Assessment of pain relief following intrauterine lignocaine in addition to paracervical block for fractional curettage

Authors

  • Meenambiga B. Department of Obstetrics and Gynecology, Raja Mirasudar Hospital, Thanjavur Medical College, Thanjavur, Tamilnadu, India
  • Haribaskar R. Department of Anaesthesiology, Raja Mirasudar Hospital, Thanjavur Medical College, Thanjavur, Tamilnadu, India

DOI:

https://doi.org/10.18203/2320-1770.ijrcog20164354

Keywords:

Fractional curettage, Intrauterine lignocaine, Pain relief

Abstract

Background: To assess the pain relief using visual analog score following intrauterine lignocaine in addition to paracervical block for fractional curettage.

Methods: This study was a prospective, double blinded randomized controlled trial conducted in 168 patients in the department of obstetrics and Gynecology, Thanjavur Medical College with abnormal uterine bleeding. All patients received either intrauterine 2% lignocaine or Normal saline along with oral misoprostol 200μg and paracervical block prior to the procedure. The primary outcome was the assessment of pain perceived at the time of curette, soon after procedure (5 mins); 30 minutes later using VAS.

Results: Both the groups were matched for age, parity, BMI, menopausal status, socioeconomic status and indication for the procedure. Patients in lignocaine group perceived less pain when compared to that in placebo group. There was no difference in both groups with respect to other outcomes.

Conclusions: Addition of intrauterine 2% lignocaine in addition to paracervical block and oral misoprostol reduces pain making fractional curettage as a patient friendly procedure.

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Published

2016-12-07

Issue

Section

Original Research Articles