Combine Serratus Anterior Plane Block Versus Erector Spinae Plane Block in Coronary Bypass Surgery

  • STATUS
    Recruiting
  • days left to enroll
    12
  • participants needed
    60
  • sponsor
    Ankara City Hospital Bilkent
Updated on 4 October 2022
analgesia
bupivacaine
pain relief
bypass graft
sternotomy
bypass surgery
pain relieving

Summary

Even though Erector Spinae Plane (ESP) Block is shown to be efficient in cardiac surgery, the Combine Serratus Anterior Plane (CSAP) Block is still controversial if it has an efficient analgesic effect for sternotomy and drain tube pain relief. This study aims to compare ESP block and CSAP block for postoperative analgesia in coronary bypass surgery patients.

Description

Acute postoperative pain after cardiac surgery originates various surgical procedures that may cause pain including the incision of tissues, sternotomy, the separation of bone-joint structures, the severity and duration of these applications, the use of chest tubes, and the patient's personal inflammatory may affect the response to these stimuli. Postoperative pain is a critical risk factor for the development of pulmonary and cardiovascular complications such as atelectasis, cardiac ischemia, and arrhythmias. Researchers claim that adding techniques to iv drugs, such as thoracic epidural anesthesia, paravertebral block, or erector spinae plane block (ESP) to multimodal analgesia regimens positively affect recovery. Although the efficacy of ESP block in providing postoperative analgesia has been demonstrated in many studies, there is no study comparing CSAP and ESP block in cardiac surgery.

Details
Condition Cardiac Surgery, Postoperative Pain, Regional Anesthesia Morbidity
Treatment ESP block, CASP block
Clinical Study IdentifierNCT05308797
SponsorAnkara City Hospital Bilkent
Last Modified on4 October 2022

Eligibility

Yes No Not Sure

Inclusion Criteria

Adult patients who will undergo coronary artery bypass grafting surgery with median sternotomy

Exclusion Criteria

Emergency surgeries
Patients with allergic reactions to anesthesia and analgesia drugs to be used
Patients who do not want to participate in the study voluntarily
Severe systemic disease (kidney, liver, pulmonary, endocrine)
Substance abuse history
History of chronic pain
Psychiatric problems and communication difficulties
Patients who need revision due to hemostasis in the postoperative period
Patients with severe hemodynamic instability due to infection, heavy bleeding, etc
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