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壓瘡
林明憲醫師臺北榮總高齡醫學中心國立陽明大學醫學系
105.08.07.
DefinitionDefinition Any lesion caused by unrelieved pressure
resulting in damage of underlying tissue Areas of local tissue trauma, usually
developing where soft tissues are compressedbetween bony prominences and any external surface for prolonged time periods
A sign of local tissue necrosis Most commonly found over bony
prominences subjected to external pressure Most common locations: sacrum, ischial
tuberosities, trochanters and heels— sacrum and heels most frequent
Synonymous terms — Pressure ulcer— Decubitus ulcer— Bedsore
EpidemiologyEpidemiology Prevalence Hospitalized elderly: 15% Patients expected to be bedridden or chair
bound > 1 week, ≥ stage II pressure ulcers: 28%
Prevalence varies by setting— Nursing home = 2.3% to 28%— Home care = 6% to 9%— Outpatient clinic = 1.6%
EpidemiologyEpidemiology
Incidence Incidence during hospitalization: 8~30% Timing: first 2 weeks of hospitalization
— The first 5 days in critical care unit
Highest incidence rate: orthopedic population (9-19%); quadriplegic (33-60%)
Morbidities associated with pressure ulcersMorbidities associated with pressure ulcers
Pain Disfigurement Septicemia Prolonged hospitalization Increased death rates quality issues
Morbidities associated with pressure ulcers-Pain
Morbidities associated with pressure ulcers-Pain
Pain—87% at dressing changes—84% at rest—42% both—18%: pain when CD, the highest level—Only 6% of them received analgesics—Stage III~IV > stage II pain? (some evidence)
Morbidities associated with pressure ulcers-Septicemia (I)
Morbidities associated with pressure ulcers-Septicemia (I)
Most severe complication Incidence 1.7/10,000 Overall mortality 48%: if pressure ulcer is the
source Transient bacteremia after debridement: 50% Infectious complication
—Wound infection—Cellulitis—Osteomyelitis
Morbidities associated with pressure ulcers-Septicemia (II)
Morbidities associated with pressure ulcers-Septicemia (II)
Among patients with nonhealing or worsening pressure ulcers—26% have underlying bone pathology, osteomyelitis—88% are colonized Pseudomonas aeruginosa—34% with Providencia species—Either pathogen should not be considered typical
colonization—Can be reservoirs for antibiotic-resistant bacteria
Morbidities associated with pressure ulcers-Death rateMorbidities associated with pressure ulcers-Death rate
Death rate among bed- or chair-bound patients—60% (PU+) vs 38% (PU-) 1 year after discharge
Nursing home resident whose pressure ulcers healed within 6 months or not—Mortality: 11%(PU healed) vs. 64%(PU not healed)
Mortality rate : 3.8 per 100,000 population—Marker for coexisting morbidity
Morbidities associated with pressure ulcers- Quality issue
Morbidities associated with pressure ulcers- Quality issue
Pressure ulcer incidence and severity are used as markers of quality care —long-term care facilities—home care agencies—acute care hospitals
Evaluate:—Each patient upon admission—Regularly thereafter for high risk group
PathophysiologyPathophysiology
Pressure ulcers are the result of mechanical injury to the skin and underlying tissues.
4 factors— Pressure— Shearing force— Friction— Moisture
PathophysiologyPathophysiology
PressurePressure
Perpendicular force or load exerted on a specific area, causing ishcemia and hypoxia of the tissues
Muscle and subcutaneous tissues are more sensitive than epidermis
High pressure area:— Supine: occiput, sacrum, heels— Sitting: ischial tuberosities— Sidelying: Trochanters
Pressure need to impair tissue perfusionPressure need to impair tissue perfusion
Closing pressures — Arteriole - 32 mm Hg — Venule - 15 mm Hg — Capillary pressure - 25 mm Hg
> 32 mmHg pressure would cause tissue ischemia
PressurePressure
Pressure under bony prominence, ex: — Buttock in lying position: 70mmHg— Sacrum and greater trochanter: 100-150mmHg— In seated persons, ischial tuberosities: 300mmHg
Factors lower the threshold— Repeated exposures to pressure— Loss of subcutaneous tissue
Shearing forcesShearing forces
Lower the amount of pressure required to cause damage to epidermis
Decrease the amount of pressure required to occlude blood vessels
Tangential forces, ex: sliding Important in development of deep tissue injury
Friction and MoistureFriction and Moisture
Friction— Cause intraepidermal blisters— Superficial erosions
Moisture— Directly lead to maceration and epidermal injury— Impact on friction forces
AssessmentAssessment
Risk assessment Assessment of pressure ulcer stage Assessment of pressure ulcer healing
Risk Assessment- FactorsRisk Assessment- Factors Immobility or severely restricted mobility being the
most important risk factors—>50 vs urine incontinence) Malnutrition Impaired mental status Altered sensation or response to pain and discomfort Increased body temperature Decreased blood pressure Advanced age
Risk Assessment - IntervalRisk Assessment - Interval
Acute care hospital: —Every 48Hrs
Home health setting: —Weekly for 4 weeks, followed by every other week
Nursing home resident: —Weekly for 4 weeks, followed by quarterly assessment
Risk Assessment – Tool (I)Risk Assessment – Tool (I)
Norton scale—Oldest, developed in 1961, in England—5 subscales: physical condition, mental state, activity,
mobility, incontinence, —Each scale 1-4, total score 5-20—≤16/20: onset of risk —≤12/20: high risk
Risk Assessment – Tool (II)Risk Assessment – Tool (II)
Braden scale— Developed in 1987, in USA— 6 subscale: sensory perception, moisture, activity,
mobility, nutrition, friction and shear— Each scale 1-4, except friction and shear 1-3— Total score 6-23— ≤16/23: at risk — 15-16/23: mild risk, 50~60% risk for stage I PU— 12-14/23: moderate risk, 65-90% risk for stage I or II PU —
1分 2分 3分 4分 分數感覺知覺程度(sensory
perception )完全昏迷對疼痛沒有反應
昏迷但對疼痛有反應
清醒但部分感官受損
清醒正常
潮濕程度(moisture ) 皮膚持續潮濕
皮膚經常潮濕,更換中單/床單每天≦3次
皮膚偶爾潮濕,更換中單/床單
每天1次乾燥、乾淨
活動力(activity) 臥床不動 受限於輪椅
可偶爾下床行走
可經常下床行走
移動力(mobility)
完全無法自行翻身
大部分需他人協助翻身
少部分需他人協助翻身
可自行翻身
營養狀態(nutrition)
禁食或進食清流質5天以上
攝取熱量每天小於1200卡
維持管灌可滿足大部分需求
正常飲食滿足需求量
摩擦力/剪力(friction/shear) 有此問題 有潛在的問題 沒有明顯問題
總分 /23
註:分數≧16分(低危險):每日皮膚評估一次。分數12~15分(中等危險):皮膚評估+每2小時翻身拍背一次。分數≦11分(高危險): 皮膚評估+每2小時翻身拍背一次+氣墊床使用。
Braden壓瘡危險因子評估表
壓瘡風險評估工具之臨床效度壓瘡風險評估工具之臨床效度
評估工具\
臨床效度
Braden量表
Norton量表
Gosnell量表
Waterlow量表
敏感度 88.0% 86.1% 46.3% 99.5%
特異性 75.1% 75.0% 90.9% 31.7%
橫斷式之調查法,在台灣地區北部、中部、南部及東部,各依人口分佈分層抽樣選取2,631住院病人為收案對象。
于博芮、李世代、林壽惠:台灣醫療院所壓瘡風險評估工具之臨床效度。台灣老年醫學雜誌 2005;1:79-88。
Assessment of Pressure Ulcer StageAssessment of Pressure Ulcer Stage
Grading or staging system based on observable depth of tissue destruction
Initial assessment: deepest layer of tissue involved
Mostly common used : —National Pressure Ulcer Advisory Panel’s (NPUAP)
classification system—(美國國家壓瘡諮詢委員會)
StagingStaging NPUAP (National Pressure Ulcer Advisory Panel) 2007 Stage I: Nonblanchable erythema
— Intact skin, usually over a bony prominence
Stage II: Partial thickness skin loss— Invulving epidermis and/or dermis
Stage III: Full thickness skin loss— Extend into subcutaneous tissues to deep fascia, but bone,
tendon, or muscle not exposed
Stage IV: Full thickness tissure loss— Exposed bone, tendon, or muscle
StagingStaging
Unstagable/Unclassified: Full thickness skin or tissue loss– depth unknown— Full-thickness injury— Actual depth obscured by slough and/or eschar— Cannot be staged until removed
Suspected Deep Tissue Injury– depth unknown— Purple or maroon localized area of discolored intact
skin or blood-filled blister — due to damage of underlying soft tissue from pressure
and/or shear
Assessment of Pressure Ulcer HealingAssessment of Pressure Ulcer Healing At a minimum:
—Location —Depth and Stage—Size —Wound bed description: necrotic tissue, exudate, wound edges for undermining and tunneling, presence or absence of granulation and epithelialization
Follow-up assessment: at least weekly Two research-based pressure ulcer assessment tools
—Bates-Jensen Wound Assessment Tool [BWAT]—NPUAP’s Pressure Ulcer Scale for Healingtool (PUSH)
Reduction in ulcer size over 1-2 week period predict healing outcome
Should improvement within 2-4 weeks If no evidence of ulcer improvement
— Consider changes in management strategy
Improvement for stage III and IV slower than II— Stage II: 75% healing in 60 days— Stage III or IV: 17% healing in 60 days
ManagementManagement
Local treatment Surgery Drugs Nutrition
Local treatmentLocal treatment
Debridement of necrotic tissue Adequate wound cleaning Application of appropriate topical therapy
DebridementDebridement Wound debridement:
—Reduce necrotic tissue burden—Decrease infection risk—Promote granulation tissue formation—NOT indicated for dry eschar on the heel or when the
pressure ulcer on an ischemic limb—5 methods of debridement: clinician preference, avalibility
Surgical or sharp debridement for extensive necrosis or when obtaining a clean wound bed quickly is important
More conservative methods (autolytic and enzymatic) for those in long-term care or home care environments
Adequate wound debridement is essential to wound bed preparation and healing.
Surgical debridementSurgical debridement
use of a scalpel, scissors, or other sharp instruments to remove nonviable tissue.
most rapid form of debridement indicated over other methods
—for removing thick, adherent, and/or large amounts of nonviable tissue
—when advancing cellulitis or signs of sepsis
Mechanical debridementMechanical debridement
Use of wet-to-dry dressings, whirlpool, lavage, or wound irrigation.
Wet-to-dry gauze dressings continue to be used for debridement
Disadvantages: —increased time/labor for application/removal of the dressings, —removing viable tissue as well as nonviable tissue —pain
Used cautiously, can traumatize new granulation tissue and epithelial tissue
Adequate analgesia should be administered
Enzymatic debridementEnzymatic debridement
Applying a concentrated, commercially preparedenzyme to the surface of the necrotic tissue
aggressively degrade necrosis by digesting devitalized tissue
3 commercially enzymes in USA: collagenase, papain-urea, and papain-urea with chorophyllin
Some of the effects attributed to autolysis Debridement faster than with autolysis More conservative than sharp debridement
Autolytic debridementAutolytic debridement Using the body’s own mechanisms to remove nonviable
tissue. Maintaining a moist wound environment allows
collection of fluid at the wound site, which allows enzymes within the wound fluid to digest necrotic tissue.
Adequate wound cleansing to wash out the partially degraded nonviable tissue.
More effective than wet-to-dry gauze dressings, —selectively removes only necrotic tissue —protects healthy tissues
May be slower to achieve a clean ulcer bed than other methods.
BiosurgeryBiosurgery
The application of maggots (disinfected fly larvae, Phaenicia sericata) to the wound
Typically at a density of 5 to 8 per cm2
May not be acceptable to all patients May not be available in all areas
Adequate wound cleaningAdequate wound cleaning General rule Pressure ulcer cleaning at changing dressing If an ulcer contains necrotic debris or is
infected, then antimicrobial activity is more important.
For wounds with large amounts of debris, more vigorous mechanical force and stronger solutions may be used
For clean wounds, less force and physiologic solutions such as normal saline should be used.
Should not use on clean pressure ulcers :— Povidone-iodine— Iodophor (易多碘)— Sodium hypochlorite (次氯酸鈉)— Hydrogen peroxide (H2O2)— Acetic acid
Toxic to fibroblast and impair wound healing
Topical therapyTopical therapy
Using moist wound healing dressings Moist wound healing allows wounds to re-
epithelialize up to 40% faster than wounds left open to air
These dressings are changed every 3 to 5 days, which allows wound fluid to gather underneath the dressing, facilitating epithelial migration
敷料種類敷料種類類別 舉例
Gauze dressing (紗布) 紗布Transparent films dressing (透明薄膜) Opisite, TegadermHydrogel (親水凝膠) DuoDerm gelHydrocolloid dressing (親水膠體敷料) DuoDermAlginate dressing (藻酸鹽敷料) Kaltostat, SeasorbHydrofiber dressing (親水纖維敷料) Aquacel, Aquacel AgFoams dressing (海綿型敷料) PU泡棉, PVA泡棉Composites dressing (複合性敷料)
Surgery Surgery
Primary closure A variety of approaches to skin graft and
myocutaneous flap Removal of underlying bony prominence Large infected pressure ulcers: more aggressive
procedures ex amputation sometimes required
Drugs - AntibioticDrugs - Antibiotic Antibiotics
—Antibiotics may be systemic or local Systemic antibiotics:
—S/S of systemic infection, sepsis or cellulitis with fever and elevated WBC
—Osteomyelitis—Prevention of bacterial endocarditis in patients
with valvular heart disease—Who require debridement of pressure ulcer
Broad-spectrum coverage—GNB, GPC, anaerobes
Drugs - AntibioticDrugs - Antibiotic Appropriate choices for antibiotic therapy
— Unasyn— Imipenem— Meropenem— Timentin— Tazocin— Combination of clindamycin or metronidazole with
ciprofloxacin, levofloxacin, or aminoglycosides— Vancomycin for MRSA
Drugs - AntibioticDrugs - Antibiotic
The most effective strategy for preventing infection and dealing with existing infection is adequate debridement of necrotic tissue
In patients with S/S of systemic infection and sepsis, the appropriate debridement method is surgical debridement.
Drugs - AntibioticDrugs - Antibiotic
Topical antibiotics (silver sulfadiazine):— For stage III or IV ulcers with evidence of local infection— For clean pressure ulcer not healing after 2-4 weeks of
optimal management
Prolonged silver release topical dressings: effective in MRSA colonization
Drugs - PainDrugs - Pain
Limited evidence to guide clinician Pressure ulcer alone: may not require routine pain
medication Medication prior to procedures is essential Opioids and/or NSAIDs 30 minutes prior to the
procedure Topical anesthetics or topical opioids
NutritionNutrition Difficult to define a causal relationship between
malnutrition and pressure ulcer development Some evidence: nutritional support to persons at
risk for pressure ulcers with relative reduction in pressure ulcer incidence of 25%
Some evidence: high-protein nutritional supplements (24-25% protein) improves pressure ulcer healing
30 to 35 kcal/kg/d 1.25 to 1.5 g/kg/d of protein
NutritionNutrition
Nutritional supplementation by tube-feeding to persons with pressure ulcers: not positive results
No evidence exists for use of supplemental vitaminsor minerals (e.g., vitamin A, E, C, zinc) in persons with pressure ulcers, except for deficiency
Persons with pressure ulcer or at risk + malnutrition: Nutritional assessment, nutrition support as indicated
Glutamine, Arginine, HMB
PreventionPrevention Scheduled turning and repositioning programs Pressure reduce/relieve support surfaces General skin care Nutritional support
Scheduled turning and repositioning programsScheduled turning and repositioning programs Patient at risk, unable to move independently Time interval: every 2 Hrs Avoid pressure on bony prominence, esp malleolus,
trochanter: 30-degree side-lying instead of 90-degree side lying
Maintain head of bed at lowest degree of elevation: decrease sacral area exposure to shearing force
Techniques: Turning sheets, draw sheets, pillows
Pressure reduce/relieve support surfaces Pressure reduce/relieve support surfaces
Static— Foam, gel, static air, water, combination— Less expensive
Dynamic— Alternating air(間歇式氣墊), low-air-loss(低壓氣浮
床墊), or air-fluidized(矽砂床)— Use if the status surface is compressed to < 1 inch or
high-risk patient has reactive hyperemia on a bony prominence despite use of static support
— Adverse effects: dehydration, sensory deprivation, loss of muscle strength, difficulty with mobilization
Pressure reduce/relieve support surfacesPressure reduce/relieve support surfaces
May reduce frequency of repositioning required in some paitents
Relative reduction in incidence of 60%
General skin careGeneral skin care Skin inspection
— Daily, esp attention to bony prominence— Reddened areas should not be massaged
Incontinence assessment and management Skin hygiene intervention
ReferenceReference
Hazzard’s Geriatric Medicine and Gerontology, 6th ed. New York: Mc Graw Hill, 2009:703-715
Textbook of Geriatric Medicine International, Souel: Argos, 2010:411-418
NPUAP (National Pressure Ulcer Advisory Panel): http://www.npuap.org/