Fluid management in emergency patient

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"fluid therapy" AND emergency

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NICE intravenous fluid therapy adults hospital guideline resuscitation 2025

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https://www.nice.org.uk/guidance/cg174/resources/intravenous…

Fluid management in the emergency patient

Fluid therapy is an emergency intervention for hypovolaemia or inadequate tissue perfusion, not a default treatment for every low blood pressure. Use an ABCDE assessment and treat the cause at the same time.

1. Immediate assessment

Look for evidence of shock or significant fluid loss:
  • Hypotension, tachycardia, cold peripheries, delayed capillary refill
  • Altered mental status, oliguria
  • Raised lactate or metabolic acidosis
  • Bleeding, vomiting, diarrhoea, burns, sepsis, dehydration
  • Signs of fluid overload: raised JVP, pulmonary crackles, peripheral oedema, hypoxia
Obtain IV or IO access, monitor ECG, SpO₂, BP, temperature, urine output, and send blood tests including CBC, electrolytes, renal function, glucose, lactate, blood gas, group and crossmatch if bleeding is possible.

2. Choose the fluid by cause

Clinical situationInitial approach
Hypovolaemia from dehydration, gastrointestinal loss, sepsisBalanced isotonic crystalloid, such as Ringer's lactate or Plasma-Lyte, is generally preferred
Haemorrhagic shockControl bleeding and activate massive haemorrhage protocol early. Give blood products rather than large crystalloid volumes
Cardiogenic shock / pulmonary oedemaAvoid routine fluid loading. Give only a carefully monitored small test bolus if true hypovolaemia is suspected
AnaphylaxisRapid isotonic crystalloid plus IM adrenaline, airway and respiratory treatment
DKA / hyperosmolar stateIsotonic crystalloid initially, with protocol-driven electrolyte and insulin management
BurnsUse a burn-resuscitation formula and specialist input, while monitoring urine output and perfusion
Head injuryAvoid hypotonic fluids and avoid hypotension. Use isotonic crystalloid; blood products if haemorrhage is the cause
Balanced crystalloids reduce chloride exposure compared with 0.9% saline. Saline remains appropriate in selected situations, but repeated large volumes can contribute to hyperchloraemic metabolic acidosis. Goldman-Cecil Medicine, Fluid Resuscitation and Acute Kidney Injury, p. 463-467.

3. Adult fluid-resuscitation method

For an adult with suspected hypovolaemic shock:
  1. Give 500 mL isotonic crystalloid over less than 15 minutes.
  2. Reassess immediately using ABCDE.
  3. If still fluid responsive and no overload, repeat 250-500 mL aliquots.
  4. If more than approximately 2 L is needed, or the cause is uncertain, escalate to senior/emergency-critical care support and reassess the diagnosis.
The NICE IV-fluid algorithm recommends 500 mL crystalloid boluses with frequent reassessment, monitoring blood pressure, capillary refill, fluid balance, weight, renal function, and electrolytes.
Reassess after every bolus, not simply after a fixed total volume:
  • Mental state and skin perfusion
  • Heart rate, BP, pulse pressure
  • Capillary refill and extremity temperature
  • Respiratory rate, SpO₂, lung auscultation
  • Urine output, usually target at least 0.5 mL/kg/hour in adults
  • Lactate trend and acid-base status
  • Bedside ultrasound where expertise is available, including cardiac function, lungs, IVC, and passive-leg-raise response

4. Do not miss the major exceptions

Haemorrhagic shock

  • Priority: haemorrhage control, rapid transport to definitive care, warming, tranexamic acid where indicated, and early blood products.
  • Avoid large crystalloid volumes because they can worsen dilutional coagulopathy, acidosis, and bleeding.
  • In uncontrolled torso haemorrhage, use permissive hypotension rather than normalising BP before surgical or interventional control, unless traumatic brain injury is present.
  • Rosen describes a reasonable systolic BP target of roughly 70-90 mmHg while awaiting haemorrhage control in selected patients with uncontrolled bleeding. ROSEN's Emergency Medicine, p. 1170.

Sepsis / septic shock

  • Give crystalloid promptly when there is hypoperfusion, but reassess repeatedly and move early to vasopressors if hypotension persists after an appropriate initial volume.
  • A fixed 30 mL/kg approach is not appropriate for every person, especially with heart failure, renal impairment, or overt overload. The 2025 ESICM guideline summary suggests up to 30 mL/kg initially in sepsis or septic shock, adjusted to context and frequent reassessment.

Cardiogenic shock

  • Fluids are not the primary treatment for left-sided cardiogenic shock and may rapidly worsen pulmonary oedema.
  • If volume status is uncertain, use small aliquots only with close reassessment and consider early ultrasound, vasopressors/inotropes, and cardiology-critical care involvement.

Traumatic brain injury

  • Prevent hypoxia and hypotension. Do not use permissive hypotension if significant brain injury is suspected.
  • Avoid hypotonic fluid and avoid glucose-containing resuscitation fluids unless treating hypoglycaemia.

5. Paediatric principle

Children require weight-based boluses and more frequent review. A common initial approach is 10-20 mL/kg isotonic crystalloid, with smaller aliquots and caution in malnutrition, congenital heart disease, severe anaemia, renal disease, or possible cardiogenic shock. Tintinalli's Emergency Medicine, p. 1011.

6. Common errors

  • Giving fluid without deciding whether the patient is actually fluid responsive
  • Delaying blood products and haemorrhage control in active bleeding
  • Repeated blind boluses in heart failure, renal failure, or pulmonary oedema
  • Not monitoring urine output and cumulative balance
  • Continuing IV fluid after oral or enteral intake becomes adequate
  • Adding potassium directly to an IV fluid bag rather than using a prepared prescription and safe infusion system

Practical emergency rule

Fluid = a monitored therapeutic trial.
Give a measured bolus, look for improved perfusion, and stop or change strategy if there is no benefit or if congestion develops.
Recent systematic reviews on early resuscitation and dynamic assessment in sepsis support an individualized, reassessment-based approach, although patient populations and protocols vary: PMIDs 40637496 and 40953281.

Fluid therapy a2z details ROSE framek work guide

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Fluid therapy: A-to-Z topic map using the ROSE framework

ROSE describes fluid therapy as four time-based phases:
  1. R - Resuscitation: rapidly restore life-saving perfusion in shock
  2. O - Optimization: fine-tune cardiac output and tissue perfusion after initial rescue
  3. S - Stabilization: maintain balance, replace measured losses, prevent accumulation
  4. E - Evacuation / De-resuscitation: remove excess fluid after the acute phase
Fluid therapy also covers:
  1. Fluid physiology: body-water compartments, tonicity, osmolality, Starling forces, capillary leak
  2. Fluid assessment: hypovolaemia, fluid responsiveness, fluid tolerance, shock classification
  3. Fluid types: balanced crystalloids, normal saline, glucose solutions, hypertonic saline, albumin, blood products
  4. Indications: dehydration, sepsis, haemorrhage, burns, DKA, perioperative loss, anaphylaxis
  5. Monitoring: clinical perfusion, urine output, lactate, blood gas, electrolytes, bedside ultrasound, fluid balance
  6. Special situations: trauma, brain injury, cardiogenic shock, renal failure, liver disease, pregnancy, children
  7. Complications: pulmonary oedema, dilutional coagulopathy, hyperchloraemic acidosis, electrolyte disorders, abdominal compartment syndrome
  8. Stopping rules and de-resuscitation: when to stop fluids, diuretics, ultrafiltration, negative fluid balance

Core principle

Fluid should be prescribed like a drug:
Right patient, right fluid, right dose, right rate, right endpoint, and repeated reassessment.
The key question is not only “Will this patient respond to fluid?” but also “Can this patient tolerate fluid?”

ROSE at a glance

PhaseClinical aimFluid strategyMain risk
R - ResuscitationReverse immediately life-threatening hypoperfusionRapid, measured isotonic crystalloid bolus or blood products when bleedingUnder-resuscitation and organ ischaemia
O - OptimizationImprove perfusion without overloadSmall repeated boluses only if fluid responsive, then consider vasoactive supportFluid accumulation
S - StabilizationMaintain homeostasis after shock is controlledMaintenance plus replacement of documented losses“Fluid creep”
E - EvacuationRemove accumulated excess fluidStop unnecessary fluid, promote negative balance with diuresis or renal replacement therapy when appropriateHypoperfusion from over-removal

Important warning

The ROSE model is primarily used in critically ill adults. It is an organizing framework, not a substitute for protocols for haemorrhage, sepsis, DKA, burns, trauma, or paediatric shock. For example, active bleeding requires haemorrhage control and blood products rather than repeated crystalloid boluses.
Which section should I expand into a detailed, exam-style guide?
  1. ROSE framework in depth
  2. Fluid types and composition
  3. Assessment and monitoring
  4. Disease-wise fluid therapy
  5. Complications and de-resuscitation

Fluid therapy

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2025 ESICM fluid therapy adult critically ill patients clinical practice guideline

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:
  1. Indication
  2. Fluid type
  3. Volume and rate
  4. Endpoint
  5. 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

FluidMain featuresTypical roleImportant cautions
Balanced crystalloid: Ringer's lactate, Hartmann's, Plasma-LyteSodium concentration closer to plasma; contains buffers such as lactate or acetate; lower chloride than salineFirst-line fluid for many resuscitation situationsCheck compatibility and clinical context; do not use blindly in all patients
0.9% salineIsotonic sodium chloride, high chloride concentrationHypochloraemia, some sodium-depletion states, selected neurological and drug-compatibility settingsLarge volumes can cause hyperchloraemic metabolic acidosis and contribute to renal vasoconstriction
5% dextroseProvides free water after glucose metabolismMaintenance component, hypoglycaemia-related indicationsNot for shock resuscitation; can worsen hyponatraemia
0.45% salineHypotonicSelected hypernatraemia or protocol-specific indicationsNot for initial resuscitation; may worsen hyponatraemia/cerebral oedema
Hypertonic salineHigh sodium concentrationSevere symptomatic hyponatraemia, selected neurocritical care indicationsRequires protocolized dosing and close sodium monitoring
AlbuminColloid oncotic agentSelected patients after large crystalloid exposure, or specific liver-related indicationsCostly; not routine first-line resuscitation fluid
Blood productsRestores oxygen-carrying capacity and haemostatic componentsActive haemorrhage / massive haemorrhageUse 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.
PhaseMeaningClinical goalFluid approach
RResuscitationReverse immediately life-threatening hypoperfusionRapid but measured resuscitation
OOptimizationImprove perfusion after immediate rescueGive only if fluid responsive and tolerated
SStabilizationMaintain equilibrium and replace ongoing lossesStop routine boluses; avoid fluid creep
EEvacuationRemove harmful accumulated fluidDe-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

  1. Stop unnecessary IV fluid.
  2. Minimize sodium and hidden fluid inputs.
  3. Aim for neutral, then negative fluid balance when stable.
  4. Consider diuretics if perfusion and renal function permit.
  5. 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

ComplicationCausesPrevention / response
Pulmonary oedemaExcess fluid, heart failure, renal failure, capillary leakStop fluid, assess congestion, oxygen/ventilatory support, diuretic or renal support where appropriate
Hyperchloraemic acidosisLarge volumes of 0.9% salineUse balanced crystalloid when suitable; monitor chloride and bicarbonate
HyponatraemiaHypotonic fluid, excess free waterAvoid hypotonic fluids in shock and brain injury; monitor sodium
HypernatraemiaInadequate water, hypertonic therapy, diabetes insipidusMatch water deficit and monitor sodium correction rate
Hypokalaemia / hyperkalaemiaPotassium-free fluids, renal dysfunction, DKA treatmentMeasure and replace or restrict potassium according to protocol
Dilutional coagulopathyLarge crystalloid volumes in bleedingEarly blood components and haemorrhage control
HypothermiaUnwarmed fluid/blood in massive resuscitationUse fluid/blood warmers
Abdominal compartment syndromeMassive resuscitation, capillary leakAvoid excessive accumulation; measure intra-abdominal pressure in high-risk cases
Tissue injury from infiltration/extravasationPeripheral IV complicationsCheck 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.
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