Observational studyBMC anesthesiology2025
Comparison of the effectiveness of transversalis fascia plane block and transversus abdominis plane block for postoperative analgesia in pediatric lower abdominal surgeries: prospective, single blinded study.
Observational study in BMC anesthesiology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT06530147 (Comparison Of The Effectiveness Of Transversalis Fascia Plane Block And Transversus Abdominis Plane Block For Postoperative Analgesia After Pediatric Lower Abdominal Surgeries), which is not on this map. Cited by 4 papers.
What it found
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The trial behind it
Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.
Comparison Of The Effectiveness Of Transversalis Fascia Plane Block And Transversus Abdominis Plane Block For Postoperative Analgesia After Pediatric Lower Abdominal Surgeries
Who cites it
4 citing papers in PubMed.
- Transversus abdominis plane block improved surgical conditions in neuromuscular blocker-free pediatric laparoscopic hernia repair: a randomized trial.Surgical endoscopy · 2026Trial
- Surgeon-guided transversalis fascia plane block vs. trocar site wound infiltration in pediatric laparoscopic appendectomy.Irish journal of medical science · 2025Trial
- Fascial plane blocks in children: Mechanisms, indications, controversies, and practical guidance: A narrative review.Indian journal of anaesthesia · 2026Review
- Efficacy of Transversus Abdominal Plane Block for Post-Operative Pain Management in Laparoscopic Appendectomy: A Narrative Review.Current pain and headache reports · 2025Review
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
2 authors.
Funding
No grant is acknowledged in the PubMed record.
Abstract
backgroundAchieving adequate postoperative analgesia in the pediatric age group is also important in terms of future pain perception and chronic pain development in the subsequent period. The primary aim of our study was to compare the effects of Transversus Abdominis Plane (TAP) and Transversalis Fascia Plane (TFP) blocks on pain scores at the 6th postoperative hour in children undergoing lower abdominal surgery. Secondary aims include the observation of pain scores over the first 24 h postoperatively, the duration until the first analgesic requirement, the presence of postoperative nausea and vomiting symptoms, and the satisfaction of parents with the provided analgesia method.
methodsPatients aged between 1 and 7 years, classified as ASA I-II, who were scheduled for elective surgery for undescended testes and inguinal hernia, were included in our study. The study was designed as a prospective observational study. The patients were divided into two groups: TAP block (n = 42) and TFP block (n = 42). Intraoperative remifentanil consumption, hemodynamic parameters, postoperative FLACC pain scores, analgesic requirements, and the time of the first analgesic need were recorded for 24 h.
resultsA total of 84 patients were included in the study. The groups were similar in terms of demographic data. No difference was found in FLACC pain scores between the groups that received both TAP and TFP blocks in patients followed for 24 h postoperatively (p > 0.05). Intraoperative remifentanil consumption was similar in TAP blocks 74 (20-100) and TFP blocks 40 (24.75-71) µg, (p: 0.268). When calculating based on the first analgesic consumption for TAP and TFP groups, it is found that the median analgesic effect durations were 12 and 9 h, respectively, for the two groups.
conclusionsIn children undergoing lower abdominal surgery, ultrasound-guided TAP and TFP blocks have shown similar effects on pain scores and analgesic requirements for 24 h postoperatively. We believe that both blocks, which we found to provide analgesia without the need for opioids after lower abdominal surgery in pediatric patients, can be safely used in this patient group. CLINICAL TRIALS REGISTRATION: NCT06530147.
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