Methods Study Inclusion Criteria: Sedated patient on the ICU > 5 days May or may not be intubated Braden score of < 16 Patients not eligible for Prevalon™ boot included in the study as control subjects with pillows used to elevate the heels. Passive ROM as ordered on all ICU patients was not withheld or viewed as a variable in the prevention of plantar flexion contractures. Procedure: 1. Skin assessment and Braden scale administered to all patients upon admission to the ICU. 2. All ICU patients meeting criteria had an initial measurement of ankle ROM done with a goniometer upon admission and prior to application of the Prevalon™ boot. Braden scale, heel skin assessment, and Ramsey sedation scale were also documented. 3. All applicable patients then had ankle ROM measured every other day. 4. Heel assessments, Braden scale, and Ramsey sedation scale were done every shift, and recorded as part of the study every other day. 5. Measurements continued until patient was either transferred, boots were discontinued by physician, or patient had a Braden scale of greater than 16. 6. Control patients also had ankle measurements, heel skin assessment, Ramsey sedation scale, and Braden scale done at admission and every other day. 7. Identified and trained ICU nurses and physical therapists performed the measurements. S S u u c c c c e e s s s s f f u u l l P P r r e e v v e e n n t t i i o o n n o o f f H H e e e e l l U U l l c c e e r r s s a a n n d d F F o o o o t t D D r r o o p p i i n n t t h h e e H H i i g g h h R R i i s s k k V V e e n n t t i i l l a a t t i i o o n n P P a a t t i i e e n n t t P P o o p p u u l l a a t t i i o o n n Tina Meyers, BSN, RN, CWOCN, ACHRN, Rejeana Pezel, ICU/CCU, Jill Bennett, RN, MSN, ICU/CCU, Vanessa Carroll, RN, ICU/CCU, Ann Russell, RN, BSN, ICU/CCU, Sharon Lagway, RN, ICU/CCU, Salvacion Ramos, RN, ICU/CCU, Eloisa Asilo, RN, ICU/CCU, Marci Green, RN, ICU/CCU nurse Conroe Regional Medical Center , Conroe TX Poster presented at the 19th Annual National Forum on Quality Improvement in Health Care : December 9-12, 2007 21040
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Successful Prevention of Heel Ulcers and Foot Drop in the ...
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Methods
Study Inclusion Criteria: � Sedated patient on the ICU >5 days
� May or may not be intubated
� Braden score of <16
� Patients not eligible for Prevalon™ boot included in the study as control subjects with pillows used to elevate the heels.
� Passive ROM as ordered on all ICU patients was not withheld or viewed as a variable in the prevention of plantar flexion contractures.
Procedure:
1. Skin assessment and Braden scale administered to all patients upon admission to the ICU.
2. All ICU patients meeting criteria had an initial measurement of ankle ROM done with a goniometer upon admission and prior to application of the Prevalon™ boot. Braden scale, heel skin assessment, and Ramsey sedation scale were also documented.
3. All applicable patients then had ankle ROM measured every other day.
4. Heel assessments, Braden scale, and Ramsey sedation scale were done every shift, and recorded as part of the study every other day.
5. Measurements continued until patient was either transferred, boots were discontinued by physician, or patient had a Braden scale of greater than 16.
6. Control patients also had ankle measurements, heel skin assessment, Ramsey sedation scale, and Braden scale done at admission and every other day.
7. Identified and trained ICU nurses and physical therapists performed the measurements.
Accepts mechanical ventilation. 3. Responds to commands only4. Brisk response to light glabellar tap or loud noise. 5. Sluggish response to light glabellar tap or loud noise. 6. No Response.
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Data Collection Tool for Conroe Hospital Prevalon II Plantar Flexion Prevention