The Efficacy of PSB and Recto-intercostal Block Combination on Postoperative Pain in Patients Undergoing Cardiac Surgery Via Sternotomy: Case Series

Trial statusNot yet recruiting
Trial phaseNot applicable
Trial typeInterventional
Biological sexAll
Age18-85
SponsorCumhuriyet University

About this trial

The aim of this study was to investigate the effectiveness of the combination of Superficial Parasternal Block and Recto-Intercostal Fascial Plane Block in patient groups undergoing cardiac surgery via sternotomy by evaluating postoperative pain scores and analgesic consumption.

Eligibility criteria

This trial does not accept healthy volunteers

Qualifiers

Adult patients over 18 years of age who will undergo cardiac surgery with sternotomy under general anesthesia and who are in classes I-II-III according to the American Society of Anesthesiologists (ASA) risk classification.

Disqualifiers

Patients who did not give consent,

patients with coagulopathy,

patients with signs of infection at the block application site,

patients using anticoagulants,

Trial design

Design model

Single group

Treatments tested in this trial

  • Parasternal Block and Recto-İntercostal Fascial Plane Block

    Other intervention

    Superficial PSB is performed with the patient in the supine position using a high-frequency linear USG probe. The probe is placed longitudinally 2 cm lateral to the sternal border to visualize the T2-T4 intercostal space and to identify the pectoralis major muscle, intercostal muscle, and pleura. 10 ml of 0.25% bupivacaine local anesthetic is administered between the pectoralis major and intercostal muscle using an in-plane approach with a 100 mm needle. In addition, a Recto-Intercostal Fascial Plane Block is performed with a high-frequency linear USG probe. The probe is placed 2-3 cm lateral to the xiphoid so that the rectus abdominis muscle and 6-7th cartilages are visualized. The needle is advanced to the plane between the costal cartilage and the rectus abdominis muscle using the in-plane technique and 1-2 ml of saline is injected. After observing the spread to the target plane, 20 ml of 0.25% bupivacaine is applied. The same process is repeated bilaterally.

Treatment groups

10 Participants
are divided into 1 treatment group
Group A: Parasternal Block and Recto-İntercostal Fascial Plane BlockOther 1 intervention

Trial outcomes

Primary outcomes

1

Comparing the numerical rating scale scores

Numerical rating scale will be used for pain assessment. The scores of the numerical rating scale changes between 0 to 10 points. 10 points mean "the most severe pain that the patient ever had". 0 point means "there is no pain." Higher scores mean worse outcome.

Time frame
Postoperative 24 hours

Secondary outcomes

1

Comparing total morphine consumption

Postoperative analgesic need

Time frame
Postoperative 24 hours

Other outcomes

Locations

This trial has no locations.

Sponsors and contacts

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