Postoperative pain is a common and significant problem following open heart surgery. Fascial plane blocks (FPBs) such as Serratus Anterior Plane Block (SAPB), Pectoral Nerve Blocks (PECS), and Pecto-Intercostal Fascial Block (PIFB) are increasingly used as part of multimodal analgesia in cardiac surgery. However, objective assessment of block quality and its relationship with clinical outcomes remains limited in the literature. This prospective observational study aims to evaluate the anatomical success of ultrasound-guided fascial plane blocks applied in elective open heart surgery (median sternotomy) using two simultaneous methods: a trained artificial intelligence (AI) model and a blinded expert anesthesiologist. Block images will be recorded in DICOM format and scored on a 3-point scale (1: incorrect anatomical placement, 2: patchy spread, 3: ideal anatomical placement). The relationship between anatomical block success scores and postoperative pain (NRS at 0, 6, 12, 24, and 48 hours), total analgesic consumption, and clinical outcomes will be investigated. Agreement between AI and blinded anesthesiologist assessments will also be analyzed.
Patients scheduled for elective open heart surgery via median sternotomy will be enrolled after obtaining written informed consent, including separate consent for AI-based image analysis. All patients will undergo routine anesthetic management including BIS monitoring, intra-arterial cannulation, standard anesthesia induction, orotracheal intubation, and central venous catheterization. Fascial Plane Block Application: Following general anesthesia induction, fascial plane blocks routinely performed in our clinic will be applied by a blinded anesthesiologist using a high-frequency linear ultrasound probe (10-15 MHz, G-brand). The blocks applied include SAPB + PIFB combination or bilateral parasternal (PIFB) block, depending on the surgical decision. All blocks will be performed using 0.25% bupivacaine (total bilaterally 30 mL) under sterile conditions with an in-plane technique. Image Recording Protocol: Block images will be recorded in a standardized manner including: pre-block anatomical scanning, video recording during needle placement, local anesthetic spread images, and post-injection final images. All images will be recorded in DICOM format (minimum 1920x1080 resolution) with standardized depth, gain, and focus settings. Patient identifiers will be anonymized. AI Model Development: A Convolutional Neural Network (CNN)-based model (U-Net or ResNet architecture) will be trained using expert-labeled ultrasound images from NYSORA references. The dataset will be divided into 70% training, 20% validation, and 10% test sets using data augmentation and cross-validation techniques. The model will evaluate anatomical landmark recognition accuracy, local anesthetic spread segmentation (Dice coefficient), and similarity to ideal block (0-100 score). Block Quality Scoring: Recorded ultrasound images will be independently scored by both the trained AI model and a blinded expert anesthesiologist using a 3-point scale: 1. Anatomically incorrect block 2. Anatomically patchy block 3. Anatomically ideal block Postoperative Follow-up: Patients will be followed postoperatively with NRS pain scores (at rest and with coughing) at 0, 6, 12, 24. Additional parameters recorded include total analgesic consumption, side effects (nausea, vomiting, pruritus), complications, mobilization time, ICU stay, and hospital length of stay. Statistical Analysis: Correlation between AI scores and postoperative pain scores will be assessed using Pearson or Spearman correlation. Factors affecting pain scores will be evaluated by multiple linear regression. Differences between block types will be analyzed using ANOVA or Kruskal-Wallis test. Agreement between AI and blinded anesthesiologist assessments will be analyzed using Cohen's kappa coefficient. Sample Size: Based on pilot study data, 120 patients are planned with 95% power.
Study Type
OBSERVATIONAL
Enrollment
120
University of Health Sciences Bursa Yüksek Ihtisas Training and Research Hospital
Bursa, Yıldırım, Turkey (Türkiye)
Postoperative Pain Score
Postoperative pain assessed using the Numerical Rating Scale (NRS) at rest and with coughing at 0, 6, 12, 24 hours after surgery. NRS ranges from 0 (no pain) to 10 (worst imaginable pain).
Time frame: 48 hours postoperatively
Agreement Between AI and Blinded Anesthesiologist Block Quality Scores
Comparison of fascial plane block anatomical success scores assigned by the trained AI model and the blinded expert anesthesiologist using a 3-point scale (1: incorrect, 2: patchy, 3: ideal). Agreement assessed by Cohen's kappa coefficient.
Time frame: Intraoperative
Total Analgesic Consumption
Total amount and type of analgesic agents consumed during the postoperative 24-hour period.
Time frame: 24 hours postoperatively
ICU Length of Stay
Duration of stay in the intensive care unit following open heart surgery.
Time frame: Through ICU discharge, approximately 1-7 days
Hospital Length of Stay
Total duration of hospital stay following open heart surgery.
Time frame: Through hospital discharge, approximately 5-10 days
Postoperative Complications
Incidence of postoperative complications including nausea, vomiting, pruritus, and other adverse events related to fascial plane blocks or analgesic use.
Time frame: 48 hours postoperatively
Time to Mobilization
Time from end of surgery to first patient mobilization.
Time frame: Through hospital discharge, approximately 5-14 days
This platform is for informational purposes only and does not constitute medical advice. Always consult a qualified healthcare professional.