Respiratory Diaphragm Part 1

By Robert Libbey, RMT

Originally published in Massage & Myotherapy Australia Journal | 12 Issue 3 | Spring 2022

In Part 1, we will be looking at the research pertaining to Phrenic Nerve and Respiratory Diaphragm to advance your knowledge and understanding in an effort to improve your outcomes with your patients.

In part 2, we will look at research documenting 2 manual techniques applied to the Respiratory Diaphragm and share video links demonstrating the techniques. As an added bonus an “Alternative” manual technique will be demonstrated to expand the therapists’ options, improving your competence and confidence no matter what patient presents to your office.

The information presented before you is an opportunity to advance and update your knowledge of an area typically misunderstood often inappropriately and ineffectively treated by well-intentioned therapists.

Working within the Biopsychosocial framework, today’s therapist strives to incorporate simple, principle based, Bottom-Up and Top-Down, evidence-informed strategies into their clinical practice, in an effort to provide treatment which maximizes positive clinical outcomes while decreasing risk of harm.

This article is not meant to be an exhaustive piece documenting all potential positive and harmful influences and effects and common rehabilitation strategies focussing on the respiratory diaphragm, but is written as an introduction to therapists to provide a better understanding of the respiratory diaphragm and how manual therapy can contribute to a patients’ maintenance and potential improvement in their quality of life. This piece will contain a blending of information obtained from published research along with my own personal experiences treating patients with various conditions, pathologies and injuries and suggestions of manual applications to a patient to best influence improved function of the respiratory diaphragm.

Structure of the Diaphragm

Drawing (view from below) shows the large central tendon, which is formed by the transverse septum. The medial and lateral arcuate ligaments are thickened fascial bands that cover the anterior psoas and quadratus lumborum muscles, respectively. Note the crura and their attachments to upper lumbar vertebral bodies. (Nason LK, et al., 2012)

(Fig 8) Diaphragmatic attachments. (a) Drawing shows diaphragmatic slips or muscle bundles (*) attached to the anterior aspects of the lower six ribs. (b) Posteroanterior radiograph shows a scalloped contour of the diaphragm caused by the slips (arrows) at their insertions on anterior ribs. Their visibility is enhanced by the flattening of the diaphragm caused by chronic obstructive pulmonary disease. (c) Sagittal CT image shows the muscle bundles near the diaphragmatic dome (arrows).

The diaphragm is both the physical barrier that separates the thorax from the abdomen and the primary muscle of ventilation. The diaphragm has multiple attachments to the body wall. The two diaphragmatic crura attach the diaphragm posteriorly to the upper lumbar vertebral bodies and disks. The crura are joined by a fibrous median arcuate ligament. (Shin MS, et al., 1985) Posterior attachments include the paired medial and lateral arcuate ligaments. (Panicek DM, et al., 1988) Diaphragmatic slips or muscle bundles attach to anterior ribs. (Fig 8). (Chavhan GB, et al., 2010; Yeh HC, et al., 1990)

The medial arcuate ligaments extend over the anterior psoas muscles as fibrous attachments between the L1 or L2 vertebral body and the transverse processes of L1. The lateral arcuate ligaments are thickened fascial bands covering the quadratus lumborum muscle and extend from the transverse processes of T12 laterally to the midportion of the 12th ribs. Anterior and lateral attachments include the inferior sternum, xiphoid process, lower six ribs, and costal cartilage. (Kleinman PK, et al., 1985)


There are three main openings in the diaphragm that allow important structures to pass between the thorax and abdomen. (Panicek DM, et al., 1988) The Inferior Vena Cava hiatus is at the T8 level and contains the Inferior Vena Cava and branches of the right phrenic nerve. It passes through the midportion of the central tendon. This opening enlarges with inspiration, drawing blood into the heart.

The esophageal hiatus is at the T10 level and contains the esophagus, vagus nerve, and sympathetic nerve branches. It passes through the crossing of the muscle fibers of the right diaphragmatic crus, which form a ring around the esophagus. This ring functions as an anatomic sphincter by constricting with inspiration and helping prevent gastroesophageal reflux.

The aortic hiatus is at the T12 level and contains the aorta, thoracic duct, and azygos and hemiazygos veins. Diaphragmatic contractions do not affect this hiatus, as it is actually retrocrural.

Fascial connections

The respiratory Diaphragm is sandwiched between the Endothoracic and Endoabdominal/ Transversalis Fascia. (Apaydin N, et al., 2008)

Phrenic Nerve

Reprinted with permission from Robert Libbey, RMT (2022)

Interesting facts about the phrenic nerve.

In medical curricular globally, students learn the phrase “C3, 4, 5 keeps the diaphragm alive.” Research has documented that this classically taught branching pattern is not always the case.

Mendelsohn et al. documented substantial variability in phrenic branching. The most frequent pattern B (absent C5 contribution) was found in 26% of the specimens (regardless of side). The classically taught branching pattern A was found in only 22% of specimens while Pattern E was found in 21% of specimens. (Mendelsohn AH, et al., 2011)

The phrenic nerve consistently arises from the root of C4 (98%) with contributions from C3 (70%) and C5 (62%).

Because the nerve arises predominantly from C4, it is formally considered part of the cervical plexus. (Bordoni, B., & Zanier, E.,2013)

The nerve crosses the upper part of the lateral border of the anterior scalene muscle and then coursed obliquely, laterally to medially, crossing the anterior surface of the anterior scalene muscle behind its fascia at approximately Erb’s point. Erb’s point has been defined as a superficial point located 2-3 cm proximal to the clavicle and the posterior border of the sternocleidomastoid muscle

The cervical plexus consists of the anterior rami of the first 4 cervical nerves.

Four cutaneous branches termed:

Lesser occipital

Greater auricular

Transverse cutaneous


It then continues posterior to the sternocleidomastoid, parallel and posterior to the internal jugular vein, then enters the thorax by passing in front of the subclavian artery.

Phrenic-stellate anastomosis

The phrenic nerve meets the stellate ganglion between the subclavian artery and the anterior side of the pleural dome (Caliot P, et al., 1984). Stellate Ganglion is involved in conditions such as chronic regional pain syndrome I and II, craniofacial hyperhidrosis, refractory angina, atypical angina, postherpetic neuralgia, phantom limb pain, chronic post-surgical pain, post-traumatic stress disorder, neuropathic pain syndromes in cancer pain, vascular headaches including cluster, headache and migraine headache, raynaud syndrome, scleroderma, upper extremity embolism, meniere syndrome, refractory cardiac arrhythmias, sympathetically mediated pain, sudden loss of hearing accompanied by tinnitus (Mehrotra M, et al., 2021).


Within the thorax, it crosses medially in front of the internal thoracic artery, although this relationship may not always be consistent, as upon entering the thorax the phrenic nerve has been recorded to cross the internal thoracic artery either superiorly, lying between the internal thoracic artery and the first rib, or inferiorly where it is held against the artery by the adjacent lung and pleura as it passes into the mediastinum. The nerve passes downward and in front of the hilum of the lung between the fibrous pericardium and mediastinal pleura and is accompanied by the pericardiophrenic vessels toward the thoracic diaphragm (Wang YJ, et al., 2016).

Location at the heart

Reprinted with permission from Robert Libbey, RMT (2022)

(Wang YJ, et al., 2016).

Anatomically, both right and left phrenic nerves are accompanied along their courses by pericardiophrenic arteries and veins, which are wrapped together inside left and right pericardiophrenic bundles. The right and left phrenic nerve will continue to descend anteriorly to the root of the lung and between the mediastinal surface of the parietal pleura and fibrous pericardium. The right phrenic nerve passes lateral to the right atrium and right ventricle and will continue to descend through the vena cava hiatus in the diaphragmatic opening at the level of T8. The left phrenic nerve descends anterior to the pericardial sac of the left ventricle and terminates at the central tendon of the diaphragm (Wang YJ, et al., 2016).

The figure illustrates an axon and synapses (in green) near muscle fibers (orange), by means of a colored micrograph under a scanning electron microscope (SEM). The image is taken from the Don Gnocchi chemistry and research laboratory in Milan.

Both nerves always divide into a variable number of branches, from two to seven. The branches vary in size and the thickness bears no relationship to the area supplied. The average finding was three to five branches separating into anterior, lateral, and posterior directions. The posteromedial branch was usually the biggest, absolutely constant, and always running in the same direction.

The phrenic nerve receives afferents from the pericardium, liver, vena cava, and peritoneum, since it contains both sensory and motor fibers (Drake R, et al., 2002; Townend RE, & McConnell P., 2012).

The brachial and cervical plexuses are located in the region of the phrenic nerve. To give some examples, the roots that may be affected by phrenic disorders are C4–C5 (ie, the dorsal nerve of the scapula), and C5–C6, specifically, the axillary nerve, suprascapular nerve, musculocutaneous nerve, and subclavian nerve (Drake R, et al., 2009).

The electrical activity of the nervous system is not restricted to the mere distribution of efferent impulses in one direction; in fact, nerves not only convey electrical impulses but also release chemobiologic, neurotrophic and, at times, immune substances (Zhao T, et al., 2012; Yampolsky C, et al., 2012) (Russell FD, et al., 2000).

Along its pathway, the phrenic nerve anastomoses to the subclavian nerve, which innervates the subclavian muscle, specifically, the first rib and the clavicle (C5–C6) (Banneheka S., 2008). If there is a phrenic disorder, it is possible to contract the subclavius muscle, raising the first rib and reproducing a thoracic outlet syndrome, with the relevant symptomatology (Zhang Z, & Dellon AL., 2008; Laulan J, et al., 2011).

The scalene muscles, which are innervated by the cervical and brachial plexuses, are equally involved (Drake R, et al., 2009). It is worth emphasizing that a brachial disorder can provoke phrenic and diaphragmatic disorders. Kehr's sign is a classic example of referred pain: irritation of the diaphragm is signaled by the phrenic nerve as pain in the area above the collarbone. This is because the supraclavicular nerves have the same cervical nerves origin as the phrenic nerve, C3 and C4 (Franko OI, et al., 2008).


Dysfunction occurs due to acute and chronic injury and or pathology to the structures involved with the attachment and function of the diaphragm. Diaphragm dysfunction can be classified as partial or total loss of diaphragmatic function and it may involve one or both hemidiaphragms.

Diaphragm dysfunction directly affects the respiratory efficiency of patients and is one of the important pathological mechanisms leading to progressive exacerbation of disease and respiratory failure (Cao et al., 2022).

Diaphragm dysfunction in patients with disease or injury can manifest in structural and functional changes, including negative changes and positive adaptive changes (Cao et al., 2022).

Diaphragm dysfunction is mainly manifested as structural changes such as diaphragm atrophy, single-fiber dysfunction, sarcomere injury and fiber type transformation, along with functional changes such as muscle strength decline, endurance change, diaphragm fatigue, decreased diaphragm mobility, etc (McCool et al., 2012).

Injuries occur from sudden falls, impacts and stresses placed upon the musculature or can occur over an extended period of time. Injuries from falls, impacts may result in skeletal fractures that contribute to muscular dysfunction impacting respiration and functional movement of not just the diaphragm and thorax but of the whole person.

Strains to the musculature can occur when there is a pressure differential created causing micro and macro tearing in the muscular tissue. Typically, these injuries occur when improper lifting occurs, involving a flexion or extension action combined with twist or torque maneuver. General health of the person and amount of weight and positional awkwardness of the lift contribute to injury of the diaphragm.

Chronic psychological stresses can result in diaphragmatic dysfunction. Psychological stresses such as anxiety, burnout, emotional exhaustion have all been associated with somatic complaints including breathing dysfunctions (Salyers, et al., 2011).

Surrounding respiratory and digestive structures associated with the diaphragm also influence its function and dysfunction. Examples can include but are not limited to various lung pathologies (cystic fibrosis, progressive systemic sclerosis), cancers (pneumonia, pneumonitis, small cell & squamous lung cancer), vascular diseases/conditions (COPD, cardiac arrest, aortic aneurism), alcoholism, septic shock, postoperative effects, intubation, mechanical ventilation small bowel obstruction, systemic inflammation, oxidative stress, muscular atrophy to name just a few (Cao et al., 2022, Laghi, F. et al., 2020; Al-Jahdali, H. et al., 2014).

Injuries to the nervous system involved in innervation of the diaphragm also occur. Spinal cord injuries (complete/incomplete) and injuries post anaesthetic blocking techniques also occur commonly (stellate ganglion block involving phrenic nerve dysfunction) (Nair, J. et al., 2017).

Treatment suggestions

If you have ever had the opportunity to be present in a dissection laboratory, you quickly learn that the anatomy presented in medical curricula text books is far from accurate. The variation of location and interconnectedness of all structures is apparent. No one structure is ever isolated or functioning unto itself separate from the whole organism. As such, treatment should be applied to the whole organism, physically, mentally, emotionally and cognitively, actively and passively by both the therapist and patient. It is an interactive experience where both participate as a team to acquire mutually agreed upon goals/outcomes.

Manual therapists have an opportunity to significantly contribute to the treatment and rehabilitation of the respiratory diaphragm. Common rehabilitation treatment methods of diaphragm dysfunction include inspiratory muscle training, exercise intervention and nutritional support (Cao, Y. et al., 2022).


A., & Tobin, M. J. (2020). Inhibition of central activation of the diaphragm: a mechanism of weaning failure. Journal of applied physiology (Bethesda, Md. : 1985), 129(2), 366–376.

Al-Jahdali, H., Rajiah, P., Allen, C., Koteyar, S. S., & Khan, A. N. (2014). Pictorial review of intrathoracic manifestations of progressive systemic sclerosis. Annals of thoracic medicine, 9(4), 193–202.

Apaydin N, Uz A, Evirgen O, Loukas M, Tubbs RS, Elhan A. The phrenico-esophageal ligament: an anatomical study. Surg Radiol Anat. 2008 Feb;30(1):29-36. doi: 10.1007/s00276-007-0279-0. Epub 2007 Dec 4. PMID: 18058057.

Banneheka S. Morphological study of the ansa cervicalis and the phrenic nerve. Anat Sci Int. 2008;83(1):31–44.

Bordoni, B., & Zanier, E. (2013). Anatomic connections of the diaphragm: influence of respiration on the body system. Journal of multidisciplinary healthcare, 6, 281–291.

Braga, D. K. A. P., Marizeiro, D. F., Florêncio, A. C. L., Teles, M. D., Silva, Ítalo C., Santos-Júnior, F. F. U., & Campos, N. G. (2016). Manual therapy in diaphragm muscle: effect on respiratory muscle strength and chest mobility. Manual Therapy, Posturology & Rehabilitation Journal, 1–5.

Brown, R. P., and Gerbarg, P. L. (2005a). Sudarshan kriya yogic breathing in the treatment of stress, anxiety, and depression: Part II—Clinical applications and guidelines. J. Altern. Complement. Med. 11, 711–717. doi: 10.1089/acm.2005. 11.711

Cahalin, L. P., Braga, M., Matsuo, Y., and Hernandez, E. D. (2002). Efficacy of diaphragmatic breathing in persons with chronic obstructive pulmonary disease: a review of the literature. J. Cardiopulm. Rehabil. 22, 7–21. doi: 10.1097/ 00008483- 200201000- 00002

Caliot P, Bousquet V, Cabanie P, Midy D. The nerve loops crossing below the subclavian artery and their anatomical variations. Anat Clin. 1984;6(3):209-13. doi: 10.1007/BF01784315. PMID: 6518114.

Cao, Y., Li, P., Wang, Y., Liu, X., & Wu, W. (2022). Diaphragm Dysfunction and Rehabilitation Strategy in Patients With Chronic Obstructive Pulmonary Disease. Frontiers in physiology, 13, 872277.

Chavhan GB, Babyn PS, Cohen RA, Langer JC. Multimodality imaging of the pediatric diaphragm: anatomy and pathologic conditions. RadioGraphics 2010;30(7):1797–1817.

Chen, Y. F., Huang, X. Y., Chien, C. H., and Cheng, J. F. (2016). The effectiveness of diaphragmatic breathing relaxation training for reducing anxiety. Perspect. Psychiatr. Care doi: 10.1111/ppc.12184 [Epub ahead of print].

Descilo, T., Vedamurtachar, A., Gerbarg, P. L., Nagaraja, D., Gangadhar, B. N., Damodaran, B., et al. (2010). Effects of a yoga breath intervention alone and in combination with an exposure therapy for post- traumatic stress disorder and depression in survivors of the 2004 South-East Asia tsunami. Acta Psychiatr. Scand. 121, 289–300. doi: 10.1111/j.1600-0447.2009.01466.x

Drake R, Vogl AW, Mitchell AWM. Gray’s Anatomy for Students, 2nd ed. New York, NY: Elsevier-Churchill-Livingstone; 2009

Franko OI, Khalpey Z, Gates J. Brachial plexus trauma: the morbidity of hemidiaphragmatic paralysis. Emerg Med J. 2008;25(9):614–615.

Hayama, Y., and Inoue, T. (2012). The effects of deep breathing on ’tension- anxiety’ and fatigue in cancer patients undergoing adjuvant chemotherapy. Complement. Ther. Clin. Pract. 18, 94–98. doi: 10.1016/j.ctcp.2011.10.001

Kleinman PK, Raptopoulos V. The anterior diaphragmatic attachments: an anatomic and radiologic study with clinical correlates. Radiology 1985;155 (2):289–293.

Laulan J, Fouquet B, Rodaix C, Jauffret P, Roquelaure Y, Descatha A. Thoracic outlet syndrome: definition, aetiological factors, diagnosis, management and occupational impact. J Occup Rehabil. 2011;21(3): 366–373.

Ma, X., Yue, Z. Q., Gong, Z. Q., Zhang, H., Duan, N. Y., Shi, Y. T., Wei, G. X., & Li, Y. F. (2017). The Effect of Diaphragmatic Breathing on Attention, Negative Affect and Stress in Healthy Adults. Frontiers in psychology, 8, 874.

Manjunath, N. K., and Telles, S. (2005). Influence of yoga and Ayurveda on self-rated sleep in a geriatric population. Indian J. Med. Res. 121, 683–690.

Marshall, R. S., Basilakos, A., Williams, T., and Love-Myers, K. (2014). Exploring the benefits of unilateral nostril breathing practice post-stroke: attention, language, spatial abilities, depression, and anxiety. J. Altern. Complement. Med. 20, 185–194. doi: 10.1089/acm.2013.0019

McCool FD, Tzelepis GE. Dysfunction of the diaphragm. N Engl J Med. 2012 Mar 8;366(10):932-42. doi: 10.1056/NEJMra1007236. Erratum in: N Engl J Med. 2012 May 31;366(22):2138. PMID: 22397655.

Mehrotra M, Reddy V, Singh P. Neuroanatomy, Stellate Ganglion. [Updated 2021 Jul 31]. In: StatPearls [Internet]. Treasure Island (FL): StatPearls Publishing; 2022 Jan-. Available from:

Mendelsohn AH, Deconde A, Lambert HW, Dodson SC, Daney BT, Stark ME, Berke GS, Wisco JJ. Cervical variations of the phrenic nerve. Laryngoscope. 2011 Sep;121(9):1920-3. doi: 10.1002/lary.21894. Epub 2011 Aug 16. PMID: 22024845.

Nair, J., Streeter, K. A., Turner, S., Sunshine, M. D., Bolser, D. C., Fox, E. J., Davenport, P. W., & Fuller, D. D. (2017). Anatomy and physiology of phrenic afferent neurons. Journal of neurophysiology, 118(6), 2975–2990.

Nair A, Alaparthi GK, Krishnan S, Rai S, Anand R, Acharya V, Acharya P. Comparison of Diaphragmatic Stretch Technique and Manual Diaphragm Release Technique on Diaphragmatic Excursion in Chronic Obstructive Pulmonary Disease: A Randomized Crossover Trial. Pulm Med. 2019 Jan 3;2019:6364376. doi: 10.1155/2019/6364376. PMID: 30719351; PMCID: PMC6335861.

Nason LK, Walker CM, McNeeley MF, Burivong W, Fligner CL, Godwin JD. Imaging of the diaphragm: anatomy and function. Radiographics. 2012 Mar-Apr;32(2):E51-70. doi: 10.1148/rg.322115127. PMID: 22411950.

Panicek DM, Benson CB, Gottlieb RH, Heitzman ER. The diaphragm: anatomic, pathologic, and radiologic considerations. RadioGraphics 1988;8(3): 385–425.

Pickering M, Jones JF. The diaphragm: two physiological muscles in one. J Anat. 2002;201(4):305–312.

Rocha T, Souza H, Brandão DC, Rattes C, Ribeiro L, Campos SL, Aliverti A, de Andrade AD. The Manual Diaphragm Release Technique improves diaphragmatic mobility, inspiratory capacity and exercise capacity in people with chronic obstructive pulmonary disease: a randomised trial. J Physiother. 2015 Oct;61(4):182-9. doi: 10.1016/j.jphys.2015.08.009. Epub 2015 Sep 19. PMID: 26386894.

Russell FD, Koishi K, Jiang Y, McLennan IS. Anterograde axonal transport of glial cell line-derived neurotrophic factor and its receptors in rat hypoglossal nerve. Neuroscience. 2000;97(3):575–580.

Salyers, M. P., Hudson, C., Morse, G., Rollins, A. L., Monroe-DeVita, M., Wilson, C., & Freeland, L. (2011). BREATHE: a pilot study of a one-day retreat to reduce burnout among mental health professionals. Psychiatric services (Washington, D.C.), 62(2), 214–217.

Shin MS, Berland LL. Computed tomography of retrocrural spaces: normal, anatomic variants, and pathologic conditions. AJR Am J Roentgenol 1985; 145(1):81–86.

Stromberg, S. E., Russell, M. E., and Carlson, C. R. (2015). Diaphragmatic breathing and its effectiveness for the management of motion sickness. Aerosp. Med. Hum. Perform. 86, 452–457. doi: 10.3357/AMHP.4152.2015

Townend RE, McConnell P. The right inferior phrenic artery: path of its ascending branch at the vena caval foramen. Clin Anat. 2012;25(5): 656–658.