When blood products are indicated.

A working reference for veterinary teams on where packed red blood cells and fresh frozen plasma have a role in small animal practice. This page describes indication categories. It is not a protocol, and it does not replace your own clinical judgement about a specific patient.

On transfusion triggers.

We have deliberately not published haematocrit thresholds on this page. The decision to transfuse rests on the whole patient: the rate of change, the presence of ongoing loss, oxygen delivery, tachycardia, lactate, mentation and anticipated trajectory. A chronically anaemic dog can be comfortable at a number that would be an emergency in an acute bleed. Treat the animal, not the value.

Packed red blood cells

When oxygen-carrying capacity is the problem.

Red cells are indicated where the patient cannot deliver enough oxygen to tissue, rather than wherever the haematocrit looks low. Packed cells rather than whole blood avoids giving volume to a patient who does not need it.

Indication

Immune-mediated haemolytic anaemia (IMHA)

Among the most common reasons a dog needs red cells. Destruction can outpace even a vigorous regenerative response, and patients often present profoundly anaemic and hypoxic. These patients need a cross-match rather than an assumption, because autoantibody complicates compatibility testing and many have been transfused before.

  • Cross-match essential. Discuss interpretation with us.

Indication

Tick-borne disease with severe anaemia

Babesiosis, ehrlichiosis and anaplasmosis are a leading cause of transfusion-requiring anaemia in Indian small animal practice. Babesia in particular can produce rapid haemolysis in an otherwise healthy young dog. Red cell support buys time while specific therapy takes effect.

  • Screen the patient. Our donors are PCR screened.

Indication

Acute haemorrhage: trauma and surgery

Road traffic accidents, splenic rupture, haemoabdomen, and intraoperative or post-operative bleeding. In acute blood loss the haematocrit lags behind the true deficit, so the clinical picture matters more than the first number you get.

  • Consider plasma alongside red cells in massive haemorrhage.

Indication

Chronic blood loss

Gastrointestinal ulceration, neoplastic bleeding, severe hookworm or flea burden. These patients compensate over weeks and can tolerate remarkably low haematocrits, so the decision to transfuse rests on clinical signs and trajectory rather than a single threshold.

  • Treat the source alongside the anaemia.

Indication

Non-regenerative anaemia

Chronic kidney disease, bone marrow disease, chronic inflammatory disease and pure red cell aplasia. Transfusion is supportive rather than curative here, and repeated transfusion raises the risk of sensitisation, which makes typing and cross-matching progressively more important.

  • Repeat transfusions: cross-match every time.

Indication

Perioperative support

Planned support for a patient going into a procedure with a marginal haematocrit, or where significant blood loss is anticipated. Planned transfusions are the ones we can prepare for best, so tell us early.

  • Give us notice where the case is elective.

Fresh frozen plasma

When the problem is clotting, or protein.

Plasma carries coagulation factors, albumin, immunoglobulins and antiproteases. It is not a volume expander and it is not a substitute for red cells, and using it as either is the most common way it gets wasted.

Indication

Anticoagulant rodenticide toxicity

A frequent emergency presentation, and one where plasma is genuinely lifesaving. Vitamin K antagonism depletes factors II, VII, IX and X, and while vitamin K1 is the definitive treatment it takes hours to restore synthesis. Plasma replaces the missing factors immediately in a patient who is already bleeding.

  • Plasma bridges the gap until vitamin K1 works.

Indication

Hepatic coagulopathy

The liver synthesises most clotting factors, so significant hepatic dysfunction produces a coagulopathy that no amount of vitamin K will fix. Relevant before liver biopsy or any invasive procedure in a patient with compromised hepatic function.

  • Consider before biopsy in hepatic patients.

Indication

Disseminated intravascular coagulation (DIC)

Consumptive coagulopathy secondary to sepsis, heatstroke, neoplasia, pancreatitis or severe trauma. Plasma replaces consumed factors and antithrombin while the underlying trigger is addressed. Plasma alone will not resolve DIC if the primary process is untreated.

  • Treat the trigger. Plasma is supportive.

Indication

Hypoproteinaemia and hypoalbuminaemia

Protein-losing enteropathy, protein-losing nephropathy, severe burns and extensive wounds. Plasma provides albumin and oncotic support, though large volumes are needed to move albumin meaningfully, so it is generally one part of a broader plan.

  • Volume required is often underestimated.

Indication

Severe acute pancreatitis

Plasma supplies alpha-macroglobulins and antiproteases alongside coagulation factors, and is used in severe cases, particularly where there is evidence of consumptive coagulopathy or significant protein loss.

  • Reserve for severe cases.

Indication

Sepsis

Septic patients frequently develop coagulopathy, hypoalbuminaemia and antithrombin depletion together. Plasma addresses several of these at once while source control and antimicrobial therapy do the definitive work.

  • Adjunctive to source control.

Indication

Congenital coagulopathies

Von Willebrand disease, haemophilia A and haemophilia B. Usually needed around surgery, dentals or trauma in a known affected animal. If you have a diagnosed patient in your practice, register them with us in advance so we are not sourcing under pressure.

  • Tell us about known patients before they bleed.

Transfusion planning

Four decisions before administration begins.

Product selection is one part of the case. Patient trajectory, compatibility, baseline observations and a monitoring plan determine whether the transfusion is managed safely.

01 — Clinical focus

Read the trajectory, not one value

Rate of change, ongoing loss, perfusion, lactate, mentation and anticipated clinical course all affect the decision. Acute and chronic anaemia cannot be interpreted the same way.

02 — Clinical focus

Establish compatibility

Type the patient and review every previous transfusion. Cross-match any previously transfused patient and any case in which immune-mediated disease complicates interpretation.

03 — Clinical focus

Record a baseline

Document PCV or haematocrit, total solids, temperature, pulse and respiratory rate before administration. Without a baseline, a reaction can be difficult to distinguish from the underlying disease.

04 — Clinical focus

Plan monitoring and reaction response

Observe closely from the start of administration, record changes, stop and assess when a reaction is suspected, and report the outcome. That record matters if the patient needs another transfusion.

Choosing a component

Quick reference.

Component selection by presenting problem
Presenting problemComponentNotes
Anaemia, no bleeding tendencyPacked red cellsAvoids unnecessary volume. Cross-match if previously transfused.
Coagulopathy, normal haematocritFresh frozen plasmaRodenticide, hepatic disease, congenital factor deficiency.
Massive acute haemorrhageBothLarge-volume red cell replacement without plasma risks a dilutional coagulopathy.
Hypoalbuminaemia, no anaemiaFresh frozen plasmaSubstantial volumes needed. Consider as part of a wider plan.
Severe babesiosisPacked red cellsAlongside specific antiprotozoal therapy. Monitor for ongoing haemolysis.
Sepsis with DICFresh frozen plasmaAdjunctive. Source control remains the definitive treatment.

Before you transfuse

Things worth doing every time.

  • Type the patient. Especially any animal likely to need repeat transfusion.
  • Cross-match if there is any transfusion history, and in any immune-mediated process.
  • Record a pre-transfusion baseline. PCV, total solids, temperature, pulse and respiratory rate. Without it you cannot tell a reaction from the underlying disease.
  • Monitor closely through the first fifteen minutes. Most acute reactions declare themselves early.
  • Report reactions to us, including mild febrile ones. It is how the service gets safer.

What we need from you

To fill a request quickly.

  • Species, breed, age and body weight
  • Presenting problem and working diagnosis
  • Current PCV or haematocrit, and total solids
  • Blood type, if known
  • Transfusion history, including anything years ago
  • Whether the case is elective or an emergency
  • Your veterinary registration details, if you are not yet registered with us
For registered veterinary practitionersThis page describes indication categories and transfusion-planning considerations. It is not a treatment protocol for an individual patient.

Recipient care, monitoring and follow-up

Talk to us about a case.

If you have a patient now, or a known coagulopathic animal you would like on our radar before they need us, get in touch. Registered practices get the current product schedule and our contact protocol for urgent requests.