From the Guidelines
The recommended initial intravenous dose of midazolam for procedural sedation in healthy adults younger than 60 years of age is 1 to 2 mg (or no more than 0.03 mg/kg) injected over 1 to 2 minutes, with additional doses of 1 mg (or 0.2-0.3 mg) administered at 2-minute intervals until adequate sedation is achieved, as supported by the most recent and highest quality study 1.
Key Considerations
- The dose of midazolam should be reduced by 20% or more in patients older than 60 and those with ASA physical status 3 or above 1.
- When midazolam is used with an opioid, a synergistic interaction occurs, and a reduction in the dose of midazolam may be indicated 1.
- A total intravenous dose greater than 6 mg is usually not required for routine endoscopic procedures 1.
- Midazolam clearance is reduced in the elderly, obese, and those with hepatic or renal impairment, which may affect the duration of action and increase the risk of adverse effects 1.
Administration and Monitoring
- Midazolam should be administered intravenously over 1 to 2 minutes, with careful monitoring of vital signs and respiratory function 1.
- Resuscitation equipment should be available, and the reversal agent flumazenil (0.2 mg IV over 15 seconds, repeated if necessary) should be prepared in case of respiratory depression 1.
- The onset of effect for midazolam is 1 to 2 minutes, and peak effect is achieved within 3 to 4 minutes, with a duration of effect of 15 to 80 minutes 1.
From the FDA Drug Label
For sedation/anxiolysis/amnesia prior to and during procedures or prior to anesthesia USUAL PEDIATRIC DOSE (NON-NEONATAL) It should be recognized that the depth of sedation/anxiolysis needed for pediatric patients depends on the type of procedure to be performed. The initial dose of midazolam should be administered over 2 to 3 minutes Since midazolam HCl is water soluble, it takes approximately three times longer than diazepam to achieve peak EEG effects; therefore, one must wait an additional 2 to 3 minutes to fully evaluate the sedative effect before initiating a procedure or repeating a dose. Pediatric patients less than 6 months of age: Limited information is available in non-intubated pediatric patients less than 6 months of age Pediatric patients 6 months to 5 years of age: Initial dose 0. 05 to 0.1 mg/kg. A total dose up to 0.6 mg/kg may be necessary to reach the desired endpoint but usually does not exceed 6 mg. Pediatric patients 6 to 12 years of age: Initial dose 0.025 to 0.05 mg/kg; total dose up to 0. 4 mg/kg may be needed to reach the desired endpoint but usually does not exceed 10 mg. Pediatric patients 12 to 16 years of age: Should be dosed as adults The dose of midazolam must be reduced in patients premedicated with opioid or other sedative agents including midazolam
The recommended dosage of midazolam for procedural sedation is as follows:
- Pediatric patients 6 months to 5 years of age: Initial dose of 0.05 to 0.1 mg/kg, with a total dose up to 0.6 mg/kg.
- Pediatric patients 6 to 12 years of age: Initial dose of 0.025 to 0.05 mg/kg, with a total dose up to 0.4 mg/kg.
- Pediatric patients 12 to 16 years of age: Should be dosed as adults.
- Adults: Initial dose of 1 mg, with a total dose not exceeding 2.5 mg for healthy adults and 1.5 mg for patients 60 or older, or debilitated or chronically ill patients. It is essential to titrate the dose slowly and monitor the patient's response to avoid respiratory depression and other adverse effects 2.
From the Research
Recommended Dosage of Midazolam for Procedural Sedation
The recommended dosage of midazolam for procedural sedation varies depending on the route of administration, patient population, and specific procedure.
- For intravenous midazolam, the dosage range is not explicitly stated in the provided studies, but it is mentioned that the median dose used in one study was 4mg 3.
- For oral midazolam, the therapeutic dose range for children is 0.3 to 0.6 mg/kg, with a maximum dose of 10 mg irrespective of the child's weight, as reported by 65% of responders in a survey 4.
- For oral midazolam in adults, the dosage range is not explicitly stated in the provided studies.
Comparison with Other Sedatives
Midazolam has been compared to other sedatives, such as propofol, in terms of efficacy and safety for procedural sedation.
- One study found that propofol was more effective and at least as safe as midazolam for procedural sedation in the emergency department 5.
- Another study found that propofol and midazolam were equally safe and effective for procedural sedation and analgesia in the emergency department, but propofol resulted in a shorter length of stay 6.
Safety and Efficacy
The safety and efficacy of midazolam for procedural sedation have been evaluated in several studies.
- One study found that midazolam resulted in a higher level of sedation than placebo, but the effect estimates for all outcomes were uncertain due to concerns about imprecision and risk of bias 3.
- Another study found that midazolam was less likely to result in moderate sedation compared to chloral hydrate in children undergoing non-invasive diagnostic procedures 3.
- A survey of physicians found that there was practice variation in midazolam dosing and cardiopulmonary monitor usage when performing minor procedures in children, highlighting the need for standardized practice guidelines 4.