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Invited Editorial
Cardiac Critical Care
8 (
4
); 181-184
doi:
10.25259/JCCC_43_2024

Value of Point-of-Care Algorithms in Pediatric Cardiac Surgery

Department of Anaesthesiology and Intensive Care Medicine, University Hospital Essen, Essen, Germany
Department of Anesthesiology and Operative Intensive Care, University Hospital Cologne, Cologne, Germany.

*Corresponding author: Klaus Görlinger, Department of Anaesthesiology and Intensive Care Medicine, University Hospital Essen, Essen, Germany. kgoerlinger@werfen.com

Licence
This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, transform, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.

How to cite this article: Görlinger K, Kammerer T. Value of Point-of-Care Algorithms in Pediatric Cardiac Surgery. J Card Crit Care TSS. 2024;8:181-4. doi: 10.25259/JCCC_43_2024

The use of point-of-care (POC) viscoelastic testing-guided bleeding management algorithms is well established in patient blood management (PBM) guidelines for adult cardiac and non-cardiac surgery with a grade 1B-R to 1A recommendation.[1,2] Here, meta-analyses of randomized controlled trials (RCTs) demonstrated a significant reduction in transfusion requirements, morbidity (e.g., acute renal failure), and mortality.[3] However, the evidence of viscoelastic testing-guided bleeding management algorithms for pediatric cardiac surgery is still low due to a limited number of studies, particularly RCTs. Up to now, two small RCTs assessed the effect of developing and implementing thromboelastometry-guided bleeding management algorithms and reported a significant reduction in post-operative bleeding, transfusion, duration of mechanical ventilation, and length of stay at the intensive care unit (ICU) but no change in in-hospital mortality.[4,5] These results have been confirmed by recent cohort studies in neonatal and infant cardiac surgery.[6] In this issue of the Journal of Cardiac Critical Care TTS, Chakraborty et al. demonstrated not only a significant reduction in chest tube drainage, transfusion requirements (packed red blood cells [PRBCs], plasma, and platelets; P < 0.001, each), postoperative complication rates (risk ratio [RR] {95% confidence interval [CI]}; 0.6467 [0.4763–0.8782]; P = 0.0052), and length of stay at the ICU but also a strong trend for reduced in-hospital mortality (RR [95% CI]; 0.4375 [0.1571–1.2187]; P = 0.1138).[7] The authors can be congratulated for their great study showing that the implementation of POC-guided bleeding management in pediatric cardiac surgery cannot only reduce bleeding and transfusion but also improve patient outcomes regarding post-operative complication rates and mortality, as shown for adult cardiac surgery.[3] Accordingly, all efforts should be made to improve patient outcomes and save the lives of our youngest patients undergoing cardiac surgery.

How can this be achieved? First of all, restrictive transfusion thresholds for all blood components must be implemented for pediatric cardiac surgery. Deng et al. reported in their systematic review and meta-analysis on packed red blood cell (PRBC) transfusion thresholds after pediatric cardiac surgery that a restrictive transfusion strategy with a hemoglobin (Hb) threshold of 7–9 g/dL is at least non-inferior to a liberal Hb threshold of 9.5–13 g/dL (RR [95% CI]; 0.49 [0.13–1.94]; P = 0.31).[8] However, a restrictive transfusion strategy must be implemented for the yellow blood products plasma and platelets, too, since they contribute significantly to transfusion-associated morbidity (transfusion-associated circulatory overload, transfusion-related lung injury, and transfusion-related immunomodulation with nosocomial infections, organ failure and sepsis and mortality).[9] Particularly, massive bleeding (blood loss of more than one total blood volume within 24 h) and transfusion (transfusion of more than 40 mL PRBCs within 24 h) should be avoided since it is associated with much higher mortality in pediatric patients compared to adults.[10]

However, PBM goes beyond restrictive blood transfusion and aims to improve patient outcomes by managing and preserving the patient’s own blood while promoting patient safety. Here, minimizing surgical, procedural, and iatrogenic blood losses and managing coagulopathic bleeding are cornerstones of the second pillar of PBM. To achieve this, the development and implementation of patient-centered, evidence-based POC thromboelastometry-guided bleeding management algorithms are important to facilitate personalized precision medicine in perioperative bleeding management as good medical practice. Here, the goal should be to administer the right hemostatic drug or intervention to the right patient at the right time, in the right dose, and in the right sequence while limiting unnecessary exposure to improve patient safety and outcomes as part of a comprehensive pediatric PBM strategy.[9,11,12]

Both with and without the use of the POC technique, PBM entails important considerations as outlined in Tables 1 and 2. Judicious Rotational thromboelastometry (ROTEM) or Thromboelastography (TEG) use can overcome many bleeding situations, as seen in Table 2 and Figure 1.[11,12]

Table 1: Important considerations when POC is not available.
  • Continue antifibrinolytics, mini-circuits, retrograde autologous priming, ultrafiltration, and the use of red cell salvage using a cell saver.

  • If at risk for postoperative bleeding, measure Hb, platelet count, fibrinogen level, and INR 30 min before separation from CPB. Notably, Clauss fibrinogen and INR can only be used on CPB if the assay is insensitive to heparin (≥5 U unfractionated heparin/mL).

  • ROTEM is an accurate and rapid tool for the analysis of coagulation pathways. Perform ROTEM/TEG during the rewarming phase of the bypass and recheck after each round of analysis. Notably, only ROTEM/TEG assays with a strong heparin inhibitor polybrene (e.g., in EXTEM, FIBTEM, and APTEM) or heparinase (e.g., in HEPTEM and heparinaseTEG) can be used already during rewarming before weaning from CPB.

  • Optimize the pre-conditions for hemostasis: Core temperature, pH (BE, lactate), and ionized calcium.

  • Low-dose tranexamic acid reduces the need for transfusions and reoperations.

  • A restrictive red blood cell transfusion policy is not inferior to a liberal transfusion policy.

  • Intraoperative hemodilution should be used on an individual basis only in patients with a high pre-operative hemoglobin level.

  • Prophylactic or empiric plasma transfusion should be avoided since it increases the need for PRBC and platelet transfusion and is associated with an increased risk of TACO, TRALI, TRIM, thrombosis, and mortality.

  • Protamine should be used in a ratio of 0.7–0.8:1 (protamine to heparin), and ratios above 1:1 should be avoided since excess protamine results in factor V inhibition and platelet dysfunction.

  • Administration of fibrinogen optimizes coagulation in case of hypofibrinogenemia but should not be routinely given as prophylaxis.

  • Prothrombin complex concentrates, but not fresh frozen plasma, should be used to reverse the effects of oral anticoagulation (vitamin Kantagonists).

  • rFVIIa should only be considered in cases of uncontrolled bleeding as the last resort, with no other therapeutic options remaining.

rFVIIa: Recombinant activated factor VII, TACO: Transfusionassociated circulatory overload, TRALI: Transfusionrelated lung injury, TRIM: Transfusionrelatedimmunomodulation, CPB: Cardiopulmonary bypass, POC: Pointofcare, Hb: Hemoglobin, INR: International normalized ratio, ROTEM/TEG: Rotational thromboelastometry / Thrombelastography; FIBTEM: Fibrin-based thromboelastometric test, APTEM: Activated Partial thromboelastometric test, HEPTEM: Heparinase assay based thromboelastometric test, EXTEM: Extrinsically activated thromboelastometric test, PRBC: Packed red blood cells, APTEM: Aprotinin based thromboelastometric test for hyperfibrinolysis

Table 2: Important considerations and intraoperative algorithm for targeted transfusion in pediatric cardiac surgery when POC testing isavailable.
S. No. Goal ROTEM delta or sigma or TEG 5000 or TEG 6s Supplement with
1. Rule out residual heparin (and avoid Protamine overdose) ACT postprotamine >1.2×ACT baseline
and
INTEM CT/HEPTEM CTratio ≥1.25
OR ACT postprotamine >1.2×ACT baseline
AND KaolinTEG Rtime >heparinaseTEG Rtime×1.25
Protamine
(0.3–0.5 mg/kg)
2. Restore fibrinogen EXTEM A5 <25 mm AND FIBTEM A5 <7 mm (FIBTEMbased dose calculation) OR RapidTEG or kaolin TEG MA <40 mm AND
TEG FF <10 mm
Fibrinogen concentrate OR cryoprecipitate
3. Restore platelets (additional platelet function testing may be considered) EXTEM A5 <25 mm
AND
FIBTEM A5 ≥7 mm
OR RapidTEG or kaolinTEG MA <40 mm AND
TEG FF ≥10 mm
Platelets
(5–10 mL/kg)
±DDAVP
(0.3 μg/kg)
4. Replace enzymatic factors (thrombin generation) EXTEM CT>90 s AND
FIBTEM A5≥7 mm (since low fibrinogen prolongs CT results but cannot be treated with FFP or 4FPCC)
OR Heparinase TEG Rtime >12 min
(Notably, TEG Rtime cannot be used to guide PCC since this requires an extrinsically activated assay)
FFP
(10–15 mL/kg)
OR
4FPCC
(10–15 U/kg)
5. Block fibrinolysis (Treat as early as suspected/detected) EXTEM A5 <25 mm OR EXTEM or FIBTEM ML >7% @ 30 min (LI30 <93%) OR EXTEM or FIBTEM ML >15% @ 60 min (LI60 <85%) OR LY30 >7.5% (Notably, TEG LY30 is 30 min after MA and ROTEM LI30 is 30 min after CT) EACA
or
TXA

POC: Pointofcare, TXA: Tranexamic acid, EACA: Epsilonaminocaproic acid, ACT: Activated clot time, DDAVP: Desmopressin acetate, FFP: Fresh frozen plasma, PCC: Prothrombin complex concentrate, EACA: Epsilon-aminocaproic acid, TXA: Tranexamic acid, ROTEM: Rotational thromboelastometry

Evidence-based thromboelastometry (ROTEM)-guided bleeding management algorithm for pediatric cardiac surgery (Courtesy of Klaus Görlinger, Essen, Germany). ML: Maximum lysis, FFP: Fresh frozen plasma, PCC: Prothrombin complex concentrate, ACT: Activated clot time, TRAPTEM: ROTEM platelet assay with Thrombin receptor-activating peptide, HEPTEM: Heparin based thromboelastometric test for hyperfibrinolysis. ADPTEM: Adenosine di-phosphate based thromboelastometric test.
Figure 1:
Evidence-based thromboelastometry (ROTEM)-guided bleeding management algorithm for pediatric cardiac surgery (Courtesy of Klaus Görlinger, Essen, Germany). ML: Maximum lysis, FFP: Fresh frozen plasma, PCC: Prothrombin complex concentrate, ACT: Activated clot time, TRAPTEM: ROTEM platelet assay with Thrombin receptor-activating peptide, HEPTEM: Heparin based thromboelastometric test for hyperfibrinolysis. ADPTEM: Adenosine di-phosphate based thromboelastometric test.

In summary, the implementation of thromboelastometry-guided bleeding management algorithms in pediatric cardiac surgery requires education, knowledge, and interdisciplinary communication, collaboration, and consensus, but – if implemented – cannot only reduce transfusion requirements and costs but also has a high potential to improve patient safety and outcomes in this vulnerable patient population. This has been demonstrated impressively by the team from AIIMS in New Delhi, India, and I hope that others will follow their path.[7]

Conflicts of interest

KG works as the Medical Director of TEM Innovations GmbH/Werfen PBM, Munich. Germany.

References

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