What is involved in a ganglion impar block procedure?

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Last updated: November 19, 2025View editorial policy

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Ganglion Impar Block Procedure

The ganglion impar block is performed by inserting a needle through the sacrococcygeal joint under fluoroscopic or ultrasound guidance to reach the retroperitoneal space anterior to the coccyx, where local anesthetic (typically 0.75% ropivacaine or bupivacaine) or neurolytic agents are injected to interrupt sympathetic and nociceptive transmission from perineal structures. 1

Anatomical Target

  • The ganglion impar (ganglion of Walther) is a solitary, unpaired retroperitoneal sympathetic structure located at the sacrococcygeal junction 2, 3
  • It represents the terminal end of the bilateral sympathetic chains and provides nociceptive and sympathetic innervation to perineal structures 2, 4
  • The ganglion is positioned anterior to the sacrococcygeal joint in the retroperitoneal space 5, 6

Clinical Indications

This block is primarily indicated for chronic pelvic and perineal pain of visceral origin, particularly when pain is refractory to conservative management. 1

  • Coccygodynia (both traumatic and idiopathic) 4
  • Chronic perineal pain syndromes 2, 3
  • Pelvic pain of visceral origin 1
  • The procedure is used as an adjuvant to decrease systemic analgesic requirements 1

Procedural Approaches

Trans-Sacrococcygeal Approach

The trans-sacrococcygeal approach is the most commonly described technique and is considered technically feasible and safe. 2

  • The needle is inserted through the sacrococcygeal joint (the first cleft below the sacral hiatus) 5, 2
  • A 23-gauge, 7 cm needle is typically used 5
  • The procedure requires 5.7-7.8 minutes on average to perform 2

Imaging Guidance Options

Fluoroscopy remains the gold standard for confirming proper needle depth and injection site, particularly for neurolytic procedures. 5, 6

  • Ultrasound guidance: A linear array transducer (5-12 MHz) can identify the sacrococcygeal joint in transverse and longitudinal views 5

    • Ultrasound is particularly helpful when the sacrococcygeal joint cannot be readily visualized on anteroposterior and lateral fluoroscopy 5
    • Real-time sonographic guidance allows accurate needle placement into the sacrococcygeal joint 5
  • Combined ultrasound and fluoroscopy: Ultrasound identifies the joint entry point, while lateral fluoroscopy confirms safe needle depth and prevents rectal injury 5, 6

  • CT guidance: Can be used for lateral approach over the Co1-Co2 coccygeal joint 3

  • Loss of resistance technique: Can be combined with ultrasound to confirm presacral space location for diagnostic or local anesthetic blocks 6

Intra-Coccygeal Joint Approach

  • An alternative approach involves needle placement through the intra-coccygeal joint 4
  • This technique also requires fluoroscopic guidance 4

Injectate Selection

Diagnostic and Therapeutic Blocks

For diagnostic and therapeutic blocks, local anesthetics are the agents of choice. 2, 3

  • 0.75% ropivacaine is commonly used 3
  • 0.125%-0.25% bupivacaine is an alternative 1
  • Volume typically ranges from 3-6 mL 2, 3

Neurolytic Blocks

Neurolytic blocks should be limited to patients with short life expectancy (typically producing blocks lasting 3-6 months). 1

  • Absolute ethanol or phenol can be used as neurolytic agents 1
  • These blocks are reserved for patients with limited prognosis due to the duration of effect 1

Efficacy Assessment

Immediate effectiveness is evaluated by measuring pain reduction 30 minutes post-procedure, with successful blocks typically achieving >50% pain reduction. 2, 3

  • In a cohort of 220 blocks, 87.7% demonstrated immediate positive response with >50% pain improvement 3
  • Complete but transient pain relief occurred in 54.1% of procedures 3
  • Visual Analogue Scale (VAS) scores show statistically significant improvement before and after blocks (P < 0.001) 3
  • Long-term follow-up at one month shows improvement in 41-43.6% of patients 3
  • In idiopathic coccygodynia cases, single blocks have achieved complete pain relief (NRS=0) lasting up to one year 4

Repeated Blocks

Repeated ganglion impar blocks can provide cumulative benefit with decreased pain intensity over time. 3

  • Three repeated blocks are commonly performed in clinical practice 3
  • VAS scores before repeated blocks show significant improvement with decreased pain intensity over time (P = 0.001) 3
  • Repeated blocks allow short-term pain reduction with moderate intermediate-term effects 3

Safety Profile

The procedure has an excellent safety profile with no major adverse events reported in prospective studies. 2, 3

  • No complications were documented in a series of 16 consecutive patients 2
  • The procedure is considered technically feasible and safe 2
  • Fluoroscopic confirmation is essential for neurolytic procedures to document needle tip position relative to the rectum and prevent rectal injury 6

Common Pitfalls and Caveats

  • Fluoroscopy limitations: The sacrococcygeal joint cannot always be readily visualized on standard AP and lateral fluoroscopy, making ultrasound assistance valuable 5
  • Neurolytic agent selection: For patients with good prognosis, neurolytic blocks may produce symptoms more difficult to control than the original pain 1
  • Rectal injury risk: Always confirm needle depth with lateral fluoroscopy before injection, especially for neurolytic procedures 5, 6
  • Transient nature: Even successful blocks typically provide temporary relief, requiring repeat procedures or transition to other pain management strategies 3

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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