University of Health Sciences, Antalya Training and Research Hospital
Antalya, Muratpaşa, Turkey (Türkiye)
NCT Number: NCT06413290
The aim of this study was to evaluate the effect of pectointercostal fascial plane block on regional haemodynamic parameters in patients undergoing cardiac surgery.
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All sexes
Observational
Antalya, Muratpaşa, Turkey (Türkiye)
Perioperative pain management has become an important component of Enhanced Recovery After Surgery (ERAS) protocols in patients undergoing cardiac surgery. Pain is most intense in the first two days after cardiac surgery. Inadequate pain control has been shown to cause an increase in pulmonary complications due to inadequate mobility and coughing, an increase in sympathetic activation, an increase in myocardial infarction and thromboembolic events, delayed wound healing, and prolonged hospital and intensive care unit stay. Non-steroidal anti-inflammatory drugs (NSAIDs), paracetamol, opioids, epidural anesthesia and ultrasound-guided fascial plane blocks are widely used for pain management after cardiac surgery. The pectointercostal fascial plane (PIFP) block is an ultrasound-guided, superficial fascial plane block that can be applied as part of multimodal postoperative analgesia, especially after cardiac surgery. PIFB block has been shown to reduce postoperative analgesic consumption and improve pain scores not only in patients undergoing cardiac surgery but also in non-cardiac surgeries and thoracic procedures. The aim of this study was to evaluate the effect of PIFP block on regional haemodynamic parameters in patients undergoing cardiac surgery.
Healthy volunteers accepted: No
Only the study team can determine whether someone qualifies for participation.
Inclusion criteria
Exclusion criteria
Ultrasound-guided PIFP block will be performed approximately 30 minutes before surgery in patients undergoing cardiac surgery
No intervention
Time frame: 1 hour
The regional haemodynamic impact of PIDB block will be evaluated by Doppler ultrasound
Time frame: 24 hours
The amount of postoperative opioid consumption will be recorded
Time frame: 24 hours
The postoperative pain intensity will be assessed with NRS pain scores (0=no pain, 10=worst possible pain)
Time frame: 5 days
The interval from the end of the surgery until the patient's discharge will be recorded.
Antalya Training and Research Hospital
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