The association of patient age, race, and demographic features on reported pain and sedation dosing during procedural abortion: A retrospective cohort study.

Contraception

School of Medicine, University of Mary land Medical Center, Baltimore, Maryland, USA; Department of OB/GYN, University of Maryland Medical Center, Baltimore, Maryland, USA.

Published: July 2023

Objectives: To explore impact of age, racial, demographic, and psychosocial factors on patients' dosage of analgesia and maximum pain score during procedural abortion.

Study Design: We performed retrospective chart review of pregnant individuals undergoing procedural abortion at our hospital-based abortion clinic from October 2019 through May 2020. Patients were stratified into age groups,<19 years, 19 to 35 years, and>35 years. We conducted the Kruskal-Wallis H test to evaluate for medication dosing or maximum pain score differences among groups.

Results: We included 225 patients in our study. We found no difference in fentanyl or midazolam dosing by age. The median fentanyl dose was 75 mcg and median midazolam dose was 2 mg in all three groups (p = 0.61, p = 0.99). White patients received higher median midazolam dosing than Black patients (2 and 3 mg, respectively, p < 0.01) despite similar pain scores. Despite no difference in pain scores, patients terminating for genetic anomaly received more fentanyl than those terminating for socioeconomic reasons (75 and 100 mcg, respectively, p < 0.01).

Conclusions: In our limited study, we found that White race and induced abortion for genetic anomaly were associated with increased medication dosing, though age was not. Multiple demographic and psychosocial factors, as well as perhaps provider bias, play into both a patient's perception of pain and the dosage of fentanyl and midazolam they receive during abortion procedures.

Implications: By acknowledging both patient factors and provider biases in medication dosing, we can provide more equitable abortion care.

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http://dx.doi.org/10.1016/j.contraception.2023.110037DOI Listing

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