Critical Care




Respiratory Failure



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Respiratory failure is commonly classified as one or both of the following:





  • 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.)






eFigure 9-2



Mechanisms of hypercapnia.





Clinical Predictors of Impending Respiratory Failure




  • 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




Management of Respiratory Failure




Oxygen Delivery Modes and Noninvasive Ventilation Modalities



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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% oxygenat 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


*The final oxygen concentration delivered by this device depends on the amount of room air that mixes with the supplemental oxygen during respiration.


**70/30 Heliox is used at our institution.


The FiO2 can be reduced by blending with room air while still maintaining the same flow rate.


‡Cognitive behavioral therapy at the beginning of therapy dramatically increases compliance up to 148%. Sleep 2007;30(5):635.





Stepwise Approach to Managing Respiratory Failure



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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





Step 1: Preparation and Intubation (STATS)





  1. Suction



  2. Tubes (anticipated ETT size + 1 size above and below)



  3. Airway adjuncts (oral airways)



  4. Tape



  5. Scopes: Laryngoscope, stethoscope




See accompanying PICU Pocket card for recommended mediations and equipment sizes.




Step 2: Pick Ventilator Mode (How the Patient and Machine Interact): Important Goals




  • Provide adequate ventilation and oxygenation.
  • Reduce the work of breathing.
  • Ensure patient comfort and synchrony with the ventilator.




Overview of Common Mechanical Ventilation Modalities



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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





Step 3: Choose Control Mode (Pressure vs. Volume)




  • 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.

  • 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)




Step 4: Choose Remaining Variables (Starting Point)




Initial SIMV Ventilator Settings for Various Ages



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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)


*Monitor chest rise and titrate to the lowest VT with adequate chest rise (lung protective strategy: 6–8 cc/kg).


Shaded boxes indicate variables that are not set in this mode; values obtained will be based on other set variables.


Large or obese adolescents may require less VT for adequate chest rise.





Step 5: Manage Patient While Intubated




Ventilator Adjustments Affecting Oxygenation and Ventilation



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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





Sedation and Analgesia




  • Consider for all intubated patients; neonates may need less than older patients to prevent patient–ventilator asynchrony and accidental extubation.




Maintenance Fluids




  • 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).




Blood Gases and Clinical Parameters




  • 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




Diuresis and Metabolic Alkalosis




  • 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.


    1. First choice: Use KCl (2–4 mEq/L) unless contraindicated (eg, renal insufficiency, hyperkalemia).



    2. Second choice: Use NaCl (2–4 mEq/kg); may cause more water retention 2/2 increased Na.



    3. 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.)




    4. 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).





Monitor for Complications of Mechanical Ventilation




  • 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.




Step 6: Wean and Extubate as Soon as Possible




Weaning



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  • 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)




Criteria for CPAP Trial Failure



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Definition of trial: 2 h on respiratory support of CPAP ≤5 cm H2O or T-piece (CPAP = 0)


Clinical Criteria



  • Diaphoresis
  • Nasal flaring
  • Increasing respiratory effort
  • Tachypnea
  • Tachycardia (increase in HR >20–40 bpm)
  • Cardiac arrhythmias
  • Hypotension
  • Apnea

Laboratory Criteria



  • Increase of PETCO2 >10 mm Hg
  • Decrease of arterial pH to <7.32
  • Absolute decline in arterial pH >0.07
  • PaO2 <60 mm Hg with FIO2 >0.40 (PaO2/FiO2 ratio <!–150)
  • SpO2 declines >5%


(Ped Crit Care Med 2009;10(1):1)





Status Asthmaticus in the Intensive Care Unit



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  • 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.




Risk Factors for ICU Admission and for Sudden Death with Status Asthmaticus




  • 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



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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)





Therapies for the Management of Status Asthmaticus



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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

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Jan 9, 2019 | Posted by in PEDIATRICS | Comments Off on Critical Care

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