Ropivacaine

DEA Class; Rx

Common Brand Names; Naropin

  • Local Anesthetics, Amides; 
  • Local Anesthetics, Parenteral

Long-acting, amide-type local anesthetic; structure and kinetics are similar to bupivacaine, however, ropivacaine appears to be less arrhythmogenic.

Indicated for local anesthesia, regional anesthesia, or surgical anesthesia.

For obstetric anesthesia or Caesarean section anesthesia.
For postoperative treatment of severe pain.
For ophthalmic anesthesia, specifically, peribulbar anesthesia and retrobulbar anesthesia.

Hypersensitivity to ropivacaine or amide-type local anesthetics, sensitivity to parabens

Bradycardia, myocardial depression, , cardiac arrhythmias, edema, hypotension, cardiovascular collapse, cardiac arrest, palpitation, tachycardia, anginal pain, hypertension (epinephrine-containing solutions)

Anxiety, apprehension, chills, headache, restlessness, nervousness, disorientation, confusion, dizziness, tremors, twitching, shivering, seizures; CNS depression manifested restlessness, tremors, drowsiness, unconsciousness, tinnitus

Nausea, vomiting

Blurred vision, miosis

Respiratory arrest, status asthmaticus

Anaphylactoid reactions (sometimes fatal)

Use caution in patients with history of malignant hyperthermia

DO NOT use solutions with epinephrine in distal areas of body (eg, digit, nose, ear)

Use preservative-free preparations for spinal or epidural anesthesia

Addition of vasoconstrictor, epinephrine, will promote local hemostasis, decrease systemic absorption, and increase duration of action

Seizures reported with systemic toxicity

This drug should be used with caution in patients receiving other local anesthetics or agents structurally related to amide-type local anesthetics since the toxic effects of these drugs are additive

Patients treated with class III antiarrhythmic drugs (eg, amiodarone) should be under close surveillance and ECG monitoring considered, since cardiac effects may be additive

The plasma concentrations of this drug may approach threshold for central nervous system toxicity after administration of 300 mg of ropivacaine for brachial plexus block; exercise caution when using 300 mg dose; the dose for a major nerve block must be adjusted according to site of administration and patient status; supraclavicular brachial plexus blocks may be associated with a higher frequency of serious adverse reactions, regardless of local anesthetic used

Major peripheral nerve blocks may result in administration of a large volume of local anesthetic in highly vascularized areas, often close to large vessels where there is increased risk of intravascular injection and/or rapid systemic absorption, which can lead to high plasma concentrations

The use of this drug in retrobulbar blocks for ophthalmic surgery has not been studied; until appropriate experience gained, the use for such surgery is not recommended

There are no adequate or well-controlled studies in pregnant women of effects of this drug on developing fetus; this drug should only be used during pregnancy if the benefits outweigh risk

One publication reported that ropivacaine is present in human milk at low levels following administration in women undergoing cesarean section; no adverse reactions were reported in the infants

The dose of local anesthetics differs with the anesthetic procedure; the area to be anesthetized; the vascularity of the tissues; the number of neuronal segments to be blocked; the intensity of the block; the degree of muscle relaxation required; the duration of anesthesia desired; individual tolerance; and the physical condition of the patient.

Adults

The maximum dosage is dependent on route of administration and indication for therapy.

Elderly

The maximum dosage is dependent on route of administration and indication for therapy.

Adolescents

Safety and efficacy have not been established.

Children

Safety and efficacy have not been established; 2.5 mg/kg using a 0.25% solution has been used for caudal anesthesia.

Ropivacaine Hydrochloride

injectable solution

  • 2mg/mL
  • 5mg/mL
  • 7.5mg/mL
  • 10mg/mL

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