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Movement, Stability & Lumbopelvic Pain. Integration of Research and Therapy PDF

610 Pages·2007·28.837 MB·English
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Contributors MA Adams BSc PhD RL DonTigny PT Senior Research Fellow, Department of Anatomy, Physical Therapist, Havre, Montana, USA University of Bristol, Bristol, UK S Gibbons BSc (Hons) PT MSc MCPA PJ Barker BAppSc(Physio) PhD Stability Physiotherapy, Mt. Pearl, Newfoundland, Senior Tutor, Department of Anatomy and Cell Biology, Canada The University of Melbourne, Victoria, Australia W Gilleard PhD M Benjamin PhD Senior Lecturer in Biomechanics, School of Exercise Professor of Musculoskeletal Biology and Sports & Sports Management, Southern Cross University, Medicine Research, School of Biosciences, Cardiff Lismore, Australia University, Cardiff, UK S Gracovetsky PhD CA Briggs BSc Dip Ed MSc PhD Retired, Concordia University, Montreal, QC, Canada Associate Professor and Deputy Head, Department of Anatomy and Cell Biology, The University of Melbourne, PW Hodges BPhty (Hons) PhD MedDr Victoria, Australia Professor and NHMRC Principal Research Fellow, Division of Physiotherapy, The University of Queensland, L Chaitow ND DO Brisbane, Australia Honorary Fellow, School of Integrated Health, University of Westminster, London, UK; Editor-in-Chief, Journal of S Holm Bodywork & Movement Therapies Professor, Department of Orthopaedics, Sahlgrenska University Hospital, Goteborg, Sweden J Cholewicki Associate Professor, Department of Orthopaedics & B Hungerford PhD Rehabilitation, Yale University School of Medicine, New Consultant Musculoskeletal Physiotherapist, Sydney Haven, CT, USA Spine & Pelvis Centre, Drummoyne, NSW, Australia HJ Dananberg DPM A Huson MD PhD Podiatrist, private practice, Catholic Medical Centre, Professor Emeritus, Maastricht University, The Bedford, New Hampshire, USA; Contributing Editor, Netherlands Journal of the American Podiatric Medical Association A Indahl MD PhD L Danneels PT PhD Consultant, Specialist in physical medicine and Professor of Rehabilitation Sciences and Physiotherapy, rehabilitation, Department of Physical Medicine and Faculty of Medicine and Health Sciences, Ghent, Rehabilitation, Hospital for Rehabilitation, Stavern, Belgium Norway C DeRosa PT PhD RE Irvin DO Professor of Physical Therapy, Northern Arizona Clinical Associate Professor, Dept of Osteopathic University, Flagstaff, Arizona, USA Manipulative Medicine, College of Osteopathic Medicine, Oklahoma State University Health Science Center, Tulsa, PF Dijkstra MD DIC PhD Oklahoma, USA Former Radiologist, Academic Medical Centre, Amsterdam, The Netherlands; Former Head of E Jurriaans BSc MBChB DTM&H FRCR(UK) FRCP(C) Department of Radiology, Jan van Breemen Institute for Associate Professor, McMaster University, Faculty of Skeletal Disease, Amsterdam, The Netherlands Health Sciences, Hamilton, Ontario, Canada; Staff Radiologist, St. Joseph’s Healthcare, Hamilton, Ontario, P Dolan PhD Canada Reader in Biomechanics, Department of Anatomy, University of Bristol, Bristol, UK PPrreelliimm--FF1100117788..iinndddd vviiiiii 1122//2211//0066 22::2288::5599 PPMM ix Contributors B Koes PhD JA Porterfi eld PT MA ATC Professor of General Practice, Head of Research Owner, Rehabilitation and Health Center, Inc., Akron, Department, Department of General Practice, Erasmus Ohio; CEO, Venture Practice Services Ltd., Akron, Ohio, MC, University Medical Centre, Rotterdam, The USA Netherlands T Ravin MD M Laslett PhD NZRP Dip MT Dip MDT Physician; President of the American Association of Senior Clinician, PhysioSouth @ Moorhouse Medical Musculoskeletal Medicine, Denver, Colorado, USA Clinic, Christchurch, New Zealand R Stoeckart PhD D Lee BSR FCAMT Department of Neuroscience, Erasmus MC, Rotterdam, Clinical and Education Consultant, Diane Lee & The Netherlands Associates, Canada B Stuge PT PhD SM Levin MD FACS Senior Researcher, Institute of Nursing & Health Director, Ezekiel Biomechanics Group, McLean, VA, USA Sciences, University of Oslo, Norway CO Lovejoy MA PhD B Sturesson MD PhD University Professor of Anthropology, Department of Head of Spine Unit, Department of Orthopaedics, Anthropology and Division of Biomedical Sciences, Kent Angelholm Hospital, Angelholm, Sweden State University and Northeast Ohio Universities College of Medicine, Ohio, USA M van Tulder PhD Professor, Institute for Research in Extramural Medicine AT Masi MD DRPH (EMGO) and Institute for Health Sciences (HIS), VU Professor of Medicine, University of Illinois College of University Medical Centre, Amsterdam, The Netherlands Medicine at Peoria (UICOMP), Illinois, USA DM Urquhart BPhysio(Hons) PhD SM McGill Dept of Epidemiology & Preventive Medicine, Monash Professor, Faculty of Applied Health Sciences, Dept of University, Victoria, Australia Kinesiology, University of Waterloo, Ontario, Canada LMG Vancleef MSc V Mooney MD Dept Medical, Clinical and Experimental Psychology, Clinical Professor of Orthopaedics, USSD, Private Maastricht University, The Netherlands Practitioner, San Diego, California, USA J Viti G Lorimer Moseley PhD BAppSc(Phty)(Hons) Assistant Professor, University of St. Augustine for Nuffi eld Medical Research Fellow, Centre for fMRI of Health Sciences, St. Augustine, Florida, USA the Brain and Dept of Human Anatomy & Genetics, University of Oxford, UK JWS Vlaeyen PhD Dept Medical, Clinical and Experimental Psychology, G Müller Maastricht University, The Netherlands Orthopaedic Surgeon, Sports Medicine, Manual Therapy, Chairman of Rueckenzentrum Am Michel, Hamburg, A Vleeming PhD Germany Clinical Anatomist and Founder, Spine and Joint Center, Rotterdam, The Netherlands JMD O’Neill MB BAO BCh MRCPI MSc FRCR(UK) Assistant Professor, McMaster University, Faculty of NK Vøllestad PhD Health Sciences, Hamilton, Ontario, Canada; Staff Professor, Head of Institute of Nursing & Health Radiologist & Director – Musculoskeletal Imaging, St. Sciences, University of Oslo, Norway Joseph’s Healthcare, Hamilton, Ontario, Canada FH Willard PhD HC Östgaard MD PhD Professor, College of Osteopathic Medicine, Family Associate Professor, Chief of Dept of Orthopaedics, Medicine, University of New England, Biddeford, Maine, Sahlgren University Hospital, Molndal, Sweden USA SV Paris PT PhD FAPTA President, University of St. Augustine for Health Sciences, St. Augustine, Florida, USA PPrreelliimm--FF1100117788..iinndddd iixx 1122//2211//0066 22::2288::5599 PPMM Preface There are a large number of books dealing with and several others. In the book they are grouped the lumbar spine and pelvis, so why this book into the following parts: on Movement, Stability and Lumbopelvic Pain? This 1. Biomechanical, clinical–anatomical and question is pertinent as there are several excellent evolutionary aspects of lumbopelvic pain and books available which cover these topics. Our dysfunction reasons are diverse. 2. Insights in function and dysfunction of the Firstly, several distinguished scientists, physicians lumbopelvic region and other specialists have lately provided evidence- 3. Diagnostic methods based, relevant new data on the lumbopelvic 4. Guidelines area. This forces us to look afresh at the adequacy 5. Effective training and treatment of current diagnostic and therapeutic methods. 6. Integrating different views and opinions when Secondly, most books deal either with the low back dealing with a complex system. or with the pelvic girdle; our aim is to collect all The studies reviewed in this book refl ect the relevant material in one book. Thirdly, most books specialties of the contributors, their back grounds, on the subject are written by one expert or by a small styles, approaches and specifi c ideas about how team of experts. This makes it diffi cult to get a grip lumbopelvic structures func tion and dysfunction. on the vast wealth of information available. Finally, Several chapters were written by authors with a and probably most importantly, notwithstanding all unique concept about the origin of pain and dys- efforts to treat patients adequately, large numbers function of lumbopelvic structures and about the of patients still suffer chronically from low back therapy requested. In a way this is hazardous since pain and/or pelvic girdle pain. It is our hope and certain authors were invited, not because of their ambition to provide, together with all contributors, evidence-based approach, but since in the opinion an integrated book that can be of help to people of the editors their audacious and sometimes involved in the diagnosis or treatment of patients controversial ideas merit attention. Their concepts with lumbopelvic pain. should invite sound research that can confi rm, The contributors to this book include scientists refute, or adapt the ideas presented. We are of internationally renowned clinical groups and convinced that the wealth of information presented departm ents dealing with basic sciences. Their by the contributors will help to create rational and contributions are from differ ent disciplines effective treatment programs for the management embracing anthropology, ortho pedic surgery, bio- of lumbopelvic pain and dysfunction. mecha nical engineering, chiropractic practice, anatomy, osteopathy, physical therapy, podiatry, Andry Vleeming, Vert Mooney and gynecology, rehabi litation medicine, epidemiology Rob Stoeckart PPrreelliimm--FF1100117788..iinndddd xx 1122//2211//0066 22::2288::5599 PPMM SECTION ONE C H A P T E R 1 The muscular, ligamentous, and neural structure of the lumbosacrum and its relationship to low back pain FH Willard INTRODUCTION The lumbosacral spinal column performs a key role in the transfer of weight from the torso and upper body into the lower extremities, both in static positions and during mobility. The primary bony structures involved in this force transduction are: five lumbar vertebrae, a sacrum, two innominate bones, and the two femoral heads. Critical to the stability of these bony components is a complex arrangement of dense connective tissue. Although typically described as separate entities in most textbooks of anatomy, these fibrous, soft-tissue structures actually form a continuous ligamentous stocking in which the lumbar vertebrae and sacrum are positioned. The major muscles representing the prime movers in this region – such as the multifidus, gluteus maximus, and biceps femoris – have various attachments to this elongated, ligamentous stocking. The muscular and ligamentous relationships composing the lumbosacral connection are of extreme importance in stabilizing the lumbar vertebrae and sacrum during the transfer of energy from the upper body to the lower extremities. This arrangement has been termed a ‘self-bracing mechanism’ (Vleeming et al 1995c) and, as such, its dysfunction is critical to the failure of the lower back. A critical relationship also exists between the neural components of the lumbosacral region and the surrounding ligamentous structures. Traumatic, infl ammatory, and degenerative disease processes affect the structure of the lumbosacral region and impact on the surrounding nerves. Current research, using immunohistochemical techniques to identify specific types of axons, suggests that all of these connective tissue structures receive a supply of small-caliber, primary afferent fibers (A(cid:98) and C-fibers), CChh0011--FF1100117788..iinndddd 55 1122//2277//0066 11::4411::1155 PPMM 6 Movement, Stability and Lumbopelvic Pain typical of those involved in nociception. Irritation Ventral Capsular Neural arch of these primary afferent nociceptive axons initiates ligaments ligaments ligaments the release of neuropeptides that interact with fibroblasts, mast cells, and immune cells present Superior articular in the surrounding connective tissue (Levine et al process 1993). The resultant cascade of events, referred to as a neurogenic infl ammatory response, is thought to Transverse play a major role in degenerative diseases and the process development of low back pain (Garrett et al 1992, Kidd et al 1990, Schaible et al 2005, Weidenbaum & Farcy 1990, Weinstein 1992). Sensitization of these small-caliber, primary afferent fibers, along with sensitization of their central connections in the dorsal horn of the spinal cord, appears to play a crucial role in the evolution of chronic painful conditions Inferior articular (Coderre et al 1993, Ji et al 2003, Woolf & Chong process Spine 1993). This chapter examines recent advances in Accessory our knowledge of the lumbosacral region structural process architecture, pathology, and innervation. Fig. 1.1 A lateral view of a lumbar vertebra illustrating the position of the neural arch ligaments, capsular ligaments, and ventral ligaments. Ligamentous structure of the lumbar region et al 1990a, 1990b) in vivo they grade together at The various ligaments of the lumbar vertebral their boundaries to unite and function as a single column form a continuous, dense, connective-tissue unit. To demonstrate this concept, the osseous stocking surrounding the vertebrae and extending components of the neural arch were removed with into the sacral area. For ease of description, the minimal disturbance to the associated ligamentous vertebral connective tissue sheath can be divided structures (Figs 1.4 and 1.5). The unitary nature into three parts: (1) the neural arch structures; of the supraspinous and intraspinous ligaments (2) the capsular structures; and (3) the ventral or and of the ligamentum fl avum is obvious because vertebral body structures (Fig. 1.1). However, it these soft tissue structures maintain their continuity should be noted that the partitions between each despite the lack of supporting osseous material. of these three divisions are for convenience only, as the connective tissue of the dorsal and ventral Ligamentum fl avum components is essentially continuous across the The ligamentum fl avum, located between individual pedicles of the vertebrae. laminae, represents a medialward continuation of the articular capsule of the facet joint (Fig. 1.4). Neural arch ligaments This elastic ligament forms a significant portion of the roof of the spinal canal. Superiorly, it attaches The neural arch of each lumbar vertebra is composed to the anterior surface of the lamina above and of the pedicles, laminae, transverse processes, inferiorly it establishes a cup-like grasp on the and spine (Figs 1.1 and 1.2). Two major ligaments superior margin of the lamina below (Olszewski et participate in surrounding the neural arch: the al 1996). The medial fibers of the ligament bridge ligamentum fl avum and the interspinous ligament; the gap between the laminae of adjacent vertebra, two additional small ligaments are also described: fusing with the interspinous ligament, whereas the supraspinous ligament posteriorly and the the lateral fibers attach to the facet joint capsule intertransverse ligament laterally. To view the (Figs 1.4B and 1.5; see also Behrsin & Briggs 1988, ligaments of the neural arch, the multifidus muscle Bogduk & Twomey 1991, Ramsey 1966). This must be completely removed from the lumbosacral distensible ligament is composed of elastic fibers region (Figs 1.2 and 1.3). Although most of these (80%) and collagenous fibers (20%), the elastic ligaments have a distinct biochemical make-up fibers imparting the ligament its yellow color when analyzed in isolation (Ballard & Weinstein and fl exible nature (Bogduk & Twomey 1991). A 1992, Fujii & Hamada 1993, Fujii et al 1993, Yahia significant function for the ligamentum fl avum is CChh0011--FF1100117788..iinndddd 66 1122//2277//0066 11::4411::1177 PPMM 7 The muscular, ligamentous, and neural structure of the lumbosacrum second component can be related to an age-related loss of elastic fibers and elasticity of the ligamentum fl avum, contributing to their progressive loss of tension in the elderly (Nachemson & Evans 1968, Ramsey 1966). Specifically, there is a decrease in Lo elastic fibers and a concomitant increase in the density of collagen fibers, along with a shift to high-molecular-weight proteoglycans (Kashiwagi S 1993, Okada et al 1993). These events favor the deposition of calcium (Kashiwagi 1993), thus nearly all fl aval ligaments in a sampling of patients with lumbar spinal stenosis had histological signs of ossification (Schrader et al 1999). Calcification of the ligament leads to its hypertrophy and to subsequent lumbar spinal stenosis (Yoshida et al 1992). These age-related changes in the liga m entum Ic fl avum have been related to spe cific neurologic sequelae such as the cauda equina syndrome and lumbar radiculopathy (Baba et al 1995, Ryan 1993). Whereas ossification of the ligament is associated with increasing age and the presence of cauda equina syndrome, chondrogenesis in the ligament appears more associated with the presence of spondylolisthesis (Okuda et al 2004). Finally, failure Mu of the elastic properties of this ligament has also been related to the development of adolescent idiopathic scoliosis (Hadley-Miller et al 1994). Unfortunately, there is little or no regenerative Fig. 1.2 The three lumbar paravertebral muscles in a capacity in the elastic tissue of the ligamentum male. On the individual’s right side is the iliocostalis muscle fl avum; thus a damaged ligament is replaced by a (Ic) laterally and the longissimus muscle (Lo) medially. Note dense connective tissue cicatrix (Ramsey 1966). that the spinalis muscle (S) does not extend into the lumbar region beyond L2 or L3. On the individual’s left side, the iliocostalis and longissimus have been removed to reveal Interspinous ligament the medially positioned multifidus muscle (Mu). Arrows The interspinous ligament extends between borders top and bottom are aligned along the spinous processes of the spines of adjacent vertebrae (Figs 1.5 and of the thoracic and lumbar vertebrae (midline). The thick 1.6). Its anterior border is a continuation of the lumbar multifidus muscle is seen differentiating into the thin, ligamentum fl avum. The posterior border of the liga- fl attened semispinalis muscle at the superior end of the lumbar vertebral column (asterisk). ment thickens to form the supraspinous liga ment, which is, in turn, anchored to the thoracolumbar fascia. The orientation of fibers in the interspinous to provide a roof for the vertebral canal that will ligament has been given multiple, confl icting not buckle during extension–fl exion movements descriptions. In humans, the ligament can best be of the vertebral column (Bogduk & Twomey 1991). described as a fan (Fig. 1.6; see also Fig. 1.11 below). At rest (in a neutral position), the ligaments have The narrow or proximal end of the fan blends with a pretension, ideally keeping the ligaments from the ligamentum fl avum and contains elastic fibers buckling (Nachemson & Evans 1968). (Yahia et al 1990b), whereas the broad end of the Despite the elasticity of the ligamentum fan extends in a posterior direction towards the fl avum, it is known to be a significant source of tips of the spines and is composed primarily of root compression in the lumbar region (Okuda et collagen fibers. In the center of the ligament, the al 2005). A component of this neural compression collagen fibers are oriented parallel to the vertebral appears to be related to buckling of the ligament spines; distally, the peripheral collagen fibers fl are inferiorly secondary to age-related intervertebral posterocranially and posterocaudally (Aspden et al disc collapse or other degenerative processes. A 1987, Hukins et al 1990). This fan-like arrangement CChh0011--FF1100117788..iinndddd 77 1122//2277//0066 11::4411::1188 PPMM 8 Movement, Stability and Lumbopelvic Pain S A B Fig. 1.3 The multifidus muscle and its bed. (A) The pyramidal-shaped multifidus muscle is demonstrated between the four arrowheads (S, lumbar spinous processes). (B) The multifidus muscle has been removed to reveal a continuous ligamentous stocking surrounding the neural arch components of the lumbar vertebrae (between arrowheads). On the sacrum, only the deepest laminae of the multifidus remain (asterisk). allows the ligament to expand without rupture as the ligament and evidence for degenerative the vertebral spines separate during fl exion. The events in the interspinous ligament has recently fibers of this ligament are described as resisting been demonstrated with CT and MRI imaging the separation of the vertebral spines during (Jinkins 2004). All of these pathologic events fl exion (Bogduk & Twomey 1991); however, the occurring to the interspinous ligament should most likely function of these ligaments, given diminish the ability of the thoracolumbar fascia to their anteroposterior fiber orientation, is to act as infl uence the alignment of the lumbar vertebrae, and an anchor, transmitting the anteroposterior pull of thereby increase their risk of destructive injury. the thoracolumbar fascia, into which it is attached via the supraspinous ligament (Hukins et al 1990), Supraspinous ligament into an increased tension in the ligamentum fl avum (Fig. 1.7). This increased tension would assist in The supraspinous ligament lies along the posterior preventing the latter ligament from buckling onto border of the interspinous ligament (Fig. 1.8). the spinal cord and would also serve to assist in Throughout its lumbar course, it is tightly adherent alignment of the lumbar vertebrae. Chondrocytes to the posterior border of the lumbar spines and are present along the osseous borders of the interspin- to the interspinous ligament. This creates an ous ligaments and age-related chondrification of interspinous–supraspinous thoracolumbar (IST) liga- the interspinous ligament occurs after the third mentous complex that anchors the major fascial decade of life (Yahia et al 1990b). Degenerative planes of the back to the lumbar spines. Traction processes in the motion segment of the vertebrae placed on the thoracolumbar fascia will destroy appear to coincide with the chondrification of the thoracolumbar sheath before it will separate CChh0011--FF1100117788..iinndddd 88 1122//2277//0066 11::4411::1188 PPMM 9 The muscular, ligamentous, and neural structure of the lumbosacrum LF FJ sd IS A B Fig. 1.4 The ligamentous stocking of the lumbar vertebrae. (A) This orientation photograph is a posterior view of the lumbar spinal column, similar to that in Fig. 1.3. The spinous processes, laminae, and inferior articular processes of the facet joint have been removed. (B) Detailed view of the ligamentous stocking illustrating the ligamentum fl avum (LF) extending between the interspinous ligament (IS) medially and the facet joint capsule (FJ) laterally. The arrowhead indicates the same facet joint capsule in both photographs. The epidural space and spinal dural (sd) can be seen between the fl aval ligaments. the IST complex (Fig. 1.8). Thus it is possible for plates surrounded by a dense connective-tissue the interspinous and supraspinous ligaments to act fibrous capsule (Lewin et al 1962). The plates are as force transducers, translating the tension of the curved such that the inferior articular process (from thoracolumbar fascia, developed in the extremities the above vertebrae) presents a convex process and torso, into the lumbar vertebral column. At to the concave superior articular process (of the lower lumbar levels, the supraspinous ligament vertebrae below) (Fig. 1.9). These joints contain a becomes progressively less organized as it grades true synovial space, a connective tissue rim and a into the distal attachments of the thoracolumbar complicated array of surrounding adipose tissue fascia, and in some individuals it might not be pads and fibroadipose menisci (Engel & Bogduk recognizable caudal to L4 (Bogduk & Twomey 1982). The articular surface of the facet joints is 1991). This ligament often presents with fatty covered with a hyaline cartilage. The joint capsule involution late in life (Heylings 1978) and can also represents a connective-tissue bridge between the ossify (Mine & Kawai 1995). neural arch ligaments and those of the vertebral body. As such, the capsule is encased in a thin Articular capsular ligament sheet of dense, irregular investing fascia, which is continuous dorsally with that surrounding the The articular processes of the lumbar vertebrae ligamentum fl avum and ventrally with the investing form the facet or zygapophyseal joints. Each joint fascia of the vertebral body. The capsule itself has consists of two opposed and vertically oriented two components: an outer layer of dense connective CChh0011--FF1100117788..iinndddd 99 1122//2277//0066 11::4411::1199 PPMM 10 Movement, Stability and Lumbopelvic Pain LS FJ IS sd SS LF LF LS IS Fig. 1.5 Lateral view of the lumbar ligamentous stocking. Fig. 1.6 A magnified view of the interspinous ligament. The facet joint (FJ) is the same as the marked FJ in Fig. The lumbar spinous processes (LS) are seen superior and 1.4B. The continuity of the fl aval ligament (LF) with the facet inferior to the ligament. Note the fan-like orientation of the joint capsule and interspinous ligament (IS) is indicated by collagenous fibers in the ligament. The proximal end of the the arrowheads. The spinal dura (sd) can be seen in the ligament is continuous with the ligamentum fl avum (LF) epidural space. and the distal end of the ligaments is embedded in the supraspinous ligament (SS). This latter structure is attached to the thoracolumbar fascia. This arrangement would serve to transform any increased tension in the thoracolumbar tissue and an inner layer composed of elastic fibers fascia into increased tension on the ligamentum fl avum, similar to the ligamentum fl avum (Yamashita et resulting in an alignment of the lumbar vertebrae al 1996). The outer layer is composed of dense, (see Fig. 1.7). regularly arranged connective tissue in which the predominant orientation of the collagenous fibers is orthogonal to the joint line, the plane on which the fl avum. It is weakest around the superior recess, two facet plates oppose each other (Fig. 1.10). The which can burst from effusion during arthrography capsule is bound tightly to the articular processes (Dory 1981). The inferior border of the capsule with the exception of its inferior and superior is continuous with the ligamentum fl avum, the recesses, each of which consists of a loosened medial border with the periosteum of the lamina, fold in the capsule wall (Figs 1.9C and 1.11). This and the lateral border with the periosteum of the arrangement of the capsule allows for a gliding pedicle and body. movement in the sagittal plane but restricts its range The intervertebral disc and its two associated of motion in the horizontal plane. Each recess has a facet joints make up a triad representing the load- small defect that is capable of transmitting fat from bearing joint surfaces at each lumbar vertebral the capsular space outward (Bogduk & Twomey level (Lewin et al 1962). Logic suggests that 1991). The capsule is reinforced dorsally by the anatomical abnormalities or degenerative changes multifidus muscle and ventrally by the ligamentum of one component would lead to changes in other CChh0011--FF1100117788..iinndddd 1100 1122//2277//0066 11::4411::1199 PPMM

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Most books are stored in the elastic cloud where traffic is expensive. For this reason, we have a limit on daily download.