Evidence map›Paper›PMID 42265792›Full record

ArticlePerioperative medicine (London, England)2026

Comparison of sacral erector spinae plane block and caudal epidural block for postoperative analgesia in pediatric hypospadias surgery: a prospective observational study.

Sümeyye Kankal, Mert Bozdana, Engin İhsan Turan, Bahadır Çiftçi, Volkan Özen

Registry-linked trialAbstract read
In one paragraph

Article in Perioperative medicine (London, England), 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT07286786 (Comparison of Analgesic Efficacy of Sacral Erector Spinae Plane Block and Caudal Epidural Block in Pediatric Patients Undergoing Hypospadias Surgery), which is not on this map. Not yet cited in PubMed.

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1 · What the graph read from it

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2 · The registry

The trial behind it

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NCT07286786 completednot on this map

Comparison of Analgesic Efficacy of Sacral Erector Spinae Plane Block and Caudal Epidural Block in Pediatric Patients Undergoing Hypospadias Surgery

TypeobservationalSponsorProf. Dr. Cemil Tascıoglu Education and Research Hospital OrganizationRan2025 to 2025Enrolled86ConditionsHypospadiasArmsCaudal Block Anesthesia, Erector Spinae Plane Block
3 · Its place in the literature

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Sümeyye KankalDepartment of Anesthesiology and Reanimation, Prof. Dr. Cemil Taşçıoğlu City Hospital, Istanbul, Turkey.
Mert BozdanaDepartment of Anesthesiology and Reanimation, Prof. Dr. Cemil Taşçıoğlu City Hospital, Istanbul, Turkey.
Engin İhsan TuranDepartment of Anesthesiology and Reanimation, Health Science University Istanbul Kanuni Sultan Süleyman Education and Training Hospital, Atakent Mahallesi Turgut Özal Bulvarı No:46/1, Istanbul, 34303, Turkey. ihsanengin.turan@sbu.edu.tr.
Bahadır ÇiftçiDepartment of Anesthesiology and Reanimation, Istanbul Medipol University, Istanbul, Turkey.
Volkan ÖzenDepartment of Anesthesiology and Reanimation, Prof. Dr. Cemil Taşçıoğlu City Hospital, Istanbul, Turkey.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundEffective postoperative analgesia is essential in pediatric urogenital surgery to reduce stress responses and opioid exposure. Caudal epidural block is widely used for hypospadias repair; however, its duration may be limited and it is associated with neuraxial-related concerns. Sacral erector spinae plane (ESP) block has recently emerged as a potential alternative regional technique. This study aimed to compare the analgesic efficacy of sacral ESP block and caudal epidural block in children undergoing hypospadias surgery.

methodsThis prospective, comparative observational study included 86 pediatric patients (aged 1-7 years, ASA I-II) undergoing elective hypospadias repair. Patients were allocated to receive either ultrasound-guided sacral ESP block or landmark-based caudal epidural block with 0.5 mL·kg⁻

resultsEighty-six patients were analyzed (43 per group), with no significant differences in baseline characteristics. Median FLACC scores were significantly lower in the sacral ESP group at all postoperative time points, including the primary endpoint at 12 h (0 [0-0] vs. 1 [0-2], p < 0.001). Time to first rescue analgesic was significantly longer in the sacral ESP group (mean 22.7 h, 95% CI 21.5-23.9) compared with the caudal group (13.7 h, 95% CI 10.9-16.6; p < 0.001). The median number of postoperative analgesic administrations was lower in the sacral ESP group (0 [0-0] vs. 1 [0-1], p < 0.001). No block-related complications were observed in either group.

conclusionsUltrasound-guided sacral erector spinae plane block was associated with lower postoperative pain scores, prolonged time to rescue analgesia, and reduced analgesic consumption compared with caudal epidural block in pediatric patients undergoing hypospadias surgery. Sacral ESP block may represent a useful alternative to caudal epidural block; however, randomized controlled studies are required to confirm these findings.

trial registrationClinicalTrials.gov, NCT07286786.

Identifiers

PMID42265792
PMCPMC13471538

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