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\n
1. Introduction
\n
Over the years, medicines and the way we approach the patient have evolved from the basic clinical situations and the way we interpret signs and symptoms to imaging technologies that help us provide a faster and more reliable diagnosis. Nonetheless, along with endoscopy appearance in daily practice, patient’s survival rate and treatment have improved, and have gradually become the mainstream of current use by introducing screening programs as in colorectal cancer (CRC) [1]. Based on the perceived balance between the necessity and benefits of endoscopy, this technique has prompted its need to be kept in current practice and has become a benchmark for human organs or cavity exploration.
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The use of endoscopy within the gastrointestinal tract has been embedded as a welcome development for both diagnosis and therapeutic paths [2]. Continuous research of available technologies has led to a groundbreaking promising foundation to explore new options for patient’s condition [3].
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A large array of therapeutic alternatives has positioned endoscopy as the cornerstone for most of the diseases of the gastrointestinal tract and gradually has become a technique that may obviate surgery in some situations. From basic tissue harvesting to real-time confocal microscopic assessment [4] or from palliative therapeutic armamentarium to procedures more close tied to surgery procedures, gastrointestinal endoscopy has become more and more popular and along with its advantages or challenges has penetrated the gastroenterology community, becoming the touchstone for this medical specialty [5].
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Modern gastroenterology is based on the availability of endoscopy and its secondary features in assessing the gastrointestinal tract. Technological development is a continuous process in our day-to-day life and has been gradually inserted into endoscopy advances along with high-resolution endoscopes, devices, or accessories. The fact that some organs could have only been accessed by surgical procedures has promoted endoscopy to a level worthy of further appraisal. Among the different steps in endoscopy, the ones that surely changed the way we tend to diagnose or treat patients in daily practice are endoscopic retrograde cholangiopancreatography [6], capsule endoscopy [7], and endoscopic ultrasound [8, 9]. Thus, a new window was opened for both patients and physicians, and allowed the concept of evidence-based medicine to be used in daily practice.
\n
Perhaps the biggest efforts in endoscopy were to improve the diagnosis of gastrointestinal tumors [10]. With various methods which are certified for cancerous gastrointestinal lesions, endoscopy has also become a valuable asset for early-stage diagnosis [10] and is still exploring new therapeutic avenues. Endoscopy screening and treatment of pre-cancerous lesions is part of a growing trend and has been increasing exponentially in many specific lesions due to new technology embedment or transposing current surgical procedures. Thus, a shift has taken place and the use of endoscopic systems has allowed technology to become part of both the physician and patient’s life.
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\n
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2. Diagnostic novelties in gastrointestinal endoscopy
\n
\n
2.1. High-definition endoscopy imaging
\n
Substantial innovations in endoscopy imaging have occurred in the last 30 years, allowing physicians to perform a more personalized therapy for patients. With an increasingly technology-driven field, the current focus is to use high-definition (HD) techniques in a platform that will eliminate all disadvantages and will enhance the gastroenterologist’s ability to provide a better diagnosis or therapeutic management [11]. Endoscopy has taken an important leap from basic imaging to digital, high-definition white-light resolution which detects and highlights mucosal changes that were not perceived by the previous techniques.
\n
The use of HD endoscopes and monitors allows substantial image improvements by producing fewer artifacts on rapid movement and when combined with the corresponding processors may reach an image quality of over 2 million pixels [12]. HD magnification endoscopes have the ability of enlarging the image up to 150× with an adjustable focus and to discriminate between lesion’s characteristics from 10 to 71 microns in diameter [13, 14]. Topical application of agents such as acetic acid, methylene blue (chromoendoscopy), congo-red, or even hematoxylin has proven beneficial [15].
\n
Narrow band imaging (NBI) was introduced for early detection of lesions. By using a narrow band filter for blue and green, it illuminates tissue at wavelengths absorbed by hemoglobin, showing microvascular patterns (Figure 1A–E). This allows better characterization of lesions, which appear darker than the surrounding tissue [16, 17]. A different solution uses algorithms based on mathematical estimations of pixels. This technique has the advantage of generating a large number of wavelength permutations with adjustable settings [18, 19]. The I-scan technology uses three algorithms which may be applied simultaneously or one at a time: surface enhancement, tone enhancement, or contrast enhancement [20, 21].
\n
Figure 1.
(A) HD endoscopy of a large colonic polyp; (B) NBI view for better characterization of the vessels; (C) HD endoscopy with NBI and magnification for pattern assessment; (D) submucosal injection of methylene blue and epinephrine 1/10,000 for elevation and enhancement in order to perform polipectomy (E).
\n
\n
\n
2.2. Confocal laser endomicroscopy
\n
Confocal laser endomicroscopy (CLE) is a cutting edge technique based on real-time image reconstruction on a subcellular level, in any endoluminal cavity by using flexible endoscopy [22]. The ability to see the microarchitecture in vivo in a non-invasive setting has opened up new windows of opportunity for a faster diagnosis. Thus, providing images of the mucosal layer will not only ensure a rapid assessment of the lesions, but will also have a role in choosing the right therapeutic management [23].
\n
Based on a low-energy light source that enables acquisition of histology-like images, CLE usually requires the use of a dye for a better characterization of morphology or vascular pattern. The most used dye is fluorescein which has a safety profile, and has the ability of highlighting the vessels. However, the direction seems to be toward individualized situations whereas specific antibodies such as CD 31, CD105, and EGFR [24, 25] might be more useful for tissue architecture description. CLE is considered a valuable tool with great potential that may overcome some of the disadvantages of classic histology such as time waiting or sampling bias, thus facilitating live diagnosis and treatment decisions. Also, its use might also lead to a lower number of biopsies, provide a real-time differential diagnosis in pancreatic tumors or access to the biliary tree, or even reduce the number of noncancerous lesions removed through endoscopic procedures [26, 27].
\n
CLE is available either in an integrated conventional endoscope (Pentax, Tokyo, Japan) or on a probe-based system which is connected to a laser unit (Mauna Kea Technologies, Paris, France). Endoscope-based CLE (eCLE) systems (Figure 2A,B) are used for both upper and lower gastrointestinal tract examinations with depth scan images from 0 to 250 μm and scan rate of 1.6 frames/s. However, eCLE is no longer commercially available [28, 29, 30]. In contrast, probe-based CLE (pCLE) consists of different confocal miniprobes (Coloflex UHD, GastroFlex UHD, CholangioFlex) which provide images at different depths depending on its use, either for gastric, colonic, or biliary tract lesions. Moreover, a special probe was designed for an endoscopic ultrasound setting through a 19 gauge needle for a real-time assessment of pancreatic tumors. All miniprobes depending on their lesions’ objective may be used for a maximum of 10 or 20 investigations.
\n
Figure 2.
(A) CLE of normal colonic mucosa—the mucosal vessels as honeycomb appearance represented by a network of capillaries circumscribing the mucosal glands. Blood cells can be observed as dark shadows in the lumen; (B) pCLE image of an ex-vivo normal pancreas. Acriflavine staining which emphasize the acini distribution.
\n
Various applications have been tested for CLE from early gastric cancer [31], Barrett’s esophagus [32], colonic polyps to inflammatory bowel disease (IBD) [33], and biliary strictures [34]. Many clinical settings have confirmed this technique as an evolutionary step and in synergy with histology have led to several atlases for pattern and morphology recognition. Surveillance CLE imaging after polyp resection or IBD therapeutic mucosal assessment has confirmed its success [35]. The advantages of CLE have been recognized by the Federal Drug Administration and it is currently used in some clinical settings and settled by insurance policies [36]. Thus, the field of endomicroscopy, a rather challenging one due to long learning curve and high costs, is on a continuous expansion with multiple methods being tested.
\n
\n
\n
2.3. Capsule endoscopy
\n
Video capsule endoscopy (VCE) has revolutionized the way we explore bowel disease, and has become the reference method for small bowel imaging diagnosis. From its commercial release in 2001, VCE surfaced as the most challenging alternative for upper endoscopy or colonoscopy [37]. However, as it turned out, its full potential is directed toward the small bowel, which until then represented an area difficult to explore.
\n
Over the years, as technology evolved, the optical lenses and image resolution have laid grounds for new improved VCE, now reaching an image resolution of 512 × 512 pixels [38]. Moreover, the use of a dedicated analysis software may enhance the picture quality and provide more details that might suggest a more accurate diagnosis. This facilitated the new ways to analyze patterns and lesions, decreasing inter-observer variability [39].
\n
The main indications are obscure gastrointestinal bleedings, with current guidelines available on Crohn’s disease initial diagnosis, suspected celiac disease, and hereditary polyposis syndromes [40, 41, 42] (Figure 3A,B). There are also some dedicated capsules for the esophagus directed to Barrett’s esophagus, esophageal varices or gastroesophageal reflux disease, or the colon, successfully used for CRC screening or adenoma detection. Colon CE (CCE) has also proven its efficiency in unsuccessful colonoscopies, or when patients willingly refused to perform a colonoscopy [43].
\n
Figure 3.
(A) VCE imaging of a telangiectasia and (B) an intestinal polyp.
\n
The major setback in VCE is the lack of biopsies. This has welcomed the implementation of virtual chromoendoscopy, color enhancement, or flexible spectral imaging. Rigorous colon preparation is required, as movements, washing, or aspiration are not possible [44]. While movement is based on bowel peristalsis or segmentation, future directions focus on systems controlled by active locomotion. Several robotic forms of CE have been developed. External magnetic systems have also been studied, either with direct control by the physician or by using external platforms with a console or robotic arm in conjunction with MRI or CT [45, 46].
\n
The future of VCE is directed to remote-controlled tools for both diagnosis and therapy as in drug delivery systems. This will provide a non-invasive and easier management for the patient with potentially less side effects and stress than ordinary procedures.
Endoscopic retrograde cholangiopancreatography (ERCP) is the standard method for therapeutic management of biliary disease [47]. Progresses have been met from stone extraction to biliary stenting for both malignant or benign stenosis and even ablation of biliary tumors. On this latter platform, the next step was set to the development of the peroral retrograde cholangioscopy, a technique that can provide direct images of bile and pancreatic duct [48, 49, 50]. A single operator device employed through the working channel of the duodenoscope has provided images that changed the way some diseases are managed [51]. It is mostly used for the differential diagnosis of biliary strictures; cholangioscopy decreases perforation and bleeding rates [51, 52, 53, 54, 55]. Spyglass digital system technology has stepped into the next generation of devices by providing high-resolution images with a field view of 110 and by eliminating degradation over excessive use [56]. With a friendly-user interface, this technique might solve the so far inaccessible path of biliary irresolute diagnosis (Figure 4).
\n
Figure 4.
Spyglass endoscopy. Cholangioscopy image with biliary stenosis and dilatation of the biliary tract.
\n
\n
\n
3.2. Endoscopic ultrasound
\n
Endoscopic ultrasound (EUS) development has opened up new horizons for diagnosis and management, especially in pancreatobiliary disease [57]. While on a continuous evolution process, EUS has been introduced as a standard diagnosis technique which provides information of structures located near the gastrointestinal tract. The arrival of fine-needle aspiration (FNA) has paved the way for various new therapeutic options that may substitute several surgical procedures or provide new options for cancer therapies [58]. EUS-drainage of fluid collections represented the grounds for novel techniques which focus on joining two cavities [59]. Along with the additional growth of the industry of endoscopy supplies, EUS has enabled novel therapeutic alternatives. Lumen-apposing metal stents are highlighting a fine line between the gastroenterology and surgical community [60] (Figure 5A,B). EUS-guided gallbladder drainage [61], EUS-choledochoduodenostomy [62], EUS-pancreaticogastrostomy [63], and the most recent EUS-gastrojejunostomy [64] represent some of the challenges that were introduced with focus on minimally invasive therapy.
\n
Figure 5.
(A) EUS of the pancreas—inhomogeneous tumor with hyperechogenic foci localized at the level of the head of the pancreas; (B) balloon-assisted EUS-gastrojejunostomy in a pig with a hot metal lumen-apposing metal stent.
\n
Cancer-directed therapy has been the EUS objective with several alternatives so far. EUS-guided radiofrequency ablation has been successfully used in pancreatic tumors, along with alcohol injection. However, the most interesting technique seems to be injection of chemotherapeutic agents either directly within the tumor or within the venous system. This setting might provide a larger volume of drugs to the tumor and enhance their effect, while avoiding systemic reactions. Pain therapy has also been a matter of discussion especially in pancreatic cancer with the EUS-guided celiac plexus neurolysis and celiac plexus block after alcohol injection [65, 66, 67].
\n
\n
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3.3. Submucosal endoscopy
\n
Greater experience in flexible endoscopy and new devices development have gradually introduced the concept of therapeutic endoscopy from endoscopic mucosal resection (EMR) to endoscopic mucosal dissection (ESD) [68, 69]. Recently, the concept of endoscopic full thickness resection (EFTR) has gained attention trying to secure the possible complications [69]. Over-the-scope clips and new suturing endoscopic devices are instruments worthy of appraisal even though it gets us closer to natural orifice transluminal surgery (NOTES) [70]. Currently, peroral endoscopic myotomy (POEM) for the treatment of achalasia represents one of the most advanced NOTES technique performed in gastroenterology, which requires a high level of skill in performing submucosal tunneling, injection, and hemostasis. POEM has prevailed as a new reference method in achalasia treatment [71].
\n
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Conflict of interest
The authors have no conflicts of interest to declare.
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Introduction",level:"1"},{id:"sec_2",title:"2. Diagnostic novelties in gastrointestinal endoscopy",level:"1"},{id:"sec_2_2",title:"2.1. High-definition endoscopy imaging",level:"2"},{id:"sec_3_2",title:"2.2. Confocal laser endomicroscopy",level:"2"},{id:"sec_4_2",title:"2.3. Capsule endoscopy",level:"2"},{id:"sec_6",title:"3. Therapeutic endoscopy",level:"1"},{id:"sec_6_2",title:"3.1. Endoscopic retrograde cholangiopancreatography (ERCP)",level:"2"},{id:"sec_7_2",title:"3.2. Endoscopic ultrasound",level:"2"},{id:"sec_8_2",title:"3.3. Submucosal endoscopy",level:"2"},{id:"sec_13",title:"Conflict of interest",level:"1"}],chapterReferences:[{id:"B1",body:'Schreuders EH, Ruco A, Rabeneck L, et al. Colorectal cancer screening: A global overview of existing programmes. Gut. 2015;64(10):1637-1649\n'},{id:"B2",body:'Hirschowitz BI, Curtiss LE, Peters CW, et al. Demonstration of a newgastroscope, the fiberscope. Gastroenterology. 1958;35(1):50; discussion 51-3\n'},{id:"B3",body:'Sivak MV. Gastrointestinal endoscopy: Past and future. Gut. 2006;55(8):1061-1064\n'},{id:"B4",body:'Zehri AH, Ramey W, Georges JF, et al. Neurosurgical confocal endomicroscopy: A review of contrast agents, confocal systems, and future imaging modalities. Surgical Neurology International. 2014;5:60\n'},{id:"B5",body:'Akarsu M, Akarsu C. Evaluation of new technologies in gastrointestinal endoscopy. Journal of the Society of Laparoendoscopic Surgeons. 2018;22(1):e2017.00053\n'},{id:"B6",body:'Aabakken L. Endoscopic retrograde cholangiopancreatography. Gastrointestinal Endoscopy. 2012;76(3):516-520\n'},{id:"B7",body:'Koulaouzidis A, Rondonotti E, Karargyris A. Small-bowel capsule endoscopy: A ten-point contemporary review. World Journal of Gastroenterology. 2013;19(24):3726-3746\n'},{id:"B8",body:'Meng FS, Zhang ZH, Ji F. Therapeutic role of endoscopic ultrasound in pancreaticobiliary disease: A comprehensive review. World Journal of Gastroenterology. 2015;21(46):12996-13003\n'},{id:"B9",body:'Longcroft-Wheaton G, Bhandari P. A review of image-enhanced endoscopy in the evaluation of colonic polyps. Expert Review of Gastroenterology & Hepatology. 2014;8(3):267-281\n'},{id:"B10",body:'Hopper AD. Early endoscopy improves survival in gastric cancer. The Practitioner. 2014;258(1773):23-27, 2\n'},{id:"B11",body:'Subramanian V, Ragunath K. Advanced endoscopic imaging: A review of commercially available technologies. Clinical Gastroenterology and Hepatology. 2014;12(3):368-376\n'},{id:"B12",body:'Rodriguez-Diaz E, Bigio IJ, Singh SK. Integrated optical tools for minimally invasive diagnosis and treatment at gastrointestinal endoscopy. Robotics and Computer-Integrated Manufacturing. 2011;27(2):249-256\n'},{id:"B13",body:'Florescu DN, Ivan ET, Ciocâlteu AM, et al. Narrow band imaging endoscopy for detection of precancerous lesions of upper gastrointestinal tract. Romanian Journal of Morphology and Embryology. 2016;57(3):931-936\n'},{id:"B14",body:'Kahi CJ, Anderson JC, Waxman I, et al. High-definition chromocolonoscopy vs. high-definition white light colonoscopy for average-risk colorectal cancer screening. The American Journal of Gastroenterology. 2010;105:1301-1307\n'},{id:"B15",body:'Subramanian V, Ramappa V, Telakis E, et al. Comparison of high definition with standard white light endoscopy for detection of dysplastic lesions during surveillance colonoscopy in patients with colonic inflammatory bowel disease. Inflammatory Bowel Diseases. 2013;19:350-355\n'},{id:"B16",body:'Ignjatovic A, East JE, Subramanian V, et al. Narrow band imaging for detection of dysplasia in colitis: A randomized controlled trial. The American Journal of Gastroenterology. 2012;107:885-890\n'},{id:"B17",body:'Sharma P, Hawes RH, Bansal A, et al. 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Efficacy of i-scan imaging for the detection and diagnosis of early gastric carcinomas. Gastroenterology Research and Practice. 2014;2014:819395\n'},{id:"B22",body:'Streba CT, Gîltan AM, Gheonea IA, et al. Utility of confocal laser endomicroscopy in pulmonology and lung cancer. Romanian Journal of Morphology and Embryology. 2016;57(4):1221-1227\n'},{id:"B23",body:'Bhutani MS, Koduru P, Joshi V, et al. EUS-guided needle-based confocal laser endomicroscopy: A novel technique with emerging applications. Gastroenterology & Hepatology (NY). 2015;11(4):235-240\n'},{id:"B24",body:'Ciocâlteu A, Săftoiu A, Pirici D, et al. Tumor neoangiogenesis detection by confocal laserendomicroscopy and anti-CD105 antibody: Pilot study. World Journal of Gastrointestinal Oncology. 2015;7(11):361-368\n'},{id:"B25",body:'Karstensen JG, Klausen PH, Saftoiu A, Vilmann P. Molecular confocal laser endomicroscopy: A novel technique for in vivo cellular characterization of gastrointestinal lesions. World Journal of Gastroenterology. 2014;20(24):7794-7800\n'},{id:"B26",body:'Maione F, Giglio MC, Luglio G, et al. Confocal laser endomicroscopy in ulcerative colitis: Beyond endoscopic assessment of disease activity. Techniques in Coloproctology. 2017;21(7):531-540\n'},{id:"B27",body:'Wang TD. Confocal microscopy from the bench to the bedside. Gastrointestinal Endoscopy. 2005;62:696-697\n'},{id:"B28",body:'Goetz M, Hoffman A, Galle PR, et al. Confocal laser endoscopy: New approach to the early diagnosis of tumors of the esophagus and stomach. Future Oncology. 2006;2:469-476\n'},{id:"B29",body:'Kiesslich R, Burg J, Vieth M, et al. Confocal laser endoscopy for diagnosing intraepithelial neoplasias and colorectal cancer in vivo. Gastroenterology. 2004;127:706-713\n'},{id:"B30",body:'Hurlstone DP, Kiesslich R, Thomson M, et al. Confocal chromoscopic endomicroscopy is superior to chromoscopy alone for the detection and characterisation of intraepithelial neoplasia in chronic ulcerative colitis. Gut. 2008;57:196-204\n'},{id:"B31",body:'Robles-Medranda C, Vargas M, Ospina J, et al. Clinical impact of confocal laser endomicroscopy in the management of gastrointestinal lesions with an uncertain diagnosis. World Journal of Gastrointestinal Endoscopy. 2017;9(8):389-395\n'},{id:"B32",body:'Kollar M, Spicak J, Honsova E, et al. The role of confocal laser endomicroscopy in patients with early esophageal neoplasia. Minerva Chirurgica. 2018;73(4):417-427. DOI: 10.23736/S0026-4733.18.07795-7\n'},{id:"B33",body:'De Palma GD, Colavita I, Zambrano G, et al. Detection of colonic dysplasia in patients with ulcerative colitis using a targeted fluorescent peptide and confocal laserendomicroscopy: A pilot study. PLoS One. 2017;12(6):e0180509\n'},{id:"B34",body:'Karia K, Kahaleh M. A review of probe-based confocal laser endomicroscopy for pancreaticobiliary disease. Clinical Endoscopy. 2016;49(5):462-466\n'},{id:"B35",body:'Karstensen JG. Evaluation of confocal laser endomicroscopy for assessment and monitoring of therapeutic response in patients with inflammatory bowel disease. Danish Medical Journal. 2016;63(11):B5301\n'},{id:"B36",body:'Technology Committee ASGE. Confocal laser endomicroscopy. Gastrointestinal Endoscopy. 2014;80(6):928-938\n'},{id:"B37",body:'Vere CC, Foarfă C, Streba CT, et al. Videocapsule endoscopy and single balloon enteroscopy: Novel diagnostic techniques in small bowel pathology. Romanian Journal of Morphology and Embryology. 2009;50(3):467-474\n'},{id:"B38",body:'Song HJ, Shim KN. Current status and future perspectives of capsule endoscopy. Intestinal Research. 2016;14(1):21-29\n'},{id:"B39",body:'Constantinescu AF, Ionescu M, Iovănescu VF, et al. A computer-aided diagnostic system for intestinal polyps identified by wireless capsule endoscopy. Romanian Journal of Morphology and Embryology. 2016;57(3):979-984\n'},{id:"B40",body:'Sealock RJ, Thrift AP, El-Serag HB, Sellin J. Long-term follow up of patients with obscure gastrointestinal bleeding examined with video capsule endoscopy. Medicine (Baltimore). 2018;97(29):e11429\n'},{id:"B41",body:'Vere CC, Streba CT, Rogoveanu I, et al. The contribution of the video capsule endoscopy in establishing the indication of surgical treatment in the tumoral pathology of the small bowel. Current Health Sciences Journal. 2012;38(2):69-73\n'},{id:"B42",body:'Parker CE, Spada C, McAlindon M, Davison C, Panter S. Capsule endoscopy—Not just for the small bowel: A review. Expert Review of Gastroenterology & Hepatology. 2015;9(1):79-89\n'},{id:"B43",body:'Bouchard S, Ibrahim M, Van Gossum A. Video capsule endoscopy: Perspectives of a revolutionary technique. World Journal of Gastroenterology. 2014;20(46):17330-17344\n'},{id:"B44",body:'Nowak T. A global perspective on capsule endoscopy. Annals of Translational Medicine. 2017;5(21):422\n'},{id:"B45",body:'Neumann H, Fry LC, Nägel A, Neurath MF. Wireless capsule endoscopy of the small intestine: A reviewwith future directions. Current Opinion in Gastroenterology. 2014;30(5):463-471\n'},{id:"B46",body:'Eliakim R. Where do i see minimally invasive endoscopy in 2020: Clock is ticking. Annals of Translational Medicine. 2017;5(9):202\n'},{id:"B47",body:'Kozarek RA. Direct cholangioscopy and pancreatoscopy at the time of endoscopic retrograde cholangiopancreaticography. The American Journal of Gastroenterology. 1988;83:55-57\n'},{id:"B48",body:'Singh A, Gelrud A, Agarwal B. Biliary strictures: Diagnostic considerations and approach. Gastroenterology Report. 2015;3:22-31\n'},{id:"B49",body:'Yasuda I, Itoi T. Recent advances in endoscopic management of difficult bile duct stones. Digestive Endoscopy. 2013;25:376-385\n'},{id:"B50",body:'Urakami Y, Seifert E, Butke H. Peroral direct cholangioscopy using routine straight-view endoscope: First report. Endoscopy. 1977;9:27-30\n'},{id:"B51",body:'Chen YK, Pleskow DK. SpyGlass single-operator peroral cholangiopancreaticogastroscopy system for the diagnosis and therapy of bile-duct disorders: A clinical feasibility study. Gastrointestinal Endoscopy. 2007;65:832-841\n'},{id:"B52",body:'Navaneethan U, Njei B, Lourdusamy V, et al. Comparative effectiveness of biliary brush cytology and intraductal biopsy for detection of malignant biliary strictures: A systematic review and meta-analysis. Gastrointestinal Endoscopy. 2015;81:168-176\n'},{id:"B53",body:'Wakai T, Shirai Y, Sakata J, et al. Clinicopathological features of benign biliary strictures masquerading as biliary malignancy. The American Surgeon. 2012;78:1388-1391\n'},{id:"B54",body:'Laleman W, Verraes K, Van Steenbergen W, et al. Usefulness of the singleoperator cholangioscopy system SpyGlass in biliary disease: A single-center prospective cohort study and aggregated review. Surgical Endoscopy. 2017;31:2223-2232\n'},{id:"B55",body:'Franzini T, Moura RN, Bonifacio P, et al. Complex biliary stones management: Cholangioscopy versus papillary large balloon dilatation—A randomized controlled trial. Endoscopy International Open. 2018;6:E131-E138\n'},{id:"B56",body:'Seicean A, Tefas C, Ungureanu B, Săftoiu A. Endoscopic ultrasound guided radiofrequency ablation in pancreas. Hepato-Gastroenterology. 2014;61(134):1717-1721\n'},{id:"B57",body:'Jenssen C, Hocke M, Fusaroli P, et al. EFSUMB guidelines on interventional ultrasound (INVUS), part IV—EUS-guided interventions: General aspects and EUS-guided sampling (short version). Ultraschall in der Medizin. 2016;37(2):157-169\n'},{id:"B58",body:'Giovannini M. Endoscopic ultrasound-guided drainage of pancreatic fluid collections. Gastrointestinal Endoscopy Clinics of North America. 2018;28(2):157-169\n'},{id:"B59",body:'Ungureanu BS, Pătrașcu Ș, Drăgoescu A, et al. Comparative study of NOTES versus endoscopic ultrasound gastrojejunostomy in pigs: A prospective study. Surgical Innovation. 2018;25(1):16-21\n'},{id:"B60",body:'Kalva NR, Vanar V, Forcione D, Bechtold ML, Puli SR. Efficacy and safety of lumen apposing self-expandable metal stents for EUS guided cholecystostomy: A meta-analysis and systematic review. Canadian Journal of Gastroenterology and Hepatology. 2018;2018:7070961\n'},{id:"B61",body:'Sandru V, Ilie M, Plotogea O, et al. Endoscopic ultrasound-guided choledochoduodenostomy using a lumen apposing metal stent for acute cholangitis. The Turkish Journal of Gastroenterology. 2018;29:511-514\n'},{id:"B62",body:'James TW, Baron TH. Antegrade pancreatoscopy via EUS-guided choledochoduodenostomy using a lumen apposing metal stent for acute cholangitis. The Turkish Journal of Gastroenterology. 2018;29:511-514\n'},{id:"B63",body:'Ungureanu BS, Pătraşcu Ş, Şurlin V, Săftoiu A. Surgical endoscopy versus endoscopic surgery for obesity. American Journal of Therapeutics. 2017;24:e579-e587\n'},{id:"B64",body:'Ungureanu BS, Pirici D, Mărgăritescu C, et al. Endoscopic ultrasound-guided radiofrequency ablation of the pancreas: An experimental study with pathological correlation. Endoscopic Ultrasound. 2015;4(4):330-335. DOI: 10.4103/2303-9027.170426\n'},{id:"B65",body:'Ungureanu BS, Pirici D, Margaritescu C, Gheonea IA, Trincu FN, Fifere A, et al. Endoscopic ultrasound guided injection of iron oxide magnetic nanoparticles for liver and pancreas: A feasibility study in pigs. Medical Ultrasonography. 2016;18(2):157-162\n'},{id:"B66",body:'Faigel D, Lake D, Landreth T, Kelman C, Marler R. Endoscopic ultrasonography-guided portal injectionchemotherapy for hepatic metastases. Endoscopic Ultrasound. 2014;3(Suppl 1):S1\n'},{id:"B67",body:'Ono H. Early gastric cancer: Diagnosis, pathology, treatment techniques and treatment outcomes. European Journal of Gastroenterology & Hepatology. 2006;18:863-867\n'},{id:"B68",body:'Sakamoto T, Mori G, Yamada M, et al. Endoscopic submucosal dissection for colorectal neoplasms: A review. World Journal of Gastroenterology. 2014;20(43):16153-16158\n'},{id:"B69",body:'Mori H, Kobara H, Nishiyama N, Masaki T. Current status and future perspectives of endoscopic full-thickness resection. Digestive Endoscopy. 2018;30(Suppl 1):25-31\n'},{id:"B70",body:'Schmidt A, Meier B, Caca K. Endoscopic full-thickness resection: Current status. World Journal of Gastroenterology. 2015;21(31):9273-9285\n'},{id:"B71",body:'Inoue H, Santi EG, Onimaru M, Kudo SE. Submucosal endoscopy: From ESD to POEM and beyond. Gastrointestinal Endoscopy Clinics of North America. 2014;24(2):257-264\n'}],footnotes:[],contributors:[{corresp:null,contributorFullName:"Costin Teodor Streba",address:null,affiliation:'
University of Medicine and Pharmacy of Craiova, Craiova, Romania
University of Medicine and Pharmacy of Craiova, Craiova, Romania
'},{corresp:null,contributorFullName:"Cristin Constantin Vere",address:null,affiliation:'
University of Medicine and Pharmacy of Craiova, Craiova, Romania
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1. Introduction
Premium multifocal intraocular lenses (IOLs) became more and more popular in modern cataract surgery after new millennium year [1, 2]. In tandem, the advances in ophthalmologic surgical approach such as femtosecond laser assisted cataract surgery (FLACS) [3], the improvement in biometry and IOL power calculation [4], the development of the intraocular lens techniques [5] led to successfully correct presbyopia, astigmatism and other refractive error through cataract or lens exchange surgery. These premium IOLs surgeries especially the presbyopia-correcting procedures can offer patients more visual and life quality without spectacle. But there are many key issues in the presbyopia-correcting procedure including proper patient selection, preoperative counseling, surgical planning and techniques which should be focused during perioperative stage.
2. Premium IOLs
Comparing with conventional IOL, premium IOLs can offer more and better visual function. But there are no standard criteria about premium IOL due to the continual evolution of the IOLs’ technology. The aspherical IOL, blue light filter IOL, toric IOL had been defined as premium IOLs in the past decades. This chapter will highlight the presbyopia correcting IOLs as the premium IOLs in the following paragraph. The presbyopia correcting IOLs can be classified into three groups: accommodative IOLs, refractive or diffractive multifocal IOLs and extended depth of focus (EDOF) IOLs according to its optical design and physical properties.
2.1 Accommodating intraocular lenses
Accommodative IOL are designated to produce a dynamic power with the change of IOL optic position, shape or refractive index by pseudoaccommodating and/or accommodating mechanisms with contraction of the ciliary muscle [6]. There are several accommodative IOLs design strategies: single-optic, dual-optic and deformable optic IOLs (Figure 1). Single-optic accommodative IOL (Crystalens, Bausch & Lomb; 1CU, Human Optics) possess the hinge design between the optic and the haptic to facilitate the anterior axial movement of effective lenses position with pressure of the capsule bag and vitreous during the accommodative stimulus. Previous studies demonstrated that 1 mm of optic movement is equivalent of 2 D of power change [7]. But the clinical studies had not demonstrated the consistent accommodation amplitude of the pseudoaccomodating IOL eyes especially in the long term follow up. Dual-optic Synchrony IOL (Abbott Medical Optics, AMO) utilize a positively powered biconvex front lens (+32D) connected to a negatively powered concave-convex lens. During the accommodative effort, the distance between the two optic elements increased that lead to increasing effective power of the overall lens [8]. The deformable optic design IOLs like FluidVision accommodating IOL (PowerVision) still underwent investigation in lab or clinical trial research. Though there are no contrast sensitivity loss or dysphotopsias issue, all these accommodative IOLs still have their limitations about the inability to consistently generate large amounts of accommodative power.
There are two type multifocal IOLs according to optical design principle: refractive and diffractive IOLs (Figure 2).
Refractive multifocal IOLs based on the different dioptic power zone with the light ray’s refraction principles. These zones provide various focal points, allowing for an improvement in distance, intermediate, and near vision. Though refractive multifocal IOL can afford good quality vision, the limitation of these symmetric multifocal lens (Array, Abbott Medical Optics; ReZoom, Abbott Medical Optics) are pupillary size and lens centration dependence. The asymmetric segmental refractive IOLs (Lentis Mplus, Oculentis) has been intended to reduce this problem and available for patients with low acceptance for dysphotopsia [9].
Diffractive multifocal IOLs rely on concentric diffractive surfaces on the optic portion of the lens, this causes constructive and destructive interference of optic wavefronts to provide two or three focality which led to bifocal or trifocal IOLs. A different approach about diffractive ring pattern, diffractive ring width and step height by different manufactures introduces different add power and light distribution. Larger ring width provides less addition power and small ring width provides more addition power, while higher steps sends more light to distant focal point and lower step sends more lights to near focal point. The IOL (Restor, Alcon) with refractive-diffractive mix pattern and apodized steps which has concentric rings of decreasing height intends to influence light distribution between distant and near focal points on pupil size [10]. Multifocal IOLs are associated with higher rates of spectacle independence than monofocal IOLs, but are more frequently associated with dysphotopsias and decreased contrast sensitivity [2].
Extended depth of focus (EDOF) IOLs are a newer category of IOLs that aims to give an elongated focus of vision, that enhances depth of focus rather than introduces several foci. It can reduce photic phenomena, glare, and halos, which have been reported in traditional multifocal IOLs. Tecnis Symfony IOL (Abbott Medical Optics) was the first EDOF IOL approved in 2016 by the U.S. Food and Drug Administration (FDA) (Figure 3). Now, there are several EDOF IOLs had been released in the market which had combined with different techniques such as diffractive optical design, spherical aberration, chromatic aberration, pinhole effect [11]. American Academy of Ophthalmology has provided consensus statement for EDOF IOL. These should have an extended far focus area which reaches the intermediate distance, providing excellent intermediate vision. Depth of focus should be at least 0.5 D wider than monofocal IOL for distance visual acuity of 0.03 logMAR [12]. Nevertheless, in practice, EDOF lenses provide excellent intermediate vision, but inadequate quality of vision for near distance [13, 14] (Table 1).
Properties of popular premium intraocular lenses (IOLs) [10, 11].
3. Patients selection
Even the IOLs technique progress offers patients the possibility of spectacle independence, the selection of presbyopia correction candidates is the most important issue which can lead to a successful surgery [16]. The right patients are the cataract or presbyopia patients who seek an intraocular IOLs solution to spectacle independence. The surgeon should understand patient’s expectations about visual task. A detailed discussion should be held to explain the limitations of premium IOLs to patient, that can establish their realistic expectation [17].
The characteristics of lifestyle or work is also an important selection criterion for premium IOL procedure. Ophthalmologists choose the correct type multifocal IOLs depending on what they do or where they live. Different cultures expressed different visual requirement on lifestyle and work. There may be a lot of time-consuming on near work with the computer, tablet, mobile phone, and on near life with book reading in Asian people, while there are more of an outdoor life in western populations. Especially, Chinese text may be very small and intricate comparing to English character, and hence a full reading add is usually needed. Furthermore, Asian people are generally shorter figure and shorter arms which cause the shorter distance between the face and the book, the mobile phone and other materials. Low add multifocal IOLs or normal monovision strategies may not be able to cope with the demands of reading in Asian people. The near vision satisfaction will be gain better in western population than Asian people. When such near vision is a high priority, high add multifocal IOLs or full-range multifocal IOL is the better solution.
Age also plays an important role in patient selection. Several conditions become more prevalent with age, such as optic neuropathy, macular degeneration and ocular surface disease, that may compound the loss of contrast sensitivity seen in multifocal IOLs. The examination of ocular disease using OCT, visual field, visual electrophysiology will provide some information about the post-operative visual quality results. These age-related diseases will be discussion in below. Multifocal IOLs implantation in pediatric cataract case is the subject of much controversy [18]. Amblyopia is common in these patients especially in unilateral pediatric cataract patients, while multifocal IOLs will reduce the contrast sensitivity and exacerbate amblyopia. Another issue is the ongoing growing of the child resulting in the question of how to calculate the power of the implanted lens, because the target refractive status depend on the age of the patient and the visual demands. There are just a few publications on this subject, we also did not have any experiences of multifocal IOLs in children [19, 20, 21].
Patients’ current visual acuity and refractive error and should be considered. Hyperopes who have significant cataracts will gain the most from presbyopia correcting IOLs, with uncorrected vision improvement at all distances. Mild myopes who have transparent crystalline lens may be dissatisfied with the result, because they often rely on their near vision for specific tasks and may have something to lose postoperatively.
Before choosing the presbyopia correcting IOLs, the surgeon should spend a lot of time in counseling with patients to access the personality, occupation and lifestyle of patients. In some clinics, a questionnaire is also helpful for evaluating patient’s needs and ranking patient’s personality from “easygoing” to “perfectionist” (Figure 4). It is important to rule out those patients who have unreasonable expectations about perfect visual needs or who have anxiety, doubt, nervousness characteristics. Those patients are more likely to be dissatisfied with presbyopia correcting IOLs. A visual behavior monitor that patients can wear on their spectacles to track their visual behavior and environment, now provides a lifestyle match index to help ophthalmologist convert that data into useful clinical information to select the best IOL for a given patient [22].
Figure 4.
Preoperative questionnaire (courtesy of dr. Takashi).
Some patients who need the specific vision requirement in their daily work and life also should be excluded out of the candidate, such as airline pilots, truck drivers, taxi drivers and anyone whose job requires activity at night or low-light conditions. The patients who often mention halos and glare disturb their jobs also should be rule out of the candidates. The diffractive or refractive multifocal IOLs will increased the photic phenomena in dim environment, while the accommodation IOL or monovision based on the monofocal IOLs should be better choice.
4. Preoperative ocular evaluation
The detailed preoperative examination of clinical ophthalmologic conditions should be done to help patients achieve good results because a successful presbyopia correcting solution often based on a health eye. Choosing the right presbyopia correcting IOLs should be considered for biometry, keratometry, topography and pupil reactivity and other eye comorbidities.
4.1 Corneal astigmatism
It is important to correct astigmatism in the premium IOLs surgery. The post-operative astigmatism should be less than 0.75D in the eye which bifocal or trifocal IOL had been implanted. Over 1.5 diopter postoperative astigmatism is one of main reasons for patient’s dissatisfaction following surgery. The larger amounts of post-operative astigmatism will cause decreasing visual function of multifocal IOLs, increasing some optical phenomena [23].
The keratometry, autorefraction and corneal topography/tomography are the helpful preoperative diagnostic devices to evaluate patients with astigmatism to select the astigmatism correction option——limbal relaxing incisions (LRI) or toric presbyopia correcting IOLs. The corneal topography provides more detailed useful information on the regularity of the corneal astigmatism than conventional keratometry or optical biometry (IOLMaster, Lenstar). Tomography devices like Pentacam address the posterior corneal astigmatism or total corneal astigmatism which deliver to more accuracy correcting astigmatism in multifocal IOLs cases (Figure 5). Another important issue in management of corneal astigmatism is surgical induced astigmatism which results from flattening in the meridian of the incision and steepening 90° away. The surgeon should evaluate his surgical induced astigmatism (SIA) via standard astigmatic vector analysis or online calculator [24].
Figure 5.
Regular corneal astigmatism and total corneal astigmatism.
Small amounts of regular astigmatism can be corrected with manual LRI or femtosecond laser LRI, the later method achieved a higher correction and lower postoperative cylinder than manual LRI patients [25]. LRI correction is determined by Abbott Medical Optics’ LRI calculator (http://www.lricalculator.com).
The toric presbyopia correcting IOLs is more predictable treatment than LRI, providing good uncorrected vision at distance and either intermediate or near, depending on the built-in add [26, 27]. The toric IOL can be calculated with online program provided by the IOL manufacturer. Most of online calculators had taken into consideration anterior corneal astigmatism, posterior corneal astigmatism and SIA, and choosing IOL toricity by using the total corneal refractive power or in-built nomogram. Some new technologies had been developed to improve toric multifocal IOLs solution flow to achieve the better outcome, including intraoperative wavefront aberrometry (ORA system, Alcon), Image Guided System like Verion(Alcon), Callisto Eye (Carl Zeiss Meditec).
Corneal with irregular astigmatism is contraindicator for multifocal IOLs. Irregular astigmatism often caused by previous corneal infection disease, trauma, dystrophies, pterygium or severe dry eye. In these conditions, poor higher-order root-mean square (HO RMS) corneal wavefront error over a 6-mm zone will present in Pentacam or other aberrometry. If this value exceeds 0.50 μm, the patient will have a high risk of halos and glare with a multifocal IOL (Figure 6).
Figure 6.
Corneal irregular astigmatism with history of corneal refractive surgery. HO RMS is 0.679 um, over 0.50 um.
4.2 Keratoconus
Cataract surgery in keratoconic eyes is not uncommon issue which need to be addressed. Proper IOL selection must be individualized for each keratoconic patient to achieve an optimal outcome. Even for monofocal IOLs implantation, IOLs power calculation is a challenging issue due to the abnormalities of both anterior and posterior corneal surface [28]. Some studies have shown promising results about toric IOL in nonprogress keratoconic patients, while in progress cases the combined procedures including intracorneal ring segment (ICRS), cross linking and toric IOL is preferred [29, 30].
But multifocal IOLs should been avoided because the loss of contrast sensitivity associated with multifocal lenses will be magnified by the corneal irregularity. Previous corneal surgical history like pterygium, PKP is an important etiology for irregular astigmatism. IOL solution in these cases is similar to the keratoconus cases.
4.3 Previous corneal refractive surgery
Patients who have undergone myopic or hyperopic LASIK/PRK/RK tend to select the premium IOLs with higher expectations regarding the refractive outcome. But intraocular lens power calculation for these patients is challenging because it is difficult to calculate the true corneal power. The optical quality of corneal is another factor to consider for IOL selection. The high order aberration is increased after the laser myopic corneal which led to decrease the visual result of multifocal IOLs and increase the photophobia like halo, glare [31]. If cornea high order aberration is higher than 1 μm especially it caused by corneal irregularities, the presence of irregular astigmatism/coma, a decentered/uneven treatment bed, the patient should not be considered as good candidate for multifocal IOL implantation [5].
The post-myopic LASIK patients who had previous treatment was less then −6 D, ablation bed was fairly well centered with no or little irregular astigmatism and did not experience problems with night vision can be considered to use presbyopia correcting IOLs. [32] Some surgeon preferred EDOF IOls (Symfony, Johnson and Johnson Vision) in these patients, because its larger size central optic and higher light transmission provides an enhanced contrast sensitivity as compared with other refractive or diffractive multifocal IOls [33, 34]. If monovision was already created with LASIK or PRK, and monovision is probably a much better way to go.
In the patients who had underwent the hyperopia laser correctio have increased negative spherical aberration and are best suited for aberration-free multifocal IOLs or IOLs with positive spherical aberration. The accommodating IOL was recommend by some surgeon if multifocal IOLs and EDOF IOLs were intolerant by the significant corneal coma.
A monofocal IOL is often the best choice in patients with previous RK who often had irregular corneal or increased corneal aberration. Now, pinhole IOLs (Xtrafocus, Morcher GmbH) is an effective presbyopia correcting solution for irregular astigmatism RK patients. It can correct of postoperative residual refraction and provide an elongated depth of focus [35].
4.4 Ocular surface disease (OSD)
Understanding the patient’s ocular surface is of critical importance because ocular surface pathologic features can lead to false corneal power, induced astigmatism and unstable bad visual acuity.
Preoperative dry eye will lead to post-operative refractive surprise, blur vision and foreign body sensation, excessive tearing, and photophobia that makes patients unhappy [36]. Surgeon and assistor should address the OSD issue as part of preoperative discussion to management the patient expectation.
The most common OSD is meibomian gland dysfunction and dye eye. A thorough evaluation of the lids and lashes, testing for lacrimal gland function and tear film should be included in preoperative examination. A symptoms questionnaire also helps to capture OSD before surgery.
The treatment is based on severity and subtype of OSD. Steroid and preservative-free lubrication can be used for improving the corneal surface. Other therapy included moisture chamber glass, punctal occlusion, and oral omega fatty acid supplements. If the ocular surface condition is not improved after advanced therapies, the multifocal IOLs is not recommend due to significantly high and persistent postoperative OSD symptoms [37]. The low tear breakup time, increased meibomian gland dropout will increase the high order aberration leading to decrease the visual quality after the premium IOLs implantation [16].
Besides OSD, there are some corneal disease inducing irregular astigmatism will affect the premium IOLs section, such as addressing anterior basement membrane dystrophy (ABMD), epithelial basement membrane dystrophy, Salzmann nodular degeneration (SND). Appropriate management of these corneal abnormalities should be performed before cataract surgery in order to gain the reliable corneal keratometry and other ocular biometry parameter.
4.5 Pupil size, angle kappa and angle alpha
Pupil size, shape and centration also have a significant influence on presbyopic IOL surgery. In diffractive multifocal IOLs, the difference of diffractive step height determined the different light energy distribution in far, intermediate and near distance. Light energy distribution of the multifocal IOLs (MIOLs) varies with different aperture. For apodized diffractive IOLs, the near reading will become difficulty due to light energy goes more to distance in dim illumination. It suggested eyes implanted with multifocal IOLs should have a photopic pupil size of 3.5 mm or less and mesopic pupil size of 5 mm or less [38]. The average pupil size of photopic and mesopic are correlated with contrast sensitivity defocus curve [38]. The photophobia phenomenon like glare and halo also more complained in the large pupil patients. For the asymmetric refractive multifocal IOLs, the pupil size is an important parameter which had a significant negative subjective impact for outcomes [39].
Angle kappa (K) is defined as the angular difference between the visual axis and the pupillary axis while angle a refers to the angular distance between the visual axis and the optical axis. Though postoperative far, intermediate, and near vision is not affected by angle K which does not include the fixation point, large angle K might play a role in the decentration of multifocal intraocular lenses (IOLs), potentially resulting in the incident of glare and hola increasing which led to patient satisfaction with multifocal IOLs [40, 41, 42, 43]. A well-centered lens in the visual axis is vital for proper functioning of presbyopic IOLs. Chord between the pupil centration and visual axis is the value to be evaluated for IOL location. It was suggested that a MIOL is unacceptable for use if the k value is greater than half of the diameter of the central optical zone. The limitation of k value is different according to the different multifocal IOLs——ReSTOR(Alcon) 0.4 mm, Tecnis multifocal IOL (Abbott Medical Optics) 0.5 mm, FineVision POD F IOL(PhysIOL) 0.6 mm [44].
Angle alpha is defined by the radial distance between the center of the limbus and the visual axis, which was found to predict the tilt of the IOL in respect to the visual axis. Wang had demonstrated that angle alpha was relatively stable whereas angle kappa changes from pre- to postoperative situation [45]. Angle alpha seems to be a better predictor for photic phenomena and patient satisfaction with multifocal IOLs [46]. But there still was different aspects on the predictive capacity of angle α on the outcome with multifocal IOLs. Piracha had concluded the angle alpha distance is larger than 0.5 mm, the eye is not suitable for multifocal IOL implantation [47], while Fu found there was no statistically significant correlation between angle alpha and the objective visual quality parameters [41] (Figure 7).
Figure 7.
Pupil size, angle kappa and angle alpha.
4.6 Glaucoma
Glaucoma patients often presented with the visual field damage, contrast sensitivity loss, small pupils and capsular and zonular issues, to affect vision outcomes must be taken into account when choosing a premium IOL.
Previous generation multifocal IOLs (Restor, Alcon; ReZoom, Abbott Medical Optics) were reported to significantly reduce the contrast sensitivity, especially in refractive multifocal IOL implantation. New advanced technology multifocal IOL or EDOF IOLs seem to mitigate the loss of contrast sensitivity [48]. And multifocal IOL also affect the visual field test and oct scan in the glaucoma patients’ follow-up.
But because of a lack of scientific evidence in the form of large trials on the impact of multifocal IOLs in glaucoma, decisions regarding the implantation in a glaucoma patient should be tailored according to the patient’ s motivation and the rate of glaucoma progression. The patient who is glaucoma suspect, ocular hypertensive, early stage with controlled and stable visual field damage is the candidate for diffractive multifocal IOLs and EDOF IOLs. The patients with severe, advanced, progressive glaucoma, or with high risk of pupil or zonular changes like chronic miotics, pseudoexfoliation, pigment dispersion will not benefit of multifocality [49].
4.7 Retinal disease
It is a controversial topic of premium IOLs application in retinal disease patients because there are varying degrees of macular lesion, ranging from drusen without visual damage to the late stages of atrophic AMD. Multifocal IOLs are strictly not recommend in retinitis pigmentosa and Stargardt’s disease, while diabetic retinopathy, age-related macular degeneration, and epiretinal membranes are relative contraindications [50]. Beside the different character of retinal diseases, the progression is an important issue to consider for premium IOLs solution [17].
For the mild or stable disease, multifocal IOLs is option for patient with careful and thoroughly consent about the prognosis including the issue of lower contrast sensitivity and long-term results with the disease progressing. Many studies had demonstrated the contrast sensitivity decreased in multifocal IOLs. Due to loss of contrast sensitivity at lower spatial frequencies is also presented even in mild forms of AMD, the EDOF IOLs is preferred in these cases. Multifocal IOLs generally are disadvised for patients with severe AMD because pre-existing pathologic features are a contraindication.
The presence of an epiretinal membrane (ERM) can lead to more unpredictability with the spherical power of the IOL selection and its refractive outcome. Multifocal IOLs in ERM patients will face to the loss of contrast sensitivity, increased risk for postoperative cystoid macular edema [51].
There are few studies addressing the multifocal IOLs and retinal disease, which report a significant improvement in visual-related outcomes than the monofocal implantation. Nevertheless, more research is needed to address the aforementioned concerns and to optimize the use of MIOLs in eyes with retinal disease.
5. Ocular biometry and IOL power calculation
Accurate measurements are critical for determining the correct power of a premium IOL before it is implanted during cataract surgery. The emmetropia is key factor of a successful refractive lens exchange to gain spectacle independence. Attaining this goal requires eliminating astigmatism and achieving a precise postoperative plano refraction within ±0.25 D.
Ocular biometry involves anatomical measurements of the eye, including the axial length (AL), keratometry, anterior chamber depth (ACD), lens thickness (LT), horizonal white to white (HWTW) which are the parameters for IOL power calculation [52].
Even the ultrasound biometry is still used in some difficult cases such as brunescent cataract, white cataract and severe subcapsular cataract. A hyperopic surprise often appeared in high myopic patients by using ultrasound biometry, because A-scan measured the deepest part of the staphyloma while macula was on the edge of the staphyloma which led to false longer axial length.
With IOLMaster (Zeiss) introduced in 1999, optical biometry technique provide a directly measurement from the macula to the corneal vertex. It becomes golden standard as it is highly accurate, easy to perform, non-invasive and comfortable for the patient. The accuracy of optical biometry, and in particular the IOLMaster 500 (Zeiss) and Lenstar 900 (Haag-Streit), have been extensively confirmed across a wide range of scientific studies [53, 54]. New generational optical biometry IOLMaster 700 (Zeiss) has integrate swept source optical coherence tomography to measure axial length. It allows for penetration of dense cataracts, determination of lens thickness (not available on the prior generations of IOLmaster), and visualization of the foveal pit to both ensure alignment of the image and possibly detect pathology like epiretinal membrane or cystoid macular edema which is influenced the premium IOLs power calculation [55].
Besides the accuracy biometry, the IOL power calculation formula choice also is critical for premium IOLs surgery. Though the third and newer generation formula can get accuracy refractive result in normal axis length and keratometry eyes, attention must be paid to the long axial length eye as well as the abnormal corneal power cases [56]. New IOL power calculation formula like Barrett, Hill-RBF and Olsen will achieve more precision and accuracy in longer and short axial length eyes [57].
The IOL power calculation in post corneal refractive surgery eyes always is a challenge issue. Whether corneal radical keratotomy or PRK/LASIK always change the corneal shape of in different ways. Errors in evaluation of the correct corneal power and errors in estimating the effective lens position with the classical thin-lens formulas lead to underestimate the IOL power and hyperopic postoperative refractive surprise. Many adjustment methods had been developed to estimate the true corneal keratometric data such as Haigis-L formula, Shammas no-history formula [58]. The new device like schiempflug or swept source OCT which can directly measure the anterior/posterior/total corneal power to obtain more accuracy results [59]. Modern IOL formulas, such as the Barrett True-K and ascrs.org web-based IOL power calculator can provide greater refractive predictability [60].
Cataract surgeon must personalize his IOL constants for premium lenses. Although the design of the IOL is the primary factor in the constant, variations in surgical technique such as the placement of the IOL, the location and design of the incision, and differences in biometry and technicians also affect the personalized lens constant. Preoperative biometric data and post-operative refractive error of 20 to 40 cases should be collected in order to personalize lens constant [52]. This process is the only way to achieve superior results with these IOLs and accuracy to within ±0.25 D for 95 percent of patients. Personalizing the lens constant is critical to eliminating the systematic variations that make excellent results and happy patients the rule with multifocal lenses.
6. Advanced technology IOL selection strategy
When the patient and ocular conditions had been fully evaluated, the surgeon can match the right advanced technology IOL to the right patients that can ensure positive outcomes. Here we present a premium IOLs decision flowchart based on the detail recommendations mentioned above.
Patients selection:
A strong desire to be independent with spectacle for near, intermediate, far distance
A positive attitude and leading an active life, not a perfectionist
A job not to require activity at night or low-light condition
Ocular Feature Checklist
Preoperative visual acuity and refractive error
Hyperopic, high myopia and plano presbyopia are good candidates for presbyopia correcting IOL surgery.
Mild myopia with presbyopia patients are typically accustomed to removing their glasses at near, so it is important to set proper expectations
Thorough education and careful counsel are needed for mild myopic patients before presbyopia correcting IOLs surgery.
Corneal conditions
Dry eye or OSD evaluation and management
Corneal astigmatism or aberration measurement by using multi-device
Address the posterior surface corneal astigmatism
Consider surgical induced astigmatism
Pupil size and centration
photopic pupil size of 3.5 mm or less and mesopic pupil size of 5 mm or less
angle Kappa greater than half of the diameter of the central optical zone
Comorbidities
Post-corneal refractive surgery
Glaucoma
Retinal disease
Biometry measurement and IOL calculation
Optical biometry is recommended, which included partial poherence interferometry (PCI) IOLMaster 500, optical low coherence reflectometry Lenstar 900 and SWEPT source OCT IOLMaster 700
Emmetropia Verifying Optical (EVO), Kane, Næser 2, Olsen, the Panacea, Pearl DGS, Radial Basis Function (RBF), T2 and VRF formulas
Special attention to post-refractive surgery IOL calculation issue
IOLs solutions
Monofocal aspheric IOLs is most common IOLs in modern phacoemulsification surgery which can neutralize the residual corneal spherical aberration and improve contrast sensitivity especially in dim light condition. For the patients with previous corneal myopic or hyperopic correction procedure or with high concern about halo, glare and night vision, the choice of aspherical IOLs should be tailored basing on the high aberration. Monofocal aspheric IOLs can used for monovision that is a simple solution for presbyopia correcting. It provides monofocal quality of vision, and many patients have been satisfied with this option. However, some patients have reported reduced depth perception, a feeling of imbalance, and limited intermediate vision. There are some modified strategies as mini-monovision or micro monovision which the non-dominant eye targeted for − 0.75 to − 1.25 D (mini-monovision) or around −0.50D (micro-monovision) of myopia to increase visual function at near and intermediate distance [62]. But monovision design may cause some potential problems such as loss of depth perception [63, 64]. A soft contact lens trial is a good predictor for simulating monovision solution, but due to cataract patients often being with worse vision, it is not always indicative of actual visual performance after cataract surgery.
Accommodating IOL is designed for allowing the IOL to move anteriorly or posteriorly, depending on the accommodative forces of the eye. It has the better contrast sensitivity and low photophobia than multifocal IOLs. However, most patients cannot achieve sufficient accommodation for functional near vision and might require reading glasses.
Multifocal IOLs by using refractive or/and diffractive optics is most popular presbyopia correcting IOLs solution in recent years. These type IOLs provide the high patient satisfaction and a better chance of spectacle independence in the refractive lens exchange procedure. Near addition powers are different in different multifocal IOLs, which is often from 1.5D to 4.0D. The higher add can offer a better near vision, but easy led to adverse effects such as dysphotopsia and a reduction in contrast sensitivity. In some aged patients, it will cost several months to neuroadapt of the multifoci images in the retina. To decide which near add power is right for a given patient, the surgeon must evaluate subjective factors (occupations, hobbies, expectations, concernabout night vision) and objective factors (preoperative visual acuity and refraction error, height/arm length).
Extended depth of focus (EDOF) IOLs are a set of intraocular lenses that extend vision instead of offering discrete close, intermediate, or distance vision. These IOLs based on diffractive, pin-hole or aberration technique, while minimizing the quality of vision compromises and night vision symptoms that are associated with multifocal lenses. The EDOF IOLs are more tolerance higher levels of cylinder error, especially for higher amounts of astigmatism in the range of 0.75D to more than 1.0D. Due to EDOF IOLs delivers less spectacle independence than trifocal IOLs, mini-monovision is common strategy with EDOF IOLs implantation. It set the nondominant eye’s target at −0.75D, which relates to an extension of the depth of focus, giving the patient the ability to read at a distance of about 45- to-50 cm, thus optimizing their potential for spectacle independence [50]. EDOF IOLs also can be considered for patients who had history of corneal refractive surgery [34] (Figure 8).
Figure 8.
Flow chart for advanced technology IOL selection.
7. Surgical techniques
Success in cataract surgery with premium IOLs lies in performing every step precisely and predictably. The surgeon team should check the patient’s information, the surgical device and material availability.
Surgeons must pay attention to preexisting or surgically induced astigmatism, because it can have a huge impact on visual outcomes with a multifocal IOL. The magnitude of astigmatism and axis should be checked by more than two device such as topography, IOLMaster, Lenstar and so on. For less than 1.0D astigmatism, the incision at steep axis is the better approach. When preoperative astigmatism is up to1.5 diopter, the limbal relaxing incisions (LRIs) can be considerable [65]. At higher levels of astigmatism than 1.5D, the best solution is toric multifocal IOLs [66]. Whether LRI or toric IOLs, the corneal limbal mark should be made before surgery. Many manual method or device had been developed, and computerized automated axis marking system also can been chosen [67].
A 5.0–5.5 mm perfectly round and centered capsulorhexis is preferred for premium IOLs surgery. The right size capsulorhexis will completely cover the optic of IOLs, let the lens center over the visual axis to get the best visual results. The capsulorhexis size depends on the different IOLs design. The precise size will be customed when femtosecond laser is available, which led to less intraocular aberration postoperatively [68, 69] (Figure 9).
Figure 9.
Trifocal IOL (Panoptix, Alcon) implantation with 5.0 mm FLACS capsulotomy.
The Healon or other viscous ophthalmic viscoelastic device (OVD) can protect the endothelium cells during the procedure. It also can flat the anterior capsule to make capsulorhexis more controlled. The OVD should be removed completely when surgery finished to prevent intraocular pressure from increasing. If the toric multifocal IOLs used, the OVD should be totally removed behind lens to avoid the accident rotation after surgery [67].
8. Management of dissatisfied patients
Even with fully preoperative examination, careful patient’s selection and precisely uneventful surgery, there are always some unhappy patients with their postoperative outcomes.
The main complaints associated with presbyopia correctiong IOLs include blurred vision, photic phenomenon. Blurred vision may be present at near, intermediate, and far distances, or specific distance. It was attributed to refractive error or residual astigmatism, posterior capsule opacification, dry eye, or coexisting ocular disease. It was also caused by loss of contrast sensitivity.
The premium IOLs very affected by small residual ametropias. Surgeon must carefully calculate IOL power by using advanced biometry formulas, customize constant according to previous experience. Any astigmatism greater than 0.75 D in a blur vision patient should be treated. The most common intervention to management of residual refractive error is spectacles or contact lens. Bioptics refractive enhancement can be performed in spherical or cylinder error patients, while IOL exchange or piggyback solution also can be used in case of important defect or if the previous solutions are not possible [17].
Another common cause of blur vision after multifocal lens implantation is ocular surface disease. The symptos can be resolved by treating with lubricating artificial tears, punctal plugs, warm compress and vectored thermal pulsation treatments.
Patients with multifocal IOLs appear more sensitive to posterior capsule opacity than with monofocal IOLs. If posterior capsule opacification is suspected to be the cause of visual disturbance, and symptoms have been worsening since surgery, the surgeon should consider Nd:YAG laser capsulotomy. If there is any chance that a lens exchange may be done, YAG capsulotomy should be delayed, as an open posterior capsule makes the exchange more difficult.
Photic phenomena can consist of glare, halos, and dysphotopsias. It also caused by IOL decentration, dry eye, posterior capsule opacification, or multifocal IOL design. During the procedure, carefully management should be taken including capsule tension ring implantation, centration of the IOLs relative to the visual axis, polishing the anterior and posterior capsule. Most case of photic phenomena will be tolerance or disappear by the time. After the reason of dry eye and PCO had be excluded, the night-time dysphotopsia and decreasing of contrast sensitivity are due to intrinsic properties of multifocal IOL. The most effective aid in managing these problems is neuroadaptation which is highly dependent on the individual and often need time to adapt. If a patient is still bothered by these problems more than three months after surgery, or if their quality of life is significantly affected, an IOL exchange for a monofocal IOL is almost always an alternative [50].
Proper management of the unhappy premium IOL patient requires time, patience, and familiarity with different medical and surgical options and techniques. The most important things are extensive preoperative patient education and avoiding the inadequate patient. Careful patient selection and clear communication regarding realistic expectations are the keys to success with premium IOLs.
9. Summary
Premium multifocal IOLs are a popular option for cataract or presbyopia patients today. Patients can achieve high levels of success and satisfaction from these IOLs. However, adequate preoperative clinical evaluation including patient selection, optical and anatomical examination is crucial to reach a success case. Based on the preoperative diagnosis including the corneal astigmatism, biometry measurement, IOL power calculation, presbyopia correcting IOLs’ indications and contraindications should be assessment for IOL selection strategy. Surgical procedure should be technically optimized to achieve the best outcomes. Adequate management of both satisfied and unsatisfied patients will improve the benefit of current premium IOLs.
\n',keywords:"premium IOL surgery, patient selection",chapterPDFUrl:"https://cdn.intechopen.com/pdfs/75474.pdf",chapterXML:"https://mts.intechopen.com/source/xml/75474.xml",downloadPdfUrl:"/chapter/pdf-download/75474",previewPdfUrl:"/chapter/pdf-preview/75474",totalDownloads:464,totalViews:0,totalCrossrefCites:0,dateSubmitted:"October 20th 2020",dateReviewed:"January 25th 2021",datePrePublished:"March 5th 2021",datePublished:"July 7th 2021",dateFinished:"March 1st 2021",readingETA:"0",abstract:"Premium multifocal IOLs are a popular option for cataract or presbyopia patients today. Patients can achieve high levels of success and satisfaction after these advanced technology IOLs implantation. However, adequate preoperative clinical evaluation including patient selection, optical and anatomical examination is crucial to reach a success case. Based on the preoperative diagnosis including the corneal astigmatism, biometry measurement, IOL power calculation, presbyopia correcting IOLs’ indications and contraindications should be assessed for IOL selection strategy. Surgical procedure should be technically optimized to achieve the best outcomes. Adequate management of both satisfied and unsatisfied patients will improve the benefit of current premium IOLs.",reviewType:"peer-reviewed",bibtexUrl:"/chapter/bibtex/75474",risUrl:"/chapter/ris/75474",signatures:"Chen Xu",book:{id:"10534",type:"book",title:"Current Cataract Surgical Techniques",subtitle:null,fullTitle:"Current Cataract Surgical Techniques",slug:"current-cataract-surgical-techniques",publishedDate:"July 7th 2021",bookSignature:"Xiaogang Wang",coverURL:"https://cdn.intechopen.com/books/images_new/10534.jpg",licenceType:"CC BY 3.0",editedByType:"Edited by",isbn:"978-1-83968-675-7",printIsbn:"978-1-83968-674-0",pdfIsbn:"978-1-83968-676-4",isAvailableForWebshopOrdering:!0,editors:[{id:"243698",title:"Dr.",name:"Xiaogang",middleName:null,surname:"Wang",slug:"xiaogang-wang",fullName:"Xiaogang Wang"}],productType:{id:"1",title:"Edited Volume",chapterContentType:"chapter",authoredCaption:"Edited by"}},authors:[{id:"336633",title:"Dr.",name:"Chen",middleName:null,surname:"Xu",fullName:"Chen Xu",slug:"chen-xu",email:"2590588576@qq.com",position:null,profilePictureURL:"//cdnintech.com/web/frontend/www/assets/author.svg",institution:{name:"Central South University",institutionURL:null,country:{name:"China"}}}],sections:[{id:"sec_1",title:"1. Introduction",level:"1"},{id:"sec_2",title:"2. Premium IOLs",level:"1"},{id:"sec_2_2",title:"2.1 Accommodating intraocular lenses",level:"2"},{id:"sec_3_2",title:"2.2 Multifocal IOL",level:"2"},{id:"sec_4_2",title:"2.3 Extended depth of focus IOLs",level:"2"},{id:"sec_6",title:"3. Patients selection",level:"1"},{id:"sec_7",title:"4. Preoperative ocular evaluation",level:"1"},{id:"sec_7_2",title:"4.1 Corneal astigmatism",level:"2"},{id:"sec_8_2",title:"4.2 Keratoconus",level:"2"},{id:"sec_9_2",title:"4.3 Previous corneal refractive surgery",level:"2"},{id:"sec_10_2",title:"4.4 Ocular surface disease (OSD)",level:"2"},{id:"sec_11_2",title:"4.5 Pupil size, angle kappa and angle alpha",level:"2"},{id:"sec_12_2",title:"4.6 Glaucoma",level:"2"},{id:"sec_13_2",title:"4.7 Retinal disease",level:"2"},{id:"sec_15",title:"5. Ocular biometry and IOL power calculation",level:"1"},{id:"sec_16",title:"6. Advanced technology IOL selection strategy",level:"1"},{id:"sec_17",title:"7. 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Changes in angle kappa and angle alpha before and after cataract surgery. J Cataract Refract Surg. 2020;46(3):365-71'},{id:"B46",body:'Grzybowski A, Eppig T. Angle alpha as predictor for improving patient satisfaction with multifocal intraocular lenses? Graefes Arch Clin Exp Ophthalmol. 2021'},{id:"B47",body:'Piracha AR. Using angle alpha in premium IOL screening. Cataract and Refractive Surgery Today. 2016:24-5'},{id:"B48",body:'Dyrda A, Martinez-Palmer A, Martin-Moral D, Rey A, Morilla A, Castilla-Marti M, et al. Clinical Results of Diffractive, Refractive, Hybrid Multifocal, and Monofocal Intraocular Lenses. J Ophthalmol. 2018;2018:8285637'},{id:"B49",body:'Ichhpujani P, Bhartiya S, Sharma A. Premium IOLs in Glaucoma. J Curr Glaucoma Pract. 2013;7(2):54-7'},{id:"B50",body:'Alio JL, Plaza-Puche AB, Fernandez-Buenaga R, Pikkel J, Maldonado M. Multifocal intraocular lenses: An overview. Surv Ophthalmol. 2017;62(5):611-34'},{id:"B51",body:'Hardin JS, Gauldin DW, Soliman MK, Chu CJ, Yang YC, Sallam AB. Cataract Surgery Outcomes in Eyes With Primary Epiretinal Membrane. JAMA Ophthalmol. 2018;136(2):148-54'},{id:"B52",body:'Olsen T. Calculation of intraocular lens power: a review. Acta Ophthalmol Scand. 2007;85(5):472-85'},{id:"B53",body:'Chen YA, Hirnschall N, Findl O. Evaluation of 2 new optical biometry devices and comparison with the current gold standard biometer. J Cataract Refract Surg. 2011;37(3):513-7'},{id:"B54",body:'Jasvinder S, Khang TF, Sarinder KK, Loo VP, Subrayan V. Agreement analysis of LENSTAR with other techniques of biometry. Eye (Lond). 2011;25(6):717-24'},{id:"B55",body:'Kunert KS, Peter M, Blum M, Haigis W, Sekundo W, Schutze J, et al. Repeatability and agreement in optical biometry of a new swept-source optical coherence tomography-based biometer versus partial coherence interferometry and optical low-coherence reflectometry. 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Comparison of the accuracy of intraocular lens power calculation formulas for eyes after corneal refractive surgery. Ann Transl Med. 2020;8(14):871'},{id:"B61",body:'Savini G, Taroni L, Hoffer KJ. Recent developments in intraocular lens power calculation methods-update 2020. Ann Transl Med. 2020;8(22):1553'},{id:"B62",body:'Mahrous A, Ciralsky JB, Lai EC. Revisiting monovision for presbyopia. Curr Opin Ophthalmol. 2018;29(4):313-7'},{id:"B63",body:'Smith CE, Allison RS, Wilkinson F, Wilcox LM. Monovision: Consequences for depth perception from large disparities. Exp Eye Res. 2019;183:62-7'},{id:"B64",body:'Burge J, Rodriguez-Lopez V, Dorronsoro C. Monovision and the Misperception of Motion. Curr Biol. 2019;29(15):2586-92 e4'},{id:"B65",body:'Freitas GO, Boteon JE, Carvalho MJ, Pinto RM. Treatment of astigmatism during phacoemulsification. Arq Bras Oftalmol. 2014;77(1):40-6'},{id:"B66",body:'Gangwani V, Hirnschall N, Findl O, Maurino V. 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Our findings showed that (1) lesions of the central amygdala inhibited the HPA axis responses to a variety of stressful stimuli. (2) Depletion of norepinephrine or serotonin in the amygdala and hypothalamus and local injections of norepinephrine and serotonin receptor antagonists into the central amygdala inhibited the HPA axis responses to neural stress. Norepinephrine and serotonin agonists injected into the amygdala caused an increase in HPA axis activity. The activation of the amygdala facilitated the in vivo release of serotonin from the paraventricular nucleus following electrical stimulation of the brainstem raphe nuclei. (3) Electrical stimulation of the amygdala impaired the glucocorticoid negative feedback action following neural stressful stimuli probably via a decrease in hippocampal corticosteroid receptors.",book:{id:"5485",slug:"the-amygdala-where-emotions-shape-perception-learning-and-memories",title:"The Amygdala",fullTitle:"The Amygdala - Where Emotions Shape Perception, Learning and Memories"},signatures:"Joseph Weidenfeld and Haim Ovadia",authors:[{id:"190851",title:"Ph.D.",name:"Haim",middleName:null,surname:"Ovadia",slug:"haim-ovadia",fullName:"Haim Ovadia"},{id:"192823",title:"Prof.",name:"Joseph",middleName:null,surname:"Weidenfeld",slug:"joseph-weidenfeld",fullName:"Joseph Weidenfeld"}]},{id:"32393",doi:"10.5772/34852",title:"The Neurochemical Anatomy of Trigeminal Primary Afferent Neurons",slug:"the-neurochemical-anatomy-of-trigeminal-primary-afferent-neurons",totalDownloads:4719,totalCrossrefCites:0,totalDimensionsCites:9,abstract:null,book:{id:"1592",slug:"neuroscience-dealing-with-frontiers",title:"Neuroscience",fullTitle:"Neuroscience - Dealing With Frontiers"},signatures:"Nikolai E. 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In particular, many neuroimaging studies find that the amygdala fails to activate in response to negative stimuli in individuals with PTSD. Several technical and design issues may explain disparate results regarding amygdala reactivity in PTSD. However, biological and symptom-based factors emerge as possible mediators of amygdala function in PTSD, leading to the conclusion that symptoms of emotional disengagement and dissociation are associated with amygdala hyporeactivity, and symptoms of hypervigilance/hyperarousal and problems with fear conditioning and extinction are reflected by amygdala hyperactivity. Therefore, treatment of PTSD should take into account the nature of amygdala dysfunction in the individual to optimize treatment outcomes.",book:{id:"5485",slug:"the-amygdala-where-emotions-shape-perception-learning-and-memories",title:"The Amygdala",fullTitle:"The Amygdala - Where Emotions Shape Perception, Learning and Memories"},signatures:"Gina L. Forster, Raluca M. Simons and Lee A. Baugh",authors:[{id:"145620",title:"Dr.",name:"Gina",middleName:null,surname:"Forster",slug:"gina-forster",fullName:"Gina Forster"},{id:"195109",title:"Dr.",name:"Raluca",middleName:null,surname:"Simons",slug:"raluca-simons",fullName:"Raluca Simons"},{id:"195110",title:"Dr.",name:"Lee",middleName:null,surname:"Baugh",slug:"lee-baugh",fullName:"Lee Baugh"}]},{id:"55211",doi:"10.5772/intechopen.68618",title:"The Amygdala and Anxiety",slug:"the-amygdala-and-anxiety",totalDownloads:2992,totalCrossrefCites:4,totalDimensionsCites:8,abstract:"The amygdala has a central role in anxiety responses to stressful and arousing situations. Pharmacological and lesion studies of the basolateral, central, and medial subdivisions of the amygdala have shown that their activation induces anxiogenic effects, while their inactivation produces anxiolytic effects. Many neurotransmitters and stress mediators acting at these amygdalar nuclei can modulate the behavioral expression of anxiety. These mediators may be released from different brain regions in response to different types of stressors. The amygdala is in close relationship with several brain regions within the brain circuitry that orchestrates the expression of anxiety. Recent developments in optogenetics have begun to unveil details on how these areas interact.",book:{id:"5485",slug:"the-amygdala-where-emotions-shape-perception-learning-and-memories",title:"The Amygdala",fullTitle:"The Amygdala - Where Emotions Shape Perception, Learning and Memories"},signatures:"Sergio Linsambarth, Rodrigo Moraga-Amaro, Daisy Quintana-\nDonoso, Sebastian Rojas and Jimmy Stehberg",authors:[{id:"144923",title:"Dr.",name:"Jimmy",middleName:null,surname:"Stehberg",slug:"jimmy-stehberg",fullName:"Jimmy Stehberg"},{id:"194182",title:"Ph.D. Student",name:"Rodrigo",middleName:null,surname:"Moraga-Amaro",slug:"rodrigo-moraga-amaro",fullName:"Rodrigo Moraga-Amaro"},{id:"194183",title:"M.Sc.",name:"Sergio",middleName:null,surname:"Linsambarth",slug:"sergio-linsambarth",fullName:"Sergio Linsambarth"}]}],mostDownloadedChaptersLast30Days:[{id:"54675",title:"The Key Role of the Amygdala in Stress",slug:"the-key-role-of-the-amygdala-in-stress",totalDownloads:2940,totalCrossrefCites:3,totalDimensionsCites:4,abstract:"Several data highlighted that stress exposure is strongly associated with several psychiatric disorders. The amygdala, an area of the brain that contributes to emotional processing, has a pivotal role in psychiatric disorders and it has been demonstrated to be highly responsive to stressful events. Here we will review evidences indicating how the amygdala changes its functionality following exposure to stress and how this contributes to the onset of anxiety disorders.",book:{id:"5485",slug:"the-amygdala-where-emotions-shape-perception-learning-and-memories",title:"The Amygdala",fullTitle:"The Amygdala - Where Emotions Shape Perception, Learning and Memories"},signatures:"Diego Andolina and Antonella Borreca",authors:[{id:"190318",title:"Dr.",name:"Diego",middleName:null,surname:"Andolina",slug:"diego-andolina",fullName:"Diego Andolina"},{id:"192832",title:"Dr.",name:"Antonella",middleName:null,surname:"Borreca",slug:"antonella-borreca",fullName:"Antonella Borreca"}]},{id:"55211",title:"The Amygdala and Anxiety",slug:"the-amygdala-and-anxiety",totalDownloads:2985,totalCrossrefCites:4,totalDimensionsCites:8,abstract:"The amygdala has a central role in anxiety responses to stressful and arousing situations. Pharmacological and lesion studies of the basolateral, central, and medial subdivisions of the amygdala have shown that their activation induces anxiogenic effects, while their inactivation produces anxiolytic effects. Many neurotransmitters and stress mediators acting at these amygdalar nuclei can modulate the behavioral expression of anxiety. These mediators may be released from different brain regions in response to different types of stressors. The amygdala is in close relationship with several brain regions within the brain circuitry that orchestrates the expression of anxiety. Recent developments in optogenetics have begun to unveil details on how these areas interact.",book:{id:"5485",slug:"the-amygdala-where-emotions-shape-perception-learning-and-memories",title:"The Amygdala",fullTitle:"The Amygdala - Where Emotions Shape Perception, Learning and Memories"},signatures:"Sergio Linsambarth, Rodrigo Moraga-Amaro, Daisy Quintana-\nDonoso, Sebastian Rojas and Jimmy Stehberg",authors:[{id:"144923",title:"Dr.",name:"Jimmy",middleName:null,surname:"Stehberg",slug:"jimmy-stehberg",fullName:"Jimmy Stehberg"},{id:"194182",title:"Ph.D. Student",name:"Rodrigo",middleName:null,surname:"Moraga-Amaro",slug:"rodrigo-moraga-amaro",fullName:"Rodrigo Moraga-Amaro"},{id:"194183",title:"M.Sc.",name:"Sergio",middleName:null,surname:"Linsambarth",slug:"sergio-linsambarth",fullName:"Sergio Linsambarth"}]},{id:"32387",title:"The Mystery of P2X7 Ionotropic Receptor: From a Small Conductance Channel to a Large Conductance Channel",slug:"the-mystery-of-p2x7-receptor-from-a-small-channel-to-a-big-pore",totalDownloads:2420,totalCrossrefCites:0,totalDimensionsCites:0,abstract:null,book:{id:"1592",slug:"neuroscience-dealing-with-frontiers",title:"Neuroscience",fullTitle:"Neuroscience - Dealing With Frontiers"},signatures:"R.X. 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Castro",authors:[{id:"107041",title:"Dr.",name:"Maite A",middleName:null,surname:"Castro",slug:"maite-a-castro",fullName:"Maite A Castro"},{id:"109692",title:"Mr.",name:"Felipe A",middleName:null,surname:"Beltran",slug:"felipe-a-beltran",fullName:"Felipe A Beltran"},{id:"109695",title:"Mr.",name:"Aníbal",middleName:"I.",surname:"Acuña",slug:"anibal-acuna",fullName:"Aníbal Acuña"},{id:"109696",title:"Ms.",name:"Maria Paz",middleName:null,surname:"Miro",slug:"maria-paz-miro",fullName:"Maria Paz Miro"}]},{id:"54509",title:"The Contribution of the Amygdala to Reward-Related Learning and Extinction",slug:"the-contribution-of-the-amygdala-to-reward-related-learning-and-extinction",totalDownloads:1742,totalCrossrefCites:3,totalDimensionsCites:3,abstract:"There has been substantial research into the role of the amygdala in fear conditioning and extinction of conditioned fear. The role of the amygdala in appetitive conditioning is relatively less explored. Here, we will review research into the role of the amygdala in reward‐related learning. Research to date suggests that the basolateral and central amygdala are responsible for learning about distinct aspects of a reinforcing event. For example, the basolateral amygdala is essential for distinguishing and choosing between specific rewards based on the specific‐sensory properties of those rewards as well as updating the relative value of specific rewarding events. In contrast, the central amygdala is involved in encoding reinforcement more generally and for regulating motivational influences on responding. 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\r\n\tTransforming our World: the 2030 Agenda for Sustainable Development endorsed by United Nations and 193 Member States, came into effect on Jan 1, 2016, to guide decision making and actions to the year 2030 and beyond. Central to this Agenda are 17 Goals, 169 associated targets and over 230 indicators that are reviewed annually. The vision envisaged in the implementation of the SDGs is centered on the five Ps: People, Planet, Prosperity, Peace and Partnership. This call for renewed focused efforts ensure we have a safe and healthy planet for current and future generations.
\r\n
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\r\n
\r\n\tThis Series focuses on covering research and applied research involving the five Ps through the following topics:
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\r\n
\r\n\t1. Sustainable Economy and Fair Society that relates to SDG 1 on No Poverty, SDG 2 on Zero Hunger, SDG 8 on Decent Work and Economic Growth, SDG 10 on Reduced Inequalities, SDG 12 on Responsible Consumption and Production, and SDG 17 Partnership for the Goals
\r\n
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\r\n\t2. Health and Wellbeing focusing on SDG 3 on Good Health and Wellbeing and SDG 6 on Clean Water and Sanitation
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\r\n\t
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\r\n\t3. Inclusivity and Social Equality involving SDG 4 on Quality Education, SDG 5 on Gender Equality, and SDG 16 on Peace, Justice and Strong Institutions
\r\n
\r\n\t
\r\n
\r\n\t4. Climate Change and Environmental Sustainability comprising SDG 13 on Climate Action, SDG 14 on Life Below Water, and SDG 15 on Life on Land
\r\n
\r\n\t
\r\n
\r\n\t5. Urban Planning and Environmental Management embracing SDG 7 on Affordable Clean Energy, SDG 9 on Industry, Innovation and Infrastructure, and SDG 11 on Sustainable Cities and Communities.
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\r\n\tThe series also seeks to support the use of cross cutting SDGs, as many of the goals listed above, targets and indicators are all interconnected to impact our lives and the decisions we make on a daily basis, making them impossible to tie to a single topic.
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She is now a lecturer at the University of Witwatersrand, South Africa, and a principal researcher at the Health Economics and Epidemiology Research Office (HE2RO), South Africa. Dr. Moolla holds a Ph.D. in Psychology with her research being focused on mental health and resilience. In her professional work capacity, her research has further expanded into the fields of early childhood development, mental health, the HIV and TB care cascades, as well as COVID. She is also a UNESCO-trained International Bioethics Facilitator.",institutionString:"University of the Witwatersrand",institution:{name:"University of the Witwatersrand",country:{name:"South Africa"}}},{id:"419588",title:"Ph.D.",name:"Sergio",middleName:"Alexandre",surname:"Gehrke",slug:"sergio-gehrke",fullName:"Sergio Gehrke",position:null,profilePictureURL:"https://s3.us-east-1.amazonaws.com/intech-files/0033Y000038WgMKQA0/Profile_Picture_2022-06-02T11:44:20.jpg",biography:"Dr. Sergio Alexandre Gehrke is a doctorate holder in two fields. The first is a Ph.D. in Cellular and Molecular Biology from the Pontificia Catholic University, Porto Alegre, Brazil, in 2010 and the other is an International Ph.D. in Bioengineering from the Universidad Miguel Hernandez, Elche/Alicante, Spain, obtained in 2020. In 2018, he completed a postdoctoral fellowship in Materials Engineering in the NUCLEMAT of the Pontificia Catholic University, Porto Alegre, Brazil. He is currently the Director of the Postgraduate Program in Implantology of the Bioface/UCAM/PgO (Montevideo, Uruguay), Director of the Cathedra of Biotechnology of the Catholic University of Murcia (Murcia, Spain), an Extraordinary Full Professor of the Catholic University of Murcia (Murcia, Spain) as well as the Director of the private center of research Biotecnos – Technology and Science (Montevideo, Uruguay). Applied biomaterials, cellular and molecular biology, and dental implants are among his research interests. He has published several original papers in renowned journals. In addition, he is also a Collaborating Professor in several Postgraduate programs at different universities all over the world.",institutionString:null,institution:{name:"Universidad Católica San Antonio de Murcia",country:{name:"Spain"}}},{id:"342152",title:"Dr.",name:"Santo",middleName:null,surname:"Grace Umesh",slug:"santo-grace-umesh",fullName:"Santo Grace Umesh",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/342152/images/16311_n.jpg",biography:null,institutionString:null,institution:{name:"SRM Dental College",country:{name:"India"}}},{id:"333647",title:"Dr.",name:"Shreya",middleName:null,surname:"Kishore",slug:"shreya-kishore",fullName:"Shreya Kishore",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/333647/images/14701_n.jpg",biography:"Dr. Shreya Kishore completed her Bachelor in Dental Surgery in Chettinad Dental College and Research Institute, Chennai, and her Master of Dental Surgery (Orthodontics) in Saveetha Dental College, Chennai. She is also Invisalign certified. She’s working as a Senior Lecturer in the Department of Orthodontics, SRM Dental College since November 2019. She is actively involved in teaching orthodontics to the undergraduates and the postgraduates. Her clinical research topics include new orthodontic brackets, fixed appliances and TADs. She’s published 4 articles in well renowned indexed journals and has a published patency of her own. Her private practice is currently limited to orthodontics and works as a consultant in various clinics.",institutionString:null,institution:{name:"SRM Dental College",country:{name:"India"}}},{id:"323731",title:"Prof.",name:"Deepak M.",middleName:"Macchindra",surname:"Vikhe",slug:"deepak-m.-vikhe",fullName:"Deepak M. Vikhe",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/323731/images/13613_n.jpg",biography:"Dr Deepak M.Vikhe .\n\n\t\n\tDr Deepak M.Vikhe , completed his Masters & PhD in Prosthodontics from Rural Dental College, Loni securing third rank in the Pravara Institute of Medical Sciences Deemed University. He was awarded Dr.G.C.DAS Memorial Award for Research on Implants at 39th IPS conference Dubai (U A E).He has two patents under his name. He has received Dr.Saraswati medal award for best research for implant study in 2017.He has received Fully funded scholarship to Spain ,university of Santiago de Compostela. He has completed fellowship in Implantlogy from Noble Biocare. \nHe has attended various conferences and CDE programmes and has national publications to his credit. His field of interest is in Implant supported prosthesis. Presently he is working as a associate professor in the Dept of Prosthodontics, Rural Dental College, Loni and maintains a successful private practice specialising in Implantology at Rahata.\n\nEmail: drdeepak_mvikhe@yahoo.com..................",institutionString:null,institution:{name:"Pravara Institute of Medical Sciences",country:{name:"India"}}},{id:"204110",title:"Dr.",name:"Ahmed A.",middleName:null,surname:"Madfa",slug:"ahmed-a.-madfa",fullName:"Ahmed A. Madfa",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/204110/images/system/204110.jpg",biography:"Dr. Madfa is currently Associate Professor of Endodontics at Thamar University and a visiting lecturer at Sana'a University and University of Sciences and Technology. He has more than 6 years of experience in teaching. His research interests include root canal morphology, functionally graded concept, dental biomaterials, epidemiology and dental education, biomimetic restoration, finite element analysis and endodontic regeneration. Dr. Madfa has numerous international publications, full articles, two patents, a book and a book chapter. Furthermore, he won 14 international scientific awards. Furthermore, he is involved in many academic activities ranging from editorial board member, reviewer for many international journals and postgraduate students' supervisor. Besides, I deliver many courses and training workshops at various scientific events. Dr. Madfa also regularly attends international conferences and holds administrative positions (Deputy Dean of the Faculty for Students’ & Academic Affairs and Deputy Head of Research Unit).",institutionString:"Thamar University",institution:null},{id:"210472",title:"Dr.",name:"Nermin",middleName:"Mohammed Ahmed",surname:"Yussif",slug:"nermin-yussif",fullName:"Nermin Yussif",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/210472/images/system/210472.jpg",biography:"Dr. Nermin Mohammed Ahmed Yussif is working at the Faculty of dentistry, University for October university for modern sciences and arts (MSA). Her areas of expertise include: periodontology, dental laserology, oral implantology, periodontal plastic surgeries, oral mesotherapy, nutrition, dental pharmacology. She is an editor and reviewer in numerous international journals.",institutionString:"MSA University",institution:null},{id:"204606",title:"Dr.",name:"Serdar",middleName:null,surname:"Gözler",slug:"serdar-gozler",fullName:"Serdar Gözler",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/204606/images/system/204606.jpeg",biography:"Dr. Serdar Gözler has completed his undergraduate studies at the Marmara University Faculty of Dentistry in 1978, followed by an assistantship in the Prosthesis Department of Dicle University Faculty of Dentistry. Starting his PhD work on non-resilient overdentures with Assoc. Prof. Hüsnü Yavuzyılmaz, he continued his studies with Prof. Dr. Gürbüz Öztürk of Istanbul University Faculty of Dentistry Department of Prosthodontics, this time on Gnatology. He attended training programs on occlusion, neurology, neurophysiology, EMG, radiology and biostatistics. In 1982, he presented his PhD thesis \\Gerber and Lauritzen Occlusion Analysis Techniques: Diagnosis Values,\\ at Istanbul University School of Dentistry, Department of Prosthodontics. As he was also working with Prof. Senih Çalıkkocaoğlu on The Physiology of Chewing at the same time, Gözler has written a chapter in Çalıkkocaoğlu\\'s book \\Complete Prostheses\\ entitled \\The Place of Neuromuscular Mechanism in Prosthetic Dentistry.\\ The book was published five times since by the Istanbul University Publications. Having presented in various conferences about occlusion analysis until 1998, Dr. Gözler has also decided to use the T-Scan II occlusion analysis method. Having been personally trained by Dr. Robert Kerstein on this method, Dr. Gözler has been lecturing on the T-Scan Occlusion Analysis Method in conferences both in Turkey and abroad. Dr. Gözler has various articles and presentations on Digital Occlusion Analysis methods. He is now Head of the TMD Clinic at Prosthodontic Department of Faculty of Dentistry , Istanbul Aydın University , Turkey.",institutionString:"Istanbul Aydin University",institution:{name:"Istanbul Aydın University",country:{name:"Turkey"}}},{id:"240870",title:"Ph.D.",name:"Alaa Eddin Omar",middleName:null,surname:"Al Ostwani",slug:"alaa-eddin-omar-al-ostwani",fullName:"Alaa Eddin Omar Al Ostwani",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/240870/images/system/240870.jpeg",biography:"Dr. Al Ostwani Alaa Eddin Omar received his Master in dentistry from Damascus University in 2010, and his Ph.D. in Pediatric Dentistry from Damascus University in 2014. Dr. Al Ostwani is an assistant professor and faculty member at IUST University since 2014. \nDuring his academic experience, he has received several awards including the scientific research award from the Union of Arab Universities, the Syrian gold medal and the international gold medal for invention and creativity. Dr. Al Ostwani is a Member of the International Association of Dental Traumatology and the Syrian Society for Research and Preventive Dentistry since 2017. He is also a Member of the Reviewer Board of International Journal of Dental Medicine (IJDM), and the Indian Journal of Conservative and Endodontics since 2016.",institutionString:"International University for Science and Technology.",institution:{name:"Islamic University of Science and Technology",country:{name:"India"}}},{id:"42847",title:"Dr.",name:"Belma",middleName:null,surname:"Işik Aslan",slug:"belma-isik-aslan",fullName:"Belma Işik Aslan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/42847/images/system/42847.jpg",biography:"Dr. Belma IşIk Aslan was born in 1976 in Ankara-TURKEY. After graduating from TED Ankara College in 1994, she attended to Gazi University, Faculty of Dentistry in Ankara. She completed her PhD in orthodontic education at Gazi University between 1999-2005. Dr. Işık Aslan stayed at the Providence Hospital Craniofacial Institude and Reconstructive Surgery in Michigan, USA for three months as an observer. She worked as a specialist doctor at Gazi University, Dentistry Faculty, Department of Orthodontics between 2005-2014. She was appointed as associate professor in January, 2014 and as professor in 2021. Dr. Işık Aslan still works as an instructor at the same faculty. She has published a total of 35 articles, 10 book chapters, 39 conference proceedings both internationally and nationally. Also she was the academic editor of the international book 'Current Advances in Orthodontics'. She is a member of the Turkish Orthodontic Society and Turkish Cleft Lip and Palate Society. She is married and has 2 children. Her knowledge of English is at an advanced level.",institutionString:"Gazi University Dentistry Faculty Department of Orthodontics",institution:null},{id:"178412",title:"Associate Prof.",name:"Guhan",middleName:null,surname:"Dergin",slug:"guhan-dergin",fullName:"Guhan Dergin",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/178412/images/6954_n.jpg",biography:"Assoc. Prof. Dr. Gühan Dergin was born in 1973 in Izmit. He graduated from Marmara University Faculty of Dentistry in 1999. He completed his specialty of OMFS surgery in Marmara University Faculty of Dentistry and obtained his PhD degree in 2006. In 2005, he was invited as a visiting doctor in the Oral and Maxillofacial Surgery Department of the University of North Carolina, USA, where he went on a scholarship. Dr. Dergin still continues his academic career as an associate professor in Marmara University Faculty of Dentistry. He has many articles in international and national scientific journals and chapters in books.",institutionString:null,institution:{name:"Marmara University",country:{name:"Turkey"}}},{id:"178414",title:"Prof.",name:"Yusuf",middleName:null,surname:"Emes",slug:"yusuf-emes",fullName:"Yusuf Emes",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/178414/images/6953_n.jpg",biography:"Born in Istanbul in 1974, Dr. Emes graduated from Istanbul University Faculty of Dentistry in 1997 and completed his PhD degree in Istanbul University faculty of Dentistry Department of Oral and Maxillofacial Surgery in 2005. He has papers published in international and national scientific journals, including research articles on implantology, oroantral fistulas, odontogenic cysts, and temporomandibular disorders. Dr. Emes is currently working as a full-time academic staff in Istanbul University faculty of Dentistry Department of Oral and Maxillofacial Surgery.",institutionString:null,institution:{name:"Istanbul University",country:{name:"Turkey"}}},{id:"192229",title:"Ph.D.",name:"Ana Luiza",middleName:null,surname:"De Carvalho Felippini",slug:"ana-luiza-de-carvalho-felippini",fullName:"Ana Luiza De Carvalho Felippini",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/192229/images/system/192229.jpg",biography:null,institutionString:"University of São Paulo",institution:{name:"University of Sao Paulo",country:{name:"Brazil"}}},{id:"256851",title:"Prof.",name:"Ayşe",middleName:null,surname:"Gülşen",slug:"ayse-gulsen",fullName:"Ayşe Gülşen",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/256851/images/9696_n.jpg",biography:"Dr. Ayşe Gülşen graduated in 1990 from Faculty of Dentistry, University of Ankara and did a postgraduate program at University of Gazi. \nShe worked as an observer and research assistant in Craniofacial Surgery Departments in New York, Providence Hospital in Michigan and Chang Gung Memorial Hospital in Taiwan. \nShe works as Craniofacial Orthodontist in Department of Aesthetic, Plastic and Reconstructive Surgery, Faculty of Medicine, University of Gazi, Ankara Turkey since 2004.",institutionString:"Univeristy of Gazi",institution:null},{id:"255366",title:"Prof.",name:"Tosun",middleName:null,surname:"Tosun",slug:"tosun-tosun",fullName:"Tosun Tosun",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/255366/images/7347_n.jpg",biography:"Graduated at the Faculty of Dentistry, University of Istanbul, Turkey in 1989;\nVisitor Assistant at the University of Padua, Italy and Branemark Osseointegration Center of Treviso, Italy between 1993-94;\nPhD thesis on oral implantology in University of Istanbul and was awarded the academic title “Dr.med.dent.”, 1997;\nHe was awarded the academic title “Doç.Dr.” (Associated Professor) in 2003;\nProficiency in Botulinum Toxin Applications, Reading-UK in 2009;\nMastership, RWTH Certificate in Laser Therapy in Dentistry, AALZ-Aachen University, Germany 2009-11;\nMaster of Science (MSc) in Laser Dentistry, University of Genoa, Italy 2013-14.\n\nDr.Tosun worked as Research Assistant in the Department of Oral Implantology, Faculty of Dentistry, University of Istanbul between 1990-2002. \nHe worked part-time as Consultant surgeon in Harvard Medical International Hospitals and John Hopkins Medicine, Istanbul between years 2007-09.\u2028He was contract Professor in the Department of Surgical and Diagnostic Sciences (DI.S.C.), Medical School, University of Genova, Italy between years 2011-16. \nSince 2015 he is visiting Professor at Medical School, University of Plovdiv, Bulgaria. \nCurrently he is Associated Prof.Dr. at the Dental School, Oral Surgery Dept., Istanbul Aydin University and since 2003 he works in his own private clinic in Istanbul, Turkey.\u2028\nDr.Tosun is reviewer in journal ‘Laser in Medical Sciences’, reviewer in journal ‘Folia Medica\\', a Fellow of the International Team for Implantology, Clinical Lecturer of DGZI German Association of Oral Implantology, Expert Lecturer of Laser&Health Academy, Country Representative of World Federation for Laser Dentistry, member of European Federation of Periodontology, member of Academy of Laser Dentistry. Dr.Tosun presents papers in international and national congresses and has scientific publications in international and national journals. He speaks english, spanish, italian and french.",institutionString:null,institution:{name:"Istanbul Aydın University",country:{name:"Turkey"}}},{id:"171887",title:"Prof.",name:"Zühre",middleName:null,surname:"Akarslan",slug:"zuhre-akarslan",fullName:"Zühre Akarslan",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/171887/images/system/171887.jpg",biography:"Zühre Akarslan was born in 1977 in Cyprus. She graduated from Gazi University Faculty of Dentistry, Ankara, Turkey in 2000. \r\nLater she received her Ph.D. degree from the Oral Diagnosis and Radiology Department; which was recently renamed as Oral and Dentomaxillofacial Radiology, from the same university. \r\nShe is working as a full-time Associate Professor and is a lecturer and an academic researcher. \r\nHer expertise areas are dental caries, cancer, dental fear and anxiety, gag reflex in dentistry, oral medicine, and dentomaxillofacial radiology.",institutionString:"Gazi University",institution:{name:"Gazi University",country:{name:"Turkey"}}},{id:"256417",title:"Associate Prof.",name:"Sanaz",middleName:null,surname:"Sadry",slug:"sanaz-sadry",fullName:"Sanaz Sadry",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/256417/images/8106_n.jpg",biography:null,institutionString:null,institution:null},{id:"272237",title:"Dr.",name:"Pinar",middleName:"Kiymet",surname:"Karataban",slug:"pinar-karataban",fullName:"Pinar Karataban",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/272237/images/8911_n.png",biography:"Assist.Prof.Dr.Pınar Kıymet Karataban, DDS PhD \n\nDr.Pınar Kıymet Karataban was born in Istanbul in 1975. After her graduation from Marmara University Faculty of Dentistry in 1998 she started her PhD in Paediatric Dentistry focused on children with special needs; mainly children with Cerebral Palsy. She finished her pHD thesis entitled \\'Investigation of occlusion via cast analysis and evaluation of dental caries prevalance, periodontal status and muscle dysfunctions in children with cerebral palsy” in 2008. She got her Assist. Proffessor degree in Istanbul Aydın University Paediatric Dentistry Department in 2015-2018. ın 2019 she started her new career in Bahcesehir University, Istanbul as Head of Department of Pediatric Dentistry. In 2020 she was accepted to BAU International University, Batumi as Professor of Pediatric Dentistry. She’s a lecturer in the same university meanwhile working part-time in private practice in Ege Dental Studio (https://www.egedisklinigi.com/) a multidisciplinary dental clinic in Istanbul. Her main interests are paleodontology, ancient and contemporary dentistry, oral microbiology, cerebral palsy and special care dentistry. She has national and international publications, scientific reports and is a member of IAPO (International Association for Paleodontology), IADH (International Association of Disability and Oral Health) and EAPD (European Association of Pediatric Dentistry).",institutionString:null,institution:null},{id:"202198",title:"Dr.",name:"Buket",middleName:null,surname:"Aybar",slug:"buket-aybar",fullName:"Buket Aybar",position:null,profilePictureURL:"https://mts.intechopen.com/storage/users/202198/images/6955_n.jpg",biography:"Buket Aybar, DDS, PhD, was born in 1971. She graduated from Istanbul University, Faculty of Dentistry, in 1992 and completed her PhD degree on Oral and Maxillofacial Surgery in Istanbul University in 1997.\nDr. Aybar is currently a full-time professor in Istanbul University, Faculty of Dentistry Department of Oral and Maxillofacial Surgery. She has teaching responsibilities in graduate and postgraduate programs. Her clinical practice includes mainly dentoalveolar surgery.\nHer topics of interest are biomaterials science and cell culture studies. 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After graduating from TED Ankara College in 1986, she attended the Hacettepe University, Faculty of Dentistry in Ankara. \nIn 1993 she attended the Gazi University, Faculty of Dentistry, Department of Orthodontics for her PhD education. After finishing the PhD education, she worked as orthodontist in Ankara Dental Hospital under the Turkish Government, Ministry of Health and in a special Orthodontic Clinic till 2011. Between 2011 and 2016, Dr. Deniz Uzuner worked as a specialist in the Department of Orthodontics, Faculty of Dentistry, Gazi University in Ankara/Turkey. In 2016, she was appointed associate professor. Dr. Deniz Uzuner has authored 23 Journal Papers, 3 Book Chapters and has had 39 oral/poster presentations. She is a member of the Turkish Orthodontic Society. 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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. 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