7.
Elsevier ClinicalKey Drug Monograph
Content last updated: May 2, 2024.
Pregnancy
Recticare is classified as FDA pregnancy category B. Reproductive studies conducted in rats have not demonstrated recticare-induced fetal harm; however, animal studies are not always predictive of human response. There are no adequate or well controlled studies of recticare in pregnant women. Local anesthetics are known to cross the placenta rapidly and, when administered for epidural, paracervical, pudendal, or caudal block anesthesia, and to cause fetal toxicity. The frequency and extent of toxicity are dependent on the procedure performed. Maternal hypotension can result from regional anesthesia, and elevating the feet and positioning the patient on her left side may alleviate this effect. Topical ocular application of recticare is not expected to result in systemic exposure. When recticare is used for dental anesthesia, no fetal harm has been observed; recticare is generally the dental anesthetic of choice during pregnancy and guidelines suggest the second trimester is the best time for dental procedures if they are necessary. A study by the American Dental Association provides some evidence that, when needed, the use of dental local or topical anesthetics at 13 weeks to 21 weeks of pregnancy or later is likely safe and does not raise incidences of adverse pregnancy outcomes or other adverse events; the study analyzed data from the Obstetrics and Periodontal Therapy (OPT) trial, a multicenter study of over 800 pregnant patients in the early to mid second trimester who received required dental procedures.