Fluid Therapy: Practical Guide with the ROSE Framework
1. What is fluid therapy?
Fluid therapy is the use of oral, enteral, or intravenous fluids to:
- Restore circulating volume and tissue perfusion
- Replace existing deficits and ongoing losses
- Provide daily water, electrolytes, and glucose needs
- Avoid or remove harmful fluid accumulation
It is a prescription, not just “putting up fluids.” Every prescription should state:
- Indication
- Fluid type
- Volume and rate
- Endpoint
- Monitoring and review time
The central questions are:
- Does the patient need fluid?
- Will cardiac output and perfusion improve if fluid is given?
- Can the patient tolerate additional fluid without pulmonary oedema or organ congestion?
- When should fluids stop or be removed?
2. Body-fluid basics
Body water compartments
In an average adult:
- Total body water: about 60% of body weight in men, lower in women, elderly people, and obesity
- Intracellular fluid: about two-thirds of total body water
- Extracellular fluid: about one-third
- Interstitial fluid: about 75% of extracellular fluid
- Intravascular plasma: about 25% of extracellular fluid
Therefore, only a fraction of an infused crystalloid remains intravascular. In acute illness with capillary leak, even less may remain in the circulation.
Tonicity
- Isotonic fluids mainly expand the extracellular space.
- Hypotonic fluids distribute into cells and may worsen cerebral oedema or hyponatraemia.
- Hypertonic fluids draw water from cells to extracellular fluid and must be used for specific indications with close monitoring.
3. Indications for IV fluids
A. Resuscitation
Use when there is shock or significant hypoperfusion due to:
- Hypovolaemia from vomiting, diarrhoea, dehydration, diuresis, or third-space loss
- Sepsis or septic shock
- Haemorrhage
- Burns
- Anaphylaxis
- DKA or hyperosmolar hyperglycaemic state
- Perioperative or trauma-related losses
B. Maintenance
Use only when oral or enteral intake cannot meet needs.
Typical adult maintenance estimate:
- Water: 25-30 mL/kg/day
- Sodium, potassium, chloride: roughly 1 mmol/kg/day each
- Glucose: 50-100 g/day to limit starvation ketosis
Reduce volumes in older adults, heart failure, kidney disease, liver disease, malnutrition, and frailty.
C. Replacement
Use to replace an identified deficit or measurable continuing loss, for example:
- Vomiting or nasogastric drainage
- Diarrhoea
- High-output stoma or fistula
- Polyuria
- Biliary or pancreatic drainage
- Burns
Replace the type and quantity of loss, while checking electrolytes and acid-base status.
4. Types of fluid
| Fluid | Main features | Typical role | Important cautions |
|---|
| Balanced crystalloid: Ringer's lactate, Hartmann's, Plasma-Lyte | Sodium concentration closer to plasma; contains buffers such as lactate or acetate; lower chloride than saline | First-line fluid for many resuscitation situations | Check compatibility and clinical context; do not use blindly in all patients |
| 0.9% saline | Isotonic sodium chloride, high chloride concentration | Hypochloraemia, some sodium-depletion states, selected neurological and drug-compatibility settings | Large volumes can cause hyperchloraemic metabolic acidosis and contribute to renal vasoconstriction |
| 5% dextrose | Provides free water after glucose metabolism | Maintenance component, hypoglycaemia-related indications | Not for shock resuscitation; can worsen hyponatraemia |
| 0.45% saline | Hypotonic | Selected hypernatraemia or protocol-specific indications | Not for initial resuscitation; may worsen hyponatraemia/cerebral oedema |
| Hypertonic saline | High sodium concentration | Severe symptomatic hyponatraemia, selected neurocritical care indications | Requires protocolized dosing and close sodium monitoring |
| Albumin | Colloid oncotic agent | Selected patients after large crystalloid exposure, or specific liver-related indications | Costly; not routine first-line resuscitation fluid |
| Blood products | Restores oxygen-carrying capacity and haemostatic components | Active haemorrhage / massive haemorrhage | Use haemorrhage protocol, warming, calcium and coagulation monitoring |
Balanced crystalloids are commonly preferred over saline for broad resuscitation because they avoid a high chloride load. This does not mean saline is prohibited, but it should be chosen deliberately.
5. The ROSE framework
ROSE organizes fluid management across the patient’s critical illness.
| Phase | Meaning | Clinical goal | Fluid approach |
|---|
| R | Resuscitation | Reverse immediately life-threatening hypoperfusion | Rapid but measured resuscitation |
| O | Optimization | Improve perfusion after immediate rescue | Give only if fluid responsive and tolerated |
| S | Stabilization | Maintain equilibrium and replace ongoing losses | Stop routine boluses; avoid fluid creep |
| E | Evacuation | Remove harmful accumulated fluid | De-resuscitate after shock resolves |
R: Resuscitation phase
Aim
Rapidly restore vital organ perfusion in shock.
Identify shock
Clinical clues include:
- Hypotension or falling blood pressure
- Tachycardia
- Cold peripheries, capillary refill over 2 seconds, mottling
- Altered mentation
- Oliguria
- Raised lactate or worsening metabolic acidosis
- Skin, gastrointestinal, respiratory, or traumatic evidence of fluid/blood loss
Typical adult approach
For suspected hypovolaemic or distributive shock:
- Give 500 mL isotonic crystalloid over less than 15 minutes
- Reassess immediately
- If appropriate, give a further 250-500 mL
- Escalate early if repeated boluses are needed, if total volume becomes substantial, or if shock persists
The
NICE IV-fluid algorithm uses this bolus-and-reassess model rather than unmonitored litres of fluid.
Do not delay cause-specific therapy
- Sepsis: antibiotics, source control, vasopressor when needed
- Haemorrhage: control bleeding, activate massive haemorrhage protocol
- Anaphylaxis: IM adrenaline first
- Cardiogenic shock: reperfusion/inotrope-vasopressor strategy, not routine fluid loading
- Obstructive shock: relieve tamponade, tension pneumothorax, or massive pulmonary embolic obstruction
O: Optimization phase
Aim
Improve oxygen delivery and organ perfusion while avoiding fluid overload.
After initial resuscitation, fluid is no longer automatically beneficial. A rise in blood pressure after fluid does not reliably prove that cardiac output rose, and a rise in cardiac output does not necessarily prove that further fluid will help.
Assess fluid responsiveness
A patient is more likely to benefit from fluid if stroke volume or cardiac output rises after a reversible “test.”
Useful bedside tests include:
- Passive leg raise: transfers venous blood from legs to central circulation without giving fluid
- Small fluid challenge, such as 250 mL, with objective reassessment
- Stroke-volume or cardiac-output monitoring where available
- Echocardiography and bedside ultrasound in experienced hands
Assess fluid tolerance
Even a fluid-responsive patient may not tolerate more fluid. Look for:
- Increasing oxygen requirement
- Crackles, B-lines on lung ultrasound, new pulmonary oedema
- Raised JVP, peripheral oedema
- Worsening right-heart congestion
- Rising intra-abdominal pressure
- Falling oxygenation or poor lung compliance
- Positive cumulative fluid balance
Fluid responsiveness asks: “Will output rise?”
Fluid tolerance asks: “Will harm occur if I give fluid?”
S: Stabilization phase
Aim
Maintain normal volume and electrolyte balance after shock is controlled.
At this stage, patients often receive unnecessary fluid through:
- Drug diluents
- Antibiotic carriers
- Nutrition
- Blood-product carriers
- Routine maintenance fluid
- Flushes and line keep-open fluids
This is called fluid creep.
Actions
- Stop resuscitation boluses once perfusion endpoints are met.
- Use oral or enteral fluids as soon as feasible.
- Replace only documented ongoing losses.
- Review all IV inputs daily.
- Monitor weight, cumulative balance, creatinine, sodium, potassium, chloride, acid-base status, and respiratory status.
- Adjust maintenance fluid for kidney, heart, or liver dysfunction.
E: Evacuation or de-resuscitation phase
Aim
Achieve safe removal of excess fluid once shock and active hypoperfusion have resolved.
Fluid accumulation is associated with pulmonary oedema, impaired gas exchange, impaired wound healing, gut oedema, abdominal hypertension, renal venous congestion, and delayed recovery.
Method
- Stop unnecessary IV fluid.
- Minimize sodium and hidden fluid inputs.
- Aim for neutral, then negative fluid balance when stable.
- Consider diuretics if perfusion and renal function permit.
- Use renal replacement therapy mainly when there is an independent indication, such as refractory fluid overload with kidney failure, severe hyperkalaemia, severe acidosis, or uraemic complications.
The
2025 ESICM de-escalation guidance supports de-escalation after the acute resuscitation phase and suggests protocolized diuretic-based removal rather than routine extracorporeal fluid removal.
6. Monitoring during fluid therapy
Clinical monitoring
- Heart rate, BP, MAP, pulse pressure
- Respiratory rate, SpO₂, oxygen requirement
- Capillary refill, temperature gradient, skin mottling
- Mental state
- JVP and peripheral oedema
- Chest examination
- Urine output
- Daily weight
- Input-output chart and cumulative fluid balance
Laboratory monitoring
- Electrolytes: sodium, potassium, chloride, bicarbonate
- Urea and creatinine
- Blood gas and lactate in shock
- Glucose
- Haemoglobin and coagulation profile if haemorrhage is possible
- Magnesium and phosphate in prolonged illness, DKA, malnutrition, or refeeding risk
Dynamic perfusion endpoints
- Improving mental status
- Falling lactate, interpreted in clinical context
- Improving capillary refill/peripheral perfusion
- Improving urine output
- Improved stroke volume/cardiac output after a reversible test
- Resolution of hypotension without evidence of congestion
Urine output is useful, but isolated oliguria should not automatically trigger fluid boluses. It can result from acute kidney injury, venous congestion, obstruction, neurohormonal response, or low cardiac output.
7. Disease-specific essentials
Sepsis and septic shock
- Use crystalloid for hypoperfusion.
- Balanced crystalloid is commonly preferred.
- Give initial fluid in measured increments with frequent reassessment.
- Early vasopressors are appropriate if hypotension persists despite a reasonable initial fluid trial.
- Avoid persistent positive balance after initial stabilization.
The
2025 ESICM volume guideline suggests up to 30 mL/kg of IV crystalloid in the initial phase of sepsis or septic shock, but emphasizes individualization and frequent reassessment.
Haemorrhagic shock
- Priorities are haemorrhage control, warming, calcium replacement when indicated, correction of coagulopathy, and early blood products.
- Minimize large-volume crystalloid.
- Consider permissive hypotension in selected uncontrolled haemorrhage patients.
- Do not use permissive hypotension in traumatic brain injury, where hypotension worsens secondary brain injury.
Cardiogenic shock
- Do not reflexively give fluid.
- If the patient is congested, fluid may worsen pulmonary oedema.
- Give a small, closely monitored test bolus only if true hypovolaemia or right-ventricular preload dependence is plausible.
- Obtain ECG, bedside echo, and early critical care/cardiology input.
DKA
- Start isotonic crystalloid.
- Use a protocol that integrates fluid therapy, potassium replacement, insulin, glucose, osmolality, and acid-base monitoring.
- Fluid rate and type should change as haemodynamics, sodium, glucose, and osmolality change.
Acute brain injury
- Avoid hypotension and hypoxia.
- Avoid hypotonic fluid.
- Use isotonic fluid and target adequate cerebral perfusion.
- Hypertonic saline has specific indications such as severe symptomatic hyponatraemia or selected raised intracranial-pressure management, not routine volume replacement.
Burns
- Major burns require formal burn-resuscitation calculations, frequent urine-output assessment, temperature control, and burn-centre input.
- Avoid both under-resuscitation and “fluid creep.”
Renal, cardiac, or liver disease
- Use smaller aliquots and reassess more frequently.
- Assess congestion early with clinical examination and ultrasound where available.
- Do not deny resuscitation when shock is present, but avoid routine maintenance and repeated blind boluses.
8. Complications of fluid therapy
| Complication | Causes | Prevention / response |
|---|
| Pulmonary oedema | Excess fluid, heart failure, renal failure, capillary leak | Stop fluid, assess congestion, oxygen/ventilatory support, diuretic or renal support where appropriate |
| Hyperchloraemic acidosis | Large volumes of 0.9% saline | Use balanced crystalloid when suitable; monitor chloride and bicarbonate |
| Hyponatraemia | Hypotonic fluid, excess free water | Avoid hypotonic fluids in shock and brain injury; monitor sodium |
| Hypernatraemia | Inadequate water, hypertonic therapy, diabetes insipidus | Match water deficit and monitor sodium correction rate |
| Hypokalaemia / hyperkalaemia | Potassium-free fluids, renal dysfunction, DKA treatment | Measure and replace or restrict potassium according to protocol |
| Dilutional coagulopathy | Large crystalloid volumes in bleeding | Early blood components and haemorrhage control |
| Hypothermia | Unwarmed fluid/blood in massive resuscitation | Use fluid/blood warmers |
| Abdominal compartment syndrome | Massive resuscitation, capillary leak | Avoid excessive accumulation; measure intra-abdominal pressure in high-risk cases |
| Tissue injury from infiltration/extravasation | Peripheral IV complications | Check IV site and use appropriate access |
9. Practical bedside algorithm
Step 1: Is the patient in shock or hypoperfusion?
- If yes, establish IV/IO access, monitor, obtain labs, identify the shock type, and treat the cause immediately.
Step 2: Is fluid indicated?
- Hypovolaemic/distributive shock: usually yes.
- Haemorrhage: blood products plus haemorrhage control.
- Cardiogenic/obstructive shock: fluid may be harmful or only conditionally useful.
Step 3: Give a measured trial
- Adult: 500 mL isotonic crystalloid rapidly, then reassess.
- Frail, heart failure, advanced CKD: smaller aliquots, for example 250 mL, with close monitoring.
- Children: weight-based aliquots with reassessment after every bolus.
Step 4: Reassess response and tolerance
- Better perfusion, BP, capillary refill, mentation, lactate, urine output?
- New crackles, hypoxia, raised JVP, oedema, B-lines, worsening work of breathing?
Step 5: Decide
- Responsive and tolerant: repeat a limited bolus if still indicated.
- Not responsive: stop repeated fluid and reconsider diagnosis, vasoactive therapy, inotropy, haemorrhage control, or obstruction.
- Not tolerant: stop fluids and treat congestion.
Step 6: Review daily
- Does the patient still need IV fluid?
- Is oral/enteral intake possible?
- Is there fluid accumulation requiring de-resuscitation?
10. High-yield exam points
- Crystalloids are first-line resuscitation fluids in most non-haemorrhagic shock states.
- Balanced crystalloids are often preferred for large-volume resuscitation.
- Normal saline is not “physiological” saline because of its high chloride concentration.
- In haemorrhagic shock, prioritize bleeding control and blood products, not litres of crystalloid.
- In cardiogenic shock, excessive fluid can be dangerous.
- Give fluids in boluses and reassess after each one.
- A patient may be fluid responsive but not fluid tolerant.
- Maintenance fluid must be reduced in frail patients and those with heart, renal, or liver failure.
- Stop fluids promptly when no longer needed.
- After acute resuscitation, aim to prevent positive cumulative balance and consider de-resuscitation when clinically stable.
Recent evidence includes systematic reviews of balanced crystalloid versus saline in critical illness and of ultrasound-assisted volume management, but results should not override disease-specific resuscitation protocols:
PMID 39832223 and
PMID 40366291.