edema or anasarca. • PEEP of 5 with Fi02 30% • Extubated in AM

More Related