Week 8 - Implant Reaction Flashcards

1
Q

sequence of events for implant reaction

A
  1. implantation
  2. blood-biomaterial interactions
  3. provisional matrix formation
  4. acute inflammation
  5. chronic inflammation
  6. granulation tissue
  7. foreign body reaction
  8. fibrosis/ fibrous capsule development
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2
Q

step 1

A

IMPLANTATION

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3
Q

step 2

A

BLOOD-BIOMATERIAL INTERACTIONS

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4
Q

what forms: PROVISIONAL MATRIX FORMATION

A
STEP 3
- forms within mins-hrs of implantation
- fibrin ( blood coagulating protein-
produced from fibrinogen)
- inflammatory products (released by complement system)
- activated blood platelets
- inflammatory cells
- endothelial cells
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5
Q

what happens: ACUTE INFLAMMATION

A

STEP 4

  • neutrophils arrive in vast numbers
  • do a lightning immunological assault
  • short duration (mins-days)
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6
Q

main features: ACUTE INFLAMMATION

A
  • release of fluid and blood plasma proteins
  • arrival of leukocytes (initially neutrophils, later macrophages)
  • resolves in a week –> longer = infection
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7
Q

role of leukocytes: ACUTE INFLAMMATION

A
  • adsorb to biomaterial
  • frustrated phagocytosis
  • -> particulate biomaterials/ wear debris, phagocytosis is successful
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8
Q

draw the graph

A

how do i insert a photo?

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9
Q

cell mediators: role and examples

A

chemicals released by damaged cells that have a role in stimulating the inflammatory response

  • histamine
  • prostoglandins
  • leukotrienes
  • kinins
  • complement
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10
Q

what happens: CHRONIC INFLAMMATION

A

STEP 5

  • macrophages (monocytes and lymphocytes) arrive –> DEFINING FEATURE
  • proliferation of blood vessels and connective tissue
  • less uniform histologically than acute
  • long term presence of lymphocytes and monocytes may indicated long-standing infection
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11
Q

what happens: GRANULATION TISSUE

A

STEP 6

  • fibroblasts and endothelial cells arrive and healing begins
  • scar tissue begins to form
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12
Q

initiation: GRANULATION TISSUE

A
  • 1 day post implant

- by action of monocytes and macrophages

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13
Q

key features: GRANULATION TISSUE

A
  • proliferation of small blood vessels –> neo-vasculatisation. angiogenesis –> proliferation, maturation and organisation of endothelial cells into capillaries
  • proliferation of fibroblasts –> activley synthesise collagen and proteoglycans of CT
  • macrophages present but not dominant
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14
Q

purpose of INFLAMMATION

A
  • contain, neutralise, dilute or wall (ward) off injurious agent or process, setting off regenerative process
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15
Q

what happens: FOREIGN BODY REACTION

A

STEP 7
macrophages form giant cells
- multinuclear macrophages
- components of granulation tissue

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16
Q

examples: FOREIGN BODY RESPONSE

A
  • silicon breast implant –> FBR 1-2 macrophage cells in thickness
  • dacron vascular implant –> FBR individual macrophages and FBGC’s
17
Q

what happens: FIBROSIS

A

fibrotic capsule development

  • immune system cannot kill or remove implant it incapsulates it
  • fibroblasts creating CT capsule to isolate implant
  • esp. for non-porous implants
  • applies to biocompatible and bioinert materials
18
Q

exceptions: FIBROSIS

A
  • porous biocompatible/ bioactive –> infuse with CT
  • nonporous bioactive –> interfaces with normal CT
  • biodegradable –> metabolised away
  • toxic –> prolonged complications and cell death
19
Q

minimising: FIBROSIS

A
  • more biocompatibl/ bioinert
  • less movement
  • leaching toxins = thicker capsule
  • bioactive coatings (HA) = eliminated capsule