Pain Control and Recovery After Thoracic Surgery Using SPSIP Block
Comparison of the Analgesic Effectiveness of Ultrasound-Guided Serratus Posterior Superior Intercostal Plane Block Among Different Thoracic Surgical Procedures: A Prospective Observational Cohort Study
Thoracic surgery is frequently associated with significant postoperative pain, which may impair respiratory function, mobilization, recovery, and patient satisfaction. The Serratus Posterior Superior Intercostal Plane (SPSIP) block is a recently described ultrasound-guided fascial plane block that may provide effective analgesia after thoracic surgery. This prospective observational cohort study will evaluate the analgesic effectiveness and postoperative recovery associated with SPSIP block in adult patients undergoing elective minor video-assisted thoracoscopic surgery (VATS), major VATS, or thoracotomy. All patients will receive SPSIP block as part of routine institutional multimodal analgesia. The primary outcome will be postoperative quality of recovery assessed using the Quality of Recovery-15 (QoR-15) questionnaire at 24 hours after surgery. Secondary outcomes will include postoperative pain intensity, opioid consumption, rescue analgesic requirements, postoperative nausea and vomiting, pulmonary complications, patient satisfaction, length of hospital stay, and chronic postoperative pain.
Aperçu de l'étude
Statut
Les conditions
Intervention / Traitement
Description détaillée
Postoperative pain remains an important clinical concern following thoracic surgery. Inadequate analgesia may adversely affect deep breathing, coughing, pulmonary toilet, early mobilization, and overall postoperative recovery. Although minimally invasive thoracic surgical techniques have reduced surgical trauma, clinically relevant postoperative pain may still occur. Regional anesthesia techniques are commonly incorporated into multimodal analgesic strategies for thoracic surgery. Fascial plane blocks have emerged as alternatives to more invasive regional techniques because of their relative technical simplicity and potential safety advantages. The Serratus Posterior Superior Intercostal Plane (SPSIP) block is a recently described ultrasound-guided fascial plane block with promising analgesic efficacy; however, evidence regarding whether its effectiveness differs according to the invasiveness of the thoracic surgical procedure remains limited.
This prospective observational cohort study will include adult patients undergoing elective thoracic surgery under general anesthesia who receive an ultrasound-guided SPSIP block as part of routine institutional multimodal analgesia. Patients will be categorized according to the surgical procedure into three predefined cohorts: minor video-assisted thoracoscopic surgery (VATS), major VATS, and thoracotomy. The SPSIP block will be performed after induction of general anesthesia according to routine institutional clinical practice using a long-acting local anesthetic. No participant will be assigned to a surgical procedure or regional anesthesia technique for research purposes.
The primary objective is to compare postoperative quality of recovery among the three surgical cohorts. Quality of recovery will be assessed using the 15-item Quality of Recovery questionnaire (QoR-15) at 24 hours after surgery, with higher scores indicating better postoperative recovery.
Secondary outcomes will include postoperative opioid consumption expressed as morphine milligram equivalents, pain intensity measured using the Numeric Rating Scale at rest and during coughing, time to first rescue analgesia, total rescue analgesic requirement, postoperative nausea and vomiting, antiemetic requirement, hemodynamic variables, pulmonary complications, time to ambulation, length of hospital stay, and patient satisfaction. Pain intensity will be evaluated in the post-anesthesia care unit and at 2, 6, 12, and 24 hours after surgery. Patients will also be followed for clinically relevant postoperative outcomes, including hospital readmission within 30 days and chronic postoperative pain at 3 and 6 months. Potential block-related complications, including local anesthetic systemic toxicity, pneumothorax, hematoma, and infection, will be recorded.
The study is designed to determine whether postoperative recovery and analgesic outcomes associated with the same SPSIP block technique differ according to the type and invasiveness of thoracic surgery.
Type d'étude
Inscription (Estimé)
Contacts et emplacements
Coordonnées de l'étude
- Nom: Ahmet Salih Tüzen, M.D.
- Numéro de téléphone: +90 535 391 55 77
- E-mail: astuzen@icloud.com
Sauvegarde des contacts de l'étude
- Nom: Murat Aksun, M.D.
- Numéro de téléphone: +90 552 363 16 14
- E-mail: murataksun@yahoo.com
Lieux d'étude
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İzmir
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Izmir, İzmir, Turquie (Türkiye), 35360
- Recrutement
- Izmir Katip Celebi University Atatürk Training and Research Hospital, Karabaglar, Izmir
-
Contact:
- Bilgesu Kaya Çalış, M.D.
- Numéro de téléphone: +90 5398795124
- E-mail: bilgesukaya2@gmail.com
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Chercheur principal:
- Murat Aksun, M.D.
-
-
Critères de participation
Critère d'éligibilité
Âges éligibles pour étudier
Accepte les volontaires sains
Sexes éligibles pour l'étude
Méthode d'échantillonnage
Population étudiée
Adults undergoing elective minor VATS, major VATS, or thoracotomy under general anesthesia who receive SPSIP block as part of routine multimodal analgesia
La description
Inclusion Criteria:
- Age 18 years or older
- American Society of Anesthesiologists (ASA) physical status I-III
- Scheduled for elective thoracic surgery
- Undergoing minor video-assisted thoracoscopic surgery (VATS), major VATS, or thoracotomy
- Planned ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block as part of routine multimodal analgesia
- Able and willing to provide written informed consent
Exclusion Criteria:
- Patient refusal
- Known allergy to amide local anesthetics
- Coagulopathy
- Therapeutic anticoagulation incompatible with regional anesthesia
- Infection at the planned block injection site
- Pregnancy
- Emergency surgery
- Chronic opioid therapy for more than 3 months
- Chronic pain syndrome
- Cognitive impairment that prevents reliable study assessments
- Inability to complete the Quality of Recovery-15 (QoR-15) questionnaire
Plan d'étude
Comment l'étude est-elle conçue ?
Détails de conception
- Modèles d'observation: COHORT
- Perspectives temporelles: PROSPECTIVE
Cohortes et interventions
Groupe / Cohorte |
Intervention / Traitement |
|---|---|
|
Minor VATS
Adult patients undergoing elective minor video-assisted thoracoscopic surgery (VATS) under general anesthesia who receive an ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block as part of routine institutional multimodal analgesia. The surgical procedure and regional analgesic technique are determined as part of routine clinical care and are not assigned by the study protocol. |
An ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block will be performed after induction of general anesthesia according to routine institutional clinical practice using a long-acting local anesthetic. |
|
Major VATS
Adult patients undergoing elective major video-assisted thoracoscopic surgery (VATS) under general anesthesia who receive an ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block as part of routine institutional multimodal analgesia. The surgical procedure and regional analgesic technique are determined as part of routine clinical care and are not assigned by the study protocol. |
An ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block will be performed after induction of general anesthesia according to routine institutional clinical practice using a long-acting local anesthetic. |
|
Thoracotomy
Adult patients undergoing elective thoracotomy under general anesthesia who receive an ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block as part of routine institutional multimodal analgesia. The surgical procedure and regional analgesic technique are determined as part of routine clinical care and are not assigned by the study protocol. |
An ultrasound-guided Serratus Posterior Superior Intercostal Plane (SPSIP) block will be performed after induction of general anesthesia according to routine institutional clinical practice using a long-acting local anesthetic. |
Que mesure l'étude ?
Principaux critères de jugement
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Quality of Recovery-15 Score at 24 Hours
Délai: 24 hours after surgery
|
Postoperative quality of recovery will be assessed using the 15-item Quality of Recovery questionnaire (QoR-15). Higher scores indicate better postoperative recovery. QoR-15 scores will be compared among the minor VATS, major VATS, and thoracotomy cohorts. |
24 hours after surgery
|
Mesures de résultats secondaires
Mesure des résultats |
Description de la mesure |
Délai |
|---|---|---|
|
Total Opioid Consumption During the First 24 Postoperative Hours
Délai: 0 to 24 hours after surgery
|
Total opioid consumption during the first 24 hours after surgery will be calculated and converted to morphine milligram equivalents (MME) to allow comparison among the three surgical cohorts. |
0 to 24 hours after surgery
|
|
Pain Intensity at Rest Upon Admission to the PACU
Délai: Upon admission to the post-anesthesia care unit (PACU)
|
Postoperative pain intensity at rest will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
Upon admission to the post-anesthesia care unit (PACU)
|
|
Pain Intensity at Rest at 2 Hours
Délai: 2 hours after the end of surgery
|
Postoperative pain intensity at rest will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
2 hours after the end of surgery
|
|
Pain Intensity at Rest at 6 Hours
Délai: 6 hours after the end of surgery
|
Postoperative pain intensity at rest will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
6 hours after the end of surgery
|
|
Pain Intensity at Rest at 12 Hours
Délai: 12 hours after the end of surgery
|
Postoperative pain intensity at rest will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
12 hours after the end of surgery
|
|
Pain Intensity at Rest at 24 Hours
Délai: 24 hours after the end of surgery
|
Postoperative pain intensity at rest will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
24 hours after the end of surgery
|
|
Pain Intensity During Coughing Upon Admission to the PACU
Délai: Upon admission to the post-anesthesia care unit (PACU)
|
Postoperative pain intensity during coughing will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
Upon admission to the post-anesthesia care unit (PACU)
|
|
Pain Intensity During Coughing at 2 Hours
Délai: 2 hours after the end of surgery
|
Postoperative pain intensity during coughing will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
2 hours after the end of surgery
|
|
Pain Intensity During Coughing at 6 Hours
Délai: 6 hours after the end of surgery
|
Postoperative pain intensity during coughing will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
6 hours after the end of surgery
|
|
Pain Intensity During Coughing at 12 Hours
Délai: 12 hours after the end of surgery
|
Postoperative pain intensity during coughing will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
12 hours after the end of surgery
|
|
Pain Intensity During Coughing at 24 Hours
Délai: 24 hours after the end of surgery
|
Postoperative pain intensity during coughing will be assessed using the 11-point Numeric Rating Scale (NRS), ranging from 0 to 10, where 0 indicates no pain and 10 indicates the worst imaginable pain. Higher scores indicate greater pain intensity and therefore a worse outcome. |
24 hours after the end of surgery
|
|
Time to First Rescue Analgesic Administration
Délai: 0 to 24 hours after surgery
|
Time from completion of surgery to the first administration of rescue analgesic medication will be recorded. |
0 to 24 hours after surgery
|
|
Total Rescue Analgesic Requirement
Délai: 0 to 24 hours after surgery
|
The total amount of rescue analgesic medication administered during the postoperative observation period will be recorded. |
0 to 24 hours after surgery
|
|
Incidence of Postoperative Nausea and Vomiting
Délai: 0 to 24 hours after surgery
|
The number of participants experiencing postoperative nausea and/or vomiting will be recorded. |
0 to 24 hours after surgery
|
|
Requirement for Rescue Antiemetic Medication
Délai: 0 to 24 hours after surgery
|
The number of participants requiring rescue antiemetic medication will be recorded. |
0 to 24 hours after surgery
|
|
Time to First Postoperative Ambulation
Délai: From the end of surgery until first postoperative ambulation or hospital discharge, whichever occurs first, assessed up to 30 days after surgery.
|
Time from the end of surgery to the patient's first postoperative ambulation will be recorded in hours. First ambulation will be defined as the first documented occasion on which the patient gets out of bed and ambulates with or without assistance. Patients who do not ambulate before hospital discharge will be considered not to have experienced the event during the observation period. |
From the end of surgery until first postoperative ambulation or hospital discharge, whichever occurs first, assessed up to 30 days after surgery.
|
|
Postoperative Length of Hospital Stay
Délai: From the end of surgery until hospital discharge, assessed up to 30 days after surgery.
|
The duration of postoperative hospitalization will be recorded in days, calculated from the end of surgery until hospital discharge. |
From the end of surgery until hospital discharge, assessed up to 30 days after surgery.
|
|
Chronic Postoperative Pain at 3 Months
Délai: 3 months after surgery
|
Chronic postsurgical pain will be defined as pain that developed or increased in intensity after surgery, is located in the surgical area or a related innervation territory, persists at 3 months after surgery, and is not better explained by infection, malignancy, a pre-existing pain condition, or another alternative cause. Pain intensity will be assessed using an 11-point Numeric Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain). |
3 months after surgery
|
|
Chronic Postoperative Pain at 6 Months
Délai: 6 months after surgery
|
Chronic postsurgical pain will be defined as pain that developed or increased in intensity after surgery, is located in the surgical area or a related innervation territory, persists at 6 months after surgery, and is not better explained by infection, malignancy, a pre-existing pain condition, or another alternative cause. Pain intensity will be assessed using an 11-point Numeric Rating Scale (NRS), ranging from 0 (no pain) to 10 (worst imaginable pain). |
6 months after surgery
|
|
Hospital Readmission Within 30 Days
Délai: Within 30 days after surgery
|
The number of participants requiring unplanned hospital readmission within 30 days after surgery will be recorded. |
Within 30 days after surgery
|
|
Incidence of SPSIP Block-Related Complications
Délai: From block performance until hospital discharge, assessed up to 30 days after surgery.
|
The number of participants who develop one or more complications related to the Serratus Posterior Superior Intercostal Plane (SPSIP) block will be recorded. Complications will include local anesthetic systemic toxicity, pneumothorax attributable to the block, hematoma at the block site, and infection at the block site. |
From block performance until hospital discharge, assessed up to 30 days after surgery.
|
|
Incidence of Postoperative Pulmonary Complications
Délai: From the end of surgery until hospital discharge, up to 30 days
|
Postoperative pulmonary complications will include pneumonia, clinically significant atelectasis requiring therapeutic intervention, bronchospasm requiring treatment, aspiration pneumonitis, acute respiratory distress syndrome, postoperative respiratory failure requiring non-invasive ventilatory support or reintubation, or an unplanned escalation in respiratory support. Participants experiencing at least one of these events will be considered to have a postoperative pulmonary complication. |
From the end of surgery until hospital discharge, up to 30 days
|
|
Patient Satisfaction With Postoperative Analgesia
Délai: 24 hours after surgery
|
Patient satisfaction with postoperative pain management will be assessed using a 5-point Likert scale: 1 = very dissatisfied, 2 = dissatisfied, 3 = neither satisfied nor dissatisfied, 4 = satisfied, and 5 = very satisfied. Higher scores indicate greater satisfaction with postoperative analgesia. |
24 hours after surgery
|
Collaborateurs et enquêteurs
Parrainer
Les enquêteurs
- Chercheur principal: Murat Aksun, M.D., Izmir Katip Celebi University Atatürk Training and Research Hospital
Dates d'enregistrement des études
Dates principales de l'étude
Début de l'étude (Réel)
Achèvement primaire (Estimé)
Achèvement de l'étude (Estimé)
Dates d'inscription aux études
Première soumission
Première soumission répondant aux critères de contrôle qualité
Première publication (Réel)
Mises à jour des dossiers d'étude
Dernière mise à jour publiée (Réel)
Dernière mise à jour soumise répondant aux critères de contrôle qualité
Dernière vérification
Plus d'information
Termes liés à cette étude
Mots clés
Termes MeSH pertinents supplémentaires
Autres numéros d'identification d'étude
- 2025-SAEK-0815
Plan pour les données individuelles des participants (IPD)
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Description du régime IPD
No individual participant data sharing is currently planned.
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