Osteomalacia
Adult rickets
Word Meaning
• Greek origin
• Osteo – bone
• Malacia - softness
Definition
• Osteomalacia is defined as a Rare
bone disorder associated with
vitamin D deficiency, resulting in
decalcification and softening of
bone.
Incidence
• Women mostly affected (Muslims)
• Its endemic in Asia
 Lack of exposure to UV rays (needed for
Vit.D synthesis)
 Drugs – anticonvulsants (phenytoin)
 GI malabsorption
 Extensive burns
 Chronic diarrhoea
 Pregnancy – multiple pregnancy
 Kidney disease
Etiology
 Excessive loss of calcium (celiac disease, biliary
tract obstruction, chronic pancreatitis)
 After surgery of gastrointestinal system
Pathophysiology
• Vit.D insufficiency
• Vit.D required for the absorption of the
calcium from the intestine
• Insufficient vit.D intake can interfere with the
normal mineralization of bone activity or
insufficient calcification of bone
• Leads to bone softening and associated
symptoms
Clinical features
• Bone become bent and flattened as they
soften
• Pathologic fracture
• Fatigue, malaise, bone pain (with tenderness)
• Difficult to walk, rise from a chair, low back
pain, progressive muscle weakness, weight
loss , deformity of spine (kyphosis), fracture
with delayed healing
Diagnostic investigation
• X-ray – generalized demineralization with
trabecular bone loss
• Bone biopsy
• Serum calcium and phosphorus levels are
reduced
• Alkaline phosphates level is moderately
elevated
Management
• Diet – vit D, calcium and phosphorous rich
• Vit.D3 (cholecalciferol), vit.D2 (ergocalciferol)
• Calcium salts and phosphorous supplements
may also prescribed
• Eggs, low fat milk, fish
• Exposure to sunlight
• Weight bearing exercises
• Orthopedic deformities may be treated with
surgery (osteotomy).
Nursing management
Assessment
• Assess for bone pain in the low back and
extremities
• Assess for fracture
• Obtain information about co existing diseases
(malabsorption syndrome) and dietary habits
• Note skeletal deformities on physical
examination
• Relieving pain – change in positions and
analgesic
• Improving body image – trusting relationship,
encourage patient to discuss any changes in
body image and methods of coping
• Encourage to use existing strength
• Allow talk with the similar successful patients
Nsg diagnosis
• Acute pain r/d to bone tenderness and
possible fracture
• Disturbed body image related to bowing of
legs, waddling gait and spinal deformities
• Deficient knowledge about disease process
and treatment
Pagets disease (osteitis deformans)
• Def - idiopathic Skeletal bone disorder in
which there is excessive bone resorption
followed by replacement of altered bone
tissue
• The new bone is larger, disorganized and
structurally weaker
• Common sites – pelvis , long bones, spine,
ribs, sternum and cranium
Etiology
• Exact cause is unknown
• Followed by viral infection (measles virus,
respiratory syncytial virus )
• Genetic (15%-30%)
• Men to women ratio – 2:1
• Seen in below 40 years
Pathophysiology
• Due to unknown causes
• Increase BONE RESORPTION
• Altered BONE TURN OVER
• As a compensatory mechanism - increase
bone formation
• Newly formed bones are large, unorganized
and weak
• Structural changes in weight bearing limbs and
other manifestation
Signs and symptoms
• Free of symptoms in the early stages
• Bone pain – deep ache – progress to severe
pain
• Fatigue
• Progressive development of waddling gait
• Become shorter
• Barrel chest
• Bowing of tibia or femur
• Changes in skin temperature
• Manifestations related to
nerve compression
• Increase bone volume in the spine can cause
spinal cord or cranial root compression leads
to head ache, blindness, vertigo, hearing loss
with tinnitus and dementia
• Pathologic fracture , osteosarcoma,
fibrosacroma and osteoclastoma tumors are
complications
• Osteoarthritis are common associated with
pagets disease
Diagnostic investigation
• X rays – shows increased bone
expansion and density.
• Bone scan
• Serum alkaline phosphates levels
increased
• N-telopeptide and C-telopeptide
they are biomarkers used to
measure the rate of bone turnover,
can be measure from urine or serum
Management
• Limited to symptoms
• Supportive care
• Correction of secondary deformity
• Calcitonin – decrease osteoclastic activity
Bisphosphonate drugs –
• Risedronate, Tidronate, Pamidronate, Ibandronate
– retard bone resorption
Calcium and vitamin D supplements
• Pain – NSAIDS, ibuprofen.
• Orthopedic surgeries for fracture, hip and knee
replacements
• Firm mattress – back support and to relieve pain
• Wear light brace
• Activity like lifting and twisting should be avoided
• Physical therapy will increase muscle strength
• Good body mechanics
• Balanced nutrition programme – vit.D, calcium
and protein
• Massage, heat therapy
Prevention
• Patient education
• Use of an assistive device

osteomalacia-with-paget-disease-don.pptx

  • 1.
  • 2.
    Word Meaning • Greekorigin • Osteo – bone • Malacia - softness
  • 3.
    Definition • Osteomalacia isdefined as a Rare bone disorder associated with vitamin D deficiency, resulting in decalcification and softening of bone.
  • 4.
    Incidence • Women mostlyaffected (Muslims) • Its endemic in Asia
  • 5.
     Lack ofexposure to UV rays (needed for Vit.D synthesis)  Drugs – anticonvulsants (phenytoin)  GI malabsorption  Extensive burns  Chronic diarrhoea  Pregnancy – multiple pregnancy  Kidney disease Etiology
  • 6.
     Excessive lossof calcium (celiac disease, biliary tract obstruction, chronic pancreatitis)  After surgery of gastrointestinal system
  • 7.
    Pathophysiology • Vit.D insufficiency •Vit.D required for the absorption of the calcium from the intestine • Insufficient vit.D intake can interfere with the normal mineralization of bone activity or insufficient calcification of bone • Leads to bone softening and associated symptoms
  • 8.
    Clinical features • Bonebecome bent and flattened as they soften • Pathologic fracture • Fatigue, malaise, bone pain (with tenderness) • Difficult to walk, rise from a chair, low back pain, progressive muscle weakness, weight loss , deformity of spine (kyphosis), fracture with delayed healing
  • 10.
    Diagnostic investigation • X-ray– generalized demineralization with trabecular bone loss • Bone biopsy • Serum calcium and phosphorus levels are reduced • Alkaline phosphates level is moderately elevated
  • 11.
    Management • Diet –vit D, calcium and phosphorous rich • Vit.D3 (cholecalciferol), vit.D2 (ergocalciferol) • Calcium salts and phosphorous supplements may also prescribed • Eggs, low fat milk, fish • Exposure to sunlight • Weight bearing exercises • Orthopedic deformities may be treated with surgery (osteotomy).
  • 12.
    Nursing management Assessment • Assessfor bone pain in the low back and extremities • Assess for fracture • Obtain information about co existing diseases (malabsorption syndrome) and dietary habits • Note skeletal deformities on physical examination
  • 13.
    • Relieving pain– change in positions and analgesic • Improving body image – trusting relationship, encourage patient to discuss any changes in body image and methods of coping • Encourage to use existing strength • Allow talk with the similar successful patients
  • 14.
    Nsg diagnosis • Acutepain r/d to bone tenderness and possible fracture • Disturbed body image related to bowing of legs, waddling gait and spinal deformities • Deficient knowledge about disease process and treatment
  • 15.
  • 16.
    • Def -idiopathic Skeletal bone disorder in which there is excessive bone resorption followed by replacement of altered bone tissue • The new bone is larger, disorganized and structurally weaker • Common sites – pelvis , long bones, spine, ribs, sternum and cranium
  • 17.
    Etiology • Exact causeis unknown • Followed by viral infection (measles virus, respiratory syncytial virus ) • Genetic (15%-30%) • Men to women ratio – 2:1 • Seen in below 40 years
  • 18.
    Pathophysiology • Due tounknown causes • Increase BONE RESORPTION • Altered BONE TURN OVER • As a compensatory mechanism - increase bone formation • Newly formed bones are large, unorganized and weak • Structural changes in weight bearing limbs and other manifestation
  • 19.
    Signs and symptoms •Free of symptoms in the early stages • Bone pain – deep ache – progress to severe pain • Fatigue • Progressive development of waddling gait • Become shorter • Barrel chest
  • 20.
    • Bowing oftibia or femur • Changes in skin temperature • Manifestations related to nerve compression
  • 21.
    • Increase bonevolume in the spine can cause spinal cord or cranial root compression leads to head ache, blindness, vertigo, hearing loss with tinnitus and dementia • Pathologic fracture , osteosarcoma, fibrosacroma and osteoclastoma tumors are complications • Osteoarthritis are common associated with pagets disease
  • 22.
    Diagnostic investigation • Xrays – shows increased bone expansion and density. • Bone scan • Serum alkaline phosphates levels increased • N-telopeptide and C-telopeptide they are biomarkers used to measure the rate of bone turnover, can be measure from urine or serum
  • 23.
    Management • Limited tosymptoms • Supportive care • Correction of secondary deformity • Calcitonin – decrease osteoclastic activity
  • 24.
    Bisphosphonate drugs – •Risedronate, Tidronate, Pamidronate, Ibandronate – retard bone resorption Calcium and vitamin D supplements • Pain – NSAIDS, ibuprofen. • Orthopedic surgeries for fracture, hip and knee replacements • Firm mattress – back support and to relieve pain • Wear light brace • Activity like lifting and twisting should be avoided
  • 25.
    • Physical therapywill increase muscle strength • Good body mechanics • Balanced nutrition programme – vit.D, calcium and protein • Massage, heat therapy Prevention • Patient education • Use of an assistive device