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B442 Regional analgesia via continuous erector spinaeplane (ESP) catheters for thoracic outlet decompression surgery in children – a retrospective case series
  1. A Koka,
  2. BP Modi,
  3. EA Nir and
  4. CA Sullivan
  1. Boston Children’s Hospital, Boston, MA, USA


Background and Aims Thoracic outlet syndrome (TOS) is an uncommon compression syndrome of the subclavian vessels or the brachial plexus that presents with pain, motor weakness, swelling, vasoactive and sensory changes in the affected limb1,2. Treatment often requires thoracic outlet decompressive surgery (TODS). We aimed to assess the efficacy of ESP catheters3,4,5in pediatric patients undergoing TODS over a 12-year period.

Methods After IRB approval, we did a retrospective chart review of pediatric patients (<18 y) who underwent TODS at a tertiary children’s hospital, between Mar 2010 and Feb 2022. We blindly matched regional analgesia group (RAg) patients with no intervention (Cg) historical controls (1:2)5. We compared baseline patient characteristics (age, weight, ASA-PS, TOS type/laterality, TODS metrics). Outcomes assessed were postoperative recovery criteria (nausea and vomiting (PONV), itching, constipation, time to floor discharge), hospital length of stay (LoS), pain scores in the first hours, and total oral morphine equivalent (OME) use in the first two days3,4,5.

Results There were no significant demographic or TODS differences between the groups (Table 1). Blocks took 17.9±7.6 min to complete. Pain scores were decreased in the RAg patients 3–24h postoperatively. Opioid analgesia administered to the RAg in 24h were less than a third than the Cg (Table 2). Non-Opioid analgesia didn’t change (Figure 1). PONV (and possibly pruritus) in the Cg were more prevalent in the first 48h compared to the RAg (p=0.006, Table 2).

Abstract B442 Table 1
Abstract B442 Table 2

Conclusions Regional analgesia continuous ESP catheters for TODS decreased pain, OME analgesic use, and some opiate adverse effects in a pediatric historical cohort.

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