Human Albumin Solution (Surgical — Volume/Oncotic)
Brand names: Albuman, Alburex, Zenalb
Human albumin solution is a colloid plasma-volume expander derived from pooled human plasma, used in the surgical setting for volume replacement and to restore oncotic pressure where crystalloids alone are inadequate.
ClinCalc Pro is rebuilding its dose data from primary open sources — the manufacturer SmPC (eMC), the WHO Model Formulary and other official references — under clinician review. This drug's structured dose is not yet published here. Confirm all doses against the product SmPC and your local formulary before prescribing.
Clinical monograph
How it works
Albumin is the major plasma protein and accounts for most of the intravascular oncotic (colloid osmotic) pressure, so an infusion draws and retains fluid within the vascular compartment to support circulating volume.
Prescribing in practice
- Infuse with caution in patients at risk of circulatory overload (cardiac failure, renal impairment) as the oncotic load can precipitate pulmonary oedema; stop the infusion at the first sign of hypervolaemia.
- Choose concentration by clinical aim — iso-oncotic solution for volume replacement, concentrated solution where fluid restriction or marked hypoalbuminaemia applies — and give through a standard infusion set without an additional filter.
- It is a blood-derived product: check the solution is clear before use, do not mix with packed red cells, protein hydrolysates or alcohol-containing solutions, and discard any unused portion of an opened container.
Monitoring
Monitor blood pressure, heart rate, urine output and signs of fluid overload during and after infusion, with haematocrit and electrolytes as guided by the clinical picture.
Counselling the patient
- Explain this is a human plasma-derived product given by drip to support blood volume during or after your operation.
- Tell staff at once if you feel breathless, flushed or develop a rash during the infusion.
Evidence & guidelines
Albumin is an established perioperative colloid; UK practice and the SPC reserve it for defined volume/oncotic indications rather than routine fluid resuscitation, where crystalloids are generally first-line.
Reference: SAFE Trial (NEJM 2004); NICE CPOC Perioperative Guidelines 2021; EASL Post-Paracentesis Guidelines; MHRA Blood Components Safety Update; Drug verified in RxNorm (NLM); confirm dosing against the manufacturer SPC (eMC). Verify against your local formulary and current prescribing references before prescribing. Monograph status: clinician-reviewed (2026-07-04).
Related
Curated clinical cross-links plus same-class fallbacks.
- Phenytoin Correction for Albumin / Renal Failure · Drug Dosing
- POSSUM Score for Surgical Morbidity and Mortality · Perioperative Risk
- SORT (Surgical Outcome Risk Tool) · Perioperative Risk
- Endotracheal Tube Depth and Tidal Volume Calculator · Airway Management
- ASA Physical Status Classification · Perioperative Risk
- Caprini Score for VTE Risk (2005) · VTE Risk
- Major Trauma — Primary Survey (ATLS) · ATLS 10th Edition; JRCALC; NICE NG39
- Major Haemorrhage / Massive Transfusion · BCSH; RCOA; RCEM; RCS — BCSH Guidelines
- Burns — TBSA Estimation & Fluid Resuscitation · British Burn Association; EMSB; RCEM 2024
- Lower Gastrointestinal Bleed · NICE; BSG; ACPGBI — Commissioning Guide
- Acute Pancreatitis · NICE; IAP/APA; ACPGBI — CG104
- Hypertrophic Pyloric Stenosis · BAPS / RCPCH