The Effect of Anxiety on Perioperative Pain: Patient and Provider Perception

Clalit Health Services

Status: Completed

Conditions: Pain

Treatments: Other: Postoperative questionnaire- Obstetrician; Other: Postoperative questionnaire; Other: Postoperative questionnaire- anesthesiologist; Other: preoperative questionnaire; Other: PACU questionnaire

Study type: Observational

Funder types: Other

Identifiers

NCT04363281

409-19

Details and patient eligibility

About

In this study we will assess the incidence and severity of intraoperative and postoperative pain and determine the effect of preoperative anxiety on intraoperative and postoperative pain incidence. Secondary outcome is to assess provider perception of pain.

Full description

This is a prospective, observational study. Following obtaining written formal consent parturients will be requested to fill out the following questionnaires

1. Three questions to predict acute pain:

   • Verbal numeric score Anxiety 0-10
   • Anticipated postoperative pain level
   • Anticipated analgesic requirements

2. Speilberger STATE-TRATE inventory index

3. Pain Catastrophizing Scale In the post anesthesia care unit (PACU) parturients will be approached and requested to fill out a questionnaire regarding intraoperative pain, medication consumption, anxiety and nausea. Furthermore parturients will also be approached at 12 hours and 48 hours postpartum and questioned regarding anxiety levels and medication consumption and requested to fill out the OBSQOR 11 questionnaire at 12 hours postpartum.

Additionally, both the attending anesthesiologist and obstetrician will be questioned regarding the parturient's level of intraoperative pain, postoperative pain levels anxiety medication consumption, uteronic management, surgical technique and management.

Enrollment: 193 patients

Sex: Female

Ages: 18+ years old

Volunteers: Accepts Healthy Volunteers

Inclusion criteria

*Women undergoing an elective cesarean section under spinal anesthesia with the ability to comply with the study requirements will be eligible for participation

Exclusion criteria

• All women unable to receive spinal anesthesia or with inadequate spinal anesthesia prior to the beginning of surgery (Less than T4 Sensory Level to pinprick assessed from blunt tip needle in caudal to cranial direction )
• All women receiving antianxiety medication
• Language barrier