Fracture Repair
- Hematoma formation
- Torn blood vessels hemorrhage
- A mass of clotted blood (hematoma) forms at the fracture site
- Site becomes swollen, painful, and inflamed
- Fibrocartilaginous callus forms
- Capillaries grow into the tissue and phagocytic cells begin cleaning debris
- Osteoblasts & fibroblasts migrate to fracture & begin reconstructing bone
- Fibroblasts secrete collagen fibers that connect broken bone ends
- Osteoblasts begin forming spongy bone
- Osteoblasts furthest from capillaries secrete an externally bulging
- Bony callus formation
- New bone trabeculae appear in the fibrocartilaginous callus
- Fibrocartilaginous callus converts into a bony (hard) callus
- Bone callus begins 3-4 weeks after injury, and continues until firm union is formed 2-3 months later
- Bone remodeling
- Excess material on the bone shaft exterior and in the medullary canal is removed
- Compact bone is laid down to reconstruct shaft walls
- Nondisplaced - bone ends retain their normal position
- Displaced - bone ends are out of normal alignment
- Complete - bone is broken all the way through
- Incomplete - bone is not broken all the way through
- Linear - the fracture is parallel to the long axis of the bone
- Transverse - the fracture is perpendicular to the long axis of the bone
- Compound (open) - bone ends penetrate the skin
- Simple (closed) - bone ends do not penetrate the skin
Homeostatic Imbalances of Bone
- Osteomalacia and Rickets
- Osteomalacia includes a number of disorders in adults in which the bone is inadequately mineralized.
- Rickets is inadequate mineralization of bones in children caused by insufficient calcium or vitamin D deficiency.
- Osteoporosis
- Group of diseases in which bone reabsorption outpaces bone deposit
- Spongy bone of the spine is most vulnerable
- Occurs most often in postmenopausal women
- Bones become so fragile that sneezing or stepping off a curb can cause fractures
- Factors that contribute to osteoporosis include a petite body form, insufficient exercise or immobility, a diet poor in calcium and vitamin D, abnormal vitamin D receptors, smoking, and certain hormone-related conditions.
- Treatment
- Calcium and vitamin D supplements
- Increased weight-bearing exercise
- Hormone (estrogen) replacement therapy (HRT) slows bone loss
- Natural progesterone cream prompts new bone growth
- Statins increase bone mineral density
- Paget's disease is characterized by excessive bone deposition and resorption, with the resulting bone abnormally high in spongy bone. It is a localized condition that results in deformation of the affected bone.
Developmental Aspects of Bones: Timing of Events
- The skeleton derives from embryonic mesenchymal cells, with ossification occurring at precise times. Most long bones have obvious primary ossification centers by 12 weeks gestation.
- At birth, most bones are well ossified, except for the epiphyses, which form secondary ossification centers.
- Throughout childhood, bone growth exceeds bone resorption; in young adults, these processes are in balance; in old age, resorption exceeds formation.
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