coagulopathy and blood component transfusion in trauma r3

18
Coagulopathy and blood component transfus ion in trauma R3 정정정

Upload: david-harris

Post on 26-Mar-2015

218 views

Category:

Documents


3 download

TRANSCRIPT

Page 1: Coagulopathy and blood component transfusion in trauma R3

Coagulopathy and blood component transfusion

in trauma

R3 정상우

Page 2: Coagulopathy and blood component transfusion in trauma R3

• Trauma– 1 in 10 death worldwide– uncontrolled bleeding

• 40% of trauma-related deaths• leading cause of potentially preventable and early in-hosp

ital death

• life-threatening bleeding– vascular injury– coagulopathy

• consumption and dilution of coagulation factors and platelets, dysfunction of platelets and the coagulation system, increased fibrinolysis, compromise of the coagulation system by the infusion of colloid, hypocalcemia, and disseminated intravascular coagulation-like syndrome

Page 3: Coagulopathy and blood component transfusion in trauma R3

Pathophysiology of coagulopathy in trauma2) Consumption coagulopathy

• precise cause is difficult to identify and multifactorial

Page 4: Coagulopathy and blood component transfusion in trauma R3

Pathophysiology of coagulopathy in trauma3) Increased fibrinolysis

• trauma pts. demonstrate both hypofibrinolytic and hyperfibrinolytic states

• severity of injury, time from injury 에 따라 달라진다

• Simmons et al.– trauma 직후 : fibrinolytic activity increase– mild~moderate inj.: 24h 이후 normal– major inj.: remain elevated– hypothermia : fibrinolytic activity 증가

Page 5: Coagulopathy and blood component transfusion in trauma R3

Pathophysiology of coagulopathy in trauma4) Hypothermia-induced coagulopathy

• significant risk factors for life-threatening coagulopathy– injury severity score > 25– systolic BP < 70mmHg– acidosis with pH < 7.10– hypothermia with BT < 34℃

• lethal triad– hypothermia, metabolic acidosis, progressive coagulo

pathy

Page 6: Coagulopathy and blood component transfusion in trauma R3

Pathophysiology of coagulopathy in trauma4) Hypothermia-induced coagulopathy

• effect of hypothermia on coagulopathy is difficult to identify by routine coagulation screening tests (PT, aPTT)

• hypothermia– impairs thrombin generation and the formation of plat

elet plugs and fibrin clots

– increase clot lysis

– results in coagulopathy and uncontrollable bleeding

Page 7: Coagulopathy and blood component transfusion in trauma R3

Pathophysiology of coagulopathy in trauma5) Decreased levels of coagulation factors and platelets• large volumes of crystalloid and colloid

• thrombocytopenia is seen commonly in pts. received massive blood transfusion

• platelets are present in whole blood

• 현재는 RBC unit 사용– negligible amounts of coagulation factors and

platelets– thrombocytopenia and subnormal levels of

coagulation factors often occur at early stage during massive RBC transfusion

Page 8: Coagulopathy and blood component transfusion in trauma R3

Pathophysiology of coagulopathy in trauma6) The effect of acute RBC loss on coagulation

• unclear

• as no data from trauma pts. are available, the effect of acute RBC loss on coagulation is unknown

Page 9: Coagulopathy and blood component transfusion in trauma R3

Effect of massive RBC transfusion on coagulation

• 과거 수혈은 주로 whole blood 에 의존 , 현재는 specific component therapy

• blood component therapy– optimizes the use of resources by allowing componen

ts to be used in different pts.– avoids potentially harmful effects caused by transfusi

on of surplus constituents– whole blood 와 비교했을 때 massive RBC transfusion

시 earlier stage 에서 coagulopathy 발생 (low levels of platelets and clotting factors)

Page 10: Coagulopathy and blood component transfusion in trauma R3

Effect of massive RBC transfusion on coagulation• relationship between volume of blood loss, repla

cement volume and the reduction in coagulation factor and platelet levels are difficult to establish

• increased acid load from RBC units may also contribute to coagulopathy– pH of an RBC unit is low, and decreases progressively

during storage from 7.0 to 6.3– plasma 의 high-buffering capacity 로 acid-base distur

bance 는 잘 일어나지 않는다– trauma pts. are already acidotic, massive transfusion

of RBCs further increase acid load, exacerbate the ongoing coagulopathy

Page 11: Coagulopathy and blood component transfusion in trauma R3

Unresolved issues regarding blood transfusion in trauma1) Optimal replacement therapy for FFP and platelets• massive RBC transfusion 시 FFP, platele

ts, fibrinogen concentrate or cryoprecipitate 를 같이 줘야한다는 건 알고 있지만 universal guideline 은 없다

• based on experts’ opinion or personal experience

Page 12: Coagulopathy and blood component transfusion in trauma R3

Unresolved issues regarding blood transfusion in trauma1) Optimal replacement therapy for FFP and platelets

• 1st approach– transfuse FFP and plts. prophylactically after

a certain number of units of RBCs– FFP:RBC → 1:10 ~ 2:3– plt:RBC → 6:10 ~ 12:10– coagulopathy 의 발생을 예방하거나 bleeding

을 줄인다는 증거는 없다– benefit 도 확실하지 않다

Page 13: Coagulopathy and blood component transfusion in trauma R3

Unresolved issues regarding blood transfusion in trauma1) Optimal replacement therapy for FFP and platelets

• 2nd approach– transfuse FFP, plt, cryoprecipate only when there is cli

nical or laboratory evidence of coagulopathy• microvascular bleeding• PT or aPTT > 1.5 times normal value• thrombocytopenia < 50000• fibrinogen concentration < 1g/L

– occult site 의 microvascular bleeding 은 발견하기 힘들다

– lab. test may take 30~60min

Page 14: Coagulopathy and blood component transfusion in trauma R3

Effect of RBC transfusion on longer-term outcome in trauma1) Multiple organ failure (MOF)• RBC transfusion has been to shown to be an ind

ependent risk factor for post-injury MOF

• 513 명의 major trauma, severe bleeding and haemorrhagic shock 환자에 대한 연구에서 injury MOF 발생한 환자는 첫 12h 이내에 RBC 13unit 수혈받음

• MOF 발생하지 않은 환자는 3.8unit

• decrease in volume of RBC transfused may decrease the risk and severity of MOF

Page 15: Coagulopathy and blood component transfusion in trauma R3

Effect of RBC transfusion on longer-term outcome in trauma2) Post-injury infection• large amounts of foreign antigens may lead to d

ownregulation of the immune system

• alternative non-immune-mediated mechanism– stored RBCs are less deformable and more rigid, onc

e transfused they may obstruct capillary blood flow, predisposing tissue to ischemia and infection as well as poor delivery of prophylactic antibiotics

Page 16: Coagulopathy and blood component transfusion in trauma R3

The need for haemostatic agents

• ideal hemostatic agent should be efficacious in a wide range of hemostatic dysfunctions, simple to store and use, and have a rapid action

• activated recombinant factor Ⅶ (rFⅦa) is a potential candidate– effective hemostasis in a wide range of bleeding conditions– significantly dcreased RBC transfusion requirement in pts.

with major trauma– optimal preconditions should be achieved before administr

ation

Page 17: Coagulopathy and blood component transfusion in trauma R3

The need for haemostatic agents

• optimal preconditions– fibrinogen concentration ≥ 0.5g/L

– platelet count ≥ 50/L

– pH ≥ 7.2

Page 18: Coagulopathy and blood component transfusion in trauma R3

Conclusions• non-surgically correctable bleeding remains a major cha

llenge

• currently, blood component replacement therapy remains the mainstay of coagulopathy-related bleeding

• although RBC transfusion can be life-saving, its negative effects on post-injury outcome have been well documented

• hemostatic agents, which can effectively control bleeding and reduce the amount of RBC required, may decrease mortality and morbidity in trauma pts. but are unlikely to replace blood transfusion completely