Tissue fluid formation & Edema
Dr Anu Priya J
Introduction
• Tissue fluid / Interstitial fluid is the fluid which
occupies the intercellular spaces.
• A medium for the exchange of substances
such as nutrients, O2, CO2, metabolic wastes,
etc., between the cells and blood.
Role of capillaries
• Fluid exchange between intravascular and
interstitial compartments occurs only at the
level of capillaries. The other parts of the
vascular system are impermeable.
• The capillaries are permeable because they
are lined by a single layer of flattened
endothelium.
Formation of tissue fluid
• Tissue fluid is derived from two sources:
1. From blood capillaries
2. From metabolism in tissues
Formation of tissue fluid
• Factors affecting the formation of tissue fluid:
a. Permeability of capillaries
b. Diffusion
c. Filtration and reabsorption
d. Metabolic activity of tissues
Filtration & Reabsorption
• Most important mechanism by which tissue fluid
is formed.
• Fluid is filtered out at the arterial end of the
capillary & is reabsorbed at its venous end.
• Starling’s forces regulate the movement of fluid
into and out of the capillaries.
Formation of tissue fluid
Drainage of tissue fluid
• 85% reabsorbed in the venular end of capillary
• 15% drained via lymph
Starling’s forces
• Hydrostatic pressure in capillary (Pc)
• Hydrostatic pressure in interstitium (Pi)
• Colloidal osmotic pressure/ Oncotic pressure
in capillary (πc)
• Colloidal osmotic pressure/ Oncotic pressure
in interstitium(πi)
Formation of tissue fluid
Formation of tissue fluid
Starling’s forces
• Filtrative force = Hydrostatic pressure gradient
(Pc – Pi)
• Absorptive force = Oncotic pressure gradient
(πc-πi)
Formation of tissue fluid
Starling’s forces
• Nf = Kf [(Pc – Pi) - (πc-πi)
• Kf = Permeability x Surface area
• Nf - Net filtration force
• Kf - Permeability coefficient
Formation of tissue fluid
Formation of tissue fluid
Pc 37 mmHg Pc 17 mmHgπc 25 mmHg
πi 0 mmHgPi 1 mmHg
Hydrostatic pressure Hydrostatic pressure
Arteriolar end
of capillary
Venular end
of capillary
Arteriolar end:
• Net filtration force = +11mmHg
• Hydrostatic pressure gradient > Oncotic pressure gradient
• Filtration of fluid
Venular end:
• Net filtration force = (-9mmHg)
• Hydrostatic pressure gradient < Oncotic pressure gradient
• Absorption of fluid
Formation of tissue fluid
Edema
• Accumulation of abnormally large amount of
fluid in the interstitial spaces
Pathophysiology of edema
i. Increased filtration of fluid
ii. Inadequate drainage of fluid
Etiology / Causes
Based on etiology:
• Cardiac edema
• Renal edema
• Inflammatory edema
• Noninflammatory-Giant/angioneurotic edema
• Heat edema
• Lymphedema
• Edema due to malnutrition
• Edema due to liver disease
• Edema due to venous obstruction
Types of edema
• Based on location
• Based on response to pressure
Types of edema
Based on location
• Localised edema
• Generalised edema
Types of edema
Based on response to pressure
Pitting edema
• pit/intendation seen after 30s pressure – due to
displacement of fluid from the area of pressure
• Inflammation, Congestive cardiac failure(CCF),
Renal diseases etc.,
Nonpitting edema
• Conditions where the swelling is not chiefly due to fluid
collection
• Myxedema, Lymphedema in filariasis, etc.,
Edema in liver disease
• Hypoproteinemia due to decreased synthesis
of proteins - decreased oncotic pressure in
the capillaries – reabsorptive force lesser than
the filtration force – accumulation of fluid in
the interstitial spaces - edema
Edema in renal failure
• Hypoproteinemia due to proteinuria
–decreased oncotic pressure in the capillaries
– reabsorptive force lesser than the filtration
force– accumulation of fluid in the interstitial
spaces - edema
Thank you
Tissue fluid formation & Edema slideshare

Tissue fluid formation & Edema slideshare

  • 1.
    Tissue fluid formation& Edema Dr Anu Priya J
  • 2.
    Introduction • Tissue fluid/ Interstitial fluid is the fluid which occupies the intercellular spaces. • A medium for the exchange of substances such as nutrients, O2, CO2, metabolic wastes, etc., between the cells and blood.
  • 3.
    Role of capillaries •Fluid exchange between intravascular and interstitial compartments occurs only at the level of capillaries. The other parts of the vascular system are impermeable. • The capillaries are permeable because they are lined by a single layer of flattened endothelium.
  • 4.
    Formation of tissuefluid • Tissue fluid is derived from two sources: 1. From blood capillaries 2. From metabolism in tissues
  • 5.
    Formation of tissuefluid • Factors affecting the formation of tissue fluid: a. Permeability of capillaries b. Diffusion c. Filtration and reabsorption d. Metabolic activity of tissues
  • 6.
    Filtration & Reabsorption •Most important mechanism by which tissue fluid is formed. • Fluid is filtered out at the arterial end of the capillary & is reabsorbed at its venous end. • Starling’s forces regulate the movement of fluid into and out of the capillaries. Formation of tissue fluid
  • 7.
    Drainage of tissuefluid • 85% reabsorbed in the venular end of capillary • 15% drained via lymph
  • 8.
    Starling’s forces • Hydrostaticpressure in capillary (Pc) • Hydrostatic pressure in interstitium (Pi) • Colloidal osmotic pressure/ Oncotic pressure in capillary (πc) • Colloidal osmotic pressure/ Oncotic pressure in interstitium(πi) Formation of tissue fluid
  • 9.
  • 10.
    Starling’s forces • Filtrativeforce = Hydrostatic pressure gradient (Pc – Pi) • Absorptive force = Oncotic pressure gradient (πc-πi) Formation of tissue fluid
  • 11.
    Starling’s forces • Nf= Kf [(Pc – Pi) - (πc-πi) • Kf = Permeability x Surface area • Nf - Net filtration force • Kf - Permeability coefficient Formation of tissue fluid
  • 12.
    Formation of tissuefluid Pc 37 mmHg Pc 17 mmHgπc 25 mmHg πi 0 mmHgPi 1 mmHg Hydrostatic pressure Hydrostatic pressure Arteriolar end of capillary Venular end of capillary
  • 13.
    Arteriolar end: • Netfiltration force = +11mmHg • Hydrostatic pressure gradient > Oncotic pressure gradient • Filtration of fluid Venular end: • Net filtration force = (-9mmHg) • Hydrostatic pressure gradient < Oncotic pressure gradient • Absorption of fluid Formation of tissue fluid
  • 14.
    Edema • Accumulation ofabnormally large amount of fluid in the interstitial spaces Pathophysiology of edema i. Increased filtration of fluid ii. Inadequate drainage of fluid
  • 15.
    Etiology / Causes Basedon etiology: • Cardiac edema • Renal edema • Inflammatory edema • Noninflammatory-Giant/angioneurotic edema • Heat edema • Lymphedema • Edema due to malnutrition • Edema due to liver disease • Edema due to venous obstruction
  • 16.
    Types of edema •Based on location • Based on response to pressure
  • 17.
    Types of edema Basedon location • Localised edema • Generalised edema
  • 18.
    Types of edema Basedon response to pressure Pitting edema • pit/intendation seen after 30s pressure – due to displacement of fluid from the area of pressure • Inflammation, Congestive cardiac failure(CCF), Renal diseases etc., Nonpitting edema • Conditions where the swelling is not chiefly due to fluid collection • Myxedema, Lymphedema in filariasis, etc.,
  • 19.
    Edema in liverdisease • Hypoproteinemia due to decreased synthesis of proteins - decreased oncotic pressure in the capillaries – reabsorptive force lesser than the filtration force – accumulation of fluid in the interstitial spaces - edema
  • 20.
    Edema in renalfailure • Hypoproteinemia due to proteinuria –decreased oncotic pressure in the capillaries – reabsorptive force lesser than the filtration force– accumulation of fluid in the interstitial spaces - edema
  • 21.

Editor's Notes

  • #4 There is constant exchange of fluid between the different fluid compartments of the body. But, fluid exchange between intravascular and interstitial compartments occurs only at the level of capillaries.
  • #7 Mvt of fluid into n out of capil first desc by Ernest Henry Starling. Hence, forces that govern the mvt.. Starling’s forces.