Foundations — the weaning journey
Start here. This gives you the mental map for the entire consultation.
🫁 What mechanical ventilation actually does
A ventilator pushes air into the lungs using positive pressure. This is the opposite of how we normally breathe — we pull air in by contracting the diaphragm, creating negative pressure. This difference matters enormously for weaning.
Positive pressure ventilation: easier on the heart (reduces preload and afterload), but causes diaphragm atrophy over time, risk of lung injury, and infection. The longer a patient stays on it, the harder it gets to come off.
Weaning = returning to negative pressure breathing. Every step in the weaning process is about transferring work from the machine back to the patient, while checking they can handle it.
🔄 The weaning trajectory: controlled → spontaneous → extubation
Think of this as a journey with three stages. ARISE currently handles Stage 3. Phase 2 adds Stages 1 and 2.
CONTROLLED
VC-AC / PC-AC
↓
Machine does all the work.
Patient's lungs are resting.
SPONTANEOUS
PSV / PAV
↓
Patient breathes on their own.
Machine gives a pressure boost.
EXTUBATION
SBT → tube out
↓
Tube removed.
HFNC or NIV if high risk.
The expert's job (and what your questions extract) is the decision logic at each arrow: what parameters trigger the step-down, and what makes them hold back?
⚖️ The supply-demand framework — the single most important concept
Weaning failure is fundamentally an imbalance between what the respiratory system needs to do (demand/load) and what it can do (supply/capacity). Every parameter in this guide sits on one side of this balance.
Supply (capacity)
- Respiratory muscle strength (NIF)
- Diaphragm function (DTF on ultrasound)
- Respiratory drive (P0.1)
- Nutritional status (protein, phosphate, Mg)
- Psychological readiness
Demand (load)
- Airway resistance (secretions, bronchospasm)
- Lung stiffness (low compliance)
- Minute ventilation need (fever, acidosis)
- Auto-PEEP (hidden threshold load)
- Dead space (wasted ventilation)
💡 Think of it this way
Imagine carrying a backpack up a hill. Supply = your leg strength and fitness. Demand = how heavy the backpack is and how steep the hill. A patient can have strong legs (good NIF) but still fail the hike if the backpack is too heavy (high resistance, stiff lungs, auto-PEEP). The expert's job is figuring out which side to fix.
📊 The three weaning categories
International consensus classifies weaning difficulty into three groups. This tells you which part of ARISE Phase 2 matters for which patient:
Simple
~65% of patients. Extubated on 1st SBT. Current ARISE handles this.
Difficult
~20%. Up to 3 SBTs or 7 days. Phase 2 SBT failure pathways target this.
Prolonged
~15%. >3 SBTs or >7 days. Phase 2 PS step-down protocol targets this.
🏥 The ventilator mode spectrum
Every ventilated patient is on a mode somewhere on a spectrum from full machine control to full patient control:
- VC-AC (Volume Control – Assist Control): Machine sets tidal volume and rate. Delivers every breath. Patient can trigger extra breaths but machine delivers each in full.
- PC-AC (Pressure Control – Assist Control): Machine sets pressure and rate. Tidal volume varies with the patient's lung compliance.
- SIMV (Synchronized Intermittent Mandatory Ventilation): Shared — machine gives mandatory breaths, patient breathes spontaneously between them. Historically used for weaning but falling out of favour.
- PSV (Pressure Support Ventilation): Patient controls everything. Machine just adds a pressure boost (e.g., PS 10 cmH₂O) to each patient-initiated breath.
- PAV+ (Proportional Assist Ventilation): Machine amplifies the patient's own effort by a set percentage (e.g., 30% assist).
- T-piece: No ventilator support at all — just humidified oxygen through the tube. Completely unassisted breathing.
💡 Think of it this way
Think of a bicycle with electric assist. VC-AC = fully electric bike (motor does all work, you just steer). PSV = pedal-assist (you pedal, motor adds boost). T-piece = regular bike (all you). Weaning = gradually turning down the motor until the patient can pedal alone.
Block 1 — Mode transition & respiratory drive
15 minutes. Show the parameter audit flowchart.
Q11, Q12, Q13, Q14, Q15 + Q28, Q29
🧠 P0.1 — airway occlusion pressure (Q12)
P0.1 is the pressure measured at the airway 100 milliseconds after the start of an inspiratory effort against a briefly occluded airway. It measures respiratory drive — how hard the brain is telling the muscles to breathe.
How it's measured: Most modern ventilators (Hamilton, Draeger, Maquet) can do this automatically. The ventilator briefly occludes the airway for 100ms at the start of a breath and measures the pressure drop. The patient doesn't notice. No special equipment — just a button press.
💡 Think of it this way
P0.1 is like measuring how hard someone stamps on the accelerator pedal in the first 0.1 seconds. A gentle press = calm driving. Slamming the pedal = panic or steep hill. It tells you about the driver's urgency, not the car's engine power.
🔢 P0.1 thresholds to know
< 1.5 cmH₂O
Low drive — over-sedation? central depression? neuromuscular weakness?
1.5 – 3.5 cmH₂O
Normal — sweet spot. Good sign for weaning.
> 4 cmH₂O
High drive — excessive load, anxiety, metabolic demand. May fatigue quickly.
> 4 in COPD
Vargas 2008: P0.1 >4 + expiratory flow limitation predicts COPD extubation failure.
💪 NIF / MIP — muscle strength (Q13)
NIF (Negative Inspiratory Force) or MIP (Maximum Inspiratory Pressure) measures the strongest breath a patient can take. It directly measures inspiratory muscle strength, primarily the diaphragm.
Important nuance: NIF is effort-dependent — the patient has to try their hardest. A sedated or confused patient may give a falsely weak reading.
🔢 NIF thresholds to know
More negative than −30
Strong muscles. Good predictor of success. (e.g., −40 cmH₂O)
−20 to −30
Borderline. May succeed with optimisation.
Weaker than −20
Weak muscles. Higher risk of failure. (e.g., −15 cmH₂O)
COPD: < −19
Elkholy 2021: specific COPD cutoff for extubation failure.
💡 Think of it this way
NIF is a grip-strength test for your breathing muscles. A strong grip (−40) means you can probably hold yourself up. A weak grip (−15) means you might drop the bar. But the test requires the patient to actually squeeze — if they're drowsy, the score doesn't reflect true strength.
📡 Triggered breaths (Q15)
On controlled modes (VC-AC, PC-AC), the machine delivers breaths at a set rate. But patients can also trigger additional breaths by making an inspiratory effort the ventilator detects.
If a patient on VC-AC set at 14 breaths/min is actually breathing at 20/min, that means 6 breaths are patient-triggered. A high percentage of triggered breaths (>50–60%) suggests the patient's respiratory drive is active and they may be ready to do more work.
Most ventilators display this but clinicians may not systematically check it. Q15 asks whether the expert uses it.
👂 Listen for in Block 1
👂
"I look at the patient" — Gestalt assessment vs checklist. If they say this, follow up: "What specifically are you reading? Accessory muscle use? Breathing pattern? Comfort level?"
👂
"triggering over the set rate" — They're describing triggered breath percentage. Ask: "What ratio makes you confident enough to step down?"
👂
"we don't really use P0.1" — Important! Ask why: training gap? ventilator doesn't support it? don't trust it? This determines if ARISE includes it as core or educational.
👂
"FiO₂ below X, PEEP below Y" — They're giving you the step-down checklist. These are the exact thresholds ARISE Phase 2 needs. Write them down precisely.
👂
"I had a patient last week who..." — Gold! Case-based reasoning reveals the nuances that checklists miss. Let them tell the story, then extract the decision logic afterwards.
⚠️ Common misunderstanding
NIF and P0.1 measure different things. P0.1 = respiratory drive (how urgently the brain wants to breathe). NIF = respiratory strength (how hard the muscles can actually pull). A patient can have high drive but low strength (brain is screaming but muscles are too weak), or low drive but adequate strength (over-sedated but muscles are fine). The combination matters more than either alone — this is what Q29 targets.
Block 2 — Respiratory mechanics & muscle assessment
15 minutes. Show the parameter audit flowchart (Categories C, D).
Q16, Q17, Q18, Q19, Q20
📐 Compliance, resistance, and driving pressure (Q17)
These are the mechanical properties of the lungs and airways — all calculated from values already on the ventilator screen.
- Static compliance (Cstat) = Vt ÷ (Pplat – PEEP). How stretchy the lungs are. Low compliance = stiff lungs (ARDS, oedema, fibrosis).
- Airway resistance (Raw) = (PIP – Pplat) ÷ flow. How narrow the airways are. High resistance = obstruction (bronchospasm, secretions, kinked ETT).
- Driving pressure (ΔP) = Pplat – PEEP. How much pressure to inflate the lungs. A key safety metric — >15 cmH₂O is associated with lung injury.
Key insight: ARISE Tab 4 already collects PIP, Pplat, and PEEP. That means ARISE can auto-calculate all three — but currently doesn't. Q17 asks if experts value this.
🔢 Mechanics thresholds to know
Compliance > 50–60
mL/cmH₂O. Good for weaning. Below 25–30 = very stiff lungs.
Resistance < 5–10
cmH₂O/L/s. Normal. Higher = airway obstruction.
Driving pressure < 15
cmH₂O. Safety threshold. >15 = lung injury risk, harder weaning.
RSBI < 105
breaths/min/L. Classic weaning predictor. COPD-specific: <85.
💡 Think of it this way
Compliance = a balloon. A new balloon (normal lungs) inflates easily. An old thick balloon (stiff lungs) needs lots of pressure for a little volume. Resistance = the straw you're blowing through. A narrow straw (blocked airway) means you blow harder for the same flow. Driving pressure = the total effort to inflate one breath — it combines both problems.
🌬️ Auto-PEEP / intrinsic PEEP (Q16)
Auto-PEEP is trapped air pressure in the lungs at end-expiration that the ventilator doesn't know about. It happens when the patient doesn't have enough time to fully exhale before the next breath starts. Air stacks up.
Why it matters: Auto-PEEP acts as a hidden threshold load. Before the patient can start inhaling, they must first overcome this trapped pressure. It's like trying to open a door with pressure pushing against it from the other side.
Common in: COPD, asthma — narrowed airways slow expiratory flow.
How to measure: Press "expiratory hold" on the ventilator — closes both valves at end-expiration. The pressure that equilibrates = total PEEP. Subtract set PEEP = auto-PEEP. If set PEEP is 5 and total is 9, auto-PEEP is 4 cmH₂O.
📷 Diaphragm ultrasound (Q18)
Bedside ultrasound of the diaphragm measures two things:
- Diaphragm Thickening Fraction (DTF): How much the diaphragm thickens during inspiration. Measured at the zone of apposition (between ribs, right side). DTF = (thickness at inspiration – thickness at expiration) ÷ expiration thickness × 100%. DTF > 30–36% predicts successful weaning.
- Excursion: How far the diaphragm moves downward. Measured with M-mode at the subcostal window. Excursion > 10–14 mm during tidal breathing is adequate.
Q18 is partly a feasibility question. Does NUH MICU have the equipment, do consultants do it, do they trust it? If "we don't do it routinely," ARISE might include it as educational prompt rather than a required input.
❤️ Weaning-induced cardiac failure (Q19, Q28)
One of the most commonly missed causes of weaning failure. Here's why:
While on positive pressure ventilation, the machine pushes air in → positive intrathoracic pressure → reduces venous return (preload) and reduces LV afterload. The heart has it easier.
During an SBT, the patient switches to negative pressure breathing → suddenly increases venous return (more blood rushes back) AND increases LV afterload. In patients with heart failure or fluid overload, this triggers acute pulmonary oedema or ischaemia.
The patient looks like they're failing for respiratory reasons (tachypnoea, desaturation) but the real problem is the heart.
💡 Think of it this way
Think of the ventilator-to-spontaneous transition like removing a dam from a river. While the dam (positive pressure) is up, the downstream town (heart) handles the water flow fine. Remove the dam and suddenly more water rushes downstream. If the town's drainage can't cope, it floods (pulmonary oedema).
🔢 Cardiac weaning failure investigations
BNP > 200–300
pg/mL. Or rise >20% during SBT = cardiac cause likely.
Troponin rise
Any rise during SBT suggests weaning-induced ischaemia.
PLR +10%
Passive leg raise increases cardiac output >10% = fluid responsive.
Echo: E/e' elevated
Bedside echo shows raised filling pressures.
🔢 Electrolyte thresholds (Q20)
Both impair respiratory muscle contraction. Easily correctable — often overlooked.
Phosphate < 0.8
mmol/L. Impairs ATP production → diaphragm weakness. IV replacement.
Magnesium < 0.7
mmol/L. Affects neuromuscular transmission → muscle weakness.
👂 Listen for in Block 2
👂
"I do an expiratory hold" — They actively check for auto-PEEP. Ask: "In which patients? Always, or only COPD/asthma?"
👂
"driving pressure" — They use this derived value. Ask: "What threshold do you aim for before stepping down?"
👂
"BNP" or "echo during SBT" — They're investigating cardiac causes. This maps directly to ARISE's Phase 2 cardiac sub-pathway.
👂
"thickening fraction" — They use diaphragm ultrasound. Ask for their threshold and how often they do it.
👂
"we always check phosphate" — Direct ARISE checklist item. Ask: "Have you seen cases where correction changed the weaning outcome?"
Block 3 — SBT failure management
20 minutes. Show the revision plan document (failure reasons 1–7).
Q21, Q22, Q23, Q24 + Q30, Q31, Q33
🚨 Reason-specific failure pathways
When a patient fails an SBT, the reason drives completely different management. This is the core of Phase 2 — you're extracting decision trees, not lists of interventions.
- Tachypnoea (RR >35) — Q21: Is the respiratory system overloaded or are muscles fatigued? Progressive PS weaning vs rest-then-retry vs IMT.
- Desaturation (SpO₂ <90%) — Q22: Oxygenation or ventilation problem? The decision tree: secretions → suction; fluid → diuresis; atelectasis → recruitment/PEEP; V/Q mismatch → positioning.
- Agitation/drowsiness — Q23: Sedation-related or delirium-related? Different paths: sedation → hold/reduce drugs; delirium → CAM-ICU, dexmedetomidine.
- Haemodynamic instability — Q28 (NEW): Preload, afterload, or pump failure? PLR, fluid challenge, echo, BNP.
⚠️ What you're actually extracting
The most valuable thing is NOT a list of interventions — it's the decision tree. Push the expert: "When you see a patient desaturate during SBT, what is your FIRST step? Then what? What makes you choose diuresis over recruitment?" The sequential logic is what ARISE needs to implement.
🔧 Prolonged weaning: PS step-down protocol (Q30)
For patients who keep failing daily SBTs, the strategy shifts from "pass/fail gate" to "gradual conditioning." This is rehabilitation — building tolerance over time.
- Start at a comfortable PS level (e.g., PS 15 cmH₂O)
- Reduce PS by 2–4 cmH₂O every 4–24 hours, as tolerated
- At each level, check: RR <30, no accessory muscles, SpO₂ >92%, no distress
- If intolerant → go back up one step and rest 4–12 hours
- When tolerating PS 5–8 → ready for SBT
Some units use "exercise and rest" cycling: 2 hours on low PS (exercise), then 4–6 hours on higher PS (rest). This mimics muscle training — work, then recover.
🔀 Patient-ventilator dyssynchrony (Q31)
Dyssynchrony = patient and ventilator are not in sync. A significant cause of distress and prolonged weaning. Each type has a specific fix:
- Trigger dyssynchrony (ineffective efforts): Patient tries to breathe, ventilator doesn't detect it. Fix → increase trigger sensitivity, reduce auto-PEEP.
- Flow dyssynchrony (flow starvation): Patient wants more airflow than ventilator delivers. The pressure curve looks "scooped out." Fix → increase peak flow or rise time.
- Cycle dyssynchrony: Ventilator ends breath too early or too late. Fix → adjust expiratory cycling threshold.
- Double-triggering: Patient's effort triggers two consecutive breaths, one stacked on another. Fix → increase inspiratory time or tidal volume.
💡 Think of it this way
Dyssynchrony is like a dance partner who is out of step. Trigger dyssynchrony = you step forward but your partner doesn't move. Flow dyssynchrony = you want to waltz but they're doing a slow shuffle. Double-triggering = they take two steps when you only took one. The fix is always adjusting the partner (ventilator) to match the patient's rhythm.
🕐 Tracheostomy timing (Q24)
When daily SBTs keep failing and prolonged weaning protocols aren't progressing, the question of tracheostomy arises. Evidence suggests timing is highly context-dependent:
- No fixed number of failed SBTs — varies by patient profile
- Earlier consideration in neuromuscular patients (may need long-term ventilation)
- Later in post-surgical patients (more likely to recover)
- Usually discussed around 10–14 days of mechanical ventilation
👂 Listen for in Block 3
👂
"first I check..." / "then I..." — Sequential decision logic. This is the decision tree ARISE needs. Write it down step by step.
👂
"I step down by 2" or "by 4" — Specific PS reduction per step. These become configurable parameters in ARISE.
👂
"exercise and rest" — They use cycling protocols. Ask for the hours: how long on low PS, how long resting?
👂
"I'd try again in the afternoon" or "wait 48 hours" — Re-attempt timing logic. Ask: "What makes you wait longer?"
👂
"ineffective efforts" — They recognise trigger dyssynchrony. Follow up: "What's your first ventilator adjustment?"
👂
"trach at day..." — Their tracheostomy timing threshold. Ask: "Does this change for neuro patients vs COPD?"
Block 4 — Sedation strategy & optimisation
10 minutes. Show live ARISE tool on tablet.
Q32, Q34
💊 Sedation during active weaning (Q32)
Sedation strategy should change as patients move through the weaning trajectory — but many teams set a RASS target and leave it. Phase 2 needs to map sedation to ventilator mode stage:
- Controlled mode (early): RASS 0 to −2. Propofol/midazolam ± fentanyl. Keep comfortable, prevent dyssynchrony.
- Transitioning to spontaneous: RASS 0 to −1. Reduce sedation, consider dexmedetomidine. Patient needs to participate more.
- Pre-SBT: RASS 0. Low-dose fentanyl + dex per MICU protocol. Comfortable but awake.
- During SBT: RASS 0 to +1. Minimal or none. Need full respiratory effort for valid test.
🧪 Dexmedetomidine — why it's special for weaning
Dexmedetomidine (dex) is an alpha-2 agonist that provides light sedation without suppressing respiratory drive. This makes it uniquely suited for weaning:
- Provides anxiolysis and comfort without depressing breathing
- Treats hyperactive delirium (a cause of SBT failure)
- Your MICU protocol already mentions it pre-SBT
- Key question for Phase 2: does the expert use it more broadly during the whole weaning trajectory?
🥗 Nutrition and mobilisation (Q34)
These run parallel to ventilator management as part of the daily optimisation checklist:
- Protein: Respiratory muscle recovery requires adequate protein intake. Some experts target 1.2–1.5 g/kg/day.
- Caloric adequacy: Underfeeding worsens muscle wasting; overfeeding increases CO₂ production (more work of breathing).
- Early mobilisation: Sitting out of bed, even while ventilated, may improve SBT pass rates and reduce ICU delirium. Growing evidence base.
🫧 Dead space and ventilation efficiency
Dead space (Vd/Vt) is the proportion of each breath that's wasted — ventilating lung areas not participating in gas exchange. Normal ~0.3 (30%). In critically ill patients: 0.5–0.7.
Clinical estimation: Vd/Vt ≈ (PaCO₂ – EtCO₂) ÷ PaCO₂. If PaCO₂ = 45 and EtCO₂ = 30, Vd/Vt ≈ 0.33 (normal). If PaCO₂ = 50 and EtCO₂ = 20, Vd/Vt ≈ 0.60 (high!).
High dead space means the patient needs more total volume just to clear CO₂. This increases work of breathing and is a hidden cause of weaning failure that standard parameters miss.
👂 Listen for in Block 4
👂
"I switch to dex when..." — The sedation transition point. This becomes a recommendation trigger in ARISE.
👂
"RASS 0 for weaning" — They have stage-specific targets. Map these to ventilator modes.
👂
"sitting out of bed" or "physio before SBT" — Mobilisation practice. Ask: "Do you think this actually changes weaning outcomes?"
Block 5 — Synthesis, waveforms & safety
10 minutes. Show full ARISE tool + protocol.
Q25, Q26, Q27
📈 Ventilator waveforms — what you need to know (Q26)
You don't need to be a waveform expert. You just need to know what the three waveforms are and what they reveal:
- Pressure-time curve: Shows airway pressure over time. Useful for: high peak pressures, plateau pressure, and dyssynchrony patterns (scooped shape = flow starvation).
- Flow-time curve: Shows airflow in/out over time. Useful for: air trapping (expiratory flow doesn't return to zero before next breath), trigger delays, and auto-PEEP detection.
- Volume-time curve: Shows tidal volume delivery over time. Useful for: air leaks (volume doesn't return to baseline), auto-cycling.
Q26 is a prioritisation question — you're asking which patterns should junior doctors learn first. The expert will likely say 2–3 high-yield ones (air trapping pattern is almost always included).
🛡️ The safety question (Q27)
This is your most important question. Save it for last, after the expert has seen everything in ARISE.
You're asking: Is there anything in ARISE that could lead a clinician to make a wrong decision? This could be an incorrect threshold, a missing safety check, or a recommendation that doesn't match evidence.
👂 Listen for in Block 5
👂
"air trapping" on the flow-time curve — Almost universally cited as the most important waveform pattern. If they describe what it looks like, that's your visual reference card content.
👂
"I'd change..." — Direct protocol improvement suggestions. These are high-impact for the EBP submission.
👂
"that threshold is too high/low" — Clinical error in ARISE. Critical — write it down with their suggested correction.
👂
"a junior might think..." — They're identifying an edge case where ARISE could mislead. This is exactly what Q27 targets.
⚠️ If they say "nothing concerns me"
Push gently: "If a first-year resident used this tool unsupervised at 3am, is there any scenario where it could point them the wrong way?" Edge cases and worst-case scenarios reveal safety issues that best-case walkthroughs miss.
Tab 5 — Weaning Engine: How to Use It
Read this before using the Weaning Engine tab. Written for junior doctors who are new to advanced ventilator parameters.
🔧 What Tab 5 does and when to use it
Tab 5 is for patients who are already awake and tolerating their tube but you're not sure they're ready to step down to less support or attempt an SBT. It's also for patients who just failed an SBT — it generates a specific 24-hour plan based on why they failed.
Think of it as answering two questions:
- "Is this patient ready to do more work?" — The assessment section identifies barriers and gives a verdict.
- "My patient just failed their SBT — what do I do for the next 24 hours?" — The SBT failure section gives a reason-specific plan.
This tab does NOT replace Tab 2 (SBT readiness) or Tab 4 (extubation readiness). It adds a layer for patients in the weaning trajectory who need more than a pass/fail decision.
1️⃣ Step 1: Select the ventilator mode — the most important first step
The mode dropdown is the master switch that controls everything else. Different modes mean different parameters matter. You must select the correct mode or the assessment won't work properly.
CONTROLLED
VC-AC or PC-AC
→
Machine controls every breath. Question: "Is the patient ready to breathe more on their own?"
HYBRID
SIMV or APRV
→
Shared control. Question: "Can we reduce mandatory breaths toward spontaneous?"
SPONTANEOUS
PSV or PAV
→
Patient drives every breath. Question: "Is the patient ready for an SBT or extubation?"
⚙️ Controlled mode inputs — what they are and why they matter
- Vt (Tidal Volume, mL): How much air the machine pushes in each breath. Normal for ICU: 400–550 mL (6–8 mL/kg ideal body weight). Too high = lung injury risk.
- Set RR (/min): How many breaths the machine delivers per minute. Standard ICU setting: 12–18/min.
- PEEP (cmH₂O): Positive End-Expiratory Pressure — pressure kept in the lungs at end of expiration to prevent alveolar collapse. Typical: 5–10 cmH₂O. Must be ≤10 before weaning trial.
- PIP (Peak Inspiratory Pressure, cmH₂O): The highest pressure during each breath. Found on the ventilator screen continuously. High PIP may mean secretions, bronchospasm, or stiff lungs.
- Pplat (Plateau Pressure, cmH₂O): Pressure at end of inspiration with no flow — measured by pressing "Inspiratory Hold" on the ventilator for 0.5 seconds. Reflects lung stiffness. Target <28.
- Triggered breaths %: What percentage of breaths the patient started themselves. If set rate is 14/min but actual rate is 20/min, then (6÷20) = 30% are triggered. Target ≥80% to confirm adequate drive.
- Auto-PEEP: Hidden trapped air pressure. Measured by pressing "Expiratory Hold" on the ventilator. Check the box if present. Important in COPD/asthma — acts as an extra load the patient must overcome to start breathing.
Auto-calculated values (appear when you enter inputs):
- Driving Pressure (DP = Pplat − PEEP): How hard the lungs are being stretched per breath. Target <15 cmH₂O. Above 15 = lung injury risk and harder to wean.
- Static Compliance (Crs = Vt ÷ DP): How stretchy the lungs are. Normal: 50–60 mL/cmH₂O. Below 25 = very stiff lungs (ARDS, fluid overload).
- Airway Resistance (Raw = (PIP−Pplat) ÷ 0.5): How narrow/obstructed the airways are. Normal: <10 cmH₂O/L/s. Above 20 = significant obstruction (secretions, bronchospasm, kinked tube).
- Mechanical Power (MP, J/min): The total energy delivered to the lungs per minute. Target <15 J/min. A combined measure of how hard the machine is working — high values correlate with lung injury and prolonged ventilation.
🫁 Spontaneous mode inputs — what they are and why they matter
- PS Level (Pressure Support, cmH₂O): The pressure boost the machine adds to each patient-triggered breath. Higher PS = machine does more work. To do an SBT you need PS ≤5–8. Above PS 12 = patient is significantly dependent. Important: if PS ≥5 cmH₂O, the RSBI interpretation changes — see RSBI below.
- PEEP during spontaneous breathing (cmH₂O): Usually 5 cmH₂O. Lower than controlled settings.
- RR (/min): The patient's spontaneous breathing rate. Enter what you see on the monitor. Target <30–35 during weaning assessment.
- Vt (Tidal Volume, mL): The volume of each spontaneous breath the patient takes. Enter from the ventilator display. Smaller Vt with high RR = shallow rapid breathing = high RSBI = bad sign.
- RSBI (auto-calculated): Rapid Shallow Breathing Index = RR ÷ Vt(L). Classic weaning predictor. Standard cutoff: <105. Key nuance: on PSV ≥5 cmH₂O, the machine is assisting each breath, so RSBI looks artificially better — use cutoff of ~75 instead (Zhang & Qin 2014).
- P0.1 (cmH₂O, optional): Airway occlusion pressure — measures how urgently the brain is telling the body to breathe. Normal: 1.5–3.5. <1.5 = low drive (over-sedated?). >4–6 = very high drive (patient is struggling, muscles may fatigue).
- NIF/MIP (cmH₂O, optional): Maximum Inspiratory Pressure — measures how strong the breathing muscles are. More negative = stronger. Target: more negative than −30 cmH₂O. Weaker than −20 = significant muscle weakness. Note: NIF requires patient cooperation — an agitated or drowsy patient may give a falsely weak reading.
2️⃣ Step 2: Fill the common readiness indicators
These are the same for all three modes. They establish baseline readiness before mode-specific assessment:
FiO₂ ≤50%
Fraction of inspired oxygen. Must be ≤50% for weaning trial — ongoing high oxygen need = lungs not ready.
P/F ≥150
PaO₂÷FiO₂. Oxygenation index. Below 150 = too hypoxaemic for weaning trial.
pH ≥7.30
Blood pH. Below 7.30 = significant acidosis. Breathing muscles work less efficiently in acidaemia.
PaCO₂ — trend
Blood CO₂. Rising PaCO₂ means the patient is retaining CO₂ — early sign of fatigue or inadequate drive.
RASS −1 to +1
Sedation score. Must be within this range — too sedated (−2 or below) or too agitated (+2 or above) = not ready.
Norad ≤0.2
Noradrenaline dose mcg/kg/min. Above 0.2 = haemodynamic instability. Switching to negative pressure breathing will stress the heart further.
3️⃣ Step 3: Advanced panel (optional but powerful)
These require extra bedside tests. Click the chevron (▼) to expand. Use them when you have the data — each adds precision to the assessment.
- DTF % (Diaphragm Thickening Fraction): Measured by bedside ultrasound. Shows whether the diaphragm is actually contracting well. DTF >30–36% = adequate. Below 20% = significant diaphragm weakness — consider inspiratory muscle training.
- Excursion (cm): How far the diaphragm moves downward during each breath. Target >1.0 cm for tidal breathing.
- E/E' ratio: From bedside echo. Measures how stiff the left ventricle is during filling. Above 7.8 = diastolic dysfunction — high risk of weaning-induced pulmonary oedema (WiPO). The heart can't handle the extra load when you switch from positive to negative pressure breathing.
- AI % (Asynchrony Index): How often the patient and ventilator are out of sync. Count asynchronous breaths ÷ total breaths × 100. AI ≥10% → 33% extubation failure rate vs 6% when synchronised (Sousa 2020).
- Phosphate and Magnesium: Low levels impair muscle contraction — including the diaphragm. Phosphate <2.5 mg/dL or Mg <1.7 mg/dL = correct before weaning trial. Often missed on routine bloods.
- CAM-ICU positive: Tick this if the patient has active delirium. Delirium is a recognised cause of SBT failure and is the target for dexmedetomidine.
4️⃣ Step 4: Reading the results — what do barriers, warnings, optimise, and strengths mean?
After clicking Assess Readiness, results appear in four colour-coded categories. Understanding these is key to using the tool correctly.
Barriers
Must resolve before weaning trial. These are hard stops — proceeding despite a barrier significantly increases failure and re-intubation risk. Example: RASS −3 means the patient cannot generate adequate effort. Fix the barrier first, then reassess.
Warnings
Non-blocking but clinically significant. Do not prevent a trial but increase risk. Monitor these closely during the trial. Example: pH 7.32 — patient isn't in severe acidosis but watch for worsening.
Optimise
Actionable targets to improve before the next attempt. Examples: phosphate is low (replete it), triggered breaths only 60% (reduce sedation to improve drive). These won't stop you from trying but fixing them increases success probability.
Strengths
Parameters that are favourable. These are the patient's weaning assets — good RSBI, adequate DTF, normal P0.1. Useful to communicate to the team ("the patient has several favourable findings") and to document in your note.
💡 Think of it this way
The assessment is like a pre-flight checklist. Barriers = the engine won't start (don't take off). Warnings = a caution light is on (proceed carefully, monitor). Optimise = you can fly but the fuel efficiency is low (fix it before the next flight). Strengths = green lights (document them in the captain's log).
5️⃣ Step 5: The verdict and what to do next
Based on the mode and barriers, the system gives a step-down recommendation:
- Controlled — READY: "Patient meets criteria for a supervised spontaneous mode trial (PSV/PAV)." → Step down to PSV 8–12 cmH₂O. Reassess in 2–4 hours. If tolerating, proceed to SBT.
- Hybrid — READY: "Consider stepping down to PSV/PAV when mandatory rate ≤4 and triggered breaths ≥80%." → Reduce SIMV rate in steps (12 → 8 → 4) over hours/days. Switch to full PSV when mandatory rate reaches 0–4.
- Spontaneous — READY: "Spontaneous parameters favourable — proceed to SBT if not yet done, then extubation readiness assessment (Tab 4)." → Confirm with Tab 2 (SBT readiness) and Tab 4 (extubation readiness).
- Any mode — NOT READY: Address the listed barriers. Re-assess when resolved.
6️⃣ The SBT Failure Section — what it is and when to use it
After any assessment, the SBT Failure — 24h Optimization Plan section appears at the bottom of Tab 5. Use it when your patient just failed an SBT.
SBT failure is not a single problem — it has different causes that need completely different responses. Treating tachypnoea the same way as desaturation or haemodynamic instability leads to incorrect management.
How to use it: Select all the signs you observed during the failed SBT. You can choose multiple reasons. The system generates a reason-specific 24-hour plan for each one.
🔢 SBT failure reasons — what to look for and what they mean
Tachypnoea (RR >35)
Respiratory muscles are overwhelmed. Either too much load (high resistance/stiffness) or too little capacity (weak muscles, low NIF). Plan: IMT, progressive PS weaning, rest-then-retry.
Tachycardia (HR >140)
May be cardiac cause — switching to negative pressure breathing increased venous return and LV afterload. Needs PLR, echo, BNP/troponin. Not always a respiratory problem.
Desaturation (SpO₂ <90%)
Oxygenation failure. Sequential approach: suction → recruitment → PEEP → fluid removal. Find the level of the problem (airway, alveolar, or vascular).
Agitation / Delirium
CAM-ICU helps differentiate delirium from anxiety/pain. Delirium → dexmedetomidine + ABCDEF bundle. Pain → analgesia. Agitation alone → anxiolytic. Do not sedate everyone the same.
Drowsiness / Over-sedation
Under-recognised cause. Patient can't generate effort because they're sedated. Check P0.1 (if <1.5 = low drive). Review all infusions. Check PaCO₂ — rising CO₂ with drowsiness = ventilatory failure due to over-sedation.
Haemodynamic Instability
Vasopressor requirement, MAP falling, heart strain during SBT. The switch from positive to negative pressure is a cardiac stress test. Needs volume assessment (PLR), echo, BNP/troponin. If cardiac cause confirmed → treat heart before re-attempting.
Apnoea / Low Drive
Patient stops breathing during SBT. Could be central (brain not sending signal) or obstructive. Most common ICU cause: residual opioids or sedation. Check P0.1 — if very low (<1) suspect pharmacological suppression. Consider naloxone cautiously.
Diaphoresis / Excess WOB
Sweating during SBT = high work of breathing — patient is struggling. The body is compensating but will fatigue. Increase PS immediately to rest, check metabolic demand (fever, sepsis), replete electrolytes (phosphate, Mg).
⚠️ The tracheostomy flag
If you select 3 or more SBT failure reasons, the plan adds a tracheostomy consideration flag. This is not a recommendation to tracheostomise immediately — it's a prompt to have the conversation.
Multiple concurrent SBT failure reasons suggest a complex, multi-system problem that is unlikely to resolve within 24–48 hours. In patients with ≥3 failure reasons who have already been on mechanical ventilation for >7–10 days, early tracheostomy may reduce complications and allow for progressive rehabilitation.
💡 The overall mental model for Tab 5
Imagine you're teaching a patient to walk again after a long illness. Tab 5 is your physiotherapy assessment:
- Mode selection = which stage of rehabilitation are they at? (bedridden → standing → walking)
- Assessment = can they do the next stage? What's stopping them?
- Barriers = they can't even stand up yet — don't try walking
- Warnings = they can stand, but their balance is shaky — watch carefully
- Optimise = they could do better with better shoes and more protein
- SBT failure plan = they fell — here's why and here's the specific rehab plan for the next 24 hours
Quick reference — glossary & cheat sheet
Keep this open during the meeting for quick look-up.
📖 Abbreviations you'll hear
P0.1Airway occlusion pressure at 100ms — measures respiratory drive
NIF / MIPNegative Inspiratory Force / Maximum Inspiratory Pressure — muscle strength
RSBIRapid Shallow Breathing Index — f/Vt, <105 favourable
CstatStatic compliance — Vt ÷ (Pplat – PEEP), lung stretchiness
RawAirway resistance — (PIP – Pplat) ÷ flow
ΔPDriving pressure — Pplat – PEEP, target <15
Auto-PEEPIntrinsic PEEP — trapped air pressure, measured by expiratory hold
DTFDiaphragm Thickening Fraction — ultrasound measure, >30–36% good
Vd/VtDead space ratio — wasted ventilation, ≈ (PaCO₂ – EtCO₂) ÷ PaCO₂
BNPB-type Natriuretic Peptide — heart strain marker
PLRPassive Leg Raise — fluid responsiveness test
SBTSpontaneous Breathing Trial — 30-minute test of unassisted breathing
SATSpontaneous Awakening Trial — daily sedation hold at 8am
PSVPressure Support Ventilation — patient-triggered, machine assists
PAV+Proportional Assist Ventilation — machine amplifies patient effort by %
VC-ACVolume Control – Assist Control — fully controlled mode
PC-ACPressure Control – Assist Control — fully controlled, pressure-targeted
SIMVSynchronized Intermittent Mandatory Ventilation — hybrid mode
RASSRichmond Agitation-Sedation Scale — −5 (comatose) to +4 (combative)
CAM-ICUConfusion Assessment Method for ICU — delirium screening
CPOTCritical-Care Pain Observation Tool — pain assessment
GCS-MGlasgow Coma Scale – Motor component — airway protection proxy
IMTInspiratory Muscle Training — threshold devices for conditioning
HFNCHigh-Flow Nasal Cannula — post-extubation support
NIVNon-Invasive Ventilation — post-extubation support (BiPAP/CPAP)
PIPPeak Inspiratory Pressure — highest pressure during breath delivery
PplatPlateau Pressure — pressure at end-inspiration (inspiratory hold)
PEEPPositive End-Expiratory Pressure — prevents alveolar collapse
FiO₂Fraction of Inspired Oxygen — 0.21 (room air) to 1.0 (100%)
P/F ratioPaO₂/FiO₂ — oxygenation index, >150–200 for weaning readiness
EtCO₂End-Tidal CO₂ — exhaled CO₂, lower than PaCO₂ by dead space margin
DexDexmedetomidine — alpha-2 agonist, sedation without respiratory depression
VtTidal volume — volume of each breath (mL). Target 6–8 mL/kg IBW on controlled modes
PIPPeak Inspiratory Pressure — highest pressure reading during breath delivery, read continuously from ventilator
PplatPlateau Pressure — measured by inspiratory hold (0.5 sec), reflects lung stiffness, target <28
DP / ΔPDriving Pressure = Pplat − PEEP. How hard lungs are stretched per breath. Target <15 cmH₂O
CrsStatic compliance = Vt ÷ DP. Lung stretchiness. Normal 50–60 mL/cmH₂O; <25 = very stiff
RawAirway resistance = (PIP − Pplat) ÷ 0.5. Normal <10 cmH₂O/L/s; high = obstruction
MPMechanical Power (J/min) — total energy delivered to lungs per minute. Target <15 J/min
AI%Asynchrony Index — % of breaths where patient and ventilator are out of sync. ≥10% = 33% extubation failure rate
DTFDiaphragm Thickening Fraction — ultrasound, >30–36% adequate, <20% = weakness
ExcursionDiaphragm movement distance on ultrasound (cm). Target >1.0 cm tidal; >1.4–1.8 deep
E/E'Echo ratio — marker of LV diastolic stiffness. >7.8 = elevated filling pressure = WiPO risk during SBT
WiPOWeaning-induced Pulmonary Oedema — cardiac flash oedema triggered by switching to negative pressure breathing
P0.1Airway occlusion pressure at 100ms — measures respiratory drive. Normal 1.5–3.5 cmH₂O; >4 = high drive/struggling; <1.5 = low drive/over-sedated
NIF / MIPNegative Inspiratory Force / Maximum Inspiratory Pressure — breathing muscle strength. Target more negative than −30 cmH₂O
PLRPassive Leg Raise — 45° leg elevation, fluid responsiveness test. MAP rise >10% = fluid responsive
📋 All thresholds at a glance
P0.1 < 4
cmH₂O. Normal respiratory drive.
NIF > −20
cmH₂O (more negative = stronger). COPD: −19.
RSBI < 105
breaths/min/L. On PSV with PS ≥8: use ~75 instead.
Compliance > 50
mL/cmH₂O. Good lung stretchiness.
Resistance < 10
cmH₂O/L/s. Normal airway calibre.
Driving ΔP < 15
cmH₂O. Safety threshold.
DTF > 30–36%
Diaphragm thickening fraction on US.
Excursion > 10–14
mm. Diaphragm movement on US.
BNP > 200–300
pg/mL during SBT = cardiac cause.
PO₄ > 0.8
mmol/L. Adequate for muscle function.
Mg > 0.7
mmol/L. Adequate for neuromuscular transmission.
Vd/Vt < 0.5
Dead space ratio. >0.5 = high, suspect ventilatory failure.
Driving ΔP < 15
cmH₂O. Above 15 = lung injury risk + harder to wean.
Crs > 40–50
mL/cmH₂O. Good compliance. <25 = very stiff (ARDS/oedema).
Raw < 10
cmH₂O/L/s. Normal airway. >20 = significant obstruction.
MP < 15
J/min. Mechanical power. >20 = high injury risk.
Triggered ≥80%
% on controlled modes. Adequate respiratory drive to step down.
AI < 10%
Asynchrony index. ≥10% → 33% extubation failure (Sousa 2020).
E/E' < 7.8
Echo ratio. Above 7.8 = diastolic dysfunction → WiPO risk.
🎯 Your role in the meeting
You're not pretending to be an expert. You're the clinical lead of a decision support tool, gathering expert knowledge to build better clinical logic. Your preparation shows respect for their time.
Ask your question, then listen. When they say something that matches a concept in this guide, you'll recognise it and can ask the right follow-up: "What threshold do you use?" or "Would you do the same for a COPD patient?"
The best interviews happen when the expert forgets they're being interviewed and starts teaching. Let that happen.