2. Details of interventional algorithms.
Author/year | Duration of intervention | Devices used | RBC trigger | FFP trigger | PLT trigger | Protamine trigger |
Cryo or fib.conc. trigger |
Antifibrinolytics trigger |
Ak 2009 | Intraoperative and until 24 hours post‐CPB | TEG | Hct < 25% (18% accepted during CPB) |
TEG‐R > 14 min | TEG‐MA < 48 mm | h‐TEG‐R < 0.5 x TEG‐R | ‐ | LY30 > 7.5% |
Avidan 2004* | Intraoperative and until 2 hours post‐CPB | TEG and PFA‐100 and Hepcon device | hb < 8g/dL | TEG‐R > 10 min (no heparin effect) and bleeding | Prolonged PFA‐100 channel closure time and persisting bleeding | Hepcon measurement | ‐ | LY30 > 7.5% and bleeding > 100 mL/hour |
Cui 2010 | Unclear | TEG, kaolin activated and functional fibrinogen | No trigger stated, the Hct was higher than 54% before operation | Not described | Not described | Protamine at standard dose (4 mg/kg) | Fibrinogen concentrate to all in TEG group 500 mg to 1000 mg | Not described |
Girdauskas 2010** | Intra‐ and postoperative | ROTEM (HEPTEM, APTEM, FIBTEM, INTEM) | Hct < 25% (hb < 8.5 g/dL) (20% (hb 6.8 g/dL) accepted during CPB) or severe haemodynamic instability |
HEPTEM‐CT > 260 sec | HEPTEM‐MCF = 35‐45 mm and FIBTEM‐MCF > 8 mm or HEPTEM‐MCF < 35 mm |
INTEM‐CT/HEPTEM‐CT > 1.5 | FIBTEM‐MCF < 8 mm | APTEM‐MCF /HEPTEM‐MCF > 1.5 (if needed beyond standard protocol) |
Kempfert 2011 | Unclear | ROTEM (4 chamber) | Not stated | Not described | Not described | Not described | Not described | Not described |
Kultufan Turan 2006 | Intra‐ and postoperative | ROTEG | Details not available | Details not available | Details not available | Details not available | ‐ | Details not available |
Nakayama 2015 | Intraoperative | ROTEM (HEPTEM, APTEM, FIBTEM, INTEM, EXTEM) | Maintain the haematocrit at 25% to 30% during CPB | EXTEM‐A10 < 30 mm and FIBTEM‐A10 ≤ 5mm | EXTEM‐A10 ≤ 30 mm and FIBTEM‐A10 > 5mm | HEPTEM‐CT/INTEM‐CT < 0.8 | Not available | Not described |
NCT00772239 | Unclear | ROTEM | Unclear | Unclear | Unclear | Unclear | Unclear | Unclear |
Nuttal 2001 | Intraoperative | TEG, Coaguchek Plus and Coulter‐MDII | Details not available | PT > 16.6 sec or aPTT > 57 sec | TEG‐MA < 48 mm or platelet count < 102,000/µL | ACT‐guided | p‐fibrinogen < 144 mg/dL | At the discretion of the anaesthesiologist |
Paniagua 2011 | Intra‐ and postoperative | ROTEM (HEPTEM, FIBTEM, INTEM, EXTEM, APTEM) | Hb < 8 g/dL | First line: EXTEM‐CT > 80 S or HEPTEM‐CT > 280 S and INTEM‐CT > 240 S Second line: EXTEM‐MCF < 50 mm and FIBTEM‐MCF < 12 mm | EXTEM‐MCF < 50 mm and FIBTEM‐MCF > 12 mm* | INTEM‐CT > 240 sec and HEPTEM‐CT normal | One patient in the ROTEM group received fibrinogen concentrate. The drug was only available during the last three months of inclusions | EXTEM‐CT >80 S, CFT > 159, EXTEM‐MCF < 50 mm and/or Lysis at 1 hour > 15% |
Rauter 2007 | Unclear | ROTEM | Unclear | Unclear | Unclear | Unclear | Unclear | Unclear |
Royston 2001 | Intraoperative | TEG and h‐TEG |
Details not available | h‐TEG‐R > 14 min | h‐TEG‐MA < 48 mm | Details not available | ‐ | LY30 > 7.5% |
Schaden 2012 | Intra‐ and postoperative | ROTEM (APTEM, FIBTEM, EXTEM) | Hb < 8 g/dL | EXTEM‐CT > 100 S | EXTEM‐A10 < 45 mm and FIBTEM‐A10 > 12 mm |
Not relevant | EXTEM‐A10 < 45 mm and FIBTEM‐A10 < 12 mm | Spindle‐shaped trace Or APTEM‐A10 >> EXTEM‐A10 or EXTEM‐LY30 > 10 % |
Shore‐Lesserson 1999 | Intraoperative | TEG and h‐TEG |
Hct < 25% (21% accepted during CPB) and bleeding (> 100 mL in 3 min or absence of visible clots) |
h‐TEG‐R > 20 min and bleeding (> 100 mL in 3 min or absence of visible clots) | TEG‐MA < 45 mm and platelet count < 100,000/µL and bleeding (> 100 mL in 3 min or absence of visible clots) | TEG‐R > 2 x h‐TEG‐R | p‐fibrinogen < 100 mg/dL and bleeding (> 100 mL in 3 min or absence of visible clots) | LY30 > 7.5% (if needed beyond standard protocol) |
Wang 2010 | Unclear/most likely only intraoperative | TEG | hb < 8 g/dL | TEG‐R > 10 min | TEG‐MA < 55 mm | ‐ | TEG‐alpha‐angle < 45 degrees | LY30, no limit stated |
Weber 2012 | Intra‐ and postoperative | ROTEM (HEPTEM, FIBTEM, INTEM, EXTEM) | Hb < 6 g/dL during CPB and < 8 g/dL after CPB | EXTEM‐CT > 80 S or HEPTEM‐CT > 240 S | EXTEM‐A10 < 40 mm and FIBTEM‐A10 > 10 mm or MULTIPLATE (TRAP < 50 AU and/or ASPI < 30 AU and/or ADP < 30 AU*) | ACT > 130 and INTEM‐CT > 240 sec and HEPTEM‐CT/INTEM‐CT < 0.8 | EXTEM‐A10 < 40 mm and FIBTEM –A10 < 10 mm | Antifibrinolytic therapy consisted of the application of 2 g tranexamic acid after the induction of anaesthesia, and another 2 g was added into the priming volume of the heart–lung machine and again during CPB |
Westbrook 2009 | Intra‐ and postoperative | TEG, h‐TEG and Platelet Mapping |
hb < 7 g/dL | h‐TEG‐R > 11 min and persisting bleeding (> 60 mL in first 30 min after protamine or > 60 mL/hour in ICU) | h‐TEG‐MA ≤ 41 mm and persisting bleeding (> 60 mL in first 30 min after protamine or > 60 mL/hour in ICU) | TEG‐R –h‐TEG‐R ≥ 3 min | h‐TEG‐MA > 45 and ‐TEG‐alpha‐angle < 45 degrees | LY30 > 15% |
*In addition: prothrombin complex concentrate if APTEM‐CT > 120 sec; **in addition: desmopressin if persisting bleeding and prolonged PFA‐100 channel closure time; ***in addition: desmopressin singular therapy approach for first time confirmed platelet dysfunction. ‐A10: ROTEM value measured early at 10 min; ACT: activated clotting time; ADP: multiplate test; APTEM: aprotinin test of ROTEM; aPTT: activated partial thromboplastin time; ASPI: multiplate test; AU: arbitrary aggregation units; CPB: cardiopulmonary bypass; ‐CT: clot formation time; EXTEM: extrinsic system screen test; FFP: fresh frozen plasma; FIBTEM: fibrinogen test of ROTEM; h‐: heparin cup; hb: haemoglobin; Hct: haematocrit; HEPTEM: heparin test of ROTEM; ICU: intensive care unit; INTEM: intrinsic system screen test; LY30: Lysis time at 30 min; ‐MCF: maximum clot firmness; p‐: plasma; PLT: platelet transfusion data; PT: prothrombin time; RBC: red blood cell; ROTEG: rotational TEG; ROTEM: rotational thromboelastometry; TEG: thromboelastography; TEG‐R: thromboelastography reaction time; TEG‐MA: thromboelastography maximum amplitude; TRAP: thrombin receptor activating peptide multiplate test;