\r\n\tMany tried to define it, and its definition is always related to those who are in power, that being explained by the fact that this power and the abuse of it precisely, gives the access to being corrupted and practicing the acts that fall under corruption.
\r\n\r\n\tWe can find various types of corruption such as bribery, lobbying, extortion, cronyism, nepotism, parochialism, patronage, influence peddling, graft, and embezzlement. Also giving or accepting bribes or inappropriate gifts, double-dealing, under-the-table transactions, manipulating elections, diverting funds, laundering money, and defrauding investors.
\r\n\tNo government is immune to corruption. According to the World Bank, “the causes of corruption are always contextual, rooted in a country's policies, bureaucratic traditions, political development, and social history”.
\r\n\tThis indeed has consequences for increasing inequality, impacts government expenditure and services, shadow economy, and crime.
\r\n\tThis book will be a collection of chapters on Corruption. It welcomes contributions related to the nature of corruption its types and how corruption is undertaken in a certain context and the ways to deal with corruption will be part of this book. We value including materials on Corruption in organizations and ways to solve it. The origins of corruption and the way to deal with corruption, how to provide solutions, and any new insights on corruption will be part of this book.
",isbn:"978-1-80356-696-2",printIsbn:"978-1-80356-695-5",pdfIsbn:"978-1-80356-697-9",doi:null,price:0,priceEur:0,priceUsd:0,slug:null,numberOfPages:0,isOpenForSubmission:!0,isSalesforceBook:!1,isNomenclature:!1,hash:"9cda6d2feaa52a6d523da74f2e2d7ffb",bookSignature:"Dr. Josiane Fahed-Sreih",publishedDate:null,coverURL:"https://cdn.intechopen.com/books/images_new/11772.jpg",keywords:"Corruption, Origins, Types, Corporate Governance, Organizational Performance, Solutions, Corruption Index, Private Sector, Lebanon, Accountability, Anti-corruption, Public Policy",numberOfDownloads:null,numberOfWosCitations:0,numberOfCrossrefCitations:null,numberOfDimensionsCitations:null,numberOfTotalCitations:null,isAvailableForWebshopOrdering:!0,dateEndFirstStepPublish:"March 23rd 2022",dateEndSecondStepPublish:"April 20th 2022",dateEndThirdStepPublish:"June 19th 2022",dateEndFourthStepPublish:"September 7th 2022",dateEndFifthStepPublish:"November 6th 2022",dateConfirmationOfParticipation:null,remainingDaysToSecondStep:"a month",secondStepPassed:!0,areRegistrationsClosed:!1,currentStepOfPublishingProcess:3,editedByType:null,kuFlag:!1,biosketch:"Dr. Fahed-Sreih is the director of the Institute of Family and Entrepreneurial Business and a chairperson in the Department of Management. She obtained a Ph.D. from Sorbonne University, France, and received the 2007 FFI International Award for outstanding achievement in furthering the understanding of family business issues between two or more countries. She is on the editorial board of the Journal of Family Business Management and a keynote speaker for corporate governance conferences.",coeditorOneBiosketch:null,coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"103784",title:"Dr.",name:"Josiane",middleName:null,surname:"Fahed-Sreih",slug:"josiane-fahed-sreih",fullName:"Josiane Fahed-Sreih",profilePictureURL:"https://mts.intechopen.com/storage/users/103784/images/system/103784.jfif",biography:"Dr. Josiane Fahed-Sreih is a full-time associate professor of Management in the School of Business, Lebanese American University. She is the founder and director of the Institute of Family and Entrepreneurial Business and a chairperson in the Department of Management at the same university. She was previously the assistant dean. She obtained a Ph.D. from Sorbonne University, Paris, France. Dr. Fahed-Sreih is the Middle East Coordinator for the Family Firm Institute (FFI), the USA, and a family wealth and family business consultant. She received the 2007 FFI International Award for outstanding achievement in furthering the understanding of family business issues that occur between two or more countries. She has participated in and organized international conferences, workshops, and seminars. She has presented at major conferences locally and internationally and consulted on management issues in many countries, including Saudi Arabia, Dubai, Jordan, Qatar, Kuwait, Syria, Bahrain, Oman, France, Cyprus, and Lebanon. She currently sits on five boards of directors as a shareholder, two as a chairman of the board, and one as an independent director in the private sector. She is also an advisor on boards of community service organizations. \n\nShe speaks regularly to trade and professional groups and presents her research at academic conferences worldwide. She is frequently invited as a keynote speaker to the recognized family business and corporate governance conferences. Her research interests are in management, family business, the functioning of boards of directors, and corporate governance. She has published three books, several book chapters, and academic articles in international journals. She is on the editorial board of the Journal of Family Business Management and is a reviewer for Family Business Review, Corporate Governance, and Journal of Management.",institutionString:"Lebanese American University",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"4",totalChapterViews:"0",totalEditedBooks:"2",institution:{name:"Lebanese American University",institutionURL:null,country:{name:"Lebanon"}}}],coeditorOne:null,coeditorTwo:null,coeditorThree:null,coeditorFour:null,coeditorFive:null,topics:[{id:"23",title:"Social Sciences",slug:"social-sciences"}],chapters:null,productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"},personalPublishingAssistant:{id:"440212",firstName:"Elena",lastName:"Vracaric",middleName:null,title:"Ms.",imageUrl:"https://mts.intechopen.com/storage/users/440212/images/20007_n.jpg",email:"elena@intechopen.com",biography:"As an Author Service Manager, my responsibilities include monitoring and facilitating all publishing activities for authors and editors. From chapter submission and review to approval and revision, copyediting and design, until final publication, I work closely with authors and editors to ensure a simple and easy publishing process. I maintain constant and effective communication with authors, editors and reviewers, which allows for a level of personal support that enables contributors to fully commit and concentrate on the chapters they are writing, editing, or reviewing. I assist authors in the preparation of their full chapter submissions and track important deadlines and ensure they are met. I help to coordinate internal processes such as linguistic review, and monitor the technical aspects of the process. As an ASM I am also involved in the acquisition of editors. 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The hippocampal neurons seem to process variety of information, such as spatial location (Wills et al., 2010), temporal information (Mitsushima et al., 2009), and emotional state (Chen et al., 2011) within specific episodes (Komorowski et al., 2009; Gelbard-Sagiv et al., 2008). However, the critical mechanism how to sustain a piece of specific memory and how to organize the memory fragment to form "episodes" is still largely unknown.
Since selective blockade of long-term potentiation (LTP) induction by NMDA receptor antagonist impairs hippocampal learning (Morris et al., 1986), LTP has been considered as a cellular model of hippocampal memory (Bliss and Lømo, 1973). In 2006,
As an endogenous trigger of LTP, we hypothesized acetylcholine (ACh) release in the hippocampus that increases during learning or exploration in freely moving animals. In fact, without electrode for tetanus stimulation, bath treatment of ACh agonist not only induces specific bursts (Fisahn et al., 1998) but also forms LTP in CA1 region of hippocampal slices (Auerbach and Segal 1996). Moreover, bilateral intra-hippocampal treatments of muscarinic receptors impair hippocampal learning (Herrera-Morales et al., 2007; Rogers and Kesner 2004). In this review, we focused on
A number of studies suggest that AChplays an important role in orchestrating major hippocampal functions (Fig. 1). In behavioural studies, ACh release increases during learning (Ragozzino et al., 1996; Stancampiano et al., 1999; Hironaka et al., 2001) and is positively correlated with learning performance (Gold, 2003; Parent and Baxter, 2004). Bilateral injections of scopolamine into the dorsal hippocampus impair spatial learning ability (Herrera-Morales et al., 2007), suggesting that muscarinic ACh receptors mediate the formation of spatial memory. At the network level, ACh generates a theta rhythm (Lee et al., 1994) that modulates the induction of long-term potentiation (LTP) in hippocampal CA1 neurons (Hyman et al., 2003). Studies exploring a genetic deficiency of muscarinic ACh receptors (M1or M2) further show the impairment of LTP in the CA1 region (Seeger et al., 2004; Shinoe et al., 2005). At the cellular level, both pyramidal and non-pyramidal neurons in the hippocampal CA1 area receive direct cholinergic afferents mediated by muscarinic receptors (Cole and Nicoll, 1983; Markram and Segal, 1990; Widmer et al., 2006).
Not only is ACh critically involved in synaptic plasticity, ACh release in the hippocampus is also responsible for neurogenesis in the dentate gyrus. Thus, neurotoxic lesions of forebrain cholinergic neurons or long-term scopolamine treatment significantly decreases the number of newborn cells in the dentate gyrus, approximately 90% of those were also positive for the neuron-specific marker NeuN (Mohapel et al., 2005; Kotani et al., 2006).
Cholinergic neurons within the basal forebrain provide the major projection to the neocortex and hippocampus (Mesulam, et al., 1983). Cortical regions receive cholinergic inputs mainly from the nucleus basalismagnocellularis(NBM) or the diagonal band of Broca, whereas the hippocampus receives cholinergic inputs mostly from the medial septum and horizontal limb of the diagonal band of Broca (Mesulam, et al., 1983). Because the cholinergic projections are necessary to maintain learning and memory (Perry et al., 1999, Sarterand Parikh, 2005), we hypothesized that
Schematic illustration of septo-hippocampal cholinergic neurons in rats. Exposure to episode induces ACh release in the hippocampus that activates hippocampal functions. Scopolamine induces amnesia in many mammalian species, including humans. For example, many people remember where they were and what they were doing when serious events occur. ACh, acetylcholine. LTP, long-term potentiation.
Experimental setup of
We first reported sex-specificACh release in the hippocampus in 2003 (Mitsushima et al., 2003). Gonadally intact male rats consistently show a greater ACh release in the hippocampus compared with diestrous or proestrous female rats, suggesting a sexually dimorphic septo-hippocampal cholinergic system. Moreover, we found that sex-dependent ACh release also shows a time-dependent 24-h profile: ACh release in the hippocampus was relatively similar in the light phase, but consistently lower in female compared with male rats in the dark phase (Masuda et al., 2005). Although ACh release clearly showed a daily rhythm in female rats, females exhibited smaller amplitude of daily change than males. However, it is necessary to rule out the possibility that the sex difference in ACh release reflects the differences in spontaneous locomotor activity levels. By simultaneous monitoring of ACh levels and spontaneous locomotor activity, we revealed a real sex difference in the "ACh release property" (Figure 3, Mitsushima et al., 2009): males showed higher ACh release than females while displaying similar levels of behavioural activity. Although female rats showed slightly higher overall spontaneous activity than intact male rats, male rats showed higher ACh release than female rats. Simple linear regression analysis was used to evaluate the relationship between ACh levels and spontaneous locomotor activity (Figure 3). Pearson\'s correlation coefficient (r) or slope of the best fit line was calculated for each rat, and sex difference was evaluated using ANOVA. We found that the data from intact males had a steeps lope of fit line, while the data from females had a gentle slope. These results suggest that sex-specific ACh release is not due to the change in spontaneous behavior, but due to actual differences in the ACh release property in gonadally intact rats (Mitsushima et al., 2009).
Sex specific ACh release property in behaving rats. Representative data from a male (#102) and a female (#175) rat were shown. Simple linear regression analysis revealed a sex-specific "ACh release property." Male rats showed higher ACh release than females undergoing similar behavioural activity levels. Although both sexes showed a high correlation, male rats showed a steeper slope than female rats in the hippocampus (see
To evaluate neuroanatomical sex difference in the septo-hippocampal cholinergic neurons, we performed immunocytochemistry. Stereological analysis showed that no sex difference was observed in the number and the distribution of choline acetyltransferaseimmunoreactive(ChAT-ir) cells in the medial septum or horizontal limb of diagonal band (Takase et al., 2009). Since the number of septo-hippocampal cholinergic neurons does not appear to be involved in the sex difference in ACh release in the hippocampus, we hypothesized that sex-specific neural circuits or substance(s) may control the endogenous release.
Neurotransmitters may be involved in expression of the sex difference in ACh release. For instance, dopaminergic neurons in the ventral tegmental area (A10) have been shown to control septo-hippocampal cholinergic neurons through the A10-septal dopaminergic pathway in male rats(Swanson, 1982; Nilsson et al., 1992; Yanai etal., 1993). A neuroanatomical study suggested that dopamine D2receptors rather than D1 receptors mediate the dopaminergic control of septo-hippocampal cholinergic neurons (Weiner et al., 1991). It has been shown that opiatergic neurons also control septo-hippocampal cholinergic neurons in male rats (Mizuno and Kimura, 1996); the injection of naloxone, a μ opioid receptor antagonist, into the medial septum markedly increased ACh release in the hippocampus, while a μ opioid receptor agonist decreased its release (Mizuno and Kimura, 1996). In contrast, GABA seems to inhibit septo-hippocampal cholinergic neurons; the injection of muscimol, a GABA receptor agonist, into the medial septum decreased ACh release in the hippocampus, while the injection of bicuculline, a GABA receptor antagonist, increased it (Moor et al., 1998). Although the neural systems are still unknown for female rats, it seems likely that neural control of septo-hippocampal cholinergic neurons is involved in the expression of sex differences in ACh release. It will be important to investigate these neural systems in female rats in future studies.
Not only neurotransmitters, but also circulating sex steroids, may regulate cholinergic neurons. In fact, neuroanatomical studies have demonstrated that, in intact male and female rats, a number of dopaminergic neurons in the A10 region have androgen receptor immunoreactivity (Kritzer,1997) and 45-60% of cholinergic neurons in the medial septum have estrogen receptor α immunoreactivity (Miettinen et al.,2002; Mufson et al., 1999). Taken together with the fact that female rats show a greater circulating estrogen concentration than male rats (Shors et al., 2001; Mitsushima et al., 2003b) and male rats show a greater circulating androgen concentration than female rats (Falvo et al., 1974; Rush and Blake, 1982), it is possible that cholinergic neurons are affected by sex steroids differently in male and female rats.
The activational effects of sex steroids on cholinergic neurons have been suggested by previous neuroanatomical and neurochemical findings. For example, male gonadectomy decreases the density of cholinergic fibers in the dorsal hippocampus, while testosterone replacement in gonadectomized male rats maintains fibre density (Nakamura et al., 2002). Also, estradiol increases the induction of choline acetyltransferase in the basal forebrain in gonadectomized female rats (Luine et al., 1986; McEwen and Alves, 1999). A previous
ACh release in the hippocampus is time-dependent, sex-specific, and hormone-dependent. Time-dependent ACh release may transmits the information such as time of day. Experiments were performed 2 weeks after gonadectomy or steroid replacement. Horizontal black bars indicate the dark phase. Gdx, gonadectomized. +T, testosterone-priming. +E, estradiol-priming. The number of animals was 6 to 8 in each group. 19h to 5h is the dark phase, shown as black bars on the x axes.(see
Moreover, we found that after gonadectomy, the positive correlation between ACh release and locomotor activity levels was severely impaired, suggesting that hippocampal function may not always be activated at low sex steroid levels (Mitsushima et al., 2009). This therefore suggests that learning impairment in gonadectomized rats (Gibbs and Pfaff, 1992; Daniel et al., 1997; Kritzer et al., 2001; Markowska et al., 2002; Luine et al., 2003) may be due to insufficient activation of hippocampus at the appropriate time. Because the replacement of sex-specific steroids restored the high positive correlation between ACh release and activity levels, the correlation appears to depend on the presence of sex steroids. These results suggest that circulating sex steroids strengthen the coupling between spontaneous behaviour and ACh release (Mitsushima et al., 2009).
The activational effect of sex steroids was sex-specific (Figure 4). Testosterone replacement in gonadectomized female rats failed to increase ACh release to levels seen in gonadectomized testosterone-primed male rats. Similarly, estradiol replacement was unable to restore ACh release in gonadectomized male rats. Moreover, estradiol consistently increases N-methyl-D-aspartate receptor binding and spine density in the CA1 area of gonadectomized female rats, although the treatment fails to increase these same parameters in gonadectomized male rats (Romeo et al., 2005; Parducz et al., 2006). These results suggest that sex-specific steroids are important for maintaining hippocampal function. Based on our data, we hypothesized that the action of sex-specific steroids is due to neonatal sexual differentiation rather than the activational effects of sex steroids in adult rats. Moreover, in the latest study, we found that neonatal androgenization in females increased ACh release to resemble that of normal males without affecting spontaneous activity levels (Mitsushima et al., 2009). These results indicate an organizational effect on sex-specific ACh release in behaving rats, and support currently accepted theories of sexual differentiation.
Because testosterone can be aromatized to estradiol in the forebrain, neonatal sex steroids activate both estrogen and androgen receptors (McEwen, 1981). In our study, both testosterone and estradiol treatment in neonatal female pups masculinized ACh release profile in adults, suggesting an estrogen receptor-mediated masculinization of septo-hippocampal cholinergic systems (Mitsushima et al., 2009). These results are consistent with the previous finding that testosterone or estradiol treatment in neonatal female pups improves their adult spatial performance, whereas neonatal gonadectomy in male pups impairs the performance (Williams and Meck, 1991). In contrast, dihydrotestosterone treatment failed to masculinize the ACh release profile. Although dihydrotestosterone has been classically considered as a prototypical androgen receptor agonist, a metabolite of dihydrotestosterone, 3β-diol, has a higher affinity for estrogen receptor β (Lund et al., 2006). Therefore, dihydrotestosterone and its metabolites may stimulate both androgen receptor and estrogen receptor β, whereas estradiol stimulates estrogen receptor α and β. Considering the action of sex steroids and their metabolites, estrogen receptor α may mediate the organizational effect on the septo-hippocampal cholinergic system.
Various environmental conditions may interact with the activational effects of sex steroids. First, we reported an interaction between stress and sex steroids. Although sex steroids did not show activational effects on baseline levels of ACh release, sex steroids clearly activated the immobility stress-induced ACh release response. In addition, we found that the contributing sex hormone effect to maintain the ACh release response was sex-specific: testosterone enhanced the ACh release response in male rats, while estradiol maintained the response in females (Mitsushima et al., 2008). Second, we reported an interaction between the light/dark cycle and sex steroids. Although sex steroids slightly enhanced ACh release during the light phase, the activational effects were much stronger during the dark phase (Figure 4). Considering the fact that the time-dependent activational effect was also sex-specific and hormone-dependent, environmental conditions seem to have complicated interactions with sex steroids (Mitsushima et al., 2009).
Some other environmental effects may affect the basal forebrain cholinergic system. Environmental conditions, such as complex or restricted(Brown, 1968; Smith, 1972),enriched or impoverished (Greenough et al., 1972), social or isolated conditions (Hymovitch,1952; Juraska et al., 1984; Seymoure et al., 1996), seem to affect spatial learning ability in a sex-specific manner. For example, male rats exhibited superior performance in learning maze tests compared with female rats if they were housed socially (Einon, 1980). But if they were housed in isolation, female rats exhibited a performance superior to that of male rats (Einon, 1980). Although few studies were performed on the relationship between the sex-specific environmental effects and ACh release in the brain, we have reported that 4-day housing in a small cage attenuates the ACh release in the hippocampus in male rats (Mitsushima et al., 1998), but not in female rats (Masuda et al., 2005). Taken together, these results suggest that housing conditions contribute to the sex difference in ACh release and spatial learning ability.
Feeding conditions after weaning also affect spatial learning ability. If fed pelleted diet (i.e. standard laboratory diet), male rats show performance superior to that of female rats (Beatty, 1984; Williams and Meck, 1991). But when fed powdered diet, female rats, but not male rats, showed improved performance (Endo et al.,1994; Takase et al., 2005a). In our study, it was found that feedingwith powdered diet after weaning increased ACh release in the hippocampus in female rats, but not in male rats(Takase et al., 2005b). 24-HACh release in female rats fed powdered diet was as high as that in male rats fed either powdered or pelleted diet, showing no sex difference. Since feeding with powdered diet improved spatial learning ability in female rats (Endo et al., 1994), the increase in the ACh release in the hippocampus in female rats fed powdered diet may partly contribute to this effect. Our findings provide evidence that environmental conditions such as housing or feeding may play a role in sex-specific hippocampal function.
Activational effects of sex steroids are very important in humans, since circulating sex steroid levels decline with age. A reduction in ACh synthesis is known as a common feature of Alzheimer\'s disease (Coyle et al., 1983), afflicting more than 18 million people worldwide (Ferri et al., 2005; Mount and Downtown 2006). The disease is the most common form of dementia (Cummings 2004) and is frequently accompanied by insomnia, poor concentration, and day/night confusion (McCurry et al., 2004; Starkstein et al., 2005). The centrally active acetylcholinesterase inhibitor (donepezil) is effective in not only mild, but also moderate to severe cases (Petersen et al., 2005; Winblad et al., 2006), proving the importance of endogenous ACh in humans. In addition, women are twice as likely to develop the disease (Swaab and Hofman 1995), and estradiol seems to play a protective role (Zandi et al., 2002; Norbury et al., 2007). A recent study using single photon emission tomography showed that estrogen replacement therapy in healthy post-menopausal women increases muscarinic M1/M4 receptor binding in the hippocampus (Norbury et al., 2007). Conversely in men, testosterone but not estradiol seems to play a protective role (Moffat et al., 2004; Rosario et al., 2004) and testosterone supplementation clearly improved hippocampal-dependent learning deficits in men with Alzheimer\'s disease (Cherrier et al., 2005). These results suggest a sex-specific activational effect of gonadal steroids on the cholinergic system in humans. Thus, there are many similarities between the rat model and human studies, supporting the idea that gonadal steroid replacement therapy or an increase in bioavailability is beneficial when there is a subthreshold level of the hormone. Based on the neonatal sexual differentiation of the septo-hippocampal cholinergic system, we may have to search for sex-specific clinical strategies for Alzheimer\'s disease.
Gonadally intact male rats consistently show a greater ACh release in the hippocampus compared with diestrous or proestrous female rats. The activational effects of sex steroids are important for sex-specific ACh release in the hippocampus, since impaired ACh release in gonadectomized rats does not show sex-specific effects. Neonatal treatment with either testosterone or estradiol clearly increased ACh release in female rats, suggesting neonatal sex differentiation of septo-hippocampal cholinergic systems. Moreover, environmental effects on the basal forebrain cholinergic system seem to be sex-specific; housing in a small cage attenuated ACh release in male ratsonly, while feeding with powdered diet after sexual maturation increases ACh release in female ratsonly. These results indicate that: (i) sex-specific circulating sex steroids are necessary for sex-specific ACh release, (ii) neonatal activation of estrogen receptors is sufficient to mediate masculinization of the septo-hippocampal cholinergic system, and (iii) sex-specific effects of environmental conditions may suggest an interaction with the effect of sex hormones.
Understanding the importance of gonadal steroids and the sex-specific effects in cognitive disorders such as Alzheimer\'s disease is essential for real improvementsin therapy.
Shoulder surgery by arthroscopy or open methods has increased in recent years. The choice of anesthetic technique depends on the patient’s conditions, the preferences of the surgical group, the position the patient is to be placed, and the experience of the anesthesiologist. General anesthesia (GA) has been considered the ideal technique for this type of surgery, but advances in regional anesthesia have gradually changed this statement. The approaches, interscalene (ISBP) block (C5 C6) or the upper trunk (UT) are the most established options; the supraclavicular approach offers optimal coverage, including the proximal arm. Patients with respiratory compromise may not tolerate hemi diaphragmatic paresis (HDP) associated with proximal approaches. Distal approaches are associated with lower rates of HDP, but coverage of the proximal upper extremity may be incomplete. The use of ultrasound guidance (USG) for nerve blocks has increased success and safety and has allowed access to more peripheral brachial plexus blocks to prevent diaphragmatic paralysis. Regional anesthesia is also an excellent supplement to GA to improve postoperative pain management and decrease the need for opioid use.
Clavicle surgery has even more controversy about the choice of the regional block, since the innervation has not been well described. But in recent years, alternative regional block methods to interscalene brachial plexus block have appeared that are suitable as single anesthesia or combined with sedation or GA.
In this chapter, we pretend to describe the innervation of the shoulder and clavicle based on current knowledge and the sonoanatomy of the neck and armpit as a guide for the performance of regional nerve blocks.
Since shoulder surgeries produce severe postoperative pain, regional anesthesia techniques could effectively control pain at rest and in motion, reduce muscle spasm and facilitate early discharge [1].
The BP is formed by the fusion of the ventral ramus of the spinal nerves C5, C6, C7, C8, and T1, with the variable contribution of C4 (15-62% of cases) and T2 (16-73% of cases). The roots emerge in the groove between the anterior scalenus and middle scalenus muscles [2]. Shoulder and proximal arm innervation are provided by branches of the BP: suprascapular nerve (SSN) (from posterior division of UT), axillary and subscapular nerves (from posterior cord), lateral pectoral nerve, and medial brachial cutaneous nerve (MBCN)) (from lateral cord), and the intercostobrachial nerve (ICBN) (originating directly from proximal intercostal nerves). SSN may be spared by an infraclavicular approach (Figure 1) [3, 4].
Brachial plexus. Roots – Start in the spinal cord. Arise from anterior rami C5-T1. Landmark: Pass inferolateral between the anterior and middle scalene muscles. Trunks
The most frequently identified innervation pattern comprises three nerve bridges consisting of articular branches from suprascapular, axillary, and lateral pectoral nerves, connecting trigger points (Figures 2 and 3) [5, 6, 7].
Distribution of shoulder articular branches. Courtesy of MF Rojas.
Shoulder structures and their related innervation.
Articular branches classified in relation to the spinoglenoid notch:
Medial branch (MSAb) originates 1.3 cm proximal to the suprascapular notch, giving branches to the coracoclavicular ligaments and the medial pole of the subacromial bursa, clavicular insertion of the acromioclavicular ligament, and motor branches to the supraspinatus muscle.
Lateral branch (LSAb) originates at the level of the suprascapular notch, giving sensory branches to the lateral subacromial pole and acromial insertion of the acromioclavicular ligament. Two subacromial branches provide medial and lateral sensory innervation (bipolar) to the subacromial bursa.
The posterior glenohumeral branch (PGHb) originates at 3 cm from the suprascapular notch, and posterior to the spinoglenoid ligament, course inferomedial towards the posterior capsule of the shoulder [8].
One or two articular branches of the main trunk travel with the anterior humeral circumflex artery between the tendons of the subscapular and latissimus dorsi muscles branching into medial branch to scapular aspect of the anteroinferior capsule and portions of the axillary recess; lateral branch to humeral portion of the anterior capsule [6]. The posterior division (after leaving the quadrangular space) gives a branch for the teres minor muscle, from which emerge 1 to 4 articular branches, to innervate the posteroinferior capsule. The branch innervating the deltoid muscle gives small multiple articular branches towards the lateral aspect of the humeral head the posterior and lateral supra-lying fascia of the shoulder capsule [6, 9, 10].
The LPN arises from two branches of the anterior divisions of the upper and middle trunks (33.8% of cases), or as a single root of the lateral cord (23.4%). It receives fibers from C5 to C7. Cross the superomedial side of the coracoid process and sends small branches to the coracoclavicular and coracoacromial ligaments, anterior acromioclavicular joint, subacromial bursa and anterosuperior portion of the glenohumeral capsule. It gives branches to the periosteum of the clavicle. Therefore, its blockade produces analgesia for distal clavicle surgery [6, 11]. The muscular branch originates from the articular branch of the LPN and innervates the deltoid muscle and skin over the subacromial region (Figure 4) [7, 11].
Lateral pectoral nerve.
A glenohumeral articular branch anastomosis with branches of the AN to innervate the long head of the biceps tendon (LHBT) and anterior capsule. The superior subscapular nerve gives 1 or 2 articular branches to innervate the anterosuperior quadrant of the glenohumeral joint [12]. Receives fibers for C5-C6.
The
Mechanoreceptors are more concentrated in the medial and lateral insertions of the anterior capsule. Nociceptors are identified primarily in the upper quadrant of the shoulder, including the subacromial bursa (SAB), glenohumeral ligaments (GHL), coracoacromial (CAL), coracoclavicular ligaments (CCL), the proximal portion of the LHBT, and the transverse humeral ligament (THL). The SAB is the area of densest and tripolar nociceptive innervation. These three nociceptive poles may correspond to the location of the lateral/medial subacromial branches of the SSN (i.e., lateral and middle poles) and the articular branch of the lateral pectoral nerve LPN (anterior pole); Thin articular branches of the AN may also participate in the innervation of the lateral pole of SAB [6].
The most painful structures in clavicle surgery include the skin over the incision area and the highly innervated periosteum. The supraclavicular nerve originates as a single trunk from the anterior ramus of cervical nerves C3-C4. It divides into medial (suprasternal), intermediate (supraclavicular), and lateral (supra-acromial) branches. The medial branch supplements the skin over the anterior aspect of the thorax, as far below as the second rib, and the sternoclavicular joint. The intermediate branch pierces the deep cervical fascia just above the clavicle and runs over the pectoralis major and deltoid muscle; supply cutaneous innervation to the skin above these muscles, as far below as the second rib. The lateral branch pierces the deep cervical fascia just above the clavicle, passes over the acromial process, to innervate skin of the upper and posterior shoulder regions (Figure 5) [13, 14].
Nerves involved in clavicular innervation.
Innervation of the clavicle itself is less well described. Different authors attribute contributions from SSN, long thoracic, nerve for the subclavian muscle, and LPN [15].
Situated posterior to the clavicular part of the pectoralis major muscle. It extends from the clavicle, costochondral joints, and coracoid process. It converges in the axilla and acts as a protective structure over the neurovascular package. The clavicular fascia splits to enclose the subclavius muscle before attaching to the clavicle, the posterior layer fuses with the deep cervical fascia which connects the omohyoid muscle to the clavicle. Medially, it is attached to the first rib before coming together with the fascia over the first two intercostal spaces. Laterally, it is attached to the coracoid process before blending with the coracoclavicular ligament. The fascia often thickens to form the costocoracoid ligament, between the first rib and coracoid process. Inferiorly, the fascia becomes thin, splits around pectoralis minor, and descends to blend with the axillary fascia and laterally with the fascia over the short head of the biceps. It is pierced by CALL [cephalic vein, artery (thoracoacromial), lateral pectoral nerve, lymphatics]. The clavipectoral fascia surrounds the clavicle, and the nerve endings of the clavicle penetrate this fascia (Figure 6) [16].
Clavipectoral fascia.
Interscalene or supraclavicular block of the BP are considered the standard technique for anesthesia and analgesia in this type of surgery. The most common adverse effect is HDP due to ipsilateral PN block in 100% of patients and a 27% decrease in forced vital capacity and forced expiratory volume at the first second [17]. At the level of the cricoid cartilage (C6 transverse process (TP)) the PN is 0.18 cm prior to the BP, but it diverges at a rate of 3 mm for each centimeter below the cricoid cartilage.
USG has allowed to decrease the anesthetic minimum volume required in 50% of patients (5-7 mL vs. 30-40 mL) using ropivacaine 0.75% or bupivacaine 0.5%, and a decrease of 50% in the incidence of paralysis of the diaphragm when the injection is performed laterally to the C5-C6 roots. If the concentration of the anesthetic is also diluted to a half or third, the HDP rate is reduced to 20% (it is still a contraindication in patients with decreased lung reserve) but carries the risk of not achieving surgical anesthesia and decreasing the duration of the blockade. According to Renes et al., if the injection is done at the C7 root level, the minimum volume required to block C5-C6 in 50% of patients was 2.9 mL (maximum volume of 6 mL), with no PN block (although there is a substantial risk of vascular lesions from punctures at this level). Renes et al. avoided PN block by administering the anesthetic in the “cornet pocket “ (intersection of the first rib with the subclavian artery and posterolateral aspect of the BP) and a volume less than 20 ml [18]. Aliste et al. compared ISB with supraclavicular block following the Renes technique, finding equal pain control, but with HDP rate of 9% [19]. Cornish found a 1% of HDP rate by advancing a catheter from the supraclavicular level and locating the tip at the infraclavicular level, inferomedial to the coracoid process [20, 21].
A combination that could be effective would be the association of a SSN block with a BP block at infraclavicular level [22] (addresses the axillary, lateral pectoral, subscapular nerves), although Petrar et al. [23] reported a 3% incidence of HDP during infraclavicular BP block (30 mL ropivacaine 0.5%).
The following paragraphs describe different techniques to achieve a selective block of the nerves supplying the shoulder.
It focuses on the anesthetic deposit near the UT, before the take of the SSN. At this level, the phrenic nerve (PN) has diverged from the BP. Compoy et al. [24] found that 5 mL of methylene blue injected around UT stains SSN, lateral pectoral nerve, and roots of C5 and C6, but not of the PN [25]. Kim et al. found analgesic equivalence between UT block and ISB, achieving equivalent surgical anesthesia and HDP incidence of 5% vs. 71% using 15 mL of injectate [26]. Ultrasound (US) examination reveals the plexus in the groove between the anterior and middle scalene muscles, deep to the prevertebral fascia. The sternocleidomastoid muscle (SCM) lies superficially, and the PN can be seen on the anterior surface of the anterior scalene muscle (ASM), crossing it towards the medial side, after the last contribution originating in the C5 root. Sonoanatomy of the transverse processes can be used to identify spinal roots. Serial images reveal the process of confirmation of the UT [27].
The blocking needle is advanced from lateral to medial, under the deep cervical fascia until its tip reaches the UT lateral edge, proximal to the exit of the SSN (it is identified as a rounded hypoechoic structure that separates laterally from the UT and runs deep to the omohyoid muscle). The needle does not pass through the middle scalene muscle (MSM), where the dorsal scapular nerve (DSN) and long thoracic nerve (LTN) are located. The injectate volume is 7 to 12 mL of local anesthetic (LA) (one-half or one-third strength). Here the nerves have a greater amount of perineural tissue, protecting against neurological dysfunction, which has been reported in about 14% of ISBP blocks and can last for up to 10 days (Figure 7).
Upper trunk and supraclavicular nerves blockade. A. C5 and C6 (bifid) roots at interscalene space, near to PN. C7 TP view. B. UT formation (inferior to C7 TP). C. Origin of supraescapular nerve (SSN). D. Back to UT - needle at its posterior surface. Local anesthetic (LA) injection at posterior surface of UT. E. Retreated needle to space between SCM-MSM. LA injected around supraclavicular nerves.
The UT provides anesthesia to nerves from the spinal cord segments C5 and C6 (originating fiber to SSN and AN, inferior subscapular nerve, and partially, to LPN) [25] and decreases the incidence and severity of PN block. HDP was observed in 97.5% in ISB vs. 76.3% of the UT block groups (P = 0.006); paresis was complete in 72.5% vs. 5.3% of the patients, respectively. The decrease in spirometry values from baseline was significantly greater in the ISB block group. UT block provides non inferior analgesia compared to ISBP block [28].
It can be supplemented with blockade of the supraclavicular nerves to anesthetize the skin over the shoulder. The needle is retracted to the space between prevertebral fascia (over the MSM) and superficial (enveloping) layer of the deep cervical fascia, under the SCM, where the supraclavicular nerves are located. A new injection of 2 to 3 mL of LA blocks nerves supplying skin over collarbone and shoulder cap and their sensitive contribution to the acromioclavicular joint.
The supraclavicular nerve trunk (C3 and C4) emerges at the posterior edge of SCM. The superficial cervical plexus (SCP) is localized by placing a transducer on the posterior edge of the SCM at the level of the upper pole of the thyroid cartilage. It can be difficult to identify the individual nerves. The greater auricular nerve (GAN) is a useful reference reliably identified as a small superficial hypoechoic round structure on SCM (Figure 8) [29].
Supraclavicular nerve trunk and SCP scan process.
The posterior approach in the suprascapular fossa (in the space between the suprascapular notch and the spinoglenoid notch) where the nerve travels through its floor under the supraspinatus muscle fascia, results in adequate flooding of SSN with minimal propagation to the BP [30] but may spare MSAb. This approach is inferior to ISBP block for pain control, at least in the first 4 hours [31, 32, 33]. The UT (C5-C6) is the major contributor to the suprascapular, axillary, and subscapular nerves. Hence, UT blockade can provide adequate control of shoulder pain, but it is still remarkably close to the PN [34, 35].
With ultrasound image, the SSN could be identified as it branches from UT, and runs laterodorsally underneath the omohyoid muscle, in 81% of cases vs. 36% in the supraspinatus fossa, at an average depth of 8 mm vs. 35 mm in the supraspinatus fossa. Peripheral nerve stimulator can help in the identification [35]. Rothe et al. studied twelve healthy volunteers; the SSN was followed into the subclavian triangle under the inferior belly of the omohyoid muscle; injecting 1 mL of lidocaine 2%, 10 blocks were performed, 8 demonstrated a reduced manual muscle-testing scale (MMT) of the supra- and infraspinatus muscles at 15 min and 30 min; increasing the injected volume, produced musculocutaneous and radial nerves blockade due to cephalic diffusion of the anesthetic (Figure 9) [36].
Scan sequence of the SSN at the supraclavicular fossa. A: Locate the transverse process of C6 vertebral vertebra and C6 and C5 roots. B: Scanning downward, locate the C7 TP and C7 root, which can be seen laterally to vertebral vessels. C: Just below the C7 transverse process, C7 root runs towards the interscalene groove. The PN is diverging from the BP, on the anterior surface ASM. Caudally to the C7 transverse process, UT and MT conformation can be imaged. D: In the supraclavicular fossa. From the UT branches the SSN. E: The SSN travels below the omohyoid muscle. F: The SSN separates from the UT, below omohyoid muscle. The nerve goes along suprascapular artery.
In 14 BP of 7 corpses, the separation between the SSN and the PN was found to be 2.5-6.4 cm, and the injection of 10 mL of solution around the SSN produced staining of the UT of the BP and its branches (SSN, anterior and posterior divisions - 14 cases, 100%), the middle trunk (MT) (13 cases, 93%), the PN (3 cases; 21.4%) [37]. In the cadaveric study by Sehmbi, the SSN and omohyoid muscle were easily identified and, with nerve injections of 5 mL, nerve staining with contrast dye was seen in 90% of dissections. The UT, MT, and LT were stained in 90%, 80% in 20% of dissections, respectively. The PN was mildly stained in 20% of the dissections [38]. Figure 9 shows the scan sequence of the SSN at the supraclavicular fossa.
The articular branch or LPN crosses the superomedial side of the coracoid process [6, 11]. The US probe is placed between the inferior border of the clavicle and the superior border of the coracoid process. Below the deltoid muscle, the acromial branch of the thoracoacromial artery and, along with it, the nerve can be found (Figure 10).
USG to locate the articular branch of LPN.
The AN provides motor innervation to subscapular, teres major and minor, and deltoids muscles. The nerve branches before entering the quadrangular space. The anterior division of the AN originates the first articular branch, which ends in the anteroinferior capsule; blocking the nerve by the posterior approach can provide incomplete analgesia.
The sensitive skin supply of the medial aspect of the arm is provided by MBCN, ICBN, and variable branches of the intercostal nerves [39].
The AN run into the inferolateral margin of the subscapular muscle and enters the quadrangular space (QS) (limits: upper, teres minor muscle; inferior, teres major muscle; medial, long head of the triceps muscle; lateral, surgical neck of the humerus; anterior, insertion of the subscapular muscle on the minor tuberosity). The subscapular muscle, the upper edge of the teres major muscle, and the humerus are the sonographic marks that lead to the identification of the AN. The ICBN originates mainly from the second intercostal nerve, with variable contributions from intercostal nerves T1, T3, and T4. It is identified in the axillary subfascial space, along.
with fat, lymph nodes, and other cutaneous branches of the upper intercostal nerves. After crossing the axillary subfascial space, it courses on the surface of the latissimus dorse muscle, covered by the superficial axillaryfascia [40].
With the arm abducted 90o, the BP is identified in the armpit (anterior to the teres major and the tendon of the latissimus dorse muscles, seen in short axis) (Position 1, Figure 11). The probe moves slightly in a proximal direction (position 2, Figure 11) towards the QS, which is identified as soon as the upper edge of the teres major muscle deepens. At this point, the AN appears as an oval honeycomb structure, accompanied by the posterior circumflex artery of the humerus (although it has an inconsistent course and presence). The elevation of the arm from 90 o to 180 o brings the nerve closest to the skin by closing the quadrangular space.
AN US images at axillary fossa. A. Transducer position 1. The US imagen corresponds to D. B. Transducer position 2. The US imagen corresponds to E. C. Anterior view of axilla showing the quadrangular space; AN emerges posterior to brachial plexus and enters the QS divided in anterior and posterior ramus. D. Scanning starts viewing the brachial plexus at the axillary level, observing the fascia of the teres major muscle. E. Moving proximally the transducer (towards the axillary fossa) shows the teres major muscle fascia deepening and the subscapular muscle tendon; the QS is seen. F. with 180° arm extension, the teres major muscle closes the QS. G and H. the axillary nerve is observed above the subscapular muscle as a hyperechoic image next to the circumflex humeral artery.
With the arm positioned parallel to the thoracic wall with internal rotation and forearm pronated on the abdomen, a US probe is placed below and parallel to the clavicula identifying the coracoid process and lesser tubercle and intertubercular (bicipital) groove; then the arm is externally rotated, pushing the subscapular muscle rostrally and identifiable under the deep lamina of the deltoid fascia; the first portion of the AN is present between the deep lamina of the deltoid fascia and the superficial lamina of the subscapular muscle, where needle tip is placed. Interfacial position is confirmed after injection of 2 mL of normal saline, then 10 mL of 0.25% bupivacaine is injected. Rotating caudally the medial side of the probe and abducting the limb permits to directly visualize the AN and posterior circumflex humeral artery.
The injection is distributed on the anterior surface of the subscapular muscle and around the proximal insertion of the coracobrachialis and biceps brachial muscles. The sensory block is detected in AN area and areas supplied by the branches of the musculocutaneous nerve, lateral pectoral nerve, lateral supraclavicular nerve, and intercostobrachial nerve.
A complete AN blockade could provide anesthesia to the anteroinferior and lateral edges, and to part of the posterior aspect. of the shoulder joint capsule. The remaining shoulder joint areas are innervated by the SSN, which must be blocked if complete anesthesia of the shoulder is to be achieved. The LPN, or its articular branches, can be blocked by PECS I block or at the space between the coracoid process and clavicle (Figure 12) [41, 42].
US-guided anterior approach to AN blockade. A. Axillary nerve and its relations to subscapular, deltoid, and pectoralis muscles, axillary and circumflex humeral arteries, coracoid process, and humerus bone. B. Sagittal oblique ultrasound anatomy of the anterior axilla. C. Ultrasound scan: Transducer between coracoid process (medial) and the lesser tubercle of the humerus. Arm adducted and internal rotation. D. Transducer parallel to the inferior border of the clavicle, ultrasound mark is lateral. E and F. arm rotated externally/no abduction; subscapular muscle appears over humeral head. G and H. full external rotation and abduction of the arm. The medial side of the transducer is rotated inferiorly to obtain a sagittal oblique view of the axilla. The subscapular muscle is pushed rostrally and is identifiable under the deep lamina of the deltoid fascia. The cephalic vein is seen in the groove between deltoid and pectoralis major muscles. The axillary artery appears in the image and laterally to it, the axillary nerve is located. The needle shows the injection around the axillary nerve, on the surface of the subscapular muscle.
Clavicle fractures account for 2.6–4% of fractures in adults and 35% of shoulder injuries. The annual incidence is estimated between 29 and 64 per 100,000, and are distributed as follows: diaphysis 69-82%, lateral end 21-28%, and medial end 2-3%. There is often caudal displacement of the lateral fragment under the shoulder weight and elevation of the medial fragment by traction by the SCM. Infrequently, posterior displacement of the medial end can cause compression of the mediastinum and main vessels requiring urgent intervention. Non-displaced fractures are managed without surgery, while surgical management is preferred in cases of displaced fractures in active adults [43].
Innervation of the skin above the second rib is supplied by the supraclavicular nerves of the SCP. Terminal branches of suprascapular, subclavian, lateral pectoral, and long thoracic nerves pass through the plane between the clavipectoral fascia and the clavicle and, theoretically, contribute to collarbone innervation.
Common approaches in anesthesia for clavicle fracture surgery are GA, regional anesthesia techniques such as ISBP block combined with SCP block. The clavipectoral fascial plane (CPB) block (Figure 13) is accomplished by injecting 10 to 15 mL of LA deep to the clavipectoral fascia on the medial and lateral side of the fracture site. A SCP or supraclavicular nerves block should be implemented to provide a sensory block of the skin of the shoulder. This nerve block can potentially involve the PN if the injection is not performed accurately in the proper subcutaneous plane and using low volumes. The block can be used for diaphysis and lateral end interventions, but as isolated block for surgical anesthesia, it only works for diaphysis fractures (Figure 13) [44].
The peri clavicular fascial plane or clavipectoral planes block (CPB). A: Scan throughout all clavicle surface, identifying the fracture site (proximal segment is displaced upward) B: Initiate the US scan in a sagittal paramedian position C: Tilting the ultrasound probe, is positioned on the upper surface of the clavicle D: Identify the anterior and posterior borders of clavicle E: 25 G needle tip positioned between bony surface and periosteum (if seen: By the fractured site, the periosteum is usually detached F: After 1-2 ml injected, the periosteum is further disengaged G: A second hyperechoic line appears, which correspond to clavipectoral fascia H: Needle tip positioned in the gap between periosteum and clavipectoral fascia I: Initial injection under clavipectoral fascia. Track Injectate spread in caudal and cephalic way along the anterior surface of clavicle I: Alternatively, Clavipectoral fascia scanning and needle in plane insertion from caudal to cephalic over clavipectoral fascia between pectoral major and minor muscles; this plane is the target for injection of local anesthetic.
For lateral fractures, including acromioclavicular and coracoacromial ligaments, articular branch of lateral pectoral nerve should be blocked. Likewise, if the surgery involves the acromioclavicular joint, the SSN should be blocked. Yamak Altinpulluk states that in the description of Ince et al., the LA was injected between the periosteum of the clavicle and the surrounding fascia (assumed as the clavipectoral fascia), but cadaveric dissections show that the spread is between the clavicle and fascia of the pectoralis major muscle in the upper and anterior aspect of the clavicle, with anesthetic spread under the deep layer of superficial cervical fascia and the superficial layer of pectoralis major fascia. The naming of this block as CPB is misleading and suggests that this block should be named as peri clavicular block (PB) [45]. The publication of a series of cases by Kukreja et al., shows the injection of the LA between the clavipectoral fascia and the pectoralis major muscle, resolving the previous objections described by Yamak Altinpulluk et al. [46].
ISBP block targets the roots and trunks of the BP in the interscalene groove between ASM and MSM, and is directed towards C5-C6 nerve roots or UT. With higher volumes, C7 and even C8 nerve roots may be blocked. The block provides analgesia and anesthesia to the shoulder, lateral two-thirds of the clavicle, proximal humerus, and shoulder joint surgeries. Continuous infusion of 0.15% bupivacaine or ropivacaine (vs GA or intravenous anesthesia) provides adequate pain relief, similar side effects, and high patient satisfaction. ISBP block is associated with a high risk of PN blockade and HDP. Persistent PN palsy after ISBP block has recently gained wider recognition (reported incidence of 1:2000). Phrenic nerve palsy could be due to direct needle trauma or intraneural injection during landmark guided ISB but this complication has not been described with USG ISBP block. More peripheral BP nerve blockades are alternatives in scenarios in which avoiding PN palsy is critical, without clinically meaningful analgesic differences compared with ISBP block, except during recovery room stay [47]. Vocal hoarseness and Horner’s syndrome are due to self-limiting temporary blockade of the ipsilateral recurrent laryngeal nerve and stellate ganglion [48]. ISBP block cannot reliably block the C8 and T1 ventral rami [48, 49].
ISBP Blockade relies on the visualization of the relevant anatomy, needle-tip position and LA spread using USG plus peripheral nerve stimulation with or without injection pressure monitoring. USG allows fewer needle passes, lower volumes of LA, and better postoperative analgesia [1].
Figure 14 shows the scan process of interscalene space: At cricoid cartilage level, with transverse scan, identify the carotid artery and move the transducer laterally to locate the sonographic image of C5 and C6 TP; C5-C6 nerve roots are seen between the anterior and posterior tubercles and are traced in the groove between ASM and MSM, deep to the prevertebral fascia. The SCM lies superficially, and the PN runs medially over the ASM, away from the C5 root. Below the C6 TP and nerve root, C7 TP appears and the C7 nerve root can be seen anteriorly as hypoechoic round structure, lateral to vertebral vessels (identified by doppler color scan); meanwhile C5 and C6 nerve trunk are merging to conform to the UT; inferiorly to C7 transverse process, C7 nerve root conforms the MT. The dorsal scapular nerve (DSN) arises from the C5 nerve root and is imaged as a hyperechoic structure traversing the MSM, accompanied by LTN. Both must be avoided not needling through MSM. The block is performed positioning the tip deep to the C6 nerve root or UT and seeking the spread of LA anterior and posterior to the nerves, within the interscalene groove, and then repositioning of the needle superficial to the C5 nerve root or UT to obtain a satisfactory spread of LA. Do not needle between C5 and C6. 10-15 mL of LA (ropivacaine 0.75%) produce surgical anesthesia. Supraclavicular nerves blockade is added aimed to provide complete anesthesia to the shoulder cap.
Interscalene brachial plexus block.
The PN diverges at a rate of 0.3 mm per cm below the cricoid cartilage. Its blockade is reported in as 100% with a traditional landmark-based approach using volumes greater than 20 mL, and between 25 and 50% with lower volumes. Forced expiratory volume in 1 s (FEV1) may be reduced by up to 40%, and patients with comorbidities (obesity and respiratory disease) may develop troublesome dyspnea. ISBP block has been associated with an incidence of temporary neurological dysfunction in up to 14% at 10 days. Hypotension and bradycardic events occur in up to 20% during shoulder surgery, typically in the sitting position, and at around 30 min after the placement of an ISBP block. High circulating catecholamine concentrations and an underfilled, hyper contractile ventricle (induced by venous pooling) stimulates intramyocardial mechanoreceptors resulting in an abrupt reduction in sympathetic tone together with increased vagal tone. Prompt treatment with an antimuscarinic (ideally atropine) with or without sympathomimetic drugs is indicated [1].
Selective trunk block (SeTB) targets injection around individual trunks, with small volumes of LA. Produces anesthesia of the entire upper extremity (C5-T1) except the ICBN innervated area (T2). Is performed as one injection targeting UT and MT at interscalene and another one targeting LT at the corner pocket of the supraclavicular fossa (Up to 25 ml of LA are used). Produces HDP similar to UT approach [49, 50].
Shoulder surgery is accompanied by severe acute postoperative pain that continues to be an unresolved problem. The gold standard for analgesia after this surgery is the ISBP. Unfortunately, this block is associated with a high incidence of ipsilateral phrenic nerve block and the consequent HDP, which restricts its use in patients with pre-existing pulmonary involvement, so it is prudent to consider the practical options to avoid or reduce the incidence of this complication. Nerve block techniques without diaphragmatic involvement such as supraclavicular blocks, upper trunk blocks, anterior suprascapular nerve blocks, costoclavicular blocks, and combined infraclavicular-suprascapular blocks are some of the possible alternatives. It has been suggested that costoclavicular blocks could provide postoperative analgesia similar to ISBP along with a 0% incidence of HDP. It is not clear whether costoclavicular blocks could achieve surgical anesthesia for shoulder surgery. The anterior suprascapular nerve blocks have been shown to provide surgical anesthesia and analgesia similar to ISBP. However, the risk of HDP has not been adequately quantified. Of the remaining nerve blocks that preserve diaphragm function, supraclavicular blocks (with injection of posterolateral local anesthetic to the brachial plexus), upper trunk blocks, and combined anterior and infraclavicular suprascapular blocks achieve analgesia similar to ISBP, along with an incidence of HDP <10% [17, 25, 51].
Orthopedic surgeries are well known to be very painful. General anesthesia or regional anesthesia, or a combination of both, are optimal options for shoulder surgery. Regional nerve blocks are essential for postoperative analgesia and can be used alone or as a complement to GA, therefore the postoperative analgesia could be prolonged for 24 hours or more [49]. Regional anesthesia in the setting of GA has a relative contraindication but, with the use of USG, this statement has been challenged [52].
ISBP blockade is the most common approach and a highly effective technique, but with a high incidence of HDP, that contraindicates it in patients with lung disease or contralateral PN paralysis [25, 51]. Supraclavicular blocks vs. ISBP, result in similar pain control and patient satisfaction, but with an incidence of HDP exceeding 60%, when LA is injected intracluster, vs. 9% depositing LA posterolateral to neural cluster (in this setting, cluster refers to the confluence of trunks and divisions of BP) [25, 28].
UT block targets C5-C6 nerve fibers traveling with SSN and AN, producing analgesia not inferior to ISBP block and a 75% incidence reduction of PN involvement [21, 22, 23, 24]. The HDP occurs with an incidence of 5% [25].
AN block (posterior access) plus SSN block (sub supraspinous muscle access) produces a good analgesic effect in minor surgeries, compared to ISBP block, but spares the AN anterior articular branches, the lateral pectoral nerve articular branch, and subscapular nerve [25, 41, 45] and is inferior in terms of analgesia when compared to ISB in major surgeries. SSN block at sub omohyoid level extends to the UT almost always and occasionally to the middle trunk, with almost no PN block [33, 34, 35, 37]. It provides surgical anesthesia and similar analgesia to ISB [25]. It remains necessary to formally quantify the incidence of HDP. Both blocks should be accompanied by a supraclavicular nerve block at the lateral edge of the SCM to give analgesia to the skin over the shoulder and its contribution to the acromioclavicular joint [29].
AN block may be performed at the axillary fossa, producing anesthesia/analgesia that includes the anterior and posterior branches, with the advantage that intercostobrachial nerve block may be performed with the same puncture [38]. Access to the AN by anterior route is easy to perform and has the possibility of extending to the musculocutaneous nerve, superior subscapular nerve, lateral pectoral nerve and through the clavipectoral fascia, to the lateral supraclavicular nerve [41]. Clavipectoral fascia and peri clavicular block can provide anesthesia and analgesia for fractures of the middle third of the clavicle, without PN paralysis [44, 45, 46].
To date, the strategy that achieves analgesic equivalence with ISB with a 0%-incidence of HDP is the costoclavicular block. In 2019, Aliste et al. [53] compared ISB and costoclavicular block in 44 patients undergoing arthroscopic surgery, finding equivalent analgesia in both groups. Moreover, there is no evidence that this block results in surgical anesthesia [25]. Supraclavicular blocks (with LA injection posterolateral to the BP), UT blocks, and combined infraclavicular-anterior suprascapular blocks have been shown to achieve similar analgesia to ISB [54], coupled with an HDP incidence <10%. Decreasing LA injectate volume could avoid HDP altogether and should also be investigated for the provision of surgical anesthesia [25].
The anesthetic challenge imposed by shoulder surgery is considerable. This chapter reviews current options for regional anesthesia in this type of surgery. A regional technique, GA, or a combination of both can be appropriately used. Performing nerve blocks distally to the ISBP approach, PN paralysis can be reduced considerably, although not eliminated, taking care when performing them in patients with lung disease or contralateral HDP.
We thank MF Rojas for Figure 2. The authors also thank Dr. Victor Whizar-Lugo for his valuable support with this chapter.
The authors declare that they have no conflicts of interest.
axillary nerve anterior scalene muscle brachial plexus clavipectoral plane block dorsal scapular nerve general analgesia great auricular nerve hemi diaphragmatic paresis intercostobrachial nerve interscalene brachial plexus intravenous analgesia Local anesthetic Long head biceps tendon lateral pectoral nerve lateral suprascapular articular branch Levator scapulae muscle lower trunk long thoracic nerve medial brachial cutaneous nerve medial pectoral nerve medial suprascapular articular Branch middle scalene muscle middle trunk peri clavicular block phrenic nerve Quadrangular space sternocleidomastoid muscle superficial cervical plexus suprascapular nerve Selective trunk block transverse process ultrasound ultrasound guidance ultrasound image upper trunk
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Biochemistry examines macromolecules - proteins, nucleic acids, carbohydrates, and lipids – and their building blocks, structures, functions, and interactions. Much of biochemistry is devoted to enzymes, proteins that catalyze chemical reactions, enzyme structures, mechanisms of action and their roles within cells. Biochemistry also studies small signaling molecules, coenzymes, inhibitors, vitamins, and hormones, which play roles in life processes. Biochemical experimentation, besides coopting classical chemistry methods, e.g., chromatography, adopted new techniques, e.g., X-ray diffraction, electron microscopy, NMR, radioisotopes, and developed sophisticated microbial genetic tools, e.g., auxotroph mutants and their revertants, fermentation, etc. More recently, biochemistry embraced the ‘big data’ omics systems. Initial biochemical studies have been exclusively analytic: dissecting, purifying, and examining individual components of a biological system; in the apt words of Efraim Racker (1913 –1991), “Don’t waste clean thinking on dirty enzymes.” Today, however, biochemistry is becoming more agglomerative and comprehensive, setting out to integrate and describe entirely particular biological systems. The ‘big data’ metabolomics can define the complement of small molecules, e.g., in a soil or biofilm sample; proteomics can distinguish all the comprising proteins, e.g., serum; metagenomics can identify all the genes in a complex environment, e.g., the bovine rumen. This Biochemistry Series will address the current research on biomolecules and the emerging trends with great promise.",coverUrl:"https://cdn.intechopen.com/series/covers/11.jpg",latestPublicationDate:"May 26th, 2022",hasOnlineFirst:!0,numberOfOpenTopics:4,numberOfPublishedChapters:289,numberOfPublishedBooks:27,editor:{id:"31610",title:"Dr.",name:"Miroslav",middleName:null,surname:"Blumenberg",fullName:"Miroslav Blumenberg",profilePictureURL:"https://mts.intechopen.com/storage/users/31610/images/system/31610.jpg",biography:"Miroslav Blumenberg, Ph.D., was born in Subotica and received his BSc in Belgrade, Yugoslavia. He completed his Ph.D. at MIT in Organic Chemistry; he followed up his Ph.D. with two postdoctoral study periods at Stanford University. Since 1983, he has been a faculty member of the RO Perelman Department of Dermatology, NYU School of Medicine, where he is codirector of a training grant in cutaneous biology. Dr. Blumenberg’s research is focused on the epidermis, expression of keratin genes, transcription profiling, keratinocyte differentiation, inflammatory diseases and cancers, and most recently the effects of the microbiome on the skin. He has published more than 100 peer-reviewed research articles and graduated numerous Ph.D. and postdoctoral students.",institutionString:null,institution:{name:"New York University Langone Medical Center",institutionURL:null,country:{name:"United States of America"}}},subseries:[{id:"14",title:"Cell and Molecular Biology",keywords:"Omics (Transcriptomics; Proteomics; Metabolomics), Molecular Biology, Cell Biology, Signal Transduction and Regulation, Cell Growth and Differentiation, Apoptosis, Necroptosis, Ferroptosis, Autophagy, Cell Cycle, Macromolecules and Complexes, Gene Expression",scope:"The Cell and Molecular Biology topic within the IntechOpen Biochemistry Series aims to rapidly publish contributions on all aspects of cell and molecular biology, including aspects related to biochemical and genetic research (not only in humans but all living beings). We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics include, but are not limited to: Advanced techniques of cellular and molecular biology (Molecular methodologies, imaging techniques, and bioinformatics); Biological activities at the molecular level; Biological processes of cell functions, cell division, senescence, maintenance, and cell death; Biomolecules interactions; Cancer; Cell biology; Chemical biology; Computational biology; Cytochemistry; Developmental biology; Disease mechanisms and therapeutics; DNA, and RNA metabolism; Gene functions, genetics, and genomics; Genetics; Immunology; Medical microbiology; Molecular biology; Molecular genetics; Molecular processes of cell and organelle dynamics; Neuroscience; Protein biosynthesis, degradation, and functions; Regulation of molecular interactions in a cell; Signalling networks and system biology; Structural biology; Virology and microbiology.",annualVolume:11410,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/14.jpg",editor:{id:"165627",title:"Dr.",name:"Rosa María",middleName:null,surname:"Martínez-Espinosa",fullName:"Rosa María Martínez-Espinosa",profilePictureURL:"https://mts.intechopen.com/storage/users/165627/images/system/165627.jpeg",institutionString:null,institution:{name:"University of Alicante",institutionURL:null,country:{name:"Spain"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"79367",title:"Dr.",name:"Ana Isabel",middleName:null,surname:"Flores",fullName:"Ana Isabel Flores",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRpIOQA0/Profile_Picture_1632418099564",institutionString:null,institution:{name:"Hospital Universitario 12 De Octubre",institutionURL:null,country:{name:"Spain"}}},{id:"328234",title:"Ph.D.",name:"Christian",middleName:null,surname:"Palavecino",fullName:"Christian Palavecino",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000030DhEhQAK/Profile_Picture_1628835318625",institutionString:null,institution:{name:"Central University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"186585",title:"Dr.",name:"Francisco Javier",middleName:null,surname:"Martin-Romero",fullName:"Francisco Javier Martin-Romero",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSB3HQAW/Profile_Picture_1631258137641",institutionString:null,institution:{name:"University of Extremadura",institutionURL:null,country:{name:"Spain"}}}]},{id:"15",title:"Chemical Biology",keywords:"Phenolic Compounds, Essential Oils, Modification of Biomolecules, Glycobiology, Combinatorial Chemistry, Therapeutic peptides, Enzyme Inhibitors",scope:"Chemical biology spans the fields of chemistry and biology involving the application of biological and chemical molecules and techniques. In recent years, the application of chemistry to biological molecules has gained significant interest in medicinal and pharmacological studies. This topic will be devoted to understanding the interplay between biomolecules and chemical compounds, their structure and function, and their potential applications in related fields. Being a part of the biochemistry discipline, the ideas and concepts that have emerged from Chemical Biology have affected other related areas. This topic will closely deal with all emerging trends in this discipline.",annualVolume:11411,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/15.jpg",editor:{id:"441442",title:"Dr.",name:"Şükrü",middleName:null,surname:"Beydemir",fullName:"Şükrü Beydemir",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003GsUoIQAV/Profile_Picture_1634557147521",institutionString:null,institution:{name:"Anadolu University",institutionURL:null,country:{name:"Turkey"}}},editorTwo:{id:"13652",title:"Prof.",name:"Deniz",middleName:null,surname:"Ekinci",fullName:"Deniz Ekinci",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYLT1QAO/Profile_Picture_1634557223079",institutionString:null,institution:{name:"Ondokuz Mayıs University",institutionURL:null,country:{name:"Turkey"}}},editorThree:null,editorialBoard:[{id:"241413",title:"Dr.",name:"Azhar",middleName:null,surname:"Rasul",fullName:"Azhar Rasul",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRT1oQAG/Profile_Picture_1635251978933",institutionString:null,institution:{name:"Government College University, Faisalabad",institutionURL:null,country:{name:"Pakistan"}}},{id:"178316",title:"Ph.D.",name:"Sergey",middleName:null,surname:"Sedykh",fullName:"Sergey Sedykh",profilePictureURL:"https://mts.intechopen.com/storage/users/178316/images/system/178316.jfif",institutionString:null,institution:{name:"Novosibirsk State University",institutionURL:null,country:{name:"Russia"}}}]},{id:"17",title:"Metabolism",keywords:"Biomolecules Metabolism, Energy Metabolism, Metabolic Pathways, Key Metabolic Enzymes, Metabolic Adaptation",scope:"Metabolism is frequently defined in biochemistry textbooks as the overall process that allows living systems to acquire and use the free energy they need for their vital functions or the chemical processes that occur within a living organism to maintain life. Behind these definitions are hidden all the aspects of normal and pathological functioning of all processes that the topic ‘Metabolism’ will cover within the Biochemistry Series. Thus all studies on metabolism will be considered for publication.",annualVolume:11413,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/17.jpg",editor:{id:"138626",title:"Dr.",name:"Yannis",middleName:null,surname:"Karamanos",fullName:"Yannis Karamanos",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002g6Jv2QAE/Profile_Picture_1629356660984",institutionString:null,institution:{name:"Artois University",institutionURL:null,country:{name:"France"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"243049",title:"Dr.",name:"Anca",middleName:null,surname:"Pantea Stoian",fullName:"Anca Pantea Stoian",profilePictureURL:"https://mts.intechopen.com/storage/users/243049/images/system/243049.jpg",institutionString:null,institution:{name:"Carol Davila University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"203824",title:"Dr.",name:"Attilio",middleName:null,surname:"Rigotti",fullName:"Attilio Rigotti",profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institutionString:null,institution:{name:"Pontifical Catholic University of Chile",institutionURL:null,country:{name:"Chile"}}},{id:"300470",title:"Dr.",name:"Yanfei (Jacob)",middleName:null,surname:"Qi",fullName:"Yanfei (Jacob) Qi",profilePictureURL:"https://mts.intechopen.com/storage/users/300470/images/system/300470.jpg",institutionString:null,institution:{name:"Centenary Institute of Cancer Medicine and Cell Biology",institutionURL:null,country:{name:"Australia"}}}]},{id:"18",title:"Proteomics",keywords:"Mono- and Two-Dimensional Gel Electrophoresis (1-and 2-DE), Liquid Chromatography (LC), Mass Spectrometry/Tandem Mass Spectrometry (MS; MS/MS), Proteins",scope:"With the recognition that the human genome cannot provide answers to the etiology of a disorder, changes in the proteins expressed by a genome became a focus in research. Thus proteomics, an area of research that detects all protein forms expressed in an organism, including splice isoforms and post-translational modifications, is more suitable than genomics for a comprehensive understanding of the biochemical processes that govern life. The most common proteomics applications are currently in the clinical field for the identification, in a variety of biological matrices, of biomarkers for diagnosis and therapeutic intervention of disorders. From the comparison of proteomic profiles of control and disease or different physiological states, which may emerge, changes in protein expression can provide new insights into the roles played by some proteins in human pathologies. Understanding how proteins function and interact with each other is another goal of proteomics that makes this approach even more intriguing. Specialized technology and expertise are required to assess the proteome of any biological sample. Currently, proteomics relies mainly on mass spectrometry (MS) combined with electrophoretic (1 or 2-DE-MS) and/or chromatographic techniques (LC-MS/MS). MS is an excellent tool that has gained popularity in proteomics because of its ability to gather a complex body of information such as cataloging protein expression, identifying protein modification sites, and defining protein interactions. The Proteomics topic aims to attract contributions on all aspects of MS-based proteomics that, by pushing the boundaries of MS capabilities, may address biological problems that have not been resolved yet.",annualVolume:11414,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/18.jpg",editor:{id:"200689",title:"Prof.",name:"Paolo",middleName:null,surname:"Iadarola",fullName:"Paolo Iadarola",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bSCl8QAG/Profile_Picture_1623568118342",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorTwo:{id:"201414",title:"Dr.",name:"Simona",middleName:null,surname:"Viglio",fullName:"Simona Viglio",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRKDHQA4/Profile_Picture_1630402531487",institutionString:null,institution:{name:"University of Pavia",institutionURL:null,country:{name:"Italy"}}},editorThree:null,editorialBoard:[{id:"72288",title:"Dr.",name:"Arli Aditya",middleName:null,surname:"Parikesit",fullName:"Arli Aditya Parikesit",profilePictureURL:"https://mts.intechopen.com/storage/users/72288/images/system/72288.jpg",institutionString:null,institution:{name:"Indonesia International Institute for Life Sciences",institutionURL:null,country:{name:"Indonesia"}}},{id:"40928",title:"Dr.",name:"Cesar",middleName:null,surname:"Lopez-Camarillo",fullName:"Cesar Lopez-Camarillo",profilePictureURL:"https://mts.intechopen.com/storage/users/40928/images/3884_n.png",institutionString:null,institution:{name:"Universidad Autónoma de la Ciudad de México",institutionURL:null,country:{name:"Mexico"}}},{id:"81926",title:"Dr.",name:"Shymaa",middleName:null,surname:"Enany",fullName:"Shymaa Enany",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002bRqB9QAK/Profile_Picture_1626163237970",institutionString:null,institution:{name:"Suez Canal University",institutionURL:null,country:{name:"Egypt"}}}]}]}},libraryRecommendation:{success:null,errors:{},institutions:[]},route:{name:"onlineFirst.detail",path:"/online-first/80185",hash:"",query:{},params:{id:"80185"},fullPath:"/online-first/80185",meta:{},from:{name:null,path:"/",hash:"",query:{},params:{},fullPath:"/",meta:{}}}},function(){var e;(e=document.currentScript||document.scripts[document.scripts.length-1]).parentNode.removeChild(e)}()