- Hypoxic (type 1): Characterized by failure of gas exchange resulting in PaO2 <50 mm Hg breathing a gas mixture of at least 50% oxygen (Figure 9-1)
- Hypercapneic (type II): Characterized as failure of ventilatory pump or chronic structural changes (BPD, cystic fibrosis) (Figure 9-2)
eFigure 9-1
Workup of hypoxemia.†Alveolar to arterial gradient (A–a) gradient = PaO2 estimated – PaO2 measured. PaO2 estimated = FiO2 × (PB– 47) – PaCO2/R (atmospheric pressure or PB at sea level is 760 mm Hg; respiratory quotient R is a unitless number representing basal metabolic rate; 0.7 is typically used in our ICU.) A normal A–a gradient is ∼10 mm Hg. (Adapted from Marino PL: The ICU Book, 2nd ed. Baltimore: Williams & Wilkins; 1990:349.)
- Early: Use of accessory muscles of respiration, markedly diminished or absent breath sounds, diaphoresis, inability to speak, AMS, irritability, cyanosis, hypercapnia
- Late: Lethargy, apnea, gasping or agonal respiration, bradycardia, hypotension
Modality | Indication | Dose and Administration | Advantages | Risks and Adverse Effects |
---|---|---|---|---|
O2 via nasal cannula (provides roughly 25%–40% oxygen)* (Use humidification system) | For non–life-threatening conditions, hypoxemia (asthma, pneumonia, bronchiolitis) | 100% oxygen†, typically no more than 4 L/min flow | Well tolerated, easy to use, readily available, no associated toxicity | Skin irritation from cannula, drying of nasal passages, nose bleeds |
O2 via simple face mask (provides roughly 35%–50% oxygen)* | For non–life-threatening conditions, hypoxemia (asthma, pneumonia, bronchiolitis) | 100% oxygen†at no less than 5 L/min, typically 5–15 L/min | Well tolerated, easy to use, readily available, no associated toxicity, provides more oxygen than nasal cannula | If flow is <5 L/min, “rebreathing” CO2 may occur |
O2 via Venturi™ mask (provides 24%–50% oxygen incrementally) | Weaning oxygen from high flow rates | The flow of 100% oxygen through the Venturi mask draws in a controlled, adjustable amount of room air (21% oxygen) | Well tolerated, easy to use, no associated toxicity, fixed and accurate concentration of oxygen | Not readily available |
O2 via partial rebreathing face mask (provides roughly 50%–100% oxygen)* | For non–life-threatening conditions, severe hypoxemia (asthma, pneumonia, bronchiolitis) | 100% oxygen, 5–15 L/min Maintain reservoir at least half full on inspiration | High-flow system readily available, provides more oxygen than simple face mask | Nitrogen washout may lead to atelectasis |
O2 via nonrebreather facemask (provides ∼80%–100% oxygen)* | Severe hypoxemia, hemodynamically stable pneumothorax (nitrogen washout) | 100% oxygen 10–15 L/min Maintain reservoir at least 2/3 full on inspiration and allow partial collapse on exhalation | Well tolerated, easy to use, readily available | Nitrogen washout may lead to atelectasis |
Heliox**, 60%–80% He with 20%–40% O2 | Upper airway obstruction (croup, bronchiolitis) May be beneficial in treatment of lower airway disease (asthma) | Can be administered via nasal cannula and face mask Do not use with oxygen tent or hood | Lower density gas decreases turbulent flow → increased O2 and medication delivery to distal airways | Beneficial effects of Helium not seen with <60%; therefore, not helpful if patient requires >40% O2 |
CPAP‡ | Acute: Respiratory distress or failure, poor lung compliance, obstructive airway disease , muscle fatigue, CHF, asthma, acute chest syndrome Chronic: OSA | Typically administer pressures of 5–10 cm H2O May give supplemental oxygen as needed | Overcomes airway resistance to maintain FRC, ↓ muscle fatigue, ↑ lung recruitment, ↓ atelectasis, ↓ V/Q mismatch Reduced risk of infection and local trauma to airway compared with ETT | Constant pressure throughout respiratory cycle; no ↑ with inspiration. Masks may cause skin breakdown with chronic use |
BiPAP‡ | (same as above for CPAP) | Administer via nose mask IPAP (8-20 cm H2O), EPAP (5-10) cm H2O, supplemental oxygen as needed | Less use of sedatives May prevent intubation | Nasal prongs and masks may cause skin breakdown with chronic use Not well tolerated by some patients Distended stomach caused by swallowed air |
Noninvasive positive pressure ventilation | Respiratory distress | Use a ventilator, set parameters (rate, Vt or PIP, PEEP) Supplemental O2 as needed | As with BiPAP May prevent intubation | As with BiPAP |
Step 1: Preparation and intubation |
Step 2: Pick ventilator mode (choose a familiar mode) |
Step 3: Choose control mode (volume vs. pressure) |
Step 4: Choose remaining variables |
Step 5: Manage patient while intubated |
Step 6: Wean and extubate as soon as possible |
Suction
Tubes (anticipated ETT size + 1 size above and below)†
Airway adjuncts (oral airways)
Tape
Scopes: Laryngoscope, stethoscope
†See accompanying PICU Pocket card for recommended mediations and equipment sizes.
Mode | Set Rate | Guaranteed Minimum MV | Support for Patient-Initiated Breaths “Over the Vent” | Notes |
---|---|---|---|---|
Controlled mechanical ventilation (CMV) | Y | Y | N | Vent delivers regular, identical breaths; no spontaneous breaths allowed Rarely used, with the exception of neonatal transport ventilators |
Assist-control ventilation (AC) | Y | Y | Y | Typically volume control; full preset TV is delivered at a preset rate; the patient may initiate additional supported cycles (also full preset VT); the patient may change MV as needed but cannot resume the work of breathing |
Intermittent mandatory ventilation (IMV) | Y | Y | N | Similar to CMV but allows patient-triggered breaths in between mandatory breaths Patient may change minute ventilation as needed and as vent rate is weaned, the patient can “take over” the work of breathing |
Synchronized intermittent mandatory ventilation (SIMV) | Y | Y | N | Similar to IMV, but internal circuitry manipulates mandatory vent delivered breaths around patient-triggered breaths |
Support mode (PS, VS) | N | N | Y | Set pressure or volume is delivered for patient-initiated cycles to support patient-initiated breaths (often combined with other modalities or as a weaning modality, i.e. SIMV + PS) |
Pressure regulated volume control (PRVC, VC+) | Y | Y | Y | On some ventilators, these are AC modes, but in others, they are SIMV modes; ask the RT Delivers preset rate and VT, but flow characteristics are regulated to deliver target volumes at the lowest possible pressure |
High-frequency oscillatory ventilation (HFOV) | N/A | N/A | N/A | Escalation of care for patients who require high and have failed conventional ventilators Consider when PEEP is 10 cm H2O or PIP is >35; better separates control of oxygenation and ventilation |
- Pressure control: Delivers a pressure-limited breath during a preset inspiratory time at the preset respiratory rate. The VT is determined by the preset pressure limit and the compliance and resistance of the patient’s respiratory system.
- Goal PIP: <35 to 40 cm H2O to reduce ventilator-induced lung injury (barotrauma).
- Does not guarantee VT.
- Pressure control may be preferentially used for ELBW or VLBW patients because of limitations in ventilator ability to consistently deliver or control extremely low VT.
- Goal PIP: <35 to 40 cm H2O to reduce ventilator-induced lung injury (barotrauma).
- Volume control: Delivers a preset VT during a preset inspiratory time at the preset respiratory rate and constant inspiratory flow.
- Guarantees VT at the expense of variations in PIP.
- Monitor PIP closely; goal is <35 to 40 cm H2O to reduce ventilator-induced lung injury(barotrauma)
- Guarantees VT at the expense of variations in PIP.
SIMV PC (Neonates) | SIMV PC (Children) | SIMV VC (Children) | SIMV VC (Adolescents) | |
---|---|---|---|---|
Rate (bpm) | 20–30 | 14–20 | 14–20 | 8–14 |
Ti (sec) | 0.2–0.5 | 0.5–0.8 | 0.5–0.8 | 0.75–1 |
VT (cc/kg)* | N/A† | N/A† | 6-8 | 6–8‡ |
PEEP (cm H2O) | 2–5 | 2–5 | 2–5 | 2–5 |
PIP (cm H2O) | 20–25 | 20–25 | N/A† | N/A† |
PS (cm H2O) | 5–10 (in addition to PEEP) | |||
FiO2 | Start at 1.0 and wean as aggressively as possible to avoid O2 toxicity (goal <0.6) |
Goal | Action | Physiology | Caveats |
---|---|---|---|
Improving oxygenation | Increase Paw by ↑ PEEP, PIP, or Ti (PEEP has greater effect); increase FiO2 | PEEP maintains FRC and ↓ V/Q mismatch; has >effect than PIP: = K(PIP-PEEP) × [Ti/(Ti + Te)] + PEEP | Overdistension with PEEP will lead to worsening oxygenation Consider HFOV if PEEP >10 |
Improving ventilation | Increase MV by ↑ RR or ↑ VT (in VC modalities) or PIP (in PC modalities) | CO2 directly related to minute ventilation. Rule of thumb: Current PaCO2 × Current respiratory rate = Desired PaCO2 × Desired respiratory rate | Allow for permissive hypercapnia (pCO2 ∼60 if pH >7.2) to reduce the potential for barotrauma With obstructive airway diseases, reducing the respiratory rate may improve ventilation by allowing for a longer Te |
- Consider for all intubated patients; neonates may need less than older patients to prevent patient–ventilator asynchrony and accidental extubation.
- For all intubated patients not on diuretics, use 75% of maintenance IVF (these patients do not have respiratory insensible loss because of the enclosed humidified ventilator circuit) and follow volume status closely.
- Nutrition: Start enteral feeds as soon as possible; if contraindicated, start TPN or PPN (ideally, the patient should start receiving adequate calories and nutrition 2–3 days after intubation).
- Follow at least qAM blood gases (preferably ABG; may use CBG, or VBG via central line).
- Follow oxygenation using pulse oximetry.
- Follow ventilation using end-tidal CO2 if feasible (may be too bulky for neonates) and correlate or recalibrate daily with pCO2 from AM blood gases.
- Follow lung compliance (want higher) and oxygenation index (want lower) daily trends
CDYN = VT/(PIP – PEEP)
CSTAT = VT/(PPLAT – PEEP
Oxygenation index = (FiO2 × Mean airway pressure)/PaO2 × 100
- Diuretics should be considered in all intubated patients given impaired lymphatic or venous return 2/2 immobility: 0.5 to 2.0 mg/kg furosemide IV Q6 to 12 h. Keep balanced intake and output (other diuretics may be used).
- Expect metabolic alkalosis. Anticipate depletion of Cl and retention of bicarbonate.
- Start replacing Cl when <90 mEq/L.
First choice: Use KCl (2–4 mEq/L) unless contraindicated (eg, renal insufficiency, hyperkalemia).
Second choice: Use NaCl (2–4 mEq/kg); may cause more water retention 2/2 increased Na.
If a and b have been exhausted and Cl <80 mEq/L, then use ammonia chloride. Dosing of mEq NH3Cl via the bicarbonate-excess method (refractory hypochloremic metabolic alkalosis):
mEq NH3Cl = 0.5 (L/kg) × wt (kg) × [Serum HCO3– – 24]
→ Give ½ to ⅔ of the calculated dose; then re-evaluate
(0.5 L/kg is the estimated bicarbonate volume of distribution, and 24 is the average normal serum bicarbonate concentration in mEq/L; use with caution in patients with hepatic insufficiency.)
After Cl >90 (or spot urine Cl suggests saline-resistant alkalosis) while pH is >7.50, use acetazolamide (5 mg/kg IV Q8h for 3 doses only; check daily lytes).
- Infection: The trachea will be colonized within ∼6 hours of intubation; monitor changes in color or quantity of secretions.
- Decreased cardiac output: Increased intrathoracic pressure impedes RV filling and decreases cardiac output, especially if the patient is hypovolemic.
- Ventilator-induced lung injury (VILI): Barotrauma: Repeated alveolar stretch (via pressure or volume) will activate the host inflammatory response. Therefore, keep VT or PIP as low as possible. Oxygen toxicity: Supplemental O2 may fuel inflammation; wean O2 aggressively.
- Pneumothorax: Results from acute changes in airway pressures. If the pneumothorax is under tension, it is a life-threatening emergency. Signs and symptoms include agitation, decreased breath sounds on the affected side, asymmetrical chest rise, tracheal or mediastinal shift away from the affected hemi-thorax, increased CVP, decreased BP, increased HR, increased PIP, increased Paw. Always assume a pneumothorax has developed with any acute or rapid deterioration in clinical status and treat swiftly with needle decompression.
- Subglottic stenosis: Results from too large of ETT, traumatic intubation, or patient agitation. Heliox may improve gas flow. Steroids may help avoid re-intubation if stridor is present upon extubation (dexamethasone 0.5 mg/kg IV Q6H (max dose 15 mg) × 4–8 doses).
- Mechanical failure or accidental extubation: Hand ventilate patient, remove the ETT.
- As the patient’s need for ventilatory support resolves, wean in the following order: FiO2 → PIP (if PC ventilation) → PEEP → Rate (ensure pressure or volume support is provided).
- Criteria for extubation readiness (Crit Care Med 2000;28(8):2991 and JAMA 2002;288(20):2561):
- PEEP ≤5
- FiO2 <40%
- Spontaneous effective VT >5 cc/kg
- Glasgow Coma Scale >8 (ie, not comatose, sedation has been weaned)
- Tracheal secretions are tolerable (ie, not thick and not requiring >Q1h suctioning)
- Appears comfortable on PEEP 5 or pressure support of 5 with no trial failure (see below)
- PEEP ≤5
Definition of trial: 2 h on respiratory support of CPAP ≤5 cm H2O or T-piece (CPAP = 0) | |
Clinical Criteria
| Laboratory Criteria
|
- Definition: An acute exacerbation of asthma that does not respond to treatment with bronchodilators and corticosteroids.
- Symptoms: Chest tightness or pain, dyspnea, dry cough, or wheezing. Patients may have nausea, vomiting, difficulty speaking or speaking in single words, or altered mental status as part of the presentation, which indicates greater severity of illness.
- Previous ICU admissions
- Previous need for mechanical ventilation with an asthma exacerbation
- Syncope during an asthma exacerbation
- Seizures during an asthma exacerbation
- History of cardiac arrest with asthma exacerbation
- Poor adherence to controller therapy
- Poor perception of severity of asthma
- Comorbid psychiatric disorder
- Rapid deterioration with current episode
- Use of more than 1 canister of home β-agonist medication per month
Clinical Respiratory Score as a Guide for Evaluating Severity of Exacerbation and Following Response to Therapy
Clinical Respiratory Score (CRS) | ||||
---|---|---|---|---|
Assess | Score 0 | Score 1 | Score 2 | Patient Score |
Respiratory Rate | < 2 mos < 50 2-12 mos < 40 1-5 yrs < 30 > 5 yrs < 20 | < 2 mos 50-60 2-12 mos 40-50 > 1-5 yrs 30-40 > 5 yrs 20-30 | < 2 mos > 60 2-12 mos > 50 > 1-5 yrs > 40 > 5 yrs > 30 | |
Auscultation | Good air movement, scattered expiratory wheezing, loose rales/crackles. | Decreased air movement, inspiratory and expiratory wheezes or rales/crackles | Diminished or absent breath sounds, severe wheezing or rales/crackles, or markedly prolonged expiration. | |
Use of Accessory Muscles | Mild to no use of accessory muscles. Mild to no retractions or nasal flaring on inspiration. | Moderate intercostal retractions, mild to moderate use of accessory muscles, nasal flaring. | Severe intercostal and substernal retractions, nasal flaring. | |
Mental Status | Normal to mildly irritable | Irritable, agitated, restless. | Lethargic | |
Room Air SpO2 | > 95% | 90 – 95 % | < 90% | |
Color | Normal | Pale to normal | Cyanotic, dusty | |
Total Score (Sum of the component scores) |
First-Line Treatment | |||
---|---|---|---|
Medication | Type and Mechanism | Route | Dose |
Albuterol | SABA (airway smooth muscle relaxation) | Inhaled (nebulized or MDI) | Nebulization: 0.15–0.5 mg/kg/h or 10–20 mg/h of continuous therapy; can give sequential nebulization × 3 (≤5 mg each) Max, 20 mg/h MDI: 4–8 puffs per dose Q20 min × 3; then Q1h |
Levalbuterol | SABA (levorotary enantiomer, airway smooth muscle relaxation) | Inhaled (nebulized or MDI) | MDI: 4–8 puffs Q20 min × 3 then Q1h |
Methylprednisolone | Steroid* (antiinflammatory) | IV | 2 mg/kg IV once; then 1 mg/kg IV Q6h Max, 60 mg/dose |
Prednisone | Steroid* (antiinflammatory) | PO | 2 mg/kg PO once; then 1–2 mg/kg/day divided Q12h Max, 60 mg/dose |
Second-Line Treatment | |||
Ipratropium bromide | Anticholinergic (airway smooth muscle relaxation) | Inhaled (nebulized or MDI) | <12 yr: Nebulization 250 mcg Q20 min × 3 then Q2–4h prn; MDI 4–8 puffs per dose >12 yr: Nebulization 500 mcg Q30 min × 3 then Q2–4h prn; MDI 4–8 puffs per dose Can “spike” the albuterol nebulization solution with ipratropium bromide dose and give as one treatment |
Magnesium sulfate | Electrolyte (smooth muscle relaxation) | IV | 40 mg/kg IV over 20 min; max 2g Although hypotension is exceedingly rare, watch for hypotension and be ready to give a 10–20 cc/kg NS bolus if it develops |
Terbutaline† | β-agonist (smooth muscle relaxation) | Sub-Q, IV | IV: 10 mcg/kg IV once; then IV infusion starting at 0.5 mcg/kg/min, titrate as HR tolerates to goal 3–6 mcg/kg/min Max, 10 mcg/kg/min |
Aminophylline‡ | Bronchodilator | IV | 6 mg/kg load over 20–30 min; then continuous infusion |
Ketamine | Dissociative anesthetic, bronchodilator | IV | 0.5–2.0 mg/kg IV; may be used as a continuous infusion May have bizarre dreams, hallucinations; watch for oversedation and need for immediate intubation Often reserved as a last medication trial or sedative before intubation |
Heliox | Gas | Inhaled | Available as 70/30 or 80/20 concentrations |