Nitroglycerin Infusion Dosing
Start intravenous nitroglycerin at 10-20 mcg/min using non-absorbing tubing and titrate upward by 5-10 mcg/min every 3-5 minutes until symptoms resolve or blood pressure response occurs, maintaining systolic blood pressure above 90 mmHg. 1, 2, 3
Initial Dosing Protocol
- Begin at 10-20 mcg/min through an infusion pump using non-PVC (non-absorbing) tubing to avoid drug absorption into the administration set 1, 2, 4
- The FDA label specifies that when using non-absorbing tubing, the initial dose should be 5 mcg/min, though clinical guidelines from the European Society of Cardiology recommend 10-20 mcg/min as the practical starting range 4, 1
- Increase by 5-10 mcg/min every 3-5 minutes based on clinical response and blood pressure tolerance 1, 5
Titration Strategy
- If no response is observed at 20 mcg/min, increase increments to 10 mcg/min 1, 5, 4
- At doses above 50 mcg/min, increments of 20 mcg/min can be used if needed 5
- Once partial blood pressure response occurs, reduce the increment size and lengthen the interval between increases to avoid precipitous hypotension 1, 4
- The typical maximum dose is 200 mcg/min, though the FDA label notes concentrations should not exceed 400 mcg/mL and prolonged infusions at 300-400 mcg/min are tolerated 1, 5, 4
Critical Blood Pressure Parameters
- Absolute contraindication if systolic BP <90 mmHg or ≥30 mmHg below baseline 1, 2, 5
- In previously normotensive patients, do not titrate systolic BP below 110 mmHg 1
- In hypertensive patients, reduce mean arterial pressure by 25-30% from baseline, but not more 1, 5
- Measure blood pressure every 3-5 minutes during active titration 3
- Consider arterial line placement for doses >50-100 mcg/min or in patients with borderline blood pressure (SBP 90-110 mmHg) 1, 3, 5
Special Considerations for Renal Dysfunction and Hypertension
- Patients with renal dysfunction are at higher risk for hypotension, which can further compromise renal perfusion—use slower titration and more frequent monitoring 1
- Hypertensive patients may require higher doses to achieve adequate preload reduction but can tolerate more aggressive blood pressure lowering (up to 25-30% reduction in MAP) 1, 5
- In hypertensive acute heart failure (SBP >160 mmHg), nitroglycerin is particularly effective and can be combined with high-dose bolus strategies in severe cases 6
Absolute Contraindications
- Phosphodiesterase inhibitor use within 24 hours of sildenafil or 48 hours of tadalafil due to risk of profound, potentially fatal hypotension 1, 2, 5
- Right ventricular infarction—these patients are critically preload-dependent and can experience life-threatening hypotension with nitrates 2, 5
- Severe aortic stenosis—marked hypotension may occur following initiation 1
Monitoring Requirements
- Continuous blood pressure and heart rate monitoring is mandatory 5, 4
- Non-invasive BP monitoring is usually adequate at lower doses (<50 mcg/min) 5
- Monitor for clinical endpoints: resolution of chest pain, dyspnea, or pulmonary congestion 1, 5
- Watch for headache (common but rarely requires discontinuation) and hypotension 1, 3
Tolerance and Duration of Therapy
- Tachyphylaxis typically develops after 24-48 hours of continuous infusion, necessitating incremental dose increases 1, 3, 5
- When patients remain symptom-free for 12-24 hours, attempt to reduce the infusion rate and transition to oral or topical nitrates with a nitrate-free interval to avoid tolerance 1, 5
- It is inappropriate to continue IV nitroglycerin in patients who remain free of ischemic signs and symptoms 1
Common Pitfalls to Avoid
- Using PVC tubing instead of non-absorbing tubing—this can result in 85% drug loss and unpredictable dosing 7
- Failing to flush or replace the infusion set when changing concentrations—this can delay delivery of the new dose by minutes to hours 4
- Administering nitrates to inferior STEMI patients without first obtaining a right-sided ECG (V3R-V4R) to rule out RV infarction 2
- Continuing the infusion beyond 24-48 hours without addressing tolerance or attempting transition to non-parenteral therapy 1