Posterior superior alveolar nerve block technique.
\r\n\t
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He is a scientist at the Leibniz-Institut für Agrartechnik und Bioökonomie working toward digitization of agriculture for food security.",coeditorOneBiosketch:"Sanaz is an Assistant Professor of Smart Farming at Virginia Tech University. Prior to this, she was an assistant professor at the University of Idaho. Her expertise lies in using advanced technologies and methodologies for economically and environmentally sustainable crops and trees monitoring and management. She integrates satellite/drone images and AI to develop methodologies for environmental monitoring, crop modeling, and water, and nutrient conservation.",coeditorTwoBiosketch:null,coeditorThreeBiosketch:null,coeditorFourBiosketch:null,coeditorFiveBiosketch:null,editors:[{id:"203413",title:"Dr.",name:"Redmond R.",middleName:null,surname:"Shamshiri",slug:"redmond-r.-shamshiri",fullName:"Redmond R. Shamshiri",profilePictureURL:"https://mts.intechopen.com/storage/users/203413/images/system/203413.png",biography:"Dr. Redmond R. Shamshiri holds a Ph.D. in agricultural automation with a focus on control systems and dynamics. He is a scientist at the Leibniz-Institut für Agrartechnik und Bioökonomie working toward digitization of agriculture for food security. His main research fields include simulation and modeling for closed-field plant production systems, LPWAN sensors, wireless control, and autonomous navigation. His work has appeared in over 100 publications, including peer-reviewed journal papers, book chapters, and conference proceedings. He is a member of the Adaptive AgroTech Consultancy Network and serves as a section editor and reviewer for various high-ranking journals in the field of smart farming.",institutionString:"Leibniz Institute of Agricultural Engineering and Bio-economy",position:null,outsideEditionCount:0,totalCites:0,totalAuthoredChapters:"7",totalChapterViews:"0",totalEditedBooks:"1",institution:{name:"Leibniz Institute for Agricultural Engineering Potsdam-Bornim",institutionURL:null,country:{name:"Germany"}}}],coeditorOne:{id:"429704",title:"Dr.",name:"Sanaz",middleName:null,surname:"Shafian",slug:"sanaz-shafian",fullName:"Sanaz Shafian",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y00003CPbhJQAT/Profile_Picture_1629955207151",biography:"Sanaz is an Assistant Professor of Smart Farming at Virginia Tech University. Prior to this she was assistant professor at University of Idaho. Her expertise lies in remote sensing research, with a focus on using advanced technologies and methodologies for economically and environmentally sustainable crops and trees monitoring and management. She integrates satellite/drone images and AI to develop methodologies for environmental monitoring, crop modeling and water and nutrient conservation and she has published widely on these topics. She has been involved in several USDA projects. With University of Idaho, she led an educational and outreach project to initiate Precision Agriculture certificate. 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Knowledge of the precise topography and distribution area of the trigeminal nerve and its branches is required to provide precise and useful anesthesia. Even more, during diverse types of surgery, it is very important to know the distribution area of the trigeminal nerve in order to predict the anesthetic area and avoid pain.
\nThe aim of this chapter is to emphasize the most relevant aspects of head and neck anatomy, specifically related to osteology and neurology, for the application of regional anesthesia techniques.
\nThis text includes the most relevant aspects of the bone and sensory anatomy, relevant for the realization of regional anesthetic techniques in the oral and maxillofacial area.
\nThe maxilla has fine external and porous corticals, with thickening in certain areas that generally do not reach thicknesses greater than 1 mm. This allows that anesthetic solution deposited through the buccal vestibules infiltrate into the maxillary bone, anesthetizing the maxillary teeth and their adjacent tissues (periodontium and gingival mucosa). However, the thickness of the palatal corticals is much greater, impeding the same infiltrative effect. This forces us to consider anesthetic block of the nerve trunks before they are introduced to the maxilla, for most effective anesthetic and of more extensive sectors.
\nFor its part, the jaw usually has a greater thickening even of all its cortical, reaching easily the 3 mm (basilar rim reaches thicknesses of up to 5 mm) [1]. These anatomical characteristics of the mandible should be considered to decide the anesthetic technique to be used, the latency time, and the required anesthetic concentration.
\nAfter the respective trigeminal branches are introduced into the maxilla and jaw and emit the branches that innervate the dental tissues, the terminal branches emerge into the skin and innervate the specific areas of the face, giving rise to the different trigeminal dermatomes [2] (see Figure 1).
\nThe major sensory dermatomes of the head and neck. B, buccal nerve; EN, external (dorsal) nasal nerve; IO, infraorbital nerve; IT, infratrochlear; ST, supratrochlear nerve; M, mental nerve; SO, supraorbital nerve; Zf, zygomaticofacial nerve; ZT, zygomaticotemporal nerve. Adapted from: Simplified Facial Rejuvenation. 1st ed. Heidelberg: Springer; 2008.
The ophthalmic nerve (V1) is the smallest of the three divisions of the trigeminal nerve. The V1 branches into the frontal, nasociliary, and lacrimal nerves as it approaches the superior orbital fissure. It supplies branches to the cornea, ciliary body, and iris; to the lacrimal gland and conjunctiva; to the upper part of the mucous membrane of the nasal cavity; and to the skin of the eyelids, eyebrow, forehead, and upper lateral nose.
\nThe frontal nerve is the largest division of the branches of the V1, courses outside and superolateral, and divides into the supratrochlear and supraorbital nerves within the orbit. The supratrochlear nerve supplies the conjunctiva and the skin of the upper eyelid and ascends dividing into branches to supply the skin of the lower forehead near the midline. The supraorbital nerve courses between the levator palpebrae muscle and orbital roof and exited the supraorbital notch or foramen; it innervates the upper eyelid, the mucous membrane of the frontal, the galea aponeurosis, and the orbicularis oculi. It ascends to the forehead, dividing into a smaller medial and a lateral branch, which supply the skin of the scalp nearly as far back as the lambdoid suture.
The nasociliary nerve is more deeply placed in the orbit. The sensory root from the nasociliary nerve passes to the globe through the short ciliary nerves and conveys sensation to cornea and globe. At the level of the fissure, the nasociliary nerve gently ascends to reach the medial part of the orbit, where it gives rise to the anterior and posterior ethmoidal nerves and infratrochlear nerve. The anterior ethmoidal nerve gives off two branches, the internal nasal and external nasal nerves. The internal nasal nerve innervates the mucous membrane of the anterior part of the nasal septum and the lateral wall of the nasal cavity. The external nasal branch innervates the skin over the apex and the
The lacrimal nerve is the smallest of the three division of the V1 and conveys sensation from the area in front of the lacrimal gland.
Anesthetic considerations:
\nThe anesthetic block of the first division of the trigeminal nerve is useful for the execution of procedures on the territories innervated by the terminal branches.
The supraorbital, supratrochlear, and infratrochlear nerves can be easily anesthetized through the location of the supraorbital notch or foramen (see Figure 2).
The supraorbital foramen is located 29 mm lateral to the midline (25–33 mm) and 5 mm below the upper margin of the supraorbital rim (range, 4–6 mm) [3]. This supraorbital notch is readily palpable in most patients and when injecting this area, it is prudent to use the free hand to palpate the orbital rim to prevent inadvertent injection into the globe. The supratrochlear nerve is located medial to the supraorbital nerve at the supraorbital rim and emerges between the trochlea and the supraorbital foramen located 16 mm lateral to the midline (range, 12–21 mm) and 7 mm below the upper margin of the supraorbital rim (range, 6–9 mm) [3]. The infratrochlear nerve can be blocked injecting local anesthetic solution at the junction of the orbit and the nasal bones.
The external nasal nerve emerges 5–10 mm from the nasal midline at the osseous junction of the inferior portion of the nasal bones (the distal edge of the nasal bones) and can be blocked subcutaneously at the osseous-cartilaginous junction of the distal nasal bones (see Figure 3).
Points to anesthetic block of the supraorbital and supratrochlear nerves. Adapted from: Simplified Facial Rejuvenation. 1st ed. Heidelberg: Springer; 2008.
Anesthetic block of external nasal branches.
The maxillary nerve (V2), the intermediate division of the trigeminal nerve, is purely sensory in function. The V2 gives innervation to all structures in and around the maxillary bone and the mid-facial region, including the skin of the mid-facial regions, the lower eyelid, side of the nose, and upper lip; nasopharyngeal mucosa, maxillary sinus, soft and hard palate, palatine tonsil, maxillary teeth, and periodontal tissues [3].
\nThe maxillary nerve leaves the endocranium through the foramen rotundum, located in the greater wing of the sphenoid bone, to enter the pterygopalatine fossa (PPF).
\nThe PPF is a pyramidal space located between the pterygoid bone posteriorly, the perpendicular plate of the palatine bone anteromedially, and maxilla anterolaterally. It opens laterally into the medial part of the infratemporal fossa through the pterygomaxillary fissure and superiorly through the medial part of the inferior orbital fissure into the orbital apex. The fossa also communicates posterolaterally with middle cranial fossa through the foramen rotundum, posteromedially with foramen lacerum through the vidian canal, medially with the nasopharynx through the palatovaginal canal, inferomedially with the oral cavity through the palatine foramina, and medially with nasal cavity through the sphenopalatine foramen.
\nThe V2, after entering the PPF, gives off ganglionic branches to the pterygopalatine ganglion (PPG). It then deviates laterally just beneath the inferior orbital fissure, giving rise to the zygomatic nerve and posterosuperior alveolar nerve.
\nAnesthetic considerations:
\nThe zygomatic nerve enters the orbit through the inferior orbital fissure, where it divides into zygomaticotemporal and zygomaticofacial nerves. These nerves give innervation to the skin on the temporal area and on the prominence of the cheek, respectively (see Figure 1).
The zygomaticofacial nerve is blocked by injecting the inferior lateral portion of the orbital rim, and the zygomaticotemporal nerve is blocked by placing the needle on the concave surface of the posterior lateral orbital rim (see Figure 4).
Image showing the needle directions for block technique of (A) zygomaticofacial nerve and (B) zygomaticotemporal nerve (copyright of authors).
In the posterior aspect of the maxillary tuberosity, one to three small holes, 1–2 mm in diameter, can be clearly seen, which are located between 10 and 25 mm above the alveolar rim and behind the second or at the height of the third upper molar. These holes are continued with small ducts or grooves that run through the posterolateral wall of the maxillary sinus until reaching the dental apices. It contains the posterosuperior alveolar vessels and nerves; it is destined to the superior molars, premolars, and neighboring tissues.
\nThe posterior superior alveolar nerve arises from the maxillary nerve before penetrating into the infraorbital canal in the PPF and descends anteriorly and inferiorly to pierce the infratemporal surface of the maxillary sinus (see Figure 5). After entering the maxillary sinus, the nerves pass forward under the mucosa of the maxillary sinus, supplying afferent innervation to these membranes. It also supplies a branch to the upper gum and the adjoining part of the cheek [3].
\nImage showing the posterior superior alveolar nerve anatomy entering at maxillary bone, true 3–4 holes in the tuberosity (copyright of authors).
The middle superior alveolar nerve leaves the infraorbital nerve (ION) in the infraorbital groove, the posterior part of the infraorbital canal. It runs down and forward in the lateral wall of the maxillary sinus and ends in small branches which link up with the superior dental plexus, supplying small rami to the upper premolar teeth [4] and first molar (Table 1).
\nAnesthetized nerves | \n\n
| \n
Anesthetized areas | \n\n
| \n
Anatomical references | \n\n
| \n
Patient/operator position | \n\n
| \n
Local anesthetic volume required | \n1.8 mL | \n
Needle required | \n\n
| \n
Needle direction | \n\n
| \n
Needle puncture depth | \n15 mm | \n
Posterior superior alveolar nerve block technique.
The pterygopalatine ganglion gives rise to: from the lower surface the greater and lesser palatine nerves; from the medial surface the sphenopalatine nerve and pharyngeal branch; and from the superior surface the orbital branch.
\nThe palatine nerves are distributed over much of the roof of the mouth, the soft palate, the amygdala, and the nasal mucosa. The major palatine nerve descends through the greater palatine canal, which begins at the lower end of the PPF, it passes through this duct, and inside, it runs down, forward, and inward, and appears in the mouth through the major palatine foramen of the maxillary. It communicates with the filaments of the nasopalatine nerve, a branch of the sphenopalatine nerve [3].
\nThe lesser palatine nerves, after leaving the PPF, descend and appear in the mouth through a lesser palatine foramen in the palatine bone and give branches to the uvula, tonsil, and soft palate. These nerves anastomose with branches of the glossopharyngeal nerve to form a tonsillar plexus around the palatine tonsil [3].
\nThe nasopalatine nerve, the largest of the nasal branches of the PPG, travels through the sphenopalatine foramen, located just below the sphenoid sinus, enters into the nasal cavity and reaches the nasal septum. It then runs anteroinferiorly between the periosteum and mucous membrane of the nasal septum, supplies a few filaments to the nasal septum, exits the nasal cavity through the incisive foramen, and ends by supplying the mucosa of the anterior part of the hard palate [3] (see Figure 6).
\nImage showing the palatal mucosal area innervated by nasopalatine nerve (copyright of authors).
Other nasal branches include medial and lateral posterior superior nasal nerves. The lateral posterior superior nasal branches innervate the mucosa of the posterior part of the superior and middle nasal conchae and the lining of the posterior ethmoidal sinuses. The medial posterior superior nasal branches supply the mucosa of the posterior part of the roof and of the nasal septum.
\nThe anterior palatine canal, also called nasopalatine, presents a Y-shape and is formed by the union of two lateral canals excavated in the palatine apophyses of the jaws, one to each side of the nasal septum, in the anterior area of the nasal floor, where they converge in one. With a top-down and back-to-front direction, its total length varies between 8 and 20 mm. Its mouth end in the palate is made through a depression or fovea, the anterior palatine foramen or incisor foramen, which may have an oval, triangular, rectangular, or racket shape, with a major axis of approximately 1 cm and a width of 5 mm. While the nasal holes that initiate this duct are located approximately 15–20 mm behind the piriform notch, the incisive foramen is located between 4 and 10 mm behind the alveolar ridge, under a thickening of the palatal mucosa, called the incisive papilla (Table 2).
\nAnesthetized nerves | \n\n
| \n
Anesthetized areas | \n\n
| \n
Anatomical references | \n\n
| \n
Patient/operator position | \n\n
| \n
Local anesthetic volume required | \n0.5 mL | \n
Needle required | \n\n
| \n
Needle direction | \n\n
| \n
Needle puncture depth | \n10 mm | \n
Nasopalatine nerve block technique.
The palatine canal, which leads to the descending palatine artery, a venous vessel and the major palatine nerve, it is an access route to the pterygomaxillary fossa from the oral cavity. The maxillary nerve block via the greater palatine canal technique will anesthetize all the terminal branches of the maxillary nerve with a single injection.
\nThe greater palatine canal is formed by the union of two excavated channels, one in the maxilla and another in the vertical sheet of the palatal bone. From the palate, its direction is outward, backward, and upright (inclinations of 5–10°, 15–20°, and 60–70°, respectively), with a length varying between 10 and 22 mm, depending on the facial biotype.
\nThe greater palatine canal emerges onto the oral cavity trough the greater palatine foramen. This foramen has an oval shape, with a larger diameter that can easily reach 5 mm. It is located in the angle that forms the horizontal portion of the palatine bone and the inner side of the maxillary alveolar ridge. In the soft tissues that cover it, a mild depression is observed, and this is an important aspect that can help in the appropriate location of the foramen for anesthetic purposes. Its posterior border lies approximately 1 cm in front of the hook of the pterygoid process and 5–6 mm in front of the border between hard and soft palate, which translates clinically as a change in the coloration of the palatal mucosa. The location of the palatine foramen in relation to the molars varies with age and individual characteristics, being able to be in front or distal to the third molar or—less frequently—between this and the second molar [4]; in young individuals who do not yet have the third molar, it is located in front of the distal side of the second; and in children less than 12 years old, it is usually in front of the distal face of the first molar (Table 3).
\nAnesthetized nerves | \n\n
| \n
Anesthetized areas | \n\n
| \n
Anatomical references | \n\n
| \n
Patient/Operator position | \n\n
| \n
Local anesthetic volume required | \n1.8 mL | \n
Needle required | \n\n
| \n
Needle direction | \n\n
| \n
Needle puncture depth | \n30–35 mm | \n
Maxillary nerve block technique via the greater palatine canal.
After entering the PPF, the V2 then turns medially as the infraorbital nerve (ION), passing through the inferior orbital fissure to enter the infraorbital groove, from where the anterior and middle superior alveolar nerves arise. The long axis of the infraorbital canal is directed forward, down, and medially through its canal lying progressively below the floor of the orbit and in the roof of the maxillary sinus, until it emerges in the face through the infraorbital foramen.
\nThe anterior superior alveolar nerve leaves the lateral side of the ION just prior to the infraorbital exit through the foramen. It traverses the canal in the anterior wall of maxillary sinus and divides into branches supplying incisor and canine teeth. In the absence of middle superior alveolar nerves, which happens in approximately 70% of cases [4], the anterior superior alveolar nerve emits a few posterior branches, which join with branches of the posterior superior alveolar nerve to form a nervous plexus also called the Auerbach dental plexus, which is distributed through the lateral wall of the maxillary sinus and innervates the premolars and the mesiobuccal root of the first molar [1] (see Figure 7).
\nImage showing the anatomical alternative with Auerbach’s plexus (circle) (copyright of authors).
The infraorbital nerve (ION) is the terminal branch of the maxillary nerve, and after emerging onto the face, it divides onto its terminal branches: inferior palpebral, nasal, and superior labial branches [5], which supply the skin and conjunctiva of the lower eyelid, the lateral skin of the nose, the movable part of the nasal septum and vestibule of the nose, the skin over the cheek and upper lip, and the related oral mucosa [5].
\nThe infraorbital notch or foramen is the facial or anterior opening of the infraorbital canal. In a generally oval shape, its major axis is oblique downward and outward, with a maximum length of 6 mm. Due to the final orientation of the infraorbital canal, the foramen has a superior cutting edge, which is notorious, whereas its lower border is imperceptible, being confused with the anterior aspect of the maxilla, which at this point forms the canine fossa.
\nThe infraorbital foramen is single in 90–97% of the cases [4]. Several authors have also described the presence of an accessory infraorbital foramen through which a branch of the ION passes. A recent systematic review showed that the frequency of skulls containing the accessory infraorbital foramen ranged from 0.8 to 27.3%, with a mean frequency of 16.9 ± 8.6%, being more frequent in left side of the skull [6]. This is important because a partial nerve blockade during anesthesia can lead to an insufficient blockage of the ION.
\nIn a study by Hu et al. [5], the accessory infraorbital foramen was found in 14% of the cases, and the nerve component that exited through the accessory infraorbital foramen was either the inferior palpebral branch, or the external nasal branch.
\nThe topography of both the canal and the infraorbital foramen is of special importance in the practice of anesthesia of the anterior superior alveolar nerves and the infraorbital nerve branches.
\nTo properly locate the infraorbital foramen, we must consider that
In the lateral sense, it is located at the junction of the inner third and the middle third of the infraorbital rim. It also corresponds to an imaginary vertical line drawn downward from the supraorbital notch, joining the infraorbital and mental foramen.
\nA successful infraorbital nerve block will anesthetize the infraorbital cheek, the lower palpebral area, the lateral nasal area, and superior labial regions (see Figure 8).
\nImage showing area innerved by infraorbital nerve (copyright of authors).
The aforementioned infraorbital nerve blocks provide anesthesia to the lateral nasal skin but do not provide anesthesia to the central portion of the nose. An external nasal nerve of the block will supplement nasal anesthesia by providing anesthesia over the area of the cartilaginous nasal dorsum and tip (Table 4).
\nAnesthetized nerves | \n\n
| \n
Anesthetized areas | \n\n
| \n
Anatomical references | \n\n
| \n
Patient/operator position | \n\n
| \n
Local anesthetic volume required | \n0.9–1.2 mL | \n
Needle required | \n\n
| \n
Needle direction | \n\n
| \n
Needle puncture depth | \n16 mm for intraoral technique | \n
Infraorbital nerve block technique.
The mandibular division (V3) is the largest branch of the trigeminal nerve. It supplies the teeth and gums of the mandible, the skin in the temporal region, part of the auricle, the lower lip, and the lower part of the face. The V3 also contains motor fiber to innervate the muscle of mastication, the mylohyoid, the anterior belly of the digastric muscle, tensor veli palatini, and tensor tympani muscle [1].
\nThe V3 is made up of two roots: a large, sensory root, which proceeds from the lateral part of the trigeminal ganglion and emerges almost immediately through the foramen ovale of the sphenoid bone and a small motor root that passes below the trigeminal ganglion and unites with the sensory root just outside the foramen ovale. This trunk it later splits into a small anterior and a large posterior division.
\nBranches from the anterior division provide motor innervation to the muscles of mastication, and sensory innervation to the mucous membrane of the cheek and buccal mucous membrane of the molars.
\nThe anterior division of V3 runs under the lateral pterygoid and then emerges between its two heads to become de buccal nerve, the only sensory component of the anterior division. Under the lateral pterygoid, this nerve gives off several motor branches; the deep temporal nerves, the masseter, and lateral pterygoid nerves.
\nAt the level of the occlusal plane of the mandibular molars, the buccal nerve crosses in front of the anterior border of the ramus and enters the cheek through the buccinator muscle. It gives innervation to the skin of the cheek, the buccal gingiva of the mandibular molars, and the mucobuccal fold in that region [1].
\nThe posterior division of V3 gives rise to sensory branches and one motor branch. It descends downward and medially to the lateral pterygoid muscle, at which points it branches into the auriculotemporal, lingual, and inferior alveolar nerves.
\nThe auriculotemporal nerve provides sensitive innervation to the skin over the helix and tragus of the ear, the external auditory meatus, the posterior portion of the temporomandibular joint, and the skin over the temporal region.
\nThe lingual nerve provides general sensation to the anterior two-thirds of the tongue and sensory innervation to the mucous membranes of the floor of the mouth and the lingual gingiva of the mandible.
\nThe inferior alveolar nerve descends medial to the lateral pterygoid muscle and lateroposterior to the lingual nerve, to the region between the sphenomandibular ligament and the medial surface of the mandibular ramus, where it is introduced into the mandibular canal at the level of the mandibular foramen. Immediately before the inferior alveolar nerve enters the mandibular foramen gives off a motor branch, the mylohyoid nerve, which supplies the mylohyoid muscle and anterior belly of the digastric muscle. Nevertheless, some fibers of the mylohyoid nerve could enter into mandibula through the retromandibular foramina and provide innervation to premolar, canine, and incisor teeth [4, 8].
\nThe inferior alveolar nerve travels anteriorly through the mandibular canal and gives off branches to the teeth, which may form a plexus between the trunk of the nerve and the roots of the teeth. The dental branches of the inferior alveolar nerve supply the molar, premolar, canine, and incisors teeth. The inferior alveolar nerve emerges in the mental foramen where it divides into the terminal branches: the incisive and mental nerve.
\nThe mental nerve, pure sensory, leaves the interior of the mandible to supply the skin of the chin and lower lip, the mucosa of the lip, and the adjacent gum.
\nA continuation of the mandibular canal, the mandibular incisive canal, is a normal structure that typically extends closer to the mandibular midline after the mental nerve emerges through the mandibular foramen [9, 10]. The mandibular incisive nerve travels within this canal and forms a nerve plexus via dental branches to supply innervation to first bicuspid, canine, and lateral and central incisors.
\nGiven that the mandibular bone is very thick, an anesthetic technique with successful nerve block of the V3 branches requires knowledge of the location of the mandibular bone repairs that allows the deposition of the anesthetic in areas close to the nerve trunks before they enter or after they leave the mandibular canal.
\nThe mandibular foramen is located in the medial surface of the mandibular ramus and is the entrance to the mandibular canal, excavated in the thickness of the mandible. This foramen acquires relevance in oral surgery since it is a critical point for the nerve block anesthesia of the inferior alveolar nerve. It has the appearance of a wide cleft, limited from the anterior side by a bony plate called the lingula of the mandible or spine of spix [8] (see Figure 9).
\nImage showing distribution of buccal, lingual, and inferior alveolar nerves at mandibular lingula or spine of spix level (arrow) (copyright of authors).
The lingula can be palpated through the mucosa of the oral cavity. It shows the way, where one should point the needle, when anesthetizing the inferior alveolar nerve [8].
\nThe location of the inferior alveolar foramen would be equidistant from the four edges of the mandibular ramus, although it is usually observed closer to the mandibular notch and to the posterior edge of the mandibular ramus [8]. In the vertical direction, the distance between the hole and the occlusal plane is correlated with the patient’s age: as the individual grows, the mandibular foramen moves cranially and positions itself in the center of the corpus [8]. In very young individuals, the mandibular foramen is located approximately at the level of the occlusal plane [11].
\nIn the mentioned foramen, the nerve lies anteriorly and medially to the inferior alveolar artery. Such a configuration occurs in 60% of the cases. In 20%, the nerve is located laterally, and in 10%, posteriorly to the artery. In 10%, the nerve is placed independently to the artery [8] (Table 5).
\nAnesthetized nerves | \n\n
| \n
Anesthetized areas | \n\n
| \n
Anatomical references | \n\n
| \n
Patient/operator position | \n\n
| \n
Local anesthetic volume required | \n1.5 mL | \n
Needle required | \n\n
| \n
Needle direction | \n\n
| \n
Needle puncture depth | \n20–25 mm | \n
Inferior alveolar, buccal, and lingual nerve block techniques.
The mandibular canal travels through the thickness of the mandible; first, close to the medial surface and then maintained equidistant and, at the anterior end, approach the external osseous table. The mental canal has an upward, backward, and lateral outward direction at an angle of 45° to the mandibular bone plane. As a consequence of this, the mental foramen regularly rounded and with a diameter of 3–5 mm has an acute lower anteroinferior border, whereas the posterosuperior half is confused with the bone plane of the mandibular body. The mental foramen may usually be found on the vertical line drawn downward from the supraorbital notch and lies below the level of premolar teeth (see Figure 10).
\nImage showing the needle direction for a successful mental anesthesia (copyright of authors).
The mental foramen has many anatomical variations not only in its size and shape but also in its location and direction of the opening [9]. In a study by Kqiku et al. [12], the most common position of the mental foramen investigated—using anatomical dissection—was between the first and second mandibular premolars in 37.75% of the cases and 27.5% in line with the long axis of the second mandibular premolar.
\nThese anatomical dispositions require that the approach of the mental foramen for anesthetic purposes consider the direction of the needle from back to front and from top to bottom. In an anteroposterior sense, the location of the mental foramen is in front of the second premolar or between both premolars, at a height—in the young adult—equidistant between the basilar border and the alveolar ridge (Table 6).
\nAnesthetized nerves | \n\n
| \n
Anesthetized areas | \n\n
| \n
Anatomical references | \n\n
| \n
Patient/operator position | \n\n
| \n
Local anesthetic volume required | \n0.6 mL | \n
Needle required | \n\n
| \n
Needle direction | \n\n
| \n
Needle puncture depth | \n23–25 mm | \n
Mental nerve block technique.
Branches of the cervical plexus could provide an additional innervation of the mandibular region. The great auricular nerve arises from the cervical plexus and provides sensory innervation of the skin over the parotid gland, the mastoid process, and the outer ears. Consequently, a separate infiltration of the great auricular may be needed to achieve total analgesia of the mandibular region when conventional anesthesia fails [4].
\nStroke is a menace to the society. All over the world, it affects countless number of people, as much as 16 million people per year [1]. Out of this number, 5.7 million die, and the rest becomes disabled for a long period, even for life. It is the second most common cause of death worldwide, after ischaemic heart disease [2, 3, 4]. The impact of stroke is mostly felt in low and middle income countries. About 85% of all stroke deaths are registered in low and middle income countries, which also account for 87% of total losses due to stroke in terms disability-adjusted life years calculated worldwide per year [2]. As the burden of stroke has shifted to the developing world, currently two-thirds of stroke mortality cases occur in sub-Saharan Africa (SSA), [2, 3, 4]. This is sad because this is the same region that poverty, malnutrition and communicable diseases also exert their greatest toll [5]. The unfortunate thing is that while the proportion of stroke is decreasing in the developed world, it is rising alarmingly in the under-developed world [6]. The World Health has predicted that by the year 2030, majority (80%) of stroke cases would be in the low-income and middle-income countries. Africa, in particular, records some of the highest rates of stroke worldwide, with an annual stroke incidence rate up to 316 per 100,000, prevalence rate up to 1460 per 100,000 and three-year fatality rate up to 84% [7, 8, 9, 10]. In Africa, stroke accounts for 4–9% of deaths and between 6.5–41% of neurological admissions, as reported in hospital-based studies [11, 12]. This is not only alarming, it is frightening; and should concern all of us. Two-thirds of stroke cases worldwide occur in SSA [13]. It is, therefore, clear that sub-Saharan Africa has become the epicentre of stroke in the world, calling for strong sustained efforts to reduce the incidence of stroke in the region. This reality should provoke increased attention to stroke issues in the world, especially in the low- and middle-income countries, in order to reverse the trend. In doing this, we must firstly identify the real problems associated with stroke in the region. For post-stroke rehabilitation effort to be effective and set goals of preventing second stroke achieved, it is important to focus attention on the real factors that predispose to stoke in the region. All factors should be taken into account, including the role of herbal centres and cultural beliefs, which have long been neglected. Great effort should be focused in reducing stroke occurrence in sub-Saharan Africa, because of the cumulative positive effect it would have on stroke reduction the world over. Fortunately and surprisingly, stroke is the most preventable of all neurological diseases as many of its risk factors, such as hypertension, high cholesterol, diabetes, and smoking can be prevented either through healthy lifestyle choices or by medication [14, 15]. In sub-Saharan Africa, therefore, psychosocial pressures and cultural beliefs should be given due attention, especially in post-stroke rehabilitation programmes.
This section discusses majorly the demographic features of 149 stroke survivors who visited Bebe Herbal Centre located in Umunomo Ihitteafoukwu, Ahiazu Mbaise, Imo state, Nigeria, for treatment and their import on stroke issues in sub-Saharan Africa. In the study [16] (Tables 1–3), it was noted that 97.3% of survivors were married while 2.7% were single. What this means is that being married is a potential source of pressure, especially for the low-income group. It was also reported that 65.1% of those married had 5 to 8 children, further strengthening our position that in SSA, having large families is potentially a big source of psychosocial pressure, which could lead to hypertension and eventual stroke. The reason is because of the low income capacity of most of these families in the region. Inability to cater for one’s family poses serious psychosocial pressure; and the larger the family, the more the pressure on parents and guardians. Cooper et al. [17] noted in their work that high blood pressure is the foundation of epidaemic cardiovascular diseases in Africa. To prevent a stroke event, especially for survivors, there is need to reduce avoidable pressures from families, for example, by limiting the number of children one caters for. Government should also help by providing social welfare programmes, including subsidising health and education for her low-income citizens. These, if done, will take a lot of pressure off low-income large families. One’s occupation in sub-Saharan Africa could also be a source of psychosocial pressure. In our work, we noted that people most commonly affected by stroke were traders (38.9%) followed by farmers and civil servants, in that order, 22.8% and 21.5% respectively. Artisans were not much affected (14.1%) while the unemployed were barely affected (2.7%). Pearson’s chi-squared test (Table 3) shows evidence of strong association between education, and occupation and gender of stroke survivors. Education had strong significant association (X2 = 12.31; df = 3, p < .006). More men than women had primary education (27.5% vs. 25.5%), secondary education (16.8% vs. 9.4%) and tertiary education (12.8% vs. 3.4%). Occupation had significant strong association with gender of the stroke survivors (X2 = 23.65; df = 4; p < .001) with more men than women being unemployed (2.7% vs. 0.7%), being artisans (19.5% vs. 3.4%) and civil servants (17.4% vs. 3.4%) while women more than men were traders (15.4% vs. 12.1%) and farmers (14.1% vs. 7.4%). By the age bracket indicated, most people in these professions would have retired from active service and be faced with the burden of lower income generation for their numerous bourgeoning responsibilities, leading to increased psychosocial pressure and hypertension. We also noted that those with primary education only were highest among the stroke survivors [53.7%], followed by secondary education and tertiary. The higher the educational level, the higher the tendency for better income and also the likelihood of better awareness of stroke risk factors. These add up to better lifestyle and low stroke incidence for those with higher education. Individuals, particularly the first-stroke ones, should be aware of these factors that fuel stroke via psychosocial pressure and hypertension. Socioeconomic status has long been identified as a risk factor for hypertension [18]. In a meta-analysis, multiple indicators of socioeconomic status (i.e., income, occupation, and education) were associated with an increased risk of hypertension. It was suggested that working conditions induce stress that is associated with increased risk of hypertension [18]. We also noted in our work that very few stroke cases were below 40 years of age while the most were between 60 and 74 years, the age group when family pressures are highest in sub-Saharan Africa. High levels of anxiety and depressive symptoms are common in adults, often comorbid with chronic illnesses such as hypertension and can have deleterious effects on individual health and quality of life. A meta-analysis of prospective studies found that depressive symptoms predict a 42% increased risk of hypertension [19]. Similarly a meta-analysis of prospective studies fund that anxiety symptoms were independent risk factor for hypertension [20]. Stressors linked with unemployment, underemployment, job conflict, or financial strain due to low wages may lead to hypertension. An explanation for this was provided by Everson-Rose et al. [21] who noted that psychosocial factors, such as hostility and job strain, are associated with higher circulating levels of catecholamines, higher cortisol levels, and increased blood pressure over time. Psychosocial factors that induce emotional stress can evoke a physiological response mediated in part by activation of the sympathetic nervous system, inflammation, and the hypothalamic–pituitary–adrenal axis (Table 4) [22, 23].
Age (years) | Frequency n (%) | Total | |
---|---|---|---|
Gender | |||
Male | Female | ||
<40 | 3 (2.0) | 3 (2.0) | 6 (4.0) |
40–44 | 2 (1.3) | 0 (0.0) | 2 (1.3) |
45–49 | 3 (2.0) | 2 (1.3) | 5 (3.4) |
50–54 | 7 (4.7) | 12 (8.1) | 19 (12.8) |
55–59 | 10 (6.7) | 9 (6.0) | 19 (12.8) |
60–64 | 13 (8.7) | 8 (5.4) | 21 (14.1) |
65–69 | 7 (4.7) | 9 (6.0) | 16 (10.7) |
70–74 | 27 (8.1) | 9 (6.0) | 36 (24.2) |
75–79 | 10 (6.7) | 7 (4.7) | 17 (11.4) |
80+ | 6 (4.0) | 2 (1.3) | 8 (5.4) |
Left | 52 (34.9) | 32 (21.5) | 84 (56.4) |
Right | 36 (24.2) | 29 (19.5) | 65 (43.6) |
Illiterate | 0 (0) | 4 (2.7) | 4 (2.7) |
Primary | 42 (28.2) | 38 (25.5) | 80 (53.7) |
Secondary | 26 (17.4) | 14 (9.4) | 40 (26.8) |
Tertiary | 20 (13.4) | 5 (3.4) | 25 (16.8) |
Unemployed | 0 (0) | 1 (1.6) | 1 (1.6) |
Trading | 19 (12.8) | 23 (15.4) | 42 (28.2) |
Artisan | 30 (20.1) | 11 (7.4) | 41 (27.5) |
Farming | 12 (8.1) | 21 (14.1) | 33 (22.1) |
Civil servant | 27 (18.1) | 5 (3.4) | 32 (21.5) |
Distribution of parameters among male and female stroke survivors (n = 149).
Nwoha et al. [16].
Variable | <45 years | 45-64 years | ≥65 years | Total |
---|---|---|---|---|
Male | 5 (3.4) | 32 (21.5) | 58 (38.9) | 95 (63.8) |
Female | 4 (2.6) | 28 (18.8) | 22 (14.8) | 54 (36.2) |
Married | 6 (4.0) | 60 (40.3) | 79 (53.0) | 145 (97.3) |
Single | 3 (2.0) | 1 (0.7) | 0 (0) | 4 (2.7) |
1–4 | 5 (3.4) | 21 (14.1) | 12 (8.1) | 38 (2.5) |
5–8 | 0 (0) | 37 (24.8) | 60 (40.3) | 97 (65.1) |
>8 | 1 (0.7) | 4 (2.7) | 9 (6.0) | 14 (9.3) |
Illiterate | 0 (0) | 1 (0.7) | 3 (2.0) | 4 (2.7) |
Primary | 2 (1.3) | 28 (18.7) | 51 (34.0) | 81 (54.0) |
Secondary | 4 (2.7) | 19 (12.7) | 11 (7.3) | 34 (22.7) |
Tertiary | 3 (2.0) | 14 (9.3) | 13 (8.7) | 30 (20.0) |
Unemployed | 1 (0.7) | 2 (1.3) | 1 (0.7) | 4 (2.7) |
Civil servants | 2 (1.3) | 15 (10.1) | 15 (10.1) | 32 (21.5) |
Artisans | 1 (0.7) | 6 (4.0) | 14 (9.4) | 21 (14.1) |
Traders | 5 (3.3) | 31 (20.8) | 22 (14.7) | 58 (38.9) |
Farmers | 0 (0) | 10 (6.7) | 24 (16.1) | 34 (22.8) |
Nov.–April (Dry) | 6 (4.0) | 46 (30.9) | 52 (34.9) | 104 (69.8) |
May–October (Wet) | 3 (2.0) | 16 (10.7) | 26 (17.4) | 45 (30.2) |
Distribution of size of variables relative to age (year) of respondents (frequency, percentage).
Nwoha et al. [16].
Variables | Male | Female | X2 | Df | P |
---|---|---|---|---|---|
n (%) | n (%) | ||||
<45 | 6 (4.0) | 3 (2.0) | |||
45-49 | 3 (2.0) | 2 (1.3) | |||
50-54 | 6 (4.0) | 12 (8.1) | |||
55-59 | 9 (6.0) | 9 (6.0) | |||
60-64 | 14 (9.4) | 8 (5.4) | |||
65-69 | 7 (4.7) | 9 (6.0) | |||
70-74 | 27 (18.1) | 9 (6.0) | |||
75-79 | 10 (6.7) | 7 (4.7) | |||
≥80 | 6 (4.0) | 2 (1.3) | |||
Primary school | 41 (27.5) | 38 (25.5) | |||
Secondary schol | 25 (16.8) | 14 (9.4) | |||
Tertiary school | 19 (12.8) | 5 (3.4) | |||
No school | 3 (2.0) | 4 (2.7) | |||
Unemployed | 4 (2.7) | 1 (0.7) | |||
Trader | 18 (12.1) | 23 (15.4) | |||
Artisan | 29 (19.5) | 11 (7.4) | |||
Farmer | 11 (7.4) | 21 (14.1) | |||
Civil servant | 26 (17.4) | 5 (3.4) | |||
Left | 52 (34.9) | 32 (21.5) | |||
Right | 36 (24.2) | 29 (19.5) | |||
No child | 4 (2.7) | 3 (2.0) | |||
01-Apr | 19 (12.8) | 16 (10.7) | |||
05-Aug | 56 (37.6) | 35 (23.5) | |||
Above 8 | 9 (6.0) | 7 (4.7) |
Descriptive characteristic of the survivors and person’s chi-squared test between male and female.
Nwoha et al. [16].
Variables | Male (n, %) | Female (n, %) | χ2 | df | p |
---|---|---|---|---|---|
Aware before stroke | 44 (29.5) | 36 (24.2) | |||
Aware after stroke | 16 (10.7) | 13 (8.7) | |||
No knowledge | 12 (8.1) | 3 (2.0) | |||
Not hypertensive | 16 (10.7) | 9 (6.0) | |||
Yes, diabetic | 24 (16.1) | 16 (10.7) | |||
No knowledge | 17 (11.4) | 11 (7.4) | |||
Not diabetic | 47 (31.5) | 34 (22.8) | |||
Yes | 67 (45.0) | 21 (14.1) | |||
Never | 21 (14.1) | 40 (26.8) | |||
Yes | 37 (24.8) | 10 (6.7) | |||
Never | 51 (34.2) | 51 (34.2) |
Stroke risk factors suffered/encountered by survivors and Pearson’s chi-squared test of association with gender.
There are traditional risk factors for stroke, including hypertension, dyslipidemia, diabetes mellitus, obesity, smoking, stress (physical and emotional), sedentary lifestyle, heavy alcohol consumption, previous stroke and family history of stroke [2, 24]. Of these, hypertension is an important risk factor for a variety of health conditions, such as cardiovascular disease, stroke, and kidney failure. Hypertension is the leading risk factor for stroke and is present in nearly 1 in 3 American adults [25]. Hypertension is a pervasive problem in the United States, with approximately a third of Americans reporting being diagnosed with hypertension by their physicians or taking antihypertensive drugs [26]. It is considered the foundation for epidaemic cardiovascular diseases in African populations [17]. In Nigeria and sub-Saharan Africa, hypertension is the most important stroke risk factor [27, 28]. Growing evidence points to multiple psychological and social factors as contributors to the onset of trajectory of hypertension. It is time to understand that greater acculturation is associated with increased risk of hypertension, independent of age, gender, race/ethnicity, education, smoking, alcohol, physical activity, body mass index, and diabetes [29]. Wrong cultural beliefs do more harm than the direct risk factors.
We have greater need to educate people that hypertension is the foremost cause of stroke in sub-Saharan Africa and that psychosocial stress is the factor mostly fuelling hypertension. If we can curtail excessive and sustained psychosocial pressures and wrong cultural beliefs, we would be curtailing stroke incidence considerably. Diabetes mellitus is second causative factor for stroke in SSA but is usually accompanied by hypertension. Rarely does it alone cause stroke. Dyslipidemia (high blood cholesterol) is a third causative factor for stroke in most developed countries but rarely noted in SSA. The remaining seven traditional risk factors, namely obesity, smoking, stress (physical and mental), sedentary lifestyle, heavy alcohol consumption, previous stroke and family history of stroke are rarely recognised in sub-Saharan Africa when issues about stroke are discussed. This observation is supported by findings in our work (Table 5) [30] in which the commonest risk factor experienced by stroke survivors was hypertension (73.1%), followed by light alcohol consumption (59.1%), smoking (31.5%) and diabetes mellitus (26.7%). It is to be noted that 15 (10.1%) of survivors had no knowledge of their hypertensive status and 28 (18.8%) none of their diabetic status. No survivor ever did blood cholesterol test. When asked to state factors that could contribute to stroke, just 19.4% mentioned hypertension while insignificant number, 0.7%, each mentioned diabetes, family history, poor diet (excessive salt intake, low vegetables and fruits intake), overweight/obesity and 2.0% mentioned high alcohol consumption. Interestingly, a large number attributed stroke in this part of the world to psychosocial stress (worry) (13.5%), spiritual attack (13.4%) and usual illness (9.4%); factors that have no empirical evidence. Still a very disturbing number (39.6%) had no idea what could cause a stroke. The aforementioned observations paint a gloomy picture of continued growth in stroke epidemic in this part of the world. If stroke survivors could be so ignorant of the cause of their stroke, then the possibility that they would engage in life-changing behaviours that would prevent future stroke is very remote. This study has strongly pointed to lack of awareness and community screening as the most pronounced common variable among the survivors. There is therefore, the strong need for awareness campaign and community screening, especially among post-stroke cases.
Variables | Male | Female | X2 | Df | P |
---|---|---|---|---|---|
N, (%) | N, (%) | ||||
Hypertension | 20 (13.4) | 9 (6.0) | |||
Diabetes | 0 (0.0) | 1 (0.7) | |||
Alcohol | 3 (2.0) | 0 (0.0) | |||
Family history of stroke | 1 (0.7) | 0 (0.0) | |||
Psychosocial stress | 8 (5.4) | 12 (8.1) | |||
Spiritual attack | 13 (8.7) | 7 (4.7) | |||
Normal Sickness | 9 (6.0) | 5 (3.4) | |||
Poor diet | 0 (0.0) | 1 (0.7) | |||
Overweight | 0 (0.0) | 1 (0.7) | |||
Don’t know | 34 (22.8) | 25 (16.8) | |||
Check blood pressure | |||||
Pray to god | 3 (2.0) | 5 (3.4) | |||
Avoid stress/worry | 7 (4.7) | 6 (4.0) | |||
Alcohol | 10 (6.7) | 9 (6.0) | |||
Medical check-up | 1 (0.7) | 0 (0.0) | |||
Good behavior | 7 (4.7) | 3 (2.0) | |||
Avoid sugar | 9 (6.0) | 2 (1.3) | |||
Visit Bebe center | 0 (0.0) | 2 (1.3) | |||
Avoid diabolical people | 1 (0.7) | 0 (0.0) | |||
No advice to give | 0 (0.0) | 1 (0.7) | |||
30 (20.1) | 24 (16.1) |
Survivors idea of causes of stroke, their advice for prevention and Pearson’s correlation with gender.
Attention should be focused on psychosocial stress as major contributing factor to stroke in this part of the world. We noted that a lot of things that contribute to pressures on the individual, including economic stress which comprises uncertainties in payment of salaries and allowances of workers to unemployment of breadwinners of families, social stress related to taking care of immediate and extended families, occupational stress resulting from uncertainty of daily outcome of market, farming, and artisan jobs. All of these converge to cause high blood pressure. The more these psychological and social pressures mount, the more the tendency to high blood pressure and hypertension. These economic anomalies may not obtain in developed countries but they are commonplace in the underdeveloped ones. Prior reviews have also identified a number of psychosocial indicators as potential risk factors for the onset and progression of hypertension [31]. Besides ignorance of actual risk factors for stroke, it is also revealing to note that many individuals, even those who have suffered a stroke, do not know the signs of an impending stroke. In our unpublished work on identifying stroke signs among stroke survivors, very few could identify the 3 cardinal signs of impending stroke, FAST (F for facial palsy, A for arm palsy, S for speech palsy and T for time to call stroke ambulance). There should be emphasis on stroke warning signs, comprising sudden disarthria (speech impairment), haemiparesis, facial palsy, dizziness/vertigo, parasthaesia, acute headache, and visual impairment. People, particularly first-ever stroke cases, should learn to avoid extreme emotional reaction to sudden painful situations in order to avoid sudden spike in blood pressure, which could lead to instant stroke. In our work, some stroke survivors recounted how their stroke occurred immediately they received painful sad news of sudden loss of loved ones, property or goods. Stroke survivors should learn to take life easy and not overreact to avoid the risk of a second stroke. For a disease such as a stroke with high incidence, this study is severely underpowered to draw any meaningful conclusions. More work in this area is needed to augment the present observations.
For effective stroke prevention and post-stroke management in sub-Saharan Africa, due attention should be paid to the contribution of herbal centres in stroke management. This aspect of health delivery has been neglected for far too long. Yet traditional healing and herbal centres seem to matter a lot in stroke management in sub-Saharan Africa. Our work on satisfactory management of stroke by herbal homes, which is the first documented of such research, is quite informative [32]. In the study of 117 survivors who patronised Bebe Herbal Centre, we found that with the onset of stroke event, 72 (61.5%) went firstly to hospital before going to Bebe Centre, 25 (21.4%) went to other places, including prayer houses, before going to the Centre while 20 (17.1%) went firstly to the Centre. Regarding satisfactory recovery of the survivors, 116 (99.1%) said they had satisfactory recovery while attending Bebe Centre; and only one person (0.9%) said he had no recovery. Regarding time taken before the satisfactory recovery, 79 (67.5%) experienced it within 1 month of attending Bebe Centre while 73 (67.5%) had theirs after 1 month but under 6 months of attendance. All the seventy-two survivors (61.5%) that firstly went to hospital said they were not satisfied with treatment received in the hospitals while the remaining that did not go said hospital was not suitable for stroke management. None of the hospitals visited by the survivors was equipped with CT scan or MRI test machines. The consensus statement by the Helsingborg Conference demands computerised tomography for all patients with symptoms suggestive of stroke [33]. With CT scan and MRI test, ischaemic is differentiated from haemorrhagic stroke, and in case of ischaemic, recombinant tissue plasminogen activator (rt-PA) can be administered early enough to open up clogged arteries and allow reflow of blood to the injured cells, hence aiding quick recovery of the cells [34]. This benefit is only for patients who arrive stroke centres within 4.5 hours of stroke icthus. In our work, out of 72 (61.5%) survivors that visited hospital first at the onset of stroke, 93.3% reached hospital within 6 hours of onset but none within 4.5 hours. Nonetheless, in the absence of CT and MRI in the hospitals visited, the survivors would not have benefitted even if they had arrived within the 4.5 hours window because of absence of neurodiagnostic machines. The above findings suggest two things namely the need for the establishment of stroke centres and units with neurodiagnostic equipment and expert personnel and the need for victims to arrive early at specialised hospitals within 4.5 hours of event. Unfortunately, only very few centers in sub-Saharan Africa have CT scan and MRI testing machines unlike in developed countries [35].
While considering factors that discourage stroke patients from seeking early hospital intervention, it should also be remembered that cultural beliefs have also become unintended setback in seeking behaviour among stroke patients in Nigeria [36]. Every ethnic group has a culture and tradition that may impact on their perception and understanding of an ailment. Stroke has been interpreted as a sign of the “gods” or “spirits” being angry [36]. Public education on risk factors will help diffuse these perceptions and hopefully increase patients being brought in for early hospital intervention in Nigeria [37], and other developing countries like Ghana [38], India [39] and even China [40]. Stroke rehabilitation services in Nigeria and most sub-Saharan Africa are limited to physiotherapy, only available in limited number of hospitals. They are rarely available outside hospital settings and certainly not in herbal homes. So there is urgent need to extend physiotherapy and other rehabilitation services to outside hospital settings, particularly to herbal homes to quicken recovery of stroke patients. The management of Bebe Centre, in our interaction, said their treatment was based purely on leaves and roots of trees and plants. If that is so, then there is the need for stroke survivors to embrace high vegetables and fruits in their diet. It is important to note the findings of Opie and Seedat [41] about risk factors for stroke in sub-Saharan Africa. They noted the impact of 6 topmost modifiable factors associated with stoke in descending order of population attributable risk (95% CI) to be hypertension 88.7%, dyslipidemia 48.2%, diabetes mellitus 22.6%, low green vegetable consumption 18.2%, stress 14.5% (Table 6).
Variables | Male (n, %) | Female (n, %) | P |
---|---|---|---|
Activity at stroke onset | |||
Sleeping | 18 (15.4) | 18 (15.4) | |
Resting | 24 (20.5) | 22 (17.1) | |
Physical activity | 15 (12.8) | 20 (17.1) | |
1st place visited after onset | |||
Hospital | 35 (29.9) | 37 (31.6) | |
Bebe center | 07 (6.0) | 13 (11.1) | |
Others | 15 (12.8) | 10 (8.5) | |
Recovery time | |||
<1 month | 40 (34.2) | 39 (33.3) | |
1–3 months | 12 (10.3) | 12 (10.3) | |
4–6 months | 01 (0.9) | 05 (4.3) | |
>6 months | 04 (3.4) | 03 (2.6) | |
No recovery | 0 | 01 (0.9) | |
After 6 months | |||
Impression Bebe Hospital (Cultural) | |||
Very satisfied | 19 (16.2) | 13 (11.1) | |
Satisfied | 34 (29.1) | 39 (33.3) | |
Fairly satisfied | 04 (03.4) | 07 (6.0) | |
Not satisfied | 0 | 01 (0.9) | |
Impression at Conventional Allopathic Hospital | |||
Not satisfied | 51 (43.6) | 21 (17.9) | |
Not suitable | 15 (12.8) | 30 (25.7) | |
BP check before stroke | |||
Once/week | 11 (9.4) | 11 (9.4) | |
>Once/week | 06 (5.1) | 11 (9.4) | |
Occasional | 20 (17.1) | 37 (31.5) | |
None | 6 (5.4) | 15 (12.7) | |
Once/week | 18 (15.4) | 12 (10.3) | |
>once/week | 20 (17.1) | 36 (30.8) | |
Occasional | 09 (7.7) | 07 (6.0) | |
None | 10 (8.5) | 05 (4.3) |
Experience of stroke survivors with hospital and Bebe Centre, Pearson’s Chi-Square test of association with sex.
P < 0.05.
Okoro et al. [32].
In conclusions, for serious and successful post-stroke effective rehabilitation in sub-Saharan Africa, there should be dedicated and sustained awareness education of stroke risk factors and warning signs, especially targeted at stroke survivors because they are at high risk of a second stroke. The awareness education should dispel erroneous beliefs about stroke in this region, emphasising the ugly relationship between psychosocial stress and hypertension as the major fuel for stroke in sub-Saharan Africa. Government should contribute to lowering stroke incidence by establishing stroke units, equipped with CT scan, MRI imaging, experts and emergency response ambulances for stroke distress calls. High risk individuals should be taught to be aware of FAST as cardinal warning signs leading eventually to stroke. Herbal centres should be upgraded to continue to provide alternative management of stroke as most stroke survivors are comfortable with treatment received from them. This also calls for the need for stroke patients to favour vegetable and fruit diets because of high fibre content for lowering diabetes and blood pressure, and for their high anti-oxidant content for mopping up excess radicals. Community Physiotherapists should be deployed to herbal centres to teach and train survivors for better treatment outcome. Overall, people, including stroke survivors, should not overstress themselves physically and emotionally, curtailing family and occupational pressures, subjecting themselves to metabolic screening. Overall, this work, conducted in one setting, is severely underpowered to draw any meaningful conclusions. The unique contribution, however, is the observation of a relation with cultural belief in obtaining stroke care. More work is advocated among stroke survivors.
The strength of this baseline study is the observation of lack of awareness and community screening, especially among stroke survivors. A study of one herbal centre is severely underpowered to draw any generalised meaningful conclusions. There is need to extend study to more survivors, and more herbal centres. One limitation here was the difficulty in having research access to most Herbal centres. The second was that majority of the herbal centres lacked proper structural organisation to allow for meaningful research work. There was also our inability to obtain body-mass index of the survivors due to lack of cooperation in this regard. This baseline study of stroke in an herbal centre should instigate more work in this area, particularly in the sub-Saharan Africa, where patronage is on the increase.
The authors wish to acknowledge the cooperation and kind support of Mr. Bebe and all staff of Bebe Herbal Centre, Umunomo, Ihitteafoukwu, Ahiazu Mbaise, Nigeria in the course of this work. We also acknowledge the contributions of Sunday Osonwa and Nkechi Chukwu in doing excellent interview work.
The authors declare that there is no conflict of interest.
Funds for this study were contributed from the private budget of the authors. There was no outside funding support.
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This chapter examines many questions that need to be considered and the role of the key individual with oversight of the GME, the designated institutional official (DIO). Topics examined are the leadership theories, practices and strategies for the DIO, dealing with change when the DIO starts, using authority versus power, effective problem-solving and decision-making, adaptive leadership style, the historical function of the DIO, as well as the many tools available to the DIO including networking. The chapter concludes with several pearls of wisdom to positively help the DIO meet the many challenges of this very important role in GME.",book:{id:"8645",slug:"contemporary-topics-in-graduate-medical-education",title:"Contemporary Topics in Graduate Medical Education",fullTitle:"Contemporary Topics in Graduate Medical Education"},signatures:"Jay M. 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We encourage the submission of manuscripts that provide novel and mechanistic insights that report significant advances in the fields. Topics can include but are not limited to: Biotechnology such as biotechnological products and process engineering; Biotechnologically relevant enzymes and proteins; Bioenergy and biofuels; Applied genetics and molecular biotechnology; Genomics, transcriptomics, proteomics; Applied microbial and cell physiology; Environmental biotechnology; Methods and protocols. Moreover, topics in biosensor technology, like sensors that incorporate enzymes, antibodies, nucleic acids, whole cells, tissues and organelles, and other biological or biologically inspired components will be considered, and topics exploring transducers, including those based on electrochemical and optical piezoelectric, thermal, magnetic, and micromechanical elements. Chapters exploring biomaterial approaches such as polymer synthesis and characterization, drug and gene vector design, biocompatibility, immunology and toxicology, and self-assembly at the nanoscale, are welcome. Finally, the tissue engineering subcategory will support topics such as the fundamentals of stem cells and progenitor cells and their proliferation, differentiation, bioreactors for three-dimensional culture and studies of phenotypic changes, stem and progenitor cells, both short and long term, ex vivo and in vivo implantation both in preclinical models and also in clinical trials.",annualVolume:11405,isOpenForSubmission:!0,coverUrl:"https://cdn.intechopen.com/series_topics/covers/9.jpg",editor:{id:"126286",title:"Dr.",name:"Luis",middleName:"Jesús",surname:"Villarreal-Gómez",fullName:"Luis Villarreal-Gómez",profilePictureURL:"https://mts.intechopen.com/storage/users/126286/images/system/126286.jpg",institutionString:null,institution:{name:"Autonomous University of Baja California",institutionURL:null,country:{name:"Mexico"}}},editorTwo:null,editorThree:null,editorialBoard:[{id:"35539",title:"Dr.",name:"Cecilia",middleName:null,surname:"Cristea",fullName:"Cecilia Cristea",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYQ65QAG/Profile_Picture_1621007741527",institutionString:null,institution:{name:"Iuliu Hațieganu University of Medicine and Pharmacy",institutionURL:null,country:{name:"Romania"}}},{id:"40735",title:"Dr.",name:"Gil",middleName:"Alberto Batista",surname:"Gonçalves",fullName:"Gil Gonçalves",profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0030O00002aYRLGQA4/Profile_Picture_1628492612759",institutionString:null,institution:{name:"University of Aveiro",institutionURL:null,country:{name:"Portugal"}}},{id:"211725",title:"Associate Prof.",name:"Johann F.",middleName:null,surname:"Osma",fullName:"Johann F. 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