Ropivacaine is FDA-approved for surgical anesthesia and acute pain management. It is used in an epidural block for surgery—such as cesarean sections. It is also used in major nerve blocks and local infiltration. In acute pain management, ropivacaine is used in epidurals (continuous infusion or intermittent bolus) for postoperative or labor pain control. More recently, ropivacaine’s use in chronic pain management has also been evaluated.

In epidural administration for cesarean section, clinical trials show that ropivacaine (0.75% or 0.5%) has a clinically similar onset of sensory and motor block to bupivacaine 0.5%. The median duration of analgesia that ropivacaine supplied to the T6-S3 dermatomes is similar to bupivacaine, but with a much shorter duration of motor block (0.9 hrs vs. 2.5 hrs). For intrathecal administration, hyperbaric solutions of ropivacaine are faster in onset and recovery than isobaric ropivacaine, but the spread and duration of the hyperbaric ropivacaine block are very variable. Co-administration with opioids reduces the amount of local anesthetic needed and prolongs analgesia without lengthening the period of the motor block.

 An outpatient study looking at bupivacaine and ropivacaine in managing chronic low back pain found there were no significant differences in analgesia, motor blockade, or hemodynamic changes between bupivacaine 0.125% and ropivacaine 0.2%. Ropivacaine was also found to be effective for severe refractory migraine through trigger point inactivation.[1][2][3]

Ropivacaine is a long-acting amide local anesthetic. It exhibits a similar mechanism of action to other local anesthetics in that it reversibly inhibits sodium ion influx in nerve fibers. Amides preferentially bind and inactivate sodium channels in the open state—thereby blocking propagation of action potentials. The dose-dependent inhibition of potassium channels potentiates this action.

Ropivacaine has a few properties that make it unique. Ropivacaine is less lipophilic than other local anesthetics, such as bupivacaine, and is less likely to penetrate large myelinated motor fibers. It therefore selectively acts on the nociceptive A, B, and C fibers over the AB (motor) fibers. Ropivacaine is also manufactured as a pure S(-) enantiomer; the S(-) enantiomer has significantly less cardiotoxicity and neurotoxicity.[4][5]

Ropivacaine is administered in incremental doses. Factors that affect the dosing of any administered local anesthetic include the area to be anesthetized, the vascularity of tissues, the number of neuronal segments to be blocked, and the depth and duration of anesthesia required.

An adequate test dose of 3-5 mL of short-acting local anesthetic with epinephrine should be used before the induction of the complete block. A repeat of the test dose should be given if the patient is moved in such a way that displacement epidural catheter may have occurred.

For lumbar surgery epidural blocks, the ropivacaine doses considered necessary to produce a successful block are 15-30 mL of 0.5% solution, 15-25 mL of 0.75% solution, 15-20 mL of 1% solution.

When used in lumbar epidural blocks for cesarean section, the doses for ropivacaine are 20-30 mL of 0.5% solution and 15-20 mL of 0.75% solution.

Dosages of ropivacaine when performing thoracic epidural blocks for surgical anesthesia are 5-15% mL dose of 0.5% solution and 5-15 mL of 0.75% solution.

When performing major nerve blocks, the dosages are 35-50 mL of 0.5% solution and 10-40 mL of 0.75% solution

For field blocks (e.g., minor nerve blocks and infiltration), ropivacaine is dosed at 1-40 mL dose of 0.5% solution.

When managing post-operative pain, peripheral nerve blocks are continuously infused at a dose of 5-10 mL/hr of 0.2% solution. For pain management through lumbar or thoracic epidurals, the continuous infusion dose of ropivacaine is at 6-14 mL/hr of 0.2% solution.

In prolonged blocks, there should be consideration of the risks of reaching a toxic plasma concentration or inducing local neural injury. A 24-hour cumulative dose of up to 770 mg ropivacaine is generally well tolerated in adults for postoperative pain management. Ropivacaine should be used with caution when administering it to debilitated patients for more than 70 hours.[6][7][8][9]

Ropivacaine is generally well tolerated. A pooled analysis from controlled clinical trials (n=1,661), in which patients received ropivacaine 0.125-1% for nerve blocks, indicates that the most common adverse reactions are hypotension (32%), nausea (17%), vomiting (7%), bradycardia (6%), and headache (7%). A similar side effect profile occurred in patients who received bupivacaine 0.25-0.75%.

Patients 61 years or older who received epidural ropivacaine 1% had a higher incidence of bradycardia than patients aged 41-60 years (58% vs. 15%); they also had a higher incidence of hypotension than patients aged 18-40 years old (74% vs. 20%).

The overall incidence of adverse reactions in children one month to 15 months is low; the most common adverse effects of ropivacaine in this age group were nausea and or vomiting.

The most common fetal or neonatal adverse reactions, following the use of ropivacaine in women undergoing cesarean section or labor, were fetal bradycardia (12%), neonatal jaundice (8%), and unspecified neonatal complications (7%).[10]

The only absolute contraindication to ropivacaine is in patients with a known hypersensitivity to ropivacaine or any amide-type local anesthetic.