Fracture & Bone Disorders PDF

Summary

This document provides a detailed overview of fracture and bone disorders. It covers topics like bone embryology, composition, and various fracture types and classifications. It also touches on healing processes and complications.

Full Transcript

MDPT FRACTURE & BONE DISORDERS I. Bone G. Salter-Harris Classification - highly specialized connective tissue composed Grade 1: epiphyseal plate, incomplete fx of cells calcified in a...

MDPT FRACTURE & BONE DISORDERS I. Bone G. Salter-Harris Classification - highly specialized connective tissue composed Grade 1: epiphyseal plate, incomplete fx of cells calcified in an organic osteoid matrix Grade 2: epiphyseal plate + triangular segment of metaphysis A. Embryology Grade 3: epiphyseal plate + epiphysis 1. Membranous Grade 4: epiphyseal plate + epiphysis + - gradual replacement of tissue into an osteoid metaphysis (all) matrix (structural framework) ○ (+) Growth arrest - connective tissue → calcification → bone Grade 5: crushed epiphyseal plate - facial bones & cranial vault 2. Endochondral *“SALTR” - mesenchymal cells will form into cartilage 1: Simple - mesenchymal cells → cartilage → bone 2: Above (the epiphyseal plate = meta) - long bones, spine, scapula, sternum, ribs 3: Lower (the epiphyseal plate = dia) 4: Through/Tatlo B. Bone cells 5: Rammed = crushed 1. Osteoblasts - bone formation 2. Osteoclasts - bone resorption *Normally, osteoblasts & osteoclasts activities II. Fracture should be equal - break / discontinuity of a bone 3. Osteocytes - “living element of bone”; carries nutrients for bone development A. Types Incomplete = (+) break / avulsion (such as C. Composition hairline fx) 1. Organic (30%) = collagen type 1 Complete = total discontinuity 2. Inorganic (70%) = hydroxyapatite a. Phosphate Open / Compound = (+) communication c b. Carbonate surrounding tissues; (+) wound 3. H2O (10%) Closed / Simple = total discontinuity D. Bone Cross-Section According to appearance: 1. Haversian System / Osteon - long patent Transverse Fx = creates a right angle along columns that are irregularly parallel along the the shaft axis of the shaft of bones Oblique Fx = creates a diagonal angle along a. Haversian canal - central spaces the shaft located in bet haversian systems Spiral Fx = 2° to torsional F; heals fastest b. Lamellae - concentric layers of Segmental Fx = broken to several segments intercellular substances that surrounds Comminuted Fx = separated into several canal fragments c. Lacunae - spaces in bet lamellae; storage of osteocytes Other types: d. Canaliculi - links the lamellae; where Avulsion Fx = 2° to strong pull of muscle processes of osteocytes happen Compression Fx = 2° to axial loading e. Volkmann’s canal - transverse / oblique Stress Fx = 2° to repetitive trauma channels that transmit blood supply Pathological Fx = 2° to underlying condition Impacted Fx = fx ends are jammed to each other; most stable fx *for open (wound coverage): Gustilo-Anderson Classification Grade 1: 1 cm but 10 cm ○ 3A: periosteal stripping, soft tissue injury E. Types of Bones ○ 3B: soft tissue injury, bony coverage; 1. Long bones - bones which length > width require flaps 2. Short bones - bones which length is almost ○ 3C: involves blood vessels (*circulatory) equal to width (cuboidal shape; capitate) 3. Sesamoid bones - sesame-shaped (patella) *for close:Tscherne Classification 4. Flat bones - flat, thin or curve (skull) 5. Complex bones - irregular shape (pelvis, *for femoral neck fx: Garden Classification vertebra) F. Bone architecture internally → externally: 1. medullary canal - hollow space 2. → endosteum 3. → diaphysis - shaft 4. → periosteum - covering of diaphysis ends of long bones: 1. Metaphysis 2. Epiphyseal plates / cartilaginous plate / growth plate 3. Epiphysis - most end MDPT FRACTURE & BONE DISORDERS B. Upper Extremity Fx D. Vertebral Fx 1. Supracondylar Fx = prox to elbow jt 1. Jefferson’s Fx = burst fx @ ring of atlas; (-) SCI - mc complication: Volkmann’s 2. Hangman’s Fx = axis, neural arch ischemic contracture (dt marked 3. Teardrop Fx = Dens / Odontoid process swelling; results to interrupted blood Types supply) a. Type 1 - fx of the tip of Odontoid; blood - mc deformity: Gunstock deformity = supply maintained cubitus varus / valgus b. Type 2 (mc) - fx of base of Odontoid; high non-union rate 2. Fx of distal radius c. Type 3 - axis is affected; HALO traction 4. Clayshoveler’s fx = fx of tip of C7 (& T1) Colle’s Fx / Poteau’s Smith’s Fx / Reverse spinous process Fx Colle’s Fx 5. Chance fx = spinal fx 2° tight seatbelts dorsal displacement volar displacement of E. Le Fort Classification for Facial Fx of distal radius distal radius 1. Le Fort 1 = low maxillary fx a. maxillary sinuses MOI: FOOSH MOI: FOBOTH / fall b. lower nasal septum on flexed hand c. pterygoid plates 2. Le Fort 2 = pyramidal / oblique fx present.: Dinner / present.: Garden a. zygomaticomaxillary sutures Silver Fork Deformity Spade Deformity b. inferior orbital rim c. nasal bridge 3. Monteggia’s Fx = fx of ulna c d/l of radial head 3. Le Fort 3 = craniofacial dysfunction Types: a. above zygomatic arch Type 1 ( mc): fx of ulnar diaphysis c ant b. med & lat orbital wall d/l of radial head Type 2: fx of ulnar diaphysis c post d/l of F. Bone Healing radial head 1. Inflammatory Phase Type 3: fx of ulnar metaphysis c ant / - hematoma formation ant+lat d/l of radial head - prostaglandin mediation (to control pain) Type 4: fx of ulna & radius c d/l of radial - neutrophils / macrophages activated to head release cytokines (for tissue repair) - days to wks 4. Galleazi’s Fx / Reverse Monteggia’s / 2. Reparative Phase Piedmont / Dupuytren’s Fx / Fx of Necessity - fibroblastic activity, for: = fx of radius c d/l of ulnar head - callus formation (soft → hard callus) - wks to mos 5. Barton’s Fx = fx &/ d/l of wrist 3. Remodeling Phase - hard callus is formed 6. Chauffeur’s Fx = fx of radial styloid process - WB status - common in automobile operators - stages (ARRFQ): - starting kickback Activation = of osteoclasts Resorption = (+) osteoclasts 7. Fx of Capitulum activity (destroy bone) a. Hahn-Steinthal Fx = complete Reversal = osteoblasts will be b. Kocher-Lorenz Fx = articular cartilage recruited Formation = (+) osteoblasts 8. Bennet’s Fx = avulsion fx of 1st MCP / thumb activity (form new bone) - APL & AdP Quiescence = bone will a. Rolando’s Fx = comminuted Bennet’s undergo dormancy until the next cycle begins 9. Boxer’s / Fist Fighters / Street Fighters Fx = 5th MCP (neck) G. Principles of Fx Healing - Treatment: 1. Reduction - replacement / realignment of fxed a. Gutter splint = 40° angulation a. Traction skin = use of adhesive rubber tips; max: *clavicular fx; displacement of the outer and middle 5-6 lbs only thirds of the bone dt pull of SCM ○ ex: Buck & Russel (for children) *DRUJ fx; focus on supination-pronation movement skeletal = drilled using screws & nails (intramedullary nail); mc: proximal tibia; C. Lower Extremity Fx max: 20-30 lbs: only very minimal 1. Femoral neck fx = interruption in blood supply / movement is allowed; additional tool to AVN prevent atrophy: Pearson attachment 2. Intertrochanteric fx = no interruption in bs (attached to the splint) 3. Walther’s fx = ischioacetabular fx ○ ex: Balance Skeletal Traction 4. Duverney’s fx = avulsion fx of iliac wing / ala b. Internal Fixation 5. Shepherd’s fx = lat tubercle of talus c. External Fixation (mc) = cast 6. Cotton fx = transmalleolar fx of the foot 3. Preservation of Reduction 7. Nutcracker fx = calcaneus & cuboid 8. March fx = stress fx of the 2nd MTT H. Anomalies in Bone Healing 9. Trimalleolar fx = dt abd, ER; add / IR 1. Delayed union - failure of fx to heal within: 10. Calcaneal fx (primary movement concern; a. UE: 3-12 wks inversion-eversion) b. LE: 12-18 wks MDPT FRACTURE & BONE DISORDERS 2. Malunion - union in an a unsatisfactory - risk factors: alignment - M (dt hormonal imbalance in 3. Non-union - failure of fx ends to unite (common F postmenopausal) in long bones) - >60 y/o: F=M - caucasians Causes: - inc caffeine intake (can inc osteoclast ○ Impaired circulation activity) ○ Interrupted stability - critical during - corticosteroids healing phase - Pharma Mx: ○ (+) infection - osteomyelitis - Bisphosphonates sequestrum = “dead bone” - Calcium: N daily dietary intake = 1,500 involucrum = thickened layer mg/day or 1,000-1,500 mg/day of bone; “living portion of bone” - Clinical features: ○ inaccurate reduction - Kyphotic ○ loss of bone substance - Dowager’s hump - Radiographic findings: - Codfish vertebra = 2° to expansion of III. Bone Disorders IVD creating a biconcavity appearance A. Achondroplasia of vertebra - mc form of short limb dwarfism - endochondral ossification retardation D. Osteogenesis Imperfecta / Brittle bones / - disproportion of trunk & limbs Fragilitas ossium - congenital disorders; autosomal dominant - a genetic connective tissue d/o caused by - features: mutation of COL1A1 & COL1A2 genes that - height seldom reaches 4 ft encode collagen type 1 - face smaller in relation to head - triad: - brachycephalic head: ant-post 1. Brittle bones diameter of head is shorter than N 2. Wedge-wood blue sclera - high & broad forehead 3. Deafness - flattened nose & depressed nose bridge - prominent lower jaw E. Progressive Myositis Ossificans - Main En Trident Deformity - gap in bet - transformation of fascia, ligaments, tendons & 3rd & 4th fingers, wrist radially shifted muscles into an immobile structures - lordotic - initially: fascia, ligaments - variants: - secondary: muscles Pseudoachondroplasia ○ features not present @ birth F. Mucopolysaccharidosis ○ head & face looks N - inherited disease Hypochondroplasia - accumulation of Mucopolysaccharides (long ○ milder form chain of sugar) ○ reaches 5 ft - lysosomal enzyme storage d/o (impaired Metaphyseal Chondrodysplasia destruction of toxic / foreign substances) ○ similarities c Rickets disease bc (HHSM(5)MS) (Vit D deficiency in children; no MPS 1: Hurler’s Syndrome (mc) calcium bone absorption) ○ (+) hurler’s / gorgoyle cells Chondroectodermal dysplasia / ○ shortened neck & trunk / spine Ellis-Van Creveld disease ○ enlarged skull & prominent forehead ○ polydactyly ○ shortening of FA ○ dysplastic fingernails ○ impaired jt mobility ○ distal shortening of FA & legs ○ hepatosplenomegaly Chondrodysplasia punctata MPS 2: Hunter’s Syndrome ○ stippled calcification in bone ○ only x-linked d/o Diastrophic Dwarfism MPS 3: San Filippo ○ multiple jt contracture ○ fatal in teens ○ external ear deformity MPS 4: Morquio’s Syndrome ○ kyphoscoliosis ○ leads to short spine dwarfism ○ clubfoot deformity ○ enlarged femoral head = hip ER ○ proximally set hitchhikers thumb ○ Waddling gait MPS 5 B. Osteosclerosis MPS 6: Maroteaux-Lamy - skeletal disease characterized by regions of inc ○ N intelligence bone density ○ corneal opacities Osteopetrosis / Marble Bones MPS 7: Sly disease ○ failure in osteoclastic activity ○ almost similar manifestation c classic ○ “bone in a bone” appearance MPS Osteopoikilosis / Spotted Bones ○ (+) ovoid spots of inc sclerosis seen in radiographs (formed by osteoblast dt IV. Amputation inactive osteoclast) - removal of a body part, a portion or the entire Osteopathia striata limb that has been severely injured, infected or ○ coarse longitudinal lines has lost its function A. Terminologies C. Osteoporosis Congenital - bone mass density falls @ -2.5 SD from N Acquired - through surgery - if 1.00-2.00 = osteopenia (less severe form) - silent disease; manifests until presence of fx Open - wound is left unclosed - DEXA / Dual Energy X-ray Absorptiometry = Close - final / definitive amputation gold standard for assessing osteoporosis MDPT FRACTURE & BONE DISORDERS Major = amputation is proximal to MCP & MTP Minor = amputation is distal to MCP & MTP Disarticulation = amputation through a jt B. Indications vascular disease / accident infection (s. aureus) trauma malignant tumor congenital anomaly (excessive growth) electrical / chemical burns C. Types of Amputation in UE Cineplastic - designed for UE for prosthetic use Krukenberg - separation of radius & ulna to create a crude pinching mechanism D. Levels of Amputation AEA / Above Elbow Amputation / Transhumeral Amputation ○ 0% = sh disarticulation / through jt ○ 0-30% = humeral neck dissection ○ 30-50% = short AEA ○ 50-90% = long AEA; standard AEA ○ 90-100% = elbow disarticulation BEA / Below Elbow Amputation / Transradial Amputation ○ 0-35% = very short BEA ○ 35-55% = short BEA (standard) ○ 55-90% = long BEA ○ 90-100% = wrist disarticulation AKA / Above Knee Amputation / Transfemoral Amputation ○ 66% = long AKA BKA / Below Knee Amputation / Transtibial Amputation ○ 50% = long BKA E. Stump Shape “BCyACo” BK = cylindrical AK = conical F. Complications Improper wound healing infection phantom sensation = can still feel the amputated segment / limb ○ telescoping: sensation of movement of amputated segment (distal) proximally phantom pain = noxious sensation on the amputated segment / limb dermatologic problems jt contractures G. Amputation in LE Lisfranc = tarsometatarsal Chopart = midtarsal Boyd = talectomy H. Others mc birth fx = clavicular fx mc limb deficiency fx = left terminal transverse radial limb / left intercalary radial limb mc fx in children = greenstick fx *Wolff’s Law = every change in forms & function is followed by a definitive change in its internal architecture; allows bone to adapt to certain stresses that is being applied to it

Use Quizgecko on...
Browser
Browser