Different Blood products

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blood products transfusion components overview

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Blood Products

Blood products (blood components) are derived from whole blood donations or by apheresis and are used to replace specific deficiencies. Modern transfusion medicine follows a component therapy approach — giving only what the patient needs.

1. Whole Blood

Rarely used today except in military/damage control settings. Modern practice fractionates it into components to maximize utility. When used, it provides RBCs, plasma, and platelets simultaneously.

2. Packed Red Blood Cells (pRBCs)

FeatureDetail
PreparationSeparated from whole blood; leukoreduced in most settings
Storage1–6°C for up to 42 days (with additive solutions)
Volume~350 mL per unit
Hematocrit~55–80%
CompatibilityABO and RhD matching required
Indications:
  • Symptomatic anemia unresponsive to medical therapy
  • Hemoglobin < 7 g/dL in stable ICU patients
  • Hemoglobin < 8 g/dL in cardiovascular disease or major orthopedic surgery
  • Active hemorrhage / hemorrhagic shock
Expected response: Each unit raises Hgb by ~1 g/dL and Hct by ~3% in a 70 kg adult.
Special preparations:
  • Leukoreduced (LR): Removes WBCs → reduces HLA alloimmunization, febrile non-hemolytic reactions (FNHTRs), and CMV transmission
  • Irradiated: Gamma-irradiation inactivates donor T-lymphocytes → prevents transfusion-associated graft-versus-host disease (TA-GvHD) in immunocompromised patients
  • CMV-negative: Used in CMV-seronegative immunosuppressed patients
  • Washed: Removes plasma proteins → for severe allergic/anaphylactic reactions or IgA deficiency

3. Platelets

FeatureDetail
PreparationPooled from 4–6 whole blood donations or single-donor apheresis
Storage20–24°C (room temperature), with continuous agitation, up to 5–7 days
Volume~50 mL (single unit) / ~250–300 mL (apheresis unit)
ABO compatibilityPreferred but not mandatory
Indications:
  • Platelet count < 10,000/µL (prophylactic in stable patients)
  • Platelet count < 50,000/µL before invasive procedures / surgery
  • Platelet count < 100,000/µL in CNS surgery or active microvascular bleeding
  • Qualitative platelet disorders with active bleeding
Key note: Apheresis platelets carry lower bacterial contamination risk than pooled units (fewer venipunctures, single donor). Platelets have the highest risk of bacterial contamination of all blood products because they are stored at room temperature.

4. Fresh Frozen Plasma (FFP)

FeatureDetail
PreparationPlasma separated and frozen within 8 hours of collection
Storage−18°C or colder, up to 12 months
Volume200–250 mL per unit
ContentsAll clotting factors, fibrinogen, natural anticoagulants (protein C, S, antithrombin)
ABO compatibilityRequired
Indications (Table 17-7, Barash):
  • Correction of inherited factor deficiencies when no specific concentrate exists (e.g., Factor V deficiency), with PT/aPTT >1.5× control or INR >2.0
  • Acquired multi-factor deficiencies with clinical bleeding (liver disease, DIC)
  • Massive transfusion / post-traumatic coagulopathy
  • Reversal of warfarin when PCCs unavailable
  • Treatment of TTP, HELLP, HUS
  • Heparin resistance from antithrombin deficiency (when AT concentrate unavailable)
  • Hereditary angioedema when C1-esterase inhibitor unavailable
Dose: Initial dose 10–20 mL/kg to achieve ≥30% factor activity.
Note: FFP is not recommended prophylactically for mild INR elevation (1.5–1.9) without clinical bleeding — evidence fails to show benefit.
Variants:
  • Thawed plasma: FFP thawed and stored at 1–6°C for up to 5 days; equivalent efficacy
  • Liquid plasma / Plasma Frozen within 24 hours (PF24): Slightly lower Factor V and VIII levels; practical for trauma centers

5. Cryoprecipitate

FeatureDetail
PreparationCold-insoluble precipitate from thawed FFP; re-frozen
Storage−18°C or colder, up to 12 months
Volume~15–20 mL per unit; typically pooled (10 units)
ContentsConcentrated fibrinogen (~150–250 mg/unit), Factor VIII, vWF, Factor XIII, fibronectin
Indications:
  • Hypofibrinogenemia (fibrinogen < 100–150 mg/dL) with active bleeding
  • DIC with fibrinogen depletion
  • Hemophilia A and vWD when specific concentrates unavailable
  • Factor XIII deficiency
  • Uremic bleeding (as bridge therapy)
Dose: 1 unit per 7–10 kg body weight; raises fibrinogen by ~50 mg/dL.

6. Fibrinogen Concentrate

A plasma-derived concentrate of fibrinogen (instead of cryoprecipitate). Advantages include:
  • Standardized dosing
  • Pathogen-reduced
  • No need for ABO matching
  • Faster to prepare than cryoprecipitate
Increasingly used in major hemorrhage protocols in Europe; growing adoption in the US.

7. Plasma Derivatives (Factor Concentrates)

ProductContentsUse
Factor VIII concentrateFactor VIII ± vWFHemophilia A
Factor IX concentrateFactor IXHemophilia B
vWF concentratevWF ± FVIIIvon Willebrand disease
Prothrombin Complex Concentrates (PCCs)Factors II, VII, IX, X (±Protein C, S)Warfarin reversal, acquired factor deficiencies
Activated PCC (aPCC / FEIBA)Activated factorsHemophilia with inhibitors
Recombinant Factor VIIa (rFVIIa)FVIIaLicensed: Hemophilia with inhibitors; Off-label: massive hemorrhage
Antithrombin (AT) concentrateAntithrombin IIIHeparin resistance from AT deficiency
AlbuminHuman albumin 5%, 25%Hypoalbuminemia, volume expansion
IVIGIgG antibodiesImmune deficiencies, immune thrombocytopenia

8. Emerging / Investigational Products

  • Pathogen-reduced platelets and plasma (e.g., Intercept system using amotosalen + UV): inactivates bacteria, viruses, and parasites
  • Cold-stored platelets (4°C): Longer shelf life, improved hemostatic function, being revisited for trauma
  • Lyophilized plasma: Freeze-dried FFP for pre-hospital and austere environments
  • Hemoglobin-based oxygen carriers (HBOCs): Still investigational
  • Reconstituted whole blood: 1:1:1 ratio of RBCs:FFP:platelets, used in massive transfusion protocols for trauma

Transfusion Triggers — Summary Table

ProductThreshold
pRBCs (stable ICU)Hgb < 7 g/dL
pRBCs (CVD / post-cardiac surgery)Hgb < 8 g/dL
Platelets (prophylactic)< 10,000/µL
Platelets (invasive procedure)< 50,000/µL
Platelets (CNS surgery / active bleeding)< 100,000/µL
FFPPT/aPTT > 1.5× control or INR > 2.0 with bleeding
CryoprecipitateFibrinogen < 100–150 mg/dL with bleeding

Compatibility Requirements

ProductABO RequiredRh Required
pRBCsYes (hemolysis risk)Yes (alloimmunization)
FFP / PlasmaYesNo
PlateletsPreferredPreferred in females of childbearing age
CryoprecipitateNot requiredNo
Emergency uncrossmatched blood: Group O RBCs (universal donor RBCs) and Group AB plasma (universal donor plasma) are used when there is no time for compatibility testing.

Source: Barash, Cullen, and Stoelting's Clinical Anesthesia, 9th ed., Chapter 17 — Blood Products and Transfusion Practice.
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