NERVOUS SYSTEM OVERVIEW
The nervous system is divided into two branches, the central nervous system and the peripheral nervous system. The central nervous system includes the brain and spinal cord and is primarily responsible for initiating, planning, and coordinating actions. The peripheral nervous system includes the nerves and ganglia (nerve clusters) that extend to the peripheral organs (i.e. muscles, glands, digestive organs, reproductive organs, etc) (1). The peripheral nervous system is further divided into two branches, the afferent (sensory) and efferent (motor or movement) divisions (2). Both the afferent and efferent divisions are subdivided into two branches, the autonomic and somatic nervous systems. The somatic nervous system is responsible for controlling skeletal muscle movements and is often referred to as the voluntary nervous system. The autonomic nervous system (ANS) regulates a wide range of involuntary physiological responses and can be further divided into two segments: the sympathetic and parasympathetic nervous systems (2).
The two branches of the ANS are responsible for producing antagonistic physiological effects, and the ganglia (nerve clusters) associated with the ANS essentially act as a junction between the nerves originating from the central nervous system and the nerves innervating their target organs in the periphery. The sympathetic ganglia deliver information to the body about stress, impending danger and fear. These ganglia are responsible for the physiological responses to these stimuli, commonly known as the “fight-or-flight” response. Alternatively, the parasympathetic ganglia produce antagonistic physiological responses in order to maintain a steady-state, commonly known as the “rest-and-digest” response.
SYMPATHETIC NERVOUS SYSTEM
The stellate ganglion (SG) is a nerve cluster associated with the sympathetic nervous system. The SG is located in the upper neck and functions to coordinate with the central nervous system to produce sympathetic physiological responses. Signals from the SG are transmitted to a wide range of peripheral targets, including the heart, eyes, sweat glands, and pain receptors (3, 4, 5). As such, the SG has a major role in carrying out sympathetic nervous system responses. In healthy, normally functioning individuals, “fight-or-flight” responses are associated with appropriate stimuli, such as an increase in sweating and heart rate when running from a bear or while slamming on the brakes to avoid a car accident. Further, mental or emotional stress has been shown to stimulate the sympathetic nervous system and elicit similar physiological responses to physical stress (6, 7, 8). The sympathetic nervous system is essential to normal functioning and survival because these physiological responses liberate extra energy and equip the body to deal with emergency situations. Despite this vital role, overstimulation of the sympathetic nervous system can result in altered SG signaling and can therefore lead to dysfunctional or inappropriate physiological responses (9).
PTSD AND SYMPATHETIC OVERDRIVE
Unfortunately, the physiological manifestations of sympathetic stimulation do not exclusively occur as a response to appropriate stimuli for individuals with Post-Traumatic Stress Disorder (PTSD) or Anxiety (10). Many studies have evidenced that both PTSD patients and patients with anxiety have overactive sympathetic reactivity and activity during mental stress and under resting conditions (10, 11, 12, 13). Individuals with overactive sympathetic reactivity experience heightened physiological responses to stressors. These magnified responses underscore the physiological basis of symptoms reported by patients with PTSD or anxiety (13). Exposure to or experiencing traumatic events can lead to debilitating and life-altering PTSD or anxiety symptoms that originate from the overactivity of the “fight-or-flight” response (12, 13). Research suggests that the recurrent trauma-related symptoms experienced by PTSD patients may be a result of enhanced and prolonged sympathetic stress responses (12, 14).
STELLATE GANGLION BLOCK FOR PTSD AND ANXIETY
Conventional treatments for PTSD and anxiety are centered around psychological therapy in combination with pharmacological treatments (i.e. antidepressants, antipsychotic drugs, and/or mood stabilizers) (15). Although some patients may find these conventional treatments adequate for symptom relief or even symptom remission, many patients with PTSD and patients with anxiety continue to struggle managing their symptoms despite seeking care. Fortunately, neuroscience research has revealed a new therapeutic avenue for individuals with PTSD and anxiety. For many years, Stellate Ganglion Blocks (SGB) has been safely and widely used as a minimally-invasive treatment option for many medical conditions ranging from peripheral vascular disease to refractory ventricular tachycardia (16, 17). More recently, however, SGBs have been shown to have significant and long-lasting symptom relief for patients with PTSD and anxiety (18, 19, 20, 21). The SGB procedure is able to successfully treat PTSD and anxiety symptoms by anesthetizing the physical source of trauma-related symptom sympathetic overdrive, the stellate ganglion nerve cluster. SGBs are able to effectively “reset” the sympathetic nervous system and restore normal biological function, providing patients with rapid and significant symptom relief of even the most severe trauma-related symptoms. When used in conjunction with trauma-focused psychotherapy, SGBs have a 70%-80% success rate in treating anxiety and PTSD symptoms (19, 22, 23).
SGBs have also been used to treat sympathetic nervous system-related conditions of the head, neck and upper body ranging from cardiac applications to complex regional pain syndrome (CRPS) (24, 25). SGBs have been shown to reduce symptoms related to sympathetic overdrive in drug-refractory electrical storms due to ventricular arrhythmia (a condition that involves recurrent ventricular arrhythmias) and inappropriate sinus tachycardia (elevated heart rate) (24, 26). As both of these cardiac conditions produce sympathetic-related symptoms that are notoriously difficult to treat because patients often do not respond to medical therapy, SGBs provide patients with an alternative treatment option that reduces morbidity and mortality (24, 26, 27). Further, SGBs can be used to treat CRPS, a chronic pain condition in which patients complain of characteristic symptoms like allodynia (extreme sensitivity to touch), hyperalgesia (extreme response to pain), sudomotor (autonomic nervous system abnormalities such as increased sweating) and vasomotor abnormalities (changes in skin temperature) following an injury, trauma or surgery (28, 29). Many CRPS symptoms involve dysregulated sympathetic nervous system responses, and CRPS is formerly known as “reflex sympathetic dystrophy” (28). As SGBs help “reset” the sympathetic nervous system, these procedures can produce long-lasting and sustained pain relief of CRPS symptoms (30, 31). In addition, SGBs have been shown to reduce acute pain and incidence of postherpetic neuralgia, the most common complication of shingles (herpes zoster virus infection) that results in prolonged burning pain after the shingles rash disappears (32). SGBs have a wide range of clinical applications and offer patients an alternative treatment option for when other therapies fail to provide adequate symptom relief.
STELLATE GANGLION BLOCK PROCEDURE
Stellate Ganglion Blocks are widely studied and highly effective minimally-invasive outpatient procedures performed under monitored care anesthesia (light sedation). Using x-ray fluoroscopy and ultrasound, a small needle is guided into the neck region that contains the stellate ganglion nerve cluster. Once the needle position is confirmed, a local numbing anesthetic (e.g. bupivacaine or lidocaine) is injected into the stellate ganglion. The entire procedure is performed under ultrasound guidance and takes an average of 20 minutes to complete (33). Although the effects of the local anesthetic wear off within 8-12 hours, a single SGB has been shown to provide immediate symptom-relief that lasts several weeks or months (21). Many patients only require a single procedure to effectively alleviate their PTSD or anxiety symptoms, but two to three procedures spread over several years is also common (33).
Conclusion
PTSD and Anxiety are chronic mental disorders that can severely impact quality of life, and traditional treatment options fail to address the physical changes that occur as a result of these conditions. Stellate Ganglion Blocks provide patients with a safe and effective treatment option for PTSD and anxiety, and clinical data has repeatedly shown that SGBs produce powerful and long-lasting symptom relief. By collaborating with mental health professionals, the Anesthesiologists at Hudson Medical offer SGBs to patients struggling to manage their PTSD and Anxiety symptoms.
Citations
- Alshak, Mark N. and Joe M Das. “Neuroanatomy, Sympathetic Nervous System.” StatPearls, StatPearls Publishing, 26 July 2021.
- Goldstein, B. “Anatomy of the peripheral nervous system.” Physical medicine and rehabilitation clinics of North America vol. 12,2 (2001): 207-36.
- Chaudhry, A et al. “Detection of the Stellate and Thoracic Sympathetic Chain Ganglia with High-Resolution 3D-CISS MR Imaging.” AJNR. American journal of neuroradiology vol. 39,8 (2018): 1550-1554. doi:10.3174/ajnr.A5698
- Kwon, Oh Jin et al. “Morphological Spectra of Adult Human Stellate Ganglia: Implications for Thoracic Sympathetic Denervation.” Anatomical record (Hoboken, N.J. : 2007) vol. 301,7 (2018): 1244-1250. doi:10.1002/ar.23797
- Yin, Zhaoyang et al. “Neuroanatomy and clinical analysis of the cervical sympathetic trunk and longus colli.” Journal of biomedical research vol. 29,6 (2015): 501-7. doi:10.7555/JBR.29.20150047
- Carter, Jason R, and David S Goldstein. “Sympathoneural and adrenomedullary responses to mental stress.” Comprehensive Physiology vol. 5,1 (2015): 119-46. doi:10.1002/cphy.c140030
- Yaribeygi, Habib et al. “The impact of stress on body function: A review.” EXCLI journal vol. 16 1057-1072. 21 Jul. 2017, doi:10.17179/excli2017-480
- Fontes, Marco Antônio Peliky et al. “Emotional stress and sympathetic activity: contribution of dorsomedial hypothalamus to cardiac arrhythmias.” Brain research vol. 1554 (2014): 49-58. doi:10.1016/j.brainres.2014.01.043
- Lipov, Eugene G et al. “A unifying theory linking the prolonged efficacy of the stellate ganglion block for the treatment of chronic regional pain syndrome (CRPS), hot flashes, and posttraumatic stress disorder (PTSD).” Medical hypotheses vol. 72,6 (2009): 657-61. doi:10.1016/j.mehy.2009.01.009
- Park, Jeanie et al. “Baroreflex dysfunction and augmented sympathetic nerve responses during mental stress in veterans with post-traumatic stress disorder.” The Journal of physiology vol. 595,14 (2017): 4893-4908. doi:10.1113/JP274269
- Wenner, Megan M. “Sympathetic activation in chronic anxiety: not just at the “height” of stress. Editorial Focus on “Relative burst amplitude of muscle sympathetic nerve activity is an indicator of altered sympathetic outflow in chronic anxiety”.” Journal of neurophysiology vol. 120,1 (2018): 7-8. doi:10.1152/jn.00220.2018
- Fonkoue, Ida T et al. “Symptom severity impacts sympathetic dysregulation and inflammation in post-traumatic stress disorder (PTSD).” Brain, behavior, and immunity vol. 83 (2020): 260-269. doi:10.1016/j.bbi.2019.10.021
- Orr, Scott P et al. “Psychophysiology of post-traumatic stress disorder.” The Psychiatric clinics of North America vol. 25,2 (2002): 271-93. doi:10.1016/s0193-953x(01)00007-7
- Sherin, Jonathan E, and Charles B Nemeroff. “Post-traumatic stress disorder: the neurobiological impact of psychological trauma.” Dialogues in clinical neuroscience vol. 13,3 (2011): 263-78. doi:10.31887/DCNS.2011.13.2/jsherin
- Miao, Xue-Rong et al. “Posttraumatic stress disorder: from diagnosis to prevention.” Military Medical Research vol. 5,1 32. 28 Sep. 2018, doi:10.1186/s40779-018-0179-0
- Kulkarni, Kalpana R et al. “Efficacy of stellate ganglion block with an adjuvant ketamine for peripheral vascular disease of the upper limbs.” Indian journal of anaesthesia vol. 54,6 (2010): 546-51. doi:10.4103/0019-5049.72645
- Rajesh, M C et al. “Stellate Ganglion Block as Rescue Therapy in Refractory Ventricular Tachycardia.” Anesthesia, essays and researches vol. 11,1 (2017): 266-267. doi:10.4103/0259-1162.194566
- Lipov, Eugene G et al. “Stellate ganglion block improves refractory post-traumatic stress disorder and associated memory dysfunction: a case report and systematic literature review.” Military medicine vol. 178,2 (2013): e260-4. doi:10.7205/MILMED-D-12-00290
- Lynch, James H. “Stellate ganglion block treats posttraumatic stress: An example of precision mental health.” Brain and behavior vol. 10,11 (2020): e01807. doi:10.1002/brb3.1807
- Summers, Mary R, and Remington L Nevin. “Stellate Ganglion Block in the Treatment of Post-traumatic Stress Disorder: A Review of Historical and Recent Literature.” Pain practice : the official journal of World Institute of Pain vol. 17,4 (2017): 546-553. doi:10.1111/papr.12503
- Mulvaney, Sean W et al. “Stellate ganglion block used to treat symptoms associated with combat-related post-traumatic stress disorder: a case series of 166 patients.” Military medicine vol. 179,10 (2014): 1133-40. doi:10.7205/MILMED-D-14-00151
- Lynch, James H et al. “Behavioral health clinicians endorse stellate ganglion block as a valuable intervention in the treatment of trauma-related disorders.” Journal of investigative medicine : the official publication of the American Federation for Clinical Research vol. 69,5 (2021): 989-993. doi:10.1136/jim-2020-001693
- Lynch, James H et al. “Effect of Stellate Ganglion Block on Specific Symptom Clusters for Treatment of Post-Traumatic Stress Disorder.” Military medicine vol. 181,9 (2016): 1135-41. doi:10.7205/MILMED-D-15-00518
- Tian, Ying et al. “Effective Use of Percutaneous Stellate Ganglion Blockade in Patients With Electrical Storm.” Circulation. Arrhythmia and electrophysiology vol. 12,9 (2019): e007118. doi:10.1161/CIRCEP.118.007118
- Datta, Rashmi et al. “A study of the efficacy of stellate ganglion blocks in complex regional pain syndromes of the upper body.” Journal of anaesthesiology, clinical pharmacology vol. 33,4 (2017): 534-540. doi:10.4103/joacp.JOACP_326_16
- Cha, Yong-Mei et al. “Stellate ganglion block and cardiac sympathetic denervation in patients with inappropriate sinus tachycardia.” Journal of cardiovascular electrophysiology vol. 30,12 (2019): 2920-2928. doi:10.1111/jce.14233
- Sahoo, Rajendra K et al. “Stellate ganglion block as rescue therapy in drug-resistant electrical storm.” Annals of cardiac anaesthesia vol. 24,3 (2021): 415-418. doi:10.4103/aca.ACA_168_19
- Albazaz, Raneem et al. “Complex regional pain syndrome: a review.” Annals of vascular surgery vol. 22,2 (2008): 297-306. doi:10.1016/j.avsg.2007.10.006
- Yucel, Istemi et al. “Complex regional pain syndrome type I: efficacy of stellate ganglion blockade.” Journal of orthopaedics and traumatology : official journal of the Italian Society of Orthopaedics and Traumatology vol. 10,4 (2009): 179-83. doi:10.1007/s10195-009-0071-5
- Singh Rana, Shiv Pratap et al. “Stellate ganglion pulsed radiofrequency ablation for stretch induced complex regional pain syndrome type II.” Saudi journal of anaesthesia vol. 9,4 (2015): 470-3. doi:10.4103/1658-354X.159480
- Datta, Rashmi et al. “A study of the efficacy of stellate ganglion blocks in complex regional pain syndromes of the upper body.” Journal of anaesthesiology, clinical pharmacology vol. 33,4 (2017): 534-540. doi:10.4103/joacp.JOACP_326_16
- Makharita, Mohamed Y et al. “Effect of early stellate ganglion blockade for facial pain from acute herpes zoster and incidence of postherpetic neuralgia.” Pain physician vol. 15,6 (2012): 467-74.
- “How SGB Works.” Stella Center, https://stellacenter.com/.