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==2013 ESA Guidelines for the Management of Severe Perioperative Bleeding (DO NOT EDIT)<ref name="Kozek-Langenecker-2013">{{Cite journal | last1 = Kozek-Langenecker | first1 = SA. | last2 = Afshari | first2 = A. | last3 = Albaladejo | first3 = P. | last4 = Santullano | first4 = CA. | last5 = De Robertis | first5 = E. | last6 = Filipescu | first6 = DC. | last7 = Fries | first7 = D. | last8 = Görlinger | first8 = K. | last9 = Haas | first9 = T. | title = Management of severe perioperative bleeding: guidelines from the European Society of Anaesthesiology. | journal = Eur J Anaesthesiol | volume = 30 | issue = 6 | pages = 270-382 | month = Jun | year = 2013 | doi = 10.1097/EJA.0b013e32835f4d5b | PMID = 23656742 }}</ref>== | ==2013 ESA Guidelines for the Management of Severe Perioperative Bleeding (DO NOT EDIT)<ref name="Kozek-Langenecker-2013">{{Cite journal | last1 = Kozek-Langenecker | first1 = SA. | last2 = Afshari | first2 = A. | last3 = Albaladejo | first3 = P. | last4 = Santullano | first4 = CA. | last5 = De Robertis | first5 = E. | last6 = Filipescu | first6 = DC. | last7 = Fries | first7 = D. | last8 = Görlinger | first8 = K. | last9 = Haas | first9 = T. | title = Management of severe perioperative bleeding: guidelines from the European Society of Anaesthesiology. | journal = Eur J Anaesthesiol | volume = 30 | issue = 6 | pages = 270-382 | month = Jun | year = 2013 | doi = 10.1097/EJA.0b013e32835f4d5b | PMID = 23656742 }}</ref>== | ||
====Coagulation Management==== | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LightGreen"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 1]] | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''1.''' We recommend treatment with [[fibrinogen]] concentrate if significant [[bleeding]] is accompanied by at least suspected low [[fibrinogen]] concentrations or function. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''2.''' We recommend that a plasma [[fibrinogen]] concentration <1.5–2.0 g/L or ROTEM/TEG signs of functional [[fibrinogen]] deficit should be triggers for [[fibrinogen]] substitution. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''3.''' We recommend that patients on oral [[anticoagulant]] therapy should be given [[prothrombin complex concentrate|prothrombin complex concentrate (PCC)]] and [[vitamin K]] before any other [[coagulation]] management steps for severe perioperative [[bleeding]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: B]])'' <nowiki>"</nowiki> | |||
|} | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 2]] | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''1.''' We suggest an initial [[fibrinogen]] concentrate dose of 25–50 mg/kg. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''2.''' We suggest that the indication for [[cryoprecipitate]] is lack of available [[fibrinogen]] concentrate for the treatment of [[bleeding]] and [[hypofibrinogenemia]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''3.''' In cases of ongoing or diffuse [[bleeding]] and low clot strength despite adequate [[fibrinogen]] concentrations, it is likely that [[Factor XIII|FXIII]] activity is critically reduced. In cases of significant [[Factor XIII|FXIII]] deficiency (i.e. < 60% activity), we suggest that [[Factor XIII|FXIII]] concentrate (30 IU/kg) can be administered. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''4.''' We suggest that [[prothrombin complex concentrate|PCC]] (20 –30 IU/kg) can also be administered to patients not on oral [[anticoagulant]] therapy in the presence of an elevated [[bleeding]] tendency and prolonged [[clotting time]]. Prolonged [[INR]]/[[PT]] alone is not an indication for [[prothrombin complex concentrate|PCC]], especially in critically ill patients. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''5.''' We suggest that off-label administration of recombinant activated [[factor VII|factor VII]] (rFVIIa) can be considered for [[bleeding]] which cannot be stopped by conventional, surgical or interventional radiological means and/or when comprehensive [[coagulation]] therapy fails. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|} | |||
====Antifibrinolytics and Tranexamic Acid==== | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LightGreen"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 1]] | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''1.''' We recommend the consideration of [[tranexamic acid]] (20 –25 mg/kg). ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | |||
|} | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 2]] | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''1.''' We suggest the use of [[DDAVP]] under specific conditions (acquired [[von Willebrand syndrome]]). There is no convincing evidence that [[DDAVP]] minimises perioperative [[bleeding]] or perioperative allogeneic blood [[transfusion]] in patients without a congenital [[bleeding disorder]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: B]])'' <nowiki>"</nowiki> | |||
|} | |||
====Correction of Confounding Factors==== | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LightGreen"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 1]] | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''1.''' We recommend maintaining perioperative normothermia because it reduces [[blood loss]] and [[transfusion]] requirements. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: B]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''2.''' While pH correction alone cannot immediately correct [[acidosis]]-induced [[coagulopathy]], we recommend that pH correction should be pursued during treatment of acidotic [[coagulopathy]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''3.''' We recommend that [[Factor VII|rFVIIa]] should only be considered alongside pH correction. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|} | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 2]] | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''1.''' We suggest that [[Factor VII|rFVIIa]] may be used in treatment of patients with hypothermic [[coagulopathy]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''2.''' We suggest that [[calcium]] should be administered during massive [[transfusion]] if Ca<sup>2+</sup> concentration is low, in order to preserve normocalcaemia (0.9 mmol/l). ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: B]])'' <nowiki>"</nowiki> | |||
|} | |||
====Emergency Radiological/Surgical Interventions to Reduce Blood Loss==== | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LemonChiffon"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 2]] | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''1.''' We suggest that endovascular [[embolization]] is a safe alternative to open surgical intervention after failed endoscopic treatment for [[upper gastrointestinal bleeding]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''2.''' We suggest super-selective [[embolization]] as primary therapy for treatment of [[angiogram]] positive [[lower gastrointestinal bleeding]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|- | |||
| bgcolor="LemonChiffon"|<nowiki>"</nowiki>'''3.''' We suggest [[embolization]] as first-line therapy for arterial complications in [[pancreatitis]]. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: C]])'' <nowiki>"</nowiki> | |||
|} | |||
====Cost Implications==== | |||
{|class="wikitable" style="width: 80%;" | |||
|- | |||
| colspan="1" style="text-align:center; background:LightGreen"|[[ESA guidelines classification scheme#Classification of Recommendations|Class 1]] | |||
|- | |||
| bgcolor="LightGreen"|<nowiki>"</nowiki>'''1.''' We recommend restricting the use of [[Factor VII|rFVIIa]] to its licensed indication because, outside these indications, the effectiveness of [[Factor VII|rFVIIa]] to reduce [[transfusion]] requirements and mortality remains unproven and the risk of arterial [[thromboembolism|thromboembolic]] events as well as costs are high. ''([[ESA guidelines classification scheme#Level of Evidence|Level of Evidence: A]])'' <nowiki>"</nowiki> | |||
|} | |||
==Sources== | ==Sources== |
Revision as of 18:47, 21 April 2014
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]
2013 ESA Guidelines for the Management of Severe Perioperative Bleeding (DO NOT EDIT)[1]
Coagulation Management
Class 1 |
"1. We recommend treatment with fibrinogen concentrate if significant bleeding is accompanied by at least suspected low fibrinogen concentrations or function. (Level of Evidence: C) " |
"2. We recommend that a plasma fibrinogen concentration <1.5–2.0 g/L or ROTEM/TEG signs of functional fibrinogen deficit should be triggers for fibrinogen substitution. (Level of Evidence: C) " |
"3. We recommend that patients on oral anticoagulant therapy should be given prothrombin complex concentrate (PCC) and vitamin K before any other coagulation management steps for severe perioperative bleeding. (Level of Evidence: B) " |
Class 2 |
"1. We suggest an initial fibrinogen concentrate dose of 25–50 mg/kg. (Level of Evidence: C) " |
"2. We suggest that the indication for cryoprecipitate is lack of available fibrinogen concentrate for the treatment of bleeding and hypofibrinogenemia. (Level of Evidence: C) " |
"3. In cases of ongoing or diffuse bleeding and low clot strength despite adequate fibrinogen concentrations, it is likely that FXIII activity is critically reduced. In cases of significant FXIII deficiency (i.e. < 60% activity), we suggest that FXIII concentrate (30 IU/kg) can be administered. (Level of Evidence: C) " |
"4. We suggest that PCC (20 –30 IU/kg) can also be administered to patients not on oral anticoagulant therapy in the presence of an elevated bleeding tendency and prolonged clotting time. Prolonged INR/PT alone is not an indication for PCC, especially in critically ill patients. (Level of Evidence: C) " |
"5. We suggest that off-label administration of recombinant activated factor VII (rFVIIa) can be considered for bleeding which cannot be stopped by conventional, surgical or interventional radiological means and/or when comprehensive coagulation therapy fails. (Level of Evidence: C) " |
Antifibrinolytics and Tranexamic Acid
Class 1 |
"1. We recommend the consideration of tranexamic acid (20 –25 mg/kg). (Level of Evidence: A) " |
Class 2 |
"1. We suggest the use of DDAVP under specific conditions (acquired von Willebrand syndrome). There is no convincing evidence that DDAVP minimises perioperative bleeding or perioperative allogeneic blood transfusion in patients without a congenital bleeding disorder. (Level of Evidence: B) " |
Correction of Confounding Factors
Class 1 |
"1. We recommend maintaining perioperative normothermia because it reduces blood loss and transfusion requirements. (Level of Evidence: B) " |
"2. While pH correction alone cannot immediately correct acidosis-induced coagulopathy, we recommend that pH correction should be pursued during treatment of acidotic coagulopathy. (Level of Evidence: C) " |
"3. We recommend that rFVIIa should only be considered alongside pH correction. (Level of Evidence: C) " |
Class 2 |
"1. We suggest that rFVIIa may be used in treatment of patients with hypothermic coagulopathy. (Level of Evidence: C) " |
"2. We suggest that calcium should be administered during massive transfusion if Ca2+ concentration is low, in order to preserve normocalcaemia (0.9 mmol/l). (Level of Evidence: B) " |
Emergency Radiological/Surgical Interventions to Reduce Blood Loss
Class 2 |
"1. We suggest that endovascular embolization is a safe alternative to open surgical intervention after failed endoscopic treatment for upper gastrointestinal bleeding. (Level of Evidence: C) " |
"2. We suggest super-selective embolization as primary therapy for treatment of angiogram positive lower gastrointestinal bleeding. (Level of Evidence: C) " |
"3. We suggest embolization as first-line therapy for arterial complications in pancreatitis. (Level of Evidence: C) " |
Cost Implications
Class 1 |
"1. We recommend restricting the use of rFVIIa to its licensed indication because, outside these indications, the effectiveness of rFVIIa to reduce transfusion requirements and mortality remains unproven and the risk of arterial thromboembolic events as well as costs are high. (Level of Evidence: A) " |
Sources
- 2013 ESA Guidelines for the Management of Severe Perioperative Bleeding[1]
References
- ↑ 1.0 1.1 Kozek-Langenecker, SA.; Afshari, A.; Albaladejo, P.; Santullano, CA.; De Robertis, E.; Filipescu, DC.; Fries, D.; Görlinger, K.; Haas, T. (2013). "Management of severe perioperative bleeding: guidelines from the European Society of Anaesthesiology". Eur J Anaesthesiol. 30 (6): 270–382. doi:10.1097/EJA.0b013e32835f4d5b. PMID 23656742. Unknown parameter
|month=
ignored (help)