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Serous Drainage
Primarily clear, serous portion of blood, watery
Sanguineous Drainage
Large number of red blood cells (bright is fresh, dark is old)
Serosanguineous Drainage
MIxture of serum and RBCs, light pink to blood tinged
Purulent Drainage
WBC, liquified dead tissue debris. Thick musty or foul smelling, yellow/green
Drains
Can be used to promote would healing of dismissal of fluids by preventing fluid accumulation (stagnant fluid causes infection), negative pressure systems promote tissue approximation, reduces swelling and pain
Cellulitis
Bacterial skin infection that affects the deep dermis and subcutaneous and inflames it. Cytokines and neutrophils go to affected area and cause erythema (redness), warmth, edema, and tenderness. This can lead to bacteremia, endocarditis, and osteomyelitis
Cellulitis Risk Factors
Anything that can cause breakdown in skin like injuries, iv site punctures, surgical incision, insects, fissures, or comorbidities
Clinical Manifestations of Cellulitis
Spreading of erythematous inflammation of the deep dermis and subcutaneous. Worsening erthema, edema, warmth and tenderness, unilateral.
Cellulitis Diagnostics
Blood work via CBC, ESR, CRP, would culture, Imaging
Cellulitis Medical Management
Antibiotics via PO for mild or IV for severe
Cellulitis Nursing Assessment
Look for warmth, erythema, edema, tenderness, look for the source of it, assess between toes and swollen lymph nodes (lymphadenopathy)
Diabetic foot ulcer
Common complication of patients who do not control their diabetes well. Cause of osteomyelitis and amputation
Pathophysiology of Diabetic Foot Ulcer
Development of callus resulting for neuropathy (sensation loss and pins and needles). Can also develop severe atherosclerosis of the small blood vessels in the legs and feet. Because of vascular compromise delayed wound care
Clinical Manifestations of Diabetic Foot Ulcers
Most common in weight bearing areas. Indicates for neuropathy (parasthesia, hypo or hyperesthesia (sensation), or anhidrosis (sweating)). Vascular insufficiency like loss of hair, shiny skin, atrophy from poor perfusion. Signs of infection
Diabetic Foot Ulcer DIagnostics
Blood work like CMP, CBC, A1c, etc.
Cultures
X ray to show osteomyelitis, air, or signs of fractures
Arterial dopplers can rule out PAD
Diabetic Foot Ulcer Management
Wound care, off loading, debridement, infection treatment, revascularization, amputation, hyperbaric oxygen therapy
Diabetic Foot Ulcer Assessment
Assess feet and lower extremities for sensation, parasthesia, anhidrosis, loss of hair, shiny skin, atrophy, purulence, erythema. Also history like fever, chills, pain, smoking, vitals, diet and exercise
Healthcare Associated Pressure Ulcer (HAPI)
Localized damage to the skin and underlying tissue that usually occurs over a bony prominence or related to the use of device and develops under care.
HAPI Basics
Sustained compression obliterates arterial and capillary perfusion to the ski, ischemic damage to underlying tissue. Reperfusion can cause injury as oxidizing agents can spark inflammatory response. Can result to necrosis
Friction
When two surfaces rub against each other and is like abrasion. Example is wrinkled sheets, pulled over sheets
Shear
When one layer of tissue slides over another layer. This will separate skin from underlying tissue
HAPI Risk Factors
Incontinence, aging skin, immobility, malnutrition, lower LOC
Stage 1 Pressure Injury
Erythema of the skin that does not blanch
Stage 2 Pressure Injury
Erythema with the loss of partial thickness of the skin that will blister
Stage 3 Pressure Injury
Full thickness ulcer that might involve the subcutaneous fat
Stage 4 Pressure Injury
Full thickness ulcer with the involvement of the muscle or bone
Braden Scale
HAPI Screening Tool that allows to identify high risk patients. Risk factors are sensory perception, moisture, activity, mobility, nutrition, and friction and shear
HAPI Diagnostics
CBC used to see if infection is setting in. Wound culture, BMP to see albumin (indicator of nutrition)
Purosanguineous
Mixed drainage of pus and blood (newly infected wound)
Hydrocolloid
Occlusive dressing that swells in the presence of exudate composed of gelatin and pectin, it forms a seal at the wound’s surface to prevent evaporation of moisture from the skin. Used to treat HAPIs
Hydrogel
Composition is mostly water. Gels after contact with exudate, promoting autolytic debridement and cooling. Rehydrates and fills dead space, used to treat HAPIs
Alginates
Nonadherent dressings that conform to the wound’s shape and absorb exudate, treats HAPIs
Collagen
Powders, pastes, granules, sheets, gels, and pastes, treats HAPIs
Vacuum Assisted Closure System
Use of foam strips laid into the wound bed with an occlusive sealed drape applied and suction tubing placed for negative pressure (suction) to occur once the tubing is connected to the systems therapy unit, used to treat HAPIs
Fistula Formation
Can occur from incision complications, abnormal passage from internal organ or vessel to outside of body or from one internal organ or vessel to another. Usually the result of infection that has developed into an abscess
Dehiscence
Partial or total separation of wound layers or as a result of excessive stress on wounds that are not healed, complication of incision
Evisceration
Most serious complication of dehiscence. Abdominal would completely separates and there is a protrusion of viscera through incision area