Sandbox vidit3
Drug | Adult dosage |
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Inhaled Short Acting β Agonists (SABA) | |
Albuterol/Bitolterol/Pirbuterol a) Nebulizer solution b) MDI | ♦ 2.5-5 mg every 20 minutes for 3 doses, then 2.5-10 mg every 1-4 hours as needed or 10-15 mg/hour continuously. ♦ 4-8 puffs every 20 mins upto 4 hours, then every 1-4 hours as needed. |
Levalbuterol a) Nebulizer solution b) MDI | ♦ 1.25-2.5 mg every 20 mins for 3 doses, then 1.25-5 mg every 1-4 hours as needed. ♦ 4-8 puffs every 20 mins upto 4 hours, then every 1-4 hours as needed. |
Anticholinergics | |
Ipratropium bromide a) Nebulizer solution b) MDI | ♦ 0.5 mg every 20 mins for 3 doses, then as needed. ♦ 8 puffs every 20 mins as needed for upto 3 hours. |
Ipratropium with albuterol a) Nebulizer solution (each 3 ml containing 0.5 mg ipratropium and 2.5 mg albuterol) b) MDI (each puff contains 18 mcg ipratropium and 90 mcg albuterol) | ♦ 3 ml every 20 mins for 3 doses, then as needed. ♦ 8 puffs every 20 mins as needed for 3 hours |
Systemic corticosteroids | |
Prednisone/Prednisolone/Methylprednisolone | ♦ 40-80 mg/day in 1 or 2 divided doses until peak expiratory flowrate (PEF) reaches 70% of personal best. |
Clinical course | Unstable |
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Physical examination | Signs of heart failure |
Functional class | IV |
6MWD | Less than 400 m |
Echocardiogram | RV Enlargement |
Hemodynamics | RAP high CI low |
BNP | Elevated/Increasing |
Treatment | Intravenous prostacyclin and/or combination treatment |
Frequency of evaluation | Q 1 to Q 3 months |
FC assessment | Every clinic visit |
6MWT | Every clinic visit |
Echocardiogram2 | Q 6 to Q 12 months/center dependent |
BNP | center dependent |
RHC | Q 6 to Q 12 months or clinical deterioration |
Management
Characterize the symptoms: Fever Hypothermia Altered mental status Mottling Ileus oliguria | |||||||||||||||||||||||||||||||||||||||||||
Examine the patient: Tachycardia Tachypnea Edema Hyperglycemia Hypotension after an initial 30 ml/Kg bolus Decreased capillary refill | |||||||||||||||||||||||||||||||||||||||||||
Order labs: Random blood sugar (RBS) Complete blood count (CBC) Plasma C reactie protein (CRP) Plasma procalcitonin Pulse oximetry Urinalysis/Renal function tests PT/INR Liver function tests Serum lactate Central venous pressure (CVP) | |||||||||||||||||||||||||||||||||||||||||||
Consider alternative diagnosis: Infections Acute pancreatitis Diabetic ketoacidosis Lower gastrointestinal bleeding Myocardial infarction | |||||||||||||||||||||||||||||||||||||||||||
Initial resuscitation: Goals to achieve in first 6 hours CVP 8-12 mm Hg Mean arterial pressure (MAP) ≥ 65 mm Hg Urine output ≥ 0/5 mL/Kg/hr Central venous O2 sat. 70% | |||||||||||||||||||||||||||||||||||||||||||
Diangosis: 2 sets of blood cultures (aerobic and anaerobic) atleast, before starting antibiotics
Imaging studies as appropriate to locate a source | |||||||||||||||||||||||||||||||||||||||||||
Antimicrobial therapy: Initiate within 1st hour of diagnosis Daily reassessment of regimen Low procalitonin level for prognosis Usual duration of therapy 10 days Longer in neutropenics, slow responders, undrainable foci, immunologically compromised | |||||||||||||||||||||||||||||||||||||||||||
Choice of antibiotics | |||||||||||||||||||||||||||||||||||||||||||
Unknown organism Empiric therapy with broad spectrum antbiotic with good tissue penetrance | Neutropenic pt with severe sepsis (goal is to cover Acinetobacter & Pseudomonas spp) Use combination empirical therapy | Severe infections + resp failure + septic shock Extended spectrum beta lactam and aminoglycoside/fluoroquinolone | Streptococcus pneumoniae Beta lactam + macrolide | Culture specific organism Shift to appropriate anti-bacterial, antiviral or antifungal | |||||||||||||||||||||||||||||||||||||||
Remove source/foci of infection: Use minimally invasive process Source removal best done in first 12 hours Remove intravascular access devices if they are a possible source Oral chlorhexidine gluconate to reduce oral contamination as a risk factor for ventilator associated pneumonia | |||||||||||||||||||||||||||||||||||||||||||
Hemodynamic support Fluid therapy: Administer crystalloids, albumin when demand for fluids is too high Use dynamic variables (change in pulse pressure, stroke volume) and static variables (arterial pressure,heart rate) to assess status Vasopressors (to achieve target MAP 65 mm Hg): Inotropic therapy: Trial of dobutamine infusion 20 μg/Kg if cardiac output low with elevated cardiac filling pressure | |||||||||||||||||||||||||||||||||||||||||||
Corticosteroids: Use continuous flow IV hydrocortisone 200 mg/day if shock doesn’t improve with fluids & vasopressor Taper when vasopressors no longer required | |||||||||||||||||||||||||||||||||||||||||||
Blood products: Transfuse blood when hemoglobin < 7.0 g/dL Transfuse platelets if < 10,000/mm3 or < 20,000/mm3 in those with high risk | |||||||||||||||||||||||||||||||||||||||||||
Mechanical ventilation for sepsis induced ARDS Target tidal volume of 6 mL/Kg Target plateau pressure ≤ 30 mm Hg Use PEEP (positive end expiratory pressure) to avoid alveolar collapse Raise patients bed to 30-45° Attempt weaning when all foll criteria are met:
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Other supportive therapy Sedation & neuromuscular blockade: Use minimal sedation/neuromuscular blockade in mechanically ventilated patients Glucose control: Renal replaement therapy: DVT prophylaxis: Stress ulcer prophylaxis Feeding: Goals of care: Discuss goals or care, patient aspirations and future directives with family with 72 hours of admission | |||||||||||||||||||||||||||||||||||||||||||